Match each clinical scenario describing a medication adverse effect or monitoring requirement in a patient with a rheumatologic condition to the most likely responsible pharmacologic agent.
- A 55-year-old woman with rheumatoid arthritis develops sudden, severe abdominal pain. Imaging reveals free intraperitoneal air indicating bowel perforation. She recently started a new biologic disease-modifying antirheumatic drug.Tocilizumab
- A 32-year-old woman with severe lupus nephritis presents with painless gross hematuria. She has been receiving monthly intravenous infusions for her lupus. Cystoscopy reveals a bladder neoplasm.Cyclophosphamide
- A 45-year-old man with ankylosing spondylitis develops a new-onset photosensitive malar rash, pleuritis, and positive anti-histone antibodies six months after starting a biologic therapy.Infliximab
- A 29-year-old woman with rheumatoid arthritis desires pregnancy. She is currently taking a non-biologic DMARD that requires an accelerated elimination procedure with cholestyramine prior to conception.Leflunomide
- A 38-year-old woman with systemic lupus erythematosus presents for her annual ophthalmologic screening, which includes spectral-domain optical coherence tomography to evaluate for maculopathy.Hydroxychloroquine
Cevap
The scenarios match with Tocilizumab (bowel perforation), Cyclophosphamide (bladder neoplasm), Infliximab (drug-induced lupus), Leflunomide (cholestyramine washout), and Hydroxychloroquine (maculopathy screening).
Each rheumatologic medication carries a distinct side effect and monitoring profile. Tocilizumab (IL-6 inhibitor) increases the risk of bowel perforation. Cyclophosphamide causes urothelial toxicity (hemorrhagic cystitis, bladder cancer) via its metabolite acrolein. Infliximab (TNF-alpha inhibitor) is classically associated with drug-induced lupus. Leflunomide is teratogenic and undergoes enterohepatic circulation, requiring cholestyramine for rapid clearance. Hydroxychloroquine causes retinal toxicity requiring rigorous OCT or visual field screening.
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Anahtar Kavram
Adverse effects and screening requirements of rheumatologic pharmacotherapy