Hyperhidrosis
Peer reviewed by Dr Toni HazellLast updated by Dr Rosalyn Adleman, MRCGPLast updated 17 Jan 2025
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Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Hyperhidrosis article more useful, or one of our other health articles.
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What is hyperhidrosis?
Hyperhidrosis (excessive sweating) may be either focal or generalised, and either primary (no underlying cause) or secondary (underlying cause identified).1 Common triggers include emotion and spicy foods.
Primary focal hyperhidrosis may affect the axillae, palms, soles or scalp, and has no underlying cause. It usually starts in childhood or adolescence, but can occur at any age. Palmar and plantar hyperhidrosis may be present at birth.
Secondary focal hyperhidrosis involves specific areas of the body, but is caused by an underlying condition.
Generalised hyperhidrosis affects the entire body and is usually caused by medical conditions or drugs.1
The prevalence of hyperhidrosis is estimated at 2-16% globally. The range is thought to be due to differences in methodology, diagnostic criteria, demographics or geography. Hyperhidrosis occurs both in children and adults. Primary hyperhidrosis has a bimodal onset, commonly starting in early childhood or at puberty.2
Causes of hyperhidrosis
Generalised hyperhidrosis1
Pregnancy.
Anxiety.
Drugs - eg, anticholinesterases (pyridostigmine, neostigmine), antidepressants, pilocarpine eye drops, bethanechol, propranolol.
Substance abuse or withdrawal (including alcohol).
Heart failure, coronary heart disease, shock.
Respiratory failure.
Infections, including tuberculosis, brucellosis, HIV, abscess, and malaria.
Malignancy, especially lymphoma.
Thyrotoxicosis, hypoglycaemia, phaeochromocytoma, acromegaly, carcinoid tumour, hyperpituitarism, obesity, gout, menopause.
Parkinson's disease, diencephalic epilepsy, hypothalamic lesions.
Familial dysautonomia (Riley-Day syndrome).
Secondary focal hyperhidrosis
Cerebrovascular disease, peripheral neuropathies, diabetic autonomic neuropathy, spinal cord lesions, and spinal tumours
Intrathoracic neoplasms - eg, mesothelioma.
Gustatory sweating (sweating induced by food or drink), which may be due to diabetic neuropathy, preauricular herpes zoster, invasion of the cervical sympathetic trunk (by tumour or injury) or surgery to the parotid gland (eg, Frey's auriculotemporal syndrome).
Compensatory hyperhidrosis: may occur with myelopathy, cerebrovascular disease, nerve trauma or after surgery. The mechanism of compensatory hyperhidrosis is not clear, but it seems to be associated with compensation for thermoregulatory function.3
Other causes include cervical rib, Raynaud's phenomenon, arteriovenous fistula, cold injury, rheumatoid arthritis, and nail-patella syndrome.
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Symptom of hyperhidrosis (presentation)1
An underlying cause should be suspected if:
There is generalised sweating.
There is sweating during sleep (suggests tuberculosis, another infection, or Hodgkin's disease).
There are symptoms and signs of systemic disease - eg, fever, weight loss, anorexia, or palpitations.
The person is taking prescribed drugs that are known to cause sweating.
There is unilateral or asymmetrical sweating (suggests a neurological lesion or tumour, an intrathoracic malignancy, or a cervical rib).
There are symptoms and signs of any other causes of secondary focal hyperhidrosis or generalised hyperhidrosis.
Assess whether anxiety may be an exacerbating factor.
Diagnose primary focal hyperhidrosis when focal, visible, excessive sweating:
Occurs in at least one of the following sites: axillae, palms, soles, or craniofacial region; and
Has lasted at least six months; and
Has no apparent cause; and
Has at least two of the following characteristics:4
Bilateral and relatively symmetrical.
Impairs daily activities.
Frequency of at least one episode per week.
Onset before 25 years of age.
Positive family history.
Cessation of local sweating during sleep.
If symptoms have lasted less than six months or onset is at 25 years of age or older, primary focal hyperhidrosis remains a likely diagnosis if other criteria are met, but extra care should be taken to exclude an underlying cause.
Diagnosing hyperhidrosis (investigations)
If the presentation is characteristic of primary focal hyperhidrosis and there is no evidence of an underlying cause, no laboratory tests are required. Any initial investigations will often depend on individual context of patient and the history and examination but often include:1
FBC; blood film for malarial parasites may be indicated.
ESR and/or CRP.
Renal function tests and electrolytes.
LFTs.
Fasting blood glucose.
TFTs.
HIV testing.
Tuberculosis testing
24 hour urinary collection for catecholamines, metanephrines (to exclude phaeochromocytoma), 5-hydroxyindoleacetic acid (to exclude carcinoid tumours).
CXR.
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Management of hyperhidrosis
Generalised hyperhidrosis
Generalised hyperhidrosis is usually due to an underlying disorder. Management is therefore directed at finding and treating any underlying cause (usually includes specialist referral).
Primary focal hyperhidrosis1
General advice:
Avoid clothes that show sweat marks readily (white or black are suitable colours). Wear loose-fitting clothing. Avoid man-made fibres - eg, nylon.
Soap substitutes reduce skin irritation.
Avoid any obvious trigger factors.
Frequently change clothing, including shoes to allow them to dry properly, and avoid heavy occlusive footwear such as boots or sports shoes.
Primary axillary hyperhidrosis: use an antiperspirant rather than a deodorant; use armpit or sweat shields to absorb excess sweat and protect clothing.
Primary plantar hyperhidrosis: changing socks at least twice daily; use absorbent soles, and use absorbent foot powder twice daily; avoid occlusive footwear such as boots or sports shoes; wear leather shoes; alternate pairs of shoes on a daily basis to allow them to dry fully.
20% aluminium chloride hexahydrate in alcohol solution should be applied to dry skin of the axillae, feet, hands, or face (avoiding the eyes) at night just before sleep, and washed off in the morning (eg, as a roll-on anti-perspirant). The solution should be applied every 1-2 days until the condition improves and then as required, which may be up to every 6 weeks. If successful, treatment can be continued indefinitely.
Consider treating any underlying anxiety with cognitive behavioural therapy (drug treatment may worsen the hyperhidrosis).
Refer to a dermatologist if the above measures are inadequate or unacceptable.
Further treatments in secondary care:
Modified topical therapy: options include emollients, topical corticosteroids, different strengths of aluminium salts (up to 50%), and topical glutaraldehyde or formaldehyde.
Topical glycopyrrolate (an antimuscarinic agent) may be useful for primary craniofacial hyperhidrosis (off-label indication).
Oral antimuscarinics, such as glycopyrronium bromide and oxybutynin, decrease sweat secretion by competitive inhibition of acetylcholine at the muscarinic receptors near eccrine sweat glands (off-label indications).
Propantheline bromide is the only licensed medication for generalised hyperhidrosis but its use is limited by anti-muscarinic side effects.
Iontophoresis:
The sites of hyperhidrosis are immersed in warm water (or a wet contact pad may be applied) through which a weak electric current is passed. It is mainly suitable for palms of the hands and soles of the feet.
Glycopyrronium bromide as a 0.05% solution is used in iontophoresis for more severe cases of hyperhidrosis affecting the plantar and palmar areas.
Some people seem to gain considerable symptom relief. Most report an improvement after 6-10 sessions. Maintenance treatment is usually required at 1- to 4-week intervals.
Botulinum type A toxin:
Botulinum A toxin-haemagglutinin complex is licensed for use intradermally for severe hyperhidrosis of the axillae unresponsive to topical antiperspirant or other antihidrotic treatment.
It is given by repeated intradermal injections into the affected area.
It has been shown to be safe and effective.
Surgery:
Usually only considered if other treatment options have failed or have not been tolerated.
Sympathectomy (division of the sympathetic chain over the neck of the ribs under general anaesthesia) is the most commonly performed procedure:4
The National Institute for Health and Care Excellence (NICE) recommends that current evidence on the efficacy and safety of endoscopic thoracic sympathectomy supports its role in the management of primary hyperhidrosis of the upper limb.5
Lumbar sympathectomy is not used for plantar hyperhidrosis because of the risk of sexual dysfunction.
Other complications include gustatory sweating, rhinitis, pneumothorax (usually resolves spontaneously), Horner's syndrome, brachial plexus injuries, postoperative neuralgia, and recurrent laryngeal nerve palsy.
MiraDry® is a non-invasive procedure that may be effective. It involves using an electromagnetic energy delivered to the skin using a specially designed handpiece.6
Complications of hyperhidrosis1
Severe hyperhidrosis can cause extreme embarrassment that may lead to social and professional isolation.
Secondary infections.
Dermatitis.
Prognosis
Further reading and references
- Hyperhidrosis; NICE CKS, September 2023 (UK access only)
- BMJ Best Practice; Hyperhydrosis 2024
- Haam SJ, Park SY, Paik HC, et al; Sympathetic nerve reconstruction for compensatory hyperhidrosis after sympathetic surgery for primary hyperhidrosis. J Korean Med Sci. 2010 Apr;25(4):597-601. doi: 10.3346/jkms.2010.25.4.597. Epub 2010 Mar 19.
- Benson RA, Palin R, Holt PJ, et al; Diagnosis and management of hyperhidrosis. BMJ. 2013 Nov 25;347:f6800. doi: 10.1136/bmj.f6800.
- Endoscopic thoracic sympathectomy for primary hyperhidrosis of the upper limb; NICE Interventional Procedure Guidance, May 2014
- miraDry®; Hyperhidrosis UK
Article history
The information on this page is written and peer reviewed by qualified clinicians.
Next review due: 16 Jan 2028
17 Jan 2025 | Latest version
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