07.01.2013 Views

Sorted By Test Name - Mayo Medical Laboratories

Sorted By Test Name - Mayo Medical Laboratories

Sorted By Test Name - Mayo Medical Laboratories

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

FHIME<br />

91376<br />

Reference Values:<br />

Negative<br />

Clinical References: 1. Centers for Disease Control and Prevention: Guidelines for counseling<br />

persons infected with human T-lymphotropic virus type I (HTLV-I) and type II (HTLV-II). MMWR<br />

Morb Mortal Wkly Rep 1993;42(RR-9):1-13 2. Murphy E, Roucoux D: The epidemiology and disease<br />

outcome of human T-lymphotropic virus type II. AIDS Rev 2004;6:144-154 3. Projetti FA,<br />

Carneiro-Projetti AB, Catalan-Soares BC, et al: Global epidemiology of HTLV-I infection and associated<br />

diseases. Oncogene 2005;24:6058-6068<br />

Humoral Immunity Evaluation Panel<br />

Reference Values:<br />

HUMORAL IMMUNITY EVALUATION<br />

DIPHTHERIA ANTITOXOID, ELISA<br />

REFERENCE RANGE: > or =0.01 IU/mL (Post-Vaccination)<br />

INTERPRETIVE CRITERIA:<br />

or =0.01 IU/mL Protective Antibody Level<br />

A minimal four-fold increase between pre-immune and post-immunization sera is considered a normal<br />

response to diphtheria toxoid.<br />

This test was developed and its performance characteristics have been determined by Focus Diagnostics.<br />

Performance characteristics refer to the analytical performance of the test.<br />

HAEMOPHILUS INFLUENZAE B VACCINE RESPONSE, ELISA<br />

REFERENCE RANGE: > or =1 ug/mL post-vaccination (protective level)<br />

INTERPRETIVE CRITERIA:<br />

or =1.0 ug/mL Protective Antibody Level<br />

IgG antibody to polyribosylribitol phosphate (PRP), the capsule polysaccharide of Haemophilus<br />

influenzae type b, is measured in micrograms/mL (ug/mL), based on correlations with a reference Farr<br />

radioimmunoprecipitation assay (RIA). The exact level of antibody needed for protection from infection<br />

has not been clarified; values ranging from 0.15 ug/mL to 1.0 ug/mL have been reported. A four-fold<br />

increase in the PRP IgG antibody level between pre-vaccination and post-vaccination sera is considered<br />

evidence of effective immunization.<br />

TETANUS ANTITOXOID, ELISA<br />

REFERENCE RANGE: > or =0.50 IU/mL (Post-Vaccination)<br />

INTERPRETIVE CRITERIA:<br />

or =0.50 IU/mL Protective Antibody Level<br />

A minimal four-fold increase between pre-immunization and post-immunization sera is considered a<br />

normal response to tetanus toxoid. Levels greater than or equal to 0.50 IU/mL are generally considered<br />

protective, whereas levels less than 0.05 IU/mL indicate a lack of protective antibody. Levels between<br />

0.05 and 0.49 IU/mL are indeterminate for the presence of protective antibody and may indicate a need<br />

for further immunization to tetanus toxoid.<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 984

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!