Treatment of Chronic Central Cerous Chorioretinopathy:

MAGNOVISION™ and Subtenon Bevacizumab + Platelet Rich Plasma Injection.

Treatment of Chronic Central Cerous Chorioretinopathy:

Complaint: A 49-year-old patient has been complaining of recurrent sudden vision decreases, contrast loss,
and macropsia in the left eye for 2 years. Attacks occur every 2-3 months, and he describes a decrease in
vision after each attack.

Treatment: Treatment was planned as a combination of Platelet-rich plasma (PRP) containing epithelial
growth factor to increase the pump function and reepitelization rate of the retinal pigment epithelium
(RPE). Antivascular endothelial growth factor (VEGF) (bevacizumab) tightens choroidal pores and prevents
new leaks from the choroid. Electromagnetic iontophoresis (MagnoVisionTM) is essential for growth factors
and AntiVEGF molecules injected into the sub-tenon space to pass into the sub-retinal space.

PRP was prepared from autologous blood. PRP was prepared by refrigerating a total of 8 ml of blood taken
from the patient relative into a sterile citrated PRP tube. After centrifuging at +4 degrees Celsius, 2500 rpm,
and 8 minutes, the lower 1/3 of the plasma formed in the tube was withdrawn into a 2.5 ml injector, totaling
1 ml of PRP. 0.5 ml of Bevacizumab was added to the syringe containing 1 ml of citrated PRP. A total of 1.5 ml
of citrate, PRP and AntiVEGF mixture was injected into the left subtenon space under topical anesthesia.
Immediately after the subtenon injection, the patient was fitted with a MagnovisionTM electromagnetic
iontophoresis helmet. Magnovision is a stimulator and iontophoresis device specifically designed for
retina/optic nerve diseases, which contains 9 coils and generates a 2000 mG magnetic field with a 42 Hertz
vibration frequency that synchronously stimulates the bulbus, visual pathways and occipital cortex. These
parameters are fixed values ​​by the manufacturer that cannot be changed for patient safety. Each session is
applied effectively and safely for 30 minutes. This process is repeated for 3 sessions in 2 months between 3
or 4 weeks interval.

After 3 sessions, VA was improved to 0.9 BCVA from 0.3

Treatment of Chronic Central Cerous Chorioretinopathy:

MAGNOVISION™ and Subtenon Bevacizumab + Platelet Rich Plasma Injection.

Treatment of Chronic Central Cerous Chorioretinopathy:

Complaint: A 43-year-old male patient has been complaining of recurrent sudden vision decreases, contrast
loss, and macropsia in the left eye for 3 years. Attacks occur every 4-5 months, and he describes a decrease
in vision after each attack.

Treatment: Treatment was planned as a combination of Platelet-rich plasma (PRP) containing epithelial
growth factor to increase the pump function and reepitelization rate of the retinal pigment epithelium
(RPE). Antivascular endothelial growth factor (VEGF) (bevacizumab) tightens choroidal pores and prevents
new leaks from the choroid. Electromagnetic iontophoresis (MagnoVisionTM) is essential for growth factors
and AntiVEGF molecules injected into the sub-tenon space to pass into the sub-retinal space.

PRP was prepared by refrigerating a total of 8 ml of blood taken from patient autologously into a sterile
citrated PRP tube. After centrifuging at +4 degrees Celsius, 2500 rpm, and 8 minutes, the lower 1/3 of the
plasma formed in the tube was withdrawn into a 2.5 ml injector, totaling 1 ml of PRP. 0.5 ml of Bevacizumab
was added to the syringe containing 1 ml of citrated PRP. A total of 1.5 ml of citrate, PRP and AntiVEGF
mixture was injected into the left subtenon space under topical anesthesia. Immediately after the subtenon
injection, the patient was fitted with a MagnovisionTM electromagnetic iontophoresis helmet. Magnovision is
a stimulator and iontophoresis device specifically designed for retina/optic nerve diseases, which contains
9 coils and generates a 2000 mG magnetic field with a 42 Hertz vibration frequency that synchronously
stimulates the bulbus, visual pathways and occipital cortex. These parameters are fixed values ​​by the
manufacturer that cannot be changed for patient safety. Each session is applied effectively and safely for
30 minutes. This process is repeated for 3 sessions in 2 months between 3 or 4 weeks interval.

After 3 sessions, VA was improved to 0.8 BCVA from 0.3. Arrows indicate thickening of the ellipsoid zone

Treatment of Chronic Central Cerous Chorioretinopathy:

MAGNOVISION™ and Subtenon Bevacizumab + Platelet Rich Plasma Injection.

Treatment of Chronic Central Cerous Chorioretinopathy:

Complaint: A 45-year-old patient has been complaining of recurrent sudden vision decreases, contrast loss,
and macropsia in the right eye for 3 years. Attacks occur every 5-6 months.

Treatment: Treatment was planned as a combination of Platelet-rich plasma (PRP) containing epithelial
growth factor to increase the pump function and reepitelization rate of the retinal pigment epithelium
(RPE). Antivascular endothelial growth factor (VEGF) (bevacizumab) tightens choroidal pores and prevents
new leaks from the choroid. Electromagnetic iontophoresis (MagnoVision™) is essential for growth factors
and AntiVEGF molecules injected into the sub-tenon space to pass into the sub-retinal space.

PRP was prepared by refrigerating a total of 8 ml of blood taken from the patient autologously into a sterile
citrated PRP tube. After centrifuging at +4 degrees Celsius, 2500 rpm, and 8 minutes, the lower 1/3 of the
plasma formed in the tube was withdrawn into a 2.5 ml injector, totaling 1 ml of PRP. 0.5 ml of Bevacizumab
was added to the syringe containing 1 ml of citrated PRP. A total of 1.5 ml of citrate, PRP and AntiVEGF
mixture was injected into the right subtenon space under topical anesthesia. Immediately after the
subtenon injection, the patient was fitted with a MagnoVision™ electromagnetic iontophoresis helmet.
MagnoVision™ is a stimulator and iontophoresis device specifically designed for retina/optic nerve diseases,
which contains 9 coils and generates a 2000 mG magnetic field with a 42 Hertz vibration frequency that
synchronously stimulates the bulbus, visual pathways and occipital cortex. These parameters are fixed
values ​​by the manufacturer that cannot be changed for patient safety. Each session is applied effectively
and safely for 30 minutes. This process is repeated for 3 sessions in 2 months between 3 or 4 weeks interval.

After 3 sessions, VA was improved to 10/10 BCVA from 4/10.

Treatment of Chronic Central Cerous Chorioretinopathy:

MANAGEMENT CENTRAL SEROUS CHOROIDORETINOPATHY

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empowering eye care professionals.

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