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1.
BMC Nephrol ; 20(1): 149, 2019 04 30.
Artículo en Inglés | MEDLINE | ID: mdl-31039759

RESUMEN

BACKGROUND: Tunnelled dialysis catheter (TC) infections are a major health complication and are associated with increased antibiotic consumption, hospital stays, health costs and mortality. Experimental data provide evidence that Ethenox, a mixture of enoxaparine 1000 U/mL in 40% v/v ethanol, could be a promising lock solution. The aim of the study is to compare an interdialytic lock solution of Ethenox with reference lock solutions, unfractionated heparin (UFH) or citrate 4% for the prevention of TCI in hemodialysis patients. METHOD: This study will monitor a multicentre, prospective, single blind, randomized, controlled, parallel group trial. The main inclusion criteria are patients > 18 years old with end-stage renal disease, treated with chronic hemodialysis/hemodiafiltration three times a week, with incident or prevalent non-impregnated internal jugular TCs inserted for at least 2 weeks and able to give informed consent. Exclusion criteria are TCI in the previous 4 weeks and anti-infective treatment for TCI in the previous 2 weeks. Patients will be randomized to receive either study treatment Ethenox in the intervention group or reference solutions in the control group, unfractionated heparin (UFH) or citrate 4% w/v according to usual practice. The primary outcome measure will be time to first TCIs assessed by an endpoint adjudication committee blinded to the study arm according to predefined criteria. Patients will receive the study treatment for up to 12 months. Intention-to-treat analysis of the primary endpoint will be performed with a marginal Cox proportional hazard model. Prospective power calculations indicate that the study will have 90% statistical power to detect a clinical significant two-fold increase in median infection-free survival if 200 patients are recruited into each arm over a period of 24 months. DISCUSSION: Firm evidence of the efficacy of the Ethenox lock in preventing TCI could be of major clinical benefit for patients. The results of this study will allow the development of new guidelines based on a high level of evidence. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03083184 , date of registration March 17 2017 and European Clinical Trials Database Identifier: EudraCT 2016-A00180-51), date of registration July 11 2016.


Asunto(s)
Antiinfecciosos Locales/administración & dosificación , Infecciones Relacionadas con Catéteres/prevención & control , Enoxaparina/administración & dosificación , Etanol/administración & dosificación , Fibrinolíticos/administración & dosificación , Ensayos Clínicos Controlados Aleatorios como Asunto , Diálisis Renal/instrumentación , Adulto , Catéteres de Permanencia/efectos adversos , Ensayos Clínicos Fase III como Asunto , Supervivencia sin Enfermedad , Combinación de Medicamentos , Francia , Humanos , Análisis de Intención de Tratar , Venas Yugulares , Fallo Renal Crónico/terapia , Estudios Multicéntricos como Asunto , Modelos de Riesgos Proporcionales , Estudios Prospectivos , Diálisis Renal/métodos , Método Simple Ciego
2.
Nephrol Ther ; 4(3): 187-95, 2008 Jun.
Artículo en Francés | MEDLINE | ID: mdl-18243835

RESUMEN

Dystrophic epidermolysis bullosa is a genetic skin disease of which the recessive subtype also named Hallopeau-Siemens is the most severe. It is due to lack of expression of type VII collagen which is essential for dermal anchoring. Severe obstructive uropathies of the urethral and bladder area may occur during the first years of life, in relation to local bullous activity. As in acquired bullous diseases, glomerular complications may occur in the dystrophic form during the second and third decade. They consist mostly in AA amylosis or mesangial immunoglobuline A glomerulonephritis, in relation to chronic inflammation and repeated cutaneous infections. End stage renal failure occurs in most cases. Only haemodialysis was used as suppletive treatment in four patients for a short period.


Asunto(s)
Epidermólisis Ampollosa Distrófica/complicaciones , Insuficiencia Renal/complicaciones , Adulto , Femenino , Humanos , Diálisis Renal , Insuficiencia Renal/terapia
3.
Nephrol Ther ; 1(1): 52-61, 2005 Mar.
Artículo en Francés | MEDLINE | ID: mdl-16895668

RESUMEN

A 29 year-old female patient developed severe arterial hypertension in the beginning of her second pregnancy. Investigations performed at 16 weeks of amenorrhea showed hypokaliemia in relation to severe hyperreninism: plasma active renin was 25 fold normal value, 94% as prorenin (prorenin representing 94% of total renin). Radiological investigations including ultrasonography and MRI disclosed an homogenous and avascular tumor in the right kidney. Its ablation confirmed renin tumor, and allowed recovery from HTA and continuation of pregnancy. This is the 75th reported case in the literature, enabling to make a new statement about diagnostic and therapeutic procedures, which are modified during pregnancy by contra-indication to X-rays and renin-angiotensin-aldosteron axis inhibitors.


Asunto(s)
Neoplasias Renales/diagnóstico , Complicaciones Cardiovasculares del Embarazo/etiología , Complicaciones Neoplásicas del Embarazo/diagnóstico , Renina/metabolismo , Adulto , Femenino , Humanos , Neoplasias Renales/diagnóstico por imagen , Neoplasias Renales/enzimología , Neoplasias Renales/patología , Neoplasias Renales/cirugía , Embarazo , Complicaciones Neoplásicas del Embarazo/diagnóstico por imagen , Complicaciones Neoplásicas del Embarazo/patología , Complicaciones Neoplásicas del Embarazo/cirugía , Radiografía , Resultado del Tratamiento
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