Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate

ABSTRACT Objective: To evaluate the emotional and social experiences of parents or caregivers of children with cleft lip and/or palate (CL/P) in a city in the Northeastern of Brazil. Material and Methods: A quantitative and cross-sectional study was conducted among parents or caregivers of children with CL/P by interviews based on a questionnaire. Interviews were conducted during the First Smile Project in Sobral, Ceará, Brazil. All participants (n=41) agreed to participate in the interview and signed an informed consent. The data was analyzed in SPSS software version 22.0. Results: The majority of participants were female (87.2%), with a mean age of 37 years, with a low level of education and low family income. The great majority (90.2%) of the parents were not prenatally diagnosed to have CL/P babies. Of those interviewed, 56.1% mentioned that the first diagnosis of cleft lip and palate was not presented by the professionals in a clarifying way to the family. Fear (36.6%) and sadness (19.5%) were the main feelings experienced when the child was diagnosed with fissure. Feeding (48.8%) was pointed out as the main concern in caring for a child with CL/P. Conclusion: The parents and caregivers interviewed faced important emotional and social problems that must be addressed by the professional team that assists the child with CL/P.

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Main Authors: Carvalho,Naiara Oliveira, Matos,Maria Franciele Soares, Belchior,Iara Freire Costa, Araújo,Marcos Bruno, Rocha,Cristiane Tomaz, Neves,Beatriz Gonçalves
Format: Digital revista
Language:English
Published: Associação de Apoio à Pesquisa em Saúde Bucal 2021
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1983-46322021000100358
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spelling oai:scielo:S1983-463220210001003582021-04-27Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or PalateCarvalho,Naiara OliveiraMatos,Maria Franciele SoaresBelchior,Iara Freire CostaAraújo,Marcos BrunoRocha,Cristiane TomazNeves,Beatriz Gonçalves Clef Palate Cleft Lip Emotions Parents Caregivers ABSTRACT Objective: To evaluate the emotional and social experiences of parents or caregivers of children with cleft lip and/or palate (CL/P) in a city in the Northeastern of Brazil. Material and Methods: A quantitative and cross-sectional study was conducted among parents or caregivers of children with CL/P by interviews based on a questionnaire. Interviews were conducted during the First Smile Project in Sobral, Ceará, Brazil. All participants (n=41) agreed to participate in the interview and signed an informed consent. The data was analyzed in SPSS software version 22.0. Results: The majority of participants were female (87.2%), with a mean age of 37 years, with a low level of education and low family income. The great majority (90.2%) of the parents were not prenatally diagnosed to have CL/P babies. Of those interviewed, 56.1% mentioned that the first diagnosis of cleft lip and palate was not presented by the professionals in a clarifying way to the family. Fear (36.6%) and sadness (19.5%) were the main feelings experienced when the child was diagnosed with fissure. Feeding (48.8%) was pointed out as the main concern in caring for a child with CL/P. Conclusion: The parents and caregivers interviewed faced important emotional and social problems that must be addressed by the professional team that assists the child with CL/P.info:eu-repo/semantics/openAccessAssociação de Apoio à Pesquisa em Saúde BucalPesquisa Brasileira em Odontopediatria e Clínica Integrada v.21 20212021-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1983-46322021000100358en10.1590/pboci.2021.058
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libraryname SciELO
language English
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author Carvalho,Naiara Oliveira
Matos,Maria Franciele Soares
Belchior,Iara Freire Costa
Araújo,Marcos Bruno
Rocha,Cristiane Tomaz
Neves,Beatriz Gonçalves
spellingShingle Carvalho,Naiara Oliveira
Matos,Maria Franciele Soares
Belchior,Iara Freire Costa
Araújo,Marcos Bruno
Rocha,Cristiane Tomaz
Neves,Beatriz Gonçalves
Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
author_facet Carvalho,Naiara Oliveira
Matos,Maria Franciele Soares
Belchior,Iara Freire Costa
Araújo,Marcos Bruno
Rocha,Cristiane Tomaz
Neves,Beatriz Gonçalves
author_sort Carvalho,Naiara Oliveira
title Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
title_short Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
title_full Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
title_fullStr Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
title_full_unstemmed Parents' Emotional and Social Experiences of Caring a Child with Cleft Lip and/or Palate
title_sort parents' emotional and social experiences of caring a child with cleft lip and/or palate
description ABSTRACT Objective: To evaluate the emotional and social experiences of parents or caregivers of children with cleft lip and/or palate (CL/P) in a city in the Northeastern of Brazil. Material and Methods: A quantitative and cross-sectional study was conducted among parents or caregivers of children with CL/P by interviews based on a questionnaire. Interviews were conducted during the First Smile Project in Sobral, Ceará, Brazil. All participants (n=41) agreed to participate in the interview and signed an informed consent. The data was analyzed in SPSS software version 22.0. Results: The majority of participants were female (87.2%), with a mean age of 37 years, with a low level of education and low family income. The great majority (90.2%) of the parents were not prenatally diagnosed to have CL/P babies. Of those interviewed, 56.1% mentioned that the first diagnosis of cleft lip and palate was not presented by the professionals in a clarifying way to the family. Fear (36.6%) and sadness (19.5%) were the main feelings experienced when the child was diagnosed with fissure. Feeding (48.8%) was pointed out as the main concern in caring for a child with CL/P. Conclusion: The parents and caregivers interviewed faced important emotional and social problems that must be addressed by the professional team that assists the child with CL/P.
publisher Associação de Apoio à Pesquisa em Saúde Bucal
publishDate 2021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1983-46322021000100358
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