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Quick Update for Healthcare Professionals on Topical Testosterone Replacement Therapy for Menopausal Women

Writer's picture: Mohammed A RashadMohammed A Rashad

Updated: Jul 22, 2024

Key Points


  • 🔍 Check Shared Care Status:


  • Verify if testosterone replacement is a shared care drug in your area. Typically initiated by menopause clinics.


  • 💼 Primary Care Responsibilities:

  • Refer patients to menopause clinic for assessment.

  • Contact specialists if concerns arise about shared care arrangements.

  • Report serious adverse reactions to MHRA and the referring specialist.

  • Continue prescribing as advised by the specialist and monitor as required.

  • Inform the specialist if the patient discontinues treatment or if there are any concerns.


Patient Selection and Treatment


  • Indication: For menopausal women with loss of libido despite conventional HRT.

  • Contraindications: Pregnancy, breastfeeding, active liver disease, hormone-sensitive breast cancer, competitive athletes, high baseline testosterone levels, hypersensitivity.

  • Side Effects: May include increased body hair, acne, voice deepening, and clitoral enlargement. Contact the specialist if these occur.


Monitoring


  • Specialist: Monitor total serum testosterone before and during treatment, and adjust as necessary.

  • Primary Care: Annual monitoring of testosterone levels, symptoms, and side effects. Ensure levels remain within normal physiological range.


Additional Information


  • Application Instructions:

  • Apply testosterone with clean hands to clean, dry skin on the lower abdomen or upper thighs.

  • Wash hands immediately after application.

  • Do not cover the skin for 3-5 minutes until dry.

  • Testogel® Sachet: Do not wash the site for 1 hour.

  • Testim® Gel: Do not wash the site for at least 6 hours.

  • Testogel® Pump Dispenser: Do not wash the site for 2 hours.

  • Tostran® Pump: Do not wash the site for at least 2 hours.


  • Precautions:


  • Avoid skin-to-skin contact with the application site to prevent testosterone transfer, especially to pregnant women and children.

  • Reduce transfer risk by washing hands after application, covering the site with clothes, or washing the site with soap and water after the recommended time.

  • MHRA Drug Safety Update: Inform patients about the risk of transfer, possible adverse effects, and precautions to minimize risk (25 Jan 2023).

  • Note: The HRT prepayment certificate, introduced on 1 April 2023, does not apply to transdermal testosterone products. It only applies to products licensed for HRT.


Resources


  • NICE Guidance: NICE NG23

  • British Menopause Society: Testosterone Replacement

  • Achillli C et al. Efficacy and safety of transdermal testosterone in postmenopausal women with hypoactive sexual desire disorder; a systematic review and meta-analysis. Fertil Steril 2017; 107(2):475-482

  • Barber RJ, Panay N, Fenton A, International Menopause Society (IMS) writing group. 2016 IMS Recommendations on women’s midlife health and hormone therapy. Climacteric. 2016; 19(2):109-150

  • Islam RM et al. Safety and efficacy of testosterone for women: a systematic review and meta-analysis of RCT data. Lancet 2019; 7 (10):754-766

  • NICE NG23: Menopause Diagnosis and management November 2015 updated December 2019 www.nice.org.uk/guidance/ng23


  • Full details of prescribing information on topical testosterone products is given in the manufacturers summary of product characteristics (SPCs), available from www.medicines.org.uk ; however, note these refer to the licensed use in male hypogonadism.


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