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阿替普酶治疗儿童中心静脉导管阻塞:一项前瞻性、开放标签、单臂研究(Cathflo Activase儿科研究)的结果

Alteplase for the treatment of central venous catheter occlusion in children: results of a prospective, open-label, single-arm study (The Cathflo Activase Pediatric Study).

作者信息

Blaney Martha, Shen Violet, Kerner John A, Jacobs Brian R, Gray Sarah, Armfield Jennifer, Semba Charles P

机构信息

Department of Vascular Medicine, Genentech, South San Francisco, CA 94080, USA.

出版信息

J Vasc Interv Radiol. 2006 Nov;17(11 Pt 1):1745-51. doi: 10.1097/01.RVI.0000241542.71063.83.

Abstract

PURPOSE

Alteplase is approved for use in the restoration of function to occluded central venous access devices (CVADs); however, there are few prospective studies in children. This study was undertaken to evaluate the safety and efficacy of alteplase in the treatment of CVAD occlusions in a pediatric population.

MATERIALS AND METHODS

A prospective, multicenter, open-label, single-arm study evaluating a maximum of two doses (< or =2 mg per dose) of alteplase was performed in pediatric patients. Inclusion criteria included patient age less than 17 years with an occluded CVAD (single-, double-, and triple-lumen catheter or implanted port). Patients with hemodialysis catheters, those with known mechanical occlusion, or those considered at high risk for bleeding or embolization were excluded. Assessment of function was made 30 and 120 minutes (if required) after each dose. The primary objective of the study was to evaluate the safety of alteplase as measured by the incidence of intracranial hemorrhage (ICH); secondary objectives included the evaluation of specific targeted serious adverse events and efficacy of alteplase in the restoration of catheter function.

RESULTS

A total of 310 patients (174 male patients, 136 female patients; mean age, 7.2 years; range, 0.04-18.3 y) were treated; 55 of the patients (17.7%) were younger than 2 years of age. No patients experienced ICH (95% CI, 0%-1.2%). Nine serious adverse events were noted in eight patients (2.6% incidence), two of which were attributed by the investigator to study drug administration (one case of sepsis and one case of a ruptured catheter lumen). The cumulative rate of restoration of CVAD function after serial administration of a maximum of two instillations of alteplase, each with a maximum dwell time of 120 minutes, was 82.9% (95% CI, 78.2%-86.9%). Similar rates of catheter function restoration were seen among all catheter types studied; there were no clinically meaningful differences among age or sex subgroups.

CONCLUSION

The administration of alteplase is safe and effective for the restoration of function to CVADs in pediatric patients.

摘要

目的

阿替普酶已被批准用于恢复阻塞的中心静脉通路装置(CVAD)的功能;然而,针对儿童的前瞻性研究较少。本研究旨在评估阿替普酶治疗儿科患者CVAD阻塞的安全性和有效性。

材料与方法

在儿科患者中进行了一项前瞻性、多中心、开放标签、单臂研究,评估最多两剂(每剂≤2mg)阿替普酶。纳入标准包括年龄小于17岁且CVAD阻塞(单腔、双腔和三腔导管或植入式端口)的患者。排除有血液透析导管的患者、已知机械性阻塞的患者或被认为有出血或栓塞高风险的患者。在每剂给药后30分钟和120分钟(如有需要)进行功能评估。本研究的主要目的是通过颅内出血(ICH)发生率评估阿替普酶的安全性;次要目的包括评估特定的严重不良事件以及阿替普酶恢复导管功能的有效性。

结果

共治疗310例患者(174例男性患者,136例女性患者;平均年龄7.2岁;范围0.04 - 18.3岁);其中55例患者(17.7%)年龄小于2岁。无患者发生ICH(95%CI,0% - 1.2%)。8例患者出现9例严重不良事件(发生率2.6%),其中2例经研究者判定与研究药物给药有关(1例败血症和1例导管腔破裂)。在最多连续两次滴注阿替普酶(每次最长停留时间120分钟)后,CVAD功能恢复的累积率为82.9%(95%CI,78.2% - 86.9%)。在所有研究的导管类型中,导管功能恢复率相似;年龄或性别亚组之间无临床意义上的差异。

结论

阿替普酶给药对于恢复儿科患者CVAD的功能是安全有效的。

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