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Case series investigates bone marrow suppression risk factors in rheumatoid arthritis patients, highlighting need for better monitoring.
This study investigated the clinical characteristics and risk factors of bone marrow suppression in rheumatoid arthritis (RA) patients treated with conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) to provide evidence for improving medication safety. We retrospectively analyzed clinical data from 30 RA inpatients with csDMARDs-induced bone marrow suppression hospitalized at the Affiliated Hospital of Zunyi Medical University between August 2022 and January 2025. Methotrexate was part of the treatment regimen for twenty-seven patients, accounting for 90% of the cohort. Medication non-adherence was identified in fifteen patients, representing 50% of cases, with unauthorized dose escalation being the primary pattern. All patients developed severe Grade III to IV bone marrow suppression. Pancytopenia was observed in twenty patients, constituting 66.7% of the total. Common complications included febrile neutropenia, oral mucositis, and gastrointestinal bleeding. Following comprehensive treatment, all patients achieved hematologic recovery and were discharged. Our findings indicate that medication non-adherence, particularly self-driven escalation of methotrexate dosage, is a critical risk factor for life-threatening bone marrow suppression in rheumatoid arthritis patients. These results underscore the necessity of enhanced patient education, strict adherence monitoring, and rigorous hematologic surveillance for high-risk individuals.
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Pan et al. (2026) studied this question.
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