[PDF][PDF] Ensuring equity and inclusion in virtual care best practices for diverse populations of youth with chronic pain

…, J Swidrovich, C Lalonde, L Tunji-Ajayi… - Healthcare Quarterly …, 2022 - researchgate.net
Poor access to care is a top patient-oriented research priority for youth with chronic pain in
Canada, and the COVID-19 pandemic has exacerbated these concerns. Our patientoriented …

Sickle cell disease in Ontario, Canada: an epidemiologic profile based on health administrative data

J Pendergrast, LT Ajayi, E Kim, MA Campitelli… - … Open Access Journal, 2023 - cmajopen.ca
Background: The number of patients with sickle cell disease in Ontario, Canada, is unknown.
In the absence of a formal registry, we performed a study to determine an approximate …

Pain management in adult patients with sickle cell disease in the emergency department: how does current practice compare with existing standards of care?

M Gulilat, L Tunji-Ajayi, S Thompson, MP Poku… - Canadian Journal of …, 2023 - Springer
Purpose Sickle cell disease (SCD) is an inherited blood disorder with a natural course
punctuated by acute complications including painful vaso-occlusive episodes. The objectives …

[PDF][PDF] Confidential

J Pendergrast, LT Ajayi, E Kim, MA Campitelli… - cmajopen.ca
Background: The number of sickle cell patients in Ontario is unknown. In the absence of a
formal registry, it may be possible to determine an approximate census via analysis of health …

An embedded mixed-methods study highlighted a lack of discussions on retention in clinical trial consultations

P Tunji-Ajayi, EM Duncan, K Gillies - Journal of Clinical Epidemiology, 2020 - Elsevier
Objectives This study investigated trial consultations to identify whether and to what extent
discussions of retention are present. Study Design and Setting This embedded mixed-…

How many sickle cell disease patients are there in Ontario? Results of a query of health services administrative databases

E Kim, E Graves, L Tunji-Ajayi… - Sickle Cell Disease …, 2018 - sicklecellanemia.ca
Method: For the period ranging from FY 2007/08-2016/17, the Ontario Discharge Abstract
Database and National Ambulatory Care Reporting System were queried for ICD9 code 2826 …

[PDF][PDF] Sickle cell disease in Ontario, Canada: an epidemiologic profile based on health administrative data

LTA MSM, MA Campitelli - 2023 - cmajopen.ca
Background: The number of patients with sickle cell disease in Ontario, Canada, is unknown.
In the absence of a formal registry, we performed a study to determine an approximate …

[HTML][HTML] Study protocol for a randomized, blinded, controlled trial of ketamine for acute painful crisis of sickle cell disease

MS Alshahrani, LP Asonto, MM El Tahan… - Trials, 2019 - Springer
Background Sickle cell disease (SCD) is an inherited hematological disorder where the
shape of red blood cells is altered, resulting in the destruction of red blood cells, anemia, and …

[PDF][PDF] Sickle cell anemia

G Poole, A Sangiorgio, S Pessione - 1932 - scholar.archive.org
Analysis of the subject matter Sickle cell disorder (scd) is a collective name for a series of
serious inherited chronic conditions that can affect all systems of the body. it is one of the most …

[HTML][HTML] PrJADENUtm (deferasirox) for the management of chronic iron overload is now available in Canada

L Lézard - lelezard.com
DORVAL, QC, May 6, 2016/CNW/-Canadians requiring treatment for chronic iron overload
have a new treatment option with the availability of JADENUtm (deferasirox) following its …