Evidence map›Paper›PMID 40504466›Full record

Trial reportInternational ophthalmology2025

Impact of residual ophthalmic viscosurgical device behind intraocular lens on postoperative intraocular pressure and refractive outcomes in cataract surgery.

Omer M Bilgic, Ozlem E Kemer

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in International ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Omer M BilgicBilkent City Hospital, University of Health Sciences, Ankara, Turkey. mustafaa.b@hotmail.com.
Ozlem E KemerBilkent City Hospital, University of Health Sciences, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to quantify the residual ophthalmic viscosurgical device (OVD) behind the intraocular lens (IOL) following cataract surgery and evaluate its impact on intraocular pressure (IOP) and refractive changes during the postoperative period. Additionally, it examines OVD regression and associated risk factors.

designProspective Clinical Trial.

methodsThirty eyes of thirty patients who underwent uncomplicated cataract surgery with monofocal posterior chamber IOL implantation were included. Postoperative assessments were conducted on days 1, 3, 5, 7, 10, and 14. Using anterior segment OCT, OVD thickness behind the IOL was measured, and correlations were analyzed between OVD reduction, IOP (via non-contact tonometry), and refractive error changes. Risk factors examined included age, gender, laterality, pseudoexfoliation (psx), surgeon experience, cataract hardness, biometric data, and phacoemulsification parameters.

resultsOn day 1, mean OVD thickness was 215.7 ± 92.7 µm. A significant decrease in OVD was noted with each follow-up, with complete resorption by day 10 (p = 0.01). Initial IOP was 18.0 ± 3.3 mmHg, showing a notable reduction over time (p = 0.01). A positive correlation was observed between OVD reduction and IOP decrease from days 1 to 3 (p = 0.01, r = 0.581) and days 1 to 5 (p = 0.017, r = 0.432). Additionally, a significant association was found between OVD reduction and myopic shift from days 3 to 5 (p = 0.014, r = 0.444). Patients with thinner lenses had higher residual OVD on day 1 (p = 0.01, r = - 0.504).

conclusionsResidual OVD behind the IOL may elevate IOP and cause refractive changes, emphasizing the need for thorough OVD removal and close postoperative monitoring, especially in patients with thinner lenses.

Indexed as

Cataract ExtractionIntraocular PressureLenses, IntraocularLens Implantation, IntraocularPhacoemulsificationRefraction, OcularAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedPostoperative PeriodProspective StudiesTomography, Optical CoherenceAnterior segment optical coherence tomographyIntraocular pressureOphthalmic viscosurgical devicesPhacoemulsificationRefraction

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.