Congenital absence, atresia and stenosis of other specified parts of small intestine
ICD-10 Q41.8 is a billable code used to indicate a diagnosis of congenital absence, atresia and stenosis of other specified parts of small intestine.
Congenital absence, atresia, and stenosis of the small intestine are serious congenital malformations that can significantly impact a child's digestive health. These conditions can lead to obstruction, malabsorption, and nutritional deficiencies. The small intestine is crucial for digestion and absorption of nutrients, and any congenital anomaly can lead to severe complications. Esophageal atresia, for instance, is a condition where the esophagus does not connect properly to the stomach, often associated with tracheoesophageal fistula. Hirschsprung disease is characterized by the absence of nerve cells in the colon, leading to severe constipation or intestinal obstruction. Imperforate anus is a defect where the anal opening is missing or blocked, requiring surgical intervention. Gastroschisis involves the intestines protruding through a hole in the abdominal wall, necessitating immediate surgical repair. Each of these conditions requires careful diagnosis and management, often involving multidisciplinary teams including pediatric surgeons, gastroenterologists, and geneticists.
Detailed clinical notes including growth parameters, feeding difficulties, and surgical history.
Management of infants with esophageal atresia requiring surgical repair and ongoing nutritional support.
Consideration of developmental milestones and long-term follow-up for growth and gastrointestinal function.
Genetic testing results, family history of congenital conditions, and syndromic associations.
Genetic counseling for families with a history of congenital malformations and assessment for syndromic conditions.
Understanding the genetic basis of congenital conditions and implications for family planning.
Used in cases of congenital atresia requiring surgical intervention.
Operative report detailing the procedure and findings.
Pediatric surgical documentation must include age-specific considerations.
Documentation should include a detailed clinical history, surgical reports, and any imaging studies that confirm the diagnosis of congenital absence, atresia, or stenosis of the small intestine. Additionally, any associated congenital anomalies should be documented to ensure accurate coding.
