We are the combination of four hospitals: the General Hospital, the Children’s Hospital, the Women’s Hospital and the Traumatology, Rehabilitation and Burns Hospital. We are part of the Vall d’Hebron Barcelona Hospital Campus: a world-leading health park where healthcare plays a crucial role.
Below we will list the departments and units that form part of Vall d’Hebron Hospital and the main diseases that we treat. We will also make recommendations based on advice backed up by scientific evidence that has been shown to be effective in guaranteeing well-being and quality of life.
We will guide you from your first visit to the centre, allowing you to find all the departments and make the most of our facilities. Whatever the reason for your visit, we will explain how to get about the hospital.
Coarctation of the aorta is a malformation in which the aorta narrows just after the outlet that supplies blood to the head and arms. This restricts the passage of fluid and the heart has to work harder to pump it to the other organs.
Some patients develop hypoplasia when the reduction involves the entire aortic arch.
Coarctation varies in different age groups depending the level of severity and its form. It is also associated with other cardiac alterations such as patent ductus arteriosus, bicuspid aortic valve, ventricular septal defect and anomalies in the mitral valve.
During the neonatal period, some patients’ blood flow may go towards the lower body, which is dependant on the ductus arteriosus. When this begins to close, circulatory collapse occurs due to the excessive load on the heart and insufficient circulation in the abdominal organs. These patients first need to be stabilized and then treated.
This is a common type of heart disease representing 5-6% of all heart pathologies. There are between 0.2 and 0.6 cases for every thousand live births.
In the neonatal period, diagnosis is via transthoracic echocardiogram, but after this stage patients do not show symptoms. For this reason, it is diagnosed when high arterial pressure is detected during a routine check up. This is usually done with an echocardiogram, but other tests tend to be carried out such as a CT angiogram or nuclear magnetic resonance imaging to define the characteristics of the coarctation.
Hypoplasia of the aortic arch is also diagnosed prenatally via echocardiogram without the need for further tests.
In the neonatal period, patients usually need surgical treatment. The operation consists of resectioning the narrow segment of the aorta and then joining it to the healthy segments. In older patients, surgery is the preferred option and the procedure is similar to that for new-borns. Techniques to expand the narrowed area such as fitting a patch can also be used,
or in other cases interventional haemodynamics is considered. If this is the case, dilatation with high pressure balloons is performed to correct the narrowing. Following this, a metal stent is implanted in the area of coarctation to keep the vessel at the correct calibre. Hypoplasia of the aortic arch is repaired in the first two weeks of life. This is done by using a patch to enlarge the narrowed section of the aorta. If there is a related ventricular septal defect, this is often closed during the same surgery. Once out of the operating room the mortality rate for this disease is 1%.
6-10% of patients will, however, go on to develop a new narrowing of the aorta (recoarctation). This will require further surgery or another procedure. In 0.5% of cases there are no serious complications associated with this disease, but in older patients there is a chance that arterial hypertension may not improve after the repair. In terms of hypoplasia of the aortic arch, 5 % of those treated require further procedures due to recoarctation.
Anatomy of the heart
Haematology and Haemotherapy
Corneal and Ocular Surface Section
Abdominal wall surgery
Oral and Maxillofacial Surgery
Uveitis and Eye Inflammation
Strokes and Cerebral Haemodynamics
Colon and Rectal Surgery
Endocrine, Metabolic, and Bariatric Surgery
Intensive care medicine
Oculoplastic and Orbital Surgery
General and Digestive Surgery
Paediatric Oncological Surgery Unit
Anaesthesia, Resuscitation and Pain Management
Hepatobiliary and Pancreatic Surgery and Transplants
Endocrinology and Nutrition
Echocardiogram and cardiac imaging unit
Hereditary Angioedema Unit
Angiology, Vascular Surgery and Endovascular Surgery
Thoracic Surgery and Lung Transplants
Diagnostic and Interventional Haemodynamics
Coronary care unit
Cardiovascular Critical Care Unit
Otolaryngology (Ear, Nose and Throat)
Congenital Heart Disease in Adolescents and Adults
Aortic pathology and Marfan syndrome
Inherited Heart Disease
Communications Management, Corporate Strategy and Citizens Advice,
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