Accuracy of Expected Symptoms and Subsequent Quality of Life Measures Among Adults With COPD

Author:

Hart Joanna L.1234,Summer Amy E.1,Ogunduyile Lon1,Lapite Folasade C.5,Hong David1,Whitman Casey1,Blette Bryan S.6,Harhay Michael O.17,Halpern Scott D.1237

Affiliation:

1. Palliative and Advanced Illness Research Center, University of Pennsylvania, Philadelphia

2. Division of Pulmonary, Allergy, and Critical Care, Department of Medicine, University of Pennsylvania, Philadelphia

3. Department of Medical Ethics and Health Policy, University of Pennsylvania, Philadelphia

4. Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania

5. Tulane University School of Medicine, New Orleans, Louisiana

6. Department of Biostatistics, Vanderbilt University, Nashville, Tennessee

7. Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia

Abstract

ImportancePatients’ expectations for future health guide their decisions and enable them to prepare, adapt, and cope. However, little is known about how inaccurate expectations may affect patients’ illness outcomes.ObjectiveTo assess the association between patients’ expectation inaccuracies and health-related quality of life.Design, Setting, and ParticipantsThis cohort study of patients with severe chronic obstructive pulmonary disease (COPD) was conducted from 2017 to 2021, which included a 24-month follow-up period. Eligible participants received outpatient primary care at pulmonary clinics of a single large US health system. Data were analyzed between 2021 and 2023.ExposureExpectation accuracy, measured by comparing patients’ self-reported expectations of their symptom burden with their actual physical and emotional symptoms 3, 12, and 24 months in the future.Main Outcome and MeasureHealth-related quality of life, measured by the St George’s Respiratory Questionnaire-COPD at 3, 12, and 24 months.ResultsA total of 207 participants were included (median age, 65.5 years [range, 42.0-86.0 years]; 120 women [58.0%]; 118 Black [57.0%], 79 White [38.2%]). The consent rate among approached patients was 80.0%. Most patients reported no or only limited discussions of future health and symptom burdens with their clinicians. Across physical and emotional symptoms and all 3 time points, patients’ expectations were more optimistic than their experiences. There were no consistent patterns of measured demographic or behavioral characteristics associated with expectation accuracy. Regression models revealed that overoptimistic expectations of future burdens of dyspnea (linear regression estimate, 4.68; 95% CI, 2.68 to 6.68) and negative emotions (linear regression estimate, −3.04; 95% CI, −4.78 to 1.29) were associated with lower health-related quality of life at 3 months after adjustment for baseline health-related quality of life, forced expiratory volume over 1 second, and interval clinical events (P < .001 for both). Similar patterns were observed at 12 months (dyspnea: linear regression estimate, 2.41; 95% CI, 0.45 to 4.37) and 24 months (negative emotions: linear regression estimate, −2.39; 95% CI, −4.67 to 0.12; dyspnea: linear regression estimate, 3.21; 95% CI, 0.82 to 5.60), although there was no statistically significant association between expectation of negative emotions and quality of life at 12 months.Conclusions and RelevanceIn this cohort study of patients with COPD, we found that patients are overoptimistic in their expectations about future negative symptom burdens, and such inaccuracies were independently associated with worse well-being over time. Developing and implementing strategies to improve patients’ symptom expectations may improve patient-centered outcomes.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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