Volume 41 Supplement 1

XXI Congress of the Italian Society of Neonatology

Open Access

Comfort care: the life has always a dignity even if it is very short and its beginning is confused with the end

  • Franca Sarracino1Email author,
  • Immacolata Como1,
  • Assia Piccolo2,
  • Annalisa Agangi2,
  • Antonio Maria Salzano3,
  • Francesco Messina1 and
  • Paolo Puggina2
Italian Journal of Pediatrics201541(Suppl 1):A40

https://doi.org/10.1186/1824-7288-41-S1-A40

Published: 24 September 2015

The comfort-care is an innovative practice introduced recently by the neonatologist Dr. Elvira Parravicini, from Columbia University Medical Center [1]. This practice in a Neonatal Intensive Care Unit (NICU) is a compassionate response that provides families with clear and relevant information and that focuses on the needs of the parents as well as the baby. On the baby side, the need to be kept warm, to be free from hunger, thirst or pain are the cornerstones of the program. On the family side, it is a viable option of care for fetus/neonates who are suffering from life-limiting conditions which takes in to account the emotional needs of the family at this difficult time [2]. When we are not able to ensure medical treatments aimed at curing the disease, we can help in a different way. Palliative care planning involves multidisciplinary team planning with professionals from (1) gynecologist (2) midwife, (3) neonatologist, (4)pediatric nurse, (5) psychologist. The multidisciplinary approach is pointed on the satisfaction of “essential needs” of both the family and the baby starting from the pre birth care to the post death care. The team's goals cover practical aspects of infant care, including pain relief, symptom relief, comfort and dignity, the management of prognostic uncertainties, but also the provision of support to families during the pregnancy, their baby's illness and afterwards when coming to terms with his loss. The target population is all infants with a life-limiting conditions (trisomy 13, trisomy 18, bilateral renal agenesis or anencephaly, etc.) for whom a decision has been made to not interrupt the pregnancy [1]. The care planning is very flexible and continuously consideres parents’ personal and/or spiritual wishes, moreover it is continuously reviewed in the best interests of the baby. Multidisciplinary discussions and decision making involving the parents and the team to plan the management are essential. At least also the staff is provided with informal and formal support during the period of providing palliative care [3, 4].

Authors’ Affiliations

(1)
Department of Neonatology and Neonatal Intensive Care Unit, “Villa Betania” Evangelical Hospital
(2)
Department of Obstetrics and Gynaecology, “Villa Betania” Evangelical Hospital
(3)
Service of Clinical Psychology, “Villa Betania” Evangelical Hospital

References

  1. Parravicini E: Is “comfort” care a “medical” care? Observations on a neonatal population. J Med Pers. 2012, 10 (1): 41-45. 10.1007/s12682-011-0108-4.View ArticleGoogle Scholar
  2. Whool C: Systematic review of the literature. Parental outcomes after diagnosis of fetal anomaly. Adv Neonatal Care. 2011, 11: 182-192. 10.1097/ANC.0b013e31821bd92d.View ArticleGoogle Scholar
  3. Whitfield JM, Siegel RE, Glicken AD, Harmon RJ, Powers LK, Goldson EJ: The application of Hospice Concepts to Neonatal Care. Am J Dis Child. 1982, 136: 421-424.PubMedGoogle Scholar
  4. Paedriatr Child Health. 2001, 6: 469-477.Google Scholar

Copyright

© Sarracino et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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