Mohammed Hemin S, Fattah Fattah H, Rahim Hawbash M, Kakamad Fahmi H, Mohammed Shvan H, Salih Rawezh Q, Salih Abdulwahid M, Naqar Sharo
Smart Health Tower, Madam Mitterrand Street, Sulaimani, Kurdistan, Iraq.
College of Medicine, University of Sulaimani, Madam Mitterrand Street, Sulaimani, Kurdistan, Iraq.
Ann Med Surg (Lond). 2022 Jun;78:103749. doi: 10.1016/j.amsu.2022.103749. Epub 2022 May 11.
Heparin-induced thrombocytopenia (HIT) is a rare and serious immune-mediated complication of heparin therapy which is seldom reported in association with COVID-19. This report aims to present a case of accelerated HIT in a severe COVID-19 patient.
A 63-year-old man presents with symptoms of COVID-19 for one week. He was conscious, ordinated, feverish, and had diffused chest crackles. Initial laboratory tests revealed elevated C-reactive protein of 87.66 mg/dL, elevated D-dimmer of 1258.9 ng/ml, elevated ferritin of 1020 ng/ml, and his platelet count was within the normal range. Polymerase chain reaction (PCR) confirmed the diagnosis of COVID-19. On the 9th day of admission, he developed a progressive worsening of dyspnea. His D-dimmer level significantly increased to 7020 ng/ml, and his interleukin-6 was 27.3 pg/ml. Hence, we started him on unfractionated heparin (UFH) for thromboprophylaxis. On the 12th day of hospitalization, the platelet count dropped from 258000 to 111000 cells/μL. He had a high probability of HIT (4Ts score = 6). As a result, we discontinued UFH and switched him to apixaban. His platelet count normalized (174000 cells/μL) within two weeks of ceasing UHF.
HIT results from the production of antibodies against platelet factor 4/heparin complexes. It is associated with a diminished platelet count within 5-10 days post heparin initiation. Because thrombocytopenia can occur in COVID-19 patients, HIT is seldom suspected.
HIT should be considered a differential diagnosis in COVID-19 patients with thrombocytopenia.
肝素诱导的血小板减少症(HIT)是肝素治疗罕见且严重的免疫介导并发症,与新型冠状病毒肺炎(COVID-19)相关的报道很少。本报告旨在介绍1例重症COVID-19患者发生的加速型HIT病例。
一名63岁男性,出现COVID-19症状一周。他神志清醒、协调,发热,双肺有弥漫性湿啰音。初始实验室检查显示C反应蛋白升高至87.66mg/dL,D-二聚体升高至1258.9ng/ml,铁蛋白升高至1020ng/ml,血小板计数在正常范围内。聚合酶链反应(PCR)确诊为COVID-19。入院第9天,他出现进行性呼吸困难加重。其D-二聚体水平显著升高至7020ng/ml,白细胞介素-6为27.3pg/ml。因此,我们开始给他使用普通肝素(UFH)进行血栓预防。住院第12天,血小板计数从258000降至111000个/μL。他发生HIT的可能性很高(4Ts评分=6)。结果,我们停用了UFH,改为阿哌沙班。停用UFH两周内,他的血小板计数恢复正常(174000个/μL)。
HIT是由针对血小板因子4/肝素复合物的抗体产生所致。它与肝素开始使用后5-10天内血小板计数减少有关。由于COVID-19患者可能出现血小板减少,HIT很少被怀疑。
对于血小板减少症的COVID-19患者,应考虑HIT作为鉴别诊断。