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Kristen A Morin

Biographic Data

ID7448666
NAMEKristen A Morin
GIVEN NAMESKristen A
FAMILY NAMEMorin
SIGNATUREMORIN K A
AFFILIATIONSNOSM University
ORCID0009-0001-4059-3475
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS0
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2022
H-INDEX0
  • Association of prescribed oral stimulants on cocaine use among patients enrolled in opioid agonist treatment

    Open Access•Mark Tatangelo, Farah Tahsin et al.•ARTICLE•Frontiers in Psychiatry•2022

    The use of oral stimulant prescriptions to treat cocaine use had no clinically significant benefit in a real-world setting. Patients who receive prescriptions for oral stimulants consume more cocaine before and after treatment compared to patients without an oral stimulant prescription. We also observed that cocaine use was reduced with increased time since treatment initiation

  • Negative Impact of Amphetamine-Type Stimulant Use on Opioid Agonist Treatment Retention in Ontario, Canada

    Open Access•Kristen A Morin, Frank Vojtesek et al.•ARTICLE•Frontiers in Psychiatry•2021

    Objective: The objective of this study was to evaluate epidemiological trends of co-use patterns of amphetamine-type stimulants and opioids and the impact of co-use patterns on Opioid Agonist Treatment (OAT) retention in Ontario, Canada. The secondary objective was to assess geographical variation in amphetamine-type stimulant use in Northern Rural, Northern Urban, Southern Rural and Southern Urban Areas of Ontario. Methods: A retrospective cohor…

  • Evidence of increased Fentanyl use during the Covid-19 pandemic among opioid agonist treatment patients in Ontario, Canada

    Open Access•Kristen A Morin, Shreedhar Acharya et al.•ARTICLE•International Journal of Drug…•2021

    The use of fentanyl increased by 108% among OAT patients in Ontario during the COVID 19 pandemic. We argue that the persistent increase of fentanyl exposure over time, specifically in the OAT population, suggests that reduced monitoring may decrease OAT's effectiveness and negatively impact patient outcomes

No prominent works on this page.

  • Negative Impact of Amphetamine-Type Stimulant Use on Opioid Agonist Treatment Retention in Ontario, Canada

    Open Access•Kristen A Morin, Frank Vojtesek et al.•ARTICLE•Frontiers in Psychiatry•2021

    Objective: The objective of this study was to evaluate epidemiological trends of co-use patterns of amphetamine-type stimulants and opioids and the impact of co-use patterns on Opioid Agonist Treatment (OAT) retention in Ontario, Canada. The secondary objective was to assess geographical variation in amphetamine-type stimulant use in Northern Rural, Northern Urban, Southern Rural and Southern Urban Areas of Ontario. Methods: A retrospective cohor…

  • Evidence of increased Fentanyl use during the Covid-19 pandemic among opioid agonist treatment patients in Ontario, Canada

    Open Access•Kristen A Morin, Shreedhar Acharya et al.•ARTICLE•International Journal of Drug…•2021

    The use of fentanyl increased by 108% among OAT patients in Ontario during the COVID 19 pandemic. We argue that the persistent increase of fentanyl exposure over time, specifically in the OAT population, suggests that reduced monitoring may decrease OAT's effectiveness and negatively impact patient outcomes

  • Association of prescribed oral stimulants on cocaine use among patients enrolled in opioid agonist treatment

    Open Access•Mark Tatangelo, Farah Tahsin et al.•ARTICLE•Frontiers in Psychiatry•2022

    The use of oral stimulant prescriptions to treat cocaine use had no clinically significant benefit in a real-world setting. Patients who receive prescriptions for oral stimulants consume more cocaine before and after treatment compared to patients without an oral stimulant prescription. We also observed that cocaine use was reduced with increased time since treatment initiation

Agonist (3 works) · Anesthesia (3 works) · Internal Medicine (3 works) · Medicine (3 works) · Opioid (3 works) · Opioid Use Disorder Treatment (3 works) · Psychiatry (2 works) · Receptor (2 works) · Amphetamine (1 work) · Attention Deficit Hyperactivity Disorder (1 work)

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