Polyuria
Peer reviewed by Dr Doug McKechnie, MRCGPLast updated by Dr Colin Tidy, MRCGPLast updated 15 Dec 2022
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What is polyuria?1 2
Polyuria is the passage of large volumes of urine with an increase in urinary frequency. A normal daily urine output in adults is about one to two litres. Polyuria is defined as a daily urine output of more than three litres.
Polyuria presents much less often than urinary frequency. Frequent passage of small amounts of urine suggests a totally different problem. It is very important to assess the frequency of micturition and volumes of urine passed. The causes of polyuria are usually also causes of polydipsia.
Nocturnal polyuria is characterised by overproduction of urine at night. It may result from abnormalities in the normal circadian variation, normal ageing or excessive evening/night-time fluid intake, but it can also be associated with various medical conditions, including congestive heart failure, diabetes mellitus, obstructive sleep apnoea, or peripheral oedema.3
Polyuria causes (aetiology)1 2
Endocrine
Cushing's syndrome, including pituitary adenomas (Cushing's disease) and ectopic adrenocorticotropic hormone (ACTH) secretion (most often due to small cell carcinoma of the lung and bronchial carcinoid tumours).
Renal
Relief of chronic urinary obstruction.
Iatrogenic
Diuretic therapy.
Alcohol.
Other drugs - eg, lithium, tetracyclines.
Metabolic
Hypercalcaemia (eg, osteoporosis treatment, multiple bony metastases, hyperparathyroidism).
Potassium depletion (eg, chronic diarrhoea, diuretics, primary hyperaldosteronism).
Psychological
Psychogenic polydipsia (compulsive water-drinking).
Polyuria is an uncommon but serious complication of psychotic illness and, if untreated, may lead to hyponatraemia, coma or even death.
Other causes
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Polyuria symptoms1 2
Thirst, increased fluid intake
Thirst will usually accompany polyuria. In psychogenic polydipsia (most often seen in adolescents), thirst with compulsive water drinking is the predominant symptom.
Nocturia
This will usually be a feature of true polyuria and secondary enuresis in children can occur.
Associated general symptoms
This includes weight loss, malaise, headache and shortness of breath, and increases the likelihood of significant pathology.
Weight loss
Rapid onset of weight loss is a feature of type 1 diabetes. Weight loss is also a feature of chronic kidney disease and may also be due to dehydration in diabetes insipidus.
Symptoms suggestive of diabetes insipidus
Daily urine output may be greater than 10 litres. A pituitary tumour may cause headaches, visual disturbance and symptoms of pituitary hormone excess or deficiency. Other brain tumours in the region of the pituitary gland may be also be responsible - eg, craniopharyngiomas.
Past medical history
Chronic kidney disease may be a consequence of diabetes mellitus, connective tissue disease such as systemic lupus erythematosus (SLE), renal vascular disease, pyelonephritis or obstructive uropathy. Cranial diabetes insipidus may be due to pituitary surgery or irradiation, infection (meningitis, cerebral abscess), sarcoidosis or head injury.
Family history
A family history of diabetes mellitus or renal problems - eg, polycystic kidneys or nephrogenic diabetes insipidus.
Signs
General - eg, dehydrated (acute presentation of type 1 diabetes, diabetes insipidus, chronic kidney disease) or anaemia (chronic kidney disease).
Blood pressure and pulse: tachycardia and postural hypotension with dehydration, bradycardia and a raised blood pressure may occur if raised intracranial pressure.
Eyes: papilloedema if raised intracranial pressure, diabetes eye complications (retinal haemorrhages, exudates, new vessel formation, cataracts). A pituitary tumour may cause a visual field defect.
Abdomen: palpable kidneys in renal disorders.
Neurology: peripheral neuropathy in diabetes mellitus or chronic kidney disease.
Investigations4
Urine tests
Urinalysis for diabetes (glucose, ketones) and signs of renal disease (proteinuria). Specific gravity is very low in diabetes insipidus and psychogenic polydipsia.
Urine osmolality: early morning urine sample in conjunction with a plasma osmolality. A high plasma osmolality and inappropriately low urine osmolality occur in diabetes insipidus; both plasma and urine osmolalities are correspondingly low in psychogenic polydipsia.
Quantification of proteinuria: 24-hour urine collection; albumin-creatinine ratio (ACR) for microalbuminuria.
Urine electrophoresis: light-chain immunoglobulins (Bence Jones' protein): myeloma may be the cause of hypercalcaemia.
Blood tests
Renal function, electrolytes: calcium, potassium, abnormalities suggesting chronic kidney disease.
Fasting (preferable) or random glucose.
FBC, ESR: anaemia found in chronic kidney disease and collagen vascular diseases. Bone marrow infiltration may be evident in myeloma. ESR raised in collagen vascular diseases, myeloma and malignancy.
Serum protein electrophoresis: for monoclonal immunoglobulin band in myeloma.
Autoantibody screen: if collagen vascular disease is a possible cause of renal failure.
Serum lithium concentration if relevant.
Further investigations
These investigations (and some of the urine and blood tests) are more likely to be part of secondary care investigations.
Imaging of the renal tract: ultrasound, X-ray, CT scan of the abdomen.
Renal biopsy.
Lateral skull X-ray: may show an enlarged pituitary fossa with pituitary tumours. Calcification is common with craniopharyngiomas.
MRI or CT scan of brain: for pituitary or other brain tumour.
Water deprivation and desmopressin test: may be performed under supervision in secondary care and is useful in distinguishing cranial and nephrogenic diabetes insipidus.
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Polyuria treatment
Admit to hospital if significantly dehydrated, whatever the likely cause. Fluid balance and electrolyte disturbance will need to be corrected.
Further management will depend on the results of initial investigations and any confirmed cause of polyuria.
Further reading and references
- Moore K, Thompson C, Trainer P; Disorders of water balance. Clin Med (Lond). 2003 Jan-Feb;3(1):28-33. doi: 10.7861/clinmedicine.3-1-28.
- Davey P, SprigingsD; Diagnosis and Treatment in Internal Medicine. Chapter 57, Polyuria. 2018
- Weiss JP; Advances in the Diagnosis and Management of Nocturnal Polyuria. Urology. 2019 Nov;133S:1-2. doi: 10.1016/j.urology.2019.06.008. Epub 2019 Jun 21.
- Douglas R et al; Algorithmic Diagnosis of Symptoms and Signs: A Cost-Effective Approach, 2012
Article history
The information on this page is written and peer reviewed by qualified clinicians.
Next review due: 15 Nov 2027
15 Dec 2022 | Latest version
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