Neonatal and Foetal Surgery
Neonatal Surgery is the sub-discipline within paediatric surgery that deals with surgically treating congenital and acquired illnesses in newborns and infants up to one month old.
This is a highly complex sub-speciality that only exists at tertiary paediatric centres. The past few decades have brought about important advances, thanks to improvements in diagnostic techniques, neonatal intensive care and anaesthetics, and surgical techniques and materials. These have radically changed the prognosis for both birth defects and acquired surgical pathologies in newborns.
Neonatal surgery requires detailed knowledge of complex pathologies in patients who also have special conditions that are different from other paediatric patients. The Neonatal and Foetal Surgery Unit covers practically every surgical neonatal pathology, and it is a reference centre both nationally and on a European level. It is part of ERNICA, the European Reference Network (ERN) for Rare Inherited and Congenital Digestive Disorders. In recent years, the Unit has been firmly committed to introducing minimally invasive surgical techniques, achieving excellent results.
We work in conjunction with the Neonatology Department. The Neonatal Intensive Care Unit (NICU) at Vall d’Hebron Hospital is one of the largest in the country and has one of the best survival rates. We have the possibility of performing surgical interventions within the NICU if transporting the newborn patient to the surgical wing would be too risky due to the instability of their condition.
Similarly, we work closely with the Foetal Medicine Unit, whose services include all the currently valid prenatal and intrapartum (EXIT technique) foetal surgery techniques.
The Unit participates in the following sessions and committees: Neonatal Medical-Surgical Session (Tuesdays at 1 pm), Paediatric Airway Committee, Birth Defects Committee.
Within our areas of interest, we highlight oesophageal atresia, a pathology for which our overall survival rate exceeds 95% in patients who do not present complex associated malformations. Patients with long-gap oesophageal atresia continue to be a challenge, as the distance between the ends is so great that a primary repair cannot be done. In these complex patients, besides applying the different classic techniques, we use the Foker technique, which consists of sustained traction on the ends to be connected in order to stimulate their growth, so that oesophageal anastomosis can finally be achieved. In those patients for whom the native oesophagus cannot be saved, we carry out oesophageal substitution via gastric pull-up, with excellent short-term and long-term results.
We have established a comprehensive treatment plan for patients affected by a congenital diaphragmatic hernia (CDH), which includes foetal treatment (using the FETO technique: Foetal Endoscopic Tracheal Occlusion) in cases where CDH has been diagnosed in the foetus and the prognosis is not good. In addition, the hospital offers every type of invasive and non-invasive respiratory support and therapy available today: synchronised mechanical ventilation, HFOV, CPAP, treatment with inhaled nitrous oxide, and ECMO (extracorporeal membrane oxygenation), providing cardiovascular and respiratory support when conventional treatment proves ineffective. In patients with large diaphragmatic defects, we use several types of patches, both synthetic and biological ones, and techniques that use autologous muscle flaps, generally from the abdominal wall.
The main abdominal wall defects we find are gastroschisis and giant omphalocele. We are especially proud of how we handle gastroschisis, which can be associated with severe medical-surgical problems due to the inflammation and thickening of the exposed intestinal loops caused by the irritation produced by the amniotic fluid at the end of gestation. Since 2002, we have been carrying out a strategy to avoid this, consisting of performing a scheduled Caesarian section at 34-35 weeks of gestation. This elective preterm C-section technique allows for the abdominal defect to be closed directly, as it reduces exposure to amniotic fluid. With more than 50 patients treated this way, we have not observed complications linked to prematurity. Instead, we have detected a decrease in the associated complications, an earlier introduction to food, and a reduced hospital stay, as well as better aesthetic outcomes, since the scar is hidden by the belly button. We have vast experience in treating giant omphalocele. For this, we use surgical techniques that employ vascularised flaps, biologic or synthetic mesh, and vacuum-assisted closure (V.A.C.®).
Our overall survival rates for acquired surgical pathologies such as necrotising enterocolitis and intestinal perforation (both in premature and LGA premature - with a birth weight of less than 750g - babies) is comparable to other European reference centres. This is thanks to the application of our philosophy of minimally aggressive surgery and conservative treatment; applying these principles is the underlying reason for our high rates of survival and preservation of native intestine.
Portfolio of services
Intrauterine or peripartum surgery
- Abdominal or thoracic malformations or tumours that require prenatal or intrapartum surgical treatment (using the EXIT technique, ex utero intrapartum treatment)
Pathologies of the disgestive tract
- Treatment of necrotising enterocolitis
- Treatment of intestinal perforation
- Surgical treatment of ileus and meconium peritonitis
- Following - Repairing oesophageal atresia, using both thoracoscopic and open approaches We specialise in complex patients (those with associated heart disease) and managing long-gap oesophageal atresia
- Oesophageal lengthening techniques to repair long-gap oesophageal atresia (the Foker technique), using both thoracoscopic and open approaches
- Oesophageal substitution via gastric pull-up, using minimally invasive and open approaches
- Congenital or acquired oesophageal stenosis, endoscopic or surgical treatment
- Gastrostomy feeding tube (open or percutaneous endoscopic techniques)
- Treatment for gastric perforation and volvulus
- Hypertrophic pyloric stenosis, pyloric and prepyloric atresia, using minimally invasive and open approaches
- Repairing congenital or acquired intestinal atresia and stenosis, using minimally invasive and open approaches
- Repairing duodenal atresia and annular pancreas, using minimally invasive and open approaches
- Treatment for intestinal duplication, using minimally invasive and open approaches
- Treatment for Meckel's diverticulum and persistent omphalomesenteric duct, using minimally invasive and open approaches
- Repairing defects involving intestinal rotation and volvulus, using minimally invasive and open approaches
Pathologies of the abdominal wall
- Repairing inguinal hernias in newborns
- Repairing gastroschisis (primary closure, Schuster technique)
- Repairing omphalocele and umbilical cord hernias
- Surgical separation of conjoined (“Siamese”) twins: joined at the thorax, abdomen, or pelvis
Pathologies of the lungs and respiratory tract
- Repairing congenital and acquired tracheoesophageal fistulas (through surgery, endoscopy, and lasers)
- Repairing congenital diaphragmatic hernia in newborns, using minimally invasive and open approaches
- Repairing diaphragmatic paralysis and/or eventration, using minimally invasive and open approaches
- Rigid and flexible bronchoscopy
- Surgical treatment of complicated congenital pulmonary pathologies in newborns (cystic adenomatoid malformation, bronchopulmonary sequestration, CPAM, congenital lobar emphysema)
- Treatment of congenital chylothorax
- Treatment for vascular malformations (including complex lymphatic malformations of the head and neck), in coordination with the Paediatric Vascular Anomalies Committee and the Foetal Surgery Unit
- Cervical teratoma and epignathus
- Treatment for intrauterine and post-natal testicular torsion
- Excision of sacrococcygeal teratoma, in coordination with the Oncology Surgery Unit and the Foetal Surgery Unit
- Temporary or permanent vascular access points
Dr. Elena Carreras, medical coordinator of the Obstetrics and Reproductive Endocrinology Department, explains how the appearance of the ultrasound revolutionised the work of staff and how new intrauterine foetal therapy techniques will mark the future of the Department.
The constant search for excellence is part of Hospital Vall d’Hebron’s nature. The biggest hospital in Catalonia and the leader in many fields, headed since February 2015 by Dr. Vicenç Martínez Ibáñez, who has a close personal and professional relationship with the Hospital. Dr. Martínez Ibáñez says that if Vall d’Hebron did not exist, it would need to be invented. The current director trained at the hospital, where he was one of the protagonists of an historic moment: the first paediatric liver transplant in Spain. Now, he is committed to continuing this legacy and, always putting the patient first, achieving excellence across all staff.
The Neonatology Department’s Sibling Project is a workshop for the siblings of new-born babies admitted to the Paediatric Intensive Care Unit in the Vall d’Hebron Maternity and Children's Hospital. Through simulated games and situations, the project prepares them to get used to seeing their younger siblings in a hospital medical setting.
Vall d’Hebron University Hospital’s kitchen serves more than 1,000 meals a day, twice a day, not counting breakfast. A reality that José Parrilla and Carmina Esteban know all too well.From three kitchens to one and from coal to gas. That is how the hospital’s catering service has evolved. A place where the needs of each patient must be taken into account and where there is room for small, juicy anecdotes.
The former head of the Thoracic Surgery Department, Dr. Mercè Canela, recently retired, recalls the important evolution of the Department to become a leader in Spain and a lung transplant pioneer. A task made possible thanks to collaboration with professionals from other departments, an added value in the personal and team environment.
Rosalia Moure arrived at Vall d’Hebron University Hospital in 1967. She spent her entire working life in the linen and laundry department of the Hospital. Rosalia Moure has witnessed the Hospital’s big transformations, from dictatorship to democracy and from analogue to digital systems.
Dr. Josep Sánchez de Toledo Codina, head of the Paediatric Haematology and Oncology Department, tells us about a Department that has laid the foundations for the specialism in Spain. He also remembers the evolution of transplants from haematopoietic stem cells and progenitors, from the beginning, buying the material at a shop in Barcelona city centre, to the more than 1,200 transplants that have now been performed.