Purpose of the Call:
Review the results of the National VTE audit
Discuss lessons learned from the audit – strengths and areas for improvement
Gather ideas for future steps for implementation of VTE prophylaxis
Mr James Downie, CEO, presented on the topic 'Moving towards value based funding' at the Healthcare reform, funding and innovation conference, hosted by AventEdge on 27 June 2017.
The document discusses the need for pharmacovigilance to improve patient safety, public health, and the assessment of medicines' benefits, harms, effectiveness, and risks. It describes the goals of India's Pharmacovigilance Program of India as ensuring the benefits of medicines outweigh the risks to safeguard public health, through monitoring adverse drug reactions, creating awareness of reporting among healthcare professionals, and supporting regulatory decisions on medicine safety.
Mr James Downie, CEO, presented on the topic 'Emergency care costing study and classification development' at the 9th Annual Emergency Department Management Conference, hosted by informa on 31 July 2017.
This presentation discusses innovative solutions to improving access to orphan drugs outside of Canada and examines their potential implications for Canada. It summarizes key developments in the US and Europe, including natural history studies, new approval pathways focusing on surrogate endpoints, value demonstration programs, reference networks, early dialogues, and proposals for cross-country price negotiations. The presentation concludes that Canada is at an inflection point and could consider a new, more flexible model incorporating value demonstration across the product lifecycle, real-world evidence generation, iterative approvals, and pan-Canadian decision-making for products treating small populations.
Mr James Downie, CEO, presented on the topic 'Moving towards value based funding' at the 2017 Activity-Based Funding Conference, hosted by the Health Service Executive, Ireland on 11 May 2017.
The document discusses liquid biopsies and next generation cancer molecular diagnostics. It summarizes that OncoCyte Corporation is focused on developing diagnostic tests for early cancer detection using liquid biopsies, with an initial focus on tests for lung cancer. Key points include that lung cancer diagnostics represents a large market opportunity and that OncoCyte's preliminary lung cancer diagnostic test shows strong performance in clinical trials with high sensitivity and specificity. The test has the potential to reduce risky follow-up procedures for patients and provide significant healthcare cost savings.
The CRO-Sponsor Interaction: Regulatory AffairsMedpace
The document discusses the evolution of relationships between clinical research organizations (CROs) and sponsors from primarily transactional to preferred partnerships and strategic integration. It outlines keys to productive alliances such as sharing objectives and expertise. The document emphasizes that early engagement between CROs and sponsors is critical for regulatory success and positive relationships. Regulatory affairs experiences a seamless transition across regions and development cycles through CRO support.
Mr James Downie, CEO, presented on the topic 'Moving towards value based funding' at the Healthcare reform, funding and innovation conference, hosted by AventEdge on 27 June 2017.
The document discusses the need for pharmacovigilance to improve patient safety, public health, and the assessment of medicines' benefits, harms, effectiveness, and risks. It describes the goals of India's Pharmacovigilance Program of India as ensuring the benefits of medicines outweigh the risks to safeguard public health, through monitoring adverse drug reactions, creating awareness of reporting among healthcare professionals, and supporting regulatory decisions on medicine safety.
Mr James Downie, CEO, presented on the topic 'Emergency care costing study and classification development' at the 9th Annual Emergency Department Management Conference, hosted by informa on 31 July 2017.
This presentation discusses innovative solutions to improving access to orphan drugs outside of Canada and examines their potential implications for Canada. It summarizes key developments in the US and Europe, including natural history studies, new approval pathways focusing on surrogate endpoints, value demonstration programs, reference networks, early dialogues, and proposals for cross-country price negotiations. The presentation concludes that Canada is at an inflection point and could consider a new, more flexible model incorporating value demonstration across the product lifecycle, real-world evidence generation, iterative approvals, and pan-Canadian decision-making for products treating small populations.
Mr James Downie, CEO, presented on the topic 'Moving towards value based funding' at the 2017 Activity-Based Funding Conference, hosted by the Health Service Executive, Ireland on 11 May 2017.
The document discusses liquid biopsies and next generation cancer molecular diagnostics. It summarizes that OncoCyte Corporation is focused on developing diagnostic tests for early cancer detection using liquid biopsies, with an initial focus on tests for lung cancer. Key points include that lung cancer diagnostics represents a large market opportunity and that OncoCyte's preliminary lung cancer diagnostic test shows strong performance in clinical trials with high sensitivity and specificity. The test has the potential to reduce risky follow-up procedures for patients and provide significant healthcare cost savings.
The CRO-Sponsor Interaction: Regulatory AffairsMedpace
The document discusses the evolution of relationships between clinical research organizations (CROs) and sponsors from primarily transactional to preferred partnerships and strategic integration. It outlines keys to productive alliances such as sharing objectives and expertise. The document emphasizes that early engagement between CROs and sponsors is critical for regulatory success and positive relationships. Regulatory affairs experiences a seamless transition across regions and development cycles through CRO support.
The document discusses strategies for successful global drug development. It focuses on navigating FDA accelerated approval programs, new frontiers in personalized medicine, and evolving regulatory paradigms for digital health. The presentation provides an overview of key FDA expedited programs like fast track designation and breakthrough therapy designation. It also examines how regulators are adapting approaches to personalized medicine and digital health technologies.
Mr James Downie, CEO, presented on the topic 'Independent Hospital Pricing Authority Update' at the HBN/CHASAN Steering Committee, hosted by Catholic Negotiating Alliance on 15 May 2017.
The document discusses risk management and pharmacovigilance in drug development and approval. It notes that some category 2 drugs approved despite safety issues identified in trials were later withdrawn, and that post-marketing studies are important as rapid uptake and direct-to-consumer advertising can compromise new drug safety. Adverse event databases and data mining are proposed to better understand safety profiles and detect toxic signals.
Pharmacovigilance Process Work Flow - Katalyst HLSKatalyst HLS
Introduction to Drug Safety & Pharmacovigilance Process Work Flow for Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
This document discusses an economics perspective on drug prices. It notes that drug development is an investment that will only occur if the revenue stream justifies costs. For small market drugs, designing a payment structure is challenging to make research attractive for companies. It provides an example of a small biopharma company developing a rare cancer drug that needs funding for later trial phases in order to continue research.
This document discusses Canada's orphan drug regulatory framework. It begins by defining orphan drugs as treatments for rare diseases affecting fewer than 5 in 10,000 people. It outlines challenges in developing and accessing orphan drugs, including small patient populations that make clinical trials difficult. Health Canada is proposing a framework to improve orphan drug availability through an accelerated review pathway, early advice to sponsors, transparency throughout the drug life cycle, and collaboration with international regulators and health technology assessment bodies. The key components of the framework include orphan drug designation, written regulatory advice, modernized market authorization applications, post-market oversight, and transparency.
Avoiding Common Pitfalls in Cell and Gene Therapy TrialsMedpace
This webinar presentation discusses operationalizing advanced therapy clinical trials using lessons learned from past experiences. The webinar covers regulatory considerations, operational challenges, and case studies. Regulatory agencies require strategic engagement, assessment of regulatory readiness, and oversight of country requirements. Investigative sites face additional committee reviews and license applications. Manufacturing complex cell and gene therapies poses challenges around process transfer, scaling, and product availability. Aligning supply chain readiness, site capabilities, and an investigational product tracking process is key to avoiding delays. Developing a global strategy requires addressing requirements for manufacturing, stability data, labeling, and supply logistics early.
The document discusses Materiovigilance, which is the monitoring of incidents involving medical devices. It aims to study device-related incidents, enable dangerous devices to be removed from the market, and improve device quality and safety for patients. The Materiovigilance Programme of India was established in 2015 after incidents involving malfunctioning medical devices caused patient deaths. It oversees monitoring centers that collect adverse event reports which are analyzed to detect safety issues and support regulatory decision-making regarding medical devices in India.
This document discusses vaccine safety surveillance systems. It describes post-marketing surveillance systems like VAERS in the US and EudraVigilance in Europe that monitor adverse events. International organizations like WHO and programs like EPI work to strengthen safety surveillance globally and help low-income countries monitor vaccines. Harmonized reporting systems, guidelines, and data sharing aim to ensure vaccine safety worldwide.
Scientific and medical literature is an important source of information for pharmacovigilance and detecting adverse drug reactions. However, marketing authorization holders face challenges in systematically reviewing literature due to a lack of harmonization across regulatory authorities and in developing effective search strategies. Literature screening is important for evaluating drug safety and can impact decisions regarding a drug's risk-benefit analysis. It is important that literature screening is done systematically and documented properly.
SCIE Investor Presentation January 2017Mike Oliver
This document discusses SpectraScience's optical biopsy technology platform and commercialization plans. The technology uses light to provide faster, non-invasive cancer detection compared to physical biopsies. Clinical studies show the technology exceeds accuracy criteria for detecting colon cancer. The company plans to commercialize the technology first in Europe, where distribution agreements are in place, to take advantage of single-payer healthcare systems and proven cost savings. Future indications for bladder, esophageal, and other cancers are also discussed.
Passive and active surveillance are two methods used to monitor health events and adverse drug reactions. Passive surveillance relies on voluntary reporting by health practitioners, while active surveillance proactively monitors for events through case validation or questioning patients and physicians. Different study designs can also be used like cohort studies which follow exposed and unexposed patient groups over time to identify risks. Registries systematically collect health information on patients with specific exposures or diseases to analyze safety. Targeted clinical investigations may further evaluate adverse reactions through pharmacokinetic or interaction studies.
This document discusses value-based pricing and "innovative agreements" between the pan-Canadian Pharmaceutical Alliance (pCPA) and pharmaceutical manufacturers. It notes that performance-based agreements that tie the price of drugs to health outcomes present both challenges and opportunities. Challenges include implementing systems to track outcomes and determining which outcomes are measurable and attributable to the drug. Opportunities include structuring agreements for small patient populations and tying rebates to uncertainty in outcomes. The document argues that value-based pricing requires involvement from public drug plans, patients, and manufacturers to address these challenges and realize the opportunities.
A risk indicator can be any metric used to identify your risk exposure over time. It becomes a KRI when it tracks an important risk, or does so especially well because of its predictive value.
Dr Andrianov, CEO Cyntegrity, discusses the importance of keeping KRIs simple, the link to specific risks, and the emerging common industry KRIs.
A full recording of this webinar is available to MCC members: https://metricschampion.org/
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.
The RACE for Children Act Will Change the Landscape for Pediatric Cancer Rese...Medpace
In this webinar, we explore the regulatory implications of the RACE for Children Act and what this law means for your development program, particularly with navigating the change in requirements for pediatric oncology trials. Furthermore, we explore the challenges of executing oncology trials in pediatric populations and offer insight into design and operational aspects to seamlessly execute these studies as part of your clinical development plan
At the Seventh Annual Health Law Year in P/Review symposium, leading experts discussed major developments during 2018 and what to watch out for in 2019. Speakers covered hot topics including health policy under the current administration, pharmaceutical policy, and public health law. Featured panels explored "Challenges Facing Health Care General Counsels" and "AI in Health Care."
For more, go to: http://petrieflom.law.harvard.edu/events/details/seventh-annual-health-law-year-in-p-review
Purpose of the Call:
Review the results of the National VTE audit day
Discuss lessons learned from the audit day – strengths and areas for improvement
Suggest future value of audits and audit tools for your organization
Gather ideas for future steps for implementation of VTE prophylaxis
Click the link below for more information and to watch the recorded webinar.
http://bit.ly/12QiAf5
Objective
Safer Healthcare Now!, a program of the Canadian Patient Safety Institute, invites you to participate in the Canadian VTE Audit, designed to establish a national perspective of VTE thromboprophylaxis rates and raise awareness of appropriate VTE prophylaxis.
VTE is one of the most common and preventable complications of hospitalization and is a Required Organizational Practice (ROP) of Accreditation Canada.
By participating in the national audit day you will be a part of a movement aimed at preventing deep vein thrombosis (DVT) and pulmonary embolism (PE) in hospital patients.
Watch the recording: http://bit.ly/1wfinCE
The document discusses strategies for successful global drug development. It focuses on navigating FDA accelerated approval programs, new frontiers in personalized medicine, and evolving regulatory paradigms for digital health. The presentation provides an overview of key FDA expedited programs like fast track designation and breakthrough therapy designation. It also examines how regulators are adapting approaches to personalized medicine and digital health technologies.
Mr James Downie, CEO, presented on the topic 'Independent Hospital Pricing Authority Update' at the HBN/CHASAN Steering Committee, hosted by Catholic Negotiating Alliance on 15 May 2017.
The document discusses risk management and pharmacovigilance in drug development and approval. It notes that some category 2 drugs approved despite safety issues identified in trials were later withdrawn, and that post-marketing studies are important as rapid uptake and direct-to-consumer advertising can compromise new drug safety. Adverse event databases and data mining are proposed to better understand safety profiles and detect toxic signals.
Pharmacovigilance Process Work Flow - Katalyst HLSKatalyst HLS
Introduction to Drug Safety & Pharmacovigilance Process Work Flow for Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
Contact:
"Katalyst Healthcares & Life Sciences"
South Plainfield, NJ, USA
info@KatalystHLS.com
This document discusses an economics perspective on drug prices. It notes that drug development is an investment that will only occur if the revenue stream justifies costs. For small market drugs, designing a payment structure is challenging to make research attractive for companies. It provides an example of a small biopharma company developing a rare cancer drug that needs funding for later trial phases in order to continue research.
This document discusses Canada's orphan drug regulatory framework. It begins by defining orphan drugs as treatments for rare diseases affecting fewer than 5 in 10,000 people. It outlines challenges in developing and accessing orphan drugs, including small patient populations that make clinical trials difficult. Health Canada is proposing a framework to improve orphan drug availability through an accelerated review pathway, early advice to sponsors, transparency throughout the drug life cycle, and collaboration with international regulators and health technology assessment bodies. The key components of the framework include orphan drug designation, written regulatory advice, modernized market authorization applications, post-market oversight, and transparency.
Avoiding Common Pitfalls in Cell and Gene Therapy TrialsMedpace
This webinar presentation discusses operationalizing advanced therapy clinical trials using lessons learned from past experiences. The webinar covers regulatory considerations, operational challenges, and case studies. Regulatory agencies require strategic engagement, assessment of regulatory readiness, and oversight of country requirements. Investigative sites face additional committee reviews and license applications. Manufacturing complex cell and gene therapies poses challenges around process transfer, scaling, and product availability. Aligning supply chain readiness, site capabilities, and an investigational product tracking process is key to avoiding delays. Developing a global strategy requires addressing requirements for manufacturing, stability data, labeling, and supply logistics early.
The document discusses Materiovigilance, which is the monitoring of incidents involving medical devices. It aims to study device-related incidents, enable dangerous devices to be removed from the market, and improve device quality and safety for patients. The Materiovigilance Programme of India was established in 2015 after incidents involving malfunctioning medical devices caused patient deaths. It oversees monitoring centers that collect adverse event reports which are analyzed to detect safety issues and support regulatory decision-making regarding medical devices in India.
This document discusses vaccine safety surveillance systems. It describes post-marketing surveillance systems like VAERS in the US and EudraVigilance in Europe that monitor adverse events. International organizations like WHO and programs like EPI work to strengthen safety surveillance globally and help low-income countries monitor vaccines. Harmonized reporting systems, guidelines, and data sharing aim to ensure vaccine safety worldwide.
Scientific and medical literature is an important source of information for pharmacovigilance and detecting adverse drug reactions. However, marketing authorization holders face challenges in systematically reviewing literature due to a lack of harmonization across regulatory authorities and in developing effective search strategies. Literature screening is important for evaluating drug safety and can impact decisions regarding a drug's risk-benefit analysis. It is important that literature screening is done systematically and documented properly.
SCIE Investor Presentation January 2017Mike Oliver
This document discusses SpectraScience's optical biopsy technology platform and commercialization plans. The technology uses light to provide faster, non-invasive cancer detection compared to physical biopsies. Clinical studies show the technology exceeds accuracy criteria for detecting colon cancer. The company plans to commercialize the technology first in Europe, where distribution agreements are in place, to take advantage of single-payer healthcare systems and proven cost savings. Future indications for bladder, esophageal, and other cancers are also discussed.
Passive and active surveillance are two methods used to monitor health events and adverse drug reactions. Passive surveillance relies on voluntary reporting by health practitioners, while active surveillance proactively monitors for events through case validation or questioning patients and physicians. Different study designs can also be used like cohort studies which follow exposed and unexposed patient groups over time to identify risks. Registries systematically collect health information on patients with specific exposures or diseases to analyze safety. Targeted clinical investigations may further evaluate adverse reactions through pharmacokinetic or interaction studies.
This document discusses value-based pricing and "innovative agreements" between the pan-Canadian Pharmaceutical Alliance (pCPA) and pharmaceutical manufacturers. It notes that performance-based agreements that tie the price of drugs to health outcomes present both challenges and opportunities. Challenges include implementing systems to track outcomes and determining which outcomes are measurable and attributable to the drug. Opportunities include structuring agreements for small patient populations and tying rebates to uncertainty in outcomes. The document argues that value-based pricing requires involvement from public drug plans, patients, and manufacturers to address these challenges and realize the opportunities.
A risk indicator can be any metric used to identify your risk exposure over time. It becomes a KRI when it tracks an important risk, or does so especially well because of its predictive value.
Dr Andrianov, CEO Cyntegrity, discusses the importance of keeping KRIs simple, the link to specific risks, and the emerging common industry KRIs.
A full recording of this webinar is available to MCC members: https://metricschampion.org/
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.
The RACE for Children Act Will Change the Landscape for Pediatric Cancer Rese...Medpace
In this webinar, we explore the regulatory implications of the RACE for Children Act and what this law means for your development program, particularly with navigating the change in requirements for pediatric oncology trials. Furthermore, we explore the challenges of executing oncology trials in pediatric populations and offer insight into design and operational aspects to seamlessly execute these studies as part of your clinical development plan
At the Seventh Annual Health Law Year in P/Review symposium, leading experts discussed major developments during 2018 and what to watch out for in 2019. Speakers covered hot topics including health policy under the current administration, pharmaceutical policy, and public health law. Featured panels explored "Challenges Facing Health Care General Counsels" and "AI in Health Care."
For more, go to: http://petrieflom.law.harvard.edu/events/details/seventh-annual-health-law-year-in-p-review
Purpose of the Call:
Review the results of the National VTE audit day
Discuss lessons learned from the audit day – strengths and areas for improvement
Suggest future value of audits and audit tools for your organization
Gather ideas for future steps for implementation of VTE prophylaxis
Click the link below for more information and to watch the recorded webinar.
http://bit.ly/12QiAf5
Objective
Safer Healthcare Now!, a program of the Canadian Patient Safety Institute, invites you to participate in the Canadian VTE Audit, designed to establish a national perspective of VTE thromboprophylaxis rates and raise awareness of appropriate VTE prophylaxis.
VTE is one of the most common and preventable complications of hospitalization and is a Required Organizational Practice (ROP) of Accreditation Canada.
By participating in the national audit day you will be a part of a movement aimed at preventing deep vein thrombosis (DVT) and pulmonary embolism (PE) in hospital patients.
Watch the recording: http://bit.ly/1wfinCE
MicroGuide app, pop up uni, 1pm, 3 september 2015NHS England
Expo is the most significant annual health and social care event in the calendar, uniting more NHS and care leaders, commissioners, clinicians, voluntary sector partners, innovators and media than any other health and care event.
Expo 15 returned to Manchester and was hosted once again by NHS England. Around 5000 people a day from health and care, the voluntary sector, local government, and industry joined together at Manchester Central Convention Centre for two packed days of speakers, workshops, exhibitions and professional development.
This year, Expo was more relevant and engaging than ever before, happening within the first 100 days of the new Government, and almost 12 months after the publication of the NHS Five Year Forward View. It was also a great opportunity to check on and learn from the progress of Greater Manchester as the area prepares to take over a £6 billion devolved health and social care budget, pledging to integrate hospital, community, primary and social care and vastly improve health and well-being.
More information is available online: www.expo.nhs.uk
This study assessed postoperative bleeding in 100 patients who underwent dental extractions while continuing their antiplatelet therapy (APT). The patients were on either mono APT (78%) or dual APT (22%). Postoperative bleeding was observed in 16 patients on mono APT at 1 hour, but in no patients at 24-48 hours. For dual APT, bleeding was observed in 10 patients at 1 hour and 1 patient at 24 hours, with no bleeding by 48 hours. Statistical analysis found the bleeding rates were significant. The results suggest that dental extractions can generally be performed safely in patients continuing APT, as postoperative bleeding is minor and can be controlled with local hemostatic measures.
Introduction of the NZ Health IT Plan enables better gout management - Reflections of an early adopter. Presented by Peter Gow, Counties Manukau DHB, at HINZ 2014, 12 November 2014, 11.37am, Plenary Room
This guideline provides updated recommendations for outpatient management of fever and neutropenia in adults treated for malignancy. Key recommendations include:
1) Using clinical judgment criteria or validated tools like MASCC or Talcott's rules to determine if patients are low risk and candidates for outpatient management.
2) For low risk patients, administering the first dose of empirical antibiotics in an outpatient setting and observing patients for at least 4 hours before discharge.
3) Recommending an oral fluoroquinolone plus amoxicillin/clavulanate (or clindamycin if penicillin allergic) as initial outpatient empirical therapy, unless fluoroquinolone prophylaxis was previously used
This document provides an updated clinical practice guideline from the American Society of Clinical Oncology (ASCO) and Infectious Diseases Society of America (IDSA) on outpatient management of fever and neutropenia in adults treated for malignancy. The guideline addresses which patients may be appropriate for outpatient treatment, recommended assessments and interventions for outpatients, and antimicrobial treatment options. A systematic review was conducted and the guideline recommendations are based on the available evidence. Key recommendations include using validated tools or clinical judgment to determine which low-risk patients are candidates for outpatient management, administering initial antibiotic doses within 1 hour and monitoring patients for at least 4 hours before discharge, and considering oral fluoroquinolone plus amo
This document summarizes Pamela Gavin's presentation on an evidence-based approach to assuring value for orphan drugs at the CEPHT Conference in Toronto. It discusses the progress made since the 1983 Orphan Drug Act, including over 700 approved orphan drugs. It then introduces the NORD-Trio partnership, which aims to ensure adequate access to orphan drugs through a patient-centric technology platform that measures stakeholder performance, defines quality measures, and advocates for patients and high performance. Finally, it provides examples of how this partnership could study the hepatitis C treatment landscape using real-world data on outcomes, access, and affordability.
RUNNING HEAD: MIS-535 Week 6 Case Study Analysis
Table of Contents
Summary………………………………………………………………………………….....Page 3
Support…………………………………………………………………………………...Pages 3-6
Evaluation………………………………………………………………………………...Pages 6-8
Questions………………………………………………………………………………....Pages 8-9
References…………………………………………………………………………………Page 10
Summary
In 2010 cardiologist by the name of Duncan Dymond complained that too many patients were arriving at his hospital at incorrect times and in far worse shape and in need of different specialists. The reason for this issue is because in 2004 the National Health Service installed a system called the choose and book system. Costing nearly 200 million pounds. At first it sounded like a plan because it would basically help all doctors with appointments and ensure that they stay on track throughout their days weeks and months. It was also supposed to help patients be on time and at the right location. But because the system was pushed out too fast it had many glitches to overcome. The major problem that came of this was that the 2 major administration systems that the hospitals were already using was not compatible with choose and book and when something isn’t compatible it just doesn’t work. Choose and book was generally geared to be the go between the 2 systems (PAS and GP). The objective of Choose and book was supposed to be able to book 90% of all referrals by December 2006 and that objective was never met. Four years later choose and book was installed into 94% of all GP surgeries it was only used to book 54%. The major role for choose and book was to make everything easier in fact 100 million pounds incentive was issued and that did not help the situation because if doctors feel that it is too hard to use or too difficult they will revert back to their old habits.
Support
According to Bio med choose and book has been a complete failure. Choose and book was supposed to not only help doctors but it was also geared to help patience. The concept was for patience to be able to go online and book an appointment when and where they so choose. Among the Choose and Book patients, 66% (31/47; 95% CI 52 to 78%) reported not being given a choice of appointment date, 66% (31/47; 95% CI 52 to 78%) reported not being given a choice of appointment time, 86% (37/43; 95% CI 74 to 94%) reported being given a choice of fewer than four hospitals in total and 32% (15/47; 95% CI 20 to 46%) reported not being given any choice of hospital. A survey was completed to see how patients liked choose and book and the results were not in the favor of the system. A total of 104 patients took part in the study between 4 May and 9 August 2006. Of these, 47 were Choose and Book patients. This represents 44% of the 107 total Choose and Book patients seen at the Hillingdon site between these dates. A further 57 patients were referred through the conventional Partial Book ...
- Surgical site infections (SSIs) develop in 2-5% of surgical patients annually in the US, accounting for 14-16% of all hospital-acquired infections and 3% of surgical mortality. They increase costs by $29,000 per patient on average.
- A survey of 103 healthcare professionals found that most facilities have protocols for preoperative skin cleansing, though compliance levels vary. The majority use chlorhexidine gluconate (CHG) products and require two or more applications.
- Improving patient education and compliance was cited as the most significant obstacle to reducing SSIs. Less than 10% of facilities used digital reminders or referred patients to informational websites.
Hemovigilance is a continuous process of monitoring blood transfusions to collect data on adverse reactions, investigate their causes, and prevent future occurrences. India launched a national Hemovigilance program in 2012 to address issues with adverse reactions from blood transfusions. The program collects reports from medical colleges on transfusion reactions and assesses causality to advise regulators on safety and provide recommendations to stakeholders. It aims to improve transfusion safety and prevent adverse events.
Realizing the potential for HIV self-testing - a summary of latest evidenceCheryl Johnson
This document summarizes the latest evidence on HIV self-testing (HIVST). It finds that HIVST is acceptable and increases testing frequency. Sensitivity and specificity of HIVST can be high, though linkage to care needs improvement. While risks like false results exist, clear messaging can mitigate them. Several countries now allow HIVST, and demand is estimated at millions of tests in 2018. The WHO is developing guidelines on HIVST to expand testing and reach undiagnosed populations. In conclusion, HIVST is an additional tool that countries should utilize alongside traditional testing to work towards ending the HIV epidemic.
This presentation has the measures to be taken for the safety of patients. It covers the 6 goals
Goal 1: Identify patients correctly
Goal 2: Improve effective communication
Goal 3: Improve the safety of high-alert medications
Goal 4: Ensure safe surgery
Goal 5: Reduce the risk of health care-associated infections
Goal 6: Reduce the risk of patient harm resulting from falls
C2 Reimbursement Perspectives on Precision MedicineEmilie Adams
This document summarizes a presentation on reimbursement perspectives for precision medicine. It discusses:
1) The promise of precision medicine in tailoring treatments to a patient's specific biomarkers or genetic profile, leading to better outcomes. Examples are given of targeted therapies approved for lung cancer subtypes.
2) Best practices from other countries in implementing precision medicine, such as France's national network of molecular testing centers to ensure equal access. Challenges discussed include getting the right test to the right patient at the right time for the right price.
3) Recommendations to optimize precision medicine in the future, such as establishing molecular testing programs and guidelines to help integrate testing into clinical practice and minimize delays in treatment. Time
- 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.
The National Confidential Enquiry into Peri-operative Deaths (NCEPOD) was established in the UK in 1988 to comprehensively and authoritatively review clinical practice surrounding deaths within 30 days of surgery. NCEPOD aims to maintain and improve standards of care for both adults and children through confidential case reviews, research, and publishing results. The National Early Warning Score (NEWS) is an excellent initiative that helps staff recognize patient deterioration earlier through standardized scoring of physiological parameters, enabling sicker patients to receive timely intensive care.
Materiovigilance Programme of India (MvPI).pptxChhavi Singh
Materiovigilance is the coordinated system of identification, collection, reporting, and analysis of any untoward occurrences associated with the use of medical devices and protection of patient's health by preventing its recurrences. Survey included.
Clinician Satisfaction Before and After Transition from a Basic to a Comprehe...Allison McCoy
Healthcare organizations are transitioning from basic to comprehensive electronic health records (EHRs) to meet Meaningful Use requirements and improve patient safety. Yet, full adoption of EHRs is lagging and may be linked to clinician dissatisfaction. In depth assessment of satisfaction before, during, and after EHR transition is rarely done. Using an adapted published tool to assess adoption and satisfaction with EHRs, we surveyed clinicians at a large, non-profit academic medical center before (baseline) and 6-12 months (short-term follow-up) and 12-24 months (long-term follow-up) after transition from a basic, locally-developed to a comprehensive, commercial EHR. Satisfaction with the EHR (overall and by component) was captured at each interval. Overall satisfaction was highest at baseline (85%), lowest at short-term follow-up (66%), and increasing at long-term follow-up (79%). This trend was similar for satisfaction with EHR components designed to improve patient safety including clinical decision support, patient communication, health information exchange, and system reliability. Conversely, at baseline, short-term and long-term follow-up, perceptions of productivity, ability to provide better care with the EHR, and satisfaction with available resources, were lower at both short- and long-term follow-up compared to baseline. Persistent dissatisfaction with productivity and resources was identified. Addressing determinants of dissatisfaction may increase full adoption of EHRs. Further investigation in larger populations is warranted.
This document discusses safe surgery practices and checklists. It notes that surgical complications occur in 3-16% of cases and deaths in 0.4-0.8% of cases, with many being preventable. Checklists can help reduce errors like operating on the wrong patient, site, or having unsafe anesthesia. The checklist has pre-operative, time-out, and post-operative components. It emphasizes marking the surgical site, checking for allergies and latest tests, taking antibiotics, and more. Junior staff have important roles like consent, markings, filling forms, and informing relatives. Effective communication and checklists can significantly improve patient safety during surgery.
Similar to National VTE Audit Day: Results and Feedback (20)
As patients and families impacted by harm, we imagine progressive approaches in responding to patient safety incidents – focused on restoring health and repairing trust.
We can change how we respond to healthcare harm by shifting the focus away from what happened, towards who has been affected and in what way. This is your opportunity to hear about innovative approaches in Canada, New Zealand, and the United States that appreciate these human impacts.
This interactive webinar is hosted by Patients for Patient Safety Canada, the patient-led program of the Canadian Patient Safety Institute and the Canadian arm of the World Health Organization Patients for Patient Safety Global Network.
This interactive webinar is part of the world tour series designed by the World Health Organization's Patients for Patient Safety (PFPS) Global Network and hosted by Patients for Patient Safety Canada, the patient-led program of the Canadian Patient Safety Institute, a WHO Collaborating Centre on Patient Safety and Patient Engagement.
The goal of this virtual discussion is to explore practical solutions for keeping seniors safe. The ideas are drawn from real life experiences noting how COVID-19 impacted seniors, their loved ones as well as healthcare workers and leaders.
The focus of the discussion is on identifying safety risks together with practical solutions for seniors who live at home, in residences and long-term care facilities.
After hearing the perspectives of patients, providers and leaders from Indigenous communities on how they perceive safety and what solutions are/ can be implemented, we will leave the session with at least one practical idea for engaging all patients, families and/or the public in improving patient safety.
Healthcare providers and leaders will address three types of silences in healthcare: organizational silence, patient-related silence, and provider to provider silence.
Read More: www.conquersilence.ca
This document discusses teamwork in healthcare and its importance for patient safety. It describes how teamwork skills are often taught through simulations but clinical experience is limited for undergraduates. The intervention described uses a film about a patient falling through the cracks followed by workshops using scenarios to practice and debrief teamwork skills. Key concepts emphasized include shared understanding of goals and plans, involving patients as part of the team, and skills like adaptation, trust, and psychological safety. The overall goal is to apply teamwork knowledge to improve patient outcomes and safety.
Enhanced Recovery After Surgery (ERAS®) is the Enhanced Recovery After Surgery (ERAS®) is the implementation of patient-focused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidence-based, interdisciplinary perioperative guidelines.
Learn more about Enhanced Recovery Canada:
http://ow.ly/hR3j30jsnjR
Dr. Dee Mangin, Professor of Family Medicine and the Associate Chair and Director, Research, at McMaster University, will join practicing pharmacist, and Vice President, Pharmacy Affairs, Sandra Hanna of the Neighbourhood Pharmacy Association of Canada to discuss medication risks, deprescribing and the dangers of polypharmacy in this one hour webinar. Learn more at www.asklistentalk.ca
Joshua Myers, Terry Brock - Fraser Health (BC) - We Want to Hear from You: Fraser Health Real-Time Experience Survey
Leading organizations in Canada invite, listen and act on feedback from patients in their care to improve the safety and quality of care. Explore the three award-winning practices linked below then join us in a conversation to learn more about each approach and reflect on how you may apply it in your organization. This webinar promises practical ideas to help you engage patients in making care safer.
Leading organizations in Canada invite, listen and act on feedback from patients in their care to improve the safety and quality of care. Explore the three award-winning practices linked below then join us in a conversation to learn more about each approach and reflect on how you may apply it in your organization. This webinar promises practical ideas to help you engage patients in making care safer.
Cathy Masuda, Leslie Louie - BC Children's Hospital, an Agency of the Provincial Health Services Authority -Patient's View: Engaging Patients and Families in Patient Safety Incident Reporting
Leading organizations in Canada invite, listen and act on feedback from patients in their care to improve the safety and quality of care. Explore the three award-winning practices linked below then join us in a conversation to learn more about each approach and reflect on how you may apply it in your organization. This webinar promises practical ideas to help you engage patients in making care safer.
Alberta Health Services: Family Volunteers or Advisors Gathering Real-time Patient Experiences
Leading organizations in Canada invite, listen and act on feedback from patients in their care to improve the safety and quality of care. Explore the three award-winning practices linked below then join us in a conversation to learn more about each approach and reflect on how you may apply it in your organization. This webinar promises practical ideas to help you engage patients in making care safer.
This final webinar will emphasise the importance of understanding the problem before brainstorming solutions to better ensure a match between barriers and the solutions.
MORE INFO: http://bit.ly/2KctiLH
This webinar provides an overview of key frameworks for identifying barriers and enablers to implementation, with a focus on the Theoretical Domains Framework (TDF). The TDF synthesizes 128 constructs from 33 theories of behavior change into 12 domains to understand factors influencing healthcare professionals' behaviors. The webinar uses a case study of improving physician hand hygiene to demonstrate how the TDF can be applied to identify potential barriers within domains like Knowledge, Skills, Social Influences, and Environmental Context & Resources.
The fifth webinar continues the momentum of the series as it focuses on providing concrete approaches for identifying barriers and enablers, emphasising behaviour change approaches.
READ MORE: http://bit.ly/2LOwbj0
Please join CPSI as we conclude our Human Factors webinar series with our final presentation Collaborative "Spaces" and Health Information Technology Design
Professor Benedetta Allegranzi,World Health Organisation
Dr. Benedetta Allegranzi is a specialist in infectious diseases, tropical medicine, infection prevention and control and hospital epidemiology. She currently works at the World Health Organization HQ (Service Delivery and Safety department), leading the "Clean Care is Safer Care" programme. Since 2013, Dr Allegranzi has gathered the title of professor of infectious diseases in the official Italian professorship list and is adjunct professor attached to the Institute of Global Health at the Faculty of Medicine, University of Geneva, Switzerland. She closely collaborates with the team at the IPC and WHO Collaborating Center on Patient Safety, University of Geneva Hospitals (Geneva, Switzerland), as well as with the Armstrong Institute for Patient Safety and Quality, John Hopkins University, (Baltimore, USA) for clinical research projects. She is currently involved in the leadership on the WHO Ebola Response in the field of IPC and supervises IPC activities in Sierra Leone and Guinea. She has experience in clinical management of infectious diseases and tropical medicine, and clinical research in healthcare settings in both developing and developed countries. She has thorough skills and experience in training and education.
She is also the author or coauthor of more than 150 scientific publications, including articles published in high-profile medical journal such as the Lancet, Lancet Infectious Diseases, New England Journal of Medicine and the WHO Bulletin, and six book chapters.
Lori Moore joined GOJO Industries in 2013 as a Clinical Application Specialist. In this position, she provided leadership and support to healthcare organizations as they implemented electronic compliance monitoring (ECM) to more accurately measure hand hygiene performance. She has been a trusted partner to hospital key stakeholders in the development, design and implementation of hand hygiene improvement efforts. Areas of expertise include root cause analysis with targeted solutions, just-in-time coaching and ECM software data analytics. In January 2017, she transitioned to the position of Clinical Educator for Healthcare.
She began her professional career in healthcare in 2010 as a registered nurse in the medical intensive care unit at the Cleveland Clinic Foundation (where she continues to work on the weekends). Her passion for patient safety and quality of care sparked her interest in infection prevention, and she worked as an infection preventionist prior to joining GOJO.
Lori has a well-rounded academic background which includes a Bachelor’s of Arts in Management from Malone College, a Bachelor’s of Science in Nursing from the University of Akron, and a Master’s degree in Public Health from the University of Akron. She is a member of the Association for Professionals in Infection Control and Epidemiology, American Society of Professionals in Patient Safety, and the American Medical Writers Association. She has also earned the credential of Certified Health Education Specialist (CHES) and Certified Professional in Patient Safety (CPPS).
The third interactive webinar in the series builds on the second session by focusing on the question: once we have evidence to justify implementing a new patient safety initiative, what next?
We are one of the top Massage Spa Ajman Our highly skilled, experienced, and certified massage therapists from different corners of the world are committed to serving you with a soothing and relaxing experience. Luxuriate yourself at our spas in Sharjah and Ajman, which are indeed enriched with an ambiance of relaxation and tranquility. We could confidently claim that we are one of the most affordable Spa Ajman and Sharjah as well, where you can book the massage session of your choice for just 99 AED at any time as we are open 24 hours a day, 7 days a week.
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LGBTQ+ Adults: Unique Opportunities and Inclusive Approaches to CareVITASAuthor
This webinar helps clinicians understand the unique healthcare needs of the LGBTQ+ community, primarily in relation to end-of-life care. Topics include social and cultural background and challenges, healthcare disparities, advanced care planning, and strategies for reaching the community and improving quality of care.
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardso...rightmanforbloodline
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
TEST BANK For Accounting Information Systems, 3rd Edition by Vernon Richardson, Verified Chapters 1 - 18, Complete Newest Version
Can coffee help me lose weight? Yes, 25,422 users in the USA use it for that ...nirahealhty
The South Beach Coffee Java Diet is a variation of the popular South Beach Diet, which was developed by cardiologist Dr. Arthur Agatston. The original South Beach Diet focuses on consuming lean proteins, healthy fats, and low-glycemic index carbohydrates. The South Beach Coffee Java Diet adds the element of coffee, specifically caffeine, to enhance weight loss and improve energy levels.
Unlocking the Secrets to Safe Patient Handling.pdfLift Ability
Furthermore, the time constraints and workload in healthcare settings can make it challenging for caregivers to prioritise safe patient handling Australia practices, leading to shortcuts and increased risks.
This particular slides consist of- what is Pneumothorax,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 a summary of Pneumothorax:
Pneumothorax, also known as a collapsed lung, is a condition that occurs when air leaks into the space between the lung and chest wall. This air buildup puts pressure on the lung, preventing it from expanding fully when you breathe. A pneumothorax can cause a complete or partial collapse of the lung.
PET CT beginners Guide covers some of the underrepresented topics in PET CTMiadAlsulami
This lecture briefly covers some of the underrepresented topics in Molecular imaging with cases , such as:
- Primary pleural tumors and pleural metastases.
- Distinguishing between MPM and Talc Pleurodesis.
- Urological tumors.
- The role of FDG PET in NET.
The facial nerve, also known as cranial nerve VII, is one of the 12 cranial nerves originating from the brain. It's a mixed nerve, meaning it contains both sensory and motor fibres, and it plays a crucial role in controlling various facial muscles, as well as conveying sensory information from the taste buds on the anterior two-thirds of the tongue.
1. www.saferhealthcarenow.ca
National VTE Audit – October 2014
RESULTS
Bill Geerts & Artemis Diamantouros
Virginia Flintoft, Anne MacLaurin and Alex Titeu
CPSI Central Measurement Team
Nov. 2014
2. www.saferhealthcarenow.ca
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audio conference toll-free number found on the Session
Info tab, and when prompted, enter the access code and
attendee ID
5. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Results - Outline
5
6. www.saferhealthcarenow.ca
• National VTE Audit: October 1-15, 2014
• Audit Sample:
– General Internal Medicine and General Surgery
• National webinar (Sept. 8) - Call to Action
• Engagement of sites & registration
• Sites contacted by CMT:
– Identification of audit sample
– Creation of data collection forms
VTE Audit - Overview
6
7. www.saferhealthcarenow.ca
• Launch of National VTE Audit:
• Data Collection: October 1 to 15
– Extension for data collection to October 31
– Data submission accepted up to November 7
• Error reports corrected and resubmitted by
Central Measurement Team (CMT)
• Data cleaning and Analyses conducted by CMT
with data from Patient Safety Metrics
(PS Metrics)
VTE Audit - Methodology
7
8. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Results - Outline
8
13. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Results - Outline
17
19. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Day Results - Outline
23
20. www.saferhealthcarenow.ca
Type of Thromboprophylaxis - Overall
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• LMWH = dalteparin; enoxaparin; fondaparinux; nadroparin; tinzaparin
• Other = apixaban; dabigatran; rivaroxaban; warfarin (2013=6%; 2014=7%)
Year
Patients
on TPX
LMWH LDH Mech
Only
2013 3,619 61% 29% 4%
2014 2,601 60% 27% 6%
21. www.saferhealthcarenow.ca
Type of Thromboprophylaxis
- by Major Patient Group
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Patient
group
Patients on
TPX
LMWH LDH Mech
Only
Gen Med 1165 64% 24% 4%
Gen Surg 758 55% 33% 8%
24. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Day Results - Outline
29
27. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Day Results - Outline
32
35. www.saferhealthcarenow.ca
• 2nd Canadian national VTE
thromboprophylaxis audit
• 110 centres and 3,809 patients
• Coast to coast representation (almost)
• Medical and surgical patients well
represented
Summary - Participation
41
36. www.saferhealthcarenow.ca
• After data cleaning 8 fewer sites participated
this year representing 858 fewer patients
• Half as many patients from Ontario and 3
times as many from AB; no data from NL but 5
sites from QC vs 0 in 2013
• 25% - 35% fewer cases reported for Gen. Med
and Gen. Surg; 50% - 68% more cases in Med-
Surg and Other Surg in 2014
Summary – 2013 vs 2014 Audits
42
37. www.saferhealthcarenow.ca
• No difference in proportional use of
Thrombolytics by type
• Slightly less use of Pre-printed Order Sets in
2014 (49% v 55%)
• Appropriateness of Thrombolytics was slightly
better in 2014
• Using Order Sets - 94% v 91%
• Not using Order Sets – 78% v 71%
Summary – 2013 vs 2014 Audits
43
39. www.saferhealthcarenow.ca
• Overall, thromboprophylaxis use = 86%
- Excellent response but still room for improvement
- 14% of patients at risk for VTE did not receive
appropriate thromboprophylaxis
• Variability in thromboprophylaxis use:
- By patient group:
– General Surgery 92%
– General Medicine 84%
- By province: 70% 96%
- By region across provinces: 55% 100%
Summary – Thromboprophylaxis Use
45
40. www.saferhealthcarenow.ca
Summary – Types of Thromboprophylaxis
46
• Types of Thromboprophylaxis:
• LMWH: 60%
• LDH: 26%
• LMWH + LDH: 87%
• Mechanical only: 5%
• Variability:
• By Patient Group:
• Medical: LMWH vs LDH (64% vs 24%)
• Surgical: LMWH vs LDH (56% and 33%)
• By province
• By region
41. www.saferhealthcarenow.ca
• Overall:
– 14% did not receive appropriate thromboprophylaxis
• Reasons:
• No thromboprophylaxis 73%
• Delay in start 8%
• Wrong dose 5%
• Modality varied from SHN recommendation 7%
Summary – Reasons for not using
Recommended Thromboprophylaxis
47
42. www.saferhealthcarenow.ca
• 49% of patients had admission / postop OS
• Huge differences by province (16% 69%) and
region
• Appropriate thromboprophylaxis more common
if OS used (94% vs 78%) – also in 2013
Summary – Order set use
48
43. www.saferhealthcarenow.ca
• Territories not represented:
– NL, NWT, Yukon, Nunavut
• Some incomplete data submitted
• Potential participation bias:
– ?good centre bias
– ?good nursing unit bias
• Snap shot Audit
Summary - Limitations
49
44. www.saferhealthcarenow.ca
1. Methodology
2. Audit participation
3. Appropriate thromboprophylaxis use
4. Types of thromboprophylaxis used
5. Reasons for not using appropriate
thromboprophylaxis
6. Use of Preprinted order sets
7. Feedback and discussion
VTE Audit Day Results - Outline
50
47. www.saferhealthcarenow.ca
Thank you / Merci
Central Measurement Team
metrics@saferhealthcarenow.ca
Virginia Flintoft – 416-946-8350
Alexandru Titeu – 416-946-3103
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