Chronic pulmonary aspergillosis: comprehensive insights into epidemiology, treatment, and unresolved challenges.

IF 3.8 Q2 INFECTIOUS DISEASES
Therapeutic Advances in Infectious Disease Pub Date : 2024-06-18 eCollection Date: 2024-01-01 DOI:10.1177/20499361241253751
Masato Tashiro, Takahiro Takazono, Koichi Izumikawa
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Abstract

Chronic pulmonary aspergillosis (CPA) is a challenging respiratory infection caused by the environmental fungus Aspergillus. CPA has a poor prognosis, with reported 1-year mortality rates ranging from 7% to 32% and 5-year mortality rates ranging from 38% to 52%. A comprehensive understanding of the pathogen, pathophysiology, risk factors, diagnosis, surgery, hemoptysis treatment, pharmacological therapy, and prognosis is essential to manage CPA effectively. In particular, Aspergillus drug resistance and cryptic species pose significant challenges. CPA lacks tissue invasion and has specific features such as aspergilloma. The most critical risk factor for the development of CPA is pulmonary cavitation. Diagnostic approaches vary by CPA subtype, with computed tomography (CT) imaging and Aspergillus IgG antibodies being key. Treatment strategies include surgery, hemoptysis management, and antifungal therapy. Surgery is the curative option. However, reported postoperative mortality rates range from 0% to 5% and complications range from 11% to 63%. Simple aspergilloma generally has a low postoperative mortality rate, making surgery the first choice. Hemoptysis, observed in 50% of CPA patients, is a significant symptom and can be life-threatening. Bronchial artery embolization achieves hemostasis in 64% to 100% of cases, but 50% experience recurrent hemoptysis. The efficacy of antifungal therapy for CPA varies, with itraconazole reported to be 43-76%, voriconazole 32-80%, posaconazole 44-61%, isavuconazole 82.7%, echinocandins 42-77%, and liposomal amphotericin B 52-73%. Combinatorial treatments such as bronchoscopic triazole administration, inhalation, or direct injection of amphotericin B at the site of infection also show efficacy. A treatment duration of more than 6 months is recommended, with better efficacy reported for periods of more than 1 year. In anticipation of improvements in CPA management, ongoing advances in basic and clinical research are expected to contribute to the future of CPA management.

慢性肺曲霉菌病:流行病学、治疗和悬而未决难题的全面见解。
慢性肺曲霉菌病(CPA)是由环境真菌曲霉菌引起的一种棘手的呼吸道感染。CPA 的预后较差,据报道 1 年死亡率为 7% 至 32%,5 年死亡率为 38% 至 52%。全面了解病原体、病理生理学、风险因素、诊断、手术、咯血治疗、药物治疗和预后对有效治疗 CPA 至关重要。尤其是曲霉菌的耐药性和隐匿菌种构成了重大挑战。CPA 缺乏组织侵袭,具有曲霉瘤等特殊特征。发生 CPA 的最关键风险因素是肺空洞症。诊断方法因 CPA 亚型而异,计算机断层扫描(CT)成像和曲霉菌 IgG 抗体是关键。治疗策略包括手术、咯血处理和抗真菌治疗。手术是治愈的选择。但据报道,术后死亡率从 0% 到 5% 不等,并发症从 11% 到 63% 不等。单纯曲霉瘤的术后死亡率通常较低,因此手术是首选。50% 的 CPA 患者会出现咯血,这是一个重要的症状,可能危及生命。支气管动脉栓塞可使64%至100%的病例止血,但50%的病例会反复咯血。抗真菌治疗对 CPA 的疗效各不相同,据报道伊曲康唑为 43-76%,伏立康唑为 32-80%,泊沙康唑为 44-61%,异黄酮唑为 82.7%,棘白菌素类为 42-77%,脂质体两性霉素 B 为 52-73%。支气管镜三唑给药、吸入或在感染部位直接注射两性霉素 B 等综合疗法也显示出疗效。建议疗程超过 6 个月,据报道超过 1 年的疗效更好。为了改善 CPA 的治疗,基础和临床研究的不断进步有望为 CPA 的未来治疗做出贡献。
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
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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