Skip to main content

The epidemiology and etiology of adhesive capsulitis in the U.S. Medicare population



Adhesive capsulitis (AC) of the shoulder, also known as frozen shoulder, causes substantial pain and disability. In cases of secondary AC, the inflammation and fibrosis of the synovial joint can be triggered by trauma or surgery to the joint followed by extended immobility. However, for primary AC the inciting trigger is unknown. The burden of the disorder among the elderly is also unknown leading to this age group being left out of therapeutic research studies, potentially receiving delayed diagnoses, and unknown financial costs to the Medicare system. The purpose of this analysis was to describe the epidemiology of AC in individuals over the age of 65, an age group little studied for this disorder. The second purpose was to investigate whether specific medications, co-morbidities, infections, and traumas are risk factors or triggers for primary AC in this population.


We used Medicare claims data from 2010–2012 to investigate the prevalence of AC and assess comorbid risk factors and seasonality. Selected medications, distal trauma, and classes of infections as potential inflammatory triggers for primary AC were investigated using a case–control study design with patients with rotator cuff tears as the comparison group. Medications were identified from National Drug codes and translated to World Health Organization ATC codes for analysis. Health conditions were identified using ICD9-CM codes.


We found a one-year prevalence rate of AC of approximately 0.35% among adults aged 65 years and older which translates to approximately 142,000 older adults in the United States having frozen shoulder syndrome. Diabetes and Parkinson’s disease were significantly associated with the diagnosis of AC in the elderly. Cases were somewhat more common from August through December, although a clear seasonal trend was not observed. Medications, traumas, and infections were similar for cases and controls.


This investigation identified the burden of AC in the US elderly population and applied case–control methodology to identify triggers for its onset in this population. Efforts to reduce chronic health conditions such as diabetes may reduce seemingly unrelated conditions such as AC. The inciting trigger for this idiopathic condition remains elusive.

Peer Review reports


Adhesive capsulitis (AC), also known as frozen shoulder, is a common and debilitating shoulder condition, yet its cause remains largely unknown. The prevalence is typically reported to be 2–5% [1, 2], although estimates range as low as 0.5% [3] or as high as 10% [4]. The condition is most common among adults aged 40 to 70 years, but reported ages range from 27 to 85 [5]. Symptoms of this condition are shoulder joint pain with motion or pain during sleep followed by stiffness and dramatically reduced range of motion. The disability in the shoulder can last over a period of one or more years during which range of motion is slowly restored. For some patients, full range of motion is not restored even after four years [5, 6]. The typical time course for AC follows three stages [2]: a painful “freezing” stage where pain precedes reduced range of motion lasting 10–36 weeks. The next stage, lasting 4–12 months, is the “frozen” stiff stage where pain is reduced but range of motion remains impaired. The final stage, lasting 5–26 months, is the “thawing” stage where range of motion is gradually improves.

The pathophysiology of AC supports the theory that the condition results from a complex chain of events starting with inflammation leading to fibrosis and contracture of the shoulder capsule, the so-called “inflammatory-fibrotic cascade” [7]. During this cascade, inflammation, with cytokine proliferation lead to increased fibroblast proliferation, increased vascularization and new nerve growth, which may explain the pain reported by patients [7,8,9,10,11,12]. These factors in turn lead to increased and dysregulated collagen fiber deposition. Collagen fibers adhere to the glenohumeral ligaments, tendons, and joint surfaces causing contracture and joint stiffening. Thus, even after the inflammation is reduced, the adhesions remain greatly restricting motion [8, 9, 12]. It remains to be discovered what the inciting factor is that triggers this cascade and leads to the acute onset of AC.

AC is typically referred to as “primary” or “secondary”. Primary AC is idiopathic AC where examination and history cannot explain the development of the condition [2] whereas secondary AC develops due to pre-existing shoulder disorders or shoulder trauma [13] or post-mastectomy from breast cancer [14]. Primary AC is idiopathic with the cause unknown. Several risk factors for primary AC have been identified including diabetes [5, 15,16,17], thyroid disorders [15, 16, 18, 19], rheumatoid arthritis [13], gout [20], hyperlipidemia [17, 21] and Parkinson’s disease [22].


Despite what is known about the pathophysiology of AC and the associated risk factors, the trigger that sets primary frozen shoulder syndrome in motion is largely unknown and few studies have been undertaken to investigate triggers. There have been several small studies that suggest that the trigger for AC may be the usage of systemic medications, distal trauma, or perhaps there is a seasonal component that directly or indirectly initiates the disorder. Much of the sparse literature related to potentially medication-associated AC is based upon case reports or small case series that merit follow-up in larger samples [23,24,25,26,27,28,29,30,31]. Trauma has been suggested to generate systemic inflammation affecting areas distant from the site of trauma [32]. Another line of evidence supporting a possible role for infection as a trigger is the suggestion of seasonal occurrence of AC. The classic investigation by Nevasier (1945) reported 7 out of 8 patients had an onset during the winter months [33], suggesting a seasonal exposure akin to seasonality observed for influenza. Spouses are reported to have AC co-occur somewhat more than siblings [5] suggesting a shared environmental exposure as a possible risk factor. This observation by Hand et al. (2008) has received little notice or follow-up. Most recently, Ascani et al. (2021) report an increase in AC after COVID-19, supporting a potential association between viral infection and AC [34].

AC has generally been described as a condition affecting late middle-aged adults, and little has been written about the condition in the elderly population. Diabetes is the best studied risk factor for AC and the prevalence of diabetes is much higher in the ≥ 65 year age group (26.8%) than in the 18–44 years (4.2%) or 45–64 year age group (17.5%) making this group potentially more at risk [35]. With a large and growing population of older adults in the US, investigating the prevalence and triggers for this condition are warranted. Therefore, in this investigation, the prevalence of AC in the US Medicare population was determined. Then, using the cases we identified as primary AC and a control group without AC, we explore the hypothesis that AC may be triggered by an infection, trauma, or medications.


Data and sample

This study used complete Medicare Part B (fee-for-service) administrative claims data from the years 2010–2012 for all Medicare beneficiaries diagnosed with AC in 2011 (N = 92,437). The use of complete Medicare administrative data enabled patient healthcare utilization to be tracked across inpatient and outpatient settings and covered patients from all states in the United States. Participants in Medicare Part C, also known as Medicare Advantage, is a separately administered program and the data were not available for analysis. This project was reviewed by the University of South Carolina Institutional Review Board and determined to be not human research.

AC prevalence cohort

Prevalence of AC (primary or secondary) in the Medicare population was determined by identifying Medicare beneficiaries with at least one diagnosis of AC in 2011 as defined by having an International Classification of Disease, Ninth Revision, Clinical Modification (ICD-9-CM) codes: 726.00, using Medicare Part B carrier claims. To calculate the denominator for prevalence estimates, the Centers for Medicare and Medicaid Services published data were used to determine the total population of Medicare beneficiaries over age 65 (40,685,908 people) and the subset of those with fee-for-service Part B coverage (26,756,183 people) [36]. Approximately two-thirds of Medicare beneficiaries over age 65 are covered by Medicare Part B.

Primary AC cohort

As this study focuses on identifying triggers for new, primary AC diagnoses, a subset of the AC prevalence cohort representing those Medicare beneficiaries with primary AC was identified. In order to best identify those beneficiaries with primary AC, a series of clinically guided inclusion criteria were applied. First, all Medicare beneficiaries with an index (first) shoulder visit in 2011 and no previous shoulder diagnoses in the 365-days prior were identified. This included 192 ICD-9-CM shoulder related diagnosis codes, including AC and RCT. The index shoulder date was defined for each beneficiary as the first date where a shoulder diagnosis was received in 2011. Of that group, individual beneficiaries with a diagnosis of AC (ICD-9-CM codes: 726.00) within 90 days of the index shoulder visit and an x-ray or MRI within 30 days of the index shoulder visit were included. Given that diagnostic imaging is routinely used in the AC diagnosing process to rule out other clinically similar shoulder diagnoses, this inclusion requirement increased the confidence in the diagnosis of AC and the likelihood the case was receiving an initial diagnosis of AC. Following the diagnostic imaging service, beneficiaries also had to have a subsequent AC diagnosis claim within 180 days of their first AC diagnosis claim. The selection of the 30, 90, and 180 day windows was based upon expertise of the investigators and the typical pattern of care when making a new diagnosis.

Given the known direct association between mastectomy and AC diagnosis [14], any beneficiaries that had a mastectomy (CPT 85.2, 85.3, 85.4) were excluded from the analysis. Patients with fracture, dislocations, and sprains involving the shoulder were also excluded as these are known causes of secondary AC [13]. Furthermore, because rotator cuff (RC) tears were used as our control group, any AC beneficiaries who had a concurrent RC diagnosis were also excluded from the study. The presence of co-morbid chronic health conditions such as diabetes were not exclusion criteria as these factors are considered risk factors and not acute triggers. Additional inclusion criteria applied to assure complete data included (1) continuous enrollment in fee-for-service Medicare Part A and Part B from 365-days prior to 365-days after the index shoulder diagnosis and no enrollment in Medicare Part C (also known as Medicare Advantage plans) during the study period, (2) aged 66 years on the index shoulder visit, and (3) residence within the continental United States or Hawaii. The final residency criteria excludes Medicare beneficiaries who may obtain medical care outside the U.S. Medicare system and thus would have incomplete data. The minimum age criterion of 66 years was used to ensure enrollment in the Medicare system for a year prior to the index shoulder diagnosis. Complete patient inclusion criteria can be found in Fig. 1. The final primary AC case cohort included 7,232 Medicare beneficiaries.

Fig. 1

Flow chart of the selection of cases and controls. FFS- Fee-for-service beneficiaries. Does not include Medicare Advantage plan participants

Rotator cuff controls selection

A group of beneficiaries with a rotator cuff tear diagnosis in 2011 were selected as controls in our study. Rotator cuff tear was selected because of its similar clinical presentation but distinct etiology, and because it has been used as a control group in two studies of AC [37, 38]. Similar inclusion criteria were applied to identify the control group using Medicare Part B claims. Individual patients with a diagnosis of rotator cuff tear (ICD-9-CM codes: 727.61, 840.3, 840.4 covering partial thickness tears, bursal-sided tears, full thickness tears, massive tears) within 90 days of the index shoulder visit and an x-ray or MRI within 30 days of the index shoulder visit were included. Medicare beneficiaries also had to have a subsequent rotator cuff tear diagnosis claim within 180 days of their first rotator cuff diagnosis claim within 2011. Patients with any shoulder diagnosis in the 365-days prior to their index shoulder diagnosis in 2011 were excluded from the study. Additionally, any beneficiaries that had a concurrent diagnosis of AC were excluded from the control cohort. Additional inclusion criteria applied to assure complete data included continuous enrollment, aged 66 years on the index shoulder data, and residence within the continental United States. The final rotator cuff tear control cohort included 70,890 eligible Medicare beneficiaries.

Case–control matching process

Controls were matched to cases in a 3:1 ratio based on beneficiary age within 4 years (± 2 years) and gender. One older case was only matched to one control due to limitations in control sample at the age range. The final matched RC control group was 21,694 beneficiaries. Cases and controls were selected according to the flow chart described in Fig. 1.

Medication and vaccine measures

Medication use in the 180 days prior to index shoulder diagnosis was obtained from Medicare National Drug Code (NDC) data and translated to the World Health Organization (WHO) Anatomical Therapeutic Chemical (ATC4) classification code [39] using the cross-reference coding developed by Kury et al. [40]. An exposure period of 180-days prior to index shoulder diagnosis was chosen to allow time for initiation of the inflammatory pathway as well as account for delays between onset of AC and accessing medical care. Prior case reports indicated wide variation in time between initiation of medication and onset of AC, such as 10 days for fluoroquinolones [26] and 3 to 5 months for primidone, metalloproteinase inhibitors, and acitretin [25, 27, 30]. Six drug classes previously noted in the literature to increase the risk of AC were studied: fluoroquinolones [25], barbiturates [24], antituberculosis agents [31], protease inhibitors [28, 29], retinoids [27], and metalloproteinase inhibitors [30]. An additional class of antiviral agents was examined to serve as a potential proxy measure for exposure to a viral agent.

The hierarchical nature of the ATC4 code allowed classification into categories of medication and specific usages. The following ATC4 codes were used: J01M to capture quinolones, J04A for antimycobacterials to treat tuberculosis including isoniazid, N03AA for any barbiturate, D05BB and D10BA for retinoids for systemic use, B02AB for proteinase inhibitors, J05AE for protease inhibitors, and J05A for antivirals. Medication utilization was identified using Part D claims. Receipt of an influenza or pneumococcal vaccine in the 180 days prior to index diagnosis was determined from Healthcare Common Procedure Coding System (HCPCS) codes in Part B claims: 90,630, 90,653, 90,654, 90,655, 90,656, 90,657, 90,658, 90,660, 90,661, 90,662, 90,672, 90,673, 90,674, 90,682, 90,685, 90,686, 90,687, 90,688, 90,689, 90,756, Q2035, Q2036, Q2037, and Q2038.

Infectious diseases and trauma exposure

Diagnosis codes were examined for infectious disease and trauma diagnoses occurring 180-days prior to the index shoulder diagnosis. Categories of infectious diseases were created following prior classification systems [13, 41, 42]. The five most common infectious disease groups, occurring in at least 3% of the study population were examined in the analysis. The minimum of 3% was selected for pragmatic reasons to identify a common trigger. With an estimate of 3% exposure in cases, the study had 99.6% power to detect an odds ratio of 1.5 or higher. The infectious disease groups included mycoses (ICD-9-CM codes 110.0–118.0), upper respiratory tract infections (ICD-9-CM codes 460.X-466.X, 475.X), lower respiratory tract infections (ICD-9-CM codes 480.X-489.X, 490.X, 510.X, 513.X), infections of the kidney and urinary tract (ICD-9-CM codes 590.0–590.9, 599.0, 595–595.9, 597.X), and skin infections (ICD-9-CM codes 680.X-686.X, 695.5).

Trauma categories excluded trauma to the shoulder and were divided into fracture, dislocation, or sprains (ICD-9-CM codes 800.X-848.X) and other traumatic injuries (ICD-9-CM codes 850.X-854.X, 870.X-879.X, 880.X-887.X, 890.X-897.X, 900.X-904.X, 920.X-924.X, 925.X-929.X, 950.X-957.X, and 959.X) based upon classification used by Peterson et al. [32].

Patient characteristics and comorbid conditions

Patient demographic characteristics were measured by cross referencing the 2011 Beneficiary Summary files from Medicare. Specific patient-level variables included age, sex, race, and dual-eligibility for Medicare and Medicaid status on the index shoulder diagnosis date. General patient health was measured using Part A and B Medicare spending in the year prior to the index shoulder date, the Charlson Comorbidity Index (CCI), and the Frailty Risk Index (FRI). CCI is a validated measure of burden of disease [43,44,45]. Comorbidities are weighted from 1 to 6 for mortality risk and disease severity and then summed to form the total CCI score [43,44,45]. The FRI score is a validated instrument for assessing frailty among older persons [46]. Comorbid conditions that have been previous associated with AC were identified using ICD-9-CM codes as follows: thyroid disorder (240–246), Type 1 and Type 2 diabetes (250.XX-250.93), hyperlipidemia (272.0–272.9), hypertension (401–405), rheumatoid arthritis (714.0), and gout (274).

Statistical analysis

Descriptive statistics were calculated for determining the overall prevalence of AC and the demographics of the AC cohort. Then descriptive statistics, followed by t-tests or Chi-square tests, were used to assess the association of AC presence and the risk factors (infections, traumas, medications, and patient demographics) individually. A P-value < 0.05 was considered statistically significant. Seasonality of AC presence was assessed by estimating the proportions of new primary AC cases diagnosed per month with 95% confidence intervals, and using the intervals to identify months that were higher or lower than typical. Logistic regression models were used next to assess the association with AC and the risk factors in a combined model. Logistic regression results were presented as 95% confidence intervals for the odds ratios. A 95% confidence interval for odds ratios that excluded 1.0 was considered to be evidence of a statistically significant association. Because the case–control matching was performed on only age and gender (and thus considered to be a loose match), unconditional logistic regression was performed [47]. A conditional model was also run to verify similar results.


Prevalence of AC in the US Medicare population

We found 92,437 individuals over age 65 with a diagnosis of AC in the Part-B beneficiary population, representing 4% of those with a shoulder claim. We estimate that the one-year prevalence for AC in the over 65-year age group to be 0.35% (92,437/26,756,183 Part-B beneficiaries). This prevalence of 0.35% translates to an estimated total 142,000 people over age 65 with AC across the U.S. (0.35% of the 40,685,908 total Medicare for the aged population). Average one-year Medicare spending, in the year prior to diagnosis, for those beneficiaries with a diagnosis of AC in 2011 was substantially higher ($14,176) than the average spending per Medicare beneficiary in 2011 ($10,756) [48].

Two thirds of AC patients were female, and the mean age of the AC cohort was 75.7 years (Table 1). White (86.3%), Black (6.7%), and Asian (2.8%) were the most common reported racial categories for patients with AC. Patients came from all regions of the United States, and two-thirds were younger than age 76 years. Using the Charlson Comorbidity Index as a measure of general health status, approximately 51.1% of individuals with AC had a CCI score of 2 or higher, indicating more co-morbidities [43, 45]. Common co-morbidities examined included diabetes (34.5%), hyperlipidemia (44.5%), hypertension (58.4%) and thyroid disorders (17.7%) while rheumatoid arthritis, gout, and Parkinson’s disease were present in less than 5% of patients (Table 1).

Table.1 Patient Characteristics for all 2011 U.S. Medicare Beneficiaries diagnosed with Adhesive Capsulitis

Case control study of incident cases of primary AC and rotator cuff tears as controls

The final sample for analysis included 7,232 individuals with newly diagnosed primary AC and 21,727 newly diagnosed rotator cuff tears matched to cases on age and gender. By design, gender and age distributions were the same with 35.8% male and a mean age of 74.8 years (Table 2). AC and rotator cuff patients came from all regions of the United States with a larger proportion of AC patients having a CCI score of 2 or more (45.3%) compared to only 41.2% of rotator cuff controls with a CCI score of two or more. Many factors reached statistical significance in comparing the two groups, but the actual differences in proportions between cases and controls were not clinically meaningful.

Table.2 Comparison of Patient Characteristics for Incident Adhesive Capsulitis Cases and Matched Rotator Cuff Tear Controls

Assessment of seasonality

The proportion of new cases diagnosed by month was plotted for AC and rotator cuff tear patients (Fig. 2). While the highest proportion of AC cases were diagnosed in the last 5 months of the year, particularly in November and December (9.6% and 9.8%, respectively), these numbers did not exceed 2 standard deviations above the mean monthly proportion of 8.3% \(\pm\) 1.6%. Similarly, there was no apparent seasonal trend for rotator cuff tears as all months were within the monthly mean of 8.3% ± 1.3%.

Fig. 2

Monthly seasonal distribution of diagnoses for adhesive capsulitis and rotator cuff tears, adults ages 65 and older, 2011 U.S. Medicare Data. Error bars show 1 SD of 0.8% for AC and 0.6% for RCT. The average line shows the expectation of 8.3% of diagnoses to occur each month if there is no monthly variation

Prevalence of comorbid health conditions

The prevalence of known co-morbid conditions and risk factors for AC were compared for primary AC cases and rotator cuff tear controls (Table 3). The odds of having AC was significantly higher for those beneficiaries with Type 1 diabetes compared to those without diabetes (odds ratios of 1.37 (95% CI 1.17–1.61) and for Type 2 diabetes (OR = 1.22 (95% CI 1.14–1.29). Parkinson’s disease, although uncommon, also showed a positive association with AC with an odds ratio of 1.58 (95% CI 1.23–2.04). Hypertension, hyperlipidemia, and thyroid disorders were prevalent for both cases and controls but no significant association was made with AC.

Table.3 Univariate and unconditional logistic regression analyses of the associations between medical comorbidities and diagnosis of adhesive capsulitis

Association with medications taken prior to diagnosis

The association with medications of a priori interest was investigated. After adjusting for age, gender, and the two significant comorbid conditions, diabetes and Parkinson’s disease, we found that odds of having AC was lower for individuals taking a quinolone antibiotic (OR = 0.88, 95% CI 0.79–0.97) in the 180-days prior to the index shoulder diagnosis (Table 4). No association was found for receiving an influenza or pneumococcal vaccination or taking a barbiturate or antiviral class of medication and having a diagnosis of AC. Recorded usage of barbiturates in the sample was low (0.3%). Too few individuals (< 10 per group) were identified who took retinoids, anti-mycobacterials, protease inhibitors, or metalloproteinase inhibitors to allow robust analysis in this investigation.

Table.4 Univariate and unconditional logistic regression analyses of the associations between medication utilization and diagnosis of adhesive capsulitis

Association with infection or trauma prior to diagnosis

Five infectious disease classes occurred in at least 3% of the population in the 180 days prior to diagnosis and were examined as potential precipitating factors for AC (Table 5). Upper respiratory tract infections were common, occurring in 10.3% of people with AC and 12% in people with rotator cuff tears. People with AC were less likely to have had an upper respiratory infection prior to diagnosis than people with rotator cuff tears (OR = 0.84, 95% CI 0.77–0.92). Lower respiratory infections were less common at 3.5% of cases and controls. No association was observed for mycoses or infections of the lower respiratory tract, kidney or urinary tract, or skin prior to diagnosis. No significant difference was observed for having a non-shoulder related fracture or sprain or other trauma prior to diagnosis in the AC group compared to rotator cuff tear group. Approximately 6–7% of cases and controls experienced these types of trauma prior to diagnosis.

Table.5 Univariate and unconditional logistic regression analyses of the associations between infectious disease triggers, trauma and diagnosis of adhesive capsulitis


Background and rationale

While AC has been studied in middle-aged adults, less is known about its epidemiology in the elderly population. In addition, little is known about the inciting trigger that leads to the development of primary AC. Therefore, this case control study was undertaken to describe AC among the elderly and explore the hypotheses that exposure to selected medications, distal traumas, or seasonal factors, may increase the risk for AC.


There were some limitations to this analysis. While three years of complete data were available, we were not able to assess trends beyond the one-year window into the year 2011. The use of claims data reflects dates of care rather than medical history. Date of claims diagnosis was used to identify date of onset, yet there may have been delay between symptom onset and seeking care. Information such as body mass index or obesity, detailed information on medication prescriptions, occurrence of infections not attended to by medical professionals, and confirmation of diagnosis of cases or controls may be less accurate using claims data than using medical records. The 7,232 new cases that were examined in detail may be an underestimate of the true number of new cases per year of primary AC, as our selection criteria required diagnostic imaging whereas not all healthcare providers order imaging to make the diagnosis. Further, patients were removed if they had any other shoulder diagnosis in the prior year which may have eliminated cases that had unrelated conditions and some cases may have been misdiagnosed with another disorder. However, the selection criteria were used in order to assess potential triggers for new cases which required a stringent selection criteria. One challenge in this analysis was selecting the most appropriate window to identify potential triggers. We selected a 6-month window prior to AC diagnosis because studies of selected medication-associated AC indicated most [25,26,27, 30], but not all [29], exposures occurred within six months of diagnosis. However, associations with long term or chronic use of medications may have been missed. Further, the window may have been too wide for association with infectious triggers given that reactive arthritis typically occurs within six weeks of infection [49]. Finally, we used patients with rotator cuff tears as a comparison group due to the similarities in presentation yet distinct etiology. Other investigations of AC have also used rotator cuff tears as comparators [37, 38]. However, the two disorders may share some underlying risk factors. In particular, fluoroquinolone [50, 51] and influenza vaccinations [52, 53] have been found to be associated with tendinopathy and rotator cuff tears. Future investigations may consider the use of additional comparison groups to investigate triggers for AC.

A strength of the study was that the prevalence of AC in the elderly population has not been well-studied to date. We included a large sample size representing all cases for an entire year across the United States among Medicare beneficiaries. The nearly universal use of Medicare among the elderly makes the findings representative of older American adults. The large sample size allowed the assessment of many potential risk factors, and the claims data included information on medications, concomitant diagnoses, and procedures.

Prevalence of AC in adults over 65 years of age

The first objective was to describe the epidemiology of AC in older adults, an age-group infrequently studied. Although AC is not typically thought to be a condition common among elderly adults, we estimate more than 140,000 Medicare beneficiaries were diagnosed with primary or secondary AC in 2011, accounting for 4% of shoulder diagnoses in this age group. We found women were more likely to have AC than men by a ratio of 1.8 to 1. Older age did not attenuate the risk for AC in women. Most people with AC in the study were white (86.3%), reflecting the demographics of the U.S. Medicare population. The patients with AC commonly had other co-morbid conditions including diabetes, hyperlipidemia, hypertension, and thyroid disorders. Rheumatoid arthritis, gout, and Parkinson’s disease were present in less than 5% of patients. These findings agree with findings from studies of younger populations [5, 15, 16], suggesting that the effects of age do not diminish the increased risk for women or those with chronic disease.

We also found that on average, Medicare annual spending for patients with AC was significantly higher than the average annual beneficiary Medicare spending in 2011 [48]. The growing elderly population and prevalence of AC in this age group suggests that AC can be a significant cause of disability for this population. Furthermore, the higher spending for beneficiaries diagnosed with AC might indicate that those beneficiaries are in worse health and require more healthcare utilization in addition to costly AC treatment.

Risk Factors for AC in adults over 65 years of age

The second objective was to investigate risk factors and potential triggers for AC. We examined newly diagnosed cases of AC and compared them to people with newly diagnosed rotator cuff tears. Age and gender were similar by study design. Elderly beneficiaries in the U.S. Medicare population are overwhelmingly white. However, a larger proportion of AC patients were non-white (11.6%) compared to those with rotator cuff tears (8.2%). This contrasts with earlier investigations which suggested a higher risk of AC for white patients [54] but is supported by more recent and larger studies which also found higher rates in non-white patients [55]. Others have observed higher rates for Asian ancestry individuals in particular [13, 56].

We found that both type 1 and type 2 diabetes as well as Parkinson’s disease were more likely in older patients with AC. Our findings corroborate that diabetes, a well-known risk factor for AC in the middle age population [13, 15,16,17, 55], is also associated with AC in the elderly population. The reason diabetes increases risk for AC is unclear, although possible biological mechanisms have been proposed. Hwang et al. identified increases in advanced glycation end products along with increased collagen density and fibroblast proliferation in capsular tissue of patients with AC and diabetes [38]. Their findings support the hypothesis that increased blood glucose levels increase the glycation of collagen proteins which then increases cross-linking of these fibers and stiffening of the joint. The association with Parkinson’s disease is less well established but confirms prior reports [22]. Contrary to initial expectations for increased risk, no association was observed for thyroid disorders.

Medication Utilization, infection and trauma as potential triggers

In addition to examining AC in the under-studied elderly population, the novel contribution of our work was to explore the association between plausible triggers (systemic medications, infections, seasonality, and inciting traumatic injury) and AC. One potentially treatment-related risk factor (use of quinolone antimicrobial treatment) was found to be significantly less common in patients with AC than rotator cuff tear controls. It is possible that fluoroquinolone exposure is associated with tendinopathy and possibly could contribute to rotator cuff tears [50]. The stronger association with rotator cuff tears prevents a true assessment of the risk of these factors on AC. A review of Medicare prescription drug usage shows approximately 20% of beneficiaries had a fluoroquinolone Part D claim in 2018 making it a potentially common risk factor. Receipt of an influenza or pneumococcal vaccination was not found to be an increased risk, contrary to prior suggestions [57, 58]. Arias et al. suggested that antigens injected into or near the synovial joint may lead to a localized inflammatory response in rare cases [58]. Other studies have reported that maladministered influenza vaccine is a risk factor for rotator cuff tears [52, 53]. Hessee et al. recommend training in proper vaccination administration techniques to ensure the injection enters the deltoid muscle and avoids the bursa, tendons, ligaments, and bones of the upper shoulder. As this association was observed for rotator cuff tears, future investigations should include a non-shoulder joint disorder as a comparison group. The general anti-viral class of medications and barbiturate medications were not found associated with AC in this analysis. Barbiturate medications were generally not covered by Medicare in 2011 [59], which may explain the small numbers of cases in the data. The other classes of investigated medications (retinoids, protease inhibitors, metalloproteinases, isoniazid) were prescribed to 0.5% or fewer of Medicare recipients at large [60] and were too infrequent in this dataset to assess as risk factors.

No positive association was found between AC diagnosis and five classes of infections in the six months prior to diagnosis. Those with an upper respiratory tract infection were less likely to be diagnosed with AC. Similarly, sustaining a non-shoulder related fracture or sprain or another injury was not associated with AC. The claims data do not allow in depth analysis, but it is possible rotator cuff tears could be due to trauma rather than these factors being protective against AC.

AC was more commonly diagnosed August through December. However, no significant seasonal trend was observed for AC, contrary to earlier suggestions [33, 61]. No medical records were available to determine whether the Medicare claim date for first AC visit reflects the date the condition began or the date when care was sought.


While this investigation did not identify specific triggers for AC, it did corroborate the long-known associations with diabetes and Parkinson’s disease in the Medicare population. Future investigations should investigate initiating triggers for the development of this common and disabling condition.

Availability of data and materials

The data that support the findings of this study are available in their original form from ResDAC but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are available from the authors upon reasonable request and with permission from the Center for Effectiveness Research in Orthopaedics and the University of South Carolina.



Adhesive capsulitis


Anatomical Therapeutic Chemical -4 Classification


Current Procedural Terminology


Fee-for-service medical care


Healthcare Common Procedure Coding System


International Classification of Disease, Ninth Revision, Clinical Modification


Magnetic resonance imaging


Rotator cuff tear


  1. 1.

    Bunker TD. Frozen shoulder: unravelling the enigma. Ann R Coll Surg Engl. 1997;79(3):210–3.

    CAS  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Hsu JE, Anakwenze OA, Warrender WJ, Abboud JA. Current review of adhesive capsulitis. J Shoulder Elbow Surg. 2011;20(3):502–14.

    PubMed  Article  PubMed Central  Google Scholar 

  3. 3.

    Thomas SJ, McDougall C, Brown ID, Jaberoo MC, Stearns A, Ashraf R, et al. Prevalence of symptoms and signs of shoulder problems in people with diabetes mellitus. J Shoulder Elbow Surg Am Shoulder Elbow Surgeons. 2007;16(6):748–51.

    Article  Google Scholar 

  4. 4.

    Walker-Bone K, Palmer KT, Reading I, Coggon D, Cooper C. Prevalence and impact of musculoskeletal disorders of the upper limb in the general population. Arthritis Rheum. 2004;51(4):642–51.

    PubMed  Article  PubMed Central  Google Scholar 

  5. 5.

    Hand C, Clipsham K, Rees JL, Carr AJ. Long-term outcome of frozen shoulder. J Shoulder Elbow Surg Am Shoulder Elbow Surgeons. 2008;17(2):231–6.

    Article  Google Scholar 

  6. 6.

    Shaffer B, Tibone JE, Kerlan RK. Frozen shoulder. A long-term follow-up. J Bone Joint Surg Am. 1992;74(5):738–46.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  7. 7.

    Rodeo SA, Hannafin JA, Tom J, Warren RF, Wickiewicz TL. Immunolocalization of cytokines and their receptors in adhesive capsulitis of the shoulder. J Orthop Res. 1997;15(3):427–36.

    CAS  PubMed  Article  Google Scholar 

  8. 8.

    Cher JZB, Akbar M, Kitson S, Crowe LAN, Garcia-Melchor E, Hannah SC, et al. Alarmins in Frozen Shoulder: A Molecular Association Between Inflammation and Pain. Am J Sports Med. 2018;46(3):671–8.

    PubMed  Article  Google Scholar 

  9. 9.

    Akbar M, McLean M, Garcia-Melchor E, Crowe LA, McMillan P, Fazzi UG, et al. Fibroblast activation and inflammation in frozen shoulder. PLoS One. 2019;14(4):e0215301.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  10. 10.

    Hand GC, Athanasou NA, Matthews T, Carr AJ. The pathology of frozen shoulder. J Bone Joint Surg Br. 2007;89(7):928–32.

    CAS  PubMed  Article  Google Scholar 

  11. 11.

    Cucchi D, Marmotti A, De Giorgi S, Costa A, D’Apolito R, Conca M, et al. Risk Factors for Shoulder Stiffness: Current Concepts. Joints. 2017;5(4):217–23.

    PubMed  PubMed Central  Article  Google Scholar 

  12. 12.

    Fields BKK, Skalski MR, Patel DB, White EA, Tomasian A, Gross JS, et al. Adhesive capsulitis: review of imaging findings, pathophysiology, clinical presentation, and treatment options. Skeletal Radiol. 2019;48(8):1171–84.

    PubMed  Article  PubMed Central  Google Scholar 

  13. 13.

    Tzeng CY, Chiang HY, Huang CC, Lin WS, Hsiao TH, Lin CH. The impact of pre-existing shoulder diseases and traumatic injuries of the shoulder on adhesive capsulitis in adult population: A population-based nested case-control study. Medicine (Baltimore). 2019;98(39):e17204.

    Article  Google Scholar 

  14. 14.

    Yang S, Park DH, Ahn SH, Kim J, Lee JW, Han JY, et al. Prevalence and risk factors of adhesive capsulitis of the shoulder after breast cancer treatment. Support Care Cancer. 2017;25(4):1317–22.

    PubMed  Article  Google Scholar 

  15. 15.

    Milgrom C, Novack V, Weil Y, Jaber S, Radeva-Petrova DR, Finestone A. Risk factors for idiopathic frozen shoulder. Israel Med Assoc J. 2008;10(5):361–4.

    Google Scholar 

  16. 16.

    Li W, Lu N, Xu H, Wang H, Huang J. Case control study of risk factors for frozen shoulder in China. Int J Rheum Dis. 2015;18(5):508–13.

    PubMed  Article  Google Scholar 

  17. 17.

    Lo SF, Chu SW, Muo CH, Meng NH, Chou LW, Huang WC, et al. Diabetes mellitus and accompanying hyperlipidemia are independent risk factors for adhesive capsulitis: a nationwide population-based cohort study (version 2). Rheumatol Int. 2014;34(1):67–74.

    CAS  PubMed  Article  Google Scholar 

  18. 18.

    Huang SW, Lin JW, Wang WT, Wu CW, Liou TH, Lin HW. Hyperthyroidism is a risk factor for developing adhesive capsulitis of the shoulder: a nationwide longitudinal population-based study. Sci Rep. 2014;4:4183.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  19. 19.

    Schiefer M, Teixeira PFS, Fontenelle C, Carminatti T, Santos DA, Righi LD, et al. Prevalence of hypothyroidism in patients with frozen shoulder. J Shoulder Elbow Surg. 2017;26(1):49–55.

    PubMed  Article  Google Scholar 

  20. 20.

    Hsu KC, Sun CH, Wu YY, Chen LC, Wu YT, Chien WC. Increased risk of adhesive capsulitis among patients with gout: A nationwide population-based matched-cohort study. Int J Rheum Dis. 2018;21(9):1716–22.

    PubMed  Article  PubMed Central  Google Scholar 

  21. 21.

    Wang JY, Liaw CK, Huang CC, Liou TH, Lin HW, Huang SW. Hyperlipidemia Is a Risk Factor of Adhesive Capsulitis: Real-World Evidence Using the Taiwanese National Health Insurance Research Database. Orthop J Sports Med. 2021;9(4):2325967120986808.

    PubMed  PubMed Central  Article  Google Scholar 

  22. 22.

    Riley D, Lang AE, Blair RD, Birnbaum A, Reid B. Frozen shoulder and other shoulder disturbances in Parkinson’s disease. J Neurol Neurosurg Psychiatry. 1989;52(1):63–6.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  23. 23.

    Mattson RH, Cramer JA, McCutchen CB. Barbiturate-related connective tissue disorders. Arch Intern Med. 1989;149(4):911–4.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  24. 24.

    Baulac M, Cramer JA, Mattson RH. Pehnobarbital and Other Barbiturates: Adverse Effects. In: Levey RH, Mattson RH, Meldrum BS, Perucca E, editors. Antiepileptic Drugs. 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2002. p. 528–40.

    Google Scholar 

  25. 25.

    Janz D, Piltz U. Frozen Shoulder Induced by Primidone. In: Oxley J, editor. Antiepileptic Therapy: Chronic Toxicity of Antiepileptic Drugs. New York: Raven Press; 1983.

  26. 26.

    Freiss S, Lecocq J, Isner ME, Vautravers P. Frozen shoulder and fluoroquinones. Two case reports. Joint Bone Spine Rev Rhum. 2000;67(3):245–9.

    CAS  Google Scholar 

  27. 27.

    Lahner M, von Schulze PC, Teske W, Lichtinger TK, von Engelhardt LV, Daniilidis K, et al. Refractory adhesive capsulitis under acitretin therapy. Technol Health Care. 2013;21(3):265–9.

    PubMed  Article  PubMed Central  Google Scholar 

  28. 28.

    Florence E, Schrooten W, Verdonck K, Dreezen C, Colebunders R. Rheumatological complications associated with the use of indinavir and other protease inhibitors. Ann Rheum Dis. 2002;61(1):82–4.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  29. 29.

    Grasland A, Ziza JM, Raguin G, Pouchot J, Vinceneux P. Adhesive capsulitis of shoulder and treatment with protease inhibitors in patients with human immunodeficiency virus infection: report of 8 cases. J Rheumatol. 2000;27(11):2642–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Hutchinson JW, Tierney GM, Parsons SL, Davis TR. Dupuytren’s disease and frozen shoulder induced by treatment with a matrix metalloproteinase inhibitor. J Bone Joint Surg Br. 1998;80(5):907–8.

    CAS  PubMed  Article  Google Scholar 

  31. 31.

    Bannwarth B. Drug-induced musculoskeletal disorders. Drug Saf. 2007;30(1):27–46.

    CAS  PubMed  Article  Google Scholar 

  32. 32.

    Peterson CY, Krzyzaniak M, Coimbra R, Chang DC. Vagus nerve and postinjury inflammatory response. Arch Surg. 2012;147(1):76–80.

    PubMed  Article  Google Scholar 

  33. 33.

    Neviaser JS. Adhesive capsulitis of the shoulder: A study of the pathological findings in periarthris of the shoulder. J Bone Joint Surg Am Vol. 1945;27(2):211–22.

    Google Scholar 

  34. 34.

    Ascani C, Passaretti D, Scacchi M, Bullitta G, De Cupis M, Pasqualetto M, et al. Can Adhesive Capsulitis of the shoulder be a consequence of COVID-19? Case series of 12 patients. J Shoulder Elbow Surg. 2021;30(7):e409-413.

  35. 35.

    Centers for Disease Control and Prevention. National Diabetes Statistics Report, 2020. Atlanta: U.S. Dept of Health and Human Services; 2020.

  36. 36.

    Center for Medicare and Medicaid Services. Medicare Enrollment 2013. Available from:

  37. 37.

    Carbone S, Napoli A, Gumina S. MRI of adhesive capsulitis of the shoulder: distension of the bursa in the superior subscapularis recess is a suggestive sign of the pathology. Eur J Radiol. 2014;83(2):345–8.

    PubMed  Article  PubMed Central  Google Scholar 

  38. 38.

    Hwang KR, Murrell GA, Millar NL, Bonar F, Lam P, Walton JR. Advanced glycation end products in idiopathic frozen shoulders. J Shoulder Elbow Surg. 2016;25(6):981–8.

    PubMed  PubMed Central  Article  Google Scholar 

  39. 39.

    World Health Organization. ATC/DDD Index 2020. 2018.

  40. 40.

    Kury FSP, Baik SH, McDonald CJ. Analysis of Healthcare Cost and Utilization in the First Two Years of the Medicare Shared Savings Program Using Big Data from the CMS Enclave. AMIA Annu Symp Proc. 2016;2016:724–33.

    PubMed  Google Scholar 

  41. 41.

    Pinner RW, Teutsch SM, Simonsen L, Klug LA, Graber JM, Clarke MJ, et al. Trends in infectious diseases mortality in the United States. JAMA. 1996;275(3):189–93.

    CAS  PubMed  Article  Google Scholar 

  42. 42.

    Kempker JA, Magee MJ, Cegielski JP, Martin GS. Associations Between Vitamin D Level and Hospitalizations With and Without an Infection in a National Cohort of Medicare Beneficiaries. Am J Epidemiol. 2016;183(10):920–9.

    PubMed  PubMed Central  Article  Google Scholar 

  43. 43.

    Roffman CE, Buchanan J, Allison GT. Charlson Comorbidities Index. J Physiother. 2016;62(3):171.

    PubMed  Article  Google Scholar 

  44. 44.

    Charlson M, Pompei P, Ales K, Mac KC. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J Chronic Dis. 1987;40(5):373–83.

    CAS  PubMed  Article  Google Scholar 

  45. 45.

    Charlson M, Szatrowski T, Peterson J, Gold J. Validation of a combined comorbidity index. J Clin Epidemiol. 1994;47(11):1245–51.

    CAS  PubMed  Article  Google Scholar 

  46. 46.

    Ng TP, Feng L, Nyunt MS, Larbi A, Yap KB. Frailty in older persons: multisystem risk factors and the Frailty Risk Index (FRI). J Am Med Dir Assoc. 2014;15(9):635–42.

    PubMed  Article  Google Scholar 

  47. 47.

    Kuo CL, Duan Y, Grady J. Unconditional or Conditional Logistic Regression Model for Age-Matched Case-Control Data? Front Public Health. 2018;6:57.

    PubMed  PubMed Central  Article  Google Scholar 

  48. 48.

    Kaiser Family Foundation. Medicare Spending Per Enrollee, by State. State Health Facts. 2011.

  49. 49.

    Hannu T. Reactive arthritis. Best Pract Res Clin Rheumatol. 2011;25(3):347–57.

    PubMed  Article  Google Scholar 

  50. 50.

    Bidell MR, Lodise TP. Fluoroquinolone-Associated Tendinopathy: Does Levofloxacin Pose the Greatest Risk? Pharmacotherapy. 2016;36(6):679–93.

    PubMed  Article  PubMed Central  Google Scholar 

  51. 51.

    Godoy-Santos AL, Bruschini H, Cury J, Srougi M, de Cesar-Netto C, Fonseca LF, et al. Fluoroquinolones and the Risk of Achilles Tendon Disorders: Update on a Neglected Complication. Urology. 2018;113:20–5.

    PubMed  Article  PubMed Central  Google Scholar 

  52. 52.

    Hesse EM, Atanasoff S, Hibbs BF, Adegoke OJ, Ng C, Marquez P, et al. Shoulder Injury Related to Vaccine Administration (SIRVA): Petitioner claims to the National Vaccine Injury Compensation Program, 2010–2016. Vaccine. 2020;38(5):1076–83.

    PubMed  Article  PubMed Central  Google Scholar 

  53. 53.

    Hibbs BF, Ng CS, Museru O, Moro PL, Marquez P, Woo EJ, et al. Reports of atypical shoulder pain and dysfunction following inactivated influenza vaccine, Vaccine Adverse Event Reporting System (VAERS), 2010–2017. Vaccine. 2020;38(5):1137–43.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  54. 54.

    Prodromidis AD, Charalambous CP. Is There a Genetic Predisposition to Frozen Shoulder?: A Systematic Review and Meta-Analysis. JBJS Rev. 2016;4(2):

  55. 55.

    Kingston K, Curry EJ, Galvin JW, Li X. Shoulder adhesive capsulitis: epidemiology and predictors of surgery. J Shoulder Elbow Surg. 2018;27(8):1437–43.

    PubMed  Article  PubMed Central  Google Scholar 

  56. 56.

    Malavolta EA, Gracitelli MEC, Ribeiro Pinto GM, Freire da Silveira AZ, Assuncao JH, Ferreira Neto AA. Asian ethnicity: a risk factor for adhesive capsulitis? Rev Bras Ortop. 2018;53(5):602–6.

    PubMed  PubMed Central  Article  Google Scholar 

  57. 57.

    Saleh ZM, Faruqui S, Foad A. Onset of Frozen Shoulder Following Pneumococcal and Influenza Vaccinations. J Chiropr Med. 2015;14(4):285–9.

    PubMed  PubMed Central  Article  Google Scholar 

  58. 58.

    Arias LHM, Fadrique RS, Gil MS, Salgueiro-Vazquez ME. Risk of bursitis and other injuries and following vaccinations Spain dysfunctions of the shoulder. Vaccine. 2017;35(37):4870–6.

    Article  Google Scholar 

  59. 59.

    Center for Medicare and Medicaid Services. Transition of Part D Coverage of Benzodiazepines and Barbiturates Beginning in 2013: Department of Health and Human Services; 2012 [updated October 2 2012]. Available from:

  60. 60.

    Center for Medicare and Medicaid Services. Medicare Part D Drug Spending Dashboard & Data 2018. Available from:

  61. 61.

    Hannafin JA, Chiaia TA. Adhesive capsulitis. A treatment approach. Clin Orthop Relat Res. 2000;372:95–109.

    Article  Google Scholar 

Download references


Not applicable.


Anatomical Therapeutic Chemical (ATC)-4 A classification system developed by the World Health Organization to classify drugs by anatomical level, therapeutic level, and then chemical or pharmacological subgroups.

Medicare – Health coverage for disabled and adults over age 65 in the United States.

Original Medicare, Part A – Fee-for-service hospital insurance

Original Medicare, Part B – Fee-for-service medical insurance. Parts A and B cover approximately two-thirds of adults over age 65 in the year 2011 and this data was available for analysis.

Medicare Part D – A prescription drug coverage. Data were available for this analysis.

Medicare Advantage, Part C – A bundled plan managed by private companies, includes hospital and medical insurance and often part D prescription plans. Approximately one-third of adults over age 65 used Medicare Advantage in the year 2011. This data is not available for analysis.

CPT code – Current Procedural Terminology CPT® codes are uniform codes for medical, services produced by the American Medical Association and used for reporting and billing.

HCPCS code – Healthcare Common Procedure Coding System – based on the CPT codes, are codes for medical procedures, supplies, products and services for use in insurance billing.

ICD-9-CM: International Classification of Disease, Ninth Revision, Clinical Modification. A standard classification of diagnoses and procedures.


This work was supported by the South Carolina Translational Research in Musculoskeletal Health, SC TRIMH P20 GM121342. Publication support was provided by the Clemson University Open Access Publishing Fund.

Author information




Conceptualization, SMS, SBF, SP; design of statistical analysis, SMS, SBF, WB; statistical analysis, SBF; writing – original draft preparation, SMS, SBF; writing –review and editing, SMS, SBF, SP, WB; supervision, SMS, funding acquisition, SMS. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sara M. Sarasua.

Ethics declarations

Ethics approval and consent to participate

The study protocol Pro00088703 was reviewed by the Institutional Review Board for the University of South Carolina and was determined that the study met the “Not Human Research” criteria set forth by the Code of Federal Regulations 45 CFR 46.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Sarasua, S.M., Floyd, S., Bridges, W.C. et al. The epidemiology and etiology of adhesive capsulitis in the U.S. Medicare population. BMC Musculoskelet Disord 22, 828 (2021).

Download citation


  • Adhesive capsulitis
  • Frozen shoulder
  • Stiff shoulder
  • Risk factors
  • Epidemiology