scholarly journals Pulmonary Mycobacterium kansasii disease in immunocompetent host: Treatment outcomes with short-course chemotherapy

2016 ◽  
Vol 34 (4) ◽  
pp. 516-519 ◽  
Author(s):  
C Padmapriyadarsini ◽  
D Nair ◽  
NS Gomathi ◽  
B Velayudham
Author(s):  
Shashikant Srivastava ◽  
Jann-Yuan Wang ◽  
Gesham Magombedze ◽  
Moti Chapagain ◽  
Hung-Ling Huang ◽  
...  

Standard therapy [isoniazid, rifampin, ethambutol], with or without a macrolide, for pulmonary Mycobacterium kansasii lasts more than a year. Therefore, shorter treatment duration regimens are required. We used data from 32 Taiwanese patients treated with standard therapy who were followed using repetitive sampling-based sputum Mkn time-to-positivity in liquid cultures to calculate kill slopes [γ] based on ordinary differential equations and time-to-extinction of each patient’s bacterial burden. The γ was 0.18 [95% Confidence Interval (CI): 0.16-0.20] log10 CFU/mL/day on standard therapy. Next, we identified Mkn time-to-extinction in the hollow fiber system model of pulmonary M. kansasii disease [HFS-Mkn] treated with standard therapy, which was a γ of 0.60 [95% CI: 0.45-0.69) log10 CFU/mL/day. The γs and time-to-extinctions between the two datasets formed structure-preserving maps based on category theory: thus, we could map them from one to the other using morphisms. This mapping identified a multistep non-linear transformation-factor for time-to-extinction from HFS-Mkn to patients. Next, a head-to-head study in the HFS-Mkn identified median time-to-extinction for standard therapy of 38.7 [95% CI: 29.1-53.2) days, isoniazid-rifampin-ethambutol-moxifloxacin of 21.7 [95% CI: 19.1-25) days, isoniazid-rifampin-moxifloxacin of 22 [96% CI: 20.1-24.5) days, and rifampin-moxifloxacin-tedizolid of 20.7 [95% CI:18.5-29) days. Our transformation-factor based translation predicted the proportion of patients of 90.7 [88.74-92.35)% achieving cure with standard therapy at 12 months, and 6-months cure rates of 99.8 [95% CI: 99.27-99.95)% for isoniazid-rifampin-ethambutol-moxifloxacin, 92.2 [90.37-93.71)% for isoniazid-rifampin-moxifloxacin, and 99.9 [99.44-99.99)% for rifampin-moxifloxacin-tedizolid. Thus, rifampin-moxifloxacin-tedizolid and isoniazid-rifampin-ethambutol-moxifloxacin are predicted to be short-course chemotherapy regimens for pulmonary M. kansasii disease.


Oncotarget ◽  
2017 ◽  
Vol 8 (66) ◽  
pp. 109889-109893
Author(s):  
Huiru An ◽  
Zhongyuan Wang ◽  
Hongbing Chen ◽  
Tao Wang ◽  
Xinjing Wang ◽  
...  

1998 ◽  
Vol 45 (3) ◽  
pp. 509
Author(s):  
Tae Hyung Kim ◽  
Kyoung A Kim ◽  
Chae Man Lim ◽  
Sang Do Lee ◽  
Youn Suck Koh ◽  
...  

2010 ◽  
Vol 35 (12) ◽  
pp. 1869-1874 ◽  
Author(s):  
Vikas Bhardwaj ◽  
Mayank Agrawal ◽  
Tarun Suri ◽  
Sumit Sural ◽  
Ravi Kashyap ◽  
...  

2012 ◽  
Vol 22 (2) ◽  
pp. 274-281 ◽  
Author(s):  
Zili Wang ◽  
Jiandang Shi ◽  
Guangqi Geng ◽  
Hongyan Qiu

1999 ◽  
Vol 81-B (3) ◽  
pp. 464-471 ◽  
Author(s):  
R. Parthasarathy ◽  
K. Sriram ◽  
T. Santha ◽  
R. Prabhakar ◽  
P. R. Somasundaram ◽  
...  

BMJ ◽  
1990 ◽  
Vol 301 (6748) ◽  
pp. 359-362 ◽  
Author(s):  
M S Jawahar ◽  
S Sivasubramanian ◽  
V K Vijayan ◽  
C V Ramakrishnan ◽  
C N Paramasivan ◽  
...  

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