Find Locations
For hours, walk-ins and appointments.Unable to load global navigation.
Find Locations
For hours, walk-ins and appointments.HIV p24 antigen/antibody with reflex to antibody differentiation; HIV-1/2 qualitative RNA; T. pallidum antibody w/reflex to RPR (with titer); Chlamydia/Gonococcus, NAA; HBV Baseline Evaluation - Hepatitis B Surface Antigen (HBsAg) screen with reflex to HBV quant DNA; Hepatitis B Surface antibody (anti-HBS); Hepatitis B Core antibody, Total (anti-HBc); Hepatitis C Virus (HCV) antibody with reflex to quantitative real-time PCR
This profile requires a dedicated, unopened, gel-barrier tube and 2 frozen (preferred) or refrigerated serum pour-off tubes.
Tests included within this profile may exhibit interference when sample is collected from a person who is consuming a supplement with a high dose of biotin (also termed as vitamin B7 or B8, vitamin H, or coenzyme R). It is recommended to ask all patients who may be indicated for testing about biotin supplementation. Patients should be cautioned to stop biotin consumption at least 72 hours prior to the collection of a sample.
2 - 3 days (testing performed daily)
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Serum and urine
10 mL serum and 2 mL of a 20 mL to 30 mL urine collection
7 mL serum (this volume does not allow for repeat testing) and 2 mL of a 15 mL urine collection
Gel-barrier tube and APTIMA® urine specimen transport
Serum specimen: Usual blood collection technique.
Urine specimen: The patient should not have urinated for at least one hour prior to specimen collection. Direct patient to provide a first-catch urine (approximately 20 to 30 mL of the initial urine stream) into a urine collection cup free of any preservatives. Collection of larger volumes of urine may result in specimen dilution that may reduce test sensitivity; lesser volumes may not adequately rinse organisms into the specimen. Add urine to the APTIMA® Combo 2 urine collection device. The final volume must be between the two black lines on the device (about 2 mL). PCR test: Centrifuge sample within 24 hours of collection. Transfer serum to a screw-cap polypropylene transport tube. Ship frozen (preferred) or refrigerated.
Serum: Gel-barrier tubes refrigerated up to 6 days
PCR test: Frozen up to 6 weeks
APTIMA® Urine: Maintain at room temperature or refrigerate (2°C to 30°C)
Temperature | Period |
---|---|
Room temperature | Urine: 30 days (stability provided by manufacturer or literature reference) |
Refrigerated | Serum: 6 days (stability provided by manufacturer or literature reference) |
Frozen | Serum: 6 weeks (stability provided by manufacturer or literature reference) |
Freeze/thaw cycles | Serum: Stable x4 (stability provided by manufacturer or literature reference) |
Patient should not have urinated for one hour prior to specimen collection.
Hemolysis; lipemia; received outside of specimen and/or storage and/or labeling requirements; aliquot received for HIV testing; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; APTIMA® urine transport >30 days from collection; APTIMA® urine transport with incorrect specimen volume
This profile aligns with current guidelines for assessment of male patients prior to the initiation of injectable HIV PrEP.
The profile includes HIV Antibody/p24 Antigen and HIV-1/2 RNA for the detection of HIV infection; Chlamydia trachomatis and Neisseria gonorrhoeae nucleic acid amplification; serologic testing for syphilis; serological assessment of HBV infection status; and reflexive testing for the detection of HCV infection.
HIV p24 antigen/antibody specimens with reactive results must be investigated by additional supplemental tests. A negative test for an individual does not preclude exposure to or infection with HIV-1 and/or HIV-2. Negative results can occur if the quantity of the marker present in the sample is too low for detection by the assay or if the marker is not present during the stage of disease in which a sample is collected.
See individual test components.
Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
---|---|---|---|---|---|---|
254972 | PrEP, BL Inj + HIV RNA (M) | 083903 | HIV Antibody/p24 Antigen | 56888-1 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 139826 | HIV-1 RNA | 25835-0 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 139827 | HIV-2 RNA | 69353-1 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 083969 | Test Information | 55752-0 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 082356 | T pallidum Antibodies | 47236-5 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 188078 | Chlamydia trachomatis, NAA | 43304-5 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 188086 | Neisseria gonorrhoeae, NAA | 43305-2 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 019054 | N/A | |||
254972 | PrEP, BL Inj + HIV RNA (M) | 006510 | HBsAg Screen | 5196-1 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 006408 | Hep B Surface Ab, Qual | 22322-2 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 006718 | Hep B Core Ab, Tot | 13952-7 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 144721 | Rfx to HBcIgM | 77202-0 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 006720 | Interpretation | 56850-1 | ||
254972 | PrEP, BL Inj + HIV RNA (M) | 144035 | HCV Ab | 40726-2 |
Reflex Table for HIV Antibody/p24 Antigen | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 083938 | HIV 1/2 Ab Differentiation | 083907 | HIV 1 Ab | 68961-2 |
Reflex Table for HIV Antibody/p24 Antigen | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 083938 | HIV 1/2 Ab Differentiation | 083908 | HIV 2 Ab | 81641-3 |
Reflex Table for T pallidum Antibodies | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 082361 | PrEP: RPR | 006097 | RPR | 20507-0 | |
Reflex 2 | 006476 | RPR, Quant | 006476 | RPR, Quant | titer | 31147-2 |
Reflex Table for T pallidum Antibodies | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 082361 | PrEP: RPR | 006097 | RPR | 20507-0 | |
Reflex 2 | 082348 | Treponemal Antibodies, TPPA | 082349 | Treponemal Antibodies, TPPA | 24312-1 |
Reflex Table for T pallidum Antibodies | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 082361 | PrEP: RPR | 006097 | RPR | 20507-0 | |
Reflex 2 | 082348 | Treponemal Antibodies, TPPA | 010003 | Interpretation: | N/A |
Reflex Table for HBsAg Screen | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 016105 | HBsAg Confirmation | 016105 | HBsAg Confirmation | 7905-3 |
Reflex Table for Rfx to HBcIgM | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 144722 | PrEP: Hep B Core Ab, IgM | 016881 | Hep B Core Ab, IgM | 24113-3 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 144030 | Interpretation: | 144030 | Interpretation: | 13955-0 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 550644 | HCV RT-PCR, Quant (Non-Graph) | 550338 | Hepatitis C Quantitation | IU/mL | 11011-4 |
Reflex 2 | 550352 | HCV RNA (International Units) | 550353 | HCV RNA (International Units) | IU/mL | 11011-4 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 550644 | HCV RT-PCR, Quant (Non-Graph) | 550338 | Hepatitis C Quantitation | IU/mL | 11011-4 |
Reflex 2 | 550352 | HCV RNA (International Units) | 550354 | HCV log10 | log10 IU/mL | 38180-6 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 550644 | HCV RT-PCR, Quant (Non-Graph) | 550339 | HCV log10 | log10 IU/mL | 38180-6 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 550644 | HCV RT-PCR, Quant (Non-Graph) | 550314 | Test Information: | 19147-8 |
Reflex Table for HCV Ab | ||||||
---|---|---|---|---|---|---|
Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
Reflex 1 | 550644 | HCV RT-PCR, Quant (Non-Graph) | 550396 | Interpretation: | 62365-2 |
© 2021 Laboratory Corporation of America® Holdings and Lexi-Comp Inc. All Rights Reserved.
CPT Statement/Profile Statement
The LOINC® codes are copyright © 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC® codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Additional information regarding LOINC® codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf