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G388

G388Management of special oral chemotherapy

OHIP Diagnostic & Therapeutic Procedures Code — DIAGNOSTIC AND THERAPEUTIC PROCEDURES · Schedule of Benefits

This is the service for the supervision of oral chemotherapy treatment for malignant disease where the agent(s) has a significant risk of toxicity in the period immediately following initiation. The physician must be available to intervene in a timely fashion for a 24 hour period following the initiation of the treatment. In addition to the Common Elements in this Schedule, this service includes the provision of the following services to the same patient: a. evaluation of any relevant laboratory, diagnostic and/or imaging investigations; and b. all discussion or advice, whether by telephone or otherwise, involving the patient, staff, patient's relative(s) or patient's representative related to the oral chemotharapy for a period of twenty-one (21) days following initiation of the agent(s).

When to Use

  • Use G388 when initiating high-toxicity oral chemotherapy agents like imatinib or capecitabine that require active monitoring for immediate adverse reactions.
  • Use this code to capture the 21-day period of follow-up care, including all telephone advice and laboratory review related to the initiation of the oral agent.

Common Pitfalls

  • Billing G388 in the same month as G382 will trigger an automatic rejection; ensure you are not claiming both for the same patient in the same billing cycle.
  • Failing to document the specific 24-hour availability window post-initiation is a frequent audit trigger for this code.

Billing Tips

  • Ensure the 21-day follow-up period is clearly tracked, as all subsequent consultations or telephone calls regarding the chemotherapy are considered included in the G388 fee.
Provider Fee$28.00

Effective: April 1, 2026

Category

J. Diagnostic and Therapeutic Procedures

Subcategory

DIAGNOSTIC AND THERAPEUTIC PROCEDURES

Service Type

ManagementFee

Code Classes

Diagnostic and Therapeutic Procedures

In addition to standard medical record requirements as per , the physician should document the initiation of the specific oral chemotherapy agent, their availability for 24 hours post-initiation, and any included follow-up activities such as evaluation of investigations and discussions with the patient or team.

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