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1.
Ann Cardiol Angeiol (Paris) ; 43(3): 160-6, 1994 Mar.
Artigo em Francês | MEDLINE | ID: mdl-8024227

RESUMO

This multicentre, randomised, open trial compared the efficacy and safety/acceptability of calcium nadroparin, a non-steroidal anti-inflammatory drug, naproxen, in the treatment of superficial venous thrombosis of the lower limbs, in 117 patients. Calcium nadroparin was given at two dosage regimens: a fixed dose (daily subcutaneous injection of 0.6 ml, i.e. 6150 anti-Xa IU, n = 38) or a dose adjusted for body weight (31.5 anti-Xa IU/kg, n = 40). The naproxen was given orally (500 mg as a single daily dose, n = 39). Treatment duration was 6 days in both groups. A very marked difference was found to the advantage of calcium nadroparin, although this difference did not reach the threshold of statistical significance with regard to repermeabilisation of the thrombosed superficial vein at the end of treatment. The most striking result concerned the regression of symptoms and signs. At the end of treatment (D7), there was a significant difference to the advantage of the calcium nadroparin groups, particularly regarding feelings of heat and redness (p < 0.001 in both cases). The persistence of symptoms and signs at 8 weeks was statistically less frequent (p = 0.007) in the calcium nadroparin groups than in the naproxen group. Efficacy did not differ between the calcium nadroparin fixed dose and calcium nadroparin weight-adjusted dose groups. No adverse events nor clinically significant laboratory abnormalities were encountered. Antithrombotic treatment of superficial venous thromboses with calcium nadroparin is well tolerated and appears to be associated with a greater improvement in symptoms and signs, in the short and mid-terms, than that obtained with an oral non-steroidal anti-inflammatory.


Assuntos
Nadroparina/uso terapêutico , Naproxeno/uso terapêutico , Tromboflebite/tratamento farmacológico , Adulto , Idoso , Assistência Ambulatorial , Relação Dose-Resposta a Droga , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Nadroparina/administração & dosagem , Nadroparina/efeitos adversos , Estudos Prospectivos , Fatores de Risco , Tromboembolia/prevenção & controle , Tromboflebite/diagnóstico por imagem , Fatores de Tempo , Ultrassonografia
2.
J Urol (Paris) ; 86(3): 167-71, 1980.
Artigo em Francês | MEDLINE | ID: mdl-7400598

RESUMO

The authors report a particularly unusual case of a 71-year-old woman with a complex renal tumour combining a clear cell nephrocarcinoma, an eosinophilic squamous carcinoma and a probably malignant angiomyolipoma. In their view this tumour is reminiscent of that described by Riopelle. Also unusually, the two daughters of this patient also had a nephrocarcinoma.


Assuntos
Neoplasias Renais/patologia , Neoplasias Primárias Múltiplas/patologia , Adenocarcinoma/patologia , Adenoma/patologia , Idoso , Feminino , Hemangioma/patologia , Humanos , Lipoma/patologia
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