Evidence map›Paper›PMID 41730284›Full record

ArticleKlinische Monatsblatter fur Augenheilkunde2026

Comparison of Biometric Measurements Between IOL Master 700 and MS-39 in Post-LASIK Myopic Eyes: Implications for IOL Selection in Cataract Surgery.

Giacomo Edoardo Bravetti, Giorgio Enrico Bravetti, Emmanouil Blavakis, Giacomo Savini, Gian Maria Cavallini

Abstract readComparative Study
In one paragraph

Article in Klinische Monatsblatter fur Augenheilkunde, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Giacomo Edoardo Bravetti *Ophthalmology Department, University Hospital Modena, Italy.
Giorgio Enrico Bravetti *Ophthalmology Department, Geneva University Hospitals, Geneva, Switzerland.ORCID 0000-0002-4756-8715
Emmanouil BlavakisOphthalmology Department, Geneva University Hospitals, Geneva, Switzerland.ORCID 0000-0002-7884-329X
Giacomo SaviniOphthalmology Department, G. B. Bietti Foundation I. R. C. C. S., Rome, Italy.
Gian Maria CavalliniOphthalmology Department, University Hospital Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abstract:

backgroundAccurate ocular biometry is essential for achieving optimal refractive outcomes in cataract surgery. In patients with prior myopic LASIK, however, biometric calculations remain particularly challenging due to altered corneal anatomy. Abstract: PURPOSE: This study aims to compare preoperative biometric measurements obtained from the Zeiss IOL Master 700 and the CSO Ray-Tracing MS-39 in patients with a history of myopic LASIK. The goal is to assess the consistency and clinical relevance of these measurements to support intraocular lens (IOL) power selection in this complex patient group. Abstract:

settingLongitudinal, monocentric, retrospective study, conducted at the Ophthalmology Department of the University Hospital of Modena. Abstract:

methodsPatients over 18 years of age scheduled for cataract surgery with a history of myopic LASIK and available preoperative biometry from both the IOL Master 700 and MS-39 were included. Exclusion criteria were incomplete clinical records, prior intraocular surgery, or significant ocular pathologies affecting measurement accuracy. The primary outcomes were differences in calculated emmetropic IOL power and predicted postoperative refraction. Secondary outcomes included comparisons of anterior chamber depth (ACD), central corneal thickness (CCT), average keratometry (K-avg), total corneal power (total keratometry [TK] from IOL Master 700 vs. mean pupil power [MMP] from MS-39), and predicted post-operative spherical equivalent (SE) by using the same IOL power, calculated from the IOL Master 700. Abstract:

resultsSeventy-six eyes from 41 patients (mean age 46.54 ± 12.70 years; 60.98% female) were analysed. The average axial length was 25.93 ± 1.55 mm. An IOL constant of 119.0 was used uniformly across both devices. Statistically significant differences were found in all biometric parameters: ACD (p = 0.00 001), CCT (p = 0.0189), K-avg (p = 0.00 009), and total keratometry (p = 0.00 001). However, no significant differences were observed in the selected IOL power for emmetropia (p = 0.72 527), the predicted postoperative SE of the IOL Master 700 vs. the MS-39 (p = 0.81 642), or the predicted postoperative SE by using the same IOL power, calculated from the IOL Master 700, (p = 0.38 938). Abstract:

conclusionsDespite statistically significant differences in individual biometric parameters between the IOL Master 700 and MS-39, these did not impact final IOL power selection or predicted refraction in post-myopic LASIK patients. Utilizing multiple biometry devices may still enhance confidence and accuracy in surgical planning for this complex group of patients.

Indexed as

BiometryCataract ExtractionKeratomileusis, Laser In SituLenses, IntraocularMyopiaAdultEquipment Failure AnalysisFemaleHumansLens Implantation, IntraocularMaleMiddle AgedRefraction, OcularReproducibility of ResultsRetrospective StudiesSensitivity and Specificity

Identifiers

PMID41730284
PMCPMC13095369

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