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Polymyxin B hemoperfusion as a feasible therapy after source control in abdominal septic shock
Jin Joo Kim1, Young Jun Park2, Ki Yoon Moon2
1Division of Trauma and Surgical Critical Care, Department of Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 137-701, South Korea.
Background:
Polymyxin B hemoperfusion (PMX-HP) has been used as a treatment for intra-abdominal septic shock by absorbing and removing endotoxins of gram-negative bacilli.
Aim:
To investigate the clinical efficacy of PMX-HP in patients with gram-negative septic shock who underwent abdominal surgery.
Methods:
From January 2012 to December 2018, patients who had septic shock secondary to peritonitis were enrolled. They were classified into PMX-HP treated and control groups based on postopreative intervention using PMX-HP. The clinical outcomes were compared using 1:1 propensity score matching methods to balance the overall distribution between the two groups.
Results:
After propensity score matching, 40 patients were analyzed (20 patients in the PMX group and 20 patients in the control group). The scores of total Sequential Organ Failure Assessment (SOFA) score, renal SOFA and coagulation SOFA were significantly improved in the PMX group but not in the control group. (from 11.2 ± 5.8 to 4.7 ± 3.5 in PMX group vs 10.0 ± 4.0 to 8.7 ± 7.3 in control group, P = 0.047 from 2.6 ± 1.0 to 0.7 ± 1.0 in PMX group vs 2.6 ± 1.5 to 2.8 ± 1.6 in control group, P = 0.000, from 1.6 ± 1.5 to 1.3 ± 1.3 in PMX group vs 1.2 ± 1.2 to 2.8 ± 1.8 in control group, P = 0.014, respectively). Further, the length of intensive care unit (ICU) stay was significantly shorter in PMX group. However, no statistically significant difference was found in ICU mortality (50% in PMX group vs 50% in control group).
Conclusion:
PMX-HP is a feasible adjunct treatment for peritonitis in ICU patients with peritonitis for improved organ impairment and to stabilize hemodynamics. It would be helpful to enhance clinical outcomes especially in patients with complete elimination of the source of gram-negative bacilli infection by surgical procedure accompanied with conventional treatment of sepsis.
Insights
Polymyxin B hemoperfusion (PMX-HP) improved organ function and reduced ICU stay in patients with gram-negative septic shock. However, PMX-HP did not significantly impact ICU mortality rates in this study.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Nephrology
Background:
- Polymyxin B hemoperfusion (PMX-HP) is utilized to treat intra-abdominal septic shock by removing endotoxins from gram-negative bacteria.
- Gram-negative bacilli are a common cause of severe infections, leading to sepsis and septic shock.
Purpose of the Study:
- To evaluate the clinical effectiveness of PMX-HP in patients experiencing gram-negative septic shock post-abdominal surgery.
- To assess the impact of PMX-HP on organ function, length of stay, and mortality in this patient population.
Main Methods:
- A cohort of patients with septic shock secondary to peritonitis was studied between January 2012 and December 2018.
- Patients were divided into PMX-HP treated and control groups, with 1:1 propensity score matching employed to balance baseline characteristics.
- Clinical outcomes, including Sequential Organ Failure Assessment (SOFA) scores and intensive care unit (ICU) mortality, were compared between groups.
Main Results:
- After propensity score matching, 40 patients (20 per group) were analyzed.
- The PMX-HP group showed significant improvements in total SOFA, renal SOFA, and coagulation SOFA scores compared to the control group.
- While the length of ICU stay was significantly shorter in the PMX-HP group, ICU mortality rates were similar between the groups (50% in both).
Conclusions:
- Polymyxin B hemoperfusion (PMX-HP) is a viable adjunctive therapy for ICU patients with peritonitis, improving organ impairment and hemodynamic stability.
- PMX-HP may enhance clinical outcomes, particularly when combined with surgical source control and conventional sepsis treatment in gram-negative infections.
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