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回顾性研究评估胸腔内注射阿替普酶治疗小儿脓胸的安全性和有效性。

A retrospective study to evaluate the safety and efficacy of intrapleural alteplase in pediatric empyema.

机构信息

Isfahan University of Medical Sciences, Isfahan, Iran.

Research Institute for Primordial Prevention of Non-communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Przegl Epidemiol. 2024 Sep 18;78(2):145-149. doi: 10.32394/pe/189711. Epub 2024 Jun 7.

Abstract

INTRODUCTION

Medical treatment of pediatric empyema consists of appropriate antibiotics, chest tube insertion, and intrapleural fibrinolytic drugs to facilitate pleural drainage. There is a lack of consensus about the drug of choice for fibrinolytic therapy, so this study was designed to evaluate the safety and efficacy of intrapleural alteplase in pediatric empyema.

MATERIAL AND METHODS

The medical records of all children with empyema treated with intrapleural alteplase at a university hospital between January 2016 and December 2020 were retrospectively reviewed. Efficacy outcomes were assessed by chest tube output before and after the first dose of alteplase, pleural fluid volume before and after therapy, a need for surgical intervention, and length of hospital stay. Safety was assessed by the frequency and severity of side effects.

RESULTS

40 children aged 2 months to 9 years hospitalized with empyema received intrapleural alteplase. Thirty patients (75%) experienced full recovery after three doses of intrapleural alteplase. The median length of hospital stay was 16 days. Chest tube output increased significantly after the first dose of alteplase. Pleural fluid volume decreased significantly after treatment. The most common side effect was pain (30%). Two patients experienced severe complications: 1 had a pulmonary hemorrhage and the other experienced a bronchopleural fistula. These patients recovered fully spontaneously.

CONCLUSIONS

According to our results, the administration of intrapleural alteplase was safe and effective in facilitating pleural drainage in pediatric patients with empyema. However, further clinical trials will be needed to determine the optimal dose, frequency, and duration of intrapleural alteplase treatment.

摘要

引言

小儿脓胸的治疗包括使用适当的抗生素、胸腔引流管插入和胸腔内纤维蛋白溶解药物,以促进胸腔引流。对于纤维蛋白溶解治疗的首选药物,目前尚未达成共识,因此本研究旨在评估胸腔内使用阿替普酶治疗小儿脓胸的安全性和疗效。

材料和方法

回顾性分析了 2016 年 1 月至 2020 年 12 月期间在一所大学医院接受胸腔内阿替普酶治疗的所有脓胸患儿的病历。通过胸腔引流管首次给药前后的引流量、治疗前后胸腔积液量、是否需要手术干预以及住院时间来评估疗效。通过副作用的频率和严重程度来评估安全性。

结果

40 名 2 个月至 9 岁的脓胸患儿接受了胸腔内阿替普酶治疗。30 名患者(75%)在接受三次胸腔内阿替普酶治疗后完全康复。中位住院时间为 16 天。胸腔引流管引流量在首次给药后显著增加。治疗后胸腔积液量明显减少。最常见的副作用是疼痛(30%)。两名患者发生严重并发症:1 例出现肺出血,另 1 例出现支气管胸膜瘘。这些患者均自发完全康复。

结论

根据我们的结果,胸腔内给予阿替普酶可安全有效地促进小儿脓胸患者的胸腔引流。然而,需要进一步的临床试验来确定胸腔内阿替普酶治疗的最佳剂量、频率和持续时间。

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