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Outcomes of Ultimpro Testing Implementation for Patients With Unexplained Recurrent Implantation Failure: A
Genevieve Genest1, Alyssa Hochberg2,3, Martine Boivin1,4
1Division of Clinical Immunology and Allergy, Department of Medicine, McGill University Health Centre, Montréal, Québec, Canada.
Unexplained recurrent implantation failure (uRIF) patients showed improved pregnancy success with the Ultimpro endometrial immunophenotype test. This test identifies immune dysregulation, guiding personalized embryo transfer protocols for better outcomes in uRIF cases.
Area of Science:
- Reproductive Immunology
- Assisted Reproductive Technology
- Genomics and Proteomics
Background:
- A subset of patients with unexplained recurrent implantation failure (uRIF) may experience endometrial immune dysregulation.
- The Ultimpro test analyzes endometrial immunophenotypes to detect and characterize immune dysregulation.
- Personalized adjustments to embryo transfer (ET) protocols can be proposed based on Ultimpro results.
Purpose of the Study:
- To evaluate the effectiveness of the Ultimpro endometrial immunophenotype test in patients with uRIF.
- To assess if Ultimpro-guided protocols improve pregnancy and live birth rates compared to standard care.
- To compare outcomes in patients with and without RIF undergoing Ultimpro testing.
Main Methods:
- A retrospective cohort study analyzed 121 patients over 2.5 years.
- Group 1 (93 patients) had uRIF and underwent Ultimpro testing; outcomes compared to a control group (94 uRIF patients).
- Group 2 (28 patients) without RIF were compared to Canadian average ongoing pregnancy rates (OPR).
Main Results:
- Group 1 (uRIF) showed a significantly higher pregnancy rate (49.5%) with Ultimpro compared to controls (33%, p=0.026).
- Patients with ≥5 failed blastocyst transfers particularly benefited (55.3% vs. 20.0%, p=0.0084).
- Group 2 (no RIF) did not show improved OPR per ET with Ultimpro recommendations compared to non-RIF averages.
Conclusions:
- Preliminary findings suggest Ultimpro recommendations improve successful outcomes in uRIF patients.
- The test did not show a benefit for patients without RIF.
- Further validation through a large-scale randomized controlled trial is warranted.
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