Welcome to the IMS Health Real-World Evidence (RWE) Solutions program of activities at the forthcoming ISPOR 18th Annual European Congress in Milan. We invite you to join us at more than 70 presentations that spotlight exciting innovations and applications of outcomes research and RWE. And please visit us at our booth to learn more about our pioneering efforts including the e360TM technology suite, RWD Catalogue with 1,800+ data sources identified, and the newly launched RWE Dictionary. Full details of our ISPOR schedule can be found in the brochure.
Real world data is no longer just for those trained in health economics and outcomes research — it can and will touch everyone in the pharma/healthcare space.
CBI asked industry's foremost RWD thought leaders a variety of questions to better understand how bio/pharmaceutical teams can collaborate and capture data in an aggregated form to continue to improve the value of products in development with real world, real-time data.
IMS Health Clinical Trial Optimization SolutionsQuintilesIMS
IMS Health's Linda T. Drumright, general manager, Clinical Trial Optimization Solutions presents at the 3rd Annual Patient Recruitment & Retention Summit 2014 - San Francisco, CA
Seamless Journey from Population Health to Precision MedicineOrion Health
Precision medicine is happening now! Join us as we examine the opportunities to leverage your initial core data sets and prepare for new data types to deliver real-time population health and precise medicine.
This webinar will demonstrate how modern healthcare organizations (HCO) are expanding clinical integration and upgrading to higher performing technology stacks on their journey to the omics-based and real-time delivery of precision medicine.
We’ll chat with Dr. Chris Hobson, CMO and CPO at Orion Health, Doctor Dylan Mordaunt, Clinical Director Research at Orion Health, and with Orion Health’s Executive Vice President of Product and Strategy, Dave Bennett about the importance of real-time data mining and re-mining, and which new computational tools and techniques you need to meet your population health goals and future proof your organization for the delivery of precision medicine.
In this webinar, we will explain:
How new models of medicine (e.g., molecular medicine, value-based medicine, etc.) are driving the immediate need for patient-specific decision support assistance
How existing and new data sets can be leveraged with integrated and real-time analytics (e.g., family history, pharmacogenics) for immediate reduction in adverse events and improved outcomes
How innovative organizations are answering this demand with high-performing technology
The role of real world data and evidence in building a sustainable & efficien...Office of Health Economics
This presentation defines RWD and RWE in the context of digital health, and looks at potential uses for RWD and RWE. It briefly sets out the current landscape in Malaysia and looks at the challenges in using RWE. In particular, the issues of access, governance and ensuring good quality are considered.
Big data, RWE and AI in Clinical Trials made simpleHadas Jacoby
Technology is slowly but surely penetrating the healthcare industry in general and the clinical trials sector in particular. New and advanced solutions offer a variety of possibilities aimed to both improving existing processes and creating new and more efficient ones. And on top of all stands the desire to make clinical trials more patient centric.
In all of this, even though some of the technologies have yet to mature enough to meet the high quality standards necessary, it is important to know them and begin imagining the promise they hold for clinical trials.
IMS Health RWES: The Future of Real-World Insights in CancerIMSHealthRWES
The document discusses IMS Health's real-world evidence solutions for cancer, including their cancer data ecosystem. The ecosystem combines various real-world data sources like medical claims, EMR data, and genomic data from over 15 million anonymous cancer patients. It provides comprehensive insights through innovative analytics to help address challenges across the cancer care continuum for clinicians, payers, pharmaceutical companies, patients, and advocacy groups.
Big Data Analytics for Treatment Pathways John CaiJohn Cai
This document discusses using real-world big data analytics to understand treatment pathways. It begins by explaining the need for real-world evidence from real-world data to assess effectiveness and outcomes beyond randomized clinical trials. It then describes the volume, variety, and velocity characteristics of real-world big data from sources like claims, EMRs, surveys, and devices. Technical challenges of reconstructing complex patient journeys are discussed. Hadoop and MapReduce are presented as a potential solution by breaking the work into mappers that extract patient data and reducers that organize it into timelines. Examples are given of how this could enable cost, pathway, and outcomes analyses to better inform decision making.
Real World Late Phase The right approach for the right questionSatish Kumar
Quintiles is a global contract research organization that provides real-world and late phase research services to biopharmaceutical companies. They have experience with over 500 real-world and late phase programs involving over 600,000 patients. Quintiles offers a comprehensive set of integrated services including scientific, strategic, operational, and technological support to help clients answer key research questions, meet regulatory requirements, and demonstrate product value. Their goal is to provide the right approach for each client's specific research needs and objectives.
NLP (Natural Language Processing) shows a great deal of potential for many applications in the healthcare industry. This document shares 6 promising use cases for NLP to manage Epilepsy treatment effectively.
mHealth Israel_Ben Echeazu_Highmark Health_ Startups Engaging with US PayersLevi Shapiro
Presentation by Ben Echeaz, Business Development Director, Highmark Health, March 25, 2019, for the mHealth Israel community: Startups Engaging with US Payers. Includes overview of the US Payerand health insurance sector, Relationship to Blue Cross Blue Shield, Challenges in addressing needs and gaps through Big Data technology, How Payers de-risk their reimbursement and coverage decisions with early stage startups, the role of Big Data in informing the movement toward value-based healthcare, Enterprise focus areas across 7 major applications: Diagnostic, Preventative, Precision Medicine, Adverse medication events, Cost reduction, Medical research Population health, etc. Highmark's VITAL has projects in the top 5 areas, these area are not mutually exclusive.
Value Based Care Model
Inadequate Evidence
Solution
Traversing “Valley of Death”
De-risking Reimbursement
Vital Innovation
Conclusion
Focus areas for evidence development
The document provides an overview of ICNet Infection Case Management & Surveillance Software. It describes ICNet as a leading provider of infection control software with over 90 NHS Trust clients in the UK and international clients. Key features of ICNet include its web-based, real-time surveillance platform that provides proactive alerts and customizable reporting. ICNet can interface with various hospital information systems and has experience implementing its software and interfaces internationally. The document outlines ICNet's training and support services and provides examples of the types of customizable reports and analyses that ICNet can generate.
Leveraging Analytics to Identify High Risk PatientsCitiusTech
A predictive analytics platform can help healthcare providers identify which patients and team members could be at the highest risk for severe illness / hospitalization.
The document summarizes a study that evaluated the acceptability of a personally controlled health record (PCHR) system called Indivo in a community-based setting. Over 300 participants were involved in formative research activities to understand awareness, beliefs and reactions. The study found moderate awareness of privacy issues and high support for patient autonomy. Results informed guidelines on design improvements, literacy tools, and safety protocols for PCHR systems. Limitations included a lack of detail on methodology and sample selection.
Purpose of the Webinar
1.Describe the process of developing an undergraduate MedRec IPE Event involving > 480 senior Medicine, Pharmacy and Nursing students;
2.Explain the logistics of conducting the event in multiple venues and urban/remote locations;
3.Discuss the successes and challenges of communicating MedRec patient safety concepts through this process; and
4.Describe future opportunities for enhancing undergraduate MedRec training in an interprofessional environment.
Watch the webinar recording: http://bit.ly/1fSqsqv
Presentation 90-10-funding-opportunity-for-health-infomation-exchangesOrion Health
How can HIEs access 90/10 and Federal funding and expand their exchange
We examined the opportunities to capture funding from CMS to develop core HIE services, public health infrastructure, electronic Clinical Quality Measurement (eCQM) infrastructure, and provider onboarding.
This webinar demonstrated how to some innovative HIEs are leveraging these grants and have elected multiple funded activities to boost growth, expand regional interoperability, and upgrade to higher performing technology stacks.
George Beckett, Chief Business Development Officer at the Cedar Bridge Group and Orion Health’s Director, Laura Young, about the process to request funding for health information exchange (HIE) infrastructure.
In this webinar, we explained:
1. The CMS 90/10 funding opportunities for private and public HIEs
2. The funding strategy used by NDHIN and their 5-year business plan
3- How NDHIN has created a solid data foundation for their data strategy and how they are expanding their infrastructure
This document introduces a new tool to assess the quality of admission medication reconciliation (MedRec) processes. The tool allows hospitals to collect patient-level data on key determinants of admission MedRec quality. It focuses on the three core steps of MedRec: collecting a best possible medication history, comparing it to admission orders, and correcting any discrepancies. The tool is designed for easy data submission and analysis through an online system. Using this tool, hospitals can identify specific areas in their MedRec processes needing improvement by quantifying how well each step is performed.
Enhancing Competitive Advantage through Improved HEDIS Reporting and NCQA Rat...CitiusTech
The objective of this document is to provide a high level understanding of the Healthcare Effectiveness Data and Information Set (HEDIS), which is a tool used by more than 90 percent of America's health plans to measure performance on important dimensions of care and service. This document helps in understanding different components of the HEDIS in terms of the measure sets (what it is meant for health plans, changes to the previous year), different methods of collecting data for HEDIS and key requirements for reporting HEDIS
IMS Health at ISPOR - Washington DC - May 2016IMSHealthRWES
This document provides information about IMS Health's activities and participation at the ISPOR 21st Annual International Meeting from May 21-25, 2016 in Washington, DC. The document outlines IMS Health's educational symposium titled "How real-world evidence (RWE) can enable pharma to partner in healthcare delivery" as well as several research posters, presentations, and workshops led by IMS Health experts on topics related to real-world evidence and its use in healthcare. Members of IMS Health's global RWE Solutions team will be available at the company's booth throughout the event.
Speech recognition and clinical knowledge systemsKlaus Stanglmayr
The document discusses combining speech recognition technology with clinical decision support tools to improve clinical documentation. It highlights how SpeechMagic speech recognition software integrates with Elsevier's clinical reference and decision support tools to allow doctors to access evidence-based medical information while dictating patient notes. The combination aims to enhance patient care by facilitating documentation while reducing errors and improving efficiency.
Planimeter Kft is a full service CRO specialized in translational medicine located in Budapest, Hungary. Their mission is to provide expertise in biostatistics for the pharmaceutical industry using rigorous quantitative methods. They have 16 employees and contractors who have experience in all phases of drug development. Their services include clinical trial design, data management, statistical analysis, and using new technologies like data mining and personalize medicine approaches.
Europe's Top 5 Effective Leaders in Healthcare Edition.pdfinsightscare
Insights Care’s team carried out its own research and found the ‘Europe's Top 5 Effective Leaders in Healthcare,’ and depicted their revolutionary tales
Beyond Speech Recognition – New approaches to Information CaptureKlaus Stanglmayr
The document discusses speech recognition technology solutions for healthcare organizations. It provides an overview of SpeechMagic, a leading speech recognition platform, and its capabilities for clinical documentation, information capture, and integration with other systems. SpeechMagic has evolved to offer interactive speech recognition that allows clinicians to instantly create structured reports at the point of care with standardized formatting and medical terminology.
AccessPoint - 9th Issue - November 2014IMSHealthRWES
This document summarizes an article from IMS Health Real-World Evidence Solutions & HEOR. It discusses three main topics:
1) How new research using real-world evidence is revealing insights into diabetes treatment outcomes and understanding patient subgroups. This is helping to improve care provision.
2) Trends in real-world evidence, including new data strategies, greater involvement of commercial teams, and increased collaboration with external stakeholders.
3) Advancements in real-world evidence, such as improved data sourcing, predictive modeling techniques, and leveraging data from Scandinavia to enable disease-level insights. This is helping to demonstrate treatment value and support care management.
SMi Group's Inaugural Big Data in Pharma conferenceDale Butler
This document provides information about a conference on big data in the pharmaceutical industry, including an agenda, speaker details, and workshop information. The two-day conference will focus on how big data can be leveraged to enhance research and development, clinical trials, and real-world evidence generation. Highlights include sessions on personalized medicine, predictive analytics, and social media strategies. Post-conference workshops will discuss the legal aspects of cloud computing and designing studies using big data to support drug development and marketing. The event aims to help pharmaceutical companies exploit big data's potential to create better medicines and new revenue streams.
Artificial Intelligence & Deep Learning - Presentation by Avner Halperin, Co-Founder & CEO of EarlySense at the NOAH Conference Tel Aviv 2018, Haoman 17 on the 14th of March 2018.
Thomas Willkens-El impacto de las ciencias ómicas en la medicina, la nutrició...Fundación Ramón Areces
El 29 de marzo de 2016 celebramos un Simposio Internacional sobre el 'Impacto de las ciencias ómicas en la medicina, nutrición y biotecnología'. Organizado por la Fundación Ramón Areces en colaboración con la Real Academia Nacional de Medicina y BioEuroLatina, abordó cómo un mejor conocimiento del genoma humano está permitiendo notables avances hacia una medicina de precisión.
mHealth Israel_Future of Integrated Individualized Healthcare_Roche DiagnosticsLevi Shapiro
Presentation by Alexandra Eberhard, Sr. Director, Global Business Development, Roche Diagnostics on the "Future of Integrated Individualized Healthcare". Includes background about Roche Diagnostics and investments in innovation. Overview of Roche products and solutions with a portfolio covering the entire spectrum of diagnostics users. Emphasis on the triple aim of healthcare- The power of data and technology to enable the transformation from volume- to value-based healthcare. Interest in data for Pharma - drive more efficient R&D; DIA - develop novel patient care Dx solutions. Focus on the needs of labs, physicians & payers for better patient health. A suite of digital solutions that improve clinical & business outcomes. Suite of solutions to optimize the lab. Translating data into insights to achieve financial goals. A move from volume- to value-based care. New opportunities in the disease continuum- Holistic solutions approach. Expanding the focus towards earlier in the patient journey. Doing now what patients need next. Contact Alexandra Vallon-Eberhard, PhD MBA; Sr. Director Global Business Development; Diagnostics Lead for Innovation in Israel; Based in Basel, Switzerland; Email: alexandra.vallon_eberhard@roche.com
IMS Health Workshop World Orphan Drug CongressIMSHealthRWES
This document provides an agenda for a workshop titled "Using real-world data to find undiagnosed patients with rare diseases" hosted by IMS Health at the World Orphan Drug Congress from April 20-22 in Washington D.C. The workshop will explore how real-world data can help address underdiagnosis of rare diseases. Speakers will discuss using large-scale real-world data to transform understanding of rare diseases, and present case studies of companies leveraging real-world data. The workshop will also cover using predictive modeling of real-world data to identify undiagnosed rare disease patients and new engagement models with healthcare providers and payers to increase rare disease treatments.
A Trust-Centric Healthcare Journey Part II | Full Presentation of PharmaLedge...PharmaLedger
In this presentation, you will find:
An introduction to the PharmaLedger project presented by Maria Eugenia (Xenia) Beltran | Project Coordinator / DRA and Use Case co-lead (Universidad Politécnica de Madrid)
Topic 1 | Clinical Trial eRecruitment | Despina Daliani (Onorach) and Ken Nessel (Pfizer)
Topic 2 | Clinical Trial eConsent | Hernando C. Giraldo (Boehringer Ingelheim) and Despina Daliani (Onorach)
Topic 3 | Health Data IoT Medical Device | Disa Lee Choun (UCB) and Francesca Rocchi (Bambino Gesù Children Hospital)
Topic 4 | Health Data Personalised Medicine | Beatriz Merino (Universidad Politécnica de Madrid) and Christos Kontogiorgis (Democritus University of Thrace)
You can also learn more about our #2 Open Webinar on Clinical Trials & Health Data by rewatching our video recording including the Q&A by clicking on the button below:
This project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 853992. This Joint Undertaking receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA.
Disclaimer: Any information on this presentation solely reflects the author’s view and neither IMI nor the European Union or EFPIA are responsible for any use that may be made of the information contained herein.
Medical Informatics World 2014 [Full Agenda]Jaime Hodges
Cambridge Healthtech Institute and Bio-IT World’s Second Annual Medical Informatics World builds upon last year’s successful inaugural launch by delivering timely programming focused on the cross-industry connections and innovative solutions needed to take biomedical research and healthcare delivery to the next level.
The 2014 meeting will bring together more than 300 senior level executives and industry leaders from each side of the discussion - providers, payers and pharma - in the fields of healthcare, biomedical sciences, health informatics, and IT. Over two days of insightful discussions and engaging presentations, leading experts will share emerging trends and solutions in population health management, payer-provider-pharma data collaborations, optimizing patient care and engagement, leveraging mobile technologies, sustaining innovation within the rapidly changing care delivery models, enhancing clinical decision support, controlling costs and improving quality, and maintaining security-privacy in healthcare. Led by key decision makers and senior executives at the forefront of healthcare information technology, the conference is a must-attend for all involved in this evolving industry.
Co-located with CHI's flagship Bio-IT World Expo, a premier event showcasing the myriad applications of IT and informatics to the life sciences enterprise, Medical Informatics World completes the week of scientific content by bridging the healthcare and life science worlds. As Bio-IT World Expo attracts more than 2,500 delegates from dozens of countries as well as more than 130 exhibiting companies, networking opportunities abound at the two events. To learn more, visit http://www.medicalinformaticsworld.com
Interviews with Dr Torsten Hoffmann (Summit Chairman), Dr Bertil Lindmark and Herbie Newell, speakers at the marcus evans Discovery Summit 2014, taking place in Lisbon, Portugal, 31 March - 1 April 2014.
1) The document describes an Insights as a Service platform that can help address multiple clinical, scientific, and economic needs by providing analytics and insights derived from large amounts of individual health data.
2) The platform establishes a standardized, industrialized process for generating insights through analytics by integrating data from various sources and providing role-based analytic tools and results.
3) Use cases for the platform include transitioning from volume-based to value-based healthcare through risk prediction and cost/utilization analytics, generating real-world evidence through large-scale analytics of electronic health data, and powering condition-specific care and population health management solutions.
Precision Medicine & Biomarkers Leaders Summit - Boston USA - 7th & 8th MayTony Couch
Tracks focus on R&D strategies, Biomarker development, Immuno-oncology, CDx development, AI and Big data analysis and approaches – Attending this Summit will provide you with the opportunity to mix and interact with experts working in all facets of Precision Medicine through the individual, panel and roundtable discussions on offer.
The document announces IMS Health's activities and presence at the ISPOR 7th Asia-Pacific Conference from September 3-6, 2016 in Singapore. IMS Health will host a symposium on how real-world evidence can enable pharmaceutical companies to partner in healthcare delivery. They will also participate in workshops, presentations, and have a booth showcasing their real-world evidence solutions and oncology research bibliography. IMS Health utilizes real-world data from electronic health records and claims to generate real-world evidence on drug safety and effectiveness to inform healthcare decisions.
Similar to IMS Health Real-World Evidence Solutions at ISPOR November 2015 (20)
How patient subpopulations are changing the commercialization of oncology pro...IMSHealthRWES
An excerpt from the latest issue of AccessPoint, looking at how genomic profiling data is transforming our understanding of patient subpopulations - a key to targeting treatments with greater precision
How predictive analytics can help find the rare disease patientIMSHealthRWES
This document discusses how predictive analytics using real-world data can help identify undiagnosed rare disease patients. It describes two case studies: 1) A screening algorithm identified potentially undiagnosed patients for a rare multi-system disease with a high risk prevalence of 20.5% compared to 0.7% of the population. 2) An analysis of a rare cardiac disease identified health system barriers like variability between diagnostic centers that could cause under diagnosis. While initial results are promising, challenges remain around data privacy, sample size, and clinician adoption of screening algorithms.
Prospective identification of drug safety signalsIMSHealthRWES
At a time of growing demand for more accurate and timely
drug safety evidence, a landmark study supports the value of
electronic medical records (EmR) for detecting new adverse
reactions.
- The document analyzes misperceptions about migraine and its treatment. It finds that while migraine affects more women, over half of diagnosed migraine patients are over age 40, contradicting the idea that it only impacts young women.
- It also finds that the majority (76%) of diagnosed adult migraine patients have cardiovascular risk factors that caution against the use of triptan medications, much higher than generally believed. Having a migraine diagnosis increases the risk of future cardiovascular events.
- Current treatment patterns show triptan use is lower in high-risk patients than others, and off-label opioid use is higher, suggesting this population is underserved by existing options.
This document describes how real-world data was used to help expand a clinical trial for a rare disease. Specifically:
1. Claims data was analyzed to identify patients diagnosed with the rare disease and their physicians, applying inclusion criteria like diagnostic tests and drug treatments. This sized the national patient population and located diagnosing/treating doctors.
2. Physicians were mapped to local hospitals to identify areas with high concentrations of relevant patients and doctors.
3. A density analysis identified the top 20 hospitals that could serve as potential new clinical trial sites based on clusters of physicians and their patient counts. This innovative use of real-world data provided new insights to strengthen the company's rare disease research program.
EMR as a highly powerful European RWD sourceIMSHealthRWES
This document discusses leveraging electronic medical record (EMR) data from multiple countries in Europe to improve clinical trial design and patient recruitment for a cardiovascular drug trial. Specifically:
EMR data from France, UK, Italy, Germany and Spain was used to 1) characterize and quantify the number of potential patients meeting the inclusion criteria, and 2) identify and pre-select high-potential clinical trial sites. This approach helped clarify the definition of "statin-intolerant patients" and ensured the number of required trial sites would be sufficient. Using real-world data in this way enhanced the clinical trial strategy and avoided potential delays or additional costs associated with insufficient patient recruitment.
As pharmaceutical manufacturers look for ways to build
stronger relationships with their Integrated Delivery Network
(IDN) clients, RWE is emerging as a desired infrastructure
capability, presenting a window of opportunity to support and
collaborate on IDN efforts. If done well, these RWE-related
partnerships should provide value for both parties involved
but require pharma to expand its mindset beyond
product-specific approaches.
Building innovative, effective RWE platformsIMSHealthRWES
As more pharmaceutical companies pursue RWE as a core
capability in their organization, they have been increasing their
investment in integrated evidence platforms.
Integrate RWE into clinical developmentIMSHealthRWES
With greater application of RWE throughout the pharmaceutical
lifecycle, learnings are emerging that offer guidance for
approaches to derive the maximum value. This article captures
the author’s experience at a leading international biotech, with
insights for smoothing RWE assimilation into clinical
development and realizing the benefits it brings.
50 Hr – Restorative Yoga Teacher Training Certificate Course
50 Hr – Restorative Yoga Teacher Training Course
Course Fee: INR 15,000 for Indian citizens only, for foreigners USD 350.
Yoga Manual (01)
Certificate
Excluded with accommodation and food
Upcoming Batches 50 Hr Non-Residential (Week-Days/Week-End)
Professional Yoga Teacher Training
Our 50 hours Restorative Yoga Teachers Training Course is beautifully programmed for those enthusiasts who desire to have a professional certificate in the future but can’t afford the time of two months in one slot.
If you have less time or you want to learn slowly, so 50-hour yoga teacher training course in Bangalore can be the perfect yoga course for you, karuna yoga offers a self-paced yoga teacher training course in Bangalore India, and you can join the other half in 1 year of time to complete 200/300 hours Teacher Training Course.
In order to obtain a professional certificate of 200/300 Hour, Teachers Training Course affiliated with the Yoga alliance one has to complete 200 Hours which is usually completed in one or two months of time, we designed this course in such a way that if any participant wants to first get introduced with the way and process of professional yoga teacher training course and have only short time then students can enroll for this yoga course.
Our 50 hours Yoga Teacher Training Course program runs along with our regular student of 200/300-hour Teacher Training Course students in the first phase, upon completion of the course if a student wants to finish remaining their balance of 150/250 hours of Teacher Training Course in the future, then students can continue the course of the second stage of Teacher Training Course to obtain 200/300-hour Teacher Training Course certificate affiliated with Yoga Alliance in order to have a professional certificate.
Our 50 hours can be accepted as continuing education from Yoga Alliance if in the future you want to continue the training from our center. Please make a note while completing 50 hour TTC you will be only provided with a certificate issued by our organization and the certificate will not be affiliated with Yoga Alliance, and only after completion of the second stage of balance 150/250 hours of TTC, which technically becomes 200/300 hours in total of training, we will issue the certificate of 200/300-hour Teacher Training Course.
Karuna Yoga Vidya Peetham is a Registered Yoga teacher training school in Bangalore, India with an affiliation of Yoga Alliance, USA which offers 50 Hour Yoga Teacher Training in Bangalore, India. If you look forward to the course then this is the best choice.
International Certification
Upon successful completion of the course, you will receive a certificate of completion of the 20 hour Hatha Yoga course, that you can count towards your continuing education. Our yoga teacher training courses are accredited by Yoga Alliance USA.
Pre-requisites:
This course is open to all students who wish to deepen their
Online Live Personal Yoga Training at Home
Home Yoga
Change is Possible!
I am ready to help you, to improve your health, reduce stress and moving towards perfect peace, happiness and joy!
Show you the difference between intentional self-care and unintentional numbing out, so that you can be fully awake for all of your life
Restore your natural physical alignment, because it is critical to your health and well-being
Help you develop a practice of intentional surrender because it brings relief from stress and will improve every aspect of your life
Show you how to take care of yourself because that is the first step toward the connection you are craving with others
Restore your mind-body connection, because decision-making is so much easier when you can hear your own intuition
Home yoga course contents
The private yoga lesson consists of Power Yoga, Dynamic Yoga, Yoga Therapy for different ailments, Yoga for stress management, yoga posture (asana), yogic breathing (pranayama), guided meditation and relaxation. Sometimes the cleansing practices like Vamana Dhouti (vomiting), Jala & Sutra Neti (nasal cleaning), Laghu Sankhaprakshalana (intestine cleansing), vyutkarma & sheetkarma kapalabhati (nasal cleansing), Trataka (eye cleansing) and MSRT (immune system enhancement) are also included depending on the requirement of the participant
If you are looking for a secluded, silent, one-on-one yoga practice with personal care and attention and without any outside disturbances, private yoga lessons are perfect for you. In private yoga lessons, you save your time and energy from traveling to a distance yoga studio and practice yoga from the comfort of your home in a personal ambiance. In private yoga lessons, you learn properly with one-on-one attention from the yoga trainer. The yoga trainer also gets enough time to understand your requirements and customizes the yoga practices accordingly for your maximum health benefit.
If you are suffering from any specific health problems, private yoga lessons are ideal for you. Yoga therapy practices cannot be done in a group, it has to be done always one-on-one basis. Because your problem is different from others. In a group yoga class, the yoga practices are not addressed according to your body conditions & requirements, some of the practices in the group might be harmful to you. Moreover, if the group yoga trainer is not a qualified yoga therapist but only a yoga instructor, he may not know the yoga practices that are useful and harmful to you. Therefore, if you are suffering from any specific health conditions, you require private yoga lessons with one-on-one attention from an experienced yoga therapist for your recovery.
How many people can join in private yoga lessons?
We allow one or, maximum of two people at a time in a private yoga lesson.
Private yoga course contents
The private yoga lesson consists of Power Yoga, Dynamic Yoga, Yoga Therapy for different ailments, Yoga for stress management, yoga post
30 – Hours Yogic Sukshma Vyayama Teacher Training Course
What is Sukshma Yoga?
Dhirendra Brahmachari formulated this system and wrote books to clearly formulate the ancient yogic science. This practice simple yet powerful series of specific exercises that improve health and enhance the strength of different organs and systems in the body, from top of head to toes.
Suksma means subtle prana, mind, and intellect: Vyayama means exercise. Suksma Vyayama is meant for the Subtle Body (Suksma Sarira), it is not meant for the Sthula Sarira (Gross Physical Body).
Need of Suksma Vyayama
In yoga, it is said that most pranic blockages start in our joints. Ayurveda says that ‘ama’ or the toxic and undigested waste material tends to settle in the empty spaces of our body, the joints. To remove these impurities we practice Suksma Vyayama, to release any such impurities in our subtle pranic body.
Three dimension of suksma Vyayama:
1.Breathing (slow or fast: Bhastrika/Bellows)
2.Point of concentration (mental concentration on Chakras)
3.Exercise (using Bandhas and Mudras)
Sukshma yoga purifies and recharges the body, mind, energy, and emotion. It prepares the well foundation for further means of Yoga practice. It includes Sukshma Vyayama (Subtle Exercise), and Vishram (Rest & Relaxation). It is itself complete package that fulfills the basic need of human being.
Sukshma Vyayama is one of the major parts for physical activity and the regulation of entire physiologies. Sukshma Vyayama is also known as a kind of warm up exercise or basic exercise or clinically anti-rheumatic group of exercise and also called body scan. The system of the physical and breathing exercise which help to sequentially work out all joints of a body, to warm it up. This system has a strong purifying effect on energy body of a human.
1.1. History of Sukshma Vyayama
We will observe visible Parampara of Sukshma Vyayama. Literal meaning of Parampara is the continuous chain of succession by Master to followers. In Parampara system, the knowledge is passed on without changes from generation to generation). Unfortunately because of the absence of enough information we are not able to find sources of this tradition.
System of Sukshma Vyayama knowledge which was unknown in the west before that was extended by one of outstanding yoga masters, Dhirendra Brahmachari (1925-1994). He received Initiation into Sukshma Vyayama techniques from Maharshi Kartikeya, the prophet and sacred great yogi who was his Master. In the preface to the book “Yogic Sukshma Vyayama” Dhirendra Brahmachari wrote about his precious Guru. Deep knowledge made him the unique expert of human characters, of their abilities and possibilities. From Maharshi Kartikeya, Dhirendra Brahmachari received a precept to spread knowledge about Sukshma Vyayama. The invaluable merit of Dhirendra Brahmachari is that he managed to accumulate knowledge in the convenient form, to make it open and understandable for the audience everywhere. The b
21. Alignment for Advanced Yoga Asana
The advance asanas that are taught during various asana classes throughout the duration of the teacher training are brought up for analytical discussions and practical sessions of methods to adjust advance postures with both verbal cues and hands-on adjustments. Learning revolves around demonstrations, observation and practicums by assisting the lead instructors during some advanced yoga classes. Students will demonstrate observe and assist lead instructors in adjusting in a basic yoga class.
Learning Objective
Be able to identify misalignments of advance postures. Be able to observe student’s capacity during adjustments. Be able to safely and gently adjust advance postures with verbal cues and with hands-on adjustments. To provide adjusting and assisting techniques of yoga asana class.
5 Must-Have’s in ePCR Software for a More PROFITABLE and EFFICIENT EMS, NEM...Traumasoft LLC
The benefits of an ePCR solution should extend to the whole EMS & NEMT organization, not just certain groups of people or certain departments.
It should benefit EMS crews – making it convenient to enter data and have the tools to increase document accuracy.
It should benefit the back-office by streamlining documentation and billing processes internally and with health facilities.
It should benefit the entire organization by improving workflow efficiency, comply with regulations, reduce costs, and contribute to generating data-driven reports.
To achieve those benefits, ePCR software must have these 5 functions.
Holistic nursing Primacy of nature in the healing process.pptxraima10
HOLISTIC NURSING
Holistic nursing is a way of treating and taking care the patient as a whole body which involves physical, social environment, psychological, cultural and religious beliefs.
This presentation tells about health education for hand wash to children. Every child should know that how to keep hand clean. And maintain the good hand washing practices. Nowadays disease are easily spread through uncleaned hands.germs are habitat in their hands and then it causes different types of diseases.so, we must give the health education for hand washing to every children. And make them practice.
Revolutionize Pain Management with Almagia’s PEMF Devices Shop Now.pptxALMAGIA INTERNATIONAL
In this blog, we will dig into some scientific studies that highlight the effectiveness of Almagia’s PEMF devices for sale and how they have transformed the landscape of pain management.
50 Hr – Hatha-Vinyasa Yoga Teacher Training Course
50 hours – Hatha-Vinyasa Yoga Teacher Training Course
Course Fee: INR 32,000 for Indian citizens only, for foreigners USD 350.
Yoga Manual (01)
Certificate
Excluded with accommodation and food
Upcoming Batches 50 Hr Non-Residential (Week-Days/Week-End)
Professional Yoga Teacher Training
Our 50 hours Yoga Teachers Training Course Hatha-Vinyasa Yoga Teacher Training Course is beautifully programmed for those enthusiasts who desire to have a professional certificate in the future but can’t afford the time of two months in one slot.
If you have less time or you want to learn slowly, so 50-hour yoga teacher training course in Bangalore can be the perfect yoga course for you, karuna yoga offers a self-paced yoga teacher training course in Bangalore India, and you can join the other half in 1 year of time to complete 200/300 hours Teacher Training Course.
In order to obtain a professional certificate of 200/300 Hour, Teachers Training Course affiliated with Yoga alliance one has to complete the 200 Hours which is usually completed in one or two months of time, we designed this course in such a way that if any participant wants to first get introduced with the way and process of professional yoga teacher training course and have only short time then students can enroll for this yoga course.
Our 50 hours Yoga Teacher Training Course program runs along with our regular student of 200/300-hour Teacher Training Course students in the first phase, upon completion of the course if a student wants to finish remaining their balance of 150/250 hours of Teacher Training Course in the future, then students can continue the course of the second stage of Teacher Training Course to obtain 200/300-hour Teacher Training Course certificate affiliated with Yoga Alliance in order to have a professional certificate.
Our 50 hours can be accepted as continuing education from Yoga Alliance if in the future you want to continue the training from our center. Please make a note while completing 50 hour TTC you will be only provided with a certificate issued by our organization and the certificate will not be affiliated with Yoga Alliance, and only after completion of the second stage of balance 150/250 hours of TTC, which technically becomes 200/300 hours in total of training, we will issue the certificate of 200/300-hour Teacher Training Course.
Karuna Yoga Vidya Peetham is a Registered Yoga teacher training school in Bangalore, India with an affiliation of Yoga Alliance, USA which offers 50 Hour Yoga Teacher Training in Bangalore, India. If you look forward to the course then this is the best choice.
International Certification
Upon successful completion of the course, you will receive a certificate of completion of the 20 hour Hatha Yoga course, that you can count towards your continuing education. Our yoga teacher training courses are accredited by Yoga Alliance USA.
Pre-requisites:
This course is open to all student
Etiologies of Bipolar disorders. Power Point Presentation ptxseri bangash
www.seribangash.com
Bipolar disorder, formerly known as manic-depressive illness, is a complex psychiatric condition characterized by extreme mood swings that include emotional highs (mania or hypomania) and lows (depression). The etiology of bipolar disorder involves a combination of genetic, biological, and environmental factors. Here's a breakdown of these etiologies:
Genetic Factors:
Family History: Bipolar disorder tends to run in families, suggesting a genetic component. Studies indicate that having a close relative with bipolar disorder increases the risk.
Genetic Studies: Research has identified specific genetic variations associated with bipolar disorder. These include genes involved in neurotransmitter signaling, ion channel function, and circadian rhythms.
Neurobiological Factors:
Neurotransmitter Imbalance: Imbalances in neurotransmitters such as dopamine, serotonin, and norepinephrine are implicated in bipolar disorder. For example, elevated dopamine levels during manic episodes and decreased levels during depressive episodes.
Neuroendocrine Factors: Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis and abnormal cortisol levels have been observed in individuals with bipolar disorder.
Neuroanatomical Factors:
Brain Structure and Function: Structural and functional abnormalities in certain brain regions are linked to bipolar disorder. These include the prefrontal cortex, amygdala, and hippocampus, which are involved in emotional regulation and cognition.
Environmental Factors:
Stress: Stressful life events, such as trauma, loss, or significant life changes, can trigger or exacerbate episodes of bipolar disorder.
Substance Abuse: Substance use, particularly stimulants or drugs that affect neurotransmitter systems, can precipitate manic episodes or worsen the course of the disorder.
Developmental Factors:
Early Life Experiences: Adverse childhood experiences, including abuse, neglect, or chronic stress, may increase susceptibility to developing bipolar disorder later in life.
Trajectories: Some individuals may have a prodromal phase marked by subthreshold symptoms or other behavioral indicators before full-blown episodes manifest.
D1 Business Opportunity Sharing Slide ( USA ) Short Version
IMS Health Real-World Evidence Solutions at ISPOR November 2015
1. ISPOR 18th Annual European Congress
7-11 November 2015, Milan, Italy
Join the IMS Health Symposium
“Enriched real-world data (RWD) studies:
Tapping into the growing use of patient-level
data to optimize observational study design
and execution”
Meet the largest expert community in RWE
– now including our new colleagues from
Cegedim Strategic Data
Discover the findings from our latest research
IMS Health Real-World Evidence Solutions
at ISPOR, November 2015
2. 2
IMS Health Our Distinctive Approach
IMS Health has taken a holistic approach to real-world evidence (RWE) in pursuit of
the most robust and insightful views of patient outcomes. With the breadth and depth
of our capabilities, we are uniquely positioned to generate and use RWE globally.
Applying the appropriate scientific and commercial lens and latest techniques to anonymous real-world
data (RWD) is critical to realizing the value of RWE in healthcare decisions.
IMS Health Real-World Evidence Solutions
IMS Health can uniquely support all elements of the
RWE ecosystem – an environment where all the components
of RWE come together for a consistent, insightful view of what
really happens in healthcare. An environment which, for the
first time, helps all functions realize its potential.
Technology-
Enabled
Analytics
Real-World
Data
Services
and
Engagement
IMS HEALTH
REAL-WORLD
EVIDENCE
SOLUTIONS
Accesstherightreal-world
da
ta
Analyzethedata
Create datasets
Apply the insights
Introducing the RWE ecosystem
Real-World Data
Identify and access the most appropriate data sources while ensuring patient privacy
•The broadest and deepest collection of scientifically-validated, anonymous patient-level data assets
•Complement fit-for-purpose data by custom data sourcing to close data gaps
Technology-Enabled Analytics
Create consistent data models empowering analyses and leveraging innovative technologies
•Extraction, analysis and visualization of RWD with IMS Health’s E360TM
technology suite
•Sophisticated data linkage and interpretation
Services and Engagement
Analyze RWD using scientific rigor, clear governance and advanced analytic and processing capabilities
•Market Access & HTA
•Health Economics
•Outcomes Research
•Pharmacoepidemiology & Drug Safety
•Commercial Analytics
3. ISPOR 18th Annual European Congress, November 2015, Milan, Italy 3
Welcome to IMS Health at ISPOR Milan, 2015
Increased emphasis on RWE and a concentrated focus on patient benefits have
placed outcomes research (OR) at the heart of healthcare decision making.
Reflecting its growing importance and potential is the need for more compelling, impactful OR across
the spectrum of evidence evaluation. Approaches that can extend existing RWD and accelerate its
power to answer critical questions are key to achieving this goal.
IMS Health is committed to innovation in data collection to overcome the limitations of traditional
methods and drive richer insights and faster results. We look forward to sharing the research this has
enabled during the ISPOR 18th Annual European Congress as progress towards “closing the gap” in
OR continues.
Please join us during the event. An overview of our activities can be found in this brochure.
We hope to see you in Milan!
#1 Partner of Choice for RWE
•Largest, international fit-for-purpose RWD
portfolio available with 500+ million anonymous
longitudinal patient data records in 25+ markets
•Partnerships and data sourcing capabilities to
bring clients data that is right for their needs
•3,500+ publications building healthcare knowledge
•Leading edge technology and analytics to
enhance understanding of patient outcomes,
healthcare costs, pharmacoepidemiology, drug
safety and product value
•Experts in 20+ markets with deep specialism in
RWE, HTA and payer requirements to translate
insights into actions
IMS Health is excited to announce that Cegedim Strategic Data has joined our Real-World
Evidence Solutions team, boosting our RWD assets and analytical expertise and confirming our
role as the partner of choice for RWE.
4. IMS Health Symposium Wednesday, 11 November
4IMS Health Real-World Evidence Solutions
“Enriched real-world data (RWD) studies: Tapping into the growing use of
patient-level data to optimize observational study design and execution”
Pharmaceutical manufacturers face a challenge in meeting increased demand for RWE through
prospective observational studies in a cost-effective and timely way. Although many are comfortable
looking purely to electronic patient data (eg, EMRs) for retrospective database analysis, they are not
always aware of how these sources can support primary data collection to generate the rich clinical
data needed.
Enriched RWD studies – observational studies supplemented by de novo data collection – are one
such alternative. These may include the use of technology embedded into an EMR system to prompt
for additional variables to be collected during patient visits and/or site or patient randomization.
Pragmatic trials with EMR follow-up can also be used to evaluate the impact of approaches to
enhancing adherence, with modest expenditures compared to RCTs. In addition, data can be collected
directly from the patient, providing missing insights about their experience when relying on
physician-reported data alone.
This symposium will discuss these processes as well as applications for enriched RWD studies,
including both for targeted use and for the creation of more enduring evidence platforms. We will
show how they can lead to more robust and efficient research, leveraging case studies to demonstrate
the benefit for stakeholders.
Members of our global Real-World Evidence Solutions team will be on hand during ISPOR to
discuss your needs in RWE and explain how we can help you address them.
Come and see us at the IMS Health stand in the exhibition area (Nos 616, 617, 700, 701) to
discover more about our expertise and capabilities, which have recently expanded with the
exciting addition of Cegedim Strategic Data.
Visit us at the IMS Health stand
5. IMS Health Symposium Agenda
IMS Health Symposium Chair
5ISPOR 18th Annual European Congress, November 2015, Milan, Italy
07:30–07:40
Introduction: RWE creating new approaches for observational research
Alison Bourke, MSc, MRPharm.S, FISPE, (Chair) Scientific Director, Real-World Evidence Solutions, IMS Health, UK
07:40–08:00
Next generation observational research: Enriched RWD studies
Joshua Hiller, MBA, Senior Principal, Real-World Evidence Solutions, IMS Health, UK
Pierre Engel, Pharm.D, MPH, PhD, Associate Director Epidemiology, Real-World & Late Phase Research, Quintiles, France
08:00–08:20
How to benefit from enriched RWD studies: Reflections from a study sponsor
Andrew Shaw, BSc, PhD, RWE Alliance Director, AstraZeneca, UK
Lance Brannman, PhD, Group Director, Health Economics & Payer Analytics, AstraZeneca, USA; Member of the
Board, Centre for Health Economics, Gothenburg University, Sweden
08:20–08:30
Moderated Q&A
Alison Bourke (Chair)
Proceedings from the symposium can be obtained from IMS Health. To receive a copy, please email Angelika Boucsein at Aboucsein@de.imshealth.com
Continental breakfast will be available for all symposium attendees
Alison Bourke, MSc, MRPharm.S, FISPE
Alison Bourke is a Scientific Director, RWE Solutions at IMS Health. She has over 25 years of experience working
with primary care patient data resources in the UK and a particular interest in their use to explore innovative
scientific methodologies. Previously, Alison headed the research team at CSD Medical Research UK, providing
primary care data and support for a range of studies, including pharmacoepidemiology and health outcomes
research. She pioneered innovative linking ‘pseudonymization at source’ technology and was instrumental in
setting up the Health Improvement Network (THIN), bringing access to 12 million pseudonymized patient
records. A trained pharmacist, Alison has also held roles at BMS where she analyzed one of the first computer-
collected safety studies, and Cegedim INPS where she supported the successful launch of GPRD.
Continued overleaf...
6. IMS Health Real-World Evidence Solutions 6
IMS Health Symposium Speakers
Joshua Hiller, MBA
Joshua Hiller is a Senior Principal, RWE Solutions at IMS Health, supporting the strategic planning and
development of the company’s capabilities for data sourcing, integration, analytics and studies. He is also
currently serving as Alliance Director in IMS Health’s collaboration with AstraZeneca for the advancement of
RWE. During a career that includes roles in market analytics, government and healthcare consulting in both the
USA and UK, Joshua has led a wide range of projects for clients in the pharmaceutical and biotech sector as well
as industry associations. He has extensive experience in pharmaceutical pricing, contracting, market landscape
development, supply management, cross border trade, lifecycle management, competitive defense, generics
market drivers and account management, with expertise across US and European markets.
Pierre Engel, Pharm.D, MPH, PhD
Dr. Pierre Engel is Associate Director Epidemiology, Real-World & Late Phase Research at Quintiles, France,
managing a team of epidemiologists involved mainly in Post Authorisation Safety Studies (PASS). He has eight
years of experience in international observational research including roles as Epidemiologist at a medium-size
CRO and at INSERM where he was in charge of developing epidemiological studies on existing data in women’s
health. Pierre has strong expertise in the design, scientific oversight, analysis and reporting of observational
studies as well as epidemiology methods, CER, pharmacoepidemiology, and database research. He is a member
of both the Steering Group and HTA Working Group at ENCePP, is actively involved as an epidemiologist on
many large international programs, and has designed numerous PASS endorsed by the EMA’s
Pharmacovigilance Risk Assessment Committee.
Andrew Shaw, BSc, PhD
Dr. Andy Shaw is RWE Alliance Director at AstraZeneca, UK, where he focuses on continuing to develop the
company’s RWE capabilities globally, particularly in the respiratory and oncology therapeutic areas. He has
established and maintained strong partnerships with many external stakeholders, including IMS Health and
Quintiles. Andy began his career as a lecturer at the University of London before moving into the pharmaceutical
industry. He has more than 18 years of experience at AstraZeneca, both in the UK and for a time in Japan, in
positions that have primarily focused on generating clinical data for regulatory submissions. More recently,
during the last 4-5 years, Andy’s focus has shifted to generating evidence outside of clinical trial settings for a
multitude of purposes.
Lance Brannman, PhD
Dr. Lance Brannman is Group Director, Health Economics & Payer Analytics for respiratory, inflammation and
autoimmune diseases at AstraZeneca, USA. He was previously responsible for cardiovascular & metabolic
diseases, CNS diseases and infection, with accountability in both roles for delivering global health economics
projects. He is also a Member of the Board at the Centre for Health Economics, Gothenburg University, Sweden.
Lance spent several years as an academic before joining the pharmaceutical industry where he has held various
senior-level positions in health economics and outcomes research at AstraZeneca and Novo Nordisk A/S. He has
extensive experience in pharmacoeconomics spanning modeling, technical writing, RWE, clinical trial design and
PRO administration, as well as expertise in microeconomic analysis, statistics & econometrics, and programming.
7. ISPOR 18th Annual European Congress, November 2015, Milan, Italy 7
Live Sessions with IMS Health
Book a demonstration of IMS Health’s E360™ technology suite
IMS Health RWE experts will be running demonstrations of our powerful
E360™ data platform technology and applications suite which allows
researchers to answer all questions – from the routine to the most challenging –
in a standardized, intuitive way.
Schedule your individual presentation at the IMS Health stand or by
emailing Peter Riebel at Priebel@de.imshealth.com
Issue Panel
• The cost of no Europe - Localized or centralized assessment of relative efficacy
– 10 November, 13:45–14:45
Workshops
• Evidence synthesis in HTA decision making – 10 November, 08:45–09:45
• Network meta analysis modeling for dose response and class effects
– 11 November, 15:00–16:00
Research Podiums
• Hospital cost and length of stay in chronic heart failure
– 9 November, 16:15–16:30
• Cost-effectiveness in COPD – 9 November, 16:30–16:45
See pages 8–11 for further details.
8. 9NOV
CV3
THE COST AND LENGTH OF STAY OF HOSPITAL EMERGENCY DEPARTMENT
VISITS FOR CHRONIC HEART FAILURE PATIENTS IN CANADA
Fischer AA, Liu N, Borelli R, Zaour N,
Barbeau M
Research
Podium
CE4
ASSESSING THE COST-EFFECTIVENESS OF USING ACLIDINIUM BROMIDE
400 µG /FORMOTEROL FUMARATE DIHYDRATE 12 µG COMPARED TO ACLIDINIUM
BROMIDE 400 µG IN THE MANAGEMENT OF MODERATE TO SEVERE CHRONIC
OBSTRUCTIVE PULMONARY DISEASE
Ramos M, Haughney J, Henry N,
Lindner L, Lamotte M
Research
Podium
PCV53
CARDIOVASCULAR EVENT RATES IN A HIGH-RISK GENERAL POPULATION
COHORT OF 340,000 INDIVIDUALS IN THE UNITED KINGDOM
Ansell D, Khan I, Proudfoot C,
Gbenedio T, Joulain F, Pockett RD,
Catterick D, Gooch K
Research
Poster
PCV63 AN ASSESMENT OF ENOXAPARINE BENEFIT ON HEALTHCARE BUDGET IN SPAIN
Delgado M, Restovic G, Planellas L,
Rubio M, Miñarro C
Research
Poster
PCV67
MEDICAL COST OF PATIENTS WITH NON-VALVULAR ATRIAL FIBRILLATION (NVAF)
AND TREATED WITH VITAMIN K ANTAGONISTS (VKAS) ACCORDING TO INR
CONTROL STATUS IN SPAIN
Postema R, Bardoulat I, Roset M,
Maurel F, Lefevre C, Evans D
Research
Poster
PCV85
AN EPIDEMIOLOGICAL EVALUATION OF THE INCIDENCE OF DEEP VENOUS
THROMBOSIS AND PULMONARY EMBOLISM IN PATIENTS WITH HIP OR KNEE
REPLACEMENT SURGERY AND OF ITS IMPACT ON THE AVERAGE LENGTH OF
STAY AND HOSPITALIZATION COST
Chevalier P, Lamotte M
Research
Poster
PCV89
A COMPARISON OF TWO LOW-MOLECULAR-WEIGHT HEPARINS (LMWHS) IN
TERMS OF COST PER PATIENT
Planellas L, Miñarro C, Restovic G,
Delgado M, Rubio M
Research
Poster
PCV90
THE COST OF ACUTE CARE HOSPITALIZATIONS ASSOCIATED WITH CHRONIC
HEART FAILURE IN CANADA
Fischer AA, Liu N, Borelli R,
Barbeau M, Zaour N
Research
Poster
PCV91
AN EPIDEMIOLOGICAL EVALUATION OF THE IMPACT OF PERCUTANEOUS
CORONARY INTERVENTIONS ON THE HOSPITALIZATION COST, LENGTH OF STAY
AND MORTALITY OF PATIENTS HOSPITALIZED WITH ACUTE CORONARY SYNDROMES
Chevalier P, Lamotte M
Research
Poster
PCV169 THE ECONOMIC BURDEN OF POOR ADHERENCE TO STATINS IN BELGIUM Ramos M, Caekelbergh K, Lamotte M
Research
Poster
PMH2
RISK FACTORS FOR DEMENTIA DIAGNOSIS IN GERMAN PRIMARY CARE
PRACTICES
Wendschlag A, Jacob L, Kostev K,
Bohlken J, Rapp MA
Research
Poster
PMH3
COGNITIVE SYMPTOMS IN MAJOR DEPRESSIVE DISORDER AND THEIR ITALIAN
PSYCHIATRISTS' PERCEPTION
Pegoraro V, Cataldo N, Albert U,
Brugnoli R, Caraci F, Dell'Osso BM,
Di Sciascio G, Tortorella A, Vampini C
Research
Poster
PMH7
TREATMENT CONTINUATION AND TREATMENT CHARACTERISTICS OF FOUR
LONG ACTING ANTIPSYCHOTIC MEDICATIONS (PALIPERIDONE PALMITATE,
RISPERIDONE MICROSPHERES, OLANZAPINE PAMOATE AND HALOPERIDOL
DECANOATE) IN THE NETHERLANDS
Denee TR, Geerts P, Sermon J,
Decuypere F, Widrich C, Rijntjes R,
Mulder CL
Research
Poster
PMH45 DRUG UTILIZATION PATTERN OF LISDEXAMFETAMINE DIMESYLATE IN EUROPE
Cook MN, Varughese S, Maxwell T,
Thun B, Ehlken B, von Bredow D, Keja J
Research
Poster
PMH48
THE ECONOMIC CONSEQUENCES OF THE USE OF ANTIDEPRESSANTS IN
BELGIUM: PRESCRIBING BEHAVIOR AND MISUSE OF ANTIDEPRESSANTS
Ramos M, Brouyère S,
Caekelbergh K, Lamotte M
Research
Poster
PMH49
THE ECONOMIC CONSEQUENCES OF THE USE OF ANTIDEPRESSANTS IN
BELGIUM
Caekelbergh K, Ramos M, Lamotte M
Research
Poster
PSS26
INTRAVITRAEL AFLIBERCEPT INJECTION FOR THE TREATMENT OF VISUAL
IMPAIRMENT DUE TO MACULAR OEDEMA SECONDARY TO BRANCH RETINAL
VEIN OCCLUSION: COST-EFFECTIVENESS VERSUS RANIBIZUMAB
Lovato E, Lloyd A, Wilson B,
Wittrup-Jensen KU
Research
Poster
8
IMS Health Activities 9 November
CODE TOPIC PRESENTERS TYPE
IMS Health Real-World Evidence Solutions
9. 9
IMS Health Activities 9 & 10 November
ISPOR 18th Annual European Congress, November 2015, Milan, Italy
CODE TOPIC PRESENTERS TYPE
9NOV10NOV
PCN10
PREVALENCE OF DEPRESSION AND ANXIETY AND THEIR RISK FACTORS IN
WOMEN WITH BREAST CANCER IN GERMAN PRIMARY CARE
Engelhard J, Bleicher L, Kostev K
Research
Poster
PCN13
THERAPY OF DEPRESSION IN CANCER AND NON-CANCER PATIENTS IN GERMAN
NEUROPSYCHIATRIC PRACTICES
Ziegelbauer K, Engelhard J, Kostev K
Research
Poster
PCN34
A DESCRIPTION OF REAL-WORLD TREATMENT WITH ABIRATERONE ACETATE IN
METASTATIC CASTRATION-RESISTANT PROSTATE CANCER PATIENTS IN THE
POST-CHEMOTHERAPY SETTING IN FRANCE AND THE NETHERLANDS
Dearden L, Musingarimi P, Shalet N,
Demuth D, Garcia Alvarez L,
Muthutantri A, Venerus A, Lasry R,
Hankins M, Maher T
Research
Poster
PCN115 THE ANALYSIS OF INPATIENTS COST OF BREAST CANCER IN CHINA, 2011 Song S, Wang Z, Zhang M
Research
Poster
PCN123
ESTIMATION OF DIRECT MEDICAL COSTS ASSOCIATED WITH TREATMENT OF
METASTATIC MELANOMA IN SWITZERLAND
Christoffersen P, Khan N, Lucas J,
Christodoulopoulou A, Del Ponte A,
Gutzwiller F
Research
Poster
PCN233
CANCER IS ASSOCIATED WITH INTRAOPERATIVE AND POSTPROCEDURAL
COMPLICATIONS AND DISORDERS
Engelhard J, Jockwig A, Kostev K
Research
Poster
PCN277
THE ITALIAN REGIONAL ACCESS OF NEW CANCER DRUGS: AN EXAMPLE IN
FOUR REGIONS
Visentin E, Heiman F, Ripellino C
Research
Poster
PCN319
4+ YEARS OF AMNOG – CLINICAL DRIVERS FOR SUCCESSFUL DOSSIER
SUBMISSIONS IN ONCOLOGY
Dehnen J, Goldhagen K, Petry D
Research
Poster
PCN353
CURRENT TREATMENT PATTERNS IN PATIENTS WITH METASTATIC MELANOMA: A
RETROSPECTIVE CLAIMS DATABASE ANALYSIS IN THE UNITED STATES (US)
Chen Y, Ma Q, Hines DM, Zhao Z,
Munakata J, Barber BL
Research
Poster
PHP47
A COMPARISON OF TIME TO LAUNCH AND REIMBURSEMENT FOR NEW
MEDICINES ACROSS DEVELOPED COUNTRIES
Hickson SS, Skinner B, Bosnic N,
Smith A, Zhang Y, Millson B
Research
Poster
PHP100
APPRAISING THE COST OF PHYSICIAN VISITS AND TECHNICAL PROCEDURES IN
FRANCE IN THE AGE OF OPEN DATA
Sherwood A, Maurel F, Colin X
Research
Poster
PHP132 THE ECONOMIC CONSEQUENCES OF THE USE OF ANTIBIOTICS IN BELGIUM Caekelbergh K, Ramos M, Lamotte M
Research
Poster
PHP136 AVOIDABLE HOSPITALIZATIONS DUE TO MEDICATION ERRORS IN BELGIUM Ramos M, Caekelbergh K, Lamotte M
Research
Poster
PHP139 LISTE-EN-SUS REFORM IN FRANCE - WHAT ARE THE CONSEQUENCES? Mitrano M, Flostrand S
Research
Poster
PHP176
ITALIAN LAW 326/2003 FOR THE REIMBURSEMENT OF ORPHAN AND LIFE SAVING
DRUGS AWAITING MARKET ENTRY: APPROVALS, REJECTIONS AND METHODS IN
AIFA'S EVALUATION PROCESS BETWEEN JANUARY 2013 AND MAY 2015
Prada M, Bertozzi C, Proietti B,
Urbinati D
Research
Poster
PHP215
FROM CENTRALIZED MARKETING AUTHORIZATION TO NATIONAL
REIMBURSEMENT – A CHALLENGING JOURNEY FOR NEW MEDICAL PRODUCTS
WITH PLACEBO CONTROLLED TRIALS
Eheberg D, Paulus G, Dannemann S,
Batscheider A
Research
Poster
PHP220
MANAGED ENTRY AGREEMENTS IN THE ITALIAN MARKET BETWEEN JUNE 2005
AND JUNE 2015
Tettamanti A, Urbinati D, Noble M
Research
Poster
PHP260
DOES CONDITIONAL MARKETING AUTHORISATION INFLUENCE MARKET ACCESS
IN FRANCE, ENGLAND, AND GERMANY?
Kaaniche A, Troubat A, Sherwood A
Research
Poster
PHP324
REFORMING DRUG PRICING AND PATIENT ACCESS SYSTEMS TO SUPPORT
UNIVERSAL COVERAGE IN DEVELOPING COUNTRIES
Shankar R, Hickson SS
Research
Poster
10. IMS Health Real-World Evidence Solutions 10
IMS Health Activities 10 & 11 November
CODE TOPIC PRESENTERS TYPE
10NOV11NOV
PIN9
PUBLIC HEALTH OUTCOMES OF PAEDIATRIC INFLUENZA VACCINATION WITH AN
INTRANASAL TETRAVALENT LIVE ATTENUATED VACCINE IN BELGIUM USING A
DYNAMIC TRANSMISSION MODEL
Gerlier L, Lamotte M, Dos Santos
Mendes S, Schwehm M, Eichner M
Research
Poster
PDB13
A CROSS-SECTIONAL STUDY ON INSULIN TREATMENTS AND GLYCEMIC
CONTROL IN TYPE 2 DIABETES IN FRANCE, ITALY, GERMANY, UK AND SPAIN
Phan T, Boutmy E, Coulombel N
Research
Poster
PDB16
CARDIOVASCULAR OUTCOMES OF ANTIDIABETIC THERAPY - RESULTS OF A
LITERATURE SEARCH
Greiner R, Eheberg D, Paulus G,
Batscheider A
Research
Poster
PDB40
HOSPITALIZATION COST AND LENGTH OF STAY ASSOCIATED WITH
OPHTHALMOLOGICAL SURGERY DEPENDING ON THE DIABETIC STATUS
Chevalier P, Lamotte M
Research
Poster
PDB56
COST-EFFECTIVENESS OF DULAGLUTIDE 1.5MG ONCE WEEKLY FOR THE
TREATMENT OF PATIENTS WITH TYPE TWO DIABETES MELLITUS IN SWEDEN
Raibouaa A, Borgeke H, Alexiou D,
Lowin J, Norrbacka K
Research
Poster
PMS3
INCREASED RISK OF OSTEOPOROSIS IN DEPRESSED PATIENTS: A REAL-WORLD
DATA STUDY CONDUCTED IN ITALY
Heiman F, Moretti R, Pegoraro V,
Cataldo N
Research
Poster
PMS7
REDUCTION IN C-REACTIVE PROTEIN WITH BIOLOGIC DRUGS IN RHEUMATOID
ARTHRITIS AND SPONDYLITIS PATIENTS IN GERMAN RHEUMATOLOGIST PRACTICES
Gossen N, Kostev K
Research
Poster
PMS68
BIOLOGICAL AGENTS FOR PATIENTS WITH RHEUMATOID ARTHRITIS WHO HAD
FAILED TREATMENT WITH METHOTREXATE IN THE SPANISH CLINICAL SETTING:
A COST-EFFECTIVENESS ANALYSIS
Sánchez R, Restovic G, Planellas L
Research
Poster
PMS90
DISPENSING FREQUENCY AMONG PATIENTS WITH RHEUMATOID ARTHRITIS
TREATED WITH RITUXIMAB IN ENGLAND
Tsoumani E, McCann E, Tham R, Yu E
Research
Poster
PSY5
HOW ARE PAIN TREATMENT RESPONSE RATES IN PRIMARY CARE INFLUENCED
BY CO-PRESCRIPTION OF CYP2D6 INHIBITORS?
Pockett RD, O'Leary CJ, Anderson P,
Nasser A, Winfield TG, Ansell D
Research
Poster
PSY45
THE BUDGET IMPACT OF ORPHAN DRUGS IN THE US AND CANADA: A 2007-2013
MIDAS SALES DATA ANALYSIS
Divino V, DeKoven M, Kim T,
Kleinrock M, Wade RL, Kaura S
Research
Poster
PSY51
ASSESSING THE BURDEN OF SYSTEMIC LUPUS ERYTHEMATOSUS IN BELGIUM
USING A LONGITUDINAL HOSPITAL DATABASE
Gerlier L, Lamotte M, Chevalier P
Research
Poster
PSY98
HEALTH-RELATED QUALITY OF LIFE (HRQOL) IN SPLENECTOMIZED IMMUNE
THROMBOCYTOPENIA (ITP) PATIENTS – A TARGETED LITERATURE REVIEW
Lebioda A, Batscheider A
Research
Poster
PSY124
THE ITALIAN 648/96 LIST: APPROVALS, REJECTIONS AND METHODS IN AIFA'S
EVALUATION PROCESS BETWEEN JANUARY 2013 AND MAY 2015
Prada M, Bertozzi C, Proietti B,
Urbinati D
Research
Poster
IP8
THE COST OF NO EUROPE: ARE THERE COSTS AND CONSEQUENCES OF
LOCALIZED OR CENTRALIZED ASSESSMENT OF RELATIVE EFFICACY?
Kent A, Rappagliosi A, Longson C,
Keja J
Issue Panel
W8
EVIDENCE SYNTHESIS BASED ON AGGREGATE AND INDIVIDUAL-LEVEL DATA:
CONSIDERATIONS FOR USE IN HTA DECISION MAKING
Reason T, Saramago Goncalves P,
Asukai Y, Abrams KR
Workshop
ENRICHED REAL-WORLD DATA (RWD) STUDIES: TAPPING INTO THE GROWING
USE OF PATIENT-LEVEL DATA TO OPTIMIZE OBSERVATIONAL STUDY DESIGN
AND EXECUTION
Bourke A, Hiller J, Engel P, Shaw A,
Brannman L
Educational
Symposium
W31
NETWORK META ANALYSIS MODELS FOR DOSE-RESPONSE AND CLASS EFFECTS
IN DECISION MAKING
Owen RK, Thorlund K, Mawdsley D,
Reason T
Workshop
PRM69
PATIENT HETEROGENEITY IN COST-EFFECTIVENESS MODELS FOR CHRONIC
OBSTRUCTIVE PULMONARY DISEASE (COPD): ARE CURRENT MODELS SUITABLE
TO EVALUATE PERSONALIZED MEDICINE
HoogendoornM,FeenstraT,AsukaiY,
BriggsA,BorgS,dalNegroR,HansenRN,
JanssonS,WackerM,RisebroughN,
SamyshkinY,LeidlR,Ruttenvan-MölkenM
Research
Poster
PRM72
CONTRASTING PREDICTIONS OF CARDIOVASCULAR INCIDENCE DERIVED FROM
ALTERNATIVE RISK PREDICTION MODELS IN TYPE 1 DIABETES
McEwan P, Foos V, Lamotte M
Research
Poster
11. ISPOR 18th Annual European Congress, November 2015, Milan, Italy 1111
IMS Health Activities 11 November
CODE TOPIC PRESENTERS TYPE
11NOV
PRM74
CONTRASTING MODEL PREDICTED LIFE EXPECTANCY IN PATIENTS WITH TYPE 2
DIABETES ACROSS DIFFERENT MORTALITY RISK PREDICTION MODELS VERSUS
DATA FROM THE CANADIAN CHRONIC DISEASE SURVEILLANCE SYSTEM
McEwan P, Foos V, Lamotte M
Research
Poster
PRM84
THE IMPORTANCE OF ACCOUNTING FOR BASELINE HYPOGLYCAEMIA
FREQUENCY WHEN MODELLING HYPOGLYCAEMIA DISUTILITY IN TYPE 1
DIABETES MELLITUS
McEwan P, Lamotte M, Foos V
Research
Poster
PRM85
VALIDATING APPROACHES TO MODELLING END-STAGE RENAL DISEASE USING
THE IMS CORE DIABETES MODEL
McEwan P, Foos V, Lamotte M
Research
Poster
PRM88
THE IMPACT OF BASELINE HBA1C AND HBA1C TRAJECTORIES ON TIME TO
THERAPY ESCALATION IN TYPE 2 DIABETES MELLITUS
McEwan P, Foos V, Lamotte M
Research
Poster
PRM98
INVESTIGATING THE IMPACT OF CONTEMPORARY RISK FACTORS FOR DIABETES
COMPLICATIONS AND THEIR EVOLUTION ON RISK PREDICTION USING THE
UKPDS 82 EQUATIONS
McEwan P, Foos V, Lamotte M
Research
Poster
PRM111
THE ROLE OF PATIENT-LEVEL DATA IN ASSESSING HEALTH ECONOMIC VALUE: A
CASE STUDY USING EDGE AND THE CORE DIABETES MODEL
Foos V, McEwan P, Evans M,
Paldanius P
Research
Poster
PRM130
USING MACHINE LEARNING TO DETECT PATIENTS WITH UNDIAGNOSED RARE
DISEASES: AN APPLICATION OF SUPPORT VECTOR MACHINES TO A RARE
ONCOLOGY DISEASE
Rigg J, Lodhi H, Nasuti P
Research
Poster
PRM228
SYSTEMATIC LITERATURE REVIEW OF ADJUNCTIVE ANTI-EPILEPTIC DRUG
TRIALS IN PATIENTS WITH PRIMARY GENERALIZED TONIC-CLONIC SEIZURES
ILLUSTRATES CHANGES IN STANDARD OF CARE OVER 12-20 YEARS
Tsong WH, Gomez-Ulloa D, Li H,
Forsythe A, Kramer L
Research
Poster
PRM246
NORDIC LONGITUDINAL DATA FROM ELECTRONIC MEDICAL RECORDS AND
FULL POPULATION NATIONAL REGISTERS: UNIQUE OPPORTUNITIES FOR NEW
INSIGHTS IN BENEFIT OF DIABETES PATIENTS
Lindh A, Persson F, Sobocki P,
Bodegard J, Lindarck N
Research
Poster
PRM250
FILLING THE GAP BETWEEN RISK/BENEFIT ASSESSMENT FOR DRUGS AND RISK
ASSESSMENT FOR CONSUMER GOODS
Hofmann-Xu L, Bonduelle D, Plantör S
Research
Poster
PRM264
VALIDATION OF SOCIAL MEDIA ANALYSIS FOR OUTCOMES RESEARCH:
IDENTIFICATION OF DRIVERS OF SWITCHES BETWEEN ORAL AND INJECTABLE
THERAPIES FOR MULTIPLE SCLEROSIS
Risson V, Saini D, Bonzani I,
Huisman A, Olson M
Research
Poster
PIH18
A COST-EFFECTIVENESS EVALUATION COMPARING BIOSIMILAR BEMFOLA TO
GONAL-F FOR THE TREATMENT OF INFERTILITY IN AN ITALIAN CONTEXT
Ripellino C, Visentin E, Gizzo S,
Bühler K
Research
Poster
PND41
COST-EFFECTIVENESS ANALYSIS OF DELAYED-RELEASE DIMETHYL FUMARATE
FOR THE TREATMENT OF RELAPSING REMITTING MULTIPLE SCLEROSIS IN SPAIN
Gasche D, Restovic G, Casado V,
Ramírez-Boix P, Martínez Lopez J
Research
Poster
PND66
COMPARISON OF COMPLIANCE AND DISCONTINUATION RATES AMONG MS
PATIENTS TREATED WITH FINGOLIMOD AND OTHER DISEASE-MODIFYING
THERAPIES: A CANADIAN RETROSPECTIVE CLAIMS ANALYSIS
Haddad P, Duquette P, Yeung M,
Lamarche A, Fraelic A, Chan S
Research
Poster
Seeking a new challenge?
We are currently looking for exceptional, talented individuals at all levels globally to join our
international Real-World Evidence Solutions team. Please ask at the IMS Health stand during ISPOR or
email our global talent acquisition manager at RWESrecruiting@imshealth.com for further information.