1. Introduction
Cardiovascular diseases (CVDs) persist globally as leading causes of disability and mortality [
1]. In Europe, CVDs account for 40% of all deaths in women and 35% in men, making it the primary cause of mortality [
2]. Within the CVD spectrum, coronary heart diseases (CHDs) are the predominant contributors to morbidity and mortality [
1,
3,
4]. CHDs are defined as diseases of the coronary arteries primarily associated with atherosclerosis leading to ischemia or myocardial infarction (MI) [
1,
5]. Sex differences in CHD diagnosis, treatment, and prognosis are undeniable and often unfavorable for women, resulting in a greater risk of poorer outcomes [
6,
7,
8]. This disparity is compounded by a lack of awareness and knowledge among healthcare professionals, exacerbating sex inequality in cardiovascular health [
6,
7,
8].
Anxiety and depression are highly prevalent and linked to poorer prognosis in CHD patients [
9,
10,
11,
12,
13]. Moreover, anxiety and depression present significant barriers to lifestyle modifications, cardiac rehabilitation (CR) participation, adherence, and completion [
2,
14,
15,
16,
17,
18]. A Swiss pre–post design study (
n = 3434) revealed that depression negatively impacts improvements in exercise capacity and quality of life in comprehensive CR [
19]. Globally, the prevalence of anxiety and depression in cardiac patients is estimated to be 32.9% and 31.3%, respectively [
20]. Among European CHD patients (
n = 7589), 26.3% reported anxiety symptoms, and 22.4% reported depression symptoms [
21]. Recent Norwegian data (
n = 10,245) indicate a 30–40% prevalence of anxiety and/or depression symptoms in MI patients [
22]. A Norwegian cohort study including 775 patients reported a 27.1% prevalence of anxiety and a 19% prevalence of depression after percutaneous coronary intervention, with higher prevalence rates in CR participants compared to non-participants [
23]. Compared with men, women with CHD exhibit a greater prevalence and more severe anxiety and depression symptoms compared to men [
14,
21,
24,
25]. Recent studies agree that women with CHD entering CR in general present with higher anxiety and/or depression symptoms levels than men do [
26,
27,
28,
29,
30,
31,
32,
33]. Despite the significant prevalence and adverse impact of these mental health conditions on cardiovascular health, and the European guidelines recommending screening and treatment, anxiety and depression in CHD patients are frequently underdiagnosed and undertreated [
15,
34]. Moreover, psychological health traditionally receives less attention than physical health [
15,
34]. Identifying and treating these mental health challenges is essential when aiming to improve patient’s prognosis [
2,
35].
CR is a comprehensive, multidisciplinary intervention aimed at improving cardiovascular health and overall well-being [
34]. The European Society of Cardiology (ESC) classifies CR as a class 1A recommendation and considers it a cost-effective intervention for secondary prevention through the assessment and treatment of cardiovascular risk factors [
2]. In Norway, CR is offered in three phases, as recommended by ESC guidelines, each supporting patients at different recovery stages (
Figure 1) [
36,
37]. Phase 2 CR is further divided into phases 2a and 2b, ensuring both early initiation and tailored multidisciplinary intervention [
36]. Phase 2b typically involves outpatient group training or inpatient services at specialized institutions, which play a critical role in slowing disease progression and promoting sustainable lifestyle changes [
36]. According to ESC guidelines, comprehensive CR should encompass assessment, physical exercise, lifestyle and risk factor management, education, counseling, and psychosocial support [
2,
34].
Exercise-only CR has been found to improve anxiety and depression symptoms in CHD patients [
30,
38]. Comprehensive CR, which synergistically integrates the advised CR elements, is however found to be most effective in facilitating positive patient outcomes; reducing CVD progression, readmission rates, and healthcare expenses, and promoting optimal physical and mental functioning for CHD patients [
2,
34,
37,
39,
40,
41,
42]. Comprehensive CR provides a suitable context for anxiety and depression screening and effective treatment of these mental health issues, contributing to symptom reduction and consequently improving patients’ quality of life and prognosis [
24,
34,
43]. While psychological interventions are found to improve depression and anxiety symptoms, uncertainty remains regarding the effect size and impact on adverse cardiac events and overall mortality of these additional psychosocial interventions to exercise-only CR [
43,
44,
45]. Although both sexes may experience reduced anxiety and depression symptoms following CR completion, research studies are inconclusive regarding sex differences in the extent of these benefits [
46]. While initial disparities in prevalence exist, with a higher prevalence in women than in men, sex differences in symptom reduction are not found in most studies following exercise-only CR [
28,
29,
30] or comprehensive CR [
26,
27]. This finding might imply that once individuals are engaged in CR, the therapeutic benefits may be similarly effective across sexes [
26,
27,
28,
29,
30]. However, the results are conflicting, with longitudinal studies indicating poorer symptom reduction in women at comprehensive CR completion [
32,
33].
To our knowledge, no Norwegian studies have examined the prevalence of anxiety and depression or changes in these symptoms during phase 2b CR, particularly with a focus on potential sex differences. The primary aim of this study is to examine the prevalence and changes in self-reported anxiety and depression symptoms among CHD patients completing phase 2b CR in Norway. Additionally, we aim to identify possible sex differences relating to anxiety and depression symptoms, accounting for possible sociodemographic and clinical confounders. Our research questions are as follows:
What is the prevalence of self-reported symptoms of anxiety and depression among CHD patients at admission and discharge from phase 2b CR, and are there sex differences?
How do self-reported anxiety and depression scores change from admission to discharge in CHD patients undergoing phase 2b CR, and are there sex differences?
Do CHD patients with anxiety and/or depression symptoms at CR admission report symptom reduction at discharge, and are there sex differences in this reduction?
2. Materials and Methods
2.1. Study Design, Setting and Intervention
This study used a retrospective pre–post quasi-experimental design. Data were collected for clinical treatment in a single phase 2b CR facility in central Norway. The data inclusion period spanned from 1 January 2022 to 30 April 2024. Patients were primarily admitted from The Central Norway Regional Health Authority. This CR facility offers a tailored inpatient program lasting three to four weeks, depending on the time of year (e.g., public holidays or seasonal breaks).
The program is designed based on an assessment of the patient’s functional and psychological status at admission. The primary objectives are to enhance functional ability, increase knowledge, and foster healthy behaviors. Additionally, psychosocial aspects regarding patients’ heart disease should be addressed. Ultimately, the program aims to motivate long-term self-care, improve coping mechanisms, manage symptoms, and reduce the risk of future cardiac issues. The comprehensive multifactorial program provides education, group guidance, individual support, medical evaluation, and daily physical training. Next of kin are involved and provided with guidance. A multidisciplinary team comprising nurses, physiotherapists, and a cardiologist are mainly responsible for coordinating patient care and managing treatment during the CR program. The physical training program includes a variety of resistance training and cardiovascular exercise, customized to individual needs and supervised by physiotherapists and/or nurses. When necessary, additional support is provided by an occupational therapist, psychiatric nurse, social worker, nutrition counsellor, or sports physiologist. Patients reporting anxiety and/or depression symptoms registered with the Hospital Anxiety and Depression Scale (HADS), with scores of ≥8, are considered to need further clinical interventions and receive additional supportive counseling during their stay, primarily from a psychiatric nurse. If necessary, they are also referred to municipal mental health services or specialized healthcare institutions for continued care.
2.2. Participants’ Characteristics, Data Collection, and Measures
Patients aged 18 years or older with a primary CHD diagnosis completing phase 2b CR were included in this study. For patients with multiple admissions during the data collection period, only data from the patient’s first stay were included to ensure that only one dataset was assessed per patient.
Sociodemographic data and information on anxiety and depression symptoms were collected primarily for clinical purposes via self-reported digital questionnaires featuring closed-ended questions. Data were collected at patient admission to CR (baseline) and at discharge (follow-up). The data were further stored in a registry database for research purposes. Additionally, details regarding the patient’s primary diagnosis, comorbidities, and medication regimen, sourced from medical records, were entered into the database. Primary diagnoses, as defined by the International Classification of Diseases (ICDs), were predominantly classified under atherosclerotic heart disease of native coronary artery (ICD-10-CM code I25.1), without further specification of CHD type or details regarding revascularization treatment. The included variables are presented in
Table 1.
The Norwegian version of a validated generic patient-reported digital questionnaire, HADS, was used to screen CR participants for self-reported anxiety and depression symptoms at admission and discharge. The HADS is widely used in both national and international research across health care levels and patient groups to assess anxiety and/or depression symptoms [
47]. The HADS comprises fourteen closed-ended questions, with seven addressing anxiety (HADS-A) and seven addressing depression (HADS-D). Each question offers four response alternatives, on a Likert-type summated rating scale from zero to three (the highest level of symptom burden) [
47]. Summing the values from each question yields a total sub-score for HADS-A and HADS-D, ranging from zero to twenty-one [
47]. This study applies an internationally recommended threshold value of ≥8, offering a good balance between sensitivity and specificity for the indication of anxiety (HADS-A) and depression (HADS-D) symptoms [
47,
48]. HADS has been shown to effectively measure psychological distress in CHD patients and has good internal consistency with the Cronbach’s alpha (HADS-A = 0.81–0.85, HADS-D = 0.78–0.88) [
15,
47].
2.3. Statistical Analysis
The included variables were assessed for normality. To describe the individual variables’ distributions, descriptive statistics and univariate analyses were utilized. The results are presented for each variable, with frequencies and percentages for categorical variables and medians and interquartile ranges (IQR) for continuous variables with skewed distributions [
49,
50]. Statistical significance for all analyses was determined at a
p-value < 0.05.
Bivariate analyses were conducted to describe the empirical relationship between two variables and identify changes in HADS-A and HADS-D scores and sex differences. The results are presented in separate models for depression and anxiety.
To assess the possible influence of missing data on representativity, Pearson’s Chi-square Test for independence (categorical variables) and the Mann–Whitney U Test (nonparametric continuous variables) were used to evaluate differences between patients who did and did not report HADS [
49].
To assess the prevalence rates of anxiety or depression symptoms, dichotomous HADS scores (≥8) were applied in univariate and bivariate analyses. McNemar’s test for repeated measures was applied to assess changes in the prevalence of anxiety and depression symptoms from admission to discharge [
49].
Possible sex differences in categorical sociodemographic factors, clinical characteristics, and dichotomous HADS-A and HADS-D scores were assessed via Pearson’s Chi-square Test. Fisher’s exact test was used when Pearson’s Chi-square test assumption was violated with cell frequencies ≤5 [
51]. The Mann–Whitney U test was used to assess sex differences in not normally distributed continuous variables, such as age, length of stay, and HADS score [
49].
The Wilcoxon signed rank test was used for within-group comparisons to assess changes in HADS-A and HADS-D scores from admission to discharge for the whole sample, for participants reporting HADS scores ≥8 at admission, and for men and women in both groups [
49].
Two multiple linear regression analyses were conducted to examine the relationships between the continuous dependent variable HADS-A or HADS-D at discharge and the independent variables HADS-A or HADS-D at admission and sex [
49]. In addition, an interaction variable that combines sex and HADS-A score at admission or sex and HADS-D score at admission was included as an independent variable in the multiple linear regression analyses to identify whether differences between men and women were related to changes in anxiety/depression scores from admission to discharge [
49]. Collinearity, multivariate outliers, normality, linearity, homoscedasticity, and independence of residuals in the multiple linear regression analyses were assessed [
49]. Statistical analyses were carried out via IBM SPSS statistics, version 30.
2.4. Ethical Considerations
This study follows the ethical principles of the Helsinki declaration [
52]. Approval was granted from the regional ethics committee for medical and healthcare research ethics (REK, 546776). All participants received comprehensive written information regarding the study’s objectives, procedures, and implications as part of an overarching research study completed at the same CR facility. Informed consent was obtained from each participant retrospectively by the institution responsible for data collection prior to the initiation of this study. The participants were explicitly informed of their right to withdraw consent. To safeguard participant anonymity and confidentiality, only deidentified data were utilized.