Do Fentanyl and Morphine Influence Body Temperature After Severe Burn Injury?

被引:7
作者
Kahn, Steven Alexander [2 ]
Beers, Ryan J. [2 ]
Lentz, Christopher W. [1 ]
机构
[1] Univ New Mexico, Dept Surg, Hlth Sci Ctr, Albuquerque, NM 87131 USA
[2] Univ Rochester, Med Ctr, Dept Surg, Rochester, NY 14642 USA
关键词
BROWN ADIPOSE-TISSUE; CARDIOPULMONARY BYPASS; RATS; MICE; THERMOREGULATION; HYPERTHERMIA; INVOLVEMENT; DEPENDENCE; LEUKOCYTES; RECEPTOR;
D O I
10.1097/BCR.0b013e31820aaf7f
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Fentanyl lacks the antiinflammatory properties of morphine. Morphine attenuates the inflammatory response through differential stimulation of mu-receptor subtypes. Patients who receive morphine during coronary artery bypass graft have been shown to experience less postoperative fever than those who receive fentanyl. Patients who receive continuous fentanyl infusions in increased room temperatures after thermal injury may be at increased risk to experience higher body temperature than those who receive morphine. The records of 28 patients with >20% TBSA burn in 30 intensive care unit rooms (13 received fentanyl and 15 received morphine or hydromorphone) and 12 trauma patients who received fentanyl in 22 degrees C intensive care unit rooms were reviewed. Mean maximum core temperature and percentage of temperature recordings > 39 degrees C in the first 48 hours of admission were compared between burn patients who received fentanyl, those who did not, and with trauma patients. Burn patients exposed to fentanyl experienced significantly higher temperatures (40.1 +/- 0.9 degrees C) compared with those given morphine (38.7 +/- 0.8 degrees C) and compared with trauma patients (37.5 +/- 2.4 degrees C), P < .01 and P < .001, respectively. Burn patients on fentanyl had temperatures > 39 degrees C for a higher percentage of time (33 +/- 27%) than those without fentanyl (7.2 +/- 13%) and trauma patients (1 +/- 2.8%), P < .01 and P < .001, respectively. No differences in other medications administered, acute physiology and chronic health evaluation II scores, or the number of infections that could account for temperature disparities between groups existed. Burn patients who receive fentanyl in 30 degrees C rooms experience higher body temperatures and are febrile for a higher percentage of time than those receiving morphine only. Morphine has well-established antiinflammatory properties and likely attenuates the postburn inflammatory response more than fentanyl, resulting in lower body temperatures. This phenomenon needs to be further investigated in additional studies. (J Burn Care Res 2011; 32: 309-316)
引用
收藏
页码:309 / 316
页数:8
相关论文
共 26 条
[1]   THE OPIOID SYSTEM AND TEMPERATURE REGULATION [J].
ADLER, MW ;
GELLER, EB ;
ROSOW, CE ;
COCHIN, J .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1988, 28 :429-449
[2]  
Adler MW, 1993, HDB EXPT PHARM, P205
[3]   Effect of morphine on lipopolysaccharide-induced tumor necrosis factor-alpha production in vivo: Involvement of the sympathetic nervous system [J].
Bencsics, A ;
Elenkov, IJ ;
Vizi, ES .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 73 (1-2) :1-6
[4]   Morphine's immunoregulatory actions are not shared by fentanyl [J].
Bilfinger, TV ;
Fimiani, C ;
Stefano, GB .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1998, 64 :S61-S66
[5]   Brown adipose tissue thermogenesis contributes to fentanyl-evoked hyperthermia [J].
Cao, WH ;
Morrison, SF .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2005, 288 (03) :R723-R732
[6]   MORPHINE HYPERTHERMIA IN RAT - ACTION ON CENTRAL THERMOSTATS [J].
COX, B ;
ARY, M ;
CHESAREK, W ;
LOMAX, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1976, 36 (01) :33-39
[7]  
GELLER EB, 1983, J PHARMACOL EXP THER, V225, P391
[8]   HIGHER ENVIRONMENTAL TEMPERATURE-INDUCED INCREASE OF BODY-TEMPERATURE - INVOLVEMENT OF CENTRAL OPIOIDERGIC-GABAERGIC INTERACTION [J].
GHOSH, S ;
PODDAR, MK .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1995, 52 (01) :73-76
[9]   Influence of fever on the hypermetabolic response in burn-injured children [J].
Gore, DC ;
Chinkes, D ;
Sanford, A ;
Hart, DW ;
Wolf, SE ;
Herndon, DN .
ARCHIVES OF SURGERY, 2003, 138 (02) :169-174
[10]  
Gore DC, 2003, ARCH SURG-CHICAGO, V138, P174