Source:http://linkedlifedata.com/resource/pubmed/id/12418296
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2002-11-6
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pubmed:abstractText |
In this prospective, randomized and controlled study, we compare complications in 2 groups of patients: group 1, enoxaparin 0.8 mg/kg, subcutaneous every 12 hours during 5 days, and group 2, intravenous unfractionated heparin during 5 days, by infusion treated to activate partial tromboplastin time 1.5-2 the upper limit of normal. Blood samples were obtained at 4, 12, 24 hours and at day 5 of treatment, to measure anti-Xa levels, and also, evaluated end points at 30 days, between groups. Univariate and multivariate logistic regression analyses were performed with clinical and angiographic variables between groups, with p < 0.05. RESULTS: 203 consecutive patients, average age of 60.5 +/- 11.2 years, and 80% men, were included. There were no differences in clinical and angiographic characteristics. All patients with enoxaparin had therapeutic levels of anti-Xa, of 0.5 to 0.67 U/mL. There was increasing risk of total bleeding in group 2 (18.7%) than in group 1 (5.6%), with RR = 1.72 (95% CI 1.29, 2.29), p = .003. Also, there was 33.3% of MACE in group 2, and only 17.8% in group 1, with RR = 1.88 (CI 95% 1.29, 2.29), p = .011. CONCLUSIONS: 1) Low doses of enoxaparine achieve therapeutic levels, since the first 4 hours of treatment. 2) A significant reduction of total bleeding occurred with the low doses of enoxaparin, with the same efficacy to reduce MACE during follow-up.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1405-9940
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pubmed:author |
pubmed-author:Barrera SánchezCarlosC,
pubmed-author:CamposJosé VictoriaJV,
pubmed-author:Cardozo ZepedaCarlosC,
pubmed-author:Chuquiure ValenzuelaEduardoE,
pubmed-author:Cortina de la RosaEvelynE,
pubmed-author:González PachecoHéctorH,
pubmed-author:Izaguirre AvilaRaúlR,
pubmed-author:Juárez HerreraUrsuloU,
pubmed-author:Lupi HerreraEuloE,
pubmed-author:Martínez SánchezCarlosC,
pubmed-author:Reyes CoronaJesúsJ,
pubmed-author:Rosas PeraltaMartínM,
pubmed-author:Vieyra HerreraGerardoG,
pubmed-author:de la Peña DíazAuroraA,
pubmed-author:de la Peña FernándezAndrésA
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pubmed:issnType |
Print
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
209-19
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12418296-Aged,
pubmed-meshheading:12418296-Angina, Unstable,
pubmed-meshheading:12418296-Anticoagulants,
pubmed-meshheading:12418296-Enoxaparin,
pubmed-meshheading:12418296-Female,
pubmed-meshheading:12418296-Hemorrhage,
pubmed-meshheading:12418296-Heparin,
pubmed-meshheading:12418296-Humans,
pubmed-meshheading:12418296-Male,
pubmed-meshheading:12418296-Middle Aged,
pubmed-meshheading:12418296-Prospective Studies,
pubmed-meshheading:12418296-Risk Factors
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pubmed:articleTitle |
[Decrease of total hemorrhage with reduced doses of enoxaparin in high risk unstable angina. ENHNFAI study. (Enoxaparin vs non-fractionated heparin in unstable angina). Preliminary report].
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pubmed:affiliation |
Unidad Coronaria del Instituto Nacional de Cardiología lgnacio Chávez, INCICH, Juan Badiano No. 1, Col. Sección XVI, Tlalpan, 14080 México, D.F.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
English Abstract,
Randomized Controlled Trial
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