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Ophthalmology Update - Cleveland Clinic

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Briefly, after everting the eyelid, the tissue is grasped<br />

within a putterman ptosis clamp and two locking<br />

0.5 forceps are placed beneath the clamp to maintain<br />

the relationship of the wound edges. then, half<br />

of the tissue in the clamp is excised, cautery is used<br />

to achieve hemostasis, the wound edges are held in<br />

approximation and the tissue glue is placed onto the<br />

dry field. then the same steps are repeated after the<br />

remaining half of the tissue is excised.<br />

the glue sets within several minutes, and the eyelid<br />

retractor is removed after checking wound security.<br />

the site is dressed with antibiotic ointment. total<br />

time for the procedure is about eight minutes per<br />

side, which represents a slight reduction in time<br />

compared with when the procedure is performed<br />

using suture closure.<br />

“average surgical time for the standard procedure is<br />

only about 11 minutes, and so increased efficiency is<br />

not a major advantage of the sutureless procedure,”<br />

notes dr. perry. Without question, however, there is<br />

less bleeding intraoperatively when the fibrin<br />

sealant is used, and as a result, ecchymoses and<br />

swelling are reduced postoperatively and resolve<br />

more quickly.<br />

“When patients return for their postoperative visit<br />

after 1 week, most have minimal bruising and swelling.<br />

there is some evidence that the fibrin sealant<br />

may accelerate healing by promoting fibroblast proliferation<br />

and accumulation of vascular endothelial<br />

growth factor, and it is likely that when a suture is<br />

placed, fluid remains trapped in the eyelid until the<br />

suture is removed,” notes dr. perry.<br />

Occasionally, patients who undergo sutureless ptosis<br />

surgery may experience a brief episode of conjunctival<br />

bleeding 4 to 5 days postoperatively. the event is<br />

painless and its onset appears consistent with the<br />

timing of degradation of the fibrin sealant.<br />

the fibrin sealant is derived in part from a human<br />

plasma donor pool. manufacturing protocols incorporate<br />

rigorous testing and vapor heat viral inactivation,<br />

and to date there are no known reported cases<br />

of viral or prion disease associated with use of the<br />

product since the manufacturer introduced pcr<br />

viral screening methodology. nevertheless, a risk of<br />

infectious disease transmission cannot be excluded.<br />

“this information is provided to patients and they are<br />

given the option of sutureless or standard surgery.<br />

however, because of its various benefits, we consider<br />

use of the fibrin sealant the method of choice in<br />

patients at increased risk for bleeding or suture<br />

morbidity as well as for patients undergoing<br />

cosmetic ptosis repair who would especially appreciate<br />

a faster and more comfortable course of healing,”<br />

dr. perry says.<br />

i n v e s t i g a t i O n s<br />

For more information, contact<br />

Julian D. Perry, M.D., at<br />

perryj1@ccf.org.<br />

c O l e e y e i n s t i t U t e c l e v e l a n d c l i n i c . O r g / e y e //

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