Why the study?
Does a fixed low-dose combination of perindopril/indapamide improve antihypertensive efficacy and surrogate markers compared to monotherapy in hypertensive patients?
Does a fixed low-dose combination of perindopril/indapamide improve antihypertensive efficacy and surrogate markers compared to monotherapy in hypertensive patients?
A fixed low-dose combination of perindopril/indapamide is an effective and safe first-line therapy for hypertension, offering advantages over monotherapy in blood pressure reduction and target organ protection.
Supports surrogate benefits of fixed low-dose perindopril/indapamide in hypertension; leaves open confirmation in outcome trials before practice change.
The association of low doses of perindopril and indapamide in a single pill has been developed to meet the criteria required for a fixed-dose combination to be used as first-line therapy. The experience accumulated so far has demonstrated a greater antihypertensive efficacy of this preparation compared with various monotherapies, but not at the expense of a worsening of tolerability. The perindopril/indapamide combination is particularly effective in lowering systolic and pulse blood pressure. Starting treatment with this fixed-dose combination improves arterial stiffness and allows a better regression of cardiac hypertrophy than angiotensin-converting enzyme-inhibition or beta-adrenoceptor blockade alone. In hypertensive patients with Type 2 diabetes, a greater reduction of urinary albumin excretion can be obtained with the perindopril/indapamide association compared with an angiotensin-converting enzyme inhibitor administered as monotherapy. There is evidence that a first-line management of hypertension based on a low-dose perindopril/indapamide combination can provide a better efficacy/safety ratio than other well-established therapeutic strategies.
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Bernard Waeber (2005) studied this question.
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