Steen V D, Blair S, Medsger T A
Ann Intern Med. 1986 May;104(5):699-705. doi: 10.7326/0003-4819-104-5-699.
We studied D-penicillamine toxicity in 259 patients with systemic sclerosis treated since 1972. The average daily dose of 635 mg was given for a mean of 1.8 years. Of patients with systemic sclerosis, 47% has side effects from D-penicillamine treatment, similar to the 56% of 807 patients with rheumatoid arthritis in seven separate series. Individual manifestations of toxicity included rash, proteinuria, gastrointestinal symptoms, dysgeusia, oral ulcers, thrombocytopenia, and neutropenia. Four episodes each of myasthenia gravis and pemphigus occurred in our patients; both were reported rarely in patients with rheumatoid arthritis. Adverse effects occurred more frequently after rapid increases in dosage. Treatment had to be discontinued due to toxicity in 29% of patients with systemic sclerosis and in 33% of those with rheumatoid arthritis. Although toxic, with a high frequency of adverse effects, D-penicillamine can be used safely in the treatment of systemic sclerosis. Pemphigus and myasthenia gravis may occur more frequently with therapy for systemic sclerosis than with that for rheumatoid arthritis.
我们研究了自1972年以来接受治疗的259例系统性硬化症患者的青霉胺毒性。平均每日剂量为635毫克,平均用药1.8年。系统性硬化症患者中,47%出现了青霉胺治疗的副作用,这与7个独立系列中807例类风湿关节炎患者的56%相似。毒性的个体表现包括皮疹、蛋白尿、胃肠道症状、味觉障碍、口腔溃疡、血小板减少和中性粒细胞减少。我们的患者中各发生了4例重症肌无力和天疱疮;在类风湿关节炎患者中这些情况均鲜有报道。剂量快速增加后不良反应更频繁发生。29%的系统性硬化症患者和33%的类风湿关节炎患者因毒性不得不停药。尽管有毒性且不良反应发生率高,但青霉胺可安全用于系统性硬化症的治疗。与类风湿关节炎治疗相比,系统性硬化症治疗可能更频繁地发生天疱疮和重症肌无力。