Journal List > J Korean Ophthalmol Soc > v.50(8) > 1008338

Gang, Jae, Woo, and Ha: Effectiveness of Preoperative Intravitreal Bevacizumab Injections in Pars Plana Vitrectomy for Proliferative Diabetic Retinopathy

Abstract

Purpose:

To evaluate the efficacy of preoperative intravitreal bevacizumab (Avastin; Genetech, San Francisco, CA, USA) injections of pars plana vitrectomy (PPV) for proliferative diabetic retinopathy (PDR).

Methods:

Thirty patients (30 eyes) who underwent PPV for treatment of PDR and received a preoperative intravitreal bevacizumab injection of 1.25 mg were retrospectively analyzed. The study group (group 1, 30 patients, 30 eyes) was compared with a control group (group 2, 29 patients, 30 eyes and matched with the study group for preoperative parameters) who underwent PPV without preoperative intravitreal bevacizumab injection.

Results:

In both groups, visual acuity improved but there was no statistical significance. Intraoperative vitreous hemorrhage occurred in 14 eyes (46.7%) from group 1 and 11 eyes (36.7%) from group 2. There was no statistical significance of intraoperative bleeding occurrence (p=0.3). Postoperative vitreous hemorrhage occurred in 4 eyes from group 1 and 14 eyes from group 2. The group 1 had a lower incidence of postoperative hemorrhage than group 2 (p=0.005).

Conclusions:

Preoperative intravitreal bevacizumab injection appears effective in decreasing early postoperative vitreous hemorrhage and maybe technically helpful in PPV for PDR.

References

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Figure 1.
Preoperative color fundus photography of one patient in group 1. Initial presentation shows extensive fibrovacular tractional membrane overlying the optic disc.
jkos-50-1221f1.tif
Figure 2.
Intraoperative fundus photography of one patient in group 1. Delamination of fibrovascular membrane with vertical scissors from the retina was technically easier than by conventional vitrectomy without preoperative intravitreal bevacizumab injection.
jkos-50-1221f2.tif
Table 1.
Preoperative characteristics of each group
  Group 1 bevacizumab (+) bevacizumab (−) Group 2 p value
No. of eyes 30 30  
No. of Patient (male) 30 (20) 29 (16)  
Mean age (year) 55.07±11.9 52.43±8.6 0.330
Duration of diabetes (year) 14.33±6.6 11.90±8.0 0.207
Duration of follow up (month) 13.43±2.27 14.10±8.48 0.854
Type 1/Type 2 DM 1/29 1/28 0.954
HbA1c (%) 7.82±1.60 8.12±2.21 0.576
Chronic renal failure (%)     0.347
  Absent 22 (73.3%) 25 (83.3%)  
  Present 8 (26.7%) 5 (16.7%)  
Hypertension (%)     0.602
  Absent 12 (40%) 14 (46.7%)  
  Present 18 (60%) 16 (56.3%)  
Preoperative PRP (%)     0.638
  Grade 0 5 (16.7%) 7 (23.3%)  
  Grade 1 8 (26.6%) 7 (23.3%)  
  Grade 2 17 (56.7%) 16 (53.4%)  
Lens status     0.559
  Phakic 21 (70%) 23 (76.7%)  
  Pseudophakic 9 (30%) 7 (23.3%)  
Surgical indication      
  Progressive fibrovascular proliferation 1 (3.3%) 0 (0%)  
  Tractional retinal detachment 6 (20.0%) 9 (30%)  
  Vitreous hemorrhage 23 (76.7%) 21 (70%)  

Data are number or mean± SD.

Ttest

Chi-square test.

Statistical significance was defined was at a p<0.05.

Table 2.
Comparison of the preoperative and postoperative BCVA
  Group 1 bevacizumab (+) Group 2 bevacizumab (−) p value
Preoperative BCVA (logMAR) 1.28±0.75 1.57±0.95 0.913
Postoperative BCVA (logMAR) 0.44±0.46 0.53±0.33  

BCVA=Best corrected visual acuity

Ttest.

Statistical significance was defined was at a p<0.05.

Table 3.
Complications in each group, number of eyes (%)
  Group 1 bevacizumab (+) Group 2 bevacizumab (−) p value
Intraoperative bleeding 14 (46.7%) 11 (36.7%) 0.3
Postoperative bleeding 4 (13.3%) 14 (46.7%) 0.005
Transient ocular hypertension 7 (23.3%) 9 (32.1%) 0.324

Chi-square test.

Statistical significance was defined was at a p<0.05.

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