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Ustekinumab and Anti-Ustekinumab Ab

Test Catalog Information

Test Catalog Synonyms

EPIC Synonyms USTEKINUMAB
UST
Ustekinumab & Anti-Ustekinumab Ab
Cerner Primary MnemonicUstekinumab & Anti-Ustekinumab Ab
EPIC Display NameUstekinumab and Anti-Ustekinumab Ab
Allscripts (AEHR) Order Name

Ustekinumab & Anti-Ustekinumab Ab

Sunrise Clinical Manager (SCM) Order Name

Ustekinumab and Anti-Ustekinumab Ab

EPIC Inpatient Orderable Yes
EPIC Outpatient Orderable Yes
Cerner Results Anti-Ustekinumab Antibody
Ustekinumab
Clinical Info

rovides ustekinumab drug concentration and anti‐ustekinumab antibodies in order to optimize treatment and facilitate clinical decision‐making. This assay may be helpful in any patients on ustekinumab therapy for Crohn's disease, psoriasis, or other autoimmune conditions. Limitations Drug concentration should be interpreted with confirmation of specimen collection timing. Non‐trough concentrations may be misleading. Trough blood collection (just before or within 24 hrs. of next dose) is suitable because target ranges and therapeutic cut‐offs have been established in clinical studies using trough concentration. The drug half‐life should be taken into consideration when interpreting results from non‐perfect trough collections. Some primary non‐responders have inadequate clinical response despite adequate trough levels. As with other biologics, the optimal ustekinumab concentration depends upon patient‐specific factors including co‐morbidities, disease and desired therapeutic endpoint. Positive anti‐ustekinumab antibodies should be interpreted in the context of the concomitant free ustekinumab drug level. High serum biotin concentrations in patients taking biotin supplements may cause an interference in this assay. Patients may be advised to stop biotin consumption at least 72 hours prior to sample collection.

Specimen Type

Blood

Container

Gold Top Tube

Collection Instructions

Container/Tube: Gold Top Tube or Red Top Tube Specimen: 2 mL serum ( 1 mL min) Transport Temperature: Refrigerated Collection: Allow a minimum clotting time of 30 to 60 minutes with serum separation within 2 hours of collection.

Transport Instructions

Specimen Stability

14 Days Room Temperature 14 Days Refrigerated 14 Days Frozen

Methodology

Electrochemiluminescence immunoassay (ECLIA)

Days Performed

TAT: 11-26 Days

Performing Laboratory

LabCorp

CPT

80299 82397

PDM

235038

Desired Epic Build Ustekinumab and Anti-Ustekinumab Ab

Cerner Primary Mnemonic: Ustekinumab & Anti-Ustekinumab Ab
PDM 235038
Informatics - WorkgroupChemistry
Synonyms *USTEKINUMAB
UST
Ustekinumab & Anti-Ustekinumab Ab
Display Name *Ustekinumab and Anti-Ustekinumab Ab
Order Entry Specimen Sources *
Order Entry Specimen Types
Specimen Navigator Specimen Types
Specimen Navigator Specimen Sources
Specimen Navigator Short Name
Ordering info (EPIC SmartText)rovides ustekinumab drug concentration and anti‐ustekinumab antibodies in order to optimize treatment and facilitate clinical decision‐making. This assay may be helpful in any patients on ustekinumab therapy for Crohn's disease, psoriasis, or other autoimmune conditions. Limitations Drug concentration should be interpreted with confirmation of specimen collection timing. Non‐trough concentrations may be misleading. Trough blood collection (just before or within 24 hrs. of next dose) is suitable because target ranges and therapeutic cut‐offs have been established in clinical studies using trough concentration. The drug half‐life should be taken into consideration when interpreting results from non‐perfect trough collections. Some primary non‐responders have inadequate clinical response despite adequate trough levels. As with other biologics, the optimal ustekinumab concentration depends upon patient‐specific factors including co‐morbidities, disease and desired therapeutic endpoint. Positive anti‐ustekinumab antibodies should be interpreted in the context of the concomitant free ustekinumab drug level. High serum biotin concentrations in patients taking biotin supplements may cause an interference in this assay. Patients may be advised to stop biotin consumption at least 72 hours prior to sample collection.
IP Orderable Yes
OP Orderable Yes
AOEs *

AP AOEs
Special History No
Build Comments
Filter *
Procedure Category Change
Cerner Results

Result DescResult displayResult PDM
UST AB Anti-Ustekinumab Antibody 235038B
USTEKINUMAB Ustekinumab 235038A

Actual Epic build

Procedure Id
Pdm
Order Display Name
Procedure Name
Procedure Master Number
Short Procedure Name
Category Code
Category Code Record Name
Synonyms
Clinically Active
Orderable
Performable
Filter Genomics
Reference Link Url
Ordering Instructions
Default Specimen Type
Specimen Type Pick List
Specimen Type List
Op Specimen Type List
Specimen Source Pick List
Specimen Source Default - Male
Specimen Source Default - Female
Specimen Source List
Op Specimen Source List
Ip Lab Test Components For Report
Op Lab Test Components For Report
Order Questions
Order Questions Record Name
Inpatient Order Questions
Inpatient Order Questions Record Name
Order Specific Question Override
Inpatient Question Override
Location Restrict List Ip
Location Restrict List Ip Record Name
Location Restrict List Include Ip
Location Restrict List Op
Location Restrict List Op Record Name
Location Restrict List Includes Op
Edp Amb Order Specific Questions Record Name
Edp Ip Order Specific Questions Record Name
Edp Ip Specimen Source
Edp Op Specimen Source
Edp Ip Specimen Type
Edp Op Specimen Type
Derived Edp Ip Buttons S
Derived Edp Ip Buttons T
Derived Edp Op Buttons S
Derived Edp Op Buttons T
Ip Orderable
Op Orderable
EPIC OP AOEs

EPIC IP AOEs

EPIC Components (results)