Singer PA, Martin DK, Kelner M. Quality end-of-life care: patients’ perspectives [see comments]. JAMA 1999; 281(2):163–168.

Solberg LI, Mosser G, McDonald S. The three faces of performance measurement: improvement, accountability, and research. Jt Comm J Qual Improv 1997; 23(3):135–147.

Solomon MZ, O’Donnell L, Jennings B, et al. Decisions near the end of life: professional views on life-sustaining treatments [see comments]. Am J Public Health 1993; 83(1):14– 23.

Spiegel D, Sands S, Koopman C. Pain and depression in patients with cancer. Cancer 1994; 74(9):2570–2578.

Steinhauser KE, Clipp EC, McNeilly M, Christakis NA, McIntyre LM, Tulsky JA. In search of a good death: observations of patients, families, and providers. Annals of Internal Medicine 2000; 132(10):825–832.

Stewart AL, Teno J, Patrick DL, Lynn J. The concept of quality of life of dying persons in the context of health care. J Pain Symptom Manage 1999; 17(2):93–108.

Strang P. Emotional and social aspects of cancer pain. Acta Oncol 1992; 31(3):323–326.

SUPPORT Principal Investigators. A controlled trial to improve care for seriously ill hospitalized patients. The Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments (SUPPORT). [published erratum appears in JAMA 1996 Apr 24; 275(16):1232]. JAMA 1995; 274(20):1591–1598.

Teno, J. Toolkit of Instruments to Measure End of Life Care, 1999: http://chcr.brown.edu/pcoc/toolkit.htm.

Teno, J. Facts on Dying: Brown Atlas Site of Death 1989–1997, 2000a; http://www.chcr.brown.edu/dying/factsondying.htm.

Teno, J. Rhode Island Partnership to Improve End-of-Life Care: Improving the Quality of Care for Our Most Vulnerable Population. 2000b; http://www.chcr.brown.edu/commstate/homepagewithframes.htm.

Teno JM, Byock I, Field MJ. Research agenda for developing measures to examine quality of care and quality of life of patients diagnosed with life-limiting illness. J Pain Symptom Manage 1999; 17(2):75–82.

Teno JM, Casey VA, Welch L, Edgman-Levitan S. Patient focused, family centered end-of-life medical care: views of the guidelines and bereaved family members. Manuscript Under Review 2001a .

Teno JM, Casey V, Edgman-Levitan S. Defining patient focused, family centered medical care. Ann Intern Med (in preparation).

Teno JM, Clarridge B, Casey V, Fowler J. Toolkit of instruments to measure end of life care bereaved family member interview—psychometric properties. Manuscript under review. 2001b.

Teno JM, Coppola KM. For every numerator, you need a denominator: a simple statement but key to measuring the quality of care of the “dying.” J Pain Symptom Manage 1999; 17(2):109–113.

Teno JM, Hakim RB, Knaus WA, et al. Preferences for cardiopulmonary resuscitation: physician-patient agreement and hospital resource use. The SUPPORT Investigators. J Gen Intern Med 1995; 10(4):179–186.

Teno JM, Stevens M, Fisher E. Variation in ICU utilizations: insights from qualitative and quantitative data. Manuscript under review. 2001e

Teno JM, Stevens M, Spernak S, Lynn J. Role of written advance directives in decision making: insights from qualitative and quantitative data. J Gen Intern Med 1998; 13(7):439–446.

Teno JM, Weitzen S, Fennell M, Mor V. Dying trajectory in the last year of life: does cancer trajectory fit other diseases? J Palliat Med. In press 2001d.



The National Academies | 500 Fifth St. N.W. | Washington, D.C. 20001
Copyright © National Academy of Sciences. All rights reserved.
Terms of Use and Privacy Statement