2021
DOI: 10.1016/j.jaip.2020.11.042
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COVID-19 affecting hereditary angioedema patients with and without C1 inhibitor deficiency

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Cited by 32 publications
(43 citation statements)
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“…These results are in line with those of Grumach et al10 Indeed, in their cohort of 13 patients, 5 (38%) experienced attacks days after SARS-CoV-2 infection, mostly affected extremities and face. Acute attacks could occur during the convalescent phase of COVID-19 illness, more commonly in patients with a history of frequent attacks.…”
supporting
confidence: 92%
“…These results are in line with those of Grumach et al10 Indeed, in their cohort of 13 patients, 5 (38%) experienced attacks days after SARS-CoV-2 infection, mostly affected extremities and face. Acute attacks could occur during the convalescent phase of COVID-19 illness, more commonly in patients with a history of frequent attacks.…”
supporting
confidence: 92%
“…23 A previously reported series of 11 young women and 2 young men taking oxandrolone or tranexamic acid for hereditary angioedema-reported COVID-19 symptom frequency of anosmia/dysgeusia of 77% and dyspnoea of 31%. 24 In a communication with the authors, at their hereditary angioedema clinic, oxandrolone is prescribed at lower dosages (4-5 mg/day) for angioedema prophylaxis, and the only woman who required hospitalisation was not using oxandrolone. We raise the possibility that DHT-derived AAS may lead to increased disease severity in a dose-dependent manner.…”
Section: Discussionmentioning
confidence: 99%
“…We collected data from 121 patients diagnosed with IEI and infected by SARS-CoV-2 between March and December 2020. The diagnosis of SARS-CoV-2 infection was con rmed by RT-PCR from nasopharyngeal or nasal swab in 82 patients (67.8%); by RT-PCR and serology, in three patients ( [26] and one common variable immunode ciency (CVID) patient was previously reported [20].…”
Section: Resultsmentioning
confidence: 99%
“…Sixty-seven patients were female (55.4%). Four out of 121 patients were previously included in Meyts et al [14], 13 patients with hereditary angioedema were included in Grumach et al [26] and one common variable immunode ciency (CVID) patient was previously reported [20].…”
Section: Resultsmentioning
confidence: 99%
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