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1.
Clin Exp Rheumatol ; 40 Suppl 134(5): 3-11, 2022 May.
Article in English | MEDLINE | ID: mdl-35349419

ABSTRACT

In order to address the main challenges related to the rare diseases (RDs) the European Commission launched the European Reference Networks (ERNs), virtual networks involving healthcare providers (HCPs) across Europe. The mission of the ERNs is to tackle low prevalence and RDs that require highly specialised treatment and a concentration of knowledge and resources. In fact, ERNs offer the potential to give patients and healthcare professionals across the EU access to the best expertise and timely exchange of lifesaving knowledge, trying to make the knowledge travelling more than patients. For this reason, ERNs were established as concrete European infrastructures, and this is particularly crucial in the framework of rare and complex diseases in which no country alone has the whole knowledge and capacity to treat all types of patients.It has been five years since their kick-off launch in Vilnius in 2017. The 24 ERNs have been intensively working on different transversal areas, including patient management, education, clinical practice guidelines, patients' care pathways and many other fundamental topics. The present work is therefore aimed not only at reporting a summary of the main activities and milestones reached so far, but also at celebrating the first 5 years of the ERN on Rare and Complex Connective Tissue and Musculo-skeletal Diseases (ReCONNET), in which the members of the network built together one of the 24 infrastructures that are hopefully going to change the scenario of rare diseases across the EU.


Subject(s)
Musculoskeletal Diseases , Rare Diseases , Connective Tissue , Europe , Health Personnel , Humans , Musculoskeletal Diseases/diagnosis , Musculoskeletal Diseases/therapy , Rare Diseases/epidemiology , Rare Diseases/therapy
2.
BMJ Case Rep ; 11(1)2018 Dec 14.
Article in English | MEDLINE | ID: mdl-30567265

ABSTRACT

Sarcoidosis is a multisystemic granulomatous disease with rare renal involvement. We describe a case of a 45-year-old female patient admitted to the hospital with severe acute kidney injury and uveitis. After clinical investigation, sarcoidosis with renal, hepatic and ocular involvement was diagnosed. Renal biopsy revealed acute granulomatous interstitial nephritis and treatment with systemic corticosteroids was started with marked improvement in renal function.


Subject(s)
Hepatomegaly/pathology , Kidney/pathology , Liver/pathology , Nephritis, Interstitial/diagnosis , Sarcoidosis/diagnosis , Uveitis/pathology , Anemia/etiology , Anorexia , Biopsy , Female , Fluid Therapy , Hepatomegaly/diagnostic imaging , Hepatomegaly/etiology , Humans , Methylprednisolone/therapeutic use , Middle Aged , Nephritis, Interstitial/physiopathology , Nephritis, Interstitial/therapy , Prednisolone/therapeutic use , Sarcoidosis/physiopathology , Sarcoidosis/therapy , Treatment Outcome , Uveitis/etiology , Vomiting
3.
Rheumatology (Oxford) ; 57(6): 997-1001, 2018 06 01.
Article in English | MEDLINE | ID: mdl-29529307

ABSTRACT

Objectives: This analysis set out to estimate the risk of opportunistic infection (OI) among patients with RA by biologic class. Methods: The British Society for Rheumatology Biologics Register for Rheumatoid Arthritis is a prospective observational cohort study established to evaluate safety of biologic therapies. The population included adults commencing biologic therapy for RA. The primary outcome was any serious OI excluding tuberculosis (TB). Event rates were compared across biologic classes using Cox proportional hazards with adjustment for potential confounders identified a priori. Analysis of the incidence of TB was performed separately. Results: In total, 19 282 patients with 106 347 years of follow-up were studied; 142 non-TB OI were identified at a rate of 134 cases/100 000 patient years (pyrs). The overall incidence of OI was not significantly different between the different drug classes; however, the rate of Pneumocystis infection was significantly higher with rituximab than with anti-TNF therapy (adjusted hazard ratio = 3.2, 95% CI: 1.4, 7.5). The rate of TB fell dramatically over the study period (783 cases/100 000 pyrs in 2002 to 38 cases/100 000 pyrs in 2015). The incidence of TB was significantly lower among rituximab users than anti-TNF users, with 12 cases/100 000 pyrs compared with 65 cases/100 000 pyrs. Conclusions: The overall rate of OI was not significantly different between drug classes; however, a subtle difference in the pattern of OI was seen between the cohorts. Patient factors such as age, gender and comorbidity were the most important predictors of OI.


Subject(s)
Arthritis, Rheumatoid/complications , Biological Products/therapeutic use , Biological Therapy/methods , Forecasting , Opportunistic Infections/complications , Registries , Rheumatology , Adult , Age Factors , Aged , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/epidemiology , Female , Follow-Up Studies , Humans , Incidence , Male , Middle Aged , Opportunistic Infections/epidemiology , Prospective Studies , Sex Factors , United Kingdom/epidemiology
4.
Case Rep Neurol ; 8(3): 251-257, 2016.
Article in English | MEDLINE | ID: mdl-28101036

ABSTRACT

Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is a rare condition characterized by emotional and behavioral disturbances, dyskinesias, and extrapyramidal signs. It occurs in young women of reproductive age and is classically described as a paraneoplastic phenomenon. We present a 36-year-old, HIV-positive female who was admitted to the hospital in an acute confusional state, with a stiff posture, periods of motor agitation, and myoclonic jerks of the hands. Her mental state progressively deteriorated. Without evidence of infection, the presence of anti-NMDAR antibodies both in serum and cerebrospinal fluid clinched the diagnosis of autoimmune encephalitis. No evidence of neoplastic disease was found, and the beneficial response to immunosuppressive therapy was exceptional. This is the first report of anti-NMDAR encephalitis in an HIV-infected individual, reminding us that autoimmune encephalitis should be included in the differential diagnosis of a young patient presenting in an acute confusional state.

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