BACKGROUND: Use of tigecycline in treating MDR Acinetobacter baumannii (MDRAB) remains controversial. OBJECTIVES: To comprehensively assess the safety and efficacy of tigecycline in pneumonia caused by Acinetobacter baumannii. METHODS: PubMed, Embase, Web of Science and Cochrane library databases were searched up to 12 March 2019. Studies were included if they compared tigecycline-based regimens with other antibiotic regimens for treating AB pulmonary infections and we pooled the clinical outcomes, microbiological response, adverse events or mortality. RESULTS: One prospective study and nine retrospective studies were included in this meta-analysis. The results showed similar clinical cure rates (OR = 1.04, 95% CI = 0.60-1.81; P = 0.89) and mortality rates (OR = 1.11, 95% CI = 0.65-1.89; P = 0.71) comparing tigecycline groups with the control groups. However, a significantly lower microbiological eradication rate was found in the tigecycline groups (OR = 0.43, 95% CI = 0.27-0.66; P = 0.0001). Incidence of nephrotoxicity in tigecycline-based regimens was significantly lower than in colistin-based regimens (OR = 0.34, 95% CI = 0.16-0.74, I2 = 35%, P = 0.006). There were no randomized controlled trials (RCTs) included; incomplete safety data and regional bias caused by the majority of the studies originating in China are the main limitations of this meta-analysis. CONCLUSIONS: Tigecycline can be used for treating MDRAB pulmonary infections owing to efficacy similar to that of other antibiotics. Moreover, tigecycline did not show a higher risk of mortality. Considering the lower microbiological eradication rate for tigecycline, which is likely to induce antimicrobial resistance, well-designed RCTs for high-dose tigecycline in treating pneumonia caused by AB are still needed.
BACKGROUND: Use of tigecycline in treating MDR Acinetobacter baumannii (MDRAB) remains controversial. OBJECTIVES: To comprehensively assess the safety and efficacy of tigecycline in pneumonia caused by Acinetobacter baumannii. METHODS: PubMed, Embase, Web of Science and Cochrane library databases were searched up to 12 March 2019. Studies were included if they compared tigecycline-based regimens with other antibiotic regimens for treating AB pulmonary infections and we pooled the clinical outcomes, microbiological response, adverse events or mortality. RESULTS: One prospective study and nine retrospective studies were included in this meta-analysis. The results showed similar clinical cure rates (OR = 1.04, 95% CI = 0.60-1.81; P = 0.89) and mortality rates (OR = 1.11, 95% CI = 0.65-1.89; P = 0.71) comparing tigecycline groups with the control groups. However, a significantly lower microbiological eradication rate was found in the tigecycline groups (OR = 0.43, 95% CI = 0.27-0.66; P = 0.0001). Incidence of nephrotoxicity in tigecycline-based regimens was significantly lower than in colistin-based regimens (OR = 0.34, 95% CI = 0.16-0.74, I2 = 35%, P = 0.006). There were no randomized controlled trials (RCTs) included; incomplete safety data and regional bias caused by the majority of the studies originating in China are the main limitations of this meta-analysis. CONCLUSIONS:Tigecycline can be used for treating MDRAB pulmonary infections owing to efficacy similar to that of other antibiotics. Moreover, tigecycline did not show a higher risk of mortality. Considering the lower microbiological eradication rate for tigecycline, which is likely to induce antimicrobial resistance, well-designed RCTs for high-dose tigecycline in treating pneumonia caused by AB are still needed.
Authors: David M P De Oliveira; Brian M Forde; Minh-Duy Phan; Bernhard Steiner; Bing Zhang; Johannes Zuegg; Ibrahim M El-Deeb; Gen Li; Nadia Keller; Stephan Brouwer; Nichaela Harbison-Price; Amanda J Cork; Michelle J Bauer; Saleh F Alquethamy; Scott A Beatson; Jason A Roberts; David L Paterson; Alastair G McEwan; Mark A T Blaskovich; Mark A Schembri; Christopher A McDevitt; Mark von Itzstein; Mark J Walker Journal: mBio Date: 2022-01-11 Impact factor: 7.867