The cornerstone of hormone therapy for trans men is testosterone. The goal of treatment is virilization – development of masculine secondary sexual characteristics.
In Ontario, options for testosterone administration include injectable and transdermal preparations (patch or gel). Injectable formulations are most commonly used, both because of their superior efficacy and lower price.
The degree and rate of physical effects is dependent on the dose and route of administration, as well as client-specific factors such as age, genetics, body habitus and lifestyle.
Desired androgenic effects of testosterone therapy include deepened voice, cessation of menses, clitoral growth, increased muscle mass, and hair growth in androgen dependent areas including facial hair. Typically, clients taking testosterone develop a male phenotype over a period of months to years. The timeframe of physiologic changes may be slightly slower with the use of transdermal preparations.
Hover over the coloured regions to view expected information on the reversibility, onset and maximum effects of physical changes
Skin oiliness and acne increases
Facial hair grows and body hair thickens.
Highly dependent on age and inheritance; may be minimal
Significantly dependent on amount of exercise
Fat redistributes from buttock/hip/thigh regions to the abdomen and mid-section.
Several pre-existing medical conditions and risk factors may increase the risks associated with testosterone administration. When these are present, a careful evaluation of risks and benefits should be completed and fully discussed with the client.
Select area of concern below
Risk factors | How to minimize risks |
---|---|
Migraines | Consider referral to neurology, consider daily migraine prophylaxis, consider transdermal route of administration |
Androgen-sensitive epilepsy | Refer to neurology |
For more information on metabolic effects please read page 24 of the full Protocols.
Risk factors | How to minimize risks |
---|---|
Uncontrolled diabetes | Identify and address barriers to optimal glycemic control, refer to dietician, encourage lifestyle modification, initiate antiglycemic agent(s), consider cardiac stress test, encourage deferral of testosterone until adequately controlled |
Uncontrolled dyslipidemia | Identify and address barriers to optimal lipid control, refer to dietician, initiate antilipemic pharmacologic therapy, consider endocrinology referral, consider cardiac stress test, encourage deferral of testosterone until addressed |
For more information on cardiovascular disease please read page 24 of the full Protocols.
Risk factors | How to minimize risks |
---|---|
Stable ischemic cardiovascular disease | Consider referral to cardiology, ensure optimal medical (including prophylactic anticoagulation) and/or surgical management as indicated, aggressive risk factor optimization, consider transdermal route of administration +/- lower dose |
Uncontrolled high blood pressure | Identify and address barriers to optimal BP control, initiate antihypertensive(s) as needed, consider cardiac stress test, encourage deferral of testosterone until adequately controlled |
Elevation of liver enzymes may occur with testosterone therapy. For more information on cardiovascular disease please read page 25 of the full Protocols.
Risk factor | How to minimize risks |
---|---|
Hepatic dysfunction | Dependent on etiology, e.g. minimize alcohol consumption, weight loss in NAFLD, consider referral to hepatology/GI |
For more information on endometrial cancer please read page 25 of the full Protocols.
Risk factors | How to minimize risks |
---|---|
Inter-menstrual bleeding | Consider pelvic ultrasound (transvaginal if possible), consider gyne referral - especially if significant risk factors for endometrial cancer |
Oligo-/amenorrhea | Consider pelvic ultrasound (transvaginal if possible), consider progesterone-induced menstrual bleed prior to testosterone initiation |
Risk factors | How to minimize risks |
---|---|
Polycythemia | Refer to hematology, identify etiology and address contributing factors, consider low-dose ASA, strongly encourage deferral until adequately managed, consider transdermal route of administration, monitor RBCs/Hct closely. More information on this on page 25 of the full Protocols |
History of deep vein thrombosis (DVT), pulmonary embolism (PE) or hypercoagulable state | Identify and minimize co-existent risk factors, monitor RBCs/Hct closely, consider transdermal route of administration |
Risks/Precautions | How to minimize risks |
---|---|
Smoker | Encourage and support smoking cessation, offer NRT and/or bupropion/varenacline, or negotiate a decrease in smoking, consider cardiac stress test especially in the presence of additional risk factors, consider transdermal route of administration |
Chronic respiratory disease that may be worsened by erythrocytosis/polycythemia | Consider referral to respirology, monitor RBCs/Hct closely, consider transdermal route of administration |
Severe/uncontrolled sleep apnea | Initiate CPAP or oral device, encourage weight loss if overweight, consider uvulopalatoplasty, monitor for changes in CPAP pressure requirements. More information on page 25 of the full Protocols |
Standard monitoring of estrogen administration should be employed at baseline, 1, 3, 6, and 12 months. This should include a functional inquiry, targeted physical exam, bloodwork, and health promotion/ disease prevention counselling.
Testosterone level may be the most useful test for monitoring in trans women; for many clients, the goal will be to achieve the suppression of testosterone into the female range. That said, the client may have clinically relevant results without total suppression of testosterone because of androgen blockade, which is not easily measured. Estradiol levels are of variable utility in monitoring feminizing therapy given the wide cyclical variation in cis women. Most clients attain considerable feminization at estradiol levels between 200-500 pmol/L. According to the Endocrine Society Guidelines, serum estradiol levels should not exceed the mean daily level for cis women (approximately 700 pmol/L).
Click on one of the tabs to find out standard monitoring suggestions at baseline, 1, 3 and 6 months.
Trans men maintained on masculinizing hormone therapy have unique preventive care needs and recommendations.
Long-term follow-up care of trans men on masculinizing hormone therapy should involve (at least) annual preventive care visits. An Adaptive Preventive Care Checklist with accompanying explanations for trans-specific recommendations can be accessed below.
Physical examinations that involve intimate body parts are discomforting to anyone. While many trans people are comfortable with their bodies others may experience body dysphoria. Some may be very uncomfortable with physical examinations or be reluctant to acknowledge or touch their own genitals.
It is best to base routine screening on the presence or absence of body parts. Sex assigned at birth and gender identity are separate things. Some women have pensises, some men have vaginas. Refrain from calling body parts ‘male’ or female’. Instead use technical terms or ask client what they prefer to call their body parts. Organs present should receive routine and preventive care.
Click on one of the tabs to find out routine care and screening suggestions.
Recommendations for clients at average risk of developing breast cancer:
Use the diagram below to find out when and what type of colon cancer screening is recommended.
Use the diagram below to find out what type of cervical cancer screening is recommended.
Analogous to cis women with elevated androgen levels, testosterone therapy in trans men may increase the risk of ovarian cancer, although evidence for this is limited. There have been a few cases of ovarian cancer in transgender men 1 but no long-term studies exist. Overall the evidence regarding the risk of ovarian cancer in trans men on testosterone is inconclusive.2 Though evidence for their benefit in screening for ovarian cancer is limited, annual bimanual exam can be considered if ovaries are present, in accordance with the provider’s routine practice with cis women.