Journal List > J Korean Ophthalmol Soc > v.50(7) > 1008302

Oh and Kim: The Effect of Preoperative Subconjunctival Injection of Mitomycin C and Triamcinolone in Recurrent Pterygium

Abstract

Purpose

To evaluate the effect of a preoperative subconjunctival injection of mitomycin C or triamcinolone in patients with recurrent pterygium.

Methods

The records of 50 eyes of 50 patients who received excision of recurrent pterygium between June 2006 and January 2007 were reviewed. The recurrence rate and postoperative fibrovascular growth were compared in the preoperative subconjunctival mitomycin C, or triamcinolone injection group and non-treated control group. Additionally, the quantitative expression level of the transforming growth factor-β1, −β2 (TGF-β1, −β2), connective tissue growth factor (CTGF), and vascular endothelial growth factor (VEGF) in excised sample of the pterygium was assessed.

Results

There was no statistically significant difference in the recurrence rate and the relative gene expression level of growth factors in the triamcinolone group and the mitomycin group when compared with the non-treated control group. Postoperative fibrovascular proliferation was more severe in the triamcinolone group than other groups.

Conclusions

Subconjunctival mitomycin C or triamcinolone as adjunctive therapy before pterygium excision did not influence the recurrence rate of pterygium.

References

1. Sanchez-Thorin JC, Rocha G, Yelin JB. Meta-analysis on the recurrence rates after bare sclera resection with and without mitomycin C use and conjunctival autograft placement in surgery for primary pterygium. Br J Ophthalmol. 1998; 82:661–5.
crossref
2. Oh TH, Choi KY, Yoon BJ. The effect of conjunctival autograft for recurrent pterygium. J Korean Ophthalmol Soc. 1994; 35:1335–9.
3. Prabhasawat P, Barton K, Burkett G, Tseng SC. Comparison of counjunctival autografts, amniotic membrane grafts and primary closure for pterygium excision. Ophthalmology. 1997; 104:974–85.
4. Kria L, Ohira A, Amemiya T. Immunohistochemical localization of basic fibroblast growth factor, platelet derived growth factor, transforming growth factor-beta and tumor necrosis factor-alpha in the pterygium. Acta Histochem. 1996; 98:195–201.
5. Lee DH, Cho HJ, Kim JT, et al. Expression of vascular endothelial growth factor and inducible nitric oxide synthase in pterygia. Cornea. 2001; 20:738–42.
crossref
6. Van Setten G, Aspiotis M, Blalock TD, et al. Connentive tissue growth factor in pterygium: simultaneous presence with vascular endothelial growth factor – possible contributing factor to connjunc-tival scarring. Graefes Arch Clin Exp Ophthalmol. 2003; 241:135–9.
7. De Keizer RJ. Pterygium excision with or without postoperative irradiation, a double-blind study. Doc Ophthalmol. 1982; 52:309–15.
crossref
8. Alanuz-Camino F. The use of postoperative beta radiation in the treatment of pterygia. Ophthalmic Surg. 1982; 13:1022–5.
9. Donnefeld ED, Perry HD, Fromer S, et al. Subconjunctival mitomycin C as adjunctive therapy before pterygium excision. Ophthalmology. 2003; 110:1012–6.
crossref
10. Cano-Parra J, Diaz-Llopis M, Maldonado MJ, et al. Prospective trial of intraoperative mitomycin C in the treatment of primary pterygium. Br J Ophthalmol. 1995; 79:439–41.
crossref
11. Cardillo JA, Alves MR, Ambrosio LE, et al. Single intraoperative application versus postoperative mitomycin C eye drops in pterygium surgery. Ophthalmology. 1995; 102:1949–52.
crossref
12. Panda A, Das GK, Tuli SW, Kumar A. Randomized trial of intraoperative mitomycin C in surgery for pterygium. Am J Ophthalmol. 1998; 125:59–63.
crossref
13. Oguz H, Basar E, Gurler B. Intaoperative application versus postoperative mitomycin C eye drops in pterygium surgery. Acta Ophthalmol Scand. 1999; 77:147–50.
14. Singh G, Wilson MR, Foster CS. Long-term follow-up studyof mitomycin eye drops as adjunctive treatment of pterygia and its comparison with conjunctival autograft transplantation. Cornea. 1990; 9:331–4.
15. Hayasaka S, Noda S, Yamanoto Y, Setogawa T. Postoperative instillation of low-dose mitomycin C in the treatment of primary pterygium. Am J Ophthalmol. 1988; 106:715–8.
crossref
16. Chen PP, Ariyasu RG, Kaza V, et al. A randomized trial comparing mitomycin C and conjunctival autograft after excision of primary pterygium. Am J Ophthalmol. 1995; 120:151–60.
crossref
17. Ma DH, See LC, Liau SB, Tsai RJ. Amniotic membrane graft for primary pterygium: comparison with conjunctival autograft and topical mitomycin C treatment. Br J Ophthalmol. 2000; 84:973–8.
crossref
18. Prabhasawat P, Tesavubul N, Leelapatranura K, Phonjan T. Efficacy of subconjunctival 5-fluorouracil and triamcinolone injection in impending recurrent pterygium. Ophthalmology. 2006; 113:1102–9.
crossref
19. Tan DT, Chee SP, Dear KB, Lim AS. Effect of pterygium morphology on pterygium recurrence in a controlled trial comparing conjunctival autografting with bare sclera excision. Arch Ophthalmol. 1997; 115:1235–40.
crossref
20. Donnenfeld ED, Perry HD, Fromer S, et al. Subconjunctival mitomycin C as adjunctive therapy before pterygium excision. Ophthalmology. 2003; 110:1012–6.
crossref
21. Chen CW, Huang HT, Bair JS, Lee CC. Trabeculectomy with simultaneous topical application of mitomycin C in refractory glaucoma. J Ocul Pharmacol. 1990; 6:175–82.
22. Govinden R, Bhoola KD. Genealogy, expressin, and cellular function of transforming growth factor-beta. Pharmacol Therap. 2003; 98:257–65.
23. Nakamura K, Kurosaka D, Yoshino M, et al. Injured corneal epithelial cells promote myodifferentiation of corneal fibroblasts. Invst Ophthalmol Vis Sci. 2002; 43:2603–8.

Figure 1.
(A) The preoperative slit lamp photograph captured by image capture system. (B) Converted image by computer program (Photoshop CS2®, Adobe sys, Inc. USA) to compare the vascularity of each pterygial tissue.
jkos-50-1005f1.tif
Figure 2.
Standard Photographs classified by the pterygial thickness. (A) T1, minimal elevation with definite confirmation of episcleral vessel in most of the elevated area. (B) T2, moderate elevation, episcleral vessel can be found in some of the elevated area. (C) T3, marked elevation, episcleral vessel cannot be found because of the pterygial fleshiness.
jkos-50-1005f2.tif
Figure 3.
Standard Photographs classified by the pterygial vascular proliferation. (A) V0, no directional vascular pattern. (B) V1, minimal vascularization with unidirectional pattern. (C) V2, moderate vascularization with unidirectional and enlarged vessels (D) V3, marked vascularization with unidirectional, engorged vessels.
jkos-50-1005f3.tif
Figure 4.
The mRNA expression profile (mean) relative to actin mRNA expression in pterygial tissue according to the preoperative treatment (TGF-β1, −β2=transforming growth factor-β1, β2; CTGF=connective tissue growth factor; VEGF=vascular endothelial growth factor). There were no statistical difference between groups in each parameters (Mann-Whitney U test, p>0.05).
jkos-50-1005f4.tif
Table 1.
The standard grading system of pterygium based on the photography captured by image capture system
Location (L)
L1 abnormal fibrovascular tissues were confined conjunctival area
L2 abnormal fibrovascular tissues were located in the limbal area (≤ 1.0 mm from the limbus)
L3 abnormal fibrovascular tissues were encroached over the limbal area (> 1.0 mm from the limbus)
Thickness (T)
T0 no elevation
T1 minimal elevation with definite confirmation of episcleral vessel in most of the elevated area
T2 moderate elevation, episcleral vessel can be found in some of the elevated area
T3 marked elevation, episcleral vessel cannot be found because of the pterygial fleshiness
Vascularity (V)
V0 no directional vascular pattern
V1 minimal vascularization with unidirectional pattern
V2 moderate vascularization with unidirectional and enlarged vessels
V3 Marked vascularization with unidirectional, engorged vessels
Table 2.
Demographic data and preoperative severity score
Non-treated group (A) Preoperative MMC* group (B) Preoperative TA group (C) p value
A-B A-C B-C
Eye (numbers) 20 8 22
Sex (Male/Female) 6/14 4/4 8/14
Age (Years) 56.85±9.74 52.38±18.52 50.82±9.58
Severity score
Thickness 2.65±0.49 2.88±0.35 2.64±0.49 0.381 0.927 0.344
Vascularization 2.70±0.47 3.00±0.00 2.68±0.48 0.237 0.900 0.202
Location 3.00±0.00 3.00±0.00 2.95±0.21 1.000 0.340 0.872
Total 8.35±0.81 8.88±0.35 8.27±0.76 0.165 0.680 0.070

* MMC=mitomycin

TA=triamcinolone

Obtained by Mann-Whitney U test.

Table 3.
Postoperative fibrovascular proliferative score and recurrence rate
Non-treated group (A) Preoperative MMC* group (B) Preoperative TA group (C) p value§
A-B A-C B-C
Post-op score
Thickness 0.70±0.98 0.63±1.19 1.50±1.14 0.709 0.021 0.087
Vascularization 0.65±0.88 0.50±1.07 1.73±1.16 0.601 0.003 0.024
Location 0.65±0.88 0.63±1.19 1.36±1.09 0.746 0.026 0.078
Total 2.0±2.63 1.75±3.41 4.59±2.87 0.709 0.004 0.045
Post-Op recurrence rate
minimal recurrence (%) 5/20 (25%) 2/8 (25%) 8/22 (36%)
Recurrence demanding 0/20 (0%) 1/8 (12.5%) 1/22 (4.5%)
reoperation (%)

* MMC=mitomycin

TA=triamcinolone

Post-op=post operation

§ Obtained by Mann-Whitney U test.

Table 4.
The mRNA expression profile (mean± SD) relative to actin mRNA expression in pterygial tissue according to the preoperative treatment
TGF-β1 TGF-β2 CTGF VEGF
Preoperative no treatment Group(A) 0.40±0.31 0.83±0.67 0.51±0.49 0.62±0.63
Preoperative mitomycin Group (B) 0.55±0.28 0.69±0.45 0.85±0.29 0.17±0.12
Preoperative triamcinolone Group (C) 0.63±0.47 0.73±0.31 0.68±0.46 0.82±0.78
p value*
A-B 0.416 0.691 0.075 0.301
A-C 0.176 0.630 0.275 0.325
B-C 0.824 0.866 0.391 0.056

* Obtained by Mann-Whitney U test.

TGF-β1, −β2=transforming growth factor-β1, β2; CTGF=connective tissue growth factor; VEGF=vascular endothelial growth factor. There were no statistical difference between groups in each parameters (Mann-Whiteny U test, p>0.05).

TOOLS
Similar articles