Tag Archives: Data Extraction

National Clinical Director for Dementia: Further Diagnosis Rates-Related Letter to CCGs (NHS England)

Posted on December 21, 2016 by Dementia and Elderly Care News

Summary Professor Alistair Burns, NHS England’s National Clinical Director for Dementia, has written another letter to CCGs about progress on national dementia diagnosis rates and priorities for post-diagnostic dementia treatment / support. National dementia diagnosis rates for November 2016 are … Continue reading →

National Clinical Director for Dementia: Letter to CCGs (NHS England)

Posted on November 26, 2016 by Dementia and Elderly Care News

Summary Professor Alistair Burns, NHS England’s National Clinical Director for Dementia, has written to CCGs about progress on national dementia diagnosis rates and priorities for post-diagnostic dementia treatment / support. The letter discusses support available from NHS England. Topics covered … Continue reading →

Posted in Commissioning, Community Care, Department of Health, Depression, Diagnosis, For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, Local Interest, Management of Condition, Mental Health, Models of Dementia Care, National, NHS, NHS England, Non-Pharmacological Treatments, Person-Centred Care, Quick Insights, Standards, Statistics, UK, Universal Interest | Tagged Alistair Burns: NHS England’s National Clinical Director for Dementia, Alistair Burns: NHS England’s National Clinical Director for Older People’s Mental Health, Anxiety, Apathy, British Association for Music Therapy, Building Research Partnerships, Calculating Quality Reporting Service (CQRS), Care City Test Bed, CCGs: Clinical Commissioning Groups, Championing Research, Clinical Commissioning Groups (CCGs), Commissioning for Research, Data Extraction, Data Extractions: National Governance, Dementia Data Extraction Processes, Dementia Diagnosis Rates, Dementia Diagnosis Rates (October 2016), Dementia: Post Diagnostic Support, Developing Research in Primary Care, Empowering Patients, Empowering Patients to Enquire About Research Participation, Empowerment, Empowerment and Dementia, Empowerment and Support, Enhanced Service CQRS: Dementia Component, Establishing a Research Culture, GP Data Extraction, Improving Dementia Diagnosis Rates, Integrating Research with Care, Join Dementia Research, Join Dementia Research National Service, Join Dementia Research Toolkit, Join Dementia Research: Clinical Trials Matchmaker Service, Join Dementia Research: Recruitment Onto Dementia Studies, Memory and Smell, Music Therapy, Music Therapy and Dementia, National Activity Providers Association (NAPA), NHS Digital Data Extract, NHS Digital Publication Calendar, Post-Diagnosis Support, Post-Diagnostic Dementia Care And Support, Post-Diagnostic Support for People with Dementia, Primary Care, Professor Alistair Burns, Restlessness, Smell & Connect Trial, Support for Improving Dementia Diagnosis Rates, Tastes and Scents, Working Collaboratively to Raise Awareness | Leave a comment

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

New Dementia Diagnosis Data Collection Requirements for GPs (HSCIC)

Posted on August 11, 2015 by Dementia and Elderly Care News

Summary Data on dementia diagnoses is collected to support the National Dementia Strategy. The aim of improving diagnosis rates was specified in the Prime Minister’s Dementia Challenge and the NHS Mandate. The Health and Social Care Information Centre (HSCIC) has … Continue reading →

Posted in Alzheimer's Society, Commissioning, Community Care, Department of Health, Diagnosis, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), Integrated Care, Local Interest, Management of Condition, Mental Health, Models of Dementia Care, National, NHS, NHS England, Patient Care Pathway, Person-Centred Care, Quick Insights, Standards, Statistics, UK | Tagged Age and Gender Differences in Diagnosis Rates, Burden Advice and Assessment Service (BAAS), Burden of Data Collection, Bureaucracy and Burnout, Case Finding, Case Finding for Patients with Dementia, Clinical Commissioning Groups (CCGs), Data Collection, Data Collection and Measurement, Data Collections Burden Reduction Service (DCBR), Data Collections: National Governance, Data Extraction, Data Extraction and Linkage, Data Extracts, Data Sharing, Dementia Care Workload, Dementia Diagnosis, Dementia Diagnosis and Care in England, Dementia Diagnosis Rates, Dementia Statistics, Dementia Statistics: By Age and Gender, Detailed Burden Assessment (DBA), Diagnosis and Referral, Diagnosis and Support, Diagnosis at Primary Care Level, Differential Impact of Dementia (Gender-Related), Early Diagnosis, Gender (Sex), Gender and Inequalities in Health in Later Life, Gender Differences in Diagnosis Rates, General Practice, General Practice in England, General Practice Performance Data, GP Data Extraction, Health and Social Care Information Centre (HSCIC), HSCIC Burden Advice and Assessment Service (BAAS), Identification and Referral, Improving Dementia Diagnosis Rates, Incentive Payments, NHS Mandate, Performance Incentives, Performance Targets, Prime Minister’s Dementia Challenge, Quality Outcomes Framework (QOF), Quality Outcomes Framework: Recorded Dementia Diagnoses, Recorded Dementia Diagnoses, Recorded Dementia Diagnoses (at Primary Care Level), Reduction in Bureaucracy, Referral and Assessment, Standardisation Committee for Care Information (SCCI), Target Culture, Target-Driven Behaviour, Timely Diagnosis, Workload in General Practice | Leave a comment

Making Best Use of Data and Technology: Promises of Success and Some Failures (BBC News / NIB / NAO / NHS England)

Posted on July 2, 2015 by Dementia and Elderly Care News

Summary The National Audit Office has criticised the General Practice Extraction Service (GPES), i.e. the GP IT system intended to improve quality and planning in the NHS, for running over budget and behind schedule. The big idea behind the GPES … Continue reading →

Dementia Data Extraction Process Revised (HSCIC)

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

Summary The Health and Social Care Information Centre (HSCIC) has introduced a different sign-up process concerning automated data extraction for the Quality and Outcomes Framework (QOF) and enhanced services. The QOF subset 2014-15 dementia extraction supports the Prime Ministerial challenge … Continue reading →

Posted in Commissioning, Community Care, Diagnosis, For Doctors (mostly), Integrated Care, Local Interest, National, NHS, Person-Centred Care, Practical Advice, Statistics, UK | Tagged Calculating Quality Reporting Service (CQRS), Data Extraction, Data Extractions: National Governance, Dementia Data Extraction Processes, Dementia Diagnosis Rates, Enhanced Services from GPs, General Practice, General Practice Extraction Service (GPES), GP Data Extraction, GPES Training Materials, GPES Website, Health and Social Care Information Centre (HSCIC), Improving Dementia Diagnosis Rates, Local Area Teams (LATs), Local Enhanced Services, NHS Area Teams (ATs), Prime Minister's Challenge on Dementia, Prime Minister’s Dementia Challenge, Quality and Outcomes Framework (QOF), Support for Improving Dementia Diagnosis Rates | Leave a comment

Consultation on the Protection of Personal Health and Care Data (Department of Health)

Posted on June 30, 2014 by Dementia and Elderly Care News

Summary The Department of Health has published a consultation document on proposals to strengthen controls and safeguards on the use of health and care data. The aim is to reassure people that their personal data will not be not open … Continue reading →

Posted in Commissioning, Department of Health, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), Integrated Care, National, NHS, Patient Care Pathway, Quick Insights, Standards, UK, Universal Interest | Tagged Accredited Safe Havens, Accredited Safe Havens (ASHs), Advisory Group for the care.data Programme, Anonymised Patient Medical Records, Anonymising Data, ASH: Accredited Safe Haven, Caldicott Principles, Caldicott Review of Information Governance, Caldicott Standards, care.data, care.data Advisory Group, Care.data: Modern Data Service for the NHS, Case Management, Commissioning Organisations, Confidentiality, Confidentiality Advisory Group (CAG), Controlling the Release of Data, Dame Fiona Caldicott: Chair of the Independent Information Governance Oversight Panel (IIGOP), Data Extraction, Data Protection Act, Data Release Review (PwC), Data Sharing Review, Department of Health Arm’s Length Bodies, Department of Health's Information Strategy, Electronic Health Records (EHRs), Electronic Medical Records, Fair Processing, Francis Inquiry Report, Future Forum, General Practice Extraction Service (GPES), General Practice [Data] Extraction Service, Government’s Information Strategy, Government’s Life Sciences Strategy, Health and Care Data, Health and Social Care Information Centre, Health and Social Care Information Centre (HSCIC), HSCIC: Health and Social Care Information Centre, Information Governance Review, Information Governance Reviews, Information Governance Toolkit Controls, Information Sharing, Information Strategy, Legal Basis for Data Extraction, Local Authorities, Modern Medicine, NHS Constitution, NHS Health and Social Care Information Centre (IC), Opt Out Procedures, Opting Out, Opting Out (care.data), Patient Confidentiality, Patient Identifiable Data, Patient Representative Groups, Personal Confidential Data, Protection of Personal Health and Care Data, Pseudonymised Data, Public Confidence, Register of Approved Data Releases, Secondary Uses Service (SUS), Secure Safe Havens, Winterbourne View | Leave a comment

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