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Fixed combination of candesartan with hydrochlorothiazide in patients with severe primary hypertension
1MEDIAN Kliniken, Herbert-Hellmann-Allee 38, 79189 Bad Krozingen, Germany. gerd.boenner@dgn.de
Insights
This study shows that combining candesartan cilexetil and hydrochlorothiazide effectively treats severe hypertension. The combination therapy demonstrated significant blood pressure reduction with no reported adverse events.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- JNC VII guidelines (2003) permit initial combination therapy for hypertension if blood pressure exceeds 20/10 mmHg.
- Severe primary hypertension requires effective and safe treatment strategies.
Purpose of the Study:
- To evaluate the efficacy and safety of candesartan cilexetil plus hydrochlorothiazide combination therapy.
- To assess treatment outcomes in patients with severe primary hypertension.
Main Methods:
- Open-label, single-group study involving 116 treatment-naive patients with severe primary hypertension (Grade III).
- 6-week treatment with 16 mg candesartan cilexetil + 12.5 mg hydrochlorothiazide daily after forced titration.
- Blood pressure measured in the morning after 15 minutes rest; median of three readings used.
Main Results:
- Mean reduction in systolic/diastolic blood pressure was 38.1/29.4 mmHg.
- 90.1% of patients were responders, with 39.6% achieving normotensive levels (< 140/< 90 mmHg).
- No drug-related adverse events or significant laboratory parameter changes were observed.
Conclusions:
- Combination therapy with candesartan cilexetil and hydrochlorothiazide shows promising efficacy and safety.
- This treatment approach appears suitable for managing severe primary hypertension.
Objective:
The new guidelines for treatment of hypertension by the JNC VII in 2003 permit the initial use of a combination therapy, if blood pressure has to be lowered more than 20/10 mmHg. The aim of this investigation was to document the efficacy and safety of a combination therapy with candesartan cilexetil and hydrochlorothiazide in severe hypertension.
Methods:
116 patients freshly diagnosed as having severe primary hypertension (Grade III) and untreated for this condition were enrolled. The study was performed without a placebo control group for ethical reasons. Thus, all patients were treated for 6 weeks with 16 mg candesartan cilexetil plus 12.5mg hydrochlorothiazide daily after forced titration with 8 and 16 mg candesartan cilexetil each for
Results:
The mean reduction in systolic/diastolic BP at the end was 38.1/29.4 mmHg. 90.1% of patients were considered to be responders, while 39.6% of patients treated became normotensive (< 140/< 90 mmHg). No drug-related adverse events or changes in laboratory parameters were reported.
Conclusion:
Although this was an open-label, single-group study, on the basis of efficacy and safety, the combination therapy appears to offer a promising treatment for patients with severe primary hypertension.
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