Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Ewurabena Simpson"'
Autor:
Sara D. Khangura, Beth K. Potter, Christine Davies, Robin Ducharme, A. Brianne Bota, Steven Hawken, Kumanan Wilson, Maria D. Karaceper, Robert J. Klaassen, Julian Little, Ewurabena Simpson, Pranesh Chakraborty
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background Newborn screening (NBS) for sickle cell disease incidentally identifies heterozygous carriers of hemoglobinopathy mutations. In Ontario, Canada, these carrier results are not routinely disclosed, presenting an opportunity to inves
Externí odkaz:
https://doaj.org/article/55c9436047534d04b6dc6dcd133ce96f
Congenital dyserythropoietic anemia type IV (CDAIV) is a rare inherited hematological disorder presenting severe anemia due to altered erythropoiesis and hemolysis, with variable needs for recurrent transfusions. We present a case of a transfusion-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e81d3d133ca40b0a00cf42c191e753
https://doi.org/10.22541/au.166505406.60948791/v1
https://doi.org/10.22541/au.166505406.60948791/v1
Autor:
R Todd Alexander, Chelsey Grimbly, Leanne M Ward, Patricia Diaz Escagedo, Jacob L Jaremko, Aisha Bruce, Nathalie Alos, Marie-Eve Robinson, Victor N Konji, Marika Page, Ewurabena Simpson, Yves D Pastore, Rose Girgis
Publikováno v:
Journal of the Endocrine Society. 6:A177-A178
Purpose To evaluate bone morbidity and the response to intravenous (IV) bisphosphonate therapy in children with Sickle Cell Disease (SCD). Methods We conducted a retrospective review of patient records from 2003 to 2019 at three Canadian pediatric te
Autor:
Adam Yan, Soumitra Tole, Lissa Bair, Amanda Wagner, Ken Tang, Melanie Kirby-Allen, Ewurabena Simpson, Suzan Williams
Publikováno v:
Journal of pediatric hematology/oncology.
Current guidelines recommend a preoperative hemoglobin of 10.0 g/dL in patients with sickle cell disease [SCD], however, this threshold continues to be an area of controversy. Previous studies demonstrating the benefits of preoperative transfusions h
Autor:
Pranesh Chakraborty, Ewurabena Simpson, Steven Hawken, Christine Davies, Maria D. Karaceper, Robert J. Klaassen, A. Brianne Bota, Kumanan Wilson, Robin Ducharme, Beth K. Potter, Sara D. Khangura, Julian Little
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 21, Iss 1, Pp 1-10 (2021)
BMC Pediatrics, Vol 21, Iss 1, Pp 1-10 (2021)
Background Newborn screening (NBS) for sickle cell disease incidentally identifies heterozygous carriers of hemoglobinopathy mutations. In Ontario, Canada, these carrier results are not routinely disclosed, presenting an opportunity to investigate th
Publikováno v:
Blood. 136:8-9
Background: Central venous catheters (CVCs) are the most frequent cause of thrombosis in acutely unwell neonates. The natural history CVC-RT remains unclear. The current guideline for symptomatic CVC-related thrombus suggests that anticoagulation lik
Autor:
Korinne Hamilton, Lehana Thabane, Mihir D. Bhatt, Ketan Kulkarni, Anthony Kam Chuen Chan, Leslie Raffini, Ewurabena Simpson
Publikováno v:
Medicine: Case Reports and Study Protocols. 2:e0053
Autor:
Isaac Odame, William T. Zempsky, Yalinie Kulandaivelu, Cynthia Nguyen, Fiona Campbell, Khush Amaria, Chitra Lalloo, Tessy George, Vicky R. Breakey, Ewurabena Simpson, Jennifer Stinson, Melanie Kirby-Allen, Richard Ward
Publikováno v:
JMIR Pediatrics and Parenting
Background Accessible self-management interventions are critical for adolescents with sickle cell disease to better cope with their disease, improve health outcomes and health-related quality of life, and promote successful transition to adult health
Publikováno v:
SickKids Handbook of Pediatric Thrombosis and Hemostasis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baf4345f88c92a1fe070fc0c47815977
https://doi.org/10.1159/000446738
https://doi.org/10.1159/000446738
Autor:
Mylene Bassal, Karen Mandel, Raveena Ramphal, Donna L. Johnston, Ewurabena Simpson, Li Peckan, Robert J. Klaassen, Jacqueline Halton
Publikováno v:
Journal of pediatric hematology/oncology. 39(6)
Providing the best care in both the inpatient and outpatient settings to pediatric oncology patients is all programs goal. Using continuous improvement methodologies, we changed from a solely team-based physician care model to a hybrid model. All pat