Polydipsia

Polydipsia
ICD-10	R63.1
ICD-9	783.5

WikiDoc Resources for Polydipsia
Articles
Most recent articles on Polydipsia Most cited articles on Polydipsia Review articles on Polydipsia Articles on Polydipsia in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Polydipsia Images of Polydipsia Photos of Polydipsia Podcasts & MP3s on Polydipsia Videos on Polydipsia
Evidence Based Medicine
Cochrane Collaboration on Polydipsia Bandolier on Polydipsia TRIP on Polydipsia
Clinical Trials
Ongoing Trials on Polydipsia at Clinical Trials.gov Trial results on Polydipsia Clinical Trials on Polydipsia at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Polydipsia NICE Guidance on Polydipsia NHS PRODIGY Guidance FDA on Polydipsia CDC on Polydipsia
Books
Books on Polydipsia
News
Polydipsia in the news Be alerted to news on Polydipsia News trends on Polydipsia
Commentary
Blogs on Polydipsia
Definitions
Definitions of Polydipsia
Patient Resources / Community
Patient resources on Polydipsia Discussion groups on Polydipsia Patient Handouts on Polydipsia Directions to Hospitals Treating Polydipsia Risk calculators and risk factors for Polydipsia
Healthcare Provider Resources
Symptoms of Polydipsia Causes & Risk Factors for Polydipsia Diagnostic studies for Polydipsia Treatment of Polydipsia
Continuing Medical Education (CME)
CME Programs on Polydipsia
International
Polydipsia en Espanol Polydipsia en Francais
Business
Polydipsia in the Marketplace Patents on Polydipsia
Experimental / Informatics
List of terms related to Polydipsia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Overview

Polydipsia is a medical condition in which the patient ingests abnormally large amounts of fluids by mouth. The word is made from the words poly meaning many and dipsia which means thirst. The fluid is usually water, though some people may think of alcohol because of the etymologically related term dipsomaniac, meaning an alcoholic.

Differential diagnosis of the causes of polydipsia

Common causes

Polydipsia is almost always associated with dehydration due to polyuria (excessive urination), if the condition is prolonged beyond a few hours in those with functioning kidneys.

It is often, and characteristically, found in diabetics, often as one of the initial symptoms, and in those who fail to take their anti-diabetic medications or whose dosages have become inadequate. It is also caused by other conditions featuring osmotic diuresis and by diabetes insipidus ("water diabetes"), and forms part of the differential diagnostic tree for them, as well. Polydipsia is also a symptom of atropine or belladonna poisoning. Another cause can be due to medication (such as diuretics) or inadvertent consumption of caffeine. One who drinks nothing but coffee or soda can be easily misdiagnosed by a medical professional as psychogenic polydipsia, as they may be unaware they are consuming diuretics.

Complete differential diagnosis of causes of polydipsia

(In alphabetical order)

• Bartter syndrome
• Beer potomania
• Cushing syndrome
• Diabetes insipidus
  • Nephrogenic diabetes insipidus
    • Amikacin
    • Amphotericin B
    • Bardet-Biedl syndrome
    • Bartter syndrome
    • Cystinosis
    • Demeclocycline
    • Diabetes insipidus, congenital nephrogenic
    • Gentamicin
    • Hypercalcaemia
    • Hypokalaemia
    • Interstitial nephritis
    • Kanamycin
    • Lithium
    • Loken Senior syndrome
    • Medullary cystic renal disease
    • Netilmicin
    • Polycystic kidney disease, adult (autosomal dominant)
    • Proximal renal tubular acidosis
    • Pyelonephritis, acute
    • Renal failure, acute
    • Renal failure, chronic
    • Sicca syndrome
    • Sickle cell disease
    • Urinary tract infection
  • Central diabetes insipidus
    • Arteriovenous malformations or aneurysms
    • Cranial surgery
    • Craniopharyngioma
    • DIDMOAD syndrome
    • Erdheim-Chester disease
    • Gestational diabetes insipidus
    • Head injury
    • Histiocytosis X
    • Hypoxic encephalopathy
    • Intracranial space-occupying lesion
    • Meningoencephalitis
    • Meningoencephalitis
    • pineal tumors
    • Pituitary tumour
    • Sarcoidosis
    • Sheehan syndrome
    • Sickle cell disease
    • Skull fracture
• Diabetes mellitus type 1 or type 2
• Fanconi syndrome
• Hyperaldosteronism
• Hyperglycemia
• Hyperthyroidism
• Maturity onset diabetes of the young
• Medications especially diuretics. see also nephrogenic diabetes insipidus
  • Bendrofluazide
  • Bumetanide
  • Conivaptan
  • Furosemide
  • Hydrochlorothiazide
  • Lithium
  • Vasopressin
  • atropine
  • belladonna poisoning
  • caffeine
• Nephronophthisis
• Osmotic diuresis
  • Diabetes mellitus type 2
  • Hyperglycaemia
  • Isosorbide
  • Mannitol
  • Sorbitol
• Primary hyperparathyroidism
• Psychogenic polydipsia
• Sicca Syndrome
• Water intoxication

Complete differential diagnosis of the causes of polydipsia

(By organ system)

Cardiovascular	No underlying causes
Chemical / poisoning	belladonna poisoning
Dermatologic	No underlying causes
Drug Side Effect	Bendrofluazide, Bumetanide, Conivaptan, Frusemide,Hydrochlorothiazide, Lithium, Vasopressin, atropine, belladonna poisoning, caffeine
Ear Nose Throat	No underlying causes
Endocrine	Cushing syndrome, Primary hyperparathyroidism, Hyperglycemia Diabetes insipidus, Water intoxication, Hyperthyroidism, Maturity onset diabetes of the young, Diabetes mellitus, Antidiuretic Hormone
Environmental	No underlying causes
Gastroenterologic	No underlying causes
Genetic	Polycystic kidney disease(autosomal dominant), Congenital nephrogenicDiabetes insipidus, Bardet-Biedl syndrome, Sickle cell disease, DIDMOAD syndrome, Fanconi syndrome
Hematologic	No underlying causes
Iatrogenic	No underlying causes
Infectious Disease	No underlying causes
Musculoskeletal / Ortho	No underlying causes
Neurologic	No underlying causes
Nutritional / Metabolic	No underlying causes
Obstetric/Gynecologic	Gestational diabetes insipidus
Oncologic	No underlying causes
Opthalmologic	No underlying causes
Overdose / Toxicity	No underlying causes
Psychiatric	Psychogenic polydipsia
Pulmonary	No underlying causes
Renal / Electrolyte	Bardet-Biedl syndrome,Bartter syndrome,Cystinosis, Congenital nephrogenicDiabetes insipidus, Hypercalcaemia, Hypokalaemia, Interstitial nephritis, Loken Senior syndrome, Medullary cystic renal disease, Polycystic kidney disease(autosomal dominant), Proximal renal tubular acidosis,Pyelonephritis,Renal failure, Urinary tract infection
Rheum / Immune / Allergy	No underlying causes
Sexual	No underlying causes
Trauma	Head trauma
Urologic	No underlying causes
Miscellaneous	No underlying causes

Polydipsia in Psychiatric Subsets

Psychogenic polydipsia is a type of polydypsia with described in patients with mental illnesses and/or the developmentally disabled. It is present in a subset of schizophrenics. These patients, most often chronic schizophrenics with a long history of illness, often exhibit enlarged ventricles and shrunken cortex on MRI, making the physiological mechanism difficult to isolate from the psychogenic. It is a serious disorder and often leads to institutionalization as it can be very difficult to manage outside the inpatient setting. It should be taken very seriously - it can be life threatening as serum sodium is diluted to an extent that seizures and cardiac arrest can occur. Patients have been known to seek fluids from any source possible.

In treatment resistant polydipsic psychiatric patients, regulation in the inpatient milieau can be accomplished by use of a weight-water protocol. First, baseline weights must be established and correlated to serum sodium levels. Weight will normally fluctuate during the day, but as the water intake of the polydipsic goes up, the weight will naturally rise. The physician can order a stepped series of interventions as the weight rises. The correlation must be individualized with attention paid to the patient's normal weight and fluctuations, diet, co-morbid disorders (such as a seizure disorder) and urinary system functioning. Progressive steps might include redirection, room restriction, and increasing levels of physical restraint with monitoring. Such plans should also progressive increases in monitoring, as well as a level at which a serum sodium level is drawn.

It is important to note that the majority of psychotropic drugs (as well as many of other classes) can cause dry mouth, but this is not to be confused with true polydipsia in which a dangerous drop in serum sodium will be seen.

While psychogenic polydipsia is generally not found outside the population of those with serious mental disorders, there is some anecdotal evidence of a milder form (typically called 'habit polydispsia' or 'habit drinking') that can occasionally be found in the absence of psychosis or other mental conditions. The excessive levels of fluid intake may result in a false diagnosis of diabetes insipidus, since the chronic ingestion of excessive water can produce diagnostic results that closely mimic those of mild diabetes insipidus.

Diagnosis

Polydipsia is a symptom, not a disease (cause). To diagnose the cause of polydipsia a fluid deprivation test is used, which may require a patient to abstain from water, and for blood and urine tests to be undertaken. Additional blood work may be required to test for the presence of diuretics, such as caffeine, or recreational drugs. Finally neurological testing may be required to determine if there has been damage to the hypothalamus ( central diabetes insipidus). These tests are routinally used in diagnosing diabetes insipidus.

Treatment

Most patients with diabetes insipidus (DI) can drink enough fluid to replace their urine losses. Losses can also be replaced with dextrose and water or IV fluid hyposmolar to the patient's serum. During replacement, avoid volume overload and a correction of hypernatremia that is too rapid. A good rule of thumb is to reduce serum sodium by 0.5 mmol/L/h. Water deficit may be calculated based on the assumption that body water is approximately 60% of body weight in kilograms. In case of inadequate thirst, desmopressin is the drug of choice. Generally, it can be administered 2-3 times per day. Patients may require hospitalization to establish fluid needs. Frequent electrolyte monitoring is recommended. Vasopressin or desmopressin acetate, modified synthetic forms of antidiuretic hormone, may be taken as a nasal spray several times a day, to maintain a normal urine output. However, taking too much of this medication can cause fluid retention and swelling and other problems. Sometimes diabetes insipidus can be controlled with drugs that stimulate production of antidiuretic hormone such as chlorpropamide, carbamazepine, clofibrate. If nephrogenic DI is caused by medication (for example, lithium), stopping the medication may help restore normal kidney function. However, after many years of lithium use, the nephrogenic DI may be permanent. Hereditary nephrogenic DI and lithium-induced nephrogenic DI are treated by drinking enough fluids to match urine output and with drugs that lower urine output. Drugs used to treat nephrogenic DI include: Anti-inflammatory medication (indomethacin)and Diuretics (hydrochlorothiazide (HCTZ) and amiloride).

Johnfanisrour 19:14, 25 January 2009 (UTC) John Fani Srour Johnfanisrour 19:14, 25 January 2009 (UTC)