Evidence map›Paper›PMID 42199330›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2026

Retrospective Evaluation of Successive Biovance

Brandon D Ayres, Nicole R Fram, Helen K Wu, Lisa Feulner, Neel R Desai

Abstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Brandon D AyresCornea Service, Wills Eye Hospital, Philadelphia, PA, USA.
Nicole R FramAdvanced Eye Care, Los Angeles, CA, USA.ORCID 0000-0002-7170-8685
Helen K WuNewton Wellesley Eye Associates, Wellesley, MA, USA.
Lisa FeulnerAdvanced Eye Care & Aesthetics, Bel Air, MD, USA.
Neel R DesaiEye Institute of West Florida, Largo, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To evaluate the clinical outcomes of serial placement of an amniotic decellularized basement membrane (DBM) graft (Biovance Methods: This retrospective study included eyes with reduced corneal sensitivity (Brill esthesiometry Levels 3-5), epithelial staining, and positive MMP-9, consistent with subclinical or Mackie Stage 1 NK. Each eye underwent serial DBM graft placement guided by clinical response over an average of 7 weeks. Corneal fluorescein staining, Brill esthesiometry, tear osmolarity, and MMP-9 status were assessed at each visit. Follow-up occurred every 1-2 weeks, with treatment advanced upon improvements in corneal staining and stabilizing biomarker trends. Outcomes included clinician-documented resolution of epithelial staining, changes in corneal sensitivity, and normalization of tear osmolarity and MMP-9. Results: A total of 936 eyes from 488 patients met enrollment criteria. Mean DBM utilization increased with disease severity (Brill 3: 3.70; Brill 4: 3.08; Brill 5: 4.30 grafts). Corneal epithelial resolution occurred in all eyes with complete follow-up. Functional corneal sensitivity improved in 0.7% of Brill 3, 31.6% of Brill 4, and 77.5% of Brill 5 eyes. Among eyes with abnormal baseline osmolarity, 70-82% normalized following treatment. MMP-9 positivity decreased across all severity groups, with 56-66% converting to negative, corresponding with improved ocular surface stability. Conclusion: Serial DBM grafting was associated with improvements in corneal staining, functional corneal sensitivity, ocular surface inflammation, and tear-film homeostasis, supporting its role in early-stage NK management. These findings suggest DBM promotes epithelial and neurosensory recovery through host-matrix interactions within the preserved basement membrane and that early intervention may help mitigate disease progression.

Indexed as

amniotic membrane tissuebiovancecorneal sensitivitydecellularized basement membraneneurotrophic keratitisocular surface disease

Identifiers

PMID42199330
PMCPMC13199709

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