Journal List > J Korean Ophthalmol Soc > v.50(6) > 1008577

Hwang and Park: The Effect of Posterior Subtenon Triamcinolone Injection in Panretinal Photocoagulation Induced Visual Dysfunction of Diabetic Retinopathy

Abstract

Purpose

To evaluate the efficacy of a prophylactic posterior sub-Tenon's capsule injection of Triamcinolone acetonide (TA) against macular edema and visual dysfunction by panretinal photocoagulation (PRP) in patients with severe nonproliferative and proliferative diabetic retinopathy.

Methods

Thirty-eight eyes of 19 patients who have diabetic retinopathy without macular edema and whose retinopathy was bilateral and symmetrical were evaluated. Triamcinolone was injected into the posterior sub-Tenon's capsule in one eye of the patients and nothing was injected in the other eye as a control. Two weeks later, PRP was performed every other week for 4 sessions on both eyes in all patients. The clinical course of visual acuity and macular edema was monitored for up to approximately 6 months after the initial PRP.

Results

There was no statistically significant difference of visual acuity before PRP in the 2 groups (p>0.05), and there was no macular edema in any patient. For a follow-up period of 6 months, visual dysfunction was more severe in the TA-injected eye than the control. However, the difference was not statistically significant (p>0.05) throughout the follow-up period except at the 20-week time point. On the other hand, macular edema occurred in 2 eyes (10.5%) of the TA-injected group, and in 4 eyes (21.1%) of the control group. IOP elevation as a complication caused by TA-injection occurred in 2 eyes (10.5%). However, IOP was controlled successfully by anti-glaucomatic eye drops.

Conclusions

Posterior sub-Tenon's capsule injection of Triamcinolone is a safe and effective treatment modality for preventing PRP-induced visual dysfunction and macular edema.

References

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Figure 1.
Line graph illustrating of the clinical course of logarithm of the minimum angle of resolution (logMAR) visual acuity between the TA-inejcted and control eyes. There was not statistically significant difference between two groups before TA injection and after 2 weeks. TA-injected group shows relatively good vision than control group through the follow-up period. But the difference was not statistically significant (p>0.05) except at 20 weeks follow-up time point (p<0.05). (* statistically significant difference between the TA-injected and control eyes at the point)
jkos-50-864f1.tif
Table 1.
Baseline clinical characteristics of 19 patients
Patients No. Age (yrs) Sex DM* duration (yrs) HbA1c (%) Hypertension Lens
1 47 M 1.5 9.8 P
2 58 F 6 7.9 P
3 47 F 3 6.9 + P
4 68 M 5 P
5 60 F 15 12.1 P
6 63 F 14 11.2 IOL
7 65 F 19 7.3 + IOL
8 62 M 28 6.8 P
9 49 F 11 P
10 67 F 1 8 P
11 54 F 11 13 P
12 57 F 12 P
13 52 M 6 13.8 P
14 67 F 23 8.3 IOL
15 64 F 3 6.9 + P
16 53 M 11 6.1 P
17 48 M 2 6.6 P
18 66 F 12 10.9 P
19 65 F 20 + P
Mean 58.53 10.71 9.04
SD** 7.46 7.78 2.55
Maximum 68 28 13.8
Minimum 47 1 6.1

* diabetes mellitus

female

intraocular lens

§ male

phakic lens

# standard deviation

** patient diagnosed with hypertension.

Table 2.
Alteration of visual acuity (logMAR*) after TA treatment
Patient No. Triamcinolone Acetonide Injected
Control
−1 week 2 weeks 24 weeks −1 week 2 weeks 24 weeks
1 0.000 0.222 0.097 0.097 0.097 0.097
2 0.301 0.222 0.301 0.222 0.301 0.222
3 0.000 0.000 0.000 0.000 0.000 0.301
4 0.046 0.097 0.046 0.097 0.046 0.155
5 0.155 0.097 0.097 0.046 0.097 0.398
6 0.155 0.155 0.222 0.155 0.222 0.222
7 0.097 0.155 0.097 0.155 0.097 0.155
8 0.097 0.523 0.155 0.000 0.155 0.222
9 0.699 0.523 1.000 0.523 1.000 0.523
10 0.301 0.523 0.398 0.699 0.398 §
11 0.155 0.222 0.155 0.155 0.155 0.301
12 0.000 0.000 0.000 0.000 0.000 0.000
13 1.222 1.398 1.222 1.398 1.222 1.699
14 0.222 0.046 0.155 0.046
15 0.222 0.222 0.222 0.222 0.222 0.222
16 0.222 0.398 0.301 0.398 0.301 0.155
17 0.222 0.097 0.097 0.222 0.097 0.398
18 0.155 0.097 0.097 0.097 0.097 0.222
19 0.155 0.155 0.155 0.222 0.155 0.222
Mean 0.233 0.284 0.248 0.256 0.259 0.309
SD 0.286 0.325 0.324 0.329 0.329 0.369
Maximum 1.222 1.398 1.000 1.398 1.222 1.699
Minimum 0.000 0.000 0.000 0.000 0.000 0.046

* logarithm of the minimum angle of resolution

standand deviation

patient was not followed

§ visual acuity was not checked.

Table 3.
Results of treatment and complication
Patient No Macular edema Outbreak (weeks) Complication Outbreak (weeks)
3 Control eye 20 IOP elevation 2
4 Control eye 20
5 Control eye 20
8 TA injected eye 24
10 IOP elevation 2
13 TA injected eye 8 (reinjection at 12 wks)
17 Control eye 22
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