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1.
Acta Paediatr ; 106(10): 1564-1568, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28580602

ABSTRACT

AIM: Alleviating pain in neonates should be the goal of all caregivers. We evaluated whether recorded maternal voices were safe and effective in limiting pain in preterm infants undergoing heel lance procedures in the neonatal intensive care unit of an Italian children's hospital. METHODS: This prospective, controlled study took place from December 2013 to December 2015. We enrolled 40 preterm infants, born at a 26-34 weeks of gestation, at a corrected gestational age 29-36 weeks and randomised them to listen or not listen to a recording of their mother's voice during a painful, routine heel lance for blood collection. Changes in the infants' Premature Infant Pain Profile, heart rate, oxygen saturation and blood pressure during the procedure were compared by analysis of variance. Possible side effects, of apnoea, bradycardia, seizures and vomiting, were also recorded. RESULTS: Both groups showed a marked increase in PIPP scores and decrease in oxygen saturation during the procedure, but infants in the treatment group had significantly lower PIPP scores (p = 0.00002) and lower decreases in oxygen saturation (p = 0.0283). No significant side effects were observed. CONCLUSION: Using recorded maternal voices to limit pain in preterm infants undergoing heel lance procedures appeared safe and effective.


Subject(s)
Intensive Care, Neonatal/methods , Pain Management/methods , Audiovisual Aids , Humans , Infant, Newborn , Infant, Premature , Maternal Behavior , Pain Measurement , Prospective Studies , Voice
2.
Lymphology ; 49(3): 150-6, 2016 Sep.
Article in English | MEDLINE | ID: mdl-29906078

ABSTRACT

There is general agreement regarding the evident need for an international, multicenter trial including long-term follow-up to establish the correct criteria for diagnosing and managing congenital chylothorax. In an attempt to identify these criteria, which could then be used to draft a prospective multicenter trial, we propose three flow-charts showing three algorithms that could be used to: 1) obtain a definitive diagnosis of pleural chylous effusion; 2) specifically focus on chyle leakage evolution and etiology of chylothorax; and 3) focus on the management of congenital chylothorax. The aim of the algorithms we propose is to build the basis on which a strongly needed multicenter trial might be structured.


Subject(s)
Algorithms , Chylothorax/congenital , Diet Therapy , Gastrointestinal Agents/therapeutic use , Octreotide/therapeutic use , Parenteral Nutrition, Total , Pleurodesis , Thoracic Duct/surgery , Chylothorax/diagnosis , Chylothorax/etiology , Chylothorax/therapy , Disease Management , Drainage , Fluid Therapy , Humans , Infant, Newborn , Ligation
3.
Int J Immunopathol Pharmacol ; 26(3): 809-16, 2013.
Article in English | MEDLINE | ID: mdl-24067483

ABSTRACT

Bronchopulmonary dysplasia (BPD) is a chronic lung disease occurring in very and extremely preterm infants undergoing mechanical ventilation. Given the altered lung vascular growth characterizing BPD, circulating angiogenic cells could be useful biomarkers to predict the risk. The objective of the study was to determine whether the percentages of circulating angiogenic cells (CD34+VEGFR-2+, CD34+CD133+VEGFR-2+, and CD45-CD34+CD133+VEGFR-2+ cells), assessed in the peripheral blood at birth by flow cytometry, could be used as markers for the risk of BPD. In one-hundred and forty-two preterm neonates (gestational age less than 32 weeks and/or birth weight less than 1500 g) admitted to our tertiary care Neonatal Intensive Care Unit between 2006 and 2009, we evaluated the percentages of circulating angiogenic cells at birth, at 7 days, and, in a subset of infants (n=40), at 28 days of life. The main outcome was the correlation between cell counts at birth and the subsequent risk of developing BPD. In our study, all the three cell populations failed to predict the development of BPD or other diseases of prematurity. We suggest that these cells cannot be used as biomarkers in preterm infants, and that research is needed to find other early predictors of BPD.


Subject(s)
Bronchopulmonary Dysplasia/diagnosis , Hematopoietic Stem Cells , Infant, Premature/blood , Infant, Very Low Birth Weight/blood , Neovascularization, Pathologic , AC133 Antigen , Antigens, CD/blood , Antigens, CD34/blood , Biomarkers/blood , Bronchopulmonary Dysplasia/blood , Bronchopulmonary Dysplasia/pathology , Flow Cytometry , Gestational Age , Glycoproteins/blood , Hematopoietic Stem Cells/metabolism , Hematopoietic Stem Cells/pathology , Humans , Leukocyte Common Antigens/blood , Leukocyte Count , Peptides/blood , Phenotype , Predictive Value of Tests , Retrospective Studies , Risk Factors , Tertiary Care Centers , Vascular Endothelial Growth Factor Receptor-2/blood
4.
J Matern Fetal Neonatal Med ; 25 Suppl 4: 97-100, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22958033

ABSTRACT

Near infrared spectroscopy (NIRS) measures the regional tissue oxygen saturation (rSO2) of various organs and provides a reflection of the balance between tissue oxygen supply and demand. Oxymetry assessed via NIRS has been proposed as a 'standard of care' and today it is already widely used in the NICU. This approach allows detection of any acute change in cerebral haemodynamics and continuous monitoring of cerebral and somatic oxygenation. This work describes three clinical cases of preterm VLBW infants which showed special points of interest during both cerebral and somatic NIRS monitoring.


Subject(s)
Cerebral Cortex/metabolism , Infant, Premature, Diseases/metabolism , Infant, Premature/metabolism , Oxygen/metabolism , Cerebral Cortex/chemistry , Female , Humans , Infant, Extremely Low Birth Weight/metabolism , Infant, Newborn , Infant, Premature, Diseases/therapy , Intensive Care Units, Neonatal , Male , Monitoring, Physiologic/methods , Oximetry/methods , Oxygen Consumption/physiology , Respiratory Therapy , Spectroscopy, Near-Infrared/methods , Tissue Distribution
5.
Minerva Pediatr ; 62(3 Suppl 1): 21-3, 2010 Jun.
Article in English | MEDLINE | ID: mdl-21089713

ABSTRACT

During the last decade, multiple techniques have been developed to isolate and quantify human endothelial progenitor cells (EPCs). In parallel, a number of studies have applied these methodologies to investigate the number and function of circulating EPCs in adult diseases characterized by vascular dysfunction. However, very little is known about different subtypes of EPCs during gestation, during the neonatal age or in neonatal diseases. Initial evidence supports the hypothesis that circulating angiogenic cells may play an important role during development, and attention has particularly focused in clarifying the function of EPCs in lung vascular development, and the role of the impairment of EPC mobilization and homing in hyperoxia-induced lung injury characteristic of bronchopulmonary dysplasia. Among different subtypes of EPCs, both the role of angiogenic mononuclear cells (triple-positive CD34+CD133+VEGFR-2+ cells and colony forming unit-Hill cells) and endothelial colony forming cells (ECFCs) in physiological vascular development and during neonatal diseases need to be elucidated. A better understanding of EPC biology during gestation, during the neonatal age and in preterm infants will unravel the pathologic basis of bronchopulmonary dysplasia and other preterm and term neonatal diseases characterized by a prominent defect in vascular growth, including retinopathy of prematurity and persistent pulmonary hypertension of the newborn.


Subject(s)
Endothelial Cells/cytology , Fetal Blood/cytology , Infant, Premature, Diseases/blood , Stem Cells/cytology , Animals , Antigens, Differentiation/analysis , Blood Cell Count , Bronchopulmonary Dysplasia/blood , Bronchopulmonary Dysplasia/pathology , Cell Differentiation , Colony-Forming Units Assay , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/pathology , Lung/blood supply , Lung/embryology , Mice , Neovascularization, Physiologic , Oxidative Stress , Oxygen/pharmacology , Stem Cells/chemistry , Stem Cells/classification , Stem Cells/drug effects
6.
Eur J Pediatr ; 168(5): 625-7, 2009 May.
Article in English | MEDLINE | ID: mdl-18726115

ABSTRACT

Subcutaneous fat necrosis of the newborn (SCFN) is a panniculitis that develops in fatty areas during the first weeks of life after foetal distress or perinatal complications. Prognosis is generally good with complete regression, but it can be complicated by metabolic abnormalities like hypoglycemia, hypertriglyceridemia, thrombocytopenia, and also potentially life-threatening hypercalcemia. We report a case of severe hypercalcemia complicating SCFN in a newborn who was treated with hyperhydration, furosemide, prednisone, and pamidronate.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Diphosphonates/therapeutic use , Fat Necrosis/complications , Hypercalcemia/drug therapy , Hypercalcemia/etiology , Child , Child, Preschool , Fat Necrosis/pathology , Female , Humans , Pamidronate
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