Ignite your medical funding opportunties emeAlan Scrase
IGNITE your.... medical funding opportunities
Presenter - Dr Lisa Douet, Senior Research Fellow, and Ellie Monks, EME Programme Manager will present about
“Research Funding: The Efficacy and Mechanism Evaluation Programme”
The EME Programme funds clinical efficacy studies. The studies it supports usually test if an intervention works as expected, in a well-defined population or group of patients. The Programmealso also provides an opportunity to use clinical studies to understand disease or treatment mechanisms, which may in turn lead to improvements in health and patient care.
Training medical policy program final version 3Emily Barton
UCare's Medical Policy Program establishes evidence-based guidelines to determine health care coverage. The program aims to improve health outcomes while meeting regulatory requirements. Medical policies are developed through a multistep process including literature review and approval by clinical committees. Finalized policies are integrated into coverage determinations and published for providers and members. Utilization is then measured and policies updated based on feedback to enhance the program over time.
This document proposes a randomized controlled trial to implement a nationally coordinated home health monitoring program for patients with long-term conditions using telemedicine. The objectives are to improve patient outcomes, reduce need for secondary care, and provide a more efficient model of care. The trial would include 400 participants across four regions and assess various health, quality of life, and utilization outcomes. It would also explore regulatory issues, costs, workforce impacts, and technology requirements of integrating telemedicine into care for long-term conditions.
This document discusses managing healthcare costs in an era of healthcare reform. It includes an agenda for a presentation on the topic with sections on the state of analytics in healthcare, strategic profit and loss statements, use cases, best practices, sample reporting, and a question and answer session. It emphasizes that healthcare transformation requires integrated clinical, financial, administrative, and research data from across healthcare providers as well as analytics. It also notes that a lack of understanding of healthcare costs is a barrier to effective reimbursement approaches and that financial decision support is a top priority for providers.
The document summarizes key themes from a webinar on developing medical policies and coverage guidelines for next generation sequencing in oncology. It discusses the challenges of evaluating genomic tests and gaining insurance coverage. Recommendations include requiring laboratories to obtain accreditation for analytic validity, covering small gene panels when clinical utility is established, and facilitating data collection to support coverage of larger tests and off-label drug use. The webinar included perspectives from various stakeholders on addressing these issues.
Maximizing Electronic Health Record Use in Physician Practices to Minimize RiskSedgwick
This document discusses maximizing the use of electronic health records (EHRs) in physician practices while minimizing risks. It provides an overview of the meaningful use incentive program and its stages of implementation. It identifies potential liability issues with transitioning to EHRs, such as communication barriers and alert fatigue. The document recommends strategies for practices to prepare for EHR implementation, including using "dummy" patients and reviewing physician experience. It stresses the importance of organizing EHR assessments, applying basic risk management principles, and developing methods to evaluate policies, charts and interviews.
Kimberly Ferrell-James has over 15 years of experience as a pharmacy technician and IT specialist with a focus on healthcare informatics. She has a Master's degree in Health Care Informatics from Grand Canyon University and a Bachelor's degree in Exercise Science from Middle Tennessee State University. She is skilled in areas such as project management, data management, quality improvement, decision making, research, and system analysis. Currently she works as a Pharmacy Technician Advanced at Vanderbilt University Medical Center where she prepares medications, fills prescriptions, researches drug interactions, trains other technicians, and works on projects to improve efficiency.
This document discusses a new drug development paradigm (NDDP) that aims to improve the efficiency and effectiveness of clinical drug development. It outlines several proposals that call for reforming the current drug development model, including using more modeling, adaptive trial designs, and integrating clinical trials into healthcare delivery systems. The NDDP proposes a more flexible framework with early patient/payer engagement, exploratory and confirmatory research phases using modern trial designs, and post-approval studies to establish relative value. Challenges for industry include conducting large simple trials, partnering to support more efficient trials, and having a clear evidentiary strategy tailored to different drug archetypes.
Ignite your medical funding opportunties emeAlan Scrase
IGNITE your.... medical funding opportunities
Presenter - Dr Lisa Douet, Senior Research Fellow, and Ellie Monks, EME Programme Manager will present about
“Research Funding: The Efficacy and Mechanism Evaluation Programme”
The EME Programme funds clinical efficacy studies. The studies it supports usually test if an intervention works as expected, in a well-defined population or group of patients. The Programmealso also provides an opportunity to use clinical studies to understand disease or treatment mechanisms, which may in turn lead to improvements in health and patient care.
Training medical policy program final version 3Emily Barton
UCare's Medical Policy Program establishes evidence-based guidelines to determine health care coverage. The program aims to improve health outcomes while meeting regulatory requirements. Medical policies are developed through a multistep process including literature review and approval by clinical committees. Finalized policies are integrated into coverage determinations and published for providers and members. Utilization is then measured and policies updated based on feedback to enhance the program over time.
This document proposes a randomized controlled trial to implement a nationally coordinated home health monitoring program for patients with long-term conditions using telemedicine. The objectives are to improve patient outcomes, reduce need for secondary care, and provide a more efficient model of care. The trial would include 400 participants across four regions and assess various health, quality of life, and utilization outcomes. It would also explore regulatory issues, costs, workforce impacts, and technology requirements of integrating telemedicine into care for long-term conditions.
This document discusses managing healthcare costs in an era of healthcare reform. It includes an agenda for a presentation on the topic with sections on the state of analytics in healthcare, strategic profit and loss statements, use cases, best practices, sample reporting, and a question and answer session. It emphasizes that healthcare transformation requires integrated clinical, financial, administrative, and research data from across healthcare providers as well as analytics. It also notes that a lack of understanding of healthcare costs is a barrier to effective reimbursement approaches and that financial decision support is a top priority for providers.
The document summarizes key themes from a webinar on developing medical policies and coverage guidelines for next generation sequencing in oncology. It discusses the challenges of evaluating genomic tests and gaining insurance coverage. Recommendations include requiring laboratories to obtain accreditation for analytic validity, covering small gene panels when clinical utility is established, and facilitating data collection to support coverage of larger tests and off-label drug use. The webinar included perspectives from various stakeholders on addressing these issues.
Maximizing Electronic Health Record Use in Physician Practices to Minimize RiskSedgwick
This document discusses maximizing the use of electronic health records (EHRs) in physician practices while minimizing risks. It provides an overview of the meaningful use incentive program and its stages of implementation. It identifies potential liability issues with transitioning to EHRs, such as communication barriers and alert fatigue. The document recommends strategies for practices to prepare for EHR implementation, including using "dummy" patients and reviewing physician experience. It stresses the importance of organizing EHR assessments, applying basic risk management principles, and developing methods to evaluate policies, charts and interviews.
Kimberly Ferrell-James has over 15 years of experience as a pharmacy technician and IT specialist with a focus on healthcare informatics. She has a Master's degree in Health Care Informatics from Grand Canyon University and a Bachelor's degree in Exercise Science from Middle Tennessee State University. She is skilled in areas such as project management, data management, quality improvement, decision making, research, and system analysis. Currently she works as a Pharmacy Technician Advanced at Vanderbilt University Medical Center where she prepares medications, fills prescriptions, researches drug interactions, trains other technicians, and works on projects to improve efficiency.
This document discusses a new drug development paradigm (NDDP) that aims to improve the efficiency and effectiveness of clinical drug development. It outlines several proposals that call for reforming the current drug development model, including using more modeling, adaptive trial designs, and integrating clinical trials into healthcare delivery systems. The NDDP proposes a more flexible framework with early patient/payer engagement, exploratory and confirmatory research phases using modern trial designs, and post-approval studies to establish relative value. Challenges for industry include conducting large simple trials, partnering to support more efficient trials, and having a clear evidentiary strategy tailored to different drug archetypes.
This document discusses a feasibility study examining whether decisions by the UK's National Institute for Health and Care Excellence (NICE) influence decisions by health technology assessment bodies in other countries. The study analyzed 29 drug-indication pairs assessed by NICE and other countries' HTAs. The results suggest NICE decisions are related to subsequent HTAs in other countries. Drugs without positive NICE recommendations had a higher probability of being not recommended by other HTAs. Additionally, the number of fully reimbursed drugs was higher before versus after NICE assessment. The consideration of NICE decisions may increase the likelihood of other HTAs issuing negative decisions. However, the small sample size means results must be interpreted cautiously and more research is needed.
‘In with the old, out with the new’ – In search of ways to help health economists break their addiction to technology adoption. CHE Seminar presented by Professor Stirling Bryan, Director, Centre for Clinical Epidemiology & Evaluation, Vancouver Coastal Health Research Institute, Professor, School of Population & Public Health, University of British Columbia. 17th October 2014
Quantification, Pricing and budgeting of Drug requirementHarishankar Sahu
The document discusses quantification and budgeting for drug procurement. It describes quantification as estimating quantities, financial requirements, and needs within constraints like finances and storage capacity. The objectives of good quantification are consistent availability, adequate supplies, minimal wastage, no overstocking, and cost-effectiveness. Quantification methods include consumption-based, morbidity-based, and analogous approaches. The document outlines the quantification process and discusses applications like procurement, forecasting, and emergency relief. It also covers price formulas, drug budgeting challenges, and concludes that a team approach can improve quantification success.
A system based on continual learning: a guide to using measurement for improvement - Phil Duncan, Patient Safety Collaborative Lead, NHS Improving Quality and Ian Chappell, Improvement Manager, NHS Improving Quality
Presentation from the Patient Safety Collaborative launch event held in London on 14 October 2014
More information at http://www.nhsiq.nhs.uk/improvement-programmes/patient-safety/patient-safety-collaboratives.aspx
This lecture discusses key attributes of data quality including consistency, currency, timeliness, granularity, precision, and relevancy. It provides examples of each attribute and recommendations for maintaining data integrity such as establishing data governance and defining standards for data collection. The lecture also notes that data quality is important for research and quality improvement efforts and that poor data quality can lead to errors.
Models of evaluation in educational technologyalsalmi
The document discusses different models for evaluating educational technology programs. It analyzes studies that evaluated continuing medical education web-based programs using Kirkpatrick's model of evaluation, which measures reaction, learning, behavior, and results. Many studies found improved learning outcomes and performance through pre-and post-testing. However, the findings suggest more research is needed to determine which web-based learning systems best enhance practice changes and impact patient health outcomes.
This document discusses effective drug supply management through quantification, which is estimating how much of each drug is needed. It describes the components of an effective system including selection, quantification, procurement, distribution, and use. Poor quantification can be seen through chronic shortages and surpluses, inequity between facilities, inadequate cost-effectiveness, irrational adjustments, and suppressed demand. The two main quantification methods described are the morbidity method based on standard treatments and episodes, and the consumption method based on past usage.
Ronan Herlihy on Engaging Clinicians with data on their ordering practicesCirdan
The appropriate ordering project uses data extracted from Electronic Medical Record to create dashboards to inform and engage clinicians in ordering practices. This presentation looks at the techniques used to create answers for the clinicians questions and discusses the purpose behind 12 dashboards. It looks at the change management approaches and challenges.
The initial pilot project has been embraced by a number of local health districts in NSW and templates have been made available along with training tools.
Implementing and Evaluating the Hospital Guide to Reducing Medicaid ReadmissionsJSI
Reducing readmissions is a growing priority in the pursuit of the Triple Aim. While much attention has been paid to Medicare readmissions, evidence demonstrates that Medicaid agencies are increasingly implementing payment penalties for readmissions, and the recent expansion of Medicaid eligibility under the Affordable Care Act (ACA) has provided millions of adults with new health coverage. Hospitals serving large numbers of Medical patients have a mounting interest in adopting strategies to reduce readmissions that address the distinct needs of this population.
The document discusses several secular trends in healthcare, including the shift towards value-based reimbursement models, increasing consumerism, and rapid advancements in technology and use of big data. Major trends include growing consolidation across healthcare sectors, 50% of Medicare payments transitioning to value-based models by 2018, a large increase in high deductible health plans, and billions in investments in digital health, technology, and analytics.
weems-Texas Medicaid Health Home Pilot Project Evaluation MethodsNASHP HealthPolicy
Leslie A. Weems, LMSW, Senior Policy Analyst and Project Manager, Medicaid/CHIP Division, Texas Health and Human Services Commission discusses Texas Medicaid Health Home Pilot Project Evaluation Methods at the New Tactics for Building Medical Homes in State Medicaid and CHIP Programs webinar
An brief introduction to the clinical data management process is described in this slides. These slides provides you the information regarding the data evaluation in the clinical trials , edit checks and data review finally data locking,then the data is submitted to the concerned regulatory body.
Presentation: Improving the regulation of generic medicines in AustraliaTGA Australia
The registration system for generic prescription medicines has not been amended since the introduction of the Streamlined Submission Process in 2010 and assigns all generics the same target timeframe of 255 working days. Amendments to the generic medicine registration process are under discussion that could provide for flexibility for certain applications and better support the timely availability of high quality generic medicines and the sustainability of the Australian health system.
Mr James Downie, CEO, presented on the topic 'IHPA 2017 and beyond' at the Enhancing Performance & Efficiency in Paediatric Care - CHA Annual Benchmarking Forum, hosted by Children's Healthcare Australasia on 25 May 2017.
This document discusses concepts of essential medicines. It begins by addressing some common misconceptions about essential medicines, such as them only being for poor people or mild diseases. It then provides the WHO definition of essential medicines as those that meet the priority health needs of most of the population and should be available and affordable. The rest of the document outlines three key concepts of essential medicines - access, quality, and rational use. It also discusses methods for quantifying medicine needs, including using morbidity data and adjusted consumption, and explains why quantifying needs is important for ensuring availability of quality medicines.
The CANS and Evidence Based Practice Implementation: Hanging Together or Just...emqff
The document discusses using the Child and Adolescent Needs and Strengths (CANS) assessment tool as the centerpiece of an integrated clinical model. The model would use CANS for assessment, outcomes tracking, assisting with evidence-based practice implementation planning, selecting common clinical elements, and tracking quality of care through a clinical dashboard. This integrated approach aims to standardize assessment, competencies, use of evidence-based practices, and continuous quality improvement.
Presented by Nick Baker
General and Community Paediatrician
Executive Clinical Director for Community Based Services, Nelson Marlborough District Health Board.
This document discusses process redesign for meaningful use objectives in healthcare. It begins by outlining the learning objectives of using software functionality and meaningful use criteria to inform process redesign in clinics. It then explains the 10 meaningful use objectives for eligible professionals, such as electronic prescribing, health information exchange, and public health reporting. For each objective, it summarizes the workflow impact, such as introducing new workflows or changing existing tasks. The document provides resources on the meaningful use specification sheets and criteria that providers must meet to receive incentives. Overall, it reviews using health IT functions to solve process problems and optimize clinical workflows in line with meaningful use objectives.
Health IT Summit Houston 2014 - Case Study "EHR Optimization for Organizational Value in a Changing Healthcare Environment"
Luis Saldana, MD, MBA, FACEP
CMIO
Texas Health Resources
iHT2 case studies and presentations illustrate challenges, successes and various factors in the outcomes of numerous types of health IT implementations. They are interactive and dynamic sessions providing opportunity for dialogue, debate and exchanging ideas and best practices. This session will be presented by a thought leader in the provider, payer or government space.
Himss m healthcomm_telehealth md exec summary recommendations_formatted final...mHealth2015
The document summarizes the perspectives of physicians on telehealth policy and reimbursement barriers. It discusses key focus areas including reimbursement issues, quality/safety concerns, and opportunities to better leverage technology. The physicians identified greatest barriers as lack of appropriate reimbursement models and flexibility in technology applications. Recommendations include expanding telehealth coverage and reimbursement through Medicare/Medicaid, addressing interstate licensure and data storage issues, and increasing education on telehealth utilities and billing.
This document discusses a feasibility study examining whether decisions by the UK's National Institute for Health and Care Excellence (NICE) influence decisions by health technology assessment bodies in other countries. The study analyzed 29 drug-indication pairs assessed by NICE and other countries' HTAs. The results suggest NICE decisions are related to subsequent HTAs in other countries. Drugs without positive NICE recommendations had a higher probability of being not recommended by other HTAs. Additionally, the number of fully reimbursed drugs was higher before versus after NICE assessment. The consideration of NICE decisions may increase the likelihood of other HTAs issuing negative decisions. However, the small sample size means results must be interpreted cautiously and more research is needed.
‘In with the old, out with the new’ – In search of ways to help health economists break their addiction to technology adoption. CHE Seminar presented by Professor Stirling Bryan, Director, Centre for Clinical Epidemiology & Evaluation, Vancouver Coastal Health Research Institute, Professor, School of Population & Public Health, University of British Columbia. 17th October 2014
Quantification, Pricing and budgeting of Drug requirementHarishankar Sahu
The document discusses quantification and budgeting for drug procurement. It describes quantification as estimating quantities, financial requirements, and needs within constraints like finances and storage capacity. The objectives of good quantification are consistent availability, adequate supplies, minimal wastage, no overstocking, and cost-effectiveness. Quantification methods include consumption-based, morbidity-based, and analogous approaches. The document outlines the quantification process and discusses applications like procurement, forecasting, and emergency relief. It also covers price formulas, drug budgeting challenges, and concludes that a team approach can improve quantification success.
A system based on continual learning: a guide to using measurement for improvement - Phil Duncan, Patient Safety Collaborative Lead, NHS Improving Quality and Ian Chappell, Improvement Manager, NHS Improving Quality
Presentation from the Patient Safety Collaborative launch event held in London on 14 October 2014
More information at http://www.nhsiq.nhs.uk/improvement-programmes/patient-safety/patient-safety-collaboratives.aspx
This lecture discusses key attributes of data quality including consistency, currency, timeliness, granularity, precision, and relevancy. It provides examples of each attribute and recommendations for maintaining data integrity such as establishing data governance and defining standards for data collection. The lecture also notes that data quality is important for research and quality improvement efforts and that poor data quality can lead to errors.
Models of evaluation in educational technologyalsalmi
The document discusses different models for evaluating educational technology programs. It analyzes studies that evaluated continuing medical education web-based programs using Kirkpatrick's model of evaluation, which measures reaction, learning, behavior, and results. Many studies found improved learning outcomes and performance through pre-and post-testing. However, the findings suggest more research is needed to determine which web-based learning systems best enhance practice changes and impact patient health outcomes.
This document discusses effective drug supply management through quantification, which is estimating how much of each drug is needed. It describes the components of an effective system including selection, quantification, procurement, distribution, and use. Poor quantification can be seen through chronic shortages and surpluses, inequity between facilities, inadequate cost-effectiveness, irrational adjustments, and suppressed demand. The two main quantification methods described are the morbidity method based on standard treatments and episodes, and the consumption method based on past usage.
Ronan Herlihy on Engaging Clinicians with data on their ordering practicesCirdan
The appropriate ordering project uses data extracted from Electronic Medical Record to create dashboards to inform and engage clinicians in ordering practices. This presentation looks at the techniques used to create answers for the clinicians questions and discusses the purpose behind 12 dashboards. It looks at the change management approaches and challenges.
The initial pilot project has been embraced by a number of local health districts in NSW and templates have been made available along with training tools.
Implementing and Evaluating the Hospital Guide to Reducing Medicaid ReadmissionsJSI
Reducing readmissions is a growing priority in the pursuit of the Triple Aim. While much attention has been paid to Medicare readmissions, evidence demonstrates that Medicaid agencies are increasingly implementing payment penalties for readmissions, and the recent expansion of Medicaid eligibility under the Affordable Care Act (ACA) has provided millions of adults with new health coverage. Hospitals serving large numbers of Medical patients have a mounting interest in adopting strategies to reduce readmissions that address the distinct needs of this population.
The document discusses several secular trends in healthcare, including the shift towards value-based reimbursement models, increasing consumerism, and rapid advancements in technology and use of big data. Major trends include growing consolidation across healthcare sectors, 50% of Medicare payments transitioning to value-based models by 2018, a large increase in high deductible health plans, and billions in investments in digital health, technology, and analytics.
weems-Texas Medicaid Health Home Pilot Project Evaluation MethodsNASHP HealthPolicy
Leslie A. Weems, LMSW, Senior Policy Analyst and Project Manager, Medicaid/CHIP Division, Texas Health and Human Services Commission discusses Texas Medicaid Health Home Pilot Project Evaluation Methods at the New Tactics for Building Medical Homes in State Medicaid and CHIP Programs webinar
An brief introduction to the clinical data management process is described in this slides. These slides provides you the information regarding the data evaluation in the clinical trials , edit checks and data review finally data locking,then the data is submitted to the concerned regulatory body.
Presentation: Improving the regulation of generic medicines in AustraliaTGA Australia
The registration system for generic prescription medicines has not been amended since the introduction of the Streamlined Submission Process in 2010 and assigns all generics the same target timeframe of 255 working days. Amendments to the generic medicine registration process are under discussion that could provide for flexibility for certain applications and better support the timely availability of high quality generic medicines and the sustainability of the Australian health system.
Mr James Downie, CEO, presented on the topic 'IHPA 2017 and beyond' at the Enhancing Performance & Efficiency in Paediatric Care - CHA Annual Benchmarking Forum, hosted by Children's Healthcare Australasia on 25 May 2017.
This document discusses concepts of essential medicines. It begins by addressing some common misconceptions about essential medicines, such as them only being for poor people or mild diseases. It then provides the WHO definition of essential medicines as those that meet the priority health needs of most of the population and should be available and affordable. The rest of the document outlines three key concepts of essential medicines - access, quality, and rational use. It also discusses methods for quantifying medicine needs, including using morbidity data and adjusted consumption, and explains why quantifying needs is important for ensuring availability of quality medicines.
The CANS and Evidence Based Practice Implementation: Hanging Together or Just...emqff
The document discusses using the Child and Adolescent Needs and Strengths (CANS) assessment tool as the centerpiece of an integrated clinical model. The model would use CANS for assessment, outcomes tracking, assisting with evidence-based practice implementation planning, selecting common clinical elements, and tracking quality of care through a clinical dashboard. This integrated approach aims to standardize assessment, competencies, use of evidence-based practices, and continuous quality improvement.
Presented by Nick Baker
General and Community Paediatrician
Executive Clinical Director for Community Based Services, Nelson Marlborough District Health Board.
This document discusses process redesign for meaningful use objectives in healthcare. It begins by outlining the learning objectives of using software functionality and meaningful use criteria to inform process redesign in clinics. It then explains the 10 meaningful use objectives for eligible professionals, such as electronic prescribing, health information exchange, and public health reporting. For each objective, it summarizes the workflow impact, such as introducing new workflows or changing existing tasks. The document provides resources on the meaningful use specification sheets and criteria that providers must meet to receive incentives. Overall, it reviews using health IT functions to solve process problems and optimize clinical workflows in line with meaningful use objectives.
Health IT Summit Houston 2014 - Case Study "EHR Optimization for Organizational Value in a Changing Healthcare Environment"
Luis Saldana, MD, MBA, FACEP
CMIO
Texas Health Resources
iHT2 case studies and presentations illustrate challenges, successes and various factors in the outcomes of numerous types of health IT implementations. They are interactive and dynamic sessions providing opportunity for dialogue, debate and exchanging ideas and best practices. This session will be presented by a thought leader in the provider, payer or government space.
Himss m healthcomm_telehealth md exec summary recommendations_formatted final...mHealth2015
The document summarizes the perspectives of physicians on telehealth policy and reimbursement barriers. It discusses key focus areas including reimbursement issues, quality/safety concerns, and opportunities to better leverage technology. The physicians identified greatest barriers as lack of appropriate reimbursement models and flexibility in technology applications. Recommendations include expanding telehealth coverage and reimbursement through Medicare/Medicaid, addressing interstate licensure and data storage issues, and increasing education on telehealth utilities and billing.
Maureen Charlebois, Chief Nursing Director and Group Director, Canada Health ...Investnet
This document summarizes Canada Health Infoway's efforts to digitally transform healthcare across Canada in 3 waves: 1) Building foundational systems, 2) Providing digital tools for clinicians, and 3) Empowering patients. It highlights achievements in areas like EMR adoption and e-prescribing, and outlines ambitions to expand telehomecare and online patient services. Clinical leadership, change management, and ensuring clinicians have necessary digital skills are emphasized as key to adoption and realizing benefits of digital health innovations.
Patient Blood Management: Impact of Quality Data on Patient OutcomesViewics
Patient blood management (PBM) has been proven to improve patient outcomes and save hospitals millions of dollars. Ensuring the quality of your data is central to decision making and critical to having a strong PBM program.
Would you like to learn how your organization can improve patient outcomes by implementing a PBM program based on accurate data?
If so, view this presentation by blood management expert Lance Trewhella. Lance presents how to develop a successful, evidence-based, multidisciplinary PBM program aimed at optimizing the care of patients who might need transfusion.
You’ll learn:
• Current recommendations for blood transfusion utilization
• The impact of quality data on PBM programs
• Best data practices in PBM
The document provides an overview of clinical analytics (CA), which involves analyzing clinical data to improve healthcare quality, safety, and efficiency. It defines CA and describes common uses like tracking quality measures. Challenges to CA include the heterogeneity of medical data and lack of data integration. The document also outlines the types of practitioners involved in CA, common tools used like data warehouses, and examples of how hospitals have leveraged CA to reduce infections, improve coding to increase revenues, and plan for public health issues. The future of CA is presented as moving from academic centers to broader healthcare and enabling personalized medicine through integrated genomic and other data.
WHO Implementation Research Program on Factors Explaining Success and Failure...RBFHealth
This document discusses implementation research on scaling up Results-Based Financing (RBF) programs from pilot schemes to integrated national health systems. It calls for case studies on RBF initiatives in select low and middle-income countries to identify factors that enable or hinder this transition. Selected proposals will examine RBF scale-up experiences in multiple countries. Next steps include a protocol development workshop to design the research and analyze findings to draw cross-cutting lessons on scaling up RBF.
Maureen Charlebois, Chief Nursing Executive and Group Director, Canada Health...Investnet
This document discusses Canada Health Infoway's efforts to digitally transform healthcare across Canada through three waves of innovation: building foundational digital health infrastructure, providing digital tools for clinicians, and empowering patients. It outlines Infoway's strategic investment model, clinical engagement strategy including peer leader networks, and goals for the next year including expanding e-prescribing and telehomecare services. The presentation emphasizes that digital health technologies can help improve care but also require leadership, change management, and integrating new competencies and ways of working into clinical practice.
How to Define Effective and Efficient Real World TrialsTodd Berner MD
This document discusses strategies for designing effective and efficient real-world clinical trials. It covers topics such as using real-world evidence to inform clinical trial design, the differences between efficacy and effectiveness, challenges around representativeness in trial populations, and the value of pragmatic clinical trials. It also discusses leveraging electronic health records for condition-specific prompts and clinical decision support to improve performance and quality of care.
How to design effective and efficient real world trials TB Evidence 2014 10.2...Todd Berner MD
This document discusses strategies for designing effective and efficient real-world clinical trials. It covers topics such as using real-world evidence to inform clinical trial design, the differences between efficacy and effectiveness, challenges in defining quality metrics, and strategies for improving performance within healthcare systems. The document provides information on pragmatic clinical trials and how real-world evidence could reduce costs compared to traditional clinical trials.
This document summarizes the findings of a review of quality assurance arrangements for NHS pathology services. Interviews were conducted with 43 participants from 12 pathology providers and commissioning organizations. The review found that quality assurance within pathology services is generally strong and driven by providers. There is variability in quality systems between providers and no agreed definition of quality. Commissioners have little involvement in monitoring or driving quality improvement in pathology. Ensuring learning from errors is shared both within and between organizations remains a challenge. Upcoming structural changes to pathology services may impact quality if not properly managed.
Point of Care Testing for Enhancing Patient Centered Planned Care DeliveryPAFP
PAFP 2013 Regional Lecture Series
Session 1 - Northeast
Presenter: Linda Thomas-Hemak, MD
The Wright Center for Primary Care
Broadcast live through the PAFP Community.
October 2nd, 2013 12pm - 1pm
CHOC Children's Hospital implemented an interdisciplinary Patient Flow Improvement Team to address issues with patient throughput and capacity. The team developed technology-enabled solutions across the continuum of care from pre-admission to discharge. This included an electronic bed board, standardized admission processes, and automated discharge workflows. Data from the systems showed improvements such as a 27% increase in ED admissions, 76-80% faster discharge times, and an 81% reduction in cancelled admissions. The initiatives helped align practices with strategic goals of ensuring timely access to care.
How to Achieve a PCMH Certification - Small Practice - Practice-centered medi...Donte Murphy
This is a PowerPoint presentation from Dr. Khan, Medical Director, MedPeds Medical Clinic. He has a small practice and is a certified PCMH. In this presentation he shares his strategy that led to his success. This is a powerful presentation for practices of all sizes, whether large or small. For more information, feel free to email us at: marketing@amazingcharts.com.
This document summarizes evidence on pay-for-performance (P4P) schemes for chronic disease management. It finds that while P4P can have positive effects, the evidence is limited and heterogeneous. Careful design is needed to avoid unintended consequences. Effective elements include incentives at multiple levels, emphasis on protocols and record-keeping, and risk-adjusting payments. More research is still needed to understand optimal incentive sizes, measures, and interactions with existing payment systems.
This document discusses regulatory approval and reimbursement for new medical technologies. It notes challenges with rising costs and uncertainty of drug development. It describes expedited FDA pathways like Fast Track, Priority Review, and Breakthrough Therapy Designation. While approval and coverage don't always align, experiences with parallel FDA/CMS review and conditional approvals in Europe aim to better link evidence standards. Adaptive pathways could approve technologies for narrow uses with commitments for further study. The goal is improving development efficiency and patients' access to promising new options.
Implementation Strategies & Outcomes: Advancing the ScienceHopkinsCFAR
This document discusses implementation science and strategies to advance the field. It begins with definitions of implementation and dissemination research. The document then discusses quality gaps in mental healthcare that implementation research aims to address. It reviews evidence-based interventions and conceptual models for measuring implementation outcomes. The rest of the document outlines theories that guide implementation strategies and provides a compilation of 68 strategies grouped into key processes like plan, educate, finance, restructure, quality management, and policy. It concludes by noting that passive dissemination is ineffective, while training is one of the most commonly used strategies.
- Patient recruitment for clinical trials is a major challenge, estimated to be a $1.2-1.8 billion market. Recruitment costs average 6% of trial costs and are a primary factor in delays.
- Less than 5% of patients are aware of clinical trials, and only 2-3% actually enroll. However, over 90% of participants have a positive experience and would participate again.
- There is significant opportunity to improve recruitment through more patient-centric approaches leveraging data, technology, and analytics to identify more eligible patients and improve the recruitment process. However, this will require changes to traditional models.
This document summarizes the implementation of the Standards Based Management and Recognition (SBM-R) approach to improve quality of child health services in Guinea and Zimbabwe. Key findings include:
1) SBM-R improved health workers' clinical skills and adherence to performance standards, but longer-term impacts on health outcomes were not measured.
2) Implementation lacked consistency with the SBM-R manual and did not sufficiently address health systems support.
3) Recommendations are to better link implementation strength and duration to results, include outcome measures, and adapt SBM-R for low-volume facilities and client perspectives.
Similar to Clahrc ps cmeeting_21st_sept2015_spacer_project_cc (20)
This document describes a comparative analysis project that evaluated whether a rapid qualitative analysis approach could deliver findings more quickly than a traditional in-depth analysis method. The rapid analysis used summary templates to analyze data within a short timeframe, while the in-depth analysis used coding and the Framework method. The results found that rapid analysis was much faster for data management but took longer for interpretation. Both methods produced similar key issues and recommendations, but the in-depth analysis provided more specific, context-informed findings. The document reflects on the applications and limitations of rapid qualitative analysis approaches.
This document discusses moving from current ad-hoc healthcare systems to a national learning health system. It outlines challenges facing healthcare like rising costs and an aging population. Current digital health data is underused. Examples show how data can enable epidemiological research, evaluate policies, and support clinical trials. Bigger efforts are needed to create a prototype national asthma learning health system. This would use various data sources to monitor asthma burden, improve outcomes and reduce deaths. The goal is an integrated system that continuously learns from patient care to drive discovery and improve value.
The document summarizes the history of healthcare development in Birmingham over the past century, from the origins of early hospitals to the planning and construction of the new Queen Elizabeth Hospital. It describes:
- The early voluntary and municipal hospitals established in Birmingham from the 18th century to treat the poor.
- The social, medical, and technological changes in the early 20th century that increased demand for hospital services.
- The controversies over proposals in the 1920s-30s to build a new united hospital center to replace overcrowded facilities.
- The planning process that ultimately led to the construction of the original Queen Elizabeth Hospital, which opened in 1938.
- The need for renewal that resulted in
This document discusses stepped wedge cluster randomized trial designs and recent related research. It provides background on cluster studies over time and describes traditional parallel and crossover cluster designs. It then explains classic and modified stepped wedge designs, issues in methodology, and recent related papers addressing topics like sample size calculations and extending CONSORT guidelines. Finally, it proposes future projects on developing CONSORT standards for stepped wedge trials and exploring designs beyond the standard stepped wedge like "dog leg" and ladder designs to improve efficiency.
4 - Further info - Setting up research in the NHS: practical and ethical cons...NIHR CLAHRC West Midlands
This document provides information about a training event on setting up research in the NHS, including practical and ethical considerations. It outlines the day's program, with a lunch break from 12-1pm, and information about an evaluation form that will be circulated by email after the event. It also provides details about an online NIHR ethics learning module, and further information sources like the CLAHRC West Midlands website and how to sign up for their news blog or email the contact listed.
3 - UoB - Setting up research in the NHS: practical and ethical considerationsNIHR CLAHRC West Midlands
Presentation by Prof Heather Draper, University of Birmingham - exploring information provided to research participants/patients during informed consent process
1 - HRA - Setting up research in the NHS: practical and ethical considerationsNIHR CLAHRC West Midlands
The Health Research Authority (HRA) was established in 2011 to simplify the process for approval of health research in the NHS in England. The HRA aims to reduce the time and cost of setting up studies through a single application process called HRA Approval. When fully implemented, HRA Approval will provide assurance to NHS organizations in England that a study can be undertaken, replacing other approval processes. The presentation provides updates on the phased implementation of HRA Approval for different study types.
CLAHARC WM Capacity Development Strategy - Nathalie Maillard and Tom MarshallNIHR CLAHRC West Midlands
Presentation to Programme Steering Committee on 14th January 2016 on the CLAHARC WM Capacity Development Strategy. Given by Nathalie Maillard and Tom Marshall.
Feedback from 'speed dating' - Postgrad / Early Career Researcher event 19th ...NIHR CLAHRC West Midlands
The document outlines the programme for a postgraduate and early career researcher event held by CLAHRC West Midlands. The programme includes sessions on ethics, collaboration and engagement, public and patient involvement, networking and peer support, and research methodology. Attendees will discuss topics like navigating ethics reviews, balancing clinical and academic work, engaging stakeholders, and designing sound studies.
The document summarizes a trial called the CO-OPS Trial which studied the effects of fatigue on radiologists' performance in breast cancer screening. It tested whether reversing the order radiologists read screening mammograms (to optimize performance patterns) and taking breaks could help address the normal vigilance decrement seen in tasks requiring sustained attention over long periods. The document outlines the trial methods, results, and interpretations that will be presented on fatigue and changing case order in breast screening radiology.
Rapid qualitative analysis vs the 'traditional approach': early findings and ...NIHR CLAHRC West Midlands
Dr Beck Taylor of Theme 1, Maternity and Child Health, presented her latest project, comparing a rapid approach to synthesising evidence from qualitative research to traditional research methods, presented at CLAHRC WM Programme Steering Committee meeting, 22nd October 2015
This document describes the SPACER study which aims to identify the benefits and disadvantages of electronic prescribing and medication administration (EPMA) compared to paper-based systems. The SPACER study will consist of 3 strands conducted over 3 years: 1) An ethnographic study to observe organizational changes and staff perspectives with EPMA implementation. 2) A data envelopment analysis study to assess the impact of EPMA on healthcare service efficiency. 3) A Drugs, Data, Decisions study to identify changes to key performance measures, processes, reporting and decision making regarding the medication process before, during and after EPMA implementation.
MBC Support Group for Black Women – Insights in Genetic Testing.pdfbkling
Christina Spears, breast cancer genetic counselor at the Ohio State University Comprehensive Cancer Center, joined us for the MBC Support Group for Black Women to discuss the importance of genetic testing in communities of color and answer pressing questions.
Exploring the Benefits of Binaural Hearing: Why Two Hearing Aids Are Better T...Ear Solutions (ESPL)
Binaural hearing using two hearing aids instead of one offers numerous advantages, including improved sound localization, enhanced sound quality, better speech understanding in noise, reduced listening effort, and greater overall satisfaction. By leveraging the brain’s natural ability to process sound from both ears, binaural hearing aids provide a more balanced, clear, and comfortable hearing experience. If you or a loved one is considering hearing aids, consult with a hearing care professional at Ear Solutions hearing aid clinic in Mumbai to explore the benefits of binaural hearing and determine the best solution for your hearing needs. Embracing binaural hearing can lead to a richer, more engaging auditory experience and significantly improve your quality of life.
DECODING THE RISKS - ALCOHOL, TOBACCO & DRUGS.pdfDr Rachana Gujar
Introduction: Substance use education is crucial due to its prevalence and societal impact.
Alcohol Use: Immediate and long-term risks include impaired judgment, health issues, and social consequences.
Tobacco Use: Immediate effects include increased heart rate, while long-term risks encompass cancer and heart disease.
Drug Use: Risks vary depending on the drug type, including health and psychological implications.
Prevention Strategies: Education, healthy coping mechanisms, community support, and policies are vital in preventing substance use.
Harm Reduction Strategies: Safe use practices, medication-assisted treatment, and naloxone availability aim to reduce harm.
Seeking Help for Addiction: Recognizing signs, available treatments, support systems, and resources are essential for recovery.
Personal Stories: Real stories of recovery emphasize hope and resilience.
Interactive Q&A: Engage the audience and encourage discussion.
Conclusion: Recap key points and emphasize the importance of awareness, prevention, and seeking help.
Resources: Provide contact information and links for further support.
R3 Stem Cell Therapy: A New Hope for Women with Ovarian FailureR3 Stem Cell
Discover the groundbreaking advancements in stem cell therapy by R3 Stem Cell, offering new hope for women with ovarian failure. This innovative treatment aims to restore ovarian function, improve fertility, and enhance overall well-being, revolutionizing reproductive health for women worldwide.
The best massage spa Ajman is Chandrima Spa Ajman, which was founded in 2023 and is exclusively for men 24 hours a day. As of right now, our parent firm has been providing massage services to over 50,000+ clients in Ajman for the past 10 years. It has about 8+ branches. This demonstrates that Chandrima Spa Ajman is among the most reasonably priced spas in Ajman and the ideal place to unwind and rejuvenate. We provide a wide range of Spa massage treatments, including Indian, Pakistani, Kerala, Malayali, and body-to-body massages. Numerous massage techniques are available, including deep tissue, Swedish, Thai, Russian, and hot stone massages. Our massage therapists produce genuinely unique treatments that generate a revitalized sense of inner serenely by fusing modern techniques, the cleanest natural substances, and traditional holistic therapists.
Gemma Wean- Nutritional solution for Artemiasmuskaan0008
GEMMA Wean is a high end larval co-feeding and weaning diet aimed at Artemia optimisation and is fortified with a high level of proteins and phospholipids. GEMMA Wean provides the early weaned juveniles with dedicated fish nutrition and is an ideal follow on from GEMMA Micro or Artemia.
GEMMA Wean has an optimised nutritional balance and physical quality so that it flows more freely and spreads readily on the water surface. The balance of phospholipid classes to- gether with the production technology based on a low temperature extrusion process improve the physical aspect of the pellets while still retaining the high phospholipid content.
GEMMA Wean is available in 0.1mm, 0.2mm and 0.3mm. There is also a 0.5mm micro-pellet, GEMMA Wean Diamond, which covers the early nursery stage from post-weaning to pre-growing.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - ...rightmanforbloodline
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
TEST BANK FOR Health Assessment in Nursing 7th Edition by Weber Chapters 1 - 34.
Healthy Eating Habits:
Understanding Nutrition Labels: Teaches how to read and interpret food labels, focusing on serving sizes, calorie intake, and nutrients to limit or include.
Tips for Healthy Eating: Offers practical advice such as incorporating a variety of foods, practicing moderation, staying hydrated, and eating mindfully.
Benefits of Regular Exercise:
Physical Benefits: Discusses how exercise aids in weight management, muscle and bone health, cardiovascular health, and flexibility.
Mental Benefits: Explains the psychological advantages, including stress reduction, improved mood, and better sleep.
Tips for Staying Active:
Encourages consistency, variety in exercises, setting realistic goals, and finding enjoyable activities to maintain motivation.
Maintaining a Balanced Lifestyle:
Integrating Nutrition and Exercise: Suggests meal planning and incorporating physical activity into daily routines.
Monitoring Progress: Recommends tracking food intake and exercise, regular health check-ups, and provides tips for achieving balance, such as getting sufficient sleep, managing stress, and staying socially active.
About this webinar: This talk will introduce what cancer rehabilitation is, where it fits into the cancer trajectory, and who can benefit from it. In addition, the current landscape of cancer rehabilitation in Canada will be discussed and the need for advocacy to increase access to this essential component of cancer care.
International Cancer Survivors Day is celebrated during June, placing the spotlight not only on cancer survivors, but also their caregivers.
CANSA has compiled a list of tips and guidelines of support:
https://cansa.org.za/who-cares-for-cancer-patients-caregivers/
Hypertension and it's role of physiotherapy in it.Vishal kr Thakur
This particular slides consist of- what is hypertension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is summary of hypertension -
Hypertension, also known as high blood pressure, is a serious medical condition that occurs when blood pressure in the body's arteries is consistently too high. Blood pressure is the force of blood pushing against the walls of blood vessels as the heart pumps it. Hypertension can increase the risk of heart disease, brain disease, kidney disease, and premature death.
This particular slides consist of- what is hypotension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is the summary of hypotension:
Hypotension, or low blood pressure, is when the pressure of blood circulating in the body is lower than normal or expected. It's only a problem if it negatively impacts the body and causes symptoms. Normal blood pressure is usually between 90/60 mmHg and 120/80 mmHg, but pressures below 90/60 are generally considered hypotensive.
1. Evaluation of the introduction of
Electronic Prescribing and
Medicines Administration (EPMA)
at Birmingham Children’s Hospital
Carole Cummins
Maternity and Child Health Theme
2. Children are not small adults
• Cognition
• Development
• Physiology
• Pharmacokinetics
• Pharmacoodynamics
• Prescribing
3. ePrescribing at Birmingham
Children’s Hospital
• UK paediatric hospitals are late adopters of ePrescribing systems
• Paediatric prescribing is more complex but with a weaker evidence
base than prescribing for adults
• Key barrier to adoption is lack of a computerised knowledge base to
inform decision support
• In order to introduce ePrescribing BCH invested in:
– Development of a drug database and procedures to review and
check drug information (now with support from NHS England)
– Adoption of the UHB NHS FT PICs platform
– Committed to the required estates changes and acquisition of
peripherals
• CEO identified ePrescribing as an area for evaluation and matched
funding in the WM CLARHC Maternity and Child Health Theme
4. BCH Business Case
Benefits Realisation
plan
We needed to
consider how an
evaluation can be
aligned against
realisation plan but
the plan requires
development.
An NHS England
Framework provides
an similar but more
extensive catalogue.
Issues: conceptual
overlap, atheoretical
Benefits Area
Anticipated Benefits
Patient
Safer = far fewer drug errors.
Charts less likely to get lost.
Easier access to previous prescriptions = saves time, effort
and fewer mistakes.
Nurse
Legible record = save time & reduce errors.
Decision support = fewer errors.
Doctor
Warnings = stop major errors.
Decision support built into system = faster & fewer errors.
Remote access = better work flows.
Pharmacist
Access to records in use = better work flows e.g. TTOs ,
clinical screening etc
Traceability of all drug prescription and administration.
Formulary control.
Full audit trail = better clinical governance, financial control
and better macro decisions about drug policy.
Operational
Easier data compliance with national standards.
Better workload planning.
Identification of prescribers and prescriber performance
indicators.
Financial
Capturing High cost drug data/PBR support reclaims.
Support continuing care claims.
5. Provisional CLAHRC view of benefits
realisation and proposed evaluation
components
• BCH data sources
– Include Board safety
report, audit data,
incident reports (Merck
classification of harm)
• University of Birmingham
– Impact on the hospital
ward: ethnographic
study
• Aston University
– Efficiency and value
Benefits
Area
Domain Evidence
Patient
Quality
and safety
Incident reports
Drug chart review
Prescription audit
Medication audit
Medication error
Qualitative research
Surveys
Nurse
Doctor
Pharmacist
Efficiency
and value
Proposed Data Envelopment Analysis
Pharmacy process
Operational
Financial
6. Proposed evaluation
• Evaluation plan covers the first stage of implementation:
• Pre-, during and post- implementation
– Will use currently available or potentially collectable measures
• Board safety report covers incident reports,
medication/prescribing audits, errors, root cause analyses
• Measurement of some metrics changes pre- and post-
intervention
• Post implementation development will allow quality improvement
innovations that are not currently possible
– Relates to benefits realisation plan
– These are likely to involve prescribing, medicines administration
and drug costs at the individual patient level –
– later CLAHRC projects? Additional funding?
7. Complexity…
• ePrescribing is a complex intervention implemented into complex
hospital systems
• Example: To Take Out (TTO) medications
– Efficient supply of TTO prescriptions is a marker of pharmacy
efficiency
– TTOs have been identified as a critical path in the discharge
pathway
– A discharge planning intervention is part of wider innovation to
improve the flow of patients through the hospital and the
efficiency of bed use
– Improved bed use will impact on the routing of patients into the
hospital via the ED, GPs and referrals
– Improved routing of patients will impact on other health providers
for children
8. A suitable theoretical model for this evaluation?
Triangle model for evaluating the effect of health information
technology on healthcare quality and safety, JS Ancker 2012
Adaptation of Donabedian model
Structure
Process
Outcomes
9. Some questions/ points for discussion:
• How/ should we link the components of the planned evaluation?
• How do we allow for complexity?
• Can we fit the evaluation into a single theoretical model?
• Is the triangle model a good fit?
• Can and should we publish an overarching protocol?
• Safety: as serious harm is rare and hard to measure, we will largely
be looking at changes in processes to mitigate risk – discuss.