This document outlines the development of a decision guide for policy makers to determine which type of health technology assessment (HTA) product is needed. It describes 3 core objectives: 1) an inventory of HTA products, 2) criteria for selecting product types, and 3) a framework for using HTA products. It also provides examples of how the framework has been applied to specific policy questions on radiofrequency ablation and hysteroscopic tubal sterilization. The framework is intended to provide consistency, define the appropriate scope and balance of information needed, and aid discussions between HTA partners and policy makers.
Implementation of Electronic Screening & Clinical Support into General Outpat...chshanah
The document discusses implementing screening and clinical support for substance use into general outpatient medical practices. It describes lessons learned from implementing screening, brief intervention, and referral to treatment (SBIRT) programs in non-research primary care settings. Key challenges included competing priorities, lack of provider training, and misaligned financial incentives in general medical practices. The document recommends that the National Institute on Drug Abuse support SBIRT implementation by establishing standardized substance use data standards, providing point-of-care training and clinical decision support tools, and leveraging electronic health records.
This document outlines the key elements to include in a research brief for pre-launch product research. It discusses researching the market, competitors, target audiences and consumer attitudes. The brief should provide background on the company and brand, key objectives, target audiences, the proposed approach (quantitative and/or qualitative), deliverables, timings, budget, project team, and next steps. The purpose is to help the agency conducting the research understand what is needed to inform the product launch strategy.
ONC Market R&D Pilot challenge Webinar finalhealth2dev
The Market R&D Pilot Challenge, brought to you by the Office of the National Coordinator for Health Information Technology (ONC), will help bridge technological gaps by bringing together health care organizations and innovative companies through $300,000 in pilot funding awards and facilitated matchmaking. This webinar provides more detail on the challenge and answers some common questions
The PRIME scheme aims to foster the development of medicines that address major unmet medical needs. It provides early and enhanced regulatory support through scientific advice and accelerated assessment. Since launching in 2016, over 50% of requests have come from small-to-medium enterprises. Of the 177 requests received, 36 products have been granted eligibility, covering a wide range of therapeutic areas. Key benefits for eligible products include early regulatory advice, a dedicated contact point, and potential for accelerated review. After two years, PRIME continues to successfully promote the development of promising medicines focused on unmet needs.
Presentation - New Business Models for Antibiotics: Where Are We Now? 16 Marc...Office of Health Economics
Speaking at the Superbugs & Superdrugs conference in London on 16 March 2016, OHE’s Jorge Mestre-Ferrandiz delivered a presentation on financial and collaborative incentives to accelerate clinical success for antibiotics.
Jorge discussed the economic challenges around antibiotics, and whether there is a need for a new business model. He reviewed of the impact of previous incentives, explaining what has worked in the past, and discussed possible new business models.
Implementation of Electronic Screening & Clinical Support into General Outpat...chshanah
The document discusses implementing screening and clinical support for substance use into general outpatient medical practices. It describes lessons learned from implementing screening, brief intervention, and referral to treatment (SBIRT) programs in non-research primary care settings. Key challenges included competing priorities, lack of provider training, and misaligned financial incentives in general medical practices. The document recommends that the National Institute on Drug Abuse support SBIRT implementation by establishing standardized substance use data standards, providing point-of-care training and clinical decision support tools, and leveraging electronic health records.
This document outlines the key elements to include in a research brief for pre-launch product research. It discusses researching the market, competitors, target audiences and consumer attitudes. The brief should provide background on the company and brand, key objectives, target audiences, the proposed approach (quantitative and/or qualitative), deliverables, timings, budget, project team, and next steps. The purpose is to help the agency conducting the research understand what is needed to inform the product launch strategy.
ONC Market R&D Pilot challenge Webinar finalhealth2dev
The Market R&D Pilot Challenge, brought to you by the Office of the National Coordinator for Health Information Technology (ONC), will help bridge technological gaps by bringing together health care organizations and innovative companies through $300,000 in pilot funding awards and facilitated matchmaking. This webinar provides more detail on the challenge and answers some common questions
The PRIME scheme aims to foster the development of medicines that address major unmet medical needs. It provides early and enhanced regulatory support through scientific advice and accelerated assessment. Since launching in 2016, over 50% of requests have come from small-to-medium enterprises. Of the 177 requests received, 36 products have been granted eligibility, covering a wide range of therapeutic areas. Key benefits for eligible products include early regulatory advice, a dedicated contact point, and potential for accelerated review. After two years, PRIME continues to successfully promote the development of promising medicines focused on unmet needs.
Presentation - New Business Models for Antibiotics: Where Are We Now? 16 Marc...Office of Health Economics
Speaking at the Superbugs & Superdrugs conference in London on 16 March 2016, OHE’s Jorge Mestre-Ferrandiz delivered a presentation on financial and collaborative incentives to accelerate clinical success for antibiotics.
Jorge discussed the economic challenges around antibiotics, and whether there is a need for a new business model. He reviewed of the impact of previous incentives, explaining what has worked in the past, and discussed possible new business models.
All patients are different, and data collected during product development or Randomised Clinical Trials (RCT) does not always paint the full picture of everyday patients. RWE insights complement the manufacturing process and RCT findings, adding more value and providing real-world impact. While together data from the manufacturing process and RWD paint a fuller picture.
Due to the limitations of the study design, data from the manufacturing process and RCTs are inadequate for demonstrating an intervention’s long-term safety and effectiveness. Moreover, it is possible to compare multiple product or interventions in RWE.
The document discusses how healthcare organizations are increasingly relying on data analytics and data scientists. It notes that while analytics can help improve patient care and reduce costs, the healthcare industry lags behind other sectors in adopting new technologies and analyzing data due to privacy concerns and differences in prioritizing risks. The document outlines some current uses of analytics including clinical decision support, fraud detection, and personalized treatment plans. It also explores challenges to wider adoption such as establishing standards and gaining access to data.
CADTH conducts Therapeutic Reviews to inform drug listing and policy decisions in Canada. Topics are chosen based on relevance and need. The reviews involve clinical researchers, health economists, and specialists. Patients and stakeholders provide input to ensure the scope reflects patient values. The Canadian Drug Expert Committee develops non-binding recommendations considering the review reports. Knowledge mobilization tools are created to disseminate the results, helping decision-makers optimize drug therapy across Canada.
Health technology assessment (HTA) is familiar as technique for gauging the value of specific medical technologies or approaches to care. As Adrian Towse points out, however, HTA has a much broader, ‘macro’ role in contributing to the efficiency of health care systems and supporting universal health coverage. This is particularly crucial in the face of increasing demands and limited budgets.
The document provides an overview of innovation and intellectual property (IP) processes at Alberta Health Services (AHS). It discusses definitions of innovation in healthcare and the importance of innovation and IP for health systems. It outlines AHS' IP policy and the processes for evaluating, managing, and commercializing innovations and IP from conception through stages of development. This includes establishing an Innovation Portal for identifying and advancing innovations, and conducting health technology assessments. A case study on a LINAC-MR radiation therapy project demonstrates applying these processes and developing a commercialization plan for an AHS-owned innovation. The document aims to provide guidance to innovators on partnering with AHS to advance healthcare innovations.
Brief Introduction to the HTA Core Model (r), Anna Nachtnebel, LBI-HTA
Presentation from the 3rd face to face training course for EUnetHTA Stakeholders organised by EUnetHTA JA2 WP2; April 23rd, 2015, Brussels.
The document discusses how healthcare organizations are increasingly using data analytics and data science. It notes that healthcare analytics aims to improve clinical care while reducing costs. Examples are given of organizations that are using analytics, such as predicting patient admissions and using inhaler trackers to identify asthma trends. The document also discusses challenges like privacy concerns with data and establishing standards. It predicts future trends will include more wearable devices generating health data and increased data sharing through electronic records.
Usage Factor is a new proposed metric to measure journal quality based on usage statistics rather than citations. It is being developed as a COUNTER project to provide a complementary measure to the Journal Impact Factor. The project conducted market research, collected and analyzed usage data from several publishers, and made recommendations for how the Usage Factor should be calculated and reported. Key findings were that authors, publishers, and librarians were generally supportive of the Usage Factor concept and saw it providing additional insights beyond citation-based measures alone.
This document summarizes a presentation given at an ISPOR conference on multi-indication pricing. It discusses the challenges of setting one price for a drug across multiple indications when the value may differ based on the indication. It provides examples showing large price differences between indications for the same drugs in different countries. Stakeholders generally support prices reflecting relative value but have concerns about implementation. UK workshop participants felt more collaboration would be needed between stakeholders if the UK pursued multi-indication pricing schemes.
This document discusses multi-indication pricing (MIP), an innovative pricing scheme where medicines can be priced differently for different approved indications. MIP aims to set prices that better reflect the value of a drug across its indications. The document outlines MIP frameworks, reviews international examples, and discusses challenges to implementing MIP in the UK healthcare system. Key challenges include whether the NHS can handle variable net prices by indication and monitor usage data. International experience shows MIP being used with different brands of the same drug or through sub-national pricing schemes. MIP warrants further exploration but requires collaboration across stakeholders and consideration of data and pricing model options.
This document summarizes a kick-off meeting for the SAFTINet project. The meeting welcomed collaborators and outlined goals of establishing a distributed research network to conduct comparative effectiveness research using electronic health data from multiple healthcare organizations. The agenda included introductions of participating organizations, presentations on comparative effectiveness research and the technical capabilities needed, and discussions around engaging partners and getting started with the work.
The document discusses regional initiatives to promote evidence-informed health policymaking. It describes the Evidence-Informed Policy Network (EVIPNet) which aims to support policymaking through partnerships between policymakers, researchers, and civil society. EVIPNet facilitates using the best scientific evidence available to develop and implement policies. It also establishes country-level teams and trains policymakers and researchers to better link research evidence to policies.
Real World Evidence - getting value from volume with metadataAnn Kelly
Anne Lapkin from Smartlogic and Bill Fox from MarkLogic webinar on Real World Evidence; the value, the opportunity, the problems and the platform of the future
This document discusses the challenges of value-based pricing for pharmaceuticals and proposes multi-indication pricing as a solution. It notes that a single price across all indications can restrict access for some patients and discourage development of new indications. Multi-indication pricing, where the price varies based on the value for each indication or patient subgroup, could increase access for more patients while still reflecting value. However, it adds complexity. The document explores options for implementing multi-indication pricing such as blended pricing or differential rebates and argues that this approach is needed as most drugs now have multiple indications.
The Green Park Collaborative (GPC) has developed a new tool to help health care decision makers confidently and consistently use Real World Evidence (RWE) when making tough coverage and care choices. Called RWE Decoder, the spreadsheet-based assessment tool lets users review and evaluate all existing studies and evidence for both rigor and relevance. Informed by these factors, users can assess study quality, and generate a visual summary to help gauge the evidence under review.
Published RWE studies developed from data-rich electronic medical records or medical claims data are increasingly available from health care systems. However, the quality of this research can vary widely, and payers, clinicians and other health care decision makers often dismiss it out of hand. RWE Decoder and its associated user guide and framework, offer a thoughtful approach to helping these decision makers assess whether RWE studies address their questions and can appropriately guide their choices.
The tool, user guide, and supporting white paper are available here: https://goo.gl/AhbHUw
This document provides a summary of the author's travels through Canada in October 2012. It describes stops in Sault Ste. Marie, Manitoulin Island, Espanola Golf and Country Club, and points of natural scenery along the way. Indigenous communities on Manitoulin Island are working to revive their culture and buy back traditional lands.
This document discusses Stewart Social Media's classes and services for real estate professionals. It focuses on using blogging and email marketing together as an effective strategy. Key points made include: setting up a blog to collect email subscribers; nurturing relationships with subscribers through weekly informative emails with calls to action; and using various "roads" like social media, SEO, and paid ads to drive traffic to the blog and grow the email list. Pricing for Stewart Social Media's products and services is also listed.
All patients are different, and data collected during product development or Randomised Clinical Trials (RCT) does not always paint the full picture of everyday patients. RWE insights complement the manufacturing process and RCT findings, adding more value and providing real-world impact. While together data from the manufacturing process and RWD paint a fuller picture.
Due to the limitations of the study design, data from the manufacturing process and RCTs are inadequate for demonstrating an intervention’s long-term safety and effectiveness. Moreover, it is possible to compare multiple product or interventions in RWE.
The document discusses how healthcare organizations are increasingly relying on data analytics and data scientists. It notes that while analytics can help improve patient care and reduce costs, the healthcare industry lags behind other sectors in adopting new technologies and analyzing data due to privacy concerns and differences in prioritizing risks. The document outlines some current uses of analytics including clinical decision support, fraud detection, and personalized treatment plans. It also explores challenges to wider adoption such as establishing standards and gaining access to data.
CADTH conducts Therapeutic Reviews to inform drug listing and policy decisions in Canada. Topics are chosen based on relevance and need. The reviews involve clinical researchers, health economists, and specialists. Patients and stakeholders provide input to ensure the scope reflects patient values. The Canadian Drug Expert Committee develops non-binding recommendations considering the review reports. Knowledge mobilization tools are created to disseminate the results, helping decision-makers optimize drug therapy across Canada.
Health technology assessment (HTA) is familiar as technique for gauging the value of specific medical technologies or approaches to care. As Adrian Towse points out, however, HTA has a much broader, ‘macro’ role in contributing to the efficiency of health care systems and supporting universal health coverage. This is particularly crucial in the face of increasing demands and limited budgets.
The document provides an overview of innovation and intellectual property (IP) processes at Alberta Health Services (AHS). It discusses definitions of innovation in healthcare and the importance of innovation and IP for health systems. It outlines AHS' IP policy and the processes for evaluating, managing, and commercializing innovations and IP from conception through stages of development. This includes establishing an Innovation Portal for identifying and advancing innovations, and conducting health technology assessments. A case study on a LINAC-MR radiation therapy project demonstrates applying these processes and developing a commercialization plan for an AHS-owned innovation. The document aims to provide guidance to innovators on partnering with AHS to advance healthcare innovations.
Brief Introduction to the HTA Core Model (r), Anna Nachtnebel, LBI-HTA
Presentation from the 3rd face to face training course for EUnetHTA Stakeholders organised by EUnetHTA JA2 WP2; April 23rd, 2015, Brussels.
The document discusses how healthcare organizations are increasingly using data analytics and data science. It notes that healthcare analytics aims to improve clinical care while reducing costs. Examples are given of organizations that are using analytics, such as predicting patient admissions and using inhaler trackers to identify asthma trends. The document also discusses challenges like privacy concerns with data and establishing standards. It predicts future trends will include more wearable devices generating health data and increased data sharing through electronic records.
Usage Factor is a new proposed metric to measure journal quality based on usage statistics rather than citations. It is being developed as a COUNTER project to provide a complementary measure to the Journal Impact Factor. The project conducted market research, collected and analyzed usage data from several publishers, and made recommendations for how the Usage Factor should be calculated and reported. Key findings were that authors, publishers, and librarians were generally supportive of the Usage Factor concept and saw it providing additional insights beyond citation-based measures alone.
This document summarizes a presentation given at an ISPOR conference on multi-indication pricing. It discusses the challenges of setting one price for a drug across multiple indications when the value may differ based on the indication. It provides examples showing large price differences between indications for the same drugs in different countries. Stakeholders generally support prices reflecting relative value but have concerns about implementation. UK workshop participants felt more collaboration would be needed between stakeholders if the UK pursued multi-indication pricing schemes.
This document discusses multi-indication pricing (MIP), an innovative pricing scheme where medicines can be priced differently for different approved indications. MIP aims to set prices that better reflect the value of a drug across its indications. The document outlines MIP frameworks, reviews international examples, and discusses challenges to implementing MIP in the UK healthcare system. Key challenges include whether the NHS can handle variable net prices by indication and monitor usage data. International experience shows MIP being used with different brands of the same drug or through sub-national pricing schemes. MIP warrants further exploration but requires collaboration across stakeholders and consideration of data and pricing model options.
This document summarizes a kick-off meeting for the SAFTINet project. The meeting welcomed collaborators and outlined goals of establishing a distributed research network to conduct comparative effectiveness research using electronic health data from multiple healthcare organizations. The agenda included introductions of participating organizations, presentations on comparative effectiveness research and the technical capabilities needed, and discussions around engaging partners and getting started with the work.
The document discusses regional initiatives to promote evidence-informed health policymaking. It describes the Evidence-Informed Policy Network (EVIPNet) which aims to support policymaking through partnerships between policymakers, researchers, and civil society. EVIPNet facilitates using the best scientific evidence available to develop and implement policies. It also establishes country-level teams and trains policymakers and researchers to better link research evidence to policies.
Real World Evidence - getting value from volume with metadataAnn Kelly
Anne Lapkin from Smartlogic and Bill Fox from MarkLogic webinar on Real World Evidence; the value, the opportunity, the problems and the platform of the future
This document discusses the challenges of value-based pricing for pharmaceuticals and proposes multi-indication pricing as a solution. It notes that a single price across all indications can restrict access for some patients and discourage development of new indications. Multi-indication pricing, where the price varies based on the value for each indication or patient subgroup, could increase access for more patients while still reflecting value. However, it adds complexity. The document explores options for implementing multi-indication pricing such as blended pricing or differential rebates and argues that this approach is needed as most drugs now have multiple indications.
The Green Park Collaborative (GPC) has developed a new tool to help health care decision makers confidently and consistently use Real World Evidence (RWE) when making tough coverage and care choices. Called RWE Decoder, the spreadsheet-based assessment tool lets users review and evaluate all existing studies and evidence for both rigor and relevance. Informed by these factors, users can assess study quality, and generate a visual summary to help gauge the evidence under review.
Published RWE studies developed from data-rich electronic medical records or medical claims data are increasingly available from health care systems. However, the quality of this research can vary widely, and payers, clinicians and other health care decision makers often dismiss it out of hand. RWE Decoder and its associated user guide and framework, offer a thoughtful approach to helping these decision makers assess whether RWE studies address their questions and can appropriately guide their choices.
The tool, user guide, and supporting white paper are available here: https://goo.gl/AhbHUw
This document provides a summary of the author's travels through Canada in October 2012. It describes stops in Sault Ste. Marie, Manitoulin Island, Espanola Golf and Country Club, and points of natural scenery along the way. Indigenous communities on Manitoulin Island are working to revive their culture and buy back traditional lands.
This document discusses Stewart Social Media's classes and services for real estate professionals. It focuses on using blogging and email marketing together as an effective strategy. Key points made include: setting up a blog to collect email subscribers; nurturing relationships with subscribers through weekly informative emails with calls to action; and using various "roads" like social media, SEO, and paid ads to drive traffic to the blog and grow the email list. Pricing for Stewart Social Media's products and services is also listed.
The document provides an annual review of initiatives to implement the Comprehensive Plan for College Station. It summarizes progress made in 2013 on neighborhood, district, and corridor plans; master plans for areas like the Medical District and parks; special projects like the BioCorridor development and Demographic Profile; and updates to the Unified Development Ordinance. It describes challenges faced and priorities for 2014 to ensure the Comprehensive Plan guides future growth.
BVSWMA, Inc. is a non-profit corporation founded in 2010 that provides solid waste disposal for Bryan and College Station through Twin Oaks Landfill and Compost facilities. It is self-funded through user fees and has 25 employees. The budget overview shows revenue projections of $6.9 million for 2013 and $6.9 million for 2014, with operating expenses of $4.9 million for 2013 and $5.3 million for 2014. Capital expenses are projected to decrease from $3.6 million in 2013 to $2.5 million in 2014. Reserves total over $4.6 million for closure and post-closure costs.
Electronic records of undesirable driving eventsOren_Musicant
This document summarizes an exploratory analysis of undesirable driving events using data collected from vehicle sensors. The analysis found that:
1) The frequency of undesirable driving events was higher at the beginning and end of trips compared to the middle of trips.
2) The frequency of events differed depending on the time of day and day of the week, with more events occurring at night and on weekdays.
3) A negative binomial model provided a better fit for the data than a Poisson model, as the variance was greater than the mean.
4) Event frequency also differed between male and female drivers depending on the time.
The document outlines an agenda and proposed next steps for the Information Exchange Workgroup. Key points include:
- Establishing two task forces focused on provider directories and public health transactions.
- Developing work plans and timelines for each task force to assess current issues, identify barriers, and make recommendations.
- Prioritizing initial areas like laboratory results, electronic prescribing, and patient summary exchange in relation to Meaningful Use.
- Coordinating activities with the HIT Policy Committee and ensuring alignment with other national health IT initiatives.
The workgroup aims to address specific challenges to information exchange and make policy recommendations to facilitate interoperability goals.
This project explored whether an aligned, forward-looking health technology assessment (HTA) process exists, or can be established. The areas of interest for modern HTA systems were identified and explored in terms of ‘future directions’, namely the HTA good practice principles that are debated or that pose implementation challenges. Based on conversations with HTA experts from high- and middle-income countries, we concluded that an aligned, modern, forward-looking HTA is not feasible but further research initiatives would be valuable to stimulate debate and provide clarity in these topic areas.
Author(s) and affiliation(s): Margherita Neri, the Office of Health Economics, Grace Hampson, the Office of Health Economics and Adrian Towse, the Office of Health Economics
Conference/meeting: ISPOR Europe 2018
Event location: Barcelona, Spain
Date: 13 November 2018
Placing the Evolution of HTA In Emerging Markets in Context of Health System ...Office of Health Economics
These slides were presented by Professor Adrian Towse at the 9th World Congress of the International Health Economics Association in July 2013. The presentation examined how the development of health care systems affect the evolution of the use of health technology assessment. Three countries provide case studies: Brazil, China and Taiwan.
ANDS health and medical data webinar 9 May. Review of the National Statement ...ARDC
Presentation by Jeremy Kenner from NHMRC on the review of the National Statement on Ethical Conduct in Human Research. Given on 9 May 2017
Full Webinar: https://www.youtube.com/watch?v=eENTF3oVVdk&t=2s
Transcript: https://www.slideshare.net/AustralianNationalDataService/transcript-webinar9517healthandmedicalshortbites
CADTH is a not-for-profit organization funded by Health Canada and provincial/territorial governments. It conducts health technology assessments of drugs and devices, employs 190 staff in Ottawa and Toronto, and is involved globally in health technology assessment. CADTH provides decision-makers with objective evidence on clinical and cost effectiveness to promote optimal use of health technologies and build domestic assessment capacity. While quality-adjusted life years are important, health technology assessment considers additional societal perspectives. Adaptive licensing and pathways prospectively plan iterative evidence gathering and regulatory/coverage adaptations to balance early access and assessment of uncertainties using real-world data across sectors.
Multi-Stakeholder Dialogues Addressing Needs, HTA Requirements and Good Pract...Office of Health Economics
This document summarizes the Asia-Pacific Policy Forum (APF), a multi-stakeholder dialogue addressing health technology assessment (HTA) needs and practices in emerging countries. The APF has met annually since 2013 in different Asia-Pacific countries to discuss topics like effective use of HTA resources, transferring HTA between countries, and overcoming barriers to universal healthcare using HTA. Key stakeholders represented include HTA agencies, health ministries, and industry. Surveys are distributed before meetings to gather data and increase awareness. Meeting discussions focus on challenges faced and learning from international colleagues. Post-meeting surveys find the opportunity for stakeholder collaboration and discussion is highly valued.
FEAST and TechFit: Rapid livestock feed assessment tools for supporting inter...ILRI
Poster prepared by Ben Lukuyu (ILRI) and Alan Duncan (ILRI) for the Agrifood chain toolkit conference: Livestock and fish value chains in East Africa, Kampala, 9-11 September 2013.
Sustainable Procurement Index for Health (SPIH) Virtual SessionUN SPHS
This document provides an overview and agenda for a session on the Sustainable Procurement Index for Health (SPIH) project. It introduces the moderator and speakers for the session. The session will include an overview of the SPIH concepts, a discussion of the piloting phase where the SPIH was tested, and feedback from the piloting phase. It will conclude with a question and answer period. The objectives of the piloting phase are outlined as understanding how easy or challenging the SPIH is for suppliers to complete and buyers to review, and gathering feedback on the SPIH structure, criteria, and implementation. An overview of the piloting process and the types of feedback requested from participants is also provided.
An introduction to conducting a systematic literature review for social scien...rosie.dunne
An introduction to conducting a systematic literature review for social scientists and health researchers presented by Luke van Rhoon Health Behaviour Change Research Group, School of Psychology, NUI Galway November 2020
This document summarizes a workshop on designing managed access programs (MAPs) for rare disease drugs. The workshop objectives were to enhance understanding of MAPs' role in patient access and work in groups to design MAPs within national pharmacare. The agenda included case study discussions, working groups to refine MAP proposals, and summarizing recommendations. Case studies examined complex therapies, gene therapies, and rare disease drugs. Groups addressed questions on stakeholder involvement, eligibility, stopping criteria, ensuring compliance, and using data for decisions. Feedback informed further discussion on feasibility and a closing discussion reflected on progress and remaining questions around health technology assessments, clinician input, expertise, and patient experiences.
The issue of open-source models in the cost-effectiveness and disease-level (collaborative) models has been brewing for many years. There has been a marked growth in open science, and funding bodies and publishers increasingly require that research data be made available. As mentioned in our previous Issue Panel, “cost-effectiveness models synthesise a wide range of evidence to facilitate extrapolation over time and from intermediate to final decision endpoints. These models are often statistically sophisticated and require assumptions that are not directly testable. This can lead to decision-makers “discounting” the results of cost-effectiveness analyses, particularly if the developer is seen as partial.” Open-source models, then, would encourage greater transparency in pharmacoeconomic modeling and the reuse and updating of the best/most useful models; they are essential if cost-effectiveness analyses are to be widely accepted to reduce bias, increase transparency, improve model access, and allow for faster access to critical knowledge. The ISPOR-SMDM guidelines and the EUnetHTA joint action projects, are supportive of these views on collaboration, transparency, confidentiality, processes and consistency offered by the availability of open-source models to improve decision-making around health care and reimbursement. With openness and sharing, however, come issues of copyright and access and a need to define how model sharing can be achieved in a fair and equitable manner. There is, therefore, a need to develop an ongoing dialog on openness, especially where the research may be considered precompetitive and not worthy of IP investment. The pros and cons of open source models and the proposed mission of the Open Source Model SIG to curate an ongoing dialog regarding issues around creating, disseminating, sharing, evaluating, and updating open source cost-effectiveness and comparative effectiveness models will be debated amongst SIG members.
Author(s) and affiliation(s): Nancy Risebrough, Senior Principal, ICON plc, Toronto, Canada Jeroen P Jansen; Innovation & Value Initiative; Precision Medicine Group; and Stanford University Lotte Steuten, Vice President & Head of Consulting, Office of Health Economics, UK Renée JG Arnold, PharmD, RPh, ICON plc, New York, NY and Icahn School of Medicine at Mount Sinai, New York, NY, USA
Event: ISPOR 2019 Annual Meeting
Date: 20/05/2019
The FDA Early Feasibility Study Pilot and the Innovation PathwayTrimed Media Group
WASHINGTON, D.C.—FDA researchers Andrew A. Farb, MD, and Dorothy B. Abel presented an overview about the potential for an FDA Early Feasibility Study pilot program in the U.S., recognizing a need for a cultural shift within the agency. However, evaluating the FDA guidance, they also recognized the challenges to the device evaluation strategy.
The document provides an overview of health technology assessment (HTA) reports produced by the Malaysian Health Technology Assessment Section (MaHTAS). It discusses MaHTAS's functions, products, and processes for conducting HTAs. Key points include that MaHTAS has produced over 550 HTA reports since 1997 covering various health technologies. The document also outlines criteria for evaluating the quality of HTA reports based on a checklist from the International Network of Agencies for HTA, focusing on transparency around methods, sources of information, and conclusions.
- The document discusses the topic selection process for the AHRQ Effective Health Care Program, which systematically reviews evidence on healthcare topics.
- It outlines principles for topic selection including stakeholder involvement, defined criteria, transparency, and process evaluation.
- An internal group reviews topic nominations using 18 selection criteria to identify important research topics in a structured, transparent manner. The process aims to prioritize topics that are relevant, non-redundant, and have sufficient evidence for review.
- Early results of the revised 2008 nomination process and ongoing challenges in identifying and prioritizing review topics are presented.
The document discusses implementing screening and clinical support for substance use into general outpatient medical practices. It describes lessons learned from implementing screening, brief intervention, and referral to treatment (SBIRT) programs in non-research primary care settings. Key challenges include a lack of standardized substance use data and clinical decision support in electronic health records. The document recommends that the National Institute on Drug Abuse support SBIRT implementation by establishing data standards, providing training and decision support tools, and helping to integrate these resources into electronic health records.
Suzanne Wait: Does benchmarking guide policyNuffield Trust
1) Benchmarking aims to guide health policy but faces challenges like measuring what is easy rather than important and indicator fatigue.
2) Benchmarking is intended to improve performance but there are questions around whether it actually influences patient choice or quality of care.
3) For benchmarking to effectively guide policy, objectives must be clear and indicators must reflect desired outcomes and priorities, with clinical and policymaker engagement.
Transitional Care for Pediatric Patients with Neuromuscular Diseases: A Healt...HTAi Bilbao 2012
Transitional Care for Pediatric Patients with Neuromuscular Diseases: A Health Technology Assessment
Jackie Tran, MD
University of Medicine and Dentistry of New Jersey, USA
HTAi 9th Annual Meeting, Bilbao
Integrated Care for a Patient Centered System
25 June, 2012
Health Technology Assessment (HTA) Report: Interventions to increase particip...HTAi Bilbao 2012
The document summarizes a Health Technology Assessment report on interventions to increase participation in organized cancer screening programs. It found that mail and phone recalls, as well as having a general practitioner's signature on the invitation letter, consistently increased participation. Fixed appointments also increased participation compared to open invitations. Self-sampling for HPV testing increased participation in non-responders relative to standard recall letters. The report evaluated interventions' efficacy, cost-effectiveness, organizational impact, and social/ethical issues.
The use of ‘colloquial evidence’ in HTA: the experience of NICE HTAi Bilbao 2012
The document summarizes a presentation given at the HTAi Annual Meeting about the National Institute for Health and Care Excellence's (NICE) use of "colloquial evidence" in developing clinical guidance. It defines colloquial evidence, explores how NICE utilizes it alongside scientific evidence at different stages of the guidance process, and discusses developing better methods for identifying and critically appraising colloquial evidence. The presentation aims to map NICE's use of colloquial evidence to an existing conceptual framework and identify variations across NICE centers.
Social values international programme: integrating research and policy to ens...HTAi Bilbao 2012
Social values international programme: integrating research and policy to ensure fair allocation of health care resources .
HTAi Conference 2012 Panel Session
Joint chairs
Professor Peter Littlejohns and Professor Albert Weale
Challenges in commissioning research on what works in integrated careHTAi Bilbao 2012
This document discusses challenges in commissioning research on integrated care and how new studies are tackling these challenges. Integrated care research is complex due to the interplay of context, mechanisms and outcomes, and difficulty tracking activity and costs across settings. New studies are using more robust methods like difference-in-difference analysis across multiple sites and person-linked data to better understand costs and impacts. They are also considering generalizability and using mixed methods to understand how micro-level integrated care can be supported at higher levels.
Building a portfolio of research findings for use by healthcare managers and ...HTAi Bilbao 2012
The document summarizes research conducted by the NIHR Health Services and Delivery Research programme on integrated care. It outlines several research projects funded through specific calls on integrated care between 2009-2011, including evaluations of case management initiatives, self-care support, and virtual wards. The research aims to identify healthcare managers' needs and generate evidence to improve services. The programme commissions applied health research to benefit the NHS based on both need and scientific merit.
This document summarizes a study exploring methods for assessing international use of UK-funded health technology assessments (HTAs). The study reviewed literature on impact assessment models and explored bibliometrics, website analytics, and citations in HTA reports. Bibliometric analysis found low international academic impact. Website analytics revealed most non-UK visits were for systematic reviews. Citations in HTA reports provided some evidence of international uptake. The study recommends a multidimensional model and further research using case studies to explore nature of HTA use internationally.
EVALUATION OF PSYCHOSOCIAL FACTORS INFLUENCING HEALTHCARE PROFESSIONAL ACCEPT...HTAi Bilbao 2012
EVALUATION OF PSYCHOSOCIAL FACTORS INFLUENCING HEALTHCARE PROFESSIONAL ACCEPTANCE OF TELEMONITORING FOR CHRONIC PATIENTS
Estibalitz Orruño1, Marie-Pierre Gagnon2-3, José Asua4, Eva Reviriego1
1 Basque Office for Health Technology Assessment (Osteba), Department of Health and Consumer Affairs, Basque Government, Vitoria-Gasteiz, Spain.
2 Faculty of Nursing Sciences, Université Laval, Québec, Canada.
3 Research Centre of the Centre Hospitalier Universitaire de Québec, Québec, Canada.
4 Direction of Knowledge Management and Evaluation, Department of Health and Consumer Affairs, Basque Government, Vitoria-Gasteiz, Spain.
The document discusses improving opportunities for patient and consumer engagement in health technology assessment (HTA) in Australia. It notes that while mechanisms exist for patient input, the overall HTA process is not well understood, advocacy groups are under-resourced, and the timeline for submissions is short. It proposes the formation of HTA_AUS, a coalition of interested parties including patient groups, government, industry and others, to address this issue and develop practical solutions like supporting patient submissions and extending deadlines. The coalition aims to increase awareness, education and support for patient engagement in HTA.
METHODS, MATHEMATICAL MODELS, DATA QUALITY ASSESSMENT AND RESULT INTERPRETATI...HTAi Bilbao 2012
METHODS, MATHEMATICAL MODELS, DATA QUALITY ASSESSMENT AND RESULT INTERPRETATION: SOLUTIONS DEVELOPED IN THE IFEDH FRAMEWORK
G. Zauner
dwh Simulation Services
Vienna , Austria
How to promote the prescription of evidence-based non-pharmacological treatme...HTAi Bilbao 2012
How to promote the prescription of evidence-based non-pharmacological treatments in France?
HTAi 2012, Bilbao
Clémence Thébaut, Olivier Scemama, Françoise Hamers, Catherine Rumeau-Pichon
Department of economic and public health evaluation
The application of Health Technology Assessment in the field of biologics: an...HTAi Bilbao 2012
This document provides a health technology assessment of etanercept for treating rheumatoid arthritis. It includes 7 chapters that evaluate the epidemiology and burden of RA, biologic drugs for RA including etanercept, the economic impacts, organizational implications, and ethical considerations of using etanercept. The assessment finds that etanercept improves quality of life when combined with methotrexate compared to methotrexate alone, and has a cost-effectiveness ratio of €25,130 per quality-adjusted life year gained, making it a reasonable treatment option.
Hospital-based HTA: does it impact on medical technologies’ expenditure and c...HTAi Bilbao 2012
This document summarizes a study on hospital-based health technology assessment (HB HTA) in Italy. The study aimed to assess the diffusion of HB HTA, its impact on hospital decisions, and potential factors influencing its effectiveness. A survey found that almost half of hospitals have an HTA commission. While few clear impacts were identified, some relationships were found between HTA characteristics and resource use. Future research should evaluate additional outcomes to better understand HB HTA's effects and inform its adoption.
Dr. Tan's Balance Method.pdf (From Academy of Oriental Medicine at Austin)GeorgeKieling1
Home
Organization
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
About AOMA: The Academy of Oriental Medicine at Austin offers a masters-level graduate program in acupuncture and Oriental medicine, preparing its students for careers as skilled, professional practitioners. AOMA is known for its internationally recognized faculty, award-winning student clinical internship program, and herbal medicine program. Since its founding in 1993, AOMA has grown rapidly in size and reputation, drawing students from around the nation and faculty from around the world. AOMA also conducts more than 20,000 patient visits annually in its student and professional clinics. AOMA collaborates with Western healthcare institutions including the Seton Family of Hospitals, and gives back to the community through partnerships with nonprofit organizations and by providing free and reduced price treatments to people who cannot afford them. The Academy of Oriental Medicine at Austin is located at 2700 West Anderson Lane. AOMA also serves patients and retail customers at its south Austin location, 4701 West Gate Blvd. For more information see www.aoma.edu or call 512-492-303434.
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Discover the benefits of homeopathic medicine for irregular periods with our guide on 5 common remedies. Learn how these natural treatments can help regulate menstrual cycles and improve overall menstrual health.
Visit Us: https://drdeepikashomeopathy.com/service/irregular-periods-treatment/
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14...Donc Test
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
- Video recording of this lecture in English language: https://youtu.be/RvdYsTzgQq8
- Video recording of this lecture in Arabic language: https://youtu.be/ECILGWtgZko
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Travel Clinic Cardiff: Health Advice for International TravelersNX Healthcare
Travel Clinic Cardiff offers comprehensive travel health services, including vaccinations, travel advice, and preventive care for international travelers. Our expert team ensures you are well-prepared and protected for your journey, providing personalized consultations tailored to your destination. Conveniently located in Cardiff, we help you travel with confidence and peace of mind. Visit us: www.nxhealthcare.co.uk
Spontaneous Bacterial Peritonitis - Pathogenesis , Clinical Features & Manage...Jim Jacob Roy
In this presentation , SBP ( spontaneous bacterial peritonitis ) , which is a common complication in patients with cirrhosis and ascites is described in detail.
The reference for this presentation is Sleisenger and Fordtran's Gastrointestinal and Liver Disease Textbook ( 11th edition ).
Computer in pharmaceutical research and development-Mpharm(Pharmaceutics)MuskanShingari
Statistics- Statistics is the science of collecting, organizing, presenting, analyzing and interpreting numerical data to assist in making more effective decisions.
A statistics is a measure which is used to estimate the population parameter
Parameters-It is used to describe the properties of an entire population.
Examples-Measures of central tendency Dispersion, Variance, Standard Deviation (SD), Absolute Error, Mean Absolute Error (MAE), Eigen Value
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
Gene therapy can be broadly defined as the transfer of genetic material to cure a disease or at least to improve the clinical status of a patient.
One of the basic concepts of gene therapy is to transform viruses into genetic shuttles, which will deliver the gene of interest into the target cells.
Safe methods have been devised to do this, using several viral and non-viral vectors.
In the future, this technique may allow doctors to treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery.
The biggest hurdle faced by medical research in gene therapy is the availability of effective gene-carrying vectors that meet all of the following criteria:
Protection of transgene or genetic cargo from degradative action of systemic and endonucleases,
Delivery of genetic material to the target site, i.e., either cell cytoplasm or nucleus,
Low potential of triggering unwanted immune responses or genotoxicity,
Economical and feasible availability for patients .
Viruses are naturally evolved vehicles that efficiently transfer their genes into host cells.
Choice of viral vector is dependent on gene transfer efficiency, capacity to carry foreign genes, toxicity, stability, immune responses towards viral antigens and potential viral recombination.
There are a wide variety of vectors used to deliver DNA or oligo nucleotides into mammalian cells, either in vitro or in vivo.
The most common vector system based on retroviruses, adenoviruses, herpes simplex viruses, adeno associated viruses.
Pictorial and detailed description of patellar instability with sign and symptoms and how to diagnose , what investigations you should go with and how to approach with treatment options . I have presented this slide in my 2nd year junior residency in orthopedics at LLRM medical college Meerut and got good reviews for it
After getting it read you will definitely understand the topic.
Helminthiasis or Worm infestation in Children for Nursing students
Which HTA Product Do I Need?
1. Which HTA Product Do I Need?
Developing a Decision Guide for Policy Makers
Ann Scott1, Christa Harstall2, Joan Berezanski3
1
Research Associate, Institute of Health Economics, 2Director of
Health Technology Assessment, Institute of Health Economics,
3
Executive Director, Clinical Advisory and Research Branch, Primary
Health Care Division, Alberta Health
Alberta, Canada
1
2. The Alberta Health Technologies
Decision Process (Decision Process)
• Mandate to develop policy regarding public provision of
non-pharmaceutical health technologies and services
using robust scientific methods
• STEP analyses
– Social and Systems Demographic
– Technological
– Economic
– Policy
• Begins with selection and prioritization of technologies or
services
• Guided by a Project Charter for each review
2
3. HTA Products
• Institute of Health Economics (IHE), Edmonton,
Alberta
– http://www.ihe.ca/
• Three Core Objectives
1. Inventory of HTA products offered by HTA agencies
2. Inventory of criteria used to determine which HTA
product type is requested for a given policy question
3. Framework for using various HTA products in the
Decision Process
3
4. Outline of Methods
• Inventory of HTA products (objective 1)
– SRs, HTAs, or narrative reviews - information used to
benchmark the IHE product line
• Inventory of criteria used for selecting product types
(objective 2)
– Articles detailing criteria used to determine which HTA
product type to use for a particular question
– SRs, HTAs, or narrative reviews detailing the criteria used to
set priorities for HTA research
• Framework for using HTA products (objective 3)
– Use information from objectives 1 and 2 to design a decision
matrix or questionnaire
4
5. Levels of HTA
• Levels of HTA products developed
• Scoping Report
– Limited search, brief synthesis
• Level 1
– Limited in scope, focused on certain main questions
• Level 2
– Broader scope of questions, may involve
administrative data
• Level 3
– Most comprehensive
– Economic modeling
– Least bias
5
6. Interface Questionnaire
• Is there more than one condition being considered?
• Is there any relevant Alberta data regarding the
technology?
• Required components of economic evaluation
– Budget impact
– Model-based evaluation
– Cost attribution
• Timeframe
6
7. Case Example: Radiofrequency
Ablation (RFA) for low back pain
• Policy Question: should RFA continue to be publicly
provided for patients with low back pain in Alberta? If so,
what is the most appropriate population?
• Technological: does it work?
• Economics: is it cost effective?
• Social: what is the demand and modes of provision in
Alberta?
• The HTA will include a comprehensive analysis of the
intervention
7
8. Case Example: Hysteroscopic
Tubal Sterilization (HTS)
• Policy Question: Should HTS be publicly funded in
Alberta as an option for patients seeking permanent
sterilization?
• Even though the Social and System Demographics was
not the major focus of this evidence review, a
comprehensive review was required for the other two
components
8
9. Advantages
• Provides a comprehensive framework to aid discussions
– Helps in addressing the right questions
– Identifies and focuses efforts on the gaps in information for
policy development
– Identifies issues that will not likely drive policy decisions
• Helps define balance in information/time tradeoff
• Consistency between HTA partners
– Clear expectations
• Objective questionnaire
– Clear questions to aid in translation between policy needs
and HTA tools
9
10. Challenges
• Early days
– Some lessons won’t be learned until the projects are
finished
• Not always easy to translate responses on the interface
questionnaire to the appropriate level of HTA
– Every policy question is different
• Conflict between comprehensiveness and timelines
– Often, a policy question that is large in scope and is of
particular political interest also requires a response in a
short timeframe
10
Editor's Notes
Thank you. For decision makers, it is a challenge to have the right information within the right timeframe. What is the right amount and type of information required to support evidence-informed decision making? What is the appropriate product to provide the information needed when it is needed? We believe that marrying the product with the policy decision can help address these questions and we want to share with you a project conducted by the Institute of Health Economics to address the need for diverse types of HTA products for government decision making on health technologies and services. I’m presenting our project to you today, but the key experts that performed the work, Christa Harstall and Ann Scott are in the audience today.
While Canada is governed at the federal and provincial levels, most healthcare-related decision making is within the jurisdiction of individual provincial governments. Alberta is one of 3 provinces in Canada that has a well established and robust process for using evidence to inform policy development for health technologies and services. The Alberta Health Technologies Decision Process involves the use of comprehensive health technology assessments, performed by internationally recognized HTA producers in Alberta, to inform decisions on health technologies and services. These HTAs are known as STE reviews and contain information on the social and systems demographic (S section), technological (T section) and economic (E section) considerations of health technologies; the Ministry then analyzes the ethical and legal aspects during policy development. Each STE review is guided by a specific Project Charter that lists the policy issues of particular interest to the Ministry. The Charter includes research-oriented questions for the STE review developed in consultation with the HTA Partner organization and an Expert Advisory Group. For the Decision Process to remain efficient, responsive and timely, it is essential to use our available HTA resources appropriately. Therefore, we needed a framework to help us choose which type of review is best suited to inform particular policy questions. Essentially, in some cases, a rapid review of lesser depth of analysis may be sufficient to address policy needs.
The Institute of Health Economics was asked to develop such a framework on responsive and timely HTA products. The Institute of Health Economics is a not-for-profit organization with key competencies in health economics, health technology assessment, decision analytic modeling, and dissemination of findings from research. They are one of three HTA partners in Alberta that have the capacity to produce these STE reviews. The three core objectives of the project were to establish an inventory of HTA products available worldwide; create an inventory of criteria for determining which HTA product is the most appropriate for answering a particular policy question; and create a framework for using the various HTA products in the Decision Process. While the framework was developed for use within the Alberta context and with the local HTA partners, the underlying concepts may be applicable to other jurisdictions and HTA agencies.
A systematic literature search was conducted up to March 2011. For objective 1, IHE looked for systematic reviews, HTAs, or narrative reviews detailing the types of products produced by HTA agencies worldwide. For objective 2, IHE looked for publications that detailed criteria or questions used to determine which HTA product type is used by healthcare decision makers to inform a given policy question or to set priorities for HTA research, because there is a potential overlap between the two sets of criteria. We found there wasn’t a significant body of published literature on the number or types of HTA products other agencies use, or detailed criteria used in the selection of HTA products. For objective 3, IHE used the information obtained from the literature searches to define a framework that could be used to guide the choice of an HTA product.
IHE developed a product line that defined what each available report type looks like methodologically, as well as the depth and type of information provided within each report. Multiple levels of HTA products were developed from short scoping reports to larger scale efforts that delve into grey literature and include comprehensive economic analyses. The HTA products were designed to vary in terms of comprehensiveness of component analyses and the timelines expected from the Ministry, without sacrificing quality. As this menu of research or HTA products was generated from the researcher’s perspective, to be useful it had to be converted into something that reflected the decision maker’s viewpoint.
The result was a questionnaire designed to serve as an interface between the evidence needs of policy makers and the menu of products available from HTA producers within the Decision Process. Its purpose is to facilitate discussion between policy makers and HTA producers on what type of HTA product should be commissioned to answer policy questions identified by the government. The questionnaire is quite comprehensive, but some examples: Whether more than one clinical condition applies If Alberta-specific administrative data is available How in-depth the economic analysis needs to be And importantly, what timeframe is required The aim is to open a detailed discussion regarding the policy needs for a particular health service, and embark on an HTA that strikes a balance between comprehensiveness and responsiveness.
I want to go over a couple of examples of how we’ve piloted the use of the questionnaire. Radiofrequency Ablation (RFA) is a service that is already being publicly provided in Alberta and involves the use of an RFA probe to disrupt nerves in the lower back to treat chronic pain. There is more demand for this service than is currently met; however, there are also concerns about the appropriateness of the population receiving the service. The policy question is whether or not it should continue. Does the evidence support its continued use? And if so, what’s the most appropriate population? Using the interface questionnaire to guide our discussions, it became apparent that an HTA that covered all three areas of consideration; social and system demographics, technological effectiveness and economic evaluation was needed. In terms of technology, we needed to understand what the evidence said about effectiveness. In terms of economics, we needed to understand if the treatment is cost-effective. We also needed to understand what demand there is in Alberta and how is it being provided currently.
Another example is hysteroscopic tubal sterilization; a non-surgical alternative to open or laparoscopic tubal ligation. The question was: Should hysteroscopic tubal sterilization (HTS) be publicly funded in Alberta as an option for patients seeking permanent sterilization? The questionnaire identified that the focus was mainly on the effectiveness/safety and economical aspects of the technology but not the social and system demographics. This meant a comprehensive systematic review of the technological safety and effectiveness evidence and a comprehensive economic analysis – budget impact and model-based evaluation, but a less in-depth summary of social and system demographics information. This is a great example where the questionnaire lead to discussions that focused our efforts and resources in informing policy.
As we continue to refine the process we have found : It helps us interact with our HTA partners and ensure we’re asking the right questions during the initiation phase of a project. It also helps the HTA partner define what are the most important pieces that deserve the most effort. The discussion guided by the interface questionnaire really allows us to get at the heart of the policy issue. Just as importantly, it helps us identify which issues can be addressed by a less in-depth analysis. It also shows us what information may be missing in the final HTA and identifies upfront the opportunity cost of tradeoffs made between comprehensiveness and timeliness. And it has the potential to create some level of consistency between the HTA partners in terms of comprehensiveness. Even if methodology varies between HTA partners, identifying the issues ahead of time helps clarify the expectations on both sides. Finally, the interface questionnaire is also clear and concise. This supports dialogue between policy-makers and researchers.
As we improve the framework and questionnaire we will continue piloting the framework. And of course, some lessons can only be learned after these trial projects are finished and we can look back and see if the final product met the policy-maker’s needs. The questionnaire has been tailored to the specific needs of the Alberta Decision Process, so it is unclear how applicable it may be to other contexts. One aspect we’re working on is the link between the interface questionnaire and the HTA product level required. Projects don’t always fit neatly within one of the HTA product levels. So it’s important to keep in mind the interface questionnaire is meant to catalyze that discussion, and not necessarily serve as a set of rigid rules. Policy issues are unique to each policy. Every project is different. Overall, there remain challenges to be addressed between the balance of quality and comprehensiveness with timeliness. Often, it is the hot button issue that a government must address with new policy that is needed in a short timeframe, but requires comprehensive research to back it up. This framework helps us in these discussions and gets us on track in making sure an appropriate HTA is performed for the policy issue at hand. It has provided a new way of navigating the gulf between the needs of policy makers and the realities of research.