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Clinical Chemistry Forum |
1 Because total and direct bilirubin are coded using the same CPT code (82251), HCFA has chosen to count the CPT codes rather than the number of tests and pay this six-test panel as though it contained only five tests. The old Hepatic Function Panel (80058) included bilirubin (total or direct), which when coded separately is 82250. The new Hepatic Function Panel includes bilirubin (total and direct), which when coded separately is 82251.
| Abstract |
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| Medicare Payment for Clinical Laboratory Services |
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Most clinical laboratory procedures are paid from laboratory fee schedules issued by individual Medicare carriers. Medicare carriers are contractors, usually large insurance companies, who administer Part B Medicare services in each state. There are 57 carriers, including one for each state and territory plus two in California and three in New York. All physician services, including pathology services not included in the laboratory fee schedule, are paid according to the Physician Fee Schedule. Unlike the laboratory fee schedule, under this schedule co-payments of 20% are collected from the beneficiary so that the actual payment received from Medicare for a given procedure is 80% of the Physician Fee Schedule amount.
Before Medicare pays for any test or diagnostic service, two basic criteria must be met: (a) the service must be covered by Medicare, and (b) the service must be medically necessary and indicated. Once these two criteria are met, Medicare pays for most clinical laboratory tests based on the applicable Laboratory Fee Schedule. Each carrier publishes a unique laboratory fee schedule and adjusts payment levels as determined by Congress during the annual budget process. Updates, when granted, are effective January 1st.
national fee limitations
National caps apply to most laboratory tests. These caps define
the maximum amount a carrier may pay for a given test. The 1998
National Limitation amounts for any given test are based on 74% of the
median amount listed on all carriers' fee schedules for a particular
laboratory test. National caps were reduced from 76% to 74% effective
January 1, 1998, resulting in a reduction of 2.63% for most clinical
laboratory tests.
Fee schedules may be adjusted only by statutory changes approved by
Congress. When the fee schedule is adjusted by a given percentage,
national caps are adjusted up or down by the same amount. Medicare
payment for clinical laboratory tests is always the lowest of the fee
schedule, the national cap, or the actual amount billed. The changes
shown in Table 1
have been made to laboratory fees since 1984, when the
Laboratory Fee Schedule was established. The dollar amounts at the
right-hand side of Table 1
show the effect of fee schedule changes on a
test that was reimbursed at $10.00 in 1984.
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Certain clinical diagnosis procedures listed in the Pathology and Laboratory sections of the Physicians' Current Procedural Terminology (CPT) (1) are not considered a part of the laboratory fee schedule. The procedures listed below are paid from the Physician Fee Schedule at 80% of the amount listed on that fee schedule. The beneficiary is responsible for the remaining 20% once the annual deductible has been met. These procedures are not subject to national limitations:
Medicare tests must be billed on an assigned basis. This means that the provider must accept the Medicare reimbursement as payment in full for any covered laboratory test. Medicare patients may not be billed for any additional amounts for covered tests. (See below for policies regarding tests that are not covered by Medicare). Medicare patients may be billed for non-covered services. The mandatory assignment requirement for laboratory tests applies regardless of whether the physician is participating (accepts assignment for all Medicare services) or non-participating (does not accept assignment for all Medicare services).
Direct billing is also required for all Medicare-reimbursed laboratory tests. Tests must be billed directly to Medicare by the laboratory or physician performing the tests. If an outside laboratory performs a test on a referral from a physician, only the reference laboratory may legally bill Medicare for the procedure.
However, hospitals and reference laboratories that send specimens to other laboratories may bill Medicare for tests performed by the other laboratories if the referring laboratory meets any one of the following three exceptions:
For the purpose of the 30% exception, each CPT code billed counts as one test. For example, when CPT code 80054 is billed, it is counted as one test although 12 tests are performed.
| The Health Care Financing Administration Common Procedure Coding System |
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Level I, which constitutes the major part of the system, is the CPT coding system. For most claims submitted, the CPT code is all that is required.
Level II, National HCPCS Codes, begin with a letter (AV) and are followed by four numbers. Most of these codes are used for describing supplies and do not apply to laboratory and pathology procedures. These codes are the same throughout the US.
Level III, Local or Intermediary HCPCS codes, begin with WZ or S and are followed by four digits. These codes are established by local Medicare carriers and are seldom used.
When code levels overlap, local codes have top priority, national codes second, and CPT codes lowest priority.
cpt codes
The procedure code is one of the most important parts of a
Medicare claim. The code used determines what and if a laboratory will
be paid for any given test or procedure. Use of CPT codes for
submitting Medicare claims became mandatory in 1987. Most other
insurance companies and third party payers also use these codes to
identify what medical procedures have been performed in the course of
any episode of illness or medical treatment.
CPT codes are revised and published annually by the American Medical Association (AMA). Of the >7000 procedures listed, ~950 apply to clinical laboratory tests and pathology services. The official AMA-published CPT manual together with its comprehensive cross index should always be used as the primary tool when searching for a particular procedure or test.
Many payers interpret and apply coding rules in unique and sometimes arbitrary ways. The only way to assure full reimbursement for any given procedure is to regularly review claims payments. The success of a coding strategy can be verified only by submitting claims, monitoring the payments received, and comparing the amounts actually paid to the Medicare fee schedules.
Laboratory tests are listed in the CPT by a common procedure name followed by additional information that describes the method, specimen source, or other details. The common procedure name is not repeated when used with more than one code. Care must be taken in reading individual entries to refer back to the common name that precedes the semicolon and to see if any subheadings apply more specifically to the test being coded than the principal code.
procedure code modifiers
Procedure code modifiers are two-digit codes added to the basic
five-digit CPT code. Modifiers are used to describe unusual
circumstances or to provide additional information regarding a test or
procedure. HCFA has created the following additional modifiers which
may be used in submitting Medicare claims.
-GA, waiver of liability statement on file.
This modifier is
used to indicate that the provider has notified a Medicare patient that
the test performed may not be reimbursed by Medicare and may be billed
to the patient. Situation- specific waivers of liability must be
obtained by a provider and signed by the patient if the patient is to
be billed for tests or other services not covered by Medicare.
-GB, distinct procedural service.
This modifier is used to
indicate that a procedure or service is distinct or separate from other
service(s) performed on the same day. For example, performance of a
follow-up test after obtaining an abnormal result from a more general
clinical test.
-QP, individually ordered automated test or panel.
This
modifier is used to indicate that automated chemistry tests or panels
containing only automated chemistry tests were ordered individually and
as such are not subject to medical necessity documentation
requirements.
-QW, CLIA waived category test.
This modifier is used to
indicate a CLIA-waived procedure was used.
-QR, repeat clinical diagnostic lab test performed on the same day
to obtain subsequent reportable test value(s) (separate specimens taken
in separate encounters).
This modifier is used when it is
necessary to obtain multiple results in the course of treatment, for
example, concentrations of drugs or hormones during treatment or
challenge tests. This modifier is not to be used when codes are
available that describe the series of results, e.g., glucose tolerance.
When a modifier is employed, additional information should be provided to support its use. In most cases, use of the modifier alone will not guarantee appropriate reimbursement. Modifiers are to be used sparingly. It is better to use a more specific primary code (with no accompanying description) to describe what was done.
| Medicare Coding Rules for Clinical Laboratory Services |
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Additional coding rules apply to test panels and profiles. If a specific code exists for a given combination of tests, that code must be used. It is considered billing fraud to unbundle a test panel to obtain higher reimbursement if a single code exists that more accurately describes the test panel.
| Specimen Collection Codes |
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For Medicare claims the following HCPCS code is used:
This code is used to avoid confusion over the inclusion of finger/heel/ear stick specimens in code 36415. Code G0001 must be used for all Medicare venipunctures (and urine collections by catheterization).
Physician laboratories may charge for specimen collection only when (a) it is accepted and prevailing practice among physicians in the locality to make a separate charge for drawing or collecting a specimen, and (b) it is the customary practice of the physician performing such a service to bill separately for specimen collection. In other words, physicians may collect the $3.00 Medicare venipuncture fee only if they also charge other payers for blood draws.
Specimen collection fees are also paid when it is medically necessary for a laboratory technician to draw a specimen from either a nursing home or homebound patient. The technician must personally draw the specimen. When a laboratory performs the specimen collection, it may receive payment both for the draw and the associated travel to obtain the specimen(s) for testing. Payment may be made to the laboratory even if the nursing facility has on-duty personnel qualified to perform the specimen collection. When the nursing home performs the specimen collection, it may receive payment only for the draw. Specimen collection performed by nursing home personnel for patients covered under Medicare Part A is paid for as part of the payment to the facility for its reasonable costs, not on the basis of the specimen collection fee.
The $3.00 Medicare specimen collection fee does not apply to non-routine venipuncture or arterial punctures. Arterial punctures for blood gas testing should be coded as CPT 36600 (arterial puncture, withdrawal of blood for diagnosis). Non-routine venipunctures, such as those common to pediatrics and those performed in atypical vein sites, should be coded using cardiovascular codes, 36400-36410 or 36420-36425. Medicare reimbursement for these procedures is paid from the Physicians' Medicare Fee Schedule rather than the Medicare Laboratory Fee Schedule.
A code for 24-h urine specimens (81050, volume measurement for timed collection, each) was added in 1993 and is used whenever a volumetric measure of urine is required to report a test result.
| Travel Allowance Codes |
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HCPCS codes used for travel allowances for Medicare claims are as follows:
| Drug Testing Codes |
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Quantitative assays should be coded using the appropriate method code or 83520 (immunoassay, other than antibody or infectious agent antigen, quantitative, not otherwise specified).
CPT code 80100 or 80101 is used for the initial screen, depending on whether the method detects multiple classes or a single class of drugs. Each confirmatory identification procedure is coded separately using 80102. These codes may be used in addition to the codes listed in the Therapeutic Drug Assay section of the CPT if the drug(s) determined qualitatively is subsequently quantified.
For example, an overdose of phenobarbital is suspected after obtaining a positive result for a urine screen for barbiturates. A quantitative serum assay for phenobarbital is then performed. Coding would be as follows:
| Evocative/Suppression Testing |
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Supplies and drugs used in performing evocative/suppression panels are reported using CPT code 99070 (supplies and materials provided by physician over and above those usually included with the office visit or other services rendered). Appropriate evaluation and management codes may be used to report physician attendance and monitoring. Prolonged physician care codes may be used if appropriate, but not for prolonged infusions reported under CPT codes 90780 and 90781.
| Allergy Testing |
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CPT code 86003 should be submitted for each allergen determined.
Other allergy testing is described under the Medicine section of the CPT using the following codes (954004-95078). These codes are not part of the laboratory fee schedule and are paid from the Physician Fee Schedule.
scratch, puncture, and prick tests
intradermal tests
other tests
CPT codes for percutaneous (scratch, puncture, or prick), intracutaneous (intradermal), and patch tests include test performance, evaluation, and correlation with the patient's history, physical examination, and other observations. The number of tests should be dependent upon history, physical findings, and clinical judgment. All patients should not receive the same number or type of sensitivity tests.
| Molecular Diagnostics Procedures |
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New antigen-specific codes are now used to describe infectious agent antigen detection and quantification using molecular diagnostic procedures (see New Codes for 1998 below).
| Antibody Identification Codes |
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For example, if antibodies to Coxsackie A and B viruses are determined using two separate assays, the following codes would be used:
If the IgM immunoglobulin class was subsequently determined for each type of virus, the same code would be used two more times:
When a specific antibody is not listed, one of the following general purpose codes or the appropriate method code should be used:
Identification of antibodies to antigens other than viruses, fungi, or bacteria are coded by method rather than analyte. For example, an immunofluorescent titer for Trichinella antibodies (a parasite) would be coded as:
| CLIA 1988 Waived Test Codes |
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Rather than continue to create new codes for each CLIA-waived product approved by the Food and Drug Administration, HCFA has chosen to use a modifier (QW) to designate waived tests. Payment, in general is the same as for the non-waived version of the same test. The following waived procedures are included in the 1998 laboratory fee schedule:
| Unlisted Procedure Codes |
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| Method Codes |
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| Changes in the 1998 CPT |
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miscellaneous laboratory procedures
automated test panels
Coding rules and medical necessity documentation requirements for automated tests and automated test panels are discussed under New Automated Multichannel Tests.
hepatitis tests
infectious agent antigens
An extensive new section covering the detection and quantification
of infection agent antigens by various methods has been added under
"Microbiology" in the Laboratory section of the CPT.
These codes replace the following general method codes, which have been
deleted.
The new codes are organized under the following seven methods:
The following individual CPT codes have been assigned to specific infectious agents under each method category. A general purpose code for unspecified agents is also included for each method.
INFECTIOUS AGENT ANTIGEN DETECTION BY DIRECT FLUORESCENT ANTIBODY TECHNIQUE: qualitative or semiquantitative, multistep method
INFECTIOUS AGENT ANTIGEN DETECTION BY ENZYME IMMUNOASSAY TECHNIQUE, qualitative or semiquantitative, multistep method
INFECTIOUS AGENT DETECTION BY IMMUNOASSAY WITH DIRECT OPTICAL OBSERVATION
A new series of CPT codes for antigen detection by nucleic acid (DNA or RNA) techniques has been created for the following infectious agents. Each infectious agent detection is classified as either by direct probe technique, amplified probe technique, or quantification.
pap smear procedures
Codes 88151 (CYTOPATHOLOGY: smears, cervical or vaginal, up to
three smears; requiring physician interpretation) and 88157
(CYTOPATHOLOGY: smears, cervical or vaginal, up to three smears, the
Bethesda System (TBS); requiring physician interpretation) have been
replaced with the single new code 88141 (CYTOPATHOLOGY: smears,
cervical or vaginal, up to three smears; any reporting system,
requiring physician interpretation).
Two new codes (88152 and 88158) have been added for automated rescreening of slides using conventional and Bethesda system techniques, and code 88142 has been created for reporting automated thin layer preparations screened by cytotechnologists under physician supervision.
embryo preparation and transfer codes
The following new codes are now available:
| Organ- or Disease-oriented Panels |
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| Use of the New Automated Test Panels |
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