Search Results - "Jego, P."
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Survival and prognosis factors in systemic sclerosis: data of a French multicenter cohort, systematic review, and meta-analysis of the literature
Published in Arthritis research & therapy (03-04-2019)“…Data on survival and prognosis factors in incident cohorts are scarce in systemic sclerosis (SStc). To describe survival, standardized mortality ratio (SMR),…”
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Is it (really) necessary to treat all postmenopausal women receiving corticosteroid therapy with bone preventive therapy?
Published in La revue de medecine interne (01-09-2021)Get full text
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Combined pulmonary fibrosis and emphysema in systemic sclerosis: A syndrome associated with heavy morbidity and mortality
Published in Seminars in arthritis and rheumatism (01-08-2019)“…The syndrome of combined pulmonary fibrosis and emphysema (CPFE) primarily due to tobacco smoking has been reported in connective tissue disease, but little is…”
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Uncertainty management and medical skills: A clinical and educational reflexion
Published in La revue de medecine interne (01-06-2019)“…Uncertainty arises when information is not sufficient to predict the prognosis or the outcome following an intervention. It is omnipresent in medical daily…”
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Diagnostic value of 18-F fluorodeoxyglucose PET/CT and bone scan in Schnitzler syndrome
Published in Autoimmunity (Chur, Switzerland) (17-11-2019)“…Introduction: Schnitzler syndrome is an auto-inflammatory disease defined by chronic urticarial eruption and monoclonal gammopathy. 18 F fluorodeoxyglucose…”
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Cessation of oral anticoagulants in antiphospholipid syndrome
Published in Lupus (01-10-2017)“…Objective To study the outcome of patients with antiphospholipid syndrome (APS) after oral anticoagulant treatment cessation. Methods We performed a…”
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Drug‐induced granulomatosis: is dupilumab the new kid on the block?
Published in Journal of the European Academy of Dermatology and Venereology (01-07-2020)“…Dupilumab is an IgG4 antibody directed toward IL-4 and IL-13, two major effectors of the Th2 immunity response. It was originally developed for severe and/or…”
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Using Rituximab Plus Fludarabine and Cyclophosphamide as a Treatment for Refractory Mixed Cryoglobulinemia Associated With Lymphoma
Published in Arthritis care & research (2010) (01-04-2013)“…Objective Treatment of refractory mixed cryoglobulinemia (MC) with severe organ involvement remains challenging. Fludarabine, cyclophosphamide, and rituximab…”
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Dépistage de l’hypertension artérielle pulmonaire au cours de la sclérodermie systémique : comparaison de l’algorithme DETECT à une discussion pluridisciplinaire en centre de compétence [Screening for pulmonary arterial hypertension in patients with systemic sclerosis: Comparison of DETECT algorithm to decisions of a multidisciplinary team, in a competence centre]
Published in La revue de medecine interne (01-08-2017)“…INTRODUCTION: Pulmonary arterial hypertension (PAH) is a severe complication of systemic sclerosis and detecting PAH efficiently remains challenging. The…”
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Libman-Sacks endocarditis under apixaban in a patient with a high-risk profile venous antiphospholipid syndrome
Published in La revue de medecine interne (01-03-2021)“…Libman-Sacks endocarditis is a rare complication of antiphospholipid syndrome. Anti-vitamin K therapy is the standard treatment, although valvular replacement…”
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Aspirin: Indications and use during pregnancy
Published in La revue de medecine interne (01-12-2017)“…Aspirin (acetylsalicylic acid) has been used ever since the Antiquity for its painkilling and anti-inflammatory effects. Its antiplatelet properties have then…”
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Illnesses unrelated to systemic sclerosis (IUSS) diagnosed throughout the patient's follow-up in a referral center: A cohort of 200 patients
Published in La revue de medecine interne (01-08-2020)“…Our work aimed to investigate the illnesses unrelated to systemic sclerosis (IUSS), diagnosed among patients with systemic sclerosis (SSc) throughout their…”
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Intra-cardiac manifestation during adult-onset Still's disease's, a tricuspid vegetation as a rare expression of systemic disease
Published in La revue de medecine interne (01-10-2018)“…Adult-onset Still's Disease is a rare multisystemic inflammatory disease characterized by fever, maculo-papular erythematous rash and arthralgia. Adult-onset…”
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A microcytic sideroblastic anemia successfully treated with B6 vitamin
Published in La revue de medecine interne (01-07-2019)“…Sideroblastic anemia is a rare cause of microcytic anemia, which is characterized by ring sideroblasts on bone marrow aspirate. This anemia can be congenital…”
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Use of a medical discharge sheet for medication reconciliation in an internal medicine department: Assessment of general practitioners' opinion
Published in La revue de medecine interne (01-06-2018)“…Medication reconciliation (MR) is a systematic and comprehensive review of all medication a patient is taking. In this study, a discharge medication sheet…”
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Use of bosentan for digital ulcers related to systemic sclerosis: a real-life retrospective French study of 89 patients treated since specific approval
Published in Scandinavian journal of rheumatology (01-10-2014)“…Objectives: Ischaemic digital ulcers (DUs) are a common complication of systemic sclerosis (SSc). This study aimed to characterize patients with SSc and…”
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Reliability and validity of a workbook for assessment of professional competencies of internal medicine residents
Published in La revue de medecine interne (01-07-2019)“…Though several assessment tools for resident professional skills based on workplace direct observation have been validated, they remain scarcely used in…”
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Hereditary thrombophilia testing and its therapeutic impact on venous thromboembolism disease: Results from a retrospective single-center study of 162 patients
Published in La revue de medecine interne (01-10-2016)“…Venous thromboembolic disease is a multifactorial, frequently recurrent pathology, whose treatment is based on anticoagulation. As part of the etiological…”
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