Glaucoma, Open-Angle, Ocular Hypertension
Conditions
Keywords
Corticosteroids, Bronchodilator Agents, Intraocular Pressure
Brief summary
The purpose of this study is to determine whether a commonly prescribed orally inhaled corticosteroid treatment will induce a clinically meaningful elevation in intraocular pressure, when administered to patients with ocular hypertension (OHT) or open-angle glaucoma (OAG). Based on the response to high-dose corticosteroids, this patient group is more likely than the normal population to demonstrate this adverse effect.
Detailed description
Systemic and topical ophthalmic steroids have long been associated with ocular effects, such as glaucoma or cataracts.\[Alfano JE; Bernstein HN et al. 1962; Bernstein HN et al. 1963; Becker B and Mills DW in Arch Ophthalm 1963; Becker B and Mills DW in JAMA 1963; Armaly MF 1963 (1); Armaly MF 1963 (2); and Buckley RJ\] Periocular steroid injections \[Herschler J; Kalina RE\] and steroids applied to periocular skin \[Aggarwal RK et al.\] have also been reported to increase intraocular pressure (IOP) and raised IOP is the major risk factor for glaucoma. Ocular hypertension (OHT) is defined as an IOP above 21mmHg in one or both eyes without detectable glaucomatous damage. Primary open-angle glaucoma (POAG) is a chronic and progressive optic neuropathy of unknown etiology characterized by disc cupping, and often associated with visual field defects and elevated IOP. This disease is one of the leading causes of blindness worldwide.\[Kwon YH et al.\] Approximately 18% to 36% of the general population are corticosteroid responders. This response is increased to 46% to 92% in patients with POAG.\[Tripathi RC et al.\] Asthma is the most common chronic respiratory illness in Canada, affecting approximately 10% of the population. For the majority of these patients, long-term inhaled corticosteroids (ICS) are standard of care to prevent acute asthma exacerbations.\[Kim H and Mazza J\] Although the systemic absorption of inhaled and nasal steroids has been established, the clinically relevant ocular side effects are poorly defined. \[Cave A et al.; Allen DB et al.\] A large prospective study in 1995 by Samiy et al reported no statistically significant increase of IOP in 187 patients without glaucoma taking inhaled steroids for various pulmonary conditions.\[Samiy N et al.\] However, six cases of increased IOP associated with combined nasal and inhaled steroid use in non-glaucomatous patients have been reported. \[Dreyer EB; Desnoeck M et al.; Opatowsky I et al.\] A large case-control study in 1997 suggested that current users of high doses of ICS prescribed regularly for 3 or more months were at increased risk of OHT or OAG (OR 1.44; 95% CI 1.01-2.06).\[Garbe E et al.\] In contrast, Gozalez et al. conducted a nested case-control study in 2010 with Quebec data which showed current and continuous use of ICS did not result in increased risk of glaucoma or raised IOP requiring treatment.\[Gonzalez AV et al.\] Similarly, Duh et al. reported no association between inhaled budesonide daily therapy and increased IOP in 1255 asthmatic patients.\[Duh MS et al.\] Further, a prospective population-based cohort study published in 2012 suggested no association between the development of OAG and ICS in the elderly.\[Marcus MW et al.\] In 2013, our group published a randomized double-masked controlled trial that showed no evidence of IOP elevation after 6 weeks use of beclomethasone nasal spray in 19 patients with OHT and POAG.\[Yuen D et al.\] The purpose of the current study protocol would be to extend the study to investigate ICS in the same patient population. To date, the effect of inhaled corticosteroids in those with pre-existing OHT or POAG remains uncertain. Considering the large number of patients on inhaled steroids, investigating the use of inhaled steroid in glaucoma patients could have significant clinical impact. This study was designed to evaluate the effect of inhaled fluticasone propionate on intraocular pressure (IOP) in patients with OHT or controlled open-angle glaucoma (OAG). Patient randomization was performed by an independent Research Coordinator in a separate physical space and kept sealed from the principal study investigators, who assessed and recorded outcome measures, until the completion of study data collection. IOP was measured in a masked fashion, using a second observer to record values. Two measurements within 1 mmHg were averaged for each data point. With a sample size of 8 patients per interventional arm, the study is powered at 0.80 to detect an elevation of 3.2 mmHg (≥20%) from mean, assuming a standard deviation of 2.5 mmHg. Baseline data will be compared between groups using the student's t test and Fisher exact test. A 2-sided p value of \<0.05 will be considered statistically significant. The primary outcome measure (mean IOP) will be assessed using a 1-sided Student t test.
Interventions
fluticasone propionate 250 µg metered-dose inhaler
saline metered dose inhaler
Sponsors
Study design
Eligibility
Inclusion criteria
* Age 18 to 85 years, inclusive * Mild-moderate open-angle glaucoma/ocular hypertension with cup:disc ratio \<0.85 vertically and humphrey visual field mean deviation \>-12.00 (BOTH EYES must meet this criteria for patient to be included) * Glaucoma well-controlled, defined by IOP \< 21 mmHg and at target with no visual field/disc progression for at least 6 months (BOTH EYES must meet this criteria for patient to be included)
Exclusion criteria
* Any form of steroid medication use within the prior 6 weeks * Any previous intra-ocular surgery or refractive surgery in the study eye * no light perception (i.e. blindness) in either eye * unwilling/unable to give consent * unwilling to accept randomization * patient potentially unavailable for follow-up visits
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean Intraocular Pressure | week 6 | Masked assessment of intraocular pressure using goldmann application tonometry. Mean of 2 measurements within 1 mmHg will be recorded. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mean Visual Acuity | week 6 | best corrected logMAR visual acuity for each eye. 20/20 vision corresponds with a logMAR score of 0, while negative logMAR scores indicate better than 20/20 vision, values \> 0.5 correspond with low vision, and values \> 1.3 correspond with blindness. |
| Side Effects | from baseline to week 6 | subjective (reported) and objective (slit lamp examination) side-effects attributable to study medications |
| Intraocular Pressure Elevation >20% From Baseline | within 6-week observation period | Participants with 2 consecutive intraocular pressure measurements exceeding 20% increase from baseline were discontinued from study. |
| Adherence | Completion of study, up to 6 weeks | Adherence was calculated from self-reported study diaries and correlated to a counter that measured number of inhaled puffs built into the placebo metered-dose inhalers |
Participant flow
Recruitment details
1,960 records of glaucoma patients with scheduled visits in a university-based glaucoma clinic were screened between August 1, 2014 and November 7, 2014.
Pre-assignment details
22 consented to participate and 20 completed the study.
Participants by arm
| Arm | Count |
|---|---|
| Fluticasone participants will be asked to use fluticasone propionate 250 µg metered-dose inhaler 1 puff twice-daily for 6 weeks. | 10 |
| Saline Placebo participants will be asked to use a saline placebo metered-dose inhaler 1 puff twice-daily for 6 weeks. | 10 |
| Total | 20 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Withdrawal by Subject | 1 | 1 |
Baseline characteristics
| Characteristic | Fluticasone | Saline Placebo | Total |
|---|---|---|---|
| Age, Continuous | 65.7 years STANDARD_DEVIATION 9 | 65.7 years STANDARD_DEVIATION 11 | 65.7 years STANDARD_DEVIATION 10 |
| Diagnosis Ocular Hypertension | 1 participants | 4 participants | 5 participants |
| Diagnosis Pigment Dispersion Glaucoma | 3 participants | 1 participants | 4 participants |
| Diagnosis Primary Open-Angle Glaucoma | 6 participants | 4 participants | 10 participants |
| Diagnosis Pseudoexfoliative Glaucoma | 0 participants | 1 participants | 1 participants |
| Mean central corneal thickness | 553.1 micrometers STANDARD_DEVIATION 31.7 | 549.1 micrometers STANDARD_DEVIATION 30.8 | 551.1 micrometers STANDARD_DEVIATION 31.25 |
| Mean cup-disc ratio | 0.49 cup:disc ratio STANDARD_DEVIATION 0.2 | 0.38 cup:disc ratio STANDARD_DEVIATION 0.2 | 0.44 cup:disc ratio STANDARD_DEVIATION 0.2 |
| Mean intraocular pressure | 14.3 mmHg STANDARD_DEVIATION 3 | 15.6 mmHg STANDARD_DEVIATION 3.6 | 15.0 mmHg STANDARD_DEVIATION 3.3 |
| Mean logMAR visual acuity | 0.19 logMAR STANDARD_DEVIATION 0.1 | 0.18 logMAR STANDARD_DEVIATION 0.1 | 0.18 logMAR STANDARD_DEVIATION 0.1 |
| Mean number of ocular hypotensive medications | 1.3 medication classes STANDARD_DEVIATION 0.7 | 1.3 medication classes STANDARD_DEVIATION 1.4 | 1.3 medication classes STANDARD_DEVIATION 1 |
| Mean visual field mean deviation | -0.72 decibels (dB) STANDARD_DEVIATION 2.6 | -1.13 decibels (dB) STANDARD_DEVIATION 2.5 | -0.92 decibels (dB) STANDARD_DEVIATION 2.6 |
| Prior laser trabeculoplasty | 1 participants | 0 participants | 1 participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 10 Participants | 10 Participants | 20 Participants |
| Race (NIH/OMB) White | 0 Participants | 0 Participants | 0 Participants |
| Region of Enrollment Canada | 10 participants | 10 participants | 20 participants |
| Sex: Female, Male Female | 4 Participants | 4 Participants | 8 Participants |
| Sex: Female, Male Male | 6 Participants | 6 Participants | 12 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 2 / 10 | 2 / 10 |
| serious Total, serious adverse events | 0 / 10 | 0 / 10 |
Outcome results
Mean Intraocular Pressure
Masked assessment of intraocular pressure using goldmann application tonometry. Mean of 2 measurements within 1 mmHg will be recorded.
Time frame: week 6
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Fluticasone | Mean Intraocular Pressure | 14.7 mmHg | Standard Deviation 2.4 |
| Saline Placebo | Mean Intraocular Pressure | 14.8 mmHg | Standard Deviation 3.8 |
Adherence
Adherence was calculated from self-reported study diaries and correlated to a counter that measured number of inhaled puffs built into the placebo metered-dose inhalers
Time frame: Completion of study, up to 6 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Fluticasone | Adherence | 93.6 percentage of required doses | Standard Deviation 7.1 |
| Saline Placebo | Adherence | 96.1 percentage of required doses | Standard Deviation 4.4 |
Intraocular Pressure Elevation >20% From Baseline
Participants with 2 consecutive intraocular pressure measurements exceeding 20% increase from baseline were discontinued from study.
Time frame: within 6-week observation period
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Fluticasone | Intraocular Pressure Elevation >20% From Baseline | elevation >20% | 1 participants |
| Fluticasone | Intraocular Pressure Elevation >20% From Baseline | no elevation >20% | 9 participants |
| Saline Placebo | Intraocular Pressure Elevation >20% From Baseline | elevation >20% | 0 participants |
| Saline Placebo | Intraocular Pressure Elevation >20% From Baseline | no elevation >20% | 10 participants |
Mean Visual Acuity
best corrected logMAR visual acuity for each eye. 20/20 vision corresponds with a logMAR score of 0, while negative logMAR scores indicate better than 20/20 vision, values \> 0.5 correspond with low vision, and values \> 1.3 correspond with blindness.
Time frame: week 6
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Fluticasone | Mean Visual Acuity | 0.15 logMAR | Standard Deviation 0.12 |
| Saline Placebo | Mean Visual Acuity | 0.15 logMAR | Standard Deviation 0.08 |
Side Effects
subjective (reported) and objective (slit lamp examination) side-effects attributable to study medications
Time frame: from baseline to week 6
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Fluticasone | Side Effects | throat discomfort | 1 participants |
| Fluticasone | Side Effects | difficulty sleeping | 0 participants |
| Fluticasone | Side Effects | headache | 1 participants |
| Fluticasone | Side Effects | no adverse effects | 8 participants |
| Fluticasone | Side Effects | lens opacity | 0 participants |
| Saline Placebo | Side Effects | no adverse effects | 8 participants |
| Saline Placebo | Side Effects | lens opacity | 0 participants |
| Saline Placebo | Side Effects | throat discomfort | 1 participants |
| Saline Placebo | Side Effects | headache | 0 participants |
| Saline Placebo | Side Effects | difficulty sleeping | 1 participants |