Journal List > J Korean Ophthalmol Soc > v.56(8) > 1010050

Kwon, Shin, Kim, and Park: Efficacy of Intravitreal Dexamethasone Implant for Macular Edema Due to Branch Retinal Vein Occlusion According to Symptom Duration

Abstract

Purpose

To evaluate the efficacy of intravitreal dexamethasone implants for the treatment of macular edema (ME) due to branch retinal vein occlusion (BRVO) according to the duration of symptoms.

Methods

Thirty-one patients who received an intravitreal dexamethasone implant for ME due to BRVO were included in this ret-rospective study. The patients were divided into 2 groups. Group A included eyes with symptom duration less than 12 weeks and Group B included eyes with symptom duration of 12 weeks or longer. The main efficacy outcomes such as best-corrected visual acui-ty (BCVA) and central macular thickness (CMT) were measured at baseline and every 4 weeks over 24 weeks. Retreatment criteria included an increased CMT of 150 µm or reduction of logarithm of the minimal angle of resolution (log MAR) scores of at least 0.2.

Results

The CMT and BCVA improved significantly at each follow-up compared with the baseline ( p < 0.001, p < 0.05, re-spectively). At 4 and 8 weeks after the first injection, CMT in Group A (285.3 ± 19.9, 276.1 ± 23.1 μ m, respectively) was less than in Group B (310.3 ± 37.5, 318.1 ± 39.6 μ m; p = 0.033, p = 0.001, respectively). At 4 weeks, the BCVA in Group A was better than in Group B ( p = 0.009). Rate and timing of recurrence were not different between the 2 groups ( p > 0.05). At 24 weeks, Group A showed less CMT and better BCVA compared with Group B ( p = 0.043, p = 0.041, respectively).

Conclusions

The intravitreal dexamethasone implant significantly reduced the CMT and improved BCVA in patients with ME due to BRVO. Patients with shorter symptom duration showed better anatomical and functional outcomes over 24 weeks. Early treatment with the intravitreal dexamethasone implant could produce better clinical results.

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Figure 1.
Central macular thickness (CMT) changes after in-travitreal dexamethasone implant. CMT changes was sig-nificantly different from the baseline at all follow-up visits. * p < 0.001.
jkos-56-1208f1.tif
Figure 2.
(A) Comparison of central macular thickness (CMT) and (B) best-corrected visual acuity (BCVA) in patients with macular edema due to retinal vein occlusion after first in-jection of intravitreal dexamethasone according to symptom duration. (A) There was a significant difference at 4 ( p = 0.033), 8 ( p = 0.001) and 24 ( p = 0.043) weeks in CMT between two groups. (B) There was a significant difference at 4 ( p = 0.009) and 24 ( p = 0.041) weeks in the BCVA. Vertical bars are standard deviation of the Group A (symptom duration <12 weeks) and Group B (symptom duration ≥12 weeks). * p < 0.05.
jkos-56-1208f2.tif
Table 1.
Clinical characteristics of the patients
Group A (16 eyes) Group B(15 eyes) p-value
Age (years) 59.7 ± 8.9 65.3 ± 8.1 0.08
Male gender (n, %) 30 (55.5) 25 (49.0) 0.20§
Symptom duration (weeks) 7.7 ± 3.0 32.1 ± 19.4 <0.001
Mean follow up (weeks) 25.7 ± 1.7 25.1 ± 1.1 0.32
Hypertension (n, %) 6 (37.5) 5 (33.3) 0.81§

Values are presented as mean ± SD unless otherwise indicated.

Symptom duration <12 weeks;

Symptom duration ≥12 weeks;

Mann-Whitney U-test;

§ Chi-square test.

Table 2.
Changes of central macular thickness and best-corrected visual acuity of total patients
Baseline Month 1 Months 2 Months 3 Months 4 Months 5 Months 6
CMT (μ m) 599.2 ± 85.3 297.4 ± 31.9 296.4 ± 38.1 403.7 ± 96.2 435.6 ± 140.9 411.7 ± 99.6 406.5 ± 109.8
p < 0.001 p < 0.001 p < 0.001 p < 0.001 p < 0.001 p < 0.001
BCVA (log MAR) 0.70 ± 0.35 0.34 ± 0.18 0.44 ± 0.13 0.53 ± 0.23 0.56 ± 0.33 0.58 ± 0.38 0.54 ± 0.22
p < 0.001 p = 0.001 p = 0.018 p = 0.017 p = 0.043 p = 0.001

Values are presented as mean ± SD unless otherwise indicated. p-value was evaluated by paired t-test and repeated measures analysis of variance.

CMT = central macular thickness; BCVA = best-corrected visual acuity; log MAR = logarithm of the minimal angle of resolution.

Table 3.
Comparison of clinical outcomes according to symptom duration
Group A (16 eyes) Group B (16 eyes) p-value
Recurrence rate (%) 56.2 60.0 0.80
Timing of recurrence (weeks) 14.7 ± 2.8 13.3 ± 2.0 0.34§
Symptom duration (weeks) 7.7 ± 3.0 32.1 ± 19.4 <0.001§
Final CMT (μ m) 364.8 ± 112.5 450.9 ± 90.6 0.043§
Final BCVA (log MAR) 0.49 ± 0.25 0.61 ± 0.17 0.041§

Values are presented as mean ± SD unless otherwise indicated.

CMT = central macular thickness; BCVA = best-corrected visual acuity; log MAR = logarithm of the minimal angle of resolution.

Symptom duration <12 weeks;

Symptom duration ≥12 weeks;

Chi-square test;

§ Mann-Whitney U-test.

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