Literature DB >> 28935629

Paediatric advance care planning survey: a cross-sectional examination of congruence and discordance between adolescents with HIV/AIDS and their families.

Maureen E Lyon1, Ronald H Dallas2, Patricia A Garvie3, Megan L Wilkins2, Ana Garcia4, Yao Iris Cheng1, Jichuan Wang1.   

Abstract

OBJECTIVES: To identify patient-reported paediatric advance care planning (pACP) needs of adolescents living with HIV and to examine the congruence with their family's perception of their needs.
METHODS: A cross-sectional survey among six paediatric hospital-based outpatient HIV specialty clinics. Participants included 48 adolescent/family dyads (n=96 participants) within a larger study facilitating pACP. The main outcome measure was the Lyon Advance Care Planning Survey - Adolescent and Surrogate Versions-Revised.
RESULTS: Adolescents' mean age was 18 years (range ≥14-<21); 54% male; 92% African-American; 27% with prior AIDS diagnosis. If dying, 92% believed in completing an advance directive; 85% preferred to die at home;88% knowing how to say good bye; 71% being off machines that extend life and 77% dying a natural death. Best timing for end-of-life (EOL) decisions was while healthy (38%), when first diagnosed (17%), when first sick from a life-threatening illness (4%), when first hospitalised (8%), if dying (4%) and all of the above (19%). Prevalence-adjusted bias-adjusted Kappa (PABAK) measured congruence in pACP needs within adolescent/family dyads. There was substantial congruence in that being free from pain (PABAK=0.83), and understanding your treatment choices (PABAK=0.92) were very important or important. There was discordance about being off machines that extend life (PABAK=0.08) and when is the best time to bring up EOL decisions (PABAK=0.32).
CONCLUSIONS: Areas of discordance were associated with life-sustaining choices and when to have the EOL conversation. Targeted, adolescent/family-centred, evidence-based pACP interventions are needed to improve family understanding of youth's EOL wishes. TRIAL REGISTRATION NUMBER: NCT01289444; Results. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  adolescent; advance care planning; chronic illness; end-of-life; palliative care

Mesh:

Year:  2017        PMID: 28935629      PMCID: PMC5862773          DOI: 10.1136/bmjspcare-2016-001224

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  29 in total

Review 1.  Are quality of life measures patient centred?

Authors:  A J Carr; I J Higginson
Journal:  BMJ       Date:  2001-06-02

Review 2.  Pediatric palliative care.

Authors:  Bruce P Himelstein; Joanne M Hilden; Ann Morstad Boldt; David Weissman
Journal:  N Engl J Med       Date:  2004-04-22       Impact factor: 91.245

3.  What do adolescents want? An exploratory study regarding end-of-life decision-making.

Authors:  Maureen E Lyon; Mary Ann McCabe; Kantilal M Patel; Lawrence J D'Angelo
Journal:  J Adolesc Health       Date:  2004-12       Impact factor: 5.012

4.  Tips for learners of evidence-based medicine: 3. Measures of observer variability (kappa statistic).

Authors:  Thomas McGinn; Peter C Wyer; Thomas B Newman; Sheri Keitz; Rosanne Leipzig; Gordon Guyatt For
Journal:  CMAJ       Date:  2004-11-23       Impact factor: 8.262

5.  End-of-life care preferences of pediatric patients with cancer.

Authors:  Pamela S Hinds; Donna Drew; Linda L Oakes; Maryam Fouladi; Sheri L Spunt; Christopher Church; Wayne L Furman
Journal:  J Clin Oncol       Date:  2005-09-19       Impact factor: 44.544

6.  The effect of discussions about advance directives on patients' satisfaction with primary care.

Authors:  W M Tierney; P R Dexter; G P Gramelspacher; A J Perkins; X H Zhou; F D Wolinsky
Journal:  J Gen Intern Med       Date:  2001-01       Impact factor: 5.128

7.  Understanding of prognosis among parents of children who died of cancer: impact on treatment goals and integration of palliative care.

Authors:  J Wolfe; N Klar; H E Grier; J Duncan; S Salem-Schatz; E J Emanuel; J C Weeks
Journal:  JAMA       Date:  2000-11-15       Impact factor: 56.272

8.  Whose quality of life? A commentary exploring discrepancies between health state evaluations of patients and the general public.

Authors:  Peter A Ubel; George Loewenstein; Christopher Jepson
Journal:  Qual Life Res       Date:  2003-09       Impact factor: 4.147

Review 9.  Key factors affecting dying children and their families.

Authors:  Pamela S Hinds; Lisa Schum; Justin N Baker; Joanne Wolfe
Journal:  J Palliat Med       Date:  2005       Impact factor: 2.947

10.  Outpatients' attitudes regarding advance directives.

Authors:  W Edinger; D R Smucker
Journal:  J Fam Pract       Date:  1992-12       Impact factor: 0.493

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  3 in total

1.  Advance Care Planning and HIV Symptoms in Adolescence.

Authors:  Maureen E Lyon; Patricia A Garvie; Lawrence J D'Angelo; Ronald H Dallas; Linda Briggs; Patricia M Flynn; Ana Garcia; Yao I Cheng; Jichuan Wang
Journal:  Pediatrics       Date:  2018-10-19       Impact factor: 7.124

2.  What Do Adults With HIV Want? End-of-Life Care Goals, Values and Beliefs by Gender, Race, Sexual Orientation.

Authors:  Katherine B Grill; Jichuan Wang; Rachel K Scott; Debra Benator; Lawrence J D'Angelo; Maureen E Lyon
Journal:  Am J Hosp Palliat Care       Date:  2021-01-19       Impact factor: 2.090

3.  Congruence Gaps Between Adolescents With Cancer and Their Families Regarding Values, Goals, and Beliefs About End-of-Life Care.

Authors:  Sarah Friebert; Daniel H Grossoehme; Justin N Baker; Jennifer Needle; Jessica D Thompkins; Yao I Cheng; Jichuan Wang; Maureen E Lyon
Journal:  JAMA Netw Open       Date:  2020-05-01
  3 in total

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