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长期药物治疗复杂肺部疾病相关的不良反应。

Adverse reactions associated with long-term drug administration in complex lung disease.

机构信息

Centre for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, Tokyo, Japan.

出版信息

Int J Tuberc Lung Dis. 2018 Dec 1;22(12):1505-1510. doi: 10.5588/ijtld.18.0171.

Abstract

SETTING

The number of patients with non-tuberculous mycobacterial lung disease (NTM-LD) worldwide has been increasing. complex lung disease (MAC-LD) accounts for 90% of NTM-LD. MAC-LD necessitates long-term treatment, but adverse reactions with long-term administration of drugs are poorly understood.

OBJECTIVE

To evaluate adverse reactions with long-term administration of drugs for MAC-LD.

DESIGN

We conducted a retrospective single-centre medical chart review of 364 patients administered two or more drugs between July 2010 and June 2015.

RESULTS

The prevalence and median time to onset of adverse reactions were as follows: hepatotoxicity 19.5%, 55 days; leucocytopaenia 20.0%, 41 days; thrombocytopaenia 28.6%, 61.5 days; cutaneous reactions 9.3%, 30 days; ocular toxicity 7.7%, 278 days; and increase in serum creatinine 12.4%, 430.5 days. Multivariate analysis showed that rifampicin use was independently associated with thrombocytopaenia, and ethambutol use was independently associated with increases in serum creatinine.

CONCLUSION

The main adverse reactions appeared within 3 months after start of treatment. Most patients were able to continue treatment with liver-supporting therapy, antihistamine agents or desensitisation therapy; however, ocular toxicity must be monitored for up to 1 year after start of treatment.

摘要

背景

全球范围内非结核分枝杆菌肺病(NTM-LD)患者数量不断增加。复杂肺病(MAC-LD)占 NTM-LD 的 90%。MAC-LD 需要长期治疗,但药物长期使用的不良反应尚不清楚。

目的

评估 MAC-LD 长期药物治疗的不良反应。

设计

我们对 2010 年 7 月至 2015 年 6 月间接受两种或两种以上药物治疗的 364 例患者进行了回顾性单中心病历回顾。

结果

不良反应的发生率和中位发病时间如下:肝毒性 19.5%,55 天;白细胞减少症 20.0%,41 天;血小板减少症 28.6%,61.5 天;皮肤反应 9.3%,30 天;眼毒性 7.7%,278 天;血清肌酐升高 12.4%,430.5 天。多变量分析表明,利福平的使用与血小板减少症独立相关,乙胺丁醇的使用与血清肌酐升高独立相关。

结论

主要不良反应出现在治疗开始后 3 个月内。大多数患者能够通过护肝治疗、抗组胺药物或脱敏治疗继续治疗;然而,必须在治疗开始后 1 年内监测眼毒性。

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