HAMDEN, Conn. (WFSB) – The family is speaking out in hopes of warning others about parechovirus.
When baby Ronan was born, he was a happy and healthy baby, but when he was about a week old his parents noticed something was wrong.
“We went from the highest high to the lowest low in a span of a month,” said Kat Delancy, Ronan’s mother.
In May, Kat and Mitch Delancy welcomed their second child, Ronan.
“He was a born May 21st a healthy full-term baby,” said Kat.
About a week after he was born, Kat noticed something wasn’t right.
“He was fussier, he wasn’t eating quite as well, and he had redness on his chest,” said Kat.
She took him to his pediatrician on a Friday and doctors said he was fine.
That night Kat says she felt something was wrong, so she brought him to Yale New Haven.
“As soon as I walked into the hospital, he stopped breathing,” said Kat.
Shortly after, Ronan started having seizures.
“Once they started seeing the seizures, they had to put him under sedation,” said Kat
Doctors couldn’t figure out what was going on with Ronan. It wasn’t until his 4th day in the hospital that Kat and Mitch got some answers.
“The more testing that they did they ended up finding this thing called parechovirus, which we had never heard of, and it sounded like a lot of the doctors had never heard of it either,” said Kat
“It was explained to us at the hospital that it’s extremely rare to find, but it might not be that rare because they don’t ever really look for it,” said Mitch, Ronan’s father.
Yale New Haven Health recently sent out a newsletter alerting other physicians about the virus, saying it “may be underdiagnosed due to lack of awareness.”
“A lot of children have no symptoms or very mild symptoms,” said Dr. Ian Michelo, CT Children’s Head of Infectious Diseases.
Dr. Michelo says he’s seen a spike in cases.
“I’m hearing through emails and other social media alerts that there is, particularly right now since the beginning of May, there are an increasing number of cases,” said Dr. Michelo.
He says most children will just suffer a fever but, in some cases, it could cause severe brain damage.
Unfortunately, Ronan had a severe case.
“I’ll never forget the doctor kneeling down and saying to me as I was in shock saying you have a very sick baby,” said Kat.
Ronan’s brain was severely damaged, and he couldn’t be saved.
“Going from the best days of our lives to having our child die in our arms,” said Kat.
Now, Kat and Mitch are hoping to warn other parents and push pediatricians to test for this disease more frequently.
“My big reason for wanting to talk about it is I want Ronan to have a legacy. I would love that. I want his name I want to keep that alive. I don’t want another family to go through this,” said Kat.
Doctors say preventing parechovirus is like any other virus, make sure to keep your hands clean and stay away from anyone who’s not feeling well.
Yale New Haven released a newsletter with more information on parechovirus that you can read here:
Parechoviruses in Neonatal Sepsis and Meningoencephalitis- Update
Parechovirus can cause neurologic disease in young infants, which can be severe, and may be underdiagnosed due to lack of awareness. This newsletter serves as a reminder of the clinical presentations in young infants and test availability since 2013 at Yale New Haven Hospital. In older children and adults, infection are usually mild or without symptoms.
In 1956, what we now call parechoviruses were first isolated from the stools of two children with diarrhea, and were designated as enteroviruses (EV), specifically echoviruses types 22 and 23 (1). However, when molecular methods were developed for pan-enterovirus diagnosis in the 1990s, these two echoviruses were not detected and thus were placed in a separate Parechovirus (PeV) genus, and a separate PCR was required for detection (2,3). Human infections are associated only with PeV species A and 18 PeV-A types have been identified.
Subclinical infections and clinical syndromes: Parechoviruses primarily cause inapparent infections in young children, and clinical syndromes similar to EV (4,5). PeV-A1 is the most commonly identified type and is primarily associated with asymptomatic or mild respiratory and gastrointestinal infections, and less frequently with CNS disease. The majority of PeV-A1 infections occur in children less than 1 year old, and almost all children are infected by age 5. Severe disease is rare.
In contrast, PeV-A3 is the most common PeV recovered from CSF and appears to have a biannual cycle. PeV-A3 has been shown to be specifically associated with sepsis and fever in young infants, especially those less than 3 months of age and with neonatal encephalitis with white matter injury (6-9). Indeed PeV-A3 has been reported as the leading cause of CNS infection in children, more common than any single EV type (10). A striking feature is that neonates with PeV-A3 encephalitis often have normal CSF findings (11). PeV-A3 was also identified as a cause of neonatal hepatitis-coagulopathy syndrome. It has been postulated that severe PeV-A3 neonatal infections may be due to lower seroprevalence of PeV-A3 antibody in women of child-bearing age and the lack of protective transplacental antibody, as well as different cellular tropism (12).
Parechovirus testing: Since July 2013, the Virology Laboratory has offered PeV PCR, including a combined PeV and EV PCR diagnostic panel intended for hospitalized children less than 5 years of age with enterovirus-like illness, in particular for neonatal sepsis and meningoencephalitis.
Test offered: The CDC Parechovirus real-time RT-PCR assay (13) is performed once a day, 5-6 days a week, and is available as both a single test and a combined EV/PeV panel. It is also now included in the febrile infant pathway.
Sample options: CSF, Blood (lavender tube), throat or nasopharyngeal swab, and stool.
For questions, contact Marie L. Landry, MD (firstname.lastname@example.org), Maureen Owen (email@example.com), or the Clinical Virology Laboratory at 203-688-3475.
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2. Stanway G, Hyypia T. Parechoviruses. J Virol 1999; 73:5249-5254.
3. Landry ML. The molecular diagnosis of parechovirus infection: has the time come? Clin Infect Dis 2010:50:362-3.
4. Harvala H, Simmonds P. Human parechoviruses: biology, epidemiology and clinical significance. J Clin Viol 2009; 45:1-9.
5. Harvala H, Wolthers KC, Simmonds P. Parechoviruses in children: understanding a new infection. Curr Opin Infect Dis. 2010; 23:224-30.
6. Boivin G, Abed Y, Boucher FD. Human parechovirus 3 and neonatal infections. Emerg Infect Dis 2005; 11:103-107.
7. Harvala H, et al. Specific association of human parechovirus type 3 with sepsis and fever in young infants, as identified by direct typing of cerebrospinal fluid samples. J Infect Dis 2009; 199:1753-60.
8. Verboon-Maciolek MA, et al. Human parechovirus causes encephalitis with white matter injury in neonates. Ann Neurol 2008; 64:266-273.
9. Wolthers KC, et al. Human parechoviruses as an important viral cause of sepsis like illness and meningitis in young children. Clin Infect Dis 2008; 47:358-63.
10. Sasidharan A, Banerjee D, Harrison CJ, Selvarangan R. Emergence of Parechovirus A3 as the Leading Cause of Central Nervous System Infection, Surpassing Any Single Enterovirus Type, in Children in Kansas City, Missouri, USA, from 2007 to 2016. J Clin Microbiol. 2021 May 19;59(6):e02935-20. doi: 10.1128/JCM.02935-20. PMID: 33692140; PMCID: PMC8316090.
11. Lane LM, McDermott MB, O’Connor P, Cronly S, O’Regan M, De Gascun CF, Morley U, Snow A, Tone S, Heffernan J, Cryan JB. Multicystic Encephalomalacia: The Neuropathology of Systemic Neonatal Parechovirus Infection. Pediatr Dev Pathol. 2021 Sep-Oct;24(5):460-466. doi: 10.1177/10935266211001645. Epub 2021 Mar 23. PMID: 33754905.
12. Klatte JM, Harrison CJ, Pate B, Queen MA, Neuhart J, Jackson MA, Selvarangan R. Maternal parechovirus A (PeV-A) shedding, serostatus, and the risk of central nervous system PeV-A infections in infants. J Clin Virol. 2021 Sep;142:104939. doi: 10.1016/j.jcv.2021.104939. Epub 2021 Aug 2. PMID: 34390928.
13. Nix WA, et al. Detection of all known parechoviruses by real-time PCR. J Clin Microbiol. 2008; 46:2519-24
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