Singapore Chapter of Rheumatologists Consensus Statement on the Eligibility for Government Subsidy of Biologic Disease Modifying Antirheumatic Agents for Treatment of Rheumatoid Arthritis (RA)

Author:

Teng Gim Gee1,Cheung Peter P1,Lahiri Manjari1,Clayton Jane A2,Chew Li Ching3,Koh Ee Tzun4,Koh Wei Howe5,Lau Tang Ching1,Ng Swee Cheng3,Thong Bernard Y4,Vasudevan Archana R5,Yoong Jon KC3,Leong Keng Hong6

Affiliation:

1. University Medicine Cluster, National University Health System, Singapore

2. Alexandra Hospital (Jurong Health), Singapore

3. Singapore General Hospital, Singapore

4. Tan Tock Seng Hospital, Singapore

5. Koh Wei Howe Arthritis & Rheumatism Medical Clinic, Mount Elizabeth Medical Centre, Singapore

6. Leong Keng Hong Arthritis and Medical Clinic, Gleneagles Medical Centre, Singapore

Abstract

Introduction: Up to 30% of patients with rheumatoid arthritis (RA) respond inadequately to conventional non-biologic disease modifying antirheumatic drugs (nbDMARDs), and may benefit from therapy with biologic DMARDs (bDMARDs). However, the high cost of bDMARDs limits their widespread use. The Chapter of Rheumatologists, College of Physicians, Academy of Medicine, Singapore aims to define clinical eligibility for government-assisted funding of bDMARDs for local RA patients. Materials and Methods: Evidence synthesis was performed by reviewing 7 published guidelines on use of biologics for RA. Using the modified RAND/UCLA Appropriateness Method (RAM), rheumatologists rated indications for therapies for different clinical scenarios. Points reflecting the output from the formal group consensus were used to formulate the practice recommendations. Results: Ten recommendations including diagnosis of RA, choice of disease activity measure, initiation and continuation of bDMARD and option of first and second-line therapies were formulated. The panellists agreed that a bDMARD is indicated if a patient has (1) active RA with a Disease Activity Score in 28 joints (DAS28) score of ≥3.2, (2) a minimum of 6 swollen and tender joints, and (3) has failed a minimum of 2 nbDMARD combinations of adequate dose regimen for at least 3 months each. To qualify for continued biologic therapy, a patient must have (1) documentation of DAS28 every 3 months and (2) at least a European League Against Rheumatism (EULAR) moderate response by 6 months after commencement of therapy. Conclusion: The recommendations developed by a formal group consensus method may be useful for clinical practice and guiding funding decisions by relevant authorities in making bDMARDs usage accessible and equitable to eligible patients in Singapore. Key words: Drug therapy, Funding, Management, Practice Guidelines

Publisher

Academy of Medicine, Singapore

Subject

General Medicine

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