Key result
Contemporary heparin-induced thrombocytopenia mortality drops to ~6%, with FcγRIIA homozygosity linked to higher thrombosis risk.
Cohort (n=144)
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Background Heparin-induced thrombocytopenia (HIT) is a rare complication of heparin treatments, and only a few large patient cohorts have been reported. In this study, biological and clinical data from 144 French patients with HIT were analyzed in comparison with the literature. Methods The diagnosis of HIT was confirmed in all patients by an immunoassay combined with serotonin release assay. In the literature, only cohorts of at least 20 HIT patients published from 1992 were selected for a comparative analysis. Results Two-thirds of patients were hospitalized in surgery and most were treated with unfractionated heparin (83.2% vs. 16.8% with low molecular weight heparin only). Thrombotic events in 54 patients (39.7%) were mainly venous (41/54). However, arterial thrombosis was more frequent after cardiac surgery (13.2% vs. 2.4% in other surgeries, p = 0.042) with a shorter recovery time (median = 3 vs. 5 days, p < 0.001). The mortality rate was lower in our series than in the 22 selected published studies (median = 6.3% vs. 15.9%). Three genetic polymorphisms were also studied and homozygous subjects FcγRIIA RR were more frequent in patients with thrombosis (37.8 vs. 18.2% in those without thrombosis, p = 0.03). Conclusion This study shows that the mortality rate due to HIT has recently decreased in France, possibly due to earlier diagnosis and improved medical care. It also confirms the strong association between polymorphism FcγRIIA H131R and thrombosis in HIT.
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Gruel et al. (2020) conducted a cohort in Heparin-induced thrombocytopenia (HIT) (n=144). French prospective HIT cohort (FRIGTIH) and FcγRIIA RR polymorphism vs. Published HIT cohorts from 1992 onward (≥20 patients) and HIT patients without thrombosis was evaluated on Mortality rate and thrombotic events. Heparin-induced thrombocytopenia patients in France had lower mortality than prior cohorts (6.3% vs 15.9%), with FcγRIIA RR homozygosity linked to thrombosis (37.8% vs 18.2%, p=0.03).
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