HIGHLIGHTS
- who: John-Michael Guest from the This experimental study was performed at the Kresge Eye Institute, Detroit, MichiganThe Institutional Review Board at Wayne State University approved the study protocol. Informed consent was not needed as there were no human subjects in our study. Participants were practicing ophthalmologists who performed at least , intravitreal injections of aflibercept per month. The ophthalmologists were educated about the proper plunger position while using the PFS (aligning the base of the dome with the target line according to the package insert) immediately prior to conducting this experiment. have published the research work: Accuracy . . .
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