1,100 results match your criteria: "centre hospitalier et universitaire[Affiliation]"

Article Synopsis
  • Whole-exome sequencing (WES) combined with testicular sperm extraction (TESE) offers valuable insights for men experiencing maturation arrest (MA) after a first unsuccessful TESE.
  • Current clinical guidelines lack predictive tests for outcomes in recurrent TESE following MA, and WES could fill this gap, aiding in decision-making.
  • The study analyzed 26 men with idiopathic non-obstructive azoospermia and identified various genetic variants that may impact spermatogenesis, suggesting potential pathways for future research and patient management.
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Objective: Anterior cranial fossa dural arteriovenous fistulas (DAVFs) have been almost exclusively considered as surgical lesions. However, new advances in endovascular technology have made the endovascular treatment (EVT) of ethmoidal DAVFs feasible. The aim of this study was to report the clinical and angiographic outcomes of patients harboring DAVFs of the anterior cranial fossa who had undergone EVT as a first-line approach.

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Introduction: In recent years, the number of patients managed by poison control centres (PCCs) has increased without a proportional increase in the number of physicians. To improve efficiency without neglecting patient follow-up, some PCCs have begun using text messages. We evaluated the difference in response rates between text messaging and traditional telephone follow-up.

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Antibody escape and global spread of SARS-CoV-2 lineage A.27.

Nat Commun

March 2022

Institute of Virology, Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

In spring 2021, an increasing number of infections was observed caused by the hitherto rarely described SARS-CoV-2 variant A.27 in south-west Germany. From December 2020 to June 2021 this lineage has been detected in 31 countries.

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Whole blood versus red cell concentrates for children with severe anaemia: a secondary analysis of the Transfusion and Treatment of African Children (TRACT) trial.

Lancet Glob Health

March 2022

Kenya Medical Research Institute, Wellcome Trust Research Programme, Kilifi, Kenya; Department of Infectious Disease, Institute of Global Health and Innovation, Imperial College London, London, UK. Electronic address:

Article Synopsis
  • The TRACT trial focused on the timing and volume of blood transfusions in children with severe anaemia (hemoglobin <6 g/dL) and assessed mortality rates within 28 days as the primary outcome.
  • A secondary analysis was conducted to investigate the safety and efficacy of different blood components (whole blood vs. red cell concentrates) in children who received immediate transfusions during the trial.
  • Results showed that children who received whole blood had a significantly better hemoglobin recovery at 8 hours compared to those who received red cell concentrates, highlighting potential differences in clinical outcomes based on the type of transfusion.
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New Therapeutic Strategies Have Changed the Natural History of Pediatric Crohn's Disease: A Two-Decade Population-Based Study.

Clin Gastroenterol Hepatol

November 2022

Gastroenterology Unit, Amiens University Hospital, Peritox, Unité Mixte de Recherche I01, Université de Picardie Jules Verne, Amiens, France.

Background & Aims: We evaluated the impact of immunosuppressants (IS) and anti-tumor necrosis factor (TNF) introduction on Crohn's disease (CD) long-term outcomes in a large population-based, pediatric-onset cohort.

Methods: All patients included in the EPIMAD registry with a diagnosis of CD occurring when they were younger than age 17 years and between 1988 and 2011 were followed up retrospectively until 2013. Three diagnostic periods were defined: 1988 to 1993 (period [P]1; pre-IS era), 1994 to 2000 (P2; pre-anti-TNF era), and 2001 to 2011 (P3; anti-TNF era).

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Objectives: Childhood maltreatment, also referred as childhood trauma, increases the severity of bipolar disorders (BD). Childhood maltreatment has been associated with more frequent mood recurrences, however, mostly in retrospective studies. Since scarce, further prospective studies are required to identify whether childhood maltreatment may be associated with the time to recurrence in BD.

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The global approach to rehabilitation following an osteoporotic fragility fracture: A review of the rehabilitation working group of the International Osteoporosis Foundation (IOF) committee of scientific advisors.

Osteoporos Int

March 2022

Department of Public Health, Epidemiology and Health Economics, WHO Collaborating Centre for Public Health Aspects of Musculo-Skeletal Health and Ageing, University of Liège, 4000, Liège, Belgium.

Purpose: To conduct a review of the current state of the evidence for rehabilitation strategies post-fragility fracture.

Methods: Narrative review conducted by the Rehabilitation Working Group of the International Osteoporosis Foundation Committee of Scientific Advisors characterizing the range of rehabilitation modalities instrumental for the management of fragility fractures.

Results: Multi-modal exercise post-fragility fracture to the spine and hip is strongly recommended to reduce pain, improve physical function, and improve quality of life.

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[Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?].

Praxis (Bern 1994)

January 2022

Centre des maladies moléculaires (CMM), Service de Médecine Génétique, Centre Hospitalier et Universitaire Vaudois (CHUV), Lausanne.

Chronic Fatigue: When to Suspect an Inherited Metabolic Disease? Chronic fatigue is a non-specific symptom, frequent in outpatient adults' consultations. Persistent physical fatigue of unknown etiology should prompt the search for rare diseases including inherited metabolic disorder (IMD) after elimination of common causes. The main characteristic of chronic fatigue in IMD is its dynamic nature, worsened by circumstances leading to an increased metabolism such as physical exertion, cold, fasting or infection.

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[Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?].

Praxis (Bern 1994)

January 2022

Zentrum für Molekularkrankheiten (CMM), Abteilung für genetische Medizin, Centre Hospitalier et Universitaire Vaudois (CHUV), Lausanne.

Chronic Fatigue: When to Suspect an Inherited Metabolic Disease? Chronic fatigue is a non-specific symptom, frequent in outpatient adults' consultations. Persistent physical fatigue of unknown etiology should prompt the search for rare diseases including inherited metabolic disorder (IMD) after elimination of common causes. The main characteristic of chronic fatigue in IMD is its dynamic nature, worsened by circumstances leading to an increased metabolism such as physical exertion, cold, fasting or infection.

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Objective: describe the ocular manifestations encounterd in chronic renal failure not on dialysis in order to ensure better management.

Methods: it is a descriptive analytical study, which took place from febrauary 2017 to june 2017. The study was carried out jointly in the Nephrology and Ophortamology departments of the Yopougon hospital and university center.

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Background: The international Choosing Wisely campaign seeks to improve the appropriateness of care, notably through large campaigns among physicians and users designed to raise awareness of the risks inherent in overmedication.

Methods: In deploying the Choosing Wisely campaign, the French Society of Geriatrics and Gerontology chose early operationalization via a tool for clinical audit over a limited area before progressive dissemination. This enabled validation of four consensual recommendations concerning the management of urinary tract infections, the prolonged use of anxiolytics, the use of neuroleptics in dementia syndromes, and the use of statins in primary prevention.

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Intra-articular injection of autologous bone marrow aspirate concentrate in the treatment of osteoarthritis of the thumb first carpometacarpal joint: A pilot study.

Hand Surg Rehabil

February 2022

Service de Chirurgie Plastique, Reconstructrice et Esthétique - Brûlés - Chirurgie de la Main, Centre Hospitalier et Universitaire de Bordeaux, Pellegrin CFXM, Place Amélie-Raba-Léon, 33076 Bordeaux, France; Collège de santé, Université́ de Bordeaux, 146 Rue Léo-Saignat, 33076 Bordeaux, France.

This study aimed to evaluate the effect of bone marrow aspirate concentrate (BMAC) in the treatment of osteoarthritis of the thumb first carpometacarpal joint. Injections were carried out in 27 thumbs. According to the Dell classification, there were 2 stage I, 11 stage II, 13 stage III and 1 stage IV cases.

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Background: Although chromosome rearrangements are responsible for spermatogenesis failure, their impact depends greatly on the chromosomes involved. At present, karyotyping and Y chromosome microdeletion screening are the first-line genetic tests for patients with non-obstructive azoospermia. Although it is generally acknowledged that X or Y chromosome rearrangements lead to meiotic arrest and thus rule out any chance of sperm retrieval after a testicular biopsy, we currently lack markers for the likelihood of testicular sperm extraction (TESE) in patients with other chromosome rearrangements.

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French Hip & Knee Society classification of short-stem hip prostheses: Inter- and intra-observer reproducibility.

Orthop Traumatol Surg Res

February 2022

Société française de chirurgie hanche et genou, 56, rue Boissonnade, 75014 Paris, France.

Introduction: In total hip replacement (THR), a short stem theoretically provides more physiological force transfer to the proximal femur, conserves bone stock and facilitates minimally invasive surgery. On the other hand, such implants involve a learning curve and incur risk of malpositioning or fracture and of secondary mobilization. There are several types of short stem, and classification is needed.

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Prolidase Deficiency Causing Recalcitrant Leg Ulcerations in Siblings.

Adv Skin Wound Care

November 2021

At the Division of Dermatology, Faculty of Medicine, Lebanese University, Beirut, Lebanon, Nancy Hajjar, MD, is Dermatology Resident; Mariam Kabbani, MD, is Dermatology Resident; and Rim Tannous, MD, is Dermatology Resident. Anne-Sophie Lebre, PhD, PharmD, is Biologist, Department of Genetics, Centre Hospitalier et Universitaire de Reims, Hôpital Maison Blanche, Reims, France. Andre Megarbane, MD, PhD, is Chair, Department of Human Genetics, Gilbert and Rose-Mary Chagoury School of Medicine, Byblos, Lebanon. Afaf Minari, MD, is Infectious Diseases Specialist, Department of Internal Medicine Infectious Diseases Division, Rafic Hariri University Hospital, Beirut. Fouad El Sayed, MD, is Professor of Dermatology, Division of Dermatology, Faculty of Medicine, Lebanese University. The authors have disclosed no financial relationships related to this article. Submitted March 16, 2021; accepted in revised form May 11, 2021.

Prolidase deficiency (PD) is a rare autosomal recessive genodermatosis with variable clinical manifestations. It results from a mutation in the peptidase-D gene that leads to abnormal activity of the prolidase enzyme, an important player in collagen catabolism. The authors report the case of two siblings presenting with dysmorphic features, disturbed blood panel, and recalcitrant leg ulcerations of several years' duration.

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[Development of a tool to help optimizing drug prescriptions in pediatric units in Côte d'Ivoire: GOPP tool].

Ann Pharm Fr

May 2022

Laboratoire de pharmacie clinique et thérapeutique, UFR sciences pharmaceutiques et biologiques, université Felix Houphouët-Boigny, Abidjan, Cote d'Ivoire; Service de pharmacologie clinique, centre hospitalier et universitaire de Cocody, Abidjan, Cote d'Ivoire.

Objective: This study aims to develop a tool for optimizing drug management related to clinical and therapeutic contexts of pediatric units in Côte d'Ivoire.

Methodology: A list of Inappropriate prescribings (IPs) was developed from prescription review of inpatients and outpatients aged 1 month to 15 years and followed in pediatric units at 4 Teaching Hospitals of Abidjan during 16 months. A two-round Delphi method was used to validate a qualitative list of IPs by experts according to their level of agreement on a six-point Likert scale of 0-5 (0, no opinion; 5, strongly agree).

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Impact of endometriosis on oocyte morphology in IVF-ICSI: retrospective study of a cohort of more than 6000 mature oocytes.

Reprod Biol Endocrinol

October 2021

Service de Gynécologie Endocrinienne Et Médecine de La Reproduction, CHU Lille, Assistance Médicale À La Procréation Et Préservation de La Fertilité, Hôpital Jeanne de Flandre, Service dAvenue Eugène Avinée, 59000, Lille, France.

Background: Infertility associated with endometriosis can be explained by several non-exclusive mechanisms. The oocyte plays a crucial role in determining embryonic competence and this is particularly relevant for in vitro fertilization (IVF) outcomes. According to some authors, the morphology of oocytes could also be a non-invasive marker of oocyte quality.

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Purpose: A Benchmark Case (BC) was performed as part of the quality assurance process of the randomized phase 2 GORTEC 2014-14 OMET study, testing the possibility of multisite stereotactic radiation therapy (SBRT) alone in oligometastatic head and neck squamous cell carcinoma (HNSCC) as an alternative to systemic treatment and SBRT.

Material And Methods: Compliance of the investigating centers with the prescription, delineation, planning and evaluation recommendations available in the research protocol was assessed. In addition, classical dosimetric analysis was supplemented by quantitative geometric analysis using conformation indices.

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ALCL is a tumor of activated T cells and possibly innate lymphoid cells with several subtypes according to clinical presentation and genetic lesions. On one hand, the expression of transcription factors and cytokine receptors triggers signaling pathways. On the other hand, ALCL tumor cells also produce many proteins including chemokines, cytokines and growth factors that affect patient symptoms.

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Introduction: despite the existence of a preventive vaccine against hepatitis B viral (HBV) infection, approximately 250 million people are infected with the virus worldwide. This study aimed at evaluating the level of knowledge, attitude and seropositivity of the disease among apparently healthy, potential blood donors at the blood service of the Bamenda Regional Hospital Blood Bank.

Methods: a cross-sectional study was carried out from March to May 2019 among 250 blood donors.

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