Facing growing criticism, the Department of
Veterans Affairs said Friday that it will not halt use of an unproven
malaria drug on veterans with COVID-19 but that fewer of its patients
are now taking it.
In responses provided to Congress and obtained by The
Associated Press, the VA said never “encouraged or discouraged” its
government-run hospitals in any way to use the drug hydroxychloroquine
on patients even as President Donald Trump heavily touted it for months
without scientific evidence.
“VA has not endorsed nor discouraged the use of
hydroxychloroquine in COVID-19 patients and has left those decisions to
providers and their patients,” the VA said. “While all drugs have the
potential for adverse events and some drugs in particular, like
hydroxychloroquine, are known to have specific risks, when they are used
carefully and judiciously, they can be managed safely.”
As of Friday, 11,883 veterans overall have been infected with the virus and 985 have died, according to VA statistics.
Responding to written questions from Sen. Jon Tester, the
top Democrat on the Senate Veterans Affairs Committee, the department
admitted it had no studies or evidence to back up Wilkie’s claim that
hydroxychloroquine had shown effectiveness in younger veterans in
particular.
“The use of hydroxychloroquine for COVID has dropped off dramatically,” the VA said.
Tester, who received VA’s responses this week, said he
remained concerned about the safety of the drug after a recent analysis
of VA hospital data showed the drug had no benefit.
“Any drug used to treat patients with COVID-19, especially
veterans living with debilitating pre-existing conditions, must be
proven safe and effective before it’s administered,” he said. “Given
recent studies from both VA and other hospitals, hydroxychloroquine
seems to fall short of those requirements.”
Major veterans’ organizations and congressional Democrats
including Senate Minority leader Charles Schumer of New York had called
on VA to explain why it allowed the use of an unproven drug on vets.
Last week, a whistleblower complaint by former HHS official Rick Bright
alleged that the Trump administration, eager for a quick fix to the
onslaught of the coronavirus, wanted to “flood” hot spots in New York
and New Jersey with the drug.
The analysis of hospital data, done by independent
researchers at two universities with VA approval, was not a rigorous
experiment. Researchers analyzed medical records of 368 older male
veterans hospitalized with confirmed coronavirus infection at VA medical
centers who died or were discharged by April 11.
About 28% of veterans who were given hydroxychloroquine plus usual care died, versus 11% of those getting routine care alone.
In its response to Congress, the department provided copies
of some of its guidance issued to VA physicians on hydroxychloroquine
from March to May. It made clear that hydroxychloroquine should be
considered mostly for use in clinical trials or when medically
appropriate after a full discussion with the patient about risks.
The VA did not explain the circumstances in which veterans
in the recent analysis of hospital data were given the drug, only
suggesting that “it is possible” they were prescribed as part of
last-ditch efforts to save a patient’s life.
“Based on the principles of patient-centric care, it would
be inappropriate to deny patients access to hydroxychloroquine under
these dire circumstances,” VA wrote. It said it had followed the
approach of the National Institute of Allergies and Infectious Diseases
by “summarizing the medical literature regarding unapproved treatments
for COVID-19 and making that available to VA clinicians in their shared
decision-making with patients.” That guidance now includes preliminary
studies on remdesivir, which has been federally approved for emergency
use to treat COVID-19.
One VA document dated March 25 and obtained by the AP, notes
to VA doctors that a few “very small cohort studies” showing possible
“beneficial effects” but adds “these data have NOT been verified in
randomized controlled trials and are extremely preliminary” and that
prescriptions should only be made “after thorough consideration of all
possible risks and benefits.”
Other VA memos, updated in April and early May, note the
drug had not been federally approved for COVID-19 and had potential
serious side effects.
The VA acknowledged to Congress it had placed bulk orders
for hydroxychloroquine from Feb. 1 to April 23 for 6.3 million tablets
worth $208,000 in anticipation of a possible shortage of the drug but
that most of it was being used for approved uses, such as treating lupus
and rheumatoid arthritis. It said it did not have breakdowns.
The department also said it planned further studies and
clinical trials on hydroxychloroquine, including whether it could help
prevent infection in veterans who were potentially exposed to COVID-19.
It currently is in discussions with Novartis to have some VA facilities
participate in a national clinical trial that will look at the
effectiveness of hydroxychloroquine in combination with azithromycin in
patients with moderate and severe disease.
Hydroxychloroquine has long been used to treat malaria and
other ailments. A few, very small preliminary studies suggested it might
help prevent the coronavirus from entering cells and possibly help
patients clear the virus sooner. But the FDA last month warned doctors
against prescribing the drug for COVID-19 outside hospitals because of
the risks of serious side effects and death.
https://www.modernhealthcare.com/providers/va-says-it-wont-stop-use-unproven-drug-vets-now
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.