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4 Policy Changes that Can Accelerate Healthcare Research

4 Policy Changes that Can Accelerate Healthcare Research

Imagine a world where groundbreaking healthcare research faces fewer hurdles and reaches patients faster. In this article, an Owner and a Physician Assistant share their perspectives on the four policy change that could revolutionize healthcare research. The discussion opens with the need to implement a fast-track approval process and concludes with the importance of making medical data publicly available. With four insightful contributions, this exploration of expert opinions offers a comprehensive look at transformative policy changes in healthcare.

  • Implement Fast-Track Approval Process
  • Enable Real-Time Collaboration
  • Mandate Comprehensive Data-Sharing
  • Make Medical Data Publicly Available

Implement Fast-Track Approval Process

One important policy change that could speed up progress in healthcare research is creating a fast-track approval process for innovative medical technologies. Right now, it can take a long time for new treatments and devices to get approved, especially for cutting-edge areas like gene editing or personalized medicine. While safety is critical, the long wait times can slow down how quickly patients get access to life-saving treatments. It goes without saying that this needs to be balanced with the safety of the devices.

A fast-track approval process would focus on technologies that show significant promise in early trials, allowing them to reach patients faster while still ensuring they are safe and effective. This change would not only help patients but also encourage more companies and researchers to invest in groundbreaking, high-risk research areas. When there's a quicker path to market, there's more incentive to develop new and innovative therapies.

Enable Real-Time Collaboration

I'd like to see more real-time collaboration between researchers and those working in the field. As a physician assistant, I see small issues daily that could have been corrected in the research-and-development phase had these teams had access to active clinics. Take, for example, device design. Too many medical devices only wind up in the hands of doctors or nurses once they're brought to market. This leads to decreased efficacy—what works in a lab can sometimes be cumbersome in practice. Additional prototypes, or even a simple conversation with end-users, could speed progress and streamline results.

Another example is sampling. Researchers have less access to patients than we do. Looping in clinicians would increase their access to larger and more appropriate sample groups. It would likely also decrease dropouts.

Carlos da Silva
Carlos da SilvaPhysician Assistant, PA Career Hub

Mandate Comprehensive Data-Sharing

I've observed that mandating comprehensive data-sharing between addiction treatment centers could revolutionize our understanding of recovery patterns and treatment efficacy. While many advocate for broader research funding, the real breakthrough would come from creating standardized protocols for tracking long-term recovery outcomes across different treatment modalities—something I've seen firsthand improve success rates in our facility's personalized treatment approaches.

The impact of this policy change would extend beyond traditional metrics, particularly in understanding the intersection of cultural factors and addiction recovery—an insight I gained through my own journey as an immigrant navigating substance abuse treatment. Currently, valuable data about how different demographic groups respond to various treatment approaches remains siloed within individual facilities. By implementing secure, anonymous data-sharing protocols, we could identify previously overlooked patterns in recovery success rates and develop more effective, culturally informed treatment strategies that address the complex nature of addiction recovery.

Make Medical Data Publicly Available

Medical data should become publicly available (anonymized) for research purposes after a certain period (a couple of years).

A regulation requires healthcare providers to store medical data (including medical imaging like CTs, MRIs, etc.) for 10-15 years after it has been produced. Some imaging, like mammographies, has to be stored for a lifetime.

If this data becomes public (or at least available for research), it will provide an excellent dataset for researchers to explore and validate various hypotheses. Right now, maybe half of the resources of any research initiative go into data-gathering and data collection. If we can reduce this overhead, researchers would be able to iterate much faster.

Andrei Blaj
Andrei BlajCo-founder, Medicai

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