Qinyuan Li , Qi Zhou , Jiangbo Fan , Siyuan Huang , Yaolong Chen , Fujian Song , Zhou Fu , Enmei Liu , Daolin Tang , Ling Zeng , Zhengxiu Luo
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Early oral switch was defined as 5–9 days for uncomplicated <em>Staphylococcus aureus</em> bacteraemia, <4 weeks for complicated <em>S. aureus</em> bacteraemia, 3–7 days for uncomplicated <em>Streptococcus</em> bacteraemia, and 3–5 days for uncomplicated <em>Enterobacterales</em> bacteraemia.</div></div><div><h3>Assessment of risk of bias</h3><div>Assessment of risk of bias includes Cochrane risk of bias tool and Newcastle-Ottawa Scale.</div></div><div><h3>Methods of data synthesis</h3><div>Random-effect models were used to pool the data. The primary outcome was treatment failure. The non-inferiority margin for treatment failure was 10%. The Grading of Recommendations Assessment, Development, and Evaluation approach was used to rate the certainty of the evidence.</div></div><div><h3>Results</h3><div>In total, 38 studies (6 RCTs, 10 adjusted cohorts, and 22 unadjusted cohorts) involving 11 566 patients were included. A primary analysis of 6 RCTs and 10 adjusted cohorts comprised 7102 patients. High-certainty evidence from six RCTs showed that early transition to oral antibiotics was non-inferior to continued IV therapy for treatment failure (<em>n</em> = 529; OR 0.89; 95% CI: 0.54–1.48). Low-certainty evidence from five adjusted cohorts also found no significant difference in treatment failure between the two groups (<em>n</em> = 929; OR 0.60; 95% CI: 0.29–1.72). Moderate-certainty evidence showed that oral switch therapy significantly reduced hospital stay (<em>n</em> = 2041; mean difference: –5.19 days; 95% CI: –8.16 to –2.22).</div></div><div><h3>Conclusions</h3><div>Early transition to oral antibiotics was non-inferior to continued IV antibiotic treatment for bacteraemia and sepsis.</div></div>","PeriodicalId":10444,"journal":{"name":"Clinical Microbiology and Infection","volume":"31 4","pages":"Pages 551-559"},"PeriodicalIF":8.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oral switch vs. continued intravenous antibiotic therapy in patients with bacteraemia and sepsis: a systematic review and meta-analysis\",\"authors\":\"Qinyuan Li , Qi Zhou , Jiangbo Fan , Siyuan Huang , Yaolong Chen , Fujian Song , Zhou Fu , Enmei Liu , Daolin Tang , Ling Zeng , Zhengxiu Luo\",\"doi\":\"10.1016/j.cmi.2024.11.035\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Bacteraemia and sepsis have traditionally required continued intravenous (IV) antibiotics.</div></div><div><h3>Objectives</h3><div>This study aims to evaluate if early transition to oral antibiotics is non-inferior to continued IV antibiotic therapy in treating patients with bacteraemia and sepsis.</div></div><div><h3>Data sources</h3><div>Data sources include MEDLINE, Embase, Web of Science, the Cochrane Library, and Wanfang databases from inception to 13 July 2024, along with clinical trial registries and <span><span>Google.com</span><svg><path></path></svg></span>.</div></div><div><h3>Study eligibility criteria</h3><div>Study eligibility criteria include randomized controlled trials (RCTs) and cohort studies.</div></div><div><h3>Participants</h3><div>Participants include patients with bacteraemia and sepsis.</div></div><div><h3>Interventions</h3><div>Interventions include early transition to oral antibiotics vs. continued IV antibiotics. Early oral switch was defined as 5–9 days for uncomplicated <em>Staphylococcus aureus</em> bacteraemia, <4 weeks for complicated <em>S. aureus</em> bacteraemia, 3–7 days for uncomplicated <em>Streptococcus</em> bacteraemia, and 3–5 days for uncomplicated <em>Enterobacterales</em> bacteraemia.</div></div><div><h3>Assessment of risk of bias</h3><div>Assessment of risk of bias includes Cochrane risk of bias tool and Newcastle-Ottawa Scale.</div></div><div><h3>Methods of data synthesis</h3><div>Random-effect models were used to pool the data. The primary outcome was treatment failure. The non-inferiority margin for treatment failure was 10%. The Grading of Recommendations Assessment, Development, and Evaluation approach was used to rate the certainty of the evidence.</div></div><div><h3>Results</h3><div>In total, 38 studies (6 RCTs, 10 adjusted cohorts, and 22 unadjusted cohorts) involving 11 566 patients were included. A primary analysis of 6 RCTs and 10 adjusted cohorts comprised 7102 patients. High-certainty evidence from six RCTs showed that early transition to oral antibiotics was non-inferior to continued IV therapy for treatment failure (<em>n</em> = 529; OR 0.89; 95% CI: 0.54–1.48). Low-certainty evidence from five adjusted cohorts also found no significant difference in treatment failure between the two groups (<em>n</em> = 929; OR 0.60; 95% CI: 0.29–1.72). 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引用次数: 0
摘要
背景:传统上,菌血症和败血症需要持续静脉注射抗生素。目的:评价在治疗菌血症和败血症患者时,早期过渡到口服抗生素是否优于继续静脉注射抗生素治疗。数据来源:MEDLINE, Embase, Web of Science, Cochrane图书馆和万方数据库,时间从开始到2024年7月13日,以及临床试验注册和google.com。研究资格标准:随机对照试验(RCTs)和队列研究。研究对象:菌血症和败血症患者。干预措施:早期过渡到口服抗生素和持续静脉注射抗生素。对于无并发症的金黄色葡萄球菌菌血症,早期口服切换定义为5-9天。数据综合方法:采用随机效应模型汇总数据。主要结局是治疗失败。治疗失败的非劣效裕度为10%。GRADE方法用于评价证据的确定性。结果:共纳入38项研究(6项随机对照试验,10个调整队列,22个未调整队列),涉及11566例患者。初步分析了6项随机对照试验和10个调整后的队列,包括7,102例患者。来自6个随机对照试验的高确定性证据显示,早期过渡到口服抗生素治疗失败并不亚于继续静脉注射治疗(n=529;或0.89;95% CI: 0.54 ~ 1.48)。来自5个校正队列的低确定性证据也发现两组治疗失败无显著差异(n=929;或0.60;95% CI: 0.29 ~ 1.72)。中等确定性证据显示,口服转换疗法显著减少住院时间(n= 2041;平均差值:-5.19天;95% CI: -8.16至-2.22)。结论:早期过渡到口服抗生素治疗菌血症和败血症的效果不逊于继续静脉注射抗生素治疗。
Oral switch vs. continued intravenous antibiotic therapy in patients with bacteraemia and sepsis: a systematic review and meta-analysis
Background
Bacteraemia and sepsis have traditionally required continued intravenous (IV) antibiotics.
Objectives
This study aims to evaluate if early transition to oral antibiotics is non-inferior to continued IV antibiotic therapy in treating patients with bacteraemia and sepsis.
Data sources
Data sources include MEDLINE, Embase, Web of Science, the Cochrane Library, and Wanfang databases from inception to 13 July 2024, along with clinical trial registries and Google.com.
Study eligibility criteria
Study eligibility criteria include randomized controlled trials (RCTs) and cohort studies.
Participants
Participants include patients with bacteraemia and sepsis.
Interventions
Interventions include early transition to oral antibiotics vs. continued IV antibiotics. Early oral switch was defined as 5–9 days for uncomplicated Staphylococcus aureus bacteraemia, <4 weeks for complicated S. aureus bacteraemia, 3–7 days for uncomplicated Streptococcus bacteraemia, and 3–5 days for uncomplicated Enterobacterales bacteraemia.
Assessment of risk of bias
Assessment of risk of bias includes Cochrane risk of bias tool and Newcastle-Ottawa Scale.
Methods of data synthesis
Random-effect models were used to pool the data. The primary outcome was treatment failure. The non-inferiority margin for treatment failure was 10%. The Grading of Recommendations Assessment, Development, and Evaluation approach was used to rate the certainty of the evidence.
Results
In total, 38 studies (6 RCTs, 10 adjusted cohorts, and 22 unadjusted cohorts) involving 11 566 patients were included. A primary analysis of 6 RCTs and 10 adjusted cohorts comprised 7102 patients. High-certainty evidence from six RCTs showed that early transition to oral antibiotics was non-inferior to continued IV therapy for treatment failure (n = 529; OR 0.89; 95% CI: 0.54–1.48). Low-certainty evidence from five adjusted cohorts also found no significant difference in treatment failure between the two groups (n = 929; OR 0.60; 95% CI: 0.29–1.72). Moderate-certainty evidence showed that oral switch therapy significantly reduced hospital stay (n = 2041; mean difference: –5.19 days; 95% CI: –8.16 to –2.22).
Conclusions
Early transition to oral antibiotics was non-inferior to continued IV antibiotic treatment for bacteraemia and sepsis.
期刊介绍:
Clinical Microbiology and Infection (CMI) is a monthly journal published by the European Society of Clinical Microbiology and Infectious Diseases. It focuses on peer-reviewed papers covering basic and applied research in microbiology, infectious diseases, virology, parasitology, immunology, and epidemiology as they relate to therapy and diagnostics.