Literature DB >> 17362765

Reducing ischemia-reperfusion injury in clinical lung transplantation.

H B Bittner1, C Binner, P Dahlberg, F W Mohr.   

Abstract

OBJECTIVE: Acute graft dysfunction secondary to ischemia-reperfusion injury (IRI) continues to be the most common cause of early mortality after lung transplantation. The perioperative management with aprotinin could decrease the incidence of severe IRI.
METHODS: A retrospective analysis was conducted of the data from 180 patients who underwent either single lung (56%) or bilateral sequential lung transplantation for similar end-stage lung disease between 1997 and 2005. The most recent 68 patients were managed perioperatively with the high-dose aprotinin infusion regimen (aprotinin group). The ISHLT grade III injury score was used for the diagnosis of severe IRI, which is based on a Pao(2)-FIo(2) ratio of less than 200 mmHg.
RESULTS: Grade III injury was observed in 18% of the patients who were not managed with aprotinin (control group, 152 grafts, 64% single transplants, 68% male, 54 +/- 8 years of age). Early ECMO support was required in 25% of these patients. The associated mortality rate was 40%. Despite significantly longer cold ischemic times (290 +/- 14 minutes vs 231 +/- 14 minutes), older donors (42 +/- 12 years of age), and more frequently observed severely elevated systolic PAP of greater than 60 mmHg (60% vs 48%) as well as more frequently required extracorporeal circulatory support (24%* vs 12%) in the aprotinin group, the incidence of severe IRI (8%) and associated mortality (9%) was markedly reduced.
CONCLUSIONS: The use of aprotinin in LTX surgery, which had strong beneficial effects on patient outcomes, significantly decreased the incidence of severe posttransplant IRI.

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Mesh:

Year:  2007        PMID: 17362765     DOI: 10.1016/j.transproceed.2006.12.005

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  6 in total

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Journal:  Am J Transl Res       Date:  2015-02-15       Impact factor: 4.060

2.  Infusion of mesenchymal stem cells protects lung transplants from cold ischemia-reperfusion injury in mice.

Authors:  Weijun Tian; Yi Liu; Bai Zhang; Xiangchen Dai; Guang Li; Xiaochun Li; Zhixiang Zhang; Caigan Du; Hao Wang
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3.  Estradiol worsens the syndrome of ischemia-reperfusion injury in an experimental lung transplantation model.

Authors:  Norberto Santana-Rodríguez; Bernardino Clavo; Pedro Llontop; Ana López; José Manuel García-Castellano; Rubén P Machín; Miguel A Ponce; María D Fiuza; Ricardo García-Herrera; Yanira Brito; Nagib Atallah Yordi; Ricardo Chirino
Journal:  Lung       Date:  2011-03-25       Impact factor: 2.584

4.  Autologous transplantation of adipose-derived mesenchymal stem cells markedly reduced acute ischemia-reperfusion lung injury in a rodent model.

Authors:  Cheuk-Kwan Sun; Chia-Hung Yen; Yu-Chun Lin; Tzu-Hsien Tsai; Li-Teh Chang; Ying-Hsien Kao; Sarah Chua; Morgan Fu; Sheung-Fat Ko; Steve Leu; Hon-Kan Yip
Journal:  J Transl Med       Date:  2011-07-22       Impact factor: 5.531

5.  A Case of Fatal Acute Lung Injury after Balloon Valvuloplasty of Pulmonary Stenosis: Case Report and Review of Literature.

Authors:  Mohammad Ali Ostovan; Maliheh Kamali; Abdolali Zolghadrasli
Journal:  J Cardiovasc Thorac Res       Date:  2015

6.  Xenogeneic and Allogeneic Mesenchymal Stem Cells Effectively Protect the Lung Against Ischemia-reperfusion Injury Through Downregulating the Inflammatory, Oxidative Stress, and Autophagic Signaling Pathways in Rat.

Authors:  Kun-Chen Lin; Jun-Ning Yeh; Yi-Ling Chen; John Y Chiang; Pei-Hsun Sung; Fan-Yen Lee; Jun Guo; Hon-Kan Yip
Journal:  Cell Transplant       Date:  2020 Jan-Dec       Impact factor: 4.064

  6 in total

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