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CPT Code

CPT code 87480 – Candida species nucleic acid detection


Code Definition

87480 is the CPT code for infectious agent detection by nucleic acid (DNA or RNA); Candida species, direct probe technique.

The test uses a non-amplified probe to find Candida DNA or RNA in a specimen, most often a vaginal swab. Amplified (PCR) Candida testing is reported with 87481, and quantification with 87482. Medicare pays 87480 on the Clinical Laboratory Fee Schedule.

Section
80047-89398 Pathology and laboratory
Subsection
87001-87999 Microbiology
Code range
87471-87801 Infectious agent detection by nucleic acid (DNA or RNA)
Billable
No
Code also known as
vaginal candida molecular test
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Key takeaways

Key takeaways

CPT code 87480 covers Candida species detection by direct (non-amplified) probe technique. Amplified NAAT or PCR testing is reported with 87481 instead.

Pair 87480 with ICD-10 B37.31 (acute candidiasis of vulva and vagina) or B37.32 (chronic) for recurrent cases. B37.3 is a non-billable header and won’t support the claim.

87480 can be co-billed with 87491 and 87591 as separately identifiable analytes. Modifier 59 or XU may be required, depending on the NCCI column indicator.

Pabau, the practice management platform we build, routes US claims through the Claim.MD clearinghouse, so each 87480 claim can be followed from submission to payment.

CPT code 87480: Official descriptor and clinical overview

The American Medical Association (AMA) defines CPT code 87480 as “Infectious agent detection by nucleic acid (DNA or RNA); Candida species, direct probe technique.” Specifically, the code reports one analyte, Candida species, detected with a non-amplified hybridization probe. Amplified testing (NAAT or PCR) is reported with 87481 instead, and culture and antigen tests have their own codes.

Clinically, 87480 supports the workup of vulvovaginal candidiasis (VVC), recurrent VVC, or vaginal discharge of unclear cause. Direct probe vaginitis assays often test one swab for Candida, Gardnerella vaginalis and Trichomonas vaginalis. As a result, each organism carries its own direct probe code: 87480, 87510 and 87660.

CodeShort descriptorCategoryAnalyte
87480Candida species, direct probe techniqueMicrobiology / Infectious agent detection by nucleic acidCandida species (DNA/RNA)
87481Candida species, amplified probe techniqueMicrobiology / Infectious agent detection by nucleic acidCandida species (DNA/RNA)
87482Candida species, quantificationMicrobiology / Infectious agent detection by nucleic acidCandida species (organism load)

CPT 87480 vs 87481 vs 87482: Choosing the right Candida code

The three Candida codes differ by laboratory method: direct probe, amplified probe, or quantification. Therefore, code the method the performing lab used, as shown on the lab report or in its test directory. In fact, payers check the reported code against that documentation, so a method mismatch is a routine cause of denials.

CodeMethodHow it worksWhen it fits
87480Direct probe (non-amplified)A labeled probe binds Candida DNA or RNA in the specimen without copying it firstDirect probe vaginitis panels that report Candida as detected or not detected
87481Amplified probe (NAAT, PCR)The target DNA or RNA is copied many times before detection, which raises sensitivityMolecular vaginitis panels and other amplified Candida assays
87482QuantificationMeasures the amount of Candida nucleic acid in the specimenLess common; verify payer policy before billing

Reporting 87480 and 87481 together: Each code describes a different method, so report the code that matches the assay the lab ran. Indeed, reporting both for one specimen tells the payer that two separate tests were performed. However, bill both only when the lab ran both methods and documented each result, and check the current NCCI procedure-to-procedure table for the pair first.

Specimen types and collection requirements

Payers and MAC Local Coverage Determinations (LCDs) tie coverage of CPT code 87480 to specific, documented specimen sources. In fact, a specimen type that is neither listed on the requisition nor consistent with the supporting ICD-10 code is a predictable denial trigger.

  • Vaginal swab: The most common specimen source for 87480. Self-collected or clinician-collected; collection method should match the lab’s validated protocol.
  • Cervical swab: Acceptable for combined vaginal pathogen panels. Additionally, document the anatomical site on the requisition.
  • Transport medium: Use the specimen transport specified by the performing lab. Otherwise, improper transport invalidates the probe result and the claim.
  • Labeling requirements: Specifically, the specimen label must include patient identifiers, collection date, collection site, and ordering provider NPI.
  • Requisition documentation: Record the specimen source explicitly. For example, vague entries such as “vaginal area” without a specific anatomical site flag the claim for additional documentation requests.

Place of service (POS) records where the test was performed. CPT code 87480 is most commonly billed by independent reference laboratories (POS 81), hospital outpatient laboratories (POS 22), or physician office laboratories (POS 11). Medicare pays 87480 on the Clinical Laboratory Fee Schedule (CLFS) in each of these settings. However, it is not priced on the Physician Fee Schedule.

ICD-10-CM codes that support medical necessity

An unlinked or mismatched diagnosis is the leading denial trigger for CPT code 87480. Every claim must carry an ICD-10-CM code that establishes the clinical reason for ordering the Candida probe test. Therefore, choosing the ICD-10 code when the test is ordered, rather than at billing, prevents the most common linkage errors.

ICD-10-CM codeDescriptionNotes
B37.31Acute candidiasis of vulva and vaginaPrimary supporting diagnosis for an acute episode; strongest medical necessity link
B37.32Chronic candidiasis of vulva and vaginaRecurrent VVC; supports repeat testing when episodes recur
N76.0Acute vaginitisUsed when cause is not yet confirmed; acceptable for screening-type orders
N76.1Subacute and chronic vaginitisRecurrent or persistent symptoms; supports repeat testing
N89.8Other specified noninflammatory disorders of vaginaUse when clinical presentation is atypical; secondary to more specific codes
R87.5Abnormal microbiological findings in specimens from female genital organsRarely primary; used when result drives further workup

When the cause isn’t confirmed yet, N76.0 supports the order until the result comes back. Additionally, check every code against the ICD-10-CM set in force on the date of service, because CMS updates it each October 1. For example, B37.3 is now a header, so claims need B37.31 or B37.32.

Medicare and commercial payer reimbursement

Medicare reimburses CPT code 87480 under the Clinical Laboratory Fee Schedule (CLFS) in every setting, including independent, physician office and hospital outpatient labs. In fact, the test is excluded from the Physician Fee Schedule, so there is no facility or non-facility rate to look up. CMS publishes one national limitation amount per code in the CMS Clinical Laboratory Fee Schedule files. Therefore, check the current quarter’s file before quoting a rate.

SettingFee scheduleNotes
Independent laboratory (POS 81)CLFS national limitation amountMost common billing context; the lab bills Medicare directly
Physician office laboratory (POS 11)CLFS national limitation amountRequires a CLIA certificate that covers the test’s complexity
Hospital outpatient laboratory (POS 22)CLFS national limitation amountPaid on the CLFS unless OPPS packages the test into the visit; there is no professional component to bill

Commercial payer coverage varies. Some payers restrict 87480 to symptomatic patients, and others require prior authorization for standalone vaginal pathogen panels. Indeed, payers that require prior auth don’t always grant it retroactively, so verify before ordering when the patient’s plan is unfamiliar. In addition, MAC Local Coverage Determinations (LCDs) govern Medicare coverage by jurisdiction, so a Novitas policy may not apply under CGS or WPS.

Pro Tip

Check the patient’s plan rules before collecting the specimen, not before submitting the claim. If the plan limits 87480 to symptomatic patients, finding out after the lab runs the sample leaves no route to retroactive authorization.

NCCI edits and codes billed alongside 87480

CPT code 87480 is often ordered on a direct probe vaginitis panel alongside Gardnerella and Trichomonas probes. Specifically, each is a separately identifiable analyte and can generally be reported on its own. Nevertheless, bundling edits can still apply, so check the current quarter’s NCCI table before you submit.

Code pair with 87480AnalyteNCCI bundle statusModifierNotes
87510Gardnerella vaginalis, direct probeGenerally separately reportable (different organism)59 or XU if edit firesSame direct probe panel
87660Trichomonas vaginalis, direct probeGenerally separately reportable (different organism)59 or XU if edit firesSame direct probe panel
87491Chlamydia trachomatis NAATGenerally separately reportable (different analyte)59 or XU if edit firesModifier indicator must be “1”
87591Neisseria gonorrhoeae NAATGenerally separately reportable (different analyte)59 or XU if edit firesDocument each result
87661Trichomonas vaginalis NAATGenerally separately reportable (different analyte)59 or XU if edit firesCheck MAC LCD frequency limits
81513Bacterial vaginosis (BV) RNA panel, BV onlyCheck current NCCI table; bundling rules varyModifier may be requiredSome LCDs require separate encounters
81514 / 81515Multiplex vaginitis panel that includes Candida speciesIncludes Candida; do not report with 87480, 87510 or 87660Not applicablePanel already covers Candida
87481Candida species, amplified probeSame organism, different methodCheck current NCCI tableBill both only if both assays ran

Modifier 59 vs X-modifiers: When a bundling edit fires, modifier 59 (distinct procedural service) may allow separate payment. In addition, the more specific X-modifiers (XE, XS, XP, XU) do the same job. Specifically, modifier 59 or XU is only valid when the NCCI column indicator is “1” (modifier allowed). Otherwise, if the indicator is “0,” the codes are never payable separately. As a result, appending one anyway creates false claim exposure.

Documentation that keeps 87480 claims clean

Overall, each element missing from the claim record maps to a specific claim adjustment reason code (CARC). A clean claim for 87480 needs these five components in place before submission.

  1. Clinical indication in the visit note: Document the patient’s symptoms (vaginal discharge, itching, odor, dyspareunia). In addition, record the clinical reason for ordering a Candida nucleic acid test rather than treating empirically. As a result, absent clinical indication is CARC 50 (not medically necessary).
  2. Correct ICD-10-CM code linked on the claim: The diagnosis must match the documented visit note. B37.31 is the preferred primary code for an acute episode, and B37.32 for recurrent cases. N76.0 is acceptable when the cause is unconfirmed. Consequently, a mismatched or absent ICD-10 code triggers CARC 11 or CARC 50.
  3. Specimen type and source on the laboratory requisition: Vague entries (“vaginal specimen”) without an anatomical site cause additional documentation requests (CARC 252). Instead, specify vaginal swab, cervical swab, or endocervical swab.
  4. Ordering provider NPI: The NPI on the requisition and on the claim must match the credentialed ordering provider. Otherwise, mismatched NPIs result in CARC 16 (claim/service lacks information).
  5. Place of service code: POS must reflect where the specimen was collected or where the testing was performed. As a result, POS errors cause claim rejections that delay reprocessing.

Common 87480 denials and how to appeal them

Overall, most 87480 denials are preventable and fall into five patterns. An effective denial management workflow maps each pattern to a specific fix before the appeal deadline runs.

Denial reasonLikely CARCFix and appeal approach
Diagnosis not supporting medical necessityCARC 50Correct ICD-10 linkage to B37.31, B37.32 or N76.0; attach visit note with symptoms documented; resubmit as corrected claim
NCCI bundling edit fired (no modifier)CARC 97Verify NCCI column indicator is “1”; if allowed, add modifier 59 or XU and resubmit; if indicator is “0,” report only the appropriate single code
Frequency limitation exceededCARC 119Pull the applicable MAC LCD for frequency limits; document recurrent symptoms clinically; appeal with medical records if testing was clinically justified
Missing prior authorizationCARC 15Contact payer to determine if retroactive auth is available; if not, write-off per plan contract or bill patient if ABN was signed
Specimen type not coveredCARC 252Resubmit with corrected requisition specifying approved specimen source; attach lab’s collection protocol if payer requests documentation

For Medicare denials, reference the AAPC Codify CPT lookup to confirm code status and any attached LCD policy notes before filing. Additionally, share the CARC denial codes reference with billing staff. Specifically, it shows how to route each denial type to the correct work queue.

CPT 87480 vs amplified and culture-based testing: When to use each

CPT code 87480 covers the direct probe approach to Candida detection. In contrast, amplified testing and culture use different CPT codes and have distinct billing and clinical trade-offs. Coders sometimes see chart orders for Candida testing that don’t name a method, and that leads to miscoding. The diagram below maps each lab method to its code.

Decision diagram for Candida testing codes
The lab’s method, not the chart order, decides the code, and a multiplex panel replaces 87480 entirely. Descriptors follow the AMA CPT code set.
MethodCPT code(s)What it reportsPayer considerations
Direct probe (non-amplified)87480 (Candida species, direct probe)Candida species detected or not detectedPaid on the CLFS; some payer policies restrict testing to symptomatic patients
Amplified probe (NAAT, PCR)87481 (Candida species, amplified probe); 87482 (quantification)Candida detected; some assays report species groups separatelyPaid on the CLFS; code only when the lab’s assay is amplified
Culture87102 (culture, fungi, isolation with presumptive identification, other source)Growth of an isolate, which allows species identification and susceptibility testingUseful in recurrent VVC when an isolate is needed to identify the species
Gardnerella direct probe87510 (Gardnerella vaginalis, direct probe)Gardnerella vaginalis detected or not detectedDistinct analyte (BV workup); not interchangeable with 87480 for Candida

The choice between probe testing and culture affects the CPT code billed and, therefore, the documentation required. When a chart notes “Candida culture ordered” but the lab runs a probe assay, a claim for 87480 or 87481 won’t match the order. That creates a medical necessity mismatch. Therefore, ensure the order, the lab requisition, and the billed code all reflect the same method.

Pro Tip

When a provider orders a ‘vaginal pathogen panel’ without naming a method, pull the lab’s test directory before coding. Many reference labs run amplified assays for every analyte in a panel, so Candida is reported with 87481, not 87480. Coding from the chart order alone without checking the lab report method is the root cause of most method-mismatch denials.

How Pabau keeps 87480 lab claims moving

Candida probe claims usually stall on small mismatches: a header ICD-10 code, a vague specimen source, or an NCCI pair billed without the right modifier. Finding them often means logging in to one payer portal after another.

Pabau sends US claims through the Claim.MD clearinghouse for electronic submission and status tracking. With claims management built in, details already on the patient record flow into the claim, so your team doesn’t re-key them.

Your billing team then sees which 87480 claims were accepted, paid or denied in one place. That view feeds your wider revenue cycle management, so a denial gets corrected and resubmitted instead of sitting unnoticed.

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Track every 87480 claim to payment

Pabau sends US claims through the Claim.MD clearinghouse and tracks each one, so your team can follow every lab claim from submission to payment.

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Conclusion

CPT code 87480 is the direct probe code for Candida, and the costliest error is treating it as the PCR code. Therefore, check the lab’s method before you choose between 87480 and 87481.

Then link B37.31 or B37.32 rather than the B37.3 header, and name the specimen source on the requisition. In addition, add a modifier only when the NCCI column indicator allows it. In short, each of those checks closes off one of the denial patterns above before the claim goes out.

If your team spends hours chasing denied lab claims, book a demo to see how Pabau tracks each one to payment.

Continue your research

Continue your research

Managing electronic claim submission for lab codes? How 837 files work in medical billing covers EDI transaction formats and how clearinghouses route claims to payers.

Getting denials with no clear CARC code? Reading electronic remittance advice (ERA) explains how to extract denial reason codes from 835 transactions for faster resolution.

Billing a full vaginal pathogen panel? Building an accurate superbill walks through how to structure multi-code lab claims so bundling edits are caught before submission.

Frequently asked questions

What does CPT code 87480 cover?

CPT code 87480 covers infectious agent detection by nucleic acid (DNA or RNA) for Candida species using a direct, non-amplified probe technique. Labs report it when a direct probe assay tests a specimen, usually a vaginal swab, for Candida. Amplified (PCR) Candida testing is reported with 87481 instead.

What is the difference between CPT 87480 and 87481?

CPT 87480 and 87481 both detect Candida species but differ by method. CPT 87480 uses a direct probe that binds the organism’s DNA or RNA without amplification. CPT 87481 uses an amplified probe technique, such as PCR, which copies the target before detection. Report the code that matches the assay the lab ran.

What are the most common denial reasons for CPT 87480?

The two most common denial reasons are a diagnosis that fails medical necessity (CARC 50) and an NCCI edit without a modifier (CARC 97). The other three are an exceeded frequency limit (CARC 119), missing prior authorization (CARC 15) and an uncovered or undocumented specimen type (CARC 252). Each has its own fix, listed in the denial table above.

Is CPT 87480 subject to NCCI edits?

Yes, CPT 87480 is subject to NCCI procedure-to-procedure edits, which CMS updates quarterly. Codes for other organisms, such as 87510, 87660, 87491 and 87591, are generally separately reportable as distinct analytes. A modifier may be required depending on the current NCCI column indicator. Before reporting 87480 with 87481, confirm the lab ran both methods and check the current edit table.

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Despina Petrushevska
Content Writer

Despina Petrushevska is a content writer covering aesthetics, dermatology, and clinic operations, known for making detailed clinical concepts clear and engaging. Outside of work, she enjoys photography, weekend getaways, and finding inspiration in everyday experiences.
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