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Cited by 753

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Catecholamines: Znediator of the Hypermetabolic Response to Thermal Injury

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WILMORE, DOUGLAS W., LONG, JAMES M., MASON, ARTHUR D., SKREEN, ROBERT W., PRUITT, BASIL A.·1974·Annals of Surgery

Abstract

Hypermetabolism characterizes the metabolic response to thermal injury and the extent of energy production is positively related to the rate of urinary catecholamine excretion. Alpha and beta adrenergic blockade decreased metabolism from 69.6 +/- 5.3 Kcal/m(2)/hr to 57.4 +/- 5.2 (p < 0.01), and infusion of 6 microgm epinephrine/minute in normal man significantly increased metabolic rate. Twenty noninfected burned adults with a mean burn size of 45% total body surface (range 7-84%) and four normal controls were studied in an environmental chamber at two or more temperatures between 19 and 33 C with vapor pressure constant at 11.88 mm Hg. All burn patients were hypermetabolic at all temperatures studied and their core and mean skin temperatures were significantly elevated above control values. Between 25 and 33 C ambient, metabolism was unchanged in controls and burns of less than 40% total body surface (48.9 +/- 4.6 Kcal/m(2)/hr vs. 48.9 +/- 4.5), but metabolic rate decreased in larger burns in the warmer environment (72.0 +/- 1.9 vs. 65.8 +/- 1.7, p < 0.001). At 21 C, metabolism and catecholamines increased, except in four nonsurvivors who became hypothermic with decreased catechol elaboration. Metabolic rate in ten patients with bacteremia was below predicted levels while catecholamines were markedly elevated suggesting interference with tissue uptake of the neurohormonal transmitters. Feeding burn patients or administering glucose and insulin improved nitrogen retention and altered substrate flow but did not significantly reduce urinary catecholamines or metabolic rate. Burned patients are internally warm, not externally cold, and catecholamines appear to mediate their increased heat production. Hypermetabolism may be modified by ambient temperature, infection, and pharmacologic means. Alterations in hypothalamic function due to injury, resulting in increased catecholamine elaboration, would explain the metabolic response to thermal injury.

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Metadata

Authors
WILMORE, D. W., LONG, J. M., MASON, A. D., SKREEN, R. W., & PRUITT, B. A.
Venue
Annals of Surgery
Published
1974-10
Volume
180
Issue
4
Pages
653-669
ISSN
0003-4932 (ISSN-L)
OpenAlex
W1967775253
Cited by
753
References
1
FWCI
18.02
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Catecholamines: Znediator of the Hypermetabolic Response to Thermal Injury. https://app.cochat.ai/papers/10.1097/00000658-197410000-00031
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WILMORE, D. W., LONG, J. M., MASON, A. D., SKREEN, R. W., & PRUITT, B. A. (1974). Catecholamines: Znediator of the Hypermetabolic Response to Thermal Injury. Annals of Surgery. https://doi.org/10.1097/00000658-197410000-00031

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