Veerabagu M P, Tuttle-Newhall J, Maliakkal R, Champagne C, Mascioli E A
Nutrition Support Service, New England Deaconess Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Nutrition. 1995 Mar-Apr;11(2):142-4.
Central venous thrombosis is a potentially life-threatening complication in patients on long-term home total parenteral nutrition (HTPN). Lack of venous access due to recurrent thromboses can prevent delivery of life-saving nutritional support. The long-term anticoagulation management to prevent thromboses in patients with central venous catheters for HTPN has not been well established. We have reviewed the role of warfarin in reducing the incidence of thromboses and its safety in our HTPN patients. Ninety consecutive HTPN patients were studied retrospectively. Twenty-two thromboses occurred during 1312 patient-mo in 53 HTPN patients on minidose warfarin. A minidose of warfarin is defined as 1-2 mg and does not prolong the prothrombin time. Seven thromboses occurred over 619 mo in 18 patients on a therapeutic dose of warfarin (minidose compared to therapeutic dose, p > 0.05). A therapeutic dose of warfarin is a dose that increases the prothrombin time to 1.2-1.5 times that of control. Twelve patients who had 18 thromboses in 323 patient-mo while on minidose warfarin were subsequently converted to therapeutic warfarin. The incidence of thromboses decreased to 2 in 369 patient-mo (p < 0.005). There were no hemorrhagic complications in the minidose warfarin group and four nonfatal hemorrhagic complications in the therapeutic dose warfarin group (p > 0.05). A therapeutic dose of warfarin is effective in reducing the incidence of thromboses in patients who experience central venous thrombosis despite minidose warfarin with a minimal increase in hemorrhagic complications.
中心静脉血栓形成是长期家庭全胃肠外营养(HTPN)患者中一种潜在的危及生命的并发症。由于反复血栓形成导致的静脉通路缺乏可能会妨碍提供挽救生命的营养支持。用于预防接受HTPN的中心静脉导管患者发生血栓形成的长期抗凝管理尚未得到充分确立。我们回顾了华法林在降低我们的HTPN患者血栓形成发生率及其安全性方面的作用。对90例连续的HTPN患者进行了回顾性研究。在53例接受小剂量华法林治疗的HTPN患者的1312个患者月期间发生了22例血栓形成。小剂量华法林定义为1 - 2毫克,且不延长凝血酶原时间。18例接受治疗剂量华法林治疗的患者在619个月期间发生了7例血栓形成(小剂量与治疗剂量相比,p>0.05)。治疗剂量的华法林是指将凝血酶原时间延长至对照值的1.2 - 1.5倍的剂量。12例在接受小剂量华法林治疗期间于323个患者月发生18例血栓形成的患者随后转为接受治疗性华法林治疗。血栓形成发生率降至369个患者月2例(p<0.005)。小剂量华法林组未发生出血并发症,治疗剂量华法林组发生4例非致命性出血并发症(p>0.05)。治疗剂量的华法林对于尽管接受小剂量华法林治疗仍发生中心静脉血栓形成的患者,在将出血并发症最小增加的情况下,可有效降低血栓形成发生率。