Primary Open Angle Glaucoma Clinical Trial
Official title:
The PAIR Study. Positive Airway Pressure and Intraocular Relationship: IOP Response to a Short-term Application of CPAP
Lowering of the pressure in the eye (intraocular pressure, IOP) is the only proven treatment
for Primary Open-angle Glaucoma (POAG). However, even effective reduction of IOP by
pharmacological or surgical means does not always change the course of the disease or prevent
the onset of glaucoma. Some people with POAG also suffer from Obstructive Sleep Apnoea (OSA),
an increasingly common sleep disorder which is known to affect heart and blood vessels, and
may contribute to glaucoma progression. OSA is treated with Continuous Positive Airway
Pressure (CPAP)Íž however using this type of breathing support may raise IOP.
This study aims to establish whether a short-term application of CPAP in awake subjects leads
to an increase in IOP. Patients with treated POAG, patients with newly diagnosed untreated
POAG and control subjects without glaucoma will be included. CPAP will be applied at several
different pressure levels for a total of 2 hours during which IOP and ocular perfusion
pressure (OPP) will be measured. If CPAP is shown to raise IOP or alter OPP it could be
necessary to assess available alternative treatment options for OSA.
Primary open-angle glaucoma (POAG) is a progressive optic neuropathy characterized by
specific optic disc changes and associated visual field defects. Estimated prevalence is
3.0%, making it the leading cause of irreversible blindness worldwide. Intraocular pressure
(IOP) is the only proven modifiable risk factor for the development and progression of POAG,
but even effective reduction of IOP by pharmacological or surgical means does not always
change the course of the disease or prevent some people from developing glaucoma.
OSA is a sleep-related breathing disorder (SBD) caused by complete (apnoea) or partial
(hypopnoea) narrowing of the upper airway, resulting in disturbed sleep and intermittent
oxygen desaturations. These in turn have negative impact on cardiovascular system and
potentially other organs. OSA is treated by continuous positive airway pressure (CPAP)
applied by a nasal or a full face mask which maintains patency of the upper airway. CPAP is
the first line treatment for moderately severe and severe OSA and, among currently used
treatment modalities, it is also the most effective one. The prevalence of OSA continues to
increase linked with the rising global incidence of obesity, though many remain undiagnosed.
A recent study from the United States estimated that 35% of people between the ages of 50 and
70 years suffer from OSA, and approximately 12% may require treatment.
OSA and OAG are, therefore, two common conditions which may coexist in a significant
proportion of patients. In fact, some studies indicate increased prevalence of OAG in
patients with OSA, which is in line with a suspected causative role of OSA in glaucoma.
People with OAG and concomitant OSA associated with the relevant symptoms, particularly
daytime sleepiness, currently receive standard treatment with CPAP. However, the impact of
CPAP on their glaucoma is unknown. There are concerns that CPAP increases IOP, currently the
only modifiable factor in glaucoma, though the evidence for this is limited. The exact
mechanisms of the possible IOP-raising effect of CPAP are not clear. The favoured hypothesis
is CPAP leads to increases in intrathoracic pressure, which in turn raises pressure in the
venous circulation and a reduction in the aqueous humour outflow through the episcleral veins
and ultimately IOP increase. A similar mechanism is believed to be responsible for IOP
elevation in the transition from an upright to supine position in which venous drainage is
reduced.
The relationship between the level of pressure used in CPAP treatment and IOP has not been
studied. It is unknown if IOP increases in correlated way to CPAP or whether there is no
straightforward correlation. If the first is true, application of CPAP only up to a certain
pressure level would be safe and perhaps the threshold to use bi-level PAP should be lower in
patients with glaucoma. If, however, IOP changes are a matter of individual response to CPAP,
perhaps dependent on the severity of OSA or BMI, a routine measurement of the pressure should
be performed once CPAP is started. This is currently not a part of standard clinical
practice. It is also possible that CPAP set within the usual pressure range does not
influence IOP or its effect is not mediated by simple mechanical pressure transmission.
Therefore understanding the influence of CPAP on IOP is important as it may inform the
management of people with OSA and concomitant glaucoma. If CPAP is shown to raise IOP or
alter ocular perfusion pressure (OPP) to levels that pose clinical risk it will be necessary
to assess available alternative treatment options for OSA.
This is a prospective physiological controlled study which will assess IOP response to
several different CPAP levels applied for short periods in wakefulness in three groups of
people: POAG patients established on treatment (treated glaucoma group), newly diagnosed
treatment naïve POAG patients (untreated glaucoma group) and control subjects without
glaucoma (control subjects).
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