Primary Sjögren's Syndrome: A Retrospective Cohort Study of Burden of Illness in Sweden.

INTRODUCTION: Primary Sjögren's syndrome (pSS) is an autoimmune disease that affects salivary and lachrymal glands and is associated with complex extraglandular manifestations. This study investigates the clinical and economic burden and disease course of pSS in Sweden.
METHODS: This retrospective cohort study utilizes data from Swedish national registries and consists of patients at least 18 years of age diagnosed in secondary care with pSS, and matched members of the Swedish general population. Healthcare resource utilization (HRU) and costs were compared. The clinical burden of pSS during follow-up was explored via year-on-year prevalence of and time-to-first extraglandular manifestation. Employment status and retirement rates were used to investigate the impact of pSS on productivity.
RESULTS: A total of 8884 patients with pSS and 88,233 general population comparators were included. Patients with pSS had significantly higher rates of HRU and higher healthcare costs than matched comparators, including twice as many outpatient visits. Costs were highest in year 1 post index before reducing in years 2 and 3 and stabilizing thereafter. Almost two-thirds of patients received their index diagnosis during an outpatient visit, and < 30% of diagnoses were from rheumatology departments. Overall, 41% of patients experienced a healthcare encounter that included a relevant extraglandular manifestation code during follow-up. Patients with pSS had significantly higher odds of early retirement than the general population at 5 years post index.
CONCLUSIONS: Patients with pSS experience a high clinical and economic disease burden in Sweden.

Key Summary Points

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Introduction

Primary Sjögren’s syndrome (pSS) is a heterogenous autoimmune disease characterized by lymphocytic infiltration of salivary and lachrymal glands [1, 2]. It predominantly affects females [1], with a reported prevalence of between 0.01 and 1.56% [3-5], and an incidence of between three and six cases per 100,000 people [6-10]. Unlike the secondary form of the disease, pSS occurs in the absence of other rheumatic diseases [11]. It has been estimated that 50% of patients with pSS experience extraglandular manifestations at diagnosis or during a mean follow-up period of 94 months; most commonly presenting as arthritis/arthralgia, but also as other systemic conditions, including Raynaud’s phenomenon, peripheral neuropathy, and some instances of interstitial lung disease [12-14]. More than a quarter of patients with pSS have been reported to develop malignancies, with 2.7–9.8% developing non-Hodgkin’s lymphoma [15], and irreversible organ damage has been observed to occur, primarily in the parotid glands and eyes [16, 17].

Regardless of organ involvement, patients with pSS experience impaired health-related quality of life to a similar degree as patients with rheumatoid arthritis or systemic lupus erythematosus (SLE) [18, 19]. In addition to dryness, patients with pSS experience significantly more severe pain and fatigue than the general population, resulting in reduced physical functioning, emotional well-being, social functioning, and cognitive impairment [18]. Fatigue is cited by patients as the most severe symptom and the one they most wish they could change [20, 21].

The heterogeneous presentations of patients with pSS can make the disease difficult to diagnose and treat. There are currently no available immunomodulatory therapies that have proven efficacy in targeting the underlying pathway(s) of pSS [22] with neither conventional standard nor biologic disease-modifying antirheumatic drugs demonstrating robust or substantial efficacy in large studies [11, 23–32].

Previous studies have revealed the high costs associated with a pSS diagnosis compared with healthy controls [33, 34]. Similar findings have been reported for Sjögren’s syndrome (SS), with or without the presence of other autoimmune conditions [35]. Patients with pSS have been estimated to have 1.6 times greater all-cause healthcare costs than patients without sicca syndrome, with these costs increasing even further for those with extraglandular manifestations [34]. These economic studies have focused on a follow-up duration of 6–24 months [33-35], and clinical studies do not provide insight to the health system burden over time. Data regarding the impact of pSS on productivity are currently limited to single academic cohorts [32, 36]. This retrospective study of administrative healthcare data aimed to increase understanding of the burden of illness over the > 10 years of follow-up, and disease course of pSS at a national level in Sweden amongst patients with pSS and matched pSS-free comparators.

Methods

Study Design

This retrospective cohort study was based on data from national registries in Sweden and consisted of patients diagnosed with pSS in secondary care plus members of the Swedish general population. The primary objective was to describe the characteristics of patients with pSS in Sweden and to investigate the associated economic burden to the healthcare system. Secondary objectives were to describe the clinical burden and employment status of patients with pSS in Sweden.

Data were collected for patients diagnosed with pSS between January 1, 2003 and December 31, 2014 (the inclusion period; Fig. 1). The index date was considered the date of diagnosis and patients were required to have 24 months of pre-index data. In addition, a 24-month pre-inclusion period (January 1, 2001 to December 31, 2002) was defined to apply the exclusion criteria and ensure that there were no prior diagnosis codes for pSS. The follow-up period lasted from the index date until emigration, death, or end of study (December 31, 2016), whichever occurred first. Patients with pSS were identified through the National Patient Register (NPR), with diagnoses based on the International Classification of Diseases, Tenth Revision (ICD-10) codes (Swedish version). Further patient data were extracted from the following national registers: National Prescribed Drug Register (NDR), Cause of Death Register (CDR), Swedish Cancer Registry (SCR), Dental Health Register (DHR), the longitudinal integration database for health insurance and labor market studies (LISA), and the Total Population Register (TPR).

Fig. 1

Study design. CDR Cause of Death Register, DHR Dental Health Register, ICD-10 International Classification of Diseases, Tenth Revision, LISA longitudinal integration database for health insurance and labor market studies, NDR National Prescribed Drug Register, NPR National Patient Register, pSS primary Sjögren’s syndrome, SCR Swedish Cancer Registry

For the general population cohort, each patient with pSS was matched with up to ten comparators on gender, age, and county of residence at index using data from the TPR. Exclusion criteria were not applied to the general population cohort. Patients included in the general population cohort who were diagnosed with pSS during the study period were censored.

Patients

Eligible patients were at least 18 years of age at the index date with either a confirmed diagnosis of ICD-10 M35.0 sicca syndrome (Sjögren’s; defined as an NPR record of M35.0 for at least two outpatient visits or at least one inpatient stay), or at least one record of ICD-10 M35.0A pSS during the inclusion period. Exclusion criteria included a diagnosis of ICD-10 M05/M06 RA, ICD-10 M32 SLE, or ICD-10 M34 systemic sclerosis up to 6 months after the index date or during the pre-index period, or of ICD-10 M35.0 sicca syndrome (Sjögren’s) during the pre-inclusion period; a record of ICD-10 M35.0B secondary SS at least once during the pre-index period; a recorded migration event in the pre-index period; and no record within TPR.

Diagnosis codes related to extraglandular manifestations were classified to the following domains based on the European League Against Rheumatism SS disease activity index (ESSDAI) [37]: constitutional, lymphadenopathy and lymphoma, articular, cutaneous, pulmonary, renal, muscular, peripheral nervous system, central nervous system, hematological, and biological, and identified by ICD-10 codes. Diagnoses in the ESSDAI glandular domain were similarly identified and reported.

Prevalence-based analyses on cost burden and healthcare resource utilization (HRU) included all patients with pSS with any index date who were in the cohort as of December 31, 2014. Incidence-based analyses were restricted to patients with pSS with an index date in 2009.

Economic Burden of pSS

Diagnosis-related group codes were used to estimate the cost per hospitalization, outpatient visit, and medical procedure reported in the NPR. All costs were adjusted to 2016 using the annual healthcare component of the Swedish Consumer Price Index. Descriptions of cost categories are detailed in the Supplementary Methods.

Mean (standard deviation [SD]) and median (interquartile range [IQR]) costs were calculated for patients with pSS and the general population comparators. Since costs were highly skewed, median (IQR) costs are presented. Wilcoxon signed-rank tests were used for statistical comparisons of per-patient median total cost burden between cohorts. For the incidence-based analyses, analysis of covariance (ANCOVA) was used to model total aggregate per-patient costs during follow-up, adjusted for age, gender, county of residence, and comorbidities at index.

Healthcare Resource Utilization

HRU was reported in terms of hospitalizations, outpatient visits, dental visits, and dental procedures. Mean (SD) and median (IQR) numbers of these healthcare interactions, and length of hospital stays were recorded. Prevalence-based analyses were used to compare HRU between cohorts. A Chi-square test was used for statistical comparisons of number of hospitalizations. T test and Wilcoxon signed-rank test were used for statistical comparisons of mean and median per-patient HRU between cohorts, respectively.

Clinical Burden Over Time

The excess mortality risk associated with pSS compared with the general population was assessed using Cox proportional hazards regression stratified on matched sets by the level of comorbidity burden. Low comorbidity burden was defined as a low Charlson Comorbidity Index (CCI) score (absence of Charlson comorbidity or a score of 0 or 1) during the pre-index period [38]. High comorbidity burden was defined as high CCI score (≥ 2) during the pre-index period. Descriptions of the disease manifestation analyses presented in the Supplementary Tables 1 and 2 are included in the Supplementary Methods.

Employment and Retirement Status Over Time

The distribution of unemployed and retired patients with pSS was described at index and at 1, 5, and 10 years after index. Conditional logistic regression was used to estimate the excess risks of unemployment and early retirement, respectively, at 5 years post index associated with pSS as compared with the general population. Descriptions of the odds ratio (OR) of unemployment and retirement analyses presented in Supplementary Table 3 is included in the Supplementary Methods.

Ethical Considerations

A copy of the study protocol and all protocol amendments (as needed) were submitted to the Ethical Review Board (ERB) in Stockholm for written approval. ERB approval was obtained before the data-extraction process was initiated. Individual informed consent was not required by Swedish law and no personally identifiable data were extracted. The study population was identified in the NPR by the National Board of Health and Welfare and in the TPR by Statistics Sweden. Personal identification numbers unique to each Swedish citizen or person registered in Sweden were used to link patient data between registers. Pseudonymized patient-level data were subsequently combined into one database and delivered to IQVIA for final creation of the study-specific database.

Results

Study Population

A total of 8884 patients with pSS and 88,233 general population comparators were included in the study. Both cohorts had a mean age at index of 63 years and were ~ 90% female. Pre-index characteristics and demographics for patients with pSS and the general population comparators are shown in Table 1. Absence of comorbidities was greater in the general population cohort compared with the pSS cohort (84 vs. 67%, respectively). Amongst CCI comorbidities, patients with pSS compared with the general population had higher relative frequencies of myocardial infarction (3.5 vs. 1.6%), congestive heart failure (3.7 vs. 1.9%), chronic pulmonary disease (8.6 vs. 2.7%), rheumatologic disease (5.7 vs. 1.7%), mild liver disease (2.3 vs. 0.4%), and malignancies (6.2 vs. 4.0%). Overall, 3.2% and 23.6% of patients with pSS had at least one diagnosis during the pre-index period within the glandular or extraglandular domain, respectively; the most common extraglandular diagnoses were in the articular (8.6%) and central nervous system (4.0%) domains (Table 1). In the pre-index period, patients with pSS also had a higher prevalence of malaise/fatigue and/or pain diagnosis codes compared with general population comparators (Table 1).

Table 1

Pre-index demographics and clinical characteristics among patients with pSS and general population comparators in the 2-year pre-index period

Characteristica	Patients with pSS (N = 8884)b	General population comparators (N = 88,233)
Age, years
Mean (SD)	62.8 (15.0)	62.9 (14.9)
Median (IQR)	63.9 (53.7–73.8)	64.0 (53.8–73.8)
Range	(18.0–99.1)	(18.0–99.7)
Gender, n (%)
Female	8033 (90.4)	79,776 (90.4)
CCI score, mean (SD)c	1.5 (1.5)	1.6 (1.7)
CCI score, n (%)c
0	631 (7.1)	3584 (4.1)
1	1055 (11.9)	3833 (4.3)
2	833 (9.4)	4847 (5.5)
3	217 (2.4)	820 (0.9)
4 +	189 (2.1)	1038 (1.2)
Absence of CC	5959 (67.1)	74,111 (84.0)
≥ 1 diagnosis within glandular domain,d n (%)	283 (3.2)	–
Lacrimal swelling	33 (0.4)	–
Submandibular swelling	22 (0.2)	–
Parotid swelling	233 (2.6)	–
≥ 1 diagnosis within extraglandular domain,d n (%)	2098 (23.6)	–
Constitutional domain	146 (1.6)	–
Lymphadenopathy domain	136 (1.5)	–
Articular domain	764 (8.6)	–
Cutaneous domain	164 (1.8)	–
Pulmonary domain	89 (1.0)	–
Renal domain	170 (1.9)	–
Muscular domain	24 (0.3)	–
Peripheral nervous system domain	200 (2.3)	–
Central nervous system domain	357 (4.0)	–
Hematological domain	296 (3.3)	–
Biological domain	42 (0.5)	–
Malaise/fatigue, n (%)	104 (1.2)	274 (0.3)
Pain, n (%)	1127 (12.7)	2988 (3.4)
Malaise/fatigue or pain, n (%)	1207 (13.6)	3225 (3.7)

CC complication or comorbidity, CCI Charlson Comorbidity Index, IQR interquartile range, pSS primary Sjögren’s syndrome, SD standard deviation

aAll characteristics assessed in the 2-year pre-index period (excluding the index date), unless otherwise indicated

bPercentages based on the total number of patients with pSS (any index date; N = 8884)

cThe CCI score was calculated for patients with at least one Charlson comorbidity present

dData for the general population comparators are not available

For the majority of the pSS cohort, the index diagnosis was recorded during an outpatient visit (n = 5784 [65.1%]; inpatient visit: n = 3100 [34.9%]). The proportion of index diagnoses received from rheumatology departments (n = 2441 [27.5%]) was higher than from ophthalmology (n = 1819 [20.5%]) and internal medicine (n = 1818 [20.5%]) departments. Additionally, almost one-third of index diagnoses occurred within 62 other medical departments (n = 2806 [31.6%]), including surgical (n = 517 [5.8%]), orthopedic (n = 478 [5.4%]), or ear, nose, and throat (n = 371 [4.2%]) departments.

Prevalent Cohort: Economic Burden of pSS and HRU in 2015

In 2015, patients with pSS in the prevalent cohort had significantly higher total costs and levels of HRU than the general population comparators (Table 2). Median per-patient drug costs for the pSS cohort were 3.3-fold higher than those of the general population. When broken down into drug categories of interest (identified based on treatment guidelines for pSS) [31, 39, 40], median costs of drugs providing symptomatic relief of dryness (e.g., eye drops of cyclosporin and pilocarpine) were higher in the pSS cohort than for the general population (Table 2). Fewer than 30% of patients in the pSS cohort were prescribed drugs in each of the other categories of interest and median costs were therefore low and not different between pSS and general population cohorts. Patients with pSS had a higher median rate of outpatient visits, dental visits, and dental procedures than the general population in 2015 (Table 2). However, 76% of patients with pSS and 85% of general population comparators were not hospitalized in 2015.

Table 2

Economic burden of pSS to the Swedish healthcare system and HRU in 2015 (prevalent cohort)a,b

	Patients with pSS and ≥ 1 dispensed prescriptions, n (%)	Per-patient median (IQR) cost, SEK
		Patients with pSS (N = 7396)	General population (N = 76,624)
Total cost	–	23,735 (9907–58,180)	8128 (2822–24,540)c
Hospitalization costs	–	0 (0–0)	0 (0–0)
Outpatient visit costs	–	7961 (2485–20,177)	2209 (0–8145)
Dental visit costs	–	1793 (0–3894)	1190 (0–2804)
Drug costs	–	5384 (2142–11,880)	1630 (400–4770)
Drugs of interestd	–	1082 (276–2685)	57 (0–475)
Biologic therapye	15 (0.2)	0 (0–0)	0 (0–0)
Antimalarials, corticosteroids, and immunosuppressantsf	2135 (28.9)	0 (0–97)	0 (0–0)
Symptomatic relief of drynessg	4386 (59.3)	165 (0–932)	0 (0–0)
Topical fluoride and chlorhexidine	1550 (21.0)	0 (0–0)	0 (0–0)

HRU healthcare resource utilization, IQR interquartile range, pSS primary Sjögren’s syndrome, SD standard deviation, SEK Swedish Krona

aBased on patients/individuals (any index date) in the cohort on December 31, 2014

bHRU reported as number of healthcare interactions unless otherwise indicated

cp < 0.0001

dBased on the European League Against Rheumatism (EULAR) and Sjögren's Foundation guidelines, and supplemented with the AECG guidelines for procedures of interest [31, 39, 40]

eRituximab, belimumab, abatacept, tocilizumab

fHydroxychloroquine, methotrexate, corticosteroids, azathioprine, cyclosporine, leflunomide, sulfasalazine

gArtificial tears (e.g., sodium hyaluronate, hypromellose), cyclosporin (ophthalmic), pilocarpine, cevimeline, topical autologous serum, methylcellulose inserts, minocycline (oral), doxycycline (oral), artificial saliva

Incident Cohort: Economic Burden of pSS Over Time

Although the mean follow-up time was similar between cohorts, the total costs to the healthcare system and the cost of hospitalizations during the follow-up period for patients diagnosed with pSS in 2009 (incident cohort) were more than double those of the general population comparators (Table 3). Hospitalizations represented most of the costs each year post index. The highest total and hospitalization costs were observed in year 1 before reducing in years 2 and 3, and remaining relatively stable thereafter. Patients with pSS had significantly higher total aggregate per-patient costs over the follow-up period when compared with the general population comparators (F = 26.50; p < 0.0001) according to adjusted ANCOVA analysis. The median costs of all drugs and drugs of interest were higher in the pSS cohort compared with the general population cohort (Table 3). Additionally, the median costs of drugs for symptomatic relief were higher than the costs of all other drug categories of interest (including antimalarials, corticosteroids, and immunosuppressants) both in year 1 and in total in patients with pSS.

Table 3

Economic burden of pSS to the healthcare system during the follow-up period among patients with pSS diagnosed in 2009 (incident cohort), by cost categories

	Per-patient median (IQR), SEK
	Patients with pSS (N = 692)			General population (N = 6859)
Mean time of follow-up, years (SD)	6.6 (2.0)			6.9 (1.7)
	Year 1	Total		Total
Total cost	38,781 (17,290–80,161)	245,556 (136,586–420,567)		99,408 (42,648–216,084)a
Hospitalizations	13,674 (0–48,026)	86,003 (17,430–204,149)		23,379 (0–102,373)
Outpatient visits	8101 (3052–16,166)	61,112 (29,967–110,956)		21,795 (7049–49,741)
Dental visits	937 (0–2408)	14,872 (4707–30,055)		11,605 (3299–23,018)
Drugs (all)	6550 (2802–14,090)	41,662 (19,453–86,637)		13,702 (4156–35,902)
Drugs of interestb	1406 (444–2961)	9290 (2917–17,948)		788 (125–3413)
Biologic therapyc	0 (0–0)	0 (0–0)		0 (0–0)
Antimalarials, corticosteroids, and immunosuppressantsd	0 (0–111)	70 (0–783)		0 (0–59)
Symptomatic relief of drynesse	400 (0–1239)		1946 (352–7672)	0 (0–120)
Topical fluoride and chlorhexidine	0 (0–24)		0 (0–335)	0 (0–0)

IQR interquartile range, pSS primary Sjögren’s syndrome, SD standard deviation, SEK Swedish Krona

ap < 0.0001

bBased on the European League Against Rheumatism (EULAR) and Sjögren's Foundation guidelines, and supplemented with the AECG guidelines for procedures of interest [31, 39, 40]

cRituximab, belimumab, abatacept, tocilizumab

dHydroxychloroquine, methotrexate, corticosteroids, azathioprine, cyclosporine, leflunomide, sulfasalazine

eArtificial tears (e.g., sodium hyaluronate, hypromellose), cyclosporin (ophthalmic), pilocarpine, cevimeline, topical autologous serum, methylcellulose inserts, minocycline (oral), doxycycline (oral), artificial saliva

Overall, 40.7% of patients with pSS had at least one recorded extraglandular domain manifestation during follow-up (Table S1). The proportion of patients with a recorded extraglandular manifestation decreased year-on-year throughout the entire follow-up period, with 0 events reported in year 10. At 5 years post index, the proportion of patients that had received a diagnosis of any extraglandular manifestation was 0.314; the articular (0.098), hematological (0.069), and central nervous system (0.064) domains had the highest cumulative incidence (Table S2).

Among those with low comorbidity burden, patients with pSS had a small (12%) but significantly greater risk of mortality than the general population comparators (hazard ratio [HR; 95% confidence interval, CI]: 1.12 [1.05–1.19]) (Table 4). In those with a high comorbidity burden, no excess risk of mortality was observed among patients with pSS compared with the general population comparators (HR [95% CI]: 0.92 [0.84–1.00]).

Table 4

Median survival and risk of death among patients with pSS compared with the general population among those with low and high comorbidity burdena

	At risk	Events	Median survival, years (95% CI)	HR (95% CI)b
Low comorbidity burdenc
General population comparators	81,652	11,515	NA	1 (reference)
Patients with pSS	7677	1173	NA	1.12 (1.05–1.19)
High comorbidity burdend
General population comparators	6581	3206	7.20 (6.92–7.53)	1 (reference)
Patients with pSS	1207	562	8.20 (7.41–8.80)	0.92 (0.84–1.00)

CCI Charlson Comorbidity Index, CI confidence interval, HR hazard ratio, IQR interquartile range, pSS primary Sjögren’s syndrome

aBased on patients/individuals with any index date (N, patients with pSS = 8884; N, general population comparators = 88,233)

bBy design of matching, HR adjusted for age, gender, and county of residence at index

cLow comorbidity burden defined as low CCI score (absence of Charlson comorbidity or CCI score 0–1) during the pre-index period

dHigh comorbidity burden defined as high CCI score (≥ 2) during the pre-index period

Impact of pSS on Productivity

At index, 11% of patients with pSS who had not already taken normal retirement were unemployed; this proportion declined over the following decade but remained at least double that of the general population (Fig. 2). The OR of unemployment within the pSS cohort was 0.91 (95% CI 0.61–1.34) compared with the general population at 5 years after index (Table S3). At index, 23.4% of patients with pSS and 12.1% of the general population had taken early retirement, while 46.4% and 47.3% had retired at or after the retirement age in Sweden (65 years of age [41]), respectively. Over the following decade, rates of early retirement were much greater in the pSS cohort than the general population, with 51.6% of patients with pSS retiring early at 10 years post index versus 1.8% in the general population. The OR of early retirement in the pSS cohort was 4.06 (95% CI 3.24–5.09) compared with the general population at 5 years after index (Table S3).

Fig. 2

Employment (a) and retirement (b) status at and over time after index among patients with pSS and general population comparators. pSS primary Sjögren’s syndrome. Unless otherwise indicated, percentages are based on the cohort at risk at each time point for assessment (i.e., excluding from the denominator the number of patients who had retired [old-age pension] or had been censored due to death, emigration, or end of study). Normal retirement was defined as having drawn an old-age pension in the calendar year of turning 65 years of age or older

Discussion

This retrospective study investigated the burden of pSS on the Swedish healthcare system using administrative healthcare data. It was found that patients with pSS have greater per-person healthcare costs and HRU than the general population and are at a greater risk of early retirement. Although most patients in both cohorts had no hospitalizations in 2015, the cost per patient per hospitalization was greater for patients with pSS. Similarly, patients with pSS had greater drug costs relating to symptomatic relief of dryness than general population comparators. Patients with pSS also had greater drug costs for symptomatic relief of dryness compared with the costs for other drug categories of interest both in year 1 and in total.

These results are consistent with previous studies into the socioeconomic burden of pSS on patients. Mandl et al. investigated rates of work disability in Sweden and found that patients with pSS have more than double the risk of sick leave or work disability 2 years after diagnosis when compared with the general population [36]. Higher levels of HRU amongst patients with pSS than the general population have also been reported [42]. A previous study in a Dutch SS population found a significantly lower employment rate compared with the general population [32]; however, we found that patients with pSS have similar odds of employment to the general population in Sweden. This suggests that the impact of pSS on work productivity in Sweden may be a result of early retirement rather than unemployment.

Patients with pSS most commonly received their index diagnosis through rheumatology, ophthalmology, and internal medicine departments. However, index diagnoses were reported for some patients in a wide range of different departments. These data indicate that the selection criteria were sensitive, despite attempts to improve selectivity. These findings also suggest that the first record of pSS in the secondary care system is the first encounter of a patient already diagnosed in primary care. Therefore, the variety of medical specialties reflects the heterogeneity of manifestations and comorbidities requiring attention in this population.

Patients with pSS experience an increase in extraglandular manifestations after diagnosis [43], highlighting the high clinical burden of the disease. In this study, the 5-year cumulative incidence of extraglandular manifestations (0.314) suggests that patients with pSS receive a diagnosis of manifestations early. This is supported by previous studies that show high healthcare costs shortly after diagnosis [33-35]. These findings indicate that few patients receive treatment for pSS within specialized care in Sweden, highlighting an unmet clinical need. In this study, patients had the highest healthcare costs in the first year after diagnosis, with these costs decreasing and stabilizing over the following 7 years. This may be due to intensive treatment efforts shortly after diagnosis, followed by stabilized treatment regimens that do not appear to reduce the disease burden, as healthcare costs do not decrease year-on-year. Decreasing healthcare costs over time could be expected to occur following the control of a patient’s disease activity with adequate therapies. However, due to the lack of effective licensed treatments for pSS, it is more likely that patients simply learn to endure their symptoms. The high levels of healthcare costs after diagnosis are consistent with those seen in a previous US study, which reported that SS is associated with 40% increased all-cause healthcare costs in the first year after diagnosis compared with the year before [35].

This study is not without limitations. Patients had a higher mean age than would be typically expected of a pSS population [42], suggesting that there may be some false–positive individuals within the population who do not truly have pSS. As with many retrospective cohort studies, patient diagnoses were based on codes within a national administrative register, meaning that there is a risk that some patients were misclassified or had other diagnoses than those described here. However, this may instead be a result of patients with pSS entering secondary care later in the disease pathway, which would mean that the burden of the disease is underestimated in this study. Similarly, the study population may be more severe than the general pSS population, as patients treated within a primary care setting were not included and would be likely to have less severe symptoms than those treated in secondary care. In addition, although relevant codes do exist for many key pSS manifestations (such as peripheral neuropathy and pulmonary interstitial fibrosis), some symptoms of pSS (including vaginal dryness) could not be analyzed, as there is no relevant ICD-10 code. In the present study, only ~ 40% of the cohort had manifestations captured by the ESSDAI domains. While, in part, this may be due to miscoding or a lack of specific diagnosis codes, it likely reflects that the most bothersome aspects of pSS (i.e., pain, dryness, and fatigue) are not well captured in secondary data sources. This is supported by the low pre-index prevalence of malaise/fatigue and/or pain in patients with pSS. Despite being reported as the most bothersome symptom of pSS [20, 21], only 1.2% of patients with pSS had a recorded diagnosis for malaise/fatigue in the pre-index period. However, the diagnosis code for malaise/fatigue had limited utility since further clinical data and laboratory data are not captured in the Swedish national patient register. Nonetheless, the data in this study reflect the total cost of this population to the secondary healthcare system, and the overall burden will incorporate all disease-related burdens regardless of whether a specific symptom can be identified. Furthermore, not all procedures may have been coded within the registries used. In particular, manifestations for which there are no specific reimbursable treatments, such as fatigue or glandular swelling, may not have been coded. Fatigue and depression in patients with pSS can contribute to a greater individual and societal burden than the classical ocular and oral symptoms of the disease [42], and therefore are likely to increase further the clinical and healthcare burden in patients with pSS. Given that some manifestations of pSS could also be captured by the CCI, general population cohorts were not matched based on this characteristic. This could be another limitation of the analysis, as the pSS cohort has a greater degree of comorbidities. However, since it is unknown whether these comorbidities are related to this diagnosis, the objective of this study was to capture all the excess burden in patients with pSS.

Further research is needed to validate the ICD-10 codes used to identify pSS and to more clearly identify which aspects of HRU might be influenced by future treatments options and unmet medical needs. In the Swedish setting, this could be achieved by combining these national register data with patient-level data reported in electronic medical records, as well as through linkage to specific pSS clinical registries. Also, it would be of interest to compare use of topical drugs in patients with pSS with patients without pSS but experiencing sicca symptoms, in order to establish the contribution of such treatments to the higher HRU in patients with pSS. This comparison could not be reliably made in the current study; it is likely that ICD-10 codes such as ‘dryness of mouth’ were underreported, since only 3.8% of the pSS cohort had a record of this diagnosis code in the 2-year pre-index period (data not shown), despite this being a cardinal symptom.

Conclusions

This retrospective study reveals the substantial economic and clinical burden associated with pSS in Sweden. Novel treatments that can alleviate the burden associated with pSS would likely be welcomed by patients and healthcare professionals alike.

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 25 KB)

Why carry out this study?

Currently, limited data are available regarding the impact of primary Sjögren’s syndrome (pSS) on productivity and gaps in the literature remain for additional contemporary evidence to describe the burden of pSS from a healthcare perspective over time.

This study aimed to investigate the long-term clinical and economic burden of pSS across the entire Swedish population and to describe the disease course (including the development of extraglandular manifestations) and the impact on productivity.

What was learned from the study?

This study found that patients with pSS experience a high clinical burden in Sweden, where more than 40% of patients with pSS had at least one extraglandular manifestation during the > 10-year follow-up period.

Patients with pSS had higher healthcare resource utilization and costs and had four times greater odds of retiring early than the general population.

While not all patients with pSS experience extraglandular involvement, there exists a high economic burden of disease including a substantial cost of drugs prescribed for symptomatic management but without disease-modifying effect.