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Irbesartan/Hydrochlorothiazide

In Moderate to Severe Hypertension

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Abstract

  • ▲ The fixed-dose combination of irbesartan/hydrochlorothiazide (HCTZ) is approved in the US for use as initial therapy in patients who are likely to need multiple agents to achieve their blood pressure (BP) goals.

  • ▲ In a 12-week, randomized, double-blind, multicentre trial in 538 patients with moderate hypertension that was untreated or uncontrolled by monotherapy, the mean reduction from baseline in seated systolic BP (SeSBP) at week 8 (primary endpoint) was significantly greater with irbesartan/HCTZ than with either irbesartan or HCTZ as monotherapy.

  • ▲ In addition, the proportion of patients with moderate hypertension achieving controlled BP (SeSBP <140 mmHg/seated diastolic BP [SeDBP] <90 mmHg) at 12 weeks was significantly greater with irbesartan/HCTZ combination therapy than with irbesartan or HCTZ monotherapy.

  • ▲ In a 7-week, randomized, double-blind, multicentre trial in 697 patients with severe hypertension that was untreated or uncontrolled by monotherapy, a significantly greater proportion achieved a trough SeDBP of <90 mmHg following 5 weeks of combination therapy with irbesartan/HCTZ compared with irbesartan monotherapy (primary endpoint).

  • ▲ Furthermore, the proportion of patients with severe hypertension achieving controlled BP of <140/ 90 mmHg was significantly greater at all timepoints of the trial compared with irbesartan monotherapy.

  • ▲ Irbesartan/HCTZ combination therapy had a similar tolerability profile to irbesartan and HCTZ monotherapy. Most adverse events were of mild to moderate intensity.

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Notes

  1. The use of trade names is for identification purposes only and does not imply endorsement.

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Acknowledgements and Disclosures

This article was reviewed by: G. Jerums, Endocrine Centre of Excellence, Austin Health, Repatriation Campus, Heidelberg, Victoria, Australia; C.E.S. Mogensen, Department of Diabetes and Endocrinology, Aarhus University Hospital, Aarhus, Denmark; G.L. Schwartz, Department of Internal Medicine, Mayo Clinic and Foundation, Rochester, Minnesota, USA; J.A. Staessen, Laboratory of Hypertension, Campus Gasthuisberg, Leuven, Belgium.

The preparation of this review was not supported by any external funding. During the peer review process, the manufacturer of the agent under review was offered an opportunity to comment on this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.

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Correspondence to Jamie D. Croxtall.

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Croxtall, J.D., Keating, G.M. Irbesartan/Hydrochlorothiazide. Drugs 68, 1465–1472 (2008). https://doi.org/10.2165/00003495-200868100-00007

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