A Comprehensive Review of the Treatment and Management of Pain in Sickle Cell Disease.
Chronic pain
Cognitive behavioral therapy
Sickle cell disease
Vasoocclusive crisis
Journal
Current pain and headache reports
ISSN: 1534-3081
Titre abrégé: Curr Pain Headache Rep
Pays: United States
ID NLM: 100970666
Informations de publication
Date de publication:
21 Mar 2020
21 Mar 2020
Historique:
entrez:
23
3
2020
pubmed:
23
3
2020
medline:
22
12
2020
Statut:
epublish
Résumé
Sickle cell disease (SCD) is a hematological disorder which leads to serious complications in multiple organ systems. While significant research has addressed many of the effects of acute pain episodes and end-organ damage connected to this disease, little has approached the chronic pain state associated with this condition. Associated chronic pain represents a significant detractor from the quality of life experienced by these patients, affecting over half of those with SCD on more days than not. Current treatment typically is centered upon preventing and responding to acute vasoocclusive crises, presumably because this is the most common reason for hospitalization in these patients. The lack of management of chronic pain symptoms leaves many with SCD in a state of suffering. In this review, the treatment methodologies of SCD patients are examined including alternative treatments, both pharmaceutical and non-pharmaceutical, as well as procedural approaches specifically aimed at reducing chronic pain in these patients.
Identifiants
pubmed: 32200490
doi: 10.1007/s11916-020-00854-y
pii: 10.1007/s11916-020-00854-y
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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