Testosterone Gel Dosing for Postmenopausal Women
For postmenopausal women with hypoactive sexual desire disorder, start with 5 mg daily of transdermal testosterone gel or less, applied to the thigh or other appropriate site, with close monitoring of side effects and hormone levels.
Evidence-Based Dosing Recommendations
The dosing of testosterone gel in postmenopausal women differs substantially from male dosing and requires careful attention to avoid supraphysiologic levels:
Starting Dose
- Begin with 5 mg daily or less of transdermal testosterone gel applied to the skin 1
- Research demonstrates that 10 mg daily of 1% testosterone gel applied to the thigh achieved adequate serum testosterone levels within the normal premenopausal range in postmenopausal women 2
- The 10 mg dose produced mean testosterone levels of 3.2 nmol/L during treatment, while 20 mg increased levels to 7.2 nmol/L, and 30 mg showed minimal further increase (7.5 nmol/L), suggesting a plateau effect 2
Clinical Indication
- The only evidence-supported indication for testosterone therapy in postmenopausal women is hypoactive sexual desire disorder (HSDD) with associated personal distress 3, 4
- Women treated with transdermal testosterone (300 mcg/day patches in clinical trials) experienced clinically meaningful improvements in satisfying sexual activity, sexual desire, and reduced distress 5
- Approximately 52% of women receiving testosterone reported meaningful treatment benefit compared to 31% on placebo 5
Critical Dosing Considerations
The Challenge of Available Formulations
- No testosterone product is specifically designed or approved for women in Europe or North America 1, 4
- Women must use preparations formulated for men, which contain much higher concentrations, making accurate dosing challenging 1
- Custom-compounded products should be used with caution due to inconsistent dosing 4
Application Technique
- Apply gel in a thin layer over approximately 15 cm² of skin on the outside of the thigh 2
- Alternative sites include the back, abdomen, or upper arms, similar to male formulations 6
- The gel must dry completely before contact with partners or children to prevent transfer 6
Monitoring Protocol
Hormone Level Monitoring
- Measure testosterone levels 2-3 months after initiation or any dose change 6
- Monitor specifically for supraphysiologic levels, not to diagnose deficiency 4
- Baseline testosterone in postmenopausal women averages approximately 1.1 nmol/L 2
- Target levels should remain within the normal premenopausal range 2
Clinical Response Assessment
- Evaluate subjective improvements in sexual desire, arousal, and satisfaction 4
- Assess for adverse effects including hirsutism and acne 4
- Continue monitoring every 6-12 months once stable 6
Safety Considerations and Contraindications
Absolute Contraindications
Adverse Effects to Monitor
- Hirsutism and acne are the most common adverse effects, though actual risks are not well-defined 4
- Mild adverse effects were reported in clinical trials 1
- The risk of breast cancer, cardiovascular disease, or thromboembolic events with testosterone therapy remains unknown 4
Important Caveats and Common Pitfalls
Concomitant Estrogen Therapy
- Testosterone therapy without concomitant estrogen cannot be recommended due to lack of evidence 4
- Most clinical trial data involve women using estrogen therapy concurrently 4
Duration of Therapy
- Use the lowest dose for the shortest time that meets treatment goals 4
- Safety and efficacy data beyond 6 months are limited 4
Diagnostic Limitations
- Do not use testosterone levels to diagnose "testosterone insufficiency" - no specific level has been linked to a clinical syndrome 4
- Clinically available laboratory assays do not accurately detect testosterone at concentrations typically found in women 4
- Rule out other causes of decreased sexual desire including physical factors, psychosocial factors, and medications before attributing symptoms to testosterone deficiency 4