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Published on: May 11, 2015
Symptomatic pulmonary hypertension in a child with sickle cell disease
Karrie Villavicencio1, Dunbar Ivy, Laura Cole
1Department of Cardiology, University of Colorado at Denver Health Sciences Center, Denver, CO, USA.
Insights
Pulmonary hypertension is a serious complication in sickle cell disease (SCD). This case report details the treatment of a child with SCD-associated pulmonary hypertension driven by hemolysis.
Area of Science:
- Pediatric Hematology
- Cardiopulmonary Medicine
- Sickle Cell Disease Research
Background:
- Pulmonary hypertension (PH) is a known complication in adult sickle cell disease (SCD).
- Limited data exist on PH development, progression, and treatment in pediatric SCD.
- Hemolysis is a suspected driver of PH in SCD.
Observation:
- A pediatric patient with homozygous sickle cell disease (SS) presented with hemolysis-driven pulmonary hypertension.
- The clinical course and treatment of this patient were documented.
Findings:
- The case highlights the potential for hemolysis to drive pulmonary hypertension in children with SCD.
- Successful management strategies for this specific complication were observed.
Implications:
- This case contributes to understanding pediatric SCD-associated PH.
- Further research into PH mechanisms and treatments in pediatric SCD is warranted.
- Early recognition and intervention for PH in pediatric SCD may improve outcomes.
Abstract:
Pulmonary hypertension is a survival-limiting complication in adults with homozygous sickle cell disease (SS), but little is known about the development, course, or best treatment of pulmonary hypertension in children with SS. We report the clinical course and treatment of a child with SS-associated, hemolysis-driven pulmonary hypertension.
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