The document discusses knowledge transfer activities in Brazil between the Federal University of Minas Gerais and the Minas Gerais State Health Authority. It describes two main activities: 1) an academic detailing pilot project to disseminate treatment protocols for Alzheimer's disease based on clinical evidence and 2) producing technical appraisals to evaluate individual treatment requests and support judicial/administrative decisions. The academic detailing project included training facilitators, visiting physicians to provide information on the Alzheimer's protocol, and found the physicians were receptive. Technical appraisals independently evaluate health technologies and provide evidence-based recommendations to inform decisions.
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
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
Our main involvement with your clinical research recruitment program concludes with processing the responses to your mailer. As our staff members direct the respondents to your site, you can begin conducting final interviews to complete the clinical trial recruitment process.
Standard of care / Standard of Practice / Clinical Guideline/ Clinical Pathway Naz Usmani
A very brief presentation to differentiate between clinical process improvement practice , guideline and pathway .
I have reflected on the basic differences between them .
Standard of care / Standard of Practice / Clinical Guideline/ Clinical Pathway Naz Usmani
A very brief presentation about the clinical process improvements including practices, standards of care , guideline and pathway . I have reflected upon the basic differences between them . Hope it is useful
FDA 2013 Clinical Investigator Training Course: The Investigator as Collabora...MedicReS
FDA 2013 Clinical Investigator Training Course: The Investigator as Collaborator in Promoting the Clinical Research Enterprise
Neil J. Weissman, M.D., MedStar Health Research Institute
Mosio's Clinical Trial Patient Recruitment and Retention Ebook (First Edition)Mosio
The first edition of Mosio's patient recruitment and retention ebook contains 68 tips and examples from clinical research industry professionals on ways to improve efforts to recruit, retain and engage clinical trial patients.
To get access to a free download of the 2nd Edition, visit http://www.mosio.com/prebook
For more information on how you can improve patient engagement while increasing workflow efficiencies in communicating with study participants using two-way text messaging, please visit us at http://www.mosio.com
ASSESSMENT OF BIOMEDICAL LITERATURE
Components of internal and external validity of controlled clinical trials
Internal validity — extent to which systematic error (bias) is minimized in clinical trials
Selection bias: biased allocation to comparison groups
Performance bias: unequal provision of care apart from treatment under evaluation
Detection bias: biased assessment of outcome
Attrition bias: biased occurrence and handling of deviations from protocol and loss to follow up
Requirements, needs
Planning, direction
Information collection
Information Assessment
- Evaluation for accuracy, correctness, relevance, usefulness
- Source reliability assessment (competency and past behavior based)
- Bias assessment (motivators, interests, funding, objectives)
- Conflicts of interest
- Sources of funding, important business relationships
- Grading of individual items (study, report, analysis, article)
Collation of information
- Exclusion of irrelevant, incorrect, and useless information
-Arrangement of information in a form which enables real-time analysis
- System for rapid retrieval of information
External validity — extent to which results of trials provide a correct basis for generalization to other circumstances
Patients: age, sex, severity of disease and risk factors, comorbidity
Treatment regimens: dosage, timing and route of administration, type of treatment within a class of treatments, concomitant treatments
Settings: level of care (primary to tertiary) and experience and specialization of care provider
Modalities of outcomes: type or definition of outcomes and duration of follow up
Patient Blood Management: Impact of Quality Data on Patient OutcomesViewics
Patient blood management (PBM) has been proven to improve patient outcomes and save hospitals millions of dollars. Ensuring the quality of your data is central to decision making and critical to having a strong PBM program.
Would you like to learn how your organization can improve patient outcomes by implementing a PBM program based on accurate data?
If so, view this presentation by blood management expert Lance Trewhella. Lance presents how to develop a successful, evidence-based, multidisciplinary PBM program aimed at optimizing the care of patients who might need transfusion.
You’ll learn:
• Current recommendations for blood transfusion utilization
• The impact of quality data on PBM programs
• Best data practices in PBM
Our main involvement with your clinical research recruitment program concludes with processing the responses to your mailer. As our staff members direct the respondents to your site, you can begin conducting final interviews to complete the clinical trial recruitment process.
Standard of care / Standard of Practice / Clinical Guideline/ Clinical Pathway Naz Usmani
A very brief presentation to differentiate between clinical process improvement practice , guideline and pathway .
I have reflected on the basic differences between them .
Standard of care / Standard of Practice / Clinical Guideline/ Clinical Pathway Naz Usmani
A very brief presentation about the clinical process improvements including practices, standards of care , guideline and pathway . I have reflected upon the basic differences between them . Hope it is useful
FDA 2013 Clinical Investigator Training Course: The Investigator as Collabora...MedicReS
FDA 2013 Clinical Investigator Training Course: The Investigator as Collaborator in Promoting the Clinical Research Enterprise
Neil J. Weissman, M.D., MedStar Health Research Institute
Mosio's Clinical Trial Patient Recruitment and Retention Ebook (First Edition)Mosio
The first edition of Mosio's patient recruitment and retention ebook contains 68 tips and examples from clinical research industry professionals on ways to improve efforts to recruit, retain and engage clinical trial patients.
To get access to a free download of the 2nd Edition, visit http://www.mosio.com/prebook
For more information on how you can improve patient engagement while increasing workflow efficiencies in communicating with study participants using two-way text messaging, please visit us at http://www.mosio.com
ASSESSMENT OF BIOMEDICAL LITERATURE
Components of internal and external validity of controlled clinical trials
Internal validity — extent to which systematic error (bias) is minimized in clinical trials
Selection bias: biased allocation to comparison groups
Performance bias: unequal provision of care apart from treatment under evaluation
Detection bias: biased assessment of outcome
Attrition bias: biased occurrence and handling of deviations from protocol and loss to follow up
Requirements, needs
Planning, direction
Information collection
Information Assessment
- Evaluation for accuracy, correctness, relevance, usefulness
- Source reliability assessment (competency and past behavior based)
- Bias assessment (motivators, interests, funding, objectives)
- Conflicts of interest
- Sources of funding, important business relationships
- Grading of individual items (study, report, analysis, article)
Collation of information
- Exclusion of irrelevant, incorrect, and useless information
-Arrangement of information in a form which enables real-time analysis
- System for rapid retrieval of information
External validity — extent to which results of trials provide a correct basis for generalization to other circumstances
Patients: age, sex, severity of disease and risk factors, comorbidity
Treatment regimens: dosage, timing and route of administration, type of treatment within a class of treatments, concomitant treatments
Settings: level of care (primary to tertiary) and experience and specialization of care provider
Modalities of outcomes: type or definition of outcomes and duration of follow up
Patient Blood Management: Impact of Quality Data on Patient OutcomesViewics
Patient blood management (PBM) has been proven to improve patient outcomes and save hospitals millions of dollars. Ensuring the quality of your data is central to decision making and critical to having a strong PBM program.
Would you like to learn how your organization can improve patient outcomes by implementing a PBM program based on accurate data?
If so, view this presentation by blood management expert Lance Trewhella. Lance presents how to develop a successful, evidence-based, multidisciplinary PBM program aimed at optimizing the care of patients who might need transfusion.
You’ll learn:
• Current recommendations for blood transfusion utilization
• The impact of quality data on PBM programs
• Best data practices in PBM
This is an attempt to explain the broad concept of and rationale behind Transfer Pricing Regulations. Also gives a high level view of the scheme of Indian Transfer Pricing Regulations as on date. Points out the TP controversies in India. Above all gives a well spirited guidance on dealing with TP in India.
Download our "2017 Transfer Pricing Overview for Hungary" for more information or simply contact our experts in Hungary if you need any additional support!
How Clinical Decision Support Systems (CDSS) is the right tool for physicians?Eurostars Programme EUREKA
We believe that CDSS delivered using information systems, ideally with the electronic medical record as the platform, will finally provide decision makers with tools making it possible to achieve large gains in performance, narrow gaps between knowledge and practice, and improve safety.
Understand what healthcare analytics is.
Identify the 5-stage Analytics Program Lifecycle (APL).
Understand how data analytics can be used in healthcare.
Check it on Experfy: https://www.experfy.com/training/courses/introduction-to-healthcare-analytics.
Increased Ethical Demands for Patient Empowerment in Personalised MedicineWolfgang Kuchinke
A Patient Empowerment tool was developed by pmedicine project, with the aim to provide help for the patient to understand medical documentation, empower the patient to make informed choices and support patients with their decisions in personalised medicine treatments. To identify and evaluate ethical issues existing, ethical concepts were assigned to the use of the patient empowerment service. Concepts from IT requirements engineering were adapted to collect ethical requirements and five ethical requirements clusters were assigned: Informed Consent, Vulnerable populations, IRB/Ethics Committee, Data privacy, Investigator related ones. The identified areas of ethical concerns cover the ethical correct presentation of medical risks and probabilities, reactions to diagnosis, truth about the patient’s medical conditions, presentation of results of false positives and false negatives, inconsistent and incomplete medical results, understanding of clinical equipoise, confidentiality and data ownership issues, data falsification, proper and justified use of new technologies.
Complex ethical problems are created by combining cancer therapies, biosampling, genetic analysis and personalised medicine method. For example, such combinations create issues of data ownership, right to data deletion, right to forget, using care data for research purposes, suitable risk assessments, ... Based on this analysis we created demands for using the Patient Empowerment Service in a ethical way: enabling patient’s understanding of whole data set that the hospital has collected; patients must be able to understand medical statements, as well as legal and ethical considerations; the empowerment tool must represent data in a comprehensible format, but in case it confronts the patient to get unfavorable information and negative diagnoses it should provide help and guidance.
Ethics and Learning Health Care: an overview of the differences between what is considered research and what is considered clinical care, and an introduction to the ethical issues that arise from this boundary being blurred.
The scientific study of methods to promote the systematic uptake of research findings and other evidence-based practices into routine practice and hence improve the quality and effectiveness of health services
A joint presentation on Real People, Real Data at the 2016 International Forum on Quality and Safety in Healthcare in Gothenburg, Sweden. Presented by Leanne Wells of the Consumers Health Forum of Australia; Sam Vaillancourt of St. Michael’s Hospital, Toronto, Canada, and; Dr Paresh Dawda of the Australian National University.
Perfil de expressão diferencial de microRNAs plasmáticos como ferramenta para...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Desinvestimento - Centro Cochrane do BrasilREBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Efetividade clínica comparativa e custo-efetividade do análogo de insulina Gl...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
ALTERAÇÕES CARDIOVASCULARES E SÍNDROME METABÓLICA EM ADULTOS E IDOSOS DE RIO ...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Desenvolvimento, implantação e análise de um sistema (web) informatizado de r...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Intervenções educacionais para aumentar o controle da pressão arterial em pac...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Análise comparativa da adesão ao tratamento anti-hipertensivo e qualidade de ...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Análise de custo-efetividade do tratamento de doenças venosas crônicas (DVC) ...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Avaliação de Riscos Potenciais em Serviços de Hemodinâmica de três Estados Br...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Avaliação de Segurança e Efetividade de Incubadoras Neonatais em Uso.REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Avaliação da parametrização para tomógrafos computadorizados e ressonância ma...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Comparação da acurácia diagnóstica de testes diagnósticos comerciais imunocro...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Estudo de Acurácia da Fotografia Digital para Rastreamento de Retinopatia Dia...REBRATSoficial
Apresentação feita no Seminário de Discussão de Avaliações de Tecnologias em Saúde de projetos financiados pelo Departamento de Ciência e Tecnologia - DECIT do Ministério da Saúde.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
HTAi 2015 - Knowledge Transfer in Brazil; Case studies from SUS Collaborating Centre.
1. KNOWLOLEDGE TRANSFER IN BRAZIL
Case studies from SUS Collaborating Centre
Prof. Augusto Guerra, PhD
Juliana de Oliveira Costa, MPH
Federal University of Minas Gerais
Brazil
Contact: augustoguerrajr@ufmg.br
contato@ccates.org.br
2. Minas Gerais State Health Authority
recently organized the State
pharmaceutical assistance and is now
facing new demands in a context of
restricted budget.
SUS COLLABORATING CENTRE
INTRODUCTION
• 19 million
people
• growing elderly
population
• crescent new-
drugs scenario
→ Need of procedures for prioritizing
and evaluating what might be
delivered for citizens.
↘ To help address these problems ↙
A partnership between Academia and
Government was established to
enforce the incorporation of clinical
evidence into decision-making
Collaborating Centre
CCATES
3. • To evaluate the compliance of individual requests for treatment with the Brazilian
or the State Protocols;
• To produce Technical Appraisals of judicial requests for medicines and specific
demands about medicines utilization;
• To support judicial and administrative decisions.
SUS COLLABORATING CENTRE
OUR MAIN ACTIVITIES
→ Academic Detailing Pilot Project: Dissemination of SUS Protocols evidence
→ Technical appraisals: To support judicial and administrative decisions
We will presente here
4. Specialized Medicines Component of
Pharmaceutical Assistance
(High cost drug program)
• Comprises high-cost treatment
– e.g.:
• Gaucher’s disease: USD 300,000.00 per patient
year
• Schizophrenia: USD 2,000.00
• Physician must fill in an administrative request explaining
the case and proving that the patient fulfills the inclusion
criteria
• CCATES team evaluate the compliance to the Brazilian or
the State Protocols of all Minas Gerais State requests for
high cost drugs (more than 100,000 per year)
5. Academic detailing for
Alzheimer’s disease
• Dementia disorders are the most common diseases among the
elderly in Brazil, reducing their social and occupational
activities.
– Alzheimer’s disease 60% of dementia cases
• Drug therapy according to Brazilian Protocols
– Cholinesterase inhibitors (donezepil, galantamine and rivastigmine)
• In 2012 - 12% of requests were denied as a result of poor filling
of the request
6. Academic detailing for
Alzheimer’s disease
• Academic detailing:
• Visit of a trained person (health
professional or not) to health professionals
in their own settings (hospital, nursing
home, office) -> one-on-one visits
• The Pilot Program
• Focus on the Clinical Protocol and
Therapeutic Guidelines for Alzheimer’s
disease to improve future prescribing
7. Academic detailing for
Alzheimer’s disease
Results
• 1st step: Seminar about the Pilot Project, the disease and its treatment
• Audience:
– Physicians 64,3%
– Residents 28,6%
– Other health professional 7,1%
Questionnaire answered
by participants of Seminar 1
• 79% of participants found the Pilot Project
relevant and were willing to receive a visit
from a CCATES facilitator
• 30% had more than one difficulty related
to the requests of Alzheimer’s treatment:
–50,0% in fullfilling the requests
–50,0% in the amount of time it requires
–28,6% had doubts about the Protocol
–14,3% other
8. • 2nd step: Study of clinical cases from both accepted and denied requests
– Revision of 165 randomly selected requests from October 2012 to
July 2013
– 80% of compliance to Clinical Protocols on 10 items evaluated
– 38% of cases were sent back to the patient/physician
– Important information lacking to analysis (e.g. educational level)
– From cases sent back, 65% were returned again, since prescribers
did little or no modification
No rejection occurred because it was not an Alzheimer's disease, but by incorrect
reporting of cognitive tests, either by incongruity between them, lack of practical
application or by non-observance of the protocol exclusion criteria.
Academic detailing for
Alzheimer’s disease
Results
9. • 3rd step: Elaboration of the material to be
delivered to physiscians:
– Handouts for patients and caregivers
– Three different bulletins for Physicians,
wich were delivered in a folder with
CCATES and UFMG logos, along with
bussiness cards.
Academic detailing for
Alzheimer’s disease
Results
In addition, we provided other material to support the visit:
‒ Clinical Protocols and Therapeutic Guidelines of the Ministry of Health, volumes 1
and 2.
‒ Book "Multidimensional Assessment of the Elderly“
‒ Pen drive containing all the material needed to request medicines in the
Specialized Component.
10. • 4th and 5th steps: Training and visiting
Academic detailing for
Alzheimer’s disease
Results
Team: eight
pharmacists with
knowledge of SUS and
evidence-based
medicine concepts.
Two-day training covering
academic detailing
techniques and principles,
Alzheimer’s disease, and
simulation of visits.
Facilitators received a
bussiness card, a badge,
the support materials
and a list of prescribers
to be visited
Physicians: selected
randomly from
CCATES database.
Criteria: requested at least
three times medicines for the
treatment of Alzheimer’s
disease during the year prior to
the study.
37 physicians were visited,
at least twice, including
psychiatrists, neurologists,
geriatricians and general
practitioners
11. Academic detailing for
Alzheimer’s disease
Results
• 6th step: Satisfaction survey by telephone evaluating acceptability, relevance
and the quality of the Academic Detailing received -> soft measures.
– 28 physicians participated
85.7% (24)
67.9% (19)
71.4% (20)
71.4% (20)
92.9% (26)
60.7% (17)
75.0% (21)
53.6% (15)
71.4% (20)
12. Academic detailing for
Alzheimer’s disease
Lessons learned
• The success of Academic Detailing depends on several factors; among the main
ones are programming and carefully training to address a topic considered
relevant to clinical practice.
• The attractiveness of visits and the support material should be targeted and
carefully planned to ensure prescriber confidence in the disseminated content
and to address the barriers identified for changing behavior.
• The physicians do not seem to be a barrier to evidence-based medicine
utilization. The barrier may be the way their practice works, since they allege to
not have time to keep-up with science publications ad the bureaucracy.
• Most of physicians were receptive to visits, which shows that they are receptive
to new information as well.
13. Academic detailing for
Alzheimer’s disease
Lessons learned
• Main evidence to use this technique was for the dissemination of clinical
protocols and compliance with its recommendations, but Academic
Detailing can also be used to track issues, challenges and suggestions of the
prescribers.
– They suggested the Protocol and the request formularies to be simplified
• In this case, the perception of the prescribers would help to update or
develop new protocols, possibly increasing their acceptability and the rate
of implementation of its recommendations.
• The prescribers’ perceptions are an important source for the identification
of problems and formulation of actions.
14. Technical Appraisals
• Used to:
– Evaluate litigated Health Tecnologies
– evaluation of the technology usefulness is needed
• Ministry of Health Guideline for Technical Apraisals
• Sumarize the cientific evidence of:
– Efficacy/Effectiveness
– Safety
– Cost-effectiveness
– Decisions of international agencies such as NICE and
CADTH.
• Quality of the evidence and strength of a
recommendation: GRADE system
– “the extent to which we can be confident that the
desirable effects of an intervention outweigh the
undesirable effects”
15. Technical Appraisals
Executive Summary
Includes the group of
patients that benefits from
the use of the technology
and if there is any alternative
available from SUS
Main part of the Technical
Appraisals
Contains the level of
recomendation of the
technology
• Weak against
• Weak in favor
• Strong against
• Strong in favor
16. Technical Appraisals
Exemples
Efficacy and safety of temozolomide in the
treatment of low grade astrocytomas
Eficacy and safety of ranibizumab and bevacizumab
in the treatment of Age-Related Macular
Degeneration
Amphotericin B formulations for the treatment of
fungal infections in patients with HIV/AIDS
Efficacy and safety of sorefenib in the
treatment of liver cancer
Efficacy and safety of rituximab for the
treatment of systemic lupus erythematosus
Efficacy and safety of zoledronic acid for the
treatment of osteoporosis
Efficacy and safety of sertraline and citalopram for
the treatment of depression
Efficacy and safety of medicines based on Cannabis
sativa extract for the treatment of epilepsy in Rett
Syndrome
Treatment of diabetic neuropathic pain:
Efficacy, safety and cost-effectiveness of pregabalin
and the association of vitamin B12, uridine and
cytidine
From 2012 to 2015: 37 Technical Apraisals were published
Efficacy and safety of drug-eluting stents in
the treatment of coronary artery disease
Ischemia time on renal graft survival:
Efficacy of perfusion machine
17. Technical Appraisals
Key points of a
Knowledge transfer
The team that develops the Technical Appraisals is
independent and free of conflicts of interests
The Technical Appraisal answers a specific question using the
evidence-based medicine principles
Gives a clear recommendation
It is written in a plain language
It is available full text at Ministry of Health and CCATES
websites