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Diagnosis, treatment and prevention of infective endocarditis: Turkish consensus report-2019.感染性心内膜炎的诊断、治疗与预防:2019年土耳其共识报告
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2
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Cardiol Ther. 2019 Dec;8(2):167-177. doi: 10.1007/s40119-019-00148-4. Epub 2019 Sep 18.
3
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Medicina (B Aires). 2019;79(4):257-264.
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Risk factors for infective endocarditis following transcatheter pulmonary valve replacement in patients with congenital heart disease.先天性心脏病患者经导管肺动脉瓣置换术后感染性心内膜炎的危险因素。
Catheter Cardiovasc Interv. 2019 Oct 1;94(4):625-635. doi: 10.1002/ccd.28474. Epub 2019 Aug 30.
7
[Current treatment of endocarditis : Innovations and controversies].[心内膜炎的当前治疗:创新与争议]
Internist (Berl). 2019 Oct;60(10):1111-1117. doi: 10.1007/s00108-019-00664-4.
8
Infective endocarditis: Beyond the usual tests.感染性心内膜炎:超越常规检查。
Cleve Clin J Med. 2019 Aug;86(8):559-567. doi: 10.3949/ccjm.86a.18120.
9
National Temporal Trend Analysis of Infective Endocarditis among Patients Infected with HIV in Spain (1997-2014): A Retrospective Study.西班牙HIV感染患者感染性心内膜炎的全国时间趋势分析(1997 - 2014年):一项回顾性研究
J Clin Med. 2019 Aug 4;8(8):1167. doi: 10.3390/jcm8081167.
10
Age, creatinine and ejection fraction (ACEF) score: a simple risk-stratified method for infective endocarditis.年龄、肌酐和射血分数(ACEF)评分:一种用于感染性心内膜炎的简单风险分层方法。
QJM. 2019 Dec 1;112(12):900-906. doi: 10.1093/qjmed/hcz191.

不同抗生素治疗方案用于感染性心内膜炎治疗的比较。

A comparison of different antibiotic regimens for the treatment of infective endocarditis.

作者信息

Martí-Carvajal Arturo J, Dayer Mark, Conterno Lucieni O, Gonzalez Garay Alejandro G, Martí-Amarista Cristina Elena

机构信息

Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE (Cochrane Ecuador), Quito, Ecuador.

School of Medicine, Universidad Francisco de Vitoria (Cochrane Madrid), Madrid, Spain.

出版信息

Cochrane Database Syst Rev. 2020 May 14;5(5):CD009880. doi: 10.1002/14651858.CD009880.pub3.

DOI:10.1002/14651858.CD009880.pub3
PMID:32407558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7527143/
Abstract

BACKGROUND

Infective endocarditis is a microbial infection of the endocardial surface of the heart. Antibiotics are the cornerstone of treatment, but due to the differences in presentation, populations affected, and the wide variety of micro-organisms that can be responsible, their use is not standardised. This is an update of a review previously published in 2016.

OBJECTIVES

To assess the existing evidence about the clinical benefits and harms of different antibiotics regimens used to treat people with infective endocarditis.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase Classic and Embase, LILACS, CINAHL, and the Conference Proceedings Citation Index - Science on 6 January 2020. We also searched three trials registers and handsearched the reference lists of included papers. We applied no language restrictions.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) assessing the effects of antibiotic regimens for treating definitive infective endocarditis diagnosed according to modified Duke's criteria. We considered all-cause mortality, cure rates, and adverse events as the primary outcomes. We excluded people with possible infective endocarditis and pregnant women.

DATA COLLECTION AND ANALYSIS

Two review authors independently performed study selection, 'Risk of bias' assessment, and data extraction in duplicate. We constructed 'Summary of findings' tables and used GRADE methodology to assess the quality of the evidence. We described the included studies narratively.

MAIN RESULTS

Six small RCTs involving 1143 allocated/632 analysed participants met the inclusion criteria of this first update. The included trials had a high risk of bias. Three trials were sponsored by drug companies. Due to heterogeneity in outcome definitions and different antibiotics used data could not be pooled. The included trials compared miscellaneous antibiotic schedules having uncertain effects for all of the prespecified outcomes in this review. Evidence was either low or very low quality due to high risk of bias and very low number of events and small sample size. The results for all-cause mortality were as follows: one trial compared quinolone (levofloxacin) plus standard treatment (antistaphylococcal penicillin (cloxacillin or dicloxacillin), aminoglycoside (tobramycin or netilmicin), and rifampicin) versus standard treatment alone and reported 8/31 (26%) with levofloxacin plus standard treatment versus 9/39 (23%) with standard treatment alone; risk ratio (RR) 1.12, 95% confidence interval (CI) 0.49 to 2.56. One trial compared fosfomycin plus imipenem 3/4 (75%) versus vancomycin 0/4 (0%) (RR 7.00, 95% CI 0.47 to 103.27), and one trial compared partial oral treatment 7/201 (3.5%) versus conventional intravenous treatment 13/199 (6.53%) (RR 0.53, 95% CI 0.22 to 1.31). The results for rates of cure with or without surgery were as follows: one trial compared daptomycin versus low-dose gentamicin plus an antistaphylococcal penicillin (nafcillin, oxacillin, or flucloxacillin) or vancomycin and reported 9/28 (32.1%) with daptomycin versus 9/25 (36%) with low-dose gentamicin plus antistaphylococcal penicillin or vancomycin; RR 0.89, 95% CI 0.42 to 1.89. One trial compared glycopeptide (vancomycin or teicoplanin) plus gentamicin with cloxacillin plus gentamicin (13/23 (56%) versus 11/11 (100%); RR 0.59, 95% CI 0.40 to 0.85). One trial compared ceftriaxone plus gentamicin versus ceftriaxone alone (15/34 (44%) versus 21/33 (64%); RR 0.69, 95% CI 0.44 to 1.10), and one trial compared fosfomycin plus imipenem versus vancomycin (1/4 (25%) versus 2/4 (50%); RR 0.50, 95% CI 0.07 to 3.55). The included trials reported adverse events, the need for cardiac surgical interventions, and rates of uncontrolled infection, congestive heart failure, relapse of endocarditis, and septic emboli, and found no conclusive differences between groups (very low-quality evidence). No trials assessed quality of life.

AUTHORS' CONCLUSIONS: This first update confirms the findings of the original version of the review. Limited and low to very low-quality evidence suggests that the comparative effects of different antibiotic regimens in terms of cure rates or other relevant clinical outcomes are uncertain. The conclusions of this updated Cochrane Review were based on few RCTs with a high risk of bias. Accordingly, current evidence does not support or reject any regimen of antibiotic therapy for the treatment of infective endocarditis.

摘要

背景

感染性心内膜炎是心脏内膜表面的微生物感染。抗生素是治疗的基石,但由于临床表现、受影响人群以及可能致病的微生物种类繁多,抗生素的使用并不规范。这是对2016年发表的一篇综述的更新。

目的

评估不同抗生素方案治疗感染性心内膜炎患者的临床益处和危害的现有证据。

检索方法

我们于2020年1月6日检索了Cochrane对照试验中心注册库(CENTRAL)、MEDLINE、Embase经典版和Embase、拉丁美洲和加勒比卫生科学数据库(LILACS)、护理学与健康领域数据库(CINAHL)以及会议论文引文索引 - 科学版。我们还检索了三个试验注册库,并手工检索了纳入论文的参考文献列表。我们没有设置语言限制。

选择标准

我们纳入了评估根据改良Duke标准诊断的确诊感染性心内膜炎的抗生素方案效果的随机对照试验(RCT)。我们将全因死亡率、治愈率和不良事件作为主要结局。我们排除了可能患有感染性心内膜炎的患者和孕妇。

数据收集与分析

两位综述作者独立进行研究选择两次、“偏倚风险”评估和数据提取。我们构建了“结果总结”表,并使用GRADE方法评估证据质量。我们对纳入的研究进行了描述性叙述。

主要结果:六项小型RCT(涉及1143名分配/632名分析参与者)符合本次首次更新的纳入标准。纳入的试验存在较高的偏倚风险。三项试验由制药公司赞助。由于结局定义的异质性以及使用的不同抗生素,数据无法合并。纳入的试验比较了各种抗生素方案,对本综述中所有预先指定的结局的影响不确定。由于偏倚风险高、事件数量极少和样本量小,证据质量低或极低。全因死亡率的结果如下:一项试验比较了喹诺酮类(左氧氟沙星)加标准治疗(抗葡萄球菌青霉素(氯唑西林或双氯西林)、氨基糖苷类(妥布霉素或奈替米星)和利福平)与单独标准治疗,报告左氧氟沙星加标准治疗组8/31(26%),单独标准治疗组9/39(23%);风险比(RR)1.12,95%置信区间(CI)0.49至2.56。一项试验比较了磷霉素加亚胺培南3/4(75%)与万古霉素0/4(0%)(RR 7.00,95% CI 0.47至10‌3.27),一项试验比较了部分口服治疗7/201(3.5%)与传统静脉治疗13/199(6.53%)(RR 0.53,95% CI 0.22至1.31)。有或无手术的治愈率结果如下:一项试验比较了达托霉素与低剂量庆大霉素加抗葡萄球菌青霉素(萘夫西林、苯唑西林或氟氯西林)或万古霉素,报告达托霉素组9/28(32.1%),低剂量庆大霉素加抗葡萄球菌青霉素或万古霉素组9/25(36%);RR 0.89,95% CI 0.42至1.89。一项试验比较了糖肽类(万古霉素或替考拉宁)加庆大霉素与氯唑西林加庆大霉素(13/23(56%)对11/11(100%);RR 0.59,95% CI 0.40至0.85)。一项试验比较了头孢曲松加庆大霉素与单独头孢曲松(15/34(44%)对21/33(64%);RR 0.69,95% CI 0.44至1.10),一项试验比较了磷霉素加亚胺培南与万古霉素(1/4(25%)对2/4(50%);RR

0.50,95% CI 0.07至3.55)。纳入的试验报告了不良事件、心脏手术干预的必要性以及未控制感染、充血性心力衰竭、心内膜炎复发和脓毒性栓子的发生率,且未发现组间有确凿差异(证据质量极低)。没有试验评估生活质量。

作者结论

本次首次更新证实了综述原版的研究结果。有限且低至极低质量的证据表明,不同抗生素方案在治愈率或其他相关临床结局方面的比较效果尚不确定。本次更新的Cochrane综述的结论基于少数偏倚风险高的RCT。因此,目前的证据不支持或拒绝任何用于治疗感染性心内膜炎的抗生素治疗方案。