Summary & Overview
CPT 84228: Quinine Level in Serum or Plasma
CPT code 84228 represents a laboratory assay that measures the concentration of quinine in patient specimens such as serum or plasma. This test is clinically relevant for therapeutic drug monitoring and for evaluating potential quinine toxicity, with implications for patient safety and medication management across ambulatory and inpatient settings. Nationally, quinine level testing is a specialized laboratory service that supports clinicians managing antimalarial therapy or assessing adverse drug effects.
Key payers included in this analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context, typical sites of service, and payer coverage considerations. The publication outlines common billing modifiers associated with laboratory services and highlights what is known about coding, utilization patterns, and areas where payers often apply medical necessity review.
This resource provides benchmarks and practical policy context for hospital and clinical laboratory administrators, billing professionals, and clinicians who order or process quinine level testing. Data not available in the input are noted where applicable. The goal is to present clear, actionable information about CPT code 84228 so readers can align billing, documentation, and clinical workflows with payer expectations and coding standards.
Billing Code Overview
CPT code 84228 describes a laboratory test performed by a lab analyst to measure the level of quinine in a patient specimen, such as serum or plasma. This service is a clinical pharmacology/toxicology assay used to assess quinine concentration for therapeutic monitoring or toxicity evaluation.
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Service type: Laboratory drug assay (quinine level)
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Typical site of service: Clinical laboratory or hospital laboratory performing blood-based specimen testing
Clinical & Coding Specifications
Clinical Context
A 48-year-old patient on chronic quinine therapy for nocturnal leg cramps or a patient presenting to the emergency department with suspected quinine toxicity after accidental overdose has a serum or plasma specimen submitted for quantitative quinine level measurement. The clinical workflow begins when the treating clinician orders 84228 to assess therapeutic concentration or toxicity risk. A phlebotomy technician collects a blood specimen (serum or plasma) following standard venipuncture procedures and labels and sends the specimen to the clinical laboratory. The laboratory accessioner logs the specimen, and a clinical laboratory scientist or toxicology analyst performs the quantitative assay using immunoassay, high-performance liquid chromatography (HPLC), or mass spectrometry methods. Results are verified by a qualified laboratory professional and reported to the ordering clinician, who interprets the value in context of symptoms, dosing history, and potential drug interactions. Typical sites of service include hospital inpatient labs, hospital outpatient laboratories, emergency departments, and independent clinical reference laboratories. Clinicians ordering this test commonly include emergency medicine physicians, internists, toxicologists, and clinical pharmacologists.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the physician interpretation or professional component of the test separate from technical work. |