A randomised trial of subcutaneous low molecular weight heparin (CY 216) compared with intravenous unfractionated heparin in the treatment of deep vein thrombosis. A collaborative European multicentre study.

Abstract:

:The standard treatment of deep vein thrombosis is given by continuous intravenous infusion of unfractionated heparin. This entails hospitalisation, nursing care, immobility and repeated laboratory tests (e.g. activated partial thromboplastin time [APTT], platelet count). In addition approximately 10% of patients suffer major haemorrhages. The potential advantages of a low molecular weight heparin (CY 216) given subcutaneously were explored in a randomised trial with blind quantitative evaluation of venograms. The study included 166 patients and both "therapeutic efficacy" and "intention to-treat" analyses showed that subcutaneous CY 216 in fixed doses based only on body weight was more effective on the Arnesen and Marder phlebographic scores than continuous i.v. standard heparin with daily dose adjustment according to results of coagulation tests. There was no increase in the risks of pulmonary embolism, haemorrhage or clot extension.

journal_name

Thromb Haemost

authors

keywords:

subject

Has Abstract

pub_date

1991-03-04 00:00:00

pages

251-6

issue

3

eissn

0340-6245

issn

2567-689X

journal_volume

65

pub_type

临床试验,杂志文章,多中心研究,随机对照试验
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    doi:

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    doi:

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    doi:

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    pub_type: 临床试验,杂志文章,随机对照试验

    doi:

    authors: David JL,Limet R

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    doi:

    authors: Journet AM,Saffaripour S,Wagner DD

    更新日期:1993-12-20 00:00:00

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    authors: van den Besselaar AM,Ram IE,Alderkamp GH,Bertina RM

    更新日期:1982-08-24 00:00:00

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    doi:

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    authors: Müller-Berghaus G,Kramer W

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    pub_type: 杂志文章,多中心研究,随机对照试验

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