Author: Rebecca Dresser
Source: Hastings Center Report; November 1995; pg. 32
Focus: Dworkin's theoretical framework concerning dementia and autonomy
Dworkin emphasizes the importance of honoring prior autonomous decisions of individuals like Margo who develop dementia.
His inquiry revolves around values such as autonomy, beneficence, and the sanctity of life.
Precedent Autonomy: Dworkin argues that individuals should retain the right to make decisions about their end-of-life care based on their prior wishes even if they lose the capacity to judge their best interests over time.
Experiential Interests
Represent momentary pleasures, e.g., activities that individuals enjoy.
Are less emphasized in Dworkin's theory due to individual variability.
Critical Interests
Associated with the meaningful pursuits that give coherence to one’s life.
Considered more important than experiential interests, especially in discussions of autonomy and individuals like Margo.
The integrity view of autonomy allows for honoring the critical interests of individuals who are unable to express their current wishes:
Dworkin supports the idea that family members should apply their understanding of the patient's critical interests when making decisions on their behalf.
He labels disregard for prior directives as an unacceptable form of moral paternalism.
Dworkin argues for the state to respect the directives set forth by individuals experiencing dementia, emphasizing a compassionate approach that supports their choice at the end of life.
The decisions made should reflect the earlier values and lifestyle of the individual, honoring the narrative of their life.
Dresser expresses skepticism about Dworkin’s theories regarding dementia, particularly focusing on the following:
Subjective Experience of Dementia: Many individuals with dementia experience varying levels of distress, which contradicts the idea that all patients experience life similarly once they become incapacitated.
Quality of Life: The quality of life for dementia patients can be significantly influenced by their environment and social interactions, which Dworkin might downplay.
Advance Directives: There is often a lack of public understanding and support in exercising advance directives, which results in many people failing to articulate their wishes prior to becoming incapable.
Change of Heart: Individuals may change their preferences over time, and rigid adherence to prior directives can undermine their current interests.
Dresser suggests that society must reassess its views on individuals with dementia and find ways to interact that allow these individuals to experience life fully and meaningfully.
Disability Perspective: A shift away from the tragic view of dementia to one that recognizes the value and enjoyment in the present moments of life is essential.
A policy aimed at enhancing the quality of life for dementia patients while respecting their critical interests would align more closely with a compassionate society.