ALESSANDRO CALISTI

Prof. Dr. ALESSANDRO CALISTI

Jepa Limmat Foundation for Advanced Education in Developing Countries, Rome, Lazio, Italy
orcid

Research Focus & Metrics

Academic Career Length

46Years (1981-Present)

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

Representative Publications

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1 March 2004 in Pediatric Surgery International
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Journal Article
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GMG. Marrocco
G. Marrocco
SVS. Vallasciani
S. Vallasciani
GFG. Fiocca
G. Fiocca
ACALESSANDRO CALISTI
ALESSANDRO CALISTI

24 October 2003 in Child's Nervous System
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Journal Article
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Luca MassimiLuca Massimi
Luca Massimi
ACALESSANDRO CALISTI
ALESSANDRO CALISTI
MKMichalis Koutzoglou
Michalis Koutzoglou
CRConcezio Di Rocco
Concezio Di Rocco

1 May 1986 in Journal of Ultrasound in Medicine
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Journal Article
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PMP Mirk
P Mirk
ACALESSANDRO CALISTI
ALESSANDRO CALISTI
AFA Fileni
A Fileni

9 April 2014 in Journal of Ultrasound
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Journal Article
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VGVincenza di Giacomo
Vincenza di Giacomo
MTMargherita Trinci
Margherita Trinci
GBGiulia van der Byl
Giulia van der Byl
VCVincenzo Davide Catania
Vincenzo Davide Catania
ACALESSANDRO CALISTI
ALESSANDRO CALISTI
VMVittorio Miele
Vittorio Miele

14 November 2011 in Italian Journal of Pediatrics
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Journal Article
Open access
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VPValentina Filomena Paradiso
Valentina Filomena Paradiso
VBVito Briganti
Vito Briganti
LOLucia Oriolo
Lucia Oriolo
RCRiccardo Coletta
Riccardo Coletta
ACALESSANDRO CALISTI
ALESSANDRO CALISTI
Background: Meconium abnormalities are characterized by a wide spectrum of severity, from the meconium plug syndrome to the complicated meconium ileus associated with cystic fibrosis. Meconium Related Ileus in absence of Cystic Fibrosis includes a combination of highly viscid meconium and poor intestinal motility, low grade obstruction, benign systemic and abdominal examination, distended loops without air fluid levels. Associated risk factors are severe prematurity and low birth weight, Caesarean delivery, Maternal MgSO4 therapy, maternal diabetes. In the last 20 yrs a new specific type of these meconium related obstructions has been described in premature neonates with low birth weight. Its incidence has shown to increase while its management continues to be challenging and controversial for the risk of complicated obstruction and perforation. Materials and methods: Among 55 newborns admitted between 1992-2008 with Meconium Related Ileus as final diagnosis, data about Low Birth Weight infants (LBW < 1500 g) were extracted and compared to those of patients ≥ 1500 g. Hischsprung's Diseases and Cystic Fibrosis were excluded by rectal biopsy and genetic probe before discharge. A softening enema with Gastrografin was the first option whenever overt perforation was not present. Temporary stoma or trans appendiceal bowel irrigation were elected after unsuccessful enema while prompt surgical exploration was performed in perforated cases. NEC was excluded in all operated cases. Data collected were perinatal history and neonatal clinical data, radiological signs, clinical course and complications, management and outcome. Results: 30 cases with BW ≥ 1500 g had an M/F ratio16/14, Mean B.W. 3052 g, Mean G.A. 37 w Caesarean section rate 40%. There were 10 meconium plug syndrome, 4 small left colon syndromes, and 16 meconium ileus without Cystic Fibrosis. Five cases were born at our institution (inborn) versus 25 referred after a mean of 2, 4 Days (1-7) after birth in another Hospital (outborn). They were managed, after a Gastrografin enema with 90% success rate, by 1 temporary Ileostomy and 2 trans appendiceal irrigation. 25 cases with BW< 1500 g (LBW) had M/F ratio 11/14, Mean B.W. 818 g, Mean G.A. 27 w, Caesarean section rate 70%, assisted ventilation 16/25. There were 8 inborn and 17 outborn. Gastrografin enema was successful in 6 out 8 inborn infants only, all referred within one week from birth. There were 12 perforations mainly among late referred LBW outborn. Conclusions: Meconium Related Ileus without Cystic Fibrosis responds to conservative management and softening enema in most of mature infants. In LBW clinical course is initially benign but as any long standing bowel obstruction management may present particular challenges. Clinical and plain radiographic criteria are reliable for making diagnosis and testing for Cystic Fibrosis may not be indicated. Enema may be resolutive when performed in a proper environment. Perforated cases may be confused with NEC which is excluded by clinical history, no signs of sepsis, lab signs missing, abdominal signs missing, typical radiological signs missing. The higher complication rate is recorded among cases delivered and initially managed in Neonatal Units without co-located Surgical Facilities. Early diagnosis and aggressive medical therapy may lead to higher success rate and help avoiding surgical interventions. Surgical therapy in uncomplicated cases, unresponsive to medical management, should be minimally aggressive.

26 June 2015 in The Journal of Maternal-Fetal & Neonatal Medicine
Verified
Journal Article
Closed access
VCVincenzo Davide Catania
Vincenzo Davide Catania
VBVito Briganti
Vito Briganti
VGVincenza Di Giacomo
Vincenza Di Giacomo
VMVittorio Miele
Vittorio Miele
FSFabrizio Signore
Fabrizio Signore
ACALESSANDRO CALISTI
ALESSANDRO CALISTI
The finding of a fetal intra-abdominal cyst is relatively common and it can be due to a wide variety of clinical conditions. The aims of this study were to determine the accuracy of the prenatal ultrasound (US) in identifying the etiology of fetal intra-abdominal cysts and to describe the neonatal outcomes. All cases of fetal intra-abdominal cystic lesion referred to our center between 2004 and 2012 were reviewed. Cysts of urinary system origin were excluded. Prenatal and postnatal data were collected. Our cohort was divided into subgroups according to the prenatal suspected origin of the lesion (ovarian, mesenteric, gastro-intestinal and other locations). For each subgroup, sensitivity, specificity, positive predictive value, false-positive rate and accuracy of fetal US were calculated. In total 47 fetuses (10/37 M/F) were identified. The mean gestational age at the time of diagnosis was 33 ± 4.9 weeks. Our cohort comprised of 25 ovarian cysts (10 simplex and 15 complex), 3 GI duplication, 6 mesenteric lesions, 4 meconium pseudocyst and 9 lesions of other origin. Surgery was performed in 38 cases (81%) at birth. The prenatally established diagnosis was exactly concordant with post-natal findings in 34 cases (72.3%). Sensitivity, specificity, positive predictive value and false-positive rate of US were 88.1%, 95.5%, 71% and 5.4%, respectively. Long-term outcome was good in almost 90% of the cases. The etiology of fetal intra-abdominal cysts can be prenatally diagnosed in about 70% cases. Despite the high risk of surgery at birth, the long-term outcome was good in most of the cases.