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Outcomes of Levofloxacin-Based Regimens in Adults With Severe Community-Acquired Pneumonia Requiring ICU Admission: A Single-Center Retrospective Cohort From Jazan, Saudi Arabia

Ahmed Hakami, Amnah Numan, Shoroog Obaidullah, Shahad Numan, Ahmad Alharbi, Hanan Hakami, Hanan Bakri, Nawal Hakami et al.

Saudi Journal of Medicine and Public Health, 2025

93 participants

Abstract

Background

Levofloxacin is widely used in combination regimens for severe community-acquired pneumonia (CAP) in the ICU; however, real-world outcome data from resource-limited settings remain scarce.

Objective:

To evaluate 28-day mortality and key clinical/safety outcomes among adults with severe CAP requiring ICU admission who received levofloxacin-based regimens at Abu-Arish General Hospital.

Methods

We conducted a retrospective cohort study that examined patient data captured through an electronic medical system at the Abu Arish General Hospital between 2021 and 2022 (Single‑center retrospective cohort (dates), Abu‑Arish General Hospital ICU). We used the repeated measures ANCOVA to investigate the effect of Levofloxacin on a wide range of medical parameters. Data analysis was performed with SPSS statistics (Version 25).

Results

A total of 93 patients were included in this study. The study examined the impact of levofloxacin on various medical parameters, including age, weight, height, BMI, initial dosage, comorbid diseases and sex. The adjusted mean differences between before and after Levofloxacin administration revealed significant changes in a variety of medical parameters, including hepatic markers and hematologic indices.

Conclusion

Levofloxacin therapy can produce change in baseline clinical characteristics of critical ill patients in the intensive care unit. We need to investigate the tolerability of this therapy in terms the severity of side effects on a large…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 93 participants or records.

How the five levels of evidence work. The level is assigned automatically from the abstract and can be wrong, so check the paper.

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