40 results match your criteria: "Centre Hospitalo-Universitaire de Strasbourg.[Affiliation]"
BMC Nephrol
October 2024
Renal Research Division, AURAL, 5 rue Henri Bergson, Strasbourg, 67087, France.
Patients with chronic kidney disease (CKD) on dialysis have a higher mortality rate associated with SARS-CoV-2 infection. Although vaccines are now available, the protective response rates and determinants of humoral response to the vaccine are poorly described in patients on peritoneal dialysis. This was a prospective observational study describing the response rates of detectable and standardized protective antibody titers one month after each mRNA vaccine dose in a cohort of 88 patients on peritoneal dialysis.
View Article and Find Full Text PDFAnaesth Crit Care Pain Med
August 2024
Centre Hospitalo-Universitaire de Nantes, Service d'Anesthésie Réanimation Chirurgicale, Hôpital Laennec, France; INSERM CIC 0004 Immunologie et infectiologie, Université de Nantes, France. Electronic address:
Background: Whether the optimization of cerebral oxygenation based on regional cerebral oxygen saturation (rSO) monitoring reduces the occurrence of cerebral ischemic lesions is unknown.
Methods: This multicenter, randomized, controlled trial recruited adults admitted for scheduled carotid endarterectomy. Patients were randomized between the standard of care or optimization of cerebral oxygenation based on rSO monitoring using near-infrared spectroscopy.
Bone Marrow Transplant
June 2024
Université de Paris Cité, AP-HP, Hôpital Robert Debré, Service de Physiologie Pédiatrique -Centre du Sommeil, INSERM NeuroDiderot, Paris, France.
The primary objective of our multicenter prospective study was to describe the incidence of late-onset non-infectious pulmonary complications (LONIPCs) in children undergoing hematopoietic cell transplantation (HCT) using sensitive criteria for pulmonary function test (PFT) abnormalities including the non-specific pattern of airflow obstruction. Secondary objectives were to assess the factors associated with LONIPC occurrence and the sensitivity of the 2014 NIH-Consensus Criteria of bronchiolitis obliterans syndrome (BOS). PFT and clinical assessment were performed prior to HCT and at 6, 12, 24, and 36 months post-HCT.
View Article and Find Full Text PDFAm J Hematol
July 2023
French Reference Center for Histiocytosis, Department of Pediatric Hematology and Oncology, Trousseau Hospital, AP-HP, Sorbonne Université, Paris, France.
The spectrum of somatic mutations in pediatric histiocytoses and their clinical implications are not fully characterized, especially for non-Langerhans cell histiocytosis (-LCH) subtypes. A cohort of 415 children with histiocytosis from the French histiocytosis registry was reviewed and analyzed for BRAF . Most BRAF samples were analyzed by next-generation sequencing (NGS) with a custom panel of genes for histiocytosis and myeloid neoplasia.
View Article and Find Full Text PDFRev Neurol (Paris)
April 2023
Service de neurologie, hôpitaux universitaires de Strasbourg, Strasbourg, France; Inserm-U964/CNRS-UMR7104, Institut de génétique et de biologie moléculaire et cellulaire (IGBMC), université de Strasbourg, Illkirch, France; Centre de référence des maladies neurogénétiques rares, Centre Hospitalo-Universitaire de Strasbourg, Strasbourg, France; Fédération de médecine translationnelle de Strasbourg (FMTS), université de Strasbourg, Strasbourg, France. Electronic address:
Clin Kidney J
September 2022
AURAL Alsace, Strasbourg, France.
Background: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is more frequent and severe in patients with chronic kidney disease (CKD) on maintenance haemodialysis (HD). Vaccines are now available, but the protective response rates and determinants of humoral response to the vaccine are poorly described.
Methods: This prospective observational study describes the response rates of detectable and protective antibody titres 1 month after each dose of an mRNA vaccine in a cohort of 851 patients on maintenance HD.
J Fr Ophtalmol
April 2022
Service d'ophtalmologie, Centre hospitalo-universitaire de Strasbourg, 1, place de l'hôpital, 67000 Strasbourg, France.
Introduction: In almost 50 % of cases, acute or chronic screen exposure is accompanied by symptoms of dry eye or binocular imbalance, known as digital eye strain. This phenomenon is described relatively little in the literature. The goal of this study is to determinate the effects of screen exposure on subjective comfort and binocular balance.
View Article and Find Full Text PDFTravel Med Infect Dis
December 2021
Grupo de Investigación Biomedicina, Faculty of Medicine, Fundación Universitaria Autónoma de las Américas, Pereira, Risaralda, Colombia; Master of Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Perú.
Background: In this cross-sectional, international study, we aimed to analyze vector-borne and zoonotic infections (VBZI), which are significant global threats.
Method: VBZIs' data between May 20-28, 2018 was collected. The 24 Participatingcountries were classified as lower-middle, upper-middle, and high-income.
J Fr Ophtalmol
December 2021
Service d'ophtalmologie, Centre hospitalo-universitaire de Strasbourg, 1, place de l'hôpital, 67000 Strasbourg, France.
The digital revolution, which has been underway since the 1980's, is disrupting our daily routines with an exponential increase in the use of screens, which has not been without consequence to our visual system. Digital eye strain (DES), or computer vision syndrome (CVS), includes all the visual symptoms secondary to the use of digital devices. DES is present in at least 50% of regular users of digital media and is defined by blurred vision, difficulty focusing, ocular irritation or burning, dry eye, visual fatigue, headaches and increased sensitivity to light.
View Article and Find Full Text PDFAnn Chir Plast Esthet
February 2021
Service de chirurgie plastique esthétique et reconstructrice, centre hospitalo-universitaire de Bordeaux, GH Pellegrin Centre François-Xavier Michelet, place Amélie-Raba-Léon, 33000 Bordeaux, France.
Introduction: The purpose of this study was to assess the efficacy of magnetic resonance imaging, ultrasound and mammography in detecting breast implant rupture.
Methods: This retrospective study included all cases of breast implant revision. Implant integrity was determined preoperatively by magnetic resonance imaging, ultrasound and mammography.
J Crohns Colitis
March 2021
INSERM, UMR1163, Laboratory of Intestinal Immunity, and Imagine Institute, Paris, France.
Br J Haematol
December 2020
French Reference Center for Langerhans Cell Histiocytosis, Trousseau Hospital, Paris, France.
The nucleoside analogue, 2-chlorodeoxyadenosine (2CDA), was reported to be an active treatment for childhood Langerhans cell histiocytosis (LCH) without risk organ (RO-) involvement. However, we lack data on long-term effects of 2CDA treatment, including the disease reactivation rate, permanent sequelae and long-term tolerance. This study included 44 children from the French LCH registry, treated for a RO- LCH with 2CDA monotherapy (median number of six courses).
View Article and Find Full Text PDFJ Gynecol Obstet Hum Reprod
September 2020
Assistance Publique-Hôpitaux de Paris, 75004, Paris, France.
Objective: To describe the course over time of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in French women from the beginning of the pandemic until mid-April, the risk profile of women with respiratory complications, and short-term pregnancy outcomes.
Methods: We collected a case series of pregnant women with COVID-19 in a research network of 33 French maternity units between March 1 and April 14, 2020. All cases of SARS-CoV-2 infection confirmed by a positive result on real-time reverse transcriptase polymerase chain reaction tests of a nasal sample and/or diagnosed by a computed tomography chest scan were included and analyzed.
Bull Cancer
May 2020
Institut Gustave-Roussy, Villejuif, France.
Ann Chir Plast Esthet
April 2020
Service de chirurgie plastique esthétique et reconstructrice, centre hospitalo-universitaire de Strasbourg, hôpital de Hautepierre, avenue Molière, 67200 Strasbourg, France.
Introduction: The need of iterative surgeries, the proximity of two anatomical areas, the combination of an aesthetic surgery with a surgery covered by health insurance are the reasons which motivated the authors to provide a simultaneous procedure on arms and breast in patients achieving massive weight loss. We propose a vertical continuation of the lateral mastopexy incision superiorly, in continuity with a simultaneous brachioplasty incision to treat the excess skin and subcutaneous tissue of the lateral chest wall, either by resection, or by increasing the breast with the patients own autologous tissue.
Methods: Between 2010 and 2017, twelve patients aged between 31 and 56 years, with 42 being the average, have undergone a technique that utilises a vertical continuation of the lateral mastopexy incision superiorly, in continuity with a simultaneous brachioplasty incision: transverse skin incisions and free nipple transplantation for correction of extreme gynaecomastia (2 cases), mastopexy with resection of the excess tissue of the lateral chest wall (8 cases), autologous breast augmentation by the use of intercostal artery perforator flaps (2 cases).
Ann Intensive Care
March 2020
Département de Néphrologie et Transplantation d'organes, Hôpital Rangueil, Intensive Care Unit, Centre Hospitalo-Universitaire de Toulouse, 1, Avenue Jean Poulhes, 31059, Toulouse, France.
Background: Rhabdomyolysis is a life-threatening disease that can lead to severe hyperkalemia, acute kidney injury (AKI) and hypovolemic shock. The predictive factors of AKI and acute to chronic kidney disease (CKD) transition remain poorly described.
Methods: This multicenter retrospective study enrolled 387 patients with severe rhabdomyolysis (CPK > 5000 U/L).
Ann Chir Plast Esthet
August 2019
Service de chirurgie plastique esthétique et reconstructrice, centre hospitalo-universitaire de Strasbourg, hôpital de Hautepierre, avenue Molière, 67200 Strasbourg, France. Electronic address:
Introduction: Breast implant-associated anaplastic large cell lymphoma is a recent pathology; the one known risk factor is breast implantation.
Methods: A retrospective study was conducted on the French BIA-ALCL cases diagnosed by the Lymphopath network and reported to the National Medical Safety Agency (ANSM). Wishing to obtain supplementary data on the prosthetic history of implants, we sent the referent surgeons a questionnaire.
Br J Haematol
September 2019
Paediatric Haematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
Outcomes in childhood T-cell acute lymphoblastic leukaemia (T-ALL) are steadily improving due to intensive therapy. Between 1989 and 2008, 599 children with newly diagnosed T-ALL were enrolled in two successive European Organization for Research and Treatment of Cancer - Children's Leukaemia Group trials (58881 and 58951), both based on the Berlin-Frankfurt-Munster protocol and without cranial irradiation. In the latter trial induction chemotherapy was intensified.
View Article and Find Full Text PDFIntroduction: Prurigo pigmentosa is a rare inflammatory, pruriginous skin disease seen predominantly in young Asian women, with average age of onset in the mid-20s.
Observation: A 25-year-old fair-skinned European woman presented with a two-year history of pruriginous skin lesions recurring fortnightly. The initial lesions were inflammatory papules, which first emerged on the back of the neck before spreading to the shoulders, below the breasts and the back.
Br J Haematol
November 2018
French Reference Centre for Langerhans Cell Histiocytosis, Trousseau Hospital, Paris, France.
Neurodegenerative (ND) complications in Langerhans cell histiocytosis (LCH) are a late-onset but dramatic sequelae for which incidence and risk factors are not well defined. Based on a national prospective registry of paediatric LCH patients, we determined the incidence rate of clinical ND LCH (cND-LCH) and analysed risk factors, taking into account disease extent and molecular characteristics. Among 1897 LCH patients, 36 (1·9%) were diagnosed with a cND-LCH.
View Article and Find Full Text PDFJ Crohns Colitis
August 2018
INSERM, UMR1163, Laboratory of Intestinal Immunity, and Imagine Institute, Paris, France.
Background And Aims: An expanding number of monogenic defects have been identified as causative of severe forms of very early-onset inflammatory bowel diseases [VEO-IBD]. The present study aimed at defining how next-generation sequencing [NGS] methods can be used to improve identification of known molecular diagnosis and to adapt treatment.
Methods: A total of 207 children were recruited in 45 paediatric centres through an international collaborative network [ESPGHAN GENIUS working group] with a clinical presentation of severe VEO-IBD [n = 185] or an anamnesis suggestive of a monogenic disorder [n = 22].
Br J Haematol
August 2017
French Reference Centre for Langerhans Cell Histiocytosis, Trousseau Hospital, Paris, France.
The BRAF mutation is reported in half of patients with Langerhans cell histiocytosis (LCH). This study investigated the detection of the BRAF allele in circulating cell-free (ccf) DNA in a paediatric LCH cohort. Children with BRAF -mutated LCH were investigated to detect ccf BRAF at diagnosis (n = 48) and during follow-up (n = 17) using a picolitre-droplet digital PCR assay.
View Article and Find Full Text PDFJ Clin Rheumatol
October 2016
Service de Rhumatologie, Centre Hospitalo-universitaire de Beni Messous, Algiers, Service de Rhumatologie, Centre Hospitalo-universitaire de Beni Messous, Algiers, Algeria. Service de Rhumatologie, Centre de Référence des Maladies Auto-immunes Rares, Centre Hospitalo-Universitaire de Strasbourg, Strasbourg, France. Département d'Immunologie, Institut Pasteur d'Algérie, Algiers, Algeria. Service de Rhumatologie, Centre de Référence des Maladies Auto-immunes Rares, Centre Hospitalo-Universitaire de Strasbourg, Strasbourg, France. Département d'Immunologie, Institut Pasteur d'Algérie, Algiers, Algeria. Service de Rhumatologie, Centre Hospitalo-universitaire de Beni Messous, Algiers, Algeria.
Br J Haematol
September 2016
Registre français des histiocytoses, Service d'Hémato-oncologie Pédiatrique Hôpital Trousseau, AP-HP, Paris, France.
The French national cohort of children with Langerhans cell histiocytosis (LCH) has included 1478 patients since it was established in 1983. LCH therapeutic strategies substantially changed in 1998, so we have divided the cohort into two 15-year periods. Starting in 1998, therapy duration increased from 6 to 12 months, repeated induction therapy was performed in cases showing a poor response to the first induction with vinblastine and steroids, and refractory disease in a risk organ (RO+) was treated with cladribine and cytarabine.
View Article and Find Full Text PDFMedicine (Baltimore)
May 2015
From the Service de Rhumatologie-Centre de Référence des Maladies Autoimmunes et Systémiques Rares (AMe, JS), Hôpitaux Universitaires de Strasbourg, Fédération de Médecine Translationnelle; Service de Physiologie et d'Explorations Fonctionnelles (AM, BG), Centre Hospitalo-Universitaire de Strasbourg; EA 3072 (AM, BG), "Mitochondrie, Stress Oxydant et Protection Musculaire", Faculté de Médecine, Université de Strasbourg et Fédération de Médecine Translationnelle (FMTS), Strasbourg; Service de Médecine Interne-Centre de Référence des Maladies Autoimmunes et Systémiques Rares (GL, EH), CHRU Lille, Université Lille 2, Lille; Service de Radiologie (GB), Hôpitaux Universitaires de Strasbourg, Strasbourg; Service de Rhumatologie (AD), Hôpital Général de Dôle, Dôle; Service de Rhumatologie (SO, OM), Hôpital Bichat, APHP, Paris; Service de Rhumatologie (AT), Hôpitaux Universitaires de Clermont-Ferrand, Clermont-Ferrand; Service de Rhumatologie (BLG), Hôpitaux Universitaires de Nantes, Nantes; Service de Rhumatologie (LM), Hôpital Général de Colmar, Colmar; Service de Médecine Interne (ALB), Hôpital Général de Douai, Douai; Service de Rhumatologie (MDB); Service de Médecine Interne (CD), Hôpitaux Universitaire de Fort de France, Fort de France; Service de Pneumologie et Réanimation Médicale (MD), Hôpital Pitié-Salpêtrière, APHP, Paris; Service de Rhumatologie et Néphrologie (PC), Centre Hospitalier de Béthune, Béthune; Department de Rhumatologie (GF), Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Avicenne-Jean Verdier-René Muret; INSERM UMR1125 (GF); Sorbonne Paris Cité-Université Paris 13 (GF), Bobigny; Service de Rhumatologie Hôpitaux Universitaires de Lille (RMF), Université de Lille 2, Lille; Service de médecine interne 2, Centre de Référence National pour le Lupus et le Syndrome des Antiphospholipides, institut E3M, Hôpital Pitié Salpêtrière, APHP, Paris, F-75013 (AMa, ZA) ; Département de médecine interne et immunologie clinique, Centre de Référence Maladies Neuro-Musculaires - DHU i2B, Hôpital Pitié- Salpêtrière, APHP, Paris, F-75013 (BH, OB) INSERM UMR-S 1135 (BH, AMa, ZA) & INSERM UMRS974 (BH, OB) Sorbonne Universités, UPMC Univ Paris 06, France.
Anticitrullinated peptide/protein antibodies (ACPA), which are highly specific for rheumatoid arthritis (RA), may be found in some patients with other systemic autoimmune diseases. The clinical significance of ACPA in patients with antisynthetase syndrome (ASS), a systemic disease characterized by the association of myositis, interstitial lung disease, polyarthralgia, and/or polyarthritis, has not yet been evaluated with regard to phenotype, prognosis, and response to treatment. ACPA-positive ASS patients were first identified among a French multicenter registry of patients with ASS.
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