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        <datestamp>2026-09-16T04:34:15Z</datestamp>
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          <dc:title>Data Sheet 1_Clinical outcomes and their relationship with tigecycline exposure in critically ill patients with drug resistant infections.pdf</dc:title>
          <dc:creator>Wei Su (89824)</dc:creator>
          <dc:creator>Shuping Song (17546933)</dc:creator>
          <dc:creator>Qing Tang (167623)</dc:creator>
          <dc:creator>Binbin Feng (2948232)</dc:creator>
          <dc:creator>Yinshan Wu (17862170)</dc:creator>
          <dc:creator>Haitao Yu (456678)</dc:creator>
          <dc:creator>Feng Guo (180529)</dc:creator>
          <dc:creator>Zhenwei Yu (3148452)</dc:creator>
          <dc:subject>Clinical Microbiology</dc:subject>
          <dc:subject>AUC</dc:subject>
          <dc:subject>carbapenem-resistant</dc:subject>
          <dc:subject>clinical response</dc:subject>
          <dc:subject>mortality</dc:subject>
          <dc:subject>tigecycline</dc:subject>
          <dc:description>Background&lt;p&gt;Dosing tigecycline, an important last resort for carbapenem-resistant organisms, should be under the guidance of pharmacokinetic/pharmacodynamic (PK/PD) theory. However, tigecycline has shown large interindividual variability in PK among different patients, and its PK/PD target has limited data support. This study aimed to evaluate the clinical outcome and the relationship with exposure in critically ill patients with drug-resistant infections.&lt;/p&gt;Methods&lt;p&gt;A single center, prospective observational, single-arm cohort study was performed to assess the outcome and its relationship with exposure in critically ill patients with drug-resistant pathogen infections. Patients were enrolled according to the inclusion and exclusion criteria. The clinical outcomes, including clinical response rate, 28-day mortality rate, and major adverse events (AEs), were followed up. Plasma concentrations in steady status were intensively collected and determined for tigecycline concentration, and the 24-hour area-under-curves (AUCs) were calculated. The exposure-clinical outcome relationship was analyzed, and multivariate logistic regressions were performed to identify risk factors that associated with outcome.&lt;/p&gt;Results&lt;p&gt;A total of 130 patients were included. The most common infection type was low respiratory tract infection (76/130), and carbapenem-resistant Acinetobacter baumannii was the most common pathogen (64/130). The median tigecycline treatment length was 12 days. The median AUC was 14.0 mg h/L. The overall response rate and 28-day mortality rate were 50.0% and 36.2%, respectively. A lower fibrinogen level was the most common AE (51/130). ALB, PLT and combined use of cefoperazone-sulbactam were independent factors associated with clinical response, but AUC was negatively associated with clinical response.&lt;/p&gt;Conclusion&lt;p&gt;The clinical outcome of tigecycline in critically ill patients with resistant pathogen infection was satisfactory, but negative relationship between tigecycline exposure and outcome was found and the PK/PD profile in these patients should be revisited.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-16T04:34:15Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fcimb.2026.1868760.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Clinical_outcomes_and_their_relationship_with_tigecycline_exposure_in_critically_ill_patients_with_drug_resistant_infections_pdf/33827866</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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