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1.
Pediatrics ; 150(1)2022 07 01.
Artigo em Inglês | MEDLINE | ID: covidwho-1817537

RESUMO

BACKGROUND: Evidence regarding the safety and efficacy of anticoagulant thromboprophylaxis among pediatric patients hospitalized for coronavirus disease 2019 (COVID-19) is limited. We sought to evaluate safety, dose-finding, and preliminary efficacy of twice-daily enoxaparin as primary thromboprophylaxis among children hospitalized for symptomatic COVID-19, including primary respiratory infection and multisystem inflammatory syndrome in children (MISC). METHODS: We performed a phase 2, multicenter, prospective, open-label, single-arm clinical trial of twice-daily enoxaparin (initial dose: 0.5mg/kg per dose; max: 60mg; target anti-Xa activity: 0.20-0.49IU/mL) as primary thromboprophylaxis for children <18 years of age hospitalized for symptomatic COVID-19. Study endpoints included: cumulative incidence of International Society of Thrombosis and Haemostasis-defined clinically relevant bleeding; enoxaparin dose-requirements; and cumulative incidence of venous thromboembolism within 30-days of hospital discharge. Descriptive statistics summarized endpoint estimates that were further evaluated by participant age (±12 years) and clinical presentation. RESULTS: Forty children were enrolled and 38 met analyses criteria. None experienced clinically relevant bleeding. Median (interquartile range) dose to achieve target anti-Xa levels was 0.5 mg/kg (0.48-0.54). Dose-requirement did not differ by age (0.5 [0.46-0.52] mg/kg for age ≥12 years versus 0.52 [0.49-0.55] mg/kg for age <12 years, P = .51) but was greater for participants with MISC (0.52 [0.5-0.61] mg/kg) as compared with primary COVID-19 (0.48 [0.39-0.51] mg/kg, P = .010). Two children (5.3%) developed central-venous catheter-related venous thromboembolism. No serious adverse events were related to trial intervention. CONCLUSIONS: Among children hospitalized for COVID-19, thromboprophylaxis with twice-daily enoxaparin appears safe and warrants further investigation to assess efficacy.


Assuntos
COVID-19 , Tromboembolia Venosa , Anticoagulantes/efeitos adversos , COVID-19/complicações , Criança , Enoxaparina/efeitos adversos , Hemorragia , Humanos , Estudos Prospectivos , Síndrome de Resposta Inflamatória Sistêmica , Resultado do Tratamento , Tromboembolia Venosa/prevenção & controle
2.
Critical Care Medicine ; 50:14-14, 2022.
Artigo em Inglês | Academic Search Complete | ID: covidwho-1598252

RESUMO

B Conclusions: b In children hospitalized for COVID-19 related illness, primary TP with subcutaneous enoxaparin twice-daily at a starting dose of 0.5 mg/kg is safe and achieves target anti-Xa levels during hospitalization in >90% of patients. Future phase 3 trials of primary TP are warranted in hospitalized children with proinflammatory conditions such as COVID-19, for which HA-VTE risk is increased. B Introduction: b Evidence is limited on the safety or efficacy of anticoagulant thromboprophylaxis (TP) against hospital-associated venous thromboembolism (HA-VTE) in children hospitalized with COVID-19 and multisystem inflammatory syndrome in children (MIS-C). [Extracted from the article] Copyright of Critical Care Medicine is the property of Lippincott Williams & Wilkins and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)

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