Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gary Rains"'
Autor:
Stephanie O. Ibemere, Paula Tanabe, Emily Bonnabeau, Gary Rains, Kern Eason, Marian F. Earls, Nirmish Shah
Publikováno v:
Journal of Primary Care & Community Health, Vol 12 (2021)
Background Sickle cell disease (SCD) is a complex chronic blood disorder characterized by severe disease complications ideally managed by both hematologists and primary care providers (PCP’s). PCP’s report knowledge gaps and discomfort with SCD m
Externí odkaz:
https://doaj.org/article/44c5499d24e34fd0834b2ed8f6723577
Autor:
Paula Tanabe, Audrey L. Blewer, Emily Bonnabeau, Hayden B. Bosworth, Denise H. Clayton, Nancy Crego, Marian F. Earls, Kern Eason, Grayson Forlines, Gary Rains, Matthew Young, Nirmish Shah
Publikováno v:
Journal of Health Economics and Outcomes Research, Vol 8, Iss 1 (2021)
**Background:** Sickle cell disease (SCD) is a genetic condition affecting primarily individuals of African descent, who happen to be disproportionately impacted by poverty and who lack access to health care. Individuals with SCD are at high likeliho
Externí odkaz:
https://doaj.org/article/e4e29c9876924490aa7287f0d9b7b71a
Autor:
Terri DeMartino, Christian Douglas, Nancy Crego, Paula Tanabe, Emily Bonnabeau, Nirmish Shah, Gary Rains, Rita V Masese
Publikováno v:
North Carolina Medical Journal. 82:312-320
BACKGROUND Sickle cell disease (SCD) is a complex disease associated with many complications and a shortened lifespan. In 2016, the National Heart, Lung and Blood Institute funded 8 centers in the United States to form the Sickle Cell Disease Impleme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca3ff8036b8431a0909763e25185a6a
https://doi.org/10.18043/ncm.82.5.312
https://doi.org/10.18043/ncm.82.5.312
Autor:
Nirmish Shah, Paula Tanabe, Emily Bonnabeau, Rita V Masese, Christian Douglas, Nancy Crego, Gary Rains
Publikováno v:
Crit Care Nurs Q
Sickle cell disease (SCD) is a common genetic blood disorder predominantly affecting African Americans in the United States. The objective of this study was to use a multimethods approach to describe how patients with SCD in North Carolina perceive t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a3725d3e4a0b0f5cb65b49e3370dddc
https://doi.org/10.1097/cnq.0000000000000350
https://doi.org/10.1097/cnq.0000000000000350
Autor:
Emily Bonnabeau, Kern Eason, Marian Earls, Elizabeth Merwin, Nancy Crego, Paula Tanabe, Gary Rains, Christian Douglas, Nirmish Shah
Publikováno v:
The Journal of the American Board of Family Medicine. 33:91-105
Background: Sickle-cell disease (SCD) causes significant morbidity, premature mortality, and high disease burden, resulting in frequent health care use. Comanagement may improve utilization and patient adherence with treatments such as Hydroxyurea. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44a2f76e55a651aac6589b278e5bc7b0
https://doi.org/10.3122/jabfm.2020.01.190143
https://doi.org/10.3122/jabfm.2020.01.190143
Autor:
Marian Earls, Emily Bonnabeau, Kern Eason, Nirmish Shah, Gary Rains, Stephanie O Ibemere, Paula Tanabe
Publikováno v:
Journal of Primary Care & Community Health
Journal of Primary Care & Community Health, Vol 12 (2021)
Journal of Primary Care & Community Health, Vol 12 (2021)
Background Sickle cell disease (SCD) is a complex chronic blood disorder characterized by severe disease complications ideally managed by both hematologists and primary care providers (PCP’s). PCP’s report knowledge gaps and discomfort with SCD m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab7fabb20e2dcf490a3a882224b4804
http://europepmc.org/articles/PMC8512219
http://europepmc.org/articles/PMC8512219
Autor:
Marian Earls, Kern Eason, Hayden B. Bosworth, Denise H. Clayton, Nirmish Shah, Gary Rains, Matthew Young, Paula Tanabe, Audrey L Blewer, Grayson Forlines, Emily Bonnabeau, Nancy Crego
Publikováno v:
Journal of Health Economics and Outcomes Research, Vol 8, Iss 1 (2021)
Journal of Health Economics and Outcomes Research
Journal of Health Economics and Outcomes Research
**Background:** Sickle cell disease (SCD) is a genetic condition affecting primarily individuals of African descent, who happen to be disproportionately impacted by poverty and who lack access to health care. Individuals with SCD are at high likeliho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52995348273378e15f93b6ed9063971e
https://jheor.scholasticahq.com/article/21535-dissemination-of-evidence-based-recommendations-for-sickle-cell-disease-to-primary-care-and-emergency-department-providers-in-north-carolina-a-cost-b.pdf
https://jheor.scholasticahq.com/article/21535-dissemination-of-evidence-based-recommendations-for-sickle-cell-disease-to-primary-care-and-emergency-department-providers-in-north-carolina-a-cost-b.pdf
Autor:
Angie Alexander, Emilia Frederick, Dominique Bulgin, Nirmish Shah, Paula Tanabe, Matthew Young, Gary Rains, Emily Bonnabeau
Publikováno v:
Journal of Emergency Nursing. 47:40-49.e1
Background Sickle cell disease is associated with frequent vaso-occlusive episode and emergency department visits. Our group developed (1) a vaso-occlusive episode treatment algorithm based on the National Heart, Lung, and Blood Institute recommendat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc62ff27e390923d6060e173dafbfea4
https://doi.org/10.1016/j.jen.2020.06.001
https://doi.org/10.1016/j.jen.2020.06.001