Johanna P. van Gemert , Sofanne J. Ravensbergen , Erik A.M. Verschuuren , Huib A.M. Kerstjens , Brigitte W.M. Willemse , Jakko van Ingen , Wouter Hoefsloot , Tji Gan , Onno W. Akkerman
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引用次数: 0
Abstract
Background
There is lack of consensus on non-tuberculous mycobacteria pulmonary disease (NTM-PD) treatment regimen and duration in patient listed for lung transplantation (LTx). We conducted a systematic review on treatment regimen and duration pre- and directly post-LTx, for patients with known NTM-PD pre-LTx. Additionally, we searched for risk factors for NTM disease development post-LTx and for mortality.
Methods
Literature was reviewed on PubMed, Embase and the Cochrane Library, for articles published from inception to January 2022. Individual patient data were sought.
Results
Sixteen studies were included reporting 92 patients. Most frequent used agents were aminoglycosides and macrolides for Mycobacterium abscessus (M. abscessus) and macrolides and tuberculostatic agents for Mycobacterium avium complex (M. avium complex). The median treatment duration pre-LTx was 10 months (IQR 6–17) and 2 months (IQR 2–8) directly post-LTx. Longer treatment duration pre-LTx was observed in children and in patients with M. abscessus. 46% of the patients with NTM-PD pre-LTx developed NTM disease post-LTx, related mortality rate was 10%. Longer treatment duration pre-LTx (p < 0.001) and sputum non-conversion pre-LTx (p = 0.003) were significantly associated with development of NTM-disease post-LTx. Longer treatment duration pre-LTx (p = 0.004), younger age (p < 0.001) and sputum non-conversion (p = 0.044) were risk factors for NTM related death.
Conclusions
The median treatment duration pre-LTx was 10 months (IQR 6–17) and 2 months (IQR 2–8) directly post-LTx. Patients with longer treatment duration for NTM-PD pre-LTx and with sputum non-conversion are at risk for NTM disease post-LTx and for NTM-related death. Children were particularly at risk for NTM related death.
背景:对于肺移植(LTx)患者的非结核分枝杆菌性肺病(NTM-PD)治疗方案和持续时间缺乏共识。我们对已知NTM-PD患者在LTx前和直接LTx后的治疗方案和持续时间进行了系统回顾。此外,我们还搜索了LTx后NTM疾病发展和死亡率的风险因素。方法:查阅PubMed、Embase和Cochrane图书馆从成立到2022年1月发表的文章。寻求个体患者数据。结果:纳入16项研究,报告92例患者。最常用的药物是用于脓肿分枝杆菌(脓肿分枝杆菌)的氨基糖苷类和大环内酯类药物,以及用于禽分枝杆菌复合物(禽分枝杆菌复合体)的大环内酯和抗结核药物。LTx前的中位治疗持续时间为10个月(IQR 6-17),LTx后直接治疗2个月(IQ R 2-8)。在儿童和脓肿分枝杆菌患者中观察到LTx前治疗持续时间更长。在LTx前的NTM-PD患者中,46%的患者在LTx后发展为NTM疾病,相关死亡率为10%。LTx前治疗持续时间更长(p结论:LTx前的中位治疗持续时间为10个月(IQR 6-17),LTx后直接治疗持续时间2个月(IQ R 2-8)。LTx前NTM-PD治疗持续时间较长且痰液未转化的患者在LTx后有患NTM疾病和NTM相关死亡的风险。儿童尤其面临NTM相关死亡的风险。
期刊介绍:
Transplantation Reviews contains state-of-the-art review articles on both clinical and experimental transplantation. The journal features invited articles by authorities in immunology, transplantation medicine and surgery.