Author: Beauverd, Yan; Adam, Yannick; Assouline, Benjamin; Samii, Kaveh
Title: COVIDâ€19 infection and treatment with hydroxychloroquine cause severe haemolysis crisis in a patient with glucoseâ€6â€phosphate dehydrogenase deficiency Cord-id: veac3zsj Document date: 2020_5_7
ID: veac3zsj
Snippet: Glucoseâ€6â€phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red cell enzymatic defects and is associated with haemolytic crisis when patients are exposed to oxidative agents (fava beans, drugs, infections). Hydroxychloroquine is suspected to trigger haemolytic crisis in G6PDâ€deficient patients, and offâ€label administration of this drug to patients infected with the novel coronavirus (SARSâ€CoVâ€2) could cause concern. We report here the first case of
Document: Glucoseâ€6â€phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red cell enzymatic defects and is associated with haemolytic crisis when patients are exposed to oxidative agents (fava beans, drugs, infections). Hydroxychloroquine is suspected to trigger haemolytic crisis in G6PDâ€deficient patients, and offâ€label administration of this drug to patients infected with the novel coronavirus (SARSâ€CoVâ€2) could cause concern. We report here the first case of severe haemolytic crisis in a patient with G6PD deficiency, initiated by severe COVIDâ€19 infection and hydroxychloroquine use. With worldwide spread of COVIDâ€19, especially in regions with a high prevalence of G6PD deficiency, our case should alert physicians to this possible correlation.
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