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羟氯喹治疗前风湿性疾病患者葡萄糖-6-磷酸脱氢酶水平筛查相关性研究

A Study on the Relevance of Glucose-6-Phosphate Dehydrogenase Level Screening in Patients with Rheumatic Diseases Prior to Initiating Treatment With Hydroxychloroquine.

作者信息

Abramova Irina, Park Kyle, Hosny Carol, Tuladhar Swosty, Yao QingPing, Patnaik Asha

机构信息

Division of Rheumatology, Department of Internal Medicine, Stony Brook University, Stony Brook, USA.

Department of Internal Medicine, Stony Brook University, Stony Brook, USA.

出版信息

Cureus. 2020 Aug 2;12(8):e9519. doi: 10.7759/cureus.9519.

Abstract

Objective Drug-induced hemolytic anemia can occur in patients with glucose-6-phosphate-dehydrogenase (G6PD) deficiency. The practice of G6PD-deficiency screening in the rheumatology field has been inconsistent. This study aimed to determine the utility of screening prior to the initiation of hydroxychloroquine and/or sulfasalazine in rheumatology patients in the ambulatory clinics at Stony Brook University Hospital, New York. Methods We conducted a retrospective chart review of cases of rheumatic diseases that were screened for G6PD deficiency at Stony Brook University Hospital ambulatory clinics. Demographic details and relevant clinical and laboratory data of the patients were collected. The data from similar studies in the literature were searched for and reviewed. Results This study consisted of 228 patients with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and Sjögren's syndrome. Among those patients, 94.7% received hydroxychloroquine, sulfasalazine, or dapsone; 41% (89/228) of patients were screened for G6PD deficiency, and the majority of them were on treatment with hydroxychloroquine. Of those patients, 7.9% (five Caucasians and two African Americans) were found to have G6PD deficiency, and two of the G6PD-deficient patients received hydroxychloroquine. There was no incidence of hemolytic anemia documented in any of the seven patients with G6PD deficiency. We reviewed the literature and found three similar studies of patients receiving hydroxychloroquine with no reported hemolytic anemia from different medical centers in the US, and the frequency of G6PD deficiency reported in these studies was 1.4%, 4.0%, and 4.2%, respectively. Conclusions Our study suggests that the frequency of G6PD deficiency in our rheumatic population is similar to that of the general population, and the risk of hemolytic anemia in G6PD deficiency associated with hydroxychloroquine is extremely rare. Hence, G6PD screening may not be recommended prior to starting treatment with hydroxychloroquine.

摘要

目的 药物性溶血性贫血可发生于葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的患者。在风湿病领域,G6PD缺乏症筛查的做法并不一致。本研究旨在确定在纽约州立大学石溪分校医院门诊对风湿病患者开始使用羟氯喹和/或柳氮磺胺吡啶之前进行筛查的效用。方法 我们对在石溪分校医院门诊接受G6PD缺乏症筛查的风湿病病例进行了回顾性病历审查。收集了患者的人口统计学细节以及相关临床和实验室数据。检索并回顾了文献中类似研究的数据。结果 本研究包括228例系统性红斑狼疮(SLE)、类风湿关节炎(RA)和干燥综合征患者。在这些患者中,94.7%接受了羟氯喹、柳氮磺胺吡啶或氨苯砜治疗;41%(89/228)的患者接受了G6PD缺乏症筛查,其中大多数正在接受羟氯喹治疗。在这些患者中,7.9%(5名白种人和2名非裔美国人)被发现存在G6PD缺乏,其中2名G6PD缺乏患者接受了羟氯喹治疗。7例G6PD缺乏患者中均未记录到溶血性贫血的发生。我们回顾了文献,发现美国不同医疗中心有三项关于接受羟氯喹治疗的患者的类似研究,均未报告溶血性贫血,这些研究报告的G6PD缺乏症发生率分别为1.4%、4.0%和4.2%。结论 我们的研究表明,我们风湿病患者群体中G6PD缺乏症的发生率与一般人群相似,与羟氯喹相关的G6PD缺乏症患者发生溶血性贫血的风险极低。因此,在开始使用羟氯喹治疗之前,可能不建议进行G6PD筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d091/7462653/000471dd1618/cureus-0012-00000009519-i01.jpg

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