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Professionalism, commitment and research by professionals on the Campus are the key elements in offering patients excellent care.
We are committed to research as a tool to provide solutions to the daily challenges we face in the field of medical healthcare.
Thanks to our healthcare, teaching and research potential, we work to incorporate new knowledge to generate value for patients, professionals and the organization itself.
We generate, transform and transmit knowledge in all areas of the health sciences, helping to train the professionals of the future.
We are defined by our vocation for communication. We invite you to share everything that happens at Vall d'Hebron Barcelona Hospital Campus, and our doors are always open.
Hospital donations
Research donations
We are the leading transplant centre in Catalonia and the second biggest centre in Spain for organ and tissue donation, one of few to provide adult and paediatric transplants. The Transplant Center project gives Vall d’Hebron a space from which to lead, integrate and optimise organ and tissue donation and transplant processes for continued improvement and professional excellence.
The Transplant Center is a shared and combined space for the coordination and strengthening of excellent practice in the area of organ donation and transplant. The prestige and potential that Vall d’Hebron has when it comes to transplants is proven, as it is the leader in transplants in Catalonia and the second biggest centre in Spain for organ and tissue donation and transplant.
The centre touches professionals, patients and the public. For the first group, the centre promotes coordinated action and collaboration. The project centres around constant improvement of clinical practice and facilitates coordination, be it between different centres and services or with different lines of research that are already researching and innovating in the field of donation and transplantation. It enables greater results orientation, while offering a space for teaching and research as instruments for continuous improvement and professional excellence.
It was conceived with the purpose of joining forces to be recognised as a leading and innovative centre for all types of transplant; a centre which helps solve patients’ problems and that stands out for the quality of its service and the excellence of its professionals. A place from which to lead, integrate and optimise organ and tissue donation and transplant processes across the whole of Vall d’Hebron Barcelona Hospital Campus.
It attempts to do so by maintaining guarantees of maximum quality, safety and efficiency, with the aim of achieving a high level of health protection (donor/recipient) and an improvement in patient survival and quality of life (adult and paediatrics). At the same time, achieving this through integrated and multidisciplinary clinical practice that is orientated around the patient and their family.
The project also opens an arena for talking about this situation, to normalise donations and transplants and make this a visible process. Vall d’Hebron understands and assumes the responsibility for training professionals and patients, but above all informing citizens. Although the transplant figures in Catalonia are more than double the European average, one out of every seven cases of delay in organ donations is due to there being no match in the family. The commitment to explaining the work conducted in this field, informing society about the processes of donation and transplantation, helps to guarantee the sustainability of first-line programmes such as the Vall d'Hebron programme. In the field of professional training, transplant coordination has been a leader in training initiatives for many years, including patient education projects.
With the patient in mind, the integrating effect the Transplant Center has for professionals and its impact on the treatment that patients receive and their experience during the donation and transplant processes should be publicised.
Vall d’Hebron understands and assumes the responsibility for training professionals and patients, but above all informing citizens.
The mission of the Coordination of Donation and Transplant Programmes Team is to lead, integrate and optimise the processes of donations and transplants. It works to offer maximum guarantees of quality, safety and efficiency, with the aim of achieving a high level of health guarantees (donor/recipient) and an improvement in quality of life of the patients who need a transplant.
Our hospital was a pioneer in creating the role of the transplant coordinator. Child and adult transplant teams are coordinated to ease the transition and integration of paediatric patients to adulthood.
In addition to providing multidisciplinary care for patients of all ages who suffer this condition, the objectives of Vall d’Hebron Hospital’s Hereditary Angioedema Unit include teaching and research in this field.
The Hereditary Angioedema Unit (UAEH) of Vall d’Hebron University Hospital’s Allergology Department has been treating patients with this disorder for more than 25 years.
UAEH outpatients are treated by allergology specialists in a multidisciplinary manner in the Outpatient Clinic in the Old Nursing School and in the Children’s and Women’s Hospital, ensuring transference and continuity of care from childhood through to adulthood for this genetic, lifelong condition.
The Unit is made up of popular, immunologists, geneticists, gynaecologists, maxillofacial surgeons, pharmacists and nurses, who are responsible for:
Depending on the type of care to be given to patients with diagnosed hereditary angioedema and their profile, they should be treated by the following divisions and/or units:
The specialists who work in the adult and paediatric allergology sections are responsible for treating patients aged 16 and under in the Children’s Hospital areas and subsequently facilitating their transfer and continuity of care with monitoring to the adult care departments in the Old Nursing School and the Allergology Day Hospital in the General Hospital.
The Hereditary Angioedema Unit (UAEH) offers an outpatient service to monitor patients with this disease: the Outpatient Clinic on the second floor of the Old Nursing School. Also, as it is a multidisciplinary unit, and depending on the type of patient (child, adult, pregnant woman), it provides care in a number of departments and units in the Children’s and Women’s Hospital, the General Hospital and A&E.
The nursing team specialises in education and specific care for patients with this disease.
Emergency care is provided at the Children’s Hospital for patients up to the age of 16 and at the General Hospital from the age of 17. The professionals who work in the A&Es have been trained to recognise the symptoms of this disease and to quickly provide its specific treatment.
When a patient needs a complex dental or maxillofacial procedure they will be assessed by the hospital’s maxillofacial surgeons and their operation will be organised with the suitable prophylaxis.
The Obstetrics, Foetal Medicine and Anaesthesia Departments have created a Working Unit for High-Risk Pregnancies for women with hereditary angioedema with the aim of monitoring the well-being of mother and child during pregnancy and of providing care during the delivery and postpartum period in accordance with a protocol specific to their type of hereditary angioedema and clinical situation. Care is also provided for high-risk postpartum cases.
In parallel to these services, there is also a reproductive counselling clinic for women with hereditary angioedema. The clinic is part of the Hereditary Angioedema Unit, and is that provided in conjunction with Gynaecology in the Outpatient Clinics of the Children’s and Women’s Hospital.
In this clinic an allergist and a gynaecologist combine their expertise to determine, in accordance with the patient’s clinical situation and type of hereditary angioedema, the possible effects of their having children. Their mission is to provide information and advice in relation to family planning and the reproductive possibilities of the patients living with this disease.
The Unit is made up of a team of specialist paediatricians, paediatric nursing staff, paediatric resident doctors working in shifts during their training, nursing assistants, paediatric nursing residents, porters, administrative and cleaning staff who share work and experiences for the sole purpose of offering the best care to the boys and girls in the Unit. We are experts in emergency care for children with complex diseases (patients with solid-organ or bone-marrow transplants, immunosuppressed patients, etc.,) in synergy with the other units in our centre. We are also part of the Paediatrics Department, offering comprehensive care to children who are poorly.
Our Paediatric Emergency Unit attends to patients up to the age of 16, except for children with chronic diseases requiring very specific treatment who may be attended to by our Unit even when they are over this age limit.
Besides making visits to assess children's emergency medical or surgical pathology, and appointments for patients who require clinical monitoring after our consultation, we also have an Observation ward for admitting patients who require hospitalisation.
Thanks to the coordination between the Nursing, Paediatric Emergency, Traumatology, Anaesthesiology, Radiology and Paediatric ICU teams and many other professionals, we are a benchmark centre in AITP (Initial Care for Paediatric Trauma).
When it comes to teaching, the Unit trains resident doctors (MIR) in Paediatrics and Family Medicine, as well as resident nurses in Paediatric Nursing. The Unit also plays a key role in training undergraduate Medical and Nursing students, as well practical training placements for nursing assistants. We take part in numerous continuous-teaching and training activities within and without the Hospital (advanced paediatrics life-support courses and AITP, joint courses with Primary Care, internal Hospital courses, sessions with several Units and Services, care simulations on children with multiple trauma and children in a critical condition, etc.).
As for research, we are part of the Spanish Society of Paediatric Emergency Medicine (SEUP) and its research network (RiSEUP), and we take part in numerous multi-centre projects and clinical trials.
The Immunology Department performs routine and complex immune system diagnostic tests, assessing and interpreting them in a clinical context. For complex testing, we act as a reference laboratory for other Catalan Health Institute centres when these centres request our help.
Most healthcare activities consist of diagnostic testing, and assessment and opinion, where applicable. Within this practice, we provide direct and continuous advice to clinical practitioners, by email, telephone as well as in person. We also design and improve diagnostic tests and protocols that allow diagnostic methods to be continually updated and bring clinical services into line with clinical requirements. Teaching and research are both crucial for the work that we are doing.
Our department includes a clinical immunology outpatients unit in which the diagnosis and follow-up of patients affected by adult immunodeficiency or immune complex pathophysiology is performed. Evaluation of the immune system’s response capacity is crucial to this activity. This unit is complementary to the Infectious Pathology and Immunodeficiencies Unit of the Paediatrics Department and the Bronchiectasis and Cystic Fibrosis Unit in the Pneumology Department.
It also actively takes part in clinical procedures within the hospital, in multidisciplinary approaches to amyloidosis, multiple myeloma, primary immunodeficiency and complex kidney diseases, as well as in the Advanced Haematology Therapies Unit.It is a reference centre, forming part of the European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune disease (ERN-RITA) and the European Reference Network for Rare Kidney Diseases (ERK-Net). It is also part of the reference unit of the Neonatal Screening Programme of the Catalan Department of Health in the field of serious combined immunodeficiency (unique in Spain).
We investigate, develop and innovate through projects in the fields of primary immunodeficiency, autoimmunity and counselling in the design and execution of research projects conducted by other groups in the hospital. We actively work alongside other departments, especially Paediatrics (Paediatric Infectious Pathology and Immunodeficiency Unit), Medicine (Allergology, Rheumatology, Systemic Medicine) and Nephrology, which is concerned with kidney infections.
Our department participates in networks to improve diagnosis and investigation in immunology, directly in collaboration with other departments and through the Catalan Immunology Society and the Spanish Immunology Society.
In recognition of our work in the promotion of Translational Immunology in our centre, i.e. applied study in patients, the Federation of Clinical Immunology Societies (FOCIS) has named the Immunology Department as Vall d'Hebron University Hospital’s Barcelona-UAB-FOCIS Centre of Excellencecoordinator www.focisnet.org.
We have also established intense bilateral relations and shared projects with, among others, the following centres:
The Immunology Department laboratories have ISO 9001 certification, as do the hospital’s other clinical laboratories.
The Immunology Department has a broad, up-to-date portfolio of diagnostic services that responds to the majority of hospital patients’ needs and those of the hospital catchment area.
The main components studied are immunoglobins, complement and regulatory proteins common to the complement and coagulation cascades. To evaluate immune response in patients with suspected immunodeficiency, the levels of immunoglobulins are measured and characterised: classes, subclasses, monoclonal components, cryoglobulins and free chains, as well as the production of IgG antibodies against polysaccharide and peptide antigens.
Complement activity along the traditional and alternative pathways is measured, as well as the main components C3, C4, C1q and C1 inhibitor. If the departments request them, special studies are conducted to measure the function of other complement pathways and the other components that make up the complement, as well as its regulatory factors.
Molecular studies have also been carried out that serve to diagnose patients with hereditary angioedema (SERPING1 and F12), patients with infections from encapsulated microorganisms (C5 and C2) and patients with abnormalities due to reduction in immune complexes (C4 haplotypes).
The laboratory has modern capillary electrophoresis, immunofixation and isoelectric focusing equipment. It also has a huge catalogue of disease samples and a digital file of cases of patients with monoclonal gammopathy, cryoglobulinaemia, etc.
This section is dedicated to the study of primary and secondary immunodeficiency, including HIV infection (secondary immunodeficiency), the results of treatment with depletion and immunomodulating agents and transplant of blood stem cells.
With this in mind, the following are conducted:
Phenotype studies and quantitative analysis of the main lymphocyte populations (T CD4+, T CD8+, NK and B lymphocytes) through flow cytometry applied above all to monitoring patients.
Phenotype studies aimed at diagnosing primary immunodeficiency by assessing naive and memory T cells (CD45RO/RA), degree of activation (CD3/HLA-DR/CD25/CD69) and minority T and NK populations such as γδ and NKT. We work with standardised panels following the FITMaN protocol (Flow Immunophenotyping Technical Meeting at NIH), which allows 30 subgroups of T, B and NK cells, monocytes and dendrites to be studied at the same time.
Research into lymphocyte function, in which the proliferation capacity, the production of cytokines, activation markers and the oxidative and cytolytic capacity of the different cell populations are assessed.
Should haemophagocytic syndromes be diagnosed, cytotoxic NK activity is studied, along with degranulation capacity, through the analysis of CD107a expression in NK cells and CD8, as well as perforin expression.
When it comes to diagnosis and monitoring of phagocytosis defects, an oxidation test and a reduction in ferricytochrome C, tests aimed at diagnosing chronic granulomatous disease, are conducted.
The department has two flow cytometers with two and three lasers respectively, with an automatic sample processing and preparation system, and the corresponding IT analysis programmes. There is also a full installation for cell cultures and another to process level 3 radioactive samples.
The Immunology Department, in collaboration with the genetics department, has a catalogue of 300 genetic studies for the diagnosis of primary immunodeficiency. These studies include severe combined immunodeficiency (SCID), antibody disorders, familial haemophagocytic lymphohistiocytosis (FHLH), innate immune defects and the main complement deficiencies.
In order to provide a highly specialised service, functional tests on the proteins associated with primary immunodeficiency are conducted using western blot or flow cytometry tests. Studies can confirm that gene mutations are pathogenic and affect the proteins they codify.
This section examines alleles and/or haplotypes associated with diseases (coeliac, ankylosing spondylitis, Behçet's disease, narcolepsy and others) and hypersensitivity to drugs (Abacavir).
The Allergy Section performs tests aimed at identifying the allergies that cause hypersensitive reactions due to IgE or IgG. The Allergy Division establishes total IgE, as well as specific IgE versus allergens originating from food and inhaled allergens of different origins, both animal and vegetable (mites, pollen, grasses, epithelial tissues of animal origin, etc.). In total there is evidence to measure specific IgEs against more than 250 allergens.
Levels of tryptase in the blood are also measured to diagnose anaphylaxis.
A group of inhaled allergens of avian or fungal origin (for example, Aspergillus fumigatus), can cause allergic pneumonitis, with a possible evolution into severe pulmonary disease. The determination of specific IgGs versus these allergens contributes to the diagnosis of this group of conditions.
The Allergy Area has Phadia 1000 and Phadia 250 equipment to automatically conduct daily allergy testing. It is anticipated that we will soon be getting ImmunoCAP ISAC technology to determine the specific IgEs against 103 allergens, indicated in polysensitised patients.
The Autoimmune Section supports the diagnosis and monitoring of autoimmune diseases, both those specific to particular organs (such as myasthenia gravis, type I diabetes, autoimmune hepatitis, etc.) and systemic diseases (such as LES, SS and scleroderma).
The screening and characterisation of antinuclear antibodies (ANA), anti-neutrophil cytoplasmic antibodies (ANCA) are performed. Anti-dsDNA antibodies, anti-cyclic citrullinated peptide and anti-transglutaminase antibodies are determined, required for the monitoring and diagnosis of systemic lupus erythematosus, rheumatoid arthritis and coeliac disease, respectively. In total there are techniques to determine autoantibodies against more than 100 antigenic specificities.
The section has equipment to automate the assembly and reading process of indirect immunofluorescence preparations, as well as specialised staff trained to read the microscope and interpret ANA, ANCA and anti-tissue immunofluorescence patterns. It also has robots for the ELISA chemiluminescent assay and immunotransfer technique for the characterisation and quantification of the different antigenic specificities. It holds an image library and collections of positive samples.
An inter-departmental functional unit that interacts with other sections in the department (immunoproteins, cell immunology, autoimmune diseases, etc.). Its objective is to monitor concentration of the biological drug, determine the presence of antibodies against the drug, study the presence of adverse effects and assess the action of the drug at the level of the immune response.
There is a catalogue of rapid response tests (response time <6 hours) in the laboratory, including Acs. Antineutrophil cytoplasmic antibodies (ANCA) for the diagnosis and monitoring of ANCA vasculitis, Acs. Antiphospholipids for catastrophic antiphospholipid syndrome, IL-6 concentration in serum for patients with sepsis or with cytokine release syndrome after treatment with immunotherapy, concentration of IL-6 in amniotic fluid in pregnant women suspected of subclinical chorioamnionitis, serum levels of soluble CD25 in patients with haemophagocytic lymphohistiocytosis and concentration of serum free chains in patients with suspected myeloma kidney.
Diagnosis and follow-up of patients affected by adult immunodeficiency or immune complex pathophysiology is performed. Evaluation of the immune system’s response capacity is crucial to this activity. The outpatient department monitors more than 200 patients and studies 100 new cases every year. There is a transition protocol to incorporate patients being treated by paediatrics when they reach adulthood. Consultation is based on specialised pneumology and digestive tract units, and the day hospital for treatment with intravenous immunoglobulins. Patients are also trained in how to self-administer endovenous immunoglobulins.
The aim of the Clinical Pharmacology Department is to promote a reasoned, safe, effective and efficient use of medication at Vall d'Hebron University Hospital. Together with the Catalan Institute of Pharmacology Foundation, we are a WHO Collaborating Centre for Pharmacoepidemiology Research and Investigation.
Our activities are split into healthcare and institutional support, research, and education and training.
Healthcare and institutional support
Research
Education and Training
See the website of the Catalan Institute of Pharmacology Foundation
The Institute for Diagnostic Imaging uses the most advanced techniques, and contributes to generalising the application of this type of diagnostics to improve care and the quality of image-based explorations and diagnoses.
The Institute for Diagnostic Imaging (IDI) is a state-owned company that is affiliated with Catsalut, and has one of its centres at the Vall d'Hebron Hospital. IDI manages, administers and executes image diagnostic services and nuclear medicine services.
At our hospital, we conduct explorations using: magnetic resonance imaging, computed tomography, nuclear medicine, PET-CT, angiography, ultrasound, mammography, densitometry, conventional radiology, and orthopantomography, among others. This centre is also charged with helping with technological innovation projects, developing research and promoting teaching, thus contributing to scientific and social progress.
IDI and Vall d'Hebron are committed to innovation. In this context, we have PET-CT equipment that allows us to analyse molecular aspects of diseases such as cancer and neurological or cardiovascular disorders. This equipment, which can carry out between 4,000 and 5,000 tests a year, also offers the possibility of introducing new radiopharmaceuticals that improve the management of diseases with a specific molecular profile.
General Hospital
Traumatology Unit
Maternity and Children's Hospital
The mission of the Dermatology Department at the Vall d'Hebron University Hospital is the diagnosis, treatment (medical and surgical) and prevention of diseases of the skin, subcutis, mucous membranes and annexes, as well as the symptoms of systemic diseases that affect the skin and systemic manifestations of skin diseases. The Department is a reference centre in complex dermatological problems that require specialised treatments.
Dermatology in Vall d'Hebron has three main areas of action:
The Department also has specialised clinics for psoriasis, cutaneous lymphomas, ampular epidermolysis, oral mucosal diseases and immuno-allergic dermatosis. We also offer diagnosis, treatment and prevention of sexually transmitted diseases.
The Clinical and Molecular Genetics department consists of: the Clinical Genetics Consultation, the Rare Diseases Functional Unit and the Genetics Laboratory.
The Clinical and Molecular Genetics department is a reference centre in Catalonia in the diagnosis and care of patients with rare genetic diseases, and we are also responsible for significant research and teaching activity.
Our clinical genetic consultation offers comprehensive care for patients with genetic illnesses and their families, based on diagnosis, monitoring, management and genetic counselling.
Our main objective is to create a functional unit around a single diagnostic process, covering everything from the clinical point of view to diagnostic testing, for genetic diseases, taking into account their complexity and the need for comprehensive, multidisciplinary treatment.
We have been officially classified as a member of the first Network of Clinical Expertise Units (XUEC) for the treatment of rare diseases in Catalonia, which is devoted to treating genetic cognitive/behavioural illnesses in children. Created by the Catalan Health Service (CatSalut). Thanks to this recognition, the Clinical Expertise Units (UEC) lead the way in diagnosing and caring for those affected by this type of disease in accordance with the criteria and requirements established by the rare diseases protocol in Catalonia.
Care for patients and relatives in the field of genetics includes four main activities:
More specifically, the clinical activity of the genetic consultation relating to diagnosis of genetic disorders is concentrated in a series of specific functional groups that include:
We pursue several lines of research that are part of Vall d'Hebron Research Institute (VHIR) research groups. This includes the Genetic Medicine Research Group and our collaboration with other groups from Oncogenetics, Mitochondrial Diseases, Endocrinology and Paediatric Pneumology.
Our teaching activity covers undergraduates, postgraduates and continuing education of professionals interested in the field, including theoretical classes, academic placements on the unit, and supervision of final year and master's degree projects. Medical staff from our department participate actively in the following master's programmes:
We also organise seminars and courses for different groups, such as nursing professionals, consultants, residents and educators.
In collaboration with the FEDER (the Spanish Rare Diseases Federation), we have set up ourWorkshops for Patients with Rare Diseases: looking beyond the disease.
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