The measurement of urine concentration provides information concerning the
kidney's ability to appropriately respond to variations in fluid homeostasi
s. It also assists in the interpretation of other tests performed on the sa
me urine specimen. The gold standard of estimating urinary concentration is
the measurement of its osmolality; however, this procedure is not readily
available to the practicing physician. Therefore, urine concentration is us
ually determined by measurement of its specific gravity (SG), which provide
s a fair estimate of urine osmolality. Over thee years numerous tests have
been developed to measure urine SG in a simple, quick, reliable and easily
available method. These tests measure SG either directly (e.g., gravimetry)
or by indirect methods (e.g., refractometry and reagent strip). All these
tests have certain limitations based on their underlying physical principle
s. Specific gravity as measured by refractometry is influenced by proteinur
ia, such that for each 10 g/l protein the SG increases by 0.003. SG is also
influenced by glucosuria such that it increases by approximately 0.002 per
10 g/l glucose when compared with urinary osmolality. Unlike osmolality, w
hich is only affected by the number of particles, refractometry is affected
by number, mass and chemical structure of the dissolved particles; hence l
arge molecules like radiographic contrast or mannitol will increase SG rela
tive to osmolality. The reagent strip is minimally affected by glucose, man
nitol or radiographic contrast. However, it is affected by urinary pH such
that only urine in the pH range of SG by reagent strip is based on the ioni
c strength of the urine and thus is significantly affected by the ionic com
position of the urine and by proteins which have an electric charge in solu
tion. In our experience, SG measured by the refractometer is consistently m
ore accurate than the reagent strip. For the clinician who is interpreting
urine SG results, it is important to be aware of these limitations and unde
rstand the reasons for possible potential errors of each particular method.