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Table 1 Characteristics of patients who underwent vitreoretinal surgery in sub-Tenon and general anesthesia

From: Safety and feasibility of sutureless pars-plana vitrectomy in sub-Tenon anesthesia (SAFE-VISA): a prospective study

Characteristics

Sub-Tenon anesthesia (N = 33/67)

General anesthesia (N = 34/67)

P value

Age (years)

72.9 ± 9.1 (59.0–91.0)

65.4 ± 8.6 (51.0–80.0)

0.002*

Sex

  

0.305

 Male

20 (60.6%)

25 (73.5%)

 

 Female

13 (39.4%)

9 (26.5%)

 

Eye

  

 > 0.999

 Right eye

14 (42.4%)

15 (44.1%)

 

 Left eye

19 (57.6%)

19 (55.9%)

 

Lens

  

 < 0.001*

 Phakic

1 (3.0%)

13 (38.2%)

 

 Pseudophakic

32 (97.0%)

21 (61.8%)

 

Time between IOL implantation and vitreoretinal surgery (years)

3.7 ± 2.8 (0.3–11.0)

3.3 ± 3.1 (0.5–11.0)

0.961

BCVA (logMAR)

 Pre surgery

1.23 ± 0.92 (NL-0.22)

0.89 ± 0.70 (3.00–0.22)

0.107

 Follow-up

0.89 ± 0.95 (NL-0.00)

0.86 ± 1.14 (3.00–0.22)

0.938

 Surgery duration (minutes)

22.7 ± 8.6 (12.0–59.0)

32.6 ± 15.1 (13.0–67.0)

0.002*

Indication for surgery

 Rhegmatogenous RD

6 (18.2%)

16 (47.1%)

 

 Macular hole/Gliosis/VMT

4 (12.1%)

6 (17.6%)

 

 Silicone oil removal

13 (39.4%)

6 (17.6%)

 

 Silicone oil removal + peeling

2 (6.1%)

0

 

 Vitreous hemorrhage

6 (18.2%)

4 (11.8%)

 

 Endophthalmitis

1 (3.0%)

0

 

 Sub-ILM hemorrhage

1 (3.0%)

1 (2.9%)

 

 CRVO

0

1 (2.9%)

 

Adverse events during follow-up

  

0.709

 RD

2 (6.1%)

2 (5.9%)

 

 Vitreous hemorrhage

1 (3.0%)

0

 

 PVR

1 (3.0%)

1 (2.9%)