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Outcomes of conbercept therapy for choroidal neovascularization secondary to pathological myopia

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AIM: To evaluate the one-year outcome of intravitreal conbercept injections for the treatment of choroidal neovascularization secondary to pathological myopia (pm-CNV) by optical coherence tomography angiography (OCTA). METHODS: The medical records of 26 consecutive eyes of 23 patients who received intravitreal injections of conbercept for pm-CNV with a follow-up of one year were retrospectively reviewed. All the patients were diagnosed by fundus fluorescein angiography (FFA) and OCTA at the first visit. All approaches were performed as “1+PRN” treatment. Outcomes included best-corrected visual acuity (BCVA), central foveal thickness (CFT) and the mean CNV area by OCTA. RESULTS: Mean Logarithm BCVA improved from (0.66±0.51) at baseline to (0.39±0.38) at one year (t=3.528, P=0.004). The CFT before treatment and after one year after were 275.08±48.74) μm and (205.15±43.74) μm respectively (t=4.630, P=0.001). The mean pm-CNV areas before treatment and after one year treatment were (0.48±0.24) mm2 and (0.15±0.11) mm2 respectively, with a significant difference among them (t=5.329, P=0.000). Twenty-one eyes had no needs after the first treatment. Four eyes received 2 injections and only one eye received 3 injections. No severe adverse events were noted relevant to the therapy. CONCLUSION: Intravitreal conbercept can improve the vision and relieve CFT and CNV area for the treatment of pm-CNV with “1+PRN” by OCTA for one year, however, long-term follow-up still need to be performed.
Title: Outcomes of conbercept therapy for choroidal neovascularization secondary to pathological myopia
Description:
AIM: To evaluate the one-year outcome of intravitreal conbercept injections for the treatment of choroidal neovascularization secondary to pathological myopia (pm-CNV) by optical coherence tomography angiography (OCTA).
METHODS: The medical records of 26 consecutive eyes of 23 patients who received intravitreal injections of conbercept for pm-CNV with a follow-up of one year were retrospectively reviewed.
All the patients were diagnosed by fundus fluorescein angiography (FFA) and OCTA at the first visit.
All approaches were performed as “1+PRN” treatment.
Outcomes included best-corrected visual acuity (BCVA), central foveal thickness (CFT) and the mean CNV area by OCTA.
RESULTS: Mean Logarithm BCVA improved from (0.
66±0.
51) at baseline to (0.
39±0.
38) at one year (t=3.
528, P=0.
004).
The CFT before treatment and after one year after were 275.
08±48.
74) μm and (205.
15±43.
74) μm respectively (t=4.
630, P=0.
001).
The mean pm-CNV areas before treatment and after one year treatment were (0.
48±0.
24) mm2 and (0.
15±0.
11) mm2 respectively, with a significant difference among them (t=5.
329, P=0.
000).
Twenty-one eyes had no needs after the first treatment.
Four eyes received 2 injections and only one eye received 3 injections.
No severe adverse events were noted relevant to the therapy.
CONCLUSION: Intravitreal conbercept can improve the vision and relieve CFT and CNV area for the treatment of pm-CNV with “1+PRN” by OCTA for one year, however, long-term follow-up still need to be performed.

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