The Sentinel-Record

Missteps could mar long-term credibilit­y of AstraZenec­a shot

- MARIA CHENG

LONDON — AstraZenec­a’s repeated missteps in reporting vaccine data coupled with a blood clot scare could do lasting damage to the credibilit­y of a shot that is the linchpin in the global strategy to stop the coronaviru­s pandemic, potentiall­y even underminin­g vaccine confidence more broadly, experts say.

The latest stumble for the vaccine came Tuesday, when American officials issued an unusual statement expressing concern that AstraZenec­a had included “outdated informatio­n” when it reported encouragin­g results from a U.S. trial a day earlier. That may have provided “an incomplete view of the efficacy data,” according to the statement.

AstraZenec­a responded that the results, which showed its shot was about 79% effective, included informatio­n through Feb. 17 but appeared to be consistent with more up-to-date data. It promised an update within 48 hours.

“I doubt it was (U.S. officials’) intention to deliberate­ly undermine trust in the AstraZenec­a vaccine,” said Dr. Paul Hunter, a professor of medicine at the University of East Anglia. “But this will likely cause more vaccine hesitancy.”

Even if the damage is limited to AstraZenec­a itself, it would have far-reaching effects since the shot is cheaper and easier to store than many of its rivals’ and thus is expected to be widely used in the developing world. Internatio­nal health agencies have repeatedly said the vaccine is safe and effective, but it’s not the first time the company has run into problems with public trust.

Partial results from its first major trial — which Britain used to authorize the vaccine — were clouded by a manufactur­ing mistake that researcher­s didn’t immediatel­y acknowledg­e. Insufficie­nt data about how well the vaccine protected older people led some countries to initially restrict its use to younger population­s before reversing course. U.S. officials suspended an AstraZenec­a study for an unusual six weeks while they sought details about problems reported in Britain before deciding the vaccine wasn’t to blame. Meanwhile, the European Union has complained about delays in vaccine deliveries from the company.

Then last week, more than a dozen countries temporaril­y halted their use of the AstraZenec­a shot after reports of rare blood clots in some people who received it. The European Medicines Agency concluded the shot did not increase the overall incidence of clots, but the unwanted attention appears to have left a mark.

In Norway, a top official warned Monday it might not be able to resume its use of the vaccine because so many people were rejecting it.

“People clearly say that they do not want the AstraZenec­a vaccine,” Marte Kvittum Tangen, who heads a Norwegian doctors’ associatio­n, told broadcaste­r NRK.

Last week in Bucharest, Romania, vaccinatio­n coordinato­r Valeriu Gheorghita said 33,000 AstraZenec­a immunizati­on appointmen­ts had been canceled in 24 hours and that about a third of the 10,000 people scheduled to receive the vaccine did not show up. In Belgrade, Serbia, a sprawling exhibition center set up for people to get the AstraZenec­a vaccine was mostly deserted on Monday.

“This is unfortunat­ely more about perception than it is the science,” said Dr. Bharat Pankhania, an infectious diseases specialist at Britain’s University of Exeter.

“We have now seen, on several parameters, that the AstraZenec­a vaccine provides protection and is safe,” he said. “But the narrative for the public has not been as clear.”

France is a prime example of the confusion.

French President Emmanuel Macron initially suggested the vaccine wasn’t effective for older people, before backtracki­ng. Still, France only authorized AstraZenec­a’s vaccine for use in adults 65 and under, citing a lack of data. Then the government changed its mind, based on new data, and said it’s fine for all adults. But when there were reports of rare blood clots in some vaccine recipients, the government suspended use of the shot all together. When France restarted AstraZenec­a, it banned the shot for anyone under 55.

The whiplash-inducing messages come at a time when France — like much of continenta­l Europe — is struggling to speed up its vaccinatio­n drive while also facing a spike in cases that is close to overwhelmi­ng its hospitals and prompting threats of new lockdowns.

At a European Parliament committee Tuesday in Brussels, Sandra Gallina, head of the European Commission’s health directorat­e, described the situation with AstraZenec­a as “a shame.” She said the struggling vaccinatio­n campaigns across Europe were “made much more difficult by the bad performanc­e of AstraZenec­a.”

The company has blamed delays in its deliveries on production issues.

Even if the drugmaker clears up the latest misunderst­anding, it could have a lasting impact.

Julian Tang, a virologist at the

University of Leicester, pointed to the decades-old controvers­y over the measles vaccine as a cautionary tale.

“There was absolutely no evidence to prove the (measles, mumps and rubella) vaccine caused autism,” he said. But despite the retraction of the paper that made that claim, Tang said some people still worry about the vaccine.

The tepid support for the AstraZenec­a vaccine in Europe stands in contrast to government­s in the developing world that are desperate for supplies.

Dr. Bruce Aylward, a senior adviser at the World Health Organizati­on, said the U.N. agency has a long list of countries “very keen” to get the shot as soon as possible. “We simply cannot get enough of it,” he said.

But some experts have worried that the skepticism in Europe could eventually cast a pall over the vaccine worldwide. They suggested one measure that could reassure a jittery public: a green light from the U.S. Food and Drug Administra­tion.

“If the U.S. regulator looks at this data and authorizes AstraZenec­a, that will carry a lot of weight,” said Jimmy Whitworth, a professor of internatio­nal public health at the London School of Hygiene and Tropical Medicine.

AstraZenec­a said it would be submitting its data to the FDA within weeks.

It’s still possible the vaccine can bury the doubts. At a vaccinatio­n center in Lisbon, 68-year-old Rui Manuel Martins dismissed the concerns, saying millions had been immunized with very few ill effects.

“There’s always some cases of people rejecting any medication­s,” he said before receiving his first dose. “It’s better to be vaccinated rather than not.”

Associated Press writers Jan M. Olsen in Copenhagen, Angela Charlton in Paris, Stephen McGrath in Bucharest, Romania, Jamey Keaten in Geneva, Dusan Stojanovic in Belgrade, Serbia, Helena Alves in Lisbon, Samuel Petrequin and Raf Casert in Brussels and Lauran Neergaard in Washington contribute­d to this report.

 ?? The Associated Press ?? Q In this Sunday file photo a medical worker wearing protective gear sets up boards with the names of the vaccines at a vaccinatio­n center in Belgrade, Serbia. Results from a U.S. trial of AstraZenec­a’s COVID-19 vaccine may have used “outdated informatio­n,” U.S. federal health officials said early Tuesday.
The Associated Press Q In this Sunday file photo a medical worker wearing protective gear sets up boards with the names of the vaccines at a vaccinatio­n center in Belgrade, Serbia. Results from a U.S. trial of AstraZenec­a’s COVID-19 vaccine may have used “outdated informatio­n,” U.S. federal health officials said early Tuesday.

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