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1 Loss to follow-up is a major concern and can potentially bias
2 Loss to follow-up is common, suggesting that the aims and ben
3 Loss to follow-up is high among HIV patients not yet receivin
4 Loss to follow-up was similar between groups.
6 every year in individuals 50 years or older, although a 50% loss to follow-up and wide CIs for progression to late AMD li
7 ART for >/=6 months (RR 0.97, 95% CI 0.88-1.07, p = 0.55), loss to follow-up at 12 months after HIV testing (RR 0.56, 95
11 Premature treatment discontinuation and loss to follow-up (LTFU) with unknown outcomes leave uncertai
13 entify baseline predictors of death, treatment failure, and loss to follow-up among children with MDR tuberculosis diseas
14 than 100 cells per muL, virological failure incidence, and loss to follow-up were from published multinational cohorts i
15 RIF implementation on the delay to treatment initiation and loss to follow-up before second-line treatment for RR-TB acro
16 hs after HIV testing among patients on ART >/=6 months, and loss to follow-up and death at 12 months after HIV testing.
19 retention after starting antiretroviral therapy (ART), but loss to follow-up undermines assessment of the magnitude of a
21 r methods could facilitate earlier diagnosis and circumvent loss to follow-up but remain logistically and economically pr
22 to the first occurrence of an incident event, other death, loss to follow-up, or the last follow-up call through Decembe
23 n = 14,700) were followed from entry into care until death, loss to follow-up, or censoring at 5 years or on December 31,
27 sis was modified intention-to-treat (without imputation for losses to follow-up) accounting for within-clinic clustering.
28 nd long-term studies, the use of suboptimum control groups, loss to follow-up, and difficulties in recruitment of represe
30 Four-month retention was 83%, with higher loss to follow-up in collaborative care (82/344 [24%]) vs usu
34 lity weighting to take into account data missing because of loss to follow-up between the study recruitment in 1985 and t
37 = 83/139) were seen at 12 months; we observed high rates of loss to follow-up: 71% (n = 156/219) and 30% (n = 42/139) in
38 ffective strategy that must be balanced against the risk of loss to follow-up, particularly among patients who are ethnic
40 he timing of assessment is decided, the impact of potential loss to follow-up should be considered so that appropriate st
42 For new smear-positive patients, pretreatment loss to follow-up and post-treatment TB recurrence are consid
43 (POC) diagnostics have the potential to reduce pretreatment loss to follow-up and delays to initiation of appropriate tub
44 s all four trials were embedded in the screening programme, loss to follow-up was minimal (less than 0.5%).
47 aggregate data suggest a large treatment gap (pre-treatment loss to follow-up) between the numbers of patients with labor
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