Developing Unique Insights From Narrative Responses to Bereaved Family Surveys.


Journal

Journal of pain and symptom management
ISSN: 1873-6513
Titre abrégé: J Pain Symptom Manage
Pays: United States
ID NLM: 8605836

Informations de publication

Date de publication:
10 2020
Historique:
received: 31 12 2019
revised: 14 04 2020
accepted: 02 05 2020
pubmed: 20 5 2020
medline: 24 6 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Although bereaved family surveys (BFS) are routinely used quantitatively for quality assessment, open-ended and narrative responses are rarely systematically analyzed. Analysis of narrative responses may identify opportunities for improving end-of-life (EOL) care delivery. To highlight the value of routine and systematic analysis of narrative responses and to thematically summarize narrative responses to the BFS of Veterans Affairs. We analyzed more than 4600 open-ended responses to the BFS for all 2017 inpatient decedents across Veterans Affairs facilities. We used a descriptive qualitative approach to identify major themes. Thematic findings clustered into three domains: patient needs, family needs, and facility and organizational characteristics. Patient needs include maintenance of veteran's hygiene, appropriately prescribing medications, adhering to patient wishes, physical presence in patient's final hours, and spiritual and religious care at EOL. Family and caregiver needs included enhanced communication with the patient's care team, assistance with administrative and logistical challenges after death, emotional support, and displays of respect and gratitude for the patient's life. Facility and organizational characteristics included care team coordination, optimal staffing, the importance of nonclinical staff to care, and optimizing facilities to be welcoming, equipped for individuals with disabilities, and able to provide high-quality food. Systematic analysis of narrative survey data yields unique findings not routinely available through quantitative data collection and analysis. Organizations may benefit from the collection and regular analysis of narrative survey responses, which facilitate identification of needed improvements in palliative and EOL care that may improve the overall experiences for patients and families.

Identifiants

pubmed: 32428664
pii: S0885-3924(20)30383-3
doi: 10.1016/j.jpainsymman.2020.05.007
pii:
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

699-708

Informations de copyright

Published by Elsevier Inc.

Auteurs

Caroline Gray (C)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA. Electronic address: caroline.gray@va.gov.

Maria Yefimova (M)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA; Office of Research, Patient Care Services, Stanford Healthcare, Stanford, California, USA.

Matthew McCaa (M)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA.

Joy R Goebel (JR)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA; School of Nursing California State University Long Beach, Long Beach, California, USA.

Scott Shreve (S)

Hospice and Palliative Care Program, US Department of Veteran Affairs, Hospice and Palliative Care Unit, Lebanon VA Medical Center, Lebanon, Pennsylvania, USA.

Karl A Lorenz (KA)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA; Division of Primary Care and Population Health, Stanford University School of Medicine, Stanford, California, USA.

Karleen Giannitrapani (K)

Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, California, USA; Division of Primary Care and Population Health, Stanford University School of Medicine, Stanford, California, USA.

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Classifications MeSH