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Glaucoma Group

Team Leader: PD Dr Plange
Team Members:
Dr. Marion Kaup

Projects:

 

Dynamic Contour Tonometry

Several recent studies have underlined the shortcomings of applanation Tonometry, mainly its dependence on the biomechanical properties of the cornea. Goldmann Tonometry provides an estimate rather than a real measurement of IOP. Classical Tonometry is based on the formula Dp = Df / A. Pressure is always indirectly determined by the measuring a certain force. This means that the eye must be distorted to a certain degree in order to determine the force required for this given deformation. Any deformation of the cornea may it be by applanation or by indentation (impression), interacts with the biomechanical properties of the cornea, especially central corneal thickness, radius and rigidity. Contour Tonometry determines pressure directly by means of a pressure sensing element, integrated into a tonometer tip with a "contoured", concave surface. It is a contact surface which comes as close as possible to the shape which the cornea assumes if pressure within and outside the eyeball were identical and if no forces were thus acting on the cornea. If this condition is met, the pressure sensor in the tip measures true IOP correctly.
Dynamic Contour Tonometry making it is easily possible to record the pressure detected by the sensor not only once at a more or less arbitrary point in time, but continuously at a high sampling rate of 100Hz. IOP is not a static property of the eye but a dynamic quantity modulated by cardiac activity. Ocular pulse amplitude (OPA) reflects the modulation of the intraocular pressure (IOP) due to the heart beat. OPA is the difference between the diastolic and systolic IOP. Currently we are investigating the correlation between OPA and the velocity of the retrobulbar vessels.

 

Working principle of the DCT:
Contour matching of the cornea surface and pressure sensor.

A: Ocular pulse amplitude messured by DCT

B: Pulse curve of the aortic artery

Cooperation partners: TechnoMed

 

 

Colour Doppler Imaging

Retinal blood flow regulation may be compromised in a variety of diseases. For example Glaucomatous optic neuropathy appears to be accompanied by changes in blood flow in the optic nerve head, retina and choroid. Therefore, we investigate the retrobulbar hemodynamic using a colour Doppler imaging device (7.5 MHz linear phased-array transducer, Siemens Sonoline Sienna, Germany). Peak systolic velocities (PSV) and end-diastolic velocities (EDV) are obtained from the velocity waveforms of each artery. The resistive index, known as Pourcelot’s ratio, is calculated by theformula (PSV-EDV) / (PSV). It characterizes peripheral vascular resistance of the studied vessels. We investigate the retrobulbar velocity in glaucoma patients, in patients with anterior ischemic optic neuropathy and other vascular high risk patients.

 

Fig 1: A Colour Doppler imaging device Siemens Sonoline Siena, B 7.5 MHz linear phased-array transducer

 

Fig. 2: CDI Examination in patient.

Fig. 3: A Colour Doppler imaging curve of the ophthalmic artery showing PSV and EDV of the artery B CDI curve of the central retinal artery showing PSV and EDV of the artery and the vein.

Selected publications on CDI

 

Contact: Dr. Niklas Plange, Dr. Marion Kaup

 

Sorry, the rest of this chapter is still under construction

 

IBT | Glaucoma | Macula | Cornea | NeuroOph | Oc Reg