Journal List > J Korean Ophthalmol Soc > v.54(10) > 1009502

Kim, Lee, Kim, Jin, and Lee: Comparison of Therapeutic Effect Between Half-Energy Photodynamic Therapy and Intravitreal Bevacizumab Injection in Chronic Central Serous Chorioretinopathy for 12 Months

Abstract

Purpose

In this study we compared the effectiveness between half energy photodynamic therapy (PDT) and intravitreal bevacizumab (IVB) injection for chronic central serous chorioretinopathy (CSC).

Methods

Forty-five eyes of 42 patients diagnosed as chronic CSC from March 2008 to April 2011 were treated with half energy PDT or IVB injection. The subjects were chosen for a retrospective study and analysis was performed on changes in best corrected visual acuity and existence of subretinal fluid, recurrence rate and changes in central macular thickness.

Results

Similar improvement of visual acuity was observed in both treatment groups 1 month after treatment and no meaningful difference was found in each stage for both groups (p = 0.001, p = 0.0012, respectively). However, 6 to 12 months after the treatment, the half energy PDT group showed more improvement in visual acuity compared to the IVB injection group (p = 0.019, p = 0.043, respectively). Nineteen out of 21 cases showed full recovery of subretinal fluid in the half energy PDT group with an average treatment period of 1.3 ± 0.8 months and 7 out of 24 cases showed full recovery in the IVB injection group with an average treatment period of 3.2 ± 2.8 months. There was a single case of recurrence in the half energy PDT group and 4 in the IVB injection group. The half energy PDT group showed a meaningful decline in central macular thickness at 1, 3, and 6 months after treatment (p = 0.001, p = 0.005, p = 0.007, respectively) compared to the IVB injection group and showed numerous cases with decline in central macular thickness below the 2 standard deviation from normal values (p = 0.002).

Conclusions

Both half energy PDT and IVB injection were effective for the treatment of chronic central serous chorioretinopathy. However, the half energy PDT group comparatively showed better anatomical and functional outcomes. The thinning of central macular thickness below normal value was also observed, thus careful choice of treatment is necessary for patients with chronic central serous chorioretinopathy.

References

1. Von Graefe A. Ueber centrale recidivirende retinitis. Albrecht von Graefes Arch Clin Exp Ophthalmol. 1866; 12:211–5.
2. Gass JDM. Pathogenesis of disciform detachment of the neuroepithelium II. Idiopathic central serous chorioretinopathy. Am J Ophthalmol. 1967; 63:587–615.
3. Gelber GS, Schatz H. Loss of vision due to central serous chorioretinopathy following psychological stress. Am J Psychiatry. 1987; 144:46–50.
4. Yannuzzi LA. Type-A behavior and central serous chorioretinopathy. Retina. 1987; 7:111–31.
crossref
5. Prünte C, Flammer J. Choroidal capillary and venous congestion in central serous chorioretinopathy. Am J Ophthalmol. 1996; 121:26–34.
6. Spaide RF, Hall L, Haas A. . Indocyanine green videoangiography of older patients with central serous chorioretinopathy. Retina. 1996; 16:203–13.
crossref
7. Yap EY, Robertson DM. The long-term outcome of central serous chorioretinopathy. Arch Ophthalmol. 1996; 114:689–92.
crossref
8. Loo RH, Scott IU, Flynn HW Jr. . Factors associated with reduced visual acuity during long-term follow-up patients with idiopathic central serous chorioretinopathy. Retina. 2002; 22:19–24.
9. Leaver P, Williams C. Argon laser photocoagulation in the treat- mentof central serous retinopathy. Br J Ophthalmol. 1979; 63:674–7.
10. Robertson DM, Ilstrup D. Direct, indirect and sham laser photocoagulation in the management of central serous chorioretinopathy. Am J Ophthalmol. 1983; 95:457–66.
crossref
11. Piccolino FC. Laser treatment of eccentric leaks in central serous chorioretinopathy resulting in disappearance of untreated juxtafo- veal leaks. Retina. 1992; 12:96–102.
12. Schmidt-Erfurth U, Laqua H, Schlötzer-Schrehard U, Viestenz A, Naumann GO. Histopathological changes following photodynamic therapy in human eyes. Arch Ophthalmol. 2002; 120:835–44.
13. Lai TY, Chan WM, Lam DS. Transient reduction in retinal function revealed by multifocal electroretinogram after photodynamic therapy. Am J Ophthalmol. 2004; 137:826–33.
crossref
14. Schlotzer-Schrehardt U, Viestenz A, Naumann GO. . Doserelated structural effects of photodynamic therapy on choroidal and retinal structures of human eyes. Graefes Arch Clin Exp Ophthalmol. 2002; 240:748–57.
15. Artunay O, Yuzbasioglu E, Rasier R. . Intravitreal bevacizumab in treatment of idiopathic persistent central serous chorioretinopathy: a prospective, controlled clinical study. Curr Eye Res. 2010; 35:91–8.
crossref
16. Schaal KB, Hoeh AE, Scheuerle A. . Intravitreal bevacizumab for treatment of chronic central serous chorioretinopathy. Eur J Ophthalmol. 2009; 19:613–7.
crossref
17. Seong HK, Bae JH, Kim ES. . Intravitreal bevacizumab to treat acute central serous chorioretinopathy: short-term effect. Ophthalmologica. 2009; 223:343–7.
crossref
18. Bouzas EA, Karadimas P, Pournaras CJ. Central serous chorioretinopathy and glucocorticoids. Surv Ophthalmol. 2002; 47:431–48.
crossref
19. Guyer DR, Yannuzzi LA, Slakter JS. . Digital indocyaine green videoangiography of central serous chorioretinopathy. Arch Ophthalmol. 1994; 112:1057–62.
20. Treatment of age-related macular degeneration with photodynamic therapy (TAP) Study Group. Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin: one-year results of 2 randomized clinical trials–TAP report. Arch Ophthalmol. 1999; 117:1329–45.
21. Verteporfin in Photodynamic Therapy Study Group. Photodynamic therapy of subfoveal choroidal neovascularization in pathologic myopia with verteporfin: one-year results of a randomized clinical trial-VIP report 1. Ophthalmology. 2001; 108:841–52.
22. Verteporfin in Photodynamic Therapy Study Group. Verteporfin therapy of subfoveal choroidal neovascularization in Age-related macular degeneration: two-year results of a randomized clinical trial including lesions with occult with no classic choroidal neo- vascularization-VIP report 2. Am J Ophthalmol. 2001; 131:541–60.
23. Chan WM, Lam DS, Lai TY. . Choroidal vascular remodelling in central serous chorioretinopathy after indocyanine green guided photodynamic therapy with verteporfin: a novel treatment at the primary disease level. Br J Ophthalmol. 2003; 87:1453–8.
crossref
24. Cardillo Piccolino F, Eandi CM, Ventre L. . Photodynamic therapy for chronic central serous chorioretinopathy. Retina. 2003; 23:752–63.
crossref
25. Tzekov R, Lin T, Zhang KM. . Ocular changes after photodynamic therapy. Invest Ophthalmol Vis Sci. 2006; 47:377–85.
crossref
26. Chang MH, Kim SW, Oh JR, Huh K. Photodynamic therapy with verteporfin using half fluence for chronic central serous chorioretinopathy. J Korean Ophthalmol Soc. 2009; 50:1326–33.
crossref
27. Kim JL, Kim HW, Yoon IH. Photodynamic therapy with verte- porfin for short time for chronic central serous chorioretinopathy. J Korean Ophthalmol Soc. 2008; 49:1078–86.
28. Chan WM, Lai TY, Lai RY. . Half-dose verteporfin photodynamic therapy for acute central serous chorioretinopathy. One-year results of a randomized controlled trial. Ophthalmology. 2008; 115:1756–65.
29. Lim SJ, Roh MI, Kwon OW. Intravitreal bevacizumab injection for central serous chorioretinopathy. Retina. 2010; 30:100–6.
crossref
30. Lim JW, Kim MU. The efficacy of intravitreal bevacizumab for idiopathic central serous chorioretinopathy. Graefes Arch Clin Ophthalmol. 2011; 249:969–74.
crossref
31. Sin BH, Jeoung JK, Park SP. A case of central serous chorioretinopathy associated with retinal detachment improved by intravitreal bevacizumab injection. J Korean Ophthalmol Soc. 2010; 51:1419–22.
crossref
32. Lee JY, Chae JB, Yang SJ. . Intravitreal bevacizumab versus the conventional protocol of photodynamic therapy for treatment of chronic central serous chorioretinopathy. Acta Ophthalmol. 2011; 89:293–4.
crossref
33. Torres-Soriano ME, Garcia-Aguirre G, Kon-Jara V. . A pilot study of intravitreal bevacizumab for the treatment of central serous chorioretinopathy (case reports). Graefes Arch Clin Exp Ophthalmol. 2008; 246:1235–9.
crossref
34. Semeraro F, Romano MR, Danzi P. . Intravitreal bevacizumab versus low-fluence photodynamic therapy for treatment of chronic central serous chorioretinopathy. Jpn J Ophthalmol. 2012; 56:608–12.
crossref
35. Huang WC, Chen WL, Tsai YY. . Intravitreal bevacizumab for treatment of chronic central serous chorioretinopathy. Eye (Lond). 2009; 23:488–9.
crossref
36. Gregori-Gisbert I, Aguirre-Balsalobre F, García-Sánchez J. . Recurrent and chronic central serous chorioretinopathy. Retina thickness evaluation one month after intravitreal bevacizumab injection. Arch Soc Esp Oftalmol. 2011; 86:407–11.
crossref

Figure 1.
Time course of mean visual acuity and visual gain during 12 months after treatment.
jkos-54-1526f1.tif
Figure 2.
Time for resolusion of subretinal fluid of patients with chronic central serous chorioretinopathy.
jkos-54-1526f2.tif
Figure 3.
Time course of central macular thickness during 12 months after treatment.
jkos-54-1526f3.tif
Table 1.
Baseline characteristics of patients with chronic central serous chorioretinopathy
Characteristic hf-PDT (n = 21 eyes) IVB (n = 24 eyes) p-value
Sex (male:female) 20:1 22:2 1.000
Age (years) 51.1 ± 9.1 51.5 ± 8.8 0.991*
Laterality (OD:OS) 13:8 11:13 0.218
Duration of chronic CSC (months) 29.4 ± 41.6 25.7 ± 42.6 0.630*
Fluoroangiographic pattern
 Focal leaking 5 15
 Diffuse, granular leaking 16 9 0.016
Follow up period (months) 8.4 ± 7.7 10.0 ± 9.0 0.498*
Number of treatment 1 1.9 ± 1.3 0.001*

Values are presented as mean ± SD unless otherwise indicate.

SD = standard deviation; CSC = central serous chorioretinopathy.

* Mann-Whitney U-test;

Fisher exact test.

Table 2.
Clinical results of patients with chronic central serous chorioretinopathy
BCVA (log MAR) hf-PDT (n = 21 eyes)
IVB (n = 24 eyes)
p-value
n BCVA Visual gain from baseline (p-value*) n BCVA Visual gain from baseline (p-value*)
Baseline 21 0.53 ± 0.31 24 0.43 ± 0.34 0.267
Post 1 month 21 0.32 ± 0.27 0.001 24 0.35 ± 0.35 0.012 0.854
Post 3 months 10 0.30 ± 0.23 0.011 16 0.24 ± 0.18 0.001 0.524
Post 6 months 5 0.11 ± 0.24 0.043 17 0.31 ± 0.25 0.091 0.12
Post 12 months 10 0.15 ± 0.22 0.005 7 0.21 ± 0.20 0.465 0.475

Values are presented as mean ± SD unless otherwise indicated.

SD = standard deviation.

* Wilcoxon signed rank test;

Mann-Whitney U-test.

Table 3.
Clinical results of patients with chronic central serous chorioretinopathy
Visual gain (log MAR) hf-PDT (n = 21eyes)
IVB (n = 24 eyes)
p-value
n Visual gain n Visual gain
Post 1 month ∼ Baseline 21 0.19 ± 0.26 24 0.10 ± 0.18 0.174
Post 3 months ∼ Baseline 10 0.32 ± 0.31 16 0.23 ± 0.24 0.494
Post 6 months ∼ Baseline 5 0.52 ± 0.33 17 0.10 ± 0.26 0.019
Post 12 months ∼ Baseline 10 0.41 ± 0.28 7 0.18 ± 0.43 0.043

Values are presented as mean ± SD unless otherwise indicated.

SD = standard deviation.

*Wilcoxon signed rank test;

Mann-Whitney U-test.

Table 4.
Subretinal fluid of patients with chronic central serous chorioretinopathy
Subretinal fluid hf-PDT (n = 21 eyes) IVB (n = 24 eyes) p-value
Location (pre)
 Subfoveal, only (<200 μm) 10 12
 Extrafoveal (> 200 μm) 11 12
 Extrafoveal, only 0 0 1.000
Remission
 Complete 19 7
 Incomplete 2 17 0.000
 Period (months) 1.3 ± 0.8 3.2 ± 2.8 0.188*

Values are presented as mean ± SD unless otherwise indicate.

SD = standard deviation.

* Mann-Whitney Latest;

Fisher exact test.

Table 5.
Central macular thinning of patients with chronic central serous chorioretinopathy
Central macular thinning hf-PDT (n = 21 eyes) IVB (n = 24 eyes) p-value
Pretreatment
 (+) 4 3
 (-) 17 21 0.591*
Posttreatment
 (+) 19 9
 (-) 2 15 0.001*

Values are presented as mean ± SD unless otherwise indicate.

SD = tandard deviation.

* Fisher exact test.

TOOLS
Similar articles