Iohexol (024)

The purpose of the scheme is to evaluate the performance of the participants’ analysis results by interlaboratory comparison (consensus value).

The scheme is aimed for clinical laboratories that measure iohexol for the examination of glomerular filtration rate.

The participants measure the iohexol concentration in the samples with the option to calculate and report the glomerular filtration rate based on additional patient information provided in the round.

The test material consists of plasma with addition of iohexol.

Test material: 2 /round

Frequency: 4/year

Reports: Normally within one month from closing date.

Examinations
P—Iohexol
Pt—GFR (Iohexol) absolute
Pt—GFR (Iohexol) relative

Swedish laboratories register on our Swedish site. Laboratories from Denmark or Norway register through their national distributors, DEKS (Denmark) or Noklus (Norway). Laboratories from other countries register through Aurevia, our distributor outside Scandinavia. Please, note that the scheme may not be available in all countries.