Impact of different modalities of continuous venovenous hemofiltration on sepsis-induced alterations in experimental pancreatitis

被引:38
作者
Yekebas, EF
Strate, T
Zolmajd, S
Eisenberger, CF
Erbersdobler, A
Saalmüller, A
Steffani, K
Busch, C
Elsner, HA
Engelhardt, M
Gillesen, A
Meins, J
The, M
Knoefel, WT
Izbicki, JR
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Surg, D-20246 Hamburg, Germany
[2] Univ Hamburg, Hosp Eppendorf, Dept Pathol, D-20246 Hamburg, Germany
[3] Univ Hamburg, Hosp Eppendorf, Dept Med Microbiol & Immunol, D-20246 Hamburg, Germany
[4] Fed Res Ctr Virus Dis Anim, D-7400 Tubingen, Germany
关键词
hemofiltration; pancreatogenic sepsis; organ failure; immunology; inflammation; multiple organ dysfunction; necrotizing pancreatitis;
D O I
10.1046/j.1523-1755.2002.00607.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Continuous venovenous hemofiltration (CVVH) is assumed to attenuate systemic complications in septic diseases. The impact of different treatment intensities of CVVH on immunologic and systemic alterations in experimental pancreatitis was evaluated. Methods. Eighty-four minipigs were allocated either to an untreated control group (group 1) or to one of six treatment groups (groups 2 to 7) that underwent CVVH in different modalities: (1): "late" CVVH, started after a decline of total peripheral resistance of 30% versus "prophylactic" CVVH started immediately after the induction of pancreatitis; (2) no change of hemofilters versus a periodic change of filters every 12 hours; (3) low-volume CVVH with a filtrate turnover of 20 mL/kg body weight (BW)/h versus high-volume CVVH (100 mL/kg/h). Pancreatitis was induced by intraductal injection of sodium-taurocholate (3%, 1 mL/kg BW) and enterokinase (2 U/kg BW). We focused on the occurrence of sepsis, serum cytokines, down-regulation of major histocompatibility complex II (MHC II) and the endotoxin receptor CD14 expression, bacterial translocation/endotoxemia, and pulmonary and renal histologic alterations. Results. CVVH delayed or definitively prevented the occurrence of sepsis. Pancreatitis was associated with a tremendous initial tumor necrosis factor-alpha (TNF-alpha) response prior to a return to near baseline levels in the late course of sepsis. Endotoxin hyporesponsiveness, suggested by the dissociation of decreasing TNF-alpha levels and increasing endotoxemia in end-stage sepsis, was favorably influenced by CVVH. Down-regulation of MHC II and CD14 expression was prevented in non-septic animals. CVVH-related sepsis-protection led to a significant attenuation of histological injury in lungs and kidneys. "Prophylactic" CVVH prevented histological changes more effectively than "late" CVVH. Conclusions. CVVH offers a therapeutic option for supportive treatment in severe pancreatitis. The efficiency of CVVH is associated with the duration of filter use and cumulative plasma turnover. Since CVVH may lead to sepsis-protection and long-term survival, further evaluation in controlled, clinical trials is warranted.
引用
收藏
页码:1806 / 1818
页数:13
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