Literature DB >> 17674097

Effects of neutrophil elastase inhibitor on progression of acute lung injury following esophagectomy.

Satoshi Ono1, Hironori Tsujimoto, Shu-Ichi Hiraki, Risa Takahata, Akifumi Kimura, Manabu Kinoshita, Takashi Ichikura, Hidetaka Mochizuki.   

Abstract

The purpose of this study was to evaluate the effect of sivelestat sodium hydrate, a selective inhibitor of neutrophil elastase in the systemic inflammatory response, pulmonary function, and the postoperative clinical course following esophagectomy. Patients with hypoxia associated with surgical stress in the intensive care unit (ICU) immediately after an esophagectomy were eligible for this study. The degree of hypoxia was calculated according to the ratio of arterial oxygen tension (PaO(2)) to the fractional concentration of inspired oxygen (FiO(2))-PaO(2)/FiO(2). Patients with PaO(2)/FiO(2) < 300 mmHg were enrolled in this study. Seven patients were treated with sivelestat, and 10 were not so treated. The degree of hypoxia, the criteria for systemic inflammatory response syndrome (SIRS), and the postoperative clinical course were compared between the two groups. The postoperative decreases in the PaO(2)/FiO(2) ratio were significantly suppressed in the sivelestat group (p < 0.05, by analysis of variance, or ANOVA). Furthermore, 9 of the 10 control group patients developed SIRS on postoperative day 2, whereas only 2 of 7 of the sivelestat group patients developed SIRS (p < 0.05). The postoperative increases in the heart rate were significantly suppressed in the sivelestat group (p < 0.05, ANOVA). The postoperative decreases in the platelet counts were significantly suppressed in the sivelestat group (p < 0.05, ANOVA). The duration of mechanical ventilation and the length of ICU stay for the sivelestat group were shorter than that for the control group. We demonstrated that the postoperative decreases in the PaO(2)/FiO(2) ratio following esophagectomy were significantly suppressed in the sivelestat-treated group. This clinical study showed that a neutrophil elastase inhibitor may thus be a potentially useful drug for treating acute lung injury following esophagectomy.

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Year:  2007        PMID: 17674097     DOI: 10.1007/s00268-007-9172-6

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  15 in total

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Authors:  K Kawabata; M Suzuki; M Sugitani; K Imaki; M Toda; T Miyamoto
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3.  Effects of a protease inhibitor on reduction of surgical stress in esophagectomy.

Authors:  S Ono; S Aosasa; H Mochizuki
Journal:  Am J Surg       Date:  1999-01       Impact factor: 2.565

4.  Activation of monocytes and endothelial cells depends on the severity of surgical stress.

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5.  Neutrophil elastase, MIP-2, and TLR-4 expression during human and experimental sepsis.

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6.  Sivelestat, a neutrophil elastase inhibitor, attenuates neutrophil priming after hepatoenteric ischemia in rabbits.

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  14 in total

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Review 2.  Effects of neutrophil elastase inhibitor in patients undergoing esophagectomy: a systematic review and meta-analysis.

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Review 3.  Neutrophil serine proteases fine-tune the inflammatory response.

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4.  A survey of the effects of sivelestat sodium administration on patients with postoperative respiratory dysfunction.

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7.  The effects of the early administration of sivelestat sodium, a selective neutrophil elastase inhibitor, on the postoperative course after radical surgery for esophageal cancer.

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8.  Preventive effect of sivelestat on postoperative respiratory disorders after thoracic esophagectomy.

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9.  Postoperative pneumonia causes the loss of skeletal muscle volume and poor prognosis in patients undergoing esophagectomy for esophageal cancer.

Authors:  Seiichiro Fujishima; Hironori Tsujimoto; Ken Nagata; Hidekazu Sugasawa; Shinsuke Nomura; Nozomi Ito; Manabu Harada; Takao Sugihara; Yusuke Ishibashi; Keita Kouzu; Hiroshi Shinmoto; Yoji Kishi; Hideki Ueno
Journal:  Gen Thorac Cardiovasc Surg       Date:  2020-09-10

10.  The alpha-lipoic acid derivative DHLHZn: a new therapeutic agent for acute lung injury in vivo.

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Journal:  Inflamm Res       Date:  2017-06-01       Impact factor: 4.575

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