Tag Archives: Public Health Improvement

NHS and Social Care Data Sharing: at the Crossroads – Again? (BBC News / Department of Health)

Posted on July 7, 2016 by Dementia and Elderly Care News

Summary The controversial care.data data-sharing project has been scrapped, after a delay of two years. The Department of Health has conducted a public consultation, in addition to two independent reviews from the National Data Guardian for Health and Care (NDG) … Continue reading →

Posted in BBC News, Commissioning, CQC: Care Quality Commission, Department of Health, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), In the News, Integrated Care, National, NHS, NHS England, Quick Insights, Standards, Statistics, UK, Universal Interest | Tagged Aggregate Level Data Sources, Aggregated Data, Analytics, Anonymised Patient Medical Records, Anonymising Data, Applications of Big Data, BBC Health News, Big Data, Big Data Analytics, Caldicott Principles, Caldicott Review of Information Governance, Care Quality Commission (CQC), care.data, Care.data: Modern Data Service for the NHS, Confidentiality, Controlling the Release of Data, Dame Fiona Caldicott: Chair of the Independent Information Governance Oversight Panel (IIGOP), Dame Fiona Caldicott: National Data Guardian for Health and Care, Dame Fiona Caldicott: National Data Guardian for Health and Care (NDG), Data Extraction, Data Extraction and Linkage, Data Linkage and Extract Service, Data Linkage to Support Surveillance, Data Protection, Data Protection Act, Data Protection Act (1998), Data Quality and Accuracy, Data Security and Identifiability, Data Security Techniques, Data Sharing Review, Digital Care Records, Digital NHS, Electronic Care Records, Epidemiology, Epidemiology and Statistics, Fair Processing, George Freeman MP: Former Life Sciences Minister, Governance of Data Access, Health and Social Care Information Centre, Health and Social Care Information Centre (HSCIC), Health Improvement, Health Informatics, HSCIC: Health and Social Care Information Centre, Increasing Efficiency, Informatics, Information Governance Reviews, Information Sharing, Information Strategy, Interoperability, Interoperability Standards, Legal Basis for Data Extraction, Legislation and Governance, Leveraging Big Data, Management of Big Data, Medical Informatics, Medical Research, National Data Guardian for Health and Care (NDG), New Data Security Standards (2016), NHS Constitution, NHS Electronic Patient Records, NHS Health and Social Care Information Centre (IC), NHS Records, Opt Out Procedures, Opting Out, Opting Out (care.data), Patient Confidentiality, Patient Identifiable Data, Personal Confidential Data, Pseudonymised Data, Public Health, Public Health and Health Improvement, Public Health Improvement, Public Health Informatics, Public Health Monitoring, Publicly-Funded UK Big Data Research, Records Management: NHS Code of Practice, Records Standards in Health and Social Care, Secondary Uses Service (SUS), Summary Care Records, Summary Level Statistics, Transparency, Transparency and Accountability, Transparency and Open Data, Transparency and Public Trust, Trust and Data Sharing, Uses of Data, Uses of Medical Records | Leave a comment

Local Health Systems: Principles of Re-Design and Performance Measurement (LGA / King’s Fund / ADASS / SOLACE / CfPS / ADPH)

Posted on October 16, 2015 by Dementia and Elderly Care News

Summary The Local Government Association has issued a list of basic principles for planning service re-design. Local systems should aim to meet these fundamental requirements for improving services to achieve better health and wellbeing outcomes. Full Text Link Reference Shared … Continue reading →

Roles of US Hospitals in Building a Culture of Health (HPOE / HRET)

Posted on October 26, 2014 by Dementia and Elderly Care News

Summary This American Hospitals in Pursuit of Excellence (HPOE) / Health Research & Educational Trust (HRET) report explores the Robert Wood Johnson Foundation’s vision of how to promote a “culture of health” and how hospitals in the USA might contribute … Continue reading →

Posted in Acute Hospitals, Charitable Bodies, For Doctors (mostly), For Researchers (mostly), International, Management of Condition, Quick Insights | Tagged Bon Secours Baltimore Health System (Baltimore: Maryland), Building Health Partnerships, Cheshire Medical Center / Dartmouth-Hitchcock Keene (Keene: New Hampshire), Collaboration, Collaborative Care, Collaborative Projects, Collaborative Working, Community Health Interventions by Hospital Role(s), Community Health Needs and Characteristics, Community Health Needs Assessment (CHNA) Process, Community Health Needs Assessments, Crozer-Keystone Health System (Springfield: Pennsylvania), Culture of Health, Encouraging Healthy Behaviour, Health Inequalities, Health Promoting Hospitals Network (HPH), Health Research & Educational Trust, Health Research & Educational Trust (HRET), HealthHospital Contributions to a Culture of Health, HealthMeasuring Culture of Health Initiatives, Healthy Behaviours, Hospital Engagement in Public Health Improvement, Hospital-Based Strategies for Culture of Health, Hospitals in Pursuit of Excellence (HPOE), Hospitals Partnering with External Organisations, INTEGRIS Health (Oklahoma City), John C. Lincoln Health Network (Phoenix: Arizona), Mt. Ascutney Hospital and Health Center (Windsor: Vermont), Multi-Agency Collaboration, Multisectoral Collaboration, Parkview Health (Fort Wayne: Indiana), Population Health: Definitions, Priority Community Health Needs (Conditions), Priority Community Health Needs (Drivers), Process and Outcome Measures for a Culture of Health, Public Health, Public Health Agenda, Public Health Improvement, Reducing Health Inequalities, Robert Wood Johnson Foundation, Robert Wood Johnson Foundation (RWJF), Spartanburg Regional Healthcare System (Spartanburg: South Carolina), St. Mary’s Regional Medical Center (Lewiston: Maine), Strategic Considerations and Hospital Roles for Building a Culture of Health, Texas Health Harris Methodist Hospital Azle (Azle: Texas), United States, United States Health Care System, United States of America, United States Public Health Service, USA | Leave a comment

Big Data and Public Health (Parliamentary Office of Science and Technology POST Note PN 474 / PN 468)

Posted on August 5, 2014 by Dementia and Elderly Care News

Summary This Parliamentary Office of Science & Technology (POST) note on “Big Data and Public Health” considers the growing use of patients’ health records and large-scale medical and administrative datasets as valuable sources of information for the study and improvement … Continue reading →

Posted in Commissioning, Department of Health, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), National, NHS, NHS England, Public Health England, Quick Insights, Standards, Statistics, UK, Universal Interest | Tagged Academic Research, Administrative Data, Administrative Data Research Network, Administrative Datasets, Aggregate Level Data Sources, Aggregated Data, Analytics, Anonymised Patient Medical Records, Applications of Big Data, Arts and Humanities Research Council, Avon Longitudinal Study of Parents & Children (ALSPAC), Be Clear on Cancer (BCOC), Big Data, Big Data Analytics, Big Data Funding and Research, Big Data Overview, Big Data: One of UK Government's Eight Great Technologies, Biotechnology and Biological Sciences Research Council, Care Act 2014, care.data, Care.data: Modern Data Service for the NHS, Clinical Audits, Clinical Commissioning Groups (CCGs), Clinical Practice Research Datalink (CPRD), Common Law Duty of Confidentiality, Data Extraction and Linkage, Data Linkage and Extract Service, Data Linkage to Support Surveillance, Data Protection Act (1998), Data Quality and Accuracy, Data Security and Identifiability, Data Security Techniques, Digital Care Records, Economic and Social Research Council, Eight Great Technologies, Electronic Care Records, Epidemiology, Epidemiology and Statistics, EU Data Protection Regulation, European Data Protection Regulation, Farr Institute, General Practice Extraction Service (GPES), Governance of Data Access, GPES Independent Advisory Group (IAG), Health and Social Care Act (2012), Health and Social Care Information Centre (HSCIC), Health Improvement, Health Informatics, Health Protection (Notification) Regulations 2010, Health Protection Agency, Health Service (Control of Patient Information) Regulations 2002, Healthcare Planning, Hospital Episode Statistics (HES), House of Commons Library, House of Commons Library POST Note PN 474, Human Rights Act (HRA), Increasing Efficiency, Informatics, Information Sharing, Innovation in Bioinformatics, Interoperability, Interoperability Standards, Legislation and Governance, Leveraging Big Data, Management of Big Data, Medical Informatics, Medical Research, National Cancer Data Repository, National Cancer Intelligence Network (NCIN), National Pupil Database, Natural Environment Research Council, NHS Electronic Patient Records, NHS Records, Office of National Statistics (ONS), Office of National Statistics Mortality Data, Office of Science & Technology POSTnote, Open Data, Open Data and Big Data, Open Data in Health and Social Care, Open Data in the NHS, Parliament, Parliamentary Office of Science & Technology, Parliamentary Office of Science & Technology (POST), Patient Records, Population Risk Stratification, POST Note PN 468, POST Note PN 474, POSTnote No.468, POSTnote No.474, POSTnotes, Primary Use Within the NHS, Pseudonymised Data, Public Health, Public Health and Health Improvement, Public Health England (PHE), Public Health Improvement, Public Health Informatics, Public Health Monitoring, Publicly-Funded UK Big Data Research, Records Management: NHS Code of Practice, Records Standards in Health and Social Care, Risk Stratification, Risk Stratification Programmes, Routes to Diagnosis (NCIN), Science and Technology Facilities Council, Secondary Use Beyond the NHS, Secondary Use Within the NHS, Secondary Uses Data Set, Secondary Uses Service (SUS), Social Epidemiology, Standardised Electronic Health Records, Summary Care Records, Summary Level Statistics, Transparency, Transparency and Accountability, Transparency and Open Data, Transparency and Public Trust, Use of Identifiable Records Without Consent: Section 251 of the National Health Service Act 2006, Uses of Data, Uses of Medical Records | Leave a comment

Government Response Health Select Committee’s Report on Public Health England (Department of Health)

Posted on July 6, 2014 by Dementia and Elderly Care News

Summary The government has responded to the House of Commons Health Select Committee (HSC) report on Public Health England, published in February 2014. The response addresses concerns about PHE’s independence, policy work and relationship with the government. PHE has to be … Continue reading →

Posted in Commissioning, Community Care, Department of Health, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, National, Non-Pharmacological Treatments, Public Health England, Quick Insights, Standards, UK, Universal Interest | Tagged Ageing Policy in the UK, Alcohol or Tobacco Withdrawal, Aspirant Director of Public Health Programme, Association of Directors of Public Health (ADPH), Behavioural Risk Factors, Change4Life, Change4Life Smart Swaps, Chief Medical Officer, Dementia Awareness, Dementia Risk Factors, Directors of Public Health, Directors of Public Health (DsPH), Emergency Preparedness, English Surveillance Programme for Antimicrobial Utilisation and Resistance, Epidemiology, Faculty of Public Health (FPH), Health and Wellbeing Framework for England, Health Determinants, Health Improvement, Health Inequalities, Health Inequalities in England, Health Policy, Health Protection, Health Protection Agency (HPA), Health Wellbeing and Independence, Healthy Ageing, Healthy Behaviours, Healthy Communities, Healthy Life Expectancy, Healthy Lifestyles, Healthy Living, House of Commons Health Committee, House of Commons Health Committee Report on Public Health England, Immunisation Programmes, Improving Local Public Health, Improving Public Health, Independence, Inequality in Healthy Life Expectancy, Information and Intelligence, Lifestyle, Lifestyle Risk Factors, Local Authority Directors of Public Health, Local Government Association: LGA, Local Health Protection, Local Health Resilience Partnerships (LHRPs), Local Public Health, Mental Health Policy, NHS Health Check, Pandemic Flu Preparedness, PHE's Relationship with Government, PHE: Public Health England, PHE’s Centre for Radiation Chemical and Environmental Hazards (CRCE), PHE’s Policy Work, Policy, Policy Context, Policy Development, Prevention of Dementia, Prevention of Dementia: Public Health England, Public Health, Public Health England (PHE), Public Health England’s Health and Wellbeing Framework, Public Health England’s Remit in 2014-15, Public Health Improvement, Reducing Health Inequalities, Royal College of Physicians: Faculty of Public Health (FPH), Smoking, Social Determinants of Health, Social Determinants of Health Inequalities, Social Epidemiology, Social Marketing, Social Policy and Society, Societal Determinants of Health, Stoptober Campaign, Tobacco Consumption, Transition to Public Health England, UK Faculty of Public Health, UK Government Dementia Awareness Campaign, Unhealthy Lifestyles, Vascular Risk Factors, Wellbeing, Wider Determinants of Health | Leave a comment

Framework for Personalised Care and Population Health (Department of Health)

Posted on July 5, 2014 by Dementia and Elderly Care News

Summary The Department of Health has published a framework to support nurses, midwives, health visitors and allied health professionals in accessing the best evidence and support for their public health role. It is also intended to act as a tool … Continue reading →

Tag Archives: Public Health Improvement

Roles of US Hospitals in Building a Culture of Health (HPOE / HRET)

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