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High Burden and Phenotype-Specific Variability of Pain Polypharmacy in Early Autoimmune Rheumatic Diseases: A 15-Year
Di Lu1, Kristen Cunanan1, James Cragun1
1Stanford University School of Medicine.
Pain medication use is high for autoimmune rheumatic diseases (ARDs) patients, with many using multiple drugs even early after diagnosis. This burden varies by specific ARD and chronic overlapping pain conditions (COPCs), highlighting a need for better pain management strategies.
Area of Science:
- Rheumatology
- Pain Management
- Pharmacology
Background:
- Pain significantly impacts disability and medication use in autoimmune rheumatic diseases (ARDs), irrespective of inflammation control.
- The prevalence of pain-related polypharmacy in ARDs, especially when co-occurring with chronic overlapping pain conditions (COPCs), is not well understood.
Purpose of the Study:
- To quantify the initial pain medication burden in the first year following an ARD diagnosis.
- To investigate how this medication burden varies based on specific ARD, presence of COPCs, and over time.
Main Methods:
- Utilized the Merative MarketScan Commercial Claims database (2008-2021).
- Identified adults with new diagnoses of rheumatoid arthritis, systemic lupus erythematosus, ankylosing spondylitis, psoriatic arthritis, Sjögren's disease, or systemic sclerosis.
- Analyzed pain medication use across ten categories in the first year post-diagnosis, assessing polypharmacy using distinct medication counts, category counts, and thresholds (≥5, ≥10 medications).
Main Results:
- Of 149,742 ARD patients, 57.6% had a COPC.
- The mean number of distinct pain medications filled in the first year was 9.0.
- 47.9% of patients used ≥5 pain medications, and 30.5% used ≥10.
- Ankylosing spondylitis showed the highest burden (mean 11.6 medications).
- Fibromyalgia patients had higher medication burden across ARDs and were the only COPC group with increased prescribing post-2015.
- Overall medication burden increased from 2008 to 2014-2015 before declining, but remained high.
Conclusions:
- Pain-related polypharmacy is prevalent early in ARD diagnoses and is influenced by disease type and pain phenotype.
- Despite recent modest decreases, the high medication burden necessitates phenotype-specific, non-pharmacologic, and deprescribing approaches in rheumatology care.
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