Ambulatory blood-pressure monitoring (ABPM) is accepted in the evaluation a
nd management of hypertension. The use of ABPM in heart failure has receive
d considerably less attention. Many patients with advanced heart failure ex
perience disabling fatigue, orthostatic dizziness and symptoms of coronary
and cerebrovascular insufficiency that may relate to periods of hypotension
. These may be exacerbated by vasodilator drug therapy and may be difficult
to evaluate by casual clinic recordings. ABPM in heart failure may help in
the following: (i) evaluating time-dependent pharmacodynamic drug effects,
such as peak and end-of-dose phenomena, tolerance and rebound; (ii) titrat
ing ACE inhibitors and other drugs to highest-tolerated doses; and (iii) co
rrelating circadian blood-pressure profiles with symptoms, quality of life,
severity of heart failure, progression of ventricular and renal dysfunctio
n, risks of stroke and myocardial infarction, and life expectancy. Devices
for ABPM have been beset by problems of inaccuracy and unreliability. Stand
ards for their manufacture and sale (including bench tests of accuracy agai
nst sphygmomanometry and intra-arterial recordings, and field tests of reli
ability) have been devised independently by several agencies, including the
British Hypertension Society (BHS) and US Association for the Advancement
of Medical Instrumentation (AAMI). A joint BHS/AAMI set of guidelines is in
preparation. These guidelines emphasize the suitability of ABPM devices fo
r hypertensive patients and those under general anesthesia, and may not be
applicable to ambulant individuals with heart failure and blood pressures a
t or below the lower end of the evaluated ranges. Prospective studies of th
e accuracy and reliability of ABPM devices, their clinical utility and rese
arch potential should be undertaken in patients with heart failure before t
heir informal and uncontrolled use in this population becomes widespread.