Literature DB >> 25200965

Barriers to care for children with orofacial clefts in North Carolina.

Cynthia H Cassell1, Paula Strassle, Dara D Mendez, Kyung A Lee, Anne Krohmer, Robert E Meyer, Ronald P Strauss.   

Abstract

BACKGROUND: Little is known about the barriers faced by families of children with birth defects in obtaining healthcare. We examined reported perceived barriers to care and satisfaction with care among mothers of children with orofacial clefts.
METHODS: In 2006, a validated barriers to care mail/phone survey was administered in North Carolina to all resident mothers of children with orofacial clefts born between 2001 and 2004. Potential participants were identified using the North Carolina Birth Defects Monitoring Program, an active, state-wide, population-based birth defects registry. Five barriers to care subscales were examined: pragmatics, skills, marginalization, expectations, and knowledge/beliefs. Descriptive and bivariate analyses were conducted using chi-square and Fisher's exact tests. Results were stratified by cleft type and presence of other birth defects.
RESULTS: Of 475 eligible participants, 51.6% (n = 245) responded. The six most commonly reported perceived barriers to care were all part of the pragmatics subscale: having to take time off work (45.3%); long waits in the waiting rooms (37.6%); taking care of household responsibilities (29.7%); meeting other family members' needs (29.5%); waiting too many days for appointments (27.0%); and cost (25.0%). Most respondents (72.3%, 175/242) felt "very satisfied" with their child's cleft care.
CONCLUSION: Although most participants reported being satisfied with their child's care, many perceived barriers to care were identified. Due to the limited understanding and paucity of research on barriers to care for children with birth defects, including orofacial clefts, additional research on barriers to care and factors associated with them are needed.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  access to health care; birth defects; cleft lip; cleft palate; health services accessibility; orofacial clefts

Mesh:

Year:  2014        PMID: 25200965      PMCID: PMC4507417          DOI: 10.1002/bdra.23303

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  27 in total

1.  Medical home access and health care use and expenditures among children with special health care needs.

Authors:  Melissa A Romaire; Janice F Bell; David C Grossman
Journal:  Arch Pediatr Adolesc Med       Date:  2011-12-05

2.  Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006.

Authors:  Samantha E Parker; Cara T Mai; Mark A Canfield; Russel Rickard; Ying Wang; Robert E Meyer; Patrick Anderson; Craig A Mason; Julianne S Collins; Russell S Kirby; Adolfo Correa
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-09-28

3.  Unmet need and problems accessing core health care services for children with autism spectrum disorder.

Authors:  Giuseppina Chiri; Marji Erickson Warfield
Journal:  Matern Child Health J       Date:  2012-07

4.  Maternal perspectives: qualitative responses about perceived barriers to care among children with orofacial clefts in North Carolina.

Authors:  Cynthia H Cassell; Dara D Mendez; Ronald P Strauss
Journal:  Cleft Palate Craniofac J       Date:  2011-07-08

Review 5.  Parents' experiences of caring for a child with a cleft lip and/or palate: a review of the literature.

Authors:  P Nelson; A-M Glenny; S Kirk; A-L Caress
Journal:  Child Care Health Dev       Date:  2011-05-30       Impact factor: 2.508

6.  Unmet dental needs and barriers to care for children with significant special health care needs.

Authors:  Linda P Nelson; Anne Getzin; Dionne Graham; Jing Zhou; Elke M Wagle; Jessie McQuiston; Suzanne McLaughlin; Akshay Govind; Matthew Sadof; Noelle L Huntington
Journal:  Pediatr Dent       Date:  2011 Jan-Feb       Impact factor: 1.874

7.  Delayed or forgone care and dissatisfaction with care for children with special health care needs: the role of perceived cultural competency of health care providers.

Authors:  Cheryl I Kerfeld; Jeanne M Hoffman; Marcia A Ciol; Deborah Kartin
Journal:  Matern Child Health J       Date:  2011-05

8.  Critical issues in craniofacial care: quality of life, costs of care, and implications of prenatal diagnosis.

Authors:  Ronald P Strauss; Cynthia H Cassell
Journal:  Acad Pediatr       Date:  2009 Nov-Dec       Impact factor: 3.107

9.  Household language use and health care access, unmet need, and family impact among CSHCN.

Authors:  Stella M Yu; Gopal K Singh
Journal:  Pediatrics       Date:  2009-12       Impact factor: 7.124

10.  Factors associated with distance and time traveled to cleft and craniofacial care.

Authors:  Cynthia H Cassell; Anne Krohmer; Dara D Mendez; Kyung A Lee; Ronald P Strauss; Robert E Meyer
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2013-09-02
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  3 in total

1.  What we don't know can hurt us: Nonresponse bias assessment in birth defects research.

Authors:  Paula D Strassle; Cynthia H Cassell; Stuart K Shapira; Sarah C Tinker; Robert E Meyer; Scott D Grosse
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2015-07-14

2.  Factors associated with the timeliness of postnatal surgical repair of spina bifida.

Authors:  Elizabeth Radcliff; Cynthia H Cassell; Sarah B Laditka; Judy K Thibadeau; Jane Correia; Scott D Grosse; Russell S Kirby
Journal:  Childs Nerv Syst       Date:  2016-05-14       Impact factor: 1.475

3.  Editorial utility of population-based birth defects surveillance for monitoring the health of infants and as a foundation for etiologic research.

Authors:  Cynthia A Moore; Edward R B McCabe
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2015-10-12
  3 in total

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