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Hospital donations
Research donations
The aim of this project is to optimise screening for sexually transmitted infections (STIs) and the human immunodeficiency virus (HIV) in the asymptomatic population. The Drassanes – Vall d’Hebron STI Unit, together with the Microbiology Laboratory, is the leading centre in Catalonia for the screening and treatment of this type of pathology, receiving around forty thousand visits per year.
The Drassanes Exprés programme provides a rapid response to demand, avoids overloading of the service and makes it easier for the vulnerable population to receive a rapid diagnosis and early treatment.
This programme has created a new fast-track HIV and STI screening service that uses state-of-the-art ICT and molecular biology technologies. It also provides easy access for asymptomatic and vulnerable users, which helps improve the efficiency of the system and reduce saturation in public health care centres.
This innovative project in the treatment and diagnosis of sexually transmitted infections (STIs) and human immunodeficiency virus (HIV) is a continuation of the pilot project launched in 2016. It is included as one of the strategic lines of the 2016-2020 Health Plan of the Regional Government of Catalonia and is subsidised by the European FEDER funds.
How does the rapid circuit work?
Users have direct access to the circuit, without needing to visit their GP first.
If you want to read more information about the rapid circuit, you may visit the Drassanes Express Department page.
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.
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