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Volume 4

Journal of Pediatric Care

ISSN: 2471-805X

Page 43

JOINT EVENT

Pediatric Critical Care 2018 &

World Pediatrics 2018

October 18- 20 , 2018

October 18- 20, 2018 Warsaw, Poland

&

6

th

International Conference on

25

th

World Pediatrics Conference

Pediatric Critical Care and Emergency Medicine

J Pediatr Care 2018, Volume 4

DOI: 10.21767/2471-805X-C4-015

PYLORIC STENOSIS

Fadumo Omar Ibrahim

Jezeera University, Somalia

P

yloric stenosis, also called infantile hypertrophic pyloric stenosis, is a condition caused by an enlarged pylorus. The pylorus

is a muscle that opens and closes to allow food to pass through the stomach into the intestine. When this muscle becomes

enlarged, feedings are blocked from emptying out of the stomach. The retained feedings cause the infant to vomit. There is no

known reason for enlargement of the pylorus. It is more common in boys than girls and usually affects children who are born at

full term. It rarely occurs in premature infants. Although not thought to be hereditary, pyloric stenosis occurs more commonly

in children of parents who had pyloric stenosis themselves as infants. Infants with pyloric stenosis typically begin vomiting

during the first month of life, but onset of symptoms may be delayed. The main symptom of pyloric stenosis is vomiting

undigested breast milk or formula soon after a feeding. Vomiting usually begins at four weeks of age but can happen as early

as two weeks after birth. Once vomiting begins it becomes more frequent, and severe, and is often described as "forceful" or

"projectile an examination of the abdomen may allow the doctor to feel the enlarged pyloric muscle (called an "olive"). If the

pylorus cannot be felt, pyloric stenosis can be diagnosed by ultrasound study or by x-rays taken after the infant drinks a liquid

called "contrast." Pyloric stenosis does not get better by itself and must be corrected with an operation. The operation is called a

"pyloromyotomy before surgery, dehydration and hypochloremic alkalosis must be corrected, generally with an initial normal

saline fluid bolus followed by infusions of half-normal saline containing 5% dextrose and potassium chloride when urine

output is observed.

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