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Open Access 01.12.2024 | Research

Status quo and factors influencing dyadic disease appraisal in chronic heart failure based on latent profile analysis in Northern Sichuan Province, China

verfasst von: Jiali Ren, Huaying Pan, Zhou Zhang, Yali Wang

Erschienen in: BMC Nursing | Ausgabe 1/2024

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Abstract

Purpose

This study explored potential categories of dyadic disease appraisal differences among patients hospitalized with chronic heart failure (CHF) in China and analyzed the main factors influencing these categories.

Methods

A survey was conducted using various tools and scales, including the Chinese version of the Memorial Heart Failure Symptom Appraisal Scale, Heart failure self-care index scale, Social Support Rating Scale, Zarit burden interview, and Self-rating anxiety scale. The data was collected from patients who were hospitalized with CHF in the cardiology department of one of two tertiary hospitals in Nanchong City, China. The dyadic disease appraisal categories were identified using latent profile analysis (LPA). Multiple logistic regression analysis was also employed to analyze the factors influencing the formation of potential categories of differences in dyadic disease appraisal in CHF patients.

Results

A total of 262 pairs of hospitalized CHF patients and their caregivers participated in this study. The dyadic disease appraisal of CHF patients was potentially categorized as the "negative difference group" (28 individuals, 10.7%) and the "positive or convergence group" (234 persons, 89.3%). The results showed that the factors influencing the categorization of dyadic disease appraisal differences included the patient's social support, disease progression, and Caregivers anxiety level, burden, gender, educational attainment, and age (p < 0.05).

Conclusion

The study findings demonstrated heterogeneity between the two groups of CHF patients in the dyadic disease appraisal. Therefore, it is necessary to focus on patients who have a brief duration of illness and limited social support. Specifically, it is important to prioritize support for female caregivers who are 65 years or older, have lower levels of educational attainment, and experience a significant burden and anxiety. Regular implementation of support person-bilateral co-management strategies can effectively reduce differences in how the disease is perceived and enhance the overall well-being of both caregivers and patients.
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Introduction

The prevalence of adult heart failure in China is about 1.3–3.5% [1], with more than 4 million people living with heart failure. CHF often leads to frequent hospitalization of patients [2], increasing the burden of disease on patients and caregivers, reducing their quality of life [3], and causing great suffering to both patients and caregivers. Studies have shown that symptom monitoring [4], daily life management, rehabilitation [5], and other aspects of CHF patients require primary assistance from caregivers, as well as monitoring patient compliance with treatment plans to improve patient self-management [6, 7]. Therefore, CHF management is a dyadic management process that requires the collaboration of patients with caregivers.
Dyadic appraisal refers to the collective appraisal of individuals and related individuals in interpersonal units towards stressful events (such as chronic diseases). The development context coping model proposed by Berg in 2007 [8] suggests that dyadic appraisal includes three aspects: disease characterization, disease affiliation, and specific stressor appraisal. Disease characterization focuses on the consistency and differences in disease appraisal by the dyadic system. The theory of dyadic illness management proposed by Lyons in 2018 [9] posits that dyadic disease appraisal refers to the synergy or difference in disease appraisal among members of a dyadic system. Differences in dyadic disease appraisal are conceptualized as the magnitude and direction of disease inconsistency (the extent to which there is a disparity in disease appraisal between patients and caregivers) and who appraises the disease as more or less severe. Consistent dyadic disease appraisal benefits partners to jointly manage diseases and promote dyadic health [10]. Many studies have shown that demographic characteristics, disease severity, comorbidity conditions, culture, relationship types, and relationship quality also contribute to dyadic disease appraisal [9]. However, a few studies have addressed the differences in the dyadic disease appraisal in CHF patients in China. As a result, further studies are needed to explore the cultural adaptability of differences in the dyadic disease appraisal.
The identification of various dyadic disease appraisal patterns, as well as modifiable individual, dyadic, and family factors that are associated with optimal and poor dyadic disease appraisal can provide valuable information on how to adjust intervention measures to promote dyadic health and dyadic management. However, the traditional approach to the study of dyadic disease appraisal in CHF patients is a variable-centered method that fails to capture the heterogeneity of dyadic disease appraisal in CHF. LPA is a promising approach for classifying subgroups within a population based on observed variables [11]. To the best of our knowledge, few studies have dealt with the heterogeneity and the factors influencing dyadic disease appraisal in CHF.
Therefore, this study aims to (1) adopt LPA to explore the potential categories of dyadic disease appraisal differences in CHF patients; (2) analyze the main factors influencing the formation of these categories; and (3) provide a theoretical basis for the development of targeted nursing care measures and optimization of caregiving disease dyadic management models for clinical healthcare professionals.

Methods

Participants and procedures

Convenience sampling was employed to select the study participants from among the CHF patients admitted to the cardiology departments of 2 tertiary hospitals in Nanchong City, China, from June 2022 to November 2022, and their caregivers. The inclusion criteria for patients were as follows: 1- formal diagnosis of HF (verified by an HF cardiologist); 2- age ≥ 18 years; 3- clear consciousness, no cognitive dysfunction, and communication disorder; 4- willingness to participate in this study; and 5- evident symptoms of HF (New York Heart Association [NYHA] class I–IV). The exclusion criteria for patients were as follows: 1- affliction with heart failure for less than a year; 2- receiving a mechanical circulatory support device, undergoing transplantation, or having another terminal condition; and 3- unwillingness of the support person to participate in the study. The inclusion criteria for caregivers were as follows: (1) age ≥ 18 years and (2) unpaid individuals who were primarily responsible for caregiving and were spending at least 4 h per day providing care in the hospital [12]. Moreover, the exclusion criteria for caregivers were as follows: (1) affliction with major physical or mental disorders; (2) suffering from cognitive impairments; and (3) not living with the patient for a minimum of one year. The sample size was calculated using the following formula: n = u1-α/2σ/δ) 2. Assuming α = 0.05, u1-α/2 = 1.96, δ = 0.1, and σ = 0.753, based on previous studies, the sample size was obtained 225.

Measures

The demographics of patients and their caregivers (i.e., age, gender, etc.) were obtained through in-person surveys. Moreover, the clinical characteristics of patients (i.e., severity of heart failure and number of hospitalizations) were obtained by reviewing their electronic medical records (Table 1).
Table 1
Survey instrument
Survey object
Survey instrument
Survey objective
Patients
Memorial Heart Failure Symptom appraisal Scale (Chinese version) (MSAS-HF)
Assess the patient 's disease symptoms
Heart failure self-care index scale (SCHFIv6.2)
Assess patients ' self-care ability
Social Support Rating Scale (SSRS)
Assess the social support status of patients
Caregivers
Memorial Heart Failure Symptom appraisal Scale (Chinese version) (MSAS-HF)
Assess the caregivers ' understanding of the patient 's disease symptoms
Zarit Burden Interview (ZBI)
Assess the caregiver burden of caregivers
Self-rating Anxiety Scale (SAS)
Assess the anxiety level of caregivers

Dyadic disease appraisal scale

The Memorial Symptom Assessment Scale-Heart Failure (MSAS-HF), developed by American scholar Zambroski [13], was employed to evaluate the symptoms that CHF patients had experienced over the past 7 days. Guo Jinyu, a Chinese scholar, adapted the MSAS-HF scale to conform to Chinese culture and customs [14]. The Chinese version of MSAS-HF measures physical symptoms, psychological symptoms, and CHF symptoms, and its items are evaluated based on the frequency, severity, and distress of the symptoms. Higher scores on this scale indicate that the patient overestimates the severity of symptoms. The Cronbach's alpha of the patient version in this study was 0.741, which is considered to indicate good internal consistency as coefficients above 0.7 are generally regarded as satisfactory. Based on the guidance of the cardiology nursing team and clinical experts, the linguistic presentation of the relevant entries was modified to develop the support person version of the scale. In terms of the number of entries and symptoms, the support person version was consistent with the patient version. The Cronbach's alpha of the support person version was obtained 0.801, indicating good reliability and validity. The dyadic disease appraisal difference in this study was defined as the discrepancy between the patient's score and the Caregivers score.

Self-care ability appraisal and social support scale for CHF patients

Self-care of heart failure index version 6.2 (SCHFI v.6.2)
Developed by Riegel [15], this index consists of three subscales: self-care maintenance, self-care management, and self-care confidence. Each subscale is converted into a standard score due to differences in the number of items and scores, where the standard score is equal to [(actual score—lowest score)/(highest score—lowest score)] * 100. Each scale uses a score of 70 as the cutoff point for sufficient self-care [16]. Wang Binqing, a Chinese scholar, adapted the SCHFIv6.2 to conform to Chinese cultural norms and practices [17]. Higher scores on this scale indicate stronger self-care abilities of the patient. In this study, Cronbach's alpha for this scale was obtained 0.894.
Social support rating scale (SSRS)
Developed by a Chinese scholar Shuiyuan Xiao [18], SSRS consists of three subscales: subjective support, objective support, and support utilization. Those who obtain a total score of 22 or less, 23 to 44, and 45 to 66 experience low, moderate, and high levels of social support, respectively. In this study, Cronbach's alpha for SSRS was equal to 0.827.

Caregivers burden and anxiety appraisal scale

Zarit burden interview (ZBI)
The ZBI was developed by Zarit in 1994 [19], and a Chinese scholar Wang Lie translated it into Chinese in 2006 [20]. The ZBI consists of 22 items in 2 dimensions: personal burden and burden of responsibility. A total score of smaller than 21, 21–40, and greater than 40 on this tool is interpreted as no or mild burden, moderate burden, and severe burden, respectively. In this study, Cronbach's alpha for this tool was obtained 0.727.
Self-rating anxiety scale (SAS)
The SAS was developed by Zung in 1971 [21], and then it was translated into Chinese and revised by a Chinese scholar Wang Zhengyu [22]. This scale consists of two dimensions: physical anxiety and mental anxiety. A total score of < 50, 50–59, 60–69, and ≥ 70 indicates no anxiety, mild anxiety, moderate anxiety, and severe anxiety, respectively. In this study, Cronbach's alpha for this scale was equal to 0.934.

Data collection and quality control

A face-to-face survey using paper-based questionnaires was conducted on hospitalized CHF patients and their caregivers in the cardiology department of two tertiary hospitals in Nanchong City, China, from June 2022 to November 2022. Before conducting the survey, the researchers provided unified training in the research topic to two nursing graduates to ensure their understanding of the experimental process and survey tools, standardize the methods of asking survey questions, and familiarize them with the necessary precautions for conducting questionnaire surveys and completing them accurately. In cases where individuals could not complete the questionnaires due to factors such as old age, impaired vision, or illiteracy, the researchers verbally presented the items and response options to the participants. The participants then provided their responses orally, and the researchers recorded their answers on their behalf. Immediately following the survey, the researchers verified the accuracy and integrity of the obtained data by promptly rectifying any missing items or misinformation. In this study, a total of 274 questionnaires were distributed among the participants. After excluding 12 questionnaires that were deemed invalid(the number of missed answers is ≥ 2/3 of the total number of questions), the data from the remaining 262 questionnaires were used for analysis, resulting in an effective rate of 95.6% (262/274).

Statistical analysis

The data obtained were analyzed statistically in SPSS 26.0. The count data were presented as frequencies and percentages, while the measurements were presented as mean ± standard deviation (x ̅ ± s). A Pearson correlation analysis was conducted. The Mplus 7.0 software was utilized to model the potential profiles. The fit indices used in this analysis include the Akaike information criterion (AIC), Bayesian information criterion (BIC), and corrected Bayesian information criterion (BIC). Smaller mean values of these indices indicate a better fit for the model. The entropy index, which ranges from 0 to 1, provides a measure of accuracy. A value closer to 1 indicates a more accurate model. Specifically, if the entropy index is greater than 0.6, it suggests that the model has better classification accuracy. To compare different models, a likelihood test called the Bootstrap-based likelihood test (BLRT) and the LMR likelihood ratio test (LMR) were performed. A significance level of P < 0.05 indicates that k-1 category models were rejected, while k-1 category models were supported. The comparison between the two groups was conducted using a two independent samples t-test if the data followed a normal distribution. For multi-group comparisons, analysis of variance (ANOVA) was used for between-group comparisons. If the data was non-normal, the rank-sum test (Kruskal–Wallis H) was used for comparison between two and multiple samples. The χ2 test was used for counting data. A multiple logistic regression analysis was conducted to examine the factors that influence the formation of potential categories of differences in dyadic disease appraisal in patients with CHF. The analysis used a significance level of P < 0.05.

Ethical approval

This study was approved by the medical ethics committee of the studied hospital (2022R375-1).

Results

Demographics of patients (Table 2)

Table 2
Demographics of patients (n = 262)
Data of Population Sociology
Items
frequency
constituent ratio (%)
Gender
Female
118
45.0
Male
144
55.0
Age
18–40
4
1.5
41–64
48
18.3
 ≥ 65
210
80.2
The level of education
Primary school and below
186
71.0
Junior high
31
11.8
High school or technical secondary school
33
12.6
College or higher
12
4.6
Combined with other chronic diseases
YES
183
69.8
NO
79
30.2

Medical data of patients (Table 3)

Table 3
Medical data of patients (n = 262)
Disease-related information
Items
Frequency
Percentage (%)
Disease course
1–4 years
89
34.0
5–10 years
38
14.5
 > 10 years
135
51.5
(NYHA)
I
7
2.7
II
53
20.2
III
149
56.9
IV
53
20.2
Number of readmission
1–2 times
95
36.3
 ≥ 3 times
167
63.7

Demographics of caregivers (Table 4)

Table 4
Demographics of caregivers (n = 262)
Data of Population Sociology
Items
Frequency
Constituent ratio (%)
gender
Female
113
43.1
Male
149
56.9
Age
18–40 years
144
55.0
41–64 years
53
20.2
 ≥ 65 years
65
24.8
The level of education
Primary school and below
47
17.9
Junior high school or technical secondary school
131
50.0
College or higher
84
32.1
Relationship with patients
Spouse
87
33.2
Other
34
13
Child
128
48.9
Parents
9
3.4
Frequency of communication with patients ' symptoms
Few
69
26.3
Sometimes
88
33.6
Often
105
40.1
Daily length of care in hospital
4-8 h
54
20.6
8-16 h
25
9.5
 > 16 h
183
69.8
Total length of care in hospital
 < three months
56
21.4
3–6 months
52
19.8
7–12 months
41
15.6
 > 12 months
113
43.1

Differences in dyadic disease appraisal between patients with CHF and caregivers (Table 5)

Table 5
Differences in dyadic disease appraisal between patients with CHF and caregivers \((\overline x\pm S)\)  
Items
Patients’ scores
Caregivers’ scores
differences
t
p
physiological symptoms
42.122 ± 12.856
43.229 ± 19.151
-1.107 ± 21.981
-0.815
0.416
psychological symptoms
10.996 ± 6.646
13.309 ± 8.752
-2.313 ± 10.665
-3.510
0.001
Symptoms of heart failure
10.164 ± 6.089
8.893 ± 7.075
-0.221 ± 9.184
2.119
0.035

Pearson correlation analysis results of patients ' self-care ability, caregivers’ social support, caregivers’ burden, caregivers’ anxiety and difference in dyadic disease appraisal (Table 6)

Table 6
Correlation between patients ' self-care ability, caregivers’ social support, caregivers’ burden, caregivers’ anxiety and difference in dyadic disease appraisal
Items
Scores
r
P
Differences in dyadic disease appraisal
-2.092 ± 29.402
-
-
Patients’ self-care ability
140.617 ± 38.914
0.707**
 < 0.01
Caregivers’social support
50.962 ± 8.399
0.285**
 < 0.01
Caregivers’ burden
29.718 ± 7.565
-0.590**
 < 0.01
Caregivers’ anxiety
49.470 ± 16.207
-0.582**
 < 0.01

Potential profile model fitting of dyadic disease appraisal difference in patients with CHF

Model fitting

In this study, 1–3 latent class models were extracted, and the fit indices of each model are shown in Table 7. The findings indicated that the AIC, BIC, and both types of latent profile models exhibited lower values compared to the one-type model. Additionally, the LMR and BLR tests yielded significant results, and the entropy measure was 0.750. Consequently, the two types of model fitting outperformed the one type model. There was no significant reduction in the AIC, BIC, or any of the three types of models compared to the two types. Additionally, the LMR and BLR tests were not significant, and the minimum category ratio was less than 5%. Therefore, the fitting of the three types of models was less satisfactory compared to that of the two types of models. Similarly, the performance of the four types of models was inferior to that of the three types of models. Consequently, the two categories of models exhibited the highest level of stability.
Table 7
Fitting information of latent profile analysis ( LPA)
Class identification number
AIC
BIC
aBIC
Entropy
LMR(p)
BLR(p)
Class probability
1
6288.492
6309.902
6290.879
-
-
-
-
2
6266.548
6302.232
6270.527
0.750
0.015
 < 0.001
10.7/89.3
3
6264.680
6314.637
6270.251
0.785
0.704
0.192
9.5/3.5/87
4
6264.196
6328.427
6271.359
0.756
0.470
0.308
20.6/75.5/0.8/3.1

Model naming

The differences in the scores of psychological symptoms, psychological symptoms, and CHF symptoms obtained from the Chinese version of the MSAS-HF for CHF patients and their caregivers are shown in Table 8 and Fig. 1. According to their characteristics, they were named the "negative difference group " (28 people, 10.7%) and the "positive or convergence group " (234 people, 89.3%).
Table 8
Differences in dyadic disease appraisal \((\overline x\pm S)\)
Items
Negative difference groups
Positive or convergence groups
Heart failure total score
-58.179 ± 17.246
4.620 ± 22.598
psychological symptoms
-10.357 ± 12.482
-1.350 ± 10.033
physiological symptoms
-41.107 ± 16.674
3.679 ± 17.138
Symptoms of heart failure
-8.107 ± 8.574
0.722 ± 8.809

Single factor analysis of the potential categories of dyadic disease appraisal differences (Table 9)

Table 9
Single factor analysis of the potential categories of dyadic disease appraisal differences ( n = 262)
 
Items
Negative difference groups
Positive or convergence groups
χ2/t
p
Patients
disease course
1–4 years
17(60.7%)
72(30.8%)
14.535
0.001
5–10 years
6(21.4%)
32(13.7%)
 > 10 years
5(17.9%)
130(55.6%)
caregivers
gender
Female
19(67.9%)
94(40.2%)
7.815
0.005
Male
9(32.1%)
140(59.8%)
Age
18–40 years
7(25.0%)
137(58.5%)
18.419
 < 0.001
41–64 years
5(17.9%)
48(20.5%)
 ≥ 65 years
16(57.1%)
49(20.9%)
The level of education
Primary school and below
14(50%)
33(14.1%)
21.936
 < 0.001
Junior high school or technical secondary school
9(32.1%)
122(52.1%)
College or higher
5(17.9%)
79(33.8%)
Relationship with patients
Spouse
13(46.4%)
74(31.6%)
10.109
0.039
Other
3(10.7%)
31(13.2%)
Child
8(28.6%)
120(51.3%)
Parents
3(10.7%)
6(2.6%)
Siblings
1(3.6%)
3(1.3%)
Frequency of communication with patients ' symptoms
Few
2(7.1%)
67(28.6%)
6.113
0.047
Sometimes
11(39.3%)
77(32.9%)
Often
15(53.6%)
90(38.5%)
Total care time
 < 3 months
14(50.0%)
42(17.9%)
16.858
0.001
3–6 months
3(10.7%)
49(20.9%)
6-1 months
5(17.9%)
36(15.4%)
 > 12 months
6(21.4%)
107(45.7%)
Patients’ dependence score
 
6.786 ± 2.043
4.966 ± 2.442
4.356a
 < 0.001
ais independent sample t test, the rest are χ2 test

Multivariate analysis of the potential categories of dyadic disease appraisal differences

A binary logistic regression analysis was conducted to examine the potential categories of differences in dyadic disease appraisal as dependent variables. The independent variables also included the patient's disease course, self-care ability, social support, Caregivers gender, age, educational attainment, relationship with the patient, frequency of communication with the patient's symptoms, patient's dependence score, Caregivers anxiety, and Caregivers burden. The findings indicated that patients who had a shorter disease course and less social support, were receiving care from female caregivers, were 65 years old, had lower educational attainment, and had higher levels of Caregivers' anxiety and burden were statistically more likely to fall into the potential category of dyadic disease appraisal (P < 0.05) (Table 10).
Table 10
Multivariate analysis of the potential categories of dyadic disease appraisal differences
 
Items
Non-standardized coefficient B
p
Exp(B)
95%CI
Lower limit
Upper limit
Patients
disease course
1–4 years
2.903
0.005
18.228
2.452
135.509
 
5–10 years
2.802
0.009
16.473
2.037
133.192
 
 > 10 years
-
-
-
-
-
Social support
 
-0.111
0.011
0.895
0.822
0.975
Caregivers
gender
Female
2.110
0.012
8.247
1.593
42.705
Male
-
-
-
-
-
Age
18–40 years
-
-
-
-
-
41–64 years
2.173
0.058
8.783
0.927
83.257
 ≥ 65 years
3.438
0.002
31.115
3.476
278.532
The level of education
Primary school and below
3.631
0.002
37.747
3.867
368.489
Junior high school or technical secondary school
0.774
0.401
2.168
0.357
13.180
College or higher
-
-
-
-
-
Anxiety
 
0.127
0.002
1.135
1.048
1.229
burden
 
0.242
 < 0.001
1.274
1.124
1.443

Discussion

This study combined patients with CHF and their caregivers as a unit of analysis and employed LPA for the first time to determine subgroups for dyadic disease appraisal in Chinese populations of CHF patients. This study enhanced the existing body of knowledge on how CHF patients perceive and evaluate diseases in their relationships. It demonstrated that different subgroups of individuals, who were assessed for various diseases in their relationships, exhibited significant differences in terms of their sociodemographic and clinical characteristics, as well as the levels of social support they received and the anxiety and burden experienced by their caregivers.

LPA of dyadic disease appraisal differences in patients with CHF.

This study combined patients with CHF and their caregivers as a unit of analysis and employed LPA for the first time to determine subgroups for dyadic disease appraisal in Chinese populations of CHF patients. This study enhanced the existing body of knowledge on how CHF patients perceive and evaluate diseases in their relationships. It demonstrated that different subgroups of individuals, who were assessed for various diseases in their relationships, exhibited significant differences in terms of their sociodemographic and clinical characteristics, as well as the levels of social support they received and the anxiety and burden experienced by their caregivers. In this study, the dyadic disease appraisal in CHF patients was divided into two potential categories: "negative difference group" and "positive or consistent group".
The mean scores of three-dimensional dyadic disease appraisal in CHF patients in the "negative difference group" were all negative. It is also possible that the inadequacy of caregivers to assist patients in coping with symptoms, provide emotional support, and facilitate decision-making may be the reason for a lower evaluation of patients' symptoms. Furthermore, caregivers may face challenges in accurately evaluating the patient's symptoms due to the patient's tendency to conceal their discomfort and their reluctance to seek assistance from caregivers [23].
The differences in the appraisal of physiological symptoms and heart failure symptoms in CHF patients in the "positive or convergence group" were divided into positive numbers, but the differences in the appraisal of psychological symptoms were divided into negative numbers, which may be related to heart failure. CHF is a persistent progressive cardiovascular disease associated with a high readmission rate, high morbidity, high mortality, and high financial burden, which often leads to common psychological disorders such as depression, anxiety, and insomnia [24]. Emotional issues are subjective feelings that are not readily apparent, and patients usually refrain from expressing their negative emotions, which makes it challenging for caregivers to identify them [25].

Caregivers’ gender

The study findings indicated that the "female support person" was a characteristic population that constitutes a "negative differential group". Specifically, the Caregivers disease appraisal was greater than the patient's self-disease appraisal. This is not consistent with the findings of Lee who showed that the difference in dyadic evaluation was relatively small when caregivers were female [26]. This can be attributed to the fact that female caregivers are more attentive and invest more time in care, which may lead to the overestimation of symptoms as a result of their increased sensitivity to changes in the disease symptoms [27]. In addition, female caregivers showed lower psychological resilience and were prone to higher levels of anxiety and care burden, which could affect disease appraisal [28]. Therefore, it is necessary to closely monitor the mental health status of female caregivers.

Caregivers’ educational attainment

This study showed that the Caregivers educational attainment was one of the factors influencing the formation of a "negative difference group". Accordingly, caregivers with lower educational attainment evaluate the disease better than the patients do. This is consistent with the findings of Sharifi et al. [29]. who studied differences between patients with heart failure and their caregivers in the evaluation of disease symptoms and found that caregivers with lower educational attainment were more likely to exhibit high differences in dyadic disease appraisal. This can be attributed to the Caregivers low level of educational attainment, resulting in a lack of comprehension of the disease and disregard for changes in the patient's condition, consequently influencing the disease appraisal [30]. Consequently, medical staff should promptly assess the health knowledge requirements of caregivers with lower levels of educational attainment, offer disease knowledge training, develop strategies for their involvement in the identification and management of patient symptoms, and mitigate disparities in dyadic disease appraisal.

Caregivers’ age

The potential classification of differences in the dyadic appraisal of CHF based on the age of the support person is a topic of controversy. Lyons found that young couples with prostate cancer were more likely to have inconsistent dyadic disease appraisal [31]. Lee reported that the dyadic disease appraisal was more pronounced when the caregivers for CHF patients were older [32]. Interestingly, this study showed that the age over 65 years for caregivers was the characteristic forming a "negative difference group". This means that the older the caregivers are, the more they overestimate the disease symptoms. Moreover, the caregivers' capacity to assess the health status of others tends to decline as they age, and they tend to overestimate the severity of the disease symptoms [32]. Furthermore, as caregivers grow older, their capacity to acquire and embrace the patient's knowledge about their disease diminishes, and their comprehension of the disease becomes ambiguous [33].

Disease course

The study findings suggested “disease course” as another factor influencing the formation of a "negative difference group", which was consistent with the results of Pickard's [34]. Patients have a lower self-appraisal of the disease because of the short disease course and a lack of understanding of their disease [35]. Therefore, to facilitate patient recovery and enhance the quality of life of patients and their caregivers, medical staff should promptly communicate with patients and caregivers, thereby increasing their comprehension of the disease symptoms, reducing their stress, and facilitating their rapid integration into the patient's disease treatment process. This will establish a positive dyadic relationship of cooperation.

Patients’ social support

This study showed that the patient's social support is one of the factors influencing the potential categories of dyadic disease appraisal differences between CHF patients and their caregivers. The lower the patient's social support, the easier it is to form a "negative difference group". This is consistent with the findings of Cameron [36]. Elderly patients with chronic diseases often rely on their home-based caregivers, such as spouses, who themselves are also patients with chronic diseases. Other family members, such as children, friends, brothers, and sisters, take care of these caregivers. The dual evaluation of symptoms of patients and their spouses may be influenced by the engagement of other caregivers [32]. Due to the reduced number of migrant workers caused by the COVID-19 pandemic during this study, the majority of caregivers were the children of patients. They communicated less and spent less time with patients, and influenced disease appraisal. Consequently, it is necessary to develop structured and family-centered health educational interventions for such patients. Participation of patients' family members in educational courses helps to establish a "hand-in-hand plan", form a "disease management knowledge sharing" model, enhance patients' social support, and mitigate discrepancies in dyadic disease appraisal [37].

Caregivers’ anxiety and burden

This study proposed “Caregivers’ anxiety and burden” as one of the factors influencing the potential categories of dyadic disease appraisal differences between CHF patients and their caregivers. The formation of a "negative difference group" is facilitated by the increased anxiety and burden of caregivers. Lyons found a significant negative correlation between the psychological health of spouses of patients with lung cancer and differences in the dyadic disease appraisal [38]. Silveira also showed that caregivers with higher levels of depression overestimate the disease symptoms, resulting in differences in the dyadic disease appraisal [25]. Schulz reviewed studies on care for patients with chronic disease and reported that caregivers’ burden and psychological distress lead to the increased perception of symptoms in patients [39]. Therefore, nursing staff should pay attention to the mental health of caregivers and provide them with educational lectures on mental health [40]. It is important to utilize modern communication technologies like telephone and social networks (e.g., WeChat) for following up the patients and their caregivers after discharge. Such a strategy can help facilitate open communication with support, allowing them to express any negative emotions they may be experiencing. Additionally, this strategy can provide them with specific measures to help alleviate these negative emotions [41].

Inspirations and suggestions for nursing research

Race and culture are the factors influencing dyadic disease appraisal differences. A study by American scholar Bidwell showed that there were differences in the consistency of the dyadic disease appraisal among different races in the US [37]. Due to differences in health literacy and knowledge structure, there is a greater difference in symptom evaluation between African American and Caucasian caregivers and patients. However, a few studies have addressed the effects of race, culture, and other factors on dyadic disease appraisal. The literature review revealed that this study is the first to use LPA to preliminarily explore the types and the factors influencing dyadic disease appraisal in Chinese CHF patients. It is important to comprehend the current state of dyadic disease appraisal disparities among CHF patients in China as well as the development of a relationship between two parties. Furthermore, this study revealed that healthcare professionals should prioritize patients and women who have a prolonged disease course, limited social support, are aged 65 years or older, have lower educational attainment, and their caregivers experience significant burden and anxiety levels. It is recommended to implement a targeted collaborative management approach that addresses the needs of both the patients and their caregivers. This should involve regularly providing a common management strategy, minimizing disparities in disease appraisal, and enhancing the overall physical and mental well-being of both parties involved in the care process.

Limitations

This cross-sectional study was conducted on hospitalized CHF patients and their caregivers. This study exclusively focused on the disparities in dyadic disease appraisal and the factors that influence it during hospitalization. Hence, in future studies, time can be included as a covariate to investigate the variations in the dyadic appraisal of CHF. Considering the need for additional management in the sick area during the COVID-19 epidemic, the reduced number of migrant workers has resulted in a change in the category of caregivers. This change affects the dyadic disease appraisal. Furthermore, the limited sample size and uneven distribution of the category group in this study were a consequence of epidemic containment management measures and other factors. Consequently, the results of this study would have been exposed to bias.

Acknowledgements

We thank all the nurses’ participants for the involved and contributed to the procedure of data collection. We thank all the hospitals and managers for their cooperation and assistance.We would like to express their gratitude to EditSprings (https://​www.​editsprings.​cn ) for the expert linguistic services provided.

Declarations

All the procedures of this study were in accordance with the Declaration of Helsinki and were approved by the Ethics Committee of Affiliated Hospital of North Sichuan Medical College (NO: 2022R375-1). The purpose and procedure of the study is explained to all participants. All of them participated in this study voluntarily and were promised to assure the anonymity of the data. Informed consent was obtained from all study participants after the participants received a written explanation of the study objectives.
Not Applicable.

Competing interests

The authors declare no competing interests.
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Metadaten
Titel
Status quo and factors influencing dyadic disease appraisal in chronic heart failure based on latent profile analysis in Northern Sichuan Province, China
verfasst von
Jiali Ren
Huaying Pan
Zhou Zhang
Yali Wang
Publikationsdatum
01.12.2024
Verlag
BioMed Central
Erschienen in
BMC Nursing / Ausgabe 1/2024
Elektronische ISSN: 1472-6955
DOI
https://doi.org/10.1186/s12912-024-02340-x