Congenital malformations of intestinal fixation
ICD-10 Q43.3 is a billable code used to indicate a diagnosis of congenital malformations of intestinal fixation.
Congenital malformations of intestinal fixation refer to a group of conditions where the intestines are improperly anchored within the abdominal cavity. This can lead to complications such as volvulus, intestinal obstruction, and impaired blood supply to the intestines. These malformations can occur in conjunction with other congenital anomalies, particularly those affecting the digestive system. Common associated conditions include esophageal atresia, where the esophagus does not connect properly to the stomach; Hirschsprung disease, characterized by the absence of nerve cells in the colon leading to severe constipation; and imperforate anus, where the anal opening is missing or blocked. Gastroschisis, a defect where the intestines protrude through a hole in the abdominal wall, is also related. These conditions often require surgical intervention and careful management in pediatric patients to ensure proper growth and development.
Detailed documentation of the patient's growth, development, and any surgical interventions performed.
Management of a newborn with esophageal atresia requiring surgical repair and follow-up care.
Consideration of the patient's overall health status and any comorbidities that may affect treatment.
Genetic testing results, family history, and any syndromic associations must be documented.
Genetic counseling for families with a history of congenital malformations.
Understanding the genetic basis of congenital conditions and their implications for family planning.
Used in cases of intestinal obstruction due to congenital malformations.
Surgical reports detailing the procedure and findings.
Pediatric surgical documentation must include age-specific considerations.
Common associated conditions include esophageal atresia, Hirschsprung disease, imperforate anus, and gastroschisis. Each of these conditions may require specific coding and documentation to accurately reflect the patient's clinical status.
