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

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...

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Main Authors: 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
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Journal of Global Antimicrobial Resistance
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Online Access:http://www.sciencedirect.com/science/article/pii/S2213716524002200
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Summary: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.
ISSN:2213-7165