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Bullous hemorrhagic dermatosis is an under-recognized side effect of full dose low-molecular weight heparin: a case report and review of the literature

机译:大疱性出血性皮肤病是全剂量低分子量肝素的一种未被充分认识的副作用:一例病例并文献复习

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摘要

Bullous hemorrhagic dermatosis (BHD) is a systemic side-effect of low molecular weight heparin, characterized by multiple intra-epidermal hemorrhages distant from the site of injection. There have been several small case series and literature reviews on BHD, but none have captured a complete set of reported patients. We sought to describe a case of BHD with late diagnosis and completely summarize the existing English and Spanish literature with searches of Pubmed, Scopus, Ovid Embase and Ovid Medline. After narrowing to 33 relevant reports, we describe 90 reported cases worldwide from 2004 to 2017, in addition to a new case from our institution as a means of comparison. We found that BHD was common in elderly men (mean age 72 ± 12; male:female, 1.9:1) and typically occurred within 7 days of administration of anticoagulation (median 7 days ± 6.4) usually with enoxaparin use (66% of cases). Lesions occurred primarily on the extremities only (67.9% of cases). Coagulation testing was most often normal before administration, and the majority of patients had coagulation testing in therapeutic range during treatment. Most practitioners stopped anticoagulation if continued therapeutic intervention was no longer required (57% of cases), or changed therapy to another anticoagulation if continued treatment was required (14.3% of cases). Therapy was continued outright in 23% of patients. The lesions usually resolved within 2 weeks (mean days, 13.0 ± 7.4). There was no difference in time to resolution between patients who continued the culprit anticoagulant or changed to a different anticoagulant, and those who discontinued anticoagulation altogether (13.9 days vs. 12.1, p = 0.49). Four deaths have been reported in this clinical context, two specified as intracranial hemorrhage. These deaths were unrelated to the occurrence of BHD. Continuation of low-molecular weight heparins appeared to be safe in patients with BHD.
机译:大疱性出血性皮肤病(BHD)是低分子量肝素的全身性副作用,其特征是远离注射部位的多次表皮内出血。关于BHD已有一些小病例系列和文献综述,但没有一例涵盖了完整的报告患者。我们试图描述一种BHD且诊断较晚的病例,并通过搜索Pubmed,Scopus,Ovid Embase和Ovid Medline来全面总结现有的英语和西班牙语文献。在将范围缩小到33个相关报告之后,我们将2004年至2017年全球90个已报告的案例进行了描述,此外我们还从机构中获得了一个新案例作为比较手段。我们发现BHD在老年男性中常见(平均年龄72±±12;男性:女性,1.9:1),通常在抗凝治疗7天内发生(中位数7天±6.4),通常使用依诺肝素(66%病例) )。病变主要发生在四肢(占病例的67.9%)。给药前凝血试验通常是正常的,并且大多数患者在治疗期间进行了治疗范围内的凝血试验。如果不再需要继续的治疗干预,大多数从业者停止抗凝治疗(占病例的57%),如果需要继续治疗,则将治疗改为另一种抗凝治疗(占病例的14.3%)。 23%的患者完全继续进行治疗。病变通常在2周内(平均日13.0±7.4)消退。继续使用罪魁祸首抗凝剂或改用其他抗凝剂的患者与完全中止抗凝剂的患者之间的解决时间没有差异(13.9天vs. 12.1,p,= 0.49)。在这种临床情况下,已报告了四例死亡,其中两例为颅内出血。这些死亡与BHD的发生无关。在BHD患者中,继续低分子肝素的治疗似乎是安全的。

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