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Real-World Effectiveness of Piperacillin/Tazobactam with and without Linezolid for Spontaneous Bacterial Peritonitis

医学 利奈唑啉 内科学 自发性细菌性腹膜炎 联合疗法 胃肠病学 哌拉西林/他唑巴坦 屎肠球菌 抗生素 哌拉西林 万古霉素 微生物学 腹水 金黄色葡萄球菌 细菌 生物 铜绿假单胞菌 遗传学
作者
Stefanie Quickert,Silvia Würstle,Philipp Reuken,Stefan Hagel,Jochen Schneider,Roland M. Schmid,Sophie Neugebauer,Andreas Stallmach,Tony Bruns
出处
期刊:Digestive Diseases [Karger Publishers]
卷期号:40 (6): 777-786 被引量:4
标识
DOI:10.1159/000522259
摘要

<b><i>Background:</i></b> Guidelines recommend empirical therapy with piperacillin/tazobactam (TZP) for spontaneous bacterial peritonitis (SBP) with low risk of multidrug-resistant organisms. Whether coverage of beta-lactam-resistant Gram-positive bacteria, such as ampicillin-resistant <i>Enterococcus faecium</i>, provides clinical benefit in such situations is unknown. <b><i>Methods:</i></b> In this observational study, we investigated the real-world effectiveness of empirical therapy with TZP monotherapy versus TZP plus linezolid (LZD) combination therapy in patients with SBP from two centers. Treatment failure, defined as the need to escalate antibiotic therapy due to in vitro resistance, lack of neutrophil decrease in ascitic fluid, or clinical decision, and 30-day survival were retrospectively assessed. <b><i>Results:</i></b> In the first cohort, 100 SBP episodes were empirically treated with TZP + LZD combination therapy (<i>n</i> = 50) or TZP monotherapy (<i>n</i> = 50). Treatment failure was recorded in 48% with TZP monotherapy compared with 16% with TZP + LZD combination therapy (<i>p</i> = 0.001), and this difference persisted after stratification for community-acquired versus hospital-acquired SBP. Although treatment failure after TZP therapy was associated with lower 30-day survival (56% vs. 82%; <i>p</i> = 0.04), 30-day survival with empirical TZP + LZD combination therapy was not different from empirical TZP monotherapy (Kaplan-Meier estimates 74% vs. 69%; <i>p</i> = 0.87). TZP concentrations in ascitic fluid were &#x3e;32 mg/L in 94% samples after continuous administration. In a second cohort of 41 patients empirically treated with TZP, treatment failure was observed in 37%, which was also higher than in episodes treated with TZP + LZD in cohort 1 (<i>p</i> = 0.03). <b><i>Conclusion:</i></b> In this retrospective analysis, empirical TZP + LZD combination therapy for SBP was associated with fewer treatment failures without impact on short-term survival.
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