Prevalence and Outcomes of D-Dimer Elevation in Hospitalized Patients With COVID-19.

Prevalence and Outcomes of D-Dimer Elevation in Hospitalized Patients With COVID-19.
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DOI:
10.1161/atvbaha.120.314872
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发表时间:
2020-10
期刊:
Arteriosclerosis, thrombosis, and vascular biology
影响因子:
--
通讯作者:
Horwitz LI
Horwitz LI
中科院分区:
其他
文献类型:
--
作者:
Berger JS;Kunichoff D;Adhikari S;Ahuja T;Amoroso N;Aphinyanaphongs Y;Cao M;Goldenberg R;Hindenburg A;Horowitz J;Parnia S;Petrilli C;Reynolds H;Simon E;Slater J;Yaghi S;Yuriditsky E;Hochman J;Horwitz LI

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补充数字内容可在文本中找到。确定2019冠状病毒病(COVID-19)住院患者D-二聚体升高的患病率、住院期间D-二聚体水平的变化轨迹及其与临床结局的相关性。确定了2020年3月1日至2020年4月8日期间在纽约市一家大型医院系统住院的SARS-CoV-2(严重急性呼吸系统综合征冠状病毒2型)聚合酶链反应检测阳性的成年人。D-二聚体升高定义为实验室特定的正常上限(>230 ng/mL)。结局包括危重病(重症监护、机械通气、出院至临终关怀或死亡)、血栓形成事件、急性肾损伤和住院期间死亡。在2377名因COVID-19和≥1次D-二聚体测量而住院的成人中,1823名(76%)在就诊时D-二聚体升高。基线D-二聚体升高的患者比D-二聚体正常的患者更容易发生危重疾病(43.9% vs 18.5%;校正比值比,2.4 [95% CI,1.9-3.1]; P<0.001),任何血栓性事件(19.4% vs 10.2%;校正比值比,1.9 [95% CI,1.4-2.6]; P<0.001),急性肾损伤(42.4%对19.0%;校正比值比,2.4 [95% CI,1.9-3.1]; P<0.001)和死亡(29.9%对10.8%;校正比值比,2.1 [95% CI,1.6-2.9]; P<0.001)。不良事件发生率随着D-二聚体升高的幅度而增加; D-二聚体>2000 ng/mL的个体发生危重病(66%)、血栓形成事件(37.8%)、急性肾损伤(58.3%)和死亡(47%)的风险最高。在COVID-19入院时经常观察到异常D-二聚体,并与危重病、血栓形成事件、急性肾损伤和死亡的发生率较高相关。COVID-19中D-二聚体升高患者的最佳管理需要进一步研究。
Supplemental Digital Content is available in the text. To determine the prevalence of D-dimer elevation in coronavirus disease 2019 (COVID-19) hospitalization, trajectory of D-dimer levels during hospitalization, and its association with clinical outcomes. Consecutive adults admitted to a large New York City hospital system with a positive polymerase chain reaction test for SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) between March 1, 2020 and April 8, 2020 were identified. Elevated D-dimer was defined by the laboratory-specific upper limit of normal (>230 ng/mL). Outcomes included critical illness (intensive care, mechanical ventilation, discharge to hospice, or death), thrombotic events, acute kidney injury, and death during admission. Among 2377 adults hospitalized with COVID-19 and ≥1 D-dimer measurement, 1823 (76%) had elevated D-dimer at presentation. Patients with elevated presenting baseline D-dimer were more likely than those with normal D-dimer to have critical illness (43.9% versus 18.5%; adjusted odds ratio, 2.4 [95% CI, 1.9–3.1]; P<0.001), any thrombotic event (19.4% versus 10.2%; adjusted odds ratio, 1.9 [95% CI, 1.4–2.6]; P<0.001), acute kidney injury (42.4% versus 19.0%; adjusted odds ratio, 2.4 [95% CI, 1.9–3.1]; P<0.001), and death (29.9% versus 10.8%; adjusted odds ratio, 2.1 [95% CI, 1.6–2.9]; P<0.001). Rates of adverse events increased with the magnitude of D-dimer elevation; individuals with presenting D-dimer >2000 ng/mL had the highest risk of critical illness (66%), thrombotic event (37.8%), acute kidney injury (58.3%), and death (47%). Abnormal D-dimer was frequently observed at admission with COVID-19 and was associated with higher incidence of critical illness, thrombotic events, acute kidney injury, and death. The optimal management of patients with elevated D-dimer in COVID-19 requires further study.