Are Survey-Based Estimates of the Burden of Drug Resistant TB Too Low? Insight from a Simulation Study

被引:16
作者
Cohen, Ted [1 ,2 ]
Colijn, Caroline [2 ]
Finklea, Bryson [2 ]
Wright, Abigail [3 ]
Zignol, Matteo [3 ]
Pym, Alexander [4 ]
Murray, Megan [1 ,2 ,5 ]
机构
[1] Brigham & Womens Hosp, Div Social Med & Hlth Inequal, Boston, MA 02115 USA
[2] Harvard Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[3] WHO, STOP TB Dept, Geneva, Switzerland
[4] S African MRC, Clin & Biomed TB Res Unit, Durban, South Africa
[5] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA USA
关键词
D O I
10.1371/journal.pone.0002363
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The emergence of tuberculosis resistant to multiple first- and second-line antibiotics poses challenges to a global control strategy that relies on standard drug treatment regimens. Highly drug-resistant strains of Mycobacterium tuberculosis have been implicated in outbreaks and have been found throughout the world; a comprehensive understanding the magnitude of this threat requires an accurate assessment of the worldwide burden of resistance. Unfortunately, in many settings where resistance is emerging, laboratory capacity is limited and estimates of the burden of resistance are obtained by performing drug sensitivity testing on a sample of incident cases rather than through the use of routine surveillance. Methodology/Principal Findings: Using an individual-based dynamic tuberculosis model to simulate surveillance strategies for drug resistance, we found that current surveys may underestimate the total burden of resistant tuberculosis because cases of acquired resistance are undercounted and resistance among prevalent cases is not assessed. We explored how this bias is affected by the maturity of the epidemic and by the introduction of interventions that target the emergence and spread of resistant tuberculosis. Conclusions: Estimates of drug resistant tuberculosis based on samples of incident cases should be viewed as a lower bound of the total burden of resistance.
引用
收藏
页数:8
相关论文
共 36 条
[1]   Epidemiology of antituberculosis drug resistance (the Global Project on Anti-tuberculosis Drug Resistance Surveillance): an updated analysis [J].
Aziz, Mohamed Abdel ;
Wright, Abigail ;
Laszlo, Adalbert ;
De Muynck, Aime ;
Portaels, Francois ;
Van Deun, Armand ;
Wells, Charles ;
Nunn, Paul ;
Blanc, Leopold ;
Raviglione, Mario .
LANCET, 2006, 368 (9553) :2142-2154
[2]  
Becerra MC, 2000, INT J TUBERC LUNG D, V4, P387
[3]   Effects of environment on compensatory mutations to ameliorate costs of antibiotic resistance [J].
Björkman, J ;
Nagaev, I ;
Berg, OG ;
Hughes, D ;
Andersson, DI .
SCIENCE, 2000, 287 (5457) :1479-1482
[4]   Understanding, predicting and controlling the emergence of drug-resistant tuberculosis: a theoretical framework [J].
Blower, SM ;
Gerberding, JL .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (09) :624-636
[5]   Fitness of antibiotic-resistant microorganisms and compensatory mutations [J].
Böttger, EC ;
Springer, B ;
Pletschette, M ;
Sander, P .
NATURE MEDICINE, 1998, 4 (12) :1343-1344
[6]   Simultaneous infection with multiple strains of Mycobacterium tuberculosis [J].
Braden, CR ;
Morlock, GP ;
Woodley, CL ;
Johnson, KR ;
Colombel, AC ;
Cave, MD ;
Yang, ZH ;
Valway, SE ;
Onorato, IM ;
Crawford, JT .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (06) :E42-E47
[7]   Modeling epidemics of multidrug-resistant M-tuberculosis of heterogeneous fitness [J].
Cohen, T ;
Murray, M .
NATURE MEDICINE, 2004, 10 (10) :1117-1121
[8]  
COHEN T, 2008, AM J RESP C IN PRESS
[9]   Exogenous re-infection and the dynamics of tuberculosis epidemics: local effects in a network model of transmission [J].
Cohen, Ted ;
Colijn, Caroline ;
Finklea, Bryson ;
Murray, Megan .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2007, 4 (14) :523-531
[10]   Genetic heterogeneity in Mycobacterium tuberculosis isolates reflected IS6110 restriction fragment length polymorphism patterns as low-intensity bands [J].
de Boer, AS ;
Kremer, K ;
Borgdorff, MW ;
de Haas, PEW ;
Heersma, HF ;
van Soolingen, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4478-4484