Presentation covers using data to improve people's health with two examples: mining social media and claims data,. Presentation to The Innovative Member Engagement Conference, Oct 22, 2015 Las Vegas
Home Healthcare + Data Science: A Prescription For Our Nation's Readmissions ...Wes Little
A result of over a year's worth of data science research and home healthcare's largest data-set, Kinnser RiskPoint was built to help solve the huge challenge of preventable patient readmissions. If this metric is a top priority for your organization- read here to learn more about the research and early results
Evaluating medical evidence for journalistsIvan Oransky
This document provides tips for journalists on evaluating medical evidence from studies. It discusses issues like the reliability of peer review and publication bias. It also covers challenges like overreliance on embargoed studies, how often studies are later found to be wrong, and the rise in retractions. The document provides advice on getting studies, assessing study quality, considering benefits and harms, and maintaining objectivity. It emphasizes the importance of reading full studies rather than just press releases or abstracts. Overall, the document aims to help journalists critically evaluate medical studies and provide accurate reporting to readers.
ML & AI in Drug development: the hidden part of the icebergPaul Agapow
This document summarizes the challenges of applying machine learning and artificial intelligence to drug development. It discusses how drug development is a long and complex process involving identifying disease targets, developing drug candidates, and testing through clinical trials. It then explains that biology is complex, data is often incomplete or biased, and there is a lack of labeled examples, making application of AI difficult. However, areas that could benefit include using AI to subtype diseases, interpret medical images like tumors, and build knowledge graphs to discover new insights. More and better quality data, along with focus on interpretability and engineering practices, are needed to further progress in this area.
- Flagship medical journals play an important role but their publishing strategy increases the risk of publishing erroneous results compared to specialized journals due to incentives and preference for novel results over replication.
- "Open publishing" and post-publication review can help mitigate these risks by allowing for rapid correction of published works.
- Journals should embrace post-publication review rather than ignore it in order to properly address concerns about published research.
Genetic algorithms and feature selection techniques are used to analyze medical diagnosis data and predict disease. The process involves obtaining patient data, selecting relevant features, and using a genetic algorithm to evolve a mathematical model for accurate prediction. Specifically, (1) medical records are collected as training data, (2) irrelevant variables are removed via filter feature selection, and (3) a genetic algorithm simulates natural selection to iteratively improve a model for predicting disease in new patient records. This automated approach helps analyze large datasets, minimize human interaction, and facilitate timely treatment recommendations.
The document provides tips for researchers on how to effectively communicate their work to health journalists. It discusses who typically covers health news and their educational backgrounds. It also outlines how Reuters Health selects and covers stories, and how other outlets cover stories. The document then provides specific tips for researchers, such as improving press releases, pitching stories by showing context, using social media to develop relationships with reporters, avoiding "disease of the month" topics, and effectively using embargoes. It encourages researchers to get to know the Association of Health Care Journalists for resources and networking.
Machine Learning for Preclinical ResearchPaul Agapow
This document summarizes a presentation on machine learning for preclinical research. It discusses how biomedical data sets are often small and discusses challenges in applying deep learning and other machine learning techniques with limited data. It proposes combining multiple smaller datasets using standards to create larger datasets for analysis. The document also notes issues with noise and bias in biomedical data and proposes careful curation and appropriate analysis methods. In conclusion, it advocates for carefully curated combined datasets, integrating different data types and sources, and validated application of machine learning to support preclinical research.
Home Healthcare + Data Science: A Prescription For Our Nation's Readmissions ...Wes Little
A result of over a year's worth of data science research and home healthcare's largest data-set, Kinnser RiskPoint was built to help solve the huge challenge of preventable patient readmissions. If this metric is a top priority for your organization- read here to learn more about the research and early results
Evaluating medical evidence for journalistsIvan Oransky
This document provides tips for journalists on evaluating medical evidence from studies. It discusses issues like the reliability of peer review and publication bias. It also covers challenges like overreliance on embargoed studies, how often studies are later found to be wrong, and the rise in retractions. The document provides advice on getting studies, assessing study quality, considering benefits and harms, and maintaining objectivity. It emphasizes the importance of reading full studies rather than just press releases or abstracts. Overall, the document aims to help journalists critically evaluate medical studies and provide accurate reporting to readers.
ML & AI in Drug development: the hidden part of the icebergPaul Agapow
This document summarizes the challenges of applying machine learning and artificial intelligence to drug development. It discusses how drug development is a long and complex process involving identifying disease targets, developing drug candidates, and testing through clinical trials. It then explains that biology is complex, data is often incomplete or biased, and there is a lack of labeled examples, making application of AI difficult. However, areas that could benefit include using AI to subtype diseases, interpret medical images like tumors, and build knowledge graphs to discover new insights. More and better quality data, along with focus on interpretability and engineering practices, are needed to further progress in this area.
- Flagship medical journals play an important role but their publishing strategy increases the risk of publishing erroneous results compared to specialized journals due to incentives and preference for novel results over replication.
- "Open publishing" and post-publication review can help mitigate these risks by allowing for rapid correction of published works.
- Journals should embrace post-publication review rather than ignore it in order to properly address concerns about published research.
Genetic algorithms and feature selection techniques are used to analyze medical diagnosis data and predict disease. The process involves obtaining patient data, selecting relevant features, and using a genetic algorithm to evolve a mathematical model for accurate prediction. Specifically, (1) medical records are collected as training data, (2) irrelevant variables are removed via filter feature selection, and (3) a genetic algorithm simulates natural selection to iteratively improve a model for predicting disease in new patient records. This automated approach helps analyze large datasets, minimize human interaction, and facilitate timely treatment recommendations.
The document provides tips for researchers on how to effectively communicate their work to health journalists. It discusses who typically covers health news and their educational backgrounds. It also outlines how Reuters Health selects and covers stories, and how other outlets cover stories. The document then provides specific tips for researchers, such as improving press releases, pitching stories by showing context, using social media to develop relationships with reporters, avoiding "disease of the month" topics, and effectively using embargoes. It encourages researchers to get to know the Association of Health Care Journalists for resources and networking.
Machine Learning for Preclinical ResearchPaul Agapow
This document summarizes a presentation on machine learning for preclinical research. It discusses how biomedical data sets are often small and discusses challenges in applying deep learning and other machine learning techniques with limited data. It proposes combining multiple smaller datasets using standards to create larger datasets for analysis. The document also notes issues with noise and bias in biomedical data and proposes careful curation and appropriate analysis methods. In conclusion, it advocates for carefully curated combined datasets, integrating different data types and sources, and validated application of machine learning to support preclinical research.
Prof Mendel Singer Big Data Meets Public Health and Medicine 2018 12-22mjbinstitute
Presentation by Prof. Mendel Singer of Case Western Reserve University, on the issue of "big data" in health care and policy research. Presented at the Myers-JDC-Brookdale Institute in Jerusalem.
The Learning Health System: Thinking and Acting Across ScalesPhilip Payne
A Learning Health System (LHS) can be defined as an environment in which knowledge generation processes are embedded into daily clinical practice in order to continually improve the quality, safety, and outcomes of healthcare delivery. While still largely an aspirational goal, the promise of the LHS is a future in which every patient encounter is an opportunity to learn and improve that patient’s care, as well as the care their family and broader community receives. The foundation for building such an LHS can and should be the Electronic Health Record (EHR), which provides the basis for the comprehensive instrumentation and measurement of clinical phenotypes, as well as a means of delivering new evidence at the patient- and population levels. In this presentation, we will explore the ways in which such EHR-derived phenotypes can be combined with complementary data across a spectrum from biomolecules to population level trends, to both generate insights and deliver such knowledge in the right time, place, and format, ultimately improving clinical outcomes and value.
Slides of the Talk Fabian Zimmer & I gave on the SIGINT 12 in Cologne. A video of the talk can be found here:
http://ftp.ccc.de/events/sigint12/mp4/vortrag_mp6_og_-_2012-05-19_20_00_-_power_to_the_patient_-_bastian_greshake_-_fabian_zimmer_-_40.mp4
Big data and machine learning techniques can be useful tools for health care marketers.
Big data refers to large and complex data sets that are difficult to analyze using traditional methods. Machine learning allows systems to learn from data to discover relationships and make predictions. Bayes' theorem provides a framework to update probabilities based on new evidence or observations. Marketers can use these techniques to better understand customers, predict behaviors, and inform strategy through data-driven insights. Questions were invited on applications of these techniques for health care marketing.
Wake up Pharma and look into your Big data Yigal Aviv
The vast volumes of medical data collected offers pharma the opportunity to harness the information in big data sets
Unlocking the potential in these data sources can ultimately lead to improved patients outcomes
This presentation describes consideration how to maximize the impact of Big Data.
its methodology, practical challenges and implications.
The document discusses the concepts of research, the scientific method, and big data. It defines research as the systematic pursuit of knowledge to describe facts and observations, explain relationships between variables, and predict outcomes based on theories and models. The scientific method is described as cumulative, iterative, and objective but also influenced by values and beliefs. The document cautions that research studies often only apply conditionally and their results may not extrapolate if the conditions change. It notes that predicting human behaviors is more difficult than chemical reactions since people can alter their actions based on research findings. Finally, the document discusses how big data and data-driven decision making are influencing many fields but that larger data also increases potential for bias.
The document discusses limitations of several medical studies and the importance of critically evaluating press releases and media coverage of new research. It provides examples of limitations that should be acknowledged, such as small sample sizes, lack of blinding, potential for bias, and lack of generalizability. The document advocates getting the full text of studies, asking authors questions to understand limitations and implications, considering alternative explanations, and finding perspectives from outside experts rather than just study authors. Reporters are advised to look at relevance, costs, existing alternatives, and other angles beyond initial claims in order to provide accurate context and avoid overstating findings.
Imogen Mitchell - Morphing the Recalcitrant ClinicianSMACC Conference
Imogen Mitchell’s SMACC Chicago talk 'Morphing the Recalcitrant Clinician’ talks us through the steps to engage the reluctant physician when implementing change.
Imogen initally touches on the stages of physician engagement from aversion, to apathy, to engaged and then outlines the steps to morphing the reluctant physician.
1. Seek out a clinical champion
2. Establish a common purpose/vision
3. Standardise what is standardisable
4. Communication, communication, communication
5. Work out barriers and overcome them
6. Deal with the ‘Whats in it for me?’WIFM
Utilizing Social Health Websites for Cognitive Computing and Clinical Decisio...CrowdTruth
Crowdsourced annotations data offers cognitive computing systems insights in lay semantics. This is especially important in health care, where medical terminology is often not aligned with patients `lay' language. However, the general crowd often has limited medical knowledge. Therefore this research investigated the opportunities of social health websites for obtaining ground truth annotations data for cognitive computing systems including clinical decision support systems. By identifying these websites and analyzing their data, it offers a starting point for the future utilization of user-generated health content for cognitive systems. However, the opportunities of social health data are currently limited by various legal regulations. Therefore this paper also dwells on the legal aspects of implementing social health data for cognitive computing systems.
From the event "Specimen Science: Ethics and Policy Implications," held at Harvard Law School on November 16, 2015.
This event was a collaboration between The Center for Child Health and Policy at Case Western Reserve University and University Hospitals Rainbow Babies & Children’s Hospital; the Petrie-Flom Center for Health Law Policy, Biotechnology, and Bioethics at Harvard Law School; the Multi-Regional Clinical Trials Center of Harvard and Brigham and Women's Hospital; and Harvard Catalyst | The Harvard Clinical and Translational Science Center. It was supported by funding from the National Human Genome Research Institute and the Oswald DeN. Cammann Fund at Harvard University.
For more information, visit our website at http://petrieflom.law.harvard.edu/events/details/specimen-science-ethics-and-policy
Sophia Zilber - Mito research and data webinar - June 3, 2021SophiaZilber
This document discusses the importance of patient registries and data sharing for mitochondrial disease research. It provides perspectives from patients on what they want from scientists and doctors, emphasizing the need to treat patients with dignity, compassion, and to not lose hope. The document also outlines best practices for patient registries, including proper governance, clear goals and communication, and recognizing patients' trust. The overall message is that patient data and participation can power future research if collected and used respectfully and for the benefit of patients.
This document summarizes a presentation on proposed changes to the informed consent process. The key proposed changes include shortening consent forms to only include the most relevant details, publicly posting consent documents for clinical trials, and allowing for broad consent for secondary use of biospecimens including de-identified samples. The goals of the proposed changes are to build more trust in the consent process and make it more meaningful. However, it is unclear if the changes will fully achieve these goals given challenges such as the open-ended nature of consent agreements. The presentation also discusses empirical studies conducted on community perspectives and issues regarding public health biobanks and consent.
This document provides an overview of health information technology (HIT). It discusses how healthcare is different from other industries due to factors like its life-or-death nature and fragmented systems. The document outlines various forms of HIT, such as electronic health records and telemedicine. It also explains how HIT can help improve the six dimensions of healthcare quality as defined by the Institute of Medicine: safety, timeliness, effectiveness, efficiency, equity, and patient-centeredness. The document emphasizes that while HIT has benefits, it does not automatically solve all healthcare issues and its impact may vary by context.
Conference Abstract: Did you know that there are measurement experts who spend their lives researching the validity of different question styles and formats? How ’bout we spend 30 minutes reviewing some of the most relevant findings in survey methods research!? During this presentation, you will learn about fascinating topics such as the validity of true/false questions, when to use “none of the above” style questions, and which question styles will help you assess the information you are actually trying to asses (read= minimize bias and error)! Participants will be asked to vote on sample question strength, and recraft “before’s” into highly valid “after’s.”
Introduction to Health Informatics and Health Information Technology (Part 2)...Nawanan Theera-Ampornpunt
This document provides an overview of health information technology (HIT) and electronic health records (EHRs). It discusses how healthcare is complex, information-rich, and prone to errors. HIT can help by providing timely access to patient information, assisting with clinical decision-making, and improving quality, safety and efficiency. However, HIT alone will not fix all healthcare issues and its benefits may vary by context. The document outlines how HIT can help achieve the six dimensions of quality healthcare as defined by the Institute of Medicine. While HIT has documented benefits, it is not a panacea and its implementation requires focus on ultimate goals like patient health rather than just technology adoption.
Jon Tilburt, MD - Assessing Health Priorities of Tribal Health Directors with...trainer2007
The document summarizes the results of a survey of tribal health directors regarding health priorities and working with researchers. It finds that while men's health was not a top priority issue, it was viewed as an important strategy for achieving other priorities by many respondents. The survey also found that most directors had a positive view of working with researchers but faced challenges of funding, staffing, and bureaucracy. It concludes that surveys provide a limited perspective and that meaningful research requires truly listening to and partnering with communities.
Approch note customer behavior towards Healthcare and WellnessBang Design
This document outlines a study to understand customer behavior and attitudes towards healthcare for the 30-45 age group. It will use qualitative research methods like interviews and observation to understand perceptions of health, hospitals, and healthy living. The goal is to gain insights that can help design new healthcare services that inspire people to lead healthier lifestyles. The research aims to identify segments within the target group and provide context to designers to create an innovative user experience. Data will be collected through discussions with customers and smaller healthcare clinics to understand perceptions, experiences, and behaviors related to health and hospitals.
This document discusses digital health transformation and the role of health information technology. It begins by exploring concepts like artificial intelligence, blockchain, cloud computing and big data. It then examines the potential for "smart" machines in healthcare while acknowledging the complexities of digitizing such a system. The document emphasizes that clinical judgment is still necessary given variations in patients. It outlines components of healthcare systems and forms of health IT both within and beyond hospitals. Finally, it discusses using health IT to support clinical decision making and reduce errors.
Integrating Design Using the Native Language of HealthcareJoyce Lee
This document discusses integrating design thinking into healthcare. It describes Joyce Lee's background in pediatrics, clinical research, and participatory design. It outlines efforts to engage students in design workshops and create apps for managing diabetes. The document proposes achieving greater adoption of design in healthcare and measuring return on investment. It presents a quality improvement project using interventions like depression screening and shared decision making to improve diabetes outcomes. Throughout, it emphasizes designing with patients and caregivers and not accepting the status quo.
Digital Health in India_Health Informatics Trained Manpower _DrDevTaneja_15.0...DrDevTaneja1
Digital India will need a big trained army of Health Informatics educated & trained manpower in India.
Presently, generalist IT manpower does most of the work in the healthcare industry in India. Academic Health Informatics education is not readily available at school & health university level or IT education institutions in India.
We look into the evolution of health informatics and its applications in the healthcare industry.
HIMMS TIGER resources are available to assist Health Informatics education.
Indian Health universities, IT Education institutions, and the healthcare industry must proactively collaborate to start health informatics courses on a big scale. An advocacy push from various stakeholders is also needed for this goal.
Health informatics has huge employment potential and provides a big business opportunity for the healthcare industry. A big pool of trained health informatics manpower can lead to product & service innovations on a global scale in India.
This particular slides consist of- what is hypotension,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is the summary of hypotension:
Hypotension, or low blood pressure, is when the pressure of blood circulating in the body is lower than normal or expected. It's only a problem if it negatively impacts the body and causes symptoms. Normal blood pressure is usually between 90/60 mmHg and 120/80 mmHg, but pressures below 90/60 are generally considered hypotensive.
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A Learning Health System (LHS) can be defined as an environment in which knowledge generation processes are embedded into daily clinical practice in order to continually improve the quality, safety, and outcomes of healthcare delivery. While still largely an aspirational goal, the promise of the LHS is a future in which every patient encounter is an opportunity to learn and improve that patient’s care, as well as the care their family and broader community receives. The foundation for building such an LHS can and should be the Electronic Health Record (EHR), which provides the basis for the comprehensive instrumentation and measurement of clinical phenotypes, as well as a means of delivering new evidence at the patient- and population levels. In this presentation, we will explore the ways in which such EHR-derived phenotypes can be combined with complementary data across a spectrum from biomolecules to population level trends, to both generate insights and deliver such knowledge in the right time, place, and format, ultimately improving clinical outcomes and value.
Slides of the Talk Fabian Zimmer & I gave on the SIGINT 12 in Cologne. A video of the talk can be found here:
http://ftp.ccc.de/events/sigint12/mp4/vortrag_mp6_og_-_2012-05-19_20_00_-_power_to_the_patient_-_bastian_greshake_-_fabian_zimmer_-_40.mp4
Big data and machine learning techniques can be useful tools for health care marketers.
Big data refers to large and complex data sets that are difficult to analyze using traditional methods. Machine learning allows systems to learn from data to discover relationships and make predictions. Bayes' theorem provides a framework to update probabilities based on new evidence or observations. Marketers can use these techniques to better understand customers, predict behaviors, and inform strategy through data-driven insights. Questions were invited on applications of these techniques for health care marketing.
Wake up Pharma and look into your Big data Yigal Aviv
The vast volumes of medical data collected offers pharma the opportunity to harness the information in big data sets
Unlocking the potential in these data sources can ultimately lead to improved patients outcomes
This presentation describes consideration how to maximize the impact of Big Data.
its methodology, practical challenges and implications.
The document discusses the concepts of research, the scientific method, and big data. It defines research as the systematic pursuit of knowledge to describe facts and observations, explain relationships between variables, and predict outcomes based on theories and models. The scientific method is described as cumulative, iterative, and objective but also influenced by values and beliefs. The document cautions that research studies often only apply conditionally and their results may not extrapolate if the conditions change. It notes that predicting human behaviors is more difficult than chemical reactions since people can alter their actions based on research findings. Finally, the document discusses how big data and data-driven decision making are influencing many fields but that larger data also increases potential for bias.
The document discusses limitations of several medical studies and the importance of critically evaluating press releases and media coverage of new research. It provides examples of limitations that should be acknowledged, such as small sample sizes, lack of blinding, potential for bias, and lack of generalizability. The document advocates getting the full text of studies, asking authors questions to understand limitations and implications, considering alternative explanations, and finding perspectives from outside experts rather than just study authors. Reporters are advised to look at relevance, costs, existing alternatives, and other angles beyond initial claims in order to provide accurate context and avoid overstating findings.
Imogen Mitchell - Morphing the Recalcitrant ClinicianSMACC Conference
Imogen Mitchell’s SMACC Chicago talk 'Morphing the Recalcitrant Clinician’ talks us through the steps to engage the reluctant physician when implementing change.
Imogen initally touches on the stages of physician engagement from aversion, to apathy, to engaged and then outlines the steps to morphing the reluctant physician.
1. Seek out a clinical champion
2. Establish a common purpose/vision
3. Standardise what is standardisable
4. Communication, communication, communication
5. Work out barriers and overcome them
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Utilizing Social Health Websites for Cognitive Computing and Clinical Decisio...CrowdTruth
Crowdsourced annotations data offers cognitive computing systems insights in lay semantics. This is especially important in health care, where medical terminology is often not aligned with patients `lay' language. However, the general crowd often has limited medical knowledge. Therefore this research investigated the opportunities of social health websites for obtaining ground truth annotations data for cognitive computing systems including clinical decision support systems. By identifying these websites and analyzing their data, it offers a starting point for the future utilization of user-generated health content for cognitive systems. However, the opportunities of social health data are currently limited by various legal regulations. Therefore this paper also dwells on the legal aspects of implementing social health data for cognitive computing systems.
From the event "Specimen Science: Ethics and Policy Implications," held at Harvard Law School on November 16, 2015.
This event was a collaboration between The Center for Child Health and Policy at Case Western Reserve University and University Hospitals Rainbow Babies & Children’s Hospital; the Petrie-Flom Center for Health Law Policy, Biotechnology, and Bioethics at Harvard Law School; the Multi-Regional Clinical Trials Center of Harvard and Brigham and Women's Hospital; and Harvard Catalyst | The Harvard Clinical and Translational Science Center. It was supported by funding from the National Human Genome Research Institute and the Oswald DeN. Cammann Fund at Harvard University.
For more information, visit our website at http://petrieflom.law.harvard.edu/events/details/specimen-science-ethics-and-policy
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This document discusses the importance of patient registries and data sharing for mitochondrial disease research. It provides perspectives from patients on what they want from scientists and doctors, emphasizing the need to treat patients with dignity, compassion, and to not lose hope. The document also outlines best practices for patient registries, including proper governance, clear goals and communication, and recognizing patients' trust. The overall message is that patient data and participation can power future research if collected and used respectfully and for the benefit of patients.
This document summarizes a presentation on proposed changes to the informed consent process. The key proposed changes include shortening consent forms to only include the most relevant details, publicly posting consent documents for clinical trials, and allowing for broad consent for secondary use of biospecimens including de-identified samples. The goals of the proposed changes are to build more trust in the consent process and make it more meaningful. However, it is unclear if the changes will fully achieve these goals given challenges such as the open-ended nature of consent agreements. The presentation also discusses empirical studies conducted on community perspectives and issues regarding public health biobanks and consent.
This document provides an overview of health information technology (HIT). It discusses how healthcare is different from other industries due to factors like its life-or-death nature and fragmented systems. The document outlines various forms of HIT, such as electronic health records and telemedicine. It also explains how HIT can help improve the six dimensions of healthcare quality as defined by the Institute of Medicine: safety, timeliness, effectiveness, efficiency, equity, and patient-centeredness. The document emphasizes that while HIT has benefits, it does not automatically solve all healthcare issues and its impact may vary by context.
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This document outlines a study to understand customer behavior and attitudes towards healthcare for the 30-45 age group. It will use qualitative research methods like interviews and observation to understand perceptions of health, hospitals, and healthy living. The goal is to gain insights that can help design new healthcare services that inspire people to lead healthier lifestyles. The research aims to identify segments within the target group and provide context to designers to create an innovative user experience. Data will be collected through discussions with customers and smaller healthcare clinics to understand perceptions, experiences, and behaviors related to health and hospitals.
This document discusses digital health transformation and the role of health information technology. It begins by exploring concepts like artificial intelligence, blockchain, cloud computing and big data. It then examines the potential for "smart" machines in healthcare while acknowledging the complexities of digitizing such a system. The document emphasizes that clinical judgment is still necessary given variations in patients. It outlines components of healthcare systems and forms of health IT both within and beyond hospitals. Finally, it discusses using health IT to support clinical decision making and reduce errors.
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Presentation made by Mat Southwell to the Harm Reduction Working Group of the English Drug and Alcohol Commissioners. Discuss stimulants, OAMT, NSP coverage and community-led approach to DCRs. Focussing on active drug user perspectives and interests
Fit to Fly PCR Covid Testing at our Clinic Near YouNX Healthcare
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2. Big Data
• Many data sources with different formats
• Data with missing values
• Text / Social Media
• Things that don’t fit in Excel
The term for a collection of data sets so large and
complex that they become difficult to process
5. Where did it all Start? Bayes
Thomas Bayes (1701 – 7 April 1761)was an English mathematician
and Presbyterian minister, known for formulating the theorem
that bears his name: Bayes' theorem
• Bayes theorem uses prior probabilities, combined with new
observations to calculate the probability of a hypothesis being true or
false
• Bayes is a natural fit to health care due to the presence of hypothesis
(diagnosis) and events (tests / observations)
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7. How can we Apply Machine Learning in
Healthcare?
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Identify patterns that humans have trouble seeing
Population
Health
Care
Optimization
Precision
Medicine
R&D
Productivity
8. What Does this Mean To Patient
Engagement?
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You are Here
12. Twitter Users Self-Described Diabetics
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•What if you could identify “real” diabetics on twitter?
• You could engage them in diabetes education, etc.
• Cost = $0
• Know things that don’t show up in claims (latency)
• Possibly alert the undiagnosed
“Lets play a game called how many times
will my relatives ask about my diabetes.
#byyyyeeee”
13. Results
• 73.5% Accuracy (ability to identify self-
described diabetics from spam, people
mentioning other people’s diabetes,
retweets, bots, etc.)
•Variables in order of importance
• #times others favorited tweets
• #followers
• #user statues
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16. MI Patients not Taking Beta Blockers
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•What patterns exist in this population?
• You had a heart attack but not taking beta
blockers
• What can we learn to effectively reach these
people
• Are they homogeneous or are there sub groups
• Preemptive activities?
17. Results
• 74% Accuracy (ability to predict
compliance with rule – take beta blockers)
•Variables in order of importance
• #primary diagnoses
• #Evaluation & Management visits
• Prior compliance with other rules
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