Kishore Amit K, Jeans Adam R, Garau Javier, Bustamante Alejandro, Kalra Lalit, Langhorne Peter, Chamorro Angel, Urra Xabier, Katan Mira, Napoli Mario Di, Westendorp Willeke, Nederkoorn Paul J, van de Beek Diederik, Roffe Christine, Woodhead Mark, Montaner Joan, Meisel Andreas, Smith Craig J
Greater Manchester Comprehensive Stroke Centre, Manchester Academic Health Science Centre, Salford Royal Foundation Trust, UK.
Division of Cardiovascular Sciences, University of Manchester, Manchester, UK.
Eur Stroke J. 2019 Dec;4(4):318-328. doi: 10.1177/2396987319851335. Epub 2019 May 27.
The microbiological aetiology of pneumonia complicating stroke is poorly characterised. In this second Pneumonia in Stroke ConsEnsuS statement, we propose a standardised approach to empirical antibiotic therapy in pneumonia complicating stroke, based on likely microbiological aetiology, to improve antibiotic stewardship.
Systematic literature searches of multiple databases were undertaken. An evidence review and a round of consensus consultation were completed prior to a final multi-disciplinary consensus meeting in September 2017, held in Barcelona, Spain. Consensus was approached using a modified Delphi technique and defined a priori as 75% agreement between the consensus group members.: No randomised trials to guide antibiotic treatment of pneumonia complicating stroke were identified. Consensus was reached for the following: (1) Stroke-associated pneumonia may be caused by organisms associated with either community-acquired or hospital-acquired pneumonia; (2) Treatment for early stroke-associated pneumonia (<72 h of stroke onset) should cover community-acquired pneumonia organisms; (3) Treatment for late stroke-associated pneumonia (≥72 h and within seven days of stroke onset) should cover community-acquired pneumonia organisms plus coliforms +/- . if risk factors; (4) No additional antimicrobial cover is required for patients with dysphagia or aspiration; (5) Pneumonia occurring after seven days from stroke onset should be treated as for hospital-acquired pneumonia; (6) Treatment should continue for at least seven days for each of these scenarios.
Consensus recommendations for antibiotic treatment of the spectrum of pneumonia complicating stroke are proposed. However, there was limited evidence available to formulate consensus on choice of specific antibiotic class for pneumonia complicating stroke.
Further studies are required to inform evidence-based treatment of stroke-associated pneumonia including randomised trials of antibiotics and validation of candidate biomarkers.
肺炎并发中风的微生物病因学特征尚不明确。在这份中风相关性肺炎共识声明的第二部分中,我们基于可能的微生物病因学,提出一种标准化的经验性抗生素治疗方法,用于中风并发肺炎的治疗,以改善抗生素管理。
对多个数据库进行了系统的文献检索。在2017年9月于西班牙巴塞罗那举行的最终多学科共识会议之前,完成了证据审查和一轮共识咨询。采用改良的德尔菲技术达成共识,事先将其定义为共识小组成员之间75%的一致意见。未发现有随机试验可指导中风并发肺炎的抗生素治疗。就以下内容达成了共识:(1)中风相关性肺炎可能由与社区获得性或医院获得性肺炎相关的病原体引起;(2)早期中风相关性肺炎(中风发作后<72小时)的治疗应覆盖社区获得性肺炎病原体;(3)晚期中风相关性肺炎(中风发作后≥72小时且在7天内)的治疗应覆盖社区获得性肺炎病原体加大肠菌群(如有危险因素则±);(4)吞咽困难或误吸患者无需额外的抗菌覆盖;(5)中风发作7天后发生的肺炎应按医院获得性肺炎治疗;(6)在每种情况下,治疗应持续至少7天。
提出了关于中风并发肺炎抗生素治疗的共识建议。然而,对于中风并发肺炎选择特定抗生素类别的问题,可用于形成共识的证据有限。
需要进一步研究以指导中风相关性肺炎的循证治疗,包括抗生素的随机试验和候选生物标志物的验证。