Factors Affecting Aqueous Humor Outflow Facility in Patients With Uveitis
| Status: | Withdrawn |
|---|---|
| Conditions: | Cervical Cancer, Ocular |
| Therapuetic Areas: | Oncology, Ophthalmology |
| Healthy: | No |
| Age Range: | 19 - 90 |
| Updated: | 9/28/2017 |
| Start Date: | April 2017 |
| End Date: | January 2018 |
Objective: To determine the clinical variables that influence aqueous outflow facility (Co)
and intraocular pressure (IOP) in uveitis.
Uveitic glaucoma is potentially blinding and occurs in 17-46% of chronic uveitis patients.
Uveitic activity causes fluctuating IOP due to decreased Co, increased uveoscleral outflow or
decreased aqueous production.
Specific Aim 1: To evaluate the risk factors for high IOP and low Co in uveitis Hypothesis:
Decreased Co and increased IOP will occur with increasing anterior chamber (AC) flare, AC
cells, degree of synechial angle closure, increased duration of disease, higher uveitis
activity and increasing steroid use Specific Aim 2: To determine prospectively the effect of
AC flare on Co and IOP in "quiescent" uveitis Hypothesis: AC flare even in the absence of AC
cells will cause progressive decline in Co.
Methods: In this proof of concept study, thirty consecutive patients with acute or chronic
uveitis will be recruited from the uveitis clinic. Ten patients with "quiescent" uveitis (no
AC cells) will be recruited for the prospective arm and followed every 2-3 months for 3
visits. Co will be measured using 2-minute pneumatonometer tonography. The effect of risk
factors on IOP and Co in uveitis will be studied using generalized linear modelling
techniques. These risk factors include AC flare (using the laser flare meter), AC cells,
degree of angle closure (by gonioscopy), duration of disease, disease activity and
corticosteroid use within the last year. In the prospective study, the patients will be
divided into subgroups with low flare (< 20ph/ms) and high flare (≥ 20 ph/msec) and the
change in Co and IOP will be analyzed.
Impact: This will be the first study to systematically analyze the risk factors for decrease
in Co and increase in IOP in uveitis and to prospectively evaluate the effect of AC flare on
Co. Proof that AC flare can damage the trabecular meshwork will corroborate previous
experimental evidence and change the paradigm of uveitis treatment. Knowledge of the risk
factors that affect Co and IOP will aid in identifying patients that may need escalation of
their uveitis or glaucoma treatment to prevent optic nerve damage.
and intraocular pressure (IOP) in uveitis.
Uveitic glaucoma is potentially blinding and occurs in 17-46% of chronic uveitis patients.
Uveitic activity causes fluctuating IOP due to decreased Co, increased uveoscleral outflow or
decreased aqueous production.
Specific Aim 1: To evaluate the risk factors for high IOP and low Co in uveitis Hypothesis:
Decreased Co and increased IOP will occur with increasing anterior chamber (AC) flare, AC
cells, degree of synechial angle closure, increased duration of disease, higher uveitis
activity and increasing steroid use Specific Aim 2: To determine prospectively the effect of
AC flare on Co and IOP in "quiescent" uveitis Hypothesis: AC flare even in the absence of AC
cells will cause progressive decline in Co.
Methods: In this proof of concept study, thirty consecutive patients with acute or chronic
uveitis will be recruited from the uveitis clinic. Ten patients with "quiescent" uveitis (no
AC cells) will be recruited for the prospective arm and followed every 2-3 months for 3
visits. Co will be measured using 2-minute pneumatonometer tonography. The effect of risk
factors on IOP and Co in uveitis will be studied using generalized linear modelling
techniques. These risk factors include AC flare (using the laser flare meter), AC cells,
degree of angle closure (by gonioscopy), duration of disease, disease activity and
corticosteroid use within the last year. In the prospective study, the patients will be
divided into subgroups with low flare (< 20ph/ms) and high flare (≥ 20 ph/msec) and the
change in Co and IOP will be analyzed.
Impact: This will be the first study to systematically analyze the risk factors for decrease
in Co and increase in IOP in uveitis and to prospectively evaluate the effect of AC flare on
Co. Proof that AC flare can damage the trabecular meshwork will corroborate previous
experimental evidence and change the paradigm of uveitis treatment. Knowledge of the risk
factors that affect Co and IOP will aid in identifying patients that may need escalation of
their uveitis or glaucoma treatment to prevent optic nerve damage.
Prospective subjects will be identified from the patient population pool in the Uveitis
Clinic at the Truhlsen Eye Institute, University of Nebraska Medical Center, Department of
Ophthalmology and Visual Sciences.
The procedures below will be performed at the first visit in all patients and at the
patient's return visit in the 10 patients recruited for the prospective arm of the study
(upto a maximum of 3 follow up visits)
The following information will be extracted from the chart. These are obtained routinely as
part of routine clinical care through history and ocular examination by slit lamp examination
and applanation tonometry for intraocular pressure measurements.
1. Age
2. Race
3. Gender
4. Diagnosis
5. Duration of disease
6. Medications, dose and duration currently and over the past year
7. Visual acuity- snellen and peripheral visual fields
8. Intraocular pressure
9. Gonioscopy: documentation of degree of synechial angle closure
10. Slit lamp examination and documentation of parameters of ocular inflammation: cells,
flare, posterior synechaie extent and clock hours
11. Fundus examination
Testing done solely for the study will involve:
1. Tonographic Outflow facility: will be assessed using the pneumatonography. A two (2)
minute tonography protocol will be used. The subject will be in a supine position as the
weighted pneumatonometer probe is placed on the eye measuring aqueous outflow. The
patient may need another drop of proparacaine prior to the test if the previous
anesthesia is insufficient. This procedure should take 3-4 minutes.
2. Aqueous flare meter: The anterior chamber flare will be measured in a non-invasive way
using the AC flare meter. This process will take 2-3 minutes and does not require any
additional topical anesthesia.
Clinic at the Truhlsen Eye Institute, University of Nebraska Medical Center, Department of
Ophthalmology and Visual Sciences.
The procedures below will be performed at the first visit in all patients and at the
patient's return visit in the 10 patients recruited for the prospective arm of the study
(upto a maximum of 3 follow up visits)
The following information will be extracted from the chart. These are obtained routinely as
part of routine clinical care through history and ocular examination by slit lamp examination
and applanation tonometry for intraocular pressure measurements.
1. Age
2. Race
3. Gender
4. Diagnosis
5. Duration of disease
6. Medications, dose and duration currently and over the past year
7. Visual acuity- snellen and peripheral visual fields
8. Intraocular pressure
9. Gonioscopy: documentation of degree of synechial angle closure
10. Slit lamp examination and documentation of parameters of ocular inflammation: cells,
flare, posterior synechaie extent and clock hours
11. Fundus examination
Testing done solely for the study will involve:
1. Tonographic Outflow facility: will be assessed using the pneumatonography. A two (2)
minute tonography protocol will be used. The subject will be in a supine position as the
weighted pneumatonometer probe is placed on the eye measuring aqueous outflow. The
patient may need another drop of proparacaine prior to the test if the previous
anesthesia is insufficient. This procedure should take 3-4 minutes.
2. Aqueous flare meter: The anterior chamber flare will be measured in a non-invasive way
using the AC flare meter. This process will take 2-3 minutes and does not require any
additional topical anesthesia.
Inclusion Criteria:
1. Subjects must be 18 years or older
2. Subjects have a diagnosis of uveitis
3. Ability to cooperate for tonography
Exclusion Criteria:
1. Any current corneal abrasion
2. Hypersensitivity to proparacaine
3. history of vitrectomy
4. hypotony (Intraocular pressure < 5 mm Hg)
5. aphakia
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