Validity of Patient-Reported Outcomes Measurement Information System Physical, Mental, and Social Health Measures After Left Ventricular Assist Device Implantation and Implications for Patient Care

Author:

Hahn Elizabeth A.1ORCID,Walsh Mary N.2,Allen Larry A.3ORCID,Lee Christopher S.4ORCID,Denfeld Quin E.5ORCID,Teuteberg Jeffrey J.6ORCID,Beiser David G.7ORCID,McIlvennan Colleen K.3ORCID,Lindenfeld JoAnn8,Klein Liviu9ORCID,Adler Eric D.10,Stehlik Josef11ORCID,Ruo Bernice10ORCID,Bedjeti Katy1ORCID,Cummings Peter D.1ORCID,Vela Alyssa M.12ORCID,Grady Kathleen L.12ORCID

Affiliation:

1. Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL. (E.A.H., K.B., P.D.C.)

2. Ascension St. Vincent Heart Center, Indianapolis, IN (M.N.W.).

3. Cardiology, University of Colorado, Aurora (L.A.A., C.K.M.).

4. Boston College William F. Connell School of Nursing, Chestnut Hill, MA (C.S.L.).

5. Oregon Health and Science University School of Nursing, Portland (Q.E.D.).

6. Falk Cardiovascular Institute, Stanford University, CA (J.J.T.).

7. Medicine, University of Chicago, IL (D.G.B.).

8. Medicine, Vanderbilt University, Nashville, TN (J.L.).

9. Medicine, University of California, San Francisco (L.K.).

10. Medicine, University of California, San Diego (E.D.A., B.R.).

11. Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City (J.S.).

12. Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL. (A.M.V., K.L.G.)

Abstract

BACKGROUND: A better understanding is needed of the burdens and benefits of left ventricular assist device (LVAD) implantation on patients’ physical, mental, and social well-being. The purpose of this report was to evaluate the validity of Patient-Reported Outcomes Measurement Information System (PROMIS) measures for LVAD patients and to estimate clinically important score differences likely to have implications for patient treatment or care. METHODS: Adults from 12 sites across all US geographic regions completed PROMIS measures ≥3 months post-LVAD implantation. Other patient-reported outcomes (eg, Kansas City Cardiomyopathy Questionnaire-12 item), clinician ratings, performance tests, and clinical adverse events were used as validity indicators. Criterion and construct validity and clinically important differences were estimated with Pearson correlations, ANOVA methods, and Cohen d effect sizes. RESULTS: Participants’ (n=648) mean age was 58 years, and the majority were men (78%), non-Hispanic White people (68%), with dilated cardiomyopathy (55%), long-term implantation strategy (57%), and New York Heart Association classes I and II (54%). Most correlations between validity indicators and PROMIS measures were medium to large (≥0.3; p <0.01). Most validity analyses demonstrated medium-to-large effect sizes (≥0.5) and clinically important differences in mean PROMIS scores (up to 14.8 points). Ranges of minimally important differences for 4 PROMIS measures were as follows: fatigue (3–5 points), physical function (2–3), ability to participate in social roles and activities (3), and satisfaction with social roles and activities (3–5). CONCLUSIONS: The findings provide convincing evidence for the relevance and validity of PROMIS physical, mental, and social health measures in patients from early-to-late post-LVAD implantation. Findings may inform shared decision-making when patients consider treatment options. Patients with an LVAD, their caregivers, and their clinicians should find it useful to interpret the meaning of their PROMIS scores in relation to the general population, that is, PROMIS may help to monitor a return to normalcy in everyday life. REGISTRATION: URL: https://clinicaltrials.gov ; Unique: identifier: NCT03044535.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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