Pii: s0895-7061(00)01235-8

Device-Guided Breathing
Exercises Reduce Blood Pressure:
Ambulatory and Home Measurements

Talma Rosenthal, Ariela Alter, Edna Peleg, and Benjamin Gavish Slow breathing practiced routinely using an interactive older patients and higher baseline BP. The results provide device has demonstrated a sustained reduction in high additional support for the efficacy of the device as an blood pressure (BP). We reevaluated the BP response of adjunctive lifestyle modification for treating hypertension.
hypertensives (n ϭ 13) to this daily treatment for 8 weeks Am J Hypertens 2001;14:74 –76 2001 American Journal using 24-h ambulatory, home, and office BP measure- ments. A clinically significant BP reduction of similarmagnitude was observed in all BP monitoring modalities Key Words: Lifestyle modification, therapeutic, ambu-
during the daytime. Greater BP reductions were found for latory blood pressure, hypertension.
Thesideeffectsandcostofantihypertensivedrugs anddigitalBPmonitoring(BPM)performedathomein
have led to the search for effective nonpharmaco- addition to standard office measurements.
logic treatment alone or as an adjunct to drug therapy.1 Recently, a randomized controlled study re- ported that device-guided slow breathing with prolonged Subjects
expiration performed daily for 2 months resulted in a The study population included 13 hypertensives, 7 men sustained office blood pressure (BP) reduction of 16.2/ and 6 women, 6 medicated with antihypertensive drugs 10.6 mm Hg from a baseline BP of 158/97 mm Hg (n ϭ with no dose change for 3 weeks before the study, and 7 65).2 A similar study with this device involved home BP unmedicated, aged 25–75 years, excluding patients with BP classified as stage III (systolic BP Ն180 mm Hg or Breathing exercises play a prominent role in behavioral diastolic BP Ն110 mm Hg) and unmedicated patients with methods such as yoga, meditation, and biofeedback, which have had some success in treating high BP.4–6 There may Study Design
be some rationale for the therapeutic effect of the breathingexercises, as the acute response to slow and stable breath- The study included only one treatment group. During the ing includes a number of beneficial effects on the cardio- study a patient visited the clinic five times. Visits 1 and 2, vascular system, both at the systemic and the microvascu- 1 day apart, were used for eligibility and baseline office lar level. These include increasing baroreflex sensitivity, and 24-h ambulatory BP measurements. Treatment and heart rate variability, microvascular flow and venous re- home BP measurement took place during the next 8 turn, and reducing BP and peripheral resistance.7–11 How- weeks. One follow-up visit (No. 3) was scheduled at the ever, some of the observed antihypertensive effect elicited end of 4 treatment weeks. Office and 24-h ambulatory BP by the breathing exercises may be attributed to placebo measurements were done at the end of treatment (visits 4 response, to which office BP measurements are sensitive, and 5, 1 day apart). An assistant trained the patient in but ambulatory and home BP monitor are relatively insen- using the device and the home BP monitor during visit 2 It is the purpose of the present study to reevaluate the Treatment
efficacy of the breathing-guiding device in reducing theBP of hypertensives using 24-h ambulatory BP monitoring Treatment consisted of 15 min daily, breathing exercisesperformed for 8 weeks, musically guided by a device Received May 25, 2000. Accepted June 6, 2000.
Address correspondence and reprint requests to Talma Rosenthal, From the Chorley Hypertension Unit, Chaim Sheba Medical Center MD, Chorley Hypertension Unit, Chaim Sheba Medical Center, Tel (TR, EP), Tel Hashomer and InterCure Ltd. (AA, BG), Neve-Ilan, Israel.
Hashomer, Israel; e-mail: talros_il@yahoo.com 2001 by the American Journal of Hypertension, Ltd. Published by Elsevier Science Inc. AJH–January 2001–VOL. 14, NO. 1 DEVICE-GUIDED BREATHING REDUCES BLOOD PRESSURE
called Respi-Low (InterCure Ltd., Neve Ilan, Israel). Thedevice consists of a belt-type respiration-movement sensormounted on the upper abdomen or chest, attached to acomputerized control unit and headphones. On the basis ofan analyzed monitored breathing pattern, the device com-poses, in real-time, music-like sound patterns with a tem-poral structure similar to the actual breathing pattern butwith prolonged “expiration” (in the sound pattern). Thebreathing pattern modification occurs as the user volun-tarily follows the sound pattern with his or her breathingmovements. This process continues until a steady state isreached at the lowest breathing rate comfortable for theuser. The device also has a data logger that stores anddisplays data including date, time, and duration of use, andperformance parameters for the purpose of technical helpby telephone. The treatment took place at home, during theafternoon or evening. No change was made in the antihy-pertensive medication throughout the study period. Treat-ment started after visit 2 and stopped before visit 4. De-vices were then collected and downloaded.
FIG. 1. Age dependence of change in 24-h ambulatory systolic
BP Measurements
blood pressure (BP) (awake) in response to treatment. Each pointcorresponds to an individual patient. The regression line is marked.
Office BP was measured in a sitting position, after the The correlation coefficient is r ϭ 0.76 and the slope is Ϫ0.46 mm patient had rested for 5 min, using a standard procedure.
The BP level for each device was taken as the average ofthe last two readings after three consecutive readings.
Twenty-four-hour ambulatory BP was determined at fre- changes were tested for being different from zero by quency of four per hour using Suntech Accutracker (Sun- one-sample t test. Dependence of BP changes on age and tech Medical Instruments, Raleigh, NC). The attached baseline values were determined using linear regression software provided the average BP in the awake and asleep models, where the P values correspond to the regression phases. Home BP was measured with Omron IC, a digital coefficients (eg, the significance of a non-zero slope as BPM that stores all data including BP, heart rate, date, and illustrated in Fig. 1). All P values were two-tailed. Statis- hour up to 350 measurements without a possibility to erase tical significance was associated with P Ͻ .05.
or replace data by the user. Patients were instructed tomeasure BP in the morning three times consecutively in acomfortable sitting position after at least 5 min of rest, and to refrain from smoking, physical exercise, or caffeine Baseline characteristics (mean Ϯ SD) were age 50.5 Ϯ during the 30 min preceding the measurement.
13.9 years and body mass index 25.0 Ϯ 5.2. Systolic/ Subject’s compliance with treatment was checked using diastolic BP were the following: for 24-h ambulatory, data stored in the data logger of the Respi-Low during the 137.1 Ϯ 6.9/82.5 Ϯ 8.4 mm Hg for awake (n ϭ 13) and study (by telephone) and after the study, when the data 117.8 Ϯ 10.3/69.4 Ϯ 10.5 mm Hg for asleep (n ϭ 12).
files were downloaded. Compliance with home BP mea- Office BP was 140.7 Ϯ 13.9/86.1 Ϯ 8.9 mm Hg and home surements was checked by the dates and times of the BP was 146.4 Ϯ 15.4/84.8 Ϯ 8.3 mm Hg. Heart rate was measurements stored in the BPM and downloaded at visits 75.2 Ϯ 6.7 beats/min. The number of patients at each BP classification was 1, 3, 7, and 2 for normal, high normal, Data Analyses and Statistics
stage I, and stage II, respectively.
The response to treatment is summarized in Table 1. In The study outcomes were the average systolic and dia- general, BP changes were similar in all monitoring meth- stolic BP changes from baseline level (visits 1 and 2 for ods. Significant systolic BP reduction was observed in the the office and 24-h ambulatory) to end level (visits 4 and 24-h ambulatory (awake) and the office BP. There was a 5). For the home measurements study outcomes were the 73% correlation between the 24-h ambulatory home mean average daily BP in the first and last 2 weeks. Heart rate arterial pressure (MAP) change (defined as: diastolic ϩ changes were defined accordingly. The primary study out- (systolic Ϫ diastolic)/3). No correlation was found be- come was the 24-h ambulatory BP changes in the awake tween office BP changes and baseline values of either phase, as outcomes of previous studies (office BP changes) ambulatory or home BP or the difference between office were defined at this time phase. The BP and heart rate and home BP, which discloses white coat effect. There was DEVICE-GUIDED BREATHING REDUCES BLOOD PRESSURE AJH–January 2001–VOL. 14, NO. 1
office systolic BP change between the present and the previous study can be explained quantitatively by its de- BP Change (mm Hg)
pendence on the baseline BP, which was higher in the BP Monitoring Modality
(n
Systolic
Diastolic
In conclusion, the present study provides additional evi- dence of the benefit of routine breathing exercises guided by the tested device as a safe and efficacious adjunctive lifestyle modification for treating hypertension.
References
* P Ͻ .05.
P Ͻ .01.
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