Antihypertensive efficacy and tolerability of lercanidipine in daily clinical practice. The ELYPSE study

被引:49
作者
Barrios, V
Navarro, A
Esteras, A
Luque, M
Romero, J
Tamargo, J
Prieto, L
Carrasco, JL
Herranz, I
Navarro-Cid, J
Ruilope, LM
机构
[1] Hosp Ramon & Cajal, Serv Cardiol, ES-28034 Madrid, Spain
[2] Recordati Spain, Madrid, Spain
[3] Pharmazan Spain, Barcelona, Spain
[4] Hosp Clin San Carlos, Madrid, Spain
[5] Univ Complutense, Sch Med, E-28040 Madrid, Spain
[6] Hosp 12 Octubre, E-28041 Madrid, Spain
关键词
arterial hypertension; calcium-channel blocker; daily clinical practice; dihydropyridine; Lercanidipine;
D O I
10.1080/08037050211265
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Aim: Lercanidipine, a long-acting dihydropyridine with a good antihypertensive efficacy and tolerability in clinical use. With the aim to determine the efficacy and tolerability of this drug in usual clinical practice we performed the ELYPSE trial. Methods: Grade 1 or 2 essential hypertensive patients in whom their physicians considered to prescribe a dihydropyridine were conferred to Lercanidipine 10 me, once daily with a 3-month follow-up; 9059 patients were included (age: 63 +/- 11 years; 58% women, 60% over 60 years, 56% grade 2 hypertensives and 69% previously treated with other antihypertensive drugs). A sub.-roup of 1267 patients (14%) who were included in the study had experienced adverse reactions with other drugs. Electronic case-report forms and a central database (Internet) were used in this trial. Results: At baseline, blood pressure (BP) was 160.1 +/- 10.2/95.6 +/- 6.6 mmHg; and heart rate (HR) 77.3 +/- 9.3 beats/min. Significant reductions in both systolic and diastolic BP were attained at 1 month with slight additional decreases 2 months later. At 3 months, BP was 141.4 +/- 11.3/83.1 +/- 6.9 mmHg, and HR 75.2 +/- 8.2 beats/min (p < 0.001 versus baseline). At the study end, 64% of the patients achieved a diastolic BP <90 mmHg, BP control (< 140/90 mmHg) was attained in 32%. In the subgroup of diabetics (n = 1269) an adequate BP control (< 130/85) was attained in only 16.4%. The overall incidence of adverse events was 6.5%, of which the most frequent were headache (2.9%), ankle oedema (1.2%), flushing (1.1%) and palpitations (0.6%). Withdrawal rate was < 1%. The efficacy and tolerability in the subgroup of patients included in the study due to adverse events with other drugs were similar to the whole study group. Conclusion: In this stud Lercanidipine has shown a good efficacy and toerability in daily clinical practice. Those findings are concordant with those reported in randomized controlled trials.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 30 条
  • [1] AMBROSIONI E, 1997, J CARDIOVASC PHAR S2, V29, pS16, DOI DOI 10.1097/00005344-199729002-00003
  • [2] [Anonymous], 1997, ARCH INTERN MED, V157, P2413, DOI [10.1001/archinte.1997.00440420033005, DOI 10.1001/ARCHINTE.1997.00440420033005]
  • [3] A comparison of observational studies and randomized, controlled trials.
    Benson, K
    Hartz, AJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (25) : 1878 - 1886
  • [4] CAFIERO M, 1997, J CARDIOVASC PHAR S2, V29, pS45
  • [5] CIRCO A, 1997, J CARDIOVASC PHAR S2, V29, pS22
  • [6] Randomized, controlled trials, observational studies, and the hierarchy of research designs.
    Concato, J
    Shah, N
    Horwitz, RI
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (25) : 1887 - 1892
  • [7] Double-blind, crossover study of lercanidipine versus amlodipine in the treatment of mild-to-moderate essential hypertension
    De Giorgio, LA
    Orlandini, F
    Malasoma, P
    Zappa, A
    [J]. CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 1999, 60 (10): : 511 - 520
  • [8] Comparative effect of lercanidipine and nifedipine gastrointestinal therapeutic system on ankle volume and subcutaneous interstitial pressure in hypertensive patients: A double-blind, randomized, parallel-group study
    Fogari, R
    Malamani, GD
    Zoppi, A
    Preti, P
    Vanasia, A
    Fogari, E
    Mugellini, A
    [J]. CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 2000, 61 (12): : 850 - 862
  • [9] GUARNERI L, 1997, J CARDIOVASC PHAR S1, V29, pS25
  • [10] Effects of intensive blood-pressure lowering and low-dose aspirin in patients with hypertension:: principal results of the hypertension optimal treatment (HOT) randomised trial
    Hansson, L
    Zanchetti, A
    Carruthers, SG
    Dahlöf, B
    Elmfeldt, D
    Julius, S
    Ménard, J
    Rahn, KH
    Wedel, H
    Westerling, S
    [J]. LANCET, 1998, 351 (9118) : 1755 - 1762