<?xml version="1.0" encoding="utf-8" ?>
<rss version="2.0">
<channel>
<title>Psychology Reports</title>
<copyright>Copyright (c) 2013 Royal College of Surgeons in Ireland All rights reserved.</copyright>
<link>http://epubs.rcsi.ie/psycholrep</link>
<description>Recent documents in Psychology Reports</description>
<language>en-us</language>
<lastBuildDate>Sat, 26 Jan 2013 22:29:00 PST</lastBuildDate>
<ttl>3600</ttl>








<item>
<title>Irish Contraception and Crisis Pregnancy Study 2010 (ICCP-2010). A Survey of the General Population.</title>
<link>http://epubs.rcsi.ie/psycholrep/50</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/50</guid>
<pubDate>Mon, 14 May 2012 05:24:36 PDT</pubDate>
<description>
	<![CDATA[
	<p>The Irish Contraception and Crisis Pregnancy Study 2010 (ICCP-2010) is a cross-sectional telephone survey of adults aged from 18 to 45 years and living in Ireland. ICCP-2010 follows on from two other national sexual health surveys: the <a href="http://epubs.rcsi.ie/psycholrep/36" target="_blank">2003 Irish Contraception and Crisis Pregnancy Study</a> (ICCP-2003) and the <a href="http://epubs.rcsi.ie/psycholrep/35" target="_blank">2006 Irish Study of Sexual Health and Relationships</a> (ISSHR). It seeks to provide: (1) data on current knowledge, attitudes and behaviours in relation to sex, contraception and pregnancy in Ireland; and (2) an opportunity to explore trends in relation to sex, contraception and pregnancy in Ireland over a number of years.</p>
<p>An overview of the main findings from ICCP-2010, as well as comparisons with ICCP- 2003, are presented in this report. Tests were conducted to explore whether differences between the two surveys were statistically significant, where appropriate, and are highlighted below and in the main report.</p>

	]]>
</description>

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


</item>






<item>
<title>Implementation of the 4th Joint Societies’ Task Force Guidelines on Cardiovascular Disease Prevention in Clinical Practice. Evaluating implementation across 13 European countries. Summary Report</title>
<link>http://epubs.rcsi.ie/psycholrep/49</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/49</guid>
<pubDate>Tue, 20 Mar 2012 03:56:08 PDT</pubDate>
<description>
	<![CDATA[
	<p>The Guidelines of the 4th Joint Societies Task Force on Cardiovascular Disease Prevention in Clinical Practice (4th JTF)* were issued in 2007, summarising and evaluating available evidence on reducing the incidence of atherosclerotic events arising from coronary heart disease, cerebrovascular disease and peripheral arterial disease. The purpose of the guidelines is to assist physicians in selecting the best strategies for managing cardiovascular disease. They are an important agreed protocol across countries and professionals that have the ultimate aim of improving outcomes from the disease. The value of these guidelines depends on the extent to which they are used by physicians in daily practice. Introducing the guidelines, the 4th JTF authors stressed that ‘implementation programmes for new guidelines form an important component of the dissemination of knowledge’.1</p>
<p>Transferring guidelines from paper into practice has proven to be frustrating for the many who endeavour to standardise the management of cardiovascular disease across Europe. The EUROASPIRE I, II and III surveys, which audited the practice of preventive cardiology in patients with coronary heart disease over a decade, illustrated that patients were not being managed to the standards set by the ESC guidelines and that limited attention was given to prevention in patients with established heart disease. Evidence of the need for more effective lifestyle management was compelling: blood pressure management remained stubbornly unchanged, and lipid targets were not achieved in almost half of patients. Other studies report disappointing levels of guideline observance among physicians; they are often unaware of recommendations given in guidelines and, even when they are, many fail to consistently apply them in treating patients.2-3 Commonly cited barriers to guideline adherence among physicians include lack of time during consultations, financial constraints and lack of confidence in patients’ motivation to comply. Physicians also find that guideline documents are difficult to translate into practice.</p>
<p>To address the gap between publication of guidelines and their use in practice, the ESC at a European level organises presentations at conferences for its member national societies and key opinion leaders. It works at a political level to promote the prevention agenda and to directly influence EU health policy, leading, for example, to the EU Commission endorsement of the European Heart Health Charter. However, such efforts must be paralleled by concerted strategies at a national level to realise implementation in the front line. The 4th JTF urged national societies to develop implementation programmes, starting with the translation of guidelines to the local language and their adaptation to the national context. It recommended that the guidelines issued by the 4th JTF be regarded as a framework from which national guidance ‘to suit local political, economic, social, and medical circumstances’ would be developed. The recalibration of the SCORE risk assessment charts to reflect mortality and risk factor distributions in individual countries as part of this adaptation was emphasised.</p>
<p>The 4th JTF saw as vital the establishment a multidisciplinary alliance of experts from national professional organisations to oversee the adaptation and to drive implementation. It was necessary that alliances would have the support of national health authorities and work with other sectors such as the medical education and business communities to advance their aims.</p>
<p>Other recommendations included:</p>
<p>An information and education programme aimed at practising doctors that would include an audit of practices and feedback. The development of supplementary materials to the guidelines, specifically electronic versions for use in hand-held devices, such as PDAs, and of A4 sheet versions of risk algorithms and treatment recommendations.</p>
<p>A population health approach addressing lifestyle risk factors in general.</p>
<p>A public information campaign explaining the concept of multiple risk assessment and treatment and intervention thresholds, as well as describing how risk can be reduced.</p>

	]]>
</description>

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


</item>






<item>
<title>Implementation of the 4th Joint Societies’ Task Force Guidelines on Cardiovascular Disease Prevention in Clinical Practice. Evaluating implementation across 13 European countries. Main report</title>
<link>http://epubs.rcsi.ie/psycholrep/48</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/48</guid>
<pubDate>Fri, 16 Mar 2012 09:57:50 PDT</pubDate>
<description>
	<![CDATA[
	<p>The Guidelines of the 4th Joint Societies Task Force on Cardiovascular Disease Prevention in Clinical Practice (4th JTF)* were issued in 2007, summarising and evaluating available evidence on reducing the incidence of atherosclerotic events arising from coronary heart disease, cerebrovascular disease and peripheral arterial disease. The purpose of the guidelines is to assist physicians in selecting the best strategies for managing cardiovascular disease. They are an important agreed protocol across countries and professionals that have the ultimate aim of improving outcomes from the disease. The value of these guidelines depends on the extent to which they are used by physicians in daily practice. Introducing the guidelines, the 4th JTF authors stressed that ‘implementation programmes for new guidelines form an important component of the dissemination of knowledge’.1</p>
<p>Transferring guidelines from paper into practice has proven to be frustrating for the many who endeavour to standardise the management of cardiovascular disease across Europe. The EUROASPIRE I, II and III surveys, which audited the practice of preventive cardiology in patients with coronary heart disease over a decade, illustrated that patients were not being managed to the standards set by the ESC guidelines and that limited attention was given to prevention in patients with established heart disease. Evidence of the need for more effective lifestyle management was compelling: blood pressure management remained stubbornly unchanged, and lipid targets were not achieved in almost half of patients. Other studies report disappointing levels of guideline observance among physicians; they are often unaware of recommendations given in guidelines and, even when they are, many fail to consistently apply them in treating patients.2-3 Commonly cited barriers to guideline adherence among physicians include lack of time during consultations, financial constraints and lack of confidence in patients’ motivation to comply. Physicians also find that guideline documents are difficult to translate into practice.</p>
<p>To address the gap between publication of guidelines and their use in practice, the ESC at a European level organises presentations at conferences for its member national societies and key opinion leaders. It works at a political level to promote the prevention agenda and to directly influence EU health policy, leading, for example, to the EU Commission endorsement of the European Heart Health Charter. However, such efforts must be paralleled by concerted strategies at a national level to realise implementation in the front line. The 4th JTF urged national societies to develop implementation programmes, starting with the translation of guidelines to the local language and their adaptation to the national context. It recommended that the guidelines issued by the 4th JTF be regarded as a framework from which national guidance ‘to suit local political, economic, social, and medical circumstances’ would be developed. The recalibration of the SCORE risk assessment charts to reflect mortality and risk factor distributions in individual countries as part of this adaptation was emphasised.</p>
<p>The 4th JTF saw as vital the establishment a multidisciplinary alliance of experts from national professional organisations to oversee the adaptation and to drive implementation. It was necessary that alliances would have the support of national health authorities and work with other sectors such as the medical education and business communities to advance their aims.</p>
<p>Other recommendations included:</p>
<p>An information and education programme aimed at practising doctors that would include an audit of practices and feedback. The development of supplementary materials to the guidelines, specifically electronic versions for use in hand-held devices, such as PDAs, and of A4 sheet versions of risk algorithms and treatment recommendations.</p>
<p>A population health approach addressing lifestyle risk factors in general.</p>
<p>A public information campaign explaining the concept of multiple risk assessment and treatment and intervention thresholds, as well as describing how risk can be reduced.</p>

	]]>
</description>

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


</item>






<item>
<title>Physical activity and core depressive symptoms in the older Irish adult population.</title>
<link>http://epubs.rcsi.ie/psycholrep/47</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/47</guid>
<pubDate>Thu, 05 Jan 2012 07:54:31 PST</pubDate>
<description>
	<![CDATA[
	<p>Research indicates that the prevalence of depression is increasing and that by 2020 depression will become the second leading cause of disease worldwide, as measured by disability adjusted life years. Interventions which involve physical activity have shown that becoming active, even at a moderate level; can be effective in treating depression. In addition, physically active individuals are less likely to develop depressive symptoms than those who are not active, making physical activity an important strategy in the prevention of ill health.</p>
<p>The aim of this study was to investigate the associations between physicalactivity levels and core depressive symptoms in Irish adults aged 50 years or more. The study used data from the Survey of Lifestyle, Attitudes and Nutrition (SLÁN) 2007, a national survey of individuals living in the Republic of Ireland (n=4,255 adults aged 50 years or older) and The Northern Ireland Health and Social Wellbeing Survey (NIHSWS), 2005-2006, a survey of individuals living in Northern Ireland (n=1,904 adults aged 50 years or older).</p>
<p>Measures of depressed mood and anhedonia (two core depressive symptoms according to diagnostic criteria (DSM IV)) were derived using items from the surveys. Physical activity patterns were categorised using the International Physical Activity Questionnaire (IPAQ) Short Form (Craig et al. 2003). Demographic factors (age, gender and social class), smoking status and health service use were also considered.</p>
<p>Just over 5% (5.4%) of SLÁN 2007 participants and 11.1% of NIHSWS 2005-2006 participants had experienced both depressed mood and anhedonia in the recent past. In the overall sample this was 7.2% of participants. Overall 45% of participants reported being moderately physically active but 36.6% of participants reported activity at low levels (SLÁN 2007: 35.6%; NIHSWS 2005-2006: 38.8%). For the overall sample, depressive symptoms were negatively associated with being male, being older and high levels of physical activity. Depressive symptoms were significantly and positively associated with being separated/divorced or widowed, and social classes 3-6. Overall, people over 50 years who were engaged in moderate to high levels of physical activity had a 50-56% reduction in the odds of having elevated depressive symptoms.</p>
<p>Consistent with other research findings, this study suggests that physical activity levels are strongly associated with depressive symptoms. Increasing levels of physical activity among adults over 50 years has the potential to improve mental health.</p>

	]]>
</description>

<author>Karen Morgan et al.</author>


</item>






<item>
<title>Pathways to child hospitalization : psychological, social and medical factors associated with the admission to hospital of children with gastroenteritis : a study of mothers and doctors.</title>
<link>http://epubs.rcsi.ie/psycholrep/46</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/46</guid>
<pubDate>Tue, 20 Sep 2011 06:49:58 PDT</pubDate>
<description>
	<![CDATA[
	<p>Gastroenteritis is a common self-limiting illness of childhood. Hospital treatment, except in severe cases, involves treatment which is the same as that given at home on medical advice or on parents' own knowledge. Nevertheless, in Ireland over 2,000 young children are hospitalized annually with this diagnosis. The objective of this study was to examine the reasons for the hospitalization of young children with gastroenteritis, with a view to decreasing the incidence of medically unnecessary admissions.</p>
<p>Doctors and mothers were interviewed. For GPs and Casualty. Doctors (the primary providers of the medical management of gastroenteritis), management decisions and the factors influencing them were systematically evaluated. Family and home circumstances of children hospitalized for gastroenteritis were compared with the circumstances of families managing gastroenteritis at home. Combining the two sources of information the major role of the individual doctor in the management of gastroenteritis emerged. The findings of the present study indicate that there is considerable scope for improvement in present. gastroenteritis management. Possible improvements have been suggested at the level of GPs' and mothers' management, and at the level of management intermediate between the GP and hospitalization. These suggestions have been made in the light of the current situation in health care in Ireland.</p>
<p>The report consists of four main sections. The problem of gastro- enteritis as it is relevant to this study is outlined in Section I. The background and the research work concerning doctors and their decision-making is presented in the next section (Section 2 ) . Following this is a detailed comparison of the child and family circumstances of those with gastroenteritis who have been managed at home and in hospital (Section 3). The final section (Section 4) presents information on the most fruitful alternatives to hospitalization as suggested by study findings and the current Irish situation. An executive summary of the main findings of the study is provided at the beginning of the report.</p>

	]]>
</description>

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


</item>






<item>
<title>Fifty plus in Ireland 2011: First results from The Irish Longitudinal Study on Ageing (TILDA)</title>
<link>http://epubs.rcsi.ie/psycholrep/45</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/45</guid>
<pubDate>Fri, 01 Jul 2011 08:45:36 PDT</pubDate>
<description>
	<![CDATA[
	<p>The Irish Longitudinal Study on Ageing (TILDA) is a large-scale, nationally representative study of people aged 50 and over in Ireland. It is the most ambitious study of ageing ever carried out in Ireland and represents a step-change in terms of data, knowledge and understanding of ageing with which to inform policy and novel research. TILDA is designed to maximise comparability with other well-established international longitudinal studies. More than 8,000 people aged 50 and over accepted the invitation to participate in the first wave of TILDA, and the majority of these also agreed to undertake a comprehensive health assessment.</p>

	]]>
</description>

<author>Alan Barrett et al.</author>


</item>






<item>
<title>The Irish Study of Sexual Health and Relationships Summary Report</title>
<link>http://epubs.rcsi.ie/psycholrep/44</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/44</guid>
<pubDate>Fri, 15 Apr 2011 01:50:09 PDT</pubDate>
<description>
	<![CDATA[
	<p>This study was commissioned by the Department of Health and Children and the Crisis Pregnancy Agency (CPA) in response to a recommendation of the National AIDS Strategy Committee.The Crisis Pregnancy Agency became involved in the project in the lightof international evidence showing that aspects of sexual health, such as contraception, crisis pregnancy and sexually transmitted infections, should be examined jointly. The study builds upon the already extensive research conducted by the CPA since its establishment. The CPA and the Department of Health and Children funded this research because the sexual health sector needs robust and comprehensive data to effectively plan sexual health policies and strategies and to inform effective approaches to promoting positive sexual health messages. The findings of this report will be considered by various organisations and will inform the future development and strategic direction of the CPA’s work in reducing the number of crisis pregnancies. The report will also provide valuable and sought-after information for individuals, organisations and policymakers working to prevent and manage crisis pregnancy and sexually transmitted infections in Ireland. It will contribute to the development of a national sexual and reproductive health strategy.</p>

	]]>
</description>

<author>Richard Layte et al.</author>


</item>






<item>
<title>The Irish Study of Sexual Health and Relationships Sub-Report 3: Sexual Knowledge, Attitudes and Behaviours - A Further Analysis.</title>
<link>http://epubs.rcsi.ie/psycholrep/43</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/43</guid>
<pubDate>Thu, 14 Apr 2011 04:48:12 PDT</pubDate>
<description>
	<![CDATA[
	<p>The ISSHR was commissioned by the Department of Health and Children and the Crisis Pregnancy Agency in response to a recommendation by the National AIDS Strategy Committee. It is the largest nationally representative study on sexual knowledge, attitudes and behaviour ever undertaken in Ireland.</p>
<p>International evidence indicates that aspects of sexual health, such as contraception, crisis pregnancy and sexually transmitted infections, should be examined jointly. To this end, the Crisis Pregnancy Agency and the Department of Health and Children instigated the ISSHR project.</p>
<p>The ISSHR findings have been outlined in a suite of reports – the Main Report, a Summary Report and three sub-reports; the latter provide detailed information in defined areas of interest. This, the third sub-report, focuses on the patterning of sexual knowledge and attitudes of people in Ireland and how these affect behaviour.</p>
<p>The Crisis Pregnancy Agency (CPA) and the sexual-health sector in general need robust evidence in order to develop sexual-health policies, to plan strategies and to inform the effective promotion of sexual-health messages. The ISSHR findings will be invaluable not only to the work of the CPA in preventing crisis pregnancy, but also to that of other organisations concerned with promoting sexual health, providing sexual-health services, preventing sexually transmitted infections, and providing sex education for young people.</p>

	]]>
</description>

<author>Grainne Cousins et al.</author>


</item>






<item>
<title>The Irish Study of Sexual Health and relationships Sub-Report 2: Sexual Health Challenges and Related Service Provision</title>
<link>http://epubs.rcsi.ie/psycholrep/42</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/42</guid>
<pubDate>Thu, 14 Apr 2011 04:24:38 PDT</pubDate>
<description>
	<![CDATA[
	<p>The ISSHR was commissioned by the Department of Health and Children and the Crisis Pregnancy Agency in response to a recommendation by the National AIDS Strategy Committee. It is the largest nationally representative study of sexual knowledge, attitudes and behaviour ever undertaken in Ireland.</p>
<p>International evidence indicates that aspects of sexual health, such as contraception, crisis pregnancy and sexually transmitted infections, should be examined jointly. To this end, the Crisis Pregnancy Agency and the Department of Health and Children instigated the ISSHR.</p>
<p>The ISSHR findings have been outlined in a suite of reports – the Main Report, the Summary Report and three sub-reports; the latter provide detailed information in defined areas of interest. This, the second sub-report, focuses on the area of sexual risk-taking and the use of relevant services.</p>
<p>The Crisis Pregnancy Agency (CPA) and the sexual-health sector in general need robust evidence in order to develop sexual-health policies, to plan strategies and to inform the effective promotion of sexual-health messages. The ISSHR findings will be invaluable not only to the work of the CPA in preventing crisis pregnancy, but also to that of other organisations concerned with promoting sexual health , providing sexual-health services, preventing sexually transmitted infections, and providing sex education for young people.</p>

	]]>
</description>

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


</item>






<item>
<title>The Irish Study of Sexual Health and Relationships Sub-Report 1: Learning About Sex and First Sexual Experiences</title>
<link>http://epubs.rcsi.ie/psycholrep/41</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/41</guid>
<pubDate>Thu, 14 Apr 2011 04:02:29 PDT</pubDate>
<description>
	<![CDATA[
	<p>The ISSHR was commissioned by the Department of Health and Children and the Crisis Pregnancy Agency in response to a recommendation by the National AIDS Strategy Committee. It is the largest nationally representative studyof sexual knowledge, attitudes and behaviour ever undertaken in Ireland.</p>
<p>International evidence indicates that aspects of sexual health, such as contraception, crisis pregnancy and sexually transmitted infections, should be examined jointly. To this end, the Crisis Pregnancy Agency and the Department of Health and Children instigated the ISSHR project.</p>
<p>The ISSHR findings have been outlined in a suite of reports – the Main Report, a Summary Report and three sub-reports; the latter provide detailed information in defined areas of interest. This, the first sub-report, focuses on the area of sexual learning and first sexual experiences.</p>
<p>The Crisis Pregnancy Agency (CPA) and the sexual-health sector in general need robust evidence in order to develop sexual-health policies, to plan strategies and to inform the effective promotion of sexual-health messages. The ISSHR findings will be invaluable not only to the work of the CPA in preventing crisis pregnancy, but also to that of other organisations concerned with promoting sexual health, providing sexual-health services, preventing sexually transmitted infections, and providing sex education for young people.</p>

	]]>
</description>

<author>Kay Rundle et al.</author>


</item>






<item>
<title>The Schedule for the Evaluation of Individual Quality of Life (SEIQoL): a Direct Weighting procedure for Quality of Life Domains (SEIQoL-DW). Administration Manual.</title>
<link>http://epubs.rcsi.ie/psycholrep/40</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/40</guid>
<pubDate>Mon, 07 Feb 2011 08:03:37 PST</pubDate>
<description>
	<![CDATA[
	<p>The Schedule for the Evaluation of Individual Quality of Life (SEIQoL) is an interviewbased instrument for the assessment of quality of life (QoL) of the individual. The interview procedure associated with the full version of the SEIQoL (McGee et al, 1991; O’Boyle et al, 1992) requires considerable time to complete (10-20 minutes) and thus may be primarily suitable for research settings or clinical situations where the instrument is being used as part of the process of having the individual consider a range of options or outcomes in evaluating QoL. The SEIQoL has been used with a variety of patient groups, but its applicability may be limited in illnesses which impair cognitive functioning or motivational state. Successful completion of the SEIQoL requires, inter alia, insight into the factors which determine one’s quality of life, the ability to think abstractly and the ability to make judgments based on information presented in diagrammatic form. Therefore, its use with patients in whom these abilities are impaired may be problematic (Coen et al, 1993). A direct weighting procedure for QoL domains that is more suitable for routine clinical use than Judgment Analysis (JA) and that may impose fewer demands on individuals with reduced cognitive function, has been developed for the SEIQoL. Psychometric information on the procedure has been obtained from a healthy adult population (Browne et al, in preparation).</p>

	]]>
</description>

<author>Ciaran O&apos;Boyle et al.</author>


</item>






<item>
<title>The Schedule for the Evaluation of Individual Quality of Life (SEIQoL). Administration Manual.</title>
<link>http://epubs.rcsi.ie/psycholrep/39</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/39</guid>
<pubDate>Mon, 07 Feb 2011 07:48:51 PST</pubDate>
<description>
	<![CDATA[
	<p>Advances in the clinical sciences this century have resulted in an impressive range of diagnostic procedures, therapies, drugs and surgical techniques which have revolutionised the management of heretofore fatal conditions. In addition to being concerned about life expectancy, people are also concerned about the quality of their lives. Partly in response to the views of patients, assessment of patient Quality of Life (QoL) is becoming increasingly important in medicine, nursing and in the behavioural sciences. It has already become an important outcome variable in assessing the impact of disease, illness and treatment (Spilker, 1990; Walker and Rosser, 1993; Bowling 1991; O'Boyle, 1992).</p>
<p>QoL is a multi-dimensional construct and there are various approaches to its evaluation. The approach varies depending on the aims of the exercise. Health economists, for example, use techniques such as the QALY (Quality Adjusted Life Year), standard gamble and time-trade-off techniques in order to incorporate QoL measures into economic analysis and clinical trials. Clinical research has utilised standardised and disease specific measures, usually in the form of questionnaires, in order to determine the impact of disease and treatment on patients' QoL. One of the problems of conducting research in this area is that there is no single agreed definition of QoL nor is there a single 'gold standard' measurement technique. However, there is broad agreement that studies of health related QoL should include assessments of physical functioning, including somatic sensations such as physical symptoms and pain; psychological function including concentration and mood; social and sexual functioning and occupational status. Many researchers also assess patients' global satisfaction and the economic impact of the condition.</p>
<p>While QoL scales and questionnaires, as well as the methods of rating and analysing them, have been developed by assessing the QoL of individuals, the specific items and the response categories do not represent the free choice of individuals who are subsequently investigated using the scale. Furthermore, the measures will often have been standardised in samples other than those currently being assessed. Results are generally presented as group statistics and provide little or no data on the QoL of individual patients.</p>

	]]>
</description>

<author>Ciaran O&apos;Boyle et al.</author>


</item>






<item>
<title>Review of Health Services Available for Persons who Contracted Hepatitis C through the Administration within the State of Blood or Blood Products. Implementation of Recommendations.</title>
<link>http://epubs.rcsi.ie/psycholrep/38</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/38</guid>
<pubDate>Thu, 27 Jan 2011 03:47:05 PST</pubDate>
<description>
	<![CDATA[
	<p>the State of infected blood and blood products. The Report examines progress on the recommendations published in 2000, and recognizes the evolution in service needs since then with the addition of 4 new recommendations. The Report will assist health service providers, the Department of Health and Children and the support groups to continue working together to ensure that the future service needs of this Hepatitis C group are met. It is timely that this review has come at a time when the health services are entering a new phase of restructuring and renewal. The Consultative Council welcomes this process and is confident that it will bring benefits to both service users and service providers. The Council has assured the Health Service Executive and the National Hospitals Office that we will be happy to co-operate with them and to continue playing a positive role in shaping Hepatitis C services for this cohort of patients in the future. As with the first Review the four support groups - Positive Action, Transfusion Positive, the Irish Haemophilia Society and the Irish Kidney Association - all of which are represented on the Consultative Council, are to be commended for the important role they play, and for encouraging their members to participate in this progress report.</p>

	]]>
</description>

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


</item>






<item>
<title>Irish contraception and Crisis Pregnancy [ICCP] Study. A Survey of the General Population. Summary</title>
<link>http://epubs.rcsi.ie/psycholrep/37</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/37</guid>
<pubDate>Thu, 27 Jan 2011 02:28:20 PST</pubDate>
<description>
	<![CDATA[
	<p>Crisis pregnancy is a complex challenge for individuals and societies alike. Its prevention and management need to be informed by up-to-date and locally applicable information on knowledge, attitudes and behaviours concerning sexual practices and contraception. Studies of aspects of sexual health in Ireland offer the prospect of vastly increasing our understanding of the pattern of health behaviours in the area of sexuality and their relationship to both the attitudes/beliefs and socio-demographic characteristics of individuals. Such surveys can also provide guidelines on where and how to intervene to improve sexual health outcomes. They offer a benchmark against which to gauge success and to plan for future work in the area of sexual health promotion in Ireland. A number of recent Government initiatives have highlighted the need for national data on sexual health issues. In October 2001, the Government established the Crisis Pregnancy Agency (CPA). Its primary focus is the development of a strategy to deal with crisis pregnancy, and more specifically to provide for: • a reduction in the number of crisis pregnancies by the provision of education, advice and contraceptive services • a reduction in the number of women with crisis pregnancies who opt for abortion by offering services and supports which make other options more attractive • the provision of counselling and medical services after crisis pregnancy. (Statutory Instrument No. 446, 2001) Information on contraceptive and crisis pregnancy service availability and utilisation, and on antecedents of crisis pregnancy, is needed for the optimal planning and evaluation of services. Research findings can provide evidence-based recommendations for planning and development of appropriate initiatives.</p>

	]]>
</description>

<author>Kay Rundle et al.</author>


</item>






<item>
<title>Irish Contraception and Crisis Pregnancy [ICCP] Study. A Survey of the General Population.</title>
<link>http://epubs.rcsi.ie/psycholrep/36</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/36</guid>
<pubDate>Wed, 26 Jan 2011 04:38:27 PST</pubDate>
<description>
	<![CDATA[
	<p>Crisis pregnancy is a complex challenge for individuals and societies alike. Its prevention and management need to be informed by up-to-date and locally applicable information on knowledge, attitudes and behaviours concerning sexual practices and contraception. Studies of aspects of sexual health in Ireland offer the prospect of vastly increasing our understanding of the pattern of health behaviours in the area of sexuality and their relationship to both the attitudes/beliefs and socio-demographic characteristics of individuals. Such surveys can also provide guidelines on where and how to intervene to improve sexual health outcomes. They offer a benchmark against which to gauge success and to plan for future work in the area of sexual health promotion in Ireland. A number of recent Government initiatives have highlighted the need for national data on sexual health issues. In October 2001, the Government established the Crisis Pregnancy Agency (CPA). Its primary focus is the development of a strategy to deal with crisis pregnancy, and more specifically to provide for: • a reduction in the number of crisis pregnancies by the provision of education, advice and contraceptive services • a reduction in the number of women with crisis pregnancies who opt for abortion by offering services and supports which make other options more attractive • the provision of counselling and medical services after crisis pregnancy. (Statutory Instrument No. 446, 2001) Information on contraceptive and crisis pregnancy service availability and utilisation, and on antecedents of crisis pregnancy, is needed for the optimal planning and evaluation of services. Research findings can provide evidence-based recommendations for planning and development of appropriate initiatives. Aim of the present study The aim of the present study was to establish nationally representative data on current attitudes, knowledge and experience of contraception, crisis pregnancy and related services in Ireland. More specifically, the research aimed to provide nationally representative data on: - current attitudes, knowledge and experience of crisis pregnancy and crisis pregnancy supports and services - current attitudes, knowledge and experience of contraception and contraceptive services - current attitudes and experiences of sex, crisis pregnancy, options facing those in crisis pregnancy and lifestyle choices - current awareness, recognition and understanding of the Crisis Pregnancy Agency's Positive Options public information campaign.</p>

	]]>
</description>

<author>Kay Rundle et al.</author>


</item>






<item>
<title>The Irish Study of Sexual Health and Relationships Main Report</title>
<link>http://epubs.rcsi.ie/psycholrep/35</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/35</guid>
<pubDate>Tue, 25 Jan 2011 10:10:52 PST</pubDate>
<description>
	<![CDATA[
	<p>SEX and sexuality are core dimensions of the human experience and an important determinant of well-being. An individual’s sexual behaviour and sexual health cannot be separated from their social and cultural context. This is brought out in the World Health Organisation’s (WHO) definition of sexual health. It is concerned not just with the absence of disease or dysfunction but with a broad definition of health: “Sexual health requires a positive and respectful approach to sexuality and sexual relationships, as well as the possibility of having pleasurable and safe sexual experiences, free of coercion, discrimination and violence.” Nonetheless, sexual behaviour can have serious consequences for physical health. These have been the subject of growing concern: Rates of sexually transmitted infections have increased by over 250% in Ireland since the mid-1990s.2 HIV notifications have increased by 243% between 1998 and 2003. Research by the Crisis Pregnancy Agency also shows that around a quarter of women who have been pregnant have experienced a ‘crisis’ pregnancy, a figure which rises to over half of all women under 26 who have been pregnant. These worrying developments demand a coordinated policy response, yet in Ireland this response has been undermined by a lack of detailed information on sexual partnerships, practices and use of contraception and protection, and the manner in which these are related to sexual attitudes, knowledge and beliefs. Research on sex in Ireland has been mainly confined to the study of sexual attitudes. Representative sources of data on sexual behaviours include: • a limited module on sexual behaviours in the 1994 International Social Survey Project • an analysis of contraceptive behaviour in the ICCP Survey • an analysis of general sexual activity, contraception and condom use using the 1998 and 2002 Slán surveys The availability or lack of representative and detailed data has an impact on the policy response. The Irish Study of Sexual Health and Relationships (ISSHR) was designed to fill the need for data. This report is one of four that detail the findings of the study. This report provides a general overview of the main findings from the ISSHR Survey. ISSHR Sub-Report 1: ‘Learning About Sex and First Sexual Experiences’ provides more detailed findings on how individuals learn about sex and on their first sexual experiences. ISSHR Sub-Report 2: ‘Sexual Health Challenges and Related Service Provision’ provides more in-depth analyses of sexual health challenges such as STIs and crisis pregnancy as well as examining associated service use. ISSHR Sub-Report 3: ‘Contemporary Sexual Knowledge, Attitudes and Behaviours in Ireland’ provides a detailed examination of contemporary Irish sexual knowledge and attitudes, and the manner in which these are related to behaviours. The ISSHR project and accompanying reports emerged from a series of developments over a number of years. In almost all countries where knowledge, attitude and behaviour (KAB) surveys have been carried out, public-health concerns have provided the impetus and legitimation for these. To a certain extent this has been true for Ireland. However, the ISSHR project, overall, emerged from a broader set of concerns and interests, such as: Chapter 1: Introducing the Irish Study of Sexual Health and Relationships • the development and findings of sexual knowledge, attitude and behaviour surveys (KABS) in other countries over the last two decades • the deliberations and recommendations of the National AIDS Strategy Committee (NASC) • a scoping study for an Irish KAB carried out in 2003 • the establishment, mandate and interests of the Crisis Pregnancy Agency in October 2001 These different influences together led to the commissioning in December 2003 of a national KAB survey for Ireland. These influences will be examined in more detail in the second section of this chapter. The chapter’s third section examines the importance of the Irish context for understanding the results of the ISSHR survey. Sexual knowledge, attitudes and behaviours can only be understood within the history and culture of an Ireland that has changed radically in recent decades. The fourth section examines the issue of socio-economic differences in health and their role in shaping sexual knowledge, attitudes and behaviours. The fifth section briefly discusses Irish legislation on sexual issues and, more importantly, how this has changed in recent decades. The sixth and last section outlines the structure of the rest of the report and briefly summarises the issues examined in the next 11 chapters.</p>

	]]>
</description>

<author>Richard Layte et al.</author>


</item>






<item>
<title>Review of health services available for persons who contracted Hepatitis C through the administration within the state of blood or blood products</title>
<link>http://epubs.rcsi.ie/psycholrep/34</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/34</guid>
<pubDate>Tue, 11 Jan 2011 07:30:52 PST</pubDate>
<description>
	<![CDATA[
	<p>Hepatitis C is a relatively common blood-borne infectious disease. It has been estimated that 3% of the world’s population is infected. Hepatitis C accounts for about 20% of cases of acute hepatitis and 70% of cases of chronic hepatitis. Its importance is that it is a major cause of cirrhosis and hepatocellular cancer1. End-stage liver disease secondary to hepatitis C virus infection is main reason for liver transplantation. Following the discovery in February 1994 that anti-D immunoglobulin manufactured by the Irish Blood Transfusion Service Board was infected with hepatitis C, a number of screening programmes were put in place to identify those persons who had been infected, either directly or indirectly. It is estimated that about 1,600 persons have been infected with hepatitis C through the administration of blood and blood products in the Republic of Ireland. Acute hospital services for persons diagnosed positive for hepatitis C were put in place in 1994 in specialist hepatology (liver) units at six designated hospitals: Beaumont Hospital, the Mater Hospital, St Vincent’s Hospital, Elm Park, and St James’s Hospital in Dublin, Cork University Hospital, and University College Hospital in Galway. More recently, St Luke’s Hospital in Kilkenny has been included in the list of hospitals funded to provide specialist hepatology services. These services, provided under the Health Act (1970), are free of charge and include access to both in-patient and out-patient treatment as required. On 23 September 1996, the Health (Amendment) Act (1996) came into effect. This legislation provided statutory entitlement to a range of primary health care services, free of charge, to persons who have contracted hepatitis C from the receipt of a blood product or blood transfusion. The services provided include general practitioner services, medicines, home nursing services, home support services, dental, opthalmic, and aural services, as well as counselling services. At the request of the then Minister for Health, each health board appointed a liaison officer to ensure the efficient delivery of services under the Act, and to serve as a contact point for individuals and various interest groups whose members can avail of services under the Act. A Health Care Package for secondary services was also agreed between Positive Action and the Department of Health and Children in 1995. This covered entitlements to hospital treatments and sought to ensure sufficient funding, staffing, and facilities to provide high quality and appropriate secondary care services to those requiring them as a consequence of hepatitis C.</p>

	]]>
</description>

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


</item>






<item>
<title>CPR 4 Schools Evaluation Study Report</title>
<link>http://epubs.rcsi.ie/psycholrep/33</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/33</guid>
<pubDate>Thu, 11 Nov 2010 07:10:53 PST</pubDate>
<description>
	<![CDATA[
	<p>CPR 4 Schools is an ambitious training programme developed by the Irish Heart Foundation (IHF) to equip post-primary school students with cardiopulmonary resuscitation (CPR) skills. In the 2008–09 school year, a pilot of the programme was rolled out to 27,000 Transition Year students. The programme is one element of the IHF’s strategy to improve survival rates from sudden cardiac arrest, which causes an estimated 5,000 deaths in Ireland every year. Most of these deaths occur at home. If there is a witness, it is most often a relative.</p>

	]]>
</description>

<author>Helen Burke et al.</author>


</item>






<item>
<title>Changing Cardiovascular Health. National Cardiovascular Health Policy 2010-2019</title>
<link>http://epubs.rcsi.ie/psycholrep/32</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/32</guid>
<pubDate>Wed, 23 Jun 2010 08:19:17 PDT</pubDate>
<description>
	<![CDATA[
	<p>The Cardiovascular Health Policy Group was established with the following terms of reference:</p>
<p>Having regard to the audit of the implementation of the cardiovascular health strategy, Building Healthier Hearts, and the audit of stroke services, Irish National Audit of Stroke Care, and consistent with developments in relation to the management of chronic diseases and the Primary Care Strategy, to develop a policy framework for the prevention, detection and treatment of cardiovascular disease, including stroke and peripheral arterial disease, which will ensure an integrated and quality-assured approach in their management.</p>
<p>This new cardiovascular policy, Changing Cardiovascular Health covering the period 2010-2019, comes a decade after the first national cardiovascular health strategy, entitled Building Healthier Hearts, was published by the Department of Health in 1999. The new policy is timely given the pace of scientific discovery and related changes in medical practice, changes in health service structures, and patterns and influences on population health behaviours in Ireland over the decade. Cardiovascular health and its maintenance is a microcosm of health more generally. A policy that can improve cardiovascular health and cardiovascular disease management will have beneficial effects for the whole healthcare system and population.</p>

	]]>
</description>

<author>Department of Health &amp; Children, Ireland et al.</author>


</item>






<item>
<title>Health Service Executive Emergency Departments. Patient Profiles, Experiences and Perceptions. Report of a National Survey among people who attended during 2006.</title>
<link>http://epubs.rcsi.ie/psycholrep/31</link>
<guid isPermaLink="true">http://epubs.rcsi.ie/psycholrep/31</guid>
<pubDate>Thu, 04 Mar 2010 04:16:09 PST</pubDate>
<description>
	<![CDATA[
	<p>Ireland has 53 publicly funded acute hospitals, 35 of which have Emergency Departments. Every day these Emergency Departments see an average of 3,300 people, the majority of whom are treated there and then and discharged without the need for in-patient admission. To better understand the service user or patients’ experience of the service, the HSE contracted an independent research company to survey, by computer aided telephone interview, 1,600 representative members of the public who had used Emergency Departments during 2006. The aim of the survey was to ask patients about their experience of attending an Emergency Department and to learn from their experiences as a basis for making improvements that matter to patients.</p>

	]]>
</description>

<author>Health Services Research Centre et al.</author>


</item>





</channel>
</rss>
