Health agencies’ credibility at risk

The credibility of two of the nation’s leading public health agencies was under fire this week.

WASHINGTON » The credibility of two of the nation’s leading public health agencies was under fire this week after controversial decisions that outside experts said smacked of political pressure from President Donald Trump as he attempts to move past the devastating toll of the coronavirus ahead of the November election.

The head of the Food and Drug Administration grossly misstated, then corrected, claims about the lifesaving power of a plasma therapy for COVID-19 authorized by his agency. Then the Centers for Disease Control and Prevention quietly updated its guidelines to suggest fewer Americans need to get tested for coronavirus, sparking outrage from scientists.

Trump’s own factual misstatements about COVID-19 are well documented, but the back-toback messaging blunders by public health officials could create new damage, eroding public trust in front-line agencies. That’s already raising concerns about whether the administration will be forthcoming with critical details about upcoming vaccines needed to defeat the pandemic.

“I do worry about the credibility of the FDA and CDC, especially at a time when the capacity of the federal government to advance public health should be a priority for all policymakers,” said Daniel Levinson, former longtime inspector general of the Department of Health and Human Services, which oversees both the FDA and the CDC.

On Friday, FDA Commissioner Stephen Hahn removed a conservative public relations official involved in the botched plasma announcement from her role heading the agency’s press office, according to a person familiar with the matter, who spoke on condition of anonymity to describe private conversations.

The move came less than two weeks after the White House tapped Emily Miller for the role. Miller previously worked as a reporter for the right-wing One America News Network and as a staffer for Sen. Ted Cruz’s reelection campaign. She did not return calls seeking comment Friday.

An FDA spokesperson said late Friday that Miller remains an appointee within the agency.

Trump administration officials said Wednesday that the CDC testing guidance was revised by the White House virus task force “to reflect current evidence,” but did not detail what that was. The new recommendations say it’s not necessary for most people who have been in close contact with infected people, but don’t feel sick, to get tested. Outside experts said that flies in the face of the scientific consensus that wide-scale testing is needed to stamp out new infections.

The week began with Hahn forced to backtrack after using an erroneous statistic describing the effectiveness of the blood plasma therapy granted emergency use for COVID-19, as Trump twisted the facts and inflated the significance of the move.

Hahn “hurt his own credibility, he hurt that of his agency and he probably hurt the credibility of the next vaccine that will get approved,” said Daniel Carpenter, a Harvard University professor of government.

The U.S. has invested billions of dollars in efforts to quickly develop multiple vaccines against COVID-19. But public fears that a vaccine is unsafe or ineffective could be disastrous, derailing the effort to vaccinate millions of Americans.

The American Medical Association urged the FDA to set up new processes to keep the medical community in the loop on vaccine developments, warning that public confidence is at stake. The group has also challenged the CDC to produce scientific data to back up its new testing recommendation.

“We need to see light,” said Dr. Susan Bailey, AMA’s president. “There is a concern that if you are not seeing the data, you have to wonder why.”

A White House spokesperson said Friday that every decision the CDC and FDA have made under the Trump administration has been “data-driven to safely save lives.”

The administration’s Sunday rollout of the news that the FDA had granted emergency authorization for blood plasma in treating COVID-19 was marred by exaggerations and inaccuracies. The plasma, taken from patients who have recovered from the coronavirus, is rich in infection-fighting antibodies, which may benefit those still battling the disease.

Trump described the move as “historic” and touted the plasma’s “incredible rate of success.” But the FDA’s own scientific memo made clear that more research is needed to prove whether it works.

Hahn echoed Trump and Health and Human Services Secretary Alex Azar in claiming that 35 more people out of 100 would survive the coronavirus if they were treated with plasma. That figure grossly overstated preliminary findings from the Mayo Clinic, which cannot be used to draw broader conclusions about survival.

The error amounted to a rookie statistical mistake, particularly egregious for a cancer specialist like Hahn. He apologized for the misstatement more than 24 hours later.

The FDA’s press statement on plasma struck an unusually political tone for the science-based agency, touting the move as “another achievement in the administration’s fight against pandemic.”

Miller’s appointment as FDA’s assistant commissioner for media affairs was also unusual, given the position is typically held by FDA civil servants, not political appointees. Her previous stints in journalism had focused primarily on gun advocacy issues, not health or medicine.

In a parallel shakeup, HHS canceled the contract of a longtime FDA communications consultant who had advised Hahn to correct the misstatements on plasma.

“I did advise the commissioner to correct the record. I think that’s the correct position to take,” said Wayne Pines, in an interview with The Associated Press. “I have always been an advocate for protecting FDA’s reputation and the trust that the American public must have in the FDA.”

Pines said he didn’t know if the cancellation of his contract was related to his advice to Hahn. An HHS official declined to comment on personnel matters.

The FDA declined to make Hahn available for an interview but pointed to comments this week in which he said he accidentally misquoted the plasma survival figure in an effort to simplify information for patients. He also denied political pressure played any role in FDA’s decision on convalescent plasma.

Dr. Jesse Goodman, FDA’s former chief scientist, said convalescent plasma probably met the bar for FDA emergency authorization, which merely requires that potential benefits outweigh risks.

But he and other former FDA staffers said they disagreed with the decision and worried that it followed pressure from Trump.

“I believe that FDA made this decision itself, however that kind of pressure is very toxic and will erode trust in FDA decisions in the future,” said Goodman, now a professor at Georgetown University.

FDA staff generally supported the decision on plasma, according to a person familiar with the deliberations, who spoke on condition of anonymity to describe private conversations. The authorization makes it easier for U.S. hospitals to use it.

But several top scientists from the National Institutes of Health weren’t yet convinced of its effectiveness. The internal debate was first reported last week by The New York Times.

Trump reacted quickly, telling reporters: “It could be a political decision because you have a lot of people over there that don’t want to rush things because they want ... to do it after Nov. 3.”

Then, on Saturday, Trump fired off a Twitter blast aimed at the “deep state, or whoever, over at the FDA.”

Pressure from Azar also ratcheted up ahead of the FDA’s Sunday authorization, the person familiar with the discussions said.

HHS did not respond to questions about whether Azar pressed the FDA. Instead a spokesperson referred to recent interviews in which Azar denied politics influenced the decision.

Events surrounding the FDA’s plasma decision resembled the agency’s March authorization of hydroxychloroquine, the anti-malaria drug vigorously promoted by Trump.

After prodding by the White House, the FDA authorized distribution of the drug despite concerns. In June, the agency reversed course after studies showed the drug was ineffective and could cause sometimes fatal heart problems.