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胸腔内纤溶酶原激活物与链激酶治疗复杂性类肺炎性胸腔积液和脓胸的前瞻性随机研究。

Intrapleural Fibrinolysis with Urokinase Versus Alteplase in Complicated Parapneumonic Pleural Effusions and Empyemas: A Prospective Randomized Study.

机构信息

Department of Internal Medicine, University Hospital Vall d'Hebron, Universitat Autónoma de Barcelona, Barcelona, Spain.

Pleural Medicine Unit, Department of Internal Medicine, Arnau de Vilanova University Hospital, Biomedical Research Institute of Lleida, Lleida, Spain.

出版信息

Lung. 2015 Dec;193(6):993-1000. doi: 10.1007/s00408-015-9807-6. Epub 2015 Sep 30.

Abstract

BACKGROUND

Pleurofibrinolysis has been reported to be potentially beneficial in the management of complicated parapneumonic effusions (CPPE) and empyemas in the adult population.

METHODS

Prospective, controlled, randomized, and double-blind study, to evaluate intrapleural alteplase 10 mg (initially 20 mg was considered but bleeding events forced dose reduction) versus 100,000 UI urokinase every 24 h for a maximum of 6 days in patients with CPPE or empyemas. The primary aim was to evaluate the success rate of each fibrinolytic agent at 3 and 6 days. Success of therapy was defined as the presence of both clinical and radiological improvement, making additional fibrinolytic doses unnecessary, and eventually leading to resolution. Secondary outcomes included the safety profile of intrapleural fibrinolytics, referral for surgery, length of hospital stay, and mortality.

RESULTS

A total of 99 patients were included, of whom 51 received alteplase and 48 urokinase. Success rates for urokinase and alteplase at 3 and 6 days were not significantly different, but when only the subgroup of CPPE was considered, urokinase resulted in a high proportion of cures. There were no differences in mortality or surgical need (overall, 3 %). Five (28 %) patients receiving 20 mg of alteplase and 4 (12 %) receiving 10 mg presented serious bleeding events.

CONCLUSIONS

If intrapleural fibrinolytics are intended to be used, urokinase may be more effective than alteplase in patients with non-purulent CPPE and have a lower rate of adverse events.

摘要

背景

已有研究报道,纤维蛋白溶解疗法可能对成人复杂性类肺炎性胸腔积液(CPPE)和脓胸的治疗有益。

方法

这是一项前瞻性、对照、随机、双盲研究,旨在评估胸腔内注射 10 mg 阿替普酶(最初考虑使用 20 mg,但出血事件迫使减少剂量)与每 24 小时注射 10 万 UI 尿激酶,最多 6 天,用于治疗 CPPE 或脓胸患者。主要目的是评估两种纤维蛋白溶解剂在第 3 天和第 6 天的成功率。治疗成功定义为临床和影像学改善,无需额外使用纤维蛋白溶解剂,最终导致缓解。次要结局包括胸腔内纤维蛋白溶解剂的安全性、手术转诊、住院时间和死亡率。

结果

共纳入 99 例患者,其中 51 例接受阿替普酶治疗,48 例接受尿激酶治疗。尿激酶和阿替普酶在第 3 天和第 6 天的成功率无显著差异,但仅考虑 CPPE 亚组时,尿激酶的治愈率较高。死亡率或手术需求无差异(总体为 3 %)。5 例(28 %)接受 20 mg 阿替普酶和 4 例(12 %)接受 10 mg 阿替普酶的患者出现严重出血事件。

结论

如果计划使用胸腔内纤维蛋白溶解剂,尿激酶在非脓性 CPPE 患者中的疗效可能优于阿替普酶,且不良事件发生率较低。

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