JAMA · 2002 · 92 citations · 43 references
Harm ReductionStep PatientsPrimary CareEnd-of-life CareSymptomatic TreatmentHealth Care TeamPhysician-assisted SuicidePublic HealthLethal PrescriptionHealth PolicyPsychiatryGeriatricsHospiceNursingPalliative CareMedical EthicsSuicidePatient SafetyEnd-of-life IssueTerminal IllnessMedicineSuicide Prevention
Studies of dying patients have shown that about half would like the option of physician-assisted suicide (PAS) to be available for possible future use. Those percentages decrease significantly with each step patients take toward action. Studies show that although about 10% of patients seriously consider PAS, only 1% of dying patients specifically request it, and 1 in 10 of those patients actually receive and take a lethal prescription. However, most patients' desires for PAS diminish as their underlying concerns are identified and addressed directly. To help identify concerns motivating a patient's request for PAS, physicians should talk with patients about their expectations and fears, options for end-of-life care, goals, family concerns and burdens, suffering or physical symptoms, sense of meaning and quality of life, and symptoms of depression. A patient with advanced amyotrophic lateral sclerosis (ALS) who requested PAS illustrates how a hasty response may adversely affect patient care and the health care team. Although physicians should remain mindful of their personal, moral, and legal concerns, these concerns should not override their willingness to explore what motivates a patient to make this request. When this approach is taken, suffering can be optimally alleviated and, in almost all cases, the patient's wishes can be met without PAS.
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