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使用全血凝血酶原时间监测仪对儿童华法林治疗进行家庭监测。

Home monitoring of warfarin therapy in children with a whole blood prothrombin time monitor.

作者信息

Massicotte P, Marzinotto V, Vegh P, Adams M, Andrew M

机构信息

Children's Hospital at Chedoke-McMaster, Hamilton, Ontario, Canada.

出版信息

J Pediatr. 1995 Sep;127(3):389-94. doi: 10.1016/s0022-3476(95)70069-2.

Abstract

We prospectively evaluated a capillary whole blood prothrombin time (PT) monitor (Biotrack, Ciba Corning) in an outpatient pediatric anticoagulation clinic (40 clinic patients) and in age-matched healthy subjects (30 control subjects). Subsequently, 23 children requiring warfarin therapy were placed on a home program (home patients) using the PT monitor; their parents were trained and the results followed by clinic staff. The PT results were reported as internationalized normalized ratios (INRs). The laboratory and PT-monitor INR values were similar for the clinic patients and the control subjects (y = 0.76x + 0.38; r = 0.93; p < 0.001). The accuracy of the PT monitor (the difference between INR values and the laboratory INR) was best at an INR of 2.5 to 3.5; 90% of paired INR values were within 0.8 INR units. The average duration of monitoring for home patients was 13 months (range, 2 to 60 months). They had an average of 3 dose measurements (range, 1 to 11 measurements) and 1.8 dose changes (range, 0.6 to 4.5 changes) per month. Of the 599 measurements, 63% were within the therapeutic range, similar to those for clinic patients; the dose requirements were also similar. There was 1 significant bleeding event, a subdural hematoma in a patient with an INR of 4.1, and 1 catheter-related thrombotic event with an INR of 1.2; both children recovered. Of the 23 families, one discontinued home monitoring because of parental discomfort, 2 children died of their primary disease, 6 completed warfarin therapy, and 14 remain on the home program. We conclude that the whole blood PT/INR monitor is safe and offers practical advantages to children requiring anticoagulation.

摘要

我们前瞻性地评估了一种毛细血管全血凝血酶原时间(PT)监测仪(Biotrack,汽巴康宁公司),研究对象为一家门诊儿科抗凝诊所的40名临床患者以及年龄匹配的30名健康受试者(对照对象)。随后,23名需要华法林治疗的儿童使用该PT监测仪开展家庭监测项目(家庭患者);对他们的父母进行了培训,诊所工作人员跟踪监测结果。PT结果以国际化标准化比值(INR)报告。临床患者和对照对象的实验室INR值与PT监测仪的INR值相似(y = 0.76x + 0.38;r = 0.93;p < 0.001)。PT监测仪的准确性(INR值与实验室INR之间的差异)在INR为2.5至3.5时最佳;90%的配对INR值在0.8个INR单位以内。家庭患者的平均监测时长为13个月(范围为2至60个月)。他们每月平均进行3次剂量测量(范围为1至11次测量)以及1.8次剂量调整(范围为0.6至4.5次调整)。在599次测量中,63%在治疗范围内,与临床患者相似;剂量需求也相似。发生了1起严重出血事件,1名INR为4.1的患者出现硬膜下血肿,以及1起INR为1.2的导管相关血栓形成事件;两名儿童均康复。在23个家庭中,1个家庭因家长感到不便而停止家庭监测,2名儿童死于原发性疾病,6名儿童完成了华法林治疗,14名儿童仍在家庭监测项目中。我们得出结论,全血PT/INR监测仪是安全的,对于需要抗凝治疗的儿童具有实际优势。

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