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차세대 완하제

New Generation Laxatives

  • 홍성노 (성균관대학교 의과대학 내과학교실) ;
  • 신정은 (단국대학교 의과대학 내과학교실) ;
  • 홍경섭 (서울대학교 의과대학 내과학교실) ;
  • 정기욱 (울산대학교 의과대학 소화기내과학교실) ;
  • 이태희 (순천향대학교 의과대학 소화기연구소) ;
  • 이봉은 (부산대학교 의과대학 내과학교실) ;
  • 박선영 (전남대학교 의과대학 내과학교실) ;
  • 김성은 (이화여자대학교 의학전문대학원 내과학교실) ;
  • 박경식 (계명대학교 의과대학 내과학교실) ;
  • 최석채 (원광대학교 의과대학 내과학교실 및 소화기질환 연구소)
  • Hong, Sung Noh (Department of Internal Medicine, Sungkyunkwan University School of Medicine) ;
  • Shin, Jeong Eun (Department of Internal Medicine, Dankook University College of Medicine) ;
  • Hong, Kyoung Sup (Department of Internal Medicine, Seoul National University College of Medicine) ;
  • Jung, Kee Wook (Department of Gastroenterology, University of Ulsan College of Medicine) ;
  • Lee, Tae Hee (Institute for Digestive Research, Soonchunhyang University College of Medicine) ;
  • Lee, Bong Eun (Department of Internal Medicine, Pusan National University School of Medicine) ;
  • Park, Sun-Young (Department of Internal Medicine, Chonnam National University Medical School) ;
  • Kim, Seong-Eun (Department of Internal Medicine, Ewha Womans University School of Medicine) ;
  • Park, Kyung Sik (Department of Internal Medicine, Keimyung University School of Medicine) ;
  • Choi, Suck Chei (Department of Internal Medicine and Digestive Disease Research Institute, Wonkwang University School of Medicine)
  • 발행 : 20150000

초록

A significant proportion of chronic constipation patients are dissatisfied with their treatment. Recently, a number of new medications have been introduced for patients refractory to conventional laxatives, such as prucalopride, lubiprostone, linaclotide, and elobixibat. Prucalopride is a novel gastrointestinal prokinetic agent that acts as a 5-hydroxytryptamine type 4 (5-HT4) agonist. Compared with older nonselective 5-HT4 agonists, the higher selectivity of prucalopride for 5-HT4 receptors can reduce the risk of significant adverse cardiovascular events. Prucalopride improves stool frequency and consistency, and reduces the need for rescue medications. Lubiprostone, a chloride channel activator, increases the secretion of intestinal fluid, improves the stool frequency and consistency, and reduces straining. Linaclotide, a guanylate cyclase-C agonist, is effective in treating patients with chronic constipation and its effect on visceral sensitivity, as shown mainly in animal studies, provides an attractive pharmaceutical option for patients with irritable bowel syndrome with constipation. Elobixibat is an ileal sodium-dependent bile acid transporter inhibitor that blocks the enterohepatic circulation of bile acids, increasing the bile acid concentration in the intestine, which accelerates colonic transit and softens the stool. A phase III trial of the treatment of chronic constipation and irritable bowel syndrome with constipation is underway. The clinical application of new-generation laxatives will contribute to the management of chronic constipation refractory to conventional laxatives.

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