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<dc:title>Venographic comparison of subcutaneous low-molecular weight heparin with oral anticoagulant therapy in the long-term treatment of deep venous thrombosis</dc:title>
<dc:creator>González Fajardo, José Antonio</dc:creator>
<dc:creator>Arreba, Emilio</dc:creator>
<dc:creator>Castrodeza Sanz, José Javier</dc:creator>
<dc:creator>Pérez Castrillon, José Luis</dc:creator>
<dc:creator>Fernández, Leopoldo</dc:creator>
<dc:creator>Agundez, Ignacio</dc:creator>
<dc:creator>Mateo, Antonio M.</dc:creator>
<dc:creator>Carrera, Santiago</dc:creator>
<dc:creator>Gutíerrez Alonso, Vicente</dc:creator>
<dc:creator>Vaquero Puerta, Carlos</dc:creator>
<dc:subject>Trombosis-Tratamiento</dc:subject>
<dc:description>Producción Científica</dc:description>
<dc:description>Purpose: The primary objective of this study was to evaluate with venography the rate of&#xd;
thrombus regression after a fixed dose of low–molecular weight heparin (LMWH) per&#xd;
day for 3 months compared with oral anticoagulant therapy for deep venous thrombosis&#xd;
(DVT). Secondary endpoints were the comparisons of the efficacy and safety of both&#xd;
treatments.&#xd;
Methods: This study was designed as an open randomized clinical study in a university hospital&#xd;
setting. Of the 165 patients finally enrolled in the study, 85 were assigned LMWH&#xd;
therapy and 80 were assigned oral anticoagulant therapy. In the group randomized to oral&#xd;
anticoagulant therapy, the patients first underwent treatment in the hospital with standard&#xd;
unfractionated heparin and then coumarin for 3 months. Doses were adjusted with&#xd;
laboratory monitoring to maintain the international normalized ratio between 2.0 and&#xd;
3.0. Patients in the LMWH group were administered subcutaneous injections of fixed&#xd;
doses of 40 mg enoxaparin (4000 anti-Xa units) every 12 hours for 7 days, and after discharge&#xd;
from the hospital, they were administered 40 mg enoxaparin once daily at fixed&#xd;
doses for 3 months without a laboratory control assay. A quantitative venographic score&#xd;
(Marder score) was used to assess the extent of the venous thrombosis, with 0 points indicating&#xd;
no DVT and 40 points indicating total occlusion of all deep veins. The rate of&#xd;
thrombus reduction was defined as the difference in quantitative venographic scores after&#xd;
termination of LMWH or coumarin therapy as compared with the scores obtained on the&#xd;
initial venographic results. The efficacy was defined as the ability to prevent symptomatic&#xd;
extension or recurrence of venous thromboembolism (documented with venograms or&#xd;
serial lung scans). The safety was defined as the occurrence of hemorrhages.&#xd;
Results: After 3 months of treatment, the mean Marder score was significantly decreased&#xd;
in both groups in comparison with the baseline score, although the effect of therapy was&#xd;
significantly better after LMWH therapy (49.4% reduction) than after coumarin therapy&#xd;
(24.5% reduction; P &lt; .001). LMWH therapy and male gender were independently&#xd;
associated with an enhanced resolution of the thrombus. A lower frequency of symptomatic&#xd;
recurrent venous thromboembolism was also shown in patients who underwent&#xd;
treatment with LMWH therapy (9.5%) than with oral anticoagulant therapy (23.7%; P&#xd;
&lt; .05), although this difference was entirely a result of recurrence of DVT. Bleeding&#xd;
complications were significantly fewer in the LMWH group than in the coumarin group&#xd;
(1.1% vs 10%; P &lt; .05). This difference was caused by minor hemorrhages. Coumarin&#xd;
therapy and cancer were independently associated with an enhanced risk of complications.&#xd;
Subcutaneous heparin therapy was well tolerated by all patients.&#xd;
Conclusion: The patients who were allocated to undergo enoxaparin therapy had a significantly&#xd;
greater improvement in their quantitative venographic score, a significantly</dc:description>
<dc:date>2013-09-18T10:19:09Z</dc:date>
<dc:date>2013-09-18T10:19:09Z</dc:date>
<dc:date>1999</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Journal of Vascular Surgery, August, vol.30, n.2. p.283-292</dc:identifier>
<dc:identifier>0741-5214</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/3443</dc:identifier>
<dc:identifier>10.1016/S0741-5214(99)70139-4</dc:identifier>
<dc:identifier>283</dc:identifier>
<dc:identifier>2</dc:identifier>
<dc:identifier>292</dc:identifier>
<dc:identifier>Journal of Vascular Surgery</dc:identifier>
<dc:identifier>30</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Unported</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/</dc:rights>
<dc:format>application/pdf</dc:format>
<europeana:object>https://uvadoc.uva.es/bitstream/10324/3443/6/vaquero31.pdf.jpg</europeana:object>
<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/</europeana:rights>
<europeana:dataProvider>UVaDOC. Repositorio Documental de la Universidad de Valladolid</europeana:dataProvider>
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