Back to HomeBeta

ICD-10 Coding for Pulmonary Arterial Hypertension(I27.0, I27.21)

Complete ICD-10-CM coding and documentation guide for Pulmonary Arterial Hypertension. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

PAHPrimary Pulmonary HypertensionIdiopathic Pulmonary Arterial Hypertension

Related ICD-10 Code Ranges

Complete code families applicable to Pulmonary Arterial Hypertension

I27.0-I27.9Primary Range

Other pulmonary heart diseases

This range includes codes for various types of pulmonary hypertension, with specific codes for primary and secondary pulmonary arterial hypertension.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
I27.0Primary pulmonary hypertensionUse when PAH is confirmed as idiopathic or heritable, validated by RHC.
  • Right heart catheterization showing mean PAP ≥20 mmHg, PAWP ≤15 mmHg, PVR ≥3 Wood units
  • Exclusion of secondary causes such as left heart disease, lung disease, or thromboembolism
I27.21Secondary pulmonary arterial hypertensionUse when PAH is secondary to another condition, confirmed by RHC.
  • RHC showing mean PAP ≥20 mmHg, PAWP ≤15 mmHg, PVR ≥3 Wood units
  • Documentation linking PAH to an underlying condition

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for pulmonary arterial hypertension

Essential facts and insights about Pulmonary Arterial Hypertension

The ICD-10 code for idiopathic or heritable pulmonary arterial hypertension is I27.0, while secondary pulmonary arterial hypertension is coded as I27.21.

Primary ICD-10-CM Codes for pulmonary arterial hypertension

Primary pulmonary hypertension
Billable Code

Decision Criteria

clinical Criteria

  • Confirmed idiopathic PAH via RHC with exclusion of secondary causes

Applicable To

  • Idiopathic pulmonary arterial hypertension
  • Heritable pulmonary arterial hypertension

Excludes

  • Pulmonary hypertension due to left heart disease (I27.22)
  • Pulmonary hypertension due to lung diseases and hypoxia (I27.23)

Clinical Validation Requirements

  • Right heart catheterization showing mean PAP ≥20 mmHg, PAWP ≤15 mmHg, PVR ≥3 Wood units
  • Exclusion of secondary causes such as left heart disease, lung disease, or thromboembolism

Code-Specific Risks

  • Misclassification if secondary causes are not excluded
  • Incorrect use without RHC confirmation

Coding Notes

  • Ensure RHC results are documented to support the use of this code.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Progressive systemic sclerosis

M34.0
Use to indicate scleroderma as an underlying cause of secondary PAH.

HIV disease

B20
Use to indicate HIV as an underlying cause of secondary PAH.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Secondary pulmonary arterial hypertension

I27.21
Use when PAH is linked to an underlying condition like connective tissue disease.

Primary pulmonary hypertension

I27.0
Use when PAH is idiopathic or heritable, not linked to another condition.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Pulmonary Arterial Hypertension to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code I27.0.

Impact

Clinical: Leads to inappropriate treatment plans., Regulatory: Non-compliance with coding standards., Financial: Potential for claim denials.

Mitigation Strategy

Always verify if PAH is primary or secondary., Document the underlying cause if secondary.

Impact

Reimbursement: May lead to denied claims due to lack of clinical validation., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate representation of patient condition.

Mitigation Strategy

Ensure RHC results are documented before coding I27.0.

Impact

Risk of coding PAH without proper clinical validation.

Mitigation Strategy

Implement regular audits of PAH cases to ensure compliance with coding 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.

Frequently Asked Questions

Common questions about ICD-10 coding for Pulmonary Arterial Hypertension, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Pulmonary Arterial Hypertension

Use these documentation templates to ensure complete and accurate documentation for Pulmonary Arterial Hypertension. These templates include all required elements for proper coding and billing.

PAH confirmed by RHC

Specialty: Pulmonology

Required Elements

  • RHC results
  • Exclusion of secondary causes
  • Linkage to underlying conditions if secondary

Example Documentation

Patient diagnosed with idiopathic PAH confirmed by RHC: mPAP 48 mmHg, PAWP 12 mmHg, PVR 5.2 Wood units.

Examples: Poor vs. Good Documentation

Poor Documentation Example
Pulmonary hypertension; refer to cardiology.
Good Documentation Example
Idiopathic PAH confirmed by RHC: mPAP 48 mmHg, PAWP 12 mmHg, PVR 5.2 Wood units, excluding CTEPH via V/Q scan.
Explanation
The good example provides specific hemodynamic data and excludes secondary causes, supporting accurate coding.

Need help with ICD-10 coding for Pulmonary Arterial Hypertension? Ask your questions below.

Ask about any ICD-10 CM code, or paste a medical note

We build tools for
clinician happiness.

Learn More at Freed.ai
Back to HomeBeta

Built by Freed

Try Freed for free for 7 days.

Learn more