Comparison of low-molecular-weight heparin with unfractionated heparin acutely and with placebo for 6 weeks in the management of unstable coronary artery disease fragmin in unstable coronary artery disease study (FRIC)

Low-molecular-weight heparin has a number of pharmacological and pharmacokinetic advantages over unfractionated heparin that make it potentially suitable, when used in combination with aspirin, for the treatment of unstable coronary artery disease. Patients with unstable angina or non-Q-wave myocard...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 1997-07, Vol.96 (1), p.61-68
Hauptverfasser: KLEIN, W, BUCHWALD, A, HILLIS, S. E, MONRAD, S, SANZ, G, TURPIE, A. G. G, VAN DER MEER, J, OLAISSON, E, UNDELAND, S, LUDWIG, K
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container_end_page 68
container_issue 1
container_start_page 61
container_title Circulation (New York, N.Y.)
container_volume 96
creator KLEIN, W
BUCHWALD, A
HILLIS, S. E
MONRAD, S
SANZ, G
TURPIE, A. G. G
VAN DER MEER, J
OLAISSON, E
UNDELAND, S
LUDWIG, K
description Low-molecular-weight heparin has a number of pharmacological and pharmacokinetic advantages over unfractionated heparin that make it potentially suitable, when used in combination with aspirin, for the treatment of unstable coronary artery disease. Patients with unstable angina or non-Q-wave myocardial infarction (1482) were included in the study, which had two phases. In an open, acute phase (days 1 to 6), patients were assigned either twice-daily weight-adjusted subcutaneous injections of dalteparin (120 i.u./kg) or dose-adjusted intravenous infusion of unfractionated heparin. In the double-blind, prolonged treatment phase (days 6 to 45), patients received subcutaneously either dalteparin (7500 i.u. once daily) or placebo. During the first 6 days, the rate of death, myocardial infarction, or recurrence of angina was 7.6% in the unfractionated heparin-treated patients and 9.3% in the dalteparin-treated patients (relative risk, 1.18; 95% confidence interval [CI], 0.84 to 1.66). The corresponding rates in the two treatment groups for the composite end point of death or myocardial infarction were 3.6% and 3.9%, respectively (relative risk, 1.07; 95% CI, 0.63 to 1.80). Revascularization procedures were undertaken in 5.3% and 4.8% of patients in unfractionated heparin and dalteparin groups, respectively (relative risk, 0.88; 95% CI, 0.57 to 1.35). Between days 6 and 45, the rate of death, myocardial infarction, or recurrence of angina was 12.3% in both the placebo and dalteparin groups (relative risk, 1.01; 95% CI, 0.74 to 1.38). The corresponding rates for death or myocardial infarction were 4.7% and 4.3% (relative risk, 0.92; 95% CI, 0.54 to 1.57). Revascularization procedures were undertaken in 14.2% and 14.3% of patients in the placebo and dalteparin groups, respectively. Our results add to previous evidence suggesting that the low-molecular-weight heparin dalteparin administered by twice-daily subcutaneous injection may be an alternative to unfractionated heparin in the acute treatment of unstable angina or non-Q-wave myocardial infarction. Prolonged treatment with dalteparin at a lower once-daily dose in our study did not confer any additional benefit over aspirin (75 to 165 mg) alone.
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E ; MONRAD, S ; SANZ, G ; TURPIE, A. G. G ; VAN DER MEER, J ; OLAISSON, E ; UNDELAND, S ; LUDWIG, K</creator><creatorcontrib>KLEIN, W ; BUCHWALD, A ; HILLIS, S. E ; MONRAD, S ; SANZ, G ; TURPIE, A. G. G ; VAN DER MEER, J ; OLAISSON, E ; UNDELAND, S ; LUDWIG, K</creatorcontrib><description>Low-molecular-weight heparin has a number of pharmacological and pharmacokinetic advantages over unfractionated heparin that make it potentially suitable, when used in combination with aspirin, for the treatment of unstable coronary artery disease. Patients with unstable angina or non-Q-wave myocardial infarction (1482) were included in the study, which had two phases. In an open, acute phase (days 1 to 6), patients were assigned either twice-daily weight-adjusted subcutaneous injections of dalteparin (120 i.u./kg) or dose-adjusted intravenous infusion of unfractionated heparin. In the double-blind, prolonged treatment phase (days 6 to 45), patients received subcutaneously either dalteparin (7500 i.u. once daily) or placebo. During the first 6 days, the rate of death, myocardial infarction, or recurrence of angina was 7.6% in the unfractionated heparin-treated patients and 9.3% in the dalteparin-treated patients (relative risk, 1.18; 95% confidence interval [CI], 0.84 to 1.66). The corresponding rates in the two treatment groups for the composite end point of death or myocardial infarction were 3.6% and 3.9%, respectively (relative risk, 1.07; 95% CI, 0.63 to 1.80). Revascularization procedures were undertaken in 5.3% and 4.8% of patients in unfractionated heparin and dalteparin groups, respectively (relative risk, 0.88; 95% CI, 0.57 to 1.35). Between days 6 and 45, the rate of death, myocardial infarction, or recurrence of angina was 12.3% in both the placebo and dalteparin groups (relative risk, 1.01; 95% CI, 0.74 to 1.38). The corresponding rates for death or myocardial infarction were 4.7% and 4.3% (relative risk, 0.92; 95% CI, 0.54 to 1.57). Revascularization procedures were undertaken in 14.2% and 14.3% of patients in the placebo and dalteparin groups, respectively. Our results add to previous evidence suggesting that the low-molecular-weight heparin dalteparin administered by twice-daily subcutaneous injection may be an alternative to unfractionated heparin in the acute treatment of unstable angina or non-Q-wave myocardial infarction. 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Reticuloendothelial system ; Dalteparin - therapeutic use ; Double-Blind Method ; Drug Administration Schedule ; Drug Therapy, Combination ; Female ; Heparin - therapeutic use ; Humans ; Injections, Intravenous ; Injections, Subcutaneous ; Male ; Medical sciences ; Middle Aged ; Myocardial Infarction - drug therapy ; Patient Compliance ; Pharmacology. Drug treatments ; Prospective Studies ; Treatment Outcome</subject><ispartof>Circulation (New York, N.Y.), 1997-07, Vol.96 (1), p.61-68</ispartof><rights>1997 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. 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G</creatorcontrib><creatorcontrib>VAN DER MEER, J</creatorcontrib><creatorcontrib>OLAISSON, E</creatorcontrib><creatorcontrib>UNDELAND, S</creatorcontrib><creatorcontrib>LUDWIG, K</creatorcontrib><title>Comparison of low-molecular-weight heparin with unfractionated heparin acutely and with placebo for 6 weeks in the management of unstable coronary artery disease fragmin in unstable coronary artery disease study (FRIC)</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Low-molecular-weight heparin has a number of pharmacological and pharmacokinetic advantages over unfractionated heparin that make it potentially suitable, when used in combination with aspirin, for the treatment of unstable coronary artery disease. Patients with unstable angina or non-Q-wave myocardial infarction (1482) were included in the study, which had two phases. In an open, acute phase (days 1 to 6), patients were assigned either twice-daily weight-adjusted subcutaneous injections of dalteparin (120 i.u./kg) or dose-adjusted intravenous infusion of unfractionated heparin. In the double-blind, prolonged treatment phase (days 6 to 45), patients received subcutaneously either dalteparin (7500 i.u. once daily) or placebo. During the first 6 days, the rate of death, myocardial infarction, or recurrence of angina was 7.6% in the unfractionated heparin-treated patients and 9.3% in the dalteparin-treated patients (relative risk, 1.18; 95% confidence interval [CI], 0.84 to 1.66). The corresponding rates in the two treatment groups for the composite end point of death or myocardial infarction were 3.6% and 3.9%, respectively (relative risk, 1.07; 95% CI, 0.63 to 1.80). Revascularization procedures were undertaken in 5.3% and 4.8% of patients in unfractionated heparin and dalteparin groups, respectively (relative risk, 0.88; 95% CI, 0.57 to 1.35). Between days 6 and 45, the rate of death, myocardial infarction, or recurrence of angina was 12.3% in both the placebo and dalteparin groups (relative risk, 1.01; 95% CI, 0.74 to 1.38). The corresponding rates for death or myocardial infarction were 4.7% and 4.3% (relative risk, 0.92; 95% CI, 0.54 to 1.57). Revascularization procedures were undertaken in 14.2% and 14.3% of patients in the placebo and dalteparin groups, respectively. Our results add to previous evidence suggesting that the low-molecular-weight heparin dalteparin administered by twice-daily subcutaneous injection may be an alternative to unfractionated heparin in the acute treatment of unstable angina or non-Q-wave myocardial infarction. Prolonged treatment with dalteparin at a lower once-daily dose in our study did not confer any additional benefit over aspirin (75 to 165 mg) alone.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Angina, Unstable - drug therapy</subject><subject>Anticoagulants - therapeutic use</subject><subject>Aspirin - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation Tests</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Dalteparin - therapeutic use</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Heparin - therapeutic use</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Patient Compliance</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>Treatment Outcome</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGL1DAUxoso6-zq1ZsQRBY9tOY1bTI9SnF1YEFY9BzS9GWma5qMScqw_6p_jRlmmIMX4cEjfL_3vSRfUbwBWgFw-ESh6jcPVccrqDg8K1bQ1k3ZtKx7XqwopV0pWF2_LK5jfMxHzkR7VVx1NeMNrFfFn97PexWm6B3xhlh_KGdvUS9WhfKA03aXyA6PhCOHKe3I4kxQOk3eqYTjRVN6SWifiHLjidtbpXHwxPhAODkg_ookc2mHZFZObXFGl44rFxeTGiwS7UM2DdkjJMxtnCKqiCTv2855NNd_2ZiW8Yl8uHvY9B9fFS-MshFfn_tN8fPuy4_-W3n__eum_3xfatbQVBrQudSAtYE1U5qtWTsYGIwwiipsxVqLjq8bzYAOnDKGtBWGmXZkIDQz7Ka4Pfnug_-9YExynqJGa5VDv0QpOmg5cJ7Bd_-Aj34JLt9N1lDzlnMKGapOkA4-xoBG7sM056dKoPKYuKQgc-Ky4xIkPw68Pbsuw4zjBT9HnPX3Z11FrWz-TaeneMFqIaAFyv4Cxwq4kw</recordid><startdate>19970701</startdate><enddate>19970701</enddate><creator>KLEIN, W</creator><creator>BUCHWALD, A</creator><creator>HILLIS, S. 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G ; VAN DER MEER, J ; OLAISSON, E ; UNDELAND, S ; LUDWIG, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-f1cf1cabe2f183ac3835bf1bf7fa0ae578c79684c310b6033e057f3f5d317c3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Angina, Unstable - drug therapy</topic><topic>Anticoagulants - therapeutic use</topic><topic>Aspirin - administration &amp; dosage</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation Tests</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Dalteparin - therapeutic use</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Heparin - therapeutic use</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Injections, Subcutaneous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Patient Compliance</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KLEIN, W</creatorcontrib><creatorcontrib>BUCHWALD, A</creatorcontrib><creatorcontrib>HILLIS, S. E</creatorcontrib><creatorcontrib>MONRAD, S</creatorcontrib><creatorcontrib>SANZ, G</creatorcontrib><creatorcontrib>TURPIE, A. G. G</creatorcontrib><creatorcontrib>VAN DER MEER, J</creatorcontrib><creatorcontrib>OLAISSON, E</creatorcontrib><creatorcontrib>UNDELAND, S</creatorcontrib><creatorcontrib>LUDWIG, K</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KLEIN, W</au><au>BUCHWALD, A</au><au>HILLIS, S. E</au><au>MONRAD, S</au><au>SANZ, G</au><au>TURPIE, A. G. G</au><au>VAN DER MEER, J</au><au>OLAISSON, E</au><au>UNDELAND, S</au><au>LUDWIG, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of low-molecular-weight heparin with unfractionated heparin acutely and with placebo for 6 weeks in the management of unstable coronary artery disease fragmin in unstable coronary artery disease study (FRIC)</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>1997-07-01</date><risdate>1997</risdate><volume>96</volume><issue>1</issue><spage>61</spage><epage>68</epage><pages>61-68</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>Low-molecular-weight heparin has a number of pharmacological and pharmacokinetic advantages over unfractionated heparin that make it potentially suitable, when used in combination with aspirin, for the treatment of unstable coronary artery disease. Patients with unstable angina or non-Q-wave myocardial infarction (1482) were included in the study, which had two phases. In an open, acute phase (days 1 to 6), patients were assigned either twice-daily weight-adjusted subcutaneous injections of dalteparin (120 i.u./kg) or dose-adjusted intravenous infusion of unfractionated heparin. In the double-blind, prolonged treatment phase (days 6 to 45), patients received subcutaneously either dalteparin (7500 i.u. once daily) or placebo. During the first 6 days, the rate of death, myocardial infarction, or recurrence of angina was 7.6% in the unfractionated heparin-treated patients and 9.3% in the dalteparin-treated patients (relative risk, 1.18; 95% confidence interval [CI], 0.84 to 1.66). The corresponding rates in the two treatment groups for the composite end point of death or myocardial infarction were 3.6% and 3.9%, respectively (relative risk, 1.07; 95% CI, 0.63 to 1.80). Revascularization procedures were undertaken in 5.3% and 4.8% of patients in unfractionated heparin and dalteparin groups, respectively (relative risk, 0.88; 95% CI, 0.57 to 1.35). Between days 6 and 45, the rate of death, myocardial infarction, or recurrence of angina was 12.3% in both the placebo and dalteparin groups (relative risk, 1.01; 95% CI, 0.74 to 1.38). The corresponding rates for death or myocardial infarction were 4.7% and 4.3% (relative risk, 0.92; 95% CI, 0.54 to 1.57). Revascularization procedures were undertaken in 14.2% and 14.3% of patients in the placebo and dalteparin groups, respectively. Our results add to previous evidence suggesting that the low-molecular-weight heparin dalteparin administered by twice-daily subcutaneous injection may be an alternative to unfractionated heparin in the acute treatment of unstable angina or non-Q-wave myocardial infarction. Prolonged treatment with dalteparin at a lower once-daily dose in our study did not confer any additional benefit over aspirin (75 to 165 mg) alone.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>9236418</pmid><doi>10.1161/01.CIR.96.1.61</doi><tpages>8</tpages></addata></record>
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source MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete
subjects Adult
Aged
Aged, 80 and over
Angina, Unstable - drug therapy
Anticoagulants - therapeutic use
Aspirin - administration & dosage
Biological and medical sciences
Blood Coagulation Tests
Blood. Blood coagulation. Reticuloendothelial system
Dalteparin - therapeutic use
Double-Blind Method
Drug Administration Schedule
Drug Therapy, Combination
Female
Heparin - therapeutic use
Humans
Injections, Intravenous
Injections, Subcutaneous
Male
Medical sciences
Middle Aged
Myocardial Infarction - drug therapy
Patient Compliance
Pharmacology. Drug treatments
Prospective Studies
Treatment Outcome
title Comparison of low-molecular-weight heparin with unfractionated heparin acutely and with placebo for 6 weeks in the management of unstable coronary artery disease fragmin in unstable coronary artery disease study (FRIC)
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