Literature DB >> 19171571

Who will speak for me? Improving end-of-life decision-making for adolescents with HIV and their families.

Maureen E Lyon1, Patricia A Garvie, Robert McCarter, Linda Briggs, Jianping He, Lawrence J D'Angelo.   

Abstract

OBJECTIVES: The purpose of this research was to test the effectiveness of a model of family/adolescent-centered advance care planning for adolescents living with HIV and their families for increasing congruence and quality of communication while decreasing decisional conflict. PATIENTS AND METHODS: Ours was a 2-group, randomized, controlled trial in 2 hospital-based outpatient clinics in Washington and Memphis from 2006 to 2008. Participants (N = 38 dyads) included medically stable adolescents aged 14 to 21 years with HIV/AIDS and surrogates/families aged > or =21 years. Three 60- to 90-minute sessions were conducted 1 week apart via a semistructured family interview with a trained/certified interviewer. Each session encompassed, respectively: (1) Lyon Advance Care Planning Survey; (2) Respecting Choices interview; and (3) Five Wishes. Controls received (1) developmental history, (2) safety tips, and (3) future plans. Family congruence was measured by the Statement of Treatment Preferences and adolescent decisional conflict by the Decisional Conflict Scale, immediately after session 2. Communication was measured by the Quality of Participant-Interviewer Communication Scale after each session.
RESULTS: Adolescent demographics were as follows: mean age was 16 years; 40% were boys; 92% were black; HIV transmission rate was 68% perinatal and 32% sexually acquired; 42% were asymptomatic; 29% were symptomatic; and 29% had a diagnosis of AIDS. Significantly increased congruence for testing the difference of the 2 kappa values for the 2 conditions was observed for intervention versus control dyads. Intervention adolescents reported feeling significantly better informed about end-of-life decisions. Intervention adolescents and all of the surrogates were more likely to feel that their attitudes and wishes were known by the interviewer over time. Intervention families, significantly more so than controls, rated the overall quality of discussion as very good to excellent.
CONCLUSIONS: Family-centered advance care planning by trained facilitators increased congruence in adolescent/surrogate preferences for end-of-life care, decreased decisional conflict, and enhanced communication quality. Families acknowledged a life-threatening condition and were willing to initiate end-of-life conversations when their adolescents were medically stable.

Entities:  

Mesh:

Year:  2009        PMID: 19171571     DOI: 10.1542/peds.2008-2379

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  36 in total

1.  Longitudinal Pediatric Palliative Care: Quality of Life & Spiritual Struggle (FACE): design and methods.

Authors:  Ronald H Dallas; Megan L Wilkins; Jichuan Wang; Ana Garcia; Maureen E Lyon
Journal:  Contemp Clin Trials       Date:  2012-06-01       Impact factor: 2.226

2.  An exploratory survey of end-of-life attitudes, beliefs, and experiences of adolescents with HIV/AIDS and their families.

Authors:  Patricia A Garvie; Jianping He; Jichuan Wang; Lawrence J D'Angelo; Maureen E Lyon
Journal:  J Pain Symptom Manage       Date:  2012-07-07       Impact factor: 3.612

3.  Effect of a disease-specific planning intervention on surrogate understanding of patient goals for future medical treatment.

Authors:  Karin T Kirchhoff; Bernard J Hammes; Karen A Kehl; Linda A Briggs; Roger L Brown
Journal:  J Am Geriatr Soc       Date:  2010-07       Impact factor: 5.562

4.  A Systematic Review and Meta-Analysis of Interventions for Orphans and Vulnerable Children Affected by HIV/AIDS Worldwide.

Authors:  Tina Thomas; Mei Tan; Yusra Ahmed; Elena L Grigorenko
Journal:  Ann Behav Med       Date:  2020-11-01

5.  FAmily CEntered (FACE) advance care planning: Study design and methods for a patient-centered communication and decision-making intervention for patients with HIV/AIDS and their surrogate decision-makers.

Authors:  Allison L Kimmel; Jichuan Wang; Rachel K Scott; Linda Briggs; Maureen E Lyon
Journal:  Contemp Clin Trials       Date:  2015-06-02       Impact factor: 2.226

Review 6.  Pediatric palliative care-when quality of life becomes the main focus of treatment.

Authors:  Eva Bergstraesser
Journal:  Eur J Pediatr       Date:  2012-04-03       Impact factor: 3.183

7.  Spirituality in HIV-infected adolescents and their families: FAmily CEntered (FACE) Advance Care Planning and medication adherence.

Authors:  Maureen E Lyon; Patricia A Garvie; Ellin Kao; Linda Briggs; Jianping He; Robert Malow; Lawrence J D'Angelo; Robert McCarter
Journal:  J Adolesc Health       Date:  2010-12-30       Impact factor: 5.012

Review 8.  Pediatric Palliative Care in Oncology.

Authors:  Jennifer Snaman; Sarah McCarthy; Lori Wiener; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2020-02-05       Impact factor: 44.544

9.  Use and Predictors of End-of-Life Care Among HIV Patients in a Safety Net Health System.

Authors:  Ramona L Rhodes; Fiza Nazir; Sonya Lopez; Lei Xuan; Ank E Nijhawan; Nicole E Alexander-Scott; Ethan A Halm
Journal:  J Pain Symptom Manage       Date:  2015-09-16       Impact factor: 3.612

10.  When silence is not golden: Engaging adolescents and young adults in discussions around end-of-life care choices.

Authors:  Lori Wiener; Sima Zadeh; Leonard H Wexler; Maryland Pao
Journal:  Pediatr Blood Cancer       Date:  2013-03-11       Impact factor: 3.167

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