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Empiric Anti-Pseudomonal β-Lactam Monotherapy Versus Fluoroquinolone Combination Therapy in Patients With
Moon Seong Baek1, Ae-Rin Baek2, Sang-Bum Hong3
1Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea.
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.
Insights
Empiric fluoroquinolone combination therapy for hospital-acquired pneumonia (HAP) did not improve survival compared to monotherapy. Routine use of fluoroquinolones in HAP patients at high risk for multidrug-resistant pathogens is not recommended.
Area of Science:
- Infectious Diseases
- Clinical Pharmacy
- Critical Care Medicine
Background:
- Limited data exists on the efficacy of empiric antibiotic combinations for hospital-acquired pneumonia (HAP).
- Investigating the impact of empiric anti-pseudomonal fluoroquinolone combination therapy on HAP patient mortality is crucial.
Purpose of the Study:
- To evaluate whether empiric anti-pseudomonal combination therapy with fluoroquinolones reduces mortality in hospital-acquired pneumonia (HAP) patients.
- To compare the survival outcomes of HAP patients receiving fluoroquinolone combination therapy versus β-lactam monotherapy.
Main Methods:
- A multicenter, retrospective cohort study involving 631 adult HAP patients in Korea.
- Patients were categorized into anti-pseudomonal non-carbapenem β-lactam monotherapy or fluoroquinolone combination therapy groups.
- Propensity score matching (PSM) was employed to control for confounding variables and assess 30-day mortality.
Main Results:
- No significant difference in 30-day mortality was observed between monotherapy (16.8%) and combination therapy (18.2%) groups, even after PSM (17.5% vs. 18.2%).
- The adjusted hazard ratio for 30-day mortality with combination therapy was 1.646 (P=0.189) post-PSM.
- Appropriateness of initial empiric antibiotics and the prevalence of multidrug-resistant (MDR) pathogens were similar between groups.
Conclusions:
- Empiric anti-pseudomonal fluoroquinolone combination therapy offers no survival advantage over β-lactam monotherapy for HAP.
- Clinicians should exercise caution when routinely combining fluoroquinolones for empiric HAP treatment, especially in patients with high risk of MDR infections.
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