Comparison of a low dose polyethylene glycol electrolyte solution with lactulose for treatment of chronic constipation

被引:169
作者
Attar, A
Lémann, M
Ferguson, A
Halphen, M
Boutron, MC
Flourié, B
Alix, E
Salmeron, M
Guillemot, F
Chaussade, S
Ménard, AM
Moreau, J
Naudin, G
Barthet, M
机构
[1] Hop St Louis, Serv Gastroenterol, F-75010 Paris, France
[2] Hop St Lazare, Serv Gastroenterol, F-75475 Paris, France
[3] Norgine Pharma, Paris, France
[4] Hop Mans, Serv Geriatr, Le Mans, France
[5] Hop Croix St Simon, Serv Gastroenterol, Paris, France
[6] Hop Claude Huriez, Serv Gastroenterol, Lille, France
[7] Hop Cochin, Serv Gastroenterol, F-75674 Paris, France
[8] Hop Rangueil, Serv Gastroenterol, Toulouse, France
[9] Hop Diaconesses, Serv Gastroenterol, Paris, France
[10] Hop St Marguerite, Serv Gastroenterol, Marseille, France
[11] Western Gen Hosp, Gastrointestinal Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
constipation; polyethylene glycol; lactulose; cathartics; randomised trial;
D O I
10.1136/gut.44.2.226
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Polyethylene glycol (PEG) 3350 is a non-absorbable, nonmetabolised osmotic agent used in lavage solutions for gut cleansing. Aims-To compare the efficacy of PEG and lactulose in chronic constipation. Methods-A total of 115 patients with chronic constipation entered a multicentre, randomised, comparative trial. They initially received two sachets containing either PEG (13 g/sachet) or lactulose (10 g/sachet) and were given an option to change the dose to one or three sachets/day, depending on response. Results-Ninety nine patients completed the trial. After four weeks, patients in the PEG group (n=50) had a higher number of stools and a lower median daily score for straining at stool than patients in the lactulose group (n=49). Overall improvement was greater in the PEG group. Clinical tolerance was similar in the two groups, but flatus was less frequently reported in the PEG group. The mean number of liquid stools was higher in the PEG group but the difference was significant only for the first two weeks. There were no serious adverse events and no significant change in laboratory tests in either group. At the end of the study, the number of sachets used by the patients was 1.6 (0.7)/day in the PEG group and 2.1 (0.7)/day in the lactulose group. Sixty one patients completed a further two months open study of one to three sachets PEG daily; there was no loss of efficacy and no serious toxicity. Conclusion-Low dose PEG 3350 was more effective than lactulose and better tolerated.
引用
收藏
页码:226 / 230
页数:5
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