Mycobacterial culture results of smear-positive patients with suspected pulmonary tuberculosis in Liverpool

被引:11
作者
Corless, JA
Stockton, PA
Davies, PDO
机构
[1] Ctr Cardiothorac, TB Res Ctr, TB Res Unit, Liverpool L4 3PE, Merseyside, England
[2] Univ Hosp, Aintree Chest Ctr, Liverpool, Merseyside, England
关键词
contact-tracing environmental mycobacteria tuberculosis;
D O I
10.1183/09031936.00.16597600
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The aim of this study was to assess the final mycobacterial culture results of patients with smear-positive sputum or bronchial washings and to investigate the efficiency of local tuberculosis (TB) contact-tracing. Retrospective analysis of mycobacterial cultures and contact-tracing was performed in every patient,vith smear-positive sputum or bronchoalveolar lavage (BAL) in two Liverpool teaching hospitals (1996-1998). Of these patients 116 with smear-positive sputum or BAL were identified, Mycobacterium tuberculosis (M. tuberculosis) was cultured in 57 (49%), environmental mycobacteria in 37 (32%) and cultures were negative in 22 (19%) of the patients. Contact-tracing information was available in 107 of the 116 (92%) patients. A total number of 1,357 contacts were screened for possible tuberculosis, Of these, 420 (31%) were contacts of patients who cultured environmental organisms or had negative cultures. In this study, 51% of smear-positive patients in Liverpool did not have tuberculosis. Inefficiencies in current contact-tracing procedures have been identified which result from screening contacts of index cases that are subsequently found not to have cultured Mycobacterium tuberculosis, The authors believe that there are clear grounds for using rapid tests to identify and type mycobacteria more quickly than current solid or liquid media methods. It is also suggested that regional variations in the frequency of infection with environmental mycobacteria should be considered when formulating tuberculosis contact-tracing procedures.
引用
收藏
页码:976 / 979
页数:4
相关论文
共 23 条
[1]  
Alcaide F, 2000, J CLIN MICROBIOL, V38, P398
[2]   ACID-FAST SMEARS IN TUBERCULOSIS DETECTION [J].
BORCHARDT, KA ;
GELBER, R ;
BOTCH, V .
ANNALS OF INTERNAL MEDICINE, 1976, 84 (03) :344-344
[3]   DECREASING RELIABILITY OF ACID-FAST SMEAR TECHNIQUES FOR DETECTION OF TUBERCULOSIS [J].
BOYD, JC ;
MARR, JJ .
ANNALS OF INTERNAL MEDICINE, 1975, 82 (04) :489-492
[4]  
*BRITH THOR ASS, 1982, BRIT MED J, V284, P1454
[5]  
Campbell I, 2000, THORAX, V55, P210
[6]  
CHAN W, 1971, B WORLD HEALTH ORGAN, V45, P551
[7]  
DOMINGUEZ J M, 1977, Tubercle, V58, P217, DOI 10.1016/0041-3879(77)90046-0
[8]   A national audit of the laboratory diagnosis of tuberculosis and other mycobacterial diseases within the United Kingdom [J].
Drobniewski, FA ;
Watt, B ;
Smith, EG ;
Magee, JG ;
Williams, R ;
Holder, J ;
Ostrowski, J .
JOURNAL OF CLINICAL PATHOLOGY, 1999, 52 (05) :334-337
[9]  
GORDIN F, 1990, ARCH PATHOL LAB MED, V114, P1025
[10]   Identification of Mycobacterium species by PCR-restriction fragment length polymorphism analyses using fluorescence capillary electrophoresis [J].
Hernandez, SM ;
Morlock, GP ;
Butler, WR ;
Crawford, JT ;
Cooksey, RC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3688-3692