Literature DB >> 23479062

Family-centered advance care planning for teens with cancer.

Maureen E Lyon1, Shana Jacobs, Linda Briggs, Yao Iris Cheng, Jichuan Wang.   

Abstract

IMPORTANCE: Advance care planning (ACP) prepares patients and their families for future health care decisions; however, the needs of adolescent oncology patients for participation in ACP have not been well studied.
OBJECTIVE: To examine the efficacy of family-centered ACP. DESIGN AND
SETTING: Two-group randomized controlled trial in a pediatric oncology program. PARTICIPANTS: Sixty adolescents aged 14 to 21 years with cancer and their surrogates or families were enrolled in the study between January 17, 2011, and March 29, 2012. INTERVENTION: Thirty dyads received 3- to 60-minute sessions 1 week apart. Intervention dyads completed (1) the Lyon Family-Centered ACP Survey, (2) the Respecting Choices interview, and (3) Five Wishes. Control subjects received standard care plus information. MAIN OUTCOME MEASURES: Statement of treatment preferences and Decisional Conflict Scale score.
RESULTS: The mean age of the adolescents was 16 years; 36 (60%) were male, 30 (50%) white, 26 (43%) black, and 4 (7%) Asian. Diagnoses were as follows: leukemia (14 patients [47%]), brain tumor (8 [27%]), solid tumor (6 [20%]), and lymphoma (2 [7%]). Significantly increased congruence was observed for intervention dyads compared with controls for 4 of the 6 disease-specific scenarios; for example, for situation 2 ("treatment would extend my life by not more than 2 to 3 months"), intervention dyads demonstrated higher congruence (κ = 0.660; P < .001) vs control dyads (κ = -0.0636; P = .70). Intervention adolescents (100%) wanted their families to do what is best at the time, whereas fewer control adolescents (62%) gave families this leeway. Intervention adolescents were significantly better informed about end-of-life decisions (t = 2.93; effect size, 0.961; 95% CI, 0.742-1.180; P = .007). Intervention families were more likely to concur on limiting treatments than controls. An ethnic difference was found in only one situation.
CONCLUSIONS: Advance care planning enabled families to understand and honor their adolescents' wishes. Intervention dyads were more likely than controls to limit treatments. Underserved African American families were willing to participate.

Entities:  

Mesh:

Year:  2013        PMID: 23479062     DOI: 10.1001/jamapediatrics.2013.943

Source DB:  PubMed          Journal:  JAMA Pediatr        ISSN: 2168-6203            Impact factor:   16.193


  56 in total

Review 1.  Palliative Care as a Standard of Care in Pediatric Oncology.

Authors:  Meaghann S Weaver; Katherine E Heinze; Katherine P Kelly; Lori Wiener; Robert L Casey; Cynthia J Bell; Joanne Wolfe; Amy M Garee; Anne Watson; Pamela S Hinds
Journal:  Pediatr Blood Cancer       Date:  2015-12       Impact factor: 3.167

Review 2.  Psychological interventions for parents of children and adolescents with chronic illness.

Authors:  Christopher Eccleston; Emma Fisher; Emily Law; Jess Bartlett; Tonya M Palermo
Journal:  Cochrane Database Syst Rev       Date:  2015-04-15

3.  Taboo Topics in Adolescent and Young Adult Oncology: Strategies for Managing Challenging but Important Conversations Central to Adolescent and Young Adult Cancer Survivorship.

Authors:  Giselle K Perez; John M Salsman; Kaitlyn Fladeboe; Anne C Kirchhoff; Elyse R Park; Abby R Rosenberg
Journal:  Am Soc Clin Oncol Educ Book       Date:  2020-03

4.  Systematic Approach to Selecting and Preparing a Medical Power of Attorney in the Gynecologic Oncology Center.

Authors:  Donna S Zhukovsky; Pamela T Soliman; Boby Mathew; Sarah Mills; Diane Bodurka; Michael Frumovitz; Larissa A Meyer; Shannon Westin; Marisa Nowitz; LaShan Archie; Shauna Fenton; Kai Lang; Janet L Williams; Valentine Boving; Eduardo Bruera
Journal:  J Oncol Pract       Date:  2019-10-15       Impact factor: 3.840

Review 5.  Establishing psychosocial palliative care standards for children and adolescents with cancer and their families: An integrative review.

Authors:  Meaghann S Weaver; Katherine E Heinze; Cynthia J Bell; Lori Wiener; Amy M Garee; Katherine P Kelly; Robert L Casey; Anne Watson; Pamela S Hinds
Journal:  Palliat Med       Date:  2015-04-28       Impact factor: 4.762

Review 6.  Identifying and addressing the needs of adolescents and young adults with cancer: summary of an Institute of Medicine workshop.

Authors:  Sharyl J Nass; Lynda K Beaupin; Wendy Demark-Wahnefried; Karen Fasciano; Patricia A Ganz; Brandon Hayes-Lattin; Melissa M Hudson; Brenda Nevidjon; Kevin C Oeffinger; Ruth Rechis; Lisa C Richardson; Nita L Seibel; Ashley W Smith
Journal:  Oncologist       Date:  2015-01-07

7.  Implementation and Impact of Patient Lay Navigator-Led Advance Care Planning Conversations.

Authors:  Gabrielle B Rocque; J Nicholas Dionne-Odom; Chao-Hui Sylvia Huang; Soumya J Niranjan; Courtney P Williams; Bradford E Jackson; Karina I Halilova; Kelly M Kenzik; Kerri S Bevis; Audrey S Wallace; Nedra Lisovicz; Richard A Taylor; Maria Pisu; Edward E Partridge; Thomas W Butler; Linda A Briggs; Elizabeth A Kvale
Journal:  J Pain Symptom Manage       Date:  2017-01-03       Impact factor: 3.612

Review 8.  Understanding death with limited experience in life: dying children's and adolescents' understanding of their own terminal illness and death.

Authors:  Alan T Bates; Julia A Kearney
Journal:  Curr Opin Support Palliat Care       Date:  2015-03       Impact factor: 2.302

Review 9.  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

10.  High Intensity of End-of-Life Care Among Adolescent and Young Adult Cancer Patients in the New York State Medicaid Program.

Authors:  Jennifer W Mack; Kun Chen; Francis P Boscoe; Foster C Gesten; Patrick J Roohan; Maria J Schymura; Deborah Schrag
Journal:  Med Care       Date:  2015-12       Impact factor: 2.983

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.