Table 1

Demographic characteristics of study group and control group

Study groupEyes (n) (patients)
(M/F)
Mean age±SD (range) years
(M/F
Mean duration of medication±SD (range) months
Group I (antiglaucoma medication with BAK)
 Group 1 A
 timolol with BAK
22
(12/10)
46±15.80 (20–65)/47±7.30
(41–60)
9.54±2.28 (7–12)
 Group I B
 timolol+PG with BAK
36
(28/8)
19.61±45 (16–74)/49.25±7.45
(40–65)
9.89±1.91 (6–12)
 Group I C
 PG with BAK
24
(14/10)
54.85±11.41 (40–68)/49.2±6.97
(41–58)
10.75±1.82 (7–13)
 Total8248±14.54 (16–74)10.05±2.02 (6–13)
Group II (antiglaucoma medication without BAK)
 Group II A
 timolol without BAK
14
(8/6)
30.5±9.24 (22–44)/44±19.37
(19–57)
11±1.66 (8–12)
 Group II B
 timolol+PG without BAK
13
(7/6)
45.86±13.50 (30–63)/55.67±4.59
(50–60)
9.46±2.47 (7–12)
 Group II C
 PG without BAK
44
(16/28)
42.62±17.15 (14–64/43.43±14.19
(24–72)
9.36±2.33 (7–14)
 Total7143.11±15.03 (14–72)9.67±2.31 (7–14)
Total study subjects
 Total number of glaucoma eyes153 (77)45.76±14.86 (14–74)9.88±2.15 (6–14)
 Control eyes30 (30)29.33±5.68 (21–47)Not applicable
  • BAK, benzalkonium chloride; PG, preservative group.