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

Q3 Medicine
Przeglad epidemiologiczny Pub Date : 2024-09-18 Epub Date: 2024-06-07 DOI:10.32394/pe/189711
Majid Keivanfar, Rasool Kermani, Mehrdad Hosseinpour, Mohsen Reisi, Bahar Poorkaramali, Sam Mirfendereski
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引用次数: 0

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.

一项回顾性研究,评估胸膜腔内阿替普酶治疗小儿肺水肿的安全性和有效性。
导言:小儿肺水肿的药物治疗包括适当的抗生素、插入胸管和胸膜腔内纤维蛋白溶解药物,以促进胸膜引流。目前对纤维蛋白溶解疗法的首选药物还缺乏共识,因此本研究旨在评估胸膜腔内阿替普酶治疗小儿肺水肿的安全性和有效性:回顾性审查了一家大学医院在2016年1月至2020年12月期间使用胸膜腔内阿替普酶治疗的所有肺水肿患儿的病历。疗效通过阿替普酶首次给药前后的胸管排量、治疗前后的胸腔积液量、手术干预需求和住院时间进行评估。安全性根据副作用的频率和严重程度进行评估:40名2个月至9岁的肺水肿住院患儿接受了胸膜腔内阿替普酶治疗。30名患者(75%)在接受了三次胸膜腔内阿替普酶治疗后完全康复。住院时间中位数为 16 天。首次使用阿替普酶后,胸腔导管输出量明显增加。治疗后胸腔积液量明显减少。最常见的副作用是疼痛(30%)。两名患者出现了严重的并发症:一名患者出现肺出血,另一名患者出现支气管胸膜瘘。这些患者都已完全自愈:根据我们的研究结果,胸膜腔内注射阿替普酶在促进儿童肺水肿患者胸膜引流方面是安全有效的。然而,要确定胸膜腔内阿替普酶治疗的最佳剂量、频率和持续时间,还需要进一步的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Przeglad epidemiologiczny
Przeglad epidemiologiczny Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
64
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