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Efficacy of tigecycline for the treatment of complicated intraabdominal infections in real-life clinical practice from five european observational studies

机译:欧洲五项观察性研究中,替加环素在现实生活中的临床实践中对复杂腹腔感染的治疗作用

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Objectives: Tigecycline is a broad-spectrum antibiotic approved for the treatment of complicated intra-abdominal infections (cIAIs). The efficacy of tigecycline when administered as monotherapy or in combination with other antibacterials in the treatment of cIAIs in routine clinical practice is described. Patients and methods: Individual patient-level data were pooled from five European observational studies (July 2006 to October 2011). Results: A total of 785 cIAI patients who received tigecycline were included (mean age 63.1+14.0 years). Of these, 56.6% were in intensive care units, 65.6% acquired their infection in hospital, 88.1% had at least one comorbidity and 65.7% had secondary peritonitis. The mean Acute Physiology and Chronic Health Evaluation (APACHE) II and Sequential Organ Failure Assessment (SOFA) scores at the beginning of treatment were 16.9+7.6 (n=614) and 7.0+4.2 (n=108), respectively, indicating high disease severity. Escherichia coli (41.8%), Enterococcus faecium (40.1%) and Enterococcus faecalis (21.1%) were the most frequently isolated pathogens; 49.1% of infections were polymicrobial and 17.5% were due to resistant pathogens. Overall, 54.8% (n=430) received tigecycline as monotherapy and 45.2% (n=355) as combination therapy for a mean duration of 10.6 days. Clinical response rates at the end of treatment were 77.4% for all patients (567/733), 80.6% for patients who received tigecycline as monotherapy (329/408), 75.2% for patients with a nosocomial infection (354/471), 75.8% for patients with an APACHE II score .15 (250/330) and 54.2% (32/59) for patients with a SOFA score =7. Conclusions: In these real-life studies, tigecycline, alone and in combination, achieved favourable clinical response rates in patients with cIAI with a high severity of illness.
机译:目的:Tigecycline是一种广谱抗生素,已被批准用于治疗复杂的腹腔内感染(cIAIs)。描述了替加环素在常规临床实践中作为单一疗法或与其他抗菌素联合治疗cIAI的功效。患者和方法:从五项欧洲观察性研究(2006年7月至2011年10月)中收集了各个患者水平的数据。结果:共纳入785名接受替加环素治疗的cIAI患者(平均年龄63.1 + 14.0岁)。其中,重症监护病房占56.6%,医院感染占65.6%,至少一种合并症占88.1%,继发性腹膜炎占65.7%。治疗开始时的平均急性生理和慢性健康评估(APACHE)II和顺序器官衰竭评估(SOFA)分数分别为16.9 + 7.6(n = 614)和7.0 + 4.2(n = 108),表明疾病高严重性。大肠杆菌(41.8%),粪肠球菌(40.1%)和粪肠球菌(21.1%)是最常见的病原体。 49.1%的感染是微生物感染,而17.5%的感染是由耐药菌引起的。总体而言,54.8%(n = 430)接受替加环素作为单一疗法,45.2%(n = 355)作为联合疗法接受平均疗程为10.6天。所有患者在治疗结束时的临床反应率分别为77.4%(567/733),接受替加环素单药治疗的患者为80.6%(329/408),医院感染患者的为75.2%(354/471),75.8对于APACHE II评分为0.15(250/330)的患者,其%;对于SOFA评分= 7的患者为54.2%(32/59)。结论:在这些现实生活中的研究中,替加环素单独或联合使用可在患有严重疾病的cIAI患者中获得良好的临床反应率。

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