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Approach to the patient with suspected hypotonic polyuria.

John D Newell-PriceJuliana Beaudette DrummondMark GurnellMiles LevyAnn I McCormackDeborah CooperJohn WassMirjam Christ-CrainJoseph G Verbalis
Published in: The Journal of clinical endocrinology and metabolism (2024)
Investigation and management of hypotonic polyura is a common challenge in clinical endocrinology. The three main causes, recently renamed to arginine vasopressin deficiency (AVP-D, formerly central diabetes insipidus), AVP-resistance (AVP-R, formerly nephrogenic diabetes insipidus), and primary polydipsia (PP) require accurate diagnosis as management differs for each. This new nomenclature more accurately reflects pathophysiology, and has now been adopted by the Systemised Nomenclature of Medicine (SNOMED). Advances in diagnosis over the last few years have centered around the use of copeptin measurement. Here, we use three patient case histories to highlight the use of this approach, and to demonstrate how it can succeed where other approaches, such as the water deprivation test, sometimes fail. We discuss the overall approach to each type of patient and the strengths and limitations of diagnostic strategies, illustrating the use of the new nomenclature.
Keyphrases
  • case report
  • type diabetes
  • cardiovascular disease
  • glycemic control
  • nitric oxide
  • pulmonary embolism
  • metabolic syndrome
  • mass spectrometry
  • adipose tissue