Journal of Global Antimicrobial Resistance (Dec 2024)

Evolution Of Multidrug-Resistant Acinetobacter Baumannii Pneumonia In Years In Terms Of Tigecycline Treatment

  • Merve Mert Vahabi,
  • Deniz Akyol,
  • Deniz Dağ,
  • Şevket Yeniyol,
  • Olcay Buse Kenanoğlu,
  • Oğuzhan Acet,
  • Ayşe Uyan Önal,
  • Uğur Önal,
  • Seichan Ketentzi,
  • Gamze Şanlıdağ,
  • Gunel Quliyeva,
  • Şükrü Dirik,
  • Cansu Bulut Avşar,
  • Derya Kaya,
  • Şöhret Aydemir,
  • Hüsnü Pullukçu,
  • Meltem Taşbakan,
  • Hilal Sipahi,
  • Bilgin Arda,
  • Oğuz Reşat Sipahi

Journal volume & issue
Vol. 39
p. 14

Abstract

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BACKGROUND-AIM: Herein, we aimed to evaluate and compare the efficacy and susceptibility patterns of tigecycline in MDR A.baumannii pneumonia (MDRABP) in a recent vs retrospective cohort. METHODS: The outcome of adult (>18 years old) patients who were consulted by Infectious Diseases consultants due to culture proven MDRABP and treated with tigecycline between March 2016 and October 2023(Group B) was compared with a similar previously published retrospective cohort from our center(Group A, Published J Chemother. 2011 dec;23(6):345-9). Statistical analysis was performed via Chi square test and a p value less then 0.05 was considered significant. RESULTS: There were total of 202 cases of MDRABP(72 patients in group a and 130 patients in Group B). Forty-seven and 81 cases were considered as VAP in group A and B, respectively. Tigecycline and netilmicin susceptibility were significantly less in group b(Table). C/S combination and tigecycline monotherapy were significantly more common in group A while any combination therapy, colistin, fosfomycin and polymyxin b combination were more common in group B (p<0.05 table). Group A EOT microbiologic eradication was significantly higher in the overall cohorts as well as HAP and VAP subgroups(Table). In the combined data of group A and B microbiological response was similar in tigecycline sensitive vs. intermediately-sensitive strains (41/94-43.6% vs.22/48-45.8% p:0.801). Not overall clinical success but clinical success in combination therapy subgroup was significantly lower in group B(Table). CONCLUSION: Our findings show that tigecycline resistance rates in MDRABP increased during years. Microbiological eradication rates but not clinical outcomes decreased significantly.

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