Skelley Jessica W, Kyle Jeffrey A, Roberts Rachel A
Department of Pharmacy Practice, McWhorter School of Pharmacy, Samford University, 800 Lakeshore Drive, Birmingham, AL, 35229, USA.
J Thromb Thrombolysis. 2016 Aug;42(2):172-8. doi: 10.1007/s11239-016-1365-0.
To review the use of the novel oral anticoagulant (NOAC) agents for the treatment of heparin-induced thrombocytopenia (HIT) from relevant clinical trial data. A MEDLINE, International Pharmaceutical Abstracts, ClinicalTrials.gov, and Google-Scholar searches (1966-March 2016) were conducted using the keywords: thrombocytopenia, NOACs, dabigatran, apixaban, rivaroxaban, edoxaban, Xa inhibitor, direct thrombin inhibitor. Articles evaluating the new oral anticoagulants for thrombocytopenia published in English and using human subjects were selected. Eight clinical trials were identified. References cited in identified articles were used for additional citations. Approximately 12 million hospitalized patients each year are exposed to heparin for thromboprophylaxis. HIT, an immune-mediated, prothrombotic adverse reaction is a potential complication of heparin therapy. As a result, heparin products must be immediately withdrawn and replaced by alternative anticoagulants to compensate for the thrombotic risk associated with HIT. Limitations exist with the only currently FDA approved heparin alternative, argatroban. NOACs have been considered as potential alternatives to traditional agents based on their pharmacologic activity. Case reports have indicated positive results in patients, with clinical outcomes and tolerability supporting the use of the NOACs as alternative agents in the treatment of HIT. Positive results have been reported for the use of NOACs in the treatment of HIT. Further robust studies are needed for definitive decision making by clinicians.
通过相关临床试验数据回顾新型口服抗凝剂(NOAC)用于治疗肝素诱导的血小板减少症(HIT)的情况。使用关键词“血小板减少症”“NOAC”“达比加群”“阿哌沙班”“利伐沙班”“依度沙班”“Xa因子抑制剂”“直接凝血酶抑制剂”在MEDLINE、国际药学文摘数据库、ClinicalTrials.gov及谷歌学术进行检索(检索时间为1966年至2016年3月)。选取以英文发表且涉及人类受试者、评估新型口服抗凝剂治疗血小板减少症的文章。共识别出8项临床试验。利用已识别文章中引用的参考文献进行额外引用。每年约有1200万住院患者接受肝素进行血栓预防。HIT是一种免疫介导的促血栓形成不良反应,是肝素治疗的潜在并发症。因此,必须立即停用肝素产品,并换用其他抗凝剂以应对与HIT相关的血栓形成风险。目前美国食品药品监督管理局(FDA)唯一批准的肝素替代药物阿加曲班存在局限性。基于其药理活性,NOAC被视为传统药物的潜在替代品。病例报告表明,患者使用NOAC取得了积极结果,临床结局和耐受性支持将NOAC用作治疗HIT的替代药物。已有关于使用NOAC治疗HIT的积极结果报道。临床医生做出明确决策还需要进一步的有力研究。