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Oral Presentations - Pathology and Laboratory Medicine - University ...

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OtherAbstract # 69Laura Book 1 , Ghada N. Al-Rawahi 1,2 , Eva Thomas 1,21Department of <strong>Pathology</strong> <strong>and</strong> <strong>Laboratory</strong> <strong>Medicine</strong>, BC Children’s Hospital, 2 Department of<strong>Pathology</strong> <strong>and</strong> <strong>Laboratory</strong> <strong>Medicine</strong>, <strong>University</strong> of British ColumbiaGhada Al-Rawahievaluation of two chromogenic media for screening ofgroup b streptococcus in pregnant womenBackround/ObjectivesTo compare the performance of StrepB Select (SBB) (Bio-Rad) <strong>and</strong> chromID Strepto B agar (STRB) (BioMerieux)media to that of our routine method for group B Streptococcus (GBS) detection in women at 35 to 37 weeksgestation.MethodsFive hundred consecutive vaginal/anal swabs were submitted directly to our microbiology laboratory for routineGBS screen between January <strong>and</strong> July 2009. The swabs were immediately emulsified in 0.5 ml of sterile saline <strong>and</strong>processed as follows:• Routine: Blood agar plate (BAP) (PML) + Group B Strep (GBS) Broth (PML).The BAPs <strong>and</strong> the GBS broths were inoculated, then incubated at 35oC for 18-24 hours. BAPs were examinedfor colonies with typical GBS morphology. Negative BAPs were re-incubated for an additional 24 hrs <strong>and</strong> thecorresponding GBS broths were sub-cultured to BAPs. All suspect colonies were confirmed by Prolex Streptococcalgrouping latex reagents (Group B) (Pro-Lab Diagnostics).• Study: SBB + STRB + GBS broth.The SBB, STRB plates <strong>and</strong> GBS broths were incubated for 24 hours at 35oC, then processed as follows: all plateswere examined for the presence of GBS colonies (SBB: blue colonies; STRB: pale pink/red colonies) followed by latexagglutination confirmation. Negative SSB/STRB plates were re-incubated for an additional 24 hours <strong>and</strong> the GBSbroth was sub-cultured to SBB <strong>and</strong> STRB. Confirmation by latex agglutination was considered the gold st<strong>and</strong>ard.ResultsA total of 109/500 samples (22%) were positive for GBS as follows: routine method detected 88/109 (80%); SBBdetected 90/109 (83%) at 24 hours, 99/109 (91%) at 48 hrs, 107/109 (98%) after selective broth culture; STRBdetected 85/109 (78%) at 24 hrs, 95/109 (87%) at 48 hours, 104/109 (95%) after selective broth culture.ConclusionBoth chromogenic media were more sensitive than our routine method for detection of GBS. The SBB was easier toread <strong>and</strong> more sensitive whilst the STRB was more specific after direct reading. However, the specificity becomes less ofan issue if all suspect colonies are confirmed by latex agglutination.80 2 0 1 0 * P o s t e r P r e s e n t a t i o n s

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