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Article

Perspectives on Knowledge, Precautionary Behaviors, and Psychological Status of Patients with Cardiovascular Diseases During the First Wave of the COVID-19 Pandemic in Lebanon: A Multicentric Cross-Sectional Study

by
Marc Machaalani
1,†,
Battoul Fakhry
1,†,
Kassem Farhat
1,†,
Juliano Haddad
1,
Youssef Rahmeh
1,
Peter Ghiya
1,2,
Diana Carolina Awad
1,3,
Aline Zaiter
1,4,
Jean G. Louka
1,5,
Layal Olaywan
1,6,
Ahmad Halawi
1,
Hassan Cherry
1,
Mohamad Ghazal
1,
Mustapha Sahili
1,
Bachir Atallah
1,
Wadih Naja
7,
Elie Chammas
8,
Roland Asmar
9,10,
Nadine Yared
11 and
Mirna N. Chahine
1,9,10,12,*
1
Department of Research, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
2
Department of Urology, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
3
Department of General Surgery, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
4
Department of Internal Medicine, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
5
Department of Orthopedic Surgery and Traumatology, Simone-Veil Hospital, 95600 Eaubonne, France
6
Department of Pulmonary and Critical Care, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
7
Department of Psychiatry, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
8
Department of Cardiology, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
9
Foundation-Medical Research Institutes (F-MRI®), Achrafieh, Beirut 1100, Lebanon
10
Foundation-Medical Research Institutes (F-MRI®), 1211 Geneva, Switzerland
11
Department of Infectious Diseases, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
12
Department of Basic Sciences, Faculty of Medical Sciences, Lebanese University, Hadath 1519, Lebanon
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
COVID 2025, 5(9), 155; https://doi.org/10.3390/covid5090155
Submission received: 22 June 2025 / Revised: 2 September 2025 / Accepted: 9 September 2025 / Published: 12 September 2025
(This article belongs to the Section COVID Public Health and Epidemiology)

Abstract

Cardiovascular diseases (CVDs) are among the most common comorbidities in COVID-19 patients. This multicenter cross-sectional study assessed knowledge, risk perception, precautionary measures, and psychological burden related to COVID-19 among Lebanese individuals with and without CVD during the pandemic’s first wave. A total of 485 CVD patients and 1033 control group (CG) participants completed standardized questionnaires, including the Patient Health Questionnaire-9 (PHQ-9), General Anxiety Disorder-7 (GAD-7), and Coronavirus Anxiety Scale. Compared to CG, CVD patients demonstrated significantly lower COVID-19-related knowledge (86.4% vs. 90.0%, p < 0.001) and adherence to preventive measures (81.5% vs. 85.7%, p < 0.001). After stratification, limited knowledge was more common among CVD patients (45.7% vs. 31.8%), as was limited precautionary behavior (70.3% vs. 54.2%). Risk perception was suboptimal in both groups, with no significant difference (41.3% vs. 38.6%, p = 0.072). Anxiety (GAD-7 ≥ 10) and depression (PHQ-9 ≥ 10) were more prevalent among CVD patients (13.4% and 11.3%) than CG participants (9.5% and 16.5%). Survey outcomes were influenced by educational, socioeconomic, and psychosocial factors. These findings highlight the need to target CVD patients in public health campaigns to enhance preparedness and mental health support during pandemics.

1. Introduction

After its detection in December 2019, the World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) a public health emergency of international concern on 30 January 2020 and elevated it to pandemic status on 11 March 2020 [1]. As of 23 August 2025, over 777 million laboratory-confirmed COVID-19 cases and approximately 7 million deaths were reported globally [2]. In Lebanon, the first confirmed COVID-19 case appeared on 21 February 2020. As of 23 August 2025, cumulative totals reached 1,243,838 confirmed cases and 10,952 deaths, equivalent to approximately 178 deaths per 100,000 population. Globally, cumulative COVID-19 deaths stood at around 7.1 million by the same date, illustrating the sustained global impact of the pandemic [2].
COVID-19 has been particularly burdensome for individuals with cardiovascular diseases (CVDs), which have emerged as the most common comorbidities and predictors of poor outcomes in infected patients [3]. CVDs encompass cerebrovascular disease, hypertension, heart failure, coronary and peripheral artery disease, arrhythmia, and thromboembolic disorders [4]. Notably, in Lebanon, the epidemiological surveillance program of the Lebanese Ministry of Public Health reported that 82% of COVID-19 deaths involved at least one comorbidity, most commonly hypertension (59.1%), reflecting the high vulnerability of patients with underlying cardiovascular risk factors [5].
SARS-CoV-2 can damage the cardiovascular system through multiple mechanisms, including direct myocardial injury, systemic inflammation, hypoxemia and hypoperfusion, endothelial dysfunction, plaque destabilization, coagulopathy, arrhythmogenesis, and stress cardiomyopathy [3,6,7,8]. In addition to acute complications, increasing evidence highlights the persistence of cardiovascular symptoms well beyond the acute phase, termed post-acute sequelae of SARS-CoV-2 infection (PASC) or long COVID. This syndrome may involve lingering symptoms such as chest pain, palpitations, exertional dyspnea, and fatigue, often accompanied by elevated cardiac biomarkers and clinical findings of myocarditis, fibrosis, and pericardial involvement months after recovery, even in previously healthy individuals [8,9,10]. The virus uses angiotensin-converting enzyme 2 (ACE-2) to infiltrate target organs which are expressed in cardiac, renal, pulmonary, and intestinal tissues [6]. This initially raised concerns regarding the safety of cardiovascular medications such as ACE inhibitors and angiotensin receptor blockers (ARBs), which may increase ACE2 expression. However, clinical evidence has not demonstrated increased risk, and both the American Heart Association (AHA) and European Society of Cardiology (ESC) have recommended continuing these therapies due to their well-established benefits in managing cardiovascular conditions [11,12]
Knowledge–attitude–practice (KAP) studies have been instrumental in understanding perceptions during the first COVID-19 wave [13], particularly among healthcare workers [14], healthy individuals [15], pregnant women [16], parents [17], and chronic disease cohorts worldwide [18,19]. In Lebanon, extensive KAP research has been conducted among the general population [20,21], pregnant women [16], parents [17], and hospital pharmacists [22]. However, until now, there has been no study specifically examining KAP among Lebanese patients with cardiovascular disease (CVD) in response to COVID-19. Previous research conducted by our team has assessed baseline KAP regarding CVD prevention in the Lebanese population [23], but the intersection of CVD and COVID-19 perspectives remains unexplored.
Beyond physical outcomes, the COVID-19 pandemic has exerted a profound psychological impact, manifesting as heightened levels of anxiety, depression, and coronavirus-specific anxiety, especially among individuals with chronic illnesses [24,25,26,27,28]. Evidence from international and regional studies indicates that psychological distress may substantially shape risk perception and precautionary practices [29,30,31]. Among patients with cardiovascular diseases, this association is particularly critical, as the coexistence of mental health difficulties and altered perceptions of risk can further compromise adherence to preventive measures and exacerbate disease management challenges [27,28].
Accordingly, this study was designed to address this gap by providing a comprehensive assessment of COVID-19-related knowledge, risk perception, precautionary behaviors, and psychological burden—including anxiety, depression, and coronavirus-related anxiety—among Lebanese patients with cardiovascular diseases during the pandemic’s first wave. By directly comparing these outcomes with those of a healthy control group, this work seeks to elucidate the multidimensional challenges faced by this vulnerable population and to generate evidence that may inform tailored public health interventions and mental health support strategies during ongoing and future health crises.

2. Materials and Methods

This study is part of a larger national project that investigates COVID-19-related knowledge, precautionary behaviors, perceptions, and psychological outcomes (anxiety and depression) in patients with various chronic diseases (cardiovascular diseases, mental disorders, lung diseases, metabolic diseases, chronic kidney diseases, cancer, and musculoskeletal disorders). The current paper focuses specifically on patients with cardiovascular diseases compared to a control group of healthy individuals.

2.1. Study Design and Population

2.1.1. Study Design and Setting

This cross-sectional study was conducted in Lebanon between 3 May and 27 May, 2020, targeting patients with cardiovascular diseases (CVDs) and healthy control participants. A structured questionnaire was administered both electronically (via Google Forms) and in printed form. Participants were recruited from various private medical clinics and hospitals located across all eight governorates of Lebanon, proportionally reflecting the population distribution in five major regions: Beirut, Mount Lebanon, Bekaa (including Baalbek-Hermel), North (including Akkar), and South (including Nabatieh). Enrollment was achieved through a combination of in-person recruitment at these healthcare facilities and remote contact via telephone interviews.

2.1.2. Study Population

We included within the case group (CVD group) all patients currently diagnosed or with a history of cardiovascular diseases (hypertension, heart failure, atherosclerosis, coronary artery disease, and thrombosis (e.g., deep vein thrombosis, pulmonary embolism)), whereas the control group (CG) included all subjects without chronic conditions (cardiovascular diseases, mental disorders, lung diseases, metabolic, chronic kidney diseases, cancer, musculoskeletal disorders).

2.1.3. Inclusion and Exclusion Criteria

All participants were required to be ≥18 years of age, residing in Lebanon, and to provide informed consent. We excluded any participant under the age of 18 or who refused to fill in the survey.

2.1.4. Sample Size Calculation

Slovin’s formula was used to calculate a representative sample of the Lebanese general population, = N 1 + N e 2 , with N representing the Lebanese population (following the Index Mundi registry, the Lebanese population was 6,100,075 in 2019), e is the p-value = 0.05. Therefore, a minimum of 400 patients had to fill out the questionnaire in order to be representative of the general population in Lebanon.
Cochran’s formula was used to calculate a representative sample of the patients suffering from CVD in the Lebanese population, n = Z 2 p q e 2 , where Z2 is the square of the confidence interval, considered 95% in this case, which corresponds to (1.96)2, p is the estimated proportion of the Lebanese population having CVD, q is (1 − p), and e represents the p-value = 0.05, The prevalence of cardiovascular comorbidities in our targeted population is around 36% [32]. Therefore, a minimum of 355 participants with CVD were needed. The population was targeted in all 8 governorates in Lebanon.

2.2. Data Collection

2.2.1. Survey Tool and Validation

The questionnaire was based on a survey executed and validated by Yale University [33]. Permission was granted for the reproduction of the questionnaire [21]. Additional questions were built according to updated guidelines and recommendations [34,35,36,37,38,39]. It was translated into Arabic using Fortin’s back-translation method and reviewed for clarity by a native Arabic speaker and bilingual medical expert [40]. A pre-test with 10 individuals ensured cultural appropriateness and comprehension. The questionnaire consisted of three main components (Appendix A):
  • Informed consent.
This section introduced the study’s purpose, outlined participants’ rights, and confirmed that participation was entirely voluntary. It also included guarantees of data confidentiality and anonymity.
2.
General questionnaire for all participants (cases and controls).
This part was composed of 103 questions divided into five key sections:
Section 1 collected sociodemographic and background data, including age, sex, region of residence, smoking status, comorbidities, and self-assessed knowledge of COVID-19.
Section 2 explored participants’ general knowledge of COVID-19, such as modes of transmission, symptoms, and prevention strategies.
Section 3 examined participants’ perceptions of the pandemic, including their beliefs about COVID-19’s severity, response measures, and personal risk.
Section 4 assessed the preventive practices adopted by participants to protect themselves against infection, such as mask-wearing, hand hygiene, and social distancing.
Section 5 included standardized psychological screening tools to assess mental health status, including the General Anxiety Disorder-7 (GAD-7) scale for anxiety symptoms, the Patient Health Questionnaire-9 (PHQ-9) for depressive symptoms, and the Coronavirus Anxiety Scale (CAS) for COVID-19-specific anxiety symptoms.
3.
Cardiovascular disease (CVD)-specific questionnaire.
This section, completed only by participants with a history of cardiovascular disease, comprised 52 questions divided into four sections:
Section 1 gathered clinical information specific to cardiovascular health, including blood pressure levels, lipid profiles, and current pharmacological treatments.
Section 2 assessed participants’ knowledge regarding the heightened risk of severe COVID-19 outcomes associated with cardiovascular conditions.
Section 3 explored the perceptions of CVD patients toward their susceptibility to COVID-19 complications.
Section 4 investigated the preventive behaviors adopted by CVD patients specifically in response to the pandemic, including medication adherence and health monitoring practices.

2.2.2. Procedure for Data Collection

Data collection took place between 3 May and 27 May 2020. Participants were enrolled through a combination of in-person recruitment at private medical clinics and hospitals and remote contact via telephone interviews. Upon confirming eligibility and obtaining informed consent, participants completed either a printed version of the questionnaire during clinic visits or an electronic version distributed via Google Forms.
Trained research coordinators provided assistance when needed, especially for older or less tech-literate participants. To ensure reliability, approximately 82% of questionnaires were completed during face-to-face or telephone interviews, with data entered directly by trained physicians. Around 18% of participants self-entered their responses through the electronic Google Form. A very small proportion of printed questionnaires were entered into the database by two independent team members using a double-entry method to verify accuracy and resolve discrepancies. All completed questionnaires, whether printed or electronic, were securely compiled into a centralized database for subsequent data cleaning and analysis. Quality control measures included real-time verification of responses by the study team and follow-up where necessary to ensure completeness.

2.2.3. Measurements and Scores

All measured variables were converted into standardized scores to enable quantitative analysis.
General knowledge about COVID-19 was assessed using 14 items answered by both cases and controls, where each correct response was awarded 1 point and incorrect or “I don’t know” responses received 0 points, resulting in a total score ranging from 0 to 14.
General perception toward COVID-19 was evaluated through 10 Likert-scale items, each scored from 1 (“strongly disagree”) to 5 (“strongly agree”), with “don’t know” assigned a score of 0. For positively framed items, “strongly agree” was designated as the highest score of 5, with “agree” scored as 4, “neutral” as 3, “disagree” as 2, and “strongly disagree” as 1. For negatively framed items, reverse scoring was applied so that “strongly disagree” received the highest score of 5 and “strongly agree” the lowest as 1. This method ensured that responses were graded rather than dichotomized, allowing for the computation of a continuous perception score ranging from 0 to 50.
General preventive practices were measured using 26 yes/no questions on behaviors related to infection control, with each correct action given 1 point and incorrect answers receiving 0 points (total range: 0–26).
Psychological status was assessed using three validated scales: the Generalized Anxiety Disorder scale (GAD-7), consisting of 7 items scored from 0 to 3 and totaling 0 to 21 points; the Patient Health Questionnaire (PHQ-9), consisting of 9 items scored on a 4-point scale to assess depressive symptoms (range: 0–27); and the Coronavirus Anxiety Scale (CAS), composed of 5 Likert-scale items assessing COVID-19-specific anxiety symptoms (range: 0–25).
CVD patients also completed a disease-specific questionnaire.
Knowledge of COVID-19 in the CVD patient section was analyzed using 16 questions. Each correct response was awarded 1 point, while incorrect and “I don’t know” answers received 0 points, for a total score ranging from 0 to 16.
Perception of COVID-19 in CVD patients included 2 questions. The questions followed a Likert scale ranging from 1 to 5 as follows: 1 “strongly disagree”, 2 “disagree”, 3 “neutral”, 4 “agree”, 5 “strongly agree” and 0 “don’t know”, resulting in a total perception score ranging from 0 to 50.
Preventions from COVID-19 in CVD patients included 6 questions about the preventive measures taken by CVD patients such as adhering to treatment and following recommendations. These questions were answered on a true/false basis with an additional “I don’t know” option. Each participant received a score of “1” on the correct answer and “0” on the false answer, yielding a total prevention score of 0 to 6.
All computed scores were subsequently categorized and sub-categorized into “Limited” (Poor, Fair) to “Adequate” (Good, Excellent) levels of knowledge and preventive measures, as shown in Table 1, using the median of the distribution and a modified version of Bloom’s taxonomy cut-off points validated by previously published studies by our team [23,41,42,43,44] and others [45].

2.3. Statistical Analysis

Data were represented as frequencies and proportions for nominal variables and as mean (±SD) for continuous variables. There were a total of 6 scores: The first 5 scores of knowledge, prevention, anxiety level (GAD-7), depression level (PHQ-9), and coronavirus anxiety level were computed for CVD patients and CG subjects, whereas a 6th score of specific knowledge was calculated from the knowledge questions addressed only to CVD patients. Internal consistency (Cronbach’s alpha) was calculated for the adapted scales. The knowledge, prevention, and perception scales demonstrated Cronbach’s alpha values of 0.707, 0.782, and 0.550, respectively. While knowledge and prevention showed acceptable reliability (α > 0.70), the perception scale had a lower alpha, likely due to the multidimensional nature of its items; however, it was retained to capture the diversity of participants’ views. For the standardized psychological instruments, internal consistency was also confirmed: CAS (α = 0.815), GAD-7 (α = 0.879), and PHQ-9 (α = 0.888), which are consistent with their established psychometric validity. In addition, Shapiro–Wilk’s test (p < 0.05) showed that the scores were not normally distributed, with a skewness and kurtoses out of the range (−1.96 and +1.96). We performed the Mann–Whitney test to compare continuous variables of two groups. The Kruskal–Wallis test was used to compare the mean of 3 or more different groups. Spearman’s tests were employed to correlate between 2 continuous variables. Categorical variables were compared using a χ2 test. Multivariate linear regression models were built including all the factors that were statistically correlated with the knowledge, prevention, PHQ-9, GAD-7, coronavirus anxiety, and specific knowledge scores. Data analysis was performed using Statistical Package for the Social Sciences (SPSS) Version 22. p < 0.05 was considered statistically significant.

2.4. Ethical Considerations

Ethical approval was granted by the Institutional Review Board of Al Hayat Hospital (number: ETC-13-2020; date: 23 April 2020). Participation in the study was entirely voluntary. Informed consent was obtained from all participants (aged ≥ 18 years) either electronically via a statement embedded in the online survey form (“Yes, I agree to participate”) or verbally with assistance from medical staff during phone-based data collection. Data collection was anonymized: personal identifiers (e.g., names, contact details, exact birth dates) were not collected, and only direct age was provided. Each participant received a designated code. Data were securely stored with restricted access limited to the researchers. The study adhered to the Declaration of Helsinki (1964) and ICH-GCP guidelines [46].

3. Results

3.1. Population Characteristics

3.1.1. General Characteristics of CVD Patients in Comparison with Control Group Subjects

We initially contacted 1706 subjects (1136 control group (CG) subjects and 570 patients suffering from CVD). The response rate was on average about 89%; thus, a total of 1518 subjects participated in this study, distributed into 1033 CG subjects without the chronic diseases cited above (Section 2) and 485 patients suffering from CVD. The mean age of the sample was 39.4 ± 19.5 years. CVD patients were predominantly males (47.6%), were significantly older (59.1 years), and had a higher body mass index (BMI) (28.5 Kg/m2) when compared to CG subjects (all p < 0.001). Patients, compared to CG subjects, had increased their consumption of cigarettes (9.3% vs. 4.75%, respectively, p < 0.001) since the start of the outbreak (all). The complete demographic details of CVD patients compared to CG subjects are presented in Table 2.

3.1.2. Clinical Characteristics of Participants in Our Study

Among the 485 patients with CVDs included in our study, hypertension was the leading diagnosis (56.2%), followed by heart rhythm disorders (15.5%), coronary artery disease (10.5%), heart failure (7.4%), thromboembolic disease (7.1%), and cerebrovascular disease (3.5%) (Supplementary Materials, Figure S1A). Blood pressure measurements revealed a 29.8% prevalence of grade 1 and 10.3% of grade 2 systolic hypertension as well as 20.2% prevalence of grade 1 and 12.1% of grade 2 diastolic hypertension in CVD patients. Additionally, 37.5% of patients reported having hyperglycemia, while total cholesterol (<200 mg/dL) and triglyceride levels (<150 mg/dL) were normal in 42.2% and 41.1% of patients, respectively (Supplementary Materials, Figure S1B). Concerning medications, 56.2% of patients were under antihypertensive medication (beta-blockers (42.2%)) and anti-coagulants (aspirin (78%)) (Supplementary Materials, Figure S1C).

3.2. General Parameters (Knowledge, Perception, Precautions About COVID-19, Coronavirus Anxiety, GAD, and Depression) in CVD Patients and CG Individuals

3.2.1. General Knowledge Score About COVID-19 and Associated Factors in CVD Patients vs. CG Individuals

The mean knowledge score of CVD patients was significantly lower than that of the CG subjects (12.1 ± 2.1/14 (86.4%) vs. 12.6 ± 1.6/14 (90.0%), p < 0.001, respectively) (Figure 1A). Almost half of the CVD patients (45.7% regrouping, 14.4% with Poor, and 31.3% with Fair knowledge scores) versus a third of CG subjects who had a “Limited” Knowledge level about COVID-19 (Figure 1B). For instance, CVD patients, when compared to CG subjects, less frequently correctly identified that asymptomatic patients carrying the virus may transmit the virus (86.6% vs. 94.3%, p < 0.001, respectively) (Figure 2A). The complete set of knowledge-related questions and the distribution of correct/incorrect responses for both groups are presented in the Supplementary Materials, Table S1. The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis showed that CVD patients knew more about COVID-19 when they were of a younger age (p = 0.001), male gender (p = 0.02), higher educational level (p < 0.001), and when they had a higher precaution score toward COVID-19 and a better specific knowledge about COVID-19 related to their disease (p < 0.001) (Supplementary Materials, Table S3).

3.2.2. General Risk Perception Toward COVID-19 and Associated Factors in CVD Patients vs. CG Individuals

CVD patients showed a poor-to-moderate general perception about COVID-19 risk, with no significant difference from CG subjects (41.3% vs. 38.6% of correct answers, respectively, p = 0.072). For instance, more than half of CVD patients, when compared to CG participants, correctly and better recognized that they should not stop their usual prescribed medication during the outbreak (p = 0.002). Very few patients correctly perceived, compared to CG subjects, that they should not worry about restricted access to their usual prescribed medications during the lockdown (p < 0.001) (8.9% vs. 15.8% of correct answers, respectively) (Figure 2B). The complete set of perception-related questions and the distribution of correct/incorrect responses for both groups are presented in the Supplementary Materials, Table S4.

3.2.3. General Precaution Score Against COVID-19 and Associated Factors in CVD Patients vs. CG Individuals

The mean precaution score of CVD patients was significantly lower than that of the CG subjects (21.2 ± 3.4 /26 (81.5%) vs. 22.3 ± 3.0/26 (85.7%), p < 0.001, respectively) (Figure 1A). Almost three-fourths of the CVD patients versus half of the CG subjects had a “Limited” precaution level towards COVID-19 (Figure 1C). Specifically, CVD patients were less likely to exercise regularly (50.7% vs. 72.6%) and to wear a mask outside home (89.5% vs. 95.4%) compared to the CG subjects (all p < 0.001) (Figure 2C). The complete set of precaution-related questions and the distribution of correct/incorrect responses for both groups are presented in the Supplementary Materials, Table S5. The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis revealed that CVD patients took more precautionary measures toward COVID-19 when they had a better socioeconomic status (p = 0.013), a higher educational level (p = 0.040), better knowledge about COVID-19 (p < 0.001), and better specific knowledge about COVID-19 in CVD patients (p < 0.001) (Supplementary Materials, Table S3).

3.2.4. Coronavirus Anxiety Scale (CAS) and Associated Factors in CVD Patients vs. CG Individuals

The mean CAS score of CVD patients was higher than that of CG subjects (1.1 ± 2.2 over 20 vs. 1.2 ± 2.3 over 20, respectively), but these means had no clinical relevance, and their differences were not statistically significant (Figure 1A). The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis revealed that CVD patients were more anxious towards COVID-19 when they had increased their alcohol consumption since the start of the outbreak (p = 0.04) and had higher GAD7 and PHQ9 scores (both p < 0.001) (Supplementary Materials, Table S3).

3.2.5. GAD-7 Score and Associated Factors in CVD Patients vs. CG Individuals

The CVD group achieved higher mean GAD-7 scores in comparison to the CG GAD-7 scores (4.7 ± 4.5/21 and 4.2 ± 4.3/21, respectively), but these means had no clinical relevance, and their differences were not statistically significant (Figure 1A). A proportion of 13.4% of CVD patients versus 9.49% of CG subjects had a clinically relevant GAD-7 score (≥10) without being diagnosed with anxiety by their physician. The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis showed that CVD patients had a significantly higher GAD-7 score when they were living outside of Beirut (p = 0.032), had a higher CAS score (p < 0.001), and had a higher PHQ-9 score (p < 0.001) (Supplementary Materials, Table S3).

3.2.6. PHQ-9 Score and Associated Factors in CVD Patients vs. CG Individuals

The mean PHQ-9 scores of CVD patients and the CG subjects were 4.84/27 (17.9%) and 5.03/27 (18.62%), respectively. The difference was not statistically significant (p > 0.05) (Figure 1A). We found that 11.3% of CVD patients versus 16.46% of CG subjects had a clinically relevant PHQ-9 score (≥10) without being diagnosed with depression by their physician. The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis demonstrated that CVD patients had a higher PHQ-9 score when they had a higher GAD-7 score (p < 0.001) and were younger (p = 0.001) (Supplementary Materials, Table S3).

3.3. Specific Parameters (Knowledge, Precautions, and Perception About COVID-19) in CVD Patients

This section was filled according to the third part of the questionnaire, completed only by CVD patients answering questions about COVID-19 that were particularly related to their disease.

3.3.1. Specific Knowledge

The mean specific knowledge score was 9.41 ± 3.77 over 14 (67.2%) for CVD patients, with 16.1% having Good and 8.9% having Excellent specific knowledge scores about COVID-19 in relation to their disease. For instance, CVD patients correctly identified that they had a higher risk of severe symptoms from COVID-19 than other individuals. However, only 35.88% knew that COVID-19 could cause blood clotting issues. Overall, the average of correct answers to questions related to specific knowledge was 61.34% (Figure 3). The bivariate analysis is shown in the Supplementary Materials, Table S2. The multivariate analysis showed that better knowledge and preventive measures positively influenced in CVD patients the specific knowledge about COVID-19 in relation to their disease (Supplementary Materials, Table S3).

3.3.2. Specific Precautions

A proportion of 93.40% of CVD patients adhered to the treatment recommended by their cardiologist. Only 32.99% of CVD patients knew that if they contracted COVID-19 while they suffered from irregular heartbeats (e.g., Long QT syndrome), they should never take hydroxychloroquine and/or azithromycin. Overall, the average of correct answers regarding questions about specific precautions was 70.34% (Figure 4).

3.3.3. Specific Perception

Only 4.12% of CVD patients correctly believed that in case they had a COVID-19 infection and a fever, they could manage the symptoms at home, since fever can be treated with paracetamol. In addition, 57.32% of patients correctly responded that in case they had a COVID-19 infection and a fever with shortness of breath, they should ask for medical help instead of managing their symptoms at home. Accordingly, the average of correct answers regarding specific risk perception questions was 30.72% (Figure 5).

4. Discussion

In this cross-sectional study, we evaluated the perspective of CVD patients in Lebanon towards COVID-19, as it has been shown that improving knowledge, risk perception, and preventive practices helps in preventing the spread of the disease and in managing symptoms of anxiety and depression during this pandemic [47]. A total of 1518 individuals participated in this survey, of which 31.9% had CVD, with the most common primary diagnosis being hypertension.

4.1. COVID-19 Knowledge

CVD patients had a reasonably fair general knowledge about COVID-19, as a few gaps existed when compared to CG subjects. More importantly, CVD patients scored poorly on specific knowledge questions related to their disease. Similar studies in the United States [18], Ethiopia [19,39], India [48], and Vietnam [47] reported a relative lack of knowledge about COVID-19 in patients with chronic diseases, including patients with heart diseases and hypertension. Some of our patients, similarly to others [19,46], failed to recognize that COVID-19 complications and death were more severe and frequent, respectively, in hypertensive patients infected with COVID-19, hence the role of the treating physician in providing better guidance and education on CVD and COVID-19. In addition, our findings, in line with others [19,39,46,48], showed that patients with a higher educational level and younger participants (healthy or suffering from a disease) were more knowledgeable about COVID-19. Moreover, males and especially those suffering from CVD demonstrated a higher knowledge level about COVID-19 than females. As the majority of patients who contracted the virus were males [49], this might explain why they would seek more information on COVID-19. Furthermore, our study demonstrated that knowledge about COVID-19 was a significant predictor of COVID-19-preventive behavior, as previously reported by others [48]. Therefore, great preventive practices toward COVID-19 can be achieved with adequate knowledge of preventive measures [24]. The poor specific knowledge among CVD patients also reflects suboptimal physician–patient communication. Previous studies have highlighted how the COVID-19 context disrupted doctor–patient communication and trust, as infection control measures created barriers in face-to-face interactions [50]. To address this challenge, ensuring clear and empathetic communication is essential, particularly for patients with chronic conditions, in order to maintain adherence to precautionary measures and treatment during the pandemic. Incorporating brief but structured counseling sessions on infection risks and comorbidity-specific vulnerabilities during outpatient visits may bridge this knowledge gap [45].

4.2. COVID-19 Risk Perception

Moreover, CVD patients disclosed high averages of wrong answers regarding COVID-19 general and specific risk perception questions. Indeed, only half of our CVD patients perceived this outbreak as a serious public health threat, which was quite in line with what other chronic disease patients (including patients with hypertension) perceived to be at high risk if infected by COVID-19 from Ethiopia (68%) [25] and from Portugal (51.6%) [29]. Only one-third of our patients worried that their family or household members would contract the virus, which was inconsistent with others’ findings from Vietnam (64.8%) [47]. More importantly, only half of our patients perceived the need to pursue their usual prescribed medication, and a quarter of them admitted to avoiding hospitals for fear of contracting the virus. These findings were in line with previously published data [30].

4.3. COVID-19-Preventive Practices

Furthermore, CVD patients adopted relatively fair preventive measures about COVID-19, as several gaps in the general preventive measures were revealed when compared to CG subjects. Most patients had a “Limited” general precautions level towards COVID-19. In line with these findings, chronic disease patients reported poor practice [19,39] as well as a decline in physical activity during the pandemic [51], in contrast to others with 98.3% adherence to face masks and an overall 77.2% good precautionary measures against COVID-19 [47]. A higher educational level and socioeconomic status in our patients correlated with a better specific knowledge about COVID-19 related to their disease. More importantly, many of our patients responded with wrong answers to the specific precautionary measures about COVID-19 in relation to their disease, with several ones who did not follow the recommendations to self-test using blood pressure machines at home for better controlling their blood pressure. Undoubtedly, the pandemic has favored remote consultation and monitoring through the use of mobile-health tools and wearables [52]. Adoption of telemedicine has become an essential step in CVD management [52]. In addition, many patients reported not adhering to their antihypertensive treatments (such as ACEI /ARB), which were initially thought to increase the risk of infection with COVID-19 [4,12] In the USA, one in eight Americans with CVD missed or delayed taking medication due to costs [53]. More drastically, in Lebanon, diminished purchasing power due to one of the worst economic crises in history, conjugated with the pandemic, has critically impeded access and adherence to medications for citizens and particularly for CVD patients.

4.4. COVID-19 Psychological Impact

Regarding the psychological impact of COVID-19 on our population, our study revealed that CVD patients and CG individuals did not show clinically relevant anxiety and depression scores. Similarly to Louvardi et al. [26], overall levels of anxiety and depression in our CVD patients and CG subjects had no clinical significance. As a matter of fact, the lack of any clinical relevance in these three scores (CAS, GAD-7, and PHQ-9) among our patients may be attributable to many possibilities: (1) The initial success of Lebanon in containing the virus and the limited number of cases and deaths among the Lebanese population at that time (May 2020) [54]. (2) CVD patients had incomplete perception of their risk of severe COVID-19, as shown in our findings and others’ [31]. Patients may have also adopted a coping strategy to deny or minimize stressors, as reported by others [31,55]. In particular, the same coping mechanism may be applied to the Lebanese general population to mitigate the disastrous period that the country is going through (unprecedented economic crisis, the August 2020 Beirut blast, etc.). That same “safety behavior” amongst individuals with high-risk diseases during the pandemic was also suggested by Kohler et al. [56]. (3) In Lebanon, anxiety and depression are still considered taboo topics to many, and some patients may avoid reaching out to their physicians to share their fears and distresses and particularly with our volunteers. Nonetheless, when classes of PHQ-9 and GAD-7 tests were closely examined, our findings revealed clinically relevant scores on both tests, with surprising rates of anxiety and depression that were not previously diagnosed by their physicians in both CG subjects and CVD patients. In particular, patients living outside of the capital Beirut had higher anxiety levels, as reported by others [27]. Younger patients manifested a higher PHQ-9 score, possibly due to isolation and limited access to healthcare, support groups, and services. Certainly, the pandemic and all its ensuing consequences, from infection, isolation, lockdowns, social distancing, working from home, and even post-COVID-19 syndrome [28], may have increased the risk of developing depression and other mental health disorders.

4.5. Limitations

This study had several limitations, mainly related to the method of data collection. The survey was made available online and was self-filled; this may have led to reporting, selection, sampling, and volunteer biases [46]. However, to reduce those biases, our team was carefully selected and well trained to address around 82% of the total number of participants (healthy individuals and our CVD patients) over face-to-face or phone interviews. Indeed, participants were randomly selected among the family, friends, and hospitalized patients. This prevented those feeling more engaged or knowledgeable about the topic to complete the survey. Nevertheless, we acknowledge that participant selection itself is a key factor that may have influenced the study outcomes, particularly given the diversity of healthcare access and sociodemographic backgrounds across Lebanon. On the other hand, direct interviews with participants, whether by phone or in-person, may have also led to a social desirability bias. A key limitation of this study is the sampling bias resulting from the demographic imbalance between the case and control groups, particularly in terms of age and gender distribution (Table 2). Patients with cardiovascular diseases are naturally older, while the control group represented a relatively younger segment of the general population. Although such differences could in principle be addressed through weighing procedures (ponderation) or by constructing matched groups, this was not the aim of our study. Our intention was to capture the perspectives of CVD patients as a high-risk population and compare them to the general Lebanese population, whose preparedness is also of public health importance. Preserving this natural demographic difference allowed us to assess vulnerabilities in older CVD patients while simultaneously identifying gaps in knowledge and behaviors among the younger general population. Nonetheless, we recognize that the absence of weighing or matching procedures could introduce bias, and this must be considered when interpreting our findings. In addition, the Likert scale used in evaluating the perception toward COVID-19 may have caused a central tendency bias, where extreme answers (e.g., strongly disagree and strongly agree that these are the correct answers) are avoided. Furthermore, due to lack of Cronbach’s alpha internal consistency, the scores of general perception as well as specific perception and specific precaution were not computed. To assess general perception, we calculated the average number of correct responses to perception-related questions for both CVD patients and control group (CG) participants. A bivariate analysis using the Mann–Whitney test was then performed to compare Likert-scale scores between the two groups. For specific perception and precaution parameters, we calculated the average number of correct responses among CVD patients regarding COVID-19 in relation to their cardiovascular condition. Finally, we failed to conduct matching and propensity scores, which might limit the generalizability of our findings.

4.6. Perspectives and Recommendations

The results of our study indicate that during the first wave of the COVID-19 pandemic in Lebanon, individuals with or without CVD experienced changes in certain lifestyle and behavioral patterns, including tobacco use, work arrangements, shopping responsibilities, and alcohol consumption. These findings underscore the importance of targeted public health strategies to address and mitigate the long-term impact of such behavioral shifts during future health crises. As assessing and improving the population’s perspective remain essential in fighting pandemics, priority should be given to older patients, females, individuals with low educational and socioeconomic status, and people living in underserved areas.
Despite reasonably fair levels of knowledge, perception, and precaution, a perfect score of 100% is required in all these parameters, since a single gap in knowledge about COVID-19 or a single flawed precautionary measure may put the individual at risk of contracting COVID-19. Meanwhile, although COVID-19 vaccines have been widely delivered worldwide, adopting the typical preventive measures (masks, social distancing, and strict hand hygiene) remains necessary. Therefore, protection is incomplete without better knowledge about the disease, responsible preventive measures, and improved risk perception. Finally, we must orient our attention to the psychological burden of this and future pandemics by encouraging patient–physician communication to mitigate any arising psychological and emotional distress, especially in vulnerable populations. The list of key points is summarized in Table 3 and Figure 6.

5. Conclusions

In conclusion, our findings suggest that a significant proportion of our CVD population had limited knowledge, perception, and practices about COVID-19. Due to the high predisposition of this population to an increased risk of complications due to COVID-19, organizing and prioritizing care for patients with CVD is of paramount importance. Thus, the perspective of CVD patients must be taken into consideration to guide future pandemic responses, and recommendations inferred from the present investigation represent a blueprint for implementing awareness campaigns to establish proper knowledge, perception, and precautionary measures along with psychological and emotional support for this vulnerable population.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/covid5090155/s1. Figure S1. (A) Chart representing the diagnoses of CVD patients by their doctor; (B) Clinical characteristics of patients with CVD. (C) Bar chart representing the medications taken by CVD patients; ACE: Angiotensin Converting Enzyme; BP: Blood Pressure; HTN: Hypertension. CVD: Cardiovascular Disease. Table S1: General Knowledge-Related Questions on COVID-19 and Distribution of Correct/Incorrect Responses Among CVD Patients and Control Participants. Table S2: Bivariate analysis of the general characteristics affecting the scores of COVID-19 knowledge, precaution, specific perception, and anxiety (CAS) as well as general anxiety (GAD-7) and depression (PHQ-9) in CVD patients: p < 0.05 was considered statistically significant. BMI: Body Mass Index; CAS: Coronavirus Anxiety Score, GAD-7: General Anxiety Disorder-7, PHQ-9: Patient Health Questionnaire-9. CVD: Cardiovascular Disease. Table S3: Multivariate analysis with Linear regression analysis of COVID-19 Knowledge, specific Perception, Precaution, and Anxiety scores, as well as GAD-7, and PHQ-9 scores in CVD patients. B: beta; Std. Error: Standard Error; t: t-test. p < 0.05 was considered statistically significant. CAS: Coronavirus Anxiety Score, GAD-7: General Anxiety Disorder-7, PHQ-9: Patient Health Questionnaire-9. CVD: Cardiovascular Disease. Table S4: General Perception-Related Questions on COVID-19 and Distribution of Correct/Incorrect Responses Among CVD Patients and Control Participants. Table S5: General Precaution-Related Questions on COVID-19 and Distribution of Correct/Incorrect Responses Among CVD Patients and Control Participants.

Author Contributions

Conceptualization, W.N., E.C., R.A., N.Y. and M.N.C.; Data curation, M.M., B.F., K.F., J.H., Y.R., P.G., D.C.A., A.Z., J.G.L., L.O., A.H., H.C., M.G., M.S. and M.N.C.; Formal analysis, B.A.; Investigation, M.M., B.F., K.F., J.H., Y.R., P.G., D.C.A., A.Z., J.G.L., L.O., A.H., H.C., M.G. and M.S.; Methodology, M.M., B.F., K.F., J.H., Y.R., P.G., D.C.A., A.Z., J.G.L., L.O., A.H., H.C., M.G., M.S., B.A., W.N., E.C., R.A., N.Y. and M.N.C.; Project administration, M.N.C.; Software, B.F. and B.A.; Supervision, W.N., E.C., R.A., N.Y. and M.N.C.; Validation, B.A.; Visualization, M.M., B.F., K.F. and M.N.C.; Writing—original draft, M.M., B.F., K.F. and J.H.; Writing—review and editing, W.N., E.C., R.A., N.Y. and M.N.C. All authors have read and agreed to the published version of the manuscript.

Funding

There has been no financial support for this work.

Institutional Review Board Statement

An IRB waiver was obtained from the ethical committee of Al-Hayat hospital (number: ETC-13-2020; 23 April 2020). Our survey was conducted in accordance with Good Clinical Practice ICH Section 3 and the principles laid down by the 18th World Medical Assembly (Helsinki, 1964) and all applicable amendments. To ensure anonymity, the survey did not require the names, phone numbers, emails, and exact date of birth (only age was provided) of the participants. All participants were provided with a designated code. Electronic records were safely stored, and access to the sheets was limited to the researchers.

Informed Consent Statement

All participants (18 years of age and older) across Lebanon have signed informed consent and accepted to fill the online survey form by choosing “yes, I agree to participate” or with the help of medical staff.

Data Availability Statement

The questionnaire is available in the Supplementary Materials. The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Acknowledgments

We are grateful for every healthy subject or patient with cardiovascular diseases who participated in our study, and we wish full recovery to all patients worldwide fighting COVID-19. We are mostly grateful for dispensaries who provided us with their list of patients to include in our study, notably Srebta Health Center and Armenian Relief Cross Lebanon Center. We thank the contribution of our undergraduate students from the Lebanese University, at the faculty of Medical Sciences and faculty of Public Health (section II), who assisted the participants to fill out the questionnaire: Aalaa Saleh, Ahmad Issawi, Ahmad El-Lakis, Ali Hamdan, Amira El Khouwayer, Atifa Kamaleddine, Carine Mina, Diana Abou Ltaif, Diana Bashashi, Dima Al Saddik, Dina Essayli, Elissa Abi Fadel, Elissa El Toum, Ennio Charchar, Emmanuel Eid, Fatima Farhat, Gaelle Ghazal, Hadi Meslem, Hadi Shammaa, Hiba El Dinnawi, Jana Ghamraoui, Joelle Kalaji, Joseph Mouawad, Karim Kheir, Maha Trad, Manar Osman, Mariane Bou Zeidan, Michel Boueiz, Mohamad Al Hajjar, Mohammad Kazzaz, Mohamad Naboulsi, Mohammad Srour, Moussa Hojeij, Mustafa Saleh, Nadia Sabbagh, Nicolas Sandakly, Ogarite Kattan, Olga Mcheileh, Omar Al Khatib, Oussama Ouzeir, Rania Makki, Raoul Al Kassis, Rawane Abdul Razzak, Rim Chehab, Rim Araoui, Rimla Abboud, Rita Chebl, Salim Yakdane, Samir Mitri, Sana Tantawi, Sawsane Ghaddar, Solay Farhat, Sondos Naous, Tia El Kazzi, Victoria Chidiac, Wafaa Bzeih, Walaa Meouch, Yara Tarhini, Yousra Antar, Yves Ghattas Damoun, Zainab Hammoud, and Zeina Ajram.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
ACE2Angiotensin-Converting Enzyme 2
ARBAngiotensin Receptor Blocker
BMIBody Mass Index
CASCoronavirus Anxiety Scale
CGControl Group
COVID-19Coronavirus Disease 2019
CVDCardiovascular Diseases
GAD-7Generalized Anxiety Disorder questionnaire
PHQ-9Patient Health Questionnaire
WHO World Health Organization

Appendix A

Questionnaire
Section 1—General Questions
A—General Characteristics of all participants
  1.
Age: ________
  2.
Gender:
Female
Male
  3.
Marital status:
Single
Married
Divorced
Widowed
  4.
Weight (kg): _______
  5.
Height(cm): _______
  6.
Nationality:
Lebanese
Other: ________________
  7.
Region of Residence:
Akkar
Baalbek-Hermel
Bekaa
Kesserouan-Ftouh-Jbeil
Mount Lebanon
South Lebanon
North Lebanon
Beirut
  8.
Do you live in a village or a city?
Village
City
  9.
Personal Monthly income (in LBP):
0–750,000LL
751,000–1,500,000LL
1,501,000–3,000,000LL
3,001,000–4,500,000LL
More than 4,500,000LL
  10.
Number of rooms in the house (excluding the kitchen and the bathroom):
1 room
2 rooms
3 rooms
4 rooms
5 rooms
6 rooms
7 rooms
8 rooms
9 rooms
10 rooms
Other: ________________
  11.
How many people live in the house?
1 person
2 persons
3 persons
4 persons
5 persons
6 persons
7 persons
8 persons
9 persons
10 persons
Other: ________________
  12.
Which school/university level did you complete?
I did not attend school
Elementary school
Middle school
Secondary school
Bachelor Degree
Master’s degree
PhD or MD diploma
  13.
Employment Status:
Housewife
Unemployed
Employed
  14.
Are you a healthcare provider (nurse, physician, pharmacist…)?
Yes
No
  15.
Since the beginning of the outbreak, were you working outside your home?
Yes
No
I am unemployed
  16.
Since the beginning of the outbreak, were you responsible for buying grocery supplies and household supplements?
Yes
No
  17.
Smoking status
Current or previous smoker
Never smoker
  18.
If ever smoker:
How many cigarettes per day do you smoke or used to smoke?
1–5
6–20
>20
I don’t smoke cigarettes
How many years have you smoked cigarettes for? ___________________
How many years have been since you quit smoking cigarettes?
<1 year
>1 year
I don’t smoke cigarettes
I still smoke cigarettes
Since the beginning of the outbreak in Lebanon did your cigarette consumption increase?
Yes
No
I don’t smoke cigarettes
  19.
If former, or current water pipe smoker:
How many water pipe sessions per day do you smoke or used to smoke?
1 session/day
>1 session/day
I don’t smoke water pipe
How many water pipe sessions per week do you smoke or used to smoke?
1–5 sessions/week
>5 sessions/week
I don’t smoke water pipe
Since the beginning of the outbreak in Lebanon, did your water pipe consumption increase?
Yes
No
I don’t smoke waterpipe
  20.
Alcohol status (drinks per day)
No alcohol consumption
1–3 drinks a day
4 drinks and more a day
  21.
Alcohol status (drinks per week)
No alcohol consumption
1–7 drinks per week
8–13 drinks per week
≥ 14 drinks per week
  ●
Since the beginning of the outbreak in Lebanon, did your alcohol consumption increase?
Yes
No
I don’t drink alcohol
  22.
Have you been tested for COVID-19 since the beginning of the outbreak in Lebanon?
No
Yes, the test result was negative
Yes, the test result was positive
Other: _________________________________
  23.
If you responded YES to Question 22, why did you seek testing for COVID-19?
Symptoms
Exposure (recent travel, contact with a confirmed case, high risk environment)
Recommended by a health professional
I haven’t been tested
  24.
If you responded Yes to Question 22, did you receive any medications? (if YES, please specify the medication in option “Other”)
Yes
No
the test result was negative
I haven’t been tested
Other: _________________________________
  25.
How would you rate your knowledge level on novel coronavirus?
Very poor
Poor
Average
Good
Very Good
B—General Knowledge about COVID-19
The following are questions about your knowledge level on novel coronavirus. Please select the answer of your choice.
  26.
Which of the following is/are correct about the definition of novel coronavirus?
COVID-19 is a viral respiratory disease caused by the novel coronavirus.
Symptoms include: fever, shortness of breath, nausea, diarrhea, dry cough, sore throat.
Usual symptoms include respiratory symptoms accompanied by fever, but infection by the novel coronavirus is not contagious.
Infection by the novel coronavirus can progress to a severe illness but never leads to death.
The novel coronavirus can cause heart diseases in healthy people
I don’t know
  27.
What are the emergency warning signs during the COVID-19 outbreak?
Severe shortness of breath and chest pain
Abdominal distention and severe headache
Syncope and greenish sputum
I don’t know
  28.
Which of the following is correct about the transmission route of the novel coronavirus?
This disease can be transmitted through respiratory droplets of an infected person released by sneezing or coughing, that land on the eyes, nose, or mouth of a nearby person or touching contaminated surfaces then touching the face
Novel coronavirus is not transmitted by close contact with people.
Sharing water pipe is not a mean of transmission for the novel coronavirus
Novel coronavirus is frequently transmitted by pets and domestic animals and humans
I don’t know
  29.
Which of the following is true about the transmission of the new Coronavirus?
The virus needs an incubation period of at least five weeks for symptoms to appear.
It takes in general a few days to two weeks for the virus symptoms to start showing.
I don’t know
  30.
May completely asymptomatic patients carrying the new coronavirus transmit it?
Yes
No
I don’t know
  31.
Physical distancing for COVID 19 is maintaining at least a distance of ------- between you and the other person.
0.5 meter
2 meters
4 meters
I don’t know
  32.
Which statement is correct about the treatment or vaccine for the novel coronavirus?
Currently, there is a treatment for novel coronavirus, but there is no vaccine
Currently, there is neither a treatment nor a vaccine
Currently, there is no treatment, but there is a vaccine
I don’t know
  33.
Regarding elderly people, which of the following statements is correct?
Persons with no symptoms can safely visit their elderly
COVID 19 is a disease of all ages not only elderly
I don’t know
  34.
Are COVID-19 complications more severe in older patients
Yes
No
I don’t know
  35.
Does mortality from COVID-19 increase with age?
Yes
No
I don’t know
  36.
In case you are having fever, cough or any respiratory symptom, you should cancel all your appointments (with everyone), refrain from grocery shopping.
True
False
I don’t know
  37.
The mortality rate from COVID19 in Lebanon is above 8%
Yes
No
I don’t know
  38.
If I get COVID-19, I should never take the anti-malarial agent, chloroquine if it is not prescribed by my doctor and administered in the hospital settings.
True
False
I don’t know
C—Perception of COVID 19
  39.
Even if I get sick from another disease, I will not go to the hospital because of risk of getting the novel coronavirus in the hospital
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  40.
I am afraid that people will label me COVID-19 victim if I get the disease
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  41.
I am afraid people will avoid me if I get the COVID-19 disease, for a long period after recovery
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  42.
I am worried about having no access to my usual prescribed medications during the lockdown so I think I should stock at least 30-days supply of my medication because there might be a shortage.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  43.
During the outbreak, I should not stop my usual prescribed medications.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  44.
I think that I am at a great risk of exposure to corona virus in public transportation.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  45.
I believe that COVID-19 outbreak is a very serious threat to public health.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  46.
I am worried that one of my family or household members will get the coronavirus.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  47.
I am worried that I may transmit the coronavirus to my family if I am going frequently to the hospital.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
  48.
During the outbreak, drugs, alcohol or cigarettes may help reduce my stress.
Strongly Disagree
Disagree
Neutral
Agree
Strongly Agree
D—Prevention from COVID-19
  49.
Since the beginning of the outbreak in Lebanon, what were the recommended preventive measures against COVID-19 infection?
  • Avoiding contact with sick people.
    Yes
    No
  • Washing hands frequently no less than 20 s.
    Yes
    No
  • Using disinfectants for household cleaning.
    Yes
    No
  • Avoiding touching my eyes, nose, and mouth with unwashed hands.
    Yes
    No
  • Taking a herbal supplement.
    Yes
    No
  • Eating healthy food and having a balanced diet
    Yes
    No
  • Using social media to stay connected with my surroundings instead of usual visits.
    Yes
    No
  • Staying busy with tasks (making a list of things you can do).
    Yes
    No
  • Recreational activity (listening to music, reading a book, crosswords, painting, drawing, etc).
    Yes
    No
  • Breathing exercise (for relaxation).
    Yes
    No
  • Getting enough rest and sleep.
    Yes
    No
  • Exercising regularly.
    Yes
    No
  • Avoiding eating raw or undercooked meat.
    Yes
    No
  • Avoiding eating outdoors and getting delivery food.
    Yes
    No
  • Avoiding crowded places.
    Yes
    No
  • Practicing physical distancing at work and when out buying food.
    Yes
    No
  • Caution when touching money.
    Yes
    No
  • Wearing a mask outside home (in a closed location or in a crowd or at the hospital).
    Yes
    No
  • Home quarantine.
    Yes
    No
  • Covering the face with a tissue when sneezing or coughing.
    Yes
    No
  • Regularly cleaning often touched surfaces like doorknobs, handles, steering wheels, or light switches, with a disinfectant.
    Yes
    No
  50.
Since the beginning of the outbreak in Lebanon, have you been using “handsfree” greeting?
Yes
No
  51.
Have you been vaccinated against the flu virus in the last 10 months?
Yes
No
  52.
Would you rely on your doctor to correct any misinformation about COVID-19?
Yes
No
  53.
If the frequency of your visits at your doctor’s office needs to be decreased during the outbreak, can you handle calls or video calls visits with your doctor for non-urgent situations and necessary follow-up?
Yes
No
  54.
Do you have an emergency contact list that includes family, friends, neighbors, and community or neighborhood resources who may be able to provide help in case of emergency?
Yes
No
E—Anxiety and depression level during COVID-19 outbreak
E1/Coronavirus Anxiety (5 Questions):
How often have you experienced the following since the beginning of the outbreak in Lebanon?
  55.
I felt dizzy, lightheaded, or fainting, when I read or listened to news about the coronavirus.
Not at all
Rare, less than a day or two
Several days
More than 7 days
Nearly every day over the last 4 weeks
  56.
I had trouble falling or staying asleep because I was thinking about the coronavirus.
Not at all
Rare, less than a day or two
Several days
More than 7 days
Nearly every day over the last 4 weeks
  57.
I felt paralyzed or frozen when I thought about or was exposed to information about the coronavirus.
Not at all
Rare, less than a day or two
Several days
More than 7 days
Nearly every day over the last 4 weeks
  58.
I lost interest in eating when I thought about or was exposed to information about the coronavirus.
Not at all
Rare, less than a day or two
Several days
More than 7 days
Nearly every day over the last 4 weeks
  59.
I felt nauseous or had stomach problems when I thought about or was exposed to information about the coronavirus.
Not at all
Rare, less than a day or two
Several days
More than 7 days
Nearly every day over the last 4 weeks
E2/Anxiety Questionnaire (7 Questions): (GAD-7)
What best describes you since the beginning of the outbreak in Lebanon?
  60.
I am feeling nervous, anxious, or on edge.
Not at all
Several days
More than half the days
Nearly every day
  61.
I am not being able to stop or control worrying.
Not at all
Several days
More than half the days
Nearly every day
  62.
I am worrying too much about different things.
Not at all
Several days
More than half the days
Nearly every day
  63.
I have trouble relaxing.
Not at all
Several days
More than half the days
Nearly every day
  64.
I am being so restless that it’s hard to sit still.
Not at all
Several days
More than half the days
Nearly every day
  65.
I am becoming easily annoyed or irritable.
Not at all
Several days
More than half the days
Nearly every day
  66.
I am feeling afraid as if something awful might happen.
Not at all
Several days
More than half the days
Nearly every day
E3/Depression Questionnaire (PHQ-9)
Since the beginning of the outbreak in Lebanon, how often have you been bothered by the following?
  67.
Little interest or pleasure in doing things.
Not at all
Several days
More than half the days
Nearly every day
  68.
Feeling down, depressed, or hopeless.
Not at all
Several days
More than half the days
Nearly every day
  69.
Trouble falling/staying asleep, sleeping too much.
Not at all
Several days
More than half the days
Nearly every day
  70.
Feeling tired or having little energy.
Not at all
Several days
More than half the days
Nearly every day
  71.
Poor appetite or overeating.
Not at all
Several days
More than half the days
Nearly every day
  72.
Feeling bad about yourself or that you are a failure or have let yourself or your family down.
Not at all
Several days
More than half the days
Nearly everyday
  73.
Trouble concentrating on things, such as reading the newspaper or watching television.
Not at all
Several days
More than half the days
Nearly every day
  74.
Moving or speaking so slowly that other people could have noticed. Or the opposite; being so fidgety or restless that you have been moving around a lot more than usual.
Not at all
Several days
More than half the days
Nearly every day
  75.
Thoughts that you would be better off dead or of hurting yourself in some way.
Not at all
Several days
More than half the days
Nearly every day
  76.
If you checked off any problem on this previous questionnaire about depression so far, how difficult have these problems made it for you to do your work, take care of things at home, or get along with other people?
Extremely difficult
Very difficult
Somewhat difficult
Not difficult at all
  77.
Are you or were you ever diagnosed BY YOUR DOCTOR with one of these cardiovascular diseases (CVD): problems with heart, vessels, blood coagulation, high blood pressure?
Yes
No
If you answered “Yes”, please proceed to section 2.
If you answered “No”, please proceed to section 3.
Section 2—Cardiovascular Diseases Questions
1. 
A/General Characteristics of Cardiovascular Disease Patients
  • What is (are) the diagnosis (diagnoses) of your cardiovascular disease(s) (CVD)?
    Cerebrovascular disease; ex: Stroke
    Hypertension
    Coronary Artery disease
    Left ventricular hypertrophy
    Heart failure
    Heart rhythm problems
    Thromboembolic disease (coagulation problem)
    None of the above
     
    If you have a cerebrovascular disease (ex: Stroke), how long have you been diagnosed for? (add number of years) ________________
    If you have hypertension, how long have you been diagnosed for? (Add number of years) ________________
    If you have coronary artery disease, how long have you been diagnosed for? (Add number of years) ________________
    If you have left ventricular hypertrophy, how long have you been diagnosed for? (Add number of years) ________________
    If you have congestive heart failure, how long have you been diagnosed for? (Add number of years) ________________
    If you have cardiac arrhythmia, how long have you been diagnosed for? (Add the number of years) ________________
    If you have thromboembolic disease, how long have you been diagnosed for? (Add the number of years) ________________
     
For questions 2 and 3, please write your blood pressure which equals SBP/DBP.
  2.
Value of your Systolic Blood pressure SBP (what is known as the highest value) (Today’s value in mmHg) ________________
  3.
Value of your Diastolic Blood pressure DBP (what is known as the lowest value) (Today’s value in mmHg) ________________
  4.
What is your heart rate? (in beats per minute) ________________
  5.
What is the average value of your Glycemia in mg/dL?
<80
80–100
101–120
121–200
201–250
>250
I don’t know
  6.
What is the value of your HbA1C in %?
<6.5%
6.5–8%
>8%
I don’t know
  7.
What is the value of your total cholesterol (in mg/dL)?
<200
200–239
>240
I don’t know
  8.
What is the value of your HDL cholesterol (in mg/dL)?
<40
41–59
>60
I don’t know
  9.
What is the value of your LDL cholesterol (in mg/dL)?
<100
100–129
130–159
160–189
>190
I don’t know
  10.
What is the value of your total triglycerides (in mg/dL)?
<150
150–199
200–499
>500
I don’t Know
  11.
What is the average value of your creatinine (in mg/dL)?
<0.84
0.84–1.21
>1.21
I don’t know
  12.
What is the value of microalbuminuria (in mg/24h)?
<30
30–300
>300
I don’t know
  13.
Do you have protein in the urine?
Yes
No
I don’t know
  14.
Do you have blood in the urine?
Yes
No
I don’t know
  15.
Did you use non-pharmacological treatments:
Diet weight loss
Yes
No
Diet- fruits- vegetable intake
Yes
No
Salt restriction
Yes
No
Alcohol restriction
Yes
No
Physical activity
Yes
No
  16.
Do you receive an anti-diabetic treatment?
No, I am not diabetic
No, I don’t receive an anti-diabetic treatment
Yes
    
If you answered “Yes”, please specify the name: ________________
  17.
Do you receive an anti-hypertensive treatment?
No, I am not hypertensive
No, I don’t receive an anti-hypertensive treatment
Yes
    
If you answered “Yes”, please specify the name: ________________
  18.
Do you receive other cardiovascular drugs?
No, I don’t have cardiovascular disease
No, I don’t receive cardiovascular drugs
Yes, Aspirin
Yes, Anticoagulant (e.g., Sintrom)
Yes, antiplatelet (e.g., Plavix)
    
If you answered “Yes”, please specify the name: ________________
  19.
Do you receive a lipid lowering treatment to decrease high cholesterol and/or triglycerides levels?
No, I don’t have high cholesterol or triglycerides
Yes
    
If you answered “Yes”, please specify the name: ________________
  20.
Do you receive any medications that decrease your immune system (steroids, cyclosporine, mycophenolate mofetil, cyclophosphamide, tacrolimus, rapamycin)?
No
Yes
I don’t know
    
If you answered “Yes”, please specify the name: ________________
  2.
B/Knowledge of COVID-19 in Cardiovascular Disease patients
  21.
How can the novel coronavirus affect my heart?
The virus causes direct damage to the lungs, which decreases the blood oxygen levels, so this pushes my heart to beat faster and harder to supply oxygen to major organs
The virus causes inflammation, which decreases the blood pressure, so this pushes my heart to beat faster and harder to supply oxygen to major organs
COVID-19 leads to rupture of atherosclerotic plaques (fatty deposits) in the coronary arteries, leading to a heart attack
I don’t know
  22.
Patients with Cardiovascular diseases have a more severe risk of symptoms from COVID-19 than others.
True
False
I don’t know
  23.
Patients who have both heart disease AND have a decrease in their immunity (ex: transplant patients, patients with cancer) are particularly at greatest risk of contracting and surrendering to the effects of the virus.
True
False
I don’t know
  24.
Elderly people or pregnant women who ALSO have heart diseases are particularly at greatest risk of contracting and surrendering to the effects of the virus.
True
False
I don’t know
  25.
Patients with the severe form of cardiac enlargement of the heart (hypertrophy) are particularly at greatest risk of contracting and surrendering to the effects of the virus.
True
False
I don’t know
 
  26.
High fever (beyond 39 °C) is extremely dangerous in patients having an abnormal electrical activity within the heart leading to fatal abnormal rhythm (arrhythmias).
True
False
I don’t know
  27.
COVID-19 complications are more severe in hypertension patients.
True
False
I don’t know
  28.
Mortality from COVID-19 is higher among hypertension patients.
True
False
I don’t know
  29.
COVID-19 complications are more severe in heart failure patients.
True
False
I don’t know
  30.
Mortality from COVID-19 is higher among heart failure patients.
True
False
I don’t know
  31.
Coronary artery disease patients are at increased risk due to COVID-19.
True
False
I don’t know
  32.
COVID-19 can cause blood clotting (coagulation) problems.
True
False
I don’t know
  33.
COVID-19 patients present a higher mortality rate due to a higher prevalence of clots (at the level of their legs and their lungs).
True
False
I don’t know
  34.
The novel coronavirus increases death among patients with both hypertension & diabetes.
True
False
I don’t know
C/Perception of COVID-19 in Cardiovascular Disease patients
Please select the answer depending on how much you agree with the statements below.
    35.
I am a patient with heart disease. In case I have a COVID-19 infection and a fever. I believe I can manage the symptoms at home. Fever can be treated with panadol.
Strongly disagree
Disagree
Neutral
Agree
Strongly agree
I don’t know
    36.
I am a patient with heart disease. In case I have a COVID-19 infection, a fever, and I feel shortness of breath. I don’t believe I can manage the symptoms at home, I should ask for medical help.
Strongly disagree
Disagree
Neutral
Agree
Strongly agree
I don’t know
D/Preventions from COVID-19 in Cardiovascular Diseases patients
     37.
I am adhering to the treatment recommended by my cardiologist.
Yes
No
     38.
My physician modified my hypertension drug because of the ongoing COVID-19 outbreak.
Yes
No
I don’t have hypertension
     39.
A patient with hypertension should adhere to their treatment (so-called ACEI nhibitors (ACEI) and Angiotensin Receptor Blockers (ARB) even if it was not proven, that it may increase both his risk of infection and the severity of infection with the coronavirus.
Yes
No
     40.
If I get the novel coronavirus infection, and I suffer from irregular heartbeats (Long QT syndrome), I should never take Hydroxychloroquine (an antimalarial agent) alone OR Azithromycin (an antibiotic agent) alone OR the combination of Hydroxychloroquine + Azithromycin as it might cause more arrhythmias, life-threatening high heart rate, and sudden death.
Yes
No
     41.
If I have blood clotting problems (due to a decrease in platelet levels) and I get COVID-19, I should stop my blood thinning medications (anticoagulants and antiplatelet drugs).
Yes
No
     42.
I am following the recommendations to self-test using blood pressure machines at home for better blood pressure control since the beginning of the outbreak in Lebanon.
Yes
No
Section 1—Continued: Other Chronic diseases
  78.
Are you or were you ever diagnosed BY YOUR PSYCHIATRIST with any anxiety OR depression?
Yes
No
  79.
Are you or were you ever diagnosed BY YOUR DOCTOR with Lung Diseases (Chronic obstructive pulmonary disease (COPD), asthma, lung fibrosis, sleep apnea or other diseases)?
Yes
No
  80.
Are you or were you ever diagnosed BY YOUR DOCTOR with metabolic diseases (diabetes, high cholesterol or triglycerides level) obesity?
Yes
No
  81.
Are you or were you ever diagnosed BY YOUR DOCTOR with chronic kidney disease?
Yes
No
  82.
Are you OR were you ever diagnosed with any type of cancer BY YOUR DOCTOR?
Yes
No
  83.
Are you or were you ever diagnosed by any musculoskeletal disease (osteoporosis, osteoarthritis, gout, rheumatoid arthritis or other diseases)?
Yes
No
  84.
In addition to all chronic diseases listed previously, do you have any of the following chronic diseases?
HIV
Any blood disorder (coagulation, anemia, etc.)
Thyroid disorders
None of the above
Other: ___________
  85.
Name all the MEDICATIONS taken regularly that were NOT LISTED IN THE PREVIOUS SECTIONS.

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Figure 1. (A) CVD patients’ and control subjects’ average scores of COVID-19 knowledge, precaution, and anxiety (CAS), as well as scores of GAD-7 and PHQ-9, according to the Mann–Whitney test, in comparison with control subjects. CAS: Coronavirus Anxiety Score; GAD-7: Generalized Anxiety Disorder-7; PHQ-9: Patient Health Questionnaire-9. CVD: cardiovascular disease. *** p < 0.001 with p < 0.05 was considered significant. (B) Percentage (%) of CVD patients versus control subjects with COVID-19 knowledge scores categorized into Poor (≤10 /14 so ≤71.4%), Fair (11/14 = 78.5% and 12/14 = 85.7%), Good (13/14 = 92.8%), and Excellent (14/14 = 100%). Almost half of the CVD patients (45.7% regrouping, 14.4% with Poor, and 31.3% with Fair knowledge scores) versus a third of CG subjects (31.8% regrouping, 6.8% with Poor, and 25.0% with Fair knowledge scores) had a “Limited” knowledge level about COVID-19. The remaining subjects (CVD: 54.4% vs. CG: 68.2%) had an ‘’Adequate” knowledge level about COVID-19 (Good and Excellent knowledge scores). (C) Percentage (%) of CVD patients versus control subjects with COVID-19 precaution scores categorized into Poor (≤19/26 so ≤73.0%), Fair (between 20/26 = 76.9% and 23/26= 84.4%), Good (between 24/26 = 92.3% and 25/26 = 96.1%), and Excellent (26/26 = 100%). Almost three-fourths of the CVD patients (70.3% regrouping, 24.9% with Poor, and 45.4% with Fair precaution scores) versus half of CG subjects (54.2% regrouping, 14.3% with Poor, and 39.9% with Fair precaution scores) had a “Limited” precaution level about COVID-19. The remaining subjects (CVD: 29.7% vs. CG: 45.8%) had an ‘’Adequate” precaution level about COVID-19 (Good and Excellent precaution scores). Categories of “Poor” and “Fair” scores = “Limited knowledge” or “Limited precautions” about COVID-19; categories of “Good” and “Excellent” scores = “Adequate knowledge” or “Adequate precautions” about COVID-19.
Figure 1. (A) CVD patients’ and control subjects’ average scores of COVID-19 knowledge, precaution, and anxiety (CAS), as well as scores of GAD-7 and PHQ-9, according to the Mann–Whitney test, in comparison with control subjects. CAS: Coronavirus Anxiety Score; GAD-7: Generalized Anxiety Disorder-7; PHQ-9: Patient Health Questionnaire-9. CVD: cardiovascular disease. *** p < 0.001 with p < 0.05 was considered significant. (B) Percentage (%) of CVD patients versus control subjects with COVID-19 knowledge scores categorized into Poor (≤10 /14 so ≤71.4%), Fair (11/14 = 78.5% and 12/14 = 85.7%), Good (13/14 = 92.8%), and Excellent (14/14 = 100%). Almost half of the CVD patients (45.7% regrouping, 14.4% with Poor, and 31.3% with Fair knowledge scores) versus a third of CG subjects (31.8% regrouping, 6.8% with Poor, and 25.0% with Fair knowledge scores) had a “Limited” knowledge level about COVID-19. The remaining subjects (CVD: 54.4% vs. CG: 68.2%) had an ‘’Adequate” knowledge level about COVID-19 (Good and Excellent knowledge scores). (C) Percentage (%) of CVD patients versus control subjects with COVID-19 precaution scores categorized into Poor (≤19/26 so ≤73.0%), Fair (between 20/26 = 76.9% and 23/26= 84.4%), Good (between 24/26 = 92.3% and 25/26 = 96.1%), and Excellent (26/26 = 100%). Almost three-fourths of the CVD patients (70.3% regrouping, 24.9% with Poor, and 45.4% with Fair precaution scores) versus half of CG subjects (54.2% regrouping, 14.3% with Poor, and 39.9% with Fair precaution scores) had a “Limited” precaution level about COVID-19. The remaining subjects (CVD: 29.7% vs. CG: 45.8%) had an ‘’Adequate” precaution level about COVID-19 (Good and Excellent precaution scores). Categories of “Poor” and “Fair” scores = “Limited knowledge” or “Limited precautions” about COVID-19; categories of “Good” and “Excellent” scores = “Adequate knowledge” or “Adequate precautions” about COVID-19.
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Figure 2. Distribution of (A) answers related to knowledge, (B) correct answers related to risk perception (Blue: Control; Red: CVD), and (C) answers related to precautionary measures concerning COVID-19 in patients with CVD versus CG subjects. The full set of knowledge/perception/precaution questions and response distributions are provided in the Supplementary Materials, Tables S1, S4, and S5, respectively. The chi square test was performed with p < 0.05 is statistically significant. CG: control group. CVD: cardiovascular disease.
Figure 2. Distribution of (A) answers related to knowledge, (B) correct answers related to risk perception (Blue: Control; Red: CVD), and (C) answers related to precautionary measures concerning COVID-19 in patients with CVD versus CG subjects. The full set of knowledge/perception/precaution questions and response distributions are provided in the Supplementary Materials, Tables S1, S4, and S5, respectively. The chi square test was performed with p < 0.05 is statistically significant. CG: control group. CVD: cardiovascular disease.
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Figure 3. Frequency (%) of correct answers to specific knowledge questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
Figure 3. Frequency (%) of correct answers to specific knowledge questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
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Figure 4. Frequency (%) of correct answers to specific precautionary measures questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
Figure 4. Frequency (%) of correct answers to specific precautionary measures questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
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Figure 5. Frequency (%) of answers to specific perception questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
Figure 5. Frequency (%) of answers to specific perception questions concerning COVID-19 in CVD patients. CVD: cardiovascular disease.
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Figure 6. Major factors affecting COVID-19 level of awareness among patients with CVD (knowledge, precaution, COVID-19 anxiety, GAD-7 (anxiety), and PHQ-9 (depression) scores). CVD: cardiovascular disease; GAD-7: Generalized Anxiety Disorder-7; PHQ-9: Patient Health Questionnaire-9. An upward-pointing arrow indicates an increase.
Figure 6. Major factors affecting COVID-19 level of awareness among patients with CVD (knowledge, precaution, COVID-19 anxiety, GAD-7 (anxiety), and PHQ-9 (depression) scores). CVD: cardiovascular disease; GAD-7: Generalized Anxiety Disorder-7; PHQ-9: Patient Health Questionnaire-9. An upward-pointing arrow indicates an increase.
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Table 1. Grading of knowledge and precautions scores about COVID-19 into categories “Limited and Adequate” and sub-categories “Poor, Fair, Good, and Excellent”.
Table 1. Grading of knowledge and precautions scores about COVID-19 into categories “Limited and Adequate” and sub-categories “Poor, Fair, Good, and Excellent”.
CategoriesSub-CategoriesKnowledgePrecautions
/14%/26%
LimitedPoor≤10≤71.40≤19≤73.00
Fair[11,12][78.50–85.70][20,21,22,23][76.90–84.40]
AdequateGood13 92.8[24,25][92.30–96.10]
Excellent1410026100
Table 2. Demographic characteristics of the control group and CVD patients. n: number of participants; p < 0.05 was considered statistically significant. BMI: body mass index; overweight (BMI: 25–29.9 Kg/m2); obesity C1 (BMI: 30–34.9 Kg/m2); obesity C2 (BMI ≥ 35 Kg/m2); CVD: cardiovascular disease. * represents statistical significance.
Table 2. Demographic characteristics of the control group and CVD patients. n: number of participants; p < 0.05 was considered statistically significant. BMI: body mass index; overweight (BMI: 25–29.9 Kg/m2); obesity C1 (BMI: 30–34.9 Kg/m2); obesity C2 (BMI ≥ 35 Kg/m2); CVD: cardiovascular disease. * represents statistical significance.
VariableControl (%)CVD (%)p-Value
Age in years30.16 ± 13.40859.10 ± 15.634<0.001 *
BMI in Kg/m224.57 ± 4.7228.5 ± 6.06<0.001 *
GenderMale354 (34.3%)231 (47.6%)<0.001 *
Female679 (65.7%)254 (52.4%)
Marital StatusSingle723 (70.0%)51 (10.5%)<0.001 *
Married295 (28.6%)362 (74.6%)
Divorced6 (0.6%)58 (12.0%)
Widowed9 (0.9%)14 (2.9%)
ObesityNormal Weight609 (59.0%)123 (25.4%)<0.001 *
Overweight298 (28.8%)204 (42.1%)
Obesity C194 (9.1%)101 (20.8%)
Obesity C232 (3.1%)57 (11.8%)
Region of ResidenceNorth Lebanon150 (14.5%)68 (14.0%)0.005 *
Bekaa132 (12.8%)86 (17.7%)
Mount Lebanon476 (46.1%)182 (37.5%)
South Lebanon117 (11.3%)73 (15.1%)
Beirut158 (15.3%)76 (15.7%)
Socioeconomic StatusLow413 (40.0%)246 (50.7%)<0.001 *
Moderate215 (20.8%)103 (21.2%)
High405 (39.2%)136 (28.1%)
Educational LevelDid not attend school0 (0.0%)45 (9.3%)<0.001 *
Elementary school13 (1.3%)86 (17.7%)
Middle school42 (4.1%)102 (21.0%)
Secondary school191 (18.5%)104 (21.4%)
Bachelor in science432 (41.8%)91 (18.8%)
Master’s degree203 (19.6%)27 (5.6%)
PhD or MD diploma152 (14.7%)30 (6.2%)
Employment StatusHousewife81 (7.8%)174 (35.9%)<0.001 *
Unemployed485 (47.0%)136 (28.0%)
Employed467 (45.2%)175 (36.1%)
Healthcare provider (nurse–physician–pharmacist)Yes350 (33.9%)30 (6.2%)<0.001 *
No683 (66.1%)455 (93.8%)
Since the beginning of the outbreak, were you working outside your home?Yes268 (25.9%)83 (17.1%)<0.001 *
No332 (32.1%)155 (32.0%)
Unemployed433 (41.9%)247 (50.9%)
Since the beginning of the outbreak, were you responsible for buying grocery supplies and household supplements?Yes458 (44.3%)273 (56.3%)<0.001 *
No575 (55.7%)212 (43.7%)
Personal assessment of knowledgeVery good243 (23.5%)64 (13.2%)<0.001 *
Good491 (47.5%)189 (39.0%)
Average268 (25.9%)178 (36.7%)
Poor25 (2.4%)37 (7.6%)
Very poor6 (0.6%)17 (3.5%)
Smoking statusEver smoked164 (15.9%)208 (42.9%)<0.001 *
Never smoked869 (84.1%)277 (57.1%)
Increased cigarette consumption since the beginning of the outbreak in LebanonYes49 (4.7%)45 (9.3%)<0.001 *
No83 (3.0%)92 (19.0%)
I don’t smoke cigarettes901 (87.2%)348 (71.8%)
Increased water-pipe consumption since the beginning of the outbreak in LebanonYes43 (4.2%)29 (6.0%)0.005 *
No77 (7.5%)6 (1.2%)
I don’t smoke waterpipe913 (88.4%)450 (92.8%)
Alcohol consumption (drinks per day)4 drinks and more a day2 (0.2%)4 (0.8%)<0.001 *
1–3 drinks a day177 (17.1%)51 (10.5%)
No alcohol consumption854 (82.7%)430 (88.7%)
Increased alcohol consumption since the beginning of the outbreak in LebanonYes27 (2.6%)7 (1.4%)0.004 *
No152 (14.7%)45 (9.3%)
I don’t drink alcohol854 (82.7%)433 (89.3%)
Table 3. Caring for patients with CVD during COVID-19 pandemic.
Table 3. Caring for patients with CVD during COVID-19 pandemic.
Caring for Patients with CVD
During COVID-19 Pandemic
1.
In patients with COVID-19, CVD increases the risk of severe complications.
2.
COVID-19 can cause blood clotting problems.
3.
Mortality from COVID-19 is higher among hypertension and heart failure patients.
4.
Patients with CVD should adhere to their medications.
5.
Elderly and pregnant CVD patients are at increased risk of severe COVID-19 symptoms.
6.
Fever in CVD patients who contract a COVID-19 infection can be managed at home.
7.
Patients with CVD who contract a COVID-19 infection and feel shortness of breath should ask for medical help.
8.
CVD patients should be encouraged to self-test their blood pressure at home for better control during the lockdown.
9.
Patients with blood clotting problems who contract COVID-19 must not discontinue their medications.
10.
CVD patients should be encouraged to stay active and exercise regularly during lockdown.
11.
CVD patients should be offered psychological support during the outbreak, especially in rural areas.
12.
The groups most affected by the economic sequelae of COVID-19 should be sustained.
13.
Approaches should be implemented that engage patients and physicians to effectively appeal and reverse denials in CVD patients
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Machaalani, M.; Fakhry, B.; Farhat, K.; Haddad, J.; Rahmeh, Y.; Ghiya, P.; Awad, D.C.; Zaiter, A.; Louka, J.G.; Olaywan, L.; et al. Perspectives on Knowledge, Precautionary Behaviors, and Psychological Status of Patients with Cardiovascular Diseases During the First Wave of the COVID-19 Pandemic in Lebanon: A Multicentric Cross-Sectional Study. COVID 2025, 5, 155. https://doi.org/10.3390/covid5090155

AMA Style

Machaalani M, Fakhry B, Farhat K, Haddad J, Rahmeh Y, Ghiya P, Awad DC, Zaiter A, Louka JG, Olaywan L, et al. Perspectives on Knowledge, Precautionary Behaviors, and Psychological Status of Patients with Cardiovascular Diseases During the First Wave of the COVID-19 Pandemic in Lebanon: A Multicentric Cross-Sectional Study. COVID. 2025; 5(9):155. https://doi.org/10.3390/covid5090155

Chicago/Turabian Style

Machaalani, Marc, Battoul Fakhry, Kassem Farhat, Juliano Haddad, Youssef Rahmeh, Peter Ghiya, Diana Carolina Awad, Aline Zaiter, Jean G. Louka, Layal Olaywan, and et al. 2025. "Perspectives on Knowledge, Precautionary Behaviors, and Psychological Status of Patients with Cardiovascular Diseases During the First Wave of the COVID-19 Pandemic in Lebanon: A Multicentric Cross-Sectional Study" COVID 5, no. 9: 155. https://doi.org/10.3390/covid5090155

APA Style

Machaalani, M., Fakhry, B., Farhat, K., Haddad, J., Rahmeh, Y., Ghiya, P., Awad, D. C., Zaiter, A., Louka, J. G., Olaywan, L., Halawi, A., Cherry, H., Ghazal, M., Sahili, M., Atallah, B., Naja, W., Chammas, E., Asmar, R., Yared, N., & Chahine, M. N. (2025). Perspectives on Knowledge, Precautionary Behaviors, and Psychological Status of Patients with Cardiovascular Diseases During the First Wave of the COVID-19 Pandemic in Lebanon: A Multicentric Cross-Sectional Study. COVID, 5(9), 155. https://doi.org/10.3390/covid5090155

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