Transdermal Testosterone Dosing for HSDD in Postmenopausal Women
For postmenopausal women with hypoactive sexual desire disorder (HSDD), the recommended dosing for transdermal testosterone is 300 μg/day, which has been shown to be effective and safe in clinical trials. 1, 2
Appropriate Formulations and Application
Recommended Dosing:
- Dose: 300 μg/day transdermal testosterone 2, 3
- Application sites: Back, abdomen, upper thighs, or upper arms 4
- Frequency: Typically applied as patches that are changed twice weekly or weekly depending on the specific product 4
Available Formulations:
Testosterone patches:
- Androderm (2 mg/24-h patch) - typically 2-6 mg/day for men, but must be adjusted to 300 μg/day for women 4
- Note: Most testosterone products are formulated for men and must be carefully dosed for women
Testosterone gels:
- Can be used with careful measurement to achieve the 300 μg/day dose
- Examples include AndroGel, Testim, and Testogel 4
- Caution: Risk of transfer to partners or children through skin contact
Monitoring and Safety
Pre-treatment Assessment:
- Baseline total testosterone level (not for diagnosis but for monitoring) 1
- Comprehensive assessment to rule out other causes of decreased libido (relationship issues, medications, mental health conditions) 1
Monitoring During Treatment:
- Total testosterone levels should be maintained in the physiologic premenopausal range 1
- Monitor after 2-3 months of treatment initiation and every 6-12 months thereafter 4
- Assess for signs of androgen excess (acne, unwanted hair growth) 1, 5
Safety Considerations:
- Short-term safety data (up to 4 years) shows minimal side effects 5
- Most common adverse events are application site reactions and mild unwanted hair growth 6, 5
- No significant changes in lipid profiles, carbohydrate metabolism, or liver function have been observed 5
- Long-term safety beyond 4 years has not been firmly established 1
Important Clinical Considerations
Efficacy:
- Transdermal testosterone at 300 μg/day has demonstrated significant improvements in:
Regulatory Status:
- Testosterone therapy for HSDD in women is currently off-label in most countries 1
- Requires informed consent and shared decision-making regarding benefits and risks 1
Cautions:
- Avoid compounded testosterone products due to lack of standardized efficacy and safety data 1
- Use cautiously in women with a history of estrogen-dependent cancers
- Testosterone patches may cause skin irritation in some women 4
- Monitor for cardiovascular effects, though short-term data suggests minimal risk 6
Treatment Algorithm
- Confirm diagnosis of HSDD not primarily related to modifiable factors
- Obtain baseline testosterone level
- Initiate transdermal testosterone at 300 μg/day
- Monitor at 2-3 months for efficacy, side effects, and testosterone levels
- Continue monitoring every 6-12 months if treatment is effective and well-tolerated
- Discontinue if:
- No improvement in symptoms after 6 months
- Development of significant side effects
- Testosterone levels exceed premenopausal range
This approach provides a structured method for safely implementing testosterone therapy for postmenopausal women with HSDD while optimizing outcomes related to sexual function and quality of life.