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Excellence
Accreditations and certifications
Among other things, the hospital's accreditations recognize the clinical experience of its units, its capacity for research, exchanging information and networking, and the training of its professionals and its facilities.

CSUR

The Reference Centres, Services and Units of the National Health System (CSUR) correspond to centres with reference units accredited by the Ministry of Health at a State level for the performance of a technique, technology or procedure or the treatment of certain pathologies or groups of pathologies that require high technology, a high level of specialization or are not very prevalent. They cover the entire national territory, regardless of the patient’s autonomous community of origin.

The Hospital Clínic de Barcelona has 23 accreditations from the Reference Centres, Services and Units (CSUR) of the Ministry of Health. 

  • Pathologies/procedures included and population served:

Adults with diseases that can cause severe alteration of the cornea, thus preventing vision, and for whom there may be an indication for ocular surface reconstruction:

    • Autoimmune diseases: pemphigus, pemphigoid, Stevens-Johnson syndrome, Lyell syndrome, etc.
    • Traumatic: caustic burns, accidents, etc.
    • Neurological: facial paralysis, trigeminal nerve anaesthesia, etc.
    • Infectious: trachoma, viral infections, etc.

Patients with aniridia who require a limbal stem cell transplant during the course of their condition are also included.

  • Pathologies/procedures included and population served:

All types of kidney transplant in recipients under 18 years of age.

  • Pathologies/procedures included and population served:

Pancreas transplantation in adult patients with insulin-dependent diabetes mellitus and end-stage kidney failure.

  • Pathologies/procedures included and population served:

Adults and children with:

CSUR Criteria for the Treatment of resistant osteoarticular infections

  • Pathologies/procedures included and population served:

Adults with congenital heart disease, including heart disease with natural survival and heart disease with some type of therapeutic intervention (surgery or percutaneous procedure) performed in paediatric patients, requiring:

  • Pathologies/procedures included and population served:

Adults with:

CSUR Criteria for Complex mitral valve repair surgery in adults

  • Pathologies/procedures included and population served:

Adults with:

  • Pathologies/procedures included and population served:

Adults and children with Refractory epilepsy.

  • Pathologies/procedures included and population served:

Conditions suitable for functional surgery for movement disorders  (Parkinson's disease, tremors of various causes and dystonia) in adult and paediatric patients who do not achieve adequate symptom control with pharmacological treatment and who meet the criteria for this intervention.

  • Pathologies/procedures included and population served:

Adults and children with:

  • Pathologies/procedures included and population served:

Adults and children with:

    • Highly contagious infections, such as viral haemorrhagic fevers or pneumonic plague.
    • Severe or atypical manifestations of certain tropical diseases such as malaria, severe dengue, or recurrent leishmaniasis (cutaneous or visceral)
    • Tropical diseases that require urgent care, including fevers of unknown origin with criteria of severity.
    • Suspected chronic tropical disease without specific diagnosis.
    • Rare tropical diseases, such as African trypanosomiasis
    • Tropical diseases in patients at special risk, such as immunocompromised individuals.
  • Accredited centre(s): Hospital Clínic de Barcelona and Hospital Sant Joan de Déu
  • Coordinator: Dr José Muñoz
  • Central multidisciplinary team, made up of professionals from the following Services/Units:
  • Contact: sifcoclinico@clinic.cat
  • Other links of interest:

CSUR Criteria for Imported tropical diseases

  • Pathologies/procedures included and population served:

Adults and children with:

  • Pathologies/procedures included:

Adults and children with:

  • Pathologies/procedures included:

Adults with:

  • Pathologies/procedures included:

Adults and children with:

  • Pathologies/procedures included:

Adults and children with:

    • Non-syndromic ichthyosis
    • Syndromic ichthyosis
    • Other rare keratinization disorders (palmoplantar keratoderma, congenital pachyonychia, erythrokeratoderma and Darier’s disease)
  • Accredited centre(s): Hospital Sant Joan de Déu and Hospital Clínic de Barcelona
  • Coordinator (at HCB): Dr Josep Riera
  • Central multidisciplinary team, made up of professionals from the following Services/Units:
  • Contact: sifcoclinico@clinic.cat
  • Other links of interest:

CSUR Criteria for Hereditary keratinization disorders

  • Pathologies/procedures included:

Adults and children with:

  • Pathologies/procedures included:

Adults and children with:

  • Pathologies/procedures included:

Adults and children with:

  • Pathologies/procedures included:

Adults and children with primary immunodeficiency in any of the following groups:

Spanish Immunology Society – Immunodeficiencies group (GISEI)

  • Pathologies/procedures included:

Adults and children with:

    • AA amyloidosis  (as a complication of an autoinflammatory disease)
    • Paediatric granulomatous arthritis
    • CAMPS (pustular psoriasis due to a mutation in the CARD14 gene)
    • Early-onset colitis due to IL-10 deficiency
    • ADA2 deficiency
    • LACC1 deficiency
    • Mevalonate kinase deficiency (mevalonic aciduria and HIDS, or hyperimmunoglobulinemia D syndrome)
    • POLA1 deficiency
    • TRNT1 deficiency
    • Epidermal growth factor receptor (EGFR) deficiency
    • HOIL1 deficiency (autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis) 
    • Familial Mediterranean fever (FMF)
    • A20 haploinsufficiency
    • Autoinflammatory disease associated with NLRP12
    • Autoinflammatory disease due to mutations in the NLRC4 gene
    • Castleman’s disease
    • Still’s disease (systemic-onset juvenile idiopathic arthritis and adult Still’s disease)
    • Autoinflammatory bone diseases: chronic recurrent multifocal osteomyelitis (CRMO) and syndrome with synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO).
    • Idiopathic recurrent pericarditis
    • Cherubism
    • Early-onset sacrcoidosis
    • APLAID syndrome (autoinflammatory syndrome with antiphospholipid deficiency and immune dysregulation associated with the PLCG2 gene)
    • Familial cold autoinflammatory syndrome (FCAS) (familial cold urticaria) (cryopyrinopathy)
    • Pyogenic autoinflammatory syndrome (no known genetic cause)
    • CANDLE syndrome (atypical neutrophilic dermatosis, lipodystrophy and elevated temperature syndrome)
    • CINCA/NOMID syndrome (NOMID: neonatal-onset multisystem inflammatory disease) (cryopyrinopathy)
    • COPA syndrome (syndrome caused by mutations in the COPA gene or autoimmune interstitial lung disease and arthritis syndrome)
    • Aicardi-Goutières syndrome (SAG)
    • Macrophage activation syndrome (as complication of autoinflammatory disease)
    • Blau syndrome
    • Majeed syndrome
    • Muckle-Wells syndrome (MWS) (cryopyrinopathy)
    • Schnitzler syndrome
    • Hyperzincemia and hypercalprotectinemia syndrome (PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome or PAMI syndrome)
    • DIRA syndrome (IL-1 receptor antagonist deficiency)
    • DITRA syndrome (IL-36 receptor antagonist deficiency)
    • H syndrome (mutations in the SLC29A3 gene)
    • PAPA syndrome (pyogenic arthritis, pyoderma gangrenosum and acne syndrome)
    • PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis and lateral cervical adenitis syndrome)
    • APLAID syndrome (autoinflammatory syndrome with antiphospholipid deficiency and immune dysregulation associated with the PLCG2 gene)
    • SAVI syndrome (STING1-associated vasculopathy of infancy)
    • TRAPS syndrome (tumour necrosis factor receptor-associated periodic syndrome)
    • VEXAS syndrome    

Undifferentiated, unspecified or unknown cause autoinflammatory syndromes (or long-standing unexplained fever/inflammatory syndrome)

    • Cryopyrin-associated periodic syndromes (CAPS) (cryropyrinopathies)

Vibratory urticaria

  • Accredited centre/s: Hospital Sant Joan de Déu and Hospital Clínic de Barcelona

Coordinator (at HCB): Dr José Hernández Rodríguez

Systemic Autoimmune Diseases Diagnosis and Treatment

  • Pathologies/procedures included:

Adults with complex hepatic vascular disease:

  • Pathologies/procedures included:

Adults with severe aortic insufficiency requiring surgery.

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