Literature DB >> 19284266

Race does not influence do-not-resuscitate status or the number or timing of end-of-life care discussions at a pediatric oncology referral center.

Justin N Baker1, Shesh Rai, Wei Liu, Kumar Srivastava, Javier R Kane, Christine A Zawistowski, Elizabeth A Burghen, Jami S Gattuso, Nancy West, Jennifer Althoff, Adam Funk, Pamela S Hinds.   

Abstract

BACKGROUND: End-of-life care (EOLC) discussions and decisions are common in pediatric oncology. Interracial differences have been identified in adult EOLC preferences, but the relation of race to EOLC in pediatric oncology has not been reported. We assessed whether race (white, black) was associated with the frequency of do-not-resuscitate (DNR) orders, the number and timing of EOLC discussions, or the timing of EOLC decisions among patients treated at our institution who died.
METHODS: We reviewed the records of 380 patients who died between July 1, 2001 and February 28, 2005. Chi(2) and Wilcoxon rank-sum tests were used to test the association of race with the number and timing of EOLC discussions, the number of DNR changes, the timing of EOLC decisions (i.e., DNR order, hospice referral), and the presence of a DNR order at the time of death. These analyses were limited to the 345 patients who self-identified as black or white.
RESULTS: We found no association between race and DNR status at the time of death (p = 0.57), the proportion of patients with DNR order changes (p = 0.82), the median time from DNR order to death (p = 0.51), the time from first EOLC discussion to DNR order (p = 0.12), the time from first EOLC discussion to death (p = 0.33), the proportion of patients who enrolled in hospice (p = 0.64), the time from hospice enrollment to death (p = 0.2) or the number of EOLC discussions before a DNR decision (p = 0.48).
CONCLUSION: When equal access to specialized pediatric cancer care is provided, race is not a significant factor in the presence or timing of a DNR order, enrollment in or timing of enrollment in hospice, or the number or timing of EOLC discussions before death.

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Mesh:

Year:  2009        PMID: 19284266      PMCID: PMC2941671          DOI: 10.1089/jpm.2008.0172

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  21 in total

1.  Comparison of hospice use and demographics among European Americans, African Americans, and Latinos.

Authors:  Merydawilda Colón; Jennifer Lyke
Journal:  Am J Hosp Palliat Care       Date:  2003 May-Jun       Impact factor: 2.500

2.  Equal participation of minority patients in U.S. national pediatric cancer clinical trials.

Authors:  W A Bleyer; H A Tejeda; S B Murphy; O W Brawley; M A Smith; R S Ungerleider
Journal:  J Pediatr Hematol Oncol       Date:  1997 Sep-Oct       Impact factor: 1.289

3.  Decision making by parents and healthcare professionals when considering continued care for pediatric patients with cancer.

Authors:  P S Hinds; L Oakes; W Furman; P Foppiano; M S Olson; A Quargnenti; J Gattuso; B Powell; D K Srivastava; D Jayawardene; J T Sandlund; C Strong
Journal:  Oncol Nurs Forum       Date:  1997-10       Impact factor: 2.172

Review 4.  Current research findings on end-of-life decision making among racially or ethnically diverse groups.

Authors:  Jung Kwak; William E Haley
Journal:  Gerontologist       Date:  2005-10

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.  Patients' race, ethnicity, language, and trust in a physician.

Authors:  Irena Stepanikova; Stefanie Mollborn; Karen S Cook; David H Thom; Roderick M Kramer
Journal:  J Health Soc Behav       Date:  2006-12

7.  Cancer-related deaths in children and adolescents.

Authors:  Glenna Bradshaw; Pamela S Hinds; Shelly Lensing; Jami S Gattuso; Bassem I Razzouk
Journal:  J Palliat Med       Date:  2005-02       Impact factor: 2.947

8.  Satisfaction with care and ease of using health care services among parents of children with special health care needs: the roles of race/ethnicity, insurance, language, and adequacy of family-centered care.

Authors:  Emmanuel M Ngui; Glenn Flores
Journal:  Pediatrics       Date:  2006-04       Impact factor: 7.124

9.  Quality indicators for end-of-life care in the intensive care unit.

Authors:  Ellen B Clarke; J Randall Curtis; John M Luce; Mitchell Levy; Marion Danis; Judith Nelson; Mildred Z Solomon
Journal:  Crit Care Med       Date:  2003-09       Impact factor: 7.598

10.  Groups potentially at risk for making poorly informed decisions about entry into clinical trials for childhood cancer.

Authors:  Christian Simon; Stephen J Zyzanski; Michelle Eder; Pauline Raiz; Eric D Kodish; Laura A Siminoff
Journal:  J Clin Oncol       Date:  2003-06-01       Impact factor: 44.544

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  16 in total

1.  Changes in medical care at a pediatric oncology referral center after placement of a do-not-resuscitate order.

Authors:  Justin N Baker; Javier R Kane; Shesh Rai; Scott C Howard; Pamela S Hinds
Journal:  J Palliat Med       Date:  2010-10-30       Impact factor: 2.947

2.  Trends in End-of-Life Care in Pediatric Hematology, Oncology, and Stem Cell Transplant Patients.

Authors:  Katharine E Brock; Angela Steineck; Clare J Twist
Journal:  Pediatr Blood Cancer       Date:  2015-10-29       Impact factor: 3.167

3.  Parent-clinician communication intervention during end-of-life decision making for children with incurable cancer.

Authors:  Pamela S Hinds; Linda L Oakes; Judy Hicks; Brent Powell; Deo Kumar Srivastava; Justin N Baker; Sheri L Spunt; Nancy K West; Wayne L Furman
Journal:  J Palliat Med       Date:  2012-06-26       Impact factor: 2.947

4.  Predictors of Late Palliative Care Referral in Children With Cancer.

Authors:  Erica C Kaye; Jonathan Jerkins; Courtney A Gushue; Samantha DeMarsh; April Sykes; Zhaohua Lu; Jennifer M Snaman; Lindsay Blazin; Liza-Marie Johnson; Deena R Levine; R Ray Morrison; Justin N Baker
Journal:  J Pain Symptom Manage       Date:  2018-02-08       Impact factor: 3.612

5.  Patterns of End-of-Life Care in Children With Advanced Solid Tumor Malignancies Enrolled on a Palliative Care Service.

Authors:  Tamara Z Vern-Gross; Catherine G Lam; Zachary Graff; Sara Singhal; Deena R Levine; Deborah Gibson; April Sykes; Doralina L Anghelescu; Ying Yuan; Justin N Baker
Journal:  J Pain Symptom Manage       Date:  2015-04-16       Impact factor: 3.612

6.  Racial and Ethnic Differences in Parental Decision-Making Roles in Pediatric Oncology.

Authors:  Bryan A Sisk; Tammy I Kang; Jennifer W Mack
Journal:  J Palliat Med       Date:  2019-08-13       Impact factor: 2.947

7.  Does phase 1 trial enrollment preclude quality end-of-life care? Phase 1 trial enrollment and end-of-life care characteristics in children with cancer.

Authors:  Deena R Levine; Liza-Marie Johnson; Belinda N Mandrell; Jie Yang; Nancy K West; Pamela S Hinds; Justin N Baker
Journal:  Cancer       Date:  2014-12-29       Impact factor: 6.860

8.  Illness and end-of-life experiences of children with cancer who receive palliative care.

Authors:  Erica C Kaye; Courtney A Gushue; Samantha DeMarsh; Jonathan Jerkins; April Sykes; Zhaohua Lu; Jennifer M Snaman; Lindsay Blazin; Liza-Marie Johnson; Deena R Levine; R Ray Morrison; Justin N Baker
Journal:  Pediatr Blood Cancer       Date:  2017-12-08       Impact factor: 3.167

9.  Predictors of Location of Death for Children with Cancer Enrolled on a Palliative Care Service.

Authors:  Erica C Kaye; Samantha DeMarsh; Courtney A Gushue; Jonathan Jerkins; April Sykes; Zhaohua Lu; Jennifer M Snaman; Lindsay J Blazin; Liza-Marie Johnson; Deena R Levine; R Ray Morrison; Justin N Baker
Journal:  Oncologist       Date:  2018-05-04

10.  Approaching the third decade of paediatric palliative oncology investigation: historical progress and future directions.

Authors:  Abby R Rosenberg; Joanne Wolfe
Journal:  Lancet Child Adolesc Health       Date:  2017-07-24
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