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Pediatric Esophageal Atresia Device Market to Reap Excessive
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Pediatric esophageal atresia is absence or abnormal narrowing of an opening
in the body. It is a congenital defect of the esophagus that occurs in early
stages of pregnancy while the baby is developing. The condition occurs due to
malformation consisting of discontinuity between the upper and lower esophageal
pouches. The defect is frequently associated with tracheoesophageal fistula. In
tracheoesophageal fistula, babies have their esophagus abnormally attached with
windpipe (trachea). In normal cases, during the early stages of fetal
development, the esophagus and windpipe forms a hollow tube joining the mouth to
stomach.

However, in newborn babies with this congenital defect Wholesale
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single hollow tube connecting the wind pipe, and instead two separate tubes are
formed. The gap between these tubes can be short or very long. This defect needs
to be corrected by surgical method to prevent fluids from the esophagus entering
the windpipe of the infant causing breathing problems. At times, other birth
defects may also co-exist, primarily in the heart and sometimes also in spinal
column, anus Wholesale
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as VACTERL association due to possible involvement of vertebral column,
anorectal, cardiac, tracheal, esophageal Wholesale
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One half of the newborn babies having esophageal atresia have associated
congenital anomalies. An estimated 1 in 25,000 babies in the U.S. is born with
this defect. On May 12, 2017, the U.S. Food and Drug Administration approved the
use of Flourish pediatric esophageal atresia device for treating infants with
esophageal atresia. The device enables doctors to repair the esophagus in
infants who were born with a defect in the esophagus without a surgery.
However Wholesale
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do not have a tracheoesophageal fistula or in whom the fistula has been
repaired.

The device uses a magnetic system to pull both the upper and lower esophagus
for closure of the gap and enabling food to enter the stomach. During this
procedure, doctors insert two catheters (flexible tubes), one from the oral
cavity and one through the stomach of the patient. Due to the magnetic
attraction between the ends of the two tubes, the esophagus is pulled together,
thereby closing the gap Wholesale
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connection from the esophagus to the stomach. The infant can be fed through the
mouth after the catheters are removed. About 3 to 13 days are required for
completion of the procedure. During this period the gap between the disconnected
esophagi gets closed.

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The global pediatric esophageal atresia device market is projected to witness
strong growth due to increase in awareness about the defect and advancement in
the field of science and technology. The device has received approval via
Humanitarian Use Device (HUD) pathway. Cook Medical has received the FDA
authorization for Flourish pediatric esophageal atresia device. However, some
complications such as ulceration or irritation in tissue around the catheter and
gastoesophageal reflux are likely to restrain the market. Moreover, high cost of
the procedure is expected to restrain the global pediatric esophageal atresia
device market.

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The global pediatric esophageal atresia device market can be segmented based
on end-user and region. In terms of end-user, the market can be divided into
pediatric clinics, hospitals Wholesale
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have shown a high prevalence of this defect in Europe. Hence, there is a wide
scope for this device in the region. The pediatric esophageal atresia device
market in other parts of the world is expected to witness significant growth
during the forecast period due to sporadic and stable prevalence of this birth
defect.

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