In clinical practice, diagnosis and follow-up of hypertension is based on b
lood pressure (BP) as measured by auscultatory method. BP is usually measur
ed using a stethoscope to auscultate the Korotkoff sounds and mercury or an
aneroid sphygmomanometer. However due to the lack of regulatory rules, the
devices are rarely checked making the quality of the measures doubtful.
Objective: to compare BP measured following the WHO recommendations, using
2 different devices: the mercury or aneroid sphygmomanometer used by the ph
ysician and a SECURUS manometer that has been calibrated just before the im
plementation of the study.
Method: The study was performed with 1694 French general practitioners. Eve
ry physician included 2 ambulatory patients: a newly diagnosed non-treated
hypertensive patient and a treated hypertensive patient. The physician was
asked to include the first patient of each category attending his office. B
P was measured sequentially with the 2 devices in a random order.
Collected data were socio-demographic parameters, cardiovascular risk facto
rs, hypertension related diseases, drug treatment for hypertension and BP l
evels.
Results: Mean BPs differ by less than 1 mmHg between the 2 devices. However
10% of the treated hypertensive patients are not classified as having norm
alised BP values (BP< 140/90 mmHg) or high BP values, in the same way by th
e 2 devices. Mean absolute difference between the 2 devices is >5 mmHg in 2
2% and 13% of the physicians for SBP and DBP respectively.
Conclusion: this pilot study emphasises the need of BP measurements of good
quality in clinical practice, because of the possible impact on the care o
f the patients and the related costs. Regulatory rules on the control of th
e devices might improve the quality of BP measurements.