Affirming Care of the Transgender Patient

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Transcription:

Mountain West AIDS Education and Training Center Affirming Care of the Transgender Patient Jessica Rongitsch, MD, FACP This presentation is intended for educational use only, and does not in any way constitute medical consultation or advice related to any specific patient.

Hormone Initiation Referral letter from trans-competent mental health provider Informed consent from prescriber: Risks and side effects Physical and emotional changes Expectations Social Impact Fertility Goals of patient/alternatives

Contraindications to Hormone Initiation Hormone-responsive cancer Untreated venous/arterial thromboembolism History suggesting untreated hypercoagulable state Consider avoiding spironolactone if on ACE I/diuretics, renal dysfunction, low blood pressure

Timeline for Physical Changes: Trans-masculine EFFECT Onset (months) Maximum (years) Skin oiliness/acne 1-6 1-2 Facial/body hair growth 6-12 4-5 Scalp hair loss 6-12 indefinite Increased muscle mass 6-12 2-5 Fat redistribution 1-6 2-5 Cessation of menses 2-6 indefinite Clitoral enlargement 3-6 1-2 Deeping of voice 6-12 1-2 Hembree et al., J Clin Endocrinol Metab, 2009

Timeline for Physical Changes: Trans-feminine Effect Onset (months) Maximum (years) Redistribution of body fat 3-6 2-3 Decrease in muscle mass 3-6 1-2 Softening skin 3-6 unknown Decreased libido 1-3 3-6 Decreased erections 1-3 3-6 Breast growth 3-6 2-3 Decreased testicular volume Decreased sperm production 3-6 2-3 unknown > 3 years Decreased hair growth 6-12 >3 years Scalp hair Voice changes No regrowth none Hembree et al., J Clin Endocrinol Metab, 2009

Common Side Effects: Trans-masculine Mood changes: irritability, anger, mood swings, anxiety Weight gain Vaginal atrophy Pelvic pain Acne Polycythemia Elevated transaminases

Common Side Effects: Trans-feminine Orthostatic hypotension/dizziness Mood issues: depression, increased emotional range, mood swings, anxiety Weight gain Fatigue Sexual dysfunction Renal dysfunction/hyperkalemia

Potential Risks Based on Limited Data VTE: 1-2% of MTF patients, risk greatest 1 st year of therapy, tobacco abuse, peri-operative period Breast cancer: no increased risk compared to general population Endometrial cancer: FTM case reports CAD risk: increased in MTF but associated with ethinyl estradiol use and other CV risk factors Worsened CV risk factors in FTM but no increased rates CV events or mortality Fenway Health: The Medical Care of Transgender Persons, 2015

Baseline Labs Transmasculine Transfeminine Comp/CMP Comp/CMP CBC CBC +/- lipid +/- lipid +/- HIV/STI screen +/- HIV/STI screen +/- testosterone if PCOS +/- testosterone +/- HCG +/- prolactin if on anti-psychotics Fenway, UCSF, The Endocrine Society

Trans-masculine Regimen Name Starting dose Standard dose range Testosterone cypionate (cottonseed) 200mg/ml Testosterone enanthate (sesame) 200mg/ml Androgel/topical testosterone Androderm patch 2 mg or 4 mg 0.15 ml 0.2 ml weekly 0.35 ml -0.5 ml weekly or 0.7 ml 1 ml q 14 days 0.15 ml 0.2 ml weekly 0.35 ml -0.5 ml weekly or 0.7ml 1 ml q 14 days 12.5 mg -25 mg TD qd 50 mg -100 mg TD qd 4mg qd 6 mg Fenway Health: The Medical Care of Transgender Persons, 2015

Trans-masculine Monitoring Parameters Q 3 months x 1 year then q 6 months Effects? Side effects? Documentation needs Risk HIV/STI, pregnancy risk Surgical gender affirmation--? Top surgery Labs: HCT/HGB, COMP/CMP, testosterone level

Testosterone Levels: Trans-masculine Goal normal male level 400 ng/dl 900 ng/dl Trough level: (around) 400 ng/dl Mid week level: 500 ng/dl 600 ng/dl

Trans-feminine Regimen: androgen blockers Name Starting dose Standard dose range Spironolactone 50 mg qd, 50 mg BID after 7 days 50 mg BID 150 mg BID Finasteride 5 mg 0.25 tab 1 tab qd 5 mg 0.25 tab 1 tab qd Prometrium (progesterone-no consensus on use) 100 mg 200 mg qd 100 mg 200 mg qd Fenway Health: The Medical Care of Transgender Persons, 2015

Trans-feminine: estradiols Name Starting dose Standard dose range Estradiol patch 0.1 mg once or twice a week depending on formulation 0.1 mg 0.4 mg once or twice a week depending on formulation Oral estradiol 2 mg qd sublingual 4 mg 8 mg qd usually divided into BID doses Injectable: estradiol valerate 40 mg/ml 0.15 ml 0.25 ml weekly 0.15 ml 0.25 ml weekly

Trans-feminine Monitoring Parameters Q 6-8 weeks if spironolactone dose increased, q 3 months x 1 year then q 6 months Effects? Side effects? Documentation needs Risk HIV/STI Surgical affirmation procedure/hair removal Labs: BUN/Cr, K, testosterone level, estradiol level

Hormone Level Goals Testosterone level goal < 50 ng/dl Estradiol levels: goal range 80-250 pg/ml

Resources UCSF: Center of Excellence for Transgender Health http://transhealth.ucsf.edu/trans?page=guidelines-home Fenway Health: The Medical Care of Transgender Persons http://transhealth.ucsf.edu/trans?page=guidelines-home Endocrine Treatment of Transsexual Persons: An Endocrine Society Clinical Practice Guideline http://press.endocrine.org/doi/pdf/10.1210/jc.2009-0345

Resources Continued Ingersoll Gender Center (Resources for patients and providers in the NW) http://ingersollcenter.org/ National Center for Transgender Equality http://www.transequality.org/