
Arthritis is a term that is used for a diverse group of painful conditions affecting the joints and surrounding structures. Arthritis is among the leading conditions causing work limitations.1 Using the National Health Interview Survey (NHIS) for 2013-2015, the estimated number of adults with doctor-diagnosed arthritis (DDA), on average, was 54.4 million,2 and is projected to reach 78.4 million, or 26% of the adult population, by 2040.3 The estimated number of adults, on average, with arthritis-attributable activity limitation (AAAL) was 23.7 million,2 projected to reach 34.6 million, or 11.4% of all adults, in 2040.3 Estimating the prevalence and burden of the various disorders that comprise arthritis and other rheumatic conditions (AORC) is important to understanding the current and growing impact of these disorders on the health care and public health systems. Equally important is identifying the gaps in our understanding of these measures and targeting potential interventions.
Arthritis is a general term that specifies inflammation in a joint although the term is sometimes used more broadly to include conditions where evidence of inflammation may be limited. Arthritis is usually associated with symptoms of joint pain and can result in activity limitation. Therefore, the following pages will reflect arthritis and other related conditions in two approaches.
First, we use the categorization developed over the years by the National Arthritis Data Workgroup and the Arthritis Program at the Centers for Disease Control and Prevention (CDC). This approach to AORC, presented in Segment 1, focuses on nine of the most common forms of arthritis plus an all other category (click HERE [3] to view the AORC categorization) and is terminology familiar to the medical and research communities. For self-report survey data, a related definition of DDA is also used. This approach largely uses the self-reported DDA definition and the AORC definition, and frequently compares the estimates for the 10 AORC subtypes to overall AORC.
The second approach, presented in Segment 2, categorizes arthritis into terminology often used with patient populations to explain their joint pain or joint disease and provides a summary and additional depth on the most familiar arthritic conditions. Using the same base data tables, analysis in this approach focuses on arthritis disorders as a share of all healthcare disorders. Included at the end of this approach is a discussion of joint pain common to all arthritis disorders, and trends in joint replacement.
An overview of the main topics within each segment is shown below. To jump to the two segments, click on the title below.
Segment 1: Arthritis and Other Rheumatic Conditions (AORC) [4]
1 Prevalence of Arthritic Conditions
2 Healthcare Utilization
3 Burden of AORC
4 Economic Burden of AORC
5 Impact of Aging
6 Key Challenges to Future
7 Unmet Needs
8 AORC ICD-9-CM Diagnosis Codes
Segment 2: Joint Disease: Arthritis in Patient Populations [5]
1 Osteoarthritis
2 Inflammatory Arthritis
A Rheumatoid Arthritis
B Spondylarthropathies
C Mixed Connective Tissue Disorders
3 Gout
4 Joint Infection
5 Fibromyalgia
6 Juvenile Arthritis
7 Joint Pain and Joint Replacement
8 Disparities
9 Key Challenges to Future
10 Unmet Needs
11 Estimated ICD-9-CM & ICD-10-CM Crosswalk Codes
Disclaimer: The findings and conclusions in this chapter are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.
Arthritis and other rheumatic conditions (AORC) comprise over 100 diseases. What most of them have in common is that they cause pain, aching, stiffness or swelling in or around a joint.
Definitions
Defining AORC to assess the burden in a population requires considering both what is important to measure and what data sources are available, such as population surveys and administrative data. Complicating any definition is the 100+ conditions that comprise what is generally thought of as “arthritis.” Furthermore, population measures need to be relatively simple and perhaps different from definitions used in clinical practice, where there is the luxury of having a medical history, physical examination, and laboratory and radiographic data. The Centers for Diseases Control and Prevention (CDC) Arthritis Program has worked with other organizations to develop case definitions, based on the best available expertise, that allow many measures of population burden to be addressed in a consistent way.1
For self-reported population surveys, doctor-diagnosed arthritis (DDA) is defined as a “yes” answer to the question “Have you EVER been told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia?” This measure aims to capture most of the major categories of arthritis and is considered valid for surveillance purposes of estimating population prevalence.2 For data sources using International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes, arthritis and other rheumatic conditions (AORC) has been defined by the National Arthritis Data Workgroup using those codes, and further divided into ten more specific subcategories defined in Arthritis and Joint Pain Codes. Both definitions were designed to exclude or minimize other major categories of musculoskeletal disease, such as osteoporosis and generic chronic back pain, even though some chronic back pain is due to arthritis. DDA is likely better for estimating what is happening in the population at large because arthritis may not be mentioned or recorded at healthcare system encounters that are typically more focused on other conditions (e.g., diabetes, heart disease). However, even with the latter limitation, AORC is likely better for estimating what is happening in the healthcare system.
A recent review of relevant data sources considers the strengths and limitations of each of the different case definitions. Using DDA criteria, four databases defined prevalence within 3 percentage points, while using ICD-9-CM criteria they had a 5 percentage point spread. This study highlights the difficulty of applying a single number for estimating prevalence of AORC and the need to consider the purpose, design, measurement methods, and statistical precision of the data source being used.3
While AORC occurs in children, it is difficult to acquire population data on them, so most of the estimates presented in this report are for adults unless otherwise noted.
In the general population, prevalence is better estimated by DDA than AORC. For the years 2013-2015, DDA affected an unadjusted average of 54.4 million adults, or 23 in 100 adults.1 Estimates show the typical distribution of higher prevalence among females and older adults, and lower prevalence among Hispanics and Asians. Absolute estimates show that most of these adults (59%, or 32.2 million) are of working age (younger than age 65).1 (Reference Table 3A.1.1 PDF [7] CSV [8])
Specific types of AORC
Clinical data are required to provide some measure of validity for estimating the prevalence of specific types of arthritis because many people are not sure what type of arthritis they have. Data from the National Arthritis Data Workgroup provided 2005 national prevalence estimates for some of the ten specific types of arthritis used in later tables.2,3 Respondents could have reported more than one type.
Osteoarthritis: Osteoarthritis (OA) is the most common type of arthritis, characterized by progressive damage to cartilage and other joint tissues. Joint injury is a risk factor for OA, but most cases occur without a specific history of injury. Obesity is a risk factor for knee OA, and to a lesser extent for hip and hand OA. Clinical OA was estimated to affect 26.9 million in 20053 and over 30 million for 2008-2011.4 The joints most affected with radiographic OA and symptomatic OA were hands, knees, and hips.3
Rheumatoid arthritis: Rheumatoid arthritis (RA) is the prototypical inflammatory arthritis. It is a chronic autoimmune disease that causes pain, aching, stiffness, and swelling in multiple joints, especially the hands, in a symmetrical fashion. In 2005, RA was estimated to affect 1.3 million adults.2
Gout and other crystal arthropathies: Gout is a recurrent inflammatory arthritis that occurs when excess uric acid collects in the body. Gout has been recognized for centuries and often affects the big toe. In 2005, an estimated 6.1 million adults reported having gout at some time, with 3.0 million affected in the past year.3 More recent studies of self-reported gout and hospitalizations show the prevalence of gout increasing in the last two decades.5,6
Joint pain/effusion/other unspecified joint disorders: Joint pain can result from several causes, including inflammation, degeneration, crystal deposition, infection, and trauma. Joint pain is often accompanied by swelling and effusion. A joint effusion is the presence of increased intra-articular fluid within the synovial compartment of a joint. Determining the cause of joint pain is primary to treatment.
Spondylarthropathies: Spondylarthropathies (or spondylarthritides) are a family of diseases that includes ankylosing spondylitis, reactive arthritis, psoriatic arthritis, enteropathic arthritis (associated with ulcerative colitis or Crohn’s disease), juvenile spondylarthritis, and undifferentiated spondylarthritis. In 2005, spondylarthropathies affected an estimated 639,000 to 2.4 million adults ages 25 and older.2
Fibromyalgia: Fibromyalgia (FM) is a syndrome of widespread pain and tenderness. The diagnosis is difficult to make, so relevant prevalence data are hard to come by. In 2005, FM was estimated to affect around 5 million adults.3 A more recent estimate by the National Fibromyalgia Association puts the estimate at 10 million people in the US, with 75%-90% of the affected adult women. However, due to the difficulty in diagnosing fibromyalgia and the potential for including other causes of pain, this estimate should be used with caution.7
Diffuse connective tissue diseases include the next four diseases.
Systemic lupus erythematosus: Systemic lupus erythematosus (SLE) is the prototypical autoimmune disease in which the body’s immune system can attack many body systems, especially the skin, kidneys, and joints. In 2005, definite and suspected SLE was conservatively estimated to affect 322,000.2 Population-based registries have provided more recent estimates for various racial/ethnic groups.8,9,10
Systemic Sclerosis: Systemic sclerosis (SSc), or scleroderma, is an autoimmune disease that primarily affects the skin, but can affect any organ system. In 2005, SSc affected an estimated 49,000 adults.2
Primary Sjögren’s Syndrome: Primary Sjögren’s Syndrome (SS) is a syndrome of dry eyes, dry mouth, and arthritis. Secondary SS can occur in association with other rheumatologic diseases such as rheumatoid arthritis and lupus. Prevalence data are very limited. In 2005, an estimated 0.4 to 3.1 million adults had SS.2
Polymyalgia rheumatica and giant cell (temporal) arteritis: Polymyalgia rheumatica (PMR) is a syndrome of sudden aching and stiffness in older adults that responds to treatment with anti-inflammatory medications (e.g., corticosteroids). Giant cell arteritis (GCA), which often occurs with PMR, is a type of vasculitis that affects medium-size arteries and results in headache, vision loss, and other symptoms. In 2005, PMR was estimated to affect 711,000 adults;3 a more recent analysis from the same data source found that the incidence of PMR had increased slightly with mortality not unlike the general population,11 suggesting that prevalence may have increased slightly as well. In 2005, GCA was estimated to affect 228,000 adults.4
Carpal tunnel syndrome: Carpal tunnel syndrome (CTS) occurs when the median nerve becomes compressed at the wrist and causes numbness, pain, or weakness in part of the hand. Thickened tendons and other rheumatic conditions are a common cause. General population prevalence has been reported between 1% and 5%.12
Soft tissue disorders (excluding back): These are a variety of problems of the tendons, bursa, muscle, ligaments, and fascia that cause pain and dysfunction. Prevalence of soft tissue disorders is difficult to determine due to the variety of conditions included.
Other specific rheumatic conditions: These are other conditions that the National Arthritis Data Workgrop considered to be rheumatic conditions.
Juvenile arthritis: Arthritis and other rheumatic conditions are relatively uncommon in children, although they can be particularly severe when they do occur. One estimate using significant pediatric arthritis and other rheumatologic conditions (SPARC) codes put the average annual prevalence at 103,000 children for the years 2001-2004 for the combined codes for rheumatoid arthritis and other inflammatory polyarthropathies, allergic purpura, arthropathy associated with infections, other and unspecified arthropathies, polyarteritis nodosa and allied conditions, and rarer inflammatory conditions.The prevalence for all SPARC codes, including synovitis and myalgia, was 294,000.13 A more in-depth discussion can be found in the Juvenile Arthritis (click HERE [11] to open new page) section later in this document.
AORC prevalence continues to increase in the aging US population, with related increases in healthcare utilization. The increase in total ambulatory care visits, together with the increasing number of joint replacements and related hospitalizations, both impact healthcare utilization. The AORC case definition is more appropriate to use within the healthcare system, which is based on health condition codes. However, the AORC case definition will miss adults with mild arthritis that is not mentioned at the visit, or for whom arthritis may not be a priority when multiple conditions are present. For estimates in the following discussions, AORC condition codes, found in ICD-9-CM Codes [13] section are used.
In 2013, AORC-related diagnoses were listed in 105.7 million healthcare visits and represented more than 10% of all healthcare visits. Hospitalizations accounted for 6% of AORC visits, while ambulatory care accounted for 94% (77% physician office, 6% outpatient, and 11% emergency department). (Reference Table 3A.3.0.1 PDF [14] CSV [15])
When looking at how the ten subtypes of AORC affect the four types of healthcare utilization below, remember that the estimates are not mutually exclusive due to the potential for multiple diagnoses in a single visit. (Reference Table 3A.3.0.2 PDF [18] CSV [19]; Table 3A3.0.3 PDF [20] CSV [21]; Table 3A.3.0.4 PDF [22] CSV [23]; and Table 3A.3.0.5 PDF [24] CSV [25])
Hospitalizations
The Healthcare Cost and Utility Project (HCUP) 2013 Nationwide Inpatient Sample (NIS) estimates that 6.4 million hospitalizations were associated with a diagnosis of AORC, or 21.4% of all hospitalizations that year. AORC was the presenting or first-listed diagnosis for only 1% of all hospitalizations, suggesting the role of AORC is more of an important comorbidity or contributor to other conditions which are the reason for the hospitalization. Nearly one-half of the 6.4 million AORC hospitalizations were associated with osteoarthritis (46%), while joint pain/effusion/other unspecified joint disorders, gout, and soft tissue disorders were each listed in more than 10% of hospitalizations. Multiple AORC diagnoses are coded in 17% of hospitalizations with an AORC diagnosis. Osteosteoarthritisrthritis is the least likely to have another AORC diagnosis, while carpal tunnel syndrome is most likely to include multiple diagnoses. (Reference Table 3A.3.0.1 PDF [14] CSV [15] and Table 3A.3.0.2 PDF [18] CSV [19])
AORC-associated hospitalizations by sex, race/ethnicity, and geographic region resembled those for all 2013 hospitalizations; however, they differed in age, skewing toward the 65 & older age group (59.1% vs. 41.7%). (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.1.0.3 PDF [30] CSV [31]; Table 3A.3.1.0.4 PDF [32] CSV [33])
Hospitalizations for specific types of AORC differed by demographic variables. Women comprised 59% of total AORC hospitalizations, but much more for hospitalizations with rheumatoid arthritis (75%), fibromyalgia (89%), and diffuse connective tissue disease (87%). Men comprised 41% of total AORC hospitalizations, but much more for hospitalizations with gout (67%) and soft tissue disorders (52%). (Reference Table 3A.3.1.0.1 PDF [26] CSV [27])
Those younger than age 65 comprised 41% of total AORC hospitalizations, but much more for hospitalizations with fibromyalgia (68%), diffuse connective tissues disease (67%), and carpal tunnel syndrome (61%). (Reference Table 3A.3.1.0.2 PDF [28] CSV [29])
Non-Hispanic blacks comprised 12% of total AORC hospitalizations, but much more for hospitalizations with gout (18%) and diffuse connective tissue disease (24%). (Reference Table 3A.3.1.0.3 PDF [30] CSV [31])
Hospitalizations for specific types of AORC did not differ much by geographic region. (Reference Table 3A.3.1.0.4 PDF [32] CSV [33])
The mean LOS for AORC-associated hospitalizations in 2013 was slightly greater than that for all hospitalizations (4.9 vs 4.7 days); differences by demographic groups were greater for AORC hospitalizations (than all hospitalizations) for women (4.8 vs 4.4 days), those 18 to 44 years (5.0 vs. 3.6 days), non-Hispanic blacks (5.6 vs 4.4 days), Hispanics (5.3 vs. 3.6 days), and those in the western geographic region (4.8 vs. 4.3 days). Among the 10 specific types of AORC the mean LOS was strikingly longer for those with soft tissue disorders and other specified rheumatic conditions both overall (6.5 and 6.5 vs. 4.9 days) and by every demographic subgroup. (Reference Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.1.2 PDF [40] CSV [41]; Table 3A.3.1.1.3 PDF [42] CSV [43]; Table 3A.3.1.1.4 PDF [44] CSV [45])
Hospital charges are based on individual record discharges. The fees included may vary from patient to patient, but generally include hospital room, supplies, medications, laboratory fees, and care staff, such as nurses. They generally do not include professional fees (doctors) and non-covered charges. Emergency charges incurred prior to admission to the hospital may be included in total charges. It is important to note that charges are not necessarily the actual amount paid by Medicare, insurers, or patients. However, they are the only medical expenditure cost available in the major databases based on ICD-9-CM diagnostic codes and provide an overall picture for comparison purposes. Because multiple diagnoses are often made with an admission, actual charges related to a specific AORC may be much smaller. This is true of cost estimates provided in the Economic Burden [48] section also.
Mean hospital charges for AORC-associated hospitalizations generally paralleled, but were consistently higher than charges for all hospitalizations, both overall (+$5,900) and for all demographic subgroups. Higher mean charges among demographic subgroups were most striking for women (+$8,200), persons 18-44 years (+$18,800), non-Hispanic whites (+$9,900), non-Hispanic blacks (+$10,900), Hispanics (+$33,700), other non-Hispanics (+$10,700), and those in the South (+$9,500) and West (+$16,100).
Total charges for AORC-associated hospitalizations were $310.9 billion in 2013, comprising 24% of all hospital charges for the year. This percentage was relatively consistent for all sex and age groups except those 18 to 44 years, where it was only 11%. Among racial/ethnic groups, AORC total charges were 19% for non-Hispanic others, while they were 30% among non-Hispanic whites. AORC-associated hospitalization total charges were 29% of all hospitalizations in the Midwest in 2013.
Among the 10 AORC subgroups, hospitalizations with osteoarthritis accounted for $138.4 billion, or 45% of total charges for AORC-associated hospitalizations, while hospitalizations with joint pain/effusion/other, gout, and soft tissue disorders accounted for 16%, 13%, and 13% respectively). (Reference Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.1.2 PDF [40] CSV [41]; Table 3A.3.1.1.3 PDF [42] CSV [43]; Table 3A.3.1.1.4 PDF [44] CSV [45])
Discharge from the hospital to long-term care, which includes skilled nursing facilities, intermediate care, and other similar facilities, or to home health care occurred more frequently among AORC-associated hospitalizations than among all hospitalizations (44% vs 29%). This was true regardless of sex, age, race/ethnicity, or region of residence. By demographic characteristics, the highest proportion of discharge to long-term care or home health care was found among females (48%), age 65 and over (55%), and residents of the Northeast region (52%).
Among the 10 AORC subgroups there were no striking differences in discharge to long-term care or home health care compared with all AORC hospitalizations. Discharge to home was more frequent, and resembled all hospitalizations (66%), among those with carpal tunnel syndrome (68%), fibromyalgia (67%), diffuse connective tissue disease (64%), and spondylarthropathies (59%). (Reference Table 3A.3.1.3.1 PDF [51] CSV [52]; Table 3A.3.1.3.2 PDF [53] CSV [54]; Table 3A.3.1.3.3 PDF [55] CSV [56];Table 3A.3.1.3.4 PDF [57] CSV [58])
Ambulatory Care Visits
From the 2013 surveys on ambulatory care, there were an estimated 99.3 million ambulatory care visits associated with a diagnosis of AORC, more than 10% of all ambulatory care visits that year, for a rate of 40.1/100 adults in the general population. An AORC-related condition was listed as the presenting (first) diagnosis for between 2.8% and 5.4% of all ambulatory care visits, depending on the healthcare site visited. Physicians’ offices accounted for 82% of all ambulatory AORC visits, vastly exceeding emergency department (12%) or outpatient (7%) sites. (see Table 3A.3.0.1 PDF [14] CSV [15]) As with hospital discharges, multiple AORC diagnoses were given in 15% to 20% of patient ambulatory visits. (Reference Table 3A.3.0.3 PDF [20] CSV [21]; Table 3A.3.0.4 PDF [22] CSV [23]; and Table 3A.3.0.5 PDF [24] CSV [25])
In 2013, AORC-associated ambulatory care visits resembled all 2013 ambulatory care visits by sex, race/ethnicity, and geographic region; they differed in age, being lower in the 18 to 44-year age group (21% vs. 32%) and higher in the 45 to 64-year age group (44% vs. 36%) and the 65 and older age group (34% vs. 32%). (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Reference Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; Table 3A.3.2.0.4 PDF [67] CSV [68]) (Note: Detailed data by type of ambulatory setting shown in Tables 3A.3.2.1.x, 3A.3.2.2.x(.1 to .4), and 3A.3.2.3.x, and can be accessed from the “Tables” tab in the upper right corner.)
Among the 10 AORC subgroups, 2 in 5 of the 99.3 million total ambulatory visits (41%) were associated with joint pain/effusion/other unspecified joint disorders or “other specified rheumatic conditions”; osteosteoarthritisrthritis and soft tissue disorders were the most common specific condition (~20% each). (Reference Table 3A.3.2.0.1 PDF [61] CSV [62])
AORC-associated ambulatory care visits for specific types of AORC differed by demographic variables. Women comprised 62% of all AORC-associated ambulatory care visits; their proportion was much higher for fibromyalgia (79%) and diffuse connective tissue disease (90%), but much lower for gout and other crystal arthropathies (27%). Men comprised 39% of all AORC-associated ambulatory care visits; their proportion was much higher for gout (72%). (Reference Table 3A3.2.0.1 PDF [61] CSV [62])
The 18 to 44-year old group comprised 21% of all AORC-associated ambulatory care visits; their proportion was a bit higher for diffuse connective tissue disease (31%), fibromyalgia (27%), and carpal tunnel syndrome (26%). Those aged 45 to 64 years comprised 44% of all AORC –associated ambulatory care visits; this proportion was similar for most specific types of AORC. Those aged 65 and older comprised 34% of all AORC-associated ambulatory care visits; their proportion was much higher for osteoarthritis (51%) and gout (50%), and much lower for fibromyalgia (20%). (Reference Table 3A.3.2.0.2 PDF [63] CSV [64])
Non-Hispanic whites (65% of the US population) comprised 73% of all AORC-associated ambulatory care visits, but only 59% of those for gout. Comparisons for other race/ethnic groups, as well as geographic regions were difficult to determine due to small sample sizes and unreliable data. (Reference Table 3A.3.2.0.3 PDF [20] CSV [21]; Table 3A.3.0.4 PDF [22] CSV [23])
Some 81 million AORC-related ambulatory care visits were physician office visits (PHYS); these accounted for 82% of all ambulatory care visits. An AORC-related condition was listed as the presenting (first) diagnosis for 5.4% of all PHYS visits. (Reference Table 3A.3.0.1 PDF [14] CSV [15])
Overall, 2013 AORC-related PHYS visits resembled those for all 2013 PHYS visits by sex, race/ethnicity, and geographic region; they differed in age, being lower in the 18 to 44-year age group (20% vs. 29%), higher in the 45 to 64-year age group (46% vs. 37%), and similar in the 65 and older age group (34%).
Among the 10 AORC subgroups, nearly 2 in 5 of the 81 million AORC-related PHYS visits (37%) were associated with joint pain/effusion/other unspecified joint disorders; osteoarthritis and soft tissue disorders were about 21% each. (Reference Table 3A.3.2.1.1 PDF [77] CSV [78])
AORC-related PHYS visits for specific types of AORC differed by demographic variables. Women comprised 61% of all AORC-associated PHYS visits; their proportion was much higher for rheumatoid arthritis (77%) and diffuse connective tissue disease (90%). Men comprised 39% of all AORC-associated PHYS visits; their proportion was much higher for gout (71%). (Reference Table 3A.3.2.1.1 PDF [77] CSV [78])
Persons aged 18 to 44 comprised 20% of all AORC-associated PHYS visits; their proportion was higher for diffuse connective tissue disease (29%) and soft tissue disorders (26%), while lower for osteoarthritis (7%) and rheumatoid arthritis (13%). Those aged 45 to 64 comprised 46% of all AORC–associated PHYS visits; their proportion pf PHYS visits was higher for fibromyalgia (55%) and carpal tunnel syndrome (50%). Those aged 65 and older comprised 34% of all AORC-associated PHYS visits; their proportion was much higher for osteoarthritis (51%) (Reference Table 3A.3.2.1.2 PDF [79] CSV [80]).
Non-Hispanic whites comprised 74% of all AORC-associated PHYS visits; their proportion was higher for rheumatoid arthritis (80%), spondylarthropathies (79%), and lower for gout (65%) and carpal tunnel syndrome (68%). Comparisons for other race/ethnic groups were difficult to determine. (Reference Table 3A.3.2.1.3 PDF [81] CSV [82])
There was little difference by geographic region. (Reference Table 3A.3.2.1.4 PDF [83] CSV [84]).
Some 6.5 million AORC-related ambulatory care visits were to outpatient (OP) clinics; these accounted for 7% of all ambulatory care visits. An AORC-related condition was listed as the presenting (first) diagnosis for 4.4% of all OP visits. (Reference Table 3A.3.0.1 PDF CSV)2013 AORC-related OP visits resembled those for all 2013 OP visits by sex, race/ethnicity, and geographic region; they differed in age, being lower in the 18 to 44-year age group (25% vs. 38%), and higher in the 45 to 64-year age group (49% vs. 39%) and the 65 and older age group (27% vs. 23%) (Reference Table 3A.3.2.2.1 PDF [85] CSV [86]).
Among the 10 AORC subgroups, more than 2 in 3 of the 6.5 million AORC-related OP visits (69%) were associated with joint pain/effusion/other unspecified joint disorders and osteoarthritis; soft tissue disorders and rheumatoid arthritis accounted for about 12% each. (Reference Table 3A.3.2.2.2 PDF [87] CSV [88])
AORC-related OP visits for specific types of AORC differed by demographic variables. Women comprised 69% of all AORC-associated OP visits; their proportion was much higher for rheumatoid arthritis (83%) and diffuse connective tissue disease (88%). Men comprised 31% of all AORC-associated OP visits; their proportion was much higher for gout (81%) and osteoarthritis (67%) (Reference Table 3A.3.2.2.1 PDF [85] CSV [86]).
Persons aged 18 to 44 comprised 25% of all AORC-associated OP visits; their proportion was higher for diffuse connective tissue disease (38%) and carpal tunnel syndrome (38%). Those aged 45 to 64 comprised 49% of all AORC-associated OP visits; their proportion was higher for rheumatoid arthritis (63%). Those aged 65 and older comprised 27% of all AORC-associated OP visits; their proportion was much higher for osteoarthritis (40%) (Reference Table 3A.3.2.2.2 PDF [87] CSV [88]).
Non-Hispanic whites comprised 58% of all AORC-associated OP visits; their proportion was higher for spondylarthropathies (71%) and fibromyalgia (70%). Comparisons for other race/ethnic groups were difficult to determine. (Reference Table 3A.3.2.2.3 PDF [89] CSV [90])
There was little difference by geographic region. (Reference Table 3A.3.2.2.4 PDF [91] CSV [92])
Emergency department (ED) visits for AORC-related diagnoses, totaling 11.7 million, accounted for 12% of all ambulatory care visits in 2013 and 11% of all emergency department visits. An AORC-related condition was listed as the presenting (first) diagnosis for 2.8% of all ED care visits. (Reference Table 3A.3.0.1 PDF [14] CSV [15])
2013 AORC-related ED visits resembled those for all 2013 ED visits by sex and geographic area; they differed in age, being lower in the 18 to 44-year age group (29% vs. 49%) and higher in the 45 to 64-year age group (34% vs. 29%) and the 65 and older age group (37% vs. 23%). (Reference Table 3A.3.2.3.2 PDF [93] CSV [94])
Among the 10 AORC subgroups, 3 in 5 of the 11.7 million AORC-related ED visits were associated with joint pain/effusion/other unspecified joint disorders and osteoarthritis; soft tissue disorders and fibromyalgia accounted for 13% and 12%, respectively. (Reference Table 3A.3.0.1 PDF [14] CSV [15])
AORC-related ED visits for specific types of AORC differed by demographic variables. Women comprised 61% of all AORC-associated ED visits; their proportion was much higher for rheumatoid arthritis (77%), fibromyalgia (79%) and diffuse connective tissue disease (90%). Men comprised 39% of all AORC-associated ED visits; their proportion was much higher for gout (69%). (Reference Table 3A.3.2.3.1 PDF [95] CSV [96])
Persons aged 18 to 44 comprised 29% of all AORC-associated ED visits; their proportion was higher for diffuse connective tissue disease (40%), fibromyalgia (43%), and carpal tunnel syndrome (51%). Those aged 45 to 64 comprised 34% of all AORC-associated ED visits; this proportion was similar for most specific types of AORC. Those aged 65 and older comprised 37% of all AORC-associated ED visits; their proportion was much higher for osteoarthritis (66%), rheumatoid arthritis (49%), gout (56%), spondylarthropathies (50%), and other specified rheumatic conditions (49%). (Reference Table 3A.3.2.3.2 PDF [93] CSV [94])
Race/ethnicity was not a defined variable in the NEDS database. There was little difference by geographic region. (Reference Table 3A.3.2.3.4 PDF [97] CSV [98])
Disease burden can be measured in many ways. This is particularly important for AORC, which has a modest effect on conveniently measured outcomes like mortality, but a much larger impact on less conveniently measured outcomes important to functionality for most people. Such outcomes include effects on work, health-related quality of life, independence, and ability to keep doing valued life activities. Three of these burdens, along with adverse life style factors that are associated with arthritis, are addressed in the estimates below.
Bed Days and Lost Work Days
Bed days are defined as spending one-half or more days in bed due to injury or illness, excluding hospitalization. Data are averaged over three years for the NHIS to achieve larger, more powerful sample sizes. For the years 2013-2015, the proportion who had bed days among adults with arthritis was higher than that for adults with any medical condition (45% vs. 41%). The 24.6 million adults with doctor-diagnosed arthritis and any bed days, 10% of the adult population, had an annual average of nearly 25 days spent in bed in the previous 12 months. This is far higher than the annual average of 14.5 bed days for the 41% of adults with bed days for any medical condition. Multiplying the 24.6 million adults by the mean bed days for arthritis resulted in 607 million bed days overall, or 55% of the 1.1 trillion bed days among adults reporting any medical condition. (Reference Table 3A.4.1.1 PDF [99] CSV [100])
Among adults with arthritis, females had a higher proportion than males of bed days (48% vs 41%) and a slightly higher mean number of days (25.6 vs. 23.1 days). Females with arthritis accounted for 65% of total bed days in 2013-2015. (Reference Table 3A.4.1.1 PDF [99] CSV [100])
Bed days are reported by a higher proportion of younger than by older adults with arthritis. Adults with arthritis had a higher proportion with bed days than adults reporting any medical condition in each age group: persons aged 18 to 44 years (59% vs. 46%), aged 45 to 64 years (50% vs. 41%), and aged 65 and older (35% vs. 31%). This was also true for the average number of bed days: 18 to 44 years (20.1 vs 9.3 days), 45 to 64 years (26.4 vs. 17.3 days), and 65 and older years (24.7 vs. 22.0 days). (Reference Table 3A.4.1.2 PDF [101] CSV [102])
Among racial/ethnic groups, those with arthritis had similar proportions reporting bed days (range 43%-47%) and a similar average number of bed days (range 21.4-25.6). (Reference Table 3A.4.1.3 PDF [103] CSV [104])
In the different geographic regions, those with arthritis had similar proportions with bed days (range 43%-47%) and a similar average number of bed days (range 22.4-27.2). (Reference Table 3A.4.1.4 PDF [105] CSV [106])
Persons in the workforce are defined as adults having worked at a job in the past 12 months. In the 2013-2015 NHIS sample, 81% of those age 18 to 44 held a job (56% of workforce), 74% of persons aged 45 to 64 years held a job (38% of workforce), and 20% of persons aged 65 and older were still working, comprising just under 6% of the workforce. Among the persons aged 65 and older, 83% were age 74 and younger. By sex, 73% of males reported being in the workforce, while 62% of females worked in the past 12 months. Males represented 52% of the workforce.
Lost work days for persons in the workforce are defined as absence from work due to illness or injury in the past 12 months, excluding maternity or family leave. For the years 2013-2015, the proportion of persons who had lost work days among adults with arthritis was lower than that for adults with any medical condition (23% vs. 30%). Among adults with doctor-diagnosed arthritis, 12.6 million in the workforce reported an average of 14.3 work days lost in the past 12 months, nearly 5 days more than the 9.4 work days reported by adults with any medical condition. This resulted in 180.9 million total lost work days among adults with arthritis who are in the workforce, or 34% of the 533.2 million work days lost among adults reporting any medical condition.
Among adults with arthritis, females and males in the workforce had similar proportions with lost work days (23%-24%) and similar mean number of lost work days (14.2-14.4). Females accounted for 57% of total arthritis-attributed lost work days per year in 2013-2013 due to the higher number of females with arthritis. (Reference Table 3A.4.1.1 PDF [99] CSV [100])
Compared with older adults, younger adults with arthritis or any medical condition had a higher proportion of lost workdays. Adults with arthritis had a higher proportion of lost work days than adults reporting any medical condition for persons aged 18 to 44 years (47% vs. 42%), but proportions were similar for the older age groups. Although, overall, the proportion of persons with DDA reporting lost work days was slightly less than was reported for any medical condition, the average number of lost work days was higher among adults with arthritis than adults with any medical condition: 18 to 44 years (13.4 vs 8.2 days), 45 to 64 years (14.6 vs. 10.8 days), and 65 and older (15.3 vs. 12.6 days). Adults aged 45 to 64 accounted for 62% of total arthritis-related lost work days even though they only comprised 38% of the workforce and 47% of those with any medical cause. (Reference Table 3A.4.1.2 PDF [101] CSV [102])
Activity Limitations
Activity limitations are included in the National Health Interview Survey in both the family database and the adult database, with slightly different response codes. Respondents are asked first if they need help performing a variety of activities of daily living (ADL), such as personal care, bathing, eating, getting in/out of chair, and walking. They are also asked if they are “limited in the kind or amount of work” they can perform. If a limitation of any type has a “yes” response, respondents are shown a list of 34 possible medical conditions and asked to identify those that cause the limitation. Multiple causes may be identified. This section uses the adult database and focuses on cases where arthritis is identified as a cause of limitations. The variable AAAL, defined in the introduction to this arthritis section, is based on a single question in the NHIS1 and produces somewhat different numbers than this more inclusive definition of activity limitations.
Limitations in any activities of daily living (ADLs) include seven components. Musculoskeletal-related ADLs include only the three limitations related to movement and action commonly associated with musculoskeletal diseases and are 1) “needing help with routine needs,” 2) ”needing help with personal care,” and 3) “having difficulty walking without equipment.” Other ADLs are related to memory, vision, hearing, and other limitations.
Of the 35.6 million adults with limitations in any ADL, 23% (8.0 million) named arthritis as a cause; the proportion jumped to 29% for those with a limitation in musculoskeletal-related ADLs. One-third (33%, 4.5 million of 13.9 million) of adults with difficulty walking identified arthritis as a cause. More than 1 in 4 attributed their need for help with routine needs (2.8 million) or personal care (1.5 million) to arthritis. (Reference Table 3A.4.2.1 PDF [111] CSV [112])
These numbers demonstrate the large impact of arthritis on adults with limitations in any ADL or in musculoskeletal related ADLs. The effect was much stronger among females than males (Reference Table 3A.4.2.1 PDF [111] CSV [112]) and among older adults. (Reference Table 3A.4.2.2 PDF [113] CSV [114])
Little difference was found between adults by race/ethnicity except for slightly higher proportion of non-Hispanic blacks attributing limitations to arthritis. (Reference Table 3A.4.2.3 PDF [115] CSV [116]). Geographic region in the US does not seem to be a factor. (Reference Table 3A.4.2.4 PDF [117] CSV [118])
Work limitations are defined here as those unable to work now due to health or limited in kind or amount of work (i.e., “unable to work” or “limited in work”). Of the 28.1 million adults with work limitations per year in 2013-2015, arthritis attributable work limitations (AAWL) affected on average 23% (6.4 million). Among those with any medical condition limiting work, 23% attributed their inability to work now to arthritis, while 22% limited in kind or amount of work did so. Higher percentages of females and older workers identified arthritis as a cause for work limitations. There was little difference seen by race/ethnicity or geographical region. (Reference Table 3A.4.2.1 PDF [111] CSV [112]; Table 3A.4.2.2 PDF [113] CSV [114]; Table 3A.4.2.3 PDF [115] CSV [116]; and Table 3A.4.2.4 PDF [117] CSV [118]).
Quality of Life and Lifestyle Factors
Among persons with DDA, compared with those without DDA, Health-Related Quality of Life (HRQoL) is worse on several scales. When assessed by self-reported health status, 27% of those with DDA reported fair/poor health compared to 12% of those without DDA. The DDA group also reported a higher mean number of days in the past month with poor physical health (6.6 vs 2.5 days), poor mental health (5.4 vs 2.8 days), or days with limitations in usual activities (4.3 vs 1.4 days).2 Using the same “unhealthy days” measures, an analysis of 2014 Humana Medicare Advantage members found that those with arthritis had more total unhealthy days, by 2.2 days per year, than those without arthritis, and that comorbid arthritis associated with hypertension, diabetes, chronic obstructive pulmonary disease, and congestive heart failure resulted in significant increases in both physically and mentally unhealthy days.3
The prevalence of DDA and of AAAL is much higher among those with the adverse lifestyle factors of obesity, insufficient or no physical activity, and fair/poor self-rated health.4 (Reference Table 3A.4.3 PDF [123] CSV [124])
The Economic Cost [129] section of this report uses the Medical Expenditures Panel Survey (MEPS), a standard source for cost of illness estimates, to estimate the total direct and indirect costs of musculoskeletal conditions and selected categories of musculoskeletal conditions, as well as the incremental direct and indirect costs specifically attributable to the selected category. Total costs are all costs for a patient regardless of the condition responsible; incremental costs are those costs attributed to a specified condition. A quick review of all economic terms used can be found by clicking HERE [130].
There are several important points to remember here. First, for arthritis and other rheumatic conditions, MEPS requires the use of selected 3-digit ICD-9-CM codes, using the 3- and 4-digit NADW AORC ICD-9-CM codes [131] to create a similar category called “arthritis and joint pain.” This approach has been used for a number of years and provides a comparative estimate of the costs of AORC. Additionally, costs estimates are per person and reported as mean per person costs. To arrive at the estimated aggregate cost, the mean per person cost is multiplied by the number of people affected, resulting in a total cost for conditions in the United States.
MEPS provides estimates of actual medical “expenditures,” meaning money changing hands, rather than medical “charges,” which are based on what is originally billed but rarely paid in full. Thus, the term direct costs, as used here, reflects actual medical expenditures. Indirect costs are those associated with lost wages. Aggregate costs for both direct and indirect costs are the sum of per-person costs across all individuals with the condition.
All-cause costs include medical expenditures or lost wages for persons with musculoskeletal disease, regardless of whether those costs are due to the musculoskeletal disease or another medical condition. Incremental costs are those estimated as attributable to musculoskeletal disease.
Direct Costs
Annual all-cause direct costs, in 2014 dollars, for arthritis and joint pain increased from a per person mean of $6,642 in the years 1996-1998 to $9,554 in 2012-2014. Incremental direct costs for arthritis and joint pain increased from a per person mean of $679 in the years 1996-1998 to a mean of $1,352 in 2012-2014, in 2014 dollars. The change in total mean costs was 44%, while incremental mean costs doubled. Incremental arthritis and joint pain costs showed a decline in 2012-2014 annual average costs compared to the previous five periods. (Reference Table 8.4.3 PDF [132] CSV [133]; Table 8.5.3 PDF [134] CSV [135])
Mean per person direct costs include ambulatory care, inpatient care, prescriptions, and other healthcare costs. In 2012-2014, ambulatory care accounted for about a third of per person direct costs, with inpatient care and prescriptions each accounting for approximately one-quarter (28% and 25%, respectively) of total cost. Over the past 18 years, prescription costs have seen the greatest change, rising nearly 140% per person in that time. Both inpatient and other healthcare costs remained steady at 9% and 11% increase, respectively. Ambulatory care increased by 59% over the same time period. (Reference Table 8.4.3 PDF [132] CSV [133])
Annual all-cause aggregate medical costs for persons with a diagnosis of arthritis and joint pain in the US increased from $192.4 billion in 1996-1998 to $626.8 billion, in 2014 dollars, for the years 2012-2014. Aggregate annual direct costs specifically attributed to arthritis and joint pain (incremental costs) in the US increased from $19.7 billion in 1996-1998 to $88.7 billion for the years 2012-2014, in 2014 dollars. While the increase over the 18-year period for total aggregate costs was more than 225%, the increase for incremental aggregate costs was greater than 350%, despite the recent decline in aggregate incremental costs. (Reference Table 8.6.3 PDF [140] CSV [141])
Annual per-person all-cause direct costs for arthritis and joint pain are highest for people age 65 and older, females, non-Hispanic whites, and residents of the Northeast region. Lower education and marital staus (divorced-widowed-separated) are also factors in higher cost. Public only insurance (Medicaid/Medicare) show the highest per person costs, in part because they serve a large share of the elderly population. (Reference Table 8.15.3 PDF [144] CSV [145])
Mean and aggregate total and incremental direct and indirect costs for osteoarthritis [146], rheumatoid arthritis [147], gout [148], and connective tissue disease [149], using the annual average for years 2008-2014 MEPS data, are calculated and shown in their respective sections.
Indirect Costs
“Indirect costs” as used in this report reflect estimates of earnings losses for persons with a work history who are unable to work due to a medical condition. They do not reflect supplemental measures, such as reduced productivity, worker replacement, or early retirement due to medical conditions.
Indirect costs are not estimated for the broad category of arthritis and joint pain.
Because many types of arthritis have a higher prevalence among older adults, we expect that the current aging of the population will increase the prevalence and impact of AORC unless new interventions are implemented within the near future. The projections of arthritis prevalence and AAAL take into account age and sex, but do not take into account potentially important factors such as the obesity epidemic and the increasing frequency of joint injuries.1 The age-adjusted percentage of AAAL among adults with arthritis increased 19% between 2002-2004 and 2013-2015.2 Previous costs of arthritis have been driven by age-related increases in prevalence,3 so future costs of arthritis are likely to be driven higher by the same age-related increase in prevalence, but also from the increasing frequency of surgical interventions.
Several data limitations exist for monitoring AORC burden in the future. First, on October 1, 2015, ICD-10-CM was required for use in clinical records; it was previously in use for death records. The current National Arthritis Data Workgroup definition of AORC uses ICD-9-CM codes. Due to significant changes in conceptualizing the new codes, a direct translation cannot be made. This means a new definition of AORC or some similar concept will be needed for analyses using ICD-based data in the future. CDC is working with ICD-10-CM translation experts and selected stakeholders to propose a draft standard ICD-10-CM based definition, which will be shared with the larger arthritis community to reach agreement on a new definition.
Second, there is a need for data on more specific conditions, for example rheumatoid arthritis, systemic lupus erythematosus, and psoriatic arthritis, to help drive clinical (eg, treatment, quality of care) and public health (eg, self-management education, safe physical activity) efforts that allow for better incidence estimates in order to better understand risk. Electronic health records may prove helpful in creating valid measures. There is also a lack of data on patient reported outcome measures (PROMs) on pain and function in electronic health records and administrative databases. These outcome measures are important to assessing the impact/burden of rheumatic and musculoskeletal diseases.
Arthritis and other rheumatic conditions are not addressed with the same priority as many other chronic conditions, perhaps because such priorities are driven more by easily available measures of mortality rather than by more challenging measures such as quality of life, disability, and impact on work. However, there is a growing policy interest in the role of multiple chronic conditions in health and health costs,1 and AORC plays a major role from this perspective for at least three reasons. First, those with priority chronic conditions are highly affected by AORC, with about half of adults with heart disease or diabetes and about a third of adults with obesity affected by DDA.2,3,4 Second, arthritis is very common condition among individuals with two or more chronic conditions, regardless of the conditions considered.5 Third, those with arthritis as one of their multiple chronic conditions fare much worse on important life domains such as social participation restriction, serious psychological distress, and work limitations.6
There are widespread and consistent professional recommendations for most types of AORC that involve increasing self-management of the disease through education, physical activity, and achieving a healthy weight, but little progress is being made.1 Such behavioral interventions offer evidence-based improvements to patients without the side effects seen with medications and other interventions. While most clinical settings are not set up to help patients achieve these recommendations effectively, increasing clinical/community linkages may offer a better approach. To see if provider referrals to community resources is a better solution, approaches such as the 1.2.3 Approach to Provider Outreach [152] and Spread the Word: Marketing Self-Management Education Through Ambassador Outreach [153] are being pilot tested in communities.
The Healthy People [154] project started with the 1979 Surgeon General’s report, Healthy People: The Surgeon General’s Report on Health Promotion and Disease Prevention. The current version of Healthy People 2020 [155] has set nine arthritis objectives for the nation to achieve by 2020, but only limited progress has occurred with the current level of investments in interventions. Currently, four new developmental objectives are included in the Arthritis, Osteoporosis, and Chronic Back Conditions [156] topic area as part of a larger effort to insure that chronic pain, regardless of the original cause, is included in Healthy People 2020.
There is a need for more conveniently measured outcomes that are important to most people. Such outcomes include effects on work, activities, health-related quality of life, independence, and ability to keep doing valued life activities.
Research funding to develop and evaluate more effective clinical and public health interventions is relatively modest, given that arthritis is the most common cause of disability and is a large and growing problem, affecting 54.4 million adults now,2 and a projected 78 million by 2040.3 This is especially frustrating because even the evidence-based interventions we have now are not reaching the people who would benefit from them. Implementation research to translate effective interventions to clinical practice and/or community settings is needed.
Although most adults with doctor-diagnosed arthritis are younger than age 65 and in their working years, the effect of their arthritis on employment and work, and the effect of reasonable workplace accommodations, have not been explored in depth. There is a need for the development and demonstration of web-based or app-based interventions for education, physical activity and achieving a healthy weight. This is an urgent issue right now and will continue to be an urgent issue as an aging workforce keeps working beyond age 65, as is anticipated.
As noted above, the use of ICD-9-CM codes for clinical and public health purposes ended with the healthcare system shift to the ICD-10-CM codes on October 1, 2015. This means the national surveys analyzed here that use ICD codes will shift to ICD-10CM as well. Standard definitions of generic and specific types of AORC need to be developed for clinical and public health researchers using the new ICD-10-CM codes; otherwise, investments in research will not be comparable and will be unable to build on each other.
Codes used in this analysis of AORC are based on the "National Arthritis Data Workgroup ICD-9-CM diagnostic codes for arthritis and other rheumatic conditions." Centers for Disease Control and Prevention, Arthritis Program, National Arthritis Data Workgroup.1
Osteoarthritis and allied disorders
715-Osteoarthritis and allied disorders
Rheumatoid arthritis
714-Rheumatoid arthritis and other inflammatory polyarthropathies
Gout and other crystal arthropathies
274-Gout
712-Crystal arthropathies
Joint pain, effusion and other unspecified joint disorders
716.1, .3-.6-.9-Other unspecified arthropathies
719.0, .4-.9-Other and unspecified joint disorders
Spondylarthropathies
720-AS/inflammatory spondylopathies
721-Spondylosis and allied disorders
99.3-Reiter’s Disease
696.0-Psoriatic arthopathy
Fibromyalgia
729.1-Myalgia and myositis unspecified
Diffuse connective tissue disease
710-Diffuse connective tissue disease [excl 710.0-.2]
710.2-Sicca syndrome (also called Sjögren's syndrome)
710.1-Systemic sclerosis (SSC, scleroderma)
710.0-Systemic lupus erythematosus (SLE)
Carpal tunnel syndrome
354.0-Carpal tunnel syndrome
Soft tissue disorders (excluding back)
726-Peripheral enthesopathies and allied disorders
727-Other disorders of synovium/tendon/bursa
728.0-.3, .6–.9-Disorders of muscle/ligament/fascia
729.0-Rheumatism, unspecified and fibrositis
729.4-Fascitis, unspecified
Other specified rheumatic conditions
95.6-Syphilis of muscle
95.7-Syphilis of synovium/tendon/bursa
98.5-Gonococcal infection of joint
136.1-Behcet’s syndrome
277.2-Other disorders purine/pyrimidine metabolism
287.0-Allergic purpura
344.6-Cauda equina syndrome
353.0-Brachial plexus/thoracic outlet lesions
355.5-Tarsal tunnel syndrome
357.1-Polyneuropathy in collagen vascular disease
390-Rheumatic fever w/o heart disease
391-Rheumatic fever w/heart disease
437.4-Cerebral arteritis
443.0-Raynaud’s syndrome
446-Polyarteritis nodosa and allied conditions [excl 446.5]
447.6-Arteritis, unspecified
711-Arthritis associated with infections
713-Arthropathy associated w/disorders classified elsewhere
716.0, .2, .8-Specified arthropathies
719.2, .3-Specified joint disorders
725-Polymyalgia rheumatica
Arthritis is an umbrella term that refers to joint pain or joint disease and encompasses more than 100 conditions. While there is no single accepted classification system for arthritis conditions, in general they are grouped as follows.
• Osteoarthritis [146]
• Inflammatory arthritis [159]
o Rheumatoid arthritis [147]
o Spondyloarthropathies [160]
o Connective tissue disease (eg, SLE, lupus) [149]
• Gout [148]
• Joint infection [161]
• Fibromyalgia [162]
• Juvenile arthritis [11]
• Joint pain/Joint replacement [163]
Osteoarthritis (OA) is widely recognized as the most common form of arthritis, and a major cause of pain and disability among US adults. Estimates of prevalence vary depending on how OA is defined: radiographic, symptomatic radiographic, or symptomatic only (self-reported presence of pain, aching, or stiffness). Radiographic OA is reported at higher prevalence levels than symptomatic, but symptomatic OA is more often cited from the self-reported databases.
From 2008 to 2014, 32.5 million US adults, or one in seven persons (14%), reported osteoarthritis and allied disorders, including joint pain with other specified or unspecified arthropathy, (herein called “osteoarthritis”) annually. Per previous research on the definition of osteoarthritis in the Medical Expenditure Panel Survey (MEPS),1 OA was defined as the presence of ICD-9-CM code 715 or a self-reported diagnosis of arthritis excluding rheumatoid arthritis and presence of ICD-9-CM 716 or ICD-9-CM 719. (Reference Table 8.13 PDF [164] CSV [165])
Across socio-demographic and health status characteristics, the following five groups represented the largest number of adults with OA by demographic classification: non-Hispanic whites (25.3 million), middle age (45-64 years) (14.8 million) or older adults (≥ 65 years) (13.8 million), those with private insurance (18.8 million), and those who were married/had a partner (17.8 million). (Reference Table 8.22 PDF [166] CSV [167])
However, total numbers do not reflect the share of the population group with OA. For example, females represent about 51% of the adult population in any given year, but comprise 78% of adults with OA. An even more disproportionate share of 18% of the population age 65 and older have OA (43%). This compares to 46% with osteoarthritis in the 34% of the population age 45 to 64 years. Non-Hispanic whites still have the highest share by race/ethnicity, comprising 65% of the population but 78% of those with OA, while Hispanics have the lowest (15% of population to 7% of adults with OA). Geographic region is not a major factor for OA, although the Midwest has a higher proportion of cases than it represents in the US population.
Share of the total OA population, however, does not give the whole picture. Since OA is closely linked to age, race/ethnicity and geographical regions with younger population segments will exhibit a lower overall share of OA patients. Both non-Hispanic black and Hispanic populations have a higher share of adults age 45 and older reporting OA than is found among non-Hispanic white adults. Hence, while non-Hispanic white adults represent the largest group of adults with OA, other race/ethnic groups have higher rates of OA. This same pattern can be seen in geographic regions, where the West has a younger population but higher rate of OA in the 65 and older population than is found in other regions. (Reference Table T3A.1.1.a PDF [172] CSV [173])
Joint Involvement in Osteoarthritis
Most OA diagnoses in both a hospital and outpatient setting do not specify the bodily site for which a healthcare visit is made. However, among those that are diagnosed with a specific site, the knee is the most common, followed by the hip. The knee accounts for about one-third (31%) of OA visits in all settings and is the only site identified in the data that meets reliability standards in all outpatient settings. Osteoarthritis in the hip accounts for 14% of hospital discharges, and 6% of physician office visits. (Reference Table 3C.1.0 PDF [176] CSV [177])
Healthcare Utilization
Osteoarthritis was diagnosed in 23.7 million healthcare visits in 2013, or 2.4% of all healthcare visits for any cause (Reference Table 3A.3.0.1 PDF [14] CSV [15]). It accounted for 10% of all hospitalizations and 2% of ambulatory visits.
Nearly 3 million hospital stays in 2013 had an OA diagnosis and it was the leading cause (46%) of hospitalization among all arthritis diagnoses. Osteoarthritis accounted for 45% of total hospital charges for arthritis diagnoses (cost charged but not necessarily paid), presumably in part because OA is the principal diagnosis associated with hip and knee joint replacements. Fewer than half (43%) of patients with an OA diagnosis were discharged to home or self-care, the lowest share of all arthritis diagnosed hospitalized patients. This is probably due to discharges to assisted living facilities or skilled nursing homes for rehabilitation following the hip or knee joint replacement. (Reference Table 3A.3.0.1 PDF [14] CSV [15]; Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52]; and Table 3A.5.3 PDF [178]CSV [179])
Females hospitalized with OA outnumber males two to one, while two in three patients were age 65 and older and hospitalized at a rate of 4.5 in 100. Non-Hispanic whites had the highest rate of hospitalization for OA (1.4 in 100 persons), while Hispanics had the lowest rate (0.4/100). Residents of the Midwest region were also more likely to be hospitalized with a diagnosis of OA (1.5/100), while those living in the West were least likely (0.9/100). Regional differences are a product of age to some degree, with the mean age of the Northeast and Midwest about 4 years older than the West. (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.1.0.3 PDF [30] CSV [31]; and Table 3A.3.1.0.4 PDF [32] CSV [33])
Osteoarthritis was diagnosed in 20.8 million outpatient visits in 2013 and accounted for one in five (21%) ambulatory care visits with any arthritis diagnosis. This was a rate of 1 in 12 (8.4%) outpatient visits for any diagnoses including an OA diagnosis. Visits per 100 were higher among females, adults 45 years and older, and non-Hispanic whites and blacks. Residents in the South had the lowest rate of outpatient visits for OA. (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; Table 3A.3.2.0.4 PDF [67] CSV [68])
Economic Burden
Combining direct and indirect costs for OA and allied disorders, average annual all-cause costs for the years 2008-2014 were $486.4 billion. Total incremental costs (direct and indirect costs directly associated with osteoarthritis) were $136.8 billion. (Reference Table 8.13 PDF [164] CSV [165])
Among all adults with osteoarthritis, annual all-cause per person direct costs were $11,502. Those reporting limitations had the highest all-cause per person direct costs: any limitation in work, housework, or school activities ($17,136) or any limitation in IADLs, ADLs, functioning, work, housework, school, vision or hearing ($14,146).
Annual total all-cause direct costs were $373.2 billion. The five socio-demographic groups with the highest total all-cause direct costs were: non-Hispanic whites ($300.7 billion); those with any limitation in IADLs, ADLs, functioning, work, housework, school, vision or hearing ($298.5 billion); any limitation in work, housework, or school activities ($213.0 billion); any private insurance ($216.5 billion); or who were married/had a partner ($200.4 billion).
Osteoarthritis incremental direct medical costs totaled $65.5 billion annually; average per person OA incremental costs were $2,018. (Reference Table 8.13 PDF [164] CSV [165], and Table 8.22 PDF [166] CSV [167])
Some 16.7 million adults of working age (18-64 years) with a work history had OA. The ratio of persons in the labor force without osteoarthritis (90%) is higher than for those with OA (69%), resulting in earnings losses due to OA.
On average, for the years 2008-2014, those without OA earned $6,783 more than those with OA, which represented a total of $113.2 billion in all-cause earnings losses for all U.S. adults with OA. Earnings losses attributable to OA were $71.3 billion; per person osteoarthritis-attributable earnings losses were $4,274. (Reference Table 8.13 PDF [164] CSV [165])
Lifetime cost attributed to knee OA in 2013 were $140,300. More than one-half (54%) of knee OA patients underwent total knee arthroplasty (TKA) an average of 13 years after diagnosis. The largest proportion of knee OA-related direct medical costs for those meeting TKA eligibility criteria was attributable to primary TKA.2
Inflammatory arthritis is a group of diseases characterized by inflammation of the synovial membrane in the joints and, often, other tissues throughout the body. Some forms of inflammatory arthritis are autoimmune diseases, conditions in which the body’s immune system attacks healthy tissue, also known as systemic autoimmune rheumatic diseases (SARD). Examples of SARDs that cause inflammatory arthritis include rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), Sjögren’s syndrome (SjS), systemic sclerosis (SSc), polymyositis (PM), and dermatomyositis (DM). Other types of inflammatory arthritis include axial spondyloarthritis (formerly called ankylosing spondylitis) and psoriatic arthritis, along with gout which is also considered a metabolic arthritis and discussed under it's own heading.
As a group, inflammatory arthritic diseases are characterized by joint pain, swelling, warmth, and tenderness in joints, and can cause deformity and loss of function of affected joints. Since these diseases are systemic, they may be associated with involvement of other tissues or organs including the skin, eye and bowel. In addition, in these diseases, blood tests provide evidence of inflammation and some conditions are useful markers that assess disease likelihood. Inflammatory arthritis conditions are sometimes difficult to diagnose and distinguish; all patients suspected of having an inflammatory arthritis should be referred to a rheumatologist for evaluation and management. Arthritis occurring in children and adolescents is referred to as juvenile idiopathic arthritis (formerly juvenile rheumatoid arthritis) and is discussed in the Juvenile Arthritis [11] heading.
Only the most common inflammatory arthritides will be discussed below. A listing of the many types of inflammatory arthritis and related conditions can be seen by clicking HERE [186].
Rheumatoid arthritis (RA) is a systemic autoimmune disease that produces inflammatory arthritis (stiff, painful, swollen joints, usually symmetrical). Rheumatoid arthritis is a form of polyarthritis and involves many joints, both large and small; it can also affect the cervical spine. Over time, RA can affect other organs (eg, eyes, lungs) and can lead to increased risk of cardiovascular disease.1
Rheumatoid arthritis is a chronic condition and, while it may occur acutely in some patients, onset is usually gradual. It can take months before a patient seeks medical attention, usually when joint pain (arthralgia) progresses to swelling and tenderness of the joint. As a systemic disease, RA is associated with symptoms such as fatigue, weight loss, and depression. In RA, inflammation of the joint can lead to erosion or damage of cartilage and bone and eventual deformity. The patient with RA characteristically produces autoantibodies called rheumatoid factors and anti-CCP. Anti-CCP (cyclic citrullinated peptide) antibodies are directed to proteins that have a modified amino acid called citrulline. These antibodies occur in approximately 70-80% of patients and are important for diagnosis and early recognition.
Rheumatoid arthritis was historically categorized based on the American Rheumatism Association Functional Class and Anatomic Stage, both proposed by Dr. Otto Steinbrocker in 1949. The former was updated by the American College of Rheumatology (ACR) in 19922 as follows:
Class I: Patient able to perform usual activities of daily living (self-care [dressing, feeding, bathing, grooming, and toileting], vocational [work, school, or homemaking] and avocational [recreational and/or leisure])
Class II: Able to perform usual self-care and vocational activities, but limited in avocational activities
Class III: Able to perform usual self-care activities but limited in vocational and avocational activities
Class IV: Limited in ability to perform usual self-care, vocational and avocational activities.
The revised classes were validated in a study of 325 patients using the Health Assessment Questionnaire (HAQ): mean HAQ disability index scores were Class I = 0.33, Class II = 1.02, Class III = 1.70 and Class IV = 2.67.
It is currently the usual practice to consider staging RA based on duration of signs and symptoms and the presence of autoantibodies and radiographic erosions. Hence, as currently defined by the ACR, RA is classified as follows:
Early RA = Signs and symptoms of < 6 months duration
Established RA = Signs and symptoms of ≥ 6 months duration or meeting the 1987 classification criteria
Seropositivity = presence of either rheumatoid factor (RF) or anti-citrullinated peptide antibodies (ACPA). Presence of erosions on radiographs of the hands/wrists.
In addition, one considers the level of disease activity at the time of the patient’s visit to inform treatment decisions. Several reliable and valid instruments are available for this purpose; most useful are the Disease Activity Score 28 [187] using either the erythrocyte sedimentation rate or the C-reactive protein marker, the Simplified Disease Activity Index [188], or the Clinical Disease Activity Index [189]. The latter does not require obtaining any laboratory tests to measure acute phase reactants. The ACR has published recommendations for the management of RA based on the above parameters, especially disease duration and disease activity.3
Although there is no cure for RA, early identification and treatment is important since current therapy can lead to significant improvement and reduce the likelihood for joint damage and progression to deformity. Therapy for RA involves a large group of medications that decrease inflammation and modify the course of disease. These agents are called DMARDS (disease modifying antirheumatic drugs) and have led to important improvement in overall outlook.
Prevalence of Rheumatoid Arthritis
As noted earlier in this report, clinical data are required to provide validity for estimating the prevalence of specific types of arthritis because the exact type of AORC causing pain and swelling is often unclear from observation. Prevalence of RA in the US is estimated to be between 1.3 and 1.5 million persons,4,5,6 roughly 0.50% of the adult population. Prevalence varies by sex, affecting 0.29%-0.31% of males and 0.73%-0.78% of females.6Also note that prevalence varies by age with highest ratios in older adults aged 65 years and older and lower ratios in declining 10-year age groups. The estimated prevalence of RA in the US population age 60 years and older is 2%.7
Healthcare Utilization
Rheumatoid arthritis effects overall health but may not be identified as the condition for which a patient is hospitalized. The NIS includes a separate variable identifying comorbidities of patients. Analyzing this variable, RA was identified as a comorbidity in 821,100 hospital discharges, or 2.7% of all hospital discharges, in 2013. However, when discharges were analyzed using the ICD9-CM codes, RA was diagnosed in only 512,600 discharges, or 1.7% of discharges for any diagnoses. Comorbidity designations are not made for all inpatients. Overall, 61% of discharges with RA diagnosed as a comorbidity also had an admitting diagnosis of RA, leaving two in five (39%) diagnosed with RA as a comorbidity but hospitalized for another cause. Common other forms of arthritis and associated diseases with RA as a comorbid condition include lupus (SLE) and fibromyalgia. (Reference graphs G3C.2.1.1 and G3C.2.1.2)
As previously noted, RA was diagnosed in slightly more than one-half million hospitalizations in 2013, representing 1.7% of discharges for any diagnoses. This is compared with the general prevalence rate of approximately 0.5%. Mean length of hospital stay and mean hospital charges were slightly higher than for all hospital discharges (106% and 109%, respectively). Nearly half (45%) of discharges with an RA diagnoses were dischared to additional care (short-term or home health), compared with 33% for all diagnoses discharges. (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52])
Rheumatoid arthritis was the first diagnoses recorded in 1.4% of total hip replacements and 0.3% of total knee replacements in 2013. (Reference Table 3A.5.3 PDF [178] CSV [179])
For RA, females outnumbered males three to one. Most RA hospitalizations occurred in those aged 65 years and older at a rate of 0.7 adults in 100 for this age group. No differences in rates were found by race/ethnic or regional group. (Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.1.0.3 PDF [30] CSV [31]; Table 3A.3.1.0.4 PDF [32] CSV [33])
Rheumatoid arthritis was diagnosed in 6.4 million ambulatory visits and accounted for 0.7% of ambulatory care visits with an arthritis diagnosis, compared with the 0.5% prevalence rate in the US population. An RA diagnosis was made in 0.6% of physician office visits and ER visits; 0.8% of outpatient visits had a RA diagnosis. (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Reference Table 3A.3.2.1.1 PDF [77] CSV [78]; Table 3A.3.2.2.1 PDF [85] CSV [86]; and Table 3A.3.2.3.1 PDF [95] CSV [96])
The distribution of ambulatory care visits by select demographic characteristics, when compared to all ambulatory visits for RA, was highest among females, and lowest among those younger than age 44 and among Black non-Hispanic and Hispanic racial/ethnic groups. (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; Table 3A.3.2.0.4 PDF [67] CSV [68])
Economic Burden
Estimates were calculated from 2008-2012 Medical Expenditures Panel Survey (MEPS) data; analysis was limited to those years because the ICD-9-CM code for RA was suppressed in the 2013 and 2014 MEPS data. MEPS respondents were classified as having RA if they met the following criteria: had a record with ICD-9-CM code 714, self-reported having ever been diagnosed with RA, and had at least five prescriptions or ambulatory care visits for RA. In the 2008–2012 period, each year, an estimated 1.7 million adults (0.8% of US adult population) had RA. Although slightly higher than the 1.3 million to 1.5 million previously cited by other sources, the numbers provide a similar rate of RA in the adult population.
Combining direct and indirect costs for RA, total average costs annually for the years 2008-2014 were $46 billion, with incremental costs, those costs directly associated with RA, of $21.6 billion. (Reference Table 8.13 PDF [164] CSV [165])
Annual average per person all-cause (diagnosis of RA along with other health condition diagnoses) medical expenditures for RA were $19,040. Across selected characteristics, the five groups with the highest all-cause per person costs were those who were college graduates ($25,526); had any limitation in work, housework, or school activities ($25,220); lived in the Northeast ($24,038); Hispanics ($22,871), and those with any limitation in IADLS, ADLs, functioning, work, housework, school, vision or hearing ($21,858). Lowest per person costs were among the uninsured ($8,674) and across the remaining subgroups, average per person costs were at least $14,387.
Total all-cause medical expenditures were $32.9 billion. Total costs include ambulatory care, inpatient care, prescriptions filled, and residual costs (ER, home health, medical devices).
For incremental medical expenditures (expenditures directly attributed to RA), mean per person expenditures for RA averaged $7,957 for the years 2008-2012. Aggregate medical expenditures (combined cost for all persons) in the United States for RA averaged $13.8 billion in each of the years of 2008-2012. (Reference Table 8.13 PDF [164] CSV [165] and Table 8.23 PDF [202] CSV [203])
The ratio of persons in the labor force without RA is higher than for those with RA in the general population, resulting in earnings losses due to RA. Among the estimated 900,746 working age adults (18-64 years) with a work history and RA, 56.1% had worked during the year compared with 87.9% of those without RA. Each year, those with RA earned, on average, $14,542 less than those without RA, which among all adults with RA totaled $13.1 billion.
For incremental medical expenditures, mean per person earnings losses attributed to RA averaged $8,748 per year in 2008-2012. Aggregate earnings losses for the United States due to RA averaged $7.9 billion in each of the years of 2008-2012. (Reference Table 8.13 PDF [164] CSV [165] and Table 8.23 PDF [202] CSV [203])
The cost of treating RA can be high. Older treatments of NSAIDS (aspirin, ibuprofen, naproxen, and celecoxib) and analgesics (acetaminophen, morphine, oxycodone) are readily available and inexpensive. However, many who suffer from RA cannot tolerate these drugs or they do not suppress the pain. A second level of drugs, the DMARDs (disease-modifying antirheumatic drugs) designed to reduce symptoms and damage, have become more affordable than previously, but still cost between $1,500 and $2,000 annually.
The newest level of drugs, the biologics, remain very expensive. Biologics are genetically engineered proteins originating from human genes targeting specific parts of the immune system that fuel inflammation. The first biologic, etanercept (Enbrel), was approved in 1998, and was used to treat RA. Actual cost estimates have a wide range, an average $18,000 to $100,000 annually, depending on the type of biologic used.8,9,10,11 In addition, because most are administered through an IV or injection administered by a healthcare professional, there are additional costs. Higher medication costs have been found to be associated with age and comorbidities.12
Spondyloarthropathy (SpA) refers to a family of inflammatory arthropathies that primarily affect the vertebral column. This group differs from other types of arthritis, especially rheumatoid arthritis, in that, rather than primarily affecting the synovial lining tissue in the joints, it involves the connective tissue where the tendons and ligaments attach to bone (entheses). Furthermore, patients with these disorders usually have negative tests for both rheumatoid factor and antibodies to citrullinated peptides (autoantibodies seen in the majority of patients with RA), often have radiographic involvement of the sacroiliac joints, and may have ocular inflammation (i.e., acute iritis or uveitis). Symptoms are often termed inflammatory back pain which is gradual in onset, worse in the morning and improves with activity. Inflammation can also affect the large joints of the lower extremities, including the knees and ankles. In the spondyloarthropathies, sacroiliac joints can fuse, and new bone can form between vertebrae. This leads to ankylosing and can cause deformity of the spine. In some patients, the spine can become rigid.
Among the conditions included in the SpA family, axial spondyloarthritis (formerly known as ankylosing spondylitis [AS]) is the most common and refers to inflammation of the spine or one or more adjacent structures of the vertebrae. Axial spondyloarthritis causes inflammation of the tissues in the spine and the root joints (shoulders and hips) and may be associated with peripheral arthritis. Over time, patients can undergo fusion of the vertebrae, limiting movement. Axial spondyloarthritis has a hereditary component and runs in families. It affects males more than females and can occur at any age. Patients with SpA frequently have a genetic marker called HLA B27. Since HLA B27 occurs commonly in the otherwise healthy population (approximately 8% of the US), it is not used as a specific diagnostic marker. HLA B27 is less common in African Americans.
In addition to AS, the more common diseases in the (SpA) family are:
• Reactive arthritis (formerly known as Reiter’s syndrome), a reaction to an infection in another part of the body;
• Psoriatic arthritis, which can occur in people with the skin disease psoriasis; and
• Enteropathic arthritis/spondylitis, a form of chronic inflammatory arthritis associated with inflammatory bowel diseases such as ulcerative colitis and Crohn’s disease. Enteropathic arthritis may be designated as axial (low back pain due to ankylosing spondylitis) or peripheral (joint involvement).
While some patients with psoriatic arthritis have a spondyloarthritis, in others, the involvement is primarily in peripheral joints. Psoriatic arthritis can resemble RA, but tests for rheumatoid factor and anti-CCP will be negative.
Prevalence of Spondylarthropathies
The prevalence of SpA in the US is difficult to determine as the diseases affect ethnic groups differently. Estimates of prevalence for SpA are 0.01%-2.5%.1,2 Current estimates of prevalence of the more common diseases are:
• Ankylosing spondylitis, 0.2%-1.7%1,2,3,4
o Axial SpA, 0.9%-1.4%2,3,4,5,6
o Advanced AS, 0.52%-0.55%2
• Psoriatic arthritis, 0.1%-0.4%1
• Reactive arthritis, no estimate found
• Enteropathic peripheral arthritis, 0.065%1
• Enteropathic axial arthritis, 0.05%-0.25%.1
Healthcare Utilization
Spondyloarthropathy was diagnosed in about one-half million hospitalizations in 2013, representing 1.6% of hospital discharges for all diagnoses, a higher proportion than prevalence in the population (1.6% of discharges vs 1.0%). No differences were found by sex, race/ethnicity, or geographic region, but age was a factor in the rate of hospitalizations for SpA. (Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.1.0.3 PDF [30] CSV [31]; Table 3A.3.1.0.4 PDF [32] CSV [33])
Among those with a diagnosis of SpA, hospital discharge rates showed higher mean charges ($60,000 per SpA discharge versus $43,000 for any diagnoses) for a similar mean length of stay (4.6 days versus 4.7 days). Discharges from the hospital to additional care (short-term or home health) was slightly higher for persons with a diagnois of SpA (40%) than for all diagnoses discharges (31%). (Reference Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52])
Spondylarthropathies accounted for 0.7% of all diagnoses ambulatory care visits. Males were slightly more likely (0.8%) to receive ambulatory health care for SpA than females, along with those age 45 to 64 years (1.0%) and those living in the South (0.9%). (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; Table 3A.3.2.0.4 PDF [67] CSV [68])
Economic Burden
Economic burden was not calculated by the BMUS project for spondyloarthropathies due to sample sizes. One study cited mean annual direct medical costs for AS of $6,500.7
Several published studies have explored the medication cost of biologics. For AS, biologic cost ranged from $1,200 to $24,200; for PSA ranged $14,200 to $32,000.7,8,9
Connective tissue disorders (CTDs) are part of the systemic autoimmune rheumatic diseases (SARD) grouping of disorders and include systemic lupus erythematosus (SLE or lupus), systemic sclerosis (SSc or scleroderma), inflammatory myositis (polymyositis and dermatomyositis), and Sjögren syndrome (SjS). They are characterized by a heterogeneous group of immune-mediated inflammatory signs and symptoms affecting multiple organ systems, including the joints.
Prevalence of Connective Tissue Disorders
The prevalence of syndromes in the CTD family are difficult to identify, and vary depending on the study duration, classification criteria, and the country in which the study was undertaken. Current estimates are based on special populations and primarily use several CDC-funded state registries. Connective tissue disorders affect all ages, but incidence is higher among women than men by a factor of at least 4:1, with estimates as high as 12:1 for SLE.1,2 Lupus generally begins during women’s children bearing years and can lead to serious kidney involvement among other complications.
The highest prevalence is for SjS, ranging between 0.5% and 3% of a given demographic population.1 Estimates of overall prevalence range from 400,000 to 3.1 million US adults.3
Recent national estimates of prevalence and incidence of SLE in the US are not available, but it is relatively uncommon. Using older meta-analysis studies, prevalence of SLE is estimated between 15 and 50 per 100,000 individuals.1 The Lupus Foundation of America estimates a total of 1.5 million Americans have some form of lupus, with an incidence of 16,000 new cases per year.4
The prevalence of SSc, also known as scleroderma, is much lower and has been reported with an incidence of 20 per one million new cases per year and a prevalence of 240 per million US adults, based on a limited US population studies published in 2003.5,6 A more recent update did not find this estimate to be changed.7
Overall prevalence and incidence of CTD is not reported in the literature, as classification criteria are not defined.1 However, the economic analysis for this report places prevalence at 0.27% for the years 2008 thru 2014. (Reference Table 8.20 PDF [216] CSV [217])
Healthcare Utilization
Connective tissue disorders represented 1% of hospital discharges and total charges for all diagnoses hospital stays in 2013. Because of the very low incidence of CTD syndromes, the prevalence is estimated at 0.3 percent or less, with use of healthcare resources much higher than the incidence ratio. Although the share of hospital discharges is higher than the share of all ambulatory visits, the rate of hospital discharges per 100 adults is much lower than the rate of ambulatory visits. Mean length of hospital stay and mean hospital charges are slightly higher than the means for all diagnoses, but patients are generally discharged to home self-care. (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52])
Hospitalizations for CTDs occurred primarily in females, those age 45-64 years, and non-Hispanic blacks compared to all diagnoses discharges. (Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.1.0.3 PDF [30] CSV [31]; Table 3A.3.1.0.4 PDF [220] CSV [33])
Connective tissue disorders accounted for 0.4% of all diagnoses for ambulatory care visits. The distribution of ambulatory care visits by select demographic characteristics, when compared to all ambulatory visits for CTDs, was highest among females and non-Hispanic blacks, and lowest among those aged 65 years and older and those living in the Midwest. Females accounted for nearly all ambulatory CTD visits. (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; Table 3A.3.2.0.4 PDF [223] CSV [68])
Data from the MEPS, used exclusively in the economic analysis of this report, show higher levels of healthcare visits than the NIS and NAMCS. In particular, the number of ambulatory physician visits is much higher in the MEPS than in the NAMCS. Differences in how conditions are classified and data coded account for some of this, as does the inclusion of ambulatory visits in settings outside a physician’s office (eg, ER or outpatient clinic).
Based on the MEPS, most individuals with a CTD (93%) incurred one or more ambulatory physician visits; among all of those with CTD, the total number of ambulatory physician visits was 9.3 million visits (average visits per person=11.2) annually. Approximately two-thirds (67.9%) of those with CTDs had at least one non-physician care visit, which include physical therapists and alternative care. The average number of non-physician visits per person was 8.5, for a total of 7.0 million non-physician visits nationally. One in five (20.7%) individuals with a CTD were hospitalized and there were 300,000 hospitalizations among all people with CTDs, with an average of 0.4 hospitalizations per person. The percentage with home health care visits was lower (14.4%) than for the other types of visits. However, those with a CTD had an average of 17.1 home health care visits per year for a total of 14.2 million visits nationally. Furthermore, those who did have a home health visit had very high home health visit utilization, with an average of 119 visits annually (data not shown). Finally, almost all individuals with a a CTD filled a prescription medication (95.8%); the total number of prescription fills each year was 39.5 million, based on average prescription fills among all of those with CTD of 47.7 fills. (Reference Table 8.20 PDF [216] CSV [217])
Economic Burden
From 2008-2014, an estimated 800,000 individuals (0.27%) in the US population had a CTD annually. Across all age groups, middle age adults (45-64 years) represented the largest percentage of those with a CTD (52% or 430,000), followed by younger adults (18-44 years) (26% or 219,000 individuals), older adults (≥ 65 years) (21% or 173,000) and children (18 years) (1% or 8,000 individuals). These numbers translate into prevalence rates shown in the graph below. (Reference Table 8.19 PDF [226] CSV [227]; Table 8.21 PDF [228] CSV [229])
Females comprised the majority of those with a CTD (767,000); at least 400,000 individuals in the following groups had a CTD: those with any limitation in IADLS, ADLs, functioning, work, housework, school, vision, or hearing (597,000); non-Hispanic Whites (542,000); those with any private insurance (503,000); and those with any limitation in work, housework, or school activities (453,000). (Reference Table 8.21 PDF [228] CSV [229])
Among all individuals with a CTD, ambulatory care represented 32% of all direct costs, followed by inpatient care (28%), prescriptions (25%), and residual costs (15%). The distribution across service category varied substantially across socio-demographic and health status characteristics suggesting very different treatment and utilization patterns across these groups. For example, there were regional differences: among those in the Northeast, ambulatory care, inpatient care, prescriptions, and other costs represented 40%, 11%, 21%, and 28%, respectively whereas in the Midwest, these categories represented 25%, 24%, 44%, and 7% of all costs, respectively.
Among all individuals with a CTD, all-cause annual per person costs were $19,702. The five groups with the highest all-cause per person costs were those who were college graduates ($30,471), had public health insurance only ($29,579), lived in the Northeast ($27,349), had never married ($27,026), or reported any limitation in work, housework, or school activities ($27,024).
The five groups with the lowest all-cause per person costs were those with no health insurance ($5,631), lived in the Midwest ($11,821), were Non-Hispanic black ($14,564), had a high school education but no college education ($14,617), or were married/had a partner ($14,735). (Reference Table 8.21 PDF [228] CSV [229])
Indirect costs (earnings losses) were not calculated for CTDs due to small numbers of cases.
Gout is caused by a buildup in the body of uric acid, in the form of monosodium urate crystals that the body cannot rid itself of quickly. This condition is characterized by hyperuricemia, referring to an elevation in the serum level of uric acid. It is not fully understood why some people with hyperuricemia develop gout and others do not. Gout is characterized by recurrent attacks of painful, red, tender, warm, and swollen joints, which generally affects only one joint at a time, often the large toe. It is more common in men, but also affects women after menopause. Repeated flares of gout can lead to chronic gouty arthritis, with involvement of multiple joints and the development of subcutaneous nodules, called tophi. While gout can be an intermittent condition, it can also lead to severe chronic arthritis and joint damage and deformity. Gout occurs frequently in patients with what is termed the metabolic syndrome and affects patients who also have diabetes, hypertension, and obesity.
Other crystal arthropathies can be caused by deposits of calcium pyrophosphate dihydrate (CPPD) crystals in the joints and have symptoms similar to gout. CPPD deposition disease is less common than gout, although radiographic chondrocalcinosis is common in older adults.
Prevalence of Gout
Prevalence estimates of gout vary for the US from 1% - 4%, depending on the data source and time frame. In 2005, an estimated 6.1 million adults reported having gout at some time, with 3.0 million affected each year.1 Estimates from the MEPS analyzed for the economic data section reported 3.1 million US adults had gout annually for the years 2008-2012, an annual prevalence rate of 1.3%.(Reference Table 8.13 PDF [164] CSV [165] and Table 8.24 PDF [239] CSV [240]) Additional studies report a higher prevalence of 3.9%, or 8.3 million adults in 2007-2008, using the NHANES as the basis of estimates.2,3,4 Another NHANES study from 2007-2010 reported a prevalence of 3.8%.5 Overall, it is believed the prevalence of gout is rising, with obesity and hypertension cited as contributors.2,4 A study of hospitalization trends using the NIS from 1993-2011 supported this, showing hospitalizations with a diagnosis of rheumatoid arthritis declining over the study period while diagnosis of gout was reported as increasing.6
Prevalence of gout is higher in males than in females, 5.9% to 2.0%, respectively,4 or at a ratio of 3-4:1. The incidence of gout increases with age, and was shown in the MEPS to be higher in the following select socio-demographic groups: non-Hispanic whites (2.3 of 3.1 million); married/had a partner (1.9 million); any private insurance (2.0 million); those with any limitation in IADLs, ADLs, functioning, work, housework, school, vision, or hearing (1.7 million). (Reference Table 8.24 PDF [239] CSV [240]).
Healthcare Utilization
More than 850,000 hospitalizations in 2013 had a diagnosis of gout, representing 2.9% of hospitals visits for any diagnoses, and accounting for 3.3% of all hospital charges billed. Gout is diagnosed along with joint pain and soft tissue disorders when multiple diagnoses are made (7% and 3.5% cross-diagnosis, respectively). At discharge, patients diagnosed with gout are more likely to be transferred to short-term or home health care than those with any diagnoses (45% vs 31%). (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.0.2 PDF [18] CSV [19]; Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52])
Gout diagnoses were made in only 0.5% of ambulatory care visits for any diagnosis, accounting for 5.3 million ambulatory visits. Ambulatory visits were made more frequently by males (72%), those aged 65 years and older (50%), non-Hispanic whites (59%), and by those living in the Northeast (rate of 2.8/100 persons versus 2.1/100 for all regions). (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; and Table 3A.3.2.0.4 PDF [67] CSV [68])
Economic Burden
Estimates for gout, defined as ICD-9-CM 274, were generated from 2008-2012 MEPS data; analysis was limited to those years because the ICD-9-CM code for gout was suppressed in 2013 and 2014 MEPS data. Combining direct and indirect costs for gout, total average costs annually for the years 2008-2012 were $26 billion. Incremental costs could not be calculated due to a small sample size. (Reference Table 8.13 PDF [164] CSV [165])
Among all adults with gout, all-cause per person direct costs were $11,936. Those with any limitation in work, housework, or school activities had the highest all-cause per person direct costs ($16,843) whereas those age 18-44 years had the lowest ($5,934). Total all-cause direct costs were $36.6 million. Direct costs attributable to gout were not reported because the relative standard errors for the estimates was greater than 30%. (Reference Table 8.13 PDF [164] CSV [165] and Table 8.24 PDF [239] CSV [240])
The percentage working during the year among adults age 18-64 years was similar for those with (85%) and without gout (88%). Per person, those with gout earned $6,810 more than those without gout; thus, overall, those with gout had negative earnings losses (aggregate of -10.0 billion). Like direct costs, earnings losses attributable to gout were not reported because the estimates were unreliable, with a relative standard error greater than 30%. (Reference Table 8.13 PDF [164] CSV [165]).
Arthritis from joint infection, known by the umbrella term as septic arthritis, can occur from an infection anywhere in the body traveling through the bloodstream. It can also occur from a penetrating injury that delivers germs directly to a joint. An infected joint is usually very tender, swollen, and painful. When caught early and treated with antibiotics it can be cleared of the joint infection. Surgical drainage of the infected joint is often necessary which can be performed arthroscopically. In some cases, the arthritis becomes chronic. Knees are most commonly affected, but septic arthritis also can affect hips, shoulders, and other joints. Often, an infected joint has been affected by another form of arthritis. Gonococcal septic arthritis, transmitted from gonorrhea bacterium, a sexually transmitted disease, can occur in otherwise healthy individuals. Lyme disease is another form of arthritis associated with infection and occurs in certain areas of the country.
The incidence of septic arthritis in industrialized countries, including the US, is estimated at six (2-10) per 100,000 population per year. In persons with underlying joint disease or prosthetic joints, incidence increases to 6-30 per 100,000 per year. The most susceptible populations are young children and the elderly.1 Infection can occur in a prosthetic joint and be a source of chronic pain. Biologics, while shown to work well for RA and other inflammatory arthritis pain, have also been associated with statistically significant higher rates of serious infections as they are designed to weaken the immune system. Serious infections included opportunistic infections as well as bacterial infections in most studies.2 These side effects of increased risk for septic arthritis are recognized and published in numerous sources.
Septic arthritis is included in the “other specific rheumatic conditions” in the AORC discussion.
Fibromyalgia does not fit within the main arthritis classifications but is considered a chronic pain condition. The primary symptoms are widespread pain throughout the body and fatigue. Recent revisions to diagnosis now focus on four criteria.1
1) Generalized pain, defined as pain in at least 4 of 5 regions is present.
2) Symptoms have been present at a similar level for at least 3 months.
3) Widespread pain index (WPI) ≥7 and symptom severity scale (SSS) score ≥5 OR WPI of 4-6 and SSS score ≥9.
4) A diagnosis of fibromyalgia is valid irrespective of other diagnoses. A diagnosis of fibromyalgia does not exclude the presence of other clinically important illnesses.
The cause of fibromyalgia is not known, but current theories include a higher sensitivity to pain. Fibromyalgia can occur by itself, although it can also accompany another form of arthritis such as rheumatoid arthritis or spondyloarthritis.
Prevalence of Fibromyalgia
Estimates of fibromyalgia range from 4 million (2% of the adult population)2 to 10 million (5% of adult population).3 Fibromyalgia is most prevalent in females, with up to 90% of incident cases females. It is also more common among older members of the population.
Healthcare Utilization
Just under one-half million (442,000) hospitalizations in 2013 had a diagnosis of fibromyalgia, representing 1.5% of hospital visits for any diagnoses, and accounting for 1.4% of all hospital charges billed. Females accounted for 89% of the hospitalizations, with those age 45 to 64 accounting for nearly half (48%) of the discharges. Fibromyalgia is diagnosed along with connective tissue disease (11.1%), joint pain (8.2%), and rheumatoid arthritis (7.1%) when multiple diagnoses are made. Hospital stays are similar to discharges for any diagnoses in length of stay and mean charges. Discharge to home is most common. (Reference Table 3A.3.1.0.1 PDF [26] CSV [27]; Table 3A.3.1.0.2 PDF [28] CSV [29]; Table 3A.3.0.2 PDF [18] CSV [19]; Table 3A.3.1.1.1 PDF [38] CSV [39]; Table 3A.3.1.3.1 PDF [51] CSV [52])
Fibromyalgia diagnoses were made in 0.8% of all ambulatory care visits for any diagnosis, accounting for 7.7 million ambulatory visits. Ambulatory visits were made more frequently by females (79%), those aged 45-64 years (52%), non-Hispanic whites (74%), and by those living in the Northeast region (rate of 3.8/100 persons versus 3.1/100 for all regions). (Reference Table 3A.3.2.0.1 PDF [61] CSV [62]; Table 3A.3.2.0.2 PDF [63] CSV [64]; Table 3A.3.2.0.3 PDF [65] CSV [66]; and Table 3A.3.2.0.4 PDF [67] CSV [68])
Economic Burden
Economic costs were not calculated for fibromyalgia.
Juvenile arthritis (JA) is an umbrella term used to describe a number of autoimmune and inflammatory conditions that can develop in children. It is the most common rheumatic disease of childhood, particularly in the Western world, with children of European descent reporting higher incidence rates.1,2
The most common form of JA is Juvenile Idiopathic Arthritis (JIA) (formally called juvenile rheumatoid arthritis (JRA) or Juvenile Chronic Arthritis (JCA)). JIA is diagnosed in a child <16 years of age with at least six weeks of persistent arthritis. There are seven distinct subtypes, each having a different presentation and association to autoimmunity and genetics.3 Subtypes also differ in typical age of onset. Certain subtypes are associated with an increased risk of inflammatory eye disease (uveitis).
Understanding the differences in the various forms of JIA, their causes, and methods to better diagnose and treat these conditions in children is important to future treatment and prevention. Among all subtypes, 40% to 45% of children with JIA still have active disease after 10 years.4
Prevalence Of Juvenile Arthritis
Due to the various forms of JA, estimates of prevalence and incidence are difficult to ascertain. Overall estimates are that 294,000 children in the United States have arthritis or another rheumatic disease.5
In 2006, the CDC Arthritis Program finalized a case definition for ongoing surveillance of significant pediatric arthritis and other rheumatologic conditions (SPARC [253]) using the current ICD-9-CM diagnostically based data systems. In response to the variations in conditions that some felt should be included, but were not, CDC generated estimates for conditions that were not included in the case definition but were felt by some should have been.
Healthcare Utilization
Using the SPARC definitions, analysis of the recent national healthcare database focusing on children, the Healthcare Cost and Utility Project (HCUP) KID, showed 104,400 children age 17 and younger were discharged from a hospital with any diagnosis of SPARC in 2012. Of those, 15,600, or 15%, had an admitting diagnosis of SPARC. Slightly more females than males were hospitalized; children age 6 and younger were more likely to be hospitalized with an admitting diagnosis of SPARC than older children, accounting for 40% of admissions.
Only a small number of children (3.8%) discharged with any diagnosis of SPARC had a diagnosis of juvenile arthritis. Females accounted for 72% of discharges with a diagnosis of JIA, with 62% of the discharges for children age 13 to 17 years.
Average hospital stays of eight days were found for any diagnosis of SPARC. The very youngest children, babies under age one, had much longer stays and higher mean hospital charges. Children with a diagnosis of JIA had hospital stays of a mean of 4.6 days, with subsequently lower mean charges.
Total hospital charges associated with any diagnoses of SPARC in the population younger than age 20 were $8.3 billion in 2012. (Reference Table 3B.1 PDF [254] CSV [255])
Emergency rooms saw 515,600 patients ages 0 to 17 with any diagnoses of SPARC in 2013. Among these patients, 6,900 had a primary diagnosis of JIA. Visits did not show major differences by sex or age.
Due to smaller sample sizes in the currently available databases for physician office visits and outpatient clinics, outpatient visits for a diagnosis of SPARC in the juvenile population are difficult to quantify. In 2013, physician visits for treatment of JA numbered 1.2 million. As with ED visits, major differences by sex or age were not seen. Due to small sample sizes, the number of visits with a diagnosis of JIA was unreliable.
Outpatient clinics saw 305,100 patients in 2011, the most recent year for outpatient data available. Patterns for distribution reflected that of other treatment sites. Due to small sample sizes, the number of visits with a diagnosis of JIA was unreliable.
From these data, an estimated 2.03 million outpatient visits for any diagnoses of SPARC occurred in the 0 to 17 years age population in 2013. (Reference Table 3B.1 PDF [254] CSV [255])
ICD-9-CM Codes for SPARC
In 2006, the CDC Arthritis Program finalized a case definition for ongoing surveillance of significant pediatric arthritis and other rheumatologic conditions (SPARC) using the current ICD-9-CM diagnostically-based data systems.
099.3 - Reactive arthritis
136.1 - Behcet's syndrome
274 - Gout
277.3 - Amyloidosis (includes Familial Mediterranean Fever)
287.0 - Allergic purpura / Henoch Schonlein purpura
390 - Rheumatic fever without heart involvement
391 - Rheumatic fever with heart involvement
437.4 - Cerebral arteritis
443.0 - Raynaud's syndrome
446 - Polyarteritis nodosa and allied conditions
447.6 - Arteritis, unspecified
695.2 - Erythema nodosum
696.0 - Psoriatic arthropathy
701.0 - Linear scleroderma / Circumscribed scleroderma / Morphea
710 - Diffuse diseases of connective tissue
711 - Arthropathy associated with infections
712 - Crystal arthropathies
713 - Arthropathy associated with other disorders classified elsewhere
714 - Rheumatoid arthritis and other inflammatory polyarthropathies
715 - Osteoarthritis and allied disorders
716 - Other and unspecified arthropathies
719.2 - Villonodular synovitis
719.3 - Palindromic rheumatism
720 - Ankylosing spondylitis and other inflammatory spondylopathies
727.0 - Tenosynovitis
729.0 - Rheumatism, unspecified and fibrositis
729.1 - Myalgia and myositis, unspecified
Joint pain is a major symptom of arthritis and non-arthritis conditions and a primary reason for seeing a medical care provider. Self-report surveys ask about joint pain but do not distinguish the cause of joint pain, which may be from arthritis, injuries, or degeneration of bone surfaces.
In 2013-2015, chronic joint pain was self-reported in the National Health Interview Survey (NHIS) by 78.9 million adults, among which 40.2 million also reported doctor-diagnosed arthritis (DDA) and 29.1 million reported activity limitations due to arthritis (AAAL). Because the latter two groups are not mutually exclusive, 30.4 million, or about 13% of the total population, have chronic joint pain but no DDA or AAAL. (Reference Table 3A.2.0 PDF [262] CSV [263])
The most common site of chronic joint pain reported by adults with DDA is the knee, reported by nearly 1 in 2 adults. Pain in the shoulder, finger, and/or hip is reported at each site by more than 1 in 4 adults with DDA. While 40% of people with DDA report joint pain in only one site, more than 20% report pain in four or more sites. (Reference Table 3A.2.1.1 PDF [264] CSV [265] and Table 3A.2.1.5 PDF [266] CSV [267])
Among adults with DDA, joint pain occurs in females more frequently than males, and in middle age more frequently than younger or older ages. Joint pain was similar by race/ethnicity and region. (Reference Table 3A.2.1.1 PDF [264] CSV [265]; Table 3A.2.1.2 PDF [268] CSV [269]; Table 3A2.1.3; PDF [270] CSV [271]; and Table 3A.2.1.4 PDF [272] CSV [273])
Joint Replacement
While in some sense, the need for a joint replacement represents failure of measures to prevent the occurrence or progression of joint problems, for those with the severe pain or poor function of end-stage joint problems, it can offer a life-altering “cure.” Joint replacements represent one of the fastest growing procedures in the US. Joint replacement procedures for hips and knees are most common, but replacements have been expanding to other joint sites in recent years.
Estimates presented come from the Healthcare Cost and Utility Project (HCUP) Nationwide Inpatient Sample (NIS). In previous editions of BMUS, estimates from the National Hospital Discharge Survey (NHDS) were also presented and are found in two tables showing trends on mean age of joint replacement patients and average length of hospital stay. The NHDS is no longer produced and not otherwise used here.
In 2013, an estimated 1.3 million inpatient joint replacement procedures were performed. Joint replacement procedures comprised about 3.6% of all inpatient procedures. More joint replacements were performed on women than men (60% vs 40%), and 95% of the procedures were performed on knees or hips. (Reference Table 3A.5.1.1 PDF [276] CSV [277])
In 2013, nearly 723,000 knee replacement procedures were performed in the U.S., comprising 56% of all joint replacement procedures. Over 90% were total knee replacements, but 8% were revision knee replacements, which occur when the original replacement fails or becomes infected. Three in five knee replacements (62%) occurred in females. More than one-half (57%) of knee replacement procedures were performed on those aged 65 years and older, but a substantial proportion (41%) were performed on persons aged 45 to 64 years. The majority (77%) of knee replacements were performed on non-Hispanic whites, with a proportion more than twice that of other racial/ethnic groups. The ratio of knee replacements to total population is higher in the Midwest region (27.2% of replacements vs. 21.4% of population) than other regions, with the Northeast having the lowest ratio of procedures (16.9% vs. 17.7%). (Reference Table 3A.5.1.1 PDF [276] CSV [277]; Table 3A.5.1.2 PDF [280] CSV [281]; Table 3A.5.1.3 PDF [282] CSV [283]; and Table 3A.5.1.4 PDF [284] CSV [285])
Trends in knee replacement procedures from 1992 to 2013 show steady increases in both total and revision knee replacements. Over the 22-year period, knee replacement procedures more than tripled, with the ratio of revisions to total remaining constant at 8% to 10%. (Reference Table 3A.5.2 PDF [286] CSV [287]).
The principal or first diagnosis associated with total knee replacement is osteoarthritis, accounting for 98% of all replacements in 2013. (Reference Table 3A.5.3 PDF [178] CSV [179]).
The 22-year mean age from 1992 to 2013 was nearly 68 years for total knee replacements, and about half a year younger for revision knee replacements. The mean age for both procedures shows a slow decline over time. (Reference Table 3A.5.4 PDF [290] CSV [291])
The average inpatient length of stay for total knee replacements has shown a remarkable decline of about 67% from a mean of nearly 8.9 days in 1992 to a mean of 3.4 days in 2013. (Reference Table 3A.5.5 PDF [292] CSV [293]).
Despite shorter hospital stays, the mean hospital charges from 1998 through 2013 showed a steady increase for all knee replacements, with revision knee replacement being more expensive than total knee replacement. Total hospitalization charges for both types of knee replacements have increased by five times over (in constant 2013 dollars) from $8.4 billion in 1998 to $41.7 billion in 2013. (Reference Table 3A.5.6 PDF [296] CSV [297])
Most adults (72%) with knee replacements are discharged to either short- or long-term care or home health care, likely due to the short hospital stay. Among persons aged 65 and older, a slightly higher proportion are discharged to either short- or long-term care or home health care (77%). (Reference Table 3A.5.7 PDF [300] CSV [301])
An estimated 493,700 hip replacement procedures were performed in 2013, comprising 39% of all joint replacement procedures. A majority, about 58%, occurred in females. Total hip replacements occurred three times as frequently as partial hip replacements, and both are far more common than revision hip replacement. A very small number of procedures, about 3,700 in 2013, were hip resurfacing, an alternative to replacement, particularly for young, active males. Females have more hip replacement procedures than males, particularly partial replacements. Hip replacements were more common among adults aged 65 years and older (61%), with most of the rest occurring among adults aged 45 to 64 years. Hip replacements by race/ethnicity paralleled that for all joint replacements, as did hip replacements by geographic region. (Reference Table 3A.5.1.1 PDF [276] CSV [277]; Table 3A.5.1.2 PDF [280] CSV [281]; Table 3A.5.1.3 PDF [282] CSV [283]; and Table 3A.5.1.4 PDF [284] CSV [285])
Trends in hip replacement procedures from 1992 to 2013 show total hip replacements increasing in number by 150%, while the number of partial replacements remained relatively stable. The ratio of revision hip to total hip replacements was about 20% from 1992 to 2002, but has consistently been around 17% since then, and dropped to 15% in 2013. (Reference Table 3A.5.2 PDF [286] CSV [287])
The principal or first listed diagnosis associated with total hip replacements was osteoarthritis (87%). The primary diagnosis for partial hip replacements was fractures (94%). (Reference Table 3A.5.3 PDF [178] CSV [179])
The 22-year mean age was about 66 years for total hip replacements and 77 years for partial hip replacements, reflecting the different underlying diagnoses. Mean ages for both procedures show a slight decline over the time period, reflecting the younger age at which joint replacements are now considered. However, in 2013, the mean age for partial hip replacements jumped to 80. (Reference Table 3A.5.4 PDF [290] CSV [291])
The mean length of stay for total hip replacements (3.0 days in 2013) showed the same remarkable decline as that for knee replacements--about 67% from 1992 through 2013. The mean lenth- of-stays for partial and revision replacements are longer, with about a 50% decline over the 22-year period. (Reference Table 3A.5.5 PDF [292] CSV [293])
Despite shorter hospital stays, mean hospital charges from 1998 through 2013 steadily increased for all hip replacements even when compared in constant 2013 dollars. Revision hip replacements are the most expensive, while total hip replacements are the least expensive. Total hospital charges for all hip replacements have tripled (in constant 2013 dollars) from $9.25 billion in 1998 to $30.7 billion in 2013, led by charges for total hip replacements. (Reference Table 3A.5.6 PDF [296] CSV [297])
Shoulder replacement procedures accounted for an estimated 45,000 procedures in 2013, comprising about 4% of all joint replacement procedures. At the same time, an estimated 19,000 other joint replacement procedures were performed for other joints in the upper and lower extremities, and the spine. More than with hip and knee replacements, these other joint replacement procedures occurred somewhat equally between females and males, and were more evenly divided between those aged 44 to 64 and those aged 65 years and older, except for shoulder replacements. Race/ethnicity and geographic regions resembled the distribution of all joint replacements. (Reference Table 3A.5.1.1 PDF [276] CSV [277]; Table 3A.5.1.2 PDF [280] CSV [281]; Table 3A.5.1.3 PDF [282] CSV [283]; and Table 3A.5.1.4 PDF [284] CSV [285])
A recent study released by the CDC Arthritis Workgroup1 reported state-level arthritis prevalence estimates for the first time. Using the 2015 Behavioral Risk Factor Surveillance System (BRFSS) self-reported doctor-diagnosed data, age-adjusted for comparison across states, the median prevalence among adults across the 50 states and District of Columbia was 23.0%. State prevalence ranged from 17.2% in Hawaii to 33.6% in West Virginia. When viewed by states in the four regions used in this report, 75% of states in the South had an age-adjusted prevalence rate above that of the national rate of 23.0%. This compares to 40% in the Northeast, 42% in the Midwest, and 31% in the West. Furthermore, five states in the South (West Virginia, Alabama, Tennessee, Kentucky, and Arkansas) and two in the Midwest (Michigan and Missouri) had a majority of counties with an arthritis prevalence rate in the highest quartile (31.2%-42.7%). A summary of state age-adjusted doctor-diagnosed arthritis prevalence rates can be found by clicking HERE [310].
The study also looked at doctor-diagnosed arthritis prevalence among adults with three comorbid conditions. At 44.5%, prevalence of arthritis was highest among those with coronary heart disease. This was followed by adults with diabetes (37.3%) and obesity (30.9%).
Leisure-time physical inactivity was also analyzed, and the median age-standardized percentage of inactive adults with arthritis was 35.0%. States in the western region tended to have the lowest prevalence of leisure-time physical inactivity with arthritis, while states in Appalachia and along the Ohio and Mississippi Rivers had the highest percentage of leisure-time physical inactivity, following the overall state prevalence rates for arthritis.
Findings from this study showed that estimated prevalence of arthritis varies by geographic area, with correlation to comorbid conditions and negative health-related characteristics. While direct causation cannot be made and further study is needed to understand why these geographic differences occur, the authors have postulated that known risk factors for arthritis such as comorbid conditions, occupation, socioeconomic status, and negative health-related characteristics may contribute. Access to medical care and medications may also be factors.
The full study of arthritis prevalence by state can be found at https://www.cdc.gov/arthritis/data_statistics/state-data-current.htm [311].
The CDC has also produced estimates of arthritis prevalence by race/ethnicity2 based on the NHIS 2013-2015 data. The lowest prevalence rate was found among non-Hispanic Asians (11.8%), with non-Hispanic multi-racial adults having the highest rate (25.2%). Among adults with arthritis, non-Hispanic Asians also reported the lowest prevalence of arthritis-attributable activity limitations (37.6%), while American Indian/Alaska Natives reported the highest prevalence of limitations (51.5%).
While medical professionals in many specialities and with a range of credentials treat patients with arthritis, those specializing in rheumatology are often at the frontline. A recently published workforce study by the American College of Rheumatology highlighted significant disparities in access to care within geographic regions of the US. Their findings showed access to care (defined as the ratio of adult rheumatology physicians to adult population) to be easiest in the Northeast (26,677 ratio) and most difficult in the Southern states (66,163 in the Southwest and 60,087 in the Southeast). This compares to a national average of rheumatologists per population of 41,658.3 Comparing this finding to the number of hospitalization and ambulatory healthcare visits, the highest number of visits, or need for care, was in the South. Furthermore, the study cited above reported the highest arthritis prevalence in the South.
In addition to regional differences, access to care based on population size is also the norm, as patients in areas with less than 50,000 population often must travel 200 or more miles to see a rheumatologist. The ratio of pediatric rheumatologists is much higher (229,442 children/physician), and it is estimated that only one-quarter of those aged 18 or younger with juvenile arthritis are currently able to see a rheumatologist.3
There are many challenges to the management of patients with arthritis that need to be addressed in the future, including, but not limited to, access to specialty care for timely and accurate diagnosis, appropriate use of non-pharmacologic modailities and pharmacotherapy, including targeted small molecule and newer biologic disease modifying anti-rheumatic drugs (DMARDs), adherence to pharmacotherapy, and addressing comorbid medical conditions in patients with various forms of arthritis.
The American College of Rheumatology (ACR) conducted a workforce study in 2015 and noted that the demand for care of patients with arthritis would continue to increase with the aging of the US population.1 Major areas that were identified include the role of primary care providers in the diagnosis and management of common forms of arthritis (eg, osteoarthritis, fibromyalgia, gout) and strategies to improve options for access to rheumatologist specialty care for patients with rheumatoid arthritis, psoriatic arthritis, spondyloarthritides, and systemic autoimmune rheumatic diseases. Training of more mid-level providers (ie, nurse practitioners and physician assistants) and more health professionals (eg, nurses, physical therapists, and occupational therapists) in the care of patients with rheumatic and musculoskeletal diseases would work to address some of this demand.
In addition to issues regarding workforce, there are potential barriers to care including insurance coverage, high co-pays, and limits on number for visits for rehabilitation services such as physical therapy and occupational therapy. Adding to the cost of non-pharmacologic and pharmacologic interventions, especially newer biologic DMARDS, and pharmacy benefit reimbursement plans, are barriers due to high co-pays and prior authorization required for newer pharmacologic interventions.
Funding of clinical trials to provide best evidence of the efficacy of treatment modalities, including non-pharmacologic interventions is needed. It is extremely important that evidence-based treatments be translated into clinical practice through the use of evidence-based recommendations published by nationally recognized professional societies. Such recommendations exist for the management of most forms of arthritis including, but not limited to, gout, osteoarthritis, rheumatoid arthritis, axial spondyloarthritis (formerly known as ankylosing spondylitis), psoriatic arthritis, and fibromyalgia. These recommendations include the use of both non-pharmacologic and pharmacologic modalities; it is felt to be important to emphasize the role of the former approaches particularly for osteoarthritis and fibromyalgia.
Virtually all forms of arthritis and systemic autoimmune rheumatic diseases are chronic conditions and effective treatments require patient participation, whether that is taking medications regularly (eg, urate-lowering therapy for gout) or making lifestyle changes such as adhering to dietary changes, a lifelong pattern of physical activity, or using cognitive behavioral therapy or mind-body techniques.
Patients with various forms of arthritis have an increased risk for cardiovascular comorbidities including coronary artery disease. While control of systemic inflammation appears to be important in ameliorating this risk, it is important for practitioners to focus on reducing other factors that contribute to increased cardiovascular disease risk including overweight and obesity, lack of physical activity, smoking, hypertension, hyperlipidemia, and poorly controlled type 2 diabetes mellitus. Depression also has been recognized as contributing to persistent pain, reduced physical function, and impaired quality of life in patients with various forms of arthritis. There is an ongoing need for care coordination between the rheumatology specialist and the primary care provider, particularly in patients who require co-management.
Meeting current and future needs will require a wealth of data currently not available or accessible. In the broad scope of musculoskeletal diseases, data currently either not available or inaccessible to BMUS analysts include treatment cost/benefits, medical workforce, geographic data at detail levels (due to small sample sizes), and outcomes.
In addition, many of the requests for additional data and analysis are beyond the scope of the current BMUS project due to staff size, staff expertise, and funding.
Major unmet needs for patients with arthritis include new, effective interventions for the safe treatment of chronic pain, improving insurance coverage for effective evidence-based, non-pharmacologic interventions, as well as newer, targeted small molecules, biologic DMARDs, and the development and approval of Disease Modifying Osteoarthritis Drugs (DMOADs) to slow or prevent progression of osteoarthritis.
Additionally, there is an ongoing need for research funding to understand the pathophysiology of the various forms of arthritis with the goal of estabilishing effective strategies for primary prevention, determining the appropriate timing for surgical intervention and the role of pre- and post-operative exercise programs to maximize functional recovery after surgical interventions, and understanding the underlying reasons for the observed sex/gender and race/ethnicity disparities in most forms of arthritis and systemic autoimmune rheumatic diseases.
Meeting future patient care needs will require increasing the workforce size of medical professionals. The 2015 Workforce Study by the American College of Rheumatology reported an excess demand for adult rheumatology care givers over current workforce projections of nearly 3200 professionals by 2030 and an excess demand of nearly 200 professionals in pediatric rheumatology.1 Other specialists in the care of arthritis likely show similar workforce demands.
The use of ICD-9-CM codes for clinical and public health purposes ended with the implementation of ICD-10-CM codes effective October 1, 2015. Standard definitions of generic and specific types of arthritis need to be developed for clinical and public health researchers using the new ICD-10-CM codes.
The crosswalk presented HERE [316] is for informational purposes only and should be carefully reviewed before used in future analysis.
Links:
[1] https://bmus.latticegroup.com/file/bmuse4g3a01png
[2] https://bmus.latticegroup.com/docs/bmus_e4_g3a.0.1.png
[3] https://bmus.latticegroup.com/docs/bmus_e4_t3.0.pdf
[4] http://www.boneandjointburden.org/fourth-edition/iiia0/arthritis-and-other-rheumatic-conditions
[5] http://www.boneandjointburden.org/fourth-edition/iiib0/joint-disease-arthritis-patient-populations
[6] http://www.cdc.gov/arthritis/data_statistics/case_definition.htm
[7] https://bmus.latticegroup.com/docs/bmus_e4_t3a.1.1.pdf
[8] https://bmus.latticegroup.com/docs/bmus_e4_t3a.1.1.csv
[9] https://bmus.latticegroup.com/file/bmuse4g3a201png
[10] https://bmus.latticegroup.com/docs/bmus_e4_g3a.2.0.1.png
[11] http://www.boneandjointburden.org/fourth-edition/iiib60/juvenile-arthritis
[12] http://www.fmaware.org/about-fibromyalgia/prevalence
[13] http://www.boneandjointburden.org/fourth-edition/iiia90/icd-9-cm-codes-aorc
[14] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.1.pdf
[15] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.1.csv
[16] https://bmus.latticegroup.com/file/bmuse4g3a301png
[17] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.0.1.png
[18] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.2.pdf
[19] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.2.csv
[20] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.3.pdf
[21] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.3.csv
[22] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.4.pdf
[23] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.4.csv
[24] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.5.pdf
[25] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.0.5.csv
[26] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.1.pdf
[27] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.1.csv
[28] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.2.pdf
[29] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.2.csv
[30] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.3.pdf
[31] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.3.csv
[32] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.4.pdf
[33] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.0.4.csv
[34] https://bmus.latticegroup.com/file/bmuse4g3a3101png
[35] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.1.0.1.png
[36] https://bmus.latticegroup.com/file/bmuse4g3a3102png
[37] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.1.0.2.png
[38] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.1.pdf
[39] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.1.csv
[40] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.2.pdf
[41] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.2.csv
[42] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.3.pdf
[43] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.3.csv
[44] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.4.pdf
[45] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.1.4.csv
[46] https://bmus.latticegroup.com/file/bmuse4g3a3111png
[47] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.1.1.1.png
[48] http://www.boneandjointburden.org/fourth-edition/iiia50/economic-burden-aorc
[49] https://bmus.latticegroup.com/file/bmuse4g3a3121png
[50] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.1.2.1.png
[51] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.1.pdf
[52] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.1.csv
[53] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.2.pdf
[54] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.2.csv
[55] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.3.pdf
[56] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.3.csv
[57] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.4.pdf
[58] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.1.3.4.csv
[59] https://bmus.latticegroup.com/file/bmuse4g3a3131png
[60] https://bmus.latticegroup.com/docs/bmus_e4_g3a.3.1.3.1.png
[61] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.2.0.1.pdf
[62] https://bmus.latticegroup.com/docs/bmus_e4_t3a.3.2.0.1.csv
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