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1 ve therapy group (antiretroviral therapy and isoniazid preventive therapy).
2 CWs to be offered antiretroviral therapy and isoniazid preventive therapy.
3 r-randomized, phased-implementation trial of isoniazid preventive therapy.
4 in 7 years of follow-up for those initiating isoniazid preventive therapy.
5 tment; if not, they were offered 9 months of isoniazid preventive therapy.
6 afe initiation of antiretroviral therapy and isoniazid preventive therapy.
7 uld have greater confidence in the safety of isoniazid preventive therapy.
8 or this purpose in assessing indications for isoniazid preventive therapy.
9  July 1992 and January 1994 and were offered isoniazid preventive therapy.
10 e test, 409 (50%) fit current guidelines for isoniazid preventive therapy, 84 (20%) we intended to tr
11 (95% CI 3.5-7.8) for empirical group and for isoniazid preventive therapy (95% CI 3.4-7.8); absolute
12 with HIV infection in Botswana receive daily isoniazid preventive therapy against tuberculosis withou
13 an help to prioritize active case finding or isoniazid preventive therapy among children exposed to T
14 f infected individuals who were eligible for isoniazid preventive therapy and the poor adherence with
15 6% received a medical examination, 91% began isoniazid preventive therapy, and 82% completed preventi
16                                              Isoniazid preventive therapy as an adjunct to ART preven
17 It is likely that antiretroviral therapy and isoniazid preventive therapy can be started safely in pe
18 nostics, reducing treatment delay, providing isoniazid preventive therapy continuously to human immun
19                                 Twice-weekly isoniazid preventive therapy for 6 months or rifampicin
20 creening, active disease treatment, and mass isoniazid preventive therapy for 9 months during 2006-20
21 gramme scenario, a combination of continuous isoniazid preventive therapy for individuals on antiretr
22                                              Isoniazid preventive therapy for latent tuberculosis (TB
23 cident cases of tuberculosis; 37 were in the isoniazid preventive therapy group (2.3 per 100 person-y
24 y and empirical tuberculosis therapy) or the isoniazid preventive therapy group (antiretroviral thera
25 ncentrations in 19 of 662 individuals in the isoniazid preventive therapy group and ten of the 667 in
26 mpirical tuberculosis therapy and 426 to the isoniazid preventive therapy group.
27 rical group and 97 (23%) participants in the isoniazid preventive therapy group.
28 rical group and 46 (11%) participants in the isoniazid preventive therapy group.
29 t would reduce early mortality compared with isoniazid preventive therapy in high-burden settings.
30 rculosis (MTB) infection and indications for isoniazid preventive therapy in HIV-infected persons.
31 omparing empirical tuberculosis therapy with isoniazid preventive therapy in HIV-positive outpatients
32 t reduce mortality at 24 weeks compared with isoniazid preventive therapy in outpatient adults with a
33 ion of systematic tuberculosis screening and isoniazid preventive therapy in outpatients with advance
34 med a phase I randomized controlled trial of isoniazid preventive therapy (IPT) before revaccination
35     The World Health Organization recommends isoniazid preventive therapy (IPT) for HIV-positive cont
36                                              Isoniazid preventive therapy (IPT) for HIV-TB coinfected
37                                    Trials of isoniazid preventive therapy (IPT) for people living wit
38 young child contacts (<5 years) who received isoniazid preventive therapy (IPT) had developed disease
39 sified tuberculosis case finding or prior to isoniazid preventive therapy (IPT) in patients infected
40 es and produced a high rate of completion of isoniazid preventive therapy (IPT) in those persons afte
41                                              Isoniazid preventive therapy (IPT) is recommended as pre
42                                              Isoniazid preventive therapy (IPT) was prescribed to <1%
43 ive tuberculin skin tests (TST) benefit from isoniazid preventive therapy (IPT) whereas those testing
44  early antiretroviral therapy (ART), 6-month isoniazid preventive therapy (IPT), or both among HIV-in
45 n control, antiretroviral therapy (ART), and isoniazid preventive therapy (IPT).
46  protection against tuberculosis provided by isoniazid preventive therapy is not known for human immu
47                                              Isoniazid preventive therapy is recommended in HIV-posit
48 rticipants were randomly assigned to receive isoniazid preventive therapy (n=662) or placebo (n=667)
49 CI, 1.57 to 22.01; p = 0.009), self-reported isoniazid preventive therapy (odds ratio, 0.18; CI, 0.04
50             We aimed to assess the effect of isoniazid preventive therapy on the risk of tuberculosis
51 ly assigned (1:1) patients to receive either isoniazid preventive therapy or a placebo for 12 months
52  eligible pregnant women living with HIV for isoniazid preventive therapy or for further investigatio
53 d a community-based tuberculin screening and isoniazid preventive therapy project among high-risk inn
54 ultivariate algorithm that predicts benefit, isoniazid preventive therapy should be recommended to al
55                                              Isoniazid preventive therapy significantly reduced tuber
56 e if they had completed at least 5 months of isoniazid preventive therapy, unless they had completed
57      We noted no evidence that the effect of isoniazid preventive therapy was restricted to patients

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