Understanding How Canadian Physicians and Public Stakeholders Rationalize MAiD Amid Bill C-7: A Critical Analysis
DOI :
https://doi.org/10.7202/1124208arMots-clés :
soins palliatifs, méthodes qualitatives, aide médicale à mourir, AMM, projet de loi C-7, Canada, point de vue des médecins, opinion publiqueLangue(s) :
AnglaisRésumé
Malgré sa légalisation, l’éthique de l’aide médicale à mourir (AMM) reste controversée en raison de l’évolution des critères d’admissibilité et des implications qui en découlent pour les personnes souffrant de maladies non terminales, notamment de troubles mentaux. Compte tenu de la disponibilité croissante de l’AMM, il est important de comparer les discours de la société et ceux des médecins afin d’éclairer l’élaboration de politiques et de lois en matière de santé qui reflètent les valeurs et les préoccupations des différentes parties prenantes. Cet article présente une analyse qualitative critique de deux types de données : 1) les réponses à des entretiens menés auprès de médecins canadiens concernant la pratique de l’aide médicale à mourir, et 2) les médias numériques canadiens, dans le but de déterminer les points de convergence et de divergence entre les discours des deux types de sources. Notre analyse a permis de dégager quatre thèmes généraux : 1) l’autonomie et le choix, 2) « mourir dans la dignité » et la réduction des risques, 3) le paternalisme et la vulnérabilité, et 4) la médicalisation de la souffrance. En général, si les médecins et les autres parties prenantes se disent attachés au principe de l’autonomie du patient, toutes les parties ont exprimé leurs préoccupations concernant les inégalités systémiques et le risque que l’AMM soit utilisée comme un substitut pour traiter les déterminants sociaux plus larges de la santé.
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© Midori Matthew 2026

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