Quality of investigations into unexpected deaths of infants and young children in England after implementation of national child death review procedures in 2008: a retrospective assessment.
Autopsy
Bereavement
Child Protective Services
/ statistics & numerical data
Child, Preschool
Death, Sudden
/ epidemiology
Delivery of Health Care
/ standards
England
/ epidemiology
Guideline Adherence
Hospice Care
/ standards
House Calls
Humans
Infant
Parents
/ psychology
Practice Guidelines as Topic
Quality of Health Care
Social Support
Sudden Infant Death
/ epidemiology
SIDS
bereavement care
child deaths
unexpected deaths
Journal
Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
15
04
2019
revised:
26
08
2019
accepted:
02
09
2019
pubmed:
29
9
2019
medline:
28
7
2020
entrez:
29
9
2019
Statut:
ppublish
Résumé
In 2008, new statutory national procedures for responding to unexpected child deaths were introduced throughout England. There has, to date, been no national audit of these procedures. Families bereaved by the unexpected death of a child under 4 years of age since 2008 were invited to participate. Factors contributing to the death and investigations after the death were explored. Telephone interviews were conducted, and coroners' documents were obtained. The nature and quality of investigations was compared with the required procedures; information on each case was reviewed by a multiagency panel; and the death was categorised using the Avon clinicopathological classification. Data were obtained from 91 bereaved families (64 infant deaths and 27 children aged 1-3 years); 85 remained unexplained after postmortem examination. Documentation of multiagency assessments was poorly recorded. Most (88%) families received a home visit from the police, but few (37%) received joint visits by police and healthcare professionals. Postmortem examinations closely followed national guidance; 94% involved paediatric pathologists; 61% of families had a final meeting with a paediatrician to explain the investigation outcome. There was no improvement in frequency of home visits by health professionals or final meetings with paediatricians between 2008-2013 and 2014-2017 and no improvement in parental satisfaction with the process. Statutory procedures need to be followed more closely. The implementation of a national child mortality database from 2019 will allow continuing audit of the quality of investigations after unexpected child deaths. An important area amenable to improvement is increased involvement by paediatricians.
Identifiants
pubmed: 31562184
pii: archdischild-2019-317420
doi: 10.1136/archdischild-2019-317420
pmc: PMC7041501
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
270-275Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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