Jodi A Worrel PharmD , Steven C Stoner PharmD, BCPP
{"title":"根除幽门螺杆菌","authors":"Jodi A Worrel PharmD , Steven C Stoner PharmD, BCPP","doi":"10.1016/S1082-7579(98)00012-0","DOIUrl":null,"url":null,"abstract":"<div><p>Since the discovery of <span><span>Helicobacter pylori</span></span><span> just over 15 years ago, the treatment of peptic ulcer disease has been revolutionized. </span><em>H. pylori</em> is an important causative factor for the development of duodenal and gastric ulcers. Because <em>H. pylori</em><span> can be eradicated with very low rates of ulcer recurrence, antibiotic therapy is now recommended by the National Institutes of Health (NIH) and the American College of Gastroenterology for all </span><em>H. pylori-</em><span>positive ulcer patients. Bismuth subsalicylate<span><span><span>, antibiotics (amoxicillin, tetracycline, </span>metronidazole, and clarithromycin), </span>proton pump inhibitors, and H</span></span><sub>2</sub> blockers are the standards for treatment. They are combined in dual, triple, and quadruple therapy regimens to produce <em>H. pylori</em> eradication. All of the phamacologic agents currently prescribed for <em>H. pylori</em> eradication are associated with bothersome adverse effects and numerous documented and potential drug interactions. Because no gold standard for <em>H. pylori</em><span> eradication exists, the treatment decision must be on the basis of efficacy, cost, compliance, tolerability, antimicrobial resistance, and potential drug interactions.</span></p></div>","PeriodicalId":100909,"journal":{"name":"Medical Update for Psychiatrists","volume":"3 4","pages":"Pages 99-104"},"PeriodicalIF":0.0000,"publicationDate":"1998-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1082-7579(98)00012-0","citationCount":"5","resultStr":"{\"title\":\"Eradication of Helicobacter Pylori\",\"authors\":\"Jodi A Worrel PharmD , Steven C Stoner PharmD, BCPP\",\"doi\":\"10.1016/S1082-7579(98)00012-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Since the discovery of <span><span>Helicobacter pylori</span></span><span> just over 15 years ago, the treatment of peptic ulcer disease has been revolutionized. </span><em>H. pylori</em> is an important causative factor for the development of duodenal and gastric ulcers. Because <em>H. pylori</em><span> can be eradicated with very low rates of ulcer recurrence, antibiotic therapy is now recommended by the National Institutes of Health (NIH) and the American College of Gastroenterology for all </span><em>H. pylori-</em><span>positive ulcer patients. Bismuth subsalicylate<span><span><span>, antibiotics (amoxicillin, tetracycline, </span>metronidazole, and clarithromycin), </span>proton pump inhibitors, and H</span></span><sub>2</sub> blockers are the standards for treatment. They are combined in dual, triple, and quadruple therapy regimens to produce <em>H. pylori</em> eradication. All of the phamacologic agents currently prescribed for <em>H. pylori</em> eradication are associated with bothersome adverse effects and numerous documented and potential drug interactions. Because no gold standard for <em>H. pylori</em><span> eradication exists, the treatment decision must be on the basis of efficacy, cost, compliance, tolerability, antimicrobial resistance, and potential drug interactions.</span></p></div>\",\"PeriodicalId\":100909,\"journal\":{\"name\":\"Medical Update for Psychiatrists\",\"volume\":\"3 4\",\"pages\":\"Pages 99-104\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1082-7579(98)00012-0\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Update for Psychiatrists\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1082757998000120\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Update for Psychiatrists","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1082757998000120","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Since the discovery of Helicobacter pylori just over 15 years ago, the treatment of peptic ulcer disease has been revolutionized. H. pylori is an important causative factor for the development of duodenal and gastric ulcers. Because H. pylori can be eradicated with very low rates of ulcer recurrence, antibiotic therapy is now recommended by the National Institutes of Health (NIH) and the American College of Gastroenterology for all H. pylori-positive ulcer patients. Bismuth subsalicylate, antibiotics (amoxicillin, tetracycline, metronidazole, and clarithromycin), proton pump inhibitors, and H2 blockers are the standards for treatment. They are combined in dual, triple, and quadruple therapy regimens to produce H. pylori eradication. All of the phamacologic agents currently prescribed for H. pylori eradication are associated with bothersome adverse effects and numerous documented and potential drug interactions. Because no gold standard for H. pylori eradication exists, the treatment decision must be on the basis of efficacy, cost, compliance, tolerability, antimicrobial resistance, and potential drug interactions.