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R74.0
ICD-10-CM
Transaminitis

Understanding transaminitis: Learn about elevated liver enzymes, AST, ALT, causes, diagnosis, ICD-10 codes (R74.8), clinical documentation improvement, and healthcare implications. Find information on liver function tests (LFTs), symptoms, treatment, and management of transaminitis for medical professionals, coders, and patients. Explore resources for accurate medical coding and compliant clinical documentation related to transaminitis.

Also known as

Elevated liver enzymes
Increased transaminase levels
elevated liver transaminases
+1 more

Diagnosis Snapshot

Key Facts
  • Definition : Elevated liver enzymes (ALT and AST) in the blood, indicating liver cell damage.
  • Clinical Signs : Often asymptomatic, but may include fatigue, nausea, abdominal pain, jaundice, dark urine.
  • Common Settings : Viral hepatitis, fatty liver disease, alcohol abuse, medication side effects, heart failure.

Related ICD-10 Code Ranges

Complete code families applicable to AAPC R74.0 Coding
R74.8

Abnormal findings of liver function tests

Indicates abnormal liver enzyme levels, including transaminases.

K70-K77

Diseases of liver

Covers various liver diseases that can cause transaminitis.

T36-T50

Poisoning by drugs, medicaments

Certain drug or medication poisonings can induce liver enzyme elevation.

Code-Specific Guidance

Decision Tree for

Follow this step-by-step guide to choose the correct ICD-10 code.

Is the transaminitis due to a specific disease?

  • Yes

    Is it due to viral hepatitis?

  • No

    Is it drug-induced?

Code Comparison

Related Codes Comparison

When to use each related code

Description
Elevated liver enzymes
Hepatitis
Non-alcoholic fatty liver disease

Documentation Best Practices

Documentation Checklist
  • Document specific transaminase levels (ALT, AST).
  • Specify the degree of elevation (mild, moderate, severe).
  • Document the onset and duration of transaminitis.
  • Exclude other causes of liver injury (e.g., viral hepatitis).
  • Correlate with relevant clinical findings (e.g., jaundice).

Coding and Audit Risks

Common Risks
  • Unspecified etiology

    Coding transaminitis without specifying the underlying cause (e.g., alcohol, medication) leads to inaccurate reporting and potential DRG misclassification.

  • Lack of specificity

    Using a non-specific transaminitis code when a more precise diagnosis (e.g., hepatitis, hepatic steatosis) is documented creates coding and billing errors.

  • Missing documentation

    Insufficient documentation of transaminitis severity and related findings (e.g., liver function tests, imaging) may lead to undercoding and lost revenue.

Mitigation Tips

Best Practices
  • Document etiology: ICD-10-CM R74.8, optimize HCC coding
  • Medication review: CDI query for drug-induced liver injury
  • Alcohol/substance use assessment: Compliance, Z72.1 ICD-10-CM
  • Liver imaging/biopsy: Correlate findings, improve CDI specificity
  • Follow-up LFTs: Monitor, document resolution for compliant billing

Clinical Decision Support

Checklist
  • Review ICD-10 codes R74.0, R74.00, R74.01 for accuracy.
  • Check AST/ALT levels documented in lab results.
  • Assess patient medications for hepatotoxicity.
  • Exclude other liver disease causes (viral, autoimmune).
  • Document transaminitis etiology and severity.

Reimbursement and Quality Metrics

Impact Summary
  • Transaminitis reimbursement hinges on accurate ICD-10 coding (R74.8) and linking to underlying cause for optimal payment.
  • Coding quality impacts transaminitis metrics reporting, affecting hospital quality scores and potential value-based payments.
  • Precise documentation of etiology improves transaminitis diagnosis coding, minimizing claim denials and maximizing revenue.
  • Proper coding and documentation enhance transaminitis data analysis, improving patient care and resource allocation.

Streamline Your Medical Coding

Let S10.AI help you select the most accurate ICD-10 codes for . Our AI-powered assistant ensures compliance and reduces coding errors.

Frequently Asked Questions

Common Questions and Answers

Q: What is the most effective differential diagnosis approach for asymptomatic transaminitis in adults, considering both common and less common causes?

A: Asymptomatic transaminitis in adults requires a systematic approach to differential diagnosis, encompassing a broad range of potential etiologies. Start by assessing the magnitude of enzyme elevation. Mild elevations (less than twice the upper limit of normal) often point to non-alcoholic fatty liver disease (NAFLD), alcoholic liver disease, or medication-induced liver injury. Consider obtaining a detailed medication history, including over-the-counter drugs and herbal supplements. For moderate to severe elevations, investigate viral hepatitis (A, B, C), autoimmune hepatitis, hemochromatosis, Wilsons disease, and alpha-1-antitrypsin deficiency. Less common causes to consider include celiac disease, thyroid disorders, and muscle disorders. A thorough patient history, physical examination, and targeted laboratory testing, including liver function tests, complete blood count, iron studies, and viral hepatitis serologies, are crucial for accurate diagnosis. Explore how imaging studies, such as ultrasound or MRI, can further aid in the evaluation. If initial testing is inconclusive, consider referral to a hepatologist for further evaluation and management. Learn more about specific diagnostic markers for each potential cause.

Q: How can I differentiate between alcoholic and non-alcoholic fatty liver disease (NAFLD) as a cause of transaminitis in a patient, given that both can present similarly?

A: Differentiating between alcoholic liver disease (ALD) and NAFLD in a patient with transaminitis can be challenging due to overlapping clinical presentations. A thorough history regarding alcohol consumption is paramount, though patient self-reporting can be unreliable. Biomarkers such as gamma-glutamyl transferase (GGT) and carbohydrate-deficient transferrin (CDT) can be helpful, but they are not always definitive. Imaging studies, like ultrasound or transient elastography, can assess liver steatosis and fibrosis, but cannot distinguish between ALD and NAFLD. Liver biopsy remains the gold standard for definitive diagnosis, providing histological evidence of the underlying pathology, including the presence of Mallory-Denk bodies suggestive of ALD. Consider implementing validated questionnaires, like the AUDIT-C, to screen for alcohol use disorders. The AST/ALT ratio can sometimes be suggestive, with a ratio >2 often seen in ALD, but this is not always reliable. Ultimately, a combination of clinical findings, laboratory data, and imaging, alongside a strong emphasis on patient history, is key to differentiating between these two etiologies. Explore how genetic testing can aid in risk stratification and personalized management of NAFLD.

Quick Tips

Practical Coding Tips
  • Code ALT/AST elevation, specify cause
  • Document liver function test results
  • R/O viral hepatitis, alcohol use
  • Consider drug-induced liver injury
  • Check biliary obstruction if indicated

Documentation Templates

Patient presents with elevated liver enzymes, indicative of transaminitis.  Symptoms include fatigue, nausea, right upper quadrant abdominal pain, and dark urine.  Physical examination reveals mild hepatomegaly.  Laboratory findings demonstrate elevated AST (aspartate aminotransferase) and ALT (alanine aminotransferase) levels, exceeding the normal range.  Differential diagnosis includes non-alcoholic fatty liver disease (NAFLD), alcoholic liver disease, viral hepatitis, drug-induced liver injury, and autoimmune hepatitis.  Further investigations such as viral hepatitis panel, liver ultrasound, and possibly liver biopsy may be necessary to determine the etiology of the transaminitis.  Initial management includes discontinuation of any potential hepatotoxic medications, lifestyle modifications including weight loss and dietary changes, and close monitoring of liver function tests.  Patient education regarding the potential causes of transaminitis, its implications, and the importance of follow-up care was provided.  ICD-10 code R74.0 (abnormal liver function tests, unspecified) is considered pending further investigation.  CPT codes for laboratory tests and imaging studies will be documented accordingly. Follow-up appointment scheduled in two weeks to review laboratory results and discuss further management based on the determined etiology.