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Moving Toward a Multimodal Analgesic Regimen for Acute Sickle Cell Pain with Non-Opioid Analgesic Adjuncts: A Narrative Review

PURPOSE OF REVIEW: Sickle cell disease (SCD) is an inherited hemoglobinopathy with potential life-threatening complications that affect millions of people worldwide. Severe and disabling acute pain, referred to as a vaso-occlusive crisis (VOC), is a fundamental symptom of the disease and the primary...

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Detalles Bibliográficos
Autores principales: Kenney, Martha O, Smith, Wally R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979590/
https://www.ncbi.nlm.nih.gov/pubmed/35386424
http://dx.doi.org/10.2147/JPR.S343069