Literature DB >> 9806109

Abciximab. An updated review of its use in ischaemic heart disease.

R H Foster1, L R Wiseman.   

Abstract

UNLABELLED: Abciximab is a glycoprotein IIb/IIIa receptor antagonist that has proven to be of significant clinical value in improving patient outcome after percutaneous coronary revascularisation. Primarily, the drug inhibits platelet aggregation, but it may also have anticoagulant activity and other beneficial effects, such as inhibiting migration and promoting apoptosis of smooth muscle cells. Large well designed studies have found administration of abciximab (as an adjunct to heparin and aspirin) during percutaneous coronary revascularisation to significantly reduce the incidence of ischaemic complications occurring in the 30 days after the procedure. Significant benefit, particularly on the incidence of myocardial infarction, was still evident after 6 months in 2 of 4 major trials. Abciximab provides particular benefit in patients with unstable angina or myocardial infarction who are undergoing percutaneous coronary revascularisation. The benefits of the drug are additive to those achieved with coronary stenting. Very preliminary data suggest that abciximab may improve coronary blood flow after myocardial infarction and allow reperfusion to be achieved with reduced thrombolytic doses. Caution is required to minimise the risk of bleeding complications with the use of abciximab in combination with heparin and aspirin. Careful patient selection, use of an appropriate heparin regimen, early vascular sheath removal and meticulous femoral artery access site care are recommended. Thrombocytopenia can occur with abciximab treatment, but severe cases are uncommon (< 2% of patients) and can be treated with platelet transfusions. The high acquisition cost of abciximab may be partly or fully offset by the costs averted by the reduced incidence of ischaemic complications and need for urgent and/or repeat revascularisation in high risk patients who receive the drug. However, if bleeding complications occur, this adds to treatment costs. Cost effectiveness analyses generally support the use of abciximab in high risk patients.
CONCLUSIONS: Abciximab can be recommended for the prevention of acute ischaemic events in most patients undergoing percutaneous coronary revascularisation, but careful patient selection and strict adherence to the recommended treatment protocol are required to reduce the risk of bleeding complications and thrombocytopenia. Its use in high risk patients is largely supported by pharmacoeconomic data. Further pharmacoeconomic information is needed to establish the drug as a standard of care for all patient groups. The indications for abciximab are likely to expand as more data on its use in acute coronary syndromes become available.

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Year:  1998        PMID: 9806109     DOI: 10.2165/00003495-199856040-00014

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  90 in total

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Journal:  Expert Opin Investig Drugs       Date:  1997-11       Impact factor: 6.206

Review 2.  Pharmacological approaches to the prevention of restenosis following angioplasty. The search for the Holy Grail? (Part I).

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Journal:  Drugs       Date:  1993-07       Impact factor: 9.546

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Journal:  Am Heart J       Date:  1998-04       Impact factor: 4.749

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Journal:  Am Heart J       Date:  1998-04       Impact factor: 4.749

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9.  Shear-induced platelet aggregation is inhibited by in vivo infusion of an anti-glycoprotein IIb/IIIa antibody fragment, c7E3 Fab, in patients undergoing coronary angioplasty.

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Journal:  Circulation       Date:  1995-03-01       Impact factor: 29.690

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Journal:  Circulation       Date:  1995-03-01       Impact factor: 29.690

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  9 in total

Review 1.  Abciximab. A pharmacoeconomic review of its use in percutaneous coronary revascularisation.

Authors:  C J Dunn; R H Foster
Journal:  Pharmacoeconomics       Date:  1999-12       Impact factor: 4.981

Review 2.  Combination of low molecular weight heparins with antiplatelet agents in non-ST elevation acute coronary syndromes: an update.

Authors:  Marc Cohen
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 3.  Abciximab: an updated review of its therapeutic use in patients with ischaemic heart disease undergoing percutaneous coronary revascularisation.

Authors:  Tim Ibbotson; Jane K McGavin; Karen L Goa
Journal:  Drugs       Date:  2003       Impact factor: 9.546

Review 4.  High-Throughput Monoclonal Antibody Discovery from Phage Libraries: Challenging the Current Preclinical Pipeline to Keep the Pace with the Increasing mAb Demand.

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Review 5.  The global landscape of approved antibody therapies.

Authors:  Xiaochen Lyu; Qichao Zhao; Julia Hui; Tiffany Wang; Mengyi Lin; Keying Wang; Jialing Zhang; Jiaqian Shentu; Paul A Dalby; Hongyu Zhang; Bo Liu
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Review 6.  Biologic Therapy and Severe Asthma in Children.

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7.  Early recovery of microvascular perfusion induced by t-PA in combination with abciximab or eptifibatide during postischemic reperfusion.

Authors:  Silva Bertuglia; Andrea Giusti
Journal:  BMC Cardiovasc Disord       Date:  2002-06-19       Impact factor: 2.298

8.  Eptifibatide is associated with significant cost savings and similar clinical outcomes to abciximab when used during primary percutaneous coronary intervention for ST-elevation myocardial infarction: An observational cohort study of 3863 patients.

Authors:  K S Rathod; S Antoniou; P Avari; N Ding; P Wright; C Knight; A K Jain; A Mathur; E J Smith; R Weerackody; A Wragg; D A Jones
Journal:  JRSM Cardiovasc Dis       Date:  2017-10-05

Review 9.  Development of therapeutic antibodies for the treatment of diseases.

Authors:  Ruei-Min Lu; Yu-Chyi Hwang; I-Ju Liu; Chi-Chiu Lee; Han-Zen Tsai; Hsin-Jung Li; Han-Chung Wu
Journal:  J Biomed Sci       Date:  2020-01-02       Impact factor: 8.410

  9 in total

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