Literature DB >> 19117852

Construction of a parent-derived questionnaire to measure end-of-life care after withdrawal of life-sustaining treatment in the neonatal intensive care unit.

Constance Williams1, Janice Cairnie, Valerie Fines, Colleen Patey, Karla Schwarzer, Jennifer Aylward, Lynne Lohfeld, Haresh Kirpalani.   

Abstract

OBJECTIVES: The objective of this study was to develop and pretest a questionnaire to assess the practice of withdrawal of life-sustaining treatment in the NICU on the basis of the experiences of bereaved parents.
METHODS: We conducted semistructured interviews with 11 parents whose infants had undergone withdrawal of life-sustaining treatment in the NICU at McMaster University Medical Centre to obtain their views on helpful practices. Interviews continued until no new items were obtained (ie, saturation point). A total of 370 items were distilled into 82 questionnaire statements on care by a multidisciplinary team and grouped for analysis into 6 domains: communication, quality of care, quality of life, shared decision-making, withdrawal of life-sustaining treatment process, and bereavement care. Respondents were asked to rank how frequently events occurred on a 7-point Likert scale anchored from 1 = never to 7 = always. A score of >5 was considered favorable. The questionnaire was distributed to a pretest sample of perinatal social workers who attended a bereavement workshop at an international conference.
RESULTS: The response rate was 48%. Respondents ranked items that pertained to the withdrawal of life-sustaining treatment process highest, indicating that items were done well. Items related to quality of care and bereavement care ranked lowest. Other domains ranked as follows: communication, shared decision-making, and quality of life. Consistency of items within domains was tested by Cronbach's alpha and split-half testing and were >0.6 for most domains.
CONCLUSIONS: Parents' views on important aspects of end-of-life care in the NICU were incorporated into a quality assurance questionnaire. Pretesting assessed the performance of the instrument and the perceptions of social workers on the effectiveness of end-of-life practices. Respondents identified that parents' practical needs were met during the withdrawal process but were not consistently met in regard to the quality of in-hospital and follow-up bereavement care.

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Mesh:

Year:  2009        PMID: 19117852     DOI: 10.1542/peds.2007-2950

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


  8 in total

Review 1.  Pediatric palliative care - The role of the patient's family.

Authors:  Carl Friedrich Classen
Journal:  World J Clin Pediatr       Date:  2012-10-08

2.  Constructing a Culturally Informed Spanish Decision-Aid to Counsel Latino Parents Facing Imminent Extreme Premature Delivery.

Authors:  Matthew J Drago; Ursula Guillén; Maria Schiaratura; Jennifer Batza; Annette Zygmunt; Anja Mowes; David Munson; John M Lorenz; Christiana Farkouh-Karoleski; Haresh Kirpalani
Journal:  Matern Child Health J       Date:  2018-07

Review 3.  Perinatal bereavement: a principle-based concept analysis.

Authors:  Kimberly Fenstermacher; Judith E Hupcey
Journal:  J Adv Nurs       Date:  2013-03-04       Impact factor: 3.187

4.  Primary palliative care in the delivery room: patients' and medical personnel's perspectives.

Authors:  L Garten; S Glöckner; J-P Siedentopf; C Bührer
Journal:  J Perinatol       Date:  2015-10-22       Impact factor: 2.521

5.  Initial development and psychometric testing of an instrument to measure the quality of children's end-of-life care.

Authors:  Kimberley Widger; Ann E Tourangeau; Rose Steele; David L Streiner
Journal:  BMC Palliat Care       Date:  2015-01-13       Impact factor: 3.234

6.  What information do parents need when facing end-of-life decisions for their child? A meta-synthesis of parental feedback.

Authors:  Vicki Xafis; Dominic Wilkinson; Jane Sullivan
Journal:  BMC Palliat Care       Date:  2015-04-30       Impact factor: 3.234

7.  Withdrawal of ventilatory support outside the intensive care unit: guidance for practice.

Authors:  Joanna Laddie; Finella Craig; Joe Brierley; Paula Kelly; Myra Bluebond-Langner
Journal:  Arch Dis Child       Date:  2014-06-20       Impact factor: 3.791

8.  Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey.

Authors:  Emily Shelkowitz; Sharon L Vessella; Patricia O'Reilly; Richard Tucker; Beatrice E Lechner
Journal:  BMC Palliat Care       Date:  2015-12-02       Impact factor: 3.234

  8 in total

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