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Grant: Partnerships for Health System Improvement (PHSI)

University of Alberta

$399,835.00

Mental Health SONAR (Study of Natural health product Adverse Reactions)

FY 2013-14

Summary
Nearly 73% Canadians use natural health products (NHPs) such as herbal medicines, vitamins and essential fatty acids etc, often assuming natural means safe. Studies show that patients who use NHPs and prescription medications concurrently are putting themselves at increased risk for adverse events that negatively affect quality of life, cost of care (more office and hospital visits, prolonged therapy), as well as potentially life-threatening events. Commonly used NHPs such as ginseng, echinacea, St. Johns wort, black cohosh, garlic, gingko, cranberry and soy may interact with medications, leading to increased adverse effects. We suggest that mental health patients experience more clinically relevant NHP-drug interactions since they are a vulnerable population at high risk for co-morbidities and also indulge in polypharmacy. We propose to implement our active surveillance program to identify serious NHP AE in mental health clinics and to partner with scientists to investigate their mechanism of action. We will ask patients coming to our participating clinics for concurrent NHP and prescription medication use, and presence/absence of adverse events by a simple questionnaire. Patients experiencing a serious, severe, or unexpected adverse reaction will be invited to participate in a telephone interview conducted by our study team and if appropriate, requested to send product samples via courier; to our participating labs for analysis. Our research team has expertise in NHP AE active surveillance, laboratory expertise to evaluate mechanism(s) of action, and the collaboration of participating clinics, including clinical expertise to adjudicate suspected adverse events. Findings from our innovative active surveillance will be relevant to policy-makers such as Health Canada, and other partnering organizations. It provides sharing of data between researchers, clinician scientists, and care providers as well as end user mental health network organization.
Program
Partnerships for Health System Improvement (PHSI)
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
298703
Name
Vohra Sunita
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Alberta Health Services; Alberta Innovates (Edmonton)
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Health systems / services
Prcname2
Partnerships for Health System Improvement
Projecttitle
Mental Health SONAR (Study of Natural health product Adverse Reactions)
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$399,835
Cihrequipment2
$0
Programname2
Partnerships for Health System Improvement (PHSI)
Keyworddelim
Active Surveillance; Adjudication; Adverse Events; Knowledge Translation And Exchange; Mental Health; Natural Health Products; Nhp Lab Analysis; Nhp-Drug Database; Nhp-Drug Interactions; Patient Safety
Abstract
Nearly 73% Canadians use natural health products (NHPs) such as herbal medicines, vitamins and essential fatty acids etc, often assuming natural means safe. Studies show that patients who use NHPs and prescription medications concurrently are putting themselves at increased risk for adverse events that negatively affect quality of life, cost of care (more office and hospital visits, prolonged therapy), as well as potentially life-threatening events. Commonly used NHPs such as ginseng, echinacea, St. Johns wort, black cohosh, garlic, gingko, cranberry and soy may interact with medications, leading to increased adverse effects. We suggest that mental health patients experience more clinically relevant NHP-drug interactions since they are a vulnerable population at high risk for co-morbidities and also indulge in polypharmacy. We propose to implement our active surveillance program to identify serious NHP AE in mental health clinics and to partner with scientists to investigate their mechanism of action. We will ask patients coming to our participating clinics for concurrent NHP and prescription medication use, and presence/absence of adverse events by a simple questionnaire. Patients experiencing a serious, severe, or unexpected adverse reaction will be invited to participate in a telephone interview conducted by our study team and if appropriate, requested to send product samples via courier; to our participating labs for analysis. Our research team has expertise in NHP AE active surveillance, laboratory expertise to evaluate mechanism(s) of action, and the collaboration of participating clinics, including clinical expertise to adjudicate suspected adverse events. Findings from our innovative active surveillance will be relevant to policy-makers such as Health Canada, and other partnering organizations. It provides sharing of data between researchers, clinician scientists, and care providers as well as end user mental health network organization.
Competitiondate
201311
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Vohra, Sunita; Urichuk, Liana J
Approvedterm
3 ans 0 mois
Cihrcontribution2
Inst of Hlth Serv & Policy Res~ $399,835~ $0~