Literature DB >> 34088752

Predictors of Palliative Care Knowledge: Findings from the Health Information National Trends Survey.

Motolani E Ogunsanya1, Elizabeth A Goetzinger2, Oluwatomi F Owopetu3, Paulette D Chandler4, Lauren E O'Connor5.   

Abstract

BACKGROUND: Palliative care plays an important role in improving the quality of life for patients with cancer and their caregivers and has been associated with increased patient satisfaction. However, palliative care knowledge in the general population is limited, and often physician referral occurs late in prognosis. The objective of this analysis was to examine factors associated with palliative care knowledge.
METHOD: Using data from the 2018 NCI's Health Information National Trends Survey (HINTS) 5 Cycle 2, descriptive statistics, bivariate analyses, and multivariable logistic regressions were used to assess factors associated with respondents' palliative care knowledge using ORs and 95% confidence intervals as measures of association. The outcome of interest was measured with the item "How would you describe your level of knowledge about palliative care?" Possible response selections were "I've never heard of it," "I know a little bit about palliative care," and "I know what palliative care is and could explain it to someone else." To reduce the risk of type 1 error, jackknife variance estimations with repeated replications were used. All analyses were conducted with the SURVEYLOGISTIC command using SAS 9.4 (SAS Institute Inc.), and the statistical significance level was set at P < 0.05.
RESULTS: A total of 3,450 respondents (weighted sample size: 249,489,772) met the inclusion criteria. About 89% (n = 3,000) of all respondents had inadequate knowledge of palliative care. Multivariable analyses indicated that frequent health care utilization as defined as ≥ 2 times per year [OR, 3.01; 95% confidence interval (CI), 2.65-3.58], female gender (OR, 2.15; 95% CI, 1.31-3.59), being married (OR, 2.02; 95% CI, 1.14-3.59), having a college degree or higher (OR, 13.83; 95% CI, 1.71-12.04), and having a regular source of care (OR, 2.67; 95% CI, 1.37-1.90) had greater odds of adequate palliative care knowledge. Those without a cancer diagnosis were less likely to have adequate knowledge of palliative care (OR, 0.49; 95% CI, 0.41-0.89).
CONCLUSIONS: Knowledge of palliative care in the United States is low, particularly for those not already actively using their available healthcare system. Public health education efforts are needed to target subgroups of the U.S. population identified by this analysis to increase palliative care knowledge. IMPACT: Healthcare providers have a major role to play in improving palliative care knowledge. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 34088752      PMCID: PMC8254767          DOI: 10.1158/1055-9965.EPI-20-1790

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.090


  34 in total

1.  Outpatient Palliative Care in Heart Failure: An Integrative Review.

Authors:  Lyndsay DeGroot; Binu Koirala; Noelle Pavlovic; Katie Nelson; Jerilyn Allen; Patricia Davidson; Martha Abshire
Journal:  J Palliat Med       Date:  2020-06-09       Impact factor: 2.947

2.  Family-centered care: a resource for social work in end-of-life and palliative care.

Authors:  Pamela J Kovacs; Melissa Hayden Bellin; David P Fauri
Journal:  J Soc Work End Life Palliat Care       Date:  2006

3.  NCCN clinical practice guidelines in oncology: palliative care.

Authors:  Michael H Levy; Anthony Back; Costantino Benedetti; J Andrew Billings; Susan Block; Barry Boston; Eduardo Bruera; Sydney Dy; Catherine Eberle; Kathleen M Foley; Sloan Beth Karver; Sara J Knight; Sumathi Misra; Christine S Ritchie; David Spiegel; Linda Sutton; Susan Urba; Jamie H Von Roenn; Sharon M Weinstein
Journal:  J Natl Compr Canc Netw       Date:  2009-04       Impact factor: 11.908

4.  Knowledge of Palliative Care Among American Adults: 2018 Health Information National Trends Survey.

Authors:  Jinhai Huo; Young-Rock Hong; Reetu Grewal; Sandhya Yadav; Isaac W Heller; Jiang Bian; Diana J Wilkie
Journal:  J Pain Symptom Manage       Date:  2019-03-26       Impact factor: 3.612

5.  Perceived knowledge of palliative care among immigrants to the United States: a secondary data analysis from the Health Information National Trends Survey.

Authors:  Amelia Barwise; Andrea Cheville; Mark L Wieland; Ognjen Gajic; Alexandra J Greenberg-Worisek
Journal:  Ann Palliat Med       Date:  2019-03-13

6.  Lack of Awareness and Common Misconceptions About Palliative Care Among Adults: Insights from a National Survey.

Authors:  Signe Peterson Flieger; Kenneth Chui; Susan Koch-Weser
Journal:  J Gen Intern Med       Date:  2020-03-10       Impact factor: 5.128

7.  Physician knowledge, attitude, and experience with advance care planning, palliative care, and hospice: results of a primary care survey.

Authors:  Sara Snyder; Susan Hazelett; Kyle Allen; Steven Radwany
Journal:  Am J Hosp Palliat Care       Date:  2012-07-12       Impact factor: 2.500

8.  Demographic factors and awareness of palliative care and related services.

Authors:  Jonathan Koffman; Geraldine Burke; Angela Dias; Bharti Raval; Judi Byrne; Juan Gonzales; Charles Daniels
Journal:  Palliat Med       Date:  2007-03       Impact factor: 4.762

9.  Effects of a Population Health Community-Based Palliative Care Program on Cost and Utilization.

Authors:  Lori Yosick; Robert E Crook; Maria Gatto; Terri L Maxwell; Ian Duncan; Tamim Ahmed; Andrew Mackenzie
Journal:  J Palliat Med       Date:  2019-04-05       Impact factor: 2.947

10.  Usage Patterns of a Web-Based Palliative Care Content Platform (PalliCOVID) During the COVID-19 Pandemic.

Authors:  Lucinda Lai; Rintaro Sato; Shuhan He; Kei Ouchi; Richard Leiter; Jane deLima Thomas; Andrew Lawton; Adam B Landman; Haipeng Mark Zhang
Journal:  J Pain Symptom Manage       Date:  2020-07-27       Impact factor: 3.612

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