Literature DB >> 385911

Predicting fatal sepsis in burn patients.

C C Baker, C L Miller, D D Trunkey.   

Abstract

The high morbidity after severe thermal insult is believed to be related partially to a resultant decrease in immunocompetence. We tested the ability of phytohemagglutinin (PHA) and Concanavalin (Con A) to stimulate lymphocyte transformation in 17 patients with moderate to severe thermal injury (greater than 25% BSA). The patients acted as their own controls and the per cent change in their mitogen response was measured over time. Eight acutely burned patients who subsequently developed severe sepsis (Group I) had decreased ability (mean, 12% of normal) to proliferate in response to PHA, and six of these died of severe sepsis. The depressed response appeared 4 to 7 days postinjury and predated clinical evidence of sepsis by 2 to 4 days. Cells from four patients who had mild infectious complications (Group II) demonstrated greatly augmented mitogen responses (mean + 243%) approximately 7 to 10 days postinjury. Five burn patients whose clinical course was sepsis free (Group III) exhibited only minimal changes in their mitogen responses (mean +30%). Although the Con A responses of the patients' cells corresponded less to their pathology, Group I patients whose cells exhibited depressed PHA responsiveness also had diminished Con A responses. Group II patients' cells also showed increases in Con A-induced stimulation. Group III patients, who had only slightly augmented PHA responses, had minimal decreases of the Con A-induced lymphocyte transformation. Many severely burned patients develop septicemia as a result of their large wound surfaces. The appearance of decreases in mitogen-induced proliferation, however, appears to characterize those patients who will be unable to handle the septic challenge.

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Year:  1979        PMID: 385911     DOI: 10.1097/00005373-197909000-00001

Source DB:  PubMed          Journal:  J Trauma        ISSN: 0022-5282


  21 in total

1.  General surgery-epitomes of progress: burn management.

Authors:  R H Demling
Journal:  West J Med       Date:  1980-12

2.  Different lymphocyte compartments respond differently to mitogenic stimulation after thermal injury.

Authors:  E A Deitch; D Z Xu; L Qi
Journal:  Ann Surg       Date:  1990-01       Impact factor: 12.969

Review 3.  The Burn Wound Microenvironment.

Authors:  Lloyd F Rose; Rodney K Chan
Journal:  Adv Wound Care (New Rochelle)       Date:  2016-03-01       Impact factor: 4.730

4.  Peripheral blood lymphocytes from thermal injury patients are defective in their ability to generate lymphokine-activated killer (LAK) cell activity.

Authors:  G R Klimpel; D H Herndon; M D Stein
Journal:  J Clin Immunol       Date:  1988-01       Impact factor: 8.317

5.  Postburn impaired cell-mediated immunity may not be due to lazy lymphocytes but to overwork.

Authors:  E A Deitch; K N Landry; J C McDonald
Journal:  Ann Surg       Date:  1985-06       Impact factor: 12.969

6.  In vitro cell-mediated immunity after thermal injury is not impaired. Density gradient purification of mononuclear cells is associated with spurious (artifactual) immunosuppression.

Authors:  D Z Xu; E A Deitch; K Sittig; L Qi; J C McDonald
Journal:  Ann Surg       Date:  1988-12       Impact factor: 12.969

7.  Longitudinal assay of lymphocyte responsiveness in patients with major burns.

Authors:  A M Munster; R A Winchurch; W J Birmingham; P Keeling
Journal:  Ann Surg       Date:  1980-12       Impact factor: 12.969

8.  Effects of azithromycin in Pseudomonas aeruginosa burn wound infection.

Authors:  David P Nichols; Silvia Caceres; Lindsay Caverly; Cori Fratelli; Sun Ho Kim; Ken Malcolm; Katie R Poch; Milene Saavedra; George Solomon; Jennifer Taylor-Cousar; Samuel Moskowitz; Jerry A Nick
Journal:  J Surg Res       Date:  2013-02-24       Impact factor: 2.192

9.  Opsonic activity of blister fluid from burn patients.

Authors:  E A Deitch
Journal:  Infect Immun       Date:  1983-09       Impact factor: 3.441

10.  Bacterial translocation from the gastrointestinal tracts of rats receiving thermal injury.

Authors:  K Maejima; E A Deitch; R D Berg
Journal:  Infect Immun       Date:  1984-01       Impact factor: 3.441

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