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Conference Paper: Seven-day rifabutin containing triple therapy versus seven-day levofloxacin containing quadruple therapy as second-line treatment for Helicobacter pylori in Chinese patients: an open label, randomized trial
Title | Seven-day rifabutin containing triple therapy versus seven-day levofloxacin containing quadruple therapy as second-line treatment for Helicobacter pylori in Chinese patients: an open label, randomized trial |
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Authors | |
Keywords | Medical sciences Gastroenterology |
Issue Date | 2015 |
Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro |
Citation | The 2015 Digestive Disease Week (DDW 2015), Washington, DC., 16-19 May 2015. In Gastroenterology, 2015, v. 148 n. 4 suppl. 1, p. S149, abstract no. 771 How to Cite? |
Abstract | INTRODUCTION: Rifabutin containing triple therapy (RIF) and levofloxacin containing quadruple therapy (QUAD) has been used as rescue therapy for resistant H. pylori infection. We compared the efficacy and tolerability of 7-day RIF with 7-day QUAD as second-line treatment for H. pylori infection. Levofloxacin was used instead of bismuth subcitrate for the quadruple therapy, as bismuth is no longer available in Hong Kong. METHODS: Patients who have failed the triple therapy (esomeprazole, amoxicillin, and clarithromycin) and remained H. pyloripositive were randomly assigned to receive either 7-day RIF (esomeprazole, rifabutin and amoxicillin) or QUAD (esomeprazole, levofloxacin, tetracycline and metronidazole) treatments. H. pylori eradication was confirmed by urea breath test at 8 weeks. The primary outcome was the eradication rates by intention-to-treat (ITT) and per-protocol (PP) analyses. RESULTS: One hundred and fifty-one patients were randomized to receive either RIF or QUAD. The PP eradication rate of the RIF and QUAD groups were 89.3% and 95.6%, respectively (P = 0.16). Base on ITT analysis, the corresponding eradication rate was 88.2% and 90.7% (P = 0.62). One patient (1.3%) in the RIF and seven (9.3%) patients in the QUAD failed to complete the treatment regime. The overall incidences of adverse events were higher in the QUAD (30.7%) than in the RIF (15.8%) group (P = 0.03). CONCLUSION: Seven-day rifabutin containing triple therapy and levofloxacin containing quadruple therapy are both highly effective and should be considered as second-line treatment for resistant H. pylori infection. |
Description | Oral Presentation |
Persistent Identifier | http://hdl.handle.net/10722/217522 |
ISSN | 2023 Impact Factor: 25.7 2023 SCImago Journal Rankings: 7.362 |
DC Field | Value | Language |
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dc.contributor.author | Hung, IFN | - |
dc.contributor.author | Liu, SHK | - |
dc.contributor.author | Tan, VP | - |
dc.contributor.author | Hsu, ASJ | - |
dc.contributor.author | Seto, WK | - |
dc.contributor.author | Tong, TSM | - |
dc.contributor.author | Leung, WK | - |
dc.date.accessioned | 2015-09-18T06:02:17Z | - |
dc.date.available | 2015-09-18T06:02:17Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | The 2015 Digestive Disease Week (DDW 2015), Washington, DC., 16-19 May 2015. In Gastroenterology, 2015, v. 148 n. 4 suppl. 1, p. S149, abstract no. 771 | - |
dc.identifier.issn | 0016-5085 | - |
dc.identifier.uri | http://hdl.handle.net/10722/217522 | - |
dc.description | Oral Presentation | - |
dc.description.abstract | INTRODUCTION: Rifabutin containing triple therapy (RIF) and levofloxacin containing quadruple therapy (QUAD) has been used as rescue therapy for resistant H. pylori infection. We compared the efficacy and tolerability of 7-day RIF with 7-day QUAD as second-line treatment for H. pylori infection. Levofloxacin was used instead of bismuth subcitrate for the quadruple therapy, as bismuth is no longer available in Hong Kong. METHODS: Patients who have failed the triple therapy (esomeprazole, amoxicillin, and clarithromycin) and remained H. pyloripositive were randomly assigned to receive either 7-day RIF (esomeprazole, rifabutin and amoxicillin) or QUAD (esomeprazole, levofloxacin, tetracycline and metronidazole) treatments. H. pylori eradication was confirmed by urea breath test at 8 weeks. The primary outcome was the eradication rates by intention-to-treat (ITT) and per-protocol (PP) analyses. RESULTS: One hundred and fifty-one patients were randomized to receive either RIF or QUAD. The PP eradication rate of the RIF and QUAD groups were 89.3% and 95.6%, respectively (P = 0.16). Base on ITT analysis, the corresponding eradication rate was 88.2% and 90.7% (P = 0.62). One patient (1.3%) in the RIF and seven (9.3%) patients in the QUAD failed to complete the treatment regime. The overall incidences of adverse events were higher in the QUAD (30.7%) than in the RIF (15.8%) group (P = 0.03). CONCLUSION: Seven-day rifabutin containing triple therapy and levofloxacin containing quadruple therapy are both highly effective and should be considered as second-line treatment for resistant H. pylori infection. | - |
dc.language | eng | - |
dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro | - |
dc.relation.ispartof | Gastroenterology | - |
dc.rights | © <year>. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ | - |
dc.subject | Medical sciences | - |
dc.subject | Gastroenterology | - |
dc.title | Seven-day rifabutin containing triple therapy versus seven-day levofloxacin containing quadruple therapy as second-line treatment for Helicobacter pylori in Chinese patients: an open label, randomized trial | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Hung, IFN: ivanhung@hkucc.hku.hk | - |
dc.identifier.email | Liu, SHK: drkliu@hku.hk | - |
dc.identifier.email | Tan, VP: vpytan@hku.hk | - |
dc.identifier.email | Hsu, ASJ: axelhsu@hku.hk | - |
dc.identifier.email | Seto, WK: wkseto@hku.hk | - |
dc.identifier.email | Tong, TSM: tongsma@hkucc.hku.hk | - |
dc.identifier.email | Leung, WK: waikleung@hku.hk | - |
dc.identifier.authority | Hung, IFN=rp00508 | - |
dc.identifier.authority | Tan, VP=rp01458 | - |
dc.identifier.authority | Seto, WK=rp01659 | - |
dc.identifier.authority | Leung, WK=rp01479 | - |
dc.identifier.hkuros | 253262 | - |
dc.identifier.volume | 148 | - |
dc.identifier.issue | 4, suppl. 1 | - |
dc.identifier.spage | S149, abstract no. 771 | - |
dc.identifier.epage | S149, abstract no. 771 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0016-5085 | - |