Physicians Have Bigger Stake In Patients' Total Care Under Medicare ACOs

One year after the passage of health care reform, recommendations around some of the more far-reaching elements of the legislation are beginning to emerge. One proposal biopharmas cannot afford to ignore: Medicare sanctioned accountable care organizations.

One year after Congressional passage of health care reform, recommendations centered around the more far-reaching elements of the legislation are beginning to emerge. One proposal biopharma companies cannot afford to ignore is tied to Medicare-sanctioned accountable care organizations (ACOs), which implement the "shared savings program" mandated by the Affordable Care Act. In a widely-anticipated document authored by the Centers for Medicare and Medicaid Services (CMS) and released March 31, the federal agency outlines a new payment model that could help solve one of the biopharmaceutical industry's thorny problems, drug compliance, which if improved, would likely boost product sales.

As outlined, the program represents a major change in the way Medicare pays for medical products and services, using financial incentives to provide higher quality and more coordinated health care through a networked group of physicians and hospitals. Encompassing hospital and physician care (including physician-administered drugs) that fall under Medicare Parts A and B, ACOs would care for fee-for-service beneficiaries and both provider and beneficiary participation would be completely voluntary. The proposal is based on a shared savings concept, in which an ACO would receive a bonus payment if cost and quality benchmarks are met but also risk payment reductions if they are not

More from Archive

Final Chance To Have Your Say: Take Our Reader Survey This Week

 

Editor’s note: This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Early Development Deals: Ipsen's Strategy For Biomarker-Driven Success

 

Mary Jane Hinrichs, Ipsen’s head of early development, talks to In Vivo about getting ahead of the competition by securing deals for candidates before they enter Phase I trials.   

Shape Our Content: Take The Reader Survey

 

Editor’s note: We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in the coverage topics, content format or the method in which you receive and access In Vivo, or if you love it how it is, now is the time to have your voice heard.

In Partnership with Cerba Research

Prioritizing Safety in CAR-T Therapy: Patient Monitoring with Cerba Research’s Testing Portfolio

The cell and gene therapy (CGT) clinical trial landscape in general and CAR-T cell clinical trials in particular are a special focus for the FDA, EMA, and other regulatory agencies. The whole industry is thus aware of the recent FDA safety investigation and requirements for labeling CAR therapy products.

More from In Vivo

NewAmsterdam’s Davidson On Reviving “Failed” Drug Class To Fill Cardiovascular Treatment Gap

 
• By 

After a string of high-profile failures by big pharma, Michael Davidson is positioning his company's CETP inhibitor as the next breakthrough in cardiovascular medicine. The body of data to support this position is growing.

Dealmaking Quarterly Statistics, Q1 2025

 
• By 

During Q1, biopharma M&A deal value reached $38.4bn and drew in $60.8bn in potential deal value from alliances. Device company M&A values reached $8.7bn.

Rising Leaders 2025: Flagship’s Jacob Rubens On Building The Next Generation Of Biotech

 
• By 

Rising Leader Jacob Rubens, who has co-founded and led several Flagship companies and is now origination partner, believes aspiring leaders should follow their bliss.