| Literature DB >> 26999505 |
Jennifer Knight-Madden1, Marc Romana1, Rinaldo Villaescusa1, Marvin Reid1, Maryse Etienne-Julan1, Laurence Boutin1, Gisèle Elana1, Narcisse Elenga1, Gillian Wheeler1, Ketty Lee1, Rosa Nieves1, Althea Jones Lecointe1, Marie-Laure Lalanne-Mistrih1, Gylna Loko1, Lisiane Keclard-Christophe1, Marie-Dominique Hardy-Dessources1.
Abstract
Sickle cell disease (SCD) is a significant problem in the Caribbean, where many individuals have African and Asian forebears. However, reliable prevalence data and specific health care programs for SCD are often missing in this region. Closer collaboration between Caribbean territories initiated in 2006 to set up strategies to promote better equity in the health care system for SCD patients led to the formation of CAREST: the Caribbean Network of Researchers on Sickle Cell Disease and Thalassemia. We present the effectiveness of collaborations established by CAREST to promote SCD newborn screening programs and early childhood care, to facilitate health worker training and approaches for prevention and treatment of SCD complications, and to carry out inter-Caribbean research studies.Entities:
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Year: 2016 PMID: 26999505 PMCID: PMC4985101 DOI: 10.2105/AJPH.2016.303078
Source DB: PubMed Journal: Am J Public Health ISSN: 0090-0036 Impact factor: 9.308