Test Catalog

Test Id : FOAPE

Ova and Parasite Exam, Fecal (Immunocompromised or Travel History)

Method Name
A short description of the method used to perform the test

Qualitative Concentration/Trichrome Stain/Microscopy

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Ova and Parasite Exam, Fecal

Aliases
Lists additional common names for a test, as an aid in searching

Ascaris

Chlonorchis sinesis

Eggs or Cysts

Fasciola

Giardia Exam

Heminths

Isospora, Isospora belli, Cystoisospora

O and P

OP FEC

Opisthrochis sinensis

Parasites

Parasitic Exam

Parasitic examination, stool

parasitic worms

Parasitology Examination

Protozoa

S. haematobium

S. japonicum

Sarcocystis

Schistosoma mansoni

Strongyloides

Specimen Type
Describes the specimen type validated for testing

Fecal

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Patient Preparation: Specimens analyzed to determine the efficacy of treatment should be collected three to four weeks after completion of therapy. Antibiotics may affect results of exam.

Specimen Type: Stool

Acceptable: AlcorFix Tube

Collection Instructions: Transfer 2 g of stool within one hour of collection into AlcorFix (Min: 1 g) and send ambient.

 

Acceptable: ECOFIX preservative (T219) (Min: 5mL)

Collection Instructions:

1. Place specimen into preservative within 30 minutes of passage or collection.

2. Follow instructions on the container as follow:

a. Mix the contents of the tube with the spoon, twist the cap tightly closed, and shake vigorously until the contents are well mixed. Refer to the fill line on the Ecofix vial for stool specimens.

b. Do not fill above the line indicated on the container.

c. Duodenal aspirates, small bowel aspirates, or colonic washings should be placed in Ecofix in a ratio of 1:1.

 

Also acceptable: Transfer 5 g of stool within one hour of collection into both 10 perfect formalin and modified PVA (10 g total). (Min: 10 g total)

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Other: Rectal swabs. Multiple specimens (more than one in 24 hours). Unpreserved specimens. Specimens containing barium, oil, or urine. Frozen specimens.

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Fecal Ambient (preferred) 270 days
Refrigerated 270 days

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Negative

Interpretation
Provides information to assist in interpretation of the test results

Method for identification of Ova and Parasites includes wet mount and trichrome stain. Due to the various shedding cycles of many parasites, three separate stool specimens collected over a 5–7-day period are recommended for ova and parasite examination. A single negative result does not rule out the possibility of a parasitic infection. The ova and parasite exam does not specifically detect Cryptosporidium, Cyclospora, Cystoisospora, and Microsporidia.

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Sunday through Saturday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

5 to 11 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

ARUP Laboratories

Fees
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

  • Authorized users can sign in to Test Prices for detailed fee information.
  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.

CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

87177

87209

LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
FOAPE Ova and Parasite Exam, Fecal 10704-5
Result Id Test Result Name Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
Z6251 Ova and Parasite, Fecal Interp 10704-5

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports

Test Update Resources

Change Type Effective Date
Test Status - Test Delay 2022-08-23
New Test 2022-07-20
New Test 2022-07-20