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  • Verified Content: Approved by the Women’s Health Clinic Clinical Team.
  • Educational Use: This is not a substitute for professional medical advice, diagnosis, or treatment.
  • Clinical Assessment: Individual suitability is determined by a clinician; results may vary.
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Dr Farzana Khan

Dr Farzana Khan

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Dr Farzana Khan qualified as an MD from the University of Copenhagen in 2003. She has worked in dermatology and obstetrics & gynaecology across the North of England and completed her MRCGP (CCT, 2013) and the Diploma of the Faculty of Sexual & Reproductive Health (2013). Her clinical focus is vaginal health—including dryness/GSM, sexual function concerns, lichen sclerosus, and comfort or volume changes. She offers careful assessment, discusses medical and conservative options first, and considers selected regenerative or aesthetic treatments where appropriate. Dr Farzana also trains clinicians as a KOL/Trainer with Neauvia, Asclepion Laser, and RegenLab (since 2023). Ongoing CPD includes IMCAS, CCR, ACE and expert training in women’s intimate fillers, PRP, and polynucleotide injectables. Her approach is simple: clear explanations, realistic expectations, and shared decision-making. Authored and medically reviewed by Dr Farzana Khan.

MD MRCGP DFFP
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Dryness & GSM faq

Who is not suitable for PRP or polynucleotides?

Who is not suitable for PRP or polynucleotides? Avoid or delay if you have active infections (BV/thrush/UTI), unexplained bleeding, fever, unhealed pelvic surgery, poorly controlled bleeding risk, severe fish allergy (for some polynucleotides), or if diagnosis is unclear. These injectables are adjuncts for genitourinary syndrome of menopause (GSM) after moisturisers, suitable lubricants, and—when acceptable—local oestrogen or DHEA. Educational only. Results vary. Not a cure.

Clinical Context

Who may suit PRP or polynucleotides? People with GSM whose main problem is entrance-focused burn/micro-tears and who remain sore despite a scheduled moisturiser and a liberal, compatible lubricant, and who either cannot use local hormones or improved on them but still have friction pain. If arousal lubrication is low, a silicone-based lubricant often gives the longest glide.

Who should avoid or delay right now? Anyone with red flags (fever, malodorous discharge, severe pelvic pain, visible haematuria, or new post-menopausal bleeding); people with active thrush/BV/UTI; those healing from pelvic/perineal surgery; and those with poorly controlled bleeding risk. Severe fish allergy generally excludes salmon-derived polynucleotides. If deep pelvic pain dominates, consider endometriosis/adenomyosis work-up rather than surface injectables.

Alternatives & next steps. Keep washing gentle (lukewarm water; bland emollient as a soap substitute), wear breathable underwear, and review irritants (perfumed washes/liners, tight kit, chlorine without rinsing). Optimise local vaginal oestrogen or DHEA placement if acceptable (a fingertip to the tender vestibule can matter). Add pelvic health physiotherapy for protective guarding. Plan a review at 6–12 weeks to adjust to the lowest effective maintenance. Educational only. Results vary. Not a cure.

Evidence-Based Approaches

Guideline first lines (UK): Patient-friendly advice on symptoms and self-care appears on the NHS page for vaginal dryness. The NICE Menopause Guideline (NG23) recommends offering information on vaginal moisturisers and lubricants and considering low-dose local vaginal oestrogen when GSM affects quality of life; local therapy can be used with or without HRT.

Prescribing/product detail: UK cautions and product information for vaginal oestrogens and prasterone (DHEA) are listed in the British National Formulary (BNF). These remain the preferred next step when non-hormonal measures are insufficient, with stronger evidence than injectables.

Comparators with stronger evidence: Systematic reviews in the Cochrane Library consistently show that local vaginal oestrogens improve dryness, soreness, dyspareunia and vaginal pH versus placebo across creams, pessaries/tablets and rings.

Emerging evidence for injectables: Peer-reviewed summaries and small studies on PRP/polynucleotides in GSM and vestibular pain are indexed on PubMed; they suggest potential benefit but note heterogeneity in preparation, dosing and follow-up, so routine use awaits more robust trials.

Applying the evidence: Follow a stepped pathway—foundations → add local therapy if needed → consider PRP or polynucleotides only as adjuncts in selected cases after informed discussion of benefits, limits, costs and maintenance. Ensure products/devices are UKCA/CE-marked for intended use and used by trained clinicians with documented consent and aftercare. ® belongs to its owner.