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Approach to the Infant with Ambiguous Genitalia Wendy Schwarz, RN CPEN, Edmonton, AB

Approach to the Infant with Ambiguous Genitalia Wendy Schwarz, RN CPEN, Edmonton, AB February 19, 2016. Disclosures. I have nothing to disclose pertaining to this presentation. Objectives.

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Approach to the Infant with Ambiguous Genitalia Wendy Schwarz, RN CPEN, Edmonton, AB

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  1. Approach to the Infant with Ambiguous Genitalia Wendy Schwarz, RN CPEN, Edmonton, AB February 19, 2016

  2. Disclosures • I have nothing to disclose pertaining to this presentation

  3. Objectives To outline key elements of the initial parent-provider interaction and the role of the multidisciplinary DSD* team To introduce the AB Children’s Hospital protocol as a resource for providers

  4. “Approach to the infant with ambiguous genitalia” ACH protocol

  5. We developed a local protocol to help any care provider know what to say, who to call, what the process is so that we can try to make these situations go as smoothly as possible for the families • It covers a bit of the terminology & classification that I won’t go in to with this group. It then outlines initial mgt process (what to tell the family), resources for parents & physicians

  6. This was a collaborative effort by endocrinology, neonatology, genetics, urology up to this point • Hopefully input from family docs, OB’s & midwives once through each OB and NICU committees • By following a standard local approach, we hope to ensure consistent messaging from all providers and create as smooth an experience as possible for the family • The principles I’m going to go through next will be included in that document

  7. Outline • Parent experience with DSD diagnosis • First steps with the family • Management process • Support & resources for parents

  8. Definition of DSD • Congenital conditions in which development of the chromosomal, gonadal or anatomical sex is atypical • Consensus Statement on Management of Intersex Disorders • Pediatrics 2006; 118; e488-500.

  9. Parental Experience • This is stressful! • Unfamiliar • Perceived stigma • Communication with friends/family • 31% of mothers, 18% of fathers report clinical levels of PTSS • Similar to published means for parents of children who have survived cancer • Crissman et al. International Journal of Pediatric Endocrinology 2011:10.Pasterski et al. Arch Sex Behav 2014; 43:369-375.

  10. HCP’s have a major influence on parent experience & impressions • Only 52% of parents completely satisfied with information provided during neonatal period • Psychosocial support is critical Crissman et al. International Journal of Pediatric Endocrinology 2011:10. Dayner et al. Journal of Urology 2004; 172:1762-1765

  11. Children with disorders of sex development: A qualitative study of early parental experience Crissman et al. International Journal of Pediatric Endocrinology 2011:10.

  12. Questionnaires & structured interviews • 41 parents of 28 children (newborn to 6 years) • 4 major themes emerged: • Gender assignment process • Surgical decision-making • Sharing information with others • Interactions with healthcare providers

  13. First Steps With the Family • Interactions with healthcare providers • Information from team helped to reduce the stress from unfamiliarity & feelings of isolation • Drawings helpful • Frustrated by lack of details, gaps in information • Overwhelmed by information online • Repeated physical examinations sometimes seen as unnecessary or exploitive

  14. Initial Management Process • Ideally, when an infant is found to have ambiguous genitalia, a consistent sequence of events should take place to address the medical needs of the patient as well as the psychosocial needs of the family • Depending on the condition, this process may take several weeks to complete. It is expected that the infant will be kept in hospital for at least 1 week • In summary, the sequence of events is as follows;

  15. When an infant is noted to have ambiguous genitalia, • The responsible physician (HCP) should: • Explain their concern to the parents as soon as it has been identified • Not sure what to say? See Scripts for some ideas. • Consult Neonatology right away to evaluate the infant and speak with the parents. Neonatology will facilitate consultation of additional subspecialties and, if necessary, patient transfer to ACH • Encourage the parents to delay naming and gender assignment

  16. Support the parent-child interaction • This is not a medical emergency. Parents should still be encouraged to bond with their newborn, breastfeed etc if the infant is otherwise stable. • Use gender-neutral terms to refer to the baby. • Eg “your baby, the baby, your little one”

  17. Engage the parents while examining the baby • Use gender neutral terms to describe anatomy: • Phallus • Single opening/two openings • Labioscrotal folds • Gonads • Examining the baby with the parents can help them understand your concern and the need for further investigation. It also promotes a sense of openness rather than shame or secrecy. • Be sensitive about repeat examinations by multiple trainees and providers.

  18. Discuss the management process in simple terms, ensuring the parents are as informed as possible about what to expect. The following information should be conveyed to the parents:

  19. The baby will need to remain in hospital for clinical observation, investigations and to be seen by the necessary subspecialties. This may take a week or more • When possible, transfer to ACH may be considered to facilitate management

  20. Subspecialties involved will include neonatology, endocrine, genetics and urology. Each of these services will need to come meet the family and examine the baby • Investigations will be recommended and facilitated by the consulting services. This will typically involve blood work and a pelvic ultrasound. The responsible physician should refrain from ordering investigations until advised by endocrinology and genetics

  21. Once results are available; • Endocrine, genetics and urology will hold a team conference to review and interpret the results. As a group they will come to an agreement on diagnosis and the recommended gender assignment, if sufficient information is available to do so (it is important to note that in certain circumstances, more extensive testing is necessary before a recommendation can be made) • The team will then hold a meeting with the family to review results and recommendations. Only then should the gender assignment be made

  22. Offer psychosocial support • The unit social worker is likely the most easily accessible initial resource to help parents cope with the shock and grief associated with the news of a possible DSD • Once endocrinology is involved, the endocrine clinic social worker will connect with families as early as possible to provide ongoing support

  23. Discuss disclosure to friends/family • Parents should be encouraged to delay a formal birth announcement until a gender assignment has been made. However, they should be encouraged to be open about their current situation with their close friends/family, depending on their degree of comfort. • Open disclosure with trusted individuals can help reduce parental feelings of isolation, shame and secrecy surrounding the diagnosis.

  24. The resources below can help families talk to others about their child’s diagnosis • www.aboutkidshealth.ca/En/HowTheBodyWorks/SexDevelopmentAnOverview • Basic information on the process of sex differentiation, with interactive visuals. Specific information on several conditions. • www.dsdfamilies.org/dsdfamilies/brochures.php • Brochure: “When your baby is born with genitals that look different”. Provides basic information regarding DSD, next steps and how to communicate with friends/family.

  25. www.dsdguidelines.org -“Handbook for Parents” • Provides much more extensive information than may be applicable to parents at the beginning, but may be helpful early on for parents who desire more information. The first chapter is particularly helpful in the early stages of diagnosis.

  26. Scripts • How to notify the parents of your concern regarding a possible DSD: • What you can say when the parents ask what to tell their friends and family:

  27. REMEMBER • DON’T assign a gender. There are many factors that impact gender assignment, and these will be taken into consideration by endocrinology, genetics and urology when they meet to review results. They will then meet with the family to discuss the recommended gender assignment. • DO identify your concern immediately. The first provider to identify ambiguous genitalia should inform the parents of their concern right away and involve the most responsible physician for further discussion. • DON’T disclose results as they become available. Results will be reviewed in the family meeting with neonatology, endocrinology, genetics and urology.

  28. Thank You • A special thanks to Dr Clare Henderson

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