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Volume 39, Issue 1, Pages 9-22 (January 2010)


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The Quality of Dying and Death Questionnaire (QODD): Empirical Domains and Theoretical Perspectives

Lois Downey, MAaCorresponding Author Informationemail address, J. Randall Curtis, MD, MPHa, William E. Lafferty, MDd, Jerald R. Herting, PhDbc, Ruth A. Engelberg, PhDa

Accepted 14 May 2009. published online 27 September 2009.

Abstract 

We used exploratory factor analysis within the confirmatory analysis framework, and data provided by family members and friends of 205 decedents in Missoula, Montana, to construct a model of latent-variable domains underlying the Quality of Dying and Death questionnaire (QODD). We then used data from 182 surrogate respondents, who were survivors of Seattle decedents, to verify the latent-variable structure. Results from the two samples suggested that survivors' retrospective ratings of 13 specific aspects of decedents' end-of-life experience served as indicators of four correlated, but distinct, latent-variable domains: Symptom Control, Preparation, Connectedness, and Transcendence. A model testing a unidimensional domain structure exhibited unsatisfactory fit to the data, implying that a single global quality measure of dying and death may provide insufficient evidence for guiding clinical practice, evaluating interventions to improve quality of care or assessing the status or trajectory of individual patients. In anticipation of possible future research tying the quality of dying and death to theoretical constructs, we linked the inferred domains to concepts from identity theory and existential psychology. We conclude that research based on the current version of the QODD might benefit from the use of composite measures representing the four identified domains, but that future expansion and modification of the questionnaire are in order.

a Division of Pulmonary and Critical Care Medicine, Department of Medicine, Harborview Medical Center, University of Washington, Seattle, Washington, USA

b Department of Psychosocial and Community Health, School of Nursing, University of Washington, Seattle, Washington, USA

c Department of Sociology, College of Arts and Sciences, University of Washington, Seattle, Washington, USA

d Office of Health Services and Public Health Outcomes Research, University of Missouri-Kansas City, Kansas City, Missouri, USA

Corresponding Author InformationAddress correspondence to: Lois Downey, MA, Division of Pulmonary and Critical Care Medicine, Department of Medicine, Harborview Medical Center, 325 Ninth Avenue, Box 359765, Seattle, WA 98104, USA.

 The following organizations provided financial support for the studies included in this article: 1) The Robert Wood Johnson Foundation—Missoula study, 2) Agency for Healthcare Quality and Research grant #R03 HS09540—hospice study, 3) National Cancer Institute grant #5 R01 CA106204—clinical trial, and 4) Lotte & John Hecht Memorial Foundation—clinical trial.

PII: S0885-3924(09)00737-4

doi:10.1016/j.jpainsymman.2009.05.012


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