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Journal of Clinical Microbiology, May 1999, p. 1579-1581, Vol. 37, No. 5
Division of Infectious Diseases,
Received 16 October 1998/Returned for modification 15 December
1998/Accepted 28 January 1999
The performance characteristics of the new signal
amplification-based Hybrid Capture (HC) II CT-ID test system (Digene,
Silver Spring, Md.) with endocervical specimens were compared to those of tissue culture and PCR (AMPLICOR CT PCR; Roche Molecular Systems, Branchburg, N.J.) for detection of Chlamydia trachomatis in
587 women. HC II CT-ID identified 62 of 65 confirmed C. trachomatis-positive patients (sensitivity of 95.4%) and was
negative for 517 of 522 patients who were negative by culture and PCR
(specificity of 99.0%). Twelve of the 65 confirmed positive patients
were negative by culture but were identified by both HC II CT-ID and
PCR (sensitivity of culture was 81.5% [P < 0.01]).
In comparison, PCR detected 59 of 65 positive specimens
(sensitivity of 90.8%) and had a specificity of 99.6% (520 of 522).
These results demonstrate that the Digene HC II CT-ID
test is a highly sensitive and specific assay for the detection of
C. trachomatis infection in endocervical specimens.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Evaluation of the Digene Hybrid Capture II CT-ID Test for
Detection of Chlamydia trachomatis in Endocervical
Specimens
*
Corresponding author. Mailing address: The Johns
Hopkins University, Division of Infectious Diseases, 720 Rutland Ave.,
Ross Research Building 1159, Baltimore, MD 21205. Phone: (410)
955-7635. Fax: (410) 614-9775. E-mail:
tquinn{at}welchlink.welch.jhu.edu.
Journal of Clinical Microbiology, May 1999, p. 1579-1581, Vol. 37, No. 5
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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