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P-168: Long term efficacy and tolerability of irbesartan in elderly hypertensive patients with renal impairment

Objective: We evaluated the blood pressure lowering activity, tolerability and safety of Irbesartan (I) in 32 elderly hypertensive (sitting diastolic blood pressure, 90 to 115 mmHg) patients with chronic renal insufficiency including mild renal insufficiency (30 to 60 ml/min x 1.73 m2; n=30), modera...

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Published in:American journal of hypertension 2001-04, Vol.14 (S1), p.86A-86A
Main Authors: De Rosa, Maria Leonarda M.L, Cardace, Piercarmine P., Rossi, Massimiliano M., de Cristofaro, Alessandro A., Baiano, Antonio A., Vigorito, Carlo C.
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container_issue S1
container_start_page 86A
container_title American journal of hypertension
container_volume 14
creator De Rosa, Maria Leonarda M.L
Cardace, Piercarmine P.
Rossi, Massimiliano M.
de Cristofaro, Alessandro A.
Baiano, Antonio A.
Vigorito, Carlo C.
description Objective: We evaluated the blood pressure lowering activity, tolerability and safety of Irbesartan (I) in 32 elderly hypertensive (sitting diastolic blood pressure, 90 to 115 mmHg) patients with chronic renal insufficiency including mild renal insufficiency (30 to 60 ml/min x 1.73 m2; n=30), moderate to severe renal insufficiency (10 to 29 ml/min x 1.73 m2; n=2) in one year trial. Design and Methods: After a 3-week placebo period, once daily I was administered for 12 months at daily dose of 150 mg. A second, non-angiotensin-converting enzyme inhibitor, antihypertensive drug was added after 8 weeks as needed. Twenty-four-hour creatinine clearance was determined and renal clearance studies of inulin and paraminohippurate were done in a subset of 11 patients. Results: Through sitting blood pressure were reduced at the end of the first week in all groups. At weeks 4, 8, 12 and after one year the reductions in systolic blood pressure/diastolic blood pressure averaged were -11.9/-8.7,-10.8/-9.4,and -14.7/-12.1mmHg in patients with mild renal insufficiency; -7.7/-6.3,-13.1/-11.8, and -14.1/-10.6 mmHg in moderate to severe renal insufficiency.Creatine clearance,glomerular filtration rate and effective renal plasma flow were stable.I was withdrawn in only 6 patients because of a clinical or laboratory adverse experience. Hyperkaliemia(>6mEq/L) requiring discontinuation of I occurred in only one(group 2)patient. Conclusion: We conclude that once-daily I given as monotherapy at dose of 150 mg or in combination with other antihypertensive drugs,was effective in reducing blood pressure in elderly hypertensive patients with chronic renal disease and that I regimens were well tolerated in all groups.
doi_str_mv 10.1016/S0895-7061(01)01813-1
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Design and Methods: After a 3-week placebo period, once daily I was administered for 12 months at daily dose of 150 mg. A second, non-angiotensin-converting enzyme inhibitor, antihypertensive drug was added after 8 weeks as needed. Twenty-four-hour creatinine clearance was determined and renal clearance studies of inulin and paraminohippurate were done in a subset of 11 patients. Results: Through sitting blood pressure were reduced at the end of the first week in all groups. At weeks 4, 8, 12 and after one year the reductions in systolic blood pressure/diastolic blood pressure averaged were -11.9/-8.7,-10.8/-9.4,and -14.7/-12.1mmHg in patients with mild renal insufficiency; -7.7/-6.3,-13.1/-11.8, and -14.1/-10.6 mmHg in moderate to severe renal insufficiency.Creatine clearance,glomerular filtration rate and effective renal plasma flow were stable.I was withdrawn in only 6 patients because of a clinical or laboratory adverse experience. Hyperkaliemia(&gt;6mEq/L) requiring discontinuation of I occurred in only one(group 2)patient. 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Design and Methods: After a 3-week placebo period, once daily I was administered for 12 months at daily dose of 150 mg. A second, non-angiotensin-converting enzyme inhibitor, antihypertensive drug was added after 8 weeks as needed. Twenty-four-hour creatinine clearance was determined and renal clearance studies of inulin and paraminohippurate were done in a subset of 11 patients. Results: Through sitting blood pressure were reduced at the end of the first week in all groups. At weeks 4, 8, 12 and after one year the reductions in systolic blood pressure/diastolic blood pressure averaged were -11.9/-8.7,-10.8/-9.4,and -14.7/-12.1mmHg in patients with mild renal insufficiency; -7.7/-6.3,-13.1/-11.8, and -14.1/-10.6 mmHg in moderate to severe renal insufficiency.Creatine clearance,glomerular filtration rate and effective renal plasma flow were stable.I was withdrawn in only 6 patients because of a clinical or laboratory adverse experience. 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ispartof American journal of hypertension, 2001-04, Vol.14 (S1), p.86A-86A
issn 0895-7061
1941-7225
1879-1905
language eng
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source Oxford Journals Online
subjects Elderly Hypertensive Patients
Irbesartan
Renal Impairment
title P-168: Long term efficacy and tolerability of irbesartan in elderly hypertensive patients with renal impairment
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