- Research article
- Open Access
- Open Peer Review
This article has Open Peer Review reports available.
Psychometric properties of the cardiac depression scale in patients with coronary heart disease
© Kiropoulos et al.; licensee BioMed Central Ltd. 2012
Received: 16 July 2012
Accepted: 27 November 2012
Published: 3 December 2012
This study examined the psychometric properties of the Cardiac Depression Scale (CDS) in a sample of coronary heart disease (CHD) patients.
A total of 152 patients were diagnosed with coronary heart disease and were administered the CDS along with the Beck Depression Inventory- 2 (BDI-2) and the State Trait Anxiety Inventory (STAI) 3.5-months after cardiac hospitalization.
The CDS’s factorial composition in the current sample was similar to that observed in the original scale. Varimax-rotated principal-components analyses extracted six factors, corresponding to mood, anhedonia, cognition, fear, sleep and suicide. Reliability analyses yielded internal consistency α - coefficients for the six subscales ranging from 0.62 to 0.82. The CDS showed strong concurrent validity with the BDI-II (r = 0.64). More patients were classified as severely depressed using the CDS. Both the CDS and the BDI-2 displayed significantly strong correlations with the STAI (r = 0.61 and r = 0.64), respectively.
These findings encourage the use of the CDS for measuring the range of depressive symptoms in those with CHD 3.5 months after cardiac hospitalization.
A high incidence of depression has been reported in those with coronary heart disease (CHD) specifically in those who have had coronary artery bypass graft surgery [1–3], those who have experienced myocardial infarction [2, 4] and following angina [5, 6]. One in every four people with CHD have been reported to meet diagnostic criteria for major depression [7–11]. Mild depression is also commonly found in those hospitalised with CHD and has been estimated to affect from one in four [9, 11] to one in three of these individuals . Depression has been found to affect the prognosis of patients with CHD even though some of these patients may not always meet the DSM-IV criteria for major depression . Those with CHD who are more likely to experience mild to moderate depression, (based on a BDI score of 10 or more), have been found to have a subsequent mortality compared with patients with BDI scores less than 10 when assessed at 6 and 18 months following the event [14–16]. Similar findings have also been found in patients with angina, (who scored greater than 10 on the BDI), who were more likely to die of a cardiac event or to experience a nonfatal cardiac event within 1 year of the initial hospital admission compared to patients with a BDI score of less than 10 . Both mild to moderate and severe depression at hospitalization have also been found to be strong predictors of depression 3 months after cardiac hospitalization . Longitudinal studies have found that individuals with CHD who are depressed are less likely to adhere to their treatment regime and lifestyle recommendations following a cardiac event  and might be at higher risk of subsequent cardiac events . Co-morbid depression and low social support has also been found to seriously impact prognosis with a 3 to 5 fold increase risk of death found in those with CHD who had poor social support .
A range of depression assessment tools have been used to measure depressive symptoms in CHD patients. These include the Beck Depression Inventory – 2 (BDI-2) , the Hospital Anxiety and Depression Scale (HADS) , the Center for Epidemiologic Studies Depression Scale (CES-D)  and the Cardiac Depression Scale (CDS) . One criticism of the use of non disease specific tools in CHD patients is that symptoms such as fatigue may be mistaken for cardiac-related symptoms which may result in under-detection of the somatic symptoms of depression which have been attributed instead to cardiac problems .
The CDS has been developed as a depression scale to accurately assess depression in cardiac patients . The original CDS has been shown to comprise of seven reliable and distinct components which include Mood, Anhedonia, Cognition, Fear, Sleep, Suicide and Hopelessness. However recent studies have found a six factor solution for the CDS [26, 27].
The CDS has been employed to assess for a range of depressive symptoms in cardiac patients with various diagnoses and at different time points including use with ambulatory cardiac outpatients with a range of diagnoses including angina, heart failure, post-myocardial infarction, valvular heart cardiac disease and arrhythmias ; those with an acute coronary syndrome (due to myocardial ischaemia or infarction) who were assessed at 2-weeks post-hospital discharge ; and a cardiac rehabilitation population which consisted of a mixed group of cardiac patients including those who had a myocardial infarction, heart failure, coronary artery bypass graft surgery, angioplasty or a stent procedure who were assessed while undergoing cardiac rehabilitation .
However, further validation of the CDS in a CHD population who are medically stable and have settled into their community surroundings after cardiac hospitalization is needed given that studies have shown that around one third of those with CHD meet criteria for depression 3–4 months after a cardiac event . The current paper presents the examination of the psychometric properties of the CDS as a measure of depressive symptoms in those who had CHD and were 3.5-months post cardiac hospitalisation, by investigating its factorial composition (as an index of its construct validity), its reliability and also comparing the CDS with the BDI-2 in its ability to discriminate those with mild, moderate and severe depression.
Participants and procedure
Characteristics of depressed and non-depressed groups
(N = 152)
(N = 93)
(N = 59)
Other health problem
Taking heart medication
Ethics approval for this study was granted by Monash University, Southern Health and Western Health Ethics Committees. Inclusion criteria included having a diagnosis of CHD and no known psychiatric problems. During their hospital stay or within a week after their hospital discharge researchers contacted participants to describe the study and ask whether potential participants would like an explanatory statement and a consent form sent out to them. Potential participants were also asked whether it would be feasible for the researcher to re-contact them at a 3 month post discharge period to undertake a 1-hour face to face interview with them at a location of their choice. Those that agreed were sent out an information pack regarding the study and a consent form with a reply paid envelope to complete and return to the researcher prior to the interview or it was collected on the day of the interview. At the 3 month post-discharge time point, the researchers re-contacted participants by phone to organise an interview time. All questionnaires were administered by way of interview for all participants. Patients were interviewed 3-months after cardiac hospitalisation to minimise any possible influence of the hospital stay on levels of depression. Interviews took place at either the researcher’s office at Monash University or in the participant’s home.
The 26-item Cardiac Depression Scale (CDS)  is designed to assess depression in adult cardiac populations. The CDS was developed as an alternative to more general depression scales that were considered to be too insensitive and unresponsive to depressive symptoms experienced by cardiac patients . Average CDS scores have been reported in different cardiac groups with higher scores observed in those with heart failure compared with those with acute myocardial infarction . All statements on the CDS are scored on a 7-point Likert-type scale ranging from ‘strongly disagree’ (1) to ‘strongly agree’ (7). Participants are asked to rate how strongly they agree or disagree with each statement. A scale point of 4 indicates neither disagreement nor agreement with the item. Seven items are reverse-scored. Higher scores on the CDS indicate more severe depression. The CDS has fewer items that refer to somatic symptoms of depression compared to the BDI-2. The total CDS score is the sum of all items and ranges from 26 to 182. Cut-off scores to indicate mild, moderate or severe depression were not provided by the original authors for the CDS. However, a cut-off score of 90 for mild depression and 100 or above has been recommended to detect individuals with more severe depression , Wise et al.]. The 21-item Beck Depression Inventory- Version 2 (BDI-2)  is a widely used measure of psychological and physical symptoms of depression in adults. Each item consists of four statements indicating the degree of severity of the symptom. The items assess cognitive, behavioural, affective and somatic symptoms. Responses to items covered ‘the past two weeks, including today’. Scores range from 0 to 3 with 0 indicating absence of the symptoms and higher values indicating greater severity of the symptom. The BDI-2 score can be grouped into mild (10–19), moderate (20–25) and severe (>25) symptoms . The internal reliability for the CDS and the BDI-2 in the current study indicated an α –coefficient of 0.91 for both scales.
The State-Trait Anxiety Inventory (state version) (STAI)  is a 20-item indictor of anxiety in adults. The scale evaluates feelings of tension, nervousness, worry and apprehension ‘in the past two weeks, including today’. Responses are on a 4-point Likert scale ranging from (0) ‘not at all’ and (3) ‘very much so’ with higher scores reflecting higher severity. In the current sample, the STAI showed excellent reliability (α = 0.93).
Quality of Life
The 26-item World Health Organisation Quality of Life scale (Brief version) (WHOQOL-BREF)  was used to measure Quality of Life. The WHOQOL-BREF asks about an individual’s quality of life in four domains including physical health, psychological health, social relationships and environment. Higher scores denote higher quality of life. The WHOQOL-BREF also contains one question about an individual’s perception of overall quality of life and a question about their perception of their overall health. The internal reliability for the four domains of the scale indicated alpha coefficients ranging from 0.81 to 0.85.
The 12-item Perceived Social Support Scale (PSSS)  assesses perceived social support from family, friends and others. Higher scores indicated higher perceived social support. The internal consistency for this scale in this sample indicated an alpha coefficient of 0.92. The 7-item Enriched Social Support Instrument (ESSI)  measures functional social support particularly emotional support in cardiac patients. Higher scores indicate higher levels of social support. The ESSI has been previously used to examine level of social support and to assess changes in patients’ social support after cardiac treatment. The alpha coefficient for the ESSI in the current sample was 0.86.
Factors extracted from the CDS by principal components analysis with varimax rotation ( N = 152)
The possibility of sudden death worries me (fear)
Things which i regret most about my life are bothering me (mood)
I become tearful more easily than before (mood)
I seem to get more easily irritated by others than before (anhedonia)
I lose my temper more easily nowadays (mood)
I feel frustrated (mood)
I get pleasure from life at present (anhedonia)
I feel independent and control in my life (anhedonia)
I have dropped many of my interests and activities (anhedonia)
I can’t be bothered doing anything much (anhedonia)
I am not the person i used to be (anhedonia)
I get hardly anything done (anhedonia)
My mind is as fast and alert as always (cognition)
I gain as much pleasure from leisure activities as i used to (anhedonia)
My memory is as good as it always was (cognition)
My concentration is as good as it ever was (cognition)
I am concerned about the uncertainty of my health (fear)
My problems are not yet over (fear)
I may not recover properly (fear)
My sleep is restless and disturbed (sleep)
I wake up in the early hours of the morning and cannot get back to sleep (sleep)
I feel in good spirits (suicide)
I am concerned about my capacity for sexual activity (fear)
I feel like im living on borrowed time (fear)
Dying is the best solution for me (suicide)
There is only misery in the future for me (suicide)
The total 26-item CDS scale showed good reliability (α = 0.91). As seen in Table 2, the Cronbach alpha coefficients for the six CDS subscales were acceptable and ranged from 0.62 (Factor 6: Suicide) to 0.82 (Factor 2: Anhedonia).
Pearson’s correlation coefficients were used to established the CDS’s concurrent validity with a moderate to high correlation between the relevant scales deemed as acceptable (r > = 0.3). A significant moderate to high correlation between the CDS and the BDI-2 scale (r = 0.65, p < 0.001) and between the BDI-2 and the STAI (r = 0.64, p < 0.001) was observed. Similarly, moderate to high correlations were found between the CDS and the STAI scale (r = 0.61, p < 0.001), the CDS and the physical QOL subdomain (r = −0.64, p < 0.001), psychological QOL subdomain (r = −0.60, p < 0.001), social QOL subdomain (r = −0.46, p < 0.001) and environmental QOL subdomain (r = −0.43, p < 0.001), and the PSSS (r = −0.42, p < 0.001). A weaker correlation was found between the CDS and the ESSI, (r = 0.18, p < 0.05).
Relationships between the CDS and the BDI-2
Summary of ANOVA results for depressed and non-depressed groups
Total sample (n = 152)
Depressed meana (SD) (n = 59)
Non-depressed mean (SD) (n = 93)
Percentages of patients with mild, moderate and severe depression according to the CDS and the BDI-2
CDS < 90
BDI-2 < 10
CDS > = 90
CDS > = 100
The aim of this study was to examine the psychometric properties of the CDS and provide further data to support the use of the CDS in a CHD population who have been medically stable and living in their usual community environment 3.5 months after cardiac hospitalisation.
Consistent with previous research examining the construct validity of the CDS in a cardiac population [26, 27] factor analysis of the CDS yielded six factors rather than the seven factor solution reported by the authors of the scale . Four of these factors were almost identical to the Mood, Anhedonia, Cognition and Sleep Disturbance factors reported originally  and by other researchers [26, 27]. Similar to previous research [24, 27], all factors except Suicidal Ideation demonstrated acceptable reliability and a potential explanation for this may be the low number of items comprising this factor .
There is growing evidence that the CDS is characterized by adequate psychometric properties when applied to cardiac samples. Reliability has been found to be high across cardiac samples when assessed in terms of internal consistency (coefficient alphas have ranged from 0.88 to 0.92). Moreover, the validity of the CDS has been used successfully to discriminate between cardiac patients diagnosed as depressed vs. nondepressed. The CDS has also been found to have good concurrent validity with the BDI-2 (ranging from 0.69 to 0.73) and the STAI (r = 0.80) [13, 26, 27]. Consistent with this, the current study also found that the CDS and the BDI-2 demonstrated good concurrent validity as seen in the significant correlations between the CDS and the BDI-2 and the anxiety, quality-of-life and social support measures [13, 24, 27]. The correlations between the CDS, BDI-2 and the STAI were within the ranges found in previous research examining the psychometric properties of the CDS . The moderate to strong correlation between the CDS and the BDI-2 scores for the current sample indicating a moderate concurrent validity suggests that the two scales are comparable. Both the BDI-2 and CDS correlated moderately to strongly with the STAI. Moderate to strong correlations obtained between depression and anxiety measures have typically been found in cardiac populations and may also be indicative of the co-morbid depressive and anxiety symptoms experienced by these populations . The internal consistency of the CDS scores in the current study was compatible with the values obtained by the original authors and other researchers.
It should be noted that the current sample of CHD patients reported a high CDS mean score compared to previous cardiac samples . This may be partly explained by the high proportion of the current sample being overseas-born who have been previously found to have higher levels of depression and anxiety  which could have contributed to the higher mean depression score. It is possible that depression could have preceded the development of CHD in these participants.
In the current study, depressed participants were determined by a BDI-2 score of 10 or more. Both the CDS and the BDI-2 identified that almost one in four patients (25% vs. 24.3%) had symptoms indicative of mild to moderate depression. These results are comparable to those reported by Wise, Harris and Carter (2006)  who found that the CDS classified 17% of their cardiac outpatient sample as mild to moderately depressed and other studies which found mild to moderate depression in 17-30% of cardiac patients [10, 34]
While the BDI-2 suggested that 14.5% had symptoms indicative of severe depression, the CDS indicated that in the same cohort, 27.6% of patients were suffering severe depression which is almost one in three patients as opposed to almost one in six by the BDI-2. This discrepancy may be due to the CDS items detecting more severe symptomatology compared to the BDI-2, the cut-off score used for detecting severe depression with the CDS and the possibility that the CDS may be overdiagnosing severe depression in this sample. However, these results are comparable to previous research which found that the CDS classified 21-25% of cardiac outpatients as severely depressed [10, 11, 15, 18, 27] and that around one-third of cardiac patients meet criteria for depression 3 to 4 months after a cardiac event .
Limitations and future directions
A major limitation of the current study is that no diagnostic interviews to assess for Major Depressive Disorder or Episode were concurrently undertaken with participants to validate the levels of depression found with the CDS and the BDI-II. The current study was not able to evaluate the sensitivity or specificity of the CDS in a fully meaningful way. Further research employing larger sample sizes is required to determine whether the CDS is a more sensitive measure of depression in the 3–4 month time period after a cardiac event or whether the CDS is yielding more false positives. The current results need to be replicated given that the current sample was less than what has been recommended for conducting factor analysis with suggestions that a minimum sample size of 200 be used . Future research should also examine the CDS with other screening measures for depression and anxiety that have fewer somatic items such as the Hospital Anxiety and Depression Scale (HADS).
Another limitation is that no information was gathered from those that declined to participate and no comparison can be made between this sample and those that agreed to participate in the current study.
Effective screening after a cardiac event and procedure has implications for the effective management of depression to assist cardiac patients in their therapeutic compliance and in their prognosis. Given that those in the current sample who were depressed also scored lower on the social support and quality of life measures, overall treatment approaches should focus on strategies to increase social supports and quality of life in these patients.
Depression has been shown to influence health outcomes in those with CHD. Accurate and timely assessment of depression in CHD patients has the potential to influence prognosis and reduce suffering in those who have been discharged after cardiac hospitalization. The current study has shown that the CDS can be used to screen and detect the range of depressive symptomatology, ranging from mild to severe, in CHD patients who are medically stable and settled in their community surroundings 3.5 months following discharge after cardiac hospitalization.
The authors would like to thank the nursing staff at Southern Health and Western Health who facilitated our efforts to recruit participants from their sites and without their help this study would not be possible. This work has been supported by a grant from beyondblue: the national depression initiative. The funding body had no involvement in the design of the study; in the collection, analysis, and interpretation of data; in the writing of the manuscript; and in the decision to submit the manuscript for publication.
- Burker EJ, Blumenthal JA, Feldman M, Burnett R, White W, Smith LR, Croughwell N, Schell R, Newman M, Reves JG: Depression in male and female patients undergoing cardiac surgery. Brit J of Clin Psychol. 1995, 13: 119-128.View ArticleGoogle Scholar
- Carney R, Rich M, Freedland K, Saini J, Tevelde A, Simeone C, Clark K: Major depressive disorders predicts cardiac events in patients with coronary artery disease. Psychosom Med. 1988, 50: 627-633.View ArticlePubMedGoogle Scholar
- Pirraglia PA, Peterson JC, Williams-Russo P, Gorkin L, Charlson ME: Depressive symptomatology in coronary artery bypass graft surgery patients. Int J Geriatr Psych. 1999, 14 (Suppl 8): 668-680.View ArticleGoogle Scholar
- Trelawny-Ross C, Russell O: Social and psychological responses to myocardial infarction: multiple determinants of outcome at months six. J Psychosom Res. 1987, 31: 125-130. 10.1016/0022-3999(87)90107-3.View ArticlePubMedGoogle Scholar
- DeVon H, Zerzic J: Symptoms of acute coronary syndromes: are there gender differences? A review of the literature. Heart Lung. 2002, 31: 235-245. 10.1067/mhl.2002.126105.View ArticlePubMedGoogle Scholar
- Lesperance F, Frasure-Smith N, Juneau M, Theroux P: Depression and 1-year prognosis in unstable angina. Arch Intern Med. 2000, 160: 1354-1360. 10.1001/archinte.160.9.1354.View ArticlePubMedGoogle Scholar
- Doerfler LA, Pbert L, De Cosimo D: Self-reported depression in patients with coronary artery disease. J Cardiopulm Rehab. 1997, 17: 163-170. 10.1097/00008483-199705000-00003.View ArticleGoogle Scholar
- Gonzalez MB, Snyderman TB, Colket JT, Arias RM, Jiang WJ, O’Connor CM, Krishnan KRR: Depression in patients with coronary artery disease. Depression. 1996, 4 (Suppl 2): 57-62.View ArticlePubMedGoogle Scholar
- Hance M, Carney RM, Freedland KE, Skala J: Depression in patients with coronary heart disease. A 12-month follow-up. Gen Hosp Psychiat. 1996, 18 (Suppl 1): 61-65.View ArticleGoogle Scholar
- Steffens DC, O’Connor CM, Jiang WJ, Pieper CF, Kuchibhatla MN, Arias RM, Look A, Davenport C, Gonzalez MB, Krishnan KRR: The effect of major depression on functional status in patients with coronary artery disease. J Am Geriat Soc. 1999, 47: 319-322.View ArticlePubMedGoogle Scholar
- Sullivan M, LaCroix A, Russo J, Swords E, Sornson M, Katon M: Depression in coronary artery disease. What is the most appropriate diagnostic threshold?. Psychosom. 1999, 40 (Suppl 4): 286-292.View ArticleGoogle Scholar
- Astin F, Jones K, Thompson DR: Prevalence and patterns of anxiety and depression in patients undergoing elective percutaneous transluminal coronary angioplasty. Heart Lung. 2005, 34: 393-401. 10.1016/j.hrtlng.2005.05.002.View ArticlePubMedGoogle Scholar
- Di Benedetto M, Lindner H, Hare DL, Kent S: Depression following acute coronary syndromes: a comparison between the cardiac depression scale and the beck depression inventory II. J Psychosom Res. 2006, 60 (Suppl 1): 13-20.View ArticlePubMedGoogle Scholar
- Barefoot J, Schroll M: Symptoms of depression, acute myocardial infarction, and total mortality in a community sample. Circulation. 1996, 93: 1976-1980. 10.1161/01.CIR.93.11.1976.View ArticlePubMedGoogle Scholar
- Frasure-Smith N, Lesperance F, Talajic M: Depression following myocardial infarct: impact on 6-month survival. JAMA. 1993, 270: 1819-1825. 10.1001/jama.1993.03510150053029.View ArticlePubMedGoogle Scholar
- Frasure-Smith N, Lesperance F, Talajic M: Depression and 18-month prognosis after myocardial infarct. Circulation. 1993, 91: 999-1005.View ArticleGoogle Scholar
- Schrader G, Cheok F, Hordacre AL, Guiver N: Predictors of depression three months after cardiac hospitalization. Psychosom Med. 2004, 66: 514-520. 10.1097/01.psy.0000128901.58513.db.View ArticlePubMedGoogle Scholar
- Ziegelstein R, Fauerbach J, Stevens S, Romanelli J, Richter D: Patients with depression are less likely to follow recommendations to reduce cardiac risk during recovery from a myocardial infarction. Arch Intern Med. 2000, 160: 1818-1823. 10.1001/archinte.160.12.1818.View ArticlePubMedGoogle Scholar
- Connerney I, Shapiro PA, McLaughlin JS, Bagiella E, Sloan RP: Relation between depression after coronary artery bypass surgery and 12-month outcome: a prospective study. Lancet. 2001, 358 (Suppl 9295): 1766-1771.View ArticlePubMedGoogle Scholar
- Joshi P, Islam S, Pais P, Reddy S, Dorairaj P, Kazmi K, Pandey MR, Haque S, Mendis S, Rangarajan S, Yusuf S: Risk factors for early myocardial infarction in south Asians compared with individuals in other countries. JAMA. 2007, 297 (Suppl 3): 286-294.View ArticlePubMedGoogle Scholar
- Beck AT, Steer RA, Brown GK: Beck depression inventory-second edition manual. 1996, San Antonio: The Psychological CorporationGoogle Scholar
- Zigmond AS, Snaith RP: The hospital anxiety and depression scale. Acta Psychiatr Scand. 1983, 67: 361-370. 10.1111/j.1600-0447.1983.tb09716.x.View ArticlePubMedGoogle Scholar
- Radloff L: The CES-D scale: A self-report depression scale for research in the general population. Appl Psych Meas. 1977, 1: 385-401. 10.1177/014662167700100306.View ArticleGoogle Scholar
- Hare DL, Davis CR: Cardiac depression scale: validation of a new depression scale for cardiac patients. J Psychosom Res. 1996, 40 (Suppl 4): 379-386.View ArticlePubMedGoogle Scholar
- Thornton L: Depression in post-acute myocardial infarction patients. J Am Acad Nurse Pract. 2001, 13: 364-367.View ArticlePubMedGoogle Scholar
- Wise FM, Harris DW, Carter LM: Validation of the cardiac depression scale in a cardiac rehabilitation population. J Psychosom Res. 2006, 65 (Suppl 2): 123-129.Google Scholar
- Gholizadeh L, Salamonson Y, Davidson PM, Parvan K, Frost SA, Chang S, Hare S: Cross-cultural validation of the cardiac depression scale in Iran. Brit J of Clin Psychol. 2010, 49: 517-528. 10.1348/014466509X478709.View ArticleGoogle Scholar
- Schleifer SJ, Macari-Hinson MM, Coyle DA, Slater WR, Kahn M, Gorlin R, Zucker HD: The nature and course of depression following myocardial infarction. Arch Intern Med. 1989, 149 (Suppl 8): 1785-1789.View ArticlePubMedGoogle Scholar
- Spielberger CD, Gorsuch RL, Lushene RE: STAI manual for the state-trait anxiety inventory. 1970, California: Consulting Psychologists PressGoogle Scholar
- WHO-QOL Group: Development of the world health organization (WHOQoL-BREF): quality of life assessment. Psychosom Med. 1998, 28: 551-554.View ArticleGoogle Scholar
- Blumenthal JA, Burg MM, Barefoot J, Williams RB, Haney T, Zimet G: Social support, type a behavior, and coronary artery disease. Psychosom Med. 1997, 49: 331-340.View ArticleGoogle Scholar
- The ENRICHD Investigators: Enhancing recovery in coronary heart disease patients (ENRICHD): study design and methods. Am Heart J. 2000, 139: 1-9.Google Scholar
- Kiropoulos LA, Klimidis S, Minas HI: Depression and anxiety: a comparison of older-aged Greek immigrants and Anglo-Australians. Aust N Z J Psychiatry. 2004, 38: 714-724. 10.1080/j.1440-1614.2004.01445.x.View ArticlePubMedGoogle Scholar
- Romanelli J, Fauerbach JA, Bush DE, Ziegelstein RC: The significance of depression in older patients after myocardial infarction. J Am Geriatr Soc. 2002, 50: 817-822. 10.1046/j.1532-5415.2002.50205.x.View ArticlePubMedGoogle Scholar
- Gorsuch RL: Factor analysis. 1974, Philadelphia: SaundersGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-244X/12/216/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.