𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The kinetics of metamizol and its metabolites in critical-care patients with acute renal dysfunction

✍ Scribed by G. Heinemeyer; H. -J. Gramm; I. Roots; R. Dennhardt; W. Simgen


Publisher
Springer
Year
1993
Tongue
English
Weight
555 KB
Volume
45
Category
Article
ISSN
0031-6970

No coin nor oath required. For personal study only.

✦ Synopsis


We have studied the clearance of monomethylaminoantipyrine (MMAAP), the pharmacologically active form of metamizol, in 46 patients in surgical intensive care with different degrees of renal dysfunction. In 23 patients without any renal impairment, mean clearance was 2.8 ml.min-1 x kg-1. Twenty-one patients with acute renal impairment had a significantly reduced clearance of MMAAP (0.83 ml.min-1 x kg-1). There was also reduced clearance in four patients with septic shock (1.0 ml.min-1 x kg-1). Kinetics of the metabolites of MMAAP (N-formylaminoantipyrine (FAAP), aminoantipyrine (AAP), and its secondary product N-acetylaminoantipyrine (AcAAP)) were calculated. FAAP and AcAAP showed delayed invasion, which can be explained by reduced hepatic metabolic activity. The product of N-demethylation, AAP, was not significantly altered. The delayed elimination of monomethylaminoantipyrine can be explained by reduced hepatic function in parallel with acute renal failure due to disturbed cardiovascular function caused by septic shock. This may also lead to disturbed hepatic macro- and microperfusion associated with altered oxygen supply and oxygen consumption.