Table 2

 Management and outcome

CharacteristicEmpirical antibiotic use
FQ(n = 79)FQ, no underlying disease(n = 37)Others(n = 218)No(n = 251)
AFS, acid-fast smear; TB, tuberculosis.
*Data presented as median (range).
†p<0.05 FQ group v no antibiotic group.
‡p<0.05 other antibiotic group v no antibiotic group.
¶p<0.05 FQ group v other antibiotic group.
Initial visit to ordering TB studies(days)*6 (0–173)†¶6 (1–173)5 (0–163)5 (0–272)
    AFS+ (n = 126)9 (1–173)4 (1–173)3 (0–78)3 (0–112)
    AFS − (n = 422)6 (0–159)6 (1–61)5 (0–163)5 (0–272)
TB study to anti-TB treatment (days)*25 (−3–231)†¶31 (−3–73)7 (−35–143)‡0 (−114–146)
    AFS+ (n = 123)5 (1–21)†4 (2–9)2 (−16–98)‡−1 (−35–55)
    AFS− (n = 363)31 (−3–231)†¶33 (−3–73)16 (−35–143)‡1 (−114–146)
Initial visit to anti-TB treatment (days)*41 (6–233)†¶38 (6–175)16 (0–198)‡7 (0–286)
    AFS+ (n = 123)15 (8–175)†¶10 (8–175)6 (0–105)‡3 (0–123)
    AFS− (n = 363)42 (6–233)†¶39 (6–96)27 (0–198)‡13 (0–286)
Ordering TB study at initial visit53 (67.1%)26 (70.3%)163 (74.8%)179 (71.3%)
TB study to identification available (days)*63 (37–85)64 (55–82)62 (36–92)62 (35–121)
    AFS+ (n = 126)63 (57–73)60 (57–62)63 (36–78)63 (50–77)
    AFS− (n = 422)63 (37–85)64 (55–82)62 (54–92)62 (35–121)
Outcome
    Completed treatment41 (51.9%)23 (62.2%)133 (61.0%)198 (78.9%)
    Ongoing treatment001 (0.5%)4 (1.6%)
    Not treated2 (2.5%)2 (5.4%)5 (2.3%)1 (0.4%)
    Lost to follow up13 (16.5%)7 (18.9%)34 (15.6%)33 (13.1%)
    Mortality23 (29.1%)5 (13.5%)45 (20.6%)15 (6.0%)
    Died of TB123221
    Died with TB1122314
Length of survival (days)*85.5 (18–448)†59 (26–448)55 (1–708)‡249 (23–902)