Leo Mimram, Jean-François Timsit, Emilie Rondinaud, Minh Le, Michael Thy
{"title":"依拉瓦环素作为危重患者难治性耐药鲍曼不动杆菌感染的最后手段:三例药代动力学报告。","authors":"Leo Mimram, Jean-François Timsit, Emilie Rondinaud, Minh Le, Michael Thy","doi":"10.1093/jacamr/dlaf095","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To describe eravacycline use as a salvage treatment for ventilator-associated pneumonia (VAP) caused by difficult-to-treat resistant (DTR) <i>Acinetobacter baumannii</i> in critically ill patients.</p><p><strong>Methods: </strong>We reported three cases of DTR <i>A. baumannii</i> VAP with multiple organ failure treated with eravacycline. Patients were critically ill with confirmed VAP by distal pulmonary cultures. Eravacycline was administered at 1 mg/kg q12h in combination with IV colistin or as primary therapy. Clinical and microbiological outcomes were assessed.</p><p><strong>Results: </strong>Eravacycline MICs ranged from 0.25 to 0.75 mg/L. Microbiological success was observed in the three cases, including one patient who was successfully weaned and discharged alive with no further samples submitted for microbiological culture, and two other patients who were repeatedly sampled and remained negative for <i>A. baumannii</i>. Clinical success could not be confirmed in one case. No adverse effects were observed. Pharmacokinetic analysis of concentrations from a single patient revealed a maximal concentration (<i>C</i> <sub>max</sub>) of 1.47 mg/L at 1 h and an AUC<sub>0-6</sub> of 2.88 mg·h/L. The epithelial lining fluid/plasma concentration ratio was 0.1.</p><p><strong>Conclusions: </strong>Eravacycline showed promise as a salvage therapy for DTR <i>A. baumannii</i> VAP in critically ill patients. Further studies are needed to confirm its efficacy and optimal dosing in this setting.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"7 3","pages":"dlaf095"},"PeriodicalIF":3.3000,"publicationDate":"2025-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12203001/pdf/","citationCount":"0","resultStr":"{\"title\":\"Eravacycline as a last resort for difficult-to-treat resistant <i>Acinetobacter baumannii</i> infections in critically ill patients: three case reports with pharmacokinetic insights.\",\"authors\":\"Leo Mimram, Jean-François Timsit, Emilie Rondinaud, Minh Le, Michael Thy\",\"doi\":\"10.1093/jacamr/dlaf095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>To describe eravacycline use as a salvage treatment for ventilator-associated pneumonia (VAP) caused by difficult-to-treat resistant (DTR) <i>Acinetobacter baumannii</i> in critically ill patients.</p><p><strong>Methods: </strong>We reported three cases of DTR <i>A. baumannii</i> VAP with multiple organ failure treated with eravacycline. Patients were critically ill with confirmed VAP by distal pulmonary cultures. Eravacycline was administered at 1 mg/kg q12h in combination with IV colistin or as primary therapy. Clinical and microbiological outcomes were assessed.</p><p><strong>Results: </strong>Eravacycline MICs ranged from 0.25 to 0.75 mg/L. Microbiological success was observed in the three cases, including one patient who was successfully weaned and discharged alive with no further samples submitted for microbiological culture, and two other patients who were repeatedly sampled and remained negative for <i>A. baumannii</i>. Clinical success could not be confirmed in one case. No adverse effects were observed. Pharmacokinetic analysis of concentrations from a single patient revealed a maximal concentration (<i>C</i> <sub>max</sub>) of 1.47 mg/L at 1 h and an AUC<sub>0-6</sub> of 2.88 mg·h/L. The epithelial lining fluid/plasma concentration ratio was 0.1.</p><p><strong>Conclusions: </strong>Eravacycline showed promise as a salvage therapy for DTR <i>A. baumannii</i> VAP in critically ill patients. Further studies are needed to confirm its efficacy and optimal dosing in this setting.</p>\",\"PeriodicalId\":14594,\"journal\":{\"name\":\"JAC-Antimicrobial Resistance\",\"volume\":\"7 3\",\"pages\":\"dlaf095\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-06-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12203001/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JAC-Antimicrobial Resistance\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/jacamr/dlaf095\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAC-Antimicrobial Resistance","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/jacamr/dlaf095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Eravacycline as a last resort for difficult-to-treat resistant Acinetobacter baumannii infections in critically ill patients: three case reports with pharmacokinetic insights.
Objectives: To describe eravacycline use as a salvage treatment for ventilator-associated pneumonia (VAP) caused by difficult-to-treat resistant (DTR) Acinetobacter baumannii in critically ill patients.
Methods: We reported three cases of DTR A. baumannii VAP with multiple organ failure treated with eravacycline. Patients were critically ill with confirmed VAP by distal pulmonary cultures. Eravacycline was administered at 1 mg/kg q12h in combination with IV colistin or as primary therapy. Clinical and microbiological outcomes were assessed.
Results: Eravacycline MICs ranged from 0.25 to 0.75 mg/L. Microbiological success was observed in the three cases, including one patient who was successfully weaned and discharged alive with no further samples submitted for microbiological culture, and two other patients who were repeatedly sampled and remained negative for A. baumannii. Clinical success could not be confirmed in one case. No adverse effects were observed. Pharmacokinetic analysis of concentrations from a single patient revealed a maximal concentration (Cmax) of 1.47 mg/L at 1 h and an AUC0-6 of 2.88 mg·h/L. The epithelial lining fluid/plasma concentration ratio was 0.1.
Conclusions: Eravacycline showed promise as a salvage therapy for DTR A. baumannii VAP in critically ill patients. Further studies are needed to confirm its efficacy and optimal dosing in this setting.