Intersectoral Partnership for the Development of an Action Plan to Guarantee the Rights to Life, Health, and Development for Newborns at Risk
Round Table – Cotroceni Presidencial Palace, 17 November 2025
On 17 November 2025, World Prematurity Day and the National Day of the Premature Child in Romania, Cotroceni Presidencial Palace hosted the Round Table entitled “Intersectoral Partnership for the Development of an Action Plan to Guarantee the Rights to Life, Health, and Development for Newborns at Risk.”
The event was organised by the Romanian Association for Long Hospitalised Newborns – ARNIS and the Romanian Neonatology Association, in partnership with the Presidential Administration and the Ministry of Health.

The meeting aimed to open a structured dialogue between institutions, healthcare professionals, and non-governmental organisations, including patient associations, to place on a shared agenda the critical issues related to the care of newborns at risk: Parental access to Neonatal Intensive Care Units (NICU), the Kangaroo Mother Care (KMC) method, early intervention, and the establishment of multidisciplinary follow-up centres for newborns at risk after discharge.
An event under a shared global message
The Round Table at Cotroceni Palace took place in the context of the official recognition by the World Health Organization (WHO) of World Prematurity Day—initiated by the Global Foundation for the Care of Newborn Infants (GFCNI)—as a day of global significance. The international campaign message for 2025 is:
“Supporting premature babies’ start in life for a better future! Access to high-quality healthcare everywhere.”
As part of the GFCNI network, ARNIS promotes this message in Romania through advocacy actions, professional training, and programmes dedicated to families of premature infants. The event at Cotroceni Palace marked the national launch of this campaign.
Why such a partnership is needed
Recent data presented on the occasion of World Prematurity Day 2025 reveal a concerning picture:
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In 2024, only 148,916 live births were registered—less than half of the number recorded in 1990 (314,746).
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Infant mortality increased to 6.7‰ in 2024, compared to 5.5‰ in 2023.
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Neonatal mortality (under 1 month) rose to 3.7‰, up from 3.3‰ in 2023.
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Approximately 10% of all births are premature (≈ 14,000/year, infants born before 37 weeks of gestation—based on semi-definitive 2024 INS data, correlated with European prematurity rates).
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Around 25% of premature infants develop a chronic condition, meaning approximately 3,500 children each year face long-term health issues.

These figures, from official sources (INS, ANPDPD, UBB studies), clearly show that early intervention and the coherent organisation of the care pathway—from Neonatal Intensive Care to follow-up in specialised centres and then into the community—can no longer be postponed.




Special guests of the event
The event would not have been possible without the involvement and openness of the institutions and professionals who committed to long-term collaboration. Key guests included:
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Mirabela Grădinaru, First Lady of Romania – host of the event, who advocated for a coordinated national effort to support children born prematurely.
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Dr. Alexandru Rogobete, Minister of Health – representing the central authority responsible for health policies and improving the quality of maternal and child health services.
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Dragoș Pîslaru, Minister of Investment and European Projects – supporter of initiatives aimed at improving medical services for mothers and children.
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Dr. Cătălin Cîrstoveanu, representative of the Neonatology Commission of the Ministry of Health, who presented progress in Neonatal Intensive Care supported through the National Recovery and Resilience Plan (PNRR) and steps towards the establishment of the Prematurity Registry.
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Prof. Dr. Manuela Cucerea, President of the Romanian Neonatology Association, who emphasised the need for data collection on premature infants, both during hospitalisation and throughout post-discharge follow-up.
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Prof. Dr. Livia Maria Ognean, Vice President of the Romanian Neonatology Association, advocate for Kangaroo Mother Care in Romania, presenting “The Road to a National Guideline.”
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Assoc. Prof. Dr. Adrian Ioan Toma, coordinator of the newly launched Ministry of Health Guideline “Follow-up of Newborns at Risk for Neurological and Developmental Sequelae.”
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Corina Croitoru, founding member and president of ARNIS, who brought forward the voice of families of premature infants: the need to improve parental access in NICU and a solution to reduce the number of children with disabilities in Romania—the establishment of multidisciplinary follow-up centres.
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Dr. Oana Blaga, lecturer at the Department of Public Health, UBB, contributing with research-based perspectives in the presentation “From Cost to Investment: Financial Insights from International Studies.”
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Dr. Uldis Mitenbergs, WHO Representative in Romania, who launched the Romanian version of the Kangaroo Mother Care guideline.
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Ileana Fălcescu, ARNIS member, who spoke from her personal experience about “The Complexity of the Recovery Process in Premature Infants.”
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Silvia Măgureanu, ARNIS member, with a moving presentation on “The Fragility of the Premature Infant and the Importance of Healthy Attachment.”
The Round Table moderator was Diana Iancu, Presidential Advisor.
Participants also included parliamentarians, representatives of health institutions, medical and therapeutic experts (neonatologists, paediatricians, neurologists, obstetricians, physiotherapists, psychotherapists, occupational therapists), representatives of NGOs active in neonatology, civil society representatives, and parents of premature infants, who provided the lived-experience perspective.


Central themes of discussion
1.Parental access in Neonatal Intensive Care Units
It was emphasised that parental presence in the NICU is not a “gesture of goodwill” but a medical and psychological necessity with direct impact on the child’s evolution and risk of complications.
2.Kangaroo Mother Care (KMC)
Data show that skin-to-skin contact can reduce infant mortality by up to 40% and shorten hospital stays when correctly and structurally implemented.
3.Multidisciplinary follow-up centres for newborns at risk
The need for early intervention to continue after discharge—through centres where children are monitored by multidisciplinary teams—was reiterated.
4.Prematurity Registry and data for public policies
Participants discussed the necessity of a national registry to monitor the evolution of premature infants, enabling evidence-based health policy decisions.
5.Expanded screening for prenatal and neonatal detectable conditions




Purple illumination of Cotroceni Presidencial Palace and activities in maternity hospitals
The Round Table was followed by press statements and the illumination of Cotroceni Presidencial Palace in purple—the international colour of prematurity promoted by GFCNI worldwide—as a gesture of solidarity for premature infants and their families.


The two working groups: directions and plans
A concrete outcome of the Cotroceni Round Table is the establishment of two working groups with clearly defined missions:
1.The Working Group on Parental Access and the Implementation of Kangaroo Mother Care (KMC) in neonatal units.
2.The Working Group on Multidisciplinary Follow-up Centres for Newborns at Risk.
In the coming period, these groups will continue their work through technical meetings, consultations with field professionals, and collaboration with relevant institutions, so that the proposals can be transformed into operational policies and programmes.
Proposals for the two Working Groups may be submitted to: [email protected]


Acknowledgements and Gratitude
ARNIS extends its gratitude to all institutions and organisations that made this meeting possible: the Presidential Administration, the Ministry of Health, the Romanian Neonatology Association, the World Health Organization – Romania Office, the Global Foundation for the Care of Newborn Infants, the universities and professional societies involved, as well as the experts, physicians, therapists, parliamentarians, and NGO representatives who engaged in this dialogue.
A special chapter is dedicated to ARNIS’s sponsors and financial partners, who consistently support programmes for premature infants and newborns at risk. Without their contribution, early intervention, professional training, psychological support, and medical recovery activities could not be carried out with the same level of consistency and impact. The full list of partners and sponsors is available in the Partners section of our website.
Through this Round Table and the formation of the two Working Groups, ARNIS and its partners take an important step from identifying problems to jointly building concrete solutions.
The goal is clear: supporting premature infants’ start in life for a better future and ensuring access to high-quality healthcare, everywhere, for every child.
