End-of-life decisions

Open Access
Location of death among children with life-threatening conditions: a national population-based observational study using the Canadian Vital Statistics Database (2008–2014)
Kimberley Widger, Sarah Brennenstuhl, Peter Tanuseputro, Katherine E. Nelson, Adam Rapoport, Hsien Seow, Harold Siden, Chris Vadeboncoeur and Sumit Gupta

April 04, 2023 11 (2) E298-E304; DOI: https://doi.org/10.9778/cmajo.20220070
Open Access
Physician perceptions of restrictive visitor policies during the COVID-19 pandemic: a qualitative study
Kirsten Wentlandt, Kayla T. Wolofsky, Andrea Weiss, Lindsay Hurlburt, Eddy Fan, Camilla Zimmermann and Sarina R. Isenberg

February 07, 2023 11 (1) E110-E117; DOI: https://doi.org/10.9778/cmajo.20220048
Open Access
Medications and dosages used in medical assistance in dying: a cross-sectional study
Igor Stukalin, Oluwatobi R. Olaiya, Viren Naik, Ellen Wiebe, Mike Kekewich, Michaela Kelly, Laura Wilding, Roxanne Halko and Simon Oczkowski

January 18, 2022 10 (1) E19-E26; DOI: https://doi.org/10.9778/cmajo.20200268
Open Access
Community implementation of the 3 Wishes Project: an observational study of a compassionate end-of-life care initiative for critically ill patients
Brenda K. Reeve, Brittany B. Dennis, William Dechert, Barbara Longo, Diane Heels-Ansdell, Alison Scholes, France J. Clarke, John R.K. Arthur and Deborah J. Cook

July 20, 2021 9 (3) E757-E764; DOI: https://doi.org/10.9778/cmajo.20200273
Open Access
Quality of end-of-life communication in 2 high-risk ICU cohorts: a retrospective cohort study
Tammy L. Pham and Allan Garland

May 21, 2021 9 (2) E570-E575; DOI: https://doi.org/10.9778/cmajo.20200146
Open Access
How the experience of medical assistance in dying changed during the COVID-19 pandemic in Canada: a qualitative study of providers
Ellen Wiebe, Michaela Kelly, Thomas McMorrow, Sabrina Tremblay-Huet, Brian Sum and Mirna Hennawy

April 16, 2021 9 (2) E400-E405; DOI: https://doi.org/10.9778/cmajo.20200163
Open Access
Assessment of capacity to give informed consent for medical assistance in dying: a qualitative study of clinicians’ experience
Ellen Wiebe, Michaela Kelly, Thomas McMorrow, Sabrina Tremblay-Huet and Mirna Hennawy

April 13, 2021 9 (2) E358-E363; DOI: https://doi.org/10.9778/cmajo.20200136
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Factors predicting the risk of loss of decisional capacity for medical assistance in dying: a retrospective database review
Debbie Selby, Christopher Meaney, Sally Bean, Elie Isenberg-Grzeda and Amy Nolen

December 08, 2020 8 (4) E825-E831; DOI: https://doi.org/10.9778/cmajo.20200052
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Evaluation of a program using a physician assistant and an electronic patient–provider communication tool to facilitate discussions about goals of care in older adults in hospital: a pilot study
Monica Monchis, Chris Martin and Giulio DiDiodato

September 14, 2020 8 (3) E577-E584; DOI: https://doi.org/10.9778/cmajo.20200022
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Quality of clinicians’ conversations with patients and families before and after implementation of the Serious Illness Care Program in a hospital setting: a retrospective chart review study
Christina Ma, Lauren E. Riehm, Rachelle Bernacki, Joanna Paladino and John J. You

June 19, 2020 8 (2) E448-E454; DOI: https://doi.org/10.9778/cmajo.20190193

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