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).
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Table 1.
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%) |
Table 2.
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 |
Table 3.
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 |