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        <identifier>oai:figshare.com:article/33950164</identifier>
        <datestamp>2026-09-21T05:41:31Z</datestamp>
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          <dc:title>Table 3_Clinical outcomes and adverse events associated with intravenous polymyxin-containing therapy in hospitalized children with resistant Gram-negative infections: a systematic review and meta-analysis.docx</dc:title>
          <dc:creator>Huilian Chen (11482906)</dc:creator>
          <dc:creator>Mure Ali (25080643)</dc:creator>
          <dc:creator>Hongyuan Huang (11256401)</dc:creator>
          <dc:creator>Junjie Ning (12424267)</dc:creator>
          <dc:creator>Shuanghong Luo (22169314)</dc:creator>
          <dc:creator>Lina Qiao (111668)</dc:creator>
          <dc:subject>Foetal Development and Medicine</dc:subject>
          <dc:subject>colistin</dc:subject>
          <dc:subject>hospitalized children</dc:subject>
          <dc:subject>nephrotoxicity</dc:subject>
          <dc:subject>pediatric intensive care</dc:subject>
          <dc:subject>polymyxin B</dc:subject>
          <dc:subject>polymyxins</dc:subject>
          <dc:subject>resistant Gram-negative infections</dc:subject>
          <dc:description>Background&lt;p&gt;Intravenous polymyxins remain salvage agents for resistant Gram-negative infections in children, but pediatric evidence on clinical outcomes and toxicity is fragmented.&lt;/p&gt;Methods&lt;p&gt;We systematically searched PubMed, Embase, Web of Science, the Cochrane Library, CNKI, Wanfang Data, SinoMed, and VIP from inception to 31 January 2025. Eligible studies reported intravenous polymyxin-containing therapy in hospitalized pediatric patients with documented or suspected resistant Gram-negative infections. Random-effects single-arm meta-analyses were used to estimate pooled outcome proportions.&lt;/p&gt;Results&lt;p&gt;Twenty-four studies comprising 1,152 reported patients or treatment units were included, most of which were single-arm observational studies. The pooled proportions were 22% [95% confidence interval (CI) 16%–27%] for all-cause mortality, 14% (95% CI 11%–17%) for infection-related mortality, 65% (95% CI 58%–72%) for clinical improvement, 13% (95% CI 9%–17%) for overall adverse events, and 10% (95% CI 7%–14%) for nephrotoxicity. Neurotoxicity and hepatotoxicity were infrequently reported. Clinical setting, dosing, outcome definitions, and units of analysis were heterogeneous.&lt;/p&gt;Conclusions&lt;p&gt;The available evidence describes outcomes observed during intravenous polymyxin-containing therapy in hospitalized children but does not establish comparative efficacy or causality for adverse events. Prospective multicenter pediatric studies using standardized dosing, outcome, and safety definitions are needed.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-21T05:41:31Z</dc:date>
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          <dc:identifier>10.3389/fped.2026.1928217.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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