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One-Year Results of a Phase I/II Randomized, Double-Masked, Placebo-Controlled Study of Processed Amniotic Fluid Drops After PRK.
Kirschenbaum, Malka Davina; Hu, Katherine S; Ip, Colin S; Lin, Amy; Pierce, Jan; Holubkov, Richard; Jensen, Hailey; Mifflin, Mark D.
Afiliación
  • Kirschenbaum MD; Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT.
  • Hu KS; Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT.
  • Ip CS; Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT.
  • Lin A; Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT.
  • Pierce J; Cell Therapy and Regenerative Medicine, University of Utah, Salt Lake City, UT; and.
  • Holubkov R; Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Jensen H; Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Mifflin MD; Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT.
Cornea ; 43(8): 955-960, 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-38277050
ABSTRACT

PURPOSE:

The aim of this study was to evaluate the 1-year outcomes of using processed amniotic fluid (pAF) postoperatively after photorefractive keratectomy (PRK).

METHODS:

Sixty-one participants were randomized to receive either placebo or pAF drops. The drops were instilled 4 times daily for 1 week after PRK along with routine postoperative medications. The primary outcome measures included uncorrected visual acuity, topographic corneal irregularity measurement, and surface staining over 1 year.

RESULTS:

A statistically significant difference in uncorrected distance visual acuity between the placebo and treatment groups was seen at 1 month post-PRK, with a visual advantage evident in the pAF group. A suggestive difference in corneal irregularity measurement was also seen between the placebo and treatment groups at 1 month postsurgery, with less irregularity noted in the pAF group. No differences in uncorrected distance visual acuity or corneal irregularity measurement were found at 3, 6, and 12 months. There was also no significant difference in corneal staining scores between the 2 groups at any of the measured time points.

CONCLUSIONS:

This 1-year study evaluating the safety and efficacy of pAF as an additional postoperative topical medication after PRK demonstrated that pAF offered a mild visual advantage at 1 month post-PRK. There were no late adverse events, and the intervention proved safe at 1 year.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Soluciones Oftálmicas / Agudeza Visual / Queratectomía Fotorrefractiva / Láseres de Excímeros / Líquido Amniótico Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male Idioma: En Revista: Cornea Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Soluciones Oftálmicas / Agudeza Visual / Queratectomía Fotorrefractiva / Láseres de Excímeros / Líquido Amniótico Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male Idioma: En Revista: Cornea Año: 2024 Tipo del documento: Article