Thursday, July 31, 2014

How to Address Commercial Ops, Commercial Contracting and Government Pricing


At MDRP 2013, Mark Linver, Director, Huron Life Sciences discusses addressing government and commercial pricing operations during mergers and divestitures. Below are two highlighted sessions from MDRP 2014 that will look into Commercial Ops, Commercial Contracting and Government Pricing.


Session Highlight:
Spillover Effects Between Government Pricing, Commercial Business & Contracting Strategies

• Discuss healthcare reforms impact on contracting & emerging contracting practices
• Evaluate the impact of government pricing changes on commercial accounts
• Reevaluate and restructure rebate and discount agreements

David Chan, Practice Leader, Compliance & Audit, Managed Markets Services, IMS Health


Session Highlight:
Improving Effectiveness of Revenue Analytics by Using GP Forecasting

The continual growth of the government channel has increased the importance of understanding the cross-channel impact of the commercial pricing and contracting decisions that drive liabilities. Along with increasing pressure to understand, forecast and accurately accrue for revenue line items as part of the GTN process, an expanding government channel means contracting and pricing functions have a greater need for pricing and forecasting outputs from the GP department. The “modern” GP team is tasked with providing “what if” analyses and forecasts for a wide variety of company specific and industry wide events, and is looked upon as a critical resource when pricing and contracting decisions are being made. Today’s GP team must be adept at developing quick yet sophisticated models to assess how any given event may affect Revenue lines that are driven by a Government payer.

This session will take a look at how to effectively incorporate commercial strategies and market events into the forecast of GP price points. We will explore how to:

• Manage and align data for analytical needs
• Consider price increases and commercial contracting strategies
• Incorporate channel shifts into forecasts
• Evaluate regulatory and market events in scenario modeling
• Identify what you know and what you don’t know, and how both should be considered and modeled

Jeffrey Baab, Senior Director, Life Sciences, daVIZta





Register by Friday 8/8 to save $300! Make sure you use the code XP1958BLOG | Register Now!




Wednesday, July 30, 2014

Complimentary Webinar | Moving and Improving: Using Data and Informatics to Inform Your Business Strategy, Save Lives and Improve Quality

A complimentary webinar from Healthcare Data Insights
 
Date: August 19th
Time: 11:00AM - 12:00PM EDT

Moving and Improving: Using Data and Informatics to Inform Your Business Strategy, Save Lives and Improve Quality




The University HealthSystem Consortium (UHC), the member organization of 120 non-profit Academic Medical Centers and their affiliates, encourages hospitals to integrate data into their business plans, in part by demonstrating how data can be used to save lives and improve quality scores. With transparent access to data from more than 400 hospitals (which includes more than 5 million inpatient discharges annually and 25 million outpatient encounters), learn how they make the case for member hospitals to “move and improve” with innovative programming based on data.

Speaker: David Levine, MD, FACEP, Vice President, Informatics, and Medical Director, UHC

In this seminar, David will show how members maximize hospital and physician data to measure efficiency and effectiveness. Work in both the inpatient and outpatient settings to capture performance over the continuum of care will be emphasized. The data challenges will be highlighted especially with cost and capturing all inputs to care.

• Key metrics being used to measure overall hospital performance
• How Academic Medical Centers are looking at physician variability
• How to identify key opportunities for cost reduction
• Importance of risk adjustment and using proper compare groups to engage clinicians in improvement
• Challenges of integrating databases and gaps in data

Register for the Webinar - Use Priority Code: W1BL




Tuesday, July 29, 2014

MDRP Lifetime Achievement Award

Each year the MDRP audience selects who should receive the “Lifetime Achievement Award.” Nominations are now open. Make sure to get your choice in for consideration now.


As the longest running MDRP conference, we are honoring the best and recognizing the dedication of those who have propelled this industry forward. Please submit your award nomination(s) here. We have divided the nominations by role in the industry, as so many have worked together to make the Medicaid Drug Rebate Program what it is today. The deadline for nominations is Monday, August 11, 2014 and the winners will be announced at the event during the networking reception on Tuesday, September 16th - So make sure you register to attend the event now. Save $300 when you register by 8/8 with the code XP1958BLOG.

To learn more about the program, download the brochure now. 

See you in Chicago this September!




Monday, July 28, 2014

Is Medicaid Expansion Feasible?

Welcome to the MDRP Podcast Series. Joining us today is Grace-Marie Turner, President, Galen Institute.




Is Medicaid Expansion Feasible?

Grace-Marie: I just think that it’s going to be very difficult to convince those other states that have resisted so far because more and more evidence is coming down to show that expanding Medicaid as a traditional program as it is currently structured is real harmful to people. And it’s really harmful to the most vulnerable citizens who are on Medicaid today. If people have many chronic conditions, many of them have no place else to go. They are basically not insurable in the private marketplace. If they are under 100 or 138% of poverty, Medicaid really is their only option. As a result, you wind up with more people competing for the same limited number of doctors who will see Medicaid patients and making it even more difficult for people on Medicaid today to find a doctor to see them.

I had a father write to me recently who has a daughter who is on Medicaid – many chronic conditions and in a wheelchair. He said: “It takes me sometimes six weeks to get an appointment with her urologist”. He said: “Do they even think about how much more difficult it’s going to be to get an appointment with the urologist if there are a million more people competing for those same appointments?” So, we must fix it so that it allows the safety net to be intact for the most vulnerable people and give those who have the option to get private coverage to do so, so that they are not competing.

And then finally, I think that the states who want to expand the program need to guarantee that providers will be paid enough that they will be able to see a Medicaid patient. In some states like New Mexico that have a very high match rate, Medicaid pays at very close to Medicare rates. In other states, a doctor may be paid $5 or $7 for an office visit – not even enough to begin to cover expenses. Doctors want to take care of these patients, but they can only keep so many and keep the lights on and pay their own bills. So, we’ve got to be able to pay providers more and that’s the kind of leverage that I think that the states would be able to have if they were not so constrained by an avalanche of federal rules and all the “Mother May I?” waiver requests that they have to get to make any changes to their plan.

If they had more flexibility, then they could make sure that patients on the program today could actually find a doctor to see them and also make sure that those who may be in an expansion population have the option of coverage that looks more like the private insurance and the private marketplace so that it’s a track and a platform to private coverage rather than the cliff that Medicaid is today – either in or out. If you make $1 too much money then you’re out of Medicaid or $1 less and you’re in. It needs to be a smoother ramp to private coverage and there are a lot of ideas to do that, including giving people the option of basically taking their Medicaid allotment as a voucher to buy into private coverage. There are a lot of ideas out there to improve this program, but we need to remember that we’re doing it for the most vulnerable citizens who are on the program today, who have no place else to go, competing for a limited number of appointments with a shrinking number of doctors to actually get appointments.

We can do so much better and I think you’re going to see many more governors actually demanding those kinds of changes and that kind of flexibility in exchange for any expansion.




Click here to download the rest of the podcast.

To hear more from Grace-Marie, make sure you join her at MDRP 2014 this September 15-17 in Chicago. As a reader you can save an extra $100 off the current rate when using the code XP1958BLOG. Register now to save!

See you in Chicago.






Thursday, July 24, 2014

How Can We Sustain the Innovation of Biopharmaceuticals?

Welcome to the Specialty Pharmacy Collaboration Summit Podcast Series. Today we are speaking with Robert Popovian, Senior Director, US Government Relations, Pfizer Pharmaceuticals.


What needs to happen in the US to sustain the innovation initiative of biopharmaceuticals?

Robert: Well, biopharmaceuticals is a complex issue and a lot of people try to make it a very simple one by saying to do regulatory reform through the FDA or provide additional NIH funding to do research. Biopharmaceutical innovation policies are very complex and inter-dependent onto one another. There is no one magic bullet.

So, there are three distinct environments that need to be addressed to really sustain the biopharmaceutical innovation marketplace in the US and that is the investment environment, which is basically appropriate and electoral property protection. For example, tax policy, ability to price medicines according to the marketplace.

There is the regulatory environment, which is the second environment, which requires that we do a better job of streamlining not only the FDA, but other regulatory bodies like the Centers for Disease Control. And then, more importantly, within the regulatory policy framework is how to better do clinical trials and clinical trial recruitment. That needs to be addressed.

Finally, it is the access, which in my opinion is the one that is short shifted a lot of times because unless you address the access environment for biopharmaceutical, no matter if you are investing a lot of money in it or you have a very deregulatory process to get the product out, if the patients are unable to access those medicines because they are too high cost regarding out-of-pocket costs or there is no meaningful way to get access to it because there is no way to communicate that information to the providers, innovation will suffer and patients will suffer long term with that.



To hear more from Robert, please join him at IIR's Specialty Pharmacy Collaboration Summit, September 15-17 in Boston. Also, you can save an EXTRA $100 off the current rate, $500 in total savings when registering by 7/25 with the code: XP1968BLOG - Register now. 

See you in Boston!




Wednesday, July 23, 2014

Attention All Health Plans | Buy One, Get One Free to the Specialty Pharmacy Collaboration Summit

 
Attention Health Plans! Join us at the Specialty Pharmacy Collaboration Summit and for a limited-time only, we're offering a Buy One, Get One offer*! 



Expiring this Friday, July 25th, purchase one pass and have a colleague attend for free! Be sure to use code: XP1968BOGO. To register, call Roxana Siu at 646-895-7452 or email rsiu@iirusa.com.


*Free Delegate Pass Eligibility Rules and Regulations:
1. Offer applies only to Health Plan executives
2. If the paying delegate cancels, the free delegate will receive an invoice for the amount of the paying delegate.
3. Tiered pricing is valid through expiration date. New pricing takes effect at specific dates indicated. All fees must be paid in full by expiration date or your price will increase to the next level tier.
4. Offer cannot be applied retroactively to confirmed paying registrants.
5. Offer cannot be combined with any other discounts or promotions.
6. All BOGO registrants and guests are subject to IIR approval.




340B Entities: Best Practices for Pricing and Compliance Methodologies


Above, you will hear John Shakow, Partner, King & Spalding speaking with MDRP TV about 340B Entities – and the best practices for pricing and compliance methodologies. To hear more insights from John, join him at MDRP 2014, where he will be speaking again. Below you can find a highlight of one of his sessions at the event.

Understand the Implications: A Business Perspective
You’ve heard the presentations and the speeches, the panels and the analysis. In this session of the conference, we will try to tie it all together and give you a 360° view of the government pricing landscape in the coming year. The emphasis will be on key takeaways, which you and your colleagues should keep top of mind as you head back home. 2014–15 promises to be a year of great change and increasing complexity in all aspects of government pricing, and with that come the inevitable compliance, legal, business and operational challenges. Secure the benefits of MDRP 2014 with this roundup of highlights and key observations.

For more session information, download the complete agenda.

And remember as a blog reader you save an extra $100 off the current rate when you register with the code XP1958BLOG - Register by 8/8 to save a total of $300!

See you in Chicago!




Tuesday, July 22, 2014

360 Perspective from BCBS, Boston Medical Center, Tufts Health Plan, Denver Health Plan and more!

 
This Friday, July 25th is your last chance to save up to $500!
Use Code: XP1968BLOG 



Due to increasing healthcare costs brought on by health care reforms and the ACA, payers need to partner with specialty pharmacies to help fill the oversight gap in compliance and to manage costs and reimbursements. Specialty Pharmacies offer their product management and patient adherence services to help fill the gaps of the payers, while meeting the needs of reduced costs.

IIR's all-new Specialty Pharmacy Collaboration Summit is the only event in the space offering you the opportunity to partner directly with all the key stakeholders in the specialty pharmacy value chain to increase patient adherence, expand distribution and improve bottom line. Learn how health plans successfully partner with specialty pharmacies and leading pharmaceutical companies and discover the impact of specialty pharmacies on bottom line profits and costs from the below experts:

The True Value of Specialty Pharmacy: A Direct Impact on Bottom Line Revenue and Profits

• Reed Melton, Executive Director, Center for Clinical Practices, Blue Cross and Blue Shield Association
• Bhavesh Shah RPh, BCOP, Clinical Pharmacy Manager, Hematology-Oncology, Coordinator - Patient Assistance Programs, Specialty Pharmacy Manager, Boston Medical Center

Payer Panel: Specialty Pharmacy Management in Commercial Health Plans

• Michelle Beozzo, PharmD, Director of Pharmacy Services, Managed Care, Denver Health Medical Plan
• David Brumley, MD, MBA, Senior Medical Director, Tufts Health Plan

Roundtables: The Specialty Pharmacy Space-Niche No More?

Independent Retail Community Pharmacies
Nick Calla, VP Industry Relations, Community Specialty Pharmacy Network
Regional and National Chains Launching Specialty at Retail Programs
Christopher Benz, Business Development Director, Armada Health Care
Brian Burke, Vice President, National Accounts, Armada Health Care
Private, Independent Specialty Pharmacies
Rebecca M. Shanahan, Esq. Chief Executive Officer, Avella Specialty Pharmacy

Download the updated brochure for the full agenda and speaker details.

Don't miss out! This Friday, July 25th is your last chance to save up to $500! Click here to register or call 888-670-8200 to register. Be sure to use code: XP1968BLOG





Monday, July 21, 2014

Best Collaborative Practices for Resolving or Avoiding Medicaid Disputes

MDRP 2014 Session Spotlight: 

Best Collaborative Practices for Resolving or Avoiding Medicaid Disputes


 

The complexities involved in identifying and resolving Medicaid disputes have only grown since the ACA with the additional claims from Managed Medicaid Organizations. In this session we will discuss some common best practices related to working collaboratively with your state contacts to either avoid disputes or resolve them quickly.

• Communications and documentation required to avoid putting units into dispute
• Key information needed by the states/manufacturers to research and resolve a disputed claim
• How best to avoid recurring unit of measure issues
• The value of informative state invoice cover letters for states and manufacturers
• An update on the work group’s efforts to standardize electronic reporting across the MDRP

Panel:
Lisa Norton, Associated Consultant, Managed Healthcare Services, Lilly USA, LLC
Kelly Geissler, Sr. Analyst, Government Rebate Operations, Johnson & Johnson Health Care Systems Inc.
Daksha Bogdon, Govt Pricing and Contracting, Genentech
Cindy Laclair, Drug Rebate Specialist (HP), Kansas
John Grotton, Sr. Director, Medicaid PBA Operations, Goold Health Systems


For more session information, download the brochure now. 

Blog readers receive an extra $100 off the current rate when you use the code XP1958BLOG. Register by 8/8 to save $300!


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Join our LinkedIn Group
 





Thursday, July 17, 2014

What is the Future of Specialty Pharmacy?

Welcome to the Specialty Pharmacy Collaboration Summit Podcast Series. Today we are speaking with Nick Calla, VP of Industry Relations, Community Specialty Pharmacy Network (CSPN)



What is the future of specialty pharmacy and the impact on the key stakeholders?

Nick: When you look at specialty pharmacy, in my mind it is still an evolving area of pharmacy. Specialty pharmacy really came into being, I would say, at least 20 years ago where it was the very beginning of specialty pharmacy with products like betaseron in the Multiple Sclerosis space, as well as products like Crixivan in the HIV space back in the mid-80s.

The model has evolved and has evolved dramatically over the last 10 years or so. At this point in time, it is really quite dominated by the Big 4, Big 5 large PBMO and health plan owned specialty pharmacies. Therefore, when you look at a model like the one that I represent or CSPN – quite honestly the smaller pharmacies are being shut out of a number of opportunities.

Now, there are a number of good reasons for that. Many retail-based or community-based pharmacies simply have not developed the infrastructure to support a specialty product which, as I mentioned earlier, is a high-touch model. Many of these pharmacies have not developed the benefit investigation needed, the reimbursement support infrastructure needed and really the clinical support needed to truly manage dictation. However in our model, for example, there are a number of community players – smaller, independent pharmacies – that have developed all of these resources. They have also developed accreditation through some of the accrediting groups like URAC and ACHC. As well, they’ve become members of organizations like NASP – National Association of Specialty Pharmacies. So, they have truly developed the model over time.

As I said, the industry is still dominated by the Big 5 and Big 6 and again, I think what’s going to happen over time as this model starts to develop is that you are going to need more pharmacies with the capabilities to handle the special dictation. There are many, many products. Development on the oncology side, for example, on the Multiple Sclerosis side and the Rheumatoid Arthritis side that I think will require a larger group of pharmacies that truly have the capability to manage that patient.

So, that’s where I see it. I see the future of specialty pharmacy really expanding and creating opportunities for stakeholders beyond the few that have truly taken advantage of this space up to this point.

Click here to download the rest of the transcript and podcast.

To hear more from Nick, please join him at IIR's Specialty Pharmacy Collaboration Summit, September 15-17 in Boston. Also, you can save an EXTRA $100 off the current rate, $500 in total savings when registering by 7/25 with the code: XP1968BLOG - Register now.

See you in Boston!




Wednesday, July 16, 2014

Obamacare May Raise Patient Costs for Specialty Drugs

Via Specialty Pharmacy Continuum

According to specialty pharmacy experts, patients who rely on specialty drugs to treat their rare and complex conditions may be forced to pay a large percentage of the drug’s cost instead of a traditional fixed copay, if they are in an Affordable Care Act (ACA) exchange health plan.

Despite some of the exchange plans having the draw of lower monthly premiums, people should prepare themselves for higher deductibles and unpredictable out of pocket costs. Even though the cost structures do vary between the exchange plans, patients may face this issue no matter what exchange plan they are enrolled in.

Avalere examined 603 unique plan designs offered by 60 different carriers in 19 states to assess whether specialty medications are being put in a higher tier with a larger percentage of coinsurance, said Jenna Stento, a senior manager at Avalere. The analysis found that 59% of silver plans on exchanges across the country use coinsurance on the specialty tier instead of a fixed copay. It also found that 23% of silver plans charged coinsurance rates of at least 30% more than the cost of the drugs on the highest formulary tier, and 60% of lower-premium bronze plans apply specialty tier coinsurance greater than 30% of the drug price.


“This examination highlights the fact that patients relying on specialty medications are going to have to lay down significant finances up front until they hit the out-of-pocket cap, which is $6,350 for most people and $2,250 if that person is 200% below the federal poverty rate,” said Ms. Stento. “The fact that patients will be paying an unknown percentage will make it harder for some to plan financially, and will raise questions about access and availability.”

With the number of underinsured and strained patients continuously growing, how can these concerns be corrected?

_________________________________________________________________


To learn more about Specialty Pharmacies, Specialty Drugs, the Affordable Care Act, and much more, join us in Boston this September for the Specialty Pharmacy Collaboration Summit. 

Register by 7/25 with the code XP1968BLOG and take an extra $100 off the current rate - that is $500 in total savings! Register here.

See you in Boston!




Tuesday, July 15, 2014

Six Cases Where Big Data Can Reduce Healthcare Costs

Via Science Daily 

As electronic health record use becomes widespread across the United States, largely due to the implementation of the Affordable Care Act, the quantity of clinical data that will become available for research and analytic purposes will also dramatically increase. Experts in healthcare have become increasingly focused on clinical analytics that analyze large quantities of data for the purpose of gathering insights that have the potential to improve the value of patient care – a process that is known as big data.

In a new research study published in Health Affairs on July 8, 2014, researchers highlight some of the clearest opportunities to reduce costs through the use of big data.

Specifically, they discuss the role of algorithms in reducing cost in the following categories: high-cost patients, readmissions, triage, decompensation (when a patient's condition worsens), adverse events, and treatment optimization for diseases affecting multiple organ systems.

"The examples we present in this study provide key insights to the 'low hanging fruit' in healthcare big data and have implications for regulatory oversight, offer suggestions for addressing privacy concerns and underscore the need for support of research on analytics," said David Bates, MD, MSc, chief quality officer at Brigham and Women's Hospital and lead author on the study.

High-cost patients

Only 5% of patients account for about half of all U.S. health care spending. Bates and his co-authors articulate the issues that need to be addressed to identify and then manage these high cost patients. They include formalizing an approach to predict which patients are likely to be high cost, what measurements can be incorporated to improve this prediction, particularly those focused on mental health, and how to make these predictions actionable. Researchers emphasize that making new analytic systems effective will rest on the ability to make these predictions easily available to clinicians in a way that does not disrupt current workflow.

Readmissions
 
Researchers write that as many as one-third of readmissions may be preventable, which provides a significant opportunity for improvement in care and reduction in cost. Bates and his coauthors suggest that all health care organizations should use algorithms to predict who is likely to be readmitted, but highlight the challenges of implementing such algorithms. They include: tailoring the intervention to the individual patient, ensuring that patients receive the interventions intended for them, monitoring specific patients after discharge to ensure they do not develop issues that would cause their condition to deteriorate, and ensuring a low ratio false positive rate of patients flagged for an intervention to patients who experience a readmission.

Triage


Effective triage is essential to estimating the risk of complications when a patient first receives care in the hospital setting. This is important in order to manage staff and bed resources, ensuring the patient is sent to the correct unit for care and overall it informs the management of the patient's care. Researchers suggest integrating a triage algorithm into clinical work flow, and underscore the importance of having a detailed guideline to clarify how specifically the algorithm will inform care. Researchers examine two pilot studies which provide lessons learned in establishing effective triage algorithms.

Decompensation

When a patient's condition worsens, there is often a period in which physiological data can be used to determine whether the patient is at risk for decompensating. Researchers explain that the initial rationale for intensive care units (ICUs) was to allow patients who were critically ill to be closely monitored for this purpose. Researchers emphasize such systems can now be used throughout the hospital, and that effective analytic systems in this area must use multiple data streams to detect decompensation, as many new technologies are becoming available that can be used to better monitor patients.

Adverse events


Adverse events, while expensive and can result in high rates of morbidity and mortality, are preventable at high rates. Researchers call out three areas, renal failure, infection and adverse drug events, as specific opportunities to utilize big data to reduce costs.

Treatment optimization for diseases affecting multiple organ systems


Chronic conditions that span more than one organ system or are systemic in nature are some of the costliest conditions to manage. Autoimmune disorders such as rheumatoid arthritis and lupus frequently fall into this category and the ability to predict the trajectory of these diseases would immensely assist the caregivers deliver expensive therapies in a more targeted way. Focusing on the usefulness of big data in this area could result in effective approaches that can combine the many measurements taken as part of routine care to predict the progression of a patient's disease and personalize treatments and therapies appropriately. Access to health records with pertinent data has been the biggest limitation in adopting the use of big data in treating chronic diseases, but as the use of electronic health records becomes widespread, advances in this area are ripe for both improving patient care and reducing costs.


Researchers emphasize that these six cases are not an exhaustive list of the ways in which big data can be useful in improving value in healthcare. Specifically, they note that these examples, which focus on inpatient settings, will likely be transferrable to the outpatient setting as well.

"Support for research that evaluates the use of analytics and big data to address these six use cases, as well as thoughtful consideration of regulation and payment is warranted," says Bates. "Additionally, as multiple streams of data become available for analytic purposes, consideration of patients' privacy and their desire to link disparate sources of data will be of the utmost importance."



Source: This story is based on materials provided by Brigham and Women's Hospital.

____________________________________________________________________

For more information about big data and healthcare costs, join us for a complimentary webinar, August 19th, 11:00AM - 12:00PM EDT - Moving and Improving: Using Data and Informatics to Inform Your Business Strategy, Save Lives and Improve Quality

For more information on the webinar, click here.

Register Now – Use Priority Code: W1BL




Monday, July 14, 2014

Medicaid Expansion and Healthcare Exchanges


Last year at MDRP, Richard Holsapple, Pharmacy Services Manager, HP Enterprise Services, Oregon MMIS, sat down with MDRP TV to discuss Medicaid Expansion and Healthcare Exchanges – watch the video above to hear what Richard had to say on this topic. And remember to join us at the 19th Annual MDRP Summit, September 15-17 in Chicago to hear Richards revised 2014 ideas and predictions…

Session Spotlight: 

Explore the Impact of Medicaid Expansion on Exchange Enrollment

Moderator: Sharon H. Greeson, R.Ph., GP Consultant, Compliance Implementation Services (CIS)

Panel:
• Jennifer Boyd, Florida
• Sam Trigillo, Illinois
• Richard Holsapple, Oregon
• Cindy Laclair, Kansas
• Andy Vasquez, Texas

Remember to register for MDRP 2014 with the code XP1958BLOG to save and EXTRA $100 off of the current rate! $300 in total savings.

See you in Chicago!




Wednesday, July 9, 2014

Rising Healthcare Costs | What are the Biggest Challenges?

 

Welcome to the Specialty Pharmacy Collaboration Summit podcast series. Joining us today is Robert Popovian, Senior Director, US Government Relations, Pfizer Pharmaceuticals


What are the biggest challenges that you face presently with rising healthcare costs?

Robert: Well, healthcare costs are increasing. We are close to about 20% of our GDP is spent on healthcare expenditures and that number is going to continuously go up, just because of the demographics in the United States.

If you look at spending and healthcare in general with regards to pharmaceuticals, pharmaceutical spending has risen slowly and overall healthcare spending – as well as other healthcare segments in the last few years – and the price increases have been pretty much in line with the other segments of healthcare.


The challenge that we have with healthcare expenditures in the United States is that we have a very dysfunctional payment mechanism in the US where we are challenged with an outdated insurance policy model where we don’t necessarily pay for the best interventions in healthcare because of the mechanisms of reimbursement where we have pharmaceuticals vs. hospital payments vs. outpatient payments vs. other services being paid separately. Because of that, no one cost beneficial intervention is the one that is put in the front of the others.



To hear more from Robert, please join him at IIR's Specialty Pharmacy Collaboration Summit, September 15-17 in Boston. Also, you can save an EXTRA $100 off the current rate when registering with the code: XP1968BLOG - Register now. 

See you in Boston!




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.





Monday, July 7, 2014

What are the biggest pain points that GP Professionals in pharma are dealing with?

Q&A with Chris Cobourn, Vice President of Regulatory Compliance, Compliance Implementation Services
 
Beyond waiting for AMP, what do you think are the biggest pain points that GP professionals in pharma are dealing with right now?

Chris: That’s a good question. I’ll hone in on that word choice – “pain point”. I think pharma compliance in general and GP specifically, we think of that term a lot. When I think “pain point” I think of what keeps CEOs or CFOs up at night. Or what keeps a GP professional up at night. So, let’s remember the intense level of compliance and accountabilities and risk – the expectation that manufacturers get this right and the risk if they don’t. The level of scrutiny out there by the Office of Inspector Generals and the Department of Justice will continue to grow and become intense. There is a huge focus on program integrity. So, the expectation is clear. Manufacturers have to get it right. The visibility across the organization increases. CEOs and CFOs understand the risk. They are certifying these calculations. That’s what we’ve seen really dramatically increase over the years.
 

The level of visibility in the organization and the understanding of the need to get this right. So, now you start introducing uncertainty and change into that, especially the C-chains that can come with AMP final rule, 340B Program integrity initiatives, constant complicated things that are hitting us – like the recent Texas reporting requirement. So, you’ve got organizations struggling with how to implement it all, understand it all, yet very high-level visibility. So, you’ve got CEOs and CFOs looking at a GP professional and saying: “You’ve got to protect the organization here. You’ve got to make sure we’re compliant. What does all this mean? How are we doing it? Tell me what to anticipate. Tell me the financial impact.” That’s, I think, the pain point at the C-level. And I think worry about some big pieces of it, especially such as will the final rule have the build-up methodology or not? We certainly hope not. But, there are a lot of changes that are going to ripple through the industry and it’s all going to start with a GP professional needing to educate their organization with what it means.
 

So, what are the biggest pain points? I think that’s what really drives people to attend conferences like this and the importance of GP professionals as a community having that dare-to-open dialogue.



To hear more from Chris, download the complete Q&A or listen to the recording.

Join us September 15-17 in Chicago for IIR's 19th Annual MDRP Summit. And when you register with the code XP1958BLOG you can take an EXTRA $100 off the current rate - Register now!




Wednesday, July 2, 2014

Moving and Improving: Using Data and Informatics to Inform Your Business Strategy, Save Lives and Improve Quality

A complimentary webinar from Healthcare Data Insights - August 19th, 11:00AM - 12:00PM EDT

Moving and Improving: Using Data and Informatics to Inform Your Business Strategy, Save Lives and Improve Quality

The University HealthSystem Consortium (UHC), the member organization of 120 non-profit Academic Medical Centers and their affiliates, encourages hospitals to integrate data into their business plans, in part by demonstrating how data can be used to save lives and improve quality scores. With transparent access to data from more than 400 hospitals (which includes more than 5 million inpatient discharges annually and 25 million outpatient encounters), learn how they make the case for member hospitals to “move and improve” with innovative programming based on data.

Speaker: David Levine, MD, FACEP, Vice President, Informatics, and Medical Director, UHC

In this seminar, David will show how members maximize hospital and physician data to measure efficiency and effectiveness. Work in both the inpatient and outpatient settings to capture performance over the continuum of care will be emphasized. The data challenges will be highlighted especially with cost and capturing all inputs to care.

• Key metrics being used to measure overall hospital performance
• How Academic Medical Centers are looking at physician variability
• How to identify key opportunities for cost reduction
• Importance of risk adjustment and using proper compare groups to engage clinicians in improvement
• Challenges of integrating databases and gaps in data

Register for the Webinar - Use Priority Code: W1BL