Johnson & Johnson COVID vaccine use in US should resume, CDC panel recommends

The pause on the Johnson & Johnson COVID-19 vaccine should be lifted with no extra warning to young women about a small risk of a rare clotting disorder, an expert advisory committee to the Centers for Disease Control and Prevention said Friday.

The recommendation by the CDC committee, called the Advisory Committee on Immunization Practices, has to be approved by the CDC and the Food and Drug Administration before becoming official government policy.

The advisory committee spent the day discussing the rare side effect, but in the end decided by a vote of 10 to 4 that the vaccine should be returned to the market without any conditions or warnings.

“This is a serious adverse event. we need to continue to ensure that awareness is raised,” said Dr. Grace Lee, a pediatrician at the Lucile Packard Children’s Hospital and Stanford University School of Medicine

in Stanford, California. “But I also think that we have to come out with a clear recommendation.”

Dr. Pablo Sanchez, a pediatrician at The Ohio State University – Nationwide Children’s Hospital in Columbus and one of the four “no” votes said he supports returning the vaccine to the market, but felt it was important to add a warning. “We have to have stronger language to ensure people are (fully informed),” he said.

CDC staff reported there have been 15 cases of the unusual disorder, among 7.89 million doses of the J&J vaccine delivered in the United States.

The rare condition includes a combination of blood clots, many in unusual locations such as the brain or abdomen, and low levels of platelets, which help wounds heal. It has been dubbed thrombosis with thrombocytopenia syndrome or TTS.

The unusual side effect, seen six to 14 days after receiving the J&J vaccine, seems to most often strike women under age 50.

Similar unusual events were seen among British and European recipients of a different COVID-19 vaccine, made by AstraZeneca and Oxford University, which uses a similar delivery system as J&J’s shots. The AstraZeneca-Oxford vaccine, which is not available in the United States, also seems to strike women more than men, though of a wider age range.

The effect has not been seen with the two other vaccines authorized for use in the U.S., by Pfizer-BioNTech and Moderna, which have so far been given to about 130 million Americans.

Resuming the use of the J&J vaccine in the United States would prevent 1,435 deaths from COVID-19 and 2,236 admissions to hospital intensive care units, according to a CDC analysis. It could cause approximately 24 cases of TTS, a CDC staffer said.

Three of the 15 known patients have died, roughly 20% of those diagnosed with TTS so far; an additional five people would be likely to die if use of the vaccine were resumed, according to a CDC analysis.

The J&J vaccine has been popular for some people because it only requires a single shot.

“Removing a vaccine that can be given as a single dose, which is a preference for Latinos in our community, would be a detriment,” said Dr. José Romero, chair of the committee and director of the Arkansas Department of Health.

The J&J shot has been especially popular for use in difficult-to-reach populations, such as people experiencing homelessness, the homebound, incarcerated individuals and college students.

“We really do depend on this ‘one dose and you’re done’ vaccine with easy storage” to reach at-risk populations, said Dr. Sandra Fryhofer, a professor of medicine at Emory University School of Medicine and liaison to the committee.

​Americans also want to have some choice about which vaccine they receive, said Dr. Beth Bell, a professor of global health at the University of Washington.

“This is a time when we need options and flexibility,” she said.

The United States remains in the middle of a COVID-19 outbreak and so needs those options now, she noted. But recommendations could change as more information about the risks and benefits of vaccines becomes available.

Several panel members praised the CDC for recognizing and acting on the safety concern so quickly.

The FDA and the CDC first recommended the pause on April 13 after several reports of the unusual blood clotting condition showed up in the CDC’s vaccine monitoring system.

Last Wednesday the advisory committee decided the pause should continue until at least Friday as the CDC gathered more information on the condition and more cases could potentially be identified. At that time, there were eight known cases of the condition.

It was very reassuring that so few additional cases have been identified since, said Dr. Grace Lee, a professor of pediatrics at Stanford University School of Medicine.

“The last 11 days for me have been reassuring in that we haven’t identified hundreds of more cases despite enhanced focus, which was my worry last week,” she said. “Last week I would have made a different decision than I would this week.”

TTS is so rare that the expert testifying before the CDC panel said he’d never seen it before.

Dr. Michael Streiff, a hematologist at the Johns Hopkins University School of Medicine, said it occurred in about 1 out of 100,000-250,000 recipients of either the J&J or AstraZeneca-Oxford vaccines.

Thrombocytopenia occurs when someone has fewer than 150,000 platelets, also known as thrombocytes, per microliter of blood. Dangerous internal bleeding can occur with platelet counts below 10,000, a figure reached by many of the patients with TTS. Such severe thrombocytopenia can cause fatal bleeding into the brain.

Most of the blood clots, also called thromboses, occurred in the brain, though several were in the abdomen.

Public health officials have warned that anyone who develops a severe headache or leg or abdominal pain a week or two after vaccination with the J&J vaccine should seek immediate attention.

This side effect is different from initial reactions to a vaccine, which start a day or two after a shot and are short-lasting.

Streiff also recommended that these patients not be given heparin, a drug commonly used to combat blood clots, as it may exacerbate symptoms. None of the three TTS patients who died received heparin, but six were given the drug before the pause.

Overall, the committee decided the benefits of the J&J vaccine still outweigh the chance of this very rare side effect.

COVID-19 itself causes 200 people to be hospitalized and leads to 30 deaths out of every million Americans, CDC numbers show, compared to 15 hospitalizations and three deaths out of more than 7 million who received the J&J vaccine.

“The overwhelming risk benefit here is ‘Get the vaccine you can get,’” said Dr. Robert Gluckman, chief medical officer of Providence Health Plans, a health network in Oregon.

Contact Elizabeth Weise at eweise@usatoday.com and Karen Weintraub at kweintraub@usatoday.

Health and patient safety coverage at USA TODAY is made possible in part by a grant from the Masimo Foundation for Ethics, Innovation and Competition in Healthcare. The Masimo Foundation does not provide editorial input.

The FDA and CDC are recommending a pause on the Johnson  & Johnson COVID vaccine after six women developed rare blood clots.

You may also like...