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EVALUATION TOOLS

Decision support tools scoring embryos according to their statistical viability by applying a number of criteria to the embryos.

Purpose: For embryo evaluation.

GET THE MOST INFORMATION TO MAKE THE BEST CHOICE

Traditional evaluation of embryos limits the amount of information about embryo development. Using time-lapse analysis, you can detect previously unseen embryo development patterns and events which have been correlated to clinical outcome. With EmbryoViewer software and Guided Annotation, you can analyse high quality videos of embryo development and easily register the information you need about each embryo to make evaluation efficient.

See what you've been missing

With EmbryoViewer software, you can achieve improved selection, or de-selection, of embryos by a combination of discovering both morphological and morphokinetic parameters. Important parameters such as the dynamic morphology, critical cleavage patterns and morphokinetics can only be observed with time-lapse technology.

Traditional embryo assessment has been reported to miss more than 70% of embryo multinucleation while more than 20% of embryos have been reported to go through an abnormal cleavage pattern. Such patterns can only be precisely determined by the use of time-lapse.1-4

Advanced software

With EmbryoViewer software, you can review, annotate and compare development of selected embryos from data acquired by the EmbryoScope and EmbryoScope+. The same EmbryoViewer software can be used for both types of incubators. The incubators’ running conditions are automatically stored with the patient data and can be observed on the EmbryoViewer software for quality assurance.

Intuitive annotation tools

With EmbryoViewer software, you can annotate cell division events, providing an easy overview of observations in developmental stages.

Improved basis for embryo selection

Use Guided Annotation in the EmbryoViewer software to efficiently get the parameters you need for embryo evaluation. Designed to provide a simplified annotation workflow.

KIDScore for efficient evaluation support

KIDScore™ decision support tools* assigns an objective score to each embryo. The scores reflect implantation potential and provide consistent and effective support for embryo evaluation. With Guided Annotation and KIDScore decision support tools you can customise to fit the workflow you like with the level of automatisation you prefer.

*KIDScore D5 has not received 510(k) clearance

Add intelligence with Guided Annotation

Guided Annotation is an added, optional tool in the EmbryoViewer software designed to provide a simplified annotation workflow. Based on artificial intelligence, Guided Annotation provides a perfect balance of control, accuracy and efficiency – ensuring fast, precise and consistent analysis of embryo development based on your needs for information before embryo selection.

Ensure consistent evaluation of embryos with Guided Annotation

With the extensive amount of image information acquired by the EmbryoScope time-lapse system, every stage of development of each embryo can be observed. Guided Annotation ensures that you collect exactly the amount and type of embryo development information that is necessary for you to evaluate which embryos are most suitable for transfer and/or freezing.

By implementing intelligent software tools and artificial intelligence, Guided Annotation makes embryo annotation fast, efficient and precise and allows you to have complete control of the level of automatisation. A confidence estimate allows you to automate annotations that have a high confidence level and prioritise validation of annotations with low confidence.

Eased workflow, efficiency and consistency

The Guided Annotation tool uses image analysis to guide you to likely timings for developmental events like division timings, morphology assessment and PN check. Simply validate or score the event by a single keyboard click.

Simplicity

Based on the annotation strategy, Guided Annotation automatically prompts you to annotate the selected variables. A continuous overview of the process is provided.

Efficiency

An efficient workflow is easily achieved by utilising customised annotation strategies in combination with the intuitive and ergonomics friendly keyboard shortcuts.

Consistency

Define an annotation strategy, or determine which predefined annotation strategy to use, and collect consistent and valuable information by all staff.

Guided Annotation and KIDScore

Guided Annotation in synergy with KIDScore optimally supports your consistent embryo evaluation process.

Benefits of KIDScore

  • • Improves the decision-making process
  • • Enhances consistency
  • • Helps you obtain better results

KIDScore™ decision support tool

KIDScore assigns an objective score to each embryo. The scores reflect implantation potential and provide consistent and effective support for embryo selection.

KIDScore for transfer on Day 3 or Day 5

The KIDScore decision support tool is developed by analysing the world’s largest database of embryo development with known clinical outcome. The models are developed by analysing how embryo morphokinetics, cleavage patterns and morphology correlates with implantation outcome after transfer.

Principles of KIDScore D3

Enjoy immediate benefits of time-lapse-based embryo analysis

  • • Improved consistency of evaluation and lower interobserver variability5
  • • Uses ‘easy-to-annotate’ variables
  • • Based on Known Implantation Data (KID) from the day of transfer
  • • A powerful tool when you have more embryos available than planned for transfer
  • • Designed to predict implantation

KIDScore D3

When to use it

  • • When deciding between embryos that reach expected stage on day 3
  • • When D3 SET is preferred
How does it work?

KIDScore D3 assigns a morphokinetic score from 1-5 to your annotated embryos. The score from 1-5 is a relative measure of the implantation potential of the embryo. The following variables need to be annotated in accordance with specific guidelines: PN assessment, PN fading, time (t) to 2, 3, 4, 5 and 8 cells.

KIDScore D3 & implantation data

The chart represents unselected embryos, embryos chosen for transfer, implanted embryos and embryos resulting in a live birth from cycles where known outcome data is available. The distribution of embryos across score groups is shown. This indicates that there is excellent concordance between the model and embryos with high implantation potential.

KIDScore D5

When to use it?

  • • When more good quality blastocysts are available than are planned for transfer
  • • When deciding which embryos are suitable for biopsy or diagnosis
How does it work?

KIDScore D5* considers the morphology and the morphokinetic traits of an embryo. For each embryo the model calculates a continuous score from 1-9.9. The score reflects the statistical chance of implantation based on development information from the five-day culture period. The higher the score, the greater the statistical chance of implantation. Only a few annotations are required to obtain a score, which further improves the worfklow.

KIDScore D5 & implantation data

KIDScore D5 scores show an increased relative implantation with higher scores. The model is based on a large database of KID blastocysts originating from a wide range of IVF clinics.

*KIDScore D5 can only be used when culturing under reduced oxygen conditions.

We have seen improved IVF outcomes since we introduced EmbryoScope time-lapse system in 2013. We owe it to our patients to use time-lapse - to give them the best possible result.

- Helen Hunter, principal embryologist, Department of Reproductive Medicine, Saint Mary's Hospital, Manchester, UK

DOWNLOAD WHITE PAPER

How can you benefit from time-lapse in IVF?

Dr. Markus Montag has written a white paper where he discusses the clinically proven results with time-lapse, as well as how time-lapse can improve the workflow in the lab and facilitate communication.

DOWNLOAD WHITE PAPER

References

1. Ergin, E.G. et al., (2014), Fertil Steril 102(4): 1029-1033 e1.

2. Data on file.

3. Rubio, I. et al., (2012), Fertil Steril 98(6): 1458-63.

4. Zhan, Q. et al., (2016) PLoS One 11(12): e0166398.

5. Sundvall, et al., (2013), Hum Reprod 28(12): 3215-21.

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