Pyloric stenosis
Template:Infobox medical condition (new) Pyloric stenosis is a narrowing of the opening from the stomach to the first part of the small intestine (the pylorus).<ref name=Ran2011/> Symptoms include projectile vomiting without the presence of bile.<ref name=Ran2011/> This most often occurs after the baby is fed.<ref name=Ran2011/> The typical age that symptoms become obvious is two to twelve weeks old.<ref name=Ran2011/>
The cause of pyloric stenosis is unclear.<ref name=Ge2012>Template:Cite journal</ref> Risk factors in babies include birth by cesarean section, preterm birth, bottle feeding, and being firstborn.<ref name=Zh2017>Template:Cite journal</ref> The diagnosis may be made by feeling an olive-shaped mass in the baby's abdomen.<ref name=Ran2011/> This is often confirmed with ultrasound.<ref name=Pan2012>Template:Cite journal</ref>
Treatment initially begins by correcting dehydration and electrolyte problems.<ref name=Ran2011/> This is then typically followed by surgery, although some treat the condition without surgery by using atropine.<ref name=Ran2011/> Results are generally good in both the short term and the long term.<ref name=Ran2011/>
About one to two per 1,000 babies are affected, and males are affected about four times more often than females.<ref name=Ran2011/> The condition is very rare in adults.<ref>Template:Cite journal</ref> The first description of pyloric stenosis was in 1888, with surgical management first carried out in 1912 by Conrad Ramstedt.<ref name=Ran2011>Template:Cite journal</ref><ref name=Ge2012/> Before surgical treatment, most babies with pyloric stenosis died.<ref name=Ran2011/>
Signs and symptoms
Babies with this condition usually present any time in the first weeks to 6 months of life with progressively worsening vomiting. It is more likely to affect the first-born with males more commonly than females at a ratio of 4 to 1.<ref name="Naffaa 2019">Template:Cite journal</ref> The vomiting is often described as non-bile stained ("non bilious") and "projectile vomiting", because it is more forceful than the usual spitting up (gastroesophageal reflux) seen at this age. Some infants present with poor feeding and weight loss but others demonstrate normal weight gain. Dehydration may occur which causes a baby to cry without having tears and to produce less wet or dirty diapers due to not urinating for hours or for a few days. Symptoms usually begin between 3 and 12 weeks of age. Findings include epigastric fullness with visible peristalsis in the upper abdomen from the infant's left to right.<ref>Template:Cite web</ref> Constant hunger, belching, and colic are other possible signs that the baby is unable to eat properly.
Causes
Rarely, infantile pyloric stenosis can occur as an autosomal dominant condition.<ref name="pmid7333028">Template:Cite journal</ref> It is uncertain whether it is a congenital anatomic narrowing or a functional hypertrophy of the pyloric sphincter muscle.Template:Citation needed
Pathophysiology
The gastric outlet obstruction due to the hypertrophic pylorus impairs emptying of gastric contents into the duodenum. As a consequence, all ingested food and gastric secretions can only exit via vomiting, which can be of a projectile nature. While the exact cause of the hypertrophy remains unknown, one study suggested that neonatal hyperacidity may be involved in the pathogenesis.<ref>Template:Cite book</ref> This physiological explanation for the development of clinical pyloric stenosis at around 4 weeks and its spontaneous long term cure without surgery if treated conservatively, has recently been further reviewed.<ref>Template:Cite journal</ref>
Persistent vomiting results in loss of stomach acid (hydrochloric acid). The vomited material does not contain bile because the pyloric obstruction prevents entry of duodenal contents (containing bile) into the stomach. The chloride loss results in a low blood chloride level which impairs the kidney's ability to excrete bicarbonate. This is the factor that prevents correction of the alkalosis leading to metabolic alkalosis.<ref name="Acidbase">Kerry Brandis, Acid-Base Physiology Template:Webarchive. Retrieved December 31, 2006.</ref>
A secondary hyperaldosteronism develops due to the decreased blood volume. The high aldosterone levels causes the kidneys to avidly retain Na+ (to correct the intravascular volume depletion), and excrete increased amounts of K+ into the urine (resulting in a low blood level of potassium).Template:Citation neededThe body's compensatory response to the metabolic alkalosis is hypoventilation resulting in an elevated arterial pCO2.
Diagnosis
Diagnosis is via a careful history and physical examination, often supplemented by radiographic imaging studies. Pyloric stenosis should be suspected in any infant with severe vomiting. On physical exam, palpation of the abdomen may reveal a mass in the epigastrium. This mass, which consists of the enlarged pylorus, is referred to as the 'olive',<ref name=Shaoul>Template:Cite journal</ref> and is sometimes evident after the infant is given formula to drink. Rarely, there are peristaltic waves that may be felt or seen (video on NEJM) due to the stomach trying to force its contents past the narrowed pyloric outlet.Template:Citation needed
Most cases of pyloric stenosis are diagnosed/confirmed with ultrasound, if available, showing the thickened pylorus and non-passage of gastric contents into the proximal duodenum. Muscle wall thickness 3 millimeters (mm) or greater and pyloric channel length of 15 mm or greater are considered abnormal in infants younger than 30 days. Gastric contents should not be seen passing through the pylorus because if it does, pyloric stenosis should be excluded and other differential diagnoses such as pylorospasm should be considered. The positions of superior mesenteric artery and superior mesenteric vein should be noted because altered positions of these two vessels would be suggestive of intestinal malrotation instead of pyloric stenosis.<ref name="Naffaa 2019"/>
Although the baby is exposed to radiation, an upper GI series (X-rays taken after the baby drinks a special contrast agent) can be diagnostic by showing the pylorus with elongated, narrow lumen and a dent in the duodenal bulb.<ref name="Naffaa 2019"/> This phenomenon caused "string sign" or the "railroad track/double track sign" on X-rays after contrast is given. Plain x-rays of the abdomen sometimes shows a dilated stomach.<ref>Template:Cite journal</ref>
Although upper gastrointestinal endoscopy would demonstrate pyloric obstruction, physicians would find it difficult to differentiate accurately between hypertrophic pyloric stenosis and pylorospasm.Template:Citation needed
Blood tests will reveal low blood levels of potassium and chloride in association with an increased blood pH and high blood bicarbonate level due to loss of stomach acid (which contains hydrochloric acid) from persistent vomiting.<ref>Template:Cite web</ref><ref>Template:Cite web</ref> There will be exchange of extracellular potassium with intracellular hydrogen ions in an attempt to correct the pH imbalance. These findings can be seen with severe vomiting from any cause.Template:Citation needed
Treatment
Infantile pyloric stenosis is typically managed with surgery;<ref name=AskewOverview>Template:Cite journal</ref> very few cases are mild enough to be treated medically.
The danger of pyloric stenosis comes from the dehydration and electrolyte disturbance rather than the underlying problem itself. Therefore, the baby must be initially stabilized by correcting the dehydration and the abnormally high blood pH seen in combination with low chloride levels with IV fluids. This can usually be accomplished in about 24–48 hours.Template:Citation needed
Intravenous and oral atropine may be used to treat pyloric stenosis. It has a success rate of 85–89% compared to nearly 100% for pyloromyotomy, however it requires prolonged hospitalization, skilled nursing and careful follow up during treatment.<ref name="pmid17210480">Template:Cite journal</ref> It might be an alternative to surgery in children who have contraindications for anesthesia or surgery, or in children whose parents do not want surgery.Template:Cn
Surgery
The definitive treatment of pyloric stenosis is with surgical pyloromyotomy known as Ramstedt's procedure (dividing the muscle of the pylorus to open up the gastric outlet). This surgery can be done through a single incision (usually 3–4 cm long) or laparoscopically (through several tiny incisions), depending on the surgeon's experience and preference.<ref>Template:Cite web</ref>
Today, the laparoscopic technique has largely supplanted the traditional open repairs which involved either a tiny circular incision around the navel or the Ramstedt procedure. Compared to the older open techniques, the complication rate is equivalent, except for a markedly lower risk of wound infection.<ref name="pmid19635317">Template:Cite journal</ref> This is now considered the standard of care at the majority of children's hospitals across the US, although some surgeons still perform the open technique. Following repair, the small 3mm incisions are difficult to see.
The vertical incision, pictured and listed above, is no longer usually required, though many incisions have been horizontal in the past years. Once the stomach can empty into the duodenum, feeding can begin again. Some vomiting may be expected during the first days after surgery as the gastrointestinal tract settles. Rarely, the myotomy procedure performed is incomplete and projectile vomiting continues, requiring repeat surgery. Pyloric stenosis generally has no long term side-effects or impact on the child's future.Template:Citation needed
Epidemiology
Males are more commonly affected than females, with firstborn males affected about four times as often, and there is a genetic predisposition for the disease.<ref name="kh">Template:Cite web</ref> It is commonly associated with people of Scandinavian ancestry, and has multifactorial inheritance patterns.<ref name="pmid7333028" /> Pyloric stenosis is more common in Caucasians than Hispanics, Blacks, or Asians. The incidence is 2.4 per 1000 live births in Caucasians, 1.8 in Hispanics, 0.7 in Blacks, and 0.6 in Asians. It is also less common amongst children of mixed race parents.<ref>Template:EMedicine</ref> Caucasian male babies with blood type B or O are more likely than other types to be affected.<ref name="kh"/>
Infants exposed to erythromycin are at increased risk for developing hypertrophic pyloric stenosis, especially when the drug is taken around two weeks of life<ref name=Erythromycin>Template:Cite journal</ref> and possibly in late pregnancy and through breastmilk in the first two weeks of life.<ref name="Kong2013">Template:Cite journal</ref> Template:Clear
References
External links
Template:Medical condition classification and resources Template:Gastroenterology Template:Congenital malformations and deformations of digestive system