Giovanna Riccipetitoni
Biographic Data
| ID | 8257075 |
|---|---|
| NAME | Giovanna Riccipetitoni |
| GIVEN NAMES | Giovanna |
| FAMILY NAME | Riccipetitoni |
| SIGNATURE | RICCIPETITONI G |
| AFFILIATIONS | University of Pavia |
| ORCID | 0000-0002-7885-2524 |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2020 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Diagnosis and Management of Congenital H-Type Tracheoesophageal Fistula
H-TEF prevalence was six cases/year, consistent with the expected rate of five cases/year in our country. The diagnosis was challenging, sometimes delayed, and, in most patients, required multiple examinations. Fistula ligation and section through cervicotomy were the most frequent treatment. Long-term outcomes are good, and recurrence is a rare event
Congenital Lung Malformations
Congenital lung malformations (CLMs) involve anomalies of the lungs and respiratory tree such as congenital pulmonary airway malformation (CPAM), pulmonary sequestration (PS), bronchogenic cysts, congenital lobar emphysema, and bronchial atresia (BA). Although symptomatic lesions require surgical resection, the appropriateness of surgery for patients with asymptomatic malformations is a matter of ongoing debate. Limited data are available concern…
Esophageal Atresia
undernutrition risk factors, beyond the type of malformation, surgery, and perinatal factors, must be early considered to personalize nutritional programming. Energy metabolism is important to monitor the nutritional requirements. The management of nutritional issues is surely a contributory factor able to counteract the poor growth of children with EA
No prominent works on this page.
Esophageal Atresia
undernutrition risk factors, beyond the type of malformation, surgery, and perinatal factors, must be early considered to personalize nutritional programming. Energy metabolism is important to monitor the nutritional requirements. The management of nutritional issues is surely a contributory factor able to counteract the poor growth of children with EA
Congenital Lung Malformations
Congenital lung malformations (CLMs) involve anomalies of the lungs and respiratory tree such as congenital pulmonary airway malformation (CPAM), pulmonary sequestration (PS), bronchogenic cysts, congenital lobar emphysema, and bronchial atresia (BA). Although symptomatic lesions require surgical resection, the appropriateness of surgery for patients with asymptomatic malformations is a matter of ongoing debate. Limited data are available concern…
Diagnosis and Management of Congenital H-Type Tracheoesophageal Fistula
H-TEF prevalence was six cases/year, consistent with the expected rate of five cases/year in our country. The diagnosis was challenging, sometimes delayed, and, in most patients, required multiple examinations. Fistula ligation and section through cervicotomy were the most frequent treatment. Long-term outcomes are good, and recurrence is a rare event
Medicine (3 works) · Surgery (3 works) · Tracheal and airway disorders (3 works) · Esophageal and GI Pathology (2 works) · Internal Medicine (2 works) · Anthropometry (1 work) · Asymptomatic (1 work) · Atresia (1 work) · Body mass index (1 work) · Congenital Diaphragmatic Hernia Studies (1 work)