The Impact Of Eliminating Kickbacks on Clinical Lab Practices In Phlebotomy

The Eliminating Kickbacks in Recovery Act (EKRA) was enacted in October 2018 as part of an effort to combat opioid abuse and fraud in healthcare. This law has far-reaching implications for a variety of Healthcare Providers, including clinical laboratories that employ phlebotomists. In this article, we will explore the potential changes that EKRA might bring into the clinical lab practices in phlebotomy.

Background of EKRA

EKRA was passed as part of the Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and Communities Act (SUPPORT Act). The primary goal of EKRA is to combat patient brokering and kickbacks related to substance abuse treatment facilities. However, the language of the law is broad and could potentially impact a wide range of Healthcare Providers, including clinical laboratories.

Potential Changes in Clinical Lab Practices

Restrictions on Referrals

One of the key provisions of EKRA is that it prohibits Healthcare Providers from making or accepting referrals for services covered by Medicare or Medicaid in exchange for any form of remuneration. This includes payments, discounts, or any other type of compensation.

Impact on Phlebotomy Services

Phlebotomy services are an essential part of clinical laboratory practices, as phlebotomists collect blood samples for testing and analysis. With the restrictions on referrals imposed by EKRA, clinical laboratories may need to reassess how they market their phlebotomy services and how they compensate phlebotomists.

Greater Transparency

Another potential change that EKRA could bring to clinical lab practices in phlebotomy is greater transparency in financial relationships. Healthcare Providers will need to carefully document any payments or compensation related to phlebotomy services and ensure that these transactions comply with EKRA guidelines.

Increased Compliance Requirements

With the passage of EKRA, clinical laboratories that employ phlebotomists will need to establish compliance programs to ensure that they are following the law. This may include training staff on EKRA requirements, conducting regular audits of financial relationships, and implementing policies to prevent kickbacks or patient brokering.

Potential Impact on Reimbursement

There is also a possibility that EKRA could impact Reimbursement for phlebotomy services. If clinical laboratories are found to be in violation of EKRA, they may face penalties, including fines and exclusion from federal healthcare programs. This could ultimately affect their ability to receive Reimbursement for services.

Challenges and Considerations

Interpretation of EKRA

One of the challenges that clinical laboratories may face in response to EKRA is interpreting the law and understanding how it applies to their specific practices. EKRA is a complex law with broad implications, and Healthcare Providers may need to seek legal counsel to ensure compliance.

Resource Allocation

Complying with EKRA may require clinical laboratories to allocate additional resources to ensure that they are following the law. This could include hiring compliance officers, conducting training for staff, and investing in new systems for tracking financial relationships.

Impact on Patient Care

There is a concern that increased compliance requirements and restrictions on referrals imposed by EKRA could impact patient care. If clinical laboratories are forced to limit their financial relationships with other Healthcare Providers, it may hinder collaboration and communication, ultimately affecting the quality of care that patients receive.

Evolving Regulatory Landscape

As with any new law, the regulatory landscape surrounding EKRA is likely to evolve over time. Clinical laboratories will need to stay informed about changes to the law and adjust their practices accordingly to ensure compliance and avoid potential penalties.

Conclusion

EKRA represents a significant shift in the healthcare regulatory landscape and has the potential to bring about changes in clinical lab practices, including those related to phlebotomy. Healthcare Providers will need to carefully review their practices, establish compliance programs, and ensure that they are following the law to avoid penalties and protect patient care.

Disclaimer: The content provided on this blog is for informational purposes only, reflecting the personal opinions and insights of the author(s) on phlebotomy practices and healthcare. The information provided should not be used for diagnosing or treating a health problem or disease, and those seeking personal medical advice should consult with a licensed physician. Always seek the advice of your doctor or other qualified health provider regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. If you think you may have a medical emergency, call 911 or go to the nearest emergency room immediately. No physician-patient relationship is created by this web site or its use. No contributors to this web site make any representations, express or implied, with respect to the information provided herein or to its use. While we strive to share accurate and up-to-date information, we cannot guarantee the completeness, reliability, or accuracy of the content. The blog may also include links to external websites and resources for the convenience of our readers. Please note that linking to other sites does not imply endorsement of their content, practices, or services by us. Readers should use their discretion and judgment while exploring any external links and resources mentioned on this blog.

Previous
Previous

What Changes Were Made to the Valid Act in the Omnibus Package

Next
Next

Adapting Lab Procedures and Protocols in a Value-Based Care Model