Summary
This 2017 guideline from the Endocrine Society, a large body of hormone doctors, recommends puberty blockers for teens at the first signs of puberty, cross-sex hormones from about 16, and hormone plans with safety checks for adults. With WPATH's standards, it is often cited as proof that youth gender medicine is 'evidence-based'. Yet its own grading rates the evidence behind every teen recommendation as low or very low quality. Some are still strong recommendations, which Gordon Guyatt, co-founder of that grading system, called a 'serious problem'. Its commissioned reviews looked only at bone and heart safety, not at whether treatment eases distress or helps mental health. Several authors created the Dutch approach it relies on, and a York review for England's Cass Review rated it low quality. It reflects expert opinion more than strong evidence.
Key findings
- Retningslinjen blev skrevet af et panel på ni eksperter, en metodeekspert og en medicinsk skribent. Den blev medstøttet af WPATH og fem andre lægeforeninger i USA og Europa.
- Den fraråder hormonbehandling før puberteten, men anbefaler pubertetsblokkere, når teenagere viser de første tegn på pubertet (brystknopper eller væksten af testikler).
- Krydskønshormoner kan tilføjes, når et team af specialister bekræfter, at lidelsen har varet ved, og teenageren kan give samtykke. Retningslinjen siger, at de fleste teenagere kan samtykke ved 16, og tillader tidligere start, mens den bemærker, at der er meget lidt offentliggjort erfaring før omkring 13,5 til 14 år.
- Ifølge dens egen gradering er evidensen bag hver eneste anbefaling til teenagere af lav eller meget lav kvalitet. For eksempel får pubertetsblokkere en stærk anbefaling baseret på evidens af lav kvalitet.
- De to evidensgennemgange, den bestilte, så kun på hormoners effekter på hjerte, kolesterol og knogler, ikke på lidelse, mental sundhed eller livskvalitet.
- For brystfjernelse hos voksne transmænd siger den, at der ikke er nok evidens til at fastsætte en mindstealder, en svag anbefaling baseret på evidens af meget lav kvalitet.
- Retningslinjen offentliggjorde to rettelser i 2018, og en opdatering rapporteres at være under udarbejdelse.
Abstract
OBJECTIVE: To update the "Endocrine Treatment of Transsexual Persons: An Endocrine Society Clinical Practice Guideline," published by the Endocrine Society in 2009. PARTICIPANTS: The participants include an Endocrine Society-appointed task force of nine experts, a methodologist, and a medical writer. EVIDENCE: This evidence-based guideline was developed using the Grading of Recommendations, Assessment, Development, and Evaluation approach to describe the strength of recommendations and the quality of evidence. The task force commissioned two systematic reviews and used the best available evidence from other published systematic reviews and individual studies. CONSENSUS PROCESS: Group meetings, conference calls, and e-mail communications enabled consensus. Endocrine Society committees, members and cosponsoring organizations reviewed and commented on preliminary drafts of the guidelines. CONCLUSION: Gender affirmation is multidisciplinary treatment in which endocrinologists play an important role. Gender-dysphoric/gender-incongruent persons seek and/or are referred to endocrinologists to develop the physical characteristics of the affirmed gender. They require a safe and effective hormone regimen that will (1) suppress endogenous sex hormone secretion determined by the person's genetic/gonadal sex and (2) maintain sex hormone levels within the normal range for the person's affirmed gender. Hormone treatment is not recommended for prepubertal gender-dysphoric/gender-incongruent persons. Those clinicians who recommend gender-affirming endocrine treatments-appropriately trained diagnosing clinicians (required), a mental health provider for adolescents (required) and mental health professional for adults (recommended)-should be knowledgeable about the diagnostic criteria and criteria for gender-affirming treatment, have sufficient training and experience in assessing psychopathology, and be willing to participate in the ongoing care throughout the endocrine transition. We recommend treating gender-dysphoric/gender-incongruent adolescents who have entered puberty at Tanner Stage G2/B2 by suppression with gonadotropin-releasing hormone agonists. Clinicians may add gender-affirming hormones after a multidisciplinary team has confirmed the persistence of gender dysphoria/gender incongruence and sufficient mental capacity to give informed consent to this partially irreversible treatment. Most adolescents have this capacity by age 16 years old. We recognize that there may be compelling reasons to initiate sex hormone treatment prior to age 16 years, although there is minimal published experience treating prior to 13.5 to 14 years of age. For the care of peripubertal youths and older adolescents, we recommend that an expert multidisciplinary team comprised of medical professionals and mental health professionals manage this treatment. The treating physician must confirm the criteria for treatment used by the referring mental health practitioner and collaborate with them in decisions about gender-affirming surgery in older adolescents. For adult gender-dysphoric/gender-incongruent persons, the treating clinicians (collectively) should have expertise in transgender-specific diagnostic criteria, mental health, primary care, hormone treatment, and surgery, as needed by the patient. We suggest maintaining physiologic levels of gender-appropriate hormones and monitoring for known risks and complications. When high doses of sex steroids are required to suppress endogenous sex steroids and/or in advanced age, clinicians may consider surgically removing natal gonads along with reducing sex steroid treatment. Clinicians should monitor both transgender males (female to male) and transgender females (male to female) for reproductive organ cancer risk when surgical removal is incomplete. Additionally, clinicians should persistently monitor adverse effects of sex steroids. For gender-affirming surgeries in adults, the treating physician must collaborate with and confirm the criteria for treatment used by the referring physician. Clinicians should avoid harming individuals (via hormone treatment) who have conditions other than gender dysphoria/gender incongruence and who may not benefit from the physical changes associated with this treatment.
Conclusion
The guideline concludes that gender affirmation is a multidisciplinary treatment in which endocrinologists play an important role. Hormone treatment is not recommended for prepubertal children. Adolescents who have entered puberty (Tanner stage G2/B2) and meet criteria should be treated with GnRH-agonist puberty suppression, and gender-affirming hormones may be added after a multidisciplinary team confirms persistent gender dysphoria and sufficient capacity to consent, which most adolescents have by age 16; there may be compelling reasons to start earlier, though published experience before 13.5–14 years is minimal. Adults should receive physiologic levels of gender-appropriate hormones with monitoring for known risks, and clinicians should avoid harming people with conditions other than gender dysphoria who may not benefit from the physical changes.