Sickle cell disease (SCD) is the most common hemoglobinopathy worldwide, characterized
by vaso-occlusive crises and ischemia that affects patients on a multi-system level. Despite …

Objective: In the absence of access to surveillance system data, single-source administrative
databases are often used to study health care utilization and health outcomes among …

Introduction Sickle cell disease is an emerging anemia in Europe leading to high morbidity
with severe acute complications requiring hospital admission and chronic consequences …

Methods: Retrospective review of electronic health records from a large, multicampus,
pediatric SCD program. Results: Of the 113 adolescents included, the mean age was 16.6 …

Introducción La drepanocitosis es una anemia emergente en Europa que condiciona una
elevada morbilidad con complicaciones agudas y crónicas. El manejo de estos pacientes es …

OBJECTIVES To assess the impact of croup guidelines on healthcare utilization and
association between guideline-recommended racemic epinephrine (RE) treatments and …

Causes and Recommendations for Fever in Sickle Cell Pediatric Patients in the Emergency
Department: A Single-Center Study Page 1 Review began 08/17/2023 Review ended 09/05/2023 …

Introduction: Individuals with sickle cell disease (SCD) have suboptimal experiences when
presenting to the emergency department (ED), especially when seeking treatment for painful …

La anemia drepanocítica o hemoglobina S constituye una enfermedad genética producida
por la mutación del gen HBB (11p15. 4) del cromosoma 11. Paciente masculino …

L'objectif de ce travail est d'évaluer l'impact du programme de dépistage néonatal universel
chez de l'anémie falciforme (AF) chez les enfants. Méthode: Nous avons procédé à une …