Elio Castagnola

Dr. Elio Castagnola

IRCCS Istituto Giannina Gaslini - Ospedale Pediatrico, 16147 Genoa, Italy
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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 November 2007 in Clinical Infectious Diseases
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Journal Article
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ECElio Castagnola
Elio Castagnola
VFVincenzo Fontana
Vincenzo Fontana
ICIlaria Caviglia
Ilaria Caviglia
SCSilvia Caruso
Silvia Caruso
MFMaura Faraci
Maura Faraci
RHRiccardo Haupt
Riccardo Haupt
Background. The purpose of our study was to evaluate the incidence and clinical characteristics of febrile episodes during neutropenia following chem

20 March 2023 in Journal of Clinical Oncology
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Journal Article
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Thomas LehrnbecherThomas Lehrnbecher
Thomas Lehrnbecher
PRPaula D. Robinson
Paula D. Robinson
RARoland A. Ammann
Roland A. Ammann
BFBrian Fisher
Brian Fisher
PPPriya Patel
Priya Patel
LSLillian Sung
Lillian Sung
PURPOSE: To update a clinical practice guideline (CPG) for the empiric management of fever and neutropenia (FN) in pediatric patients with cancer and hematopoietic cell transplantation recipients. METHODS: The International Pediatric Fever and Neutropenia Guideline Panel reconvened to conduct the second update of this CPG. We updated the previous systematic review to identify new randomized controlled trials (RCTs) evaluating any strategy for the management of FN in pediatric patients. Using the Grading of Recommendations Assessment, Development and Evaluation framework, evidence quality was classified as high, moderate, low, or very low. The panel updated recommendations related to initial management, ongoing management, and empiric antifungal therapy. Changes from the 2017 CPG were articulated, and good practice statements were considered. RESULTS: We identified 10 new RCTs in addition to the 69 RCTs identified in previous FN CPGs to inform the 2023 FN CPG. Changes from the 2017 CPG included two conditional recommendations regarding (1) discontinuation of empiric antibacterial therapy in clinically well and afebrile patients with low-risk FN if blood cultures remain negative at 48 hours despite no evidence of marrow recovery and (2) pre-emptive antifungal therapy for invasive fungal disease in high-risk patients not receiving antimold prophylaxis. The panel created a good practice statement to initiate FN CPG-consistent empiric antibacterial therapy as soon as possible in clinically unstable febrile patients. CONCLUSION: The updated FN CPG incorporates important modifications on the basis of recently published trials. Future work should focus on addressing knowledge gaps, improving CPG implementation, and measuring the impact of CPG-consistent care.

1 April 2005 in Annals of Oncology
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GFG. Fratino
G. Fratino
Angelo Claudio MolinariAngelo Claudio Molinari
Angelo Claudio Molinari
SPStefano Parodi
Stefano Parodi
SLS. Longo
S. Longo
PSP. Saracco
P. Saracco
RHR. Haupt
R. Haupt
Background: The use of indwelling central venous catheters (CVCs) has become commonplace in the management of children undergoing anticancer treatment. Several types of CVC are available, while information on complications observed in children is scarce. We describe the experience of two tertiary care centers in Italy that prospectively followed up three types of CVC used at both institutions over a 30-month period. Patients and methods: Between January 2000 and May 2002, double-lumen (DL) or single-lumen (SL) Hickman–Broviac (HB) catheters, and single-lumen pressure-activated safety valve (PASV) catheters were used and prospectively evaluated. Four types of possible complication were defined a priori: mechanical, thrombotic, malfunctioning and infectious. Results: Four hundred and eighteen CVCs (180 SL-HB, 162 DL-HB and 76 PASV) were inserted in 368 children, for a total of 107 012 catheter days at risk of complication. At least one complication occurred while using 169 of the devices (40%): 46% of the DL-HB, 46% of the PASV and 33% of the SL-HB (P=0.02) catheters. Subjects with hematological malignancies or non-malignant diseases had significantly more complications than those with solid tumors (P <0.0001). Overall, 234 complications were documented: 93 infectious [complication rate per 1000 catheter days at risk (CR)=0.87], 84 malfunctioning (CR=0.78), 48 mechanical (CR=0.45) and nine thrombotic (CR=0.08). SL-HB had statistically fewer infectious complications, while PASV had more mechanical complications. In a multivariate regression model, the most significant risk factors for having a CVC complication were hematological disease [relative risk (RR)=3.0; 95% confidence interval (CI) 1.8–4.8] and age <6 years at CVC insertion (RR=2.5; 95% CI 1.5–4.1). As for the type of CVC, compared with SL-HB, the DL-HB catheter had a statistically significant two-fold increased risk of any complication (RR=2.1; 95% CI 1.2–3.6), while the PASV catheter had a borderline RR of 1.8 (95% CI 1.0–3.6). Analysis by tumor type showed a higher risk of any kind of complication in patients with solid malignancies who had received a DL-HB catheter as compared with an SL-HB catheter (RR=7.2; 95% CI 2.8–18.7). Conclusions: CVCs may cause complications in up to 40% of patients, with type of CVC, underlying disease and patient age being the three main factors that affect the incidence of CVC-related complications. SL-HB catheters have the best performance.

9 October 2003 in European Journal of Haematology
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Journal Article
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ECElio Castagnola
Elio Castagnola
FFFrancesca Fioredda
Francesca Fioredda
The aim of the present work was to summarise in a single paper all the options for prevention of life‐threatening infections due to encapsulated bacteria in patients with hyposplenism or asplenia. Prevention of these infections should be obtained in all patients with 1) patient and family education, 2) prophylaxis by means of vaccination against Haemophilus influenzae and Streptococcus pneumoniae, 3) antibiotic prophylaxis, based primarily on penicillin, 4) delay of elective splenectomy or use methods of tissue salvage in splenic trauma. Vaccination is not effective against all serotypes of S. pneumoniae and Neisseria meningitidis causing life‐threatening infections in hypo/asplenic patients. Moreover, antibacterial prophylaxis could select antibacterial‐resistant pathogens and is highly conditioned by patient's compliance. Therefore, empirical antibacterial therapy of fever and/or suspected infection should be recommended to all splenectomised patients independently from time elapsing from splenectomy, vaccinal status and assumption of antibacterial prophylaxis.

1 October 1999 in Annals of Allergy, Asthma & Immunology
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ECElio Castagnola
Elio Castagnola
GRGiovanni A. Rossi
Giovanni A. Rossi
SCSimonetta Cozzani
Simonetta Cozzani
GPGrazia Pulvirenti
Grazia Pulvirenti
LFLilia Fasce
Lilia Fasce

2 August 2010 in Pediatric Blood & Cancer
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Journal Article
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ECElio Castagnola
Elio Castagnola
MRMario R. Rossi
Mario R. Rossi
Simone CesaroSimone Cesaro
Simone Cesaro
SLSusanna Livadiotti
Susanna Livadiotti
MGMareva Giacchino
Mareva Giacchino
RHRiccardo Haupt
Riccardo Haupt