Evidence-Based Complementary and Alternative Medicine
Volume 2020 (2020), Article ID 8171549, 10 pages
https://doi.org/10.1155/2020/8171549

Research Article

Effect of Baduanjin Sequential Therapy on the Quality of Life and Cardiac Function in Patients with AMI After PCI: A Randomized Controlled Trial

Ming-Gui Chen, Xuefei Liang, Lili Kong, Jingjing Wang, Fangfang Wang, Xiyan Hu, Jianzhuo He, Rui-Xiang Zeng, Shuai Mao, Liheng Guo, Min-Zhou Zhang, and Xiaoxuan Zhang

Division of Chest Pain Center, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou 510120, China

Correspondence should be addressed to Min-Zhou Zhang; minzhouzhang@aliyun.com and Xiaoxuan Zhang; zhxiaoxuan2003@163.com

Received 21 March 2020; Accepted 2 June 2020; Published 4 July 2020

Academic Editor: Avni Sali

Copyright © 2020 Ming-Gui Chen 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.

Abstract.

Purpose. The purpose of this study was to examine the effects of Baduanjin sequential therapy (BST) on the quality of life and cardiac function in patients with AMI after PCI. Subjects. 96 patients with AMI after PCI were randomly assigned as subjects to two groups: BST group who received 24 weeks of BST training and control group who received no training. Methods. The methods used in this study included the changes in SF-36 subscales, the measures of left ventricular ejection fraction (LVEF), N-terminal pro-B-type natriuretic peptide (NT-pro-BNP), the body mass index (BMI), and the abdominal circumference. Results. Of the 96 participants, 82 total patients completed the entire study. At 12 weeks, role physical and health transition of SF-36 were significantly different between the two groups, with a difference of 26.12 (95% CI, 11.59 to 40.64) in role physical and a difference of 15.94 (95% CI, 5.60 to 26.28) in health transition (). However, there were statistically significant differences in all aspects of SF-36 between the two groups at 24 weeks (). The BST also lowered abdominal circumference and BMI as compared with the control group. In the 24-week follow-up, a significant difference was found in the decline of the LVEF in the control group (), while there was a nonsignificant difference in the BST group (). Compared with the control group, the BST group reduced 50 pg/ml on the NT-pro-BNP at 24 weeks (). The effects of BST exercise were maintained at 24 weeks after the intervention. No serious adverse events were observed. Conclusions. The BST appears to improve the quality of life in patients with AMI after PCI, with additional benefits of lowered abdominal circumference and BMI and improved level of cardiac function. This trial is registered with NCT02693795.

1. Introduction

Acute myocardial infarction (AMI) is one of the leading causes of death around the world, with the potential for substantial morbidity and mortality [1, 2]. From 2001 to 2011, the number of AMI in China increased by four times [3]. Based on the estimation of the Markov model, 21 million new acute coronary events and 7 million cardiac deaths will occur in China in the next 20 years [4]. Although technical advances in percutaneous coronary intervention (PCI) are becoming better and more effective medical therapy, most patients still suffer from angina pectoris, anxiety, depression, and reduced cardiac function after PCI [5–8]. At least 5–10% of survivors die within the first 12 months after the MI and close to 50% need hospitalization within the same year [9, 10].

Previous studies have shown that myocardial ischemia-reperfusion (IR) injury can cause ventricular cell death and is a major pathological event leading to morbidity and mortality in those with acute myocardial infarction [11, 12]. Interestingly, appropriate exercise can rapidly produce a cardiac phenotype that resists IR-induced myocardial injury. It can also relax the heart blood vessels, promote the regeneration of microvessel, and regulate the balance of the autonomic nervous system of the heart [13–15]. As a result, many studies have confirmed that exercise can reduce cardiovascular diseases and significantly decrease the incidence of angina and cardiac events [16, 17]. Exercise also improves patient survival and improves patients’ quality of life [18, 19]. However, most exercise programs are complicated and require supervision, and they may even result in an overload of the heart in patients with AMI. A simple easy-to-learn, free-of-charge, and appropriate home-based exercise program is necessary to improve adherence to exercise and help patients with AMI maintain a physically active lifestyle.

Baduanjin exercise, as an important component of Chinese Qigong exercises, is easy to learn and can be performed at home without any assistive equipment [20]. Previous studies have found that Baduanjin exercise is beneficial to health, leading to improvement of strength, physical fitness, and depression [21–23]. However, many studies have focused on the effects of standing Baduanjin on chronic diseases. Baduanjin sequential therapy (BST) which has been developed by our team consists of sitting and standing forms as shown in Supplementary Appendix Figures 1(a) and 1(b). It is simple and effective in clinical practice and the program emphasizes early rehabilitation interventions and continued rehabilitation after discharge. However, there exists few data from large-scale randomized trials that have addressed the effect of Baduanjin exercise on the quality of life and cardiac function in the patient with AMI after PCI. The primary aim of this study was to examine the quality of life and the level of cardiac function in AMI patients after PCI over time in response to a 24-week BST.

2. Materials and Methods

2.1. Research Design

This study was a parallel, randomized controlled trial (RCT) with a longitudinal research design. Participants were randomly assigned to either the BST group or the control group. Our study strictly complies with the guidelines of the CONSORT 2010 checklist. The study received ethical approval from the Guangdong Provincial Hospital of Chinese Medicine’s Human Research Ethics Committee (approval number B2015–41-01), and it was registered with the clinicaltrials.gov (protocol: NCT02693795). This study complies with the principles outlined in the Helsinki Declaration and the relevant regulations of the national regulatory agency.

2.2. Participants and Procedures

Recruitment took place in 2016 and 2017, primarily via the screening of hospitalized patients. Eligibility criteria included patients with a clinical diagnosis of AMI, aged 18 to 80 years, performed PCI, and signed an informed consent form. The AMI diagnostic criteria are a reference to the third universal definition of myocardial infarction [24]. Exclusion criteria were current participation in any other behavioral or pharmacological study or instructor-led exercise program, cardiogenic shock, severe heart failure (NYHA cardiac function class IV or LVEF ≤ 35%), malignant arrhythmia (ventricular fibrillation, ventricular tachycardia, and frequent ventricular premature beats), or active bleeding. Patients with poor underlying conditions such as those suffering from bone and joint disease or nervous system disorders that would impede full participation in the study and unavailability during the study period were also excluded.

Patients were randomized to either the BST group or to the control group in a 1 : 1 allocation ratio. Biostatisticians randomized assignments using a sequence randomly generated in the R statistical package. These assignments were put into sealed, opaque envelopes with the date and signature labels placed over the seals of the envelopes. After baseline evaluation of patients, the study coordinator opened the consecutive randomization envelopes and informed the individuals of their group assignments.

Given the nature of the exercise intervention, it was impossible that study participants and exercise instructors could be unaware of the randomization allocation throughout the entire duration of this trial. However, the investigators conducting the outcome assessments and the biostatisticians responsible for the analysis were blinded to the assignment.

The patients in the BST group were asked to complete attendance forms as well as class sign-in sheets for the BST intervention once a month and the patients in the control group would be requested to maintain their original habit of lifestyle. They were also asked to maintain Baduanjin exercise or regular aerobic exercise throughout the follow-up period. Adherence was measured after intervention by telephone calls or WeChat during which research assistants inquired about the frequency and duration of the patients’ participation in the BST exercise and general aerobic exercise.

2.3. Sample Size

The sample size was calculated on the basis of the changes in SF-36 after 24 weeks of intervention between comparison groups with a significance level of 5% and a two-tailed critical region. According to previous research, the control group can increase the average score of SF-36 by 9 points. Baduanjin can increase the average score of SF-36 by 23 points, and the standard deviation is about 29. According to the formula, . The sample size of each group is about 40 cases and a total of 80 cases in the two groups. Considering the situation of dropout and loss of follow-up, it is estimated that the dropout (loss of follow-up) of 20% will require 96 cases.

2.4. Interventions

2.4.1. BST Exercise

BST has been developed by our team based on the characteristics of patients with myocardial infarction (Supplementary Appendix Video 1). It consists of the sitting form and the standing form (Supplementary Appendix Figures 1(a) and 1(b)) because the goal is to allow patients with AMI to be also rehabilitated during hospitalization. On the second day after the standard treatment (blood revascularization + drug therapy), patients began the sitting Baduanjin exercises (30 min/session, twice a day, 3 days). After discharge, the patients did the standing Baduanjin exercises (30 min/session, fifth weekly, lasting up to 24-weeks). Patients were provided with a picture-based educational brochure describing the Baduanjin exercises including practicing techniques and safety precautions. Scheduled telephone follow-ups were also provided to reinforce patients’ adherence to the 24-week follow-up assessments.

We had strict monitoring indicators and the therapy would be terminated if patients had any of the following conditions. (1) The patient felt laborious and had physical discomforts such as chest pain, dizziness, sweating, and severe dyspnoea. The oxygen saturation was <90%. (2) The FIO₂ was >60% and breathing was >35 breaths per minute. (3) The systolic blood pressure was <90 or >200 mmHg and mean arterial pressure < 65 mmHg. (4) The patient had unstable heart rhythm or needed to use antiarrhythmic drugs or vasoactive medicines.

2.5. Outcome Measures

All outcomes were measured at baseline (week 0) and midterm (week 12) and study completion (week 24). The primary outcome was the SF-36. The secondary outcomes included changes in LVEF, NT-pro-BNP, BMI, and abdominal circumference.

2.5.1. SF-36

The SF-36 health survey scale was developed by the health research institute of New England medical center in Boston, USA, and the Chinese version was successfully developed by the team of Li et al. in 2002, with good reliability and validity [25]. The SF-36 is a widely used, standard instrument for evaluating HRQoL. It is a self-assessment health status questionnaire containing 36 items (questions) about sociodemographic data, health, and personal behavior, grouped into 8 multi-item domains. It measures the following: (1) physical functioning (10 items), (2) social functioning (2 items), (3) role limitations because of physical problems (4 items), (4) role limitations because of emotional problems (3 items), (5) mental health (5 items), (6) energy and vitality (4 items), (7) bodily pain (2 items), and (8) general health perception (5 items). Each of the scores for the domains was coded, summed in an Excel chart, and later transformed in the statistical program SPSS. The results were presented from 0 (worst possible health) to 100 (best imaginable health).

2.5.2. LVEF

The LVEF was obtained through echocardiography. Participants were asked to undergo echocardiographic measurements on the first day of admission, at 12 and 24 weeks after discharge.

2.5.3. NT-pro-BNP

The NT-pro-BNP was determined by sampled blood. All participants were tested for the NT-pro-BNP on admission. The participants were also notified by telephone or WeChat to have blood tests at 12 and 24 weeks after discharge. The laboratory instrument we used was ROCHE, the model was cobae e602, and the reagent batch number was 37537600.

2.5.4. BMI

The BMI is the weight in kilograms divided by the square of the height in meters. Participants were instructed to remove their shoes for measuring their height and weight, and the staff used consistent methods with each patient measurement.

2.5.5. The Abdominal Circumference

The abdominal circumference was measured by tapeline. Patients were asked to stand up and naturally relaxed. The staff measured the abdominal circumference at the navel level 3 times. The results were averaged to derive a range for each measure.

2.6. Statistical Analysis

Data were reported as mean and standard deviation for continuous variables and as percentages for categorical variables. All analyses were undertaken in SPSS version 22 (IBM Corp). Independent t-tests and chi-square (χ²) tests were used to examine the homogeneity of demographic and clinical information and the quality of life between the two groups at baseline. Values are presented as mean ± SD and percentage (%) in tables and median with the interquartile range in figures. Repeated measures analysis of variance (ANOVA) was used to test for change over time (i.e., baseline, 12 weeks, and 24 weeks) in the quality of life and NT-pro-BNP for the intervention and control groups. Group comparisons were made by the Mann–Whitney U test for continuous variables and the chi-square test for categorical variables. A value of <0.05 was considered significant.

3. Results

3.1. Characteristics at Baseline between the Two Groups

During the study period from July 2016 to August 2017, a total of 110 patients with AMI who underwent PCI were recruited according to the inclusion criteria. Of these patients, 10 refused to participate, and 4 were unable to play videos at home. Most participants who refused to participate in this study did so for personal reasons, including being too busy, having no motivation or interest, and feeling inconvenienced or uncomfortable. 96 patients were randomly assigned to either the BST group (n = 48) or the control group (n = 48). 14 patients withdrew due to personal reasons (n = 12), loss of contact (n = 1), and death (n = 1). Of the 96 participants, 82 total patients completed the entire study, yielding an attrition rate of 14.58% (Figure 1).

Figure 1: Inclusion and exclusion criteria for this study.

We obtained complete data from 82 cases as shown in Table 1. Table 1 shows the baseline characteristics of the study population. The groups were well matched about baseline characteristics, including age, sex, BMI, NT-pro-BNP, baseline study outcomes of drug treatment, and procedural characteristics ().

Table 1: Baseline clinical and procedural characteristics.

Variable
Control group (n = 39)
BST group (n = 43)
value

Clinical characteristics

Age (years)
61.49 ± 11.54
59.98 ± 10.86
0.543

Male, n (%)
30 (76.9)
29 (67.4)
0.34

Body mass index (kg/m²)
24.62 ± 2.86
23.95 ± 2.35
0.25

Hypertension, n (%)
22 (56.4)
26 (60.5)
0.71

Dyslipidaemia, n (%)
11 (28.2)
14 (32.6)
0.669

History of smoker, n (%)
25 (64.1)
22 (51.2)
0.237

History of CAD, n (%)
1 (2.6)
6 (14)
0.148

Diabetes, n (%)
10 (25.6)
9 (20.9)
0.614

LVEF (%)
63.74 ± 8.52
61.07 ± 9.64
0.189

LVEDD (mm)
46.54 ± 3.73
44.83 ± 4.68
0.073

LVESD (mm)
29.77 ± 5.52
29.82 ± 5.71
0.97

NT-pro-BNP (pg/ml)
374 (108–1093)
408 (191–921)
0.66

WBC (10⁹/L)
10.55 ± 3.12
10.97 ± 3.51
0.574

TG (mmol/L)
1.51 (1.09–2.19)
1.53 (1.10–2.30)
0.795

TC (mmol/L)
4.86 ± 0.85
4.87 ± 1.13
0.971

HDL-C (mmol/L)
1.10 ± 0.28
1.12 ± 0.44
0.856

LDL-C (mmol/L)
3.38 ± 0.78
3.53 ± 0.92
0.425

Drug treatment

Statins, n (%)
39 (100)
43 (100)

Aspirin, n (%)
39 (100)
43 (100)

Clopidogrel, n (%)
39 (100)
43 (100)

b-Blockers, n (%)
16 (41)
20 (46.5)
0.617

Calcium blockers, n (%)
6 (15.4)
5 (11.6)
0.618

ACE inhibitors, n (%)
6 (15.4)
3 (7)
0.388

ARBs, n (%)
6 (15.4)
14 (32.6)
0.71

Diuretics, n (%)
4 (10.3)
3 (7)
0.893

Procedural characteristics

Transradial access, n (%)
36 (92.3)
39 (90.7)
1

Target vessel

Left main
1 (2.6)
1 (2.6)
1

Left anterior descending
32 (82.1)
33 (76.7)
0.554

Left circumflex
20 (51.3)
19 (44.2)
0.521

Right coronary artery
23 (59)
25 (58.1)
0.939

Lesion location

Proximal
24 (61.5)
29 (67.4)
0.577

Middle
27 (69.2)
27 (62.8)
0.539

Distal
4 (10.3)
7 (16.3)
0.424

Branch
13 (33.3)
13 (30.2)
0.763

Preoperative TIMI 0
17 (43.6)
18 (41.9)
0.874

Preoperative TIMI 1
2 (5.1)
1 (2.3)
0.931

Preoperative TIMI 2
1 (2.6)
2 (4.7)
1

Preoperative TIMI 3
19 (48.7)
22 (51.2)
0.825

Postoperative TIMI 3
39 (100)
43 (100)

Lesion classification

Number of stents implanted
1.18 ± 0.389
1.09 ± 0.294
0.263

BMI, body mass index; CAD, coronary artery disease; NT-pro-BNP, N-terminal pro-brain natriuretic peptide; TG, triglyceride; TC, total cholesterol; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; ACE, angiotensin-converting enzyme; ARBs, angiotensin receptor blockers. The BMI is the weight in kilograms divided by the square of the height in meters. Values are expressed as the mean ± SD, the median with interquartile range, or n (%). values were calculated by t-test for continuous variables and by the chi-square test or Fisher’s exact test for categorical variables.

3.2. Primary Outcomes

Mean (±SD) differences between groups in outcome visits at baseline, 12 weeks, and 24 weeks were shown in Table 2. Pairwise comparison and data analysis showed that there was no statistically significant difference between the two groups at the time of enrollment (). At 12 weeks, role physical and health transition of SF-36 were significantly different between the two groups, with a difference of 26.12 (95% CI, 11.59 to 40.64) in role physical and a difference of 15.94 (95% CI, 5.60 to 26.28) in health transition (). However, there were statistically significant differences in physical functioning, role physical, bodily pain, general health, vitality, social function, role emotional, mental health, and health transition of SF-36 between the two groups at 24 weeks ().

Table 2: The changes of SF-36 subscales during the 24 weeks.

Measure
Control group (n = 39)
BST (n = 43)
BST vs. control group (95% CI)
value

Physical functioning

Baseline
77.05 ± 17.15
71.51 ± 17.27
−5.54 (−13.12 to 2.04)
0.150

12 weeks
80.13 ± 16.60
86.33 ± 10.73
6.20 (0.11 to 12.28)
0.051

24 weeks
82.69 ± 12.34
90.11 ± 10.72
7.42 (2.35 to 12.49)
0.005

Role physical

Baseline
35.89 ± 32.34
34.88 ± 38.76
−1.01 (−16.79 to 14.76)
0.899

12 weeks
44.23 ± 33.67
70.34 ± 32.39
26.12 (11.59 to 40.64)
0.001

24 weeks
69.87 ± 40.63
90.11 ± 16.49
20.24 (6.85 to 33.64)
0.004

Bodily pain

Baseline
61.90 ± 21.61
56.44 ± 25.09
−5.46 (−15.80 to 4.88)
0.297

12 weeks
80.97 ± 17.70
79.30 ± 13.59
−1.67 (−8.57 to 5.23)
0.631

24 weeks
80.35 ± 19.89
90.05 ± 11.81
9.69 (2.58 to 16.80)
0.008

General health

Baseline
56.92 ± 15.08
52.00 ± 14.33
−4.92 (−11.38 to 1.54)
0.134

12 weeks
65.28 ± 16.27
59.58 ± 19.81
−5.70 (−13.72 to 2.31)
0.161

24 weeks
63.54 ± 18.73
77.84 ± 16.19
14.30 (6.62 to 21.98)
<0.001

Vitality

Baseline
59.23 ± 14.31
55.58 ± 12.21
−3.65 (−9.48 to 2.18)
0.216

12 weeks
62.18 ± 14.99
67.21 ± 9.96
5.03 (−0.64 to 10.70)
0.081

24 weeks
62.31 ± 8.57
73.95 ± 8.42
11.65 (7.91 to 15.38)
<0.001

Social function

Baseline
83.97 ± 24.15
77.61 ± 26.10
−6.36 (−17.45 to 4.73)
0.257

12 weeks
71.28 ± 24.62
72.56 ± 20.94
1.28 (−8.74 to 11.29)
0.801

24 weeks
71.79 ± 24.37
82.32 ± 12.87
10.53 (1.78 to 19.28)
0.019

Role emotional

Baseline
61.53 ± 42.26
47.98 ± 38.04
−13.55 (−31.20 to 4.09)
0.130

12 weeks
69.23 ± 40.74
81.39 ± 25.51
12.16 (−3.02 to 27.34)
0.114

24 weeks
70.08 ± 38.08
96.12 ± 10.81
26.04 (13.31 to 38.77)
<0.001

Mental health

Baseline
71.28 ± 16.51
66.32 ± 17.07
−4.96 (−12.35 to 2.44)
0.186

12 weeks
78.97 ± 15.78
80.19 ± 13.38
1.21 (−5.20 to 7.62)
0.708

24 weeks
74.87 ± 15.27
82.23 ± 17.38
7.36 (0.14 to 14.58)
0.046

Health transition

Baseline
36.54 ± 26.19
44.19 ± 24.90
7.65 (−3.58 to 18.87)
0.179

12 weeks
44.87 ± 22.34
60.81 ± 24.49
15.94 (5.60 to 26.28)
0.003

24 weeks
51.28 ± 22.18
82.56 ± 19.31
31.28 (21.99 to 40.56)
<0.001

Data are presented as mean ± SD. values were calculated by t-test for continuous variables.

3.3. Secondary Outcomes

Significant differences between groups were observed after 24 weeks. The BST group had significantly better performance on the abdominal circumference and BMI (Table 3). In the 12 weeks and 24 weeks, the participants in the BST group had a mean decrease of 3.45 centimeters and 4.29 centimeters in abdominal circumference compared with the control group (). Regarding BMI, although the 2 groups had no significant improvements during the 12 weeks, there was a considerable improvement in the BST group compared with the control group at 24 weeks (23.40 ± 2.30 and 24.60 ± 2.82, respectively, ).

Table 3: The changes of abdominal circumference and BMI during the 24 weeks.

Measure
Control group (n = 39)
BST (n = 43)
BST vs. control group (95% CI)
value

Abdominal circumference

Baseline
90.84 ± 9.44
87.87 ± 6.68
−2.96 (−6.61 to 0.68)
0.109

12 weeks
90.34 ± 7.00
86.89 ± 5.25
−3.45 (−6.25 to −0.65)
0.016

24 weeks
90.26 ± 7.10
85.98 ± 5.79
−4.29 (−7.18 to −1.39)
0.004

BMI

Baseline
24.62 ± 2.86
23.95 ± 2.35
−0.67 (−1.81 to 0.48)
0.249

12 weeks
24.57 ± 2.77
23.94 ± 2.33
−0.63 (−1.75 to 0.49)
0.268

24 weeks
24.60 ± 2.82
23.40 ± 2.30
−1.21 (−2.34 to −0.09)
0.035

BMI, body mass index. Data are presented as mean ± SD.

In the 24-week follow-up, the LVEF of the BST group and the control group was baseline (61.06 ± 9.64 and 63.74 ± 8.51, respectively), 12-week outcome (60.34 ± 9.20 and 60.48 ± 9.64, respectively), and 24-week outcome (58.74 ± 10.10 and 57.79 ± 9.56, respectively) (Figure 2). A significant difference was found in the decline of the LVEF in the control group (). A nonsignificant difference was found in the decline of the LVEF in the BST group (). Besides, we also found that the BST group and the control group had a significant decrease in the NT-pro-BNP level at the 24-week outcome (105 [67–244], 155 [108–293], respectively, ) (Figure 3);

Figure 2: The changes of cardiac function during the 24 weeks. In the 24-week follow-up, the LVEF of the BST group and the control group was baseline (61.06 ± 9.64 and 63.74 ± 8.51, respectively), 12-week outcome (60.34 ± 9.20 and 60.48 ± 9.64, respectively), and 24-week outcome (58.74 ± 10.10 and 57.79 ± 9.56, respectively). A significant difference was found in the decline of the LVEF in the control group (). A nonsignificant difference was found in the decline of the LVEF in the BST group ().

(a)

(b)

(c)

Figure 3: The changes of NT-pro-BNP during the 24 weeks. Values are presented as median with the interquartile range. A significant difference was found in the NT-pro-BNP between the BST and control groups at 24 weeks (); a nonsignificant difference was found between the BST and control groups at baseline and 12 weeks ().

3.4. Adverse Events

During the study period, 1 patient died of cardiac arrest during hospitalization in the control group, and 1 patient withdrew from the study because of a new diagnosis of non-Hodgkin'’s lymphoma during follow-up in the BST group. None of these events could be related to the interventions. 4 patients withdrew from the BST group, and 8 patients were removed from the control group for personal reasons.

4. Discussion

The results of this study showed that the 24-week BST program was effective for improving the quality of life and cardiac function in patients with AMI after PCI. It could also significantly decrease BMI and abdominal circumference. No serious adverse events were observed during BST training, indicating the safety and usefulness of early intervention for patients with AMI who underwent PCI.

AMI is a common cardiac emergency with a high mortality rate [1]. Although PCI and drugs are currently effective in treating patients, many studies have shown that even after treatment, there is still a high risk of cardiovascular disease recurrence and death after PCI, especially within 1 year after surgery [26, 27]. Therefore, there is considerable concern about this problem. Relevant literature reports that nearly 60% of patients after PCI are severely deficient in exercise, and about 84% of patients after PCI have associated anxiety symptoms, while 67% have associated depressive symptoms [26, 28]. Previous studies have shown that myocardial ischemia-reperfusion (IR) injury can cause ventricular cell death and is a major pathological event leading to morbidity and mortality in those with acute myocardial infarction [11, 12]. Interestingly, appropriate exercise can rapidly produce a cardiac phenotype that resists IR-induced myocardial injury. It is essential for the prognosis of patients with myocardial infarction [13, 15]. Goel and his colleagues counted the proportion of patients with cardiac stents participating in cardiac rehabilitation in a state in the United States and found that poststent exercise rehabilitation had become a trend [8]. Exercise training is beneficial to the patient’s cardiac rehabilitation.

To the best of our knowledge, our study is the first RCT to investigate the effect of BST exercise in patients with AMI who underwent PCI. Chen and his colleagues [29] have indicated that Baduanjin exercise can effectively improve the quality of life in patients with heart failure. A meta-analysis of nineteen studies [30] also showed that Baduanjin practice is beneficial for the quality of life. But the benefits of Baduanjin on the quality of life are more evident in older adults and individuals with chronic conditions. In our study, we were studying more severely ill patients with AMI and the results showed that the patients in the BST group performed significantly better than those in the control group at the 24-week outcome visit. Nine aspects of SF-36 were improved compared to the control group. These results were also similar to the findings of Tsang et al. [31].

As we have known, Baduanjin is a low-intensity, aerobic exercise and it is easy to learn because it is less demanding of physical and cognitive skills [32]. Several recent studies have demonstrated other benefits of Baduanjin exercise, including preventing ischaemic stroke, relieving pain and stiffness, and improving sleep quality and psychological well-being [21, 22, 33]. The BST consists of the sitting and the standing Baduanjin. It is developed by our team based on the characteristics of patients with myocardial infarction. The sitting Baduanjin exercise conforms to the aspects of low-intensity and long-term aerobic activity, which is very suitable for the rehabilitation training of patients with AMI after PCI. It was conducted twice a day in the hospital, for 30 min/session. The standing Baduanjin is more suitable for patients with sequential rehabilitation after discharge. Previous studies have shown that the reduction of LVEF following AMI is a result of infarcted myocardium and may involve dysfunctional but viable myocardium [20, 34]. In our study, a nonsignificant difference was found in the decline of the LVEF in the BST group. This shows that BST exercise can prevent the decline of cardiac function. The BST also reduced 50 pg/ml on the NT-pro-BNP at 24 weeks, compared with the control group. Regarding BMI, there was no improvement between the two groups at 12 weeks. However, the participants in the BST group had a mean decrease of 1.21 in BMI compared with the control group at the 24 weeks, which was consistent with a study by An et al. [35], who reported that the BMI values of patients with knee osteoarthritis were significantly improved after one year of Baduanjin exercise. The BST group also had significantly better abdominal circumference after the 12 weeks and 24 weeks of intervention. The results of the analysis indicated that prolonged BST exercise was of benefit to the health of the patients with AMI who underwent PCI.

The performance of BST can systematically enhance cardiopulmonary functions and concurrently modulate mind and spirit, ultimately achieving the integration of the mind and body. However, the mechanisms behind the therapeutic change remain less understood and warrant future exploration.

4.1. Study Limitations

This study has some limitations. First, this is a single-center study. Second, because they were given behavior-based treatments, the participants were aware of their intervention assignments. Moreover, we are unable to provide a definitive physiological mechanism for the effects of the Baduanjin exercise. Nonetheless, this study offers informative data from the first large-scale clinical trial of BST in patients with AMI after PCI.

5. Conclusions

The BST appears to improve the quality of life in patients with AMI after PCI, with additional benefits of lowered abdominal circumference and BMI and improved level of cardiac function.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Disclosure

This paper represents independent research. The views expressed are those of the author(s) and not necessarily those of the National Health Service, the NIHR, or the Department of Health and Social Care.

Conflicts of Interest

The author(s) declare no potential conflicts of interest for the research, authorship, and/or publication of this article.

Authors’ Contributions

Ming-Gui Chen and Xuefei Liang contributed equally to this work.

Acknowledgments

The authors gratefully acknowledge the contributions of all the investigators and participants of the carers. This work was funded by a grant (2014A020221092), from the Department of Science and Technology, Guangdong Provincial Academy of Medicine Joint Research Projects. This research was also financially supported by the Science Foundation of Guangdong Province (Nos. 2015A030310437, 2015A030306049, 2014A030313402, and 2014A020221048) and the Scientific and Technological Research of Traditional Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine (No. YN2016HL03).

Supplementary Materials

Supplementary Appendix Figure 1: (a) the introduction of the sitting Baduanjin exercises by the intensive care unit of Guangdong Provincial Hospital of Chinese Medicine. (b) the introduction of the standing Baduanjin exercises by the intensive care unit of Guangdong Provincial Hospital of Chinese Medicine. Supplementary Appendix Video 1: cardiac rehabilitation exercises of the Baduanjin sequential therapy. (Supplementary Materials)

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