TY - JOUR
T1 - Comparison of telemetric and tail-cuff blood pressure monitoring in adrenocorticotrophic hormone-treated rats
AU - Fraser, Tafline B.
AU - Turner, Steven W.
AU - Mangos, George J.
AU - Ludbrook, John
AU - Whitworth, Judith A.
PY - 2001
Y1 - 2001
N2 - 1. The aim of the present study was to validate a telemetric blood pressure (BP) monitoring system against tail-cuff blood pressure in both adrenocorticotrophic hormone (ACTH)- and sham-treated rats. In the statistical analyses, we first tested whether there was a detectable effect on systolic blood pressure (SBP) of 10 days treatment with ACTH compared with saline. Second, we compared results of telemetered and tail-cuff measurements and, third, we developed a novel method for estimating the relative power of the two techniques. 2. Twenty-three male Sprague-Dawley rats were randomly divided into two groups: (i) ACTH (100 μg/kg per day, s.c.; n=12) treated; or (ii) sham treated (0.9% saline, s.c.; n=11). Systolic BP was measured by the telemetric system (sampled for 10 s every 2 min) continuously for 4 h (n=16) or for 30 min (n=23) and also by the indirect tail-cuff method daily (n=23). Data were compared within and between groups; ordinary least products (OLP) regression analysis was then performed to test for bias between the two methods. Sample size/power estimations were also performed. 3. Adrenocorticotrophic hormone treatment raised telemetered SBP by 11 mmHg (P<0.001) compared with 14 mmHg (P<0.001) using the tail-cuff method. There was no fixed or proportional bias between the two methods of measurement, as shown by regression analysis. Power calculations indicate that a minimum sample size of six gives a power of telemetered to tail-cuff of 0.84/0.86=0.98. The power of 4 h versus 30 min BP measurements was 0.99/0.82=1.2. 4. Telemetry gave very similar results to the tail-cuff method. Telemetry allows for a longer period of measurement, giving greater power to the study so that fewer animals are needed.
AB - 1. The aim of the present study was to validate a telemetric blood pressure (BP) monitoring system against tail-cuff blood pressure in both adrenocorticotrophic hormone (ACTH)- and sham-treated rats. In the statistical analyses, we first tested whether there was a detectable effect on systolic blood pressure (SBP) of 10 days treatment with ACTH compared with saline. Second, we compared results of telemetered and tail-cuff measurements and, third, we developed a novel method for estimating the relative power of the two techniques. 2. Twenty-three male Sprague-Dawley rats were randomly divided into two groups: (i) ACTH (100 μg/kg per day, s.c.; n=12) treated; or (ii) sham treated (0.9% saline, s.c.; n=11). Systolic BP was measured by the telemetric system (sampled for 10 s every 2 min) continuously for 4 h (n=16) or for 30 min (n=23) and also by the indirect tail-cuff method daily (n=23). Data were compared within and between groups; ordinary least products (OLP) regression analysis was then performed to test for bias between the two methods. Sample size/power estimations were also performed. 3. Adrenocorticotrophic hormone treatment raised telemetered SBP by 11 mmHg (P<0.001) compared with 14 mmHg (P<0.001) using the tail-cuff method. There was no fixed or proportional bias between the two methods of measurement, as shown by regression analysis. Power calculations indicate that a minimum sample size of six gives a power of telemetered to tail-cuff of 0.84/0.86=0.98. The power of 4 h versus 30 min BP measurements was 0.99/0.82=1.2. 4. Telemetry gave very similar results to the tail-cuff method. Telemetry allows for a longer period of measurement, giving greater power to the study so that fewer animals are needed.
KW - Adrenocorticotrophic hormone
KW - Blood pressure
KW - Experimental hypertension
KW - Rats
KW - Telemetry
UR - http://www.scopus.com/inward/record.url?scp=0034773858&partnerID=8YFLogxK
U2 - 10.1046/j.1440-1681.2001.03531.x
DO - 10.1046/j.1440-1681.2001.03531.x
M3 - Article
SN - 0305-1870
VL - 28
SP - 831
EP - 835
JO - Clinical and Experimental Pharmacology and Physiology
JF - Clinical and Experimental Pharmacology and Physiology
IS - 10
ER -