SciELO - Scientific Electronic Library Online

vol.27 issue4Tratamiento quirúrgico de las fracturas acetabulares: resultado clínico-radiológico y sus complicacionesAproximación clínica al consumo de sodio author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand



Related links


Revista Médica del Uruguay

On-line version ISSN 1688-0390


BERNADA, Mercedes et al. Características de una población de niños hospitalizados con condiciones de salud pasibles de cuidados paliativos pediátricos: primeros pacientes de la Unidad de Cuidados Paliativos Pediátricos del Centro Hospitalario Pereira Rossell (UCPP-CHPR). Rev. Méd. Urug. [online]. 2011, vol.27, n.4, pp.220-227. ISSN 1688-0390.

Summary Introduction: Law 18,335 provides that: "All individuals have the right to receive comprehensive health services ... including palliative care". The World Health Organization (WHO) defined pediatric palliative care as "a global model for health care services both for the child with a disease that limits and/or threatens his life, and his family". Pereira Rossell Hospital Center has created a Pediatric Palliative Care Unit to provide attention and train professionals in these health care services. Objective: to describe the main characteristics of the first patients seen in the above mentioned unit. Method: We conducted a retrospective, descriptive study of the characteristics of the children seen from December 30, 2008 through December 30, 2010, based on their files and medical records. All children hospitalized in the intermediate health care in the Department of Pediatrics were included in the study. Results: 87 patients were seen, 54 of them were girls. Median age was three years old (ranging from 28 days until 16 years old). Health conditions requiring palliative care were varied, mainly non-progressive severe neurological disorders. The most frequent cause of hospitalization was respiratory infections, although several other biological, psychological and social problems were seen. 25% of the children died, most of them in the hospital. Conclusions: pediatric palliative care is a right. Thus, all health professionals working with children must be familiar with the problems presented and receive training for a comprehensive approach of the condition, since it is an obligation of the health system to guarantee this right.


        · abstract in Spanish | Portuguese     · text in Spanish     · Spanish ( pdf )


Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License