Literature DB >> 8986688

Frozen-thawed epididymal spermatozoa for intracytoplasmic sperm injection.

C A Holden1, G F Fuscaldo, P Jackson, A Cato, G J Southwick, R Hauser, P D Temple-Smith, R I McLachlan.   

Abstract

OBJECTIVE: To report the fertilization rate and pregnancy results for intracytoplasmic sperm injection (ICSI) cycles using frozen-thawed epididymal spermatozoa.
DESIGN: Retrospective analysis of consecutive ICSI cycles.
SETTING: Tertiary referral center for infertility. PATIENT(S): Infertile couples in whom 39 patients (59 ICSI cycles) required the use of frozen-thawed epididymal spermatozoa. As no cycles were performed using fresh epididymal spermatozoa, outcomes were compared with those of 130 couples (170 ICSI cycles) using fresh ejaculated spermatozoa for severe oligoasthenozoospermia-teratozoospermia, in which < 200,000 motile spermatozoa were retrieved after Percoll density gradient centrifugation. INTERVENTION(S): Epididymal sperm aspiration during microsurgery, followed by ICSI. MAIN OUTCOME MEASURE(S): Fertilization, embryo cleavage, ET, and clinical pregnancy rates (PRs). RESULT(S): A total of 484 metaphase II oocytes were injected with frozen-thawed epididymal spermatozoa, resulting in a two-pronuclear fertilization rate per injected metaphase II oocyte of 47%, significantly lower than in cycles using fresh ejaculated spermatozoa (73%). Embryo implantation rates (12.0% versus 13.3%) and clinical PRs per transfer (18.4% versus 27.0%) were not different. When the prefreeze vitality was > 20%, compared with lower vitality, both the fertilization (56% versus 22%) and embryo cleavage (91% versus 57%) rates were significantly greater. CONCLUSION(S): The routine collection and cryopreservation of epididymal spermatozoa at microsurgery allows multiple ICSI treatment cycles with success rates similar to those of ejaculated spermatozoa. However, when the vitality of aspirated spermatozoa is < 20%, the poor fertilization rates indicate the need to consider an alternative source of viable spermatozoa.

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Mesh:

Year:  1997        PMID: 8986688     DOI: 10.1016/s0015-0282(97)81860-2

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  5 in total

1.  Is early embryo development as observed by time-lapse microscopy dependent on whether fresh or frozen sperm was used for ICSI? A cohort study.

Authors:  Jessica Eastick; Christos Venetis; Simon Cooke; Ashleigh Storr; Daisy Susetio; Michael Chapman
Journal:  J Assist Reprod Genet       Date:  2017-04-29       Impact factor: 3.412

2.  Performing testicular or epididymal sperm retrieval prior to the injection of hCG.

Authors:  B Urman; C Alatas; S Aksoy; A Nuhoglu; A Sertac; B Balaban
Journal:  J Assist Reprod Genet       Date:  1998-03       Impact factor: 3.412

3.  Postmortem recovery and cryopreservation of spermatozoa from the vas deferens of rhesus macaques (Macaca mulatta).

Authors:  K Goff; J Liukkonen; H M Kubisch
Journal:  Theriogenology       Date:  2009-07-30       Impact factor: 2.740

4.  Minimal volume vitrification of epididymal spermatozoa results in successful in vitro fertilization and embryo development in mice.

Authors:  Fabrizzio Horta; Hamida Alzobi; Sutthipat Jitanantawittaya; Sally Catt; Penny Chen; Mulyoto Pangestu; Peter Temple-Smith
Journal:  Asian J Androl       Date:  2017 Jan-Feb       Impact factor: 3.285

Review 5.  Severe male factor in in vitro fertilization: definition, prevalence, and treatment. An update.

Authors:  Rossella Mazzilli; Alberto Vaiarelli; Lisa Dovere; Danilo Cimadomo; Nicolò Ubaldi; Susanna Ferrero; Laura Rienzi; Francesco Lombardo; Andrea Lenzi; Herman Tournaye; Filippo Maria Ubaldi
Journal:  Asian J Androl       Date:  2022 Mar-Apr       Impact factor: 3.285

  5 in total

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