Description, clinical impact and early outcome of S. maltophilia respiratory tract infections after lung transplantation, A retrospective observational study

IF 2.2 4区 医学 Q3 RESPIRATORY SYSTEM
Benoît Pilmis , Claire Rouzaud , Deborah To-Puzenat , Anne Gigandon , Gaelle Dauriat , Séverine Feuillet , Delphine Mitilian , Justin Issard , Alban Le Monnier , Olivier Lortholary , Elie Fadel , Jérôme Le Pavec
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引用次数: 0

Abstract

Background and research question

S. maltophilia infections are associated with significant morbidity and mortality. Little is known regarding its presentation, management, and outcome in lung transplant recipients.

Study design and Methods

This retrospective case control study reviewed S. maltophilia respiratory tract infection in lung transplant recipients (01/01/2011-31/01/2020) and described the clinical, microbiological and outcome characteristics matched with lung transplant recipients without respiratory tract infection.

Results and interpretation

We identified 63 S. maltophilia infections in lung transplant recipients. Among them none were colonized before transplantation. Infections occurred a median of 177 (IQR: 45- 681) days post transplantation. Fifty-four (85.7 %) patients received trimethoprim-sulfamethoxazole (400/80 mg three times a week) to prevent Pneumocystis jirovecii pneumonia (PJP). S. maltophilia strains were susceptible to trimethoprim-sulfamethoxazole, levofloxacin, minocycline and ceftazidime in respectively 85.7 %, 82.5 %, 96.8 % and 34.9 % of cases. Median duration of treatment was 9 days (IQR 7–11.5). Clinical and microbiological recurrence were observed in respectively 25.3 % and 39.7 % of cases. Combination therapy was not associated with a decrease in the risk of recurrence and did not prevent the emergence of resistance. S. maltophilia respiratory tract infection was associated with a decline in FEV-1 at one year.

Conclusion

S. maltophilia is an important cause of lower respiratory tract infection in lung transplant recipients. Trimethoprim-sulfamethoxazole use as prophylaxis for PJP doesn't prevent S. maltophilia infection among lung transplant recipients. Levofloxacin and trimethoprim-sulfamethoxazole appear to be the two molecules of choice for the treatment of these infections and new antibiotic strategies (cefiderocol, aztreonam/avibactam) are currently being evaluated for multi-resistant S. maltophilia infections.

肺移植术后嗜麦芽汁酵母菌呼吸道感染的描述、临床影响和早期预后:一项回顾性观察研究
背景和研究问题嗜麦芽糖浆菌感染与严重的发病率和死亡率有关。这项回顾性病例对照研究回顾了肺移植受者(01/01/2011-31/01/2020)中嗜麦芽梭菌呼吸道感染的情况,并描述了与无呼吸道感染的肺移植受者相匹配的临床、微生物学和结果特征。其中没有人在移植前就已感染。感染发生的时间中位数为移植后 177 天(IQR:45- 681 天)。54名患者(85.7%)接受了三甲双胍-磺胺甲噁唑治疗(400/80 毫克,每周三次),以预防肺孢子虫肺炎(PJP)。分别有 85.7%、82.5%、96.8% 和 34.9% 的病例中,嗜麦芽糖球菌菌株对三甲双胍-磺胺甲恶唑、左氧氟沙星、米诺环素和头孢他啶敏感。中位治疗时间为 9 天(IQR 7-11.5)。临床和微生物复发率分别为 25.3% 和 39.7%。联合疗法并不能降低复发风险,也不能防止耐药性的产生。结论嗜麦芽梭菌是肺移植受者下呼吸道感染的一个重要原因。使用三甲氧苄啶-磺胺甲噁唑预防 PJP 并不能预防肺移植受者感染嗜麦芽梭菌。左氧氟沙星和三甲氧苄氨嘧啶-磺胺甲噁唑似乎是治疗这些感染的首选药物,目前正在对治疗嗜麦芽糖酵母菌多重耐药性感染的新抗生素策略(头孢羟氨苄、阿曲南/阿维巴坦)进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine and Research
Respiratory Medicine and Research RESPIRATORY SYSTEM-
CiteScore
2.70
自引率
0.00%
发文量
82
审稿时长
50 days
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