7 results on '"Bourdain, F."'
Search Results
2. Urinary tract infection after acute stroke: Impact of indwelling urinary catheterization and assessment of catheter-use practices in French stroke centers.
- Author
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Net P, Karnycheff F, Vasse M, Bourdain F, Bonan B, and Lapergue B
- Subjects
- Aged, Aged, 80 and over, Female, France epidemiology, Health Care Surveys, Humans, Incidence, Male, Prospective Studies, Urinary Bladder diagnostic imaging, Urinary Retention etiology, Catheters, Indwelling adverse effects, Catheters, Indwelling statistics & numerical data, Stroke complications, Stroke therapy, Urinary Catheterization adverse effects, Urinary Catheterization statistics & numerical data, Urinary Tract Infections epidemiology
- Abstract
Introduction: Urinary catheterization and acute urinary retention increase the risk of urinary tract infection (UTI). Our study aimed to investigate the incidence of UTI following acute stroke at our stroke center (SC) and to assess urinary catheter-care practices among French SCs., Methods: Stroke patients hospitalized within 24h of stroke onset were prospectively enrolled between May and September 2013. Neurological deficit level was assessed on admission using the US National Institutes of Health Stroke Scale (NIHSS). Patients were followed-up until discharge. Indwelling urinary catheterization (IUC) was the only technique authorized during the study. An electronic survey was also conducted among French SCs to assess their practices regarding urinary catheterization in acute stroke patients., Results: A total of 212 patients were included, with 45 (21.2%) receiving indwelling urinary catheters. The overall estimated incidence of UTI was 14.2%, and 18% among patients receiving IUC. On univariate analysis, IUC was significantly associated with older age, longer hospital stays and higher NIHSS scores. Of the 30 SCs that responded to our survey, 19 (63.3%) declared using IUC when urinary catheterization was needed. The main argument given to justify its use was that it was departmental policy to adopt this technique. Also, 27 participants (90%) stated that conducting a study to assess the impact of urinary catheterization techniques on UTI rates in acute stroke patients would be relevant., Discussion: Our results are in accord with previously reported data and confirm the high burden of UTI among acute stroke subjects. However, no association was found between IUC and UTI on univariate analysis due to a lack of statistical power. Also, our survey showed high heterogeneity in catheter-use practices among French SCs, but offered no data to help determine the best urinary catheterization technique., Conclusion: Urinary catheterization is common after acute stroke and a well-known risk factor of UTI. However, as high heterogeneity in catheter-use practices is found among French SCs, randomized studies comparing the efficacy of urinary catheterization techniques in terms of UTI prevention in acute stroke patients are now warranted., (Copyright © 2018 Elsevier Masson SAS. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
3. Posterior reversible encephalopathy syndrome (PRES) and hypomagnesemia: A frequent association?
- Author
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Chardain A, Mesnage V, Alamowitch S, Bourdain F, Crozier S, Lenglet T, Psimaras D, Demeret S, Graveleau P, Hoang-Xuan K, and Levy R
- Subjects
- Adult, Child, Comorbidity, Female, Humans, Hypercalciuria blood, Hypercalciuria complications, Male, Middle Aged, Nephrocalcinosis blood, Nephrocalcinosis complications, Posterior Leukoencephalopathy Syndrome complications, Prevalence, Renal Tubular Transport, Inborn Errors blood, Renal Tubular Transport, Inborn Errors complications, Retrospective Studies, Young Adult, Hypercalciuria epidemiology, Magnesium blood, Nephrocalcinosis epidemiology, Posterior Leukoencephalopathy Syndrome blood, Posterior Leukoencephalopathy Syndrome epidemiology, Renal Tubular Transport, Inborn Errors epidemiology
- Abstract
Posterior reversible encephalopathy syndrome (PRES) is a serious neurological condition encountered in various medical fields. Pathophysiological factor(s) common to PRES cases of apparently unrelated etiologies are yet to be found. Based on the hypothesis that hypomagnesemia might participate in the cascade leading to PRES, our study sought to verify whether hypomagnesemia is frequently associated with PRES regardless of etiology. From a retrospective study of a cohort of 57 patients presenting with PRES of different etiologies, presented here are the findings of 19 patients with available serum magnesium levels (SMLs) during PRES. In the acute phase of PRES, hypomagnesemia was present in all 19 patients in spite of differences in etiology (including immunosuppressive drugs, hypertensive encephalopathy, eclampsia, systemic lupus erythematosus, iatrogenic etiology and unknown). SMLs were within normal ranges prior to PRES and below normal ranges during the first 48h of PRES, with a significant decrease in SMLs during the acute phase. In this retrospective study, constant hypomagnesemia was observed during the acute phase of PRES regardless of its etiology. These results now require larger studies to assess the particular importance of acute hypomagnesemia in PRES and especially the possible need to treat PRES with magnesium sulfate., (Copyright © 2016 Elsevier Masson SAS. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
4. [Multiple system atrophy and Alzheimer's disease: a case report of a rare association of two neuro-degenerative disorders].
- Author
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Rusina R, Bourdain F, and Matej R
- Subjects
- Brain pathology, Cerebellum pathology, Cerebral Cortex pathology, Fatal Outcome, Female, Humans, Immunohistochemistry, Magnetic Resonance Imaging, Middle Aged, Plaque, Amyloid pathology, Alzheimer Disease complications, Alzheimer Disease pathology, Multiple System Atrophy complications, Multiple System Atrophy pathology
- Abstract
Multiple system atrophy (MSA) is a neurodegenerative disorder typically characterised by cerebellar dysfunction, parkinsonism, pyramidal signs and dysautonomy. Cognitive impairement is usually limited to a moderate subcortical dysexecutive syndrom. We report the case of a 62-year-old woman suffering from MSA who progressively developed severe dementia. Neuropathological examination confirmed the diagnosis of definite MSA and also showed histopathological hallmarks of Alzheimer's disease. This association is extremely rare in the literature. Our observation confirmes that franc dementia in MSA should prompt a search for another associated cause and underlines the usefulness of neuropathological verifications in atypical clinical pictures.
- Published
- 2007
- Full Text
- View/download PDF
5. [Pupil-sparing painful oculomotor neuropathy due to a carotico-cavernous aneurysm].
- Author
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Meliksetyan G, Bourdain F, Rodesch G, Condette-Auliac S, Decroix JP, and Graveleau P
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- Aged, Blepharoptosis etiology, Carotid Artery Diseases diagnosis, Carotid Artery Diseases diagnostic imaging, Carotid Artery Diseases therapy, Carotid Artery, Internal, Cerebral Angiography, Diplopia etiology, Embolization, Therapeutic, Female, Humans, Intracranial Aneurysm diagnosis, Intracranial Aneurysm diagnostic imaging, Intracranial Aneurysm therapy, Ischemia etiology, Magnetic Resonance Angiography, Nerve Compression Syndromes etiology, Oculomotor Nerve blood supply, Remission Induction, Strabismus etiology, Carotid Artery Diseases complications, Cavernous Sinus pathology, Intracranial Aneurysm complications, Nerve Compression Syndromes diagnosis, Oculomotor Nerve Diseases etiology, Pupil physiology
- Abstract
Introduction: In third cranial nerve palsy, the lack of mydriasis evokes a noncompressive mechanism. Case report. We report a case of a slightly painful, pure extrinsic third-nerve palsy, complete except for the partial ptosis secondary to the compression by an intracavernous carotid aneurysm. Percutaneous endovascular embolization was followed by complete regression of the palsy within 4 weeks. The pupil may have been spared by the mechanism of compression after the separation of the pupillomotor and extrinsic fibers or the ischemia of the third nerve by its arterial trunk lesion., Conclusion: This case report underlines that brain radiological explorations are necessary in some third-nerve pupil-sparing palsies.
- Published
- 2006
- Full Text
- View/download PDF
6. [Resolution of choreic movements associated with HIV encephalitis with anti-retroviral therapy].
- Author
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Trocello JM, Blanchet A, Bourdain F, Meyohas MC, and Vidailhet M
- Subjects
- AIDS Dementia Complex drug therapy, AIDS Dementia Complex pathology, Adult, Anti-HIV Agents administration & dosage, Anti-HIV Agents pharmacology, Anticonvulsants administration & dosage, Anticonvulsants therapeutic use, Basal Ganglia physiopathology, Chorea drug therapy, Chorea physiopathology, Drug Therapy, Combination, Epilepsy, Tonic-Clonic drug therapy, Epilepsy, Tonic-Clonic etiology, Epilepsy, Tonic-Clonic physiopathology, HIV Protease Inhibitors administration & dosage, HIV Protease Inhibitors therapeutic use, HIV Reverse Transcriptase antagonists & inhibitors, Humans, Magnetic Resonance Imaging, Male, Mental Disorders etiology, Recovery of Function, Reverse Transcriptase Inhibitors administration & dosage, Reverse Transcriptase Inhibitors therapeutic use, Viral Load, AIDS Dementia Complex complications, Anti-HIV Agents therapeutic use, Chorea etiology
- Abstract
Introduction: Infection of the central nervous system with human immunodeficiency virus (HIV) can be associated with movement disorders., Case Report: A case of chorea during HIV encephalitis which responded well to antiretroviral therapy is reported. Choreic movements disappeared with a decrease of MRI lesions observed in basal ganglia., Conclusion: The efficacy of anti-retroviral therapy in choreic movements, a rare syndrome with HIV encephalitis, can be underlined.
- Published
- 2006
- Full Text
- View/download PDF
7. [Guillain-Barré syndrome: from the original description to the modern concepts].
- Author
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Raphael JC, Sharshar T, Bourdain F, and Léger JM
- Subjects
- Electrophysiology, Humans, Polyradiculoneuropathy diagnosis, Polyradiculoneuropathy physiopathology, Polyradiculoneuropathy therapy
- Abstract
Since the original report, acute paralysis and albuminocytologic dissociation have remained hallmarks of the Guillain-Barré syndrome but the initially described favorable outcome with complete motor recovery is not always observed. Guillain-Barré syndrome can be complicated by early respiratory distress, dysautonomia and late functional impairment. The conduction block induced by acute demyelination accounts for the spontaneous neurological improvement. On the other hand, early axonal damage or sustained demyelination can be responsible for residual deficit. The cause and mechanism of the disease still remain unclear. For these patients, general care is essential and should be provided in appropriate hospital units. Today, specific treatment consists of either plasma exchange or high-dose intravenous immunoglobulins; the choice depends on their respective contraindications.
- Published
- 1999
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