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Institution

Saskatchewan Health

GovernmentRegina, Saskatchewan, Canada
About: Saskatchewan Health is a government organization based out in Regina, Saskatchewan, Canada. It is known for research contribution in the topics: Population & Health care. The organization has 442 authors who have published 489 publications receiving 7728 citations.


Papers
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Journal ArticleDOI
TL;DR: A population-based study to estimate the incidence of hospitalizations for aplastic anemia and agranulocytosis and to evaluate associations between these disorders and antecedent prescription drug use was performed using the Saskatchewan administrative health care databases.

45 citations

Journal ArticleDOI
TL;DR: Evidence of high prevalence and a 3-fold comorbid association between CUD with MD and Cud with GAD is confirmed, which confirms the evidence of evidence-based policy interventions with effective, integrated management ofComorbid CUDs with psychiatric disorders may contribute to positive patient outcomes.

45 citations

Journal ArticleDOI
TL;DR: Neither ATP13A2 genetic variability nor quantitative gene expression in brain appears to contribute to familial parkinsonism or nonfamilial PD.
Abstract: Recessively inherited mutations in ATP13A2 result in Kufor-Rakeb syndrome, whereas genetic variability and elevated ATP13A2 expression have been implicated in Parkinson disease (PD). Given this background, ATP13A2 was comprehensively assessed to support or refute its contribution to PD. Sequencing of ATP13A2 exons and intron-exon boundaries was performed in 89 probands with familial parkinsonism from Tunisia. The segregation of mutations with parkinsonism was subsequently assessed within pedigrees. The frequency of genetic variants and evidence for association was also examined in 240 patients with non-familial PD and 372 healthy controls. ATP13A2 mRNA expression was also quantified in brain tissues from 38 patients with non-familial PD and 38 healthy subjects from the US. Sequencing analysis revealed 37 new variants; seven missense, six silent and 24 that were noncoding. However, no single ATP13A2 mutation segregated with familial parkinsonism in either a dominant or recessive manner. Four markers showed marginal association with non-familial PD, prior to correction for multiple testing. ATP13A2 mRNA expression was marginally decreased in PD brains compared with tissue from control subjects. In conclusion, neither ATP13A2 genetic variability nor quantitative gene expression in brain appears to contribute to familial parkinsonism or non-familial PD.

45 citations

Journal ArticleDOI
TL;DR: The study emphasises the need to provide language assistance during medical consultations to address language barriers among immigrants and recommends the development of guidelines for recruitment, training, and effective engagement of language interpreters during medical consultation to ensure high quality, equitable and client-centered care.
Abstract: Background Immigrants from culturally, ethnically, and linguistically diverse countries face many challenges during the resettlement phase, which influence their access to healthcare services and health outcomes. The "Healthy Immigrant Effect" or the health advantage that immigrants arrive with is observed to deteriorate with increased length of stay in the host country. Methods An exploratory qualitative design, following a community-based research approach, was employed. The research team consisted of health researchers, clinicians, and community members. The objective was to explore the barriers to healthcare access among immigrants with limited English language proficiency. Three focus groups were carried out with 29 women and nine men attending English language classes at a settlement agency in a mid-sized city. Additionally, 17 individual interviews were carried out with healthcare providers and administrative staff caring for immigrants and refugees. Results A thematic analysis was carried out with transcribed focus groups and healthcare provider interview data. Both the healthcare providers and immigrants indicated that limited language proficiency often delayed access to available healthcare services and interfered with the development of a therapeutic relationship between the client and the healthcare provider. Language barriers also impeded effective communication between healthcare providers and clients, leading to suboptimal care and dissatisfaction with the care received. Language barriers interfered with treatment adherence and the use of preventative and screening services, further delaying access to timely care, causing poor chronic disease management, and ultimately resulting in poor health outcomes. Involving untrained interpreters, family members, or others from the ethnic community was problematic due to misinterpretation and confidentiality issues. Conclusions The study emphasises the need to provide language assistance during medical consultations to address language barriers among immigrants. The development of guidelines for recruitment, training, and effective engagement of language interpreters during medical consultation is recommended to ensure high quality, equitable and client-centered care.

44 citations

Journal ArticleDOI
TL;DR: A reassortant influenza A(H 1N1) virus of swine origin distinct from the pandemic H1N1 2009 strain was isolated from 3 patients, all of whom worked at the same large hog operation in Saskatchewan, Canada, and was the product of a genetic reassortment between seasonal H1n1 and triple-reassortant flu virus that emerged in North American swine during the late 1990s.
Abstract: A reassortant influenza A(H1N1) virus of swine origin distinct from the pandemic H1N1 2009 strain was isolated from 3 patients, all of whom worked at the same large hog operation in Saskatchewan, Canada. The genomic composition of the isolates has not been previously reported, to our knowledge, and was the product of a genetic reassortment between seasonal H1N1 and triple-reassortant influenza virus that emerged in North American swine during the late 1990s. The neuraminidase and hemagglutinin genes of A/ Saskatchewan/5350/2009, A/Saskatchewan/5351/2009, and A/ Saskatchewan/5131/2009 were derived from human H1N1 virus and were closely related to those of A/Brisbane/59/2007.

42 citations


Authors

Showing all 449 results

NameH-indexPapersCitations
Gary R. Hunter7133716410
Lisa M. Lix5946213778
Peter O'Hare551269246
Edward D. Chan542249014
Paul Babyn5430711466
Roland N. Auer521208564
Paul N. Levett441378486
Alan A. Boulton391835253
Carl D'Arcy381295002
Vikram Misra371164363
Andrew W. Lyon281092449
Denis C. Lehotay27521756
Gary F. Teare26612749
Greg B. Horsman25491727
Emina Torlakovic24961899
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20232
20221
2021116
202088
201959
201836