TY - JOUR
T1 - Potential survival benefit of polymyxin B hemoperfusion in patients with septic shock
T2 - A propensity-matched cohort study
AU - and Japan Septic Disseminated Intravascular Coagulation (JSEPTIC DIC) study group
AU - Nakamura, Yoshihiko
AU - Kitamura, Taisuke
AU - Kiyomi, Fumiaki
AU - Hayakawa, Mineji
AU - Hoshino, Kota
AU - Kawano, Yasumasa
AU - Yamasaki, Reiko
AU - Nishida, Takeshi
AU - Mizunuma, Mariko
AU - Ishikura, Hiroyasu
AU - Saito, Shinjiro
AU - Uchino, Shigehiko
AU - Kudo, Daisuke
AU - Mayumi, Toshihiko
AU - Azuhata, Takeo
AU - Ito, Fumihito
AU - Yoshihiro, Shodai
AU - Katsura, Hayakawa
AU - Nakashima, Tsuyoshi
AU - Ogura, Takayuki
AU - Noda, Eiichiro
AU - Sekine, Ryosuke
AU - Yamakawa, Kazuma
AU - Yoshikawa, Yoshiaki
AU - Sekino, Motohiro
AU - Ueno, Keiko
AU - Okuda, Yuko
AU - Watanabe, Masayuki
AU - Tampo, Akihito
AU - Saito, Nobuyuki
AU - Kitai, Yuya
AU - Takimoto, Kohei
AU - Takahashi, Hiroki
AU - Kobayashi, Iwao
AU - Kondo, Yutaka
AU - Sanui, Masamitsu
AU - Iizuka, Yusuke
AU - Matsunaga, Wataru
AU - Nachi, Sho
AU - Miike, Toru
AU - Takahashi, Hiroshi
AU - Takauji, Shuhei
AU - Umakoshi, Kensuke
AU - Todaka, Takafumi
AU - Kodaira, Hiroshi
AU - Andoh, Kohkichi
AU - Kasai, Takehiko
AU - Iwashita, Yoshiaki
AU - Arai, Hideaki
AU - Murata, Masato
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/6/7
Y1 - 2017/6/7
N2 - Background: The purpose of this study was to investigate whether polymyxin B hemoperfusion (PMX-HP) improves the survival of patients with septic shock. Methods: This was a retrospective, multicenter study conducted on patients treated during a 3-year period. We performed propensity-score analyses of the Japan Septic Disseminated Intravascular Coagulation (JSEPTIC DIC) study database. The study included data on 1723 patients with septic shock aged 16 years or older. Furthermore, we divided patients into to PMX-HP- and non-PMX-HP-treated groups. The primary endpoint was all-cause hospital mortality; secondary endpoints included intensive care unit (ICU) mortality and number of ICU-free days (ICUFDs) in the first 28 days. Results: Of 1,723 eligible patients, 522 had received PMX-HP. Propensity score matching created 262 matched pairs (i.e., 262 patients in each of the non-PMX-HP and PMX-HP groups). The proportion of all-cause hospital mortality was significantly lower in the PMX-HP group than in the non-PMX-HP group (32.8% vs. 41.2%; odds ratio (OR): 0.681; 95% confidence interval (CI): 0.470-0.987; P = 0.042). The number of ICUFD in the first 28 days was significantly higher in the PMX-HP group than in the non-PMX-HP group (18 (0-22) vs. 14 (0-22) days, respectively; P = 0.045). On the other hand, there was no significant difference in ICU mortality between the two groups (21.8% vs. 24.4%; OR: 0.844; CI: 0.548-1.300; P = 0.443). Conclusions: Our results strongly suggest that PMX-HP reduces all-cause hospital mortality and length of ICU stay in patients with septic shock.
AB - Background: The purpose of this study was to investigate whether polymyxin B hemoperfusion (PMX-HP) improves the survival of patients with septic shock. Methods: This was a retrospective, multicenter study conducted on patients treated during a 3-year period. We performed propensity-score analyses of the Japan Septic Disseminated Intravascular Coagulation (JSEPTIC DIC) study database. The study included data on 1723 patients with septic shock aged 16 years or older. Furthermore, we divided patients into to PMX-HP- and non-PMX-HP-treated groups. The primary endpoint was all-cause hospital mortality; secondary endpoints included intensive care unit (ICU) mortality and number of ICU-free days (ICUFDs) in the first 28 days. Results: Of 1,723 eligible patients, 522 had received PMX-HP. Propensity score matching created 262 matched pairs (i.e., 262 patients in each of the non-PMX-HP and PMX-HP groups). The proportion of all-cause hospital mortality was significantly lower in the PMX-HP group than in the non-PMX-HP group (32.8% vs. 41.2%; odds ratio (OR): 0.681; 95% confidence interval (CI): 0.470-0.987; P = 0.042). The number of ICUFD in the first 28 days was significantly higher in the PMX-HP group than in the non-PMX-HP group (18 (0-22) vs. 14 (0-22) days, respectively; P = 0.045). On the other hand, there was no significant difference in ICU mortality between the two groups (21.8% vs. 24.4%; OR: 0.844; CI: 0.548-1.300; P = 0.443). Conclusions: Our results strongly suggest that PMX-HP reduces all-cause hospital mortality and length of ICU stay in patients with septic shock.
KW - Intensive care unit-free days
KW - Mortality
KW - Polymyxin B hemoperfusion
KW - Propensity score matching
KW - Septic shock
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U2 - 10.1186/s13054-017-1712-3
DO - 10.1186/s13054-017-1712-3
M3 - Article
C2 - 28592318
AN - SCOPUS:85020460491
SN - 1364-8535
VL - 21
JO - Critical Care
JF - Critical Care
IS - 1
M1 - 134
ER -