Core Concepts
Prescribing compounded bioidentical hormone therapy for menopause poses legal risks and lacks scientific backing.
Abstract
The content discusses the risks associated with prescribing compounded bioidentical hormone therapy (cBHT) for menopause. It highlights the lack of FDA approval, quality issues, and unsubstantiated marketing claims surrounding cBHT. The article emphasizes the importance of evidence-based practice and informed decision-making in hormone therapy for menopausal symptoms.
Highlights:
- Legal risks for physicians prescribing cBHT
- Lack of scientific evidence supporting cBHT
- Quality problems and variations in cBHT ingredients
- Higher side effects in cBHT compared to FDA-approved HRT
- Financial implications for patients due to lack of insurance coverage
- Importance of informed consent and documentation for prescribing cBHT
Stats
Clinicians write an estimated 26 to 33 million prescriptions for compounded bioidentical hormone therapy (cBHT) every year.
Side effects were significantly higher in the cBHT group (57.6% vs 14.8%; P < .0001).
Quotes
"There is a public perception that this is natural, safer, and anti-aging."
"They're being hyped as safer and more effective when in reality, we don't have any studies that show that information."