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Biomedical Research

An International Journal of Medical Sciences

Research Article - Biomedical Research (2016) Volume 27, Issue 4

Clinical values of electrocardiogram (ECG) in diagnosing cardiac autonomic dysfunction

Yimeng Wang and Jinyi Xu*

Department of Electrocardiogram Room, Henan Provincial People’s Hospital, Zhengzhou 450000, PR China

*Corresponding Author:
Jinyi Xu
Department of Electrocardiogram Room, Henan Provincial People’s Hospital, Zhengzhou, China

Accepted on April 17, 2016

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Abstract

This study aims to analyse the clinical efficacies of electrocardiogram (ECG) in diagnosing cardiac autonomic dysfunction (CAD) and to explore the clinical values of this method. A total of 82 CAD patients clinically diagnosed and confirmed were selected for the traditional Chinese medical treatment and psychological intervention. After three courses of treatment, their ECG were monitored, and the diagnostic results before and after the treatment were then compared. Before the treatment, the abnormality rate of the patients ECG diagnosis was 100%; while after the treatment, the rate was reduced to 10.98% (9/82). The intragroup comparison showed that the post-treatment abnormal ECG rate was significantly reduced and exhibited statistically significant difference with that before the treatment (P<0.05). Meanwhile, after the treatment, such clinical symptoms as palpitation, shortness of breath, or precordialgia were significantly improved, and the symptoms in 73 patients totally disappeared. The application of ECG in the clinical diagnosis of CAD was non-invasive and simple, and had high detection rate and accuracy; therefore, it had high clinical values and was suitable for wide promotion.

Keywords

Electrocardiogram, Clinical diagnosis, Cardiac autonomic dysfunction, Clinical value.

Introduction

Cardiac autonomic dysfunction (CAD) is the syndromes of cardiovascular dysfunction caused by the cardiac autonomic function disorders [1,2], though it does not belong to cardiac organic disease, its incidence has been significantly increased in recent years, and the incidence focuses in young adults at the age of 20 ~ 40 years old; the incidence in female is slightly higher than that in male. Because the clinical manifestations of CAD were palpitation, shortness of breath, and precordialgia [3], which were very similar to those of organic cardiac diseases, not only the difficulties of clinical diagnosis were increases, but also the patients would have more psychological burdens because of the doubts about the disease, and these were not conducive to the treatment of CAD [4]. Dynamic electrocardiogram (ECG) could diagnose CAD accurately and simply [4]. In order to accurately diagnose CAD and perform the symptomatic treatment as early as possible, we sampled 82 CAD patients to analyse the diagnostic values of their ECG results, and the study was reported below.

Materials and Methods

General information

A total of 82 CAD patients clinically diagnosed and confirmed in our hospital from January 2013 to January 2015 were selected. All the 82 patients met the following inclusion criteria: 1). had different degrees of palpitation, shortness of breath, and precordialgia, and these symptoms lasted for >150 days [2]; 2). Between 20 and 40 years old; 3). ECG results revealed abnormalities of ST wave band, T wave, and heart rate variability. Meanwhile, through blood routine, urine routine, and hepatonephric function examinations, patients with heart diseases, myocarditis, and diabetes were excluded [3]. Among the 82 qualified patients selected, 35 were males and 47 were females, with the average age as (32.6 ± 3.2) years (Table 1). This study was conducted in accordance with the declaration of Helsinki. This study was conducted with approval from the Ethics Committee of Henan Provincial People’s Hospital. Written informed consent was obtained from all participants.

S.No. Gender Age Type of abnormality in this monitoring Symptoms disappeared completely
1 male 33 Supraventricular extrasystole and emergency ventricular extrasystole Yes
2 male 37 Supraventricularextrasystole and emergency ventricular extrasystole Yes
3 male 32 Complex heart rhythm abnormality Yes
4 male 36 Multiple ventricular extrasystole Yes
5 male 29 Multiple ventricular extrasystole Yes
6 male 29 Supraventricularextrasystole andemergency ventricular extrasystole Yes
7 male 36 Supraventricularextrasystole and emergency ventricular extrasystole Yes
8 male 33 Supraventricularextrasystole andemergency ventricular extrasystole Yes
9 male 32 Complex heart rhythm abnormality No
10 male 36 Supraventricularextrasystole andemergency ventricular extrasystole Yes
11 male 26 Multiple ventricular extrasystole Yes
12 male 29 Multiple ventricular extrasystole Yes
13 male 35 Supraventricularextrasystole andemergency ventricular extrasystole Yes
14 male 36 Multiple ventricular extrasystole Yes
15 male 35 Supraventricularextrasystole andemergency ventricular extrasystole Yes
16 male 34 Multiple ventricular extrasystole No
17 male 35 Supraventricularextrasystole andemergency ventricular extrasystole Yes
18 male 32 Multiple ventricular extrasystole Yes
19 male 29 Multiple ventricular extrasystole Yes
20 male 28 Supraventricularextrasystole andemergency ventricular extrasystole Yes
21 male 28 Multiple ventricular extrasystole No
22 male 37 Complex heart rhythm abnormality Yes
23 male 30 Supraventricularextrasystole andemergency ventricular extrasystole Yes
24 male 35 Atrioventricular conduction disorder Yes
25 male 36 Supraventricularextrasystole andemergency ventricular extrasystole Yes
26 male 30 Supraventricularextrasystole andemergency ventricular extrasystole Yes
27 male 32 Supraventricularextrasystole andemergency ventricular extrasystole Yes
28 male 33 Multiple ventricular extrasystole Yes
29 male 28 Supraventricularextrasystole andemergency ventricular extrasystole Yes
30 male 32 Multiple ventricular extrasystole Yes
31 male 30 Supraventricularextrasystole andemergency ventricular extrasystole Yes
32 male 28 Multiple ventricular extrasystole Yes
33 male 38 Supraventricularextrasystole andemergency ventricular extrasystole Yes
34 male 36 Supraventricularextrasystole andemergency ventricular extrasystole Yes
35 male 36 Complex heart rhythm abnormality Yes
36 female 36 Supraventricularextrasystole andemergency ventricular extrasystole Yes
37 female 28 Supraventricularextrasystole andemergency ventricular extrasystole No
38 female 29 Multiple ventricular extrasystole Yes
39 female 36 Supraventricularextrasystole and emergency ventricular extrasystole Yes
40 female 32 Multiple ventricular extrasystole Yes
41 female 37 Normal Yes
42 female 32 Supraventricularextrasystole and emergency ventricular extrasystole Yes
43 female 28 Atrioventricular conduction disorder Yes
44 female 29 Multiple ventricular extrasystole Yes
45 female 28 Atrioventricular conduction disorder Yes
46 female 36 Supraventricularextrasystole and emergency ventricular extrasystole Yes
47 female 33 Supraventricularextrasystole and emergency ventricular extrasystole Yes
48 female 29 Supraventricular extrasystole and emergency ventricular extrasystole Yes
49 female 35 Complex heart rhythm abnormality Yes
50 female 32 Normal Yes
51 female 29 Supraventricular extrasystole and emergency ventricular extrasystole Yes
52 female 29 Supraventricular extrasystole and emergency ventricular extrasystole Yes
53 female 35 Multiple ventricular extrasystole Yes
54 female 35 Multiple ventricular extrasystole Yes
55 female 37 Supraventricular extrasystole and emergency ventricular extrasystole Yes
56 female 38 Multiple ventricular extrasystole Yes
57 female 36 Supraventricular extrasystole and emergency ventricular extrasystole Yes
58 female 30 Multiple ventricular extrasystole Yes
59 female 32 Multiple ventricular extrasystole No
60 female 36 Multiple ventricular extrasystole Yes
61 female 35 Supraventricular extrasystole and emergency ventricular extrasystole No
62 female 30 Supraventricular extrasystole and emergency ventricular extrasystole Yes
63 female 31 Complex heart rhythm abnormality Yes
64 female 32 Multiple ventricular extrasystole Yes
65 female 32 Complex heart rhythm abnormality Yes
66 female 28 Atrioventricular conduction disorder Yes
67 female 35 Multiple ventricular extrasystole Yes
68 female 32 Normal Yes
69 female 26 Supraventricular extrasystole and emergency ventricular extrasystole Yes
70 female 36 Supraventricular extrasystole and emergency ventricular extrasystole Yes
71 female 32 Multiple ventricular extrasystole No
72 female 34 Multiple ventricular extrasystole No
73 female 37 Supraventricular extrasystole and emergency ventricular extrasystole Yes
74 female 33 Supraventricular extrasystole and emergency ventricular extrasystole Yes
75 female 28 Normal Yes
76 female 35 Multiple ventricular extrasystole Yes
77 female 33 Multiple ventricular extrasystole Yes
78 female 35 Supraventricular extrasystole and emergency ventricular extrasystole Yes
79 female 36 Supraventricular extrasystole and emergency ventricular extrasystole No
80 female 30 Atrioventricular conduction disorder Yes
81 female 32 Supraventricular extrasystole and emergency ventricular extrasystole Yes
82 female 31 Normal Yes

Table 1. General information of patients and some results in this study.

ECG diagnosis

All the patients were performed 24 h dynamic ECG monitoring twice after admission (model: MSLVE02, manufacturer: Guangzhou Yilujiuge Co., China), and were recorded the detailed monitoring results.

Treatment methods

The main treatment was psychotherapy, aiming to eliminate the patient's fear and pressure. Meanwhile, necessary medical treatment was supplemented according to the principles of reinforcing Heart and tranquilization; the traditional Chinese medicine Ganmai dazao decoction was used for the treatment, with 10 days as a course for three courses [5].

Dynamic ECG monitoring

At the end of the three treatment courses, dynamic ECG monitoring was performed three times, and the duration should be >20 h; the ECG monitoring results were recorded.

Observation indexes

The abnormal indexes before the treatment and at the end of the 3rd ECG monitoring were observed to compare the abnormality rates. Meanwhile, the changes of clinical symptoms before and after the treatment were observed and compared.

Statistical analysis

SPASS 17.0 software was used for the data analysis; the counting data were expressed as% and performed the χ2 test; the measurement data were expressed as mean ± standard deviation ( ± s) and performed the t-test, with P<0.05 considered as statistically significant difference.

Results

Results of 24h dynamic ECG monitoring

There were 77 cases of cardiac index abnormality in this monitoring, including 32 males and 45 females; there was no statistically significant difference in the detection rate between the genders (P>0.05). Among these cases, 38 cases were supraventricular extrasystole and emergency ventricular extra systole, accounting for 49.35%; 27 cases were multiple ventricular extra systole, accounting for 35.06%; seven cases were complex heart rhythm abnormality, accounting for 9.09%; five cases were atrioventricular conduction disorder, accounting for 6.49% (Table 1, Figure 1).

biomedres-dynamic-ECG-monitoring

Figure 1. Results of 24th dynamic ECG monitoring.

Abnormality rate of ECG

Before the treatment, all the 82 patients exhibited ECG abnormality, with the abnormality rate as 100%. After the treatment, only nine patients showed abnormal ECG, with the abnormality rate as 10.98%. The intragroup comparison showed that the post-treatment abnormal ECG rate was significantly reduced and exhibited statistically significant difference with that before the treatment (χ2=12.6968, P=0.0004<0.05) (Table 2).

Before the treatment After the treatment Statistical result
The normality rate 0% (n=0) 89.02% (n=73) χ2=12.6968, P=0.0004
The abnormality rate 100% (n=82) 10.98% (n=9)

Table 2. Abnormality rate of ECG between before the treatment and after the treatment.

Changes of clinical symptoms

After the treatment, such clinical symptoms as palpitation, shortness of breath, and precordialgia in this study were significantly improved. Of these, the symptoms in 73 patients disappeared completely, and the clinical improvement rate was 89.02% (Table 1, Figure 2).

biomedres-Clinical-symptoms-changes

Figure 2. Clinical symptoms changes.

Discussion

The syndromes of cardiovascular dysfunction caused by the autonomic dysfunction while without heart organic disease are named CAD [6,7]. With the accelerated pace of life and the gradually increased pressure, the incidence of ACD is continuously increased and shows the trend towards younger adults; women between 20 and 40 years has become the highrisk population of CAD [8,9]. This study investigated the clinical values of ECG in diagnosing CAD, aiming to lay solid foundations for further clinical diagnostic work.

Because CAD belongs to a kind of psychological illness, so the focus of clinical treatment should be put onto caring the patient's psychological problems. But from the current status of the clinical treatments of CAD, it was usually treated as the diseases of the cardiovascular system, so many doctors just treated the clinical symptoms while did not care about the psychological status of the patients [10-12] or this issue had not caused sufficient attention, so it would easily lead to repeated medical treatment, which not only was a waste of medical resources but also would increase the economic and psychological pressure of the patients.

From the pathogenesis of CAD, fast pace of life, lack of sleep, or too much pressure were important factors towards the occurrence of CAD [13,14]. Under the joint effects of these factors, the body's sympathetic nerve and autonomic nerve might difficultly maintain the balance, so it would be easy to result in the dysfunction. Palpitation, shortness of breath, and precordialgia are the main clinical manifestations of CAD; meanwhile, patients might produce intense and other negative emotions because of pain, which virtually increased the psychological pressure of patients [15]. and would have some impacts on their normal work and lives.

Currently, there is still lack of unified and standard diagnostic criteria towards CAD, and what detection method should be used to confirm this issue is still a big controversy among medical fields. Based on this situation, we mainly used the symptom diagnosis and exclusion diagnosis to confirm the diagnosis. Dynamic ECG monitoring is simple and noninvasive, and could be easily accepted by patients; therefore, it could be used as the diagnostic evidence of CAD. In addition, other examination methods such as patient’s medical history, enzymology, ultrasound, or x-rays could be combined for the comprehensive judgment and correct diagnosis, which could then eliminate patient’s psychological fear of heart disease, improve the mental condition, facilitate physicians to achieve symptomatic treatment, and make the patient recovered as soon as possible [16,17].

Because ECG was the main signal detection way for heart diseases, which could quickly and accurately capture the instantaneous heart rate changes and waveform abnormalities [18,19], it could provide certain basis for the diagnose of CAD. This study investigated the clinical significance of ECG in diagnosing CAD.

The twice 24 h dynamic ECG monitoring towards the 82 patients revealed that a total of 77 patients exhibited abnormal heart rate indexes and waveforms, with a little higher abnormality rate as 93.9%. The abnormality rates in ST wave band or T wave were higher, and most of them appeared when the heart rate increased, so the frequency of the abnormality rate was positively correlated with the heart rate. Meanwhile, comparing the ECG monitoring results before and after the treatment revealed that the post-treatment abnormality rate was significantly reduced than that before the treatment, and the difference was statistically significant (P<0.05). In addition, after the treatment, such clinical symptoms as palpitation, shortness of breath, or precordialgia were significantly improved, and the symptoms in 73 patients totally disappeared; the clinical improvement rate was 89.02%. These results fully demonstrated that the clinical data of dynamic ECG could be used as the diagnostic evidence of CAD, consistent with Corazza et al. [20], indicating that ECG had high clinical values in diagnosing CAD. In summary, the application of ECG in clinically diagnosing CAD was non-invasive and simple, and had high detection rate and accuracy; therefore, it had high clinical values and was suitable for wide promotion.

References