A5039714214- Childhood Cancer Survivors' Quality of Life
- Palliative Care and End-of-Life Issues
- Mitochondrial Function and Pathology
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
- COVID-19 and healthcare impacts
- Congenital Diaphragmatic Hernia Studies
- Child and Adolescent Health
- Family and Patient Care in Intensive Care Units
- Metabolism and Genetic Disorders
- Epilepsy research and treatment
- Anesthesia and Sedative Agents
- Click Chemistry and Applications
- Infant Nutrition and Health
- Clinical Nutrition and Gastroenterology
- Neonatal Health and Biochemistry
- Biotin and Related Studies
- COVID-19 Clinical Research Studies
- Intensive Care Unit Cognitive Disorders
- Advanced biosensing and bioanalysis techniques
Ospedale di Bolzano
2014-2023
Accurate estimation of the specialized pediatric palliative care (PPC) burden and definition extent quality PPC service in Italy represent urgent needs to enable proper allocation resources prevention educational plans. The PalliPed project aimed provide first comprehensive assessment characteristics Italian patients requiring PPC, regional networks/facilities, number dedicated resources. In this paper, we present results second part project, regarding implementation services Italy.
Abstract Background The PalliPed project is a nationwide, observational, cross-sectional study designed with the aim of providing constantly updated national database for census and monitoring specialized pediatric palliative care (PPC) activities in Italy. This paper presents results first phase project, which was developed through 2022–2023 study, to update current knowledge on provision PPC services Methods Italian centers/facilities were invited participate asked complete self-reporting,...
<h3>Objective</h3> In previous cases, we have observed occasional hypoglycaemic episodes in preterm infants after initial intensive care. this prospective study, determined the frequency and severity of abnormal tissue glucose (TG) clinically stable on full enteral nutrition. <h3>Methods</h3> Preterm born at <1000 g (n=23; G1) birth weight 1000–1500 (n=18; G2) were studied a postmenstrual age 32±2 weeks (G1) 33±2 (G2). Infants fed two or three hourly, according to standard bolus-nutrition...
Introduction: Biotinidase deficiency (BD) is an autosomal recessive disease causing a defect in the biotin-releasing enzyme. Newborn screening (NBS) allows early diagnosis and treatment, ensuring excellent prognosis. The aim of this study was to describe our experience diagnosis, follow-up showing key strategies unsolved questions management BD patients. Methods: We analyzed data patients identified by Regional Centre for Screening Verona followed Inherited Metabolic Disease Unit Neonatal...
Mitochondrial fatty acid oxidation disorders (FAODs) are a heterogeneous group of hereditary autosomal recessive diseases included in newborn screening (NBS) program Italy. The aim this study was to analyse FAODs cases, identified either clinically or by NBS,for clinical and genetic characterization evaluate five years' experience NBS, the attempt figure out complexity genotype-phenotype correlation confirm impact NBS our centre experience.We analysed patients diagnosed clinically, followed...
Fig. 1 Chest x-ray showing widespread opacification of both lungs.Key Points Children show a milder course COVID-19 infection than adults.2 The impact in paediatric patients with chronic or degenerative diseases is not known.3 Dedicated guidelines should be developed for these and their families.