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A Nationwide Study to Evaluate Accessibility to Specialized Pediatric Palliative Care in Italy-Patients, Needs, and
Franca Benini1, Anna Mercante2, Sara Di Nunzio3
1Department of Women's and Children's Health, Pediatric Palliative Care, Pain Service, University of Padua, Padua, Italy.
Insights
The PalliPed project reveals a significant need for enhanced pediatric palliative care (PPC) services in Italy. Findings highlight gaps in service availability, referral processes, and family support, emphasizing the need for improved healthcare provider communication.
Area of Science:
- Pediatric Palliative Care
- Healthcare Network Analysis
- Clinical Needs Assessment
Background:
- Pediatric palliative care (PPC) is crucial for children with complex needs.
- Existing PPC services in Italy lack comprehensive national data.
- Understanding current PPC access and resource allocation is essential.
Purpose of the Study:
- To describe characteristics of patients accessing specialized pediatric palliative care (PPC) in Italy.
- To assess the extent, quality, and resources of regional PPC networks.
- To identify areas for improvement in PPC service delivery and family support.
Main Methods:
- Nationwide project involving all Italian PPC centers.
- Inclusion of pediatric patients receiving specialized PPC as of October 24, 2022.
- Data collection via online survey, using the ACCAPED Scale and multidisciplinary assessment.
Main Results:
- 867 patients were analyzed, revealing inadequate specialized PPC services.
- Identified need for improved referrals, especially for infants and oncology patients.
- Highlighted necessity for enhanced family support, particularly for mothers, and improved communication skills.
Conclusions:
- The PalliPed project provides the first national census of specialized PPC activities in Italy.
- Results underscore critical gaps in PPC service provision and resource allocation.
- The research model can inform and compare PPC models internationally.
Abstract:
PalliPed is the first Italian nationwide project aimed at describing the characteristics of patients accessing specialized pediatric palliative care (PPC) and their families, in the main care settings (hospice, home care, and hospital). The project's secondary aim is to assess the extent and quality of regional PPC networks/facilities and the number of dedicated resources. In this article, we present the results of the first part of the project. All Italian PPC centers/facilities were invited to participate in the project. Children and young adults in the care of the specialized PPC networks/structures as of 24 October, 2022, including prenatal care, were involved. Children's eligibility for specialized PPC was assessed according to the Assessment Form for Complex Clinical Needs in Pediatrics (ACCAPED Scale) and after a multidisciplinary assessment by the healthcare team. Data were collected through an online survey. A total of 867 patients were described. The lack of adequate specialized PPC service emerged, according to the available estimate of specialized PPC needs, as well as the need for improved referral to PPC by pediatricians or territorial services, particularly for infants and oncological patients. More family support measures also seem necessary, particularly for the mothers. Healthcare providers' communication skills should be improved to ensure greater involvement of patients and families in care decisions. This analysis represents the first step toward defining a constantly updated database for the census and monitoring of specialized PPC activities at the national level. This research model can be extended to other realities in different countries, allowing comparison of different care models.
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