My question concerns my 8 y/o son with POAG diagnosis. Diagnosis in Dec '06, followed by a regime of drops.
PressuresPressure ulcer seemed to be controlled ou. OS IOP at onset was ~40 mmHg, OD ~ 25mmHg. Post trtmnt with
AlphaganAlphagan
Alphagan p
Alphagan-p P BID ou,
Azopt BID os
pressuresPressure ulcer were ~15 ou. Last week os iop spiked to 50 (od ~ 16).
DiamoxDiamox
Diamox sequels ,
timopticTimoptic ocudose
Timoptic ocumeter
Timoptic ocumeter plus
Timoptic-xe xe, travatan were added ( Azopt stopped). All exams show clear corneas, open angles, normal vf, corrected vision 20/20 od, 20/30 os, c/d ratio slightly worse in os (can't recall what they were)---otherwise healthy kid. Next step would presumably be surgery. I would like to exhaust all other options before sx. Could the unilateral nature of this be indicative of some sort of something (venous flow problem)? In the abscence of any systemic issues (sturge-weber, others typically seen with glauc)) or other ocular issues are there other avenues to diagnose and/or rule out. Would an MRI or MRA tell us anything? Could there be some sort of -oma lurking in there somewhere? We are recieving excellent care and advice form our OD and Ophthalmologist, but would like to get additional input.
Any resources or advice you can offer is appreciated
surgery is probably your best option IMO.
not sure what IMO is?
thanks for your input.
and a bleb is pretty much a last resort. no way your 8 year old gets a bleb as a 1st option. he's going to get SLT or ALT:
http://www.glaucoma.org/treating/surgery.html?section=152
its relatively painless and highly likely to work well. i have an 8 year old and i guarantee that if my 8 year old had high iop/glaucoma, laser would be my 1st choice.
unlikely IMO to be an "underlying" systemic condition.