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Heparin-induced thrombocytopenia in patients with COVID-19: a systematic review and meta-analysis

Heparin thromboprophylaxis is routinely administered during hospitalization for COVID-19. Because of the immune stimulation related to COVID-19, there is ongoing concern regarding a heightened incidence of heparin-induced thrombocytopenia (HIT). We performed a literature search using PubMed, EMBASE,...

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Detalles Bibliográficos
Autores principales: Uaprasert, Noppacharn, Tangcheewinsirikul, Nuanrat, Rojnuckarin, Ponlapat, Patell, Rushad, Zwicker, Jeffrey I., Chiasakul, Thita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455241/
https://www.ncbi.nlm.nih.gov/pubmed/34543382
http://dx.doi.org/10.1182/bloodadvances.2021005314
Descripción
Sumario:Heparin thromboprophylaxis is routinely administered during hospitalization for COVID-19. Because of the immune stimulation related to COVID-19, there is ongoing concern regarding a heightened incidence of heparin-induced thrombocytopenia (HIT). We performed a literature search using PubMed, EMBASE, Cochrane, and medRxiv database to identify studies that reported clinical and laboratory characteristics and/or the incidence of HIT in patients with COVID-19. The primary aim was to systematically review the clinical features and outcomes of patients with COVID-19 with confirmed HIT. The secondary objective was to perform a meta-analysis to estimate the incidence of HIT in hospitalized patients with COVID-19. A meta-analysis of 7 studies including 5849 patients revealed the pooled incidence of HIT in COVID-19 of 0.8% (95% confidence interval [CI], 0.2%-3.2%; I(2) = 89%). The estimated incidences were 1.2% (95% CI, 0.3%-3.9%; I(2) = 65%) vs 0.1% (95% CI, 0.0%-0.4%; I(2) = 0%) in therapeutic vs prophylactic heparin subgroups, respectively. The pooled incidences of HIT were higher in critically ill patients with COVID-19 (2.2%; 95% CI, 0.6%-8.3%; I(2) = 72.5%) compared with noncritically ill patients (0.1%; 95% CI, 0.0%-0.4%: I(2) = 0%). There were 19 cases of confirmed HIT and 1 with autoimmune HIT for clinical and laboratory characterization. The median time from heparin initiation to HIT diagnosis was 13.5 days (interquartile range, 10.75-16.25 days). Twelve (63%) developed thromboembolism after heparin therapy. In conclusion, the incidence of HIT in patients with COVID-19 was comparable to patients without COVID-19, with higher incidences with therapeutic anticoagulation and in critically ill patients.