View All Issues
Awareness of Parents on the Nature of Cleft Lip and Palate (CLP) | Journal of All India Institute of Speech and Hearing

ISSN


ISSN

Vol 30 No 1 (2011)
Speech

Awareness of Parents on the Nature of Cleft Lip and Palate (CLP): an Exploratory Study

How to Cite
Indu Thammaiah, Jasmine Lydia, & M, P. (1). Awareness of Parents on the Nature of Cleft Lip and Palate (CLP). Journal of All India Institute of Speech and Hearing, 30(1), 15-22. Retrieved from http://203.129.241.91/jaiish/index.php/aiish/article/view/945

Abstract

Cleft lip and palate (CLP) is a congenital anomaly which requires a multidimensional medical care by multidisciplinary team of professionals. Extensive information and appropriate knowledge is required for the parents of Child with CLP. This study is an endeavor to assess the parental awareness of the condition of cleft lip and palate. The present study is aimed to assess the parental awareness on nature of CLP on various aspects such as cause, associated problems, assessment and treatment of CLP. 30 parents of children with CLP who visited the unit of structural orofacial anomalies (USOFA), All India
Institute of Speech and Hearing (AIISH), Mysore served as participants of the study. A Questionnaire was developed with five subdivisions on seven domains which consisted of five myths and five facts.
The participants were asked to mark YES or NO for correct or incorrect statements respectively. On exploring the responses, the results revealed that the parents having a child with CLP believe more in
the myths about the causes rather than facts and the awareness on treatment schedule and the role of team members are limited. The results also indicate better awareness on the associated problems and
also showed a greater need to sensitize the parents on assessment and treatment of CLP. The results obtained could be attributed to the facts that the medical guidance provided for the parents having
child with CLP was limited or in spite of having the child with CLP, the efforts taken to understand the condition is not adequate. The results of the present study warrant developing more systematic
programs towards creating awareness on CLP among parents and various health care professionals. 

References

American Cleft Palate-Craniofacial Association (2008,
Accessed November 10, 2009). Standards for
cleft palate and craniofacial teams. Retrieved
from http:// www.acpa-cpf.org.Broder, H., Trier,
W. C. (1985). Effectiveness of genetic counseling
for families with craniofacial anomalies. Cleft
Palate Journal, 22 (3), 157–162.
Bull, R., & Rumsey, N. (1988). The social psychology
of facial disfigurement. Journal of cross cultural
psychology. 17. 99-108.
Byrnes, A. L., Berk, N. W., Cooper, M. E., &
Marazita, M. L. (2003). Parental evaluation of
informing interviews for cleft lip and/or palate.
Pediatric, 112, 308–313.
Grow, J. L., & Lehman, J. A. (2002). A Local
perspective on the initial management of children
with cleft lip and palate by primary care
physicians. Cleft Palate Craniofacial Journal,
39(5), 535–540.
Hafner, M., Bartsch, A., Trimbach, G., Zobel, I., &
Witt, E. (1987). Parental reactions following the
birth of a cleft child. Journal of Orofacial
Orthopedics, 58 (2), 124–133.
Horner, M. M., Rawlins, P., & Giles, K. (1987). How
parents of children with chronic conditions
perceive their own needs. MCN: American
Journal of Maternal Child Nursing, 12, 40–44.
Johansson, B., & Ringsberg, K. (2004). Parents’
experiences of having a child with cleft lip and
palate. Journal of Advanced Nursing, 47(1), 165–
173.
Lansdown, R., Lloyd, J., & Hunter, J. (1991). Facial
deformity in childhood: severity and
psychological adjustment. Child Care Health
Development, 17, 165-71.
Latta, L. C., Dick, R., Parry, C., & Tamura, G. S.
(2008). Parental responses to involvement in
rounds on a pediatric inpatient unit at a teaching
hospital: a qualitative study. Academic Medicine,
83, 292–297.
Pannbacker, M., & Scheuerle, J. (1993). Parents’
attitudes toward family involvement in cleft
palate treatment. The Cleft Palate-Craniofacial
Journal, 30(1), 87–89.
Raju, S. (2000). In search of a smile-study of children
born with cleft lip and palate in India. Tata
Institute of Social Sciences: Mumbai. Available
from: http://www.smiletrain.org [last cited on
2009 Aug 15]
Simon, K. (2004). Psychological issues in cleft lip and
palate. Clinics in Plastic Surgery, 31(2), 347-52.
Sinko, K., Jagsch, R., Prechtl, V., Watzinger, F.,
Hollmann, K., & Baumann, A. (2005). Evaluation
of Esthetic, Functional, and Quality-Of-Life
Outcome in Adult Cleft Lip and Palate Patients.
Cleft Palate–Craniofacial Journal, 42 (4), 355-
361.
White, R. C., Eiserman, W., Beddoe, M., &
Vanderberg, R. (2006). Perceptions,
Expectations, and Reactions to Cleft Lip and
Palate Surgery in Native Populations: A Pilot
Study in Rural India. Cleft Palate–Craniofacial
Journal, 42 (5), 560-564.
World Health Organization. (2001). Global registry
and database on craniofacial anomalies: Report of
a WHO registry meeting of craniofacial
anomalies. WHO library cataloguing.
Wyszynski, D. F. (2002). Cleft lip and palate. In
Elavenil, et al. (2010). Origin to treatment.(pp.
458-67). Oxford: Oxford University Press.
Young, J. L. (2001). What information do parents of
newborns with cleft lip, palate or both want to
know?. Cleft Palate Craniofacial Journal, 38(1).
55–58.