This appears to be the first report of the use of intracameral phenylephrine for controlling intraocular bleeding during cataract surgery. Physiologically, the observed cessation of bleeding makes sense in light of the known potent vasoconstrictive properties of phenylephrine. Phenylephrine injected intravitreally in rabbits has been shown to result in iris-ciliary vessel vasoconstriction [4].
Topical phenylephrine or Mydriasert® ophthalmic insert was used pre-operatively in all three cases. The latter is removed from the conjunctival fornix a few minutes before the surgery. Animal models have shown that phenylephrine is present in the aqueous humor for at least 2 h following topical drops instillation [5]. Despite this, intraocular bleeding occurred, and was only stopped when phenylephrine was injected intracamerally. There are several explanations for this. Firstly, irrigation and aspiration of anterior chamber fluid may have washed out residual pre-operative phenylephrine. The duration of vasoconstriction has not been studied as far as we know after phenylephrine washout. However, further irrigation and aspiration after intracameral phenylephrine injection (to stop bleeding), did not result in re-bleeding. The efficacy of intracameral phenylephrine may therefore be due to the higher concentration achieved in the aqueous as compared to pre-operative topical application. It is interesting that case 2 had intracameral phenylephrine at the start of surgery yet developed iris bleeding towards the end of surgery. The operation was not prolonged (20 min), suggesting that short duration of action of the first intracameral phenylephrine injection is less likely to explain the bleeding occurring towards the end of surgery. One hypothesis is therefore that the efficacy of phenylephrine is due to the direct vasoconstrictive effect on the exposed bleeding vessel.
There are theoretical concerns regarding vasodilation of the vessel after initial vasoconstriction leading to further intraocular bleeding. This was not observed intraoperatively in these cases, and no hyphema was seen in any of the post-operative visits.
Intraocular adrenaline 0.1% is known to have a vasoconstrictive effect on iris vessels in rat eyes [6]. All three surgical cases had 0.5 ml of adrenaline 1:1000 infused into 500 ml of balanced saline solution (BSS) irrigation solution (i.e., adrenaline 0.1%). Irrigation and aspiration of the anterior segment with this solution did not succeed in halting the bleeding. This case series suggests that intracameral phenylephrine is much more effective in controlling significant intraoperative intraocular bleeding.
Albeit a few sporadic case reports, no significantly increased risk of systemic or post-operative ophthalmological complications have been reported with intracameral phenylephrine 2.5% use [2, 3, 7]. A concentration of 2.5% has been recommended for operating room use [8].
In our case series, 0.3 ml injection of 2.5% phenylephrine was used. A retrospective study found that a 0.6 ml intracameral injection of diluted phenylephrine (0.3 ml phenylephrine 2.5% mixed with 0.3 ml BSS) was not found to be associated with complications in the short- and medium term [7]. Phenylephrine is a vasopressor, however, and there are case reports of cardiovascular complications [9]. Circulatory monitoring of patients for increased blood pressure and heart rate/rhythm changes is therefore advisable.
Although intracameral phenylephrine was not found to be associated with post-operative complications, no corneal endothelial cell counts nor corneal thickness measurements were performed to assess for endothelial toxicity. Also, as this is not a controlled study, it is not possible to state how much faster the bleeding is controlled with phenylephrine as compared with observation.