21st Century Cures Act

21st Century Cures Act
Great Seal of the United States
Other short titles Helping Families in Mental Health Crisis Reform Act of 2016
Increasing Choice, Access, and Quality in Health Care for Americans Act
Long title An Act to accelerate the discovery, development, and delivery of 21st century cures, and for other purposes.
Enacted by the 114th United States Congress
Citations
Public law 114 - 255 Pub.L. 114 – 255
Legislative history

The 21st Century Cures Act is a United States law enacted by the 114th United States Congress in December 2016. It authorized $6.3 billion in funding, mostly for the National Institutes of Health.[1] The act was supported especially by large pharmaceutical manufacturers and was opposed especially by consumer organizations.[2]

The bill included the Helping Families In Mental Health Crisis Act, a landmark mental health reform bill which, according to Fortune, "increase the availability of psychiatric hospital beds, establish a new assistant secretary for mental health and substance use disorders in the Department of Health and Human Services (HHS), and boost treatment for young mental health patients, among other provisions."[3] This mental health component was the most significant attempt at mental health reform in decades.[4]

Content

Research and drug development

Division A, which shares the title “21st Century Cures Act,” contains provisions related to National Institutes of Health funding and administration, reducing opioid abuse, medical research, and drug development.[5]

Opioid epidemic

The Comprehensive Addiction and Recovery Act (CARA) was passed a few months earlier. This act authorized many harm-reduction strategies, including increased access to the overdose reversal drug naloxone, for the opioid crisis, but didn't provide any federal funding for implementation.[6] The 21st Century Cures Act designated $1 billion in grants for states over two years to fight the opioid epidemic.[6][7] The money may be used to improve prescription drug monitoring programs,[7] to make treatment programs more accessible, to train healthcare professionals in best practices of addiction treatment, and to research the most effective approaches to prevent dependency.[6][7]

FDA drug approval process

The 21st Century Cures Act modified the FDA Drug Approval process. It was intended to expedite the process by which new drugs and devices are approved by easing the requirements put on drug companies looking for FDA approval on new products or new indications on existing drugs. For instance, under certain conditions, the act allows companies to provide "data summaries" and "real world evidence" such as observational studies, insurance claims data, patient input, and anecdotal data rather than full clinical trial results.[6][8][9]

The 21st Century Cures Act allows researchers to waive the requirement for "informed consent" in specific cases where the devices being tested don't pose any health risks beyond those of normal everyday life and wouldn't direct a patient's care in any way. An example that has been given is a high-tech bandage that monitors blood flow from a serious wound, which functions just like a regular bandage but only has this added benefit of possibly monitoring blood flow. Ordinarily, researchers would obtain the patient's permission before testing any new device on them. However, in this example, researchers might want to test the bandage in a real-world scenario where patients may not be conscious. In such circumstances, researchers may waive an informed consent requirement, since it would be difficult or impossible to obtain, and the patient is still getting the standard, medically accepted care of blood pressure and heart rate monitoring. Researchers will still need to obey standard research protocols including institutional review boards to approve their research design and ethics.[6]

Medical research

The act allocates $4.8 billion to the National Institutes of Health for precision medicine and biomedical research.[1][6][8] Of this, $1.5 billion is earmarked for research on brain disease.[1] Another $1.8 billion is dedicated to cancer research in what is called the "Beau Biden Cancer Moonshot" initiative, named in honor of Vice President Joe Biden's son, who died of brain cancer in 2015.[1][6][10][11]

Strategic Petroleum Reserve sales

The act requires sale of 25 million barrels of crude oil (10,000,000 in 2017, 9,000,000 in 2018, and 6,000,000 in 2019) from the Strategic Petroleum Reserve.[12][13] Revenue from these sales will provide part of the NIH funding provided in the law.[14]

Behavioral health

Division B of the law, the “Helping Families in Mental Health Crisis Reform Act of 2016,” addresses the prevention and treatment of mental illnesses and substance abuse, treatment coverage, communication permitted by HIPAA, and interactions with law enforcement and the criminal justice system.[15]

The law strengthens mental health parity regulation,[7] which require insurance companies to cover mental health treatments to the same extent and in the same way as medical treatments. It also includes grants to provide community mental health resources, suicide prevention and intervention programs, and de-escalation training for law enforcement.[6] It also provides five-year grants for a demonstration program in which psychiatry residents and other mental health clinicians will practice in underserved areas.[7]

Some of these provisions were originally proposed in earlier bills, including the Mental Health Reform Act of 2016 (S. 2680); the Mental Health and Safe Communities Act of 2015 (H.R. 3722, S. 2002); the Helping Families in Mental Health Crisis Act of 2016 (H.R. 2646); the Comprehensive Justice and Mental Health Act of 2015 (H.R. 1854, S. 993); the Mental Health Awareness and Improvement Act of 2015 (H.R. 5327, S. 1893); the Justice and Mental Health Collaboration Act of 2015 (H.R. 731); and the Behavioral Health Care Integration Act of 2016 (H.R. 4388).[16]

Healthcare access and quality improvement

Division C of the law, the “Increasing Choice, Access, and Quality in Health Care for Americans Act,” concerns Medicare programs and federal tax laws related to health plans for small employers.[17]

Legislative history

Another bill with the same name, H.R. 6, was introduced by Fred Upton (R–MI) on May 19, 2015. It passed the House on July 10, 2015. but in the Senate, it died in committee.[18]

More than 1,400 registered lobbyists worked on this bill, representing more than 400 different organizations,[9] mostly pharmaceutical companies.[8] The bill passed the House first by a wide margin.[19] Only five senators voted against it: Elizabeth Warren of Massachusetts, Bernie Sanders of Vermont, Ron Wyden and Jeff Merkley, both of Oregon, all Democrats, and Mike Lee, a Republican of Utah.[20] Warren, Sanders and Merkley, in particular, objected to the pharmaceutical industry's influence on the bill.[2] In early December 2016, the act had support from both houses of congress.[21][22]

President Obama signed the act on December 13, 2016.[23] The reasons stated for his support included counting opioid abuse, advancing cancer research, advancing the BRAIN Initiative, advancing the Precision Medicine Initiative, and addressing bipartisan health issues.[23]

Reception

Stakeholders who praised the passing of the act include drug companies; medical device manufacturers; the National Institutes of Health; people advocating for lowered barriers to collecting human subject research data; Representatives Fred Upton (R-MI), Diana DeGette (D-CO), Timothy F. Murphy (R-PA); Senator Lamar Alexander (R-TN); and Vice President Joe Biden.[8] Hospitals and universities,[9] as well as the American Cancer Society Action Network, Research!America, and FasterCures supported the bill for its commitment toward funding research.[8] The American Psychological Association supported the bill due to its mental health provisions.[24] The Advanced Medical Technology Association supported the bill for easing the process of introducing new medical technologies.[8] The American Society of Human Genetics (ASHG) commended the passage of the bill for strengthened genetic privacy for research participants.[25][26][27] Prison Fellowship supported the bill due to its inclusion of the Comprehensive Justice and Mental Health Act, a portion designed to encourage collaboration among criminal justice, juvenile justice, mental health treatment, and substance abuse systems.[28][29]

Stakeholders who criticized the passing of the act include the FDA, advocates for strong protections in clinical research, consumer organizations, and advocates of regenerative medicine.[8] The expedited drug approval process has been one topic of concern and debate[1] The Public Citizen’s Health Research Group and the National Center for Health Research campaigned against the Cures Act in fear that it will endanger public health by weakening FDA standards.[8] Senator Elizabeth Warren said that the bill had been “hijacked” by the pharmaceutical industry. She said the legislation watered down safety requirements for new drugs and devices and then, as a trade-off, called for research funding — at levels that must be appropriated on an annual basis.[8] John LaMattina, former head of Pfizer research and development and current commentator on the pharmaceutical industry, said that full clinical trials are necessary to prove effectiveness, and suggests some drugs may now be approved based on early data and only later proved ineffective.[9] The Public Citizen’s Health Research Group says the designation of “breakthrough” devices is too broad, and could lead to clearance of devices that aren’t ready for the market.[8]

Lupkin points out that the NIH’s funding will need to be appropriated each year through the normal budget process, and therefore may be reduced from what this bill promised.[9] The NIH funding was actually less than many advocates hoped for,[8][9] and earlier versions of the bill had promised.

See also

References

  1. 1 2 3 4 5 "Learn from Cures Act bipartisanship". Editorial. Asbury Park Press. Asbury Park, NJ: Gannett. 17 December 2016. Retrieved 31 December 2016.
  2. 1 2 Mukherjee, Sy (7 December 2016). "Everything You Need to Know About the Massive Health Reform Law That Just Passed Congress". Fortune. Retrieved 14 December 2016.
  3. ↑ Congress Is on the Verge of Passing a Landmark Mental Health Bill
  4. ↑ House Passes Most Significant Mental Health Reform Bill in Decades
  5. ↑ H.R. 34 Division A—21st Century Cures
  6. 1 2 3 4 5 6 7 8 Jacoby, Sarah (December 16, 2016). "What The Controversial 21st Century Cures Act Means For You". Refinery29. Retrieved 31 December 2016.
  7. 1 2 3 4 5 Levin, Aaron (December 30, 2016). "Obama Signs Landmark Legislation With Major Mental Health Provisions". Psychiatric News. doi:10.1176/appi.pn.2017.1a10.
  8. 1 2 3 4 5 6 7 8 9 10 11 Kaplan, Sheila (5 December 2016). "Winners and losers of the 21st Century Cures Act". STAT News. Retrieved 31 December 2016.
  9. 1 2 3 4 5 6 Franz, Julia (December 25, 2016). "America's new 21st Century Cures Act will speed up drug approvals. Is that a good thing?". PRI. Retrieved 31 December 2016.
  10. ↑ Biden, Joe; Obama, Barack (13 December 2016). "Remarks by the President and the Vice President at the 21st Century Cures Act Bill Signing" (Press release). Washington, DC: The White House, Office of the Press Secretary. Retrieved 31 December 2016.
  11. ↑ "AACR Commends President Obama for Signing the 21st Century Cures Act" (Press release). Philadelphia, PA: American Association for Cancer Research. 13 December 2016. Retrieved 2016-12-31.
  12. ↑ "This Week in Petroleum". US Department of Energy. 21 December 2016. Retrieved 21 December 2016.
  13. ↑ H.R. 34, Sec. 5010. Strategic Petroleum Reserve Drawdown.
  14. ↑ Lupkin, Sydney (25 November 2016). "Legislation That Would Shape FDA And NIH Triggers Lobbying Frenzy". Shots: Health News from NPR. National Public Radio.
  15. ↑ H.R. 34 Division B—Helping Families in Mental Health Crisis
  16. ↑ "H.R. 34 (114th): 21st Century Cures Act". GovTrack. Civic Impulse, LLC. Retrieved January 10, 2017.
  17. ↑ H.R. 34 Division C—Increasing Choice, Access, and Quality in Health Care for Americans
  18. ↑ "Actions - H.R.6 - 114th Congress (2015-2016): 21st Century Cures Act". Congress.gov. Library of Congress. July 13, 2015. Retrieved January 10, 2017.
  19. ↑ Kaplan, Sheila (30 November 2016). "House approves the 21st Century Cures Act, sending landmark bill to Senate". Stat.
  20. ↑ Johnson, Lorie (13 December 2016). "Enormous, Expensive 21st Century Cures Act Signed Into Law". CBN News. Retrieved 31 December 2016.
  21. ↑ Pear, Robert (8 December 2016). "Cures Act Gains Bipartisan Support That Eluded Obama Health Law". The New York Times. Retrieved 14 December 2016.
  22. ↑ Ornstein, Norm. "Congress Achieves a Rare Bipartisan Victory for Science". The Atlantic. Retrieved 14 December 2016.
  23. 1 2 Somanader, Tanya (13 December 2016). "3 Letters That Explain Why President Obama Is Signing the Cures Act". whitehouse.gov. Retrieved 14 December 2016.
  24. ↑ Sliwa, Jim (1 December 2016). "APA Hails House Passage Of Mental Health Provisions In 21st Century Cures Act" (Press release). Washington, DC: American Psychological Association. Retrieved 31 December 2016.
  25. ↑ Padmanabhan, Nalini (7 December 2016). "ASHG Supports Genetic Privacy Provisions in 21st Century Cures Act" (Press release). Bethesda, MD: American Society of Human Genetics. Retrieved 2 January 2017.
  26. ↑ Thompson, Dennis (8 December 2016). "Congress passes 21st Century Cures Act with billions for new research, treatments". CBS News. CBS Interactive Inc. Retrieved 2 January 2017.
  27. ↑ Enzi, Mike (15 December 2016). "Congress acts to protect the most personal data – genetic information". Opinion. Pine Bluffs Post. 108 (50). Pine Bluffs, WY. Retrieved 2 January 2017.
  28. ↑ DeRoche, Craig (29 November 2016). "Urgent need for support for 21st Century Cures Act". PrisonTalk.com. Retrieved 22 February 2017.
  29. ↑ DeRoche, Craig (14 December 2016). "Dear Scotty". New Abolitionists Radio. Retrieved 22 February 2017.
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