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Inspired by Dr Doan's return and desire to revive this forum thought I'd post this to start some discussion.
Got a flyer in the mail about an upcoming conference and one of the topics to be discussed is limiting your malpractice risk. And one of the subtopics they are going to cover is informed consent for steroid drops.
What do the rest of you do when starting steroid drops on patients. I do discuss with them the risk of glaucoma and cataracts and the importance of returning for appointments to monitor for these side effects. But does anybody actually have them sign informed consent forms?
Clearly steroid drops are indicated and necessary in some cases but often can be considered elective. For example, I saw a patient last year was being treated for blepharitis with Tobradex who came in with a painful eye and an IOP of 45.
Thoughts?
Got a flyer in the mail about an upcoming conference and one of the topics to be discussed is limiting your malpractice risk. And one of the subtopics they are going to cover is informed consent for steroid drops.
What do the rest of you do when starting steroid drops on patients. I do discuss with them the risk of glaucoma and cataracts and the importance of returning for appointments to monitor for these side effects. But does anybody actually have them sign informed consent forms?
Clearly steroid drops are indicated and necessary in some cases but often can be considered elective. For example, I saw a patient last year was being treated for blepharitis with Tobradex who came in with a painful eye and an IOP of 45.
Thoughts?