Jamie R. Daw
University of British Columbia
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Publication
Featured researches published by Jamie R. Daw.
Pharmacoepidemiology and Drug Safety | 2011
Jamie R. Daw; Gillian E. Hanley; Devon Greyson; Steven G. Morgan
To review the literature describing patterns of outpatient prescription drug use during pregnancy by therapeutic category, potential for fetal harm, and overall.
Health Policy | 2012
Jamie R. Daw; Steven G. Morgan
OBJECTIVES To describe recent changes and identify emergent trends in public drug benefit policies in Canada from 2000 to 2010. METHODS For each province, we tracked pharmacare design (namely eligibility, premiums, and patient cost-sharing) over time for three beneficiary groups: social assistance recipients, seniors, and the general non-senior population. We assess which plan designs are emerging as a national standard, where the gaps in public coverage remain, and implications for progress towards national pharmacare. RESULTS Expansion of public drug coverage has been limited. For social assistance recipients, first-dollar coverage is the standard. Seniors coverage remains varied, though means testing of eligibility or cost-sharing is common. Seniors benefits were significantly expanded in only one province. As of 2010, six provinces have embraced age irrelevant catastrophic income-based coverage, in some, resulting in the elimination of seniors drug benefits. CONCLUSIONS Universal income-based catastrophic coverage appears to be emerging as an implicit national standard for provincial pharmacare. However, due to the variation and high level of patient cost-sharing required under these programs, convergence on this model does not equate to substantial progress towards expanding coverage or reducing interprovincial disparities. Leverage of federal spending power to promote standards for public drug coverage is necessary to uniformly protect Canadians against high drug costs.
Clinical Therapeutics | 2012
Jamie R. Daw; Barbara Mintzes; Michael R. Law; Gillian E. Hanley; Steven G. Morgan
BACKGROUND Owing to the paucity of evidence available on the risks and benefits of drug use in pregnancy, the use of prescription medicines is a concern for both pregnant women and their health care providers. OBJECTIVE The aim of this study was to measure the frequency, timing, and type of medicines used before, during, and after pregnancy in a Canadian population. METHODS This retrospective cohort analysis used population-based health care data from all pregnancies ending in live births in hospitals in British Columbia from April 2001 to June 2006 (n = 163,082). Data from hospital records were linked to those in outpatient prescription-drug claims. Data from prescriptions filled from 6 months before pregnancy to 6 months postpartum were analyzed. Drugs were classified by therapeutic category and US Food and Drug Administration (FDA) pregnancy risk categories. RESULTS Prescriptions were filled in 63.5% of pregnancies. Evidence on safety is limited for many of the medicines most frequently filled in pregnancy, including codeine, salbutamol, and betamethasone. At least 1 prescription for a category D or X medicine was filled in 7.8% of pregnancies (5.5% category D; 2.5% category X). The most frequently filled prescriptions for category D drugs were benzodiazepines and antidepressants. The most frequently filled prescriptions for category X drugs were oral contraceptives and ovulation stimulants filled in the first trimester. CONCLUSIONS The majority of pregnant women in British Columbia filled at least 1 prescription, and ~1 in 13 filled a prescription for a drug categorized as D or X by the FDA. The prevalence of maternal prescription drug use emphasizes the need for postmarketing evaluation of the risk-benefit profiles of pharmaceuticals in pregnancy. Future research on prenatal drug use based on administrative databases should examine maternal treatment adherence and the determinants of maternal drug use, considering maternal health status, sociodemographics, and the characteristics and providers of prenatal care.
Canadian Medical Association Journal | 2015
Steven G. Morgan; Michael R. Law; Jamie R. Daw; Liza Abraham; Danielle Martin
Background: With the exception of Canada, all countries with universal health insurance systems provide universal coverage of prescription drugs. Progress toward universal public drug coverage in Canada has been slow, in part because of concerns about the potential costs. We sought to estimate the cost of implementing universal public coverage of prescription drugs in Canada. Methods: We used published data on prescribing patterns and costs by drug type, as well as source of funding (i.e., private drug plans, public drug plans and out-of-pocket expenses), in each province to estimate the cost of universal public coverage of prescription drugs from the perspectives of government, private payers and society as a whole. We estimated the cost of universal public drug coverage based on its anticipated effects on the volume of prescriptions filled, products selected and prices paid. We selected these parameters based on current policies and practices seen either in a Canadian province or in an international comparator. Results: Universal public drug coverage would reduce total spending on prescription drugs in Canada by
Health Affairs | 2013
Steven G. Morgan; Jamie R. Daw; Paige A. Thomson
7.3 billion (worst-case scenario
C.D. Howe Institute Commentary | 2013
Steve Morgan; Jamie R. Daw; Michael R. Law
4.2 billion, best-case scenario
Health Policy | 2013
Michael R. Law; Jamie R. Daw; Lucy Cheng; Steven G. Morgan
9.4 billion). The private sector would save
Clinical Research and Regulatory Affairs | 2015
Carolyn Edelstein; Zain Kassam; Jamie R. Daw; Mark B. Smith; Colleen R. Kelly
8.2 billion (worst-case scenario
BMC Health Services Research | 2013
Steven G. Morgan; Paige A. Thomson; Jamie R. Daw; Melissa K. Friesen
6.6 billion, best-case scenario
Health Services Research | 2018
Jamie R. Daw; Laura A. Hatfield
9.6 billion), whereas costs to government would increase by about