The Journal of Pediatrics
Volume 160, Issue 2 , Page A3, February 2012

Pain crises in children with sickle cell anemia

Sickle cell anemia (SCA) illustrates some of the challenges of keeping current with the management of a chronic illness. As improvements in standard care are incorporated into practice, one needs to periodically reexamine the natural history of the condition, which may be modified by the new therapies. Thus, even in a disease studied as well as SCA, there is an ongoing need for continuing well-characterized multicenter studies.

 

PII: S0022-3476(11)01267-4

doi:10.1016/j.jpeds.2011.12.017

Refers to article:

  • Markers of Severe Vaso-Occlusive Painful Episode Frequency in Children and Adolescents with Sickle Cell Anemia , 05 September 2011

    Deepika S. Darbari, Onyinye Onyekwere, Mehdi Nouraie, Caterina P. Minniti, Lori Luchtman-Jones, Sohail Rana, Craig Sable, Gregory Ensing, Niti Dham, Andrew Campbell, Manuel Arteta, Mark T. Gladwin, Oswaldo Castro, James G. Taylor, Gregory J. Kato, Victor Gordeuk
    The Journal of Pediatrics February 2012 (Vol. 160, Issue 2, Pages 286-290)

The Journal of Pediatrics
Volume 160, Issue 2 , Page A3, February 2012