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Donor Sperm / Donor Insemination (DI) A. The male partner has no sperm present (azoospermia), or very low number of sperm present (severe oligospermia), or other significant sperm abnormalities. Evaluation of the Female Recipient Evaluation for possible tubal or peritoneal abnormalities Patients who fail to conceive after three donor sperm inseminations may be candidates for a hysterosalpingogram (HSG), laparoscopy, or other appropriate tests to detect possible causes for their failure to conceive including fallopian tube blockage or disease. Pretreatment HSG or laparoscopy may be indicated by the history and/or physical findings.
The decision to proceed with donor insemination is complex and patients and their partners may benefit from psychological counseling to aid in this decision. At PREG, we offer psychological counseling by a qualified mental health professional to all couples who desire counseling. Recipients of donor gametes may receive counseling about the potential psychological implications, about their subsequent feelings concerning the medical conditions that necessitated the use of donor gametes, address the impact of successful treatment: feelings during pregnancy, positive and negative aspects of disclosure and nondisclosure with offspring, potential impact of multiple pregnancy, transition to parenthood, parenting at an older age (if applicable), and non-biological parenting issues. The impact of treatment failure should also be addressed: coping with treatment termination, the grieving process, and developing alternatives for the future. In cases involving known donors, related issues, such as the potential impact of the relationship between donor and recipient, should be explored. The recipients should be informed about the screening and testing required of the donor. The couple should be made aware that a donor may be deemed unsuitable for donation and that the practice may refuse to use these gametes for treatment. If the recipient couple elects to use a donor who is deemed unsuitable, then additional counseling must involve risk management and an agreement that the recipient couple understands and assumes the risk. Couples should be informed that the records related to the screening and testing of the donor will be stored. The storage of this information is relevant to the recipients because it relates to other information-sharing decisions they may make. Directed donation (use of known sperm donors) Directed (non-anonymous or known) donation is acceptable if all parties agree. Known donors must undergo the same screening and testing as anonymous donors and this must be done through a FDA approved commercial sperm bank (not done at PREG). PREG’s policy regarding directed sperm donors follows ASRM guidelines in that directed-donor specimens should be treated in the same manner as anonymous-donor specimens. Results of screening or testing that would exclude an anonymous donor also should exclude a directed donor. All directed-donor specimens will be quarantined (sperm samples frozen) for at least 6 months (180 days), with the donor then retested for STI’s as described above and if the donor still tests negative, the specimen is released in the same manner required for anonymous-donor specimens per FDA regulations. PREG would also highly recommend that legal paper work regarding potential responsibilities (if any) of the known donor to the offspring be clearly outlined and documented. PREG does NOT allow the use of fresh semen for any donor inseminations. Sexually intimate couples Although there is no FDA or legal requirement for sexually transmitted infection (STI) testing of sexually intimate partners undergoing fertility treatment, such testing can help to ensure that appropriate precautions are taken to minimize risk of STI transmission to partners and offspring. PREG does not perform inseminations using sperm obtained from men testing positive for HIV, Hepatitis B, or Hepatitis C. Couples in which one or both partners test positive for HIV, Hepatitis B or C should be treated by fertility centers having the appropriate laboratory resources. PREG does not have a specific sperm bank that we require you to use. We recommend that you do an internet search for an FDA licensed and approved commercial sperm bank. Review the sperm bank’s website, contact their customer representatives, look at their donor profiles and carefully choose your donor. It may be helpful to contact several of the commercial sperm banks. Some of the different sperm banks used by our patients include Cryogenics Laboratories, Fairfax Cryobank http://www.fairfaxcryobank.com/, Xytex http://www.xytex.com/ , and California Cryobank http://www.cryobank.com/ (these are just some of the examples and are not meant to be an endorsement for any the companies and is certainly not an inclusive list). When doubt exists about timing of ovulation, other tests of ovulation such as serum progesterone level, basal body temperature, luteinizing hormone (LH) surge detection, and ultrasound monitoring of follicular maturation can be used. Appropriate timing of the insemination procedure optimizes chances for success. At PREG, we recommend ovulation monitoring with ovulation predictor kits and transvaginal ultrasound mid-cycle follicle scans to help time your inseminations. Women who do not conceive after several spontaneous cycle inseminations or who do not have regular ovulatory cycles may benefit from taking fertility medications, such as Clomid (Clomiphene) or Femara (Letrozole), to ensure optimal ovulation and improve their chance of conception. These fertility medications do have about a 10% risk of multiple gestations. Use of other medications such as hCG 10,000 units or Ovidrel (these are a single injection or shot) may be recommended to trigger or boost ovulation and also help with the timing of your insemination. Self-Pay Costs (insurance not billed or no insurance coverage): Medications* (approximate costs): Clomid/Letrozole (Fertility drugs) - $40-50.00; hCG 10,000 units or Ovidrel (Ovulation triggering medications) - $40-50.00
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