N-acetylcysteine increases cerebral perfusion pressure in pigs with fulminant hepatic failure

Citation
Lm. Ytrebo et al., N-acetylcysteine increases cerebral perfusion pressure in pigs with fulminant hepatic failure, CRIT CARE M, 29(10), 2001, pp. 1989-1995
Citations number
33
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
29
Issue
10
Year of publication
2001
Pages
1989 - 1995
Database
ISI
SICI code
0090-3493(200110)29:10<1989:NICPPI>2.0.ZU;2-Y
Abstract
Objective. Intravenous administration of N-acetylcysteine beyond 15 hrs red uces mortality rates in patients suffering from paracetamol-induced fulmina nt hepatic failure, although the mechanism of the therapeutic benefit remai ns unclear. We hypothesized increased survival to be caused by improved hem odynamic performance. The main objective for the study was to explore the e ffect of Af-acetylcysteine on hemodynamics, oxygen transport, and regional blood flow in pigs with fulminant hepatic failure. Design: Prospective, randomized, controlled trial. Setting. Surgical research laboratory in a university hospital. Subjects., Female Norwegian Landrace pigs. Interventions: Fulminant hepatic failure was induced by a total liver devas cularization procedure. Five hours later, the pigs were allocated to N-acet ylcysteine treatment (150 mg.kg(-1) in 100 mL of 0.9% saline over 15 mins, followed by 50 mg.kg(-1) in 500 mL of 0.9% saline over a period of 4 hrs) o r placebo. Measurements and Main ResultsMean arterial pressure stabilized in the N-ace tylcysteine group and increased slightly during the last 2 hrs (P-GT = .009 ). Thus, mean arterial pressure was significantly higher compared with plac ebo after 3 hrs (p = .01). Cerebral perfusion pressure was significantly hi gher during the last 2 hrs in the N-acetylcysteine group (POT = .033). Comm on carotid artery flow also increased and was maintained at a higher level compared with placebo (p(GT) = .027). Systemic vascular resistance index in itially decreased but then gradually increased (PGT < .001). Cardiac index increased after 15 mins of N-acetylcysteine infusion, causing a significant interaction (PGT = .038), but did not differ after 3 hrs. No significant d ifferences in hindleg and mesentery hemodynamics were found. A short-lived increase in oxygen delivery caused by a temporary increase in cardiac index was observed but without any corresponding increase in oxygen consumption. Conclusions. Intravenous N-acetylcysteine infusion increases cerebral perfu sion pressure in pigs with fulminant hepatic failure. Earlier reported effe cts on oxygen transport and uptake could not be confirmed.