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1.
Pediatr Blood Cancer ; 68(7): e28975, 2021 07.
Artículo en Inglés | MEDLINE | ID: mdl-33661561

RESUMEN

We report the clinical and laboratory coagulation characteristics of 27 pediatric and young adult patients (2 months to 21 years) treated for symptomatic COVID-19 at a children's hospital in the Bronx, New York, between March 1 and May 31, 2020. D-Dimer was > 0.5 µg/mL (upper limit of normal) in 25 (93%) patients at admission; 11 (41%) developed peak D-dimer > 5 µg/mL during admission. Seven (26%) patients developed venous thromboembolism: three with deep vein thrombosis and four with pulmonary embolism. Requirement of increased ventilatory support was a risk factor for thrombosis (P = 0.006). Three of eight (38%) patients on prophylactic anticoagulation developed thrombosis; however, no patients developed VTE on low-molecular-weight heparin prophylaxis titrated to anti-Xa level. Manifestation of COVID-19 disease was severe or critical in 16 (59%) patients. Four (15%) patients died of COVID-19 complications: all had comorbidities. Elevated D-dimer and increased VTE rate were observed in this young cohort, particularly in those with severe respiratory complications, suggesting thrombotic coagulopathy. More data are needed to guide thromboprophylaxis in this age group.


Asunto(s)
Anticoagulantes/uso terapéutico , Trastornos de la Coagulación Sanguínea/epidemiología , COVID-19/complicaciones , Hospitalización/estadística & datos numéricos , SARS-CoV-2/aislamiento & purificación , Tromboembolia Venosa/epidemiología , Adolescente , Adulto , Trastornos de la Coagulación Sanguínea/tratamiento farmacológico , Trastornos de la Coagulación Sanguínea/virología , COVID-19/virología , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , New York/epidemiología , Factores de Riesgo , Tromboembolia Venosa/tratamiento farmacológico , Tromboembolia Venosa/virología , Adulto Joven
2.
Complement Ther Med ; 52: 102481, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32951731

RESUMEN

Sickle Cell Disease (SCD) is a chronic hemolytic disorder associated with frequent pain episodes, end organ damage and a shortened lifespan. Currently there exist no disease specific targeted therapies for the treatment of acute vaso-occlusive crisis (VOC) and management with analgesics and hydration is purely supportive. Improvement in understanding of disease pathophysiology has resulted in a great interest in disease modifying novel therapies and many are being evaluated in clinical trials. Here we report the results from the pre-specified mid-point analysis of the Phase 2 study of Intravenous Gamma Globulin (IVIG) for the treatment of acute VOC in patients with SCD and lessons learned.


Asunto(s)
Anemia de Células Falciformes/tratamiento farmacológico , Inmunoglobulinas Intravenosas/uso terapéutico , Manejo del Dolor/métodos , gammaglobulinas/uso terapéutico , Adolescente , Adulto , Anemia de Células Falciformes/complicaciones , Niño , Método Doble Ciego , Femenino , Humanos , Factores Inmunológicos/uso terapéutico , Masculino , Adulto Joven
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