4.02.503 Infertility and Reproductive Services
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Educational Objectives Current IVF Practice
2/23/2015 Update from the IVF Lab: Preimplantation Genetic Testing Janet McLaren Bouknight, MD Reproductive Endocrinology and Infertility Department of Obstetrics & Gynecology Educational Objectives • Gain familiarity with the procedures and pregnancy outcomes of current in vitro fertilization practices. • Understand the application of Preimplantation Genetic Diagnosis (PGD) for single‐gene disorders. • Appreciate the role of Preimplantation Genetic Screening (PGS) in maximizing IVF cycle efficiency and encouraging elective single embryo transfer. Current IVF Practice 1 2/23/2015 Current IVF Practice 150,000 cycles 65,000 livebirths Current IVF Practice Current IVF Practice All SART Clinics 2012 <35 35‐37 38‐40 41‐42 >42 Pregnancy Rate 47% 38% 30% 20% 9% Live Birth Rate 41% 31% 22% 12% 4% # embryos transfer 1.9 2.0 2.4 2.9 2.9 % Twins 30% 25% 20% 13% 9% • What are the advanced that have contributed to an increase in success in the IVF Lab? • Improved lab conditions • Extended embryo culture • Improvements in embryo cryopreservation 2 2/23/2015 Current IVF Practice: Improved Lab Conditions Current IVF Practice: Improved Lab Conditions Current IVF Practice: Improved Lab Conditions 3 2/23/2015 Current IVF Practice: Extended Embryo Culture Day 3: Cleavage Stage Day 5: Blastocyst Stage • 8‐cells • 200‐300 cells • 30% implantation rate • 50% implantation rate Increased live birth rates seen in “good prognosis” patients who undergo a Day 5 transfer Current IVF Practice: Extended Embryo Culture Current IVF Practice: Extended Embryo Culture • Supports blastocyst transfer for “good prognosis” patients • Opportunity to consider single embryo transfer • May be associated with a small increased risk of monozygotic twinning 4 2/23/2015 Current IVF Practice: Embryo Cryopreservation Cycles • Improvements in freezing techniques (vitrification) have increased success of cryopreserved embryos. -
Oocyte Or Embryo Donation to Women of Advanced Reproductive Age: an Ethics Committee Opinion
ASRM PAGES Oocyte or embryo donation to women of advanced reproductive age: an Ethics Committee opinion Ethics Committee of the American Society for Reproductive Medicine American Society for Reproductive Medicine, Birmingham, Alabama Advanced reproductive age (ARA) is a risk factor for female infertility, pregnancy loss, fetal anomalies, stillbirth, and obstetric com- plications. Oocyte donation reverses the age-related decline in implantation and birth rates of women in their 40s and 50s and restores pregnancy potential beyond menopause. However, obstetrical complications in older patients remain high, particularly related to oper- ative delivery and hypertensive and cardiovascular risks. Physicians should perform a thorough medical evaluation designed to assess the physical fitness of a patient for pregnancy before deciding to attempt transfer of embryos to any woman of advanced reproductive age (>45 years). Embryo transfer should be strongly discouraged or denied to women of ARA with underlying conditions that increase or exacerbate obstetrical risks. Because of concerns related to the high-risk nature of pregnancy, as well as longevity, treatment of women over the age of 55 should generally be discouraged. This statement replaces the earlier ASRM Ethics Committee document of the same name, last published in 2013 (Fertil Steril 2013;100:337–40). (Fertil SterilÒ 2016;106:e3–7. Ó2016 by American Society for Reproductive Medicine.) Key Words: Ethics, third-party reproduction, complications, pregnancy, parenting Discuss: You can discuss -
Cryopreserved Oocyte Versus Fresh Oocyte Assisted Reproductive Technology Cycles, United States, 2013
HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Fertil Steril Manuscript Author . Author manuscript; Manuscript Author available in PMC 2018 January 01. Published in final edited form as: Fertil Steril. 2017 January ; 107(1): 110–118. doi:10.1016/j.fertnstert.2016.10.002. Cryopreserved oocyte versus fresh oocyte assisted reproductive technology cycles, United States, 2013 Sara Crawford, Ph.D.a, Sheree L. Boulet, Dr.P.H., M.P.H.a, Jennifer F. Kawwass, M.D.a,b, Denise J. Jamieson, M.D., M.P.H.a, and Dmitry M. Kissin, M.D., M.P.H.a aDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Emory University, Atlanta, Georgia bDivision of Reproductive Endocrinology and Infertility, Department of Gynecology and Obstetrics, Emory University, Atlanta, Georgia Abstract Objective—To compare characteristics, explore predictors, and compare assisted reproductive technology (ART) cycle, transfer, and pregnancy outcomes of autologous and donor cryopreserved oocyte cycles with fresh oocyte cycles. Design—Retrospective cohort study from the National ART Surveillance System. Setting—Fertility treatment centers. Patient(s)—Fresh embryo cycles initiated in 2013 utilizing embryos created with fresh and cryopreserved, autologous and donor oocytes. Intervention(s)—Cryopreservation of oocytes versus fresh. Main Outcomes Measure(s)—Cancellation, implantation, pregnancy, miscarriage, and live birth rates per cycle, transfer, and/or pregnancy. -
Social Freezing: Pressing Pause on Fertility
International Journal of Environmental Research and Public Health Review Social Freezing: Pressing Pause on Fertility Valentin Nicolae Varlas 1,2 , Roxana Georgiana Bors 1,2, Dragos Albu 1,2, Ovidiu Nicolae Penes 3,*, Bogdana Adriana Nasui 4,* , Claudia Mehedintu 5 and Anca Lucia Pop 6 1 Department of Obstetrics and Gynaecology, Filantropia Clinical Hospital, 011171 Bucharest, Romania; [email protected] (V.N.V.); [email protected] (R.G.B.); [email protected] (D.A.) 2 Department of Obstetrics and Gynaecology, “Carol Davila” University of Medicine and Pharmacy, 37 Dionisie Lupu St., 020021 Bucharest, Romania 3 Department of Intensive Care, University Clinical Hospital, “Carol Davila” University of Medicine and Pharmacy, 37 Dionisie Lupu St., 020021 Bucharest, Romania 4 Department of Community Health, “Iuliu Hat, ieganu” University of Medicine and Pharmacy, 6 Louis Pasteur Street, 400349 Cluj-Napoca, Romania 5 Department of Obstetrics and Gynaecology, Nicolae Malaxa Clinical Hospital, 020346 Bucharest, Romania; [email protected] 6 Department of Clinical Laboratory, Food Safety, “Carol Davila” University of Medicine and Pharmacy, 6 Traian Vuia Street, 020945 Bucharest, Romania; [email protected] * Correspondence: [email protected] (O.N.P.); [email protected] (B.A.N.) Abstract: Increasing numbers of women are undergoing oocyte or tissue cryopreservation for medical or social reasons to increase their chances of having genetic children. Social egg freezing (SEF) allows women to preserve their fertility in anticipation of age-related fertility decline and ineffective fertility treatments at older ages. The purpose of this study was to summarize recent findings focusing on the challenges of elective egg freezing. -
The Disposition of Cryopreserved Embryos: Why Embryo Adoption Is an Inapposite Model for Application to Third-Party Assisted Reproduction Elizabeth E
William Mitchell Law Review Volume 35 | Issue 2 Article 1 2009 The Disposition of Cryopreserved Embryos: Why Embryo Adoption Is an Inapposite Model for Application to Third-Party Assisted Reproduction Elizabeth E. Swire Falker Follow this and additional works at: http://open.mitchellhamline.edu/wmlr Recommended Citation Falker, Elizabeth E. Swire (2009) "The Disposition of Cryopreserved Embryos: Why Embryo Adoption Is an Inapposite Model for Application to Third-Party Assisted Reproduction," William Mitchell Law Review: Vol. 35: Iss. 2, Article 1. Available at: http://open.mitchellhamline.edu/wmlr/vol35/iss2/1 This Article is brought to you for free and open access by the Law Reviews and Journals at Mitchell Hamline Open Access. It has been accepted for inclusion in William Mitchell Law Review by an authorized administrator of Mitchell Hamline Open Access. For more information, please contact [email protected]. © Mitchell Hamline School of Law Falker: The Disposition of Cryopreserved Embryos: Why Embryo Adoption Is THE DISPOSITION OF CRYOPRESERVED EMBRYOS: WHY EMBRYO ADOPTION IS AN INAPPOSITE MODEL FOR APPLICATION TO THIRD-PARTY ASSISTED REPRODUCTION † Elizabeth E. Swire Falker, Esq. I. THE DEBATE OVER THE DISPOSITION OF CRYOPRESERVED EMBRYOS FOR FAMILY BUILDING ............................................ 491 II. THE “TYPICAL” EMBRYO ADOPTION/DONATION IN THE UNITED STATES ...................................................................... 498 III. DEFINING THE TERM EMBRYO ............................................... -
Should the U.S. Approve Mitochondrial Replacement Therapy?
SHOULD THE U.S. APPROVE MITOCHONDRIAL REPLACEMENT THERAPY? An Interactive Qualifying Project Report Submitted to the Faculty of WORCESTER POLYTECHNIC INSTITUTE In partial fulfillment of the requirements for the Degree of Bachelor of Science By: ____________________ ____________________ ____________________ Daniela Barbery Emily Caron Daniel Eckler IQP-43-DSA-6594 IQP-43-DSA-7057 IQP-43-DSA-5020 ____________________ ____________________ Benjamin Grondin Maureen Hester IQP-43-DSA-5487 IQP-43-DSA-2887 August 27, 2015 APPROVED: _________________________ Prof. David S. Adams, PhD WPI Project Advisor 1 ABSTRACT The overall goal of this project was to document and evaluate the new technology of mitochondrial replacement therapy (MRT), and to assess its technical, ethical, and legal problems to help determine whether MRT should be approved in the U.S. We performed a review of the current research literature and conducted interviews with academic researchers, in vitro fertility experts, and bioethicists. Based on the research performed for this project, our team’s overall recommendation is that the FDA approve MRT initially for a small number of patients, and follow their offspring’s progress closely for a few years before allowing the procedure to be done on a large scale. We recommend the FDA approve MRT only for treating mitochondrial disease, and recommend assigning parental rights only to the two nuclear donors. In medical research, animal models are useful but imperfect, and in vitro cell studies cannot provide information on long-term side-effects, so sometimes we just need to move forward with closely monitored human experiments. 2 TABLE OF CONTENTS Title Page ……………………………….……………………………………..……. 01 Abstract …………………………………………………………………..…………. 02 Table of Contents ………………………………………………………………..… 03 Acknowledgements …………………………………………………………..……. -
Donor Eggs for the Treatment of Infertility
CLINICAL Caitlin Dunne, MD, FRCSC Donor eggs for the treatment of infertility Using donated eggs can be a remarkably successful fertility treatment in the right circumstances. Though donor egg pregnancies may carry some increased obstetrical risks, the risks are manageable and can offer women a chance at pregnancy when there is no other option. ABSTRACT: Egg donation is a common treatment the right time to recover the resulting embryo, Columbia has the highest age of first birth in for infertility. It is most often used for women with which was transferred into the intended moth- Canada at 30.5 years versus 30.3 years in On- premature menopause, advanced reproductive er’s uterus.2,3 tario.10 According to Statistics Canada, 2010 age, or a history of unsuccessful in vitro fertilization In the early 1980s, assisted reproductive marked the first time that more women in their attempts. Because egg donors are generally in their technology was developing rapidly in Canada 30s were having children compared to women 20s, pregnancy success rates are high. In many cas- and around the world.4 Fertility pioneers used in their 20s.11 es, donor eggs give women a chance at pregnancy laparoscopy to retrieve donor eggs for fertiliza- The possible consequences of delaying child- when there would be no other option. Donor egg tion in vitro.3,5,6 These early “third-party repro- bearing are infertility, embryo aneuploidy, and pregnancies may carry some increased obstetrical duction” techniques were groundbreaking at miscarriage. These are largely attributed to aging risks related to preeclampsia and advanced mater- the time, given that the world’s first IVF baby, oocytes with failing meiotic spindles and other nal age. -
Triggering Final Oocyte Maturation with Gonadotropin-Releasing
J Assist Reprod Genet (2014) 31:927–932 DOI 10.1007/s10815-014-0248-6 FERTILITY PRESERVATION Triggering final oocyte maturation with gonadotropin-releasing hormone agonist (GnRHa) versus human chorionic gonadotropin (hCG) in breast cancer patients undergoing fertility preservation: an extended experience Jhansi Reddy & Volkan Turan & Giuliano Bedoschi & Fred Moy & Kutluk Oktay Received: 5 February 2014 /Accepted: 5 May 2014 /Published online: 23 May 2014 # Springer Science+Business Media New York 2014 ABSTRACT Conclusions GnRHa trigger improved cycle outcomes as evi- Purpose To analyze the cycle outcomes and the incidence of denced by the number of mature oocytes and cryopreserved ovarian hyperstimulation syndrome (OHSS), when oocyte embryos, while significantly reducing the risk of OHSS in maturation was triggered by gonadotropin-releasing hormone breast cancer patients undergoing fertility preservation. agonist (GnRHa) versus human chorionic gonadotropin (hCG) in breast cancer patients undergoing fertility preservation. Keywords Fertility preservation . Breast cancer . Trigger . Methods One hundred twenty-nine women aged≤45 years, GnRH agonist . hCG diagnosed with stage≤3 breast cancer, with normal ovarian reserve who desired fertility preservation were included in the retrospective cohort study. Ovarian stimulation was achieved utilizing letrozole and gonadotropins. Oocyte maturation was Introduction triggered with GnRHa or hCG. Baseline AMH levels, number of oocytes, maturation and fertilization rates, number of em- Breast cancer is the most common malignancy diagnosed in bryos, and the incidence of OHSS was recorded. women worldwide. Early detection and improvements in Results The serum AMH levels were similar between GnRHa screening have increased the number of premenopausal women and hCG groups (2.7±1.9 vs. -
Science of Mitochondrial Donation and Related Matters Submission 20
+- Associate Professor Catherine Mills Monash Bioethics Centre Monash University [email protected] +61 3 9905 3207 Committee Secretary Senate Standing Committees on Community Affairs PO Box 6100 Parliament House Canberra ACT 2600 11 May 2018 Dear Committee Members. Thank you for the opportunity to contribute to the Inquiry into the Science of Mitochondrial Donation and Other Matters. We are the Chief Investigators of an ongoing Australian Research Council-funded study into ‘The legal and ethical aspects of the inheritable genetic modification of humans: The Australian context’ (ARC DP170100919). This project focuses on the ethical and legal aspects of mitochondrial donation and CRISPR-Cas9. We hope our research to date assists the Committee in considering the legal and ethical aspects of mitochondrial donation and associated matters. Sincerely, Associate Professor Catherine Mills Lead Investigator Monash Bioethics Centre Monash University Associate Professor Karinne Ludlow Faculty of Law Monash University Professor Robert Sparrow Department of Philosophy Monash University Dr Narelle Warren School of Social Sciences Monash University INQUIRY INTO THE SCIENCE OF MITOCHONDRIAL DONATION AND OTHER MATTERS | 1 OVERVIEW Mitochondrial donation is a relatively new scientific advance in the sphere of assisted reproductive technologies. It allows for the replacement of mitochondrial DNA affected by mutations in a human egg (ovum) or zygote by transferring the nuclear DNA into a healthy donated egg that is not affected. The aim of this is to stop the transmission of mitochondrial disease that is inherited from the maternal line. In 2015, the British Parliament legalised the clinical use of mitochondrial donation. Significantly, these techniques allow for interventions that may be inherited by all subsequent generations of offspring of the person that the modified embryo may grow to be. -
Oocyte Warming and Insemination Consent Form
Oocyte Warming and Insemination Process, Risk, and Consent While embryos and sperm have been frozen and thawed with good results for many years, eggs have proved much more difficult to manage. Newer egg freezing methods have been more successful, at least in younger women, the main population in which the techniques have been studied. Egg freezing takes place by one of two methods: a slow freeze protocol, or a different “flash freeze” method known as vitrification. USF IVF uses the newer vitrification technology exclusively. There are two sources of frozen eggs. Some women may have chosen to have had their eggs frozen for the purpose of fertility preservation at some time prior to warming. Other women may have obtained frozen eggs donated by an egg donor. This consent reviews the Oocyte warming process from start to finish, including the risks that this treatment might pose to you and your offspring. While best efforts have been made to disclose all known risks, there may be risks of oocyte freezing, subsequent warming, and the IVF process, that are not yet clarified or even suspected at the time of this writing. Oocyte warming and subsequent embryo transfer typically includes the following steps or procedures: Medications to prepare the uterus to receive embryos Oocyte warming Insemination of eggs that have survived warming with sperm, using intracytoplasmic sperm injection (ICSI) Culture of any resulting fertilized eggs (embryos) Placement (transfer) of one or more embryos into the uterus Support of the uterine lining with hormones to permit and sustain pregnancy In certain cases, these additional procedures can be employed: Assisted hatching of embryos to potentially increase the chance of embryo attachment (implantation) Cryopreservation (freezing) of embryos Is pregnancy achieved as successfully with frozen eggs as with fresh eggs? As mentioned, most studies have looked at success rates using either donor eggs or women who produced larger numbers of eggs. -
MG Infertility Services Commercial
Infertility Services — Commercial Last Review Date: June 11, 2021 Number: MG.MM.ME.53f Medical Guideline Disclaimer Property of EmblemHealth. All rights reserved. The treating physician or primary care provider must submit to EmblemHealth the clinical evidence that the patient meets the criteria for the treatment or surgical procedure. Without this documentation and information, EmblemHealth will not be able to properly review the request for prior authorization. The clinical review criteria expressed below reflects how EmblemHealth determines whether certain services or supplies are medically necessary. EmblemHealth established the clinical review criteria based upon a review of currently available clinical information (including clinical outcome studies in the peer reviewed published medical literature, regulatory status of the technology, evidence-based guidelines of public health and health research agencies, evidence-based guidelines and positions of leading national health professional organizations, views of physicians practicing in relevant clinical areas, and other relevant factors). EmblemHealth expressly reserves the right to revise these conclusions as clinical information changes and welcomes further relevant information. Each benefit program defines which services are covered. The conclusion that a particular service or supply is medically necessary does not constitute a representation or warranty that this service or supply is covered and/or paid for by EmblemHealth, as some programs exclude coverage for services or supplies that EmblemHealth considers medically necessary. If there is a discrepancy between this guideline and a member's benefits program, the benefits program will govern. In addition, coverage may be mandated by applicable legal requirements of a state, the Federal Government or the Centers for Medicare & Medicaid Services (CMS) for Medicare and Medicaid members. -
Attitudes Towards Embryo Donation Among Healthcare Professionals Working in Child Healthcare
Armuand et al. BMC Pediatrics (2019) 19:209 https://doi.org/10.1186/s12887-019-1578-4 RESEARCH ARTICLE Open Access Attitudes towards embryo donation among healthcare professionals working in child healthcare: a survey study Gabriela Armuand1* , Gunilla Sydsjö1,2, Agneta Skoog Svanberg3 and Claudia Lampic4 Abstract Background: The aim of this study was to investigate attitudes towards embryo donation and embryo donation families among professionals working in primary child healthcare, and their experiences of these families. Methods: A cross-sectional online survey was conducted in Sweden between April and November 2016. A total of 712 primary healthcare physicians, registered nurses and psychologists were approached to participate in this study. The study-specific questionnaire measured attitudes and experiences in the following four domains: legalisation and financing, the family and the child’s health, clinical experience of meeting families following embryo donation, and knowledge of embryo donation. Results: Of the 189 women and 18 men who completed the questionnaire (response rate 29%), relatively few (13%) had clinical experience of caring for families following embryo donation. Overall, 69% supported legalisation of embryo donation for infertile couples, and 54% agreed it should be publicly funded. The majority (88%) agreed the child should have the right to know the donors’ identity. Respondents did not believe that children conceived through embryo donation are as healthy as other children (50%), citing the risks of poor mental health (17%) and social stigmatization (18%). Approximately half reported low confidence in their own knowledge of embryo donation (47%) and wanted to know more (58%). Conclusions: These results indicate relatively large support among healthcare professionals in Sweden for the legalisation of embryo donation.