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By Andrea Shalal-Esa
WASHINGTON (Reuters) - US-based Advanced
Bionics Corp. on Thursday warned that the inner-ear implants it makes to
help deaf people hear may also put them at greater risk for potentially
fatal meningitis and urged its customers to get vaccinated.
"We're making very strong recommendations
to all of the individuals who use our cochlear system to be vaccinated
against various pneumococcal diseases," said Douglas Lynch, spokesman
for the Valencia, California-based company, one of three manufacturers
of the devices.
The Food and Drug Administration issued a
public health notification on Wednesday noting that 25 adults and
children with cochlear implants had been diagnosed with meningitis
worldwide and it was aware of nine deaths in these cases.
Surveys of cochlear implant centers
currently under way suggested that there were additional, unreported
cases of meningitis among cochlear implant patients, the FDA said.
The FDA recommended that physicians
consider giving patients antibiotics before implantation and urged them
to diagnose and treat ear infections promptly in implant patients.
"Cochlear implant candidates, as well as
those already implanted, may benefit from vaccinations against organisms
that commonly cause bacterial meningitis, particularly streptococcus
pneumoniae and haemophilus influenzae," the FDA said, urging prompt
reporting of any cases of meningitis.
The FDA said the onset of meningitis
symptoms ranged from less than 24 hours to greater than 5 years from the
time of implantation. It said some 60,000 people worldwide had received
the implants, which contain electrodes that are positioned in the inner
ear, or cochlea, to activate auditory nerve fibers to allow transmission
of sound signals to the brain.
Advanced Bionics has sold some 10,000
cochlear implants since the FDA first approved the device in 1996.
Australian manufacturer Cochlear Ltd., the
leading manufacturer of the devices, has sold over 40,000 devices in the
past 20 years.
Jim Miller, president of Cochlear Americas,
the US division, said he was not aware of any meningitis-related deaths
linked to the company's products in that entire period.
ANTIBIOTIC TREATMENT ENCOURAGED
Miller noted meningitis was a complication
of any inner-ear surgery, and some deaf patients were at even greater
risk due to malformations of the inner ear. But he said his company's
research showed the incidence of meningitis in implant patients was not
greater than that of the general public.
Still, Miller lauded the FDA's effort to
raise awareness about the risks of meningitis, and said his company
routinely recommended prophylactic antibiotic treatment in the period
immediately before and after implantation surgery.
No comment was immediately available from
the third manufacturer of cochlear implants, Austrian-based MED-EL.
Advanced Bionics first raised the issue of
a possible increased risk for meningitis with the FDA on June 28, Lynch
said, noting that the company had launched an independent investigation
after observing "a few cases of meningitis."
Lynch said there was still no evidence of
"a definitive link," but the company was reviewing its device and
components to determine if they could be linked to an increased risk.
He noted that the company already warned
patients about the risks of contracting meningitis as a result of the
surgery.
"We want to educate everyone who gets
implanted. It's prudent to get vaccinated," said Lynch. "It makes good
sense."
Meningitis is an infection of the membranes
surrounding the brain that can be treated when diagnosed early. It can
be deadly in some cases, especially if diagnosed late. The disease can
be difficult to diagnose in young children, whose symptoms include
fever, irritability, lethargy and loss of appetite.
Older children and adults may also have
headaches, stiff necks, nausea and vomiting. Younger patients and the
elderly were the most vulnerable to meningitis, the FDA said.
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