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Algorithms for differentiating the three major types of diabetes insipidus (DI). In a patient with polydipsia and polyuria, a 24-hour urine osmolarity less than 300 mOsm/L and a negative test for glucosuria, there are two ways to determine the type of DI. One is to measure plasma arginine vasopressin (AVP) under conditions of unrestricted fluid intake. If it is high (>2.5 pg/mL) when the urine is dilute, the patient has renal (nephrogenic) DI and an MRI of the brain is not necessary. However, if plasma AVP is low (<1 pg/mL), a brain MRI to determine if the hyperintense signal (“bright spot”) normally emitted by the posterior pituitary (PP) is present or absent will indicate whether the patient has primary polydipsia or pituitary DI. It may also reveal evidence of pathology responsible for the disorder. The other way to differentiate DI is to perform a fluid deprivation test with hourly measurements of urine osmolarity Source: Disorders of Water Metabolism, Pediatric Endocrinology and Inborn Errors of Metabolism, 2e as well as plasma osmolarity or plasma sodium. If the urine osmolarity does not rise above 300 mOsm/L before plasma osmolarity or sodium reach the Sarafoglou K, range, Hoffmann GF, polydipsia Roth KS. Pediatric Endocrinology Inborn Errors Metabolism, 20172 Available at:the injection of upper limit ofCitation: the normal reference primary is excluded and repeat and measurements of of urine osmolarity2e; 1 and hours after http://mhmedical.com/ Accessed: June 10, 2017 desmopressin suffice to determine if the patient has severe pituitary or severe nephrogenic DI. However, if fluid deprivation results in concentration of the © 2017 McGraw-Hill Education. All rights urine before Copyright plasma osmolarity or sodium reach the upper limit reserved of normal, repeat measurements of plasma AVP as well as plasma and urine osmolarity before and after an infusion of 3% saline will be necessary to reliably distinguish between primary polydipsia, partial pituitary DI, and partial nephrogenic DI