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Parenting a child with congenital cytomegalovirus infection: A qualitative study

Parenting a child with congenital cytomegalovirus infection: A qualitative study
Parenting a child with congenital cytomegalovirus infection: A qualitative study
Background Congenital cytomegalovirus (CMV) is the most common infectious cause of congenital disability, which can cause lifelong impairments including sensorineural hearing loss and developmental delay. This study aimed to explore the experiences of parenting a child with congenital CMV and the impact this has on families.

Methods Ten parents living with a child with congenital CMV in the UK participated in semistructured interviews and data were analysed using thematic analysis.

Results The findings illustrate that delays in making the diagnosis of congenital CMV are associated with parental distress and lack of knowledge about CMV among medical professionals can exacerbate this distress. Parents expressed frustration about not knowing about CMV infection during their pregnancies and therefore not having the opportunity to take measures to reduce their risk of acquiring CMV while pregnant. The uncertainty about the long-term outcomes of children with congenital CMV adds additional emotional burden for parents. Family and wider societal networks have the potential to facilitate coping and alleviate stress, but the lack of awareness of CMV acts as a barrier to receiving support from family and friends.

Conclusions There is a need to increase awareness of CMV among medical professionals, pregnant women and wider society to improve the diagnostic process and to provide better support for families caring for children with congenital CMV infection.
Vandrevala, Tushna
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Barber, Victoria
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Mbire-Chigumba, Evas
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Calvert, Anna
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Star, Caroline
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Khalil, Asma
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Griffiths, Paul
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Book, Alexander S.
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Book, Gayle M.
f929c0b2-bf34-43b7-bb38-543a109e8aa8
Heath, Paul
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Jones, Christine E
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Vandrevala, Tushna
45ccaf5a-cb30-40df-ba91-1ef166672468
Barber, Victoria
f8c6d6ff-ab0a-4e3d-9997-8b310bfb40f6
Mbire-Chigumba, Evas
68d3ad8f-b5d0-4a75-b534-7e012712a03a
Calvert, Anna
2a51489e-8ea4-4b6c-a439-ef1df57999bb
Star, Caroline
6c77cbfa-699d-47a1-a8d5-d0bbef7e86a6
Khalil, Asma
4a8ca35d-4afc-49ed-a295-1e8f1b8441bb
Griffiths, Paul
bf1dfc3d-551e-4ea0-b763-6f7010e96b7f
Book, Alexander S.
0f9feee8-ce83-401e-ab69-701a1120b1d8
Book, Gayle M.
f929c0b2-bf34-43b7-bb38-543a109e8aa8
Heath, Paul
b4513946-a286-46e5-9c5f-8d2071f367a3
Jones, Christine E
48229079-8b58-4dcb-8374-d9481fe7b426

Vandrevala, Tushna, Barber, Victoria, Mbire-Chigumba, Evas, Calvert, Anna, Star, Caroline, Khalil, Asma, Griffiths, Paul, Book, Alexander S., Book, Gayle M., Heath, Paul and Jones, Christine E (2020) Parenting a child with congenital cytomegalovirus infection: A qualitative study. BMJ Paediatrics Open, 4 (1), [e000844]. (doi:10.1136/bmjpo-2020-000844).

Record type: Article

Abstract

Background Congenital cytomegalovirus (CMV) is the most common infectious cause of congenital disability, which can cause lifelong impairments including sensorineural hearing loss and developmental delay. This study aimed to explore the experiences of parenting a child with congenital CMV and the impact this has on families.

Methods Ten parents living with a child with congenital CMV in the UK participated in semistructured interviews and data were analysed using thematic analysis.

Results The findings illustrate that delays in making the diagnosis of congenital CMV are associated with parental distress and lack of knowledge about CMV among medical professionals can exacerbate this distress. Parents expressed frustration about not knowing about CMV infection during their pregnancies and therefore not having the opportunity to take measures to reduce their risk of acquiring CMV while pregnant. The uncertainty about the long-term outcomes of children with congenital CMV adds additional emotional burden for parents. Family and wider societal networks have the potential to facilitate coping and alleviate stress, but the lack of awareness of CMV acts as a barrier to receiving support from family and friends.

Conclusions There is a need to increase awareness of CMV among medical professionals, pregnant women and wider society to improve the diagnostic process and to provide better support for families caring for children with congenital CMV infection.

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More information

Accepted/In Press date: 19 October 2020
e-pub ahead of print date: 12 November 2020

Identifiers

Local EPrints ID: 446953
URI: http://eprints.soton.ac.uk/id/eprint/446953
PURE UUID: a7fdb6df-86ad-4d61-8140-fe22d07e5df0
ORCID for Evas Mbire-Chigumba: ORCID iD orcid.org/0009-0003-6281-128X
ORCID for Christine E Jones: ORCID iD orcid.org/0000-0003-1523-2368

Catalogue record

Date deposited: 26 Feb 2021 17:35
Last modified: 17 Mar 2024 03:45

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Contributors

Author: Tushna Vandrevala
Author: Victoria Barber
Author: Evas Mbire-Chigumba ORCID iD
Author: Anna Calvert
Author: Caroline Star
Author: Asma Khalil
Author: Paul Griffiths
Author: Alexander S. Book
Author: Gayle M. Book
Author: Paul Heath

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