TY - JOUR
T1 - Intravitreal plasmin without associated vitrectomy as a treatment for refractory diabetic macular edema
AU - Diaz-Llopis, Manuel
AU - Udaondo, Patricia
AU - Arevalo, Fernando
AU - Salom, David
AU - Garcia-Delpech, Salvador
AU - Quijada, Arturo
AU - Romero, Francisco Javier
PY - 2009/8/1
Y1 - 2009/8/1
N2 - Objective: To determine the effectiveness of a low-dose intravitreal injection of autologous plasmin enzyme (APE), without the performance of a vitrectomy, as a treatment for refractory diffuse diabetic macular edema (DDME). Design: Prospective, comparative, interventional case series. Patients: Sixteen patients with bilateral DDME who had not responded to prior laser photocoagulation. All patients received an injection in 1 eye, while the other eye served as a control. Intervention: Intravitreal 0.2 mL APE injection under topical anesthesia. The APE was obtained using a simplified method. Main Outcome Measures: Central macular thickness (CMT) at 1 and 6 months, determined by optical coherence tomography (OCT) and best corrected visual acuity (BCVA). Results: All patients underwent a 1-month follow-up. Prior to injection, CMT in the eye about to receive the injection was 541 ± 79 μm (mean ± standard deviation [SD]) versus 535 ± 76 μm in the control eye. One month after injection, CMT was 241 ± 47 μm in injected eyes and 530 ± 85 μm in control eyes (P < 0.001, bilateral Wilcoxon test for paired samples). The macular edema (ME) improved in all injected eyes (100%), with complete resolution in 7 patients (44%). The mean BCVA of treated eyes was 0.618 ± 0.27 (mean ± SD) at baseline and 0.45 ± 0.24 four weeks after injection (paired samples t-test, P < 0.001). No adverse effects were observed in any of the patients. BCVA and CMT were stable when evaluated at 6-month follow-up (0.43 ± 0.242 and 244 ± 46 μm, respectively). Conclusions: Intravitreal APE injection effectively reduces macular thickening due to DDME in cases that fail to respond to conventional laser photocoagulation, and improves visual acuity in a short term, and this results remain stable in a medium term what is very important. Further investigation is warranted in order to assess long-term efficacy and safety.
AB - Objective: To determine the effectiveness of a low-dose intravitreal injection of autologous plasmin enzyme (APE), without the performance of a vitrectomy, as a treatment for refractory diffuse diabetic macular edema (DDME). Design: Prospective, comparative, interventional case series. Patients: Sixteen patients with bilateral DDME who had not responded to prior laser photocoagulation. All patients received an injection in 1 eye, while the other eye served as a control. Intervention: Intravitreal 0.2 mL APE injection under topical anesthesia. The APE was obtained using a simplified method. Main Outcome Measures: Central macular thickness (CMT) at 1 and 6 months, determined by optical coherence tomography (OCT) and best corrected visual acuity (BCVA). Results: All patients underwent a 1-month follow-up. Prior to injection, CMT in the eye about to receive the injection was 541 ± 79 μm (mean ± standard deviation [SD]) versus 535 ± 76 μm in the control eye. One month after injection, CMT was 241 ± 47 μm in injected eyes and 530 ± 85 μm in control eyes (P < 0.001, bilateral Wilcoxon test for paired samples). The macular edema (ME) improved in all injected eyes (100%), with complete resolution in 7 patients (44%). The mean BCVA of treated eyes was 0.618 ± 0.27 (mean ± SD) at baseline and 0.45 ± 0.24 four weeks after injection (paired samples t-test, P < 0.001). No adverse effects were observed in any of the patients. BCVA and CMT were stable when evaluated at 6-month follow-up (0.43 ± 0.242 and 244 ± 46 μm, respectively). Conclusions: Intravitreal APE injection effectively reduces macular thickening due to DDME in cases that fail to respond to conventional laser photocoagulation, and improves visual acuity in a short term, and this results remain stable in a medium term what is very important. Further investigation is warranted in order to assess long-term efficacy and safety.
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U2 - 10.1089/jop.2008.0118
DO - 10.1089/jop.2008.0118
M3 - Article
C2 - 19650710
AN - SCOPUS:68549096118
SN - 1080-7683
VL - 25
SP - 379
EP - 384
JO - Journal of Ocular Pharmacology and Therapeutics
JF - Journal of Ocular Pharmacology and Therapeutics
IS - 4
ER -