National Health Care Network for children with oral clefts: organization, functioning, and preliminary outcomes

Agustina Cassinelli1, Nadia Pauselli2, Agustina Piola1

  • 1Red Nacional de Anomalías Congénitas, Centro Nacional de Genética Médica (Administración Nacional de Laboratorios e Institutos de Salud -ANLIS-, Malbrán), Ministerio de Salud de la Nación, Ciudad Autónoma de Buenos Aires.

Insights

Argentina established a national oral clefts health care network in 2015. The network connects maternity centers with 61 accredited treatment facilities, aiming to improve care for affected newborns.

Area of Science:

  • Public Health
  • Pediatric Congenital Anomalies
  • Health Care Networks

Background:

  • Oral clefts are significant congenital anomalies affecting lip and/or palate, with an approximate prevalence of 15 per 10,000 births in Argentina.
  • In 2015, Argentina's Ministry of Health launched a national health care network for children with oral clefts.
  • This initiative involved collaboration with the National Registry of Congenital Anomalies (RENAC) and the SUMAR Program.

Purpose of the Study:

  • To describe the structure of the newly established national health care network for oral clefts in Argentina.
  • To report on the preliminary outcomes of this network in managing affected newborns.

Main Methods:

  • Accreditation and identification of 61 centers providing comprehensive oral clefts treatment.
  • Establishment of a network connecting maternity centers with treating centers through designated nodes.
  • Data collection on newborn infants covered by the public health care system between March 2015 and February 2016.

Main Results:

  • 550 newborn infants with oral clefts were identified within the public health system.
  • Cleft lip and palate occurred in 62% of cases, cleft lip in 18%, and cleft palate only in 20%.
  • 75% of cases were isolated oral clefts, while 25% were associated with other congenital anomalies.

Conclusions:

  • Approximately 70% of children with oral clefts are being assessed and treated by certified institutions.
  • The network aims to enhance data systematization and broaden center participation.
  • Future goals include strengthening interdisciplinary teamwork and promoting high-quality treatment standards.
Abstract

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