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Prothrombin (PTR) Mutation Molecular Detection

Test Catalog Information

Test Catalog Synonyms
EPIC Synonyms FACTOR II
Venous thrombosis
Factor II G20210A mutation testing
FACTOR 2
Cerner Primary MnemonicxMGPTR
EPIC Display NameProthrombin (PTR) Mutation Molecular Detection
Allscripts (AEHR) Order Name

Not Orderable

Sunrise Clinical Manager (SCM) Order Name

Not Orderable

EPIC Inpatient Orderable Yes
EPIC Outpatient Orderable Yes
Cerner Results DNA Isolation
Prothrombin Gene Indication
Prothrombin Gene Result
PTR INTERP
Clinical Info

The prothrombin (Factor II) mutation refers to a base change from guanine (G) to adenine (A) at nucleotide position 20210 in the prothrombin gene. The G20210A mutation is associated with an elevation of prothrombin levels to about 30 percent above normal in heterozygotes and to 70 percent above normal in homozygotes. The mutation is the second most common inherited risk factor for thrombosis. In the United States, the prevalence of the mutant allele is 1.1 percent in Caucasians and Hispanics and 0.3 percent in African Americans. This mutation is present in about 2 percent of the population and in 6 percent or more of patients who present with a first venous thromboembolism (VTE).

Specimen Type

Blood

Container

Lavender Top Tube

Collection Instructions

Transport Instructions

Specimen Stability

Methodology

Days Performed

Performing Laboratory

NSLIJ Manhasset

CPT

PDM

5160177xx

Desired Epic Build Prothrombin (PTR) Mutation Molecular Detection

Cerner Primary Mnemonic: xMGPTR
PDM 5160177
Informatics - WorkgroupMolpath inhouse
Synonyms *FACTOR II
Venous thrombosis
Factor II G20210A mutation testing
FACTOR 2
Display Name *Prothrombin (PTR) Mutation Molecular Detection
Order Entry Specimen Sources *
Order Entry Specimen Types
Blood
Specimen Navigator Specimen Types
Specimen Navigator Specimen Sources
Specimen Navigator Short Name
Ordering info (EPIC SmartText)The prothrombin (Factor II) mutation refers to a base change from guanine (G) to adenine (A) at nucleotide position 20210 in the prothrombin gene. The G20210A mutation is associated with an elevation of prothrombin levels to about 30 percent above normal in heterozygotes and to 70 percent above normal in homozygotes. The mutation is the second most common inherited risk factor for thrombosis. In the United States, the prevalence of the mutant allele is 1.1 percent in Caucasians and Hispanics and 0.3 percent in African Americans. This mutation is present in about 2 percent of the population and in 6 percent or more of patients who present with a first venous thromboembolism (VTE).
IP Orderable Yes
OP Orderable Yes
AOEs *

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

Result DescResult displayResult PDM
DNA ISO DNA Isolation 5160192
PTR IND Prothrombin Gene Indication 5160014
RES PTR Prothrombin Gene Result 5160194
PTR INTERP PTR INTERP 5160222

Actual Epic build

Procedure Id 64734
Pdm 5160177
Order Display Name Prothrombin (PTR) Mutation Molecular Detection
Procedure Name PROTHROMBIN GENE MUTATION
Procedure Master Number LAB834
Short Procedure Name PROTHROMBIN GENE MUTATIO
Category Code 21.0
Category Code Record Name LAB MOLECULAR DIAGNOSTICS ORDERABLES
Synonyms FACTOR II VENOUS THROMBOSIS FACTOR II G20210A MUTATION TESTING FACTOR 2
Clinically Active Yes
Orderable Yes
Performable Yes
Filter Genomics Generic Genomics Procedure
Reference Link Url https://labs.northwell.edu/epic/test/64734
Ordering Instructions
Default Specimen Type Blood
Specimen Type Pick List Blood
Specimen Type List
Op Specimen Type List
Specimen Source Pick List Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous
Specimen Source Default - Male Blood, Venous
Specimen Source Default - Female Blood, Venous
Specimen Source List Blood, Venous Blood, Central Line Blood, Arterial Blood, Capillary
Op Specimen Source List
Ip Lab Test Components For Report HLXPTRFR
Op Lab Test Components For Report HLXPTRFR
Order Questions ["3048500000", "3045300170", "3045300171", "3045300173"]
Order Questions Record Name NH IP PATIENT COMPLETED CONSENT NH IP HOME COLLECT DATE NH IP HOME COLLECT DAYS NH IP HOME COLLECT MEDICALLY NECESSARY
Inpatient Order Questions ["3048500000", "3048500000"]
Inpatient Order Questions Record Name NH IP PATIENT COMPLETED CONSENT
Order Specific Question Override Yes
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 NH IP PATIENT COMPLETED CONSENT
Edp Ip Order Specific Questions Record Name NH IP PATIENT COMPLETED CONSENT
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 1
Op Orderable 1
EPIC OP AOEs

Question IDQuestion NameQuestionResponse TypeResponse ListRequire Response
3045300170 NH IP HOME COLLECT DATE Start Date Date Yes
3045300171 NH IP HOME COLLECT DAYS Days Custom List Monday
Tuesday
Wednesday
Thursday
Friday
Saturday
Sunday
Yes
3045300173 NH IP HOME COLLECT MEDICALLY NECESSARY Medically Necessary? Yes/No Yes
3048500000 NH IP PATIENT COMPLETED CONSENT Patient completed consent? Yes/No Yes
EPIC IP AOEs

Question IDQuestion NameQuestionResponse TypeResponse ListRequire Response
3048500000 NH IP PATIENT COMPLETED CONSENT Patient completed consent? Yes/No Yes
EPIC Components (results)