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1 antituberculosis therapy using intermittent directly observed therapy.
2 sis, confirming the efficacy of intermittent directly observed therapy.
3 ended by the World Health Organization under directly observed therapy.
4 11-5.43) were less likely to receive IPTp by directly observed therapy.
5 ecause of improved access to health care and directly observed therapy.
6 onadherence and should have been assigned to directly observed therapy.
7 coadministered with methadone using modified directly observed therapy.
8 otal of 150 patients were ordered to undergo directly observed therapy, 139 patients to be detained d
9 zithromycin (AZ) or placebo, administered as directly observed therapy 4 times per year between Augus
11 trol measures in the homeless should include directly observed therapy and incentive approaches, trea
13 initiation, previous tuberculosis treatment, directly observed therapy, and acid-fast-bacilli smear-p
14 rvised strategies and modified approaches to directly observed therapy, are unlikely to achieve this
19 erence to medication in persons using WOT or directly observed therapy (DOT) during TB treatment.
20 model to estimate the cost-effectiveness of directly observed therapy (DOT) for individuals with new
23 PrEP was administered to women through daily directly observed therapy (DOT) for ten consecutive days
26 zid and rifapentine (3HP) administered under directly observed therapy (DOT) might increase treatment
27 idual treatment (SIT), group treatment (GT), directly observed therapy (DOT), and no intervention for
28 signed (1:1:1) to receive 3HP by facilitated directly observed therapy (DOT), facilitated self-admini
29 ed strategies for delivering 3HP-facilitated directly observed therapy (DOT), facilitated self-admini
31 treatment failure/death were the absence of directly observed therapy (DOT; adjusted hazard ratio [a
33 was compared with 2- and 4-week samples from Directly Observed Therapy Dried Blood Spots (DOT-DBS) St
34 supervision could be a viable alternative to directly observed therapy for a substantial proportion o
35 conclude that treatment plans that emphasize directly observed therapy from the start of therapy have
36 ly assigned 259 participants to the modified directly observed therapy group (n=129) or the standard-
38 was 25.1% (95% CI 17.7-32.4) in the modified directly observed therapy group and 17.3% (10.8-23.7) in
39 laboratory abnormality (n=21 in the modified directly observed therapy group and n=15 in the standard
41 ment, good cooperation between services, and directly observed therapy improved treatment outcome and
42 nd tolerability of 12 weeks of INH/RPT given directly observed therapy in 17 consecutive SOT candidat
43 on receiving some portion of treatment under directly observed therapy increased from 27.3% to 59.1%
45 randomized trial of a partner-based modified directly observed therapy (mDOT) compared with standard
46 l measures such as uniform implementation of directly observed therapy might reduce the proportion of
47 fference in standard of care versus modified directly observed therapy of -6.6% (95% CI -16.5% to 3.2
50 pot urine and plasma samples during a 6-week directly observed therapy period and a 4-week washout pe
52 use of case management strategies (including directly observed therapy), regimen and dosing selection
53 didates, combination INH/RPT weekly given as directly observed therapy seems to be reasonably well to
56 Hair strands from volunteers enrolled in a directly observed therapy study were analyzed by IR-MALD
57 966 to August 1, 1996) with original data on directly observed therapy, supervised therapy, complianc
59 As compared with patients ordered to receive directly observed therapy, the patients who were detaine
60 003), and cavitary disease in the absence of directly observed therapy throughout therapy (OR, 2.65;
65 s based on a patient-centered approach using directly observed therapy with multiple enablers and enh
66 ner-based support intervention with modified directly observed therapy would improve outcomes with se