Scott L Keith, Grier Laurie R, Conrad Steven A
ECLS Program, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA.
Pediatr Crit Care Med. 2006 May;7(3):255-7. doi: 10.1097/01.PCC.0000200966.56379.95.
Heparin-induced thrombocytopenia (HIT) is rare in the pediatric population, with a majority occurring in the pediatric intensive care unit setting. All reported cases have been associated with the use of unfractionated heparin. Because unfractionated heparin is the anticoagulant of choice for extracorporeal life support, the development of HIT in these patients can be devastating. We report a case of HIT with evidence of small-vessel arterial thromboembolism in a 17-month-old child receiving extracorporeal membrane oxygenation and continuous renal replacement therapy successfully treated with argatroban.
The patient was a 17-month-old boy with severe respiratory failure secondary to asthma and mucus plugging that failed conventional and unconventional ventilation. Venovenous extracorporeal membrane oxygenation was initiated, and within 24 hrs, there was a precipitous decrease in the platelet count, with the development of cutaneous ischemia involving his lower limbs. Heparin-associated antibodies were positive. Argatroban was started, and the child maintained on extracorporeal membrane oxygenation and continuous renal replacement therapy, with resolution of the cutaneous ischemia and rebound of the thrombocytopenia.
HIT is rare in the pediatric population. Recognition of HIT is vital because withdrawal of heparin is the first and most important therapy. For patients on extracorporeal membrane oxygenation or continuous renal replacement therapy who develop HIT, synthetic thrombin inhibitors (hirulogs) have been reported as an alternative. However, little information on their use in extracorporeal life support has been published, particularly in the pediatric population.
This report documents a pediatric case of HIT successfully treated with argatroban, allowing continuation of the venovenous extracorporeal membrane oxygenation and continuous renal replacement therapy, with resolution of the thromboembolic ischemia and thrombocytopenia.
肝素诱导的血小板减少症(HIT)在儿科人群中较为罕见,大多数病例发生在儿科重症监护病房。所有报道的病例均与使用普通肝素有关。由于普通肝素是体外生命支持的首选抗凝剂,这些患者发生HIT可能是灾难性的。我们报告一例17个月大接受体外膜肺氧合和持续肾脏替代治疗的儿童发生HIT并伴有小血管动脉血栓栓塞的病例,该患儿用阿加曲班成功治疗。
该患者是一名17个月大的男孩,因哮喘和黏液阻塞继发严重呼吸衰竭,常规和非常规通气均失败。开始进行静脉-静脉体外膜肺氧合,24小时内血小板计数急剧下降,出现累及下肢的皮肤缺血。肝素相关抗体呈阳性。开始使用阿加曲班,患儿继续接受体外膜肺氧合和持续肾脏替代治疗,皮肤缺血得到缓解,血小板减少症出现反弹。
HIT在儿科人群中罕见。认识到HIT至关重要,因为停用肝素是首要且最重要的治疗方法。对于接受体外膜肺氧合或持续肾脏替代治疗并发生HIT的患者,已报道合成凝血酶抑制剂(水蛭素)可作为替代药物。然而,关于它们在体外生命支持中的应用,特别是在儿科人群中的应用,发表的信息很少。
本报告记录了一例用阿加曲班成功治疗的儿科HIT病例,使得静脉-静脉体外膜肺氧合和持续肾脏替代治疗得以继续,血栓栓塞性缺血和血小板减少症得到缓解。