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Triple Therapy, Sequential Therapy, and Concomitant Therapy for Helicobacter pylori Infection in Korea: A Multicenter, Randomized Controlled Trial

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The Korean Journal of Internal Medicine Vol. 29, No. 5 (Suppl. 1)

WCIM 2014 SEOUL KOREA 485

Slide Session

K-UG-28 Upper GI Tract

Triple Therapy, Sequential Therapy, and Concomitant Therapy for Helicobacter pylori Infection in Korea: A Multicenter, Randomized Controlled Trial

Byung-Wook Kim1, Joon Sung Kim1, Hyung Gil Kim2, Byoung Wook Bang2, Su Jin Hong3, Jae Pil Han3, Chang Whan Kim4

The Catholic University of Korea, Incheon St. Mary`s Hospital, Korea1, Inha Unversity, Korea2, Soon- ChunHyang University, Korea3, The Catholic University of Korea, Bucheon St. Mary`s Hospital, Korea4 Background: Eradication of Helicobacter pylori infection with triple therapy (TT) has been reported to achieve unacceptable rates in Korea. Sequential therapy (ST) and concomitant therapy (CT) has been suggested as alternatives to the TT regimen. The aim of this study was to compare the effi cacy of ST and CT with that of TT in Korea.

Methods: For this multicentre, randomized trial, patients (=20 years of age) with H.

pylori infection from 5 centers in Korea were recruited. Patients were randomly allo- cated to TT (PPI, amoxicillin and clarithromycin for 10 days), ST (PPI and amoxicillin for the fi rst 5 days, followed by PPI, clarithromycin and metronidazole for the next 5 days) or CT (PPI, amoxicillin, clarithromycin and metronidazole for 10 days). The prima- ry outcome was the eradication rate of each treatment by intention-to-treat (ITT) and per-protocol (PP) analysis.

Results: From March, 2013 a total of 151 patients were enrolled in our study. Sixty one patients were allocated to the TT, 49 patients to CT group, and 29 patients to the ST group. For ITT analysis, the eradication rates of TT, ST and CT were 67.2% (41/61), 59.2% (29/49), 68.3% (28/41), respectively. For PP analysis, the eradication rates were 91.1% (41/45), 82.9% (29/35), 93.3% (28/30), respectively. We recorded no signifi cant difference in the occurrence of adverse effects or in compliance between the three groups.

Conclusions: TT and CT regimens seem to achieve higher eradication rates than the ST regimen in Korea. Additional study results from more patients are expected.

K-UG-29 Upper GI Tract

Serum Pepsinogen Assay is Not Valuable in Reinfected Subjects After H. pylori Eradication

Sang Hee An1, Sun-Young Lee1, Sang Pyo Lee1, Jeong Hwan Kim1, In-Kyung Sung1, Hyung Seok Park1, Chan Sup Shim1, Choon Jo Jin1

Department of Internal Medicine, Konkuk University School of Medicine, Korea1

Background: The serum titer of anti-Helicobacter pylori immunoglobulin G (IgG) an- tibody starts to increase again when reinfection occurs after a successful eradication.

The aim of this study was to evaluate whether the serum pepsinogen (PG) assay is effective for the diagnosis of gastric atrophy after reinfection.

Methods: This study included consecutive Korean adults who had a remote H. pylori eradication therapy, but showed positive serum anti-H. pylori IgG antibody test on the day of upper gastrointestinal endoscopy and serum PG test at our center. Advanced chronic atrophic gastritis on endoscopy was defi ned as either closed- or open-type atrophy. Serologic atrophy was defi ned as PG I/II ratio <3.0 and PG I level < 70 ng/ml.

Results: Of the 131 subjects who fulfi lled the study inclusion criteria, 50 showed high bacterial loads (serum anti-H. pylori antibody titer =150 AU/ml) and 28 showed low bacterial loads (<50 AU/ml). The high bacterial load group showed highest PG levels and lowest PG I/II ratio (Table 1). Although serologic atrophy was more frequent in the high bacterial load group (p=0.034), this group showed the highest serum PG I levels (p=0.001).

Conclusions: The severity of gastric atrophy cannot be assessed by serum PG assay after reinfection, as suggested by our fi nding that PG I/II ratio is inversely related to the PG I level. Higher bacterial load induces a larger increase in PG II level than PG I level due to severe infl ammatory reaction upon reinfection. Therefore, a decreased PG I/II ratio is no longer valuable for detecting serologic atrophy in the reinfected subjects after a successful H. pylori eradication.

K-UG-30 Upper GI Tract

Effect of Helicobacter pylori Eradication on the Development of Metachronous Gastric Cancer After Resection of Early Gastric Cancer: A Systematic Review and Meta-Analysis

Chang Seok Bang1, Gwang Ho Baik1, Hyo Sun Kim1, Sang Hyun Park1, Eun Jin Kim1, Jin Bong Kim1, Ki Tae Suk1, Jai Hoon Yoon1, Yeon Soo Kim1, Dong Joon Kim1 Department of Internal Medicine, Hallym University College of Medicine, Korea1

Background: There still remains controversies about effect of Helicobacter pylori eradication on the development of metachronous gastric cancer after endoscopic re- section of early gastric cancer (EGC). The aim of this study was to assess the effi cacy of Helicobacter pylori eradication for the prevention of metachronous recurrecne after endoscopic resection of EGC.

Methods: A systematic literature review was conducted using the core databases (Pu- bMed, EMBASE, and the Cochrane Library). Metachronous gastric cancer recurrence rates between Helicobacter pylori eradicated vs. non-eradicated group were extracted and analyzed using risk ratios (RRs). A random effect model was applied. The meth- odological quality of the enrolled studies was assessed by the Risk of Bias table and Newcastle-Ottawa Scale. Publication bias was evaluated through the funnel plot, trim and fi ll method, Egger’s test, and rank correlation test.

Results: A total of 5914 patients with EGC or dysplasia was enrolled from 10 studies.

Overall, Helicobacter pylori eradicated group showed a RR of 0.467 (95% CI: 0.362- 0.602, P<0.001) for the development of metachronous recurrence after endoscopic resection of EGC. Sensitivity analyses showed consistent results. Publication bias was not detected.

Conclusions: In this analysis, Helicobacter pylori eradication reduces the occurrence of metachronous gastric cancer after endoscopic resection of EGC.

K-UG-31 Upper GI Tract

Korea’s Contribution to Endoscopic Submucosal Dissection: A Bibliographic Analysis

Eun Jin Kim1, Chang Seok Bang1, Gwang Ho Baik1, Hyo Sun Kim1, Sang Hyun Park1, Jin Bong Kim1, Ki Tae Suk1, Jai Hoon Yoon1, Yeon Soo Kim1, Dong Joon Kim1 Department of Internal Medicine, Hallym University College of Medicine, Korea1

Background: To evaluate the articles published by Korean endoscopists in the MED- LINE between 1971 and 2014.

Methods: A systematic literature review was conducted using the MEDLINE database (through PubMed). The searching keyword was ‘endoscopic submucosal dissection’.

Analyzed parameters included the total number of articles, journal, institution, country, published year, and number of citation. The number of citation was measured by the Institute for Scientifi c Information Web of Knowledge-Web of Science (SCIE) database on July 2014.

Results: A total of 1791 papers were searched in 244 journals (941 articles in SCI journal, 525 articles in SCIE journal, and 325 non-SCI, SCIE articles). Among the total articles, Korea’s contribution was 15.6% (n=304) and ranked 2nd in the world.

The journals in the order of number of articles were as follows; Endoscopy (n=206), Gastrointest Endosc (n=187), Dig Endosc (n=137), Surg Endosc (n=134), and World J Gastroenterol (n=82). Among the literatures written by Korean authors, the journals in the order of number of articles were as follows; Surg Endosc (n=38), Clin Endosc (n=35), Gastrointest Endosc (n=31), and Endoscopy (n=24). The mean citation number was 12.1 ± 25 in the total literatures. However, the number was decreased in the articles written by Korean authors; 7 ± 14.2. The most cited article written by Korean authors was ‘Therapeutic outcomes in 1000 cases of endoscopic submucosal dissection for early gastric neoplasms: Korean ESD Study Group multicenter study’ published in 2009, which was cited 153 times until now.

Conclusions: Korea’s contribution to endoscopic submucosal dissection has been in- creasing.

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