Hypervolemia

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Hypervolemia
ICD-10	E 87.7
ICD-9	276.6

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

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

Overview

Hypervolemia (or "Fluid overload") is the medical condition where there is too much fluid in the blood. The fluid can either be intravascular or extravascular and result in edema.

The opposite condition is Hypovolemia (too little fluid volume in the blood).

Related chapters

volume status
edema
anasarca (swelling of skin)
ascites (excess fluid in the peritoneal cavity)
pleural effusion (excess fluid in the pleural cavity)

Resources

CRISP Thesaurus 00004009
DDB 6534

v • d • e Metabolic pathology / Inborn error of metabolism (E70-90, 270-279)
Amino acid	Aromatic (Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism, Histidinemia) - Branched chain (Maple syrup urine disease, Propionic acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency, Citrullinemia, Argininosuccinic aciduria, Hyperammonemia) - Glutaric acidemia type 1 - Sarcosinemia
Carbohydrate	Lactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) - other intestinal carbohydrate absorption (Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria
Lipid storage	Sphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)
Other lipid	Lipoprotein/lipidemias: Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia Fatty acid: Adrenoleukodystrophy - Carnitine (Primary, I, II)
Mineral	Cu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO₄³⁻ Hypophosphatemia/Hypophosphatasia - Mg²⁺ Hypermagnesemia/Hypomagnesemia - Ca²⁺ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism
Fluid, electrolyte and acid-base balance	Electrolyte disturbance - Na⁺ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base balance - H₂O Dehydration/Hypervolemia - K⁺ Hypokalemia/Hyperkalemia - Cl⁻ Hyperchloremia/Hypochloremia
Purine and pyrimidine	Hyperuricemia - Lesch-Nyhan syndrome - Xanthinuria
Porphyrin	Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate
Bilirubin	Unconjugated (Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome)
Glycosaminoglycan	Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly
Glycoprotein	Mucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
Other	Alpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia