z-logo
Premium
Association of type II secretory phospholipase A 2 and surfactant protein D with the pulmonary oxygenation potential in patients with septic shock during polymyxin‐B immobilized fiber‐direct hemoperfusion
Author(s) -
Ishibe Yoriko,
Shibata Shigehiro,
Takahashi Gaku,
Suzuki Yasushi,
Inoue Yoshihiro,
Endo Shigeatsu
Publication year - 2017
Publication title -
journal of clinical apheresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.697
H-Index - 46
eISSN - 1098-1101
pISSN - 0733-2459
DOI - 10.1002/jca.21507
Subject(s) - hemoperfusion , ards , medicine , septic shock , polymyxin b , gastroenterology , pulmonary surfactant , sepsis , lung , immunology , anesthesia , biochemistry , chemistry , antibiotics , hemodialysis
This study was undertaken to analyze the association of type II secretory phospholipase A 2 (sPLA 2 ‐II) and surfactant protein D (SP‐D) with the pulmonary oxygenation potential in patients with septic shock during polymyxin‐B immobilized fiber‐direct hemoperfusion (PMX‐DHP). The study was conducted in 25 patients with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). PMX‐DHP lowered the blood endotoxin level in all patients. Following PMX‐DHP, there were decreases from day 0 → day 1 → day 2 in both the mean plasma sPLA 2 ‐II level (340 → 260 → 189 ng/mL) and plasma SP‐D level (483 → 363 → 252 ng/mL). The PaO2/FiO2 ratio ( P/F ratio) rose (210 → 237 → 262) in all patients. Upon the onset of ALI or ARDS, there was a significant negative correlation between the sPLA 2 ‐II level and the P/F ratio. Furthermore, there was a significant positive correlation between the sPLA 2 ‐II and TNF‐α levels. The results suggest that as the blood endotoxin levels were lowered by the PMX‐DHP, the inflammatory reactions were suppressed, with suppressed formation of sPLA 2 ‐II and improved pulmonary oxygenation potential. The results also suggested possible involvement of TNF‐α in the production of sPLA 2 ‐II.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here