Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management

ScientificWorldJournal. 2012:2012:949535. doi: 10.1100/2012/949535. Epub 2012 Aug 1.

Abstract

The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of the β globin gene resulting in the substitution of glutamic acid by valine at position 6 of the β globin polypeptide chain. Although the molecular lesion is a single-point mutation, the sickle gene is pleiotropic in nature causing multiple phenotypic expressions that constitute the various complications of sickle cell disease in general and sickle cell anemia in particular. The disease itself is chronic in nature but many of its complications are acute such as the recurrent acute painful crises (its hallmark), acute chest syndrome, and priapism. These complications vary considerably among patients, in the same patient with time, among countries and with age and sex. To date, there is no well-established consensus among providers on the management of the complications of sickle cell disease due in part to lack of evidence and in part to differences in the experience of providers. It is the aim of this paper to review available current approaches to manage the major complications of sickle cell disease. We hope that this will establish another preliminary forum among providers that may eventually lead the way to better outcomes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anemia, Sickle Cell / complications*
  • Anemia, Sickle Cell / genetics
  • Blood Transfusion / methods*
  • Clinical Trials as Topic
  • Disease Management*
  • Gastrointestinal Diseases / drug therapy
  • Gastrointestinal Diseases / etiology
  • Gastrointestinal Diseases / therapy
  • Humans
  • Hydroxyurea / pharmacology
  • Hypertension, Pulmonary / drug therapy
  • Hypertension, Pulmonary / etiology
  • Hypertension, Pulmonary / physiopathology
  • Muscular Diseases / drug therapy
  • Muscular Diseases / etiology
  • Muscular Diseases / therapy
  • Nervous System Diseases / drug therapy
  • Nervous System Diseases / etiology
  • Nervous System Diseases / therapy
  • Pain / drug therapy
  • Pain / etiology
  • Pain / physiopathology
  • Phenotype
  • Piperazines / pharmacology
  • Purines / pharmacology
  • Retinal Diseases / drug therapy
  • Retinal Diseases / etiology
  • Retinal Diseases / therapy
  • Sildenafil Citrate
  • Sulfones / pharmacology
  • Treatment Outcome

Substances

  • Piperazines
  • Purines
  • Sulfones
  • Sildenafil Citrate
  • Hydroxyurea