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Concept · philosophy

End-of-life ethics

4 studiesEvidence last moved Sep 3, 2026

End-of-life ethics asks who may forgo life-sustaining treatment, how autonomy is shared with family and clinicians, and whether dying well means erasing all suffering.

Destination LVADs, East Asian statutes and palliative-care metrics all pressure the simple picture of an isolated chooser who wants zero pain.

Studies

4

Findings

4

4 supporting · 0 challenging · 0 qualifying citations

Open tensions

1

Latest change

Concept page published

End-of-life ethics

Currently

What we know

  1. Respect for autonomy remains central at the end of life, but decisions are better understood relationally in clinical context than as isolated choice characteristics.
  2. Japan, Korea, Taiwan and England regulate forgoing life-sustaining treatment differently, including how family is treated.
  3. Den Hartogh argues dying well can require respecting some suffering rather than only removing it as a symptom list.
  4. LVAD as destination therapy prolongs life in transplant-ineligible heart failure but reshapes dying, consent and caregiver burden.

Largest unresolved question

Relational-autonomy authors keep autonomy central; comparative statute work shows jurisdictions that still lack a forgoing-LST law or treat family as the decision site.

Common misconceptions

  • Palliative care’s aim is to drive suffering to zero.

    Den Hartogh says studies cite Cassell then measure suffering like symptoms; dying well can include respecting some suffering.

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