Literature DB >> 33273250

Health-Related Quality of Life Declines Over 3 Years for Congenital Heart Disease Survivors.

Jamie L Jackson, Jennifer DeSalvo, Carine E Leslie, Joseph R Rausch.   

Abstract

BACKGROUND: Because of medical advancements, many congenital heart disease (CHD) survivors are relatively symptom-free until adulthood, at which time complications may occur. Worsening health status likely drives a change in patient-reported outcomes, such as health-related quality of life (HRQoL), although change in HRQoL has not been investigated among adolescent and young adult CHD survivors.
OBJECTIVE: The aims of the current mixed cross-sectional and longitudinal study were to (1) examine changes in HRQoL over 3 years and (2) identify any demographic (age, sex, estimated family income, and distance from medical center) and medical predictors (functional status and number of cardiac-related medications) of that change.
METHODS: Baseline and 3-year follow-up data were obtained via an online survey of 172 CHD survivors (15-39 years old at baseline; 25% simple, 45% moderate, 30% complex) recruited from a pediatric hospital and an adult hospital. Medical predictors were abstracted from electronic medical records.
RESULTS: After controlling for New York Heart Association functional class, mixed-effects models identified significant declines in all subscales of the Research and Development Corporation 36-Item Health Survey 1.0 across the 3-year timeframe. A lower estimated family income (≤$35 000) predicted more decline in physical functioning (b = 0.5, 95% confidence interval, 0.2-0.8; P = .001) and emotional functioning (b = 0.3, 95% confidence interval, 0.1-0.5; P = .017). No other significant demographic or medical predictors were identified.
CONCLUSIONS: Study findings highlight the importance of tracking patient-reported outcomes over time, suggesting that medical staff should discuss HRQoL with CHD survivors during late adolescence and early adulthood before decline.
Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

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Mesh:

Year:  2021        PMID: 33273250      PMCID: PMC7878288          DOI: 10.1097/JCN.0000000000000764

Source DB:  PubMed          Journal:  J Cardiovasc Nurs        ISSN: 0889-4655            Impact factor:   2.083


  31 in total

1.  Missing data: our view of the state of the art.

Authors:  Joseph L Schafer; John W Graham
Journal:  Psychol Methods       Date:  2002-06

2.  Medical factors that predict quality of life for young adults with congenital heart disease: What matters most?

Authors:  Jamie L Jackson; Lauren Hassen; Gina M Gerardo; Kathryn Vannatta; Curt J Daniels
Journal:  Int J Cardiol       Date:  2015-09-30       Impact factor: 4.164

3.  Quality of life in adults with congenital heart disease: biopsychosocial determinants and sex-related differences.

Authors:  Chun-An Chen; Shih-Cheng Liao; Jou-Kou Wang; Chung-I Chang; Ing-Sh Chiu; Yih-Sharng Chen; Chun-Wei Lu; Ming-Tai Lin; Hsin-Hui Chiu; Shuenn-Nan Chiu; Yu-Chuan Hua; Hung-Chi Lue; Mei-Hwan Wu
Journal:  Heart       Date:  2010-10-26       Impact factor: 5.994

4.  Cardiovascular health: the importance of measuring patient-reported health status: a scientific statement from the American Heart Association.

Authors:  John S Rumsfeld; Karen P Alexander; David C Goff; Michelle M Graham; P Michael Ho; Frederick A Masoudi; Debra K Moser; Véronique L Roger; Mark S Slaughter; Kim G Smolderen; John A Spertus; Mark D Sullivan; Diane Treat-Jacobson; Julie J Zerwic
Journal:  Circulation       Date:  2013-05-06       Impact factor: 29.690

5.  Health-related Quality of Life in children and adolescents after invasive treatment for congenital heart disease.

Authors:  A W Spijkerboer; E M W J Utens; W B De Koning; A J J C Bogers; W A Helbing; F C Verhulst
Journal:  Qual Life Res       Date:  2006-05       Impact factor: 4.147

6.  Readmissions after adult congenital heart surgery: Frequency and risk factors.

Authors:  Yuli Y Kim; Wei He; Thomas E MacGillivray; Oscar J Benavidez
Journal:  Congenit Heart Dis       Date:  2016-12-19       Impact factor: 2.007

Review 7.  Quality of life of adult congenital heart disease patients: a systematic review of the literature.

Authors:  Theodora Fteropoulli; Jan Stygall; Shay Cullen; John Deanfield; Stanton P Newman
Journal:  Cardiol Young       Date:  2013-02-06       Impact factor: 1.093

8.  Perceptions of Disease-Related Stress: A Key to Better Understanding Patient-Reported Outcomes Among Survivors of Congenital Heart Disease.

Authors:  Jamie L Jackson; Gina M Gerardo; Curt J Daniels; Kathryn Vannatta
Journal:  J Cardiovasc Nurs       Date:  2017 Nov/Dec       Impact factor: 2.083

9.  Patient-reported outcomes in adults with congenital heart disease: Inter-country variation, standard of living and healthcare system factors.

Authors:  Philip Moons; Adrienne H Kovacs; Koen Luyckx; Corina Thomet; Werner Budts; Junko Enomoto; Maayke A Sluman; Hsiao-Ling Yang; Jamie L Jackson; Paul Khairy; Stephen C Cook; Raghavan Subramanyan; Luis Alday; Katrine Eriksen; Mikael Dellborg; Malin Berghammer; Bengt Johansson; Andrew S Mackie; Samuel Menahem; Maryanne Caruana; Gruschen Veldtman; Alexandra Soufi; Susan M Fernandes; Kamila White; Edward Callus; Shelby Kutty; Liesbet Van Bulck; Silke Apers
Journal:  Int J Cardiol       Date:  2017-10-21       Impact factor: 4.164

10.  Reduced health-related quality of life in older patients with congenital heart disease: a cross sectional study in 2360 patients.

Authors:  Jan Müller; Anne Berner; Peter Ewert; Alfred Hager
Journal:  Int J Cardiol       Date:  2014-06-18       Impact factor: 4.164

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