Report on Progress in the Australian National Blood Pressure Study (NBPS)

1976 ◽  
Vol 51 (s3) ◽  
pp. 645s-647s
Author(s):  
J. D. Abernethy ◽  
J. L. Baker ◽  
M. U. Bullen ◽  
M. L. Lamb ◽  
M. R. Stewart

1. The National Blood Pressure Study (NBPS) is a single blind trial designed to test the efficacy of active drug treatment in reducing complications from mild hypertension (mean diastolic pressure = 95–109 mmHg). 2. Between 1973 and 1975, four centres screened about 104 000 subjects aged 30–69 years, yielding an estimated prevalence of hypertension (≥95 mmHg diastolic) of 16% and of moderate-to-severe hypertension (≥110 mmHg diastolic) of 1·3%. 3. Some 4000 subjects selected for untreated uncomplicated mild hypertension were randomized to either active treatment (chlorothiazide + α-methyldopa and/or a β-adrenoreceptor antagonist as required) or to matching placebos. 4. At 1 year mean pressures had fallen significantly below entry pressures in both groups but in the active group the fall was greater by a margin of 14·4±1·3 (sem) mmHg systolic and 71 ±0·7 mmHg diastolic. At 1 year 5% of subjects in the placebo group had been placed on active treatment on the ethical grounds that pressure had exceeded the mild hypertension limit. 5. Trial end-points (death, morbidity from stroke, hypertensive heart and renal disease, and ischaemic heart disease) number 106 (nine deaths) thus far, of which ischaemic heart disease accounts for 71% and stroke 19%. 6. The duration of trial may need to be extended beyond the original estimate of 5 years.

1977 ◽  
Vol 5 (4) ◽  
pp. 236-242 ◽  
Author(s):  
V H Yajnik ◽  
J S Nandi ◽  
S C Patel ◽  
H V Doshi ◽  
S H Patel

A pilot single-blind placebo controlled crossover within-patient study was undertaken in essential hypertension. In ten patients single daily doses of 25 mg and 50 mg and in two patients 25 mg, 50 mg and 100 mg were used. Satisfactory reductions in both systolic and diastolic blood pressure in the supine and erect postures were observed. Reduction in heart rate was of the order of 6·32%, there being no correlation between reductions in blood pressure and decrements in heart rate. Three patients were dropped from the final analyses. Seventy-eight per cent (7/9) of patients had a final diastolic pressure (lying) of 90 mm Hg or less. Single doses of penbutolol controlled blood pressure for at least twenty-four hours. At the end of two weeks on placebo medication, following nine weeks of active drug medication, blood pressure had reverted to near pre-treatment levels. Penbutolol was well tolerated.


BMJ ◽  
1982 ◽  
Vol 284 (6323) ◽  
pp. 1148-1151 ◽  
Author(s):  
L Harris ◽  
H J Dargie ◽  
P G Lynch ◽  
C J Bulpitt ◽  
D M Krikler

1998 ◽  
Vol 60 (1) ◽  
pp. 105
Author(s):  
D. Carroll ◽  
G. Davey Smith ◽  
G. Willemsen ◽  
D. Sheffield ◽  
P.M. Sweetnam ◽  
...  

1992 ◽  
Vol 10 (10) ◽  
pp. 1273-1278 ◽  
Author(s):  
Christopher J. Bulpitt ◽  
Alison J. Palmer ◽  
Astrid E. Fletcher ◽  
D Gareth Beevers ◽  
Edward C. Coles ◽  
...  

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