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Policies
POLICY
STATEMENT FROM MAYO MEDICAL LABORATORIES ABOUT ANALYTE-SPECIFIC REAGENTS
(ASR): Mayo Medical Laboratories
The ordering of tests which utilize ASRs is limited to
physicians and other persons authorized by applicable state law to order such
tests. As required by the Food and Drug Administration, HHS, the following
comment will appear on the test report when ASRs are utilized to perform the
test: “This test was developed and its
performance characteristics determined by Laboratory Medicine and Pathology,
Mayo Clinic Rochester. It has not been cleared or approved by the U.S. Food and
Drug Administration.”
POLICY
STATEMENT FROM ST. LOUIS CHILDREN'S HOSPITAL ABOUT ANALYTE-SPECIFIC REAGENTS
(ASR): St. Louis Children’s Hospital
Clinical Laboratory
As required by the Food and Drug Administration, HHS,
the following comment will appear on the test report when ASRs are utilized to
perform the test: “This test was developed and its performance characteristics
determined by St. Louis Children’s Hospital Clinical Laboratory. It has not
been cleared or approved by the U.S. Food and Drug Administration.”
We do not accept animal specimens for laboratory
testing except by special arrangement with the appropriate Laboratory Director
or Supervisor approval.
Cancellations received prior to testing will be
honored at no charge.
St. Louis Children’s Hospital Laboratory is dedicated
to providing quality healthcare services to our patients. By following laws, regulations and ethical
obligations, we earn the trust and respect of our patients and our community. We respect the confidentiality of our
Patient's health information. We have
policies and guidelines in place to ensure that laboratory results are being
released within the requirements of the law. We appreciate your assistance in
helping St. Louis Children's Hospital Laboratory preserve patient
confidentiality. When requesting the
release of patient results the provision of appropriate identifiers will
greatly assist in a prompt and accurate response.
It is your responsibility to determine the correct CPT
codes to use for billing. While this catalog lists CPT codes in an effort to
provide some guidance, the CPT codes listed reflect only our interpretation of
CPT coding requirements and may not necessarily be correct. Particularly, in
the case of a test involving several component tests, this catalog attempts to
provide a comprehensive list of the CPT codes for all of the possible
components of the test. Only a subset of the component tests may be performed
on your specimen. You should verify the accuracy of the codes listed; and where
multiple codes are listed, you should select the codes for the tests actually
performed on your specimen.
St. Louis Children's Hospital uses Mayo Medical
Laboratories (MML) for certain reference testing services. Many of the laboratory tests, panels, and
profiles that MML performs for St. Louis Children's Hospital Laboratory are
identified and listed in this test catalog.
The MML tests, panels, and profiles have been established by MML in
accordance with their policies and procedures.
Any listed MML profile that contains multiple CPT codes should be
treated as a profile for purposes of Medicare.
Therefore, the ordering physician should order the profile only if all
of its components are medically necessary for the particular patient. If all of the components are not medically
necessary, the physician should order only the necessary tests. For further reference, please consult the CPT
Coding Manual published by the American Medical Association; and if you have
any questions regarding the use of a code, please contact your local Medicare
carrier.
Specimen Labeling Requirements
All specimens submitted to the
St. Louis Children's Hospital Laboratory for analysis must follow the
collection process for identification of the patient and be properly labeled.
Specimens are considered
properly collected according to the following criteria:
·
Specimens are labeled at the point of collection. This must be done by the person
obtaining the specimen.
·
The unique identifiers obtained from the patient must match those on the
requisition and the specimen label.
Specimens are considered
properly labeled according to the following criteria:
·
Specimens are
labeled with the patient=s first and last name and another unique patient
identifier :
i.e. Medical record number
Date of birth
Social
security number
Financial
number
Specimens for trauma
patients may be labeled with an alpha numeric identifier and do not require
a
second
unique identifier. Patient
identification for trauma patients shall remain unchanged for the first
24 hours of the patient’s
admission.
·
Blood Bank specimens require the above information as
well as date of collection, and initials or signature of the individual drawing
the specimen.
Specimens with trauma number designations may only be
used for compatibility testing for 24 hours
provided the requests for transfusion use the
Trauma Number. After 24 hours, a new
specimen shall
be collected for compatibility testing upon
updating the patient’s demographics.
Each separate tube or container
collected must have its own label affixed to the specimen.
·
Specimens will be
considered unlabeled or mislabeled and not acceptable for analysis if any label
requirements are missing, illegible, or inaccurate.
·
Each separate
tube or container collected must have it=s own
label affixed to the specimen (one label around two tubes is not acceptable).
Specimens must also be
sealed and properly contained. Examples
of specimens not properly contained:
·
Leaky urines.
·
Tubes of blood not sealed correctly.
·
Any other body
fluid not contained properly.
IMPROPERLY
LABELED SPECIMENS SUBMITTED FOR ANALYSIS
Specimens will be considered unlabeled or mislabeled
and not acceptable for analysis if:
·
The patient's
name and/ or unique identifier (Medical record number, financial number, Date
of Birth, social security number) is missing from the specimen container.
Requisition Requirements
Testing orders should be
requested on a St. Louis Children’s Hospital requisition. Providing complete information on each
laboratory requisition is necessary to ensure accurate ordering, timely
reporting and correct billing. The
following information is required on the requisition:
When a third party is to be billed the following
additional information is necessary.
Patient's complete address,
diagnosis, commercial insurance plan name and address, name of subscriber and
certificate and group numbers.
Note: A
photocopy of both sides of the patient's insurance card attached to the
requisition is sufficient for the required insurance information.
Supplies
Mailing cartons, specimen vials, special specimen
collection containers and kits, sterile vials, stool containers, and request
forms are supplied without charge.
Contact Laboratory Customer Service at (314) 454-4161.
All tests are unique in their collection and testing
requirements. To avoid specimen rejection or delayed turnaround times, please
check the “Specimen Required” field within each test.
You will be notified of rejected or problem specimens upon receipt.
Please review the following conditions prior to
submitting a specimen to St. Louis Children’s Hospital:
• Any timed urine collections (e.g. 12 hour, 24 hour,
etc.)
• pH of urine
• Lack of hemolysis/lipemia
• Specimen
type (plasma, serum, whole blood, etc.)
• Specimen
volume
• Patient
information requested
• Patient/specimen
properly identified
• Specimen
container (metal-free, separation gel, appropriate preservative, etc.)
• Transport
medium
• Temperature
(ambient, frozen, refrigerated)
Reference
Lab Testing
The main reference laboratory used by St. Louis
Children's Hospital is Mayo Medical Laboratories.
October 2009