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dc.contributor.authorFlabeau, Olivier-
dc.contributor.authorBisson, Thomas-
dc.date.accessioned2022-10-18T07:10:44Z
dc.date.available2022-10-18T07:10:44Z
dc.date.issued2021
dc.identifier.citationFlabeau, Olivier ; Bisson, Thomas ; Le suivi multidisciplinaire de patients adultes atteints de dystrophie myotonique de type 1 dans le Sud Aquitain, Med Sci (Paris), Vol. 37, N° HS ; p. 32-35 ; DOI : 10.1051/medsci/2021190
dc.identifier.issn1958-5381
dc.identifier.urihttp://hdl.handle.net/10608/11975
dc.description.abstractDM1 is characterized by a multisystemic involvement. Our objective was to determine the proportion of adequate follow-up for each affected organ in DM1 patients based on the recently published American and Spanish recommendations. To this end, we conducted a descriptive cross-sectional survey by phone in adult, genetically proven DM1 patients followed in the two French neuromuscular centers of Bayonne and Hendaye located in South Aquitaine, France. The questionnaire selected the most stringent criteria of the two international recommendations for each item of follow-up. Seventy-three patients were included, 55% of which were women (mean age of 48 years) with an average number of 467 CTG repeats. The proportion of patients receiving clinical follow-up in accordance with the recommendations was 90% in cardiology, 60% in neurology, 68% in ophthalmology, 53% in physiotherapy, 23% in pneumology, and 12% in rehabilitation. The high rate of neurological, cardiological, and ophthalmological monitoring might be explained by a locally dense medical demography whereas low rate of respiratory follow up and rehabilitation may reflect an incomplete knowledge of both the disease and the questionnaire. These results should be carefully interpretated as cognitive status may influence such a declarative study. Our study nevertheless disclosed important disparities according to the recommended multidisciplinary follow-up criteria in this French cohort of adult DM1 patients. These results highlight the major role of a multidisciplinary care and monitoring in DM1.en
dc.language.isofr
dc.publisherEDP Sciences
dc.relation.ispartofPrise en charge
dc.rightsArticle en libre accèsfr
dc.rightsMédecine/Sciences - Inserm - SRMSfr
dc.rights.uri
dc.sourceM/S. Médecine sciences [ISSN papier : 0767-0974 ; ISSN numérique : 1958-5381], Vol. 37, N° HS; p. 32-35
dc.subject.meshAdultefr
dc.subject.meshÉtudes de cohortesfr
dc.subject.meshÉtudes transversalesfr
dc.subject.meshFemellefr
dc.subject.meshFrancefr
dc.subject.meshHumainsfr
dc.subject.meshAdulte d'âge moyenfr
dc.subject.meshDystrophie myotoniquefr
dc.subject.meshTechniques de physiothérapiefr
dc.subject.meshthérapiefr
dc.titleLe suivi multidisciplinaire de patients adultes atteints de dystrophie myotonique de type 1 dans le Sud Aquitainfr
dc.title.alternativeMultidisciplinary care of patients with Myotonic Dystrophy type 1 (DM1) in South Aquitaineen
dc.typeArticle
dc.contributor.affiliationCentre de Compétence des Maladies Neuromusculaires de Bayonne, France
dc.contributor.affiliationCentre de Compétence des Maladies Neuromusculaires de Hendaye, France
dc.identifier.doi10.1051/medsci/2021190
dc.identifier.pmid34878392


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