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Number of results

Journal

2012 | 7 | 4 | 475-480

Article title

Statins and hemoperfusion improve 28-day survival in septic shock patients

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EN

Abstracts

EN
Uncontrolled inflammation and endotoxin play a central role in septic shock. Statins may possess anti-inflammatory properties, and removal of endotoxin by hemoperfusion with polymyxin B-immobilized fiber (PMX-F) could have favorable effects on sepsis. We examined retrospectively whether pre-existing statin and hemoperfusion with PMX-F at the time of admission were separately and independently associated with decreased overall 28-day mortality in septic shock patients. Consecutive 173 patients with septic shock (71.2±10.7 years old, 115 male and 58 female) were included in the present study. All patients underwent a complete history and physical examination, determination of blood chemistries. Multiple stepwise regression analysis revealed that albumin, creatinine (inversely), statin use, hemoperfusion with PMX-F and HDL-cholesterol were independently correlated to 28-day survival in septic shock patients (R2=0.464). Our present study suggests that pre-existing statin use and hemoperfusion with PMX-F may separately and independently contribute to blunt the process of septic shock.

Keywords

Publisher

Journal

Year

Volume

7

Issue

4

Pages

475-480

Physical description

Dates

published
1 - 8 - 2012
online
24 - 5 - 2012

Contributors

  • Division of Nephrology, Department of Internal Medicine, Shinmatsudo Central General Hospital, Matsudo, 270-0034, Japan
author
  • Division of Nephrology, Department of Internal Medicine, Shinmatsudo Central General Hospital, Matsudo, 270-0034, Japan
  • Division of Nephrology, Department of Internal Medicine, Shinmatsudo Central General Hospital, Matsudo, 270-0034, Japan
  • Division of Nephrology, Department of Internal Medicine, Shinmatsudo Central General Hospital, Matsudo, 270-0034, Japan
author
  • Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume, 830-0011, Japan
  • Department of Chemistry, Keio University School of Medicine, Yokohama, 223-8521, Japan
  • Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume, 830-0011, Japan

References

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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11536-011-0169-z
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