Therapeutic Outcomes of Shelf-Stable, Cryopreserved Amniotic Membrane in Recalcitrant Keratopathy

Milanka Stevanovic,1,2 Gina Ciarmiello,1 Robert Eden,1 Robert Schultze1 1Department of Eye Care, Center for Eye Care Excellence, Slingerlands, NY, USA; 2Department of Ophthalmology, Albany Medical College, Albany, NY, USACorrespondence: Milanka Stevanovic, Department of Eye Care, Center for Eye Care Excellence, 9 Vista Blvd #100, Slingerlands, NY, USA, Tel +1 518 475 1515, Email [email protected]: Keratopathy can be caused by multiple factors including neuropathy, inflammation, radiation, among others. Amniotic membrane (AM) is known to have anti-inflammatory and anti-scarring properties, which helps promote epithelialization. Herein, we assessed application of AM to promote epithelialization in the treatment of recalcitrant keratopathy.Patients and Methods: A single-center, retrospective review was performed of consecutive patients with recalcitrant keratopathy that failed to respond to conservative treatment who were subsequently treated with shelf-stable cryopreserved AM. Corneal staining, corneal sensitivity, tear osmolarity, uncorrected visual acuity (UCVA), and complications were assessed before treatment as well as one-week, one-month, and three-months post-treatment.Results: A total of 34 eyes of 18 subjects were included in the analysis. All eyes were diagnosed with recalcitrant keratopathy (n=34), of which 7 (20.6%) eyes had reduced corneal sensation. Eyes were treated with shelf-stable AM for an average of 2.0 ± 0.6 days. Corneal staining scores significantly improved from 1.52 ± 0.68 at baseline to 0.50 ± 0.85 at 1 week (p=0.01), 0.25 ± 0.43 at 1 month (p< 0.001), and 0.47 ± 0.91 at 3 months (p=0.007). The percentage of eyes with no corneal staining was 70.0% at 1-week, 72.7% at 1-month, and 73.7% at 3-months. Corneal sensitivity improved from 2.3 ± 1.4 at baseline to 1.6 ± 0.9 at 1 week (p=0.31), 1.38 ± 0.7 at 1 month (p< 0.001), and 1.11 ± 0.32 at 3 months (p=0.002). UCVA changed from 0.24 ± 0.26 at baseline to 0.14 ± 0.16 at 1 week (p=0.41), 0.18 ± 0.23 at 1 month (p=0.013), and 0.11 ± 0.08 at 3 months (p=0.08). Tear osmolarity did not significantly change from baseline at any timepoint. No complications or adverse events were noted.Conclusion: Shelf-stable cryopreserved AM transplantation led to a significant improvement in corneal epithelization, corneal sensitivity, and visual acuity in patients with recalcitrant keratopathy.Keywords: amniotic membrane, cryopreservation, dry eye disease, neurotrophic keratopathy, keratopathy, superficial punctate keratopathy

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Dove Medical Press (Taylor and Francis Group)
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2025-12-09
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Corneal Surgery and Treatments
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article

Therapeutic Outcomes of Shelf-Stable, Cryopreserved Amniotic Membrane in Recalcitrant Keratopathy

Dove Medical Press (Taylor and Francis Group)
Corneal Surgery and Treatments
article

Therapeutic Outcomes of Shelf-Stable, Cryopreserved Amniotic Membrane in Recalcitrant Keratopathy

article en

Abstract

Milanka Stevanovic,1,2 Gina Ciarmiello,1 Robert Eden,1 Robert Schultze1 1Department of Eye Care, Center for Eye Care Excellence, Slingerlands, NY, USA; 2Department of Ophthalmology, Albany Medical College, Albany, NY, USACorrespondence: Milanka Stevanovic, Department of Eye Care, Center for Eye Care Excellence, 9 Vista Blvd #100, Slingerlands, NY, USA, Tel +1 518 475 1515, Email [email protected]: Keratopathy can be caused by multiple factors including neuropathy, inflammation, radiation, among others. Amniotic membrane (AM) is known to have anti-inflammatory and anti-scarring properties, which helps promote epithelialization. Herein, we assessed application of AM to promote epithelialization in the treatment of recalcitrant keratopathy.Patients and Methods: A single-center, retrospective review was performed of consecutive patients with recalcitrant keratopathy that failed to respond to conservative treatment who were subsequently treated with shelf-stable cryopreserved AM. Corneal staining, corneal sensitivity, tear osmolarity, uncorrected visual acuity (UCVA), and complications were assessed before treatment as well as one-week, one-month, and three-months post-treatment.Results: A total of 34 eyes of 18 subjects were included in the analysis. All eyes were diagnosed with recalcitrant keratopathy (n=34), of which 7 (20.6%) eyes had reduced corneal sensation. Eyes were treated with shelf-stable AM for an average of 2.0 ± 0.6 days. Corneal staining scores significantly improved from 1.52 ± 0.68 at baseline to 0.50 ± 0.85 at 1 week (p=0.01), 0.25 ± 0.43 at 1 month (p< 0.001), and 0.47 ± 0.91 at 3 months (p=0.007). The percentage of eyes with no corneal staining was 70.0% at 1-week, 72.7% at 1-month, and 73.7% at 3-months. Corneal sensitivity improved from 2.3 ± 1.4 at baseline to 1.6 ± 0.9 at 1 week (p=0.31), 1.38 ± 0.7 at 1 month (p< 0.001), and 1.11 ± 0.32 at 3 months (p=0.002). UCVA changed from 0.24 ± 0.26 at baseline to 0.14 ± 0.16 at 1 week (p=0.41), 0.18 ± 0.23 at 1 month (p=0.013), and 0.11 ± 0.08 at 3 months (p=0.08). Tear osmolarity did not significantly change from baseline at any timepoint. No complications or adverse events were noted.Conclusion: Shelf-stable cryopreserved AM transplantation led to a significant improvement in corneal epithelization, corneal sensitivity, and visual acuity in patients with recalcitrant keratopathy.Keywords: amniotic membrane, cryopreservation, dry eye disease, neurotrophic keratopathy, keratopathy, superficial punctate keratopathy

Dove Medical Press (Taylor and Francis Group)
Openalex Percentile: Top 33%
Corneal Surgery and Treatments
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Therapeutic Outcomes of Shelf-Stable, Cryopreserved Amniotic Membrane in Recalcitrant Keratopathy · Dove Medical Press (Taylor and Francis Group) (2025) | TGRS Research Map | TGRS