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<title>Psychology Articles</title>
<copyright>Copyright (c) 2013 Royal College of Surgeons in Ireland All rights reserved.</copyright>
<link>http://epubs.rcsi.ie/psycholart</link>
<description>Recent documents in Psychology Articles</description>
<language>en-us</language>
<lastBuildDate>Thu, 16 May 2013 01:51:37 PDT</lastBuildDate>
<ttl>3600</ttl>


	
		
	







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<title>The MacNew Heart Disease health-related quality of life instrument: a summary.</title>
<link>http://epubs.rcsi.ie/psycholart/57</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/57</guid>
<pubDate>Tue, 14 May 2013 07:25:28 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: The measurement of health, the effects of disease, and the impact of health care include not only an indication of changes in disease frequency and severity but also an estimate of patients' perception of health status before and after treatment. One of the more important developments in health care in the past decade may be the recognition that the patient's perspective is as legitimate and valid as the clinician's in monitoring health care outcomes. This has lead to the development of instruments to quantify the patients' perception of their health status before and after treatment.</p>
<p>METHODS: We review evidence supporting the measurement properties of the MacNew Heart Disease Health-related Quality of Life [MacNew] Questionnaire which was designed to evaluate how daily activities and physical, emotional, and social functioning are affected by coronary heart disease and its treatment.</p>
<p>RESULTS: Reliability was demonstrated by using internal consistency and the intraclass correlation coefficients for the three domains in the Dutch, English, Farsi, German, and Spanish versions of the MacNew. With internal consistency and intraclass correlation coefficients =>0.73, reliability is high. Validity of the MacNew was examined with factor analysis and three core underlying factors, physical, emotional, and social, were identified, explaining 63.0 - 66.5% of the observed variance and replicated in the translations with psychometric data. Construct validity of the MacNew was further demonstrated by extensive substantiation of the logical relationships, defined a priori, between items and other comparison tools. The MacNew is responsive and sensitive to changes in HRQL following various interventions for patients with heart disease with 11 of 13 effect size statistics >0.80. Taking an average of 10 minutes or less to complete, the respondent-burden for the MacNew is low and its acceptability is demonstrated by response rates of over 90%. Normative data are available for patients with myocardial infarction, angina, and heart failure in the English version.</p>
<p>CONCLUSION: The MacNew may be a valuable tool for assessing and evaluating health related quality of life in patients with heart disease.</p>

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<author>Stefan Höfer et al.</author>


<category>Attitude to Health</category>

<category>Female</category>

<category>Health Status</category>

<category>Heart Diseases</category>

<category>Humans</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Psychometrics</category>

<category>Quality of Life</category>

<category>Questionnaires</category>

<category>Sickness Impact Profile</category>

<category>Translations</category>

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<title>Through doctors&apos; eyes: A qualitative study of hospital doctor perspectives on their working conditions.</title>
<link>http://epubs.rcsi.ie/psycholart/56</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/56</guid>
<pubDate>Tue, 07 May 2013 08:22:03 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Hospital doctors face significant challenges in the current health care environment, working with staff shortages and cutbacks to health care expenditure, alongside increased demand for health care and increased public expectations. OBJECTIVE: This article analyses challenges faced by junior hospital doctors, providing insight into the experiences of these frontline staff in delivering health services in recessionary times. DESIGN: A qualitative methodology was chosen. METHODS: Semi-structured in-depth interviews were conducted with 20 doctors from urban Irish hospitals. Interviews were recorded via note taking. Full transcripts were analysed thematically using NVivo software. RESULTS: Dominant themes included the following: (1) unrealistic workloads: characterised by staff shortages, extended working hours, irregular and frequently interrupted breaks; (2) fatigue and its impact: the quality of care provided to patients while doctors were sleep-deprived was questioned; however, little reflection was given to any impact this may have had on junior doctors own health; (3) undervalued and disillusioned: insufficient training, intensive workloads and a perceived lack of power to influence change resulted in a sense of detachment among junior doctors. They appeared immune to their surroundings. CONCLUSION: Respondents ascribed little importance to the impact of current working conditions on their own health. They felt their roles were underappreciated and undervalued by policy makers and hospital management. Respondents were concerned with the lack of time and opportunity for training. This study highlighted several 'red flags', which need to be addressed in order to increase retention and sustain a motivated junior medical workforce. STATEMENT OF CONTRIBUTION: What is already known on this subject? Loss of public funding in Ireland has led to large numbers of Irish trained doctors emigrating. Research indicates the likelihood of medical graduates returning depends on improvements to working conditions. Good working conditions are likely to encourage doctor retention yet little research has been conducted in this area. What does this study add? Intense workplace demands reduce confidence and productivity among doctors. Junior doctors were reluctant to reflect on the impact current working conditions had on their own health. Early warning signs of burnout appear to resonate with many of the issues raised by junior doctors in this study.</p>

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<author>Yvonne McGowan et al.</author>


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<title>The new open access journal on health psychology and behavioral medicine: why do we need it?</title>
<link>http://epubs.rcsi.ie/psycholart/55</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/55</guid>
<pubDate>Wed, 17 Apr 2013 08:14:01 PDT</pubDate>
<description>
	<![CDATA[
	<p>On behalf of the editorial board, it is our pleasure to introduce Health Psychology and Behavioral Medicine: an Open Access Journal (HPBM), which we hope will become a leading international journal in these areas. HPBM will be interdisciplinary and global in scope, offering studies in a wide range of forms including systematic and critical reviews, meta-analyses, ethnographic and qualitative studies, quantitative studies, program evaluation, policy studies, case studies, and research protocols. Individually and in combination, these publications will contribute to the development and integration of psychosocial, behavioral, and biomedical knowledge to promote and maintain health, to prevent, treat, and manage physical and psychological illness, and to identify etiological and diagnostic correlates of health and illness. Discrete but related topics including assessment, prevention, diagnosis, treatment, prognosis, and rehabilitation that contribute to health will be featured. The need for this new journal stems from both recent developments in the fields of health psychology and behavioral medicine, and the recent revolutionary movement of academic publishing into online dissemination.</p>

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<author>Xiaoming Li et al.</author>


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<title>The association between self-reported lifestyle changes and health-related quality of life in coronary patients: the EUROASPIRE III survey.</title>
<link>http://epubs.rcsi.ie/psycholart/54</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/54</guid>
<pubDate>Mon, 04 Feb 2013 07:18:52 PST</pubDate>
<description>
	<![CDATA[
	<p>Patients with coronary heart disease often suffer from an impaired health-related quality of life (HRQoL). A healthier lifestyle not only extends individuals' lengths of life but might also improve their HRQoL. The aim of this study was to explore the relation between self-reported lifestyle changes and HRQoL in European coronary patients.MethodsData on 8745 coronary patients, from 22 countries, participating in the EUROASPIRE III survey (2006-2007) were used. These patients hospitalized for coronary artery bypass graft, percutaneous coronary intervention, acute myocardial infarction, or myocardial ischaemia were interviewed and examined at least 6 months and no later than 3 years after their hospital admission to gather information on their HRQoL, self-reported lifestyle changes, and risk factors.ResultsSignificantly better HRQoL scores were found in ex-smokers compared to current smokers. Patients who made an attempt to increase their physical activity level had a better HRQoL compared to those who had not made an attempt. Furthermore dietary changes were associated with HRQoL, with better outcomes in patients who tried to reduce fat and salt intake and increase fish, fruit, and vegetable intake. The intention to change behaviour was not associated with HRQoL.ConclusionsBetter HRQoL scores were found in those coronary patients who adopted a healthier lifestyle. The actual lifestyle changes - smoking cessation, increasing physical activity, and adopting a healthy diet - and not the intention to change are associated with better HRQoL outcomes.</p>

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<author>Delphine De Smedt et al.</author>


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<title>Screening for depression in medical research: ethical challenges and recommendations.</title>
<link>http://epubs.rcsi.ie/psycholart/53</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/53</guid>
<pubDate>Mon, 14 Jan 2013 06:52:11 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Due to the important role of depression in major illnesses, screening measures for depression are commonly used in medical research. The protocol for managing participants with positive screens is unclear and raises ethical concerns. The aim of this article is to identify and critically discuss the ethical issues that arise when a positive screen for depression is detected, and offer some guidance on managing these issues. DISCUSSION: Deciding on whether to report positive screens to healthcare practitioners is both an ethical and a pragmatic dilemma. Evidence suggests that reporting positive depression screens should only be considered in the context of collaborative care. Possible adverse effects, such as the impact of false-positive results, potentially inappropriate labelling, and potentially inappropriate treatment also need to be considered. If possible, the psychometric properties of the selected screening measure should be determined in the target population, and a threshold for depression that minimises the rate of false-positive results should be chosen. It should be clearly communicated to practitioners that screening scores are not diagnostic for depression, and they should be informed about the diagnostic accuracy of the measure. Research participants need to be made aware of the consequences of the detection of high scores on screening measures, and to be fully informed about the implications of the research protocol. SUMMARY: Further research is needed and the experiences of researchers, participants, and practitioners need to be collated before the value of reporting positive screens for depression can be ascertained. In developing research protocols, the ethical challenges highlighted should be considered. Participants must be agreeable to the agreed protocol and efforts should be made to minimise potentially adverse effects.</p>

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<author>Aisling M. Sheehan et al.</author>


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<title>Secular trends in child and adult sexual violence--one decreasing and the other increasing: a population survey in Ireland.</title>
<link>http://epubs.rcsi.ie/psycholart/52</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/52</guid>
<pubDate>Wed, 09 Jan 2013 04:05:29 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Sexual violence is a worldwide problem affecting children and adults. Knowledge of trends in prevalence is essential to inform the design and evaluation of preventive and intervention programmes. We aimed to assess the prevalence of lifetime sexual violence for both sexes and to document the prevalence of adult and child abuse by birth year in the general population.</p>
<p>METHODS: National cluster-randomized telephone interview study of 3120 adults in Ireland was done.</p>
<p>RESULTS: Child sexual abuse involving physical contact was reported by 20% of women and 16% of men. In adulthood, figures were 20% and 10% for women and men, respectively. Prevalence of any form of sexual violence across the lifespan was 42% (women) and 38% (men). Analysis by year of birth indicated a curvilinear pattern for child sexual abuse with lower prevalence in the oldest and youngest participants. Sexual violence in young adulthood showed a linear pattern with higher prevalence in the youngest participants.</p>
<p>CONCLUSION: The trend of lower rates of experience of child sexual abuse in younger adults in the sample is in keeping with findings from other countries. The trend of higher rates of adult sexual violence in younger adults is worrying, particularly since the same participants reported less experience of child sexual abuse than the preceding generations. There is a paucity of international data addressing the issue of cohort differences in exposure to sexual violence. Within-study analysis, and follow-up studies designed to maximize replicability, are needed to inform discussion about societal trends in different types of sexual violence.</p>

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</description>

<author>Hannah McGee et al.</author>


<category>Adolescent</category>

<category>Adult</category>

<category>Age Factors</category>

<category>Aged</category>

<category>Child Abuse, Sexual</category>

<category>Cohort Studies</category>

<category>Female</category>

<category>Humans</category>

<category>Ireland</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Prevalence</category>

<category>Sex Factors</category>

<category>Sex Offenses</category>

<category>Young Adult</category>

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<title>Health related quality of life in coronary patients and its association with their cardiovascular risk profile: Results from the EUROASPIRE III survey.</title>
<link>http://epubs.rcsi.ie/psycholart/51</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/51</guid>
<pubDate>Tue, 11 Dec 2012 03:35:09 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Cardiovascular patients are likely to have an impaired health-related quality of life (HRQoL) due to functional and psycho-social limitations. The main objective of this study was to assess the distribution of HRQoL scores in coronary heart disease (CHD) patients across 22 European countries and to identify factors associated with the variation between patients. METHODS: Data from the EUROASPIRE III survey (European Action on Secondary and Primary Prevention by Intervention to Reduce Events), on 8734 patients, were used. Patients with a diagnosis of CHD (coronary artery bypass graft (CABG), percutaneous coronary intervention (PCI), acute myocardial infarction (AMI) or myocardial ischemia) were interviewed and examined at least 6months after their acute coronary event. Quality of life of each patient was measured using 2 standardized questionnaires: the EuroQoL-5D (EQ-5D) and the 12-item short-form health survey (SF-12v2). RESULTS: HRQoL values differed significantly across countries. Lower HRQoL estimates were found in women, older patients, less educated patients, patients with myocardial infarction or ischemia as recruiting diagnosis, patients with a history of stroke and patients who suffered from a recurring CHD event. In addition, HRQoL was significantly associated with current smoking, central obesity, lack of exercise and inappropriate HbA1c control in patients with diabetes. Furthermore the number of risk factors is inversely associated with HRQoL. CONCLUSION: Overall, a large heterogeneity was observed in HRQoL values between countries and patient groups. There seems to be a significant association between quality of life and patient characteristics with lifestyle risk factors as important determinants of HRQoL.</p>

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<author>Delphine De Smedt et al.</author>


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<title>The Hospital Anxiety and Depression Scale: A meta confirmatory factor analysis</title>
<link>http://epubs.rcsi.ie/psycholart/50</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/50</guid>
<pubDate>Wed, 21 Nov 2012 02:36:57 PST</pubDate>
<description>
	<![CDATA[
	<p>Objective: To systematically evaluate the latent structure of the Hospital Anxiety and Depression Scale (HADS) through reanalysis of previous studies and meta confirmatory factor analysis (CFA).</p>
<p>Method: Data from 28 samples were obtained from published studies concerning the latent structure of the HADS. Ten models were considered, including eight previously identified models and two bifactor models. The fit of each model was assessed separately in each sample and by meta CFA. Meta CFA was conducted using all samples and using subgroups consisting of community samples, cardiovascular disease samples and samples from studies administering the English language version of the HADS.</p>
<p>Results: A bifactor model including all items loading onto a general distress factor and two orthogonal anxiety and depression group factors provided the best fit for the majority of samples. Meta CFA provided further support for the bifactor model with two group factors. This was the case using all samples, as well as all subgroup analyses. The general distress factor explained 73% of the covariance between items, with the (autonomic) anxiety and (anhedonic) depression factors explaining 11% and 16%, respectively.</p>
<p>Conclusion: A bifactor structure provides the most acceptable empirical explanation for the HADS correlation structure. Due to the presence of a strong general factor, the HADS does not provide good separation between symptoms of anxiety and depression. We recommend it is best used as a measure of general distress.</p>

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<author>Sam Norton et al.</author>


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<title>Community-based post-stroke service provision and challenges: a national survey of managers and inter-disciplinary healthcare staff in Ireland.</title>
<link>http://epubs.rcsi.ie/psycholart/49</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/49</guid>
<pubDate>Tue, 13 Nov 2012 04:28:28 PST</pubDate>
<description>
	<![CDATA[
	<p>ABSTRACT: BACKGROUND: The extent of stroke-related disability typically becomes most apparent after patient discharge to the community. Maximising rehabilitation input at this point can minimise the impact of disability. As part of the Irish National Audit of Stroke Care (INASC), a national survey of community-based allied health professionals and public health nurses was conducted. The aim was to document the challenges to service availability for patients with stroke in the community and to identify priorities for service improvement. METHODS: The study was a cross-sectional tailored interview survey with key managerial and service delivery staff. As comprehensive listings of community-based health professionals involved in stroke care were not available, a cascade approach to information gathering was adopted. Representative regional managers for services incorporating stroke care (N=7) and disciplinary allied health professional and public health nurse managers (N=25) were interviewed (94% response rate). RESULTS: Results indicated a lack of formal, structured community-based services for stroke, with no designated clinical posts for stroke care across disciplines nationally. There was significant regional variation in availability of allied health professionals. Considerable inequity was identified in patient access to stroke services, with greater access, where available, for older patients (>65 years). The absence of a stroke strategy and stroke prevalence statistics were identified as significant impediments to service planning, alongside organisational barriers limiting the recruitment of additional allied health professional staff, and lack of sharing of discipline-specific information on patients. CONCLUSIONS: This study highlighted major gaps in the provision of inter-disciplinary team community-based services for people with stroke in one country. Where services existed, they were generic in nature, rarely inter-disciplinary in function and deficient in input from salient disciplines. Challenges to optimal care included the need for strategic planning; increased funding of healthcare staff; increased team resources and teamwork; and removal of service provision barriers based on age. There were notably many challenges beyond funding. Similar evaluations in other healthcare systems would serve to provide comparative lessons to serve to tackle this underserved aspect of care for patients with stroke and their families.</p>

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<author>Anne Hickey et al.</author>


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<title>The validation of a French-language version of the Aging Perceptions Questionnaire (APQ) and its extension to a population aged 55 and over.</title>
<link>http://epubs.rcsi.ie/psycholart/48</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/48</guid>
<pubDate>Tue, 13 Nov 2012 03:54:06 PST</pubDate>
<description>
	<![CDATA[
	<p>UNLABELLED: ABSTRACT:</p>
<p>BACKGROUND: Several studies have shown the influence of the perceptions of aging on the cognitive functioning and the mental and physical health of older people. These relationships have not to date been studied in France where validated instruments are lacking. The primary objective of this study was to validate a French-language version of the Aging Perceptions Questionnaire (APQ) in the French general population aged 65 and over. The secondary objective was to study the stability of the dimensions of this instrument among participants aged 55 to 64.</p>
<p>METHODS: The study was proposed to the cohort of the Observatoire Régional du Vieillissement (OPREVI) (observatory of aging), located in a small town in Poitou-Charentes (western France). An anonymous questionnaire including the APQ was sent by mail to inhabitants aged 55 and over. The original English language APQ was described with adults aged 65 and older. It has 32 items distributed on 7 dimensions: timeline chronic and cyclical, positive and negative consequences, positive and negative control and emotional representations.</p>
<p>RESULTS: 656 adults participated in this survey (286 men, 370 women). Among those aged 65 and over (n = 394), the seven-factor structure estimated by confirmatory factor analysis was coherent with original findings. Internal consistency as evaluated by Cronbach alpha, was between 0.83 for consequences negative and 0.52 for control negative. Several dimensions were strongly correlated. Among participants aged 55 to 64 (n = 262), the same factorial model yielded an acceptable fit. Multi-group confirmatory factor analysis concluded to approximate factorial invariance between the two age groups with a null delta in comparative fit index.</p>
<p>CONCLUSION: This study among French people aged 65 and over, added further evidence of the multidimensional structure of the French version of the APQ which is superimposed to the dimensions of the original Irish version. The same factorial structure applies acceptably to the younger group (aged 55-64). The OPREVI study is ongoing, and will collect data on the physical, material and social characteristics of participants. It will therefore be possible to analyse the variables associated with the perceptions of aging. On the basis of an individual's perceptions of aging as captured by this questionnaire, and his or her clinical profile, tailored multi-dimensional assistance could be made available aiming to provide incentives to anticipate or to adapt to difficulties.</p>

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<author>Isabelle Ingrand et al.</author>


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<title>A 10-year (2000-2010) systematic review of interventions to improve quality of care in hospitals.</title>
<link>http://epubs.rcsi.ie/psycholart/47</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/47</guid>
<pubDate>Mon, 17 Sep 2012 08:54:51 PDT</pubDate>
<description>
	<![CDATA[
	<p>ABSTRACT: BACKGROUND: Against a backdrop of rising healthcare costs, variability in care provision and an increased emphasis on patient satisfaction, the need for effective interventions to improve quality of care has come to the fore. This is the first ten year (2000--2010) systematic review of interventions which sought to improve quality of care in a hospital setting. This review moves beyond a broad assessment of outcome significance levels and makes recommendations for future effective and accessible interventions. METHODS: Two researchers independently screened a total of 13,195 English language articles from the databases PsychInfo, Medline, PubMed, EmBase and CinNahl. There were 120 potentially relevant full text articles examined and 20 of those articles met the inclusion criteria. RESULTS: Included studies were heterogeneous in terms of approach and scientific rigour and varied in scope from small scale improvements for specific patient groups to large scale quality improvement programmes across multiple settings. Interventions were broadly categorised as either technical (n = 11) or interpersonal (n = 9). Technical interventions were in the main implemented by physicians and concentrated on improving care for patients with heart disease or pneumonia. Interpersonal interventions focused on patient satisfaction and tended to be implemented by nursing staff. Technical interventions had a tendency to achieve more substantial improvements in quality of care. CONCLUSIONS: The rigorous application of inclusion criteria to studies established that despite the very large volume of literature on quality of care improvements, there is a paucity of hospital interventions with a theoretically based design or implementation. The screening process established that intervention studies to date have largely failed to identify their position along the quality of care spectrum. It is suggested that this lack of theoretical grounding may partly explain the minimal transfer of health research to date into policy. It is recommended that future interventions are established within a theoretical framework and that selected quality of care outcomes are assessed using this framework. Future interventions to improve quality of care will be most effective when they use a collaborative approach, involve multidisciplinary teams, utilise available resources, involve physicians and recognise the unique requirements of each patient group.</p>

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<author>Mary C. Conry et al.</author>


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<title>Differential Predictive Value of Depressive Versus Anxiety Symptoms in the Prediction of 8-Year Mortality After Acute Coronary Syndrome.</title>
<link>http://epubs.rcsi.ie/psycholart/46</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/46</guid>
<pubDate>Thu, 30 Aug 2012 06:44:38 PDT</pubDate>
<description>
	<![CDATA[
	<p>ObjectiveBoth depression and anxiety have been associated with poor prognosis in patients with acute coronary syndrome (ACS). However, certain symptoms and how they are measured may be more important than others. We investigated three different scales to determine their predictive validity.MethodsPatients with ACS (N = 598) completed either the Hospital Anxiety and Depression Scales (HADS-A, HADS-D; n = 316) or the Beck Depression Inventory-Fast Screen (n = 282). Their all-cause mortality status was assessed at 8 years.ResultsDuring follow-up, 20% (121/598) of participants died. Cox proportional hazards modeling showed that the HADS-D was predictive of mortality (hazard ratio [HR] = 1.11, 95% confidence interval [CI] = 1.04-1.19), and this association remained significant after adjustment for major clinical/demographic factors, whereas the HADS-A (HR = 0.96, 95% CI = 0.85-1.09) and the Beck Depression Inventory-Fast Screen (HR = 0.99, 95% CI = 0.91-1.08) were not. The following depression items from the HADS-D predicted mortality: "I still enjoy the things I used to enjoy" (HR = 1.38, 95% CI = 1.05-1.82), "I can laugh and see the funny side of things" (HR = 1.48, 95% CI = 1.11-1.96), "I feel as if I am slowed down" (HR = 1.66, 95% CI = 1.24-2.22), and "I look forward with enjoyment to things" (HR = 1.36, 95% CI = 1.08-1.72).ConclusionsDepressive symptoms related to lack of enjoyment or pleasure and physical or cognitive slowing, as measured by the HADS-D, predicted all-cause mortality at 8 years ACS patients, whereas other depressive and anxiety symptoms did not. Whether symptoms of distress predict prognosis in ACS seems to be dependent on the measures and items used.</p>

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<author>Frank Doyle et al.</author>


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<title>The HeartQoL: Part II. Validation of a new core health-related quality of life questionnaire for patients with ischemic heart disease.</title>
<link>http://epubs.rcsi.ie/psycholart/45</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/45</guid>
<pubDate>Tue, 24 Jul 2012 07:57:34 PDT</pubDate>
<description>
	<![CDATA[
	<p>Background: Evaluation of health-related quality of life (HRQL) is important in improving the quality of patient care. The aim of this study was to determine the psychometric properties of the HeartQoL in patients with ischemic heart disease (IHD), specifically angina, myocardial infarction (MI), or ischemic heart failure.Methods: Data for the validation of the HeartQoL questionnaire were collected in (a) a cross-sectional survey and (b) a prospective substudy of patients undergoing either a percutaneous coronary intervention (PCI) or referred to cardiac rehabilitation (CR) were then analyzed to determine the reliability, validity, and responsiveness of the HeartQoL questionnaire.Results: We enrolled 6384 patients (angina, n = 2111, 33.1%; MI, n = 2351, 36.8%; heart failure, n = 1922, 30.1%) across 22 countries speaking 15 languages in the cross-sectional study and 730 patients with IHD in the prospective substudy. The HeartQoL questionnaire comprises 14-items with physical and emotional subscales and a global score (range 0-3 (poor to better HRQL). Cronbach's α was consistently ≥0.80; convergent validity correlations between similar HeartQoL and SF-36 subscales were significant (r ≥ 0.60, p < 0.001); discriminative validity was confirmed with predictor variables: health transition, anxiety, depression, and functional status. HeartQoL score changes following either PCI or CR were significant (p < 0.001) with effect sizes ranging from 0.37-0.64.Conclusion: The HeartQoL questionnaire is reliable, valid, and responsive to change allowing clinicians and researchers to (a) assess baseline HRQL, (b) make between-diagnosis comparisons of HRQL, and (c) evaluate change in HRQL in patients with angina, MI, or heart failure with a single IHD-specific HRQL instrument.</p>

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<author>Neil Oldridge et al.</author>


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<title>The HeartQoL: Part I. Development of a new core health-related quality of life questionnaire for patients with ischemic heart disease.</title>
<link>http://epubs.rcsi.ie/psycholart/44</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/44</guid>
<pubDate>Tue, 24 Jul 2012 04:17:19 PDT</pubDate>
<description>
	<![CDATA[
	<p>Background: Evaluation of health-related quality of life (HRQL) is important in improving the quality of patient care.Methods: The HeartQoL Project, with cross-sectional and longitudinal phases, was designed to develop a core ischemic heart disease (IHD) specific HRQL questionnaire, to be called the HeartQoL, for patients with angina, myocardial infarction (MI), or ischemic heart failure. Patients completed a battery of questionnaires and Mokken scaling analysis was used to identify items in the HeartQoL questionnaire.Results: We enrolled 6384 patients (angina, n = 2111, 33.1%; MI, n = 2351, 36.8%; heart failure, n = 1922, 30.1%) across 22 countries and 15 languages. The HeartQoL questionnaire comprises 14-items with 10-item physical and 4-item emotional subscales which are scored from 0 (poor HRQL) to 3 (better HRQL) with a global score if needed. The mean baseline HeartQoL global score was 2.2 (±0.5) in the total group and was different (p < 0.001) by diagnosis (MI, 2.4 ± 0.5; angina, 2.2 ± 0.6; and heart failure, 2.1 ± 0.6).Conclusion: The HeartQoL questionnaire, with global and subscale scores, has the potential to allow clinicians and researchers to (a) assess baseline HRQL, (b) make between-diagnosis comparisons of HRQL, and (c) evaluate change in HRQL in patients with angina, MI, or heart failure with a single IHD-specific HRQL instrument.</p>

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<author>Neil Oldridge et al.</author>


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<title>Validity and reliability of three commonly used Quality of Life measures in a large European population of coronary heart disease patients.</title>
<link>http://epubs.rcsi.ie/psycholart/43</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/43</guid>
<pubDate>Wed, 20 Jun 2012 07:28:01 PDT</pubDate>
<description>
	<![CDATA[
	<p>Objective: To investigate the validity and reliability of the EuroQol (EQ-5D), the Short form health survey (SF-12v2), and the Hospital Anxiety and Depression Scale (HADS) in a stable coronary population.</p>
<p>Study Design: Cross-sectional study EUROPASPIRE III</p>
<p>Setting: Quality of Life data (Qol) were available on 8745 patients hospitalized for coronary artery bypass graft (CABG), percutaneous coronary intervention (PCI) or acute myocardial infarction (AMI). They were interviewed and examined at least 6 months after their hospital admission. Reliability and validity of the 3 instruments were tested. Internal consistency, and discriminative, convergent, criterion and construct validity were assessed.</p>
<p>Results: Cronbach's alpha indicated good internal consistency for all measures (0.73 to 0.87). Discriminative validity analyses confirmed significant QoL differences between known groups: age, gender, educational level. In addition, all hypothesized correlations between QoL constructs (convergent validity) and items (criterion validity) were confirmed with significant correlations. Confirmatory factor analyses indicated good construct validity for HADS and SF-12v2. On country-specific level, results were roughly similar.</p>
<p>Conclusion: The EQ-5D as well as the SF-12v2 and the HADS are reliable and valid instruments for use in a stable coronary population, both on aggregate European level as on country-specific level. However, our results must be generalized with caution, because EUROASPIRE III patients might not be representative for all patients with stable coronary heart disease.</p>

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<author>Delphine De Smedt et al.</author>


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<title>Why the HADS is still important: Reply to Coyne &amp; van Sonderen</title>
<link>http://epubs.rcsi.ie/psycholart/42</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/42</guid>
<pubDate>Mon, 28 May 2012 02:23:39 PDT</pubDate>
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<author>Frank Doyle et al.</author>


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<title>Recruitment using mobile telephones in an Irish general population sexual health survey: challenges and practical solutions.</title>
<link>http://epubs.rcsi.ie/psycholart/41</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/41</guid>
<pubDate>Mon, 14 May 2012 06:01:06 PDT</pubDate>
<description>
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	<p>BACKGROUND: Non-coverage of households without a landline telephone is a major concern of telephone survey researchers. Sampling mobile telephone users in national surveys is vital in order to gain access to the growing proportion of households that use mobile telephones extensively or exclusively. The complex logistics of conducting surveys with mobile telephones have been discussed in the literature. This paper outlines the actual challenges encountered during a recent national sexual health survey in Ireland, which utilized a mobile telephone sampling frame to recruit approximately half of the sample.</p>
<p>METHOD: The 2010 Irish Contraception and Crisis Pregnancy Survey (ICCP-2010) is a nationally representative sample of adults aged 18-45 years living in Ireland (n = 3002; 1416 recruited by landline telephone and 1586 recruited by mobile telephone). The overall response rate for the survey was 69% (79% for the landline telephone strand; 61% for the mobile telephone strand). All interviews were conducted using computer-assisting telephone interviewing.</p>
<p>RESULTS: During the 18-week fieldwork period, five main challenges relating to the use of mobile telephones were encountered: (1) explaining to respondents how random digit dialling works in relation to mobile telephones; (2) establishing the respondent's eligibility; (3) calling the respondent with the Caller ID blocked or withheld; (4) calling the respondent when they are in any number of locations or situations; and (5) explaining to respondents the importance of refusal conversion calls for the response rate calculation. Details of how the survey protocols and procedures were monitored and adapted throughout the study to ensure a high response rate are outlined.</p>
<p>CONCLUSION: It is undeniably more challenging to recruit respondents using mobile telephones as opposed to landline telephones. Respondents are generally not familiar with being contacted on their personal mobile telephone for the purposes of being recruited for a research study. The main challenge for survey methodologists and interviewers is to devise simple protocols to explain to respondents why they are being contacted on a mobile telephone. Recommendations for survey researchers interested in using this methodological approach in the future are discussed.</p>

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<author>Orla McBride et al.</author>


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<title>Understanding communication of health information: a lesson in health literacy for junior medical and physiotherapy students</title>
<link>http://epubs.rcsi.ie/psycholart/40</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/40</guid>
<pubDate>Tue, 03 Apr 2012 03:57:22 PDT</pubDate>
<description>
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	<p>Healthcare professional students should be engaged in best practice regarding communication with patients, including using good quality patient information leaflets (PILs) on health behaviours. A cross-sectional survey of 337 junior medical and physiotherapy students investigated the readability, health psychology theory content, and quality and reliability ratings of nine international PILs on smoking. Estimates of readability, theory content and quality/reliability ratings varied considerably across PILs. Importantly, additional theory-based content, as proposed by students, had no detrimental effect on readability scores. Results are discussed with regard to their potential for improving interactions between future healthcare providers and service users.</p>

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</description>

<author>Frank Doyle et al.</author>


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<item>
<title>Predictors of utilisation of dental care services in a nationally representative sample of adults.</title>
<link>http://epubs.rcsi.ie/psycholart/39</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/39</guid>
<pubDate>Mon, 26 Mar 2012 08:45:30 PDT</pubDate>
<description>
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	<p>OBJECTIVE: The objective of this study was to identify the predictors of utilisation of dental care services in Ireland.</p>
<p>PARTICIPANTS: The 2007 Irish Survey of Lifestyle, Attitudes and Nutrition is a cross-sectional study, conducted in 2006/2007 (n = 10,364), by interviews at home to a representative sample of adults aged 18 years or over.</p>
<p>MAIN OUTCOME MEASURES: Multivariate logistic regression was used to investigate the influence of socioeconomic, predisposing and enabling factors on the odds of males and females having a dental visit in the past year.</p>
<p>RESULTS: The significant predictors of visiting the dentist in the past year were for males: having 3rd level education, employment status, earning 50,000 euros or more, location of residence, use of a car, brushing frequently, and dentition status. For females, the predictors were being between 25-34 or 55-64 years-old, education level, earning 50,000 euros or more, location of residence, use of a car, brushing frequently and dentition status.</p>
<p>CONCLUSIONS: Predictors of the use of dental services vary by gender. Predictors common to both genders were education level, higher income, location of residence, use of a car, brushing frequently and dentition status. Many of the predictors of dental visiting in the past year are also related to social inequalities in health. These predictors may be useful markers of impact for policies designed to address inequalities in access to oral health services.</p>

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<author>Helena Guiney et al.</author>


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<title>Measuring population mental health and social well-being.</title>
<link>http://epubs.rcsi.ie/psycholart/38</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholart/38</guid>
<pubDate>Thu, 22 Mar 2012 05:17:29 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVES: This paper examines the relationships between indicators of positive and negative dimensions of mental health, social well-being and physical health. METHODS: The paper reports on data collected in the third National Survey of Lifestyle, Attitudes and Nutrition (SLÁN 2007), a cross-sectional survey conducted with a representative sample of 10,364 Irish adults. The survey included measures of positive mental health and non-specific psychological distress from the SF-36 questionnaire, together with measures of social well-being, subjective health, and selected health behaviours. RESULTS: Positive mental health is predicted by lower levels of loneliness and higher levels of social support. Better self-rated health, positive health behaviours and lower GP consultation rates are associated with higher levels of positive mental health. Lower levels of social well-being, were found to be the strongest predictors of negative mental health. CONCLUSIONS: Social well-being and health behaviours correlate with both positive and negative mental health. These findings highlight the need to endorse comprehensive approaches to population mental health promotion. The inclusion of both positive and negative mental health indicators in future population health surveys is supported by the findings.</p>

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<author>Eric Van Lente et al.</author>


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