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1.
Rev Mal Respir ; 33(1): 5-16, 2016 Jan.
Article in French | MEDLINE | ID: mdl-26163395

ABSTRACT

COLIBRI-COPD is a francophone consultation web portal accessible to pulmonologists in the hospital and in the community. We present this observation which describes the phenotype of COPD patients entered (anthropometry, exposures, addictions, functional impairments, questionnaires: MRC, DIRECT, CAT, HAD, Epworth, co-morbidities, incidence of exacerbations, drug treatment or other treatments). The results of the first 1079 patients show a high level of completeness for the main data items. A comparison of patients seen in outpatient consultations shows significant variability between patients with the same GOLD stage, regarding the incidence of exacerbations, signs of anxiety-depression, of diabetes mellitus, or the prescriptions of anticholinergics and inhaled corticosteroids. These initial results suggest that data collection in real life gives a reliable database to obtain longitudinal data on various aspects of COPD. The data quality (completeness, reliability) is partly related to the usability of the web tool and to the possibility of doing self-assessment of practitioners' own recorded data.


Subject(s)
Databases, Factual , Internet , Pulmonary Disease, Chronic Obstructive , Feasibility Studies , Humans , Quality Improvement
2.
Rev Med Interne ; 35(11): 752-6, 2014 Nov.
Article in French | MEDLINE | ID: mdl-25217794

ABSTRACT

INTRODUCTION: The diagnosis of the antiphospholipid syndrome (APS) is based on clinical and biological criteria including the persistent presence of antiphospholipid antibodies and thrombotic events or pregnancy morbidity. Heparins relayed by vitamin K antagonists (VKA) are the gold standard treatment for thrombosis. CASE REPORT: We report a 17-year-old man who presented with an initially seronegative antiphospholipid syndrome, in whom the diagnosis was late, only obtained after anticoagulation withdrawing, when a catastrophic antiphospholipid syndrome (CAPS) with cutaneous lesions and disseminated intravascular coagulation syndrome occurred. For personal convenience, this patient was initially treated with fondaparinux followed by a new oral anticoagulant (rivaroxaban) before to return to the conventional VKA treatment. CONCLUSION: The "seronegative" APS is a controversial concept reflecting the heterogeneity of antigenic targets for aPL. This diagnosis may be considered after a rigorous work-up, with the help of haemostasis laboratories testing new emerging aPL assays. In APS, the new anticoagulants represent an attractive option needing nevertheless prospective studies to evaluate their safety and efficacy. Lupus anticoagulant detection in patients treated by new oral anticoagulants is not easy by usually recommended coagulation tests.


Subject(s)
Antibodies, Antiphospholipid/blood , Antiphospholipid Syndrome/diagnosis , Antiphospholipid Syndrome/drug therapy , Disseminated Intravascular Coagulation/etiology , Adolescent , Anticoagulants/therapeutic use , Disseminated Intravascular Coagulation/drug therapy , Factor Xa Inhibitors/therapeutic use , Fondaparinux , Humans , Male , Morpholines/therapeutic use , Polysaccharides/therapeutic use , Rivaroxaban , Thiophenes/therapeutic use
3.
Rev Med Interne ; 33(5): e28-30, 2012 May.
Article in French | MEDLINE | ID: mdl-21821322

ABSTRACT

Neutrophilic diseases may have various clinical presentations but share common histopathological manifestations with an aseptic infiltrate of polymorphonuclears neutrophils. The association with various diseases is frequent and must be systematically discussed. We report a patient who presented three different synchronous clinical manifestations of neutrophilic disease: pyoderma gangrenosum, subcorneal pustular dermatosis and aseptic spleen abscesses.


Subject(s)
Abscess/etiology , Neutrophils , Pyoderma Gangrenosum/etiology , Skin Diseases, Vesiculobullous/etiology , Splenic Diseases/etiology , Aged, 80 and over , Humans , Male , Pyoderma Gangrenosum/complications , Skin Diseases, Vesiculobullous/complications , Splenic Diseases/complications
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