Marabani M, Madhok R, Capell H A, Hunter J A
Centre for Rheumatic Diseases, Glasgow Royal Infirmary.
Ann Rheum Dis. 1989 Jun;48(6):505-7. doi: 10.1136/ard.48.6.505.
Leucopenia appears to be a more frequent complication of sulphasalazine treatment in rheumatoid arthritis than in inflammatory bowel disease and poses a management problem. In this study leucopenia was found in 20 patients, 14 of whom were participating in prospective studies (252 patients), giving an incidence of 5.6%. Treatment had to be discontinued in half of these patients. Most (14) episodes of leucopenia occurred early in treatment (less than 24 weeks) but some occurred late and sustained monitoring seems necessary. No predictive factors for leucopenia were elucidated. All patients recovered fully with dose adjustment or, in more severe cases, after withdrawal of sulphasalazine and appropriate supportive therapy. The incidence of leucopenia may be higher in Glasgow than in other units in Britain.
白细胞减少症似乎是类风湿性关节炎患者使用柳氮磺胺吡啶治疗时比炎性肠病更常见的并发症,并且带来了治疗管理上的问题。在本研究中,20名患者出现白细胞减少症,其中14名参与了前瞻性研究(共252名患者),发生率为5.6%。这些患者中有一半不得不停止治疗。大多数(14例)白细胞减少症发作发生在治疗早期(少于24周),但也有一些发生在后期,因此似乎有必要进行持续监测。未阐明白细胞减少症的预测因素。所有患者通过调整剂量或在更严重的情况下停用柳氮磺胺吡啶并给予适当的支持性治疗后均完全康复。格拉斯哥的白细胞减少症发生率可能高于英国其他医疗机构。