Diabetes insipidus is an uncommon condition characterized by polyuria
and polydipsia. The symptoms and biochemical changes of this condition
result from either a lack of antidiuretic hormone or renal insensitiv
ity to its effect. Failure to produce or release antidiuretic hormone
may result from cranial pathology, including trauma and surgery. The r
enal insensitivity to antidiuretic hormone that occurs in patients wit
h nephrogenic diabetes insipidus may be caused by genetic factors, dru
gs (especially lithium) or specific disease processes. Patients may co
mpensate for polyuria and nocturia by excessive water intake but show
marked decreases in urine specific gravity and osmolality. Patients wi
th severe and uncompensated symptoms develop marked dehydration, neuro
logic symptoms and encephalopathy. The water deprivation test is usefu
l in diagnosing diabetes insipidus and in differentiating neurogenic f
rom nephrogenic cases. Neurogenic diabetes insipidus may respond to na
sal administration of desmopressin. Nephrogenic diabetes insipidus req
uires good hydration and monitoring of body chemistry. Thiazides and a
miloride may relieve symptoms.