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革兰氏阴性菌感染住院患者的适当初始抗生素治疗:系统评价与荟萃分析

Appropriate initial antibiotic therapy in hospitalized patients with gram-negative infections: systematic review and meta-analysis.

作者信息

Raman Gowri, Avendano Esther, Berger Samantha, Menon Vandana

机构信息

Center for Clinical Evidence Synthesis, Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Box 63, 800 Washington Street, Boston, MA, 02111, USA.

Tufts University School of Medicine, 145 Harrison Avenue, Boston, MA, 02111, USA.

出版信息

BMC Infect Dis. 2015 Sep 30;15:395. doi: 10.1186/s12879-015-1123-5.

Abstract

BACKGROUND

The rapid global spread of multi-resistant bacteria and loss of antibiotic effectiveness increases the risk of initial inappropriate antibiotic therapy (IAT) and poses a serious threat to patient safety. We conducted a systematic review and meta-analysis of published studies to summarize the effect of appropriate antibiotic therapy (AAT) or IAT against gram-negative bacterial infections in the hospital setting.

METHODS

MEDLINE, EMBASE, and Cochrane CENTRAL databases were searched until May 2014 to identify English-language studies examining use of AAT or IAT in hospitalized patients with Gram-negative pathogens. Outcomes of interest included mortality, clinical cure, cost, and length of stay. Citations and eligible full-text articles were screened in duplicate. Random effect models meta-analysis was used.

RESULTS

Fifty-seven studies in 60 publications were eligible. AAT was associated with lower risk of mortality (unadjusted summary odds ratio [OR] 0.38, 95 % confidence interval [CI] 0.30-0.47, 39 studies, 5809 patients) and treatment failure (OR 0.22, 95 % CI 0.14-0.35; 3 studies, 283 patients). Conversely, IAT increased risk of mortality (unadjusted summary OR 2.66, 95 % CI 2.12-3.35; 39 studies, 5809 patients). In meta-analyses of adjusted data, AAT was associated with lower risk of mortality (adjusted summary OR 0.43, 95 % CI 0.23-0.83; 6 studies, 1409 patients). Conversely, IAT increased risk of mortality (adjusted summary OR 3.30, 95 % CI 2.42-4.49; 16 studies, 2493 patients). A limited number of studies suggested higher cost and longer hospital stay with IAT. There was considerable heterogeneity in the definition of AAT or IAT, pathogens studied, and outcomes assessed.

DISCUSSION

Using a large set of studies we found that IAT is associated with a number of serious consequences,including an increased risk of hospital mortality. Infections caused by drug-resistant, Gram-negative organisms represent a considerable financial burden to healthcare systems due to the increased costs associated with the resources required to manage the infection, particularly longer hospital stays. However, there were insufficient data that evaluated AAT for the outcome of costs among patients with nosocomialGram-negative infections.

CONCLUSIONS

IAT in hospitalized patients with Gram-negative infections is associated with adverse outcomes. Technological advances for rapid diagnostics to facilitate AAT along with antimicrobial stewardship, surveillance, infection control, and prevention is needed.

摘要

背景

多重耐药菌在全球的迅速传播以及抗生素效力的丧失增加了初始不恰当抗生素治疗(IAT)的风险,并对患者安全构成严重威胁。我们对已发表的研究进行了系统评价和荟萃分析,以总结恰当抗生素治疗(AAT)或IAT针对医院环境中革兰氏阴性菌感染的效果。

方法

检索MEDLINE、EMBASE和Cochrane CENTRAL数据库至2014年5月,以识别关于AAT或IAT在住院革兰氏阴性病原体患者中使用情况的英文研究。感兴趣的结局包括死亡率、临床治愈、成本和住院时间。对文献引用和符合条件的全文文章进行双人筛选。采用随机效应模型进行荟萃分析。

结果

60篇出版物中的57项研究符合条件。AAT与较低的死亡风险相关(未调整的汇总比值比[OR]为0.38,95%置信区间[CI]为0.30 - 0.47,39项研究,5809例患者)以及治疗失败风险(OR为0.22,95%CI为0.14 - 0.35;3项研究,283例患者)。相反,IAT增加了死亡风险(未调整的汇总OR为2.66,95%CI为2.12 - 3.35;39项研究,5809例患者)。在调整数据的荟萃分析中,AAT与较低的死亡风险相关(调整后的汇总OR为0.43,95%CI为0.23 - 0.83;6项研究,1409例患者)。相反,IAT增加了死亡风险(调整后的汇总OR为3.30,95%CI为2.42 - 4.49;16项研究,2493例患者)。少数研究表明IAT会导致更高的成本和更长的住院时间。在AAT或IAT的定义、所研究的病原体以及评估的结局方面存在相当大的异质性。

讨论

通过大量研究我们发现,IAT与许多严重后果相关,包括医院死亡率增加。由耐药革兰氏阴性菌引起的感染给医疗系统带来了相当大的经济负担,因为管理感染所需资源的成本增加,尤其是住院时间延长。然而,对于医院获得性革兰氏阴性菌感染患者成本结局方面评估AAT的数据不足。

结论

住院革兰氏阴性菌感染患者的IAT与不良结局相关。需要快速诊断的技术进步以促进AAT,同时还需要抗菌药物管理、监测、感染控制和预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae3/4589179/0090cc8dc00f/12879_2015_1123_Fig1_HTML.jpg

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