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Dive into the research topics where S. Barbarot is active.

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Featured researches published by S. Barbarot.


British Journal of Dermatology | 2011

Topical corticosteroid phobia in atopic dermatitis: a study of its nature, origins and frequency

Hélène Aubert-Wastiaux; Leïla Moret; A. Le Rhun; A.M. Fontenoy; J.M. Nguyen; Christophe Leux; L. Misery; P. Young; M. Chastaing; N. Danou; Pierre Lombrail; F. Boralevi; J.P. Lacour; J. Mazereeuw-Hautier; J.-F. Stalder; S. Barbarot

Background  Topical corticosteroids remain the mainstay of atopic dermatitis therapy. Many atopic dermatitis therapeutic failures appear to be attributable to poor adherence to treatment due to topical corticosteroid phobia.


Allergy | 2011

Patient‐Oriented SCORAD (PO‐SCORAD): a new self‐assessment scale in atopic dermatitis validated in Europe

J-F Stalder; S. Barbarot; Andreas Wollenberg; E A Holm; L De Raeve; Stefania Seidenari; Arnold P. Oranje; Mette Deleuran; F. Cambazard; Åke Svensson; Dagmar Simon; E Benfeldt; T Reunala; J Mazereeuv; F Boralevi; B. Kunz; L. Misery; Charlotte Gotthard Mortz; Ulf Darsow; Carlo Gelmetti; Thomas L. Diepgen; Johnny Ring; M Moehrenschlager; Uwe Gieler; Alain Taïeb

To cite this article: Stalder J‐F, Barbarot S, Wollenberg A, Holm EA, De Raeve L, Seidenari S, Oranje A, Deleuran M, Cambazard F, Svensson A, Simon D, Benfeldt E, Reunala T, Mazereeuv J, Boralevi F, Kunz B, Misery L, Mortz CG, Darsow U, Gelmetti C, Diepgen T, Ring J, Moehrenschlager M, Gieler U, Taïeb A, for the PO‐SCORAD Investigators Group. Patient‐Oriented SCORAD (PO‐SCORAD): a new self‐assessment scale in atopic dermatitis validated in Europe. Allergy 2011; 66: 1114–1121.


British Journal of Dermatology | 2007

Idiopathic facial aseptic granuloma: a multicentre prospective study of 30 cases.

F. Boralevi; Christine Léauté-Labrèze; S. Lepreux; S. Barbarot; J. Mazereeuw‐Hautier; C. Eschard; Alain Taïeb

Background  Idiopathic facial aseptic granuloma (IFAG) was recently described in a single‐centre retrospective study as a skin condition that occurs specifically in childhood.


Pediatric Dermatology | 2013

Therapeutic Patient Education in Atopic Dermatitis: Worldwide Experiences

J.-F. Stalder; C. Bernier; Alan Ball; Linda De Raeve; Uwe Gieler; Mette Deleuran; Danielle Marcoux; Lawrence F. Eichenfield; Peter A. Lio; Sue Lewis-Jones; Carlo Gelmetti; Roberto Takaoka; C. Chiaverini; L. Misery; S. Barbarot

Therapeutic patient education (TPE) has proven effective in increasing treatment adherence and improving quality of life (QoL) for patients with numerous chronic diseases, especially atopic dermatitis (AD). This study was undertaken to identify worldwide TPE experiences in AD treatment. Experts from 23 hospitals, located in 11 countries, responded to a questionnaire on 10 major items. Patients in TPE programs were mainly children and adolescents with moderate to severe AD or markedly affected QoL. Individual and collective approaches were used. Depending on the center, the number of sessions varied from one to six (corresponding to 2 to 12 hours of education), and 20 to 200 patients were followed each year. Each centers education team comprised multidisciplinary professionals (e.g., doctors, nurses, psychologists). Evaluations were based on clinical assessment, QoL, a satisfaction index, or some combination of the three. When funding was obtained, it came from regional health authorities (France), insurance companies (Germany), donations (United States), or pharmaceutical firms (Japan, Italy). The role of patient associations was always highlighted, but their involvement in the TPE process varied from one country to another. Despite the nonexhaustive approach, our findings demonstrate the increasing interest in TPE for managing individuals with AD. In spite of the cultural and financial differences between countries, there is a consensus among experts to integrate education into the treatment of eczema.


Pediatric Dermatology | 2013

Therapeutic patient education in children with atopic dermatitis: position paper on objectives and recommendations

S. Barbarot; C. Bernier; Mette Deleuran; Linda De Raeve; Lawrence F. Eichenfield; May El Hachem; Carlo Gelmetti; Uwe Gieler; Peter A. Lio; Danielle Marcoux; Marie Morren; Antonio Torrelo; J.-F. Stalder

Poor adherence is frequent in patients with atopic dermatitis (AD), leading to therapeutic failure. Therapeutic patient education (TPE) helps patients with chronic disease to acquire or maintain the skills they need to manage their chronic disease. After a review of the literature, a group of multispecialty physicians, nurses, psychologists, and patients worked together during two international workshops to develop common recommendations for TPE in AD. These recommendations were structured as answers to nine frequently asked questions about TPE in AD: What is TPE and what are its underlying principles? Why use TPE in the management of AD? Who should benefit from TPE in AD? How can TPE be organized for AD? What is the assessment process for TPE in AD? What is the evidence of the benefit of TPE in AD? Who are the people involved in TPE? How should TPE be funded in dermatology? What are the limits of the TPE process?


Journal of The International Neuropsychological Society | 2010

Executive dysfunction in children with neurofibromatosis type 1: a study of action planning.

Arnaud Roy; Jean-Luc Roulin; Valérie Charbonnier; Philippe Allain; Luciano Fasotti; S. Barbarot; J.-F. Stalder; Anne Terrien; Didier Le Gall

In this study, we tested the hypothesis that action planning is impaired in children with neurofibromatosis type 1 (NF1). Thirty-six children with NF1 were pair-matched to 36 healthy controls (HC) on age (range, 7-12 years), sex, and parental education level, and both groups were administered three action-planning tasks. To examine the relation of task performance to attention deficit hyperactivity disorder (ADHD), the NF1 group was divided into subsets of children who met or did not meet criteria for ADHD. Children with NF1 performed less well than HC on all planning tasks, and differences remained when controlling for IQ or a measure of visuospatial skill. Both the NF1 with ADHD subset and NF1 without ADHD subset performed more poorly than HC on two of the tasks, whereas only the NF1 with ADHD subset performed worse than HC on the third planning task. The results underscore the importance of evaluating executive function in children with NF1 and suggest that deficits in this domain may be only partially related to ADHD. Planning deficits in children with NF1 may be part of their cognitive phenotype. Identifying these deficits is relevant in determining factors contributing to learning problems and in developing appropriate interventions.


British Journal of Dermatology | 2013

Propranolol-resistant infantile haemangiomas

S. Caussé; H. Aubert; M. Saint‐Jean; E. Puzenat; A.‐C. Bursztejn; C. Eschard; E. Mahé; Annabel Maruani; J. Mazereeuw-Hautier; I. Dreyfus; J. Miquel; C. Chiaverini; O. Boccara; S. Hadj-Rabia; J.‐F. Stalder; S. Barbarot

Propranolol is now widely used to treat severe infantile haemangiomas (IHs). Very few cases of propranolol‐resistant IH (PRIH) are mentioned in the literature.


British Journal of Dermatology | 2015

Psoriasis and obesity in French children: a case–control, multicentre study

E. Mahé; Alain Beauchet; C. Bodemer; A. Phan; A.‐C. Bursztejn; F. Boralevi; A.‐L. Souillet; C. Chiaverini; E. Bourrat; J. Miquel; P. Vabres; S. Barbarot; D. Bessis; C. Eschard; S. Hadj-Rabia

Obesity is more common in adults with psoriasis than in the general population, but there is a lack of data available regarding this association in children.


British Journal of Dermatology | 2012

Factors influencing quality of life in patients with inherited ichthyosis: a qualitative study in adults using focus groups.

J. Mazereeuw-Hautier; I. Dreyfus; S. Barbarot; L. Serrentino; E. Bourdon-Lanoy; Khaled Ezzedine; A. Maza; Isabelle Aujoulat; Anne Le Rhun

Background  There is limited information regarding quality of life in patients with inherited ichthyosis.


Orphanet Journal of Rare Diseases | 2012

Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study

E. Sbidian; Smail Hadj-Rabia; Vincent M. Riccardi; Laurence Valeyrie-Allanore; S. Barbarot; Olivier Chosidow; Salah Ferkal; Diana Rodriguez; P. Wolkenstein; Sylvie Bastuji-Garin

ObjectiveTo identify clinical characteristics associated with internal neurofibromas in children with NF1, as a means of ensuring the early identification of patients at high risk for malignant peripheral nerve-sheath tumors developed from preexisting internal neurofibromas.Patients and methodsWe used data from two NF1 populations, in France and North America, respectively. The French database comprised 1083 patients meeting NIH diagnostic criteria for NF1 and the Neurofibromatosis Institute Database of North America comprised 703 patients. Patients younger than 17 years of age were eligible for our study if they had been evaluated for internal neurofibromas using computed tomography and/or magnetic resonance imaging. Clinical characteristics associated with internal neurofibromas by univariate analysis (P ≤ 0.15) were entered into a multiple logistic regression model after checking for potential interactions and confounding. Multiple imputation was used for missing values.ResultsAmong the 746 children in the two databases, 357 (48%) met our inclusion criteria. Their mean age was 7.7 ± 5.0 years and there were 192 (53.8%) males. Internal neurofibromas were present in 35 (9.8%) patients. Internal neurofibromas developed earlier in females than in males and their prevalence increased during adolescence. Factors independently associated with internal neurofibromas were age (OR = 1.16 [1.07-1.27]), xanthogranulomas (OR = 5.85 [2.18-15.89]) and presence of both subcutaneous and plexiform neurofibromas (OR = 6.80 [1.52-30.44]).ConclusionsSeveral easily recognizable clinical characteristics indicate a high risk of internal neurofibromas in children with NF1 and, therefore, a need for very close monitoring.

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E. Mahé

Necker-Enfants Malades Hospital

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P. Vabres

Necker-Enfants Malades Hospital

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F. Boralevi

Boston Children's Hospital

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D. Bessis

University of Montpellier

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I. Dreyfus

Paul Sabatier University

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