Caterina Agosto
University of Padua
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Publication
Featured researches published by Caterina Agosto.
The Clinical Journal of Pain | 2004
Franca Benini; Manuela Trapanotto; Daniela Gobber; Caterina Agosto; Giovanna Carli; Paola Drigo; Jo Eland; Franco Zacchello
Objectives:Little attention has been paid to the assessment of pain in children with developmental delay. The aim of this study was to explore several methods for assessing pain during venipuncture in this population of children, using classic and modified scales to evaluate the children’s response to simplified tools. Methods:Sixteen children with mild or moderate developmental delay were evaluated using three standard self-rating scales (Visual Analog Scale [VAS], Eland Scale, and Faces Scale) and three modified methods (Cube Test, Modified Eland Scale, and Modified Faces Scale), recording subjective self-ratings and behavioral expressions of pain during a venipuncture procedure, apart from the initial fear. The children’s pain and reaction time were assessed by an outside observer, while their pain and fear were also evaluated by the parents. Results:The VAS was used without difficulty by all the children and revealed a good consistency with the Cube Test. The parents’ and neutral observer’s indirect pain assessment was also consistent with the child’s evaluations. The Eland Scale proved difficult to use, especially for Down’s syndrome children, while its modified version was easier. Results emerging from the original and modified Faces Scales were inconsistent. Frightened children attributed higher pain scores, demonstrating that negative emotions exacerbate the experience of pain in developmentally delayed children. The patients showed a limited capacity for verbal and behavioral expression in reaction to the painful stimulus (especially the Down’s cases). Discussion:These findings support the conviction that even developmentally delayed children can use self-rating methods effectively. This sector demands further, more extensive study, including the development of simplified tools, to ensure an adequate pain assessment and optimal antalgic approach to this particular pediatric population.
Acta Paediatrica | 2014
Franca Benini; Filomena Pierri; Katy Vecchiato; Luca Ronfani; Caterina Agosto; Alessandro Ventura; Orazio Genovese; Egidio Barbi
The aim of this study was to determine the safety and the efficacy of paediatrician‐administered propofol in children undergoing different painful procedures.
Acta Paediatrica | 2012
Maria Immacolata Farina; Roberto Scarani; Chiara Po; Caterina Agosto; Giancarlo Ottonello; Franca Benini
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder typically presenting in infants with an impaired automatic control of breathing, particularly during sleep, and often associated with variable patterns of autonomic nervous system dysregulations. We studied three children who had CCHS associated with episodes of severe hypoglycaemia and hyperinsulinaemia; we discuss the possible relationship with impaired dopamine‐beta‐hydroxylase function.
Supportive Care in Cancer | 2012
Chiara Po; Franca Benini; Laura Sainati; Maria Immacolata Farina; Simone Cesaro; Caterina Agosto
PurposeThe quality of life of children with cancer can be affected by the experience of cancer-related pain, treatment-related pain, procedural pain, generalized pain, and long-term chronic pain, and the consequences may be permanent. Treatment-related pain and procedural pain are often reportedly the most painful experiences relating to their illness. Procedural pain treatment is therefore now considered essential. This multicenter survey investigated how procedural pain is managed at Italian Pediatric Hematology–Oncology Centers.MethodsFrom April to October 2010, questionnaires were collected from the directors and/or referent of the Italian Centers of Pediatric Hematology–Oncology about the management of lumbar punctures, bone marrow aspirates, and biopsies.ResultsWe received responses from 67% of the centers (which performed a total of 13,271 procedures per year). Fifty percent of the procedures were performed in the operating room. The sedation–analgesia was provided “almost always” for 84% of procedures. Non-pharmacological treatments were used in 55% of the centers. The specialist who practiced analgesia was the anesthetist in 83.3% of the cases.ConclusionsA nationwide multicentre survey has been conducted for the first time to verify the management of procedural pain in Pediatric Hematology–Oncology patients. The results indicate that many aspects in the management of procedural pain appear consistent with the international guidelines. Some problems still remain, including the inability to ensure adequate sedation–analgesia in all the patients—often due to the lack of adequate staff, the frequent use of the operating room, and an underdeveloped use of non-pharmacological therapies.
European Journal of Pain | 1998
Franca Benini; D. Gobber; Paola Lago; Caterina Agosto; Giovanna Carli; Franco Zacchello
The aim of the present study was to evaluate the efficacy of EMLA cream (containing a eutectic mixture of local anaesthetics) in controlling pain due to arteriovenous fistula cannulation in teenagers undergoing chronic haemodialysis. The study was conducted in two phases, one prospective, the other a blind randomized trial, at the Paediatric Haemodialysis service of the Paediatrics Department of Padua University, Italy. It involved six teenagers, aged 12–18 years. Pain was measured using the visual analogue scale, indirect evaluation by nurses and a four‐category verbal rating scale.
Intensive Care Medicine | 2007
Maria Martha Martinez Toledo; Angela Amigoni; Giorgia Martini; Caterina Agosto; Andrea Pettenazzo
Juvenile dermatomyositis (JDM) is a multisystemic disease of children that affects primarily muscle and skin. The prevalence of pulmonary involvement is not well known but seems to be rarer than in adult patients with dermatomyositis/polymyositis (DM/PM) [1–3]. A wide spectrum of clinical presentations have been described, ranging from asymptomatic patients with merely abnormal pulmonary function tests [4] to severe, potentially fatal cases refractory to immunosuppressive and supportive therapy [5-9]. Here we present the case of a child with JDM and severe interstitial lung disease (ILD) successfully treated with immunosuppressive drugs and extracorporeal membrane oxygenation (ECMO).
Pediatric Research | 1999
Paola Lago; Franca Benini; Sabrina Salvadori; Tiziana Bettiol; Caterina Agosto; Franco Zacchello
Effect of Administering Low-Dose Fentanyl Infusion on Respiratory Dynamics in the Premature Ventilated for Respiratory Distress Syndrome-A Randomized Double-Blind Trial
Case reports in pediatrics | 2016
Sabrina Congedi; Silvia Spadini; Chiara Di Pede; Martina Ometto; Tatiana Franceschi; Valentina De Tommasi; Caterina Agosto; Pierina Lazzarin; Franca Benini
We report our clinical experience on the effect of Scrambler Therapy (ST) for a child with acute mixed pain refractory to pharmacological treatment. ST, recently proposed as an alternative treatment for chronic neuropathic pain in adults, is a noninvasive approach to relieve pain, by changing pain perception at brain level. It is safe and has no side effects. Further research is needed to assess its efficacy for acute pain and for paediatric population.
Case reports in pediatrics | 2016
Chiara Di Pede; Sabrina Congedi; Sara Rossin; Antuan Divisic; Alesandra De Gregorio; Caterina Agosto; Igor Catalano; Alessandro Mazza; Leonardo Sartori; Stefano Masiero; Franca Benini
We describe a case of a paediatric patient affected by mandibular fibrous dysplasia (FD) with severe and chronic pain who was successfully treated with zoledronic acid (ZOL): a third-generation bisphosphonate. Further research is needed to assess its safety and efficacy as a treatment option for FD in the paediatric population.
Acta Paediatrica | 2018
Chiara Di Pede; Caterina Agosto; Valentina De Tommasi; Alessandra De Gregorio; Franca Benini
This study described end‐of‐life care for children affected by spinal muscular atrophy type 1 (SMA1), which is characterised by progressive muscle weakness and develops in the first six months of life.