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SAT0219 (2020)
PATIENT CHARACTERISTICS, TREATMENT PATTERNS, AND RESOURCE UTILIZATION OF SJOGREN’S SYNDROME PATIENTS IN A LARGE US HEALTH NETWORK
P. J. Mease1, J. Zhuo2, R. Weerasinghe3, Q. Xia2, C. Samal4, N. Sharma4
1Swedish Medical Center/Providence St. Joseph Health, Seattle, United States of America
2Bristol-Myers Squibb, Lawrenceville, United States of America
3Providence St. Joseph Health, Renton, United States of America
4Mu-Sigma, Bangalore, India

Background: Sjogren’s syndrome (SS) is a chronic progressive autoimmune disorder which occurs as primary (pSS) or secondary SS (sSS). With no approved disease modifying therapy, there is limited information on the treatment patterns and resource utilization among these patients (pts).


Objectives: To describe pts characteristics, treatment patterns and healthcare resource utilization (HCRU) using electronic health records (EHR) of pts with pSS and sSS treated at the Providence St. Josephs Health system (PSJH).


Methods: Pts ≥18 years of age with at least one clinical encounter with ICD-9-CM or ICD-10-CM diagnosis of SS, between Jan 2013 and Mar 2019 were included. Date of first encounter with SS diagnosis (index date) was used to assess pts demographics. Pt baseline comorbidities were evaluated during the 24 months pre-index period. Treatment patterns and HCRU were assessed during the 12 months post-index follow-up. Descriptive statistics were used to describe pts’ demographic and clinical characteristics, and medications use in the baseline and follow up.


Results: Study cohort included 9,108 SS pts of which 76.5% had sSS diagnosis on index date. Majority of SS pts were women, Caucasian, with mean age of 58.3 yrs, and from western states in the US ( Table 1 ). Endocrine conditions including hypo- and hyperthyroidism, and diabetes was the most common (45.5%) comorbidity at baseline, followed by rheumatologic disorders (25.6%) and neurological conditions (22.2%). Among patients with treatment information (4088, 44.88%), 42.95% were using symptomatic treatments for dry eye and mouth at baseline ( Table 1 ). In the follow-up, SS pts had average 5.8 healthcare visits per patient per year (PPPY), including 0.6 inpatient and 3.4 outpatient visit respectively. About 40% of the SS pts (53.8% pSS and 35.8% sSS) were diagnosed by rheumatologists. Majority of the SS pts initiated treatment with cDMARDs (82%) and remained on the same treatment during 1 year follow-up ( Fig 2 ).

Baseline Demographic and Clinical Pts Characteristics

SS Pts (n=9,108 )
Demographics
Age (years) on index date, mean (SD) 58.3 (15.1)
Female, n (%) 8,338 (91.6)
Caucasian, n (%) 6.936 (76.2)
Western Region, n (%) 8,998 (98.8)
Married, n (%) 5,164 (56.7)
Never Smoked, n (%) 4,847 (53.2)
Primary diagnosis, n (%) 2,137 (23.5)
Comorbidities, n (% )
Cardiovascular 1,408 (17.2)
Endocrine 3,733 (45.5)
Oncology 800 (9.8)
Blood disorders 1,221 (14.9)
Pulmonary 1,802 (22.0)
Neurological 1,821 (22.2)
Liver/Kidney 1,782 (21.7)
Rheumatologic disorders 2,096 (25.6)
Autoimmune/ Immune related 1,527 (18.6)
Baseline Medications, n (% )
Symptomatic 1 1,756 (43.0)
NSAIDs 2 1,578 (38.6)
cDMARDs 3 1,435 (35.1)
Corticosteroid 4 1,393 (34.1)
bDMARDs 5 266 (6.5)

1 cevimeline, pilocarpine hydrochloride, ophthalmic insert etc; 2 aspirin, ibuprofen, naproxen; 3 methotrexate, hydroxychloroquine, sulfasalazine, leflunomide, myophenolate mofetil, azathioprine; 4 prednisone; 5 sarilumab, belimumab, ustekinumab, infliximab, adalimumab, certolizumab pegol, golimumab, etanercept, abatacept, tocilizumab, rituximab, tofacitinib, baricitinib

HCRU for pSS and sSS Pts

Treatment Sequencing for pSS and sSS Pts. Note: Discontinued: pts who discontinued and didn’t advance to any therapy; same treatment: pts continued on index treatment till we have information.


Conclusion: Observation of higher comorbidities suggests substantial burden of SS pts on healthcare system, with majority of pts being diagnosed outside of rheumatology offices.


Acknowledgments : We acknowledge the contributions of Manasi Suryavanshi towards drafting and reviewing the abstract.


Disclosure of Interests: Philip J Mease Grant/research support from: Abbott, Amgen, Biogen Idec, BMS, Celgene Corporation, Eli Lilly, Novartis, Pfizer, Sun Pharmaceutical, UCB – grant/research support, Consultant of: Abbott, Amgen, Biogen Idec, BMS, Celgene Corporation, Eli Lilly, Novartis, Pfizer, Sun Pharmaceutical, UCB – consultant, Speakers bureau: Abbott, Amgen, Biogen Idec, BMS, Eli Lilly, Genentech, Janssen, Pfizer, UCB – speakers bureau, Joe Zhuo Shareholder of: Bristol-Myers Squibb, Employee of: Bristol-Myers Squibb, Roshanthi Weerasinghe Grant/research support from:., Qian Xia Shareholder of: I own shares of Bristol-Myers Squibb Company, Employee of: I am a paid employee of Bristol-Myers Squibb Company, Chidananda Samal Consultant of: I work as a consultant for Bristol-Myers Squibb Company, Niyati Sharma Consultant of: I work as a consultant for Bristol-Myers Squibb Company


Citation: Ann Rheum Dis, volume 79, supplement 1, year 2020, page 1048
Session: SLE, Sjön’s and APS - clinical aspects (other than treatment) (Poster Presentations)