Randomized trial of low-volume PEG solution versus standard PEG plus electrolytes for bowel cleansing before colonoscopy

被引:206
|
作者
Ell, Christian [1 ]
Fischbach, Wolfgang [2 ]
Bronisch, Hans-Joachim [3 ]
Dertinger, Stefan [4 ]
Layer, Peter [5 ]
Ruenzi, Michael [6 ]
Schneider, Thomas [7 ]
Kachel, Guenther [8 ]
Grueger, Joerg [9 ]
Koellinger, Michael [10 ]
Nagell, Waltraud [11 ]
Goerg, Karl-Josel [12 ]
Wanitschke, Roland [13 ]
Gruss, Hans-Juergen [14 ]
机构
[1] Dr Horst Schmidt Kliniken GmbH, Chefrzt Innere Med 2, D-65199 Wiesbaden, Germany
[2] Klinikum Aschaffenburg, Aschaffenburg, Germany
[3] Katho Krankenhaus St Johann Nepomuk, Erfurt, Germany
[4] Kreiskrankenhaus Tirschenreuth, Tirschenreuth, Germany
[5] Israelit Krankenhaus, Hamburg, Germany
[6] Krankenhaus St Josef gGmbH, Kliniken Essen Sud Kathol, Essen, Germany
[7] Klinikum Furth, Furth, Germany
[8] Klinikum Dachau, Dachua, Germany
[9] Stadt Kliniken Frankfurt Hochst, Frankfurt, Germany
[10] Klinikum St Marien, Amberg, Germany
[11] Burgerhosp Frankfurt Main eV, Frankfurt, Germany
[12] Klinikum St Antonius, Wuppertal, Germany
[13] Johannes Gutenberg Univ Mainz, Mainz, Germany
[14] Norgine Ltd, R&D Div, Harefield, Middx, England
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2008年 / 103卷 / 04期
关键词
D O I
10.1111/j.1572-0241.2007.01708.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Polyethylene glycol (PEG)-based gut lavage solutions are safe and effective, but require consumption of large volumes of fluid. We compared a new 2 L solution of PEG plus ascorbic acid (PEG + Asc) with standard 4 L PEG with electrolytes (PEG + E) for bowel cleansing before colonoscopy to determine efficacy, safety, and patient acceptability. METHODS: Consenting adult inpatients scheduled to undergo colonoscopy were randomized to receive either 2 L PEG + Asc or 4 L PEG + E. Preparations were taken as split doses the evening before colonoscopy and the following morning. The PEG + Asc group took 1 L at each administration (i.e., total dose of 2 L). The PEG + E group took 2 L at each administration (i.e., total dose of 4 L). Bowel cleansing success was assessed via videotapes by independent, blinded raters. Statistical noninferiority was predefined as a difference of < 15% in the lower limit of the 97.5% confidence interval for treatment difference. Patient views on the preparations were elicited. Adverse events were noted. RESULTS: Successful gut cleansing was achieved in 136 of 153 (88.9%) cases of the PEG + Asc group and 147 of 155 (94.8%) cases of the 4 L PEG + E group (mean difference -5.9 [-12.0-infinity]). The difference fell within the predefined limit for noninferiority. Clinical and laboratory parameters showed no difference in safety profile. Patient ratings of acceptability and taste were better for the PEG + Asc group than for the PEG + E group (P < 0.025). CONCLUSIONS: The combination of ascorbic acid and PEG-based bowel preparation reduces the volume patients have to drink without compromising efficacy or safety. The low-volume PEG + Asc preparation was more acceptable to patients, and should, therefore, improve effectiveness in routine practice.
引用
收藏
页码:883 / 893
页数:11
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