Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/859
Title: Treatment of female pattern hair loss with low dose minoxidil.
Epworth Authors: Sinclair, Rodney
Keywords: Alopecia
Poster 41
Baldness
Hair Loss
FPHL
Hypertrichosis
Female Pattern Hair Loss
Minoxidil
Spironolactone
Hair Shedding
Hyperkalaemia
Urticaria
Chair of Dermatology, Epworth HealthCare, Victoria, Australia
Head & Neck Clinical Institute, Epworth HealthCare, Victoria, Australia
Issue Date: Jul-2016
Citation: Poster 41
Conference: Research Week 2016.
Conference Location: Epworth Research Institute, Epworth Richmond.
Abstract: Background: The oral antihypertensive minoxidil stimulates hair growth, but its use in the treatment of female pattern hair loss (FPHL) is limited by the potential adverse events of postural hypotension, fluid retention and hypertrichosis, Spironolactone is another antihypertensive used to treat FPHL. Method: To investigate the safety and effectiveness of a single once daily oral capsule containing minoxidil 0.25mg and spironolactone 25mg in the treatment of FPHL, women with a Sinclair stage 2-5 FPHL were treated once daily for 12 months. Hair shedding was scored using a 6 point visual analogue scale. Patients were reviewed 3 monthly and blood pressure an side-effects documented. Full blood count, renal function, electrolytes and liver function were monitored at 3 monthly intervals. Results: 100 women were enrolled. mean age was 48.44 years (range 18-80). mean hair loss severity at baseline was Sinclair 2.79(range 1-5). mean hair shedding score at baseline was 4.82. mean reduction in hair loss severity score was 0.85 at 6 months and 1.3 at 12 months. Side effects were seen in 8 of women but were generally mild. No patients developed hyperkalaemia or any other blood test abnormality. Six of these women continued treatment and 2 women who developed urticaria discontinued treatment. Discussion: Once daily minoxidil / spironolactone appears to be safe and effective in the treatment of FPHL. Placebo controlled to investigate this further are warranted.
URI: http://hdl.handle.net/11434/859
Type: Conference Poster
Type of Clinical Study or Trial: Cohort Study
Appears in Collections:Head & Neck
Dermatology

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