Showing posts with label IIR. Show all posts
Showing posts with label IIR. Show all posts

Tuesday, June 2, 2015

MDRP 2015 Brochure is Now Available for Download


Don't miss out on the largest MDRP event in the space, with the most speakers, government representations and MDRP executives all under one roof!

Ensure you have the most comprehensive educational experience over three days with unparalleled access to government officials creating regulatory rules, the industry leaders interpreting them, and the pharmaceutical executives implementing them.

Join us and celebrate 20 years of MDRP this September 30-October 2, at the Chicago Marriott Downtown Magnificent Mile in Chicago, IL. See What's New for 2015!

Deep Dive Pre-Conference Summits: 
• Fundamentals of Government Pricing Programs + MDRP 101
• Pharmaceutical VA Contracting and Compliance Summit
• Town Hall between Manufacturers and States

Tailor-Made Content: 
• State Policy Changes and Updates
• Executive Leadership Boardroom
• Business Leadership Workshop on "Embracing Generational Diversity"

Interactive Session Formats: 
• Think Tanks/Innovator Showcase
• Fireside Chats
• Roundtable Discussions
• Rapid-Fire Sessions
• Benchmark Best Practices

AND MORE! Download the Full Brochure For More Information.

Register now with the code XP2058BLOG and save $100 off the current rate | Register today and lock in a $500 savings, click here to register.

This is your opportunity to benchmark best practices and gain solutions to overcome new operational challenges brought on by AMP Final Rule, 340B, Medicaid Expansion, Class of Trade, Fair Market Value, FSS, VA, OIG, and other critical government programs. Reserve your seat today at the most comprehensive MDRP event to date!
 




Monday, March 16, 2015

Look Who's Attending IIR's 7th Annual Government Programs Summit

Sneak-Peek List of the 2015 Attendees Below
 
IIR's 7th Annual Government Programs Summit is just 2 weeks away! Get the most comprehensive, up-to-date information on the key government programs affecting your operations including an update from CMS on operational issues affecting the Medicaid Pharmacy Program and HRSA on key 340B updates.

In addition, you will gain critical insights on Medicare Part D & Coverage Gap, Part B, MDRP, TRICARE, VA, OIG and more. Register now to reserve your seat at this leading industry event.

Everyone who's anyone is here! Here's just a snapshot of companies already confirmed to be in Arlington,with many more slated to join us: (as of 3/11/15)

• Actavis
• Actelion Pharmaceuticals
• Afaxys Inc
• Amneal Pharmaceuticals
• Ariad Pharmaceuticals
• Baxter International Inc
• Bayer HealthCare Pharmaceuticals
• Bristol Myers Squibb
• Celgene Corporation
• Chiesi USA
• Daiichi Sankyo Inc
• Eli Lilly & Co
• Ferring Pharmaceuticals Inc
• Fresenius Kabi
• Genentech
• GlaxoSmithKline
• Glenmark Generics Inc USA
• Health Resources & Services Adminstration    •    Hospira
• Impax Laboratories
• Jazz Pharmaceuticals
• Johnson & Johnson
• Mylan Inc
• National Association of Chain Drug
• National Council for Prescription Drug Programs NCPDP
• Novartis Pharmaceuticals
• Salix Pharmaceuticals Inc
• Sanofi
• Shire
• Sunovion
• Taro Pharmaceuticals USA Inc
• United Therapeutics
• US GAO

Add your name to this list and join in on this one-stop-shop for all things government programs in Arlington on March 23-25, 2015.

Register online now to receive 50% off! Be sure to use XP205150OFF




Tuesday, January 6, 2015

Prevention, Incentives and Medicare Costs

By Nalini K Pande, JD

A little over a year ago at my previous consulting job, I served as the project director for a very interesting prevention project.   The project was for the Bipartisan Policy Center’s (BPC) Health Care Cost Containment Initiative1.   BPC had asked us to develop a financial model of the costs and benefits of a diabetes Type 2 prevention program.  Our report illustrated how the financial incentives for three different payors  (commercial plans, Medicare, and ACOs) vary given different assumptions of who would pay for these prevention services and the age at which individuals would first receive prevention services. We chose to model Type 2 diabetes prevention services given that Type 2 diabetes is reversible and given the tremendous amount that the US spends on Type 2 diabetes2 .   What we learned was fascinating.

Prevention Efforts Can Yield Cost Savings

The key finding from our report was that a diabetes prevention program “can produce overall cost savings which increase over time for an individual.” Given this, why wouldn’t we roll out these prevention programs on a widespread basis?  Well, the answer may surprise you.  To delve into this, you will need to understand three key issues:
  • - First, who pays for the diabetes prevention program? 
  • - Second, who benefits?
  • - Third, when do the savings kick in?
Our report showed that if private commercial plans bear the cost of the diabetes prevention program, they may not reap all the benefits.  This is because of two reasons.  First, if individuals switch health plans over time, another plan would reap the benefits – allowing for only small benefits for the plan that implemented the prevention program.  Second, if you’re 55 or older, there is no incentive for a private commercial plan to cover your participation in a diabetes prevention program.  Simply put, by the time the cost savings would kick in (10 years), you would be on Medicare and Medicare, not the plan, would reap the benefits. 

So, what if Medicare paid private plans to cover these diabetes prevention programs?  Perhaps, then, we would all win.  Those with private commercial plans would benefit from diabetes prevention services and Medicare would benefit from healthier beneficiaries who save the program money. Our report found that while the Government does recoup savings when it pays for the program, it only did so for those who are near 60.  In fact, the Government receives very little savings from a younger population who would stay with the private sector and continue to be with a commercial plan during the timeframe when most of the savings would be realized over a 25-year period.

Where does this leave us?

In essence, what we have is a scenario where payors are reluctant to pay for prevention services since they won’t benefit completely.  Has our patchwork system of health care created disincentives around prevention?  Not quite.  Our study found that if patients could join an ACO when they are under 65 (as a commercial ACO) and then stay in the same ACO when they are over 65 (as a Medicare ACO with shared savings between the ACO and Medicare), perhaps the ACO would get the best of both worlds.  In this scenario, an ACO could invest in its patients through prevention programs and recoup the benefits, assuming limited plan switching.

Investing in prevention appears to be a game of “what’s in it for me?” How do we change it to a “win-win” scenario? The answer is simple.  We do so by utilizing new systems like ACOs that allow payors to reap long-term savings. 

Nalini Pande, Managing Director, Sappho Health Strategies has nearly 20 years of experience in healthcare policy and reform.  She has considerable experience in Medicare and Medicaid, prevention, population health, and emerging payment models including accountable care organizations and patient-centered medical homes. Ms. Pande also has strong expertise in dual eligibles and the specific issues facing this unique population.  Ms. Pande is a graduate of Harvard Law School and Princeton's Woodrow Wilson School of Public and International Affairs.




                                           

1 Under the leadership of former Senate Majority Leaders Tom Daschle (D-SD) and Bill Frist (R-TN), former Senator Pete Domenici (R-NM), and former White House and Congressional Budget Office Director Dr. Alice Rivlin, BPC’s Health Care Cost Containment Initiative  “explored and evaluated strategies to contain health care cost growth on a system-wide basis, while enhancing health care quality and value.” 
 2 In Appendix D of our report, we noted a study by Dall and colleagues that estimated the costs associated with Type 2 diabetes as $105 billion for medical costs (along with $54 billion for non-medical costs such as lost work days).  




Tuesday, July 8, 2014

The 5 Biggest Challenges for Stakeholders in the Oncology Value Chain

Interview with Rebecca M. Shanahan, CEO of Avella Specialty Pharmacy, a speaker at IIR's upcoming Annual Summit for Oncology Management, July 21-23, in Philadelphia.
 
What are the 5 biggest challenges for stakeholders in the Oncology Value Chain? And why?

Despite tremendous advancements, there remain significant challenges in the Oncology Value Chain.

First, there remains a lack of meaningful integration of the stakeholders.

The silos that exist in this area of healthcare limit communication and, ultimately, patient health outcomes, whether by virtue of geography, subspecialization, organizational structure or fragmented data. 

One area this is evident in is the duplication of existing services capabilities by hospital networks. For example, primary care network management, pharmacy services, hospice, and other services lines are often redundant with those already existent in the provider community. “Big data” capabilities remain in repositories that are not driving insights to improve healthcare across provider segments.  Informatics pointed toward patients communicate/replicate medical terminology without flags, links or explanations comprehensible by the most highly educated laypeople.

Pharmaceutical manufacturers with patient assistance and nursing support programs, interactions with PBMs and Plans regarding formulary management, and aligned economic incentives are hampered by the “silo” approach when they tailoreprograms and pricing to differeing classes of trade, sometimes to their detriment.  As an example, a manufacturer of a new oral medication treating a disease previously less well treated by infused therapies experiences 75% dose titration in its clinical trial. To roll the drug out, it conducts Physician Advisory Boards, Physician Clinical Education and Healthcare Economic Outcomes Reviews of Prescribing Patterns.  As the drug is an oral therapy and most likely dispensed by a pharmacy, the manufacturer also established an 8 pharmacy Limited Distribution Network for the drug.  However, no program was instituted for the pharmacies and the prescribing physicians to share information and ask questions regarding dose titration.  Real world dose titration was 27%, thereby resulting in lower uptake of the drug and less benefit for patients.

Once data becomes ubiquitous and the tools to access and comment on the data are available through a user-friendly system, we will move to risk-sharing model that would benefit all stakeholders.

Second, there remains a lack of novel approaches to therapy management that improve patient empowerment. 

Value-based care has historically worked well with diabetic & cardiovascular patients.  Pitney Bowes and Safeway both have successfully implemented programs to align the interests and needs of employers and employees.  Similar practices could be further leveraged within the oncology treatment process.

Shoppers Drug Mart created a pharmacy benefit plan based upon a retail pharmacy services model wherein enrollees could qualify for a progressively enhanced series of incentives, benefits & rewards if they (i) completed an Health Sstatus Assessment, (ii) elected to participate in health management programs for one of 5 high cost diseases which they evidenced experiencing, (iii) progressed through milestones associated with disease-specific therapy management and (iv) sustained their health gains over a period of time.

Cardinal Health and P4 Pathways, as well as Wellpoint Aim, established Pathways Programs in Oncology wherein NCCN guideline-based Formulary, Interventions and Outcomes metrics drove Best Practices and savings at a rate of 5 to 15 percent, depending upon the flexibility of the pathway, the pre-existing Clinical Best Practices approach, etc.  Using a series of interventions, the program managed and documented cadence and content, exchanged generics for brands where appropriate, managed dosing, reduced combination therapy in later stages of therapy and provided regular clinical checks for patients.  These novel programs could gain more widespread utilization within the industry, provided collaboration occurs real time amongst physicians, pharmacists and disease therapy management providers.

Third, there is not a clear intersection / integration for providers, payors, patients and pharmaceutical manufacturers on healthcare coverage issues. 

There needs to be a shift from “Class of Trade” thinking to “Patient Engagement” thinking by the stakeholders.  There should be a standard of care, regardless of class of trade.  The appropriate treating provider based on clinical expertise, patient location and unique patient healthcare and socio-economic needs would have the data accessible to delivera consistently measured and reported standard of care.

Fourth, the cost of oncology therapy and care management continues to rise dramatically.
 
Currently, care management spending is $100B annually and is projected to be $200B by 2020.  This is compounded with the cost of specialty medications that, at $100B, represent 25% of pharmacy spend today.  By 2015, this is projected to reach over $180B and could trend over $400B by 2020.  A large driver of this cost is hepatitis-C treatment, but oncology is also making tremendous impact.
While  costs may be fueling  tremendous medication advancements, more focus needs to be place on the HEOR (health economics outcomes research) to better understand the end-to-end measurement of costs and health outcomes.  With greater transparency of data to measure results of therapy, we could better align incentives and savings and service models. 

Fifth, across all stakeholders, there needs to be an improved knowledge of the oncology value chain.

We are seeing gains in this challenge.  An example is the (recent) traction of the oral parity laws that ensure equal coverage for infused oncology therapies versus oral oncology therapies.  In a study done by Prime Therapeutics, it was found that one in six cancer patients with high out-of-pocket costs abandon their medication.  The same study found that patients with an out-of pocket cost greater than $200 were at least 3 times more likely to not refill prescriptions than those with OOP costs of $100 or less.  The technology has evolved, but because of cost differentials, patients may not reap the rewards of these advancements.

Improved knowledge would benefit the oncology community in the areas of drug safety, specifically pharmaco-vigilence programs and than transparency of reporting to provider and pharmacies.

How do specialty pharmacies like Avella assist with these issues?   

Specialty pharmacies are in a unique position to connect the stakeholders in the Oncology Value Chain.  Leveraging their position of having meaningful interactions with the many oncology stakeholders (patients, payors, manufacturers, healthcare providers), specialty pharmacies should serve as a “hub” for the stakeholders.  Formulary management, step therapy implementation, HIPAA-protected real time data collection and reporting, access to performance of patients across providers, payers and therapies – all these in one tool-based repository are available through Avella and its clinical pharmacy team.

With a deeper connection between the stakeholders, the data each group is collecting and measuring becomes more transparent and useful.  Harnessing the data, specialty pharmacies can become a leader in health economics outcomes research and ultimately find additional cost savings solutions.

Finally, through increasingly meaningful patient engagement, specialtypharmacies can improve communication, adherence levels, patient literacy levels, and clinical outcomes.  This short video highlights several of the ways Avella and specialties pharmacies benefit patients:  https://avella.wistia.com/medias/fksa6j9ntg


About Rebecca M. Shanahan:


As Chief Executive Officer of Avella Specialty Pharmacy, Ms. Shanahan brings extensive healthcare and specialty pharmacy experience to Avella Specialty Pharmacy. Ms. Shanahan served as Executive Vice President and Head of the Aetna Specialty Pharmacy from 2005 - 2007 and as a member of Avella Specialty Pharmacy’s board of directors from 2010 – 2013.

Prior to joining Avella Specialty Pharmacy, Ms. Shanahan was president of Shanahan Capital Ventures, LLC, (SVC) a consulting firm that built strategic business initiatives and programs for a number of healthcare entities in the United States and Canada. SVC clients included Cardinal Healthcare Specialty Solutions, Shoppers Drug Mart, Rite Aid Pharmacy, US BioServices, Bayer Pharmaceuticals, Bristol-Myers Squibb, Inspirational Biologics, MedSolutions, and Reliant Rehabilitation.

To learn more about Rebecca and the other members of Avella leadership, please visit www.avella.com/leadership. 

Rebecca will be a speaker at the upcoming Oncology Management Summit held July 21-23, 2014 in Philadelphia. Register now and save 15% when you use the code: XP1914BLOG.





Tuesday, June 17, 2014

Hear from CMO of BCBSA on Rising Cancer Care Costs

 America's National Institute of Health predicts that spending on all cancer treatment assuming a 5 percent annual increase in these costs raises the projection to $207 billion.

Due to an aging population, increased cancer diagnosis, rising cancer care expenses, and a demanding payer market, new strategies need to be addressed for pharmaceutical companies to maintain, commercialize, and increase oncology access in the marketplace. It is imperative to learn from experts who are able to deliver affordable cancer care, while improving quality and bend the cost curve downward

At IIR’s Annual Summit for Oncology Management taking place July 21-23 in Philadelphia, you will hear from Dr. Trent Haywood, MD, JD SVP Office of Clinical Affairs and Chief Medical Officer at BlueCross BlueShield Association, a trend-setter in this space. Dr. Haywood will be discussing the so-called “cancer conundrums”, focusing on the current issues and challenges your industry is facing and shed light on some of the successful strategies that have worked for BCBSA.

Download the brochure to view Dr. Haywood’s sessions and more.

Register now to meet and collaborate with all the key stakeholders across the oncology management landscape including BCBSA, Aetna, Astellas Pharma, Eli Lilly and more! Save $200 by Friday, 6/20. Please use your code XP1914BLOG

Dr. Trent Haywood, MD 
 As the BCBSAs’ chief medical officer, Dr. Haywood supports the innovation of Blue Cross and Blue Shield companies in communities around the country as they improve the choices of healthcare quality and patient safety for their members. He is responsible for the Office of Clinical Affairs, which includes the Center for Clinical Effectiveness, Center for Clinical Practices, and the Center for Clinical Value. Collectively, the Office of Clinical Affairs supports opportunities between Blue Cross and Blue Shield companies and stakeholders to improve the choices of affordable, high quality healthcare provided to members.





Friday, April 25, 2014

Decode Big Data to Drive Decisions | Register for HDI by Friday to Save $500!

 According to PricewaterhouseCoopers, big data and predictive analytics help companies better understand their audiences and how to engage them.

We're not talking to the "data guy". We're talking to YOU-the person making informed decisions based on data that is material to your business (claims data, member feedback, clinical data, etc.) By translating this information into actionable insights, you have the power to make more efficient and effective business decisions.

Don't fall behind as more and more companies grow increasingly data-driven and are more willing to apply analytics-derived insights to key business operations. Join us in Chicago this June 23-25 at IIR's all-new Healthcare Data Insights, where you will hear from speakers who successful implement big data analytics into their business strategy.

Discover how to make the best data-driven decisions for your company with speakers including:
•    Elizabeth Benz, Associate VP of Community Outreach & Engagement, Molina Healthcare of Wisconsin   
•    Greg Poulsen, Senior Vice President, Chief Strategy Officer, Intermountain Healthcare   
•    Bob Gladden, Vice President of Decision, Support & Informatics, CareSource   
•    Dan Munro, Contributor of Healthcare IT, Innovation and Policy, Forbes

Register by Friday 4/25 to save $400! Plus take an extra $100 off when registering with the code: XP1902BLOG

That is $500 in total savings, register today!

Learn more about Healthcare Data Insights here.




Friday, April 11, 2014

Download Gorman Health Group’s expert summary of the 2015 Final Rate Announcement from CMS

John Gorman predicted that -- if the rate announcement was enacted as outlined in the draft call letter -- it would be "just about a worst-case scenario for flabby, distracted, uncommitted health plans in Medicare."  John declared "there is no question that the 2015 call letter is an evolutionary event and some inferior species will be eliminated."

Now that the Final Rate Announcement has been released we can finally get some concrete answers. Gorman Health Group's renowned financial and policy experts Bill MacBain and Jean LeMasurier are teaming up to provide a detailed analysis and summary of the final regulation.

While Jean and Bill are finalizing the Summary of the Final Call Letter, you can request a copy and we will notify you as soon as it is ready.  But while you wait, enjoy access to some additional resources.  Request a copy of the Summary here.

As an added bonus, Bill and Jean will also be hosting a complimentary webinar today from 2:00PM – 3:30PM to offer insight on the Final Rate Announcement from CMS. You will walk away from this session with critical to-do items and issues to tackle in order to ensure your success in 2015 and beyond. Register now. 

                                                                                              



Reminder – Don’t miss IIR’s Healthcare Data Insights taking place June 23-25 in Chicago. Register by Friday 4/25 to save $400 on the standard conference rate.  For more information, click here.

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Tuesday, April 14, 2009

OFFICIAL CALL FOR PRESENTERS PATIENT ASSISTANCE PROGRAMS


Official Call For Presenters

PATIENT ASSISTANCE PROGRAMS
From: Courtney Leonard, Conference Producer
Re: Call for Speakers & Presentations
Event Date: October 26-27, 2009
Event Venue: Capital Hilton, Washington, DC

INDUSTRY ALERT: OFFICIAL CALL FOR PAPERS

The Institute for International Research (IIR) is currently seeking presenters for the 2009 Patient Assistance Programs event. This 2-day event will take place October 26-27, 2009 in Washington, DC. We invite you to submit a proposal for a speaking opportunity directly to Courtney Leonard, by May 01, 2009. Please send to cleonard@iirusa.com.

Submission Guidelines & Details

CUSTOMIZE YOUR CONFERENCE AGENDA!

We are currently recruiting pharmaceutical and biotech professionals who can share first-hand perspective, insights, and real-world case studies on what has worked at their organizations. Some of the topics to be addressed at the 2009 event are:

• Improve and enhance medication assistance programs
• Improving State wide medication assistance programs; Best practices from other states
• Web based PAP enrollment
• Medicare Part D
• PAPS Automating the PAP enrollment process
• How to utilize patient profile data
• How to survive an audit
• Legal consideration in PAP administration
• Bulk Replacement Programs
• Growing need for copay assistance
• Expansions of PAP programs
• Oncology driven PAP Programs
• Ensuring PAP compliance with changing government regulations
• Effective PAP marketing strategies
• Specialty pharmacy role and management in PAPS

MAKE SURE YOUR BIGGEST ISSUES ARE ADDRESSED!

Are your biggest issues not addressed here?
Contact Courtney Leonard to ensure that your pressing issue gets the attention it deserves! cleonard@iirusa.com or 919.518.8294.

Do you want to reach this audience?

We have a limited number of slots available for solution providers/consultants.
People who wish to become part of the program should contact , Andrew Sinetar, Sponsorship Manager, at 646.895.7484 or e-mail asinetar@iirusa.com.
Sessions will be 30-45 minutes including Q & A.