Keywords
Depression, Hypertension, Diabetes Mellitus, Chronic Obstructive, Renal Insufficiency, Chronic, Heart Diseases, Nepal
Depression, Hypertension, Diabetes Mellitus, Chronic Obstructive, Renal Insufficiency, Chronic, Heart Diseases, Nepal
Depression is a major evolving health problem imposing a significant disease burden globally and is one of the leading causes of morbidity and mortality worldwide across all age groups. In addition, it is one of the important risk factors for increasing the incidence of suicides, drug abuse, and social and educational dysfunctions.1 Furthermore, depression is more common in women, more so over in younger age groups, in people with low socioeconomic backgrounds, and people who spend their life alone.2
With lifestyle modifications, the prevalence of chronic physical illnesses has been sharply rising, which causes an increase in depression in these patients. People with chronic physical illnesses like diabetes, hypertension, chronic obstructive pulmonary disease (COPD), and so on experience a greater risk for comorbid depression than those who do not have these diseases. Moreover, depression over time impair the quality of life and alters treatment adherence compared to those without depression.3–5
A meta-analysis by Solano et al., shows a prevalence of depression between 13 and 79% in people with different chronic physical diseases (cancer, heart disease, renal disease, and COPD).6 Other studies show the prevalence of depression among chronic kidney disease (CKD) patients is 44.1%,7 26.8% among hypertensive patients,3 and 33.3% among COPD patients.8 In addition, studies in Nepal shows the prevalence of diabetes mellitus (DM) type II is 29.2%,9 among COPD patient is 69.2%.10
In developing countries like Nepal, where health care facilities and human resources are limited, no conclusive research explains depression in this region. Therefore, the general objective of this research is to determine the prevalence and correlation of depressive symptoms in patients with chronic physical illness and relation to attributes of depressive symptoms. Thus, this research will help provide baseline information on depression among patients with chronic diseases and its characteristics, which will help recognize and treat underlying depression early, improve patient quality of life, lower morbidity, and mortality of the disease, hence lower the burden of depression.
All the participants were explained about the research, and the process was carried out only after obtaining informed written consent from the patient and the primary caretaker. The study was conducted following the protocol and approval by the Ethical Review Committee of the Nepalese Army Institute of Health Sciences (NAIHS; Reference no: 385).
This cross-sectional analytical study was conducted among the patients receiving out-patient and in-patient services for chronic medical illnesses from the medical department of the Shree Birendra Hospital, a multidisciplinary tertiary-level hospital. It is a 635 bedded central and referral hospital that caters for the medical and healthcare needs of people affiliated to the Nepalese army and their dependents. This hospital was selected for the survey as this is a multidisciplinary well equipped tertiary level referral center with adequate patient flow from all over Nepal especially for the Nepalese army and their families, and also a working center for most of the authors. Data for the analysis was collected over four months (February - May 2021). This survey was made among the patients who visit the medical OPD for regular follow-up and those who get admitted to the medical ward with complications because of the disease condition mentioned above. At the time of data collection, all the participants were informed about the study and its objectives, and informed written consent was obtained from those participants who were willing to volunteer for the study (Extended data/ file 1).11 As the participants were surveyed once, a follow-up session of cases was not done. The authors had surveyed the participants physically using the pre-structured interview questionnaire in an English format by translating it into Nepali without disturbing the actual meaning of the sentence (Extended data/ file 3).11 Translation of the questionnaire was completed by the authors. A semi-structured proforma and Kuppuswamy’s scale modified for Nepalese context by Joshi and Acharya (2019)12 was used to obtain the socio-demographic and clinical variables (Extended data/ file 2).11 To assess the prevalence of depressive symptoms the Beck depression Inventory-II questionnaire, a 21-item self-reporting questionnaire was used (Extended data/file 2).11,13
The sample size was 326, which was determined using Cochran’s formula:
Where p is the prevalence of depression in chronic physical illness taken from the previous study by Sharma S et al., i.e., 69.2%,10 z is 1.96 at 95% confidence level, q is (1-p), and e is the margin of error, i.e., 5%.
After reviewing the Shree Birendra Hospital annual record sheet, patients diagnosed with hypertension, DM, COPD, CKD, and congestive heart disease (CHD) (the five most prevalent chronic illnesses at this hospital) were included. Participants who were diagnosed by the treating physician of Shree Birendra Hospital and receiving medication for at least a year who could respond/express well and give consent were eligible for participation. The patients too unwell to participate were excluded from the study. The cases were selected by simple random sampling adopting the lottery method from the medical in-patient and out-patient departments of Shree Birendra Hospital. Participants were interviewed physically by authors at the outpatient and inpatient department respectively using the pre-structured interview questionnaire. Collected data were then entered in IBM SPSS statistics data editor, and then analysis was done partly using SPSS version 26 and STATA version 15 (https://www.stata.com/).
Demographic and socio-economic variables such as gender (male/female), residence (rural/urban), education (illiterate/literate/primary/secondary/higher secondary), marital status (married/widowed/separated/unmarried), religion (Hindu/Buddhist/Christian/Others), Kuppuswamy’s score (upper middle/lower middle/upper lower/lower), physical activity (sedentary/non-sedentary), sleep (adequate/inadequate), substance abuse (alcohol/smoking/both/none/missing), comorbidities (Hypertension/DM/COPD/CKD/CHD/multiple comorbidities), duration of illness (1-5 years/6-10 years/11 years and above), and past history of depression (yes/no) were included in the survey questionnaire (Extended data/file 2).11
This study used the BDI-II questionnaire13 along with the socio-demographic questionnaire.11 The internal consistency BDI-II questionnaire was positively correlated with the Hamilton depression rating scale.14 The BDI can be used for ages 13 to 80.13 The validity and reliability of the BDI have been tested across populations, worldwide.15–19
The inventory contains items on a four-point scale ranging from zero to three (symptoms absent to severe symptoms), and the total score varies from 0 to 63. Thus total score in patients diagnosed with depression is classified as (0–13) minimal, (14-19) mild, (20-28) moderate, and (29-63) severe depression.13,14 Cases with scores 14 and above were considered to have some form of depression in our study.
The socio-demographic questionnaire was standardized based on 13 variables as provided by GESIS survey guidelines20 and harmonization of the questionnaire was based on the socio-cultural practice of Nepal.
Since Nepal does not have a standardized socio-economic scale for its population, Kuppuswamy’s scale modified for the Nepalese context by Joshi and Acharya, 2019 was used.11,12 It comprises three parameters with a score range for education (1-7), occupation of the head of the family (1-10), and total monthly family income (1-12). The modified Kuppuswamy scale differs from Kuppuswamy socioeconomic scale (1976) only in the context of total monthly family income which has been updated using the latest national consumer price index of Kathmandu valley (NCPI) provided by the Nepal Rastra Bank. The total scores vary from 3 to 29 and based on the scoring the population is grouped into five different socio-economic classes: upper (26-29), upper-middle (16-25), lower-middle (11-15), upper-lower (5-10), and lower (less than 5).12
Data analysis was done partly using a statistical package for the social sciences (SPSS) version 26 and STATA version 15. This analysis can be made alternatively with PSPPIRE data editor (PSPP) a freely accessible statistical software. First, a simple descriptive analysis was done, and socio-demographic variables determining the depression were presented in table and text as appropriate. Then chi-square/Fisher’s exact test was employed to check the association between Beck scales-based diagnosis of depression with other independent socio-demographic variables studied. Finally, multivariate logistic regression was performed considering the diagnosis of depression as an outcome of interest (with 1 = depression and 0 = no depression). Gender, education, residential setting, other socio-demographic variables, and chronic illness were considered independent variables, and diagnosis of depression was taken as the dependent variable. The pseudo-R2 value for the logistic model was 0.2341, indicating an acceptable model fit.
The treatment record book of the patients was thoroughly studied and those cases receiving treatment for additional comorbidities other than the aforementioned diseases were excluded which helped to minimize the confounding bias. As the selected cases in the study were not followed-up, there was an increasing chance of repetition of the cases which was avoided by asking every participant if they had participated in the same study recently. Furthermore, a meticulous study of all the data set recorded aided in preventing case repetition.
A total of 326 patients took part in the survey.21 All socio-demographic variables and outcomes are presented in frequency distribution (Table 1). Out of 326 patients, 175 (53.7%) were male while 151 (46.3%) were female, 189 (59%) were residents of rural regions and 137 (42%) from urban regions. The majority of the patients were illiterate 142 (43.6%), while 95 (29.1%) were literate, 32 (9.8%) had primary level education, 38 (11.7%) had secondary level education, and only 19 (5.8%) had higher secondary level education. More than 260 (79.8%) patients were married, while 66 (20.2%) were widowed. The bulk of patients, 300 (92%), were Hindu by religion, followed by 22 (6.7%) Buddhism, 3 (0.9%) Christian. On the Kuppuswamy scale, 164 (50.3%) fall under the upper lower class category and 139 (42.6%) under the lower middle class. 173 (53.1%) had a sedentary lifestyle while 153 (46.9%) had a non-sedentary lifestyle. On sleep habits, 180 (55.2%) had adequate sleep while the remaining 146 (44.8%) had inadequate sleep (< 7 hours a day). About substance abuse, in most of the cases, 161 (49.4%) didn’t use any abusive substance, followed by 80 for cigarette smoking (24.5%), 47 with both smoking and alcohol abuse (14.4%), and 32 for alcohol (9.8%). From the cases we had selected, the majority of the patients suffered from multiple comorbidities in the study with 92 (28.2%) followed by hypertension 81 (24.8%), COPD 68 (20.9%), CKD 40 (12.3%), DM 30 (9.2%) and CHD 15 (4.6%). The majority of the patients, 169 (51.8%), have had their disease for 1-5 years, and 318 (97.5%) have had a history of depression in the past. With the use of the BDI-II screening tool for depression, we found that 170 (52.1%) had minimal depression, 55 (16.9%) had a mild form of depression, 61 (18.7%) had a moderate form of depression, and 40 (12.3%) had severe depression. In total 47.9% of the study population had some form of depression.
Data evaluation with cross-tabulation of depression with nature of illness of individuals, the prevalence of depression among hypertension, diabetes mellitus, chronic obstructive pulmonary disease, chronic kidney disease, congestive heart disease was 30.9%, 43.3%, 45.6%, 77.5%, and 60.0%, respectively. While the prevalence of depression among patients with multiple comorbidities (more than one disease mentioned above) was 51.1% (Table 2).
Data evaluation with cross-tabulation of depression with a duration of illness, the prevalence of depression among patients with duration of illness 1 to 5 years, 6 to 10 years, and 11 years and above was found to be 45.6%, 48.3%, and 52.9% respectively (Table 3).
Duration of illness (Years) | No. of patients (N) | Minimal or no depression [n (%)] | Depressed [n (%)] |
---|---|---|---|
1-5 | 169 | 92 (54.4) | 77 (45.6) |
6-10 | 89 | 46 (51.7) | 43 (48.3) |
11 years and above | 68 | 32 (47.1) | 36 (52.9) |
Using chi-square/Fisher’s exact test to check the association between depression (dependent variable) and other independent variables showed a statistically significant association between education, physical activities, sleep, substance abuse, and comorbidities (p<0.05). Both male and female with (23.9%), living in the rural region (27.6%), illiterate (23.6%), married (37.7%), following Hindu religion (44.5%), falling under Kaposi scale of lower/upper lower class (22.7%), with a sedentary lifestyle (32.8%). Furthermore, those having inadequate sleep (30.1%) and not using any form of substance abuse (21.6%) with multiple comorbidities (14.4%) and a duration of illness about 1-5 years (23.6%) and no history of depression (46.9%) were found to be depressed (Table 4).
Variables | Depression | p-value | ||
---|---|---|---|---|
Minimal or no depression | Depressed | |||
Gender | Male | 97(29.8) | 78(23.9) | .202 |
Female | 73(22.4) | 78(23.9) | ||
Residency | Rural | 99(30.4) | 90(27.6) | .921 |
Urban | 71(21.8) | 66(20.2) | ||
Education | Illiterate | 65(19.9) | 77(23.6) | .017 |
Literate | 47(14.4) | 48(14.7) | ||
Primary | 17(5.2) | 15(4.6) | ||
Secondary | 26(8.0) | 12(3.7) | ||
Higher secondary | 15(4.6) | 4(1.2) | ||
Marital status | Married | 137(42.0) | 123(37.7) | .696 |
Widowed | 33(10.1) | 33(10.1) | ||
Religion | Hindu | 155(47.5) | 145(44.5) | .965* |
Buddhist | 12(3.7) | 10(3.1) | ||
Christian | 2(.6) | 1(.3) | ||
Others | 1(.3) | 0(0.0) | ||
KS | Upper middle | 8(2.5) | 9(2.8) | .653* |
Lower middle | 70(21.5) | 69(21.2) | ||
Upper lower | 90(27.6) | 74(22.7) | ||
Lower | 2(.6) | 4(1.2) | ||
Physical activity | Sedentary | 66(20.2) | 107(32.8) | .000 |
Non Sedentary | 104(31.9) | 49(15.0) | ||
Sleep | Adequate (> 7 hours a day) | 122(37.4) | 58(17.8) | .000 |
Inadequate (< 7 hours a day) | 48(14.7) | 98(30.1) | ||
Substance abuse | Alcohol | 16(5.0) | 16(5.0) | .048 |
Smoking | 43(13.4) | 37(11.6) | ||
Both | 16(5.0) | 31(9.7) | ||
None | 92(28.8) | 69(21.6) | ||
Comorbidities | Hypertension (HTN) | 56(17.2) | 25(7.7) | .000 |
Diabetes Mellitus (DM) | 17(5.2) | 13(4.0) | ||
Chronic obstructive pulmonary disease (COPD) | 37(11.3) | 31(9.5) | ||
Chronic kidney disease (CKD) | 9(2.8) | 31(9.5) | ||
Congestive heart disease (CHD) | 6(1.8) | 9(2.8) | ||
Multiple comorbidities | 45(13.8) | 47(14.4) | ||
Duration of illness | 1-5 years | 92(28.2) | 77(23.6) | .586 |
6-10 years | 46(14.1) | 43(13.2) | ||
11 years and above | 32(9.8) | 36(11.0) | ||
Past history of depression | Yes | 5(1.5) | 3(.9) | .725* |
No | 165(50.6) | 153(46.9) |
Multivariate logistic regression analysis showed, in comparison to illiterate patients, those with secondary and higher secondary level education had 72% (aOR, 0.28; 95% CI, 0.096-0.82) and 89% (aOR, 0.11, 95% CI, 0.025-0.52) lower odds for depression. Similarly, compared to those with active lifestyles, individuals living sedentary lifestyles had 2.97 higher odds of having depression (95% CI, 1.67-5.29). Additionally, individuals with inadequate sleeping (< 7 hours a day) had 4.34 higher odds of having depression (95% CI, 2.47-7.61) in comparison to those with adequate sleep. Interestingly, people with CKD only seem to have a higher rate of depression than people with hypertension; however, for other comorbidities, no significant differences were observed (Table 5).
This study divulged that most patients with chronic physical illness had minimal depression followed by mild depression. In the present study, the prevalence of depressive symptoms was equal among males and females (23.9%) and was more prevalent among illiterate individuals (23.6 %); however, a study by Lam M et al., among adults of Nepal reported a higher prevalence of depressive symptoms among females (24.1%) and disclosed that adults who had no formal education had a higher prevalence of depression (28.8%).22 Moreover, this study revealed that 23.6% of the patients with chronic medical illness developed symptoms of depression within 1-5 years of diagnosis.
Here, we found that the depression rate was higher among participants with multiple illnesses, i.e., 14.4%, than those with a single illness. In this study, 45.6% of participants with COPD were depressed, and this finding was compared to the finding from the study by Sharma S et al., in 2018 in which 69.2% of participants had depression.10 Also, the study by Negi H et al. reported 53.9% of participants were depressed.8 In this study, 77.5% of participants with CKD had depressive symptoms. A cross-sectional study by Ahlawat R et al. revealed that 44.8 % of patients with CKD were depressed.7
According to this study, 43.3% of participants with type 2 diabetes mellitus had depressive symptoms similar to the finding from the study by Joshi S et al. in 2015, where 44.1 % of participants had depressive symptoms.23 A cross-sectional study done among persons with type 2 diabetes mellitus by Niraula K et al., revealed that 40.3 % of participants had clinical depression, which supported this study.24 A cross-sectional study conducted among persons with hypertension in urban Nepal by Neupane D et al. disclosed that 15 % of participants had undiagnosed depression,25 which was lower than this study where 30.9% of participants with hypertension had depressive symptoms.
In the present study, 60% of participants with chronic heart disease showed depressive symptoms; this finding was found to be higher than the finding of a study done among patients with cardiac disease in public health institute in 2019 by Bahall M which revealed 40% of hospitalized patients with cardiac disease had clinically significant depression.26 According to a study by Dhital P et al., all among patients with coronary artery disease, 23.8% of participants had depression.27
Our study showed a higher prevalence of depressive symptoms among patients with CKD; therefore, CKD patients have higher odds of having depressive symptoms in comparison to hypertensive patients. Moreover, participants with secondary education have more odds of having depression than illiterate ones. In addition, people with a sedentary lifestyle and inadequate sleep have more odds of acquiring depression when compared to the ones with a non-sedentary lifestyle and adequate sleep, respectively. The findings from our study were similar to other studies conducted in Nepal and those conducted in other countries. In the present study, we evaluated socioeconomic, clinical, and behavioral factors for the prevalence of depressive symptoms among patients with chronic physical illness. In addition, the presence of such symptoms was evaluated using the BDI-II scale.
Our study is a small single-center study; therefore, the findings might not be applicable around the country/globally. Also, this simple cross-sectional study could not establish the determining causal relationship. Furthermore, the lack of comparison groups limits its control over unobserved heterogeneity among the respondents. Chronic physical illness includes a myriad of diseases; therefore, it was only feasible for us to include the top five chronic physical illnesses prevalent in Shree Birendra Hospital. Many chronic diseases were bound to be missed in this study.
In conclusion, this study established that depressive symptoms were more prevalent among illiterate and married individuals with chronic illnesses living in rural areas. People with inadequate sleep and following a sedentary lifestyle are prone to be depressed. Patients with multiple illnesses were more depressed than those with only one illness but the symptoms were found to be higher among CKD and CHD patients. Hence, patients with CKD have a higher odds ratio of having depressive symptoms in comparison to hypertension. Similarly, patients with a history of duration of illness 1-5 years were more depressed but the symptoms were found to be higher among patients with a history of duration of illness of 11 years and above.
Figshare: Prevalence of depressive symptoms in patients with chronic physical illness: A single institutional cross-sectional study from Nepal. DOI: https://doi.org/10.6084/m9.figshare.19032668.v3.21
The project contains the following underlying data:
• Working data.sav: (Data set with quantitative data on age, gender, residence, chronic illness, socioeconomic status, BDI-II score, past history of depression, physical activities, sleep, substance abuse, education, marital status, and religion data gathered in this study)
Data are available under the terms of the Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
Figshare: Prevalence of depressive symptoms in patients with chronic physical illness: A single institutional cross-sectional study from Nepal. DOI: https://doi.org/10.6084/m9.figshare.17307074.v611
The project contains the following extended data:
• File 1: Informed consent form (in English and Nepali)
• File 2: Questionnaire English format (socio-demographic and BDI-II questionnaire and Kuppuswamy’s socioeconomic scale in context to Nepal used in this study in English)
• File 3: Questionnaire Nepali Format (socio-demographic and BDI-II questionnaire and Kuppuswamy’s socioeconomic scale in context to Nepal used in this study in Nepali)
Data are available under the terms of the Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: internal medicine
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | ||
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Version 1 11 Mar 22 |
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