Pyloric stenosis is a condition that affects infants, typically between three to five weeks of age, causing severe and progressive vomiting. This condition occurs when the pylorus, the muscle between the stomach and the small intestine, thickens and obstructs food from passing through.
Though relatively rare, pyloric stenosis requires prompt medical attention to prevent complications such as dehydration and weight loss.
This blog aims to provide a comprehensive overview of pyloric stenosis, including its symptoms, diagnosis, and treatment options.
Pyloric stenosis, also known as infantile hypertrophic pyloric stenosis (IHPS), is a condition in which the pyloric muscle thickens, leading to a narrowing of the pyloric canal. This narrowing hinders the passage of stomach contents into the small intestine, causing severe vomiting and other related symptoms.
While the exact cause of pyloric stenosis is not entirely understood, both genetic and environmental factors are believed to play a role.
The symptoms of pyloric stenosis usually become apparent between the third and fifth weeks of an infant’s life. Key symptoms include:
While the exact cause of pyloric stenosis remains unclear, several factors are thought to contribute to its development:
Early diagnosis of pyloric stenosis is important for several reasons:
Timely diagnosis and treatment are crucial in preventing complications such as severe dehydration, electrolyte imbalances, and failure to thrive in infants.
Providing accurate and timely diagnosis can help alleviate parental anxiety and offer a clear treatment plan for the infant’s recovery.
Early diagnosis enables prompt surgical intervention, resulting in improved outcomes and faster recovery for the infant.
The diagnosis of pyloric stenosis typically involves a combination of medical history, physical examination, and diagnostic tests:
The first step in diagnosing pyloric stenosis is a detailed review of the infant’s symptoms. Parents often report frequent and severe vomiting, which is typically projectile and happens shortly after feeding. They may also note persistent hunger, weight loss, and signs of dehydration.
The healthcare provider will ask about the infant’s feeding habits and growth patterns. Poor weight gain or weight loss despite regular feedings is a significant red flag. A family history of pyloric stenosis can increase the likelihood of the condition, so the doctor will enquire about any relatives who have had the condition.
During the physical examination, the doctor will palpate the infant’s abdomen to feel an olive-shaped mass in the upper right quadrant. This mass is the hypertrophied pyloric muscle, which is a classic sign of pyloric stenosis.
The doctor may observe visible waves of peristalsis moving from left to right across the infant’s abdomen after feeding, indicating the stomach’s efforts to push food past the obstructed pylorus.
An abdominal ultrasound is the most commonly used and effective diagnostic tool for pyloric stenosis. It can visualise the thickened pyloric muscle and measure its dimensions. A pyloric muscle thickness greater than 3-4 mm and a pyloric channel length greater than 15-18 mm are indicative of pyloric stenosis.
In some cases, if the ultrasound results are inconclusive, a barium swallow test may be performed. The infant drinks a barium solution, and X-rays are taken to observe the passage of the liquid through the digestive tract. A “string sign,” where the barium flows through a narrow pyloric canal, can confirm the diagnosis.
Blood tests are performed to assess the infant’s electrolyte levels and hydration status. Frequent vomiting can lead to dehydration and electrolyte imbalances, such as low potassium and chloride levels and elevated bicarbonate levels. These findings help in planning the necessary preoperative management.
Occasionally, an upper GI series may be used to evaluate the stomach and intestines. The infant ingests a contrast material, and a series of X-rays are taken to visualise the upper digestive tract. This test can help identify the narrowed pyloric canal and other possible abnormalities.
Pyloric stenosis is a condition that necessitates prompt medical intervention to prevent complications and ensure the health of the affected infant. The primary treatment for pyloric stenosis is surgical, but preoperative management to stabilise the infant is also important.
Let’s look at this in more detail:
Before surgery, the infant’s condition needs to be stabilised to address dehydration and electrolyte imbalances caused by persistent vomiting. This involves:
The definitive treatment for pyloric stenosis is a surgical procedure called pyloromyotomy. There are two main surgical approaches:
In an open pyloromyotomy, the surgeon makes a small incision in the infant’s abdomen, typically on the right upper quadrant, to access the pylorus. The thickened pyloric muscle is then split longitudinally without cutting the inner lining of the stomach, widening the passage to allow food to pass through.
This traditional approach is straightforward and has a high success rate. It involves a larger incision, which can result in a longer recovery time and more visible scarring compared to laparoscopic surgery.
In a laparoscopic pyloromyotomy, the surgeon makes several small incisions and uses a laparoscope (a thin, flexible tube with a camera) and specialised instruments to perform the surgery. The pyloric muscle is split in the same manner as in the open approach.
This minimally invasive technique typically results in smaller incisions, less postoperative pain, shorter hospital stays, and faster recovery times. It requires specialised equipment and expertise, and in rare cases, it may need to be converted to an open procedure if complications arise.
After the surgical procedure, the infant requires careful monitoring and supportive care to ensure a smooth recovery.
Immediately after the surgery, the infant is closely monitored in the recovery room for any immediate postoperative complications such as bleeding, infection, or anaesthesia-related issues.
Feeding usually resumes a few hours after surgery, starting with small amounts of clear liquids (such as an electrolyte solution) to ensure that the infant can tolerate fluids without vomiting. Gradually, the feedings are increased in volume and transitioned to breast milk or formula. The process typically spans 24 to 48 hours, intending to return to normal feeding patterns.
Pain relief is provided using medications such as acetaminophen. It’s important to manage pain effectively to keep the infant comfortable and facilitate recovery.
Monitoring for Complications: During the post-operative time, the healthcare team monitors the infant closely for potential complications such as:
Parents are provided with instructions on how to care for the incision site, recognise signs of complications, and gradually reintroduce regular feeding. They are also informed about follow-up appointments to monitor the infant’s recovery and growth.
While there are no definitive preventive measures for pyloric stenosis, early recognition of symptoms and prompt medical attention are pivotal. Parents should be aware of the signs of pyloric stenosis and seek medical advice if their infant exhibits persistent vomiting, poor weight gain, or other related symptoms.
Parents play a vital role in supporting their infant’s recovery after pyloromyotomy. Key steps include:
Pyloric stenosis is a condition that can cause significant distress for both infants and their parents. However, with early diagnosis and prompt surgical treatment, the prognosis is excellent. Understanding the symptoms, diagnosis, and treatment options for pyloric stenosis is crucial for parents and caregivers to ensure timely and effective medical care for affected infants.
By working closely with healthcare providers and following postoperative care instructions, parents can support their infant’s recovery and help them return to a healthy, thriving state.
The main cause of pyloric stenosis is not entirely understood, but it involves a combination of genetic and environmental factors.
The warning signs of pyloric stenosis include projectile vomiting after feeding, persistent hunger, and poor weight gain.
If left untreated, pyloric stenosis can become life-threatening due to severe dehydration and electrolyte imbalances.
Dr Syariz Izry Sehat
Consultant Paediatric Surgeon
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