1990
DOI: 10.1001/archsurg.1990.01410200129021
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Cardiovascular and Neurohumoral Responses Following Burn Injury

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Cited by 57 publications
(16 citation statements)
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“…Other differences between the patterns of hormone release in children and adults are manifested in A II release. Whereas in children the peak of A II release was reached 6 h after admission, the peak of A II release in adults was not reached until the third day after injury ( Crum et al ., 1988 , 1990). The increase in A II concentration between 85 and 108 h in our study is also different from the adult response, but may be related to the severity of injury, since the surge in A II occurred more in the children with the biggest burns.…”
Section: Discussioncontrasting
confidence: 99%
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“…Other differences between the patterns of hormone release in children and adults are manifested in A II release. Whereas in children the peak of A II release was reached 6 h after admission, the peak of A II release in adults was not reached until the third day after injury ( Crum et al ., 1988 , 1990). The increase in A II concentration between 85 and 108 h in our study is also different from the adult response, but may be related to the severity of injury, since the surge in A II occurred more in the children with the biggest burns.…”
Section: Discussioncontrasting
confidence: 99%
“…With the exception of one study ( Crum et al ., 1990 ), the mean plasma concentration of AVP in admission blood samples was higher in our burn‐injured children than values reported for adults ( Shirani et al ., 1983 ; Morgan et al ., 1980 ; Crum et al ., 1988 ), although the mean burn size of the patients in this study was lower (20.5%). In spite of the high admission concentrations, AVP levels in the children returned to just above normal levels by 24–36 h after admission, earlier than reported in adults.…”
Section: Discussioncontrasting
confidence: 54%
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“…Numerous immunologic and endocrine factors have been found to be drastically different in serum obtained from burn patients when compared to control serum, such as: complement, C-reactive protein, interferon γ, TNF-α, interleukins-1β, 2, 4, 5, 6, 7, 8, 10, 12, 13, and 17, catecholamines, insulin-like growth factor-1 (IGF-1), IGF-1 binding protein-3 (IGFBP-3), growth hormone (GH), testosterone, thyroxine (T4), and cortisol (Crum et al, 1990; Jeffries and Vance, 1992; Jeschke et al, 2008; Merritt et al, 2012). Our data suggest that, despite large increases in circulating TNF-α and IL-6, the rise in these pro-inflammatory cytokines is not enough to activate downstream NFκB and STAT3 signaling in skeletal muscle for a prolonged period of time.…”
Section: Discussionmentioning
confidence: 99%