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Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching
BACKGROUND: There is insufficient data on the benefits of empiric antibiotic combinations for hospital-acquired pneumonia (HAP). We aimed to investigate whether empiric anti-pseudomonal combination therapy with fluoroquinolones decreases mortality in patients with HAP. METHODS: This multicenter, ret...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593602/ https://www.ncbi.nlm.nih.gov/pubmed/37873633 http://dx.doi.org/10.3346/jkms.2023.38.e353 |
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author | Baek, Moon Seong Baek, Ae-Rin Hong, Sang-Bum Bae, Soohyun Park, Hye Kyeong Kim, Changhwan Lee, Hyun-Kyung Cho, Woo Hyun Kim, Jin Hyoung Chang, Youjin Lee, Heung Bum Gil, Hyun-Il Shin, Beomsu Yoo, Kwang Ha Moon, Jae Young Oh, Jee Youn Min, Kyung Hoon Jeon, Kyeongman |
author_facet | Baek, Moon Seong Baek, Ae-Rin Hong, Sang-Bum Bae, Soohyun Park, Hye Kyeong Kim, Changhwan Lee, Hyun-Kyung Cho, Woo Hyun Kim, Jin Hyoung Chang, Youjin Lee, Heung Bum Gil, Hyun-Il Shin, Beomsu Yoo, Kwang Ha Moon, Jae Young Oh, Jee Youn Min, Kyung Hoon Jeon, Kyeongman |
author_sort | Baek, Moon Seong |
collection | PubMed |
description | BACKGROUND: There is insufficient data on the benefits of empiric antibiotic combinations for hospital-acquired pneumonia (HAP). We aimed to investigate whether empiric anti-pseudomonal combination therapy with fluoroquinolones decreases mortality in patients with HAP. METHODS: This multicenter, retrospective cohort study included adult patients admitted to 16 tertiary and general hospitals in Korea between January 1 and December 31, 2019. Patients with risk factors for combination therapy were divided into anti-pseudomonal non-carbapenem β-lactam monotherapy and fluoroquinolone combination therapy groups. Primary outcome was 30-day mortality. Propensity score matching (PSM) was used to reduce selection bias. RESULTS: In total, 631 patients with HAP were enrolled. Monotherapy was prescribed in 54.7% (n = 345) of the patients, and combination therapy was prescribed in 45.3% (n = 286). There was no significant difference in 30-day mortality between the two groups (16.8% vs. 18.2%, P = 0.729) or even after the PSM (17.5% vs. 18.2%, P = 0.913). After the PSM, adjusted hazard ratio for 30-day mortality from the combination therapy was 1.646 (95% confidence interval, 0.782–3.461; P = 0.189) in the Cox proportional hazards model. Moreover, there was no significant difference in the appropriateness of initial empiric antibiotics between the two groups (55.0% vs. 56.8%, P = 0.898). The proportion of multidrug-resistant (MDR) pathogens was high in both groups. CONCLUSION: Empiric anti-pseudomonal fluoroquinolone combination therapy showed no survival benefit compared to β-lactam monotherapy in patients with HAP. Caution is needed regarding the routine combination of fluoroquinolones in the empiric treatment of HAP patients with a high risk of MDR. |
format | Online Article Text |
id | pubmed-10593602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-105936022023-10-25 Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching Baek, Moon Seong Baek, Ae-Rin Hong, Sang-Bum Bae, Soohyun Park, Hye Kyeong Kim, Changhwan Lee, Hyun-Kyung Cho, Woo Hyun Kim, Jin Hyoung Chang, Youjin Lee, Heung Bum Gil, Hyun-Il Shin, Beomsu Yoo, Kwang Ha Moon, Jae Young Oh, Jee Youn Min, Kyung Hoon Jeon, Kyeongman J Korean Med Sci Original Article BACKGROUND: There is insufficient data on the benefits of empiric antibiotic combinations for hospital-acquired pneumonia (HAP). We aimed to investigate whether empiric anti-pseudomonal combination therapy with fluoroquinolones decreases mortality in patients with HAP. METHODS: This multicenter, retrospective cohort study included adult patients admitted to 16 tertiary and general hospitals in Korea between January 1 and December 31, 2019. Patients with risk factors for combination therapy were divided into anti-pseudomonal non-carbapenem β-lactam monotherapy and fluoroquinolone combination therapy groups. Primary outcome was 30-day mortality. Propensity score matching (PSM) was used to reduce selection bias. RESULTS: In total, 631 patients with HAP were enrolled. Monotherapy was prescribed in 54.7% (n = 345) of the patients, and combination therapy was prescribed in 45.3% (n = 286). There was no significant difference in 30-day mortality between the two groups (16.8% vs. 18.2%, P = 0.729) or even after the PSM (17.5% vs. 18.2%, P = 0.913). After the PSM, adjusted hazard ratio for 30-day mortality from the combination therapy was 1.646 (95% confidence interval, 0.782–3.461; P = 0.189) in the Cox proportional hazards model. Moreover, there was no significant difference in the appropriateness of initial empiric antibiotics between the two groups (55.0% vs. 56.8%, P = 0.898). The proportion of multidrug-resistant (MDR) pathogens was high in both groups. CONCLUSION: Empiric anti-pseudomonal fluoroquinolone combination therapy showed no survival benefit compared to β-lactam monotherapy in patients with HAP. Caution is needed regarding the routine combination of fluoroquinolones in the empiric treatment of HAP patients with a high risk of MDR. The Korean Academy of Medical Sciences 2023-10-16 /pmc/articles/PMC10593602/ /pubmed/37873633 http://dx.doi.org/10.3346/jkms.2023.38.e353 Text en © 2023 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Baek, Moon Seong Baek, Ae-Rin Hong, Sang-Bum Bae, Soohyun Park, Hye Kyeong Kim, Changhwan Lee, Hyun-Kyung Cho, Woo Hyun Kim, Jin Hyoung Chang, Youjin Lee, Heung Bum Gil, Hyun-Il Shin, Beomsu Yoo, Kwang Ha Moon, Jae Young Oh, Jee Youn Min, Kyung Hoon Jeon, Kyeongman Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title | Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title_full | Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title_fullStr | Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title_full_unstemmed | Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title_short | Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With Hospital-Acquired Pneumonia: A Multicenter Cohort Study With Propensity Score Matching |
title_sort | empiric anti-pseudomonal β-lactam monotherapy versus fluoroquinolone combination therapy in patients with hospital-acquired pneumonia: a multicenter cohort study with propensity score matching |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593602/ https://www.ncbi.nlm.nih.gov/pubmed/37873633 http://dx.doi.org/10.3346/jkms.2023.38.e353 |
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