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1.
Andes Pediatr ; 93(3): 383-391, 2022 Jun.
Artigo em Espanhol | MEDLINE | ID: mdl-35857009

RESUMO

INTRODUCTION: Annually, 7.9 million neonates in the world have developmental anomalies. Together with prema turity, they constitute the main causes of mortality during the first year of life in developed and de veloping countries. In Chile, the estimated prevalence is 3.9% of all live births. There are no reports on the prevalence of malformations in the Araucanía Region. OBJECTIVE: to estimate the prevalence of congenital malformations at birth in neonates hospitalized in a Neonatology Service. PATIENTS AND METHOD: cross-sectional study. Reference population: 54,241 live births at the Regional Hospi tal of Temuco over a 10-year period. Cases came from the neonatology hospital discharge database according to the ICD 10 classification, from January 1, 2009, to December 31, 2018. Descriptive and analytical statistics were performed with the STATA 15 software. RESULTS: 949 neonates with one or more congenital malformations were identified. The overall prevalence of neonates with malforma tions was 1.7%, the most prevalent being ventricular septal defect 40.9 x 10,000 live newborns (LNB), atrial septal defect 21.5 x 10,000 LNB, cleft lip and palate 14.0 x 10,000 LNB, congenital hypertrophic cardiomyopathies 8.1 x 10,000 LNB, and congenital rectal atresia and stenosis or absence of the anus 7.9 x 10,000 LNB. CONCLUSIONS: the overall prevalence of malformations is similar to that reported for the country. When analyzing by type, we found significantly higher incidences than those repor ted in previous studies.


Assuntos
Anormalidades Congênitas , Actinas/deficiência , Chile/epidemiologia , Fenda Labial/epidemiologia , Fissura Palatina/epidemiologia , Anormalidades Congênitas/epidemiologia , Estudos Transversais , Comunicação Interatrial/epidemiologia , Humanos , Recém-Nascido , Prevalência
2.
Rev. chil. pediatr ; 84(6): 650-658, dic. 2013. tab
Artigo em Espanhol | LILACS | ID: lil-703288

RESUMO

Objetivo: La Unidad de Neonatología, se propuso mejorar la calidad de la atención de la familia del recién nacido que fallece. Pacientes y Método: Tras constituirse un Comité de Manejo del Duelo Neonatal, se capacitó al personal al inicio y luego anualmente. Se elaboró un Manual de Procedimientos, aplicado desde marzo de 2000. Se presenta el análisis cuantitativo de los resultados de la aplicación del Manual y el análisis cualitativo del impacto del programa en el personal y en los padres. Resultados: Fallecieron 440 niños entre el 1 de marzo de 2000 hasta el 31 de diciembre de 2009. El aviso de muerte inminente se realizó en el 98,8 por ciento de los casos, la presencia de los padres en el momento de la muerte llegó a un 85,9 por ciento, lo que estuvo determinado significativamente por el lugar de residencia y la hora del fallecimiento. El 87,8 por ciento de los padres abrazaron a su hijo, mientras que el 5,8 por ciento sólo lo miraron. Se describe, además, el impacto del programa sobre el personal y las opiniones de los padres en una conversación post-mortem. Conclusión: El programa del Duelo Neonatal mejoró la calidad de la atención a los padres del recién nacido moribundo.


Objective: A Neonatal Unit decided to improve the family quality care of dying newborns. Patients and Method: After a Neonatal Grief Management Committee was established, care providers were immediately trained and followed by annually training programs. A Procedures Manual was elaborated and implemented since March 2000. A quantitative analysis of the Manual application results and a qualitative analysis regarding the program impact on care providers and parents are presented. Results: 440 children died between March 1, 2000 and December 31, 2009. The new of imminent death was delivered in 98.8 percent of cases; the presence of parents at the time of death reached 85.9 percent which was significantly determined by the place of residence and time of death. 87.8 percent of parents hugged their child, while 5.8 percent only looked at him. The program's impact on care providers and the views of parents in post-mortem conversations are described. Conclusion: The Neonatal Grief Program improved the quality care of the parents of dying newborns.


Assuntos
Humanos , Adulto , Recém-Nascido , Atitude Frente a Morte , Pesar , Pais/psicologia , Atitude do Pessoal de Saúde , Entrevistas como Assunto , Apego ao Objeto , Relações Pais-Filho , Relações Profissional-Família , Assistência Terminal , Revelação da Verdade
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