RETRACTED: Effects of postoperative sedation with propofol and midazolam on pancreatic function assessed by pancreatitis-associated protein (Retracted article. See vol. 66, pg. 646, 2011)

被引:18
作者
Piper, SN [1 ]
Kumle, B [1 ]
Maleck, WH [1 ]
Suttner, SW [1 ]
Fent, MT [1 ]
Boldt, J [1 ]
机构
[1] Klinikum Stadt Ludwigshafen, Dept Anaesthesiol & Intens Care Med, D-67063 Ludwigshafen, Germany
关键词
sedation; propofol; midazolam pancreatitis : pancreatitis-associated protein;
D O I
10.1046/j.1365-2044.2001.02175.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
This prospective randomised controlled study evaluated the effects of postoperative sedation with propofol and midazolam on pancreatic function. We studied 42 intensive care unit patients undergoing elective major surgery who were expected to be sedated postoperatively. Patients were randomly assigned to a propofol group (n = 21) or a midazolam group (n = 21). To assess pancreatic function, the following parameters were measured: pancreatitis-associated protein, amylase, lipase, cholesterol and triglyceride prior to start of sedation on the intensive care unit, 4 h after the sedation was started and at the first postoperative day. Patients in the propofol group received on average (SD) 1292 (430) mg propofol and were sedated for 9.03 (4.26) h. The midazolam group received 92 (36) mg midazolam and were sedated for 8.81 (4.68) h. Plasma cholesterol concentrations did not differ significantly between groups. Triglyceride plasma levels 4 h after the start of infusion were significantly higher in the propofol group (140 (54) mg.dl(-1)) than the midazolam-treated patients (81 (29) mg.dl(-1)), but were within normal limits. There were no significant differences between the two groups regarding amylase, lipase and pancreatitis-associated protein plasma concentrations at any time. No markers of pancreatic dysfunction were outside the normal range. We conclude that postoperative sedation with propofol induced a significant increase of serum triglyceride levels but that pancreatic function is unchanged with standard doses of propofol.
引用
收藏
页码:836 / 840
页数:5
相关论文
共 25 条
[1]  
BEHNE M, 1994, ANASTH INTENSIVMED, V35, P101
[2]   PROPOFOL VS MIDAZOLAM IN SHORT-TERM, MEDIUM-TERM, AND LONG-TERM SEDATION OF CRITICALLY ILL PATIENTS - A COST-BENEFIT-ANALYSIS [J].
CARRASCO, G ;
MOLINA, R ;
COSTA, J ;
SOLER, JM ;
CABRE, L .
CHEST, 1993, 103 (02) :557-564
[3]   Comparative study of propofol versus midazolam in the sedation of critically ill patients: Results of a prospective, randomized, multicenter trial [J].
Chamorro, C ;
deLatorre, FJ ;
Montero, A ;
SanchezIzquierdo, JA ;
Jareno, A ;
Moreno, JA ;
Gonzalez, E ;
Barrios, M ;
Carpintero, JL ;
MartinSantos, F ;
Otero, B ;
Ginestal, R .
CRITICAL CARE MEDICINE, 1996, 24 (06) :932-939
[4]   Is pancreatitis a complication of propofol infusion? [J].
Dönmez, A ;
Arslan, G ;
Pirat, A ;
Demirhan, B .
EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 1999, 16 (06) :367-370
[5]   PROPOFOL - AN OVERVIEW OF ITS PHARMACOLOGY AND A REVIEW OF ITS CLINICAL EFFICACY IN INTENSIVE-CARE SEDATION [J].
FULTON, B ;
SORKIN, EM .
DRUGS, 1995, 50 (04) :636-657
[6]   EFFECT OF PROLONGED SEDATION WITH PROPOFOL ON SERUM TRIGLYCERIDE AND CHOLESTEROL CONCENTRATIONS [J].
GOTTARDIS, M ;
KHUNLBRADY, KS ;
KOLLER, W ;
SIGL, G ;
HACKL, JM .
BRITISH JOURNAL OF ANAESTHESIA, 1989, 62 (04) :393-396
[7]   Propofol reduces the migration of human leukocytes through endothelial cell monolayers [J].
Hofbauer, R ;
Frass, M ;
Salfinger, H ;
Moser, D ;
Hornykewycz, S ;
Gmeiner, B ;
Kapiotis, S .
CRITICAL CARE MEDICINE, 1999, 27 (09) :1843-1847
[8]   SERUM LEVELS OF PANCREATITIS-ASSOCIATED PROTEIN AS INDICATORS OF THE COURSE OF ACUTE-PANCREATITIS [J].
IOVANNA, JL ;
KEIM, V ;
NORDBACK, I ;
MONTALTO, G ;
CAMARENA, J ;
LETOUBLON, C ;
LEVY, P ;
BERTHEZENE, P ;
DAGORN, JC .
GASTROENTEROLOGY, 1994, 106 (03) :728-734
[9]   AN ADDITIONAL SECRETORY PROTEIN IN THE RAT PANCREAS [J].
KEIM, V ;
ROHR, G ;
STOCKERT, HG ;
HABERICH, FJ .
DIGESTION, 1984, 29 (04) :242-249
[10]   Advances in the laboratory diagnostics of acute pancreatitis [J].
Kemppainen, EAJ ;
Hedström, JI ;
Puolakkainen, PA ;
Haapianinen, RK ;
Stenman, UH .
ANNALS OF MEDICINE, 1998, 30 (02) :169-175