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Medical Billing • CPT Modifiers • Laboratory Billing

Modifier 91

Repeat Clinical Diagnostic Laboratory Test

Learn what Modifier 91 means, when it is appropriate, when it should not be used, how it differs from Modifiers 59, 76 and 90, common denial scenarios, AR investigation steps and practical laboratory billing examples.

91
Repeat Clinical Diagnostic Laboratory Test

Modifier 91 at a Glance

The essential points every medical biller, coder and AR caller should know.

91

Repeat Laboratory Test

Used when the same clinical diagnostic laboratory test is performed more than once on the same day for the same patient when medically necessary.

SAME

Same Day

Modifier 91 is specifically associated with repeat laboratory testing performed on the same date of service.

MED

Medical Necessity

The repeat test must be necessary to obtain subsequent reportable results during the course of treatment.

NO

Not for Reruns

Do not use Modifier 91 for laboratory errors, quality-control reruns or confirmation of initial results.

What Is Modifier 91?

Understanding repeat clinical diagnostic laboratory testing.

Simple Definition

Modifier 91 is used to identify a repeat clinical diagnostic laboratory test performed on the same patient on the same day when the repeat test is medically necessary to obtain subsequent reportable results.

CMS explains that the modifier is appropriate when the physician needs a repeat clinical diagnostic laboratory test that is distinct or separate from other laboratory services and is performed to obtain medically necessary subsequent test values.

Easy Way to Remember

Think:

“91 = Same lab test, same patient, same day, medically necessary repeat result.”

The key question is not simply whether the laboratory test was performed twice. The reason for repeating the test matters.

The 4 Core Rules of Modifier 91

Check all four before reporting the modifier.

01

Same Patient

The repeated laboratory test is performed for the same patient.

02

Same Day

The repeat test occurs on the same date of service.

03

Medically Necessary

The repeat result is needed during the patient’s treatment.

04

Subsequent Result

The repeat test is performed to obtain another medically necessary reportable result.

CMS Rule

CMS states that Modifier 91 is for repeat laboratory testing on the same day when multiple results are medically necessary. It should not be used when testing is repeated merely to confirm the initial result or because of testing problems.

When Should Modifier 91 Be Used?

The clinical reason for the repeat test is the most important consideration.

YES

Treatment Monitoring

A laboratory test is repeated during treatment because another result is needed to monitor the patient’s condition.

YES

Multiple Clinical Results

The provider needs additional results during the same day to guide ongoing clinical management.

YES

Repeat Component Test

A component of a laboratory panel is repeated as a medically reasonable and necessary service on the same date.

YES

Subsequent Values

Additional reportable values are required during the course of treatment.

YES

Sequential Monitoring

The patient’s condition requires laboratory monitoring at different points during the same day.

YES

Separate Reportable Result

The second test produces a clinically needed result rather than simply repeating the first test because of a technical problem.

When Should Modifier 91 NOT Be Used?

These situations are especially important for denial prevention.

Do Not Use

Confirming Initial Results

Do not use Modifier 91 when the test is repeated simply to confirm the initial result.

Do Not Use

Laboratory Error

Do not use it when the original test needs to be rerun because of a laboratory error.

Do Not Use

Specimen Problem

Do not use it merely because there was a problem with the specimen or equipment.

Do Not Use

Quality Control

Internal quality-control reruns are not the intended use of Modifier 91.

Do Not Use

One Reportable Result

Do not use the modifier when only one normal, reportable result is required.

Do Not Use

Test Series Already Described

Do not use Modifier 91 when another CPT code already describes the series of test results.

CMS Warning

CMS specifically excludes repeat testing performed to confirm initial results, because of specimen or equipment problems, or when a normal one-time reportable result is all that is required.

Modifier 91 Decision Workflow

Use this workflow before appending Modifier 91.

1 Was the laboratory test performed more than once?
2 Was it performed for the same patient?
3 Were the tests performed on the same date of service?
4 Was the second test medically necessary during treatment?
5 Was another reportable result required?
6 Was the repeat test NOT caused by laboratory error, QC, specimen problems or confirmation of the first result?
7 Does another CPT code already describe the testing series?
8 If all applicable conditions support it, evaluate Modifier 91.

Modifier 90 vs Modifier 91

These two laboratory modifiers address completely different situations.

Feature Modifier 90 Modifier 91
Main purpose Identifies a referred/outside laboratory service. Identifies an appropriate repeat clinical diagnostic laboratory test.
Key issue Who performed the test? Why was the test repeated?
Same day requirement Not the defining concept. Yes.
Medical necessity Still subject to coverage requirements. Critical to appropriate use.
Laboratory error Not the defining issue. Do not use Modifier 91 for this reason.
Basic memory trick Outside laboratory. Repeat laboratory result.

Modifier 91 vs Modifier 59

One of the most important distinctions for laboratory billing.

Modifier 91

  • Repeat clinical diagnostic laboratory test.
  • Same patient.
  • Same day.
  • Medically necessary subsequent result.
  • Used for appropriate repeat laboratory testing.

Modifier 59

  • Identifies a distinct procedural service.
  • Different clinical circumstances must support distinctness.
  • Can involve separate encounters, sites, structures or other circumstances depending on the service.
  • Not simply a replacement for Modifier 91.
  • Must be supported by appropriate documentation.

CMS NCCI Guidance

CMS identifies Modifier 91 among the modifiers that may be used under appropriate circumstances with NCCI edits. CMS separately describes Modifier 91 as the appropriate modifier for repeating a component laboratory test from a panel when the repeat is medically reasonable and necessary on the same date.

Modifier 91 vs Modifier 76

Modifier Meaning Typical Service Key Question
76 Repeat procedure/service by same physician or other qualified healthcare professional. General procedures/services. Was the procedure repeated by the same provider?
77 Repeat procedure/service by another physician or other qualified healthcare professional. General procedures/services. Was the procedure repeated by another provider?
91 Repeat clinical diagnostic laboratory test. Laboratory testing. Was the laboratory test repeated for a medically necessary subsequent result?

AR Tip

Do not automatically replace Modifier 91 with Modifier 76. Determine whether the service is a clinical diagnostic laboratory test and then determine why it was repeated.

Modifier 91 and Laboratory Panels

A common CMS example involves repeating one component of a laboratory panel.

Example

A laboratory performs all tests included in an applicable laboratory panel.

During the same date of service, the provider needs one of the component tests repeated because another medically necessary result is required during treatment.

The applicable component CPT code may be reported again with Modifier 91 when the CMS requirements are met.

Coding Concept

Panel:

Laboratory Panel

Repeat component:

Component CPT + 91

CMS specifically gives this type of scenario as an example of appropriate Modifier 91 use.

Modifier 91 Billing Examples

Practical examples for billers, coders and AR callers.

Example 1 — Repeat Test During Treatment

A patient is receiving treatment and the provider needs another laboratory value later the same day to guide ongoing care.

CPT CPT-91

The second laboratory service may be reported with Modifier 91 when the applicable requirements are satisfied.

Example 2 — Panel Component Repeated

The laboratory performs a complete panel. One component must be repeated later that day to obtain a medically necessary subsequent value.

Panel CPT Component CPT-91

CMS specifically identifies this type of repeat component testing as an example for Modifier 91.

Example 3 — Laboratory Error

The laboratory repeats the test because the first specimen was compromised or there was a testing problem.

CPT

Do not use Modifier 91 merely to report the technical rerun.

Example 4 — Confirming Initial Result

The first laboratory result is unexpected and the laboratory repeats the test only to confirm the original result.

CPT

Modifier 91 should not be used when the test is rerun merely to confirm the initial result.

Example 5 — Multiple Clinical Values

Multiple laboratory values are needed during the same day’s treatment because the patient’s condition is changing.

CPT CPT-91

Modifier 91 may be appropriate when the repeated testing produces medically necessary subsequent reportable results.

Example 6 — Test Series Code

Another CPT code already describes a series of laboratory results.

Series CPT

Do not automatically report repeated individual tests with Modifier 91 when another code already describes the series.

Common Modifier 91 Denials

Common claim problems involving repeat clinical diagnostic laboratory testing.

Denial 01

Modifier Not Supported

The documentation does not establish that the repeat laboratory test was medically necessary.

Denial 02

Repeat Test Not Allowed

The payer does not consider the reported repeat laboratory service separately payable under the submitted circumstances.

Denial 03

Confirmation Testing

The second test was performed only to confirm the initial result.

Denial 04

Laboratory Error

The second test was required because of specimen, equipment or laboratory testing problems.

Denial 05

Duplicate Service

The payer considers the repeated laboratory service duplicative rather than a medically necessary subsequent test.

Denial 06

Wrong Modifier

Another modifier or coding approach may be applicable depending on the actual circumstances.

Denial 07

Missing Documentation

The medical record does not support why the repeat test was required.

Denial 08

Frequency Limitation

The payer’s policy may limit the number or frequency of separately payable laboratory services.

Denial 09

Medical Necessity

The diagnosis or clinical documentation does not support the repeat service under the payer’s policy.

AR Caller Workflow for Modifier 91 Denials

A practical denial-management workflow for repeat laboratory services.

1

Review ERA / EOB

Identify the exact denial message, CARC, RARC, adjustment and affected laboratory claim line.

2

Identify the CPT / HCPCS

Determine which laboratory test was billed more than once.

3

Verify Date of Service

Confirm whether the repeated laboratory services occurred on the same date.

4

Compare Claim Lines

Review the original line and repeated line, including units and modifiers.

5

Verify Modifier 91

Determine whether the second laboratory service has Modifier 91 and whether the clinical circumstances support it.

6

Determine Why It Was Repeated

Find out whether the repeat was medically necessary for treatment, a confirmation test, QC rerun, specimen issue or another reason.

7

Review Medical Documentation

Verify that the medical record supports the clinical reason for obtaining another result.

8

Check Laboratory Policy

Review Medicare, MAC, Medicaid, Medicare Advantage or commercial payer requirements.

9

Check NCCI / MUE

Determine whether an NCCI edit or MUE affects the service and whether the applicable modifier rules support separate reporting.

10

Identify Root Cause

Determine whether the denial resulted from coding, documentation, medical necessity, frequency, duplicate billing or payer policy.

11

Correct or Appeal

Submit a corrected claim or appeal only when supported by the payer’s requirements and documentation.

12

Document Follow-Up

Record payer instructions, representative name, reference number, filing deadline and next action.

AR Caller Script for Modifier 91

Questions to ask the payer when investigating a repeat laboratory denial.

“I’m calling regarding a clinical laboratory claim where the repeat laboratory service was submitted with Modifier 91.”

“Could you please provide the exact denial reason and the applicable CARC and RARC codes?”

“Can you confirm whether the denial is related to Modifier 91 or to the laboratory service itself?”

“Can you confirm whether your policy allows this laboratory test to be reported more than once on the same date of service?”

“Can you confirm what documentation is required to support the medical necessity of the repeat test?”

“Does your policy distinguish between medically necessary repeat testing and testing performed to confirm an initial result?”

“Can you confirm whether an NCCI or MUE edit affected this claim line?”

“If a corrected claim is required, could you please confirm the exact correction and filing deadline?”

“If an appeal is appropriate, what documentation should be submitted?”

“May I have the call reference number for our records?”

Documentation Checklist

What the billing and AR team should be able to establish.

01

First Test

Identify the original laboratory test and result.

02

Repeat Test

Identify the second laboratory test and its result.

03

Same Date

Verify that the repeat service occurred on the same date of service.

04

Clinical Reason

Document why the subsequent laboratory result was needed.

05

Medical Necessity

Establish that the repeat test was necessary during the course of treatment.

06

Reportable Result

Establish that the repeat test generated a clinically needed subsequent reportable result.

Root Causes of Modifier 91 Denials

01

Wrong Modifier

Modifier 91 was reported when the circumstances do not support it.

02

Confirmation Test

The laboratory repeated the test only to confirm the first result.

03

Technical Rerun

The second test resulted from a specimen, equipment or laboratory problem.

04

No Medical Necessity

The record does not support why another result was required.

05

Duplicate Service

The payer considers the second test duplicative.

06

Frequency Issue

The payer’s policy limits the frequency or number of separately payable tests.

07

Wrong CPT

Another CPT code may describe the laboratory testing series.

08

Missing Documentation

The claim does not have adequate support for the repeat service.

Modifier 91 and Medicare NCCI

Modifier 91 can have an important role when laboratory edits are involved.

NCCI Considerations

  • Review the applicable NCCI PTP edit.
  • Check whether the same CPT/HCPCS code appears on multiple claim lines.
  • Determine the MUE Adjudication Indicator when applicable.
  • Confirm that Modifier 91 is clinically supported.
  • Review the current NCCI Policy Manual.

CMS NCCI Guidance

CMS identifies Modifier 91 as one of the modifiers that can be used under appropriate circumstances with NCCI edits. CMS also explains that when an applicable MUE is adjudicated as a claim line edit, certain modifiers can allow separate lines to be adjudicated separately.

However, the existence of a modifier does not automatically justify its use. The clinical circumstances must support the modifier.

Modifier 91 and MUEs

What AR Should Know

A Medically Unlikely Edit, or MUE, represents a maximum number of units of a service that a provider would typically report for the same beneficiary on the same date of service under the applicable MUE methodology.

CMS explains that when a HCPCS/CPT code has an MUE adjudicated as a claim-line edit, certain appropriate modifiers—including 91—may allow separate claim lines to be adjudicated separately. This does not mean every repeat service should receive Modifier 91.

Modifier 91 and Medicaid

Medicaid Review Checklist

  • Identify the state Medicaid program.
  • Verify whether Modifier 91 is recognized.
  • Review the state Medicaid laboratory policy.
  • Check Medicaid NCCI requirements.
  • Verify frequency and medical-necessity requirements.
  • Check the applicable Medicaid MCO policy.

Important

Medicaid requirements can vary by state. Medicaid managed-care organizations may also have additional billing policies.

CMS notes that Medicaid NCCI policies can apply Modifier 91 in appropriate laboratory circumstances, but providers should also check the applicable state Medicaid agency requirements.

Modifier 91 and Commercial Insurance

01

Verify Payer Policy

Confirm whether the payer recognizes Modifier 91 and under what circumstances.

02

Verify Medical Necessity

Determine whether the payer requires documentation supporting the repeat test.

03

Check Frequency

Review payer-specific frequency limitations.

04

Check NCCI

Determine whether an applicable coding edit affected payment.

05

Review Documentation

Confirm the clinical reason for the subsequent laboratory result.

06

Follow Appeal Rules

Use the payer’s current corrected-claim and appeal process.

How to Prevent Modifier 91 Denials

01

Capture Clinical Reason

Document why another laboratory result was needed.

02

Confirm Same Day

Verify the repeated service occurred on the same date of service.

03

Avoid Confirmation Reruns

Do not use Modifier 91 simply to confirm the first result.

04

Avoid QC Reruns

Separate internal quality-control testing from medically necessary patient testing.

05

Check CPT Series

Confirm another CPT code does not already describe the testing series.

06

Audit Denials

Track Modifier 91 denials by payer, CPT, reason and root cause.

Modifier 91 Quick Cheat Sheet

  • Modifier 91 = Repeat Clinical Diagnostic Laboratory Test.
  • The test is repeated for the same patient.
  • The repeat test occurs on the same date of service.
  • Another medically necessary reportable result is required.
  • The repeat test is part of the patient’s course of treatment.
  • Do not use Modifier 91 for laboratory errors.
  • Do not use it for quality-control reruns.
  • Do not use it merely to confirm the initial result.
  • Do not use it when only one normal reportable result is needed.
  • Check whether another CPT code already describes the testing series.
  • Check applicable NCCI and MUE rules.
  • Medical necessity documentation may be required.
  • Modifier 91 does not guarantee payment.
  • Always verify the applicable payer policy before appealing.

Before You Bill Modifier 91

  • Confirm the laboratory test was performed more than once.
  • Confirm the same patient was tested.
  • Confirm the same date of service.
  • Confirm the repeat was medically necessary.
  • Confirm another reportable result was needed.
  • Confirm the repeat was not caused by laboratory error.
  • Confirm it was not simply a confirmation test.
  • Confirm it was not a quality-control rerun.
  • Check whether another CPT describes the test series.
  • Review applicable NCCI/MUE rules.
  • Verify payer-specific requirements.
  • Maintain documentation supporting the repeat service.

Modifier 91 FAQs

What is Modifier 91?

Modifier 91 identifies an appropriate repeat clinical diagnostic laboratory test performed on the same patient on the same day when another medically necessary reportable result is required.

What does Modifier 91 mean in medical billing?

It means an appropriate laboratory test was repeated on the same day to obtain a subsequent medically necessary result.

Can Modifier 91 be used on the same day?

Yes. Same-day repeat laboratory testing is the specific circumstance addressed by Modifier 91.

Can Modifier 91 be used for the same patient?

Yes. The modifier applies when the same laboratory test is performed more than once on the same patient on the same day under the applicable circumstances.

Can Modifier 91 be used to confirm an initial result?

No. CMS specifically says Modifier 91 must not be used when testing is repeated to confirm the initial result.

Can Modifier 91 be used for laboratory errors?

No. Modifier 91 should not be used when the test is rerun because of laboratory, specimen or equipment problems.

Can Modifier 91 be used for quality control?

No. Quality-control reruns are not the intended use of Modifier 91.

Can Modifier 91 be used when only one result is needed?

No. CMS excludes situations where a normal one-time reportable result is all that is required.

Can Modifier 91 be used with a laboratory panel?

When a laboratory performs all tests in an applicable panel and one component is repeated as a medically reasonable and necessary service on the same date, CMS states that the component CPT code may be reported with Modifier 91.

What is the difference between Modifier 91 and Modifier 90?

Modifier 90 identifies a referred or outside laboratory service. Modifier 91 identifies an appropriate repeat clinical diagnostic laboratory test.

What is the difference between Modifier 91 and Modifier 59?

Modifier 91 addresses appropriate repeat clinical diagnostic laboratory testing. Modifier 59 identifies a distinct procedural service. They should not be treated as interchangeable modifiers.

What is the difference between Modifier 91 and Modifier 76?

Modifier 76 is used for an appropriate repeat procedure or service by the same physician or other qualified healthcare professional. Modifier 91 specifically addresses repeat clinical diagnostic laboratory testing.

Does Modifier 91 guarantee payment?

No. Modifier 91 only identifies the applicable repeat laboratory circumstance. Coverage, medical necessity, frequency limits, NCCI edits and payer policy still apply.

Can Modifier 91 bypass an NCCI edit?

Modifier 91 is among the modifiers that CMS recognizes for appropriate NCCI circumstances, but it must be clinically supported. It should never be added simply to bypass an edit.

What should an AR caller check first?

Start with the ERA/EOB denial reason, then review the CPT, date of service, claim lines, Modifier 91, clinical reason for the repeat test, documentation and payer policy.

What documentation supports Modifier 91?

Documentation should support that the repeat test was clinically necessary during treatment and that another reportable result was needed. The exact documentation requirements can vary by payer and policy.

Can Modifier 91 be used for a test repeated because of a bad specimen?

Generally no. CMS specifically excludes repeat testing caused by testing problems involving specimens or equipment.

What if another CPT code already describes a series of results?

Modifier 91 should not be used to separately report repeated tests when another code already describes the testing series.

Does Medicare use Modifier 91 for laboratory tests?

Yes. CMS Medicare guidance specifically addresses Modifier 91 for laboratory tests paid under the Clinical Laboratory Fee Schedule when the applicable repeat-testing circumstances are met.

Where can I find official CMS laboratory guidance?

CMS maintains a Clinical Labs Information Center containing Medicare Claims Processing Manual laboratory guidance, NCCI resources, Clinical Laboratory Fee Schedule information and other laboratory billing resources.

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