Stay up to date with notifications from The Independent

Notifications can be managed in browser preferences.

AFM: Mysterious polio-like illness affects children in 22 US states

Rare condition confuses doctors and researchers who fail to identify cause of paralysing disease

Wednesday 14 November 2018 15:58 GMT
Comments
CBS News medical contributor Dr. Tara Narula lists symptoms that herald onset of AFM

Your support helps us to tell the story

From reproductive rights to climate change to Big Tech, The Independent is on the ground when the story is developing. Whether it's investigating the financials of Elon Musk's pro-Trump PAC or producing our latest documentary, 'The A Word', which shines a light on the American women fighting for reproductive rights, we know how important it is to parse out the facts from the messaging.

At such a critical moment in US history, we need reporters on the ground. Your donation allows us to keep sending journalists to speak to both sides of the story.

The Independent is trusted by Americans across the entire political spectrum. And unlike many other quality news outlets, we choose not to lock Americans out of our reporting and analysis with paywalls. We believe quality journalism should be available to everyone, paid for by those who can afford it.

Your support makes all the difference.

US health officials are worried about an increase in a mysterious and rare condition that mostly affects children and can paralyse arms and legs, with more than 120 confirmed or suspected cases reported.

Of those, 62 cases of acute flaccid myelitis, or AFM, have been confirmed in 22 states, according to Nancy Messonnier, a top official at the Centers for Disease Control and Prevention (CDC).

More than 90 per cent of the confirmed cases have been in children 18 and younger, with the average age being four-years-old.

The surge in cases has baffled health officials, who on Tuesday took the unusual step of announcing a change in the way the agency will count cases in the future.

They also wanted to raise awareness about the frightening condition so parents can seek medical care if their child develops symptoms and so reports of the illness can be quickly relayed back to the CDC.

“We understand that people, particularly parents, are concerned about AFM,” said Ms Messonnier, director of the National Center for Immunisation and Respiratory Diseases. Despite extensive laboratory and other testing, CDC has not been able to find the cause for the majority of the cases. “There is a lot we don’t know about AFM, and I am frustrated that despite all of our efforts, we haven’t been able to identify the cause of this mystery illness.”

The increase in cases has been happening since 2014, usually in August and September, but only in 2014 and 2016, Ms Messonnier said in a news briefing with reporters. The CDC knows of one child who died with the disorder in 2017.

Since officials have been unable so far to determine how the disease spreads, they are starting to count suspected cases as well as confirmed to better anticipate increases in confirmed cases over the coming months, she said.

There is no specific treatment for the disorder and long-term outcomes are unknown. The rare but serious disorder affects a person’s nervous system, specifically the spinal cord. Neurological conditions like it have a variety of causes, such as viruses, environmental toxins and genetic disorders.

Among the cases under investigation are five reported to Maryland health officials in recent weeks, a health department spokeswoman said. Maryland’s first case was reported on 21 September. No known cases have been reported in Virginia or the District this year, but there were three confirmed cases in Virginia in 2016, health department officials said.

“We know this can be frightening for parents and I know many parents want to know what signs and symptoms they should be looking out for in their children,” Ms Messonnier said. Parents should seek medical care right away if their child develops sudden weakness or loss of muscle tone in the arms and legs.

Some patients diagnosed with this condition have recovered quickly, but some continue to have paralysis and require ongoing care, she said.

CDC began tracking the condition in 2014, when there were 120 confirmed cases. Then in 2016, there were 149 confirmed cases. Officials said it is too early to know whether the total for 2018 will surpass those previous years. But the data reported on Tuesday represents “a substantially larger number than in previous months this year,” Ms Messonnier said.

She said it was important for parents and clinicians to remember that this is a rare condition, affecting fewer than one in one million people under 18. “As a parent myself, I understand what it’s like to be scared for your child,” she said. “Parents need to know that AFM is rare even with the increase in cases we are seeing now.”

Still, because this is a “pretty dramatic disease”, Ms Messonnier said health officials want to raise awareness about the symptoms to make sure parents seek medical care immediately if their children show a sudden onset of weakness in their arms and legs.

The agency knows that poliovirus is not the cause of these cases, because CDC has tested every single stool specimen from patients, and none have tested positive for poliovirus. Ms Messonnier said West Nile virus, which had been listed as a possible cause on CDC’s website, is not causing the illnesses.

In some individuals, health officials have determined that the condition was from infection with a type of virus that causes severe respiratory illness.

So far, the CDC has found no relationship between vaccines and children diagnosed with AFM from the 2014 cases.

Officials will be conducting additional analysis on this year’s cases. “Our medical team has been reviewing vaccine records when available during this year’s investigation and do not see a correlation,” said CDC spokeswoman Kristen Nordlund. The disorder has been diagnosed in children who have received some of their recommended vaccinations and in unvaccinated children, she said.

The agency does not know who may be at higher risk of developing this condition or the reasons they may be at higher risk. CDC has tested many different specimens from patients with this condition for a wide variety of pathogens, or germs, which can cause AFM. But so far, no pathogen has been consistently detected in the patients’ spinal fluid.

Parents can best protect their children from serious diseases by taking prevention steps, such as washing their hands, staying up to date on recommended vaccines and using insect repellent to prevent mosquito bites, Ms Messonnier said.

There is no specific treatment for AFM, but neurologists who specialise in treating brain and spinal cord illnesses may recommend certain interventions, such as physical or occupational therapy, on a case-by-case basis.

Benjamin Greenberg, a neurologist who has treated children with AFM at the University of Texas Southwestern in Dallas, said AFM is “exquisitely rare”.

But, if their child is diagnosed, parents should prepare for extensive physical therapy – therapy that is not always covered by insurance, he said. Some children paralysed by AFM have eventually regained their ability to walk, but need time.

“Families really sticking with it are seeing slow but steady recovery,” he said.

CDC is not releasing a list of the 22 states with confirmed and suspected cases because of privacy issues. But some state health departments have been making public their reported cases. States are not required to provide this information to CDC, but they have been voluntarily reporting their data.

The Washington Post

Join our commenting forum

Join thought-provoking conversations, follow other Independent readers and see their replies

Comments

Thank you for registering

Please refresh the page or navigate to another page on the site to be automatically logged inPlease refresh your browser to be logged in