Sources of concern about the patient self-determination act

S. M. Wolf, P. Boyle, D. Callahan, J. J. Fins, B. Jennings, J. L. Nelson, J. A. Barondess, D. W. Brock, R. Dresser, L. Emanuel, S. Johnson, J. Lantos, D. R. Mason, M. Mezey, D. Orentlicher, F. Rouse

Research output: Contribution to journalArticlepeer-review

139 Scopus citations

Abstract

ON December 1, 1991, the Patient Self-Determination Act of 1990 (PSDA)1 went into effect. This is the first federal statute to focus on advance directives and the right of adults to refuse life-sustaining treatment. The law applies to all health care institutions receiving Medicare or Medicaid funds, including hospitals, skilled-nursing facilities, hospices, home health and personal care agencies, and health maintenance organizations (HMOs). The statute requires that the institution provide written information to each adult patient on admission (in the case of hospitals or skilled-nursing facilities), enrollment (HMOs), first receipt of care (hospices), or before the patient comes under an …

Original languageEnglish (US)
Pages (from-to)1666-1671
Number of pages6
JournalNew England Journal of Medicine
Volume325
Issue number23
DOIs
StatePublished - Dec 5 1991

ASJC Scopus subject areas

  • General Medicine

Fingerprint

Dive into the research topics of 'Sources of concern about the patient self-determination act'. Together they form a unique fingerprint.

Cite this