Endotoxin adsorption therapy for septic shock using polymyxin B-immobilized fibers (PMX): Evaluation by high-sensitivity endotoxin assay and measurement of the cytokine production capacity

被引:41
作者
Kojika, M
Sato, N
Yaegashi, Y
Suzuki, Y
Suzuki, K
Nakae, H
Endo, S
机构
[1] Iwate Med Univ, Sch Med, Dept Crit Care Med, Morioka, Iwate 0200807, Japan
[2] Iwate Med Univ, Sch Med, Dept Anesthesiol, Morioka, Iwate 0200807, Japan
[3] Akita Univ, Sch Med, Dept Integrated Med, Div Emergency & Crit Care Med, Akita 010, Japan
关键词
endotoxin; PMX; sepsis; shock; TNF-alpha;
D O I
10.1111/j.1744-9987.2006.00340.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Because of its low sensitivity, the conventional measurement method for endotoxin (ET) is not the most appropriate for monitoring the effect of ET adsorption therapy. Thus, the efficacy of ET adsorption therapy was investigated using a newly developed high-sensitivity ET assay method. The changes in the cytokine production capacity of whole blood were also examined. We treated 24 peritonitis patients who had developed postoperative septic shock with ET adsorption therapy using a column of polymyxin B-immobilized fibers (PMX) and their serum ET levels were measured using the high-sensitivity ET assay based on the kinetic turbidimetric Limulus assay. In addition, the changes in the tumor necrosis factor-(TNF-alpha) production capacity of whole blood following lipopolysaccharide (LPS) stimulation and clinical outcome in the study patients were also examined. The 28-day mortality rate was 12%. PMX-direct hemoperfusion (PMX-DHP) was associated with elevation of the mean arterial pressure and urine output, reduction in the mean dose requirement of vasopressor agents, and recovery from the shock state in all the patients. The PaO2/FIO2 ratio also showed significant improvement. Using the high-sensitivity ET assay, ET was detected in the blood of 20 out of the 24 patients (80%) before the PMX-DHP, and a significant reduction in the ET level was noted after the PMX-DHP. The TNF-alpha production capacity of whole blood, which was found to be lower in the septic shock patients than in healthy subjects, was significantly increased after PMX-DHP. Elimination of ET by PMX-DHP in septic shock patients was confirmed by the high-sensitivity ET assay. PMX-DHP is thus considered to be a useful adjuvant therapeutic technique in the treatment of septic shock. Also, PMX-DHP might alleviate the immunosuppression associated with severe sepsis.
引用
收藏
页码:12 / 18
页数:7
相关论文
共 24 条
[1]   E5 murine monoclonal antiendotoxin antibody in gram-negative sepsis - A randomized controlled trial [J].
Angus, DC ;
Birmingham, MC ;
Balk, RA ;
Scannon, PJ ;
Collins, D ;
Kruse, JA ;
Graham, DR ;
Dedhia, HV ;
Homann, S ;
MacIntyre, N .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (13) :1723-1730
[2]   A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotropin [J].
Annane, D ;
Sébille, V ;
Troché, G ;
Raphaël, JC ;
Gajdos, P ;
Bellissant, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (08) :1038-1045
[3]  
[Anonymous], 1963, JAMA
[4]   ASSOCIATION BETWEEN PROTECTIVE EFFICACY OF ANTI-LIPOPOLYSACCHARIDE (LPS) ANTIBODIES AND SUPPRESSION OF LPS-INDUCED TUMOR NECROSIS FACTOR-ALPHA AND INTERLEUKIN-6 [J].
BAUMGARTNER, JD ;
HEUMANN, D ;
GERAIN, J ;
WEINBRECK, P ;
GRAU, GE ;
GLAUSER, MP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (03) :889-896
[5]   CONTINUOUS VENOVENOUS HEMOFILTRATION WITH DIALYSIS REMOVES CYTOKINES FROM THE CIRCULATION OF SEPTIC PATIENTS [J].
BELLOMO, R ;
TIPPING, P ;
BOYCE, N .
CRITICAL CARE MEDICINE, 1993, 21 (04) :522-526
[6]  
BLINZLER L, 1991, CONTRIB NEPHROL, V93, P234
[7]   A CONTROLLED CLINICAL-TRIAL OF HIGH-DOSE METHYLPREDNISOLONE IN THE TREATMENT OF SEVERE SEPSIS AND SEPTIC SHOCK [J].
BONE, RC ;
FISHER, CJ ;
CLEMMER, TP ;
SLOTMAN, GJ ;
METZ, CA ;
BALK, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (11) :653-658
[8]  
CDC, 1990, JAMA-J AM MED ASSOC, V263, P937
[9]   Effect of hemoperfusion with polymyxin B-immobilized fiber on plasma endothelin-1 and endothelin-1 mRNA in monocytes from patients with sepsis [J].
Ebihara, I ;
Nakamura, T ;
Shimada, N ;
Shoji, H ;
Koide, H .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (06) :953-961
[10]  
EZOE E, 2001, JPN J CRIT CARE ENDO, V5, P150