Fugate Susan, Chiappe Julia
Department of Pharmacy, Clinical and Administrative Sciences, College of Pharmacy, University of Oklahoma, 1110 North Stonewall, P.O. Box 26901, Oklahoma City, OK 73126, USA.
Am J Health Syst Pharm. 2008 Feb 15;65(4):334-9. doi: 10.2146/ajhp070086.
An evidence-based heparin- induced thrombocytopenia (HIT) treatment protocol to standardize the management of confirmed or suspected HIT was developed.
In a retrospective review of 10 patients with known or suspected HIT over a two-year period, medical records were evaluated for baseline laboratory results, treatment selection, initial dosing and monitoring, discontinuation of heparin, and alternative therapies chosen. Six of 10 patients had antibody-confirmed HIT at admission. Nine patients received alternative anticoagulation therapy with one of two formulary direct thrombin inhibitor (DTI) agents, lepirudin and argatroban; 1 patient was given fondaparinux. Medical record analyses revealed deficiencies in both initial and transitional dose administration and renal function monitoring, order omissions, infusion-related medication errors, and treatments that were unsubstantiated, inappropriate, or lacking in regulatory approval. The new treatment protocol developed to assist physicians, pharmacists, and nurses with HIT management focused primarily on the two agents labeled for HIT, lepirudin and argatroban. The protocol established baseline levels for the selection of anticoagulation therapy as well as guidance in DTI selection, use, and monitoring. Guidelines for initial dosing and continuous infusion rates based on weight and detailed instructions in all aspects of therapy discontinuation (transition) were included. HIT treatments unsupported by data ensuring the efficacy and safety of therapies were excluded. Careful review of the relevant literature led to the inclusion of alternative anticoagulant treatments based on issues of safety, efficacy, cost, and convenience of dose forms.
A treatment protocol for HIT was developed and implemented in a tertiary care hospital in an effort to improve the management of patients suffering from this complication.
制定一项基于证据的肝素诱导的血小板减少症(HIT)治疗方案,以规范确诊或疑似HIT的管理。
在对两年内10例已知或疑似HIT患者的回顾性研究中,评估了病历中的基线实验室检查结果、治疗选择、初始剂量和监测、肝素停用情况以及所选择的替代疗法。10例患者中有6例入院时抗体确诊为HIT。9例患者接受了两种处方直接凝血酶抑制剂(DTI)药物之一(来匹卢定和阿加曲班)的替代抗凝治疗;1例患者使用了磺达肝癸钠。病历分析显示,初始和过渡剂量给药以及肾功能监测存在不足,医嘱遗漏,输液相关用药错误,以及治疗缺乏依据、不恰当或未获监管批准。为协助医生、药剂师和护士管理HIT而制定的新治疗方案主要聚焦于两种被标记用于HIT的药物,即来匹卢定和阿加曲班。该方案确定了抗凝治疗选择的基线水平以及DTI选择、使用和监测的指导原则。包括基于体重的初始剂量和持续输注速率指南以及治疗停药(过渡)各方面的详细说明。排除了无数据支持疗效和安全性的HIT治疗方法。对相关文献的仔细审查导致纳入了基于安全性、疗效、成本和剂型便利性问题的替代抗凝治疗方法。
一家三级护理医院制定并实施了HIT治疗方案,以努力改善患有这种并发症患者的管理。