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1.
Neurourol Urodyn ; 34(1): 32-6, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24115110

RESUMO

AIMS: Lower urinary tract dysfunctions (LUTD) are very common in Multiple Sclerosis (MS), have a significant social impact, while the organic impact is discussed. We studied urinary complications and their risk factors in our cohort of MS patients, in order to improve the management of LUTD in MS. METHODS: Between 2004 and 2009, all patients affected by MS and managed for LUTD were included in a retrospective study. We studied the epidemiological data (age, gender), the clinical data (duration of MS, EDSS score, progression of MS) and the paraclinical data (urinary creatinine clearance, urine culture, urinary tract ultrasonography and in some cases urodynamic assessment and cystography). We then identified the urinary complications and their risk factors. RESULTS: Three hundred twenty eight patients, mean age 49.9 ± 12.3 years, with a MS for 14.3 ± 10 years on average and with a median EDSS score equal to 6 (1-9), were managed for LUTD. One hundred seventy eight (54%) patients developed one or more urinary complications. We identified duration of MS greater than 8.5 years and an EDSS above 7 as risk factors. CONCLUSION: Urinary complications are common in symptomatic MS, these results imply screening and specialized care to limit the impact on the quality of life but also to prevent urinary complications.


Assuntos
Sintomas do Trato Urinário Inferior/etiologia , Esclerose Múltipla/complicações , Adulto , Fatores Etários , Estudos de Coortes , Progressão da Doença , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Qualidade de Vida , Estudos Retrospectivos , Fatores de Risco
2.
Urology ; 80(4): 852-7, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22939550

RESUMO

OBJECTIVE: To assess the morbidity, mortality, and impact on quality of life and renal function after laparoscopic cystectomy and ileal conduit in patients with multiple sclerosis with lower urinary tract symptom refractory to conservative management. MATERIALS AND METHODS: A prospective study was conducted between February 2004 and December 2010 on 44 consecutive patients with multiple sclerosis who underwent laparoscopic cystectomy and ileal conduit for lower urinary tract symptom. Median Expanded Disability Status Scale score was 8 (6.5-8.5). Mean duration of multiple sclerosis was 19.3 ± 7.9 years. The quality of life was determined using the validated Qualiveen questionnaire preoperatively and at minimum 6 months after the surgery. RESULTS: No conversion to open surgery was required. Postoperative morbidity rate was 18.2%; minor (Clavien ≤ 2) and major (Clavien ≥ 3) complications occurred in 13.6% and 6.8%, respectively. Mean follow-up was 44.5 ± 20.6 months. Complications noted were asymptomatic ureteroileal stenosis (n = 6) and pyelonephritis (n = 3). Neurological status and Expanded Disability Status Scale score remained stable throughout. Renal function remained unchanged. Limitations, constraints, and specific urinary impact index subscores of the Qualiveen were significantly improved at 6 months time. CONCLUSION: Laparoscopic cystectomy and ileal conduit for lower urinary tract symptom in advanced multiple sclerosis is a safe procedure with low complications. Neurological status and renal function remain stable and quality of life improves and continues to remain improved during long-term follow-up, suggesting this to be an attractive option in patients with advanced multiple sclerosis with lower urinary tract symptom refractory to conservative treatment.


Assuntos
Cistectomia , Sintomas do Trato Urinário Inferior/cirurgia , Esclerose Múltipla/complicações , Qualidade de Vida , Derivação Urinária , Adulto , Constrição Patológica/etiologia , Cistectomia/efeitos adversos , Avaliação da Deficiência , Feminino , Humanos , Rim/fisiologia , Laparoscopia/efeitos adversos , Sintomas do Trato Urinário Inferior/etiologia , Masculino , Pessoa de Meia-Idade , Esclerose Múltipla/fisiopatologia , Exame Neurológico , Pielonefrite/etiologia , Inquéritos e Questionários , Ureter/patologia , Derivação Urinária/efeitos adversos
3.
Ann Neurol ; 58(6): 958-63, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16240368

RESUMO

The heterozygous R445H mutation in OPA1 was found in five patients with optic atrophy and deafness. Audiometry suggested that the sensorineural deafness resulted from auditory neuropathy. Skin fibroblasts showed hyperfragmentation of the mitochondrial network, decreased mitochondrial membrane potential, and adenosine triphosphate synthesis defect. In addition, OPA1 was found to be widely expressed in the sensory and neural cochlear cells of the guinea pig. Thus, optic atrophy and deafness may be related to energy defects due to a fragmented mitochondrial network.


Assuntos
GTP Fosfo-Hidrolases/genética , Perda Auditiva Neurossensorial/genética , Atrofia Óptica Autossômica Dominante/genética , Mutação Puntual , Adolescente , Adulto , Animais , Audiometria , Criança , Cóclea/metabolismo , Cricetinae , Feminino , Fibroblastos/metabolismo , Genótipo , Perda Auditiva Neurossensorial/metabolismo , Humanos , Masculino , Mitocôndrias/metabolismo , Atrofia Óptica Autossômica Dominante/metabolismo , Consumo de Oxigênio , Fenótipo , Pele/citologia
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