CONTINUOUS ARTERIOVENOUS HEMOFILTRATION THERAPY FOR STAPHYLOCOCCUS-AUREUS-INDUCED SEPTICEMIA IN IMMATURE SWINE

Citation
Pa. Lee et al., CONTINUOUS ARTERIOVENOUS HEMOFILTRATION THERAPY FOR STAPHYLOCOCCUS-AUREUS-INDUCED SEPTICEMIA IN IMMATURE SWINE, Critical care medicine, 21(6), 1993, pp. 914-924
Citations number
24
Categorie Soggetti
Emergency Medicine & Critical Care
Journal title
ISSN journal
00903493
Volume
21
Issue
6
Year of publication
1993
Pages
914 - 924
Database
ISI
SICI code
0090-3493(1993)21:6<914:CAHTFS>2.0.ZU;2-Q
Abstract
Objectives. The goals of this study were: a) to evaluate the efficacy of controlled, continuous arteriovenous hemofiltration in improving mo rbidity and mortality rates in an immature swine model of Staphylococc us aureus-induced septicemia; b) to determine if ultrafiltrate from se ptic animals contained mediators that produce pathophysiologic changes observed in untreated S. aureus septic pigs. Design: Prospective, ran domized, controlled study with age-matched controls. Setting. U.S. Dep artment of Agriculture-licensed biomedical research facility.Subjects: Sixty-five weaned Poland-China swine (4 to 6 wks of age; 5 to 10 kg). Interventions. Part 1: Animals received a lethal dose of live S. aure us (8 x 10(9) colony-forming units/kg) over 1 hr. The three treatment groups included: hemofiltration group 1 (eight filtered, eight nonfilt ered animals), plasma filtration fraction = 5.5%; hemofiltration group 2 (six filtered, six nonfiltered animals), filtration fraction = 16.6 %; and hemofiltration group 3 (six filtered, six nonfiltered animals), filtration fraction = 33.4%. A control, nonseptic group of animals (n = 4) was filtered to obtain 'clean' ultrafiltrate (hemofiltration gro up 4). Part 2: Sterile ultrafiltrate concentrate batches obtained from each group of filtered, septic animals were concentrated and infused into healthy, nonseptic pigs (reinfusion groups 1 through 3). Measurem ents and Main Results. Physiologic, biochemical, and hematologic varia bles were measured in all animals every 1 to 3 hrs. Overall length of survival was also recorded. In hemofiltration groups 1 through 3, filt ered animals survived significantly longer than matched, nonfiltered ( sham-filtered) animals. Increments in survival time increased directly with filtration fraction. Ultrafiltrate concentrate from septic pigs produced death (LD41) and disease similar to those rates observed in u ntreated S. aureus-septic pigs. Infusion of clean ultrafiltrate concen trate produced no response. Conclusions: Continuous arteriovenous hemo filtration significantly improved survival rates in swine with S. aure us-induced sepsis. Resultant ultrafiltrate concentrate contained media tors responsible for some pathophysiologic responses observed in this animal model.