肝素诱发的静脉和动脉血栓栓塞性疾病:病例报告和文献资料

N. Mahoungou-Mackonia
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引用次数: 0

摘要

HIT源于f4p特异性IgG抗体的产生。它通常在开始肝素治疗后5-14天开始,血小板计数比预处理值下降50%以上,与两名静脉和/或动脉血栓形成并发症患者中有一名相关。这是一种罕见的问题,发生在1-5%的UFH和0.1-0.2%的低分子肝素中,需要及时治疗。47岁患者,每日3克酒精摄入10年,因APO合并乙基性CMD住院,150次/分钟ACFA过速LVEF 33%。患者给予速尿和利索当治疗。注射可达酮和低分子肝素(治疗剂量),连续7天。发展的标志是窦性心律恢复,一周后耳鸣消失,但血栓形成22000/mm3,肺栓塞,左腘窝DVT和髂动脉血栓形成,然后是左股动脉血栓形成。抗pf4抗体与血小板活化试验相结合,证实了HIT 2型的诊断。停用低分子肝素,10天后给予Fondaparinux 7.5mg/d至血小板恢复正常,待临床改善,动静脉多普勒超声及胸部血管检查恢复正常后,改用利伐沙班治疗6个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heparin-Induced Venous and Arterial Thromboembolic Disease: Case Report and Literature Data
HIT results from the development of F4P-specific IgG antibodies. It usually begins 5-14 days after initiation of heparin therapy with a drop in platelet count of more than 50% from a pretreatment value, associated in one in two patients with venous and/or arterial thrombotic complications. This is a rarer problem that occurs in 1-5% with UFH and 0.1-0.2% with LMWH and requires prompt management. Forty-seven-year-old patient, alcoholic at 3g/d for 10 years, hospitalized for APO complicating an ethylic CMD, LVEF 33% in tachy ACFA at 150batt/min. The patient was treated with furosemide and risordan. Injectable Cordarone was administered and LMWH in curative dose for 7 days. The evolution was marked by a resumption of sinus rhythm, disappearance of crepitus rales, after one week, but an installation of thrombenia at 22000/mm3, a pulmonary embolism, left popliteal DVT and thrombosis of the iliac and then left femoral arteries. The diagnosis of HIT type 2 was confirmed by the presence of anti-PF4 antibodies in association with the platelet activation test. LMWH was stopped, the patient received Fondaparinux 7.5mg/d until platelets normalized after 10 days and then substituted with rivaroxaban for 6 months after clinical improvement and normalization of arteriovenous Doppler ultrasound and chest angioscan.
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