CE: Understanding the Complications of Sickle Cell Disease.
Journal
The American journal of nursing
ISSN: 1538-7488
Titre abrégé: Am J Nurs
Pays: United States
ID NLM: 0372646
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
entrez:
29
5
2019
pubmed:
29
5
2019
medline:
21
1
2020
Statut:
ppublish
Résumé
: Sickle cell disease (SCD) is an autosomal recessive genetic condition that alters the shape and function of the hemoglobin molecule in red blood cells. While the overall survival rate among children with SCD has improved in recent years, pediatric rates of hospitalization, ED use, and mortality from complications of SCD remain high. Among patients ages 18 and older, hospital admission and ED usage are even greater-and the median age at death of people with SCD is considerably lower than that of the general population. Nurses who care for patients with SCD have an opportunity to improve health outcomes and quality of life for these patients by recognizing the major SCD-associated complications and providing patients and their caregivers with appropriate educational information. The authors discuss the genetic, hematologic, and clinical features of SCD and describe the major associated health complications. In addition, they review the nursing implications of each complication and provide online links to resources for clinicians, patients, and caregivers.
Identifiants
pubmed: 31135428
doi: 10.1097/01.NAJ.0000559779.40570.2c
pii: 00000446-201906000-00023
pmc: PMC6674980
mid: NIHMS1033669
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
26-35Subventions
Organisme : Intramural CDC HHS
ID : CC999999
Pays : United States
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