Complete ICD-10-CM coding and documentation guide for Acromegaly. Includes clinical validation requirements, documentation requirements, and coding pitfalls.
Also known as:
Complete code families applicable to Acromegaly
Disorders of other endocrine glands
This range includes disorders related to the pituitary gland, including acromegaly.
Essential facts and insights about Acromegaly
Additional codes that should be used in conjunction with the main diagnosis codes when applicable.
Benign neoplasm of pituitary gland
D35.2Alternative codes to consider when ruling out similar conditions to the primary diagnosis.
Carcinoid syndrome
E34.0Avoid these common documentation and coding issues when documenting Acromegaly to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code E22.0.
Clinical: Incomplete clinical picture, Regulatory: Potential audit risk, Financial: Missed reimbursement opportunities
Review patient history for comorbidities, Ensure all relevant conditions are coded
Reimbursement: Incorrect DRG assignment, Compliance: Non-compliance with coding guidelines, Data Quality: Inaccurate clinical data representation
Always sequence E22.0 before comorbid conditions.
Incorrect sequencing of primary and secondary codes.
Regular training on ICD-10 guidelines.
Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.
Common questions about ICD-10 coding for Acromegaly, with expert answers to help guide accurate code selection and documentation.
Use these documentation templates to ensure complete and accurate documentation for Acromegaly. These templates include all required elements for proper coding and billing.
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