• 作者：F. Botet ; ^{fbotet@clinic.ub.es} ; J. Figueras Aloy ; I. Echaniz Urcelay ; S. Rite ; J. Moreno ; J.R. Ferná ; ndez Lorenzo ; G. Herranz Carrillo ; E. Salguero ; M. Sá ; nchez Luna
• 关键词：Sistemas de informació ; n ; Informació ; n ; salud ; Salud comunitaria ; Registro electró ; nico de salud ; Recié ; n nacido
• 刊名：Anales de Pediatr¨ªa
• 出版年：2013
• 出版时间：May, 2013
• 年：2013
• 卷：78
• 期：5
• 页码：336.e1-336.e4
• 全文大小：175 K

The aim is to provide a framework for data collection in the health area of newborn infants allowing harmonization of their care. This requires knowing the population served, and the greatest difficulty is the absence of a data collection system and standards of care for all conditions of the newborn infant. It is essential to have a single record with the main perinatal and neonatal data of all newborn infants. The Spanish Society of Neonatology (SEN) should be responsible for the database, which must meet all legal requirements of privacy and confidentiality. It is possible to determine the relative weight of the pathology treated using Diagnostic Related Groups (DRG) and the results from a quality care perspective. Guidelines for diagnosis and treatment may be established by comparative analysis (benchmarking studies¡­).

Conclusion and Recommendation. It is necessary to know the newborn population served, and define criteria for diagnosis and treatment to improve quality of care. The SEN wishes to address those responsible for the care in hospitals, and to ask for their support and cooperation in the implementation of these recommendations.