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小儿多房性脓胸的胸膜内纤维蛋白溶解治疗

Intrapleural fibrinolytic treatment of multiloculated pediatric empyemas.

作者信息

Ulkü Refik, Onen Abdurrahman, Onat Serdar, Kilinç Nihal, Ozçelik Cemal

机构信息

Department of Thoracic Surgery, Dicle University School of Medicine, 21280, Diyarbakir, Turkey.

出版信息

Pediatr Surg Int. 2004 Jul;20(7):520-4. doi: 10.1007/s00383-004-1214-7. Epub 2004 Jun 8.

Abstract

Our objective was to compare the efficacy of adjunctive intrapleural fibrinolytic agents (IPFA) (streptokinase, urokinase) on fibrinopurulent stage empyema and chronic stage empyema in children. IPFA were used in 78 pediatric patients with empyema (36 fibrinopurulent stage empyemas, 42 chronic stage empyemas) between December 1994 and September 2002. Pleural biopsy was done for staging in all cases. Streptokinase 250,000 units in 100 ml normal saline (62 patients) or 100,000 units urokinase in 100 ml normal saline (16 patients) was instilled daily into the patient's chest tube, and the tube was clamped for 4 h, followed by suction. This treatment was continued daily for 2-8 days until resolution was demonstrated by chest radiographs and/or computed chest tomography. Success of treatment was 97.2% (complete response 24/36, partial response 11/36) in the fibrinopurulent stage and 9.4% (complete response 2/42, partial response 2/42) in chronic empyema cases. In one patient with fibrinopurulent empyema, the treatment was stopped due to allergic reaction and pleural hemorrhage; this patient died 1 day later in a septic condition. Although an invasive method, the pleural biopsy technique may be an alternative way of more properly staging thoracic empyema in selected children in whom staging based on radiographic and biochemical findings is doubtful. Intrapleural fibrinolytic treatment is an effective and safe therapy of choice and may have significant benefit in most children with fibrinopurulent phase empyema, except for those with bronchopleural fistula. IPFA do not seem to be effective in children with chronic phase empyema.

摘要

我们的目的是比较辅助性胸膜内纤维蛋白溶解剂(IPFA)(链激酶、尿激酶)对儿童纤维脓性期脓胸和慢性期脓胸的疗效。1994年12月至2002年9月期间,78例小儿脓胸患者(36例纤维脓性期脓胸,42例慢性期脓胸)使用了IPFA。所有病例均进行胸膜活检以分期。将25万单位链激酶溶于100 ml生理盐水中(62例患者)或10万单位尿激酶溶于100 ml生理盐水中(16例患者)每日经胸管注入患者胸腔,胸管夹闭4小时,然后进行抽吸。这种治疗每天持续2 - 8天,直到胸部X线片和/或胸部计算机断层扫描显示脓胸消退。纤维脓性期治疗成功率为97.2%(完全缓解24/36,部分缓解11/36),慢性脓胸病例为9.4%(完全缓解2/42,部分缓解2/42)。1例纤维脓性脓胸患者因过敏反应和胸膜出血停止治疗;该患者1天后因脓毒症死亡。尽管胸膜活检技术是一种侵入性方法,但对于根据影像学和生化检查结果进行分期存疑的特定儿童,它可能是更准确地对胸腔脓胸进行分期的另一种方法。胸膜内纤维蛋白溶解治疗是一种有效且安全的治疗选择,对大多数纤维脓性期脓胸儿童可能有显著益处,但有支气管胸膜瘘的儿童除外。IPFA对慢性期脓胸儿童似乎无效。

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