Evidence map›Paper›PMID 42085515›Full record

Observational studyReproduction & fertility2026

Media temperature control: a potentially important quality control parameter in human oocyte vitrification.

Munevver Serdarogullari, Zafer Atayurt, Georges Raad, Yaren Yilancilar, Omar Ammar, Zalihe Yarkiner, Beril Yuksel, Marcos Meseguer, George Liperis

Abstract readObservational Study
In one paragraph

Observational study in Reproduction & fertility, 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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0citing papers 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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

9 authors.

Munevver SerdarogullariVentus IVF Center, Embryology Laboratory, Nicosia, Cyprus.
Zafer AtayurtVentus IVF Center, Embryology Laboratory, Nicosia, Cyprus.
Georges RaadFaculty of Medicine and Medical Sciences, Holy Spirit University of Kaslik, Jounieh, Lebanon.
Yaren YilancilarVentus IVF Center, Embryology Laboratory, Nicosia, Cyprus.
Omar AmmarDepartment of Obstetrics and Gynaecology, College of Medicine, University of Anbar, Ramadi, Iraq.
Zalihe YarkinerDepartment of Basic Sciences and Humanities, Faculty of Arts and Sciences, Cyprus International University, Northern Cyprus, Turkey.
Beril YukselVentus IVF Center, Embryology Laboratory, Nicosia, Cyprus.
Marcos MeseguerIVIRMA Global Research Alliance, IVI Foundation, Instituto de Investigación Sanitaria La Fe IIS La Fe, Valencia, Spain.
George LiperisUniversity of Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0001-9588-3392

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abstract: The purpose of this study was to evaluate the role of controlling media temperature during human oocyte vitrification. This retrospective study compared fertilisation rates, cleavage-stage embryo development, and blastulation between two separate periods defined by uncontrolled versus controlled media temperature during oocyte vitrification. A retrospective observational study was conducted at Ventus IVF Center, Cyprus, evaluating the effect of vitrification solution temperature during vitrification on oocyte survival and embryological outcomes. Oocytes were vitrified either under uncontrolled ambient conditions (n = 87 oocytes) or with temperature control (n = 83 oocytes), with the experimental groups assessed asynchronously. Vitrification and equilibration solution temperatures were recorded using a calibrated UNI-T UT322 thermometer. There were no significant differences in baseline characteristics of oocyte donors between the controlled and uncontrolled temperature groups (P > 0.05). During vitrification, vitrification media temperature was significantly higher in the controlled group (23.85 ± 0.43°C) compared to the uncontrolled group (19.65 ± 0.43°C; P < 0.001). No significant differences were observed in oocyte survival post-warming (82/83 vs 80/87; P = 0.08) or fertilisation rates (69/82 vs 70/87; P = 0.67) between groups. Compared to the controlled group, the uncontrolled group showed markedly higher developmental arrest at the pronuclear (10/70 vs 0/69; P < 0.001), post-pronuclear (20/70 vs 0/69; P < 0.001), and cleavage (35/70 vs 0/69; P < 0.001) stages, and significantly reduced blastocyst formation (5/70 vs 56/69; P < 0.001). Maintaining vitrification solution temperature rather than relying on ambient conditions significantly improves oocyte vitrification efficiency and pre-implantation embryo development parameters. Lay summary: Freezing human eggs is widely used in fertility treatment and fertility preservation, but small laboratory factors can strongly influence success. This study investigated whether controlling the temperature of the freezing solutions during egg freezing into a glass-like state affects how well eggs survive and develop into embryos. Eggs from donor cycles were frozen either under room conditions or by controlling the freezing solution temperature at a stable temperature. Although egg survival and fertilisation rates were similar in both groups, eggs frozen without temperature control showed very high rates of early embryo development failure and produced very few embryos following a five-day culture. In contrast, eggs frozen with controlled solution temperatures developed into embryos following the five-day culture far more often. These findings show that maintaining the temperature of freezing solutions is a critical but often overlooked laboratory quality control factor and that simple temperature control measures could significantly improve the success of egg freezing in fertility clinics. Graphical Abstract:

Indexed as

CryopreservationCulture MediaOocytesVitrificationAdultCell SurvivalEmbryonic DevelopmentFemaleFertilization in VitroHumansQuality ControlRetrospective StudiesTemperatureCulture Mediaembryo developmentoocyte vitrificationpronuclear arrestquality controltemperature control

Identifiers

PMID42085515
PMCPMC13193071

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