Beruflich Dokumente
Kultur Dokumente
Research Article
Effectiveness of Acupressure on the Taichong Acupoint
in Lowering Blood Pressure in Patients with Hypertension:
A Randomized Clinical Trial
Copyright © 2016 Gan-Hon Lin et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Objectives. To evaluate the effectiveness of acupressure on the Taichong acupoint in lowering systolic and diastolic blood
pressure (BP) in hypertensive patients. Methods. Eighty patients with hypertension attending a cardiology outpatient department
in central Taiwan were included in this randomized clinical trial. Acupressure was applied to the Taichong acupoint in the
experimental group ( = 40) and to the first metatarsal (sham acupoint) in the control group ( = 40). Blood pressure was
measured by electronic monitoring before and immediately 15 min and 30 min after acupressure. Results. The average age of
the experimental and control participants was 59.3 ± 9.2 years and 62.7 ± 8.4 years, respectively. The two groups were similar
for demographics and antihypertensive drug use. Mean systolic and diastolic BP in the experimental group decreased at 0, 15,
and 30 min after acupressure (165.0/96.3, 150.4/92.7, 145.7/90.8, and 142.9/88.6 mmHg); no significant changes occurred in
the control group. There was a significant difference in systolic and diastolic BP between the experimental and control groups
immediately and 15 and 30 min after acupressure ( < 0.05). Conclusion. Acupressure on the Taichong acupoint can lower BP
in hypertensive patients and may be included in the nursing care plan for hypertension. However, additional studies are needed
to determine the optimal dosage, frequency, and long-term effects of this therapy.
2.4. Sample Size. The sample size was calculated from the ±2 g and was used to train researchers to apply acupressure
findings of a pilot study that included 8 participants (4 men, 4 steadily and effectively. The training regime was performed
women). The mean and standard deviation for the difference over 2 consecutive weeks. The researcher was trained to
in systolic BP before and 15 min after acupressure between the apply pressure in a perpendicular manner with the right
two groups (effect size) were entered into G Power v.3.1.2 thumb to the middle of the surface of the Digital Baby
software [26] and set to t-test. A priori analysis was performed Scale 30 times consecutively until 3 kg of pressure could be
to calculate the sample size with the following input consistently applied and the error kept within 0.5 kg.
parameters: two tails, error probability = 0.05, and power (1 −
error probability) = 0.8. The required sample size was 2.6.4. Validity and Reliability of Acupressure Staff.
calculated to be 60. Using an estimated 20% drop-out rate, we Acupres-sure staff received 180 h of training in traditional
would need 80 subjects. Forty subjects were recruited for the Chinese medicine nursing courses. The training included
experimental group and 40 for the control group. All meridian and acupoint theory as well as practical sessions.
participants enrolled completed the study. Prior to starting the study, the researcher was instructed on
correct acupressure skills and the location of the Taichong
2.5. Randomization. In this study, a gender-stratified acupoint by two Chinese physicians.
random assignment, conducted by nonteam members prior
to the beginning of the study, was used to exclude the 2.7. Data Collection. Personal information and BP were
potential effect of sex on BP and acupressure [3, 27–30]. recorded for each participant by the same researcher. The
The ran-domization process included the following: (1) 20 effectiveness of acupressure was evaluated by measuring
strips of paper labeled “control group” and 20 labeled BP in the right upper arm [31] before and immediately after
“experimental group” being placed individually in opaque acupressure and 15 and 30 min later. Participant
envelopes; (2) the envelopes being placed in a box labeled information was collected by verbal inquiry and a search of
“male group” and each qualifying male participant the medical records while waiting for BP to be measured.
receiving an enve-lope randomly picked from the box; (3)
each participant being assigned to the experimental group 2.8. Data Analysis. The statistical analysis was performed
or control group depending on the labeled strip in the using SPSS version 22.0 for Windows (IBM Corp., Armonk,
envelope. For female participants, the random assignment NY, USA). The frequency, percentage, mean, and standard
steps were identical to those used in the male participants. deviation were used as descriptive statistics. The chi-square
test and independent t-test were used to evaluate the homo-
2.6. Measures geneity of the baseline demographics of participants in both
groups and to evaluate the difference in BP in both groups
2.6.1. Validity and Reliability of Participant Data Record before and after the acupressure intervention. The paired t-test
Sheet. The following data were recorded: basic information for was used to evaluate the dif ference in BP at baseline and after
each participant, BP prior to and following acupressure, intervention. The linear mixed-effect model for repeated
medical conditions, current medications, and any other factors measures was used to analyze the effect of the intervention on
that may influence BP. Next, a 6-person panel comprising BP under conditions where confounding factors such as
Western physicians, Chinese medicine physicians, and nurse gender, age, and medications were controlled.
special-ists performed content validity tests. The content
validity index for all items ranged from 0.83 to 1.00. 2.9. Ethical Considerations. The research protocol was
reviewed and approved by the institutional review board of
2.6.2. Validity and Reliability of Electronic BP Monitor. An Taichung Veterans Hospital in central Taiwan (number
oscillometric electronic BP monitoring device (CAS740, CAS CF12105). Before recruitment, the study protocol was
Medical Systems, Inc., Branford, CT, USA) was used to described to the subjects in detail, after which they signed
measure BP prior to and following acupressure. According to consent forms. Participants were informed that they could
the manufacturer, the device has a precision of ±5 mmHg and withdraw from the study at any time and that withdrawal
a standard deviation not greater than 8 mmHg. The accuracy would not affect their treatment. After completion of the
of the electronic BP monitor was calibrated and tested study, the researcher taught the controls how to locate the
regularly by the hospital medical engineering personnel. The Taichong acupoint and apply self-acupressure.
reliability of the monitor was tested using the same monitor
and measurement method in the study site. The monitor was
set to automatically measure BP four times at 1-minute 3. Results
intervals and the test was conducted on 5 subjects. Thereafter, 3.1. Participant Information. This study was conducted
the coefficient of variation was 1.1%–2.1% and 1.3%–4.1% between August 2012 and January 2013. Of the 220 patients
for systolic and diastolic BP, respectively. who met the inclusion and exclusion criteria, 80 agreed to
participate and completed the study (Figure 2). The reasons for
2.6.3. Validity and Reliability of Digital Baby Scale. The refusal to participate included the following: family members
Digital Baby Scale (Model 727, Seca GmbH & Co. KG, or friends were waiting to take the patient home ( = 70, 50%);
Hamburg, Germany) used in this study had a precision of other work to attend to ( = 42, 30%); and lack
4 Evidence-Based Complementary and Alternative Medicine
Refused (n = 140)
Reasons for refusal:
(1) Family members or friends waiting (n = 70)
(2) Other work to attend to (n = 42)
(3) Lack of willingness in participation (n = 28)
Randomized individuals (n = 80)
Table 1: Distribution and analysis of demographic characteristics and factors affecting blood pressure in both groups.
Table 2: Changes in blood pressure before and after acupressure in both groups.
BP, gender, age, interactions between groups, and time and 30 min after acupressure in the experimental group was
between measures were significantly different ( <0.05). Group, greater than in the control group.
time between measures, and medication use were not
significantly different ( >0.05, Table 4). The effectiveness of 4. Discussion
acupressure in lowering systolic and diastolic BP in the
experimental group was significantly different from that in the The results of this study demonstrated that acupressure on the
control group after adjusting for confounding factors, Taichong acupoint was much more effective than acupressure
including gender, age, and medication use. Specifically, the on a sham acupoint in lowering systolic and diastolic BP in
decrease in systolic and diastolic BP immediately and 15 min patients with hypertension. Further, acupressure on the
6 Evidence-Based Complementary and Alternative Medicine
Table 3: Linear mixed-effect model analysis of factors affecting systolic blood pressure change.
15 min after /before (before = 0.00 1.20 0.00 1.000 −2.36 2.36
0)
−1.13 0.86 −1.31 0.192 −2.82 0.57
Immediately after /before
(before = 0) −23.03 2.04 −11.28 <0.001 −27.04 −19.01
Group ∗time 3 (30 min after
/before )
Group ∗time 2 (15 min after
−19.25 1.69 −11.37 <0.001 −22.58 −15.92
/before )
Group ∗time 1 (immediately
−13.50 1.22 −11.11 <0.001 −15.90 −11.11
after /before )
Linear mixed-effect model for repeated measures; < 0.05. time 1, time between preacupressure and immediately after acupressure; time 2, time between
preacupressure and 15 min after acupressure; time 3, time between preacupressure and 30 min after acupressure. CI, confidence interval; , acupressure.
Table 4: Linear mixed-effect model analysis of factors affecting diastolic blood pressure change.
15 min after /before (before = −1.08 0.84 −1.28 0.203 −2.73 0.58
0)
−0.93 0.60 −1.54 0.126 −2.11 0.26
Immediately after /before
(before = 0) −7.53 1.44 −5.22 <0.001 −10.37 −4.69
Group ∗time 3 (30 min after
/before )
Group ∗time 2 (15 min after
−4.48 1.19 −3.76 <0.001 −6.82 −2.13
/before )
Group ∗time 1 (immediately
−2.68 0.85 −3.14 0.002 −4.35 −1.00
after /before )
Linear mixed-effect model for repeated measures < 0.05. Time 1, time between preacupressure and immediately after acupressure; time 2, time between
preacupressure and 15 min after acupressure; time 3, time between preacupressure and 30 min after acupressure. , acupressure; CI, confidence interval; SE,
standard error.
8 Evidence-Based Complementary and Alternative Medicine
INFLAMMATION
BioMed
PPAR Research Research International
Hindawi Publishing Corporation Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014 http://www.hindawi.com Volume 2014
Journal of
Obesity
Evidence-Based
Journal of Stem Cells Complementary and Journal of
Ophthalmology
Hindawi Publishing Corporation
International
Hindawi Publishing Corporation
Alternative Medicine
Hindawi Publishing Corporation Hindawi Publishing Corporation
Oncology
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014 http://www.hindawi.com Volume 2014 http://www.hindawi.com Volume 2014 http://www.hindawi.com Volume 2014 http://www.hindawi.com Volume 2014
Parkinson’s
Disease
Computational and
Mathematical Behavioural AIDS Oxidative Medicine and
Methods in Medicine
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014
Neurology
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014
Research and Treatment
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014
Cellular Longevity
Hindawi Publishing Corporation
http://www.hindawi.com Volume 2014