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Rapid Plasma Reagin (RPR)

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Accredited by the Standards Council of Canada to Laboratory no. 594 - CAN-P-4E (ISO/IEC 17025)

Requisition Forms

Reference Details

Description:

Rapid plasma reagin (RPR) test for the determination of lipoidal antibody titres present in sera as a result of infection by treponemes or other nontreponemal diseases that cause tissue damage.

Test Category:
Serology
Pathogen:
Treponema pallidum subspecies pallidum
Illnesses and Diseases:
  • Syphilis
Specimen:

Serum – minimum of 0.5 mL. Maximum of 1.0 mL – same serum sample is used for all required syphilis testing.

Collection Method:

N/A

Specimen Processing, Storage and Shipping:
Store samples refrigerated or frozen until shipped for testing. Ship frozen samples on dry ice, and refrigerated samples on wet ice
Transportation of Dangerous Goods:

Shipping of specimens shall be done by a TDG certified individual in accordance with TDG regulations. For additional information regarding classification of specimens for the purposes of shipping, consult either Part 2 Appendix 3 of the TDG Regulations or section 3.6.2 of the IATA Dangerous Goods Regulations as applicable.

Patient Criteria:

Suspected of syphilis infection.

Accompanying Documentation:

Completed Syphilis requisition form including sender lab name, address and telephone number. Patient identifier (specimen reference #), date of birth and sex. Date collected and test requested.

Comments:

N/A

Methods and Interpretation of Results:

See reference below.

Turnaround Time:

20 calendar days. Contact the laboratory prior to submission of urgent clinical specimens.

Contact:
Phone #: (204) 789-2130 or (204) 789-6017
Fax: (204) 789-2018
References:
  1. A Manual of Tests for Syphilis 9th Edition. Edited by S. A. Larsen, V. Pope, R. E. Johnson, E. J. Kennedy Jr. American Public Health Association. Washington, D.C. 1998.
Guidelines: