Skip Navigation

European Journal of Heart Failure 1999 1(1):73-79; doi:10.1016/S1388-9842(98)00002-6
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Cleland, J. G.F.
Right arrow Articles by Rydén, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cleland, J. G.F.
Right arrow Articles by Rydén, L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1999 European Society of Cardiology

Baseline clinical characteristics of patients recruited into the assessment of treatment with lisinopril and survival study

John G.F. Cleland*, P. Armstrong, J.D. Horowitz, B. Massie, M. Packer, P.A. Poole-Wilson and L. Rydén1

University of Hull, Department of Cardiology, Castle Hill Hospital Castle Rd, Cottingham, Kingston-upon-Hull, East Yorkshire, HU16 5JQ, UK

* Corresponding author. University of Hull, Castle Hill Hospital, Department of Cardiology, Castle Rd., Cottingham, Kingston-upon-Hull, East Yorkshire, HU16 5JQ, UK


   Abstract

Background: The beneficial effect of ACE inhibitors on mortality has been established in a series of trials. However, in clinical practice, ACE inhibitors are commonly administered in doses much lower than those shown to be effective in the landmark trials.

Aims: This report describes the baseline characteristics of the patients recruited into the ATLAS study by age and gender sub-groups.

Methods: The ATLAS study compared the effects of ‘low’ dose (2.5–5.0 mg/day) to ‘high’ dose (32.5–55.0 mg/day) lisinopril in a double-blind study of 5164 patients with moderate to severe heart failure and left ventricular ejection fraction < 30% during a mean follow-up period of 46 months. The primary end-point was all cause mortality and the principal secondary end-point a composite of all-cause hospitalisation or all-cause mortality.

Results: Among patients with heart failure selected for the presence of left ventricular systolic function there were few differences among age groups or between genders. Older patients were not so heavy, were more likely to have ischaemic heart disease, hypertension and atrial fibrillation contributing to their heart failure and had a higher blood urea. Women were not so heavy as men. Age and gender had no major influence on mean ejection fraction or baseline treatment in the ATLAS study.

Conclusions: Weight and renal function may alter the plasma concentration of any given dose of an ACE inhibitor. Potential interactions between dose of lisinopril, weight and renal function will be explored after the study is completed.

Key Words: ACE inhibitors • Lisinopril • Patients with heart failure • Dose


1 On behalf of the ATLAS investigators. The ATLAS study is supported by Zeneca Pharmaceuticals.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
HeartHome page
P A Poole-Wilson, B F Uretsky, K Thygesen, J G F Cleland, B M Massie, and L Ryden
Mode of death in heart failure: findings from the ATLAS trial
Heart, January 1, 2003; 89(1): 42 - 48.
[Abstract] [Full Text] [PDF]


Home page
HeartHome page
J G F Cleland
Contemporary management of heart failure in clinical practice
Heart, October 1, 2002; 88(90002): ii5 - 8.
[Full Text] [PDF]


Home page
Eur Heart JHome page
J.G.F. Cleland, K. Thygesen, B.F. Uretsky, P. Armstrong, J.D. Horowitz, B. Massie, M. Packer, P.A. Poole-Wilson, L. Ryden, and on behalf of the ATLAS investigators
Cardiovascular critical event pathways for the progression of heart failure; a report from the ATLAS study
Eur. Heart J., September 1, 2001; 22(17): 1601 - 1612.
[Abstract] [PDF]


Home page
Eur Heart JHome page
L Ryden, P.W Armstrong, J.G.F Cleland, J.D Horowitz, B.M Massie, M Packer, and P.A Poole-Wilson
Efficacy and safety of high-dose lisinopril in chronic heart failure patients at high cardiovascular risk, including those with diabetes mellitus. Results from the ATLAS trial
Eur. Heart J., December 1, 2000; 21(23): 1967 - 1978.
[Abstract] [PDF]


Home page
CirculationHome page
M. Packer, P. A. Poole-Wilson, P. W. Armstrong, J. G. F. Cleland, J. D. Horowitz, B. M. Massie, L. Ryden, K. Thygesen, and B. F. Uretsky
Comparative Effects of Low and High Doses of the Angiotensin-Converting Enzyme Inhibitor, Lisinopril, on Morbidity and Mortality in Chronic Heart Failure
Circulation, December 7, 1999; 100(23): 2312 - 2318.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.