Publications by authors named "Parisot A"

Purpose: To investigate the efficacy and tolerance of systemic treatments for the prevention of HLA-B27-associated acute uveitis (AU) recurrence.

Methods: Retrospective review of patients with HLA-B27-associated uveitis followed in our tertiary center over a 15-year period. Systemic treatments were prescribed to patients with frequent (more than 2 flares per year) or severe uveitis, according to a step-up strategy.

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Article Synopsis
  • The study aimed to evaluate the cost and effectiveness of a standardized approach versus an open approach for diagnosing uveitis.
  • A total of 903 uveitis patients were analyzed, with the standardized strategy costing an average of 182.97 euros per patient, significantly lower than the 251.75 euros for the open strategy.
  • The standardized method resulted in fewer patient visits, radiological procedures, and laboratory tests, making it a more efficient and economical option for diagnosing uveitis.
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Purpose: To describe the characteristics of de novo uveitis in patients ≥ 60 years old.

Methods: Retrospective review of patients with uveitis followed in our tertiary center over a 14-year period. Patients aged 60-70 years and patients aged > 70 years were compared.

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Aim: To assess the usefulness of F-fluorodeoxyglucose positron emission tomography (F-FDG PET/CT) and the predictive factors for the diagnosis of sarcoidosis in patients with uveitis who have normal thoracic tomography.

Methods: We retrospectively reviewed 67 consecutive patients with uveitis of unknown aetiology or a suspected sarcoidosis. All patients with normal thoracic tomography underwent an F-FDG PET/CT, which was blindly reinterpreted.

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Purpose: To describe patients with new onset sarcoid uveitis occurring after an ophthalmic procedure and compare them with patients with sarcoid uveitis without ocular procedure.

Methods: Retrospective analysis of case records from patients with postophthalmic procedure sarcoid uveitis seen at our institution between April 2004 and October 2016. Patients with a previous history of uveitis were not included.

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Article Synopsis
  • The study investigated the effects of brain atrophy on early neurological deterioration (END) and outcomes for severe ischemic strokes treated with intravenous thrombolysis.
  • It included 137 patients with significant stroke severity, analyzing factors influencing both END and long-term recovery.
  • Findings showed that while factors like age, diabetes, and hemorrhage were predictors for END, brain atrophy did not significantly impact risk or outcomes at three months post-treatment.
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Purpose: ULISSE is the only study that prospectively assessed the efficiency of a standardized strategy, compared to an open strategy for the etiologic diagnosis of uveitis. Our aim was to evaluate the diagnostic yield of the tests prescribed in the ULISSE study to clarify their relevance.

Methods: ULISSE is a non-inferiority, prospective, multicenter and cluster randomized study.

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Purpose: To prospectively assess the efficiency of a standardized diagnostic approach, compared to an open strategy, for the etiologic diagnosis of uveitis.

Design: Noninferiority, prospective, multicenter, clustered randomized controlled trial.

Methods: Consecutive patients with uveitis, who visited 1 of the participating departments of ophthalmology, were included.

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Upper respiratory tract (URT) involvement in sarcoidosis may be refractory to corticosteroids and immunosuppressants. Whether TNF-antagonists are efficient and safe in such phenotype is unknown. STAT is a French national drug registry including patients presenting sarcoidosis treated with TNF alpha antagonists.

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Purpose: The sarcoidosis-lymphoma syndrome is a recognised entity. However, the presence of granulomas in patients with a haematological disease should not lead too easily to a diagnosis of sarcoidosis. The presence of granulomatous lesions during the follow-up of these patients raises diagnostic and therapeutic issues.

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Pituitary dysfunction is a rare manifestation of granulomatosis with polyangiitis (GPA) (Wegener). The main aim of this multicenter retrospective study was to describe the characteristics and outcomes of pituitary manifestations in patients with GPA included in the French Vasculitis Study Group database.Among the 819 GPA patients included in the database, 9 (1.

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Spontaneous emergence of phenotypic heterogeneity in cultures of genetically identical cells is a frequently observed phenomenon that provides a simple in vitro experimental system to model the problems of in vivo differentiation. In the present study, we have investigated whether stochastic variation of gene expression levels could contribute to phenotypic change in human cells. We have applied the two fluorescence-coding gene method and the expression variability of the two reporter genes to human cells in culture.

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