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Published on: November 6, 2014
Cleft lip and/or palate in the west of Ireland, 1980-1996
1Regional Orthodontic Department, Merlin Park Hospital, Galway, Ireland. hewson@iol.ie
Insights
This study identified 106 children with cleft lip/palate (CL/P) in Ireland from 1980-1996. Establishing a national CL/P register could improve data collection and care coordination.
Area of Science:
- Pediatric Epidemiology
- Craniofacial Anomalies
- Public Health
Background:
- Cleft lip and/or palate (CL/P) are common congenital anomalies requiring specialized care.
- Understanding the epidemiology of CL/P is crucial for public health planning and resource allocation.
- Previous epidemiological data for CL/P in Ireland during this period is limited.
Purpose of the Study:
- To identify and investigate the incidence and characteristics of children born with CL/P in the Western Health Board region of Ireland between 1980 and 1996.
- To analyze epidemiological trends including cleft type, gender, family history, and geographical distribution.
- To provide evidence for improving data collection and care coordination for CL/P.
Main Methods:
- Retrospective cohort study identifying children with CL/P.
- Data collection over a 17-year period (1980-1996).
- Analysis of incidence rates, epidemiological factors, and comparison with international trends.
Main Results:
- One hundred and six children with CL/P were identified.
- The incidence rate was 1.14 per thousand live births (1:871).
- Epidemiological findings aligned with established international patterns for CL/P.
Conclusions:
- The incidence of CL/P in the studied region aligns with global trends.
- A national register for CL/P with mandatory reporting is recommended for Ireland.
- Improved data consistency and care coordination are potential benefits of a national register.
Abstract:
The aim of this study was to identify and investigate care for children born, over a 17-year period (1980-1996), with cleft lip and/or palate (CL/P) in the Western Health Board region of Ireland. One hundred and six cleft-affected children were identified. The incidence was 1.14 per thousand (1:871) live births. Epidemiological findings in relation to cleft type, gender, family history, and location followed international trends. The establishment of a national Register with mandatory reporting of children with CL/P in Ireland would ensure greater consistency in data collection and may help improve co-ordination of care.
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