109 results match your criteria: "Centre Hospitalier Universitaire de Fort de France[Affiliation]"

Long-term weight gain in children with craniopharyngioma.

Eur J Endocrinol

May 2024

Paediatric Endocrinology, Diabetology, Gynaecology Department, Necker-Enfants Malades University Hospital, AP-HP Centre, Paris 75015, France.

Objective: Adamantinomatous craniopharyngioma mainly affects children. Excessive weight gain is a major long-term complication. The primary objective of this study was to assess long-term weight changes in children treated for craniopharyngioma.

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[Bilateral congenital blue sclera: Case report].

J Fr Ophtalmol

December 2023

Service d'ophtalmologie, centre hospitalier universitaire de Fort-de-France, hôpital Pierre-Zobda-Quitman, BP 632 Fort de France 97261, Martinique, France.

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Zolpidem is a sedative drug that has been shown to induce a paradoxical effect, restoring brain function in wide range of neurological disorders. The underlying functional mechanism of the effect of zolpidem in the brain in clinical improvement is still poorly understood. Thus, we aimed to investigate rest brain function to study zolpidem-induced symptom improvement in a patient who developed postoperative pediatric cerebellar mutism syndrome, a postoperative complication characterized by delayed onset transient mutism/reduced speech that can occur after medulloblastoma resection.

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Objective: The aim of this study was to determine the cognitive profile of children with a temporal arachnoid cyst (TAC) and its impact on daily life.

Methods: The authors prospectively analyzed the cognitive and psychological profiles of 100 consecutive children relative to age and cyst characteristics (side, cyst size, and cyst shape: convex or nonconvex) and their outcome 4 years later.

Results: Mean IQs were normal but with high heterogeneity on Full Scale IQ (FSIQ; range 59-150); 29% of children had at least one Wechsler index below the norm, in particular, Processing Speed and Working Memory Indexes.

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Objective: The authors' objective was to study clinical, imaging, and neuropsychological changes in children who underwent surgery for a temporal arachnoid cyst (TAC).

Methods: Thirty-four children were prospectively assessed similarly at diagnosis and postoperatively (mean 14 months) with clinic visits, images, cognitive tests, and parental questionnaires on mood/behavior and executive functions. The scores were compared pre- and postoperatively for the entire cohort and individually.

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Prescription of Aminoglycosides in 23 French Neonatal Intensive Care Units.

Antibiotics (Basel)

November 2021

Centre D'Etudes Périnatales de L'Océan Indien (UR 7388), Université de La Réunion, 97410 Saint-Pierre, France.

Article Synopsis
  • * The exposure rates for gentamicin and amikacin were 31.7% and 9.1%, respectively, with a significant majority of treatments starting within the first week of life, and changes in average daily doses noted over the years.
  • * The study found low rates of overdose and underdose for both antibiotics, with factors such as year of admission and prematurity influencing gentamicin overdose rates, suggesting the effectiveness of a
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[Posterior polar hemispheric choroidal dystrophy: Report of a case followed for ten years].

J Fr Ophtalmol

February 2022

Service d'ophtalmologie, centre hospitalier universitaire de Fort-de-France, hôpital Pierre-Zobda-Quitman, BP 632, 97261 Fort-de-France cedex, Martinique, France (French West Indian).

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Bitot's spot in an adult without vitamin A deficiency.

J Fr Ophtalmol

October 2021

Service d'ophtalmologie, hôpital Pierre-Zobda-Quitman, centre hospitalier universitaire de Fort-de-France, CS 90632-97261, 97261 Fort-de-France Cedex, Martinique, France.

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Objectives: The primary objective of this study is to determine the current level of patient medication exposure in Level 3 Neonatal Wards (L3NW). The secondary objective is to evaluate in the first month of life the rate of medication prescription not cited in the Summary of Product Characteristics (SmPC). A database containing all the medication prescriptions is collected as part of a prescription benchmarking program in the L3NW.

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A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management.

Neurology

February 2019

From CHRU de Tours (E.L.), Université François Rabelais de Tours, INSERM U1253, Tours; Neuromuscular Reference Center (C.D., M.D.A., R.G.), AP-HP, Hôpital Pitié-Salpêtrière, Paris; Inserm UMRS872 (M.D.A.), team22, Centre de recherche des Cordeliers, Paris; Service de neurologie pédiatrique (F.A.), pneumologie pédiatrique et médecine infantile, Hôpital de La Timone, Marseille; Service de pédiatrie médicale (N.B.), pôle Femme Enfant, CHU, Caen; Consultation myologie (C.B., I.D.), Cliniques des maladies du développement, Hôpital Necker-Enfants Malades, Paris; Centre hospitalier universitaire de Fort de France (R.B.), unité de neuromyologie, Fort de France; Service de pédiatrie-Neurologie Pôle enfants (C.C.), Hôpital des enfants, CHU Purpan, Toulouse; Service de neurologie pédiatrique (B.C.), pneumologie pédiatrique et médecine infantile, Hôpital de La Timone, Marseille; Service de Neuropédiatrie et Centre de Référence Maladies Neuromusculaires (J.-M.C.), Hôpital Roger-Salengro, Lille; Pôle mère-enfant (J.D.), neuropédiatrie et neurochirgurgie de l'enfant, CHU d'Angers; Service de pédiatrie médicale (C.E.), Hôpital Pellegrin, Bordeaux; Pôle de pédiatrie médico-chirurgicale et génétique Clinique (M.F.), CHU de Rennes-Hôpital Sud, Rennes; Centre de Référence Déficiences Intellectuelles (D. Héron), Département de Génétique et INSERM U975, Groupe hospitalier Pitié-Salpétrière, Paris; Service de neuropédiatrie et pathologie du développement (A.I., M.M.), Hôpital Trousseau, Paris; Service de neurophysiologie enfants et adultes (A.J.-P.), Hôpital F. Mitterrand, Dijon; Centre hospitalier Bretagne Atlantique (H.J.), Vannes; Hôpital de la mère et de l'enfant (C.L.-R.), Dominique Larrey, Limoges; Service de pédiatrie 1 (V.L.), Centre de référence pour les maladies neuromusculaires CENRNEST, Hôpital de Hautepierre-Hôpitaux Universitaires de Strasbourg; CHU Nantes (A.M., Y.P., J.P.-B.), Centre de Référence Maladies Neuromusculaires Nantes-Angers, Hôtel-Dieu, Nantes; Service d'Epileptologie Clinique (V.M.), des Troubles du Sommeil et de Neurologie Fonctionnelle de l'Enfant, Hôpital Femme Mère Enfant, Lyon; Département de pédiatrie et département de génétique médicale (S.P.), Hôpital Morvan, Brest; Département de pédiatrie (S.Q.-R.), Hôpital Raymond Poincaré, Garches; Service d'explorations fonctionnelles pédiatriques (S.R.-M.), Hôpital de Brabois, Vandœuvre-Lès-Nancy; Service de de pédiatrie et de neuropédiatrie (C.R.), Hôpital l'Archet 2, Pôle Femme Mère Enfant, Nice; Département de neuropédiatrie (F.R., U.W.-L.), Hôpital Gui de Chauliac, Montpellier; Service de pédiatrie A-Unité de neurologie pédiatrique (P.S.), American Memorial Hospital, Reims; Centre de référence des neuropathies rares et pathologies neuromusculaires (C.S.), Centre hospitalo-universitaire de Clermont-Ferrand, Clermont-Ferrand; Pôle de Psychiatrie (H.T.), Neurologie et Rééducation Neurologique, CHU Grenoble Alpes, Grenoble; Service de neurologie pédiatrique (C.V.), Pavillon Femme, mère et enfant, Hôpital Charles Nicolle, Rouen; Inserm UMR U955 E10 et Université Paris-Est Créteil (R.G.); Direction de la Recherche et de l'Innovation (D. Hamroun), CHRU de Montpellier; Sorbonne Université (G.B.), INSERM, UMRS974, Neuromuscular Reference Center, AP-HP, Hôpital Pitié-Salpêtrière, Paris; and FILNEMUS (E.L., C.D., M.D.A., F.A., N.B., C.B., R.B., C.C., B.C., J.-M.C., I.D., J.D., C.E., M.F., D. Héron, A.I., A.J.-P., H.J., C.L.-R., V.L., A.M., V.M., M.M., Y.P., J.P.-B., S.P., S.Q.-R., S.R.-M., C.R., F.R., P.S., C.S., H.T., C.V., U.W.-L., R.G., D. Hamroun, G.B.), French Neuromuscular Reference Centers, France.

Objective: To genotypically and phenotypically characterize a large pediatric myotonic dystrophy type 1 (DM1) cohort to provide a solid frame of data for future evidence-based health management.

Methods: Among the 2,697 patients with genetically confirmed DM1 included in the French DM-Scope registry, children were enrolled between January 2010 and February 2016 from 24 centers. Comprehensive cross-sectional analysis of most relevant qualitative and quantitative variables was performed.

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[Bilateral cystoid macular edema on Paclitaxel: Case report].

J Fr Ophtalmol

January 2019

Service d'ophtalmologie, hôpital Pierre-Zobda-Quitman, centre hospitalier universitaire de Fort-de-France, BP 632, 97261 Fort-de-France cedex, Martinique.

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Purpose: To determine whether there is an optic neuropathy (ON) in patients with human T-cell lymphotropic virus type 1 (HTLV-1) infection.

Methods: We included HTLV-1 asymptomatic carriers (a.c.

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Multifocal tuberculosis revealed by spinal tuberculosis in an eleven-year-old Guianese child.

Bull Soc Pathol Exot

October 2017

Service de médecine et chirurgie pédiatrique, centre hospitalier Andrée-Rosemon de Cayenne, F-97306, Cayenne cedex, Guyane française, France.

Multifocal tuberculosis in a child is rare event. Here we report a case of multifocal tuberculosis revealed by spinal tuberculosis in an eleven-year-old French Guianese girl. This observation underlines the difficulties, the consequences of delay, and the necessity of an early diagnosis of this disease for children.

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Background: N-acetylcysteine (NAC) has been suggested to prevent relapse to cocaine seeking. However, the psychological processes underlying its potential therapeutic benefit remain largely unknown.

Methods: We investigated the hallmark features of addiction that were influenced by chronic NAC treatment in rats given extended access to cocaine: escalation, motivation, self-imposed abstinence in the face of punishment, or propensity to relapse.

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European guidelines recommend the routine offer of an HIV test in patients with a number of AIDS-defining and non-AIDS conditions believed to share an association with HIV; so called indicator conditions (IC). Adherence with this guidance across Europe is not known. We audited HIV testing behaviour in patients accessing care for a number of ICs.

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[Pseudo-Coats diagnosed in 58-year-old woman].

J Fr Ophtalmol

November 2015

Service d'ophtalmologie, hôpital Pierre-Zobda-Quitman, centre hospitalier universitaire de Fort-de-France, BP 632, 97261 Fort-de-France cedex, Martinique.

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17th International Conference on Human Retroviruses: HTLV and Related Viruses.

Retrovirology

March 2016

Centre d’Études d’Agents Pathogènes et Biotechnologies pour la Santé, CNRS FRE 3689, Université Montpellier 1, Université Montpellier 2, Montpellier, France

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Myocarditis in Patients With Antisynthetase Syndrome: Prevalence, Presentation, and Outcomes.

Medicine (Baltimore)

July 2015

From the Service de Maladies Infectieuses et Maladies du Sang, Centre Hospitalier de Rochefort (CD); Service de Médecine Interne, Centre Hospitalier Universitaire de Fort de France (CD); Service de Rhumatologie, Centre National de Référence des Maladies Autoimmunes et Systémiques Rares, Hôpitaux Universitaires de Strasbourg (AM, JS); Service de Radiologie Vasculaire et Interventionnelle (PC); Département de Médecine Interne et d'Immunologie Clinique, Centre national de Référence des Maladies Neuromusculaires, DHU I2B, Hôpital Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, Paris (NC, DS, OB, BH); Service de Médecine Interne - Centre national de Référence des Maladies Autoimmunes et Systémiques Rares, Hôpital Claude Huriez, Université de Lille, Lille (GL, EH); and Service de Médecine Interne, Hôpital Haut-Lévêque, Pessac, France (J-LP).

Article Synopsis
  • Antisynthetase syndrome (aSS) involves inflammatory myopathy with myositis-specific autoantibodies and has been associated with myocarditis in about 3.4% of patients.
  • Twelve cases of myocarditis were identified through increased troponin levels and cardiac imaging, with symptoms ranging from asymptomatic to acute cardiac failure.
  • Despite the good overall prognosis, with 75% recovering, myocarditis remains a serious condition that requires careful monitoring in active aSS patients.
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International consensus diagnostic criteria for neuromyelitis optica spectrum disorders.

Neurology

July 2015

From the Departments of Neurology (D.M.W.) and Library Services (K.E.W.), Mayo Clinic, Scottsdale, AZ; the Children's Hospital of Philadelphia (B.B.), PA; the Departments of Neurology and Ophthalmology (J.L.B.), University of Colorado Denver, Aurora; the Service de Neurologie (P.C.), Centre Hospitalier Universitaire de Fort de France, Fort-de-France, Martinique; Department of Neurology (W.C.), Sir Charles Gairdner Hospital, Perth, Australia; the Department of Neurology (T.C.), Massachusetts General Hospital, Boston; the Department of Neurology (J.d.S.), Strasbourg University, France; the Department of Multiple Sclerosis Therapeutics (K.F.), Tohoku University Graduate School of Medicine, Sendai, Japan; the Departments of Neurology and Neurotherapeutics (B.G.), University of Texas Southwestern Medical Center, Dallas; The Walton Centre NHS Trust (A.J.), Liverpool, UK; the Molecular Neuroimmunology Group, Department of Neurology (S.J.), University Hospital Heidelberg, Germany; the Center for Multiple Sclerosis Investigation (M.L.-P.), Federal University of Minas Gerais Medical School, Belo Horizonte, Brazil; the Department of Neurology (M.L.), Johns Hopkins University, Baltimore, MD; Portland VA Medical Center and Oregon Health and Sciences University (J.H.S.), Portland; the Department of Neurology (S.T.), National Pediatric Hospital Dr. Juan P. Garrahan, Buenos Aires, Argentina; the Department of Medicine (A.L.T.), University of British Columbia, Vancouver, Canada; Nuffield Department of Clinical Neurosciences (P.W.), University of Oxford, UK; and the Department of Neurology (B.G.W.), Mayo Clinic, Rochester, MN.

Neuromyelitis optica (NMO) is an inflammatory CNS syndrome distinct from multiple sclerosis (MS) that is associated with serum aquaporin-4 immunoglobulin G antibodies (AQP4-IgG). Prior NMO diagnostic criteria required optic nerve and spinal cord involvement but more restricted or more extensive CNS involvement may occur. The International Panel for NMO Diagnosis (IPND) was convened to develop revised diagnostic criteria using systematic literature reviews and electronic surveys to facilitate consensus.

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[Pseudotumor cerebri in children with sickle cell disease].

J Fr Ophtalmol

January 2015

Service d'ophtalmologie, centre hospitalier universitaire de Fort-de-France, hôpital Pierre-Zobda-Quitman (French West Indies), BP 632, 97261 Fort-de-France cedex, Martinique.

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Evaluation of four commercial real-time RT-PCR kits for the detection of dengue viruses in clinical samples.

Virol J

September 2014

Laboratoire de Virologie, Centre Hospitalier Universitaire de Fort-de-France, and EA 4537, Université des Antilles et de la Guyane, Martinique, France.

Background: Dengue is the most frequent arthropod-borne viral disease worldwide. Because dengue manifestations are similar to those of many other febrile syndromes, the availability of dengue-specific laboratory tests is useful for the differential diagnosis. Timely and accurate diagnosis of dengue virus (DENV) infection is important for appropriate management of complications, pathophysiological studies, epidemiological investigations and optimization of vector-control measures.

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Objective: In accordance with the European Association of Urology guidelines, a second transurethral resection of the bladder (TURB) is recommended for high-grade or T1-category tumors. This practice brings into question the benefit of photodynamic diagnosis (PDD) in reducing the residual disease after TURB in patients with positive results on urine cytology showing high-grade cancer cells.

Methods And Materials: A prospective, bicentric, randomized study comparing white light cystoscopy (WLC)+PDD with hexaminolevulinate arm with WLC alone (control arm) during the first TURB in patients with primary non-muscle-invasive bladder cancer and with positive results on urine cytology showing high-grade cancer cells.

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[Torpedo maculopathy: anatomic and functional description].

J Fr Ophtalmol

January 2014

Service d'ophtalmologie, hôpital Pierre-Zobda-Quitman, centre hospitalier universitaire de Fort-de-France, BP 632, 97261 Fort-de-France cedex, Martinique.

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[An atypical case of cat scratch disease (Bartonellosis)].

J Fr Ophtalmol

February 2014

Service d'ophtalmologie, centre hospitalier universitaire de Fort-de-France, hôpital Pierre-Zobda-Quitman, BP 632, 97261 Fort-de-France cedex, France.

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