Other interstitial lung diseases of childhood
ICD-10 J84.848 is a billable code used to indicate a diagnosis of other interstitial lung diseases of childhood.
J84.848 refers to other interstitial lung diseases of childhood, which encompass a variety of pulmonary conditions characterized by inflammation and scarring of the lung interstitium. Clinically, children may present with symptoms such as persistent cough, wheezing, shortness of breath, and exercise intolerance. The anatomy involved includes the alveoli and surrounding connective tissue, which can become thickened or damaged due to various etiologies, including environmental exposures, infections, or genetic factors. Disease progression can vary widely; some conditions may be acute and reversible, while others can lead to chronic respiratory failure and require long-term management. Diagnostic considerations include a thorough clinical history, physical examination, imaging studies such as chest X-rays or CT scans, and pulmonary function tests. In some cases, lung biopsy may be necessary to confirm the diagnosis and rule out other conditions. Early identification and management are crucial to improving outcomes in affected children.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
J84.848 encompasses a range of interstitial lung diseases in children, including but not limited to hypersensitivity pneumonitis, sarcoidosis, and pulmonary alveolar proteinosis. Each condition has specific diagnostic criteria based on clinical, radiological, and histopathological findings.
J84.848 should be used when a child presents with interstitial lung disease that does not fit the criteria for more specific codes like J84.1 or J84.9. It is essential to document the clinical rationale for selecting this code, ensuring that the specific interstitial lung disease is accurately captured.
Documentation for J84.848 should include a detailed clinical history, results from imaging studies, pulmonary function tests, and any relevant laboratory findings. A clear narrative explaining the diagnosis and treatment plan is also critical to support the use of this code.
