2025 ICD-10-CM code E84.1
(Active) Effective Date: N/A Endocrine, nutritional and metabolic diseases - Disorders of amino-acid metabolism 4 Feed
Cystic fibrosis with intestinal manifestations.
Medical necessity is established by the diagnosis of cystic fibrosis, a genetic disorder requiring ongoing medical management.The intestinal manifestations necessitate interventions to maintain adequate nutrition and prevent complications like DIOS.
Clinicians diagnose this condition based on patient history, symptoms, physical exam, and laboratory tests (including blood tests, stool tests, sweat tests, and genetic testing). Treatment focuses on managing symptoms, improving nutrition, and addressing the underlying CFTR gene mutation.
In simple words: Cystic fibrosis is a genetic condition where the body produces thick, sticky mucus. When this affects the intestines, it can cause problems with digestion and absorbing nutrients from food.
Cystic fibrosis with intestinal manifestations is a genetic disorder characterized by the buildup of thick mucus, primarily affecting the lungs, pancreas, and other organs.In the intestines, this mucus can block ducts, impairing digestion and nutrient absorption.
Example 1: A newborn infant presents with meconium ileus, a bowel obstruction caused by thick meconium, and is subsequently diagnosed with cystic fibrosis., A child experiences chronic digestive problems, including greasy stools, weight loss, and abdominal pain, leading to a diagnosis of cystic fibrosis with intestinal manifestations., An adult with cystic fibrosis develops distal intestinal obstruction syndrome (DIOS) due to the accumulation of thick stool and mucus in the intestines.
Documentation should include details of the patient's symptoms (e.g., greasy stools, abdominal pain, failure to thrive), diagnostic test results (sweat chloride test, genetic testing), and treatment plans.
- Specialties:Gastroenterology, Pulmonology, Pediatrics, General Practice
- Place of Service:Inpatient Hospital, Outpatient Hospital, Office, Home