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Tedizolid Versus Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infection: A Systematic Review and Meta-Analysis

机译:Tedizolid与Linezolid联合治疗急性细菌性皮肤和皮肤结构感染:系统评价和荟萃分析

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摘要

This meta-analysis aims to assess the efficacy and safety of tedizolid, compared to linezolid, in the treatment of acute bacterial skin and skin structure infection (ABSSSI). PubMed, Web of Science, EBSCO (Elton B. Stephens Co.), Cochrane Library, Ovid Medline and Embase databases were accessed until 18 July 2019. Only randomized controlled trials (RCTs) comparing the efficacy of tedizolid with linezolid for adult patients with ABSSSIs were included. The outcomes included the clinical response, microbiological response, and risk of adverse events (AEs). A total of four RCTs involving 2056 adult patients with ABSSSI were enrolled. The early clinical response rate was 79.6% and 80.5% for patients receiving tedizolid and linezolid, respectively. The pooled analysis showed that tedizolid had a non-inferior early clinical response rate to linezolid (odds ratio (OR) = 0.96, 95% confidence interval (CI) = 0.77–1.19, I2 = 0%). The early response rate was similar between tedizolid and linezolid among patients with cellulitis/erysipelas (75.1% vs. 77.1%; OR = 0.90, 95% CI = 0.64–1.27, I2 = 25%), major cutaneous abscess (85.1% vs. 86.8%; OR = 0.93, 95% CI = 0.42–2.03, I2 = 37%) and wound infection (85.9% vs. 82.6%; OR = 1.29, 95% CI = 0.66–2.51, I2 = 45%). For methicillin-resistant Staphylococcus aureus patients, tedizolid had a favorable microbiological response rate of 95.2% which was comparable to linezolid (94%) (OR = 1.19, 95% CI = 0.49–2.90, I2 = 0%). In addition to the similar risk of treatment-emergent AEs (a serious event, the discontinuation of the study drug due to AEs and mortality between tedizolid and linezolid), tedizolid was associated with a lower risk of nausea, vomiting and abnormal neutrophil count than linezolid. In conclusion, once-daily tedizolid (200 mg for six days) compared to linezolid (600 mg twice-daily for 10 days) was non-inferior in efficacy in the treatment of ABSSSI. Besides, tedizolid was generally as well tolerated as linezolid, and had a lower incidence of gastrointestinal AEs and bone marrow suppression than linezolid.
机译:这项荟萃分析旨在评估与替尼唑胺相比,替地唑胺在治疗急性细菌性皮肤和皮肤结构感染(ABSSSI)中的功效和安全性。 PubMed,Web of Science,EBSCO(Elton B.Stephens Co。),Cochrane图书馆,Ovid Medline和Embase数据库的访问日期截止至2019年7月18日。仅比较了替硝唑与利奈唑胺治疗成人ABSSSIs疗效的随机对照试验(RCT)。被包括在内。结果包括临床反应,微生物反应和不良事件(AE)的风险。总共招募了4个RCT,涉及2056名成年ABSSSI患者。接受替硝唑和利奈唑胺治疗的患者的早期临床反应率为79.6%和80.5%。汇总分析显示,替硝唑对利奈唑胺的早期临床反应率不差(优势比(OR)= 0.96,95%置信区间(CI)= 0.77-1.19,I 2 = 0% )。在蜂窝织炎/丹毒患者中,替硝唑和利奈唑胺的早期反应率相似(75.1%比77.1%; OR = 0.90,95%CI = 0.64-1.27,I 2 = 25%),严重皮肤脓肿(85.1%vs. 86.8%; OR = 0.93,95%CI = 0.42-2.03,I 2 = 37%)和伤口感染(85.9%vs. 82.6%; OR = 1.29 ,则95%CI = 0.66-2.51,I 2 = 45%)。对于耐甲氧西林的金黄色葡萄球菌患者,泰地齐德的良好微生物反应率为95.2%,与利奈唑胺(94%)相当(OR = 1.19,95%CI = 0.49–2.90,I 2 = 0%)。除了出现类似的出现治疗性AE的风险(严重事件,由于AE导致的研究药物停药以及替替利德和利奈唑胺之间的死亡率)外,替利唑德的恶心,呕吐和异常嗜中性粒细胞计数风险也比利奈唑胺更低。总之,与利奈唑胺(600 mg,每天两次,连续10天)相比,每天一次替地唑德(每天200毫克,连续6天)在ABSSSI的治疗中疗效不差。此外,泰替唑酯通常与利奈唑胺一样耐受,并且胃肠道不良事件和骨髓抑制的发生率比利奈唑胺低。

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