Literature DB >> 10869822

The relationship between tumor necrosis factor (TNF)-alpha and survival following granulocyte-colony stimulating factor (G-CSF) administration in burn sepsis.

E Arslan1, M Yavuz, C Dalay.   

Abstract

Blood levels of tumor necrosis factor (TNF)-alpha were determined in 78 patients with burn sepsis. Of these patients, 51 were managed with additional administration of granulocyte colony-stimulating factor (G-CSF) in addition to routine treatment procedures (group A), while 27 received only routine treatment (group B). G-CSF was administrated for at least nine and at most 14 days; doses were gradually decreased in each 3 day period. On the 1st, 4th, 7th, 10th and 15th days, blood levels of TNF-alpha were determined. We sought to determine whether TNF alpha levels had a prognostic value in the management of burn induced sepsis that was treated with G-CSF. In our study, patients with gradually decreasing TNF-alpha levels in the second 3 day period, were strong candidates for survival, because TNF-alpha levels decreased little in nonsurvivors but decreased greatly in survivors. The survival rate was 42/51 (82.3%) in group A and 9/27 (33.3%) in group B. In conclusion, G-CSF had positive effects on survival, and TNF-alpha was a predictor of prognosis in burn-induced sepsis.

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Year:  2000        PMID: 10869822     DOI: 10.1016/s0305-4179(00)00024-3

Source DB:  PubMed          Journal:  Burns        ISSN: 0305-4179            Impact factor:   2.744


  7 in total

1.  Innate immunity SNPs are associated with risk for severe sepsis after burn injury.

Authors:  Robert C Barber; Ling-Yu E Chang; Brett D Arnoldo; Gary F Purdue; John L Hunt; Jureta W Horton; Corinne C Aragaki
Journal:  Clin Med Res       Date:  2006-12

Review 2.  The systemic immune response to pediatric thermal injury.

Authors:  Racheal A Devine; Zachary Diltz; Mark W Hall; Rajan K Thakkar
Journal:  Int J Burns Trauma       Date:  2018-02-05

3.  TLR4 and TNF-alpha polymorphisms are associated with an increased risk for severe sepsis following burn injury.

Authors:  R C Barber; C C Aragaki; F A Rivera-Chavez; G F Purdue; J L Hunt; J W Horton
Journal:  J Med Genet       Date:  2004-11       Impact factor: 6.318

4.  Regulation of Key Immune-Related Genes in the Heart Following Burn Injury.

Authors:  Jake J Wen; Keyan Mobli; Geetha L Radhakrishnan; Ravi S Radhakrishnan
Journal:  J Pers Med       Date:  2022-06-20

5.  Adenosine triphosphate hydrolysis reduces neutrophil infiltration and necrosis in partial-thickness scald burns in mice.

Authors:  Jill Bayliss; Sara Delarosa; Jianfeng Wu; Jonathan R Peterson; Oluwatobi N Eboda; Grace L Su; Mark Hemmila; Paul H Krebsbach; Paul S Cederna; Stewart C Wang; Chuanwu Xi; Benjamin Levi
Journal:  J Burn Care Res       Date:  2014 Jan-Feb       Impact factor: 1.845

6.  Magnolol protects against acute gastrointestinal injury in sepsis by down-regulating regulated on activation, normal T-cell expressed and secreted.

Authors:  Shi-Hao Mao; Dan-Dan Feng; Xi Wang; Yi-Hui Zhi; Shu Lei; Xi Xing; Rong-Lin Jiang; Jian-Nong Wu
Journal:  World J Clin Cases       Date:  2021-12-06       Impact factor: 1.337

7.  Predicting and managing sepsis in burn patients: current perspectives.

Authors:  Omar Nunez Lopez; Janos Cambiaso-Daniel; Ludwik K Branski; William B Norbury; David N Herndon
Journal:  Ther Clin Risk Manag       Date:  2017-08-29       Impact factor: 2.423

  7 in total

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