Javascript must be enabled to continue!
Intravitreal bevacizumab for vitreous hemorrhage
View through CrossRef
Abstract Purpose Vitreous hemorrage is one of the major complications of ischemic retinopathies such as diabetic retinopathy. Our purpose was to describe the clinical outcome of patients who underwent a less invasive intervention than vitrectomy for therapy of persisting vitreous hemorrage Methods Our clinical interventional case series study included 10 patients (n=11 eyes) who presented with vitreous hemorrage due to proliferative diabetic retinopathy (n=10 eyes)or ischemic retinal vein occlusions (n=1). The hemorrage had persisted for at least 3 months. Mean age was 62,1+/‐14,5 years (median 58.4 years; range 45.8‐90.8 years) and mean visual acuity was 1,65+/‐0.97 logMAR. The mean intraocular pressure was 14.6+/‐3.6 mm Hg. All eyes received an intravitreal injection of 1.25 mg bevacizumab, which was repeated in 2 eyes (17%). All patients were fully informed about the experimental character of the treatment and signed an informed consent. Results At the end of follow‐up at 3.9+/‐2.3 months (range 1‐6 months) after the first injection, the vitreous hemorrage had cleared without any further intervention in all but 1 (9%) eye. Visual acuity improved significantly (p=0.02) from 1.65+/‐0.97 logMAR to 0.98+/‐0.67 logMAR. The intraocular pressure remained in the normal range (mean 14.6+/‐3.5 mm Hg) with no significant difference to the baseline values (p=0.94). We did not observe any sign of intraocular inflammation or other changes that could be regardesd as side‐effects of the intravitreal injecion. 4 (36%) eyes underwent panretinal laser coagulation after clearing of the vitreous hemorrage. Conclusion The present study may suggest to extend the intravitreal use of bevacizumab to persisting vitreous hemorrage due to ischemic retinopathies.
Title: Intravitreal bevacizumab for vitreous hemorrhage
Description:
Abstract Purpose Vitreous hemorrage is one of the major complications of ischemic retinopathies such as diabetic retinopathy.
Our purpose was to describe the clinical outcome of patients who underwent a less invasive intervention than vitrectomy for therapy of persisting vitreous hemorrage Methods Our clinical interventional case series study included 10 patients (n=11 eyes) who presented with vitreous hemorrage due to proliferative diabetic retinopathy (n=10 eyes)or ischemic retinal vein occlusions (n=1).
The hemorrage had persisted for at least 3 months.
Mean age was 62,1+/‐14,5 years (median 58.
4 years; range 45.
8‐90.
8 years) and mean visual acuity was 1,65+/‐0.
97 logMAR.
The mean intraocular pressure was 14.
6+/‐3.
6 mm Hg.
All eyes received an intravitreal injection of 1.
25 mg bevacizumab, which was repeated in 2 eyes (17%).
All patients were fully informed about the experimental character of the treatment and signed an informed consent.
Results At the end of follow‐up at 3.
9+/‐2.
3 months (range 1‐6 months) after the first injection, the vitreous hemorrage had cleared without any further intervention in all but 1 (9%) eye.
Visual acuity improved significantly (p=0.
02) from 1.
65+/‐0.
97 logMAR to 0.
98+/‐0.
67 logMAR.
The intraocular pressure remained in the normal range (mean 14.
6+/‐3.
5 mm Hg) with no significant difference to the baseline values (p=0.
94).
We did not observe any sign of intraocular inflammation or other changes that could be regardesd as side‐effects of the intravitreal injecion.
4 (36%) eyes underwent panretinal laser coagulation after clearing of the vitreous hemorrage.
Conclusion The present study may suggest to extend the intravitreal use of bevacizumab to persisting vitreous hemorrage due to ischemic retinopathies.
Related Results
Abstract 2099: Model-riven optimization of anti-angiogenics combined with chemotherapy: application to bevacizumab + pemetrexed/cisplatin doublet in NSCLC-bearing mice
Abstract 2099: Model-riven optimization of anti-angiogenics combined with chemotherapy: application to bevacizumab + pemetrexed/cisplatin doublet in NSCLC-bearing mice
Abstract
Bevacizumab-containing protocols are all based upon the concomitant administration of the drugs given in a row. Bevacizumab is expected to induce a transien...
Reflux after intravitreal injection: an anterior segment optical coherence tomography study
Reflux after intravitreal injection: an anterior segment optical coherence tomography study
Purpose: To investigate the intraocular pressure and conjunctival thickness changes following the intravitreal injection Methods: Sixty eyes of 60 patients having intravitreal inj...
Immediate Effect of Intravitreal Bevacizumab Injection on Intraocular Pressure
Immediate Effect of Intravitreal Bevacizumab Injection on Intraocular Pressure
Purpose: Raised intra ocular pressure following intravitreal Bevacizumabis a potential side effect which can be clinically significant. The aim of the study was to evaluate short ...
Intravitreal brimonidine inhibits form-deprivation myopia in guinea pigs
Intravitreal brimonidine inhibits form-deprivation myopia in guinea pigs
Abstract
Background
The use of ocular hypotensive drugs has been reported to attenuate myopia progression. This study explores whether brimonidine c...
The Auckland Endophthalmitis Study
The Auckland Endophthalmitis Study
Purpose: To report on the incidence and management of endophthalmitis following intravitreal bevacizumab in Auckland, New Zealand. Method: A survey of facilities in Auckland perfor...
99mTc-Labeled Bevacizumab via HYNIC for Imaging of Melanoma
99mTc-Labeled Bevacizumab via HYNIC for Imaging of Melanoma
Vascular endothelial growth factor (VEGF) is one of the classic factors to tumour-induced angiogenesis in several types, including melanoma. Bevacizumab, a monoclonal antibody ant...
Efficacy of bevacizumab with cisplatin and gemcitabine in Asian patients with advanced or recurrent non‐squamous non‐small cell lung cancer who have not received prior chemotherapy: A substudy of the Avastin in Lung trial
Efficacy of bevacizumab with cisplatin and gemcitabine in Asian patients with advanced or recurrent non‐squamous non‐small cell lung cancer who have not received prior chemotherapy: A substudy of the Avastin in Lung trial
AbstractAim: The phase III AVAiL study evaluated the efficacy and safety of the anti‐vascular epidermal growth factor agent bevacizumab combined with platinum‐based chemotherapy a...
Effect of intravitreal bevacizumab injection in central serous chorioretinopathy
Effect of intravitreal bevacizumab injection in central serous chorioretinopathy
AbstractPurposeTo investigate the effect of intravitreal bevacizumab injection on the type of central serous chorioretinopathy.MethodsWe performed a retrospective analysis of 43 pa...

