Pyloric StenosisSkip to the navigation
What is pyloric stenosis?
Pyloric stenosis is a problem with a baby's stomach that causes forceful vomiting. It happens when the baby's pylorus, which connects the stomach and the small intestine, swells and thickens. This can keep food from moving into the intestine.
A baby may get pyloric stenosis anytime between birth and 5 months of age. Boys are more likely than girls to get it. It usually starts about 3 weeks after birth. If your baby was born early (premature), symptoms may start later.
What causes pyloric stenosis?
Experts don't know what causes pyloric stenosis. It may be passed down through families.
What are the symptoms?
A baby with pyloric stenosis may:
- Vomit soon after a feeding.
- Have a full, swollen upper belly after a feeding.
- Act fussy and hungry a lot of the time.
- Have fewer and harder stools than normal.
- Pass less urine than normal.
Vomiting usually starts gradually. As the pylorus becomes tighter, the vomiting may become more frequent and more forceful.
As the vomiting continues, your baby may:
- Lose weight.
- Become dehydrated.
- Be sleepier than normal and very fussy when awake.
How is pyloric stenosis diagnosed?
Your doctor will do a physical exam and ask about your baby's symptoms. If your baby has pyloric stenosis, the doctor may be able to feel a small lump in the upper part of the belly.
How is it treated?
Pyloric stenosis is treated with surgery to widen the opening between the stomach and the small intestine. Surgery rarely causes problems, and almost all babies recover completely. After surgery, your baby probably won't get pyloric stenosis again.
Your baby likely will be ready to go home within 2 days after surgery. Being involved in your baby's care while he or she is in the hospital may help you feel more comfortable when you take your baby home. Talk with the doctor about how to feed your baby and what to expect. It's normal to feel nervous, but don't be afraid to hold and handle your baby.
Frequently Asked Questions
Learning about pyloric stenosis:
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Other Works Consulted
- Greenup RA, Calkins CM (2011). Infantile hypertrophic pyloric stenosis. In CD Rudolph et al., eds., Rudolph’s Pediatrics, 22nd ed., pp. 1420–1421. New York: McGraw-Hill.
- Hoffenberg E, et al. (2014). Gastrointestinal tract. In WW Hay Jr et al., eds., Current Diagnosis and Treatment: Pediatrics, 22nd ed., pp. 651–691. New York: McGraw-Hill.
- Hunter AK, Liacouras CA (2011). Pyloric stenosis and other congenital anomalies of the stomach. In RM Kliegman et al., eds., Nelson Textbook of Pediatrics, 19th ed., pp. 1274–1276. Philadelphia: Saunders.
- Middlesworth W, Kadenhe-Chiweshe A (2006). Neonatal intestinal obstruction. In FD Burg et al., eds., Current Pediatric Therapy, 18th ed., pp. 289–293. Philadelphia: Saunders Elsevier.
- Semrin MG, Russo MA (2010). Anatomy, histology, embryology, and developmental anomalies of the stomach and duodenum. In M Feldman et al., eds., Sleisenger and Fordtran’s Gastrointestinal and Liver Disease, 9th ed., vol. 1, pp. 773–788. Philadelphia: Saunders.
Primary Medical Reviewer John Pope, MD - Pediatrics
Specialist Medical Reviewer Brad W. Warner, MD - Pediatric Surgery
Current as ofNovember 20, 2015
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