Improved sensitivity of nucleic acid amplification for rapid diagnosis of tuberculous meningitis

被引:16
作者
Johansen, IS
Lundgren, B
Tabak, F
Petrini, B
Hosoglu, S
Saltoglu, N
Thomsen, VO
机构
[1] Statens Serum Inst, Int Reference Lab Mycobacteriol, DK-2300 Copenhagen S, Denmark
[2] Hvidovre Univ Hosp, Dept Clin Microbiol, Copenhagen, Denmark
[3] Istanbul Univ, Dept Infect Dis & Clin Microbiol, Cerrahpasa Med Fac, Istanbul, Turkey
[4] Dicle Univ Hosp, Dept Infect Dis, Diyarbakir, Turkey
[5] Cukurova Univ, Dept Infect Dis & Clin Microbiol, Adana, Turkey
[6] Cukurova Univ, Fac Med, Adana, Turkey
[7] Karolinska Hosp & Inst, Dept Clin Microbiol, Stockholm, Sweden
关键词
D O I
10.1128/JCM.42.7.3036-3040.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Early diagnosis of tuberculous meningitis (TBM) is essential for a positive outcome; but present microbiological diagnostic techniques are insensitive, slow, or laborious. We evaluated the standard BDProbeTec ET strand displacement amplification method (the standard ProbeTec method) for the detection of Mycobacterium tuberculosis complex organisms in parallel with the ProbeTec method with a modified pretreatment procedure with 101 prospectively collected cerebrospinal fluid specimens from 94 patients with suspected TBM. By the modified method, the sample-washing step was omitted. A definitive diagnosis was attained by culture. Thirteen specimens from 12 patients were culture positive for M. tuberculosis complex organisms; three specimens (23%) were microscopy positive for acid-fast bacilli. Among the culture-positive specimens, the standard ProbeTec method was positive for 8 (61.5%) and the modified assay was positive for 10 (76.9%). The overall specificity by both procedures was 98.8% compared to the results of culture. After discrepancy analysis, conducted by reviewing the patients' previous laboratory data, the specificity increased to 100%. If the cutoff value for respiratory specimens was adjusted from the recommended value of 3,400 to 1,000, the sensitivity of the modified procedure increased to 84.7%, with unchanged specificity. Results were obtained in 3 to 4 h. The new pretreatment procedure with the ProbeTec assay described here provides a rapid, simple, and sensitive tool for the diagnosis of TBM.
引用
收藏
页码:3036 / 3040
页数:5
相关论文
共 32 条
[1]   DIAGNOSTIC-CRITERIA FOR TUBERCULOUS MENINGITIS AND THEIR VALIDATION [J].
AHUJA, GK ;
MOHAN, KK ;
PRASAD, K ;
BEHARI, M .
TUBERCLE AND LUNG DISEASE, 1994, 75 (02) :149-152
[2]   Clinical evaluation of the BDProbeTec ET system for rapid detection of Mycobacterium tuberculosis [J].
Bergmann, JS ;
Keating, WE ;
Woods, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :863-865
[3]   Tuberculous meningitis in a country with a low incidence of tuberculosis:: Still a serious disease and a diagnostic challenge [J].
Bidstrup, C ;
Andersen, PH ;
Skinhoj, P ;
Andersen, ÅB .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2002, 34 (11) :811-814
[4]   Use of Roche AMPLICOR Mycobacterium tuberculosis PCR in early diagnosis of tuberculous meningitis [J].
Bonington, A ;
Strang, JIG ;
Klapper, PE ;
Hood, SV ;
Rubombora, W ;
Penny, M ;
Willers, R ;
Wilkins, EGL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (05) :1251-1254
[5]   Role of IS6110-targeted PCR, culture, biochemical, clinical, and immunological criteria for diagnosis of tuberculous meningitis [J].
Caws, M ;
Wilson, SM ;
Clough, C ;
Drobniewski, F .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (09) :3150-3155
[6]  
Chedore P, 2002, INT J TUBERC LUNG D, V6, P913
[7]   Diagnosis of extrapulmonary tuberculosis by Gen-Probe amplified Mycobacterium tuberculosis direct test [J].
Ehlers, S ;
Ignatius, R ;
Regnath, T ;
Hahn, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (09) :2275-2279
[8]   Comparison of T-cell-based assay with tuberculin skin test for diagnosis of Mycobacterium tuberculosis infection in a school tuberculosis outbreak [J].
Ewer, K ;
Deeks, J ;
Alvarez, L ;
Bryant, S ;
Waller, S ;
Andersen, P ;
Monk, P ;
Lalvani, A .
LANCET, 2003, 361 (9364) :1168-1173
[9]   Strand displacement amplification and the polymerase chain reaction for monitoring response to treatment in patients with pulmonary tuberculosis [J].
Hellyer, TJ ;
Fletcher, TW ;
Bates, JH ;
Stead, WW ;
Templeton, GL ;
Cave, MD ;
Eisenach, KD .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (04) :934-941
[10]  
Hosoglu S, 2002, INT J TUBERC LUNG D, V6, P64