Efficacy of Azithromycin and Meropenem in Pediatric XDR Salmonella Typhi: A Retrospective Study from Abbottabad, Pakistan

Khyal Muhammad, Kalsoom Kalsoom, Amna Khan, Anis Ur Rehman, Khadija Bibi
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Abstract

Objective: To evaluate the efficacy of azithromycin as a first-line therapy and the combination of meropenem and azithromycin as the second-line therapy in treating pediatric patients with extensively drug-resistant (XDR) Salmonella Typhi in Abbottabad, Pakistan. Methods: This retrospective cross-sectional study was conducted at Department of Pediatrics, Abbottabad International Medical Complex, Pakistan from May 2022 to January 2024. Children aged 1-15 years clinically diagnosed with typhoid fever were enrolled if subsequent blood cultures confirmed XDR Salmonella Typhi infection. Initial treatment comprised azithromycin. If there was no response to azithromycin, patients received a combination therapy of meropenem alongside continued azithromycin. Primary outcomes were clinical recovery, recurrence within 30 days post-treatment, and treatment-related adverse effects. Results: Of total 67 pediatric patients, the mean age of the patients was 10.02 ±2.76 years. The overall mean duration of defervescence was 6.01 ±2.98 days. Initially, all patients were treated with azithromycin alone. Most patients recovered clinically 57 (85.1%). For the 10 (14.9%) who did not respond, meropenem was added to azithromycin, resulting in recovery for all. The mean duration of defervescence found significantly low in patients who received azithromycin monotherapy as compared to patients who received combination therapy i.e., 4.80 ±0.58 days vs. 12.90 ±1.10 days (p-value <0.001). Mild nausea was the only adverse event observed in 29 patients (43.3%) during treatment. Conclusion: Azithromycin monotherapy demonstrated a high clinical recovery rate, with a significant reduction in fever duration compared to combination therapy with meropenem. Mild nausea was the only treatment-related adverse effect observed.
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阿奇霉素和美罗培南对小儿 XDR 伤寒沙门氏菌的疗效:巴基斯坦阿伯塔巴德的一项回顾性研究
目的评估阿奇霉素作为一线疗法以及美罗培南和阿奇霉素联合疗法作为二线疗法治疗巴基斯坦阿伯塔巴德广泛耐药(XDR)伤寒沙门氏菌儿科患者的疗效。研究方法这项回顾性横断面研究于 2022 年 5 月至 2024 年 1 月在巴基斯坦阿伯塔巴德国际医疗中心儿科进行。临床诊断为伤寒的 1-15 岁儿童,如果随后的血液培养证实感染了 XDR 伤寒沙门氏菌,则被纳入研究范围。初始治疗包括阿奇霉素。如果患者对阿奇霉素无反应,则在继续接受阿奇霉素治疗的同时接受美罗培南联合治疗。主要结果是临床康复、治疗后 30 天内复发以及与治疗相关的不良反应。结果67名儿童患者的平均年龄为(10.02±2.76)岁。总平均延期时间为(6.01±2.98)天。最初,所有患者都只接受了阿奇霉素治疗。大多数患者临床痊愈 57 例(85.1%)。对于 10 例(14.9%)无反应的患者,在阿奇霉素的基础上加用美罗培南,结果所有患者均痊愈。与接受联合疗法的患者相比,接受阿奇霉素单一疗法的患者的平均缓解期明显较短,即 4.80 ±0.58 天对 12.90 ±1.10 天(P 值 <0.001)。治疗期间,29 名患者(43.3%)出现轻度恶心,这是唯一的不良反应。结论与美罗培南联合疗法相比,阿奇霉素单药治疗临床痊愈率高,发热持续时间显著缩短。轻度恶心是唯一观察到的与治疗相关的不良反应。
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来源期刊
Journal of the Dow University of Health Sciences
Journal of the Dow University of Health Sciences Health Professions-Health Professions (miscellaneous)
CiteScore
0.30
自引率
0.00%
发文量
22
审稿时长
14 weeks
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