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  1. Book ; Thesis: Renin system activity in essential hypertension

    Allikmets, Kristina

    associations with atherothrombogenic cardiovascular risk factors and with the efficacy of calcium antagonist treatment

    (Dissertationes medicinae Universitatis Tartuensis ; 25)

    1996  

    Author's details Kristina Allikmets
    Series title Dissertationes medicinae Universitatis Tartuensis ; 25
    Collection
    Language English
    Size 140 S. : graph. Darst.
    Publisher Tartu Univ. Press
    Publishing place Tartu
    Publishing country Estonia
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Tartu, Univ., Diss., 1996
    Note Zsfassung in estn. Sprache
    HBZ-ID HT007632299
    ISBN 9985-56-208-9 ; 978-9985-56-208-6
    Database Catalogue ZB MED Medicine, Health

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  2. Article: Aliskiren--an orally active renin inhibitor. Review of pharmacology, pharmacodynamics, kinetics, and clinical potential in the treatment of hypertension.

    Allikmets, Kristina

    Vascular health and risk management

    2007  Volume 3, Issue 6, Page(s) 809–815

    Abstract: The importance of renin-angiotensin-aldosterone system (RAAS) in diseases such as hypertension, congestive heart failure and chronic renal failure has long ago been recognized. It has also been established that inhibition of RAAS, using inhibitors of the ...

    Abstract The importance of renin-angiotensin-aldosterone system (RAAS) in diseases such as hypertension, congestive heart failure and chronic renal failure has long ago been recognized. It has also been established that inhibition of RAAS, using inhibitors of the angiotensin-converting enzyme (ACE) or angiotensin II receptor blockers (ARB), is an effective way to intervene with the pathogenesis of these disorders. Renin inhibitors block the RAAS at the highest level, at its origin, and might thus offer a new exciting approach for pharmacotherapy of arterial hypertension. Aliskiren is the first in a new class of orally active, non-peptide, low molecular weight renin inhibitors, and so far the only renin inhibitor that has progressed to phase III clinical trials. This review summarizes the available data on the pharmacokinetic and pharmacodynamic properties of aliskiren and its clinical development for treatment of arterial hypertension.
    MeSH term(s) Amides/pharmacology ; Amides/therapeutic use ; Antihypertensive Agents/pharmacology ; Antihypertensive Agents/therapeutic use ; Drug Interactions ; Fumarates/pharmacology ; Fumarates/therapeutic use ; Humans ; Hypertension/drug therapy ; Renin/antagonists & inhibitors
    Chemical Substances Amides ; Antihypertensive Agents ; Fumarates ; aliskiren (502FWN4Q32) ; Renin (EC 3.4.23.15)
    Language English
    Publishing date 2007-11-28
    Publishing country New Zealand
    Document type Journal Article ; Review
    ZDB-ID 2186568-1
    ISSN 1178-2048 ; 1176-6344
    ISSN (online) 1178-2048
    ISSN 1176-6344
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Aliskiren (Speedel).

    Allikmets, Kristina

    Current opinion in investigational drugs (London, England : 2000)

    2002  Volume 3, Issue 10, Page(s) 1479–1482

    Abstract: Speedel Pharma is developing aliskiren (formerly CGP-60536), a renin inhibitor under license from Novartis, for the potential treatment of several cardiovascular disorders. By October 2001, a phase IIb study in hypertension had been completed, and phase ... ...

    Abstract Speedel Pharma is developing aliskiren (formerly CGP-60536), a renin inhibitor under license from Novartis, for the potential treatment of several cardiovascular disorders. By October 2001, a phase IIb study in hypertension had been completed, and phase III studies for this indication were anticipated for 2002; at this time, phase II studies in congestive heart failure and chronic renal failure were ongoing.
    MeSH term(s) Amides ; Animals ; Antihypertensive Agents/therapeutic use ; Clinical Trials as Topic ; Fumarates/adverse effects ; Fumarates/metabolism ; Fumarates/therapeutic use ; Humans ; Renin/antagonists & inhibitors
    Chemical Substances Amides ; Antihypertensive Agents ; Fumarates ; aliskiren (502FWN4Q32) ; Renin (EC 3.4.23.15)
    Language English
    Publishing date 2002-10
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2027913-9
    ISSN 2040-3429 ; 1472-4472 ; 0967-8298
    ISSN (online) 2040-3429
    ISSN 1472-4472 ; 0967-8298
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Sampatrilat Shire.

    Allikmets, Kristina

    Current opinion in investigational drugs (London, England : 2000)

    2002  Volume 3, Issue 4, Page(s) 578–581

    Abstract: Sampatrilat is a dual inhibitor of neutral endopeptidase (NEP) and angiotensin converting enzyme (ACE), which is under development by Pfizer and Shire (previously Roberts Pharmaceutical) for the potential treatment of hypertension. As of 1995, Pfizer had ...

    Abstract Sampatrilat is a dual inhibitor of neutral endopeptidase (NEP) and angiotensin converting enzyme (ACE), which is under development by Pfizer and Shire (previously Roberts Pharmaceutical) for the potential treatment of hypertension. As of 1995, Pfizer had taken the compound into phase II clinical trials [179233]. In April 1997, Roberts Pharmaceutical, through its wholly owned subsidiary Roberts Laboratories Inc, received an exclusive license from Pfizer to develop and market sampatrilat for the treatment of essential hypertension and congestive heart failure. The agreement provided for transfer of data and the awarding of patent rights to Roberts [240809]. Although in June 2000, Shire confirmed it had discontinued all development of this drug [372652], by December 2000 it had recommenced studies with a reformulation of sampatrilat that achieved a 4-fold increase in oral bioavailability. A clinical trial with the new formulation was to be initiated in 2001, with results expected during the second quarter of 2001. The company also revealed that it was seeking a licensing partner at this time [394238]. In November 2001, Shire confirmed that while the project was undergoing further development with a view to outlicensing, it was unlikely to take this project into phase II alone [429562].
    MeSH term(s) Angiotensin-Converting Enzyme Inhibitors/adverse effects ; Angiotensin-Converting Enzyme Inhibitors/pharmacology ; Clinical Trials as Topic ; Contraindications ; Endopeptidases/metabolism ; Heart Failure/drug therapy ; Humans ; Hypertension/drug therapy ; Mesylates/adverse effects ; Mesylates/pharmacology ; Protease Inhibitors/adverse effects ; Protease Inhibitors/pharmacology ; Structure-Activity Relationship ; Tyrosine/adverse effects ; Tyrosine/analogs & derivatives ; Tyrosine/pharmacology
    Chemical Substances Angiotensin-Converting Enzyme Inhibitors ; Mesylates ; Protease Inhibitors ; Tyrosine (42HK56048U) ; Endopeptidases (EC 3.4.-) ; sampatrilat (V7O29949TG)
    Language English
    Publishing date 2002-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2027913-9
    ISSN 2040-3429 ; 1472-4472 ; 0967-8298
    ISSN (online) 2040-3429
    ISSN 1472-4472 ; 0967-8298
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Comparative cost-effectiveness of anticoagulation with bivalirudin or heparin with and without a glycoprotein IIb/IIIa-receptor inhibitor in patients undergoing percutaneous coronary intervention in Sweden: a decision-analytic model.

    Borg, Sixten / Persson, Ulf / Allikmets, Kristina / Ericsson, Karin

    Clinical therapeutics

    2006  Volume 28, Issue 11, Page(s) 1947–1959

    Abstract: Objective: This study modeled the comparative costs and effectiveness of anticoagulation with bivalirudin alone, heparin alone, and heparin combined with a glycoprotein IIb/IIIa-receptor inhibitor (GPI) in patients undergoing percutaneous coronary ... ...

    Abstract Objective: This study modeled the comparative costs and effectiveness of anticoagulation with bivalirudin alone, heparin alone, and heparin combined with a glycoprotein IIb/IIIa-receptor inhibitor (GPI) in patients undergoing percutaneous coronary intervention (PCI) in Sweden.
    Methods: GPIs are prescribed for -40% to 50% of patients undergoing PCI in Sweden. However, because treatment practices vary between hospitals, the model analyzed a cohort in which different proportions of patients (0%-100%) would receive a GPI in addition to heparin and the remaining patients would receive heparin monotherapy. This mixed cohort was compared with a cohort treated with bivalirudin. Abciximab was used as the GPI comparator, as this is the only GPI currently approved in Sweden for patients undergoing PCI. Pooled data from 3 studies (REPLACE-2 [second Randomized Evaluation of PCI Linking Angiomax to Reduced Clinical Events], ESPRIT [European/Australasian Stroke Prevention in Reversible Ischaemia Trial], and EPISTENT [Evaluation of Platelet IIb/IIIa Inhibitor for Stenting]) were used as the source for the probabilities of myocardial infarction (MI), urgent revascularization (UR), major and minor bleeding (Thrombolysis in Myocardial Infarction study definitions), and death. Treatment costs associated with these complications were obtained from 4 Swedish hospitals, and official drug prices were obtained from the Swedish Pharmacopoeia. All costs were presented in 2006 Swedish kronor (SEK). The model was evaluated over a 30-day time frame from the perspective of a Swedish hospital. The modeled patient population was 63 years old, weighed 78 kg, and was 75% male.
    Results: Compared with a pattern in which heparin plus a GPI was used in 50% of all PCIs and heparin alone was used in the remaining 50%, bivalirudin treatment was associated with a significant reduction in all complications in the model (P < 0.05), including a mean of 18.2 fewer MIs, 1.6 fewer URs, 15.3 fewer bleeding events, and 1.3 fewer deaths per 1000 treated patients. Bivalirudin therapy also was associated with a significant reduction in total drug and health care costs per patient (SEK -1301; 95% Cl, -1367 to -1229). The benefit of bivalirudin was sensitive to the rate of GPI use: additional reductions in rates of MI, UR, and death were seen at lower rates of GPI use, and additional reductions in rates of bleeding and costs of drugs and health care utilization were seen at higher rates of GPI use.
    Conclusions: In this model, anticoagulation with bivalirudin in patients undergoing PCI was cost-effective compared with heparin alone and heparin plus a GPI. In a hypothetical Swedish hospital unit using equal proportions of heparin alone and heparin plus a GPI, a switch to bivalirudin would reduce the risk of both ischemic events and bleeding events, resulting in savings in total drug and health care costs.
    MeSH term(s) Angioplasty, Balloon, Coronary/economics ; Cost-Benefit Analysis ; Decision Making ; Female ; Hemorrhage/economics ; Hemorrhage/prevention & control ; Heparin/administration & dosage ; Heparin/economics ; Hirudins/administration & dosage ; Hirudins/economics ; Humans ; Ischemia/economics ; Ischemia/prevention & control ; Male ; Middle Aged ; Models, Theoretical ; Peptide Fragments/administration & dosage ; Peptide Fragments/economics ; Platelet Aggregation Inhibitors/administration & dosage ; Platelet Aggregation Inhibitors/economics ; Platelet Glycoprotein GPIIb-IIIa Complex ; Prospective Studies ; Randomized Controlled Trials as Topic ; Recombinant Proteins/administration & dosage ; Recombinant Proteins/economics ; Sweden
    Chemical Substances Hirudins ; Peptide Fragments ; Platelet Aggregation Inhibitors ; Platelet Glycoprotein GPIIb-IIIa Complex ; Recombinant Proteins ; Heparin (9005-49-6) ; bivalirudin (TN9BEX005G)
    Language English
    Publishing date 2006-11
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 603113-4
    ISSN 1879-114X ; 0149-2918
    ISSN (online) 1879-114X
    ISSN 0149-2918
    DOI 10.1016/j.clinthera.2006.11.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Ischaemic events and bleeding in patients undergoing percutaneous coronary intervention with concomitant bivalirudin treatment.

    Madsen, Jan Kyst / Chevalier, Bernard / Darius, Harald / Rutsch, Wolfgang / Wójcik, Jaroslaw / Schneider, Steffen / Allikmets, Kristina

    EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology

    2009  Volume 3, Issue 5, Page(s) 610–616

    Abstract: Aims: The European ImproveR registry aimed to characterise the patient population undergoing percutaneous coronary intervention (PCI) with bivalirudin treatment in a routine clinical setting and to evaluate associated ischaemic and bleeding events.: ... ...

    Abstract Aims: The European ImproveR registry aimed to characterise the patient population undergoing percutaneous coronary intervention (PCI) with bivalirudin treatment in a routine clinical setting and to evaluate associated ischaemic and bleeding events.
    Methods and results: A total of 3,799 evaluable patients, aged > 18 years, were enrolled in 102 centres across 12 European countries from January 2005 to June 2006. The population was elderly (median age, 67.2 years; 24% > 75 years) and comprised 27.1% female patients, 27.9% with diabetes and 14.9% with renal impairment. Forty-nine percent of patients presented with acute coronary syndromes (ACS), 22% of these with ST-segment elevation myocardial infarction (STEMI). In-hospital and 30-day rates of major adverse cardiac events (death, myocardial infarction or urgent revascularisation) were 2.3% and 5.6%, respectively. In-hospital ischaemic complications were associated with a STEMI diagnosis and age > 65 years. In-hospital significant bleeding occurred in 1.7% of patients and was associated with renal impairment, female gender and glycoprotein IIb/IIIa inhibitor use.
    Conclusion: The ImproveR registry population is characterised by a high proportion of elderly patients and patients with diabetes, renal impairment and ACS. In clinical practice, bivalirudin effectively suppresses ischaemic complications while maintaining a low rate of haemorrhagic consequences, as expected from randomised trials.
    Language English
    Publishing date 2009-07-13
    Publishing country France
    Document type Journal Article
    ZDB-ID 2457174-X
    ISSN 1969-6213 ; 1774-024X
    ISSN (online) 1969-6213
    ISSN 1774-024X
    DOI 10.4244/eijv3i5a109
    Database MEDical Literature Analysis and Retrieval System OnLINE

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