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Dive into the research topics where Ai-Wen Kao is active.

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Featured researches published by Ai-Wen Kao.


Alimentary Pharmacology & Therapeutics | 2005

Esomeprazole 40 mg twice daily in triple therapy and the efficacy of Helicobacter pylori eradication related to CYP2C19 metabolism

Bor-Shyang Sheu; Ai-Wen Kao; Hui Chuan Cheng; S.-F. Hunag; T.-W. Chen; Cheng Chan Lu; Jiunn-Jong Wu

Aim : To determine whether an increased dosage of esomeprazole 40 mg twice daily in triple therapy improved the Helicobacter pylori eradication rate for patients with different genotypes of S‐mephenytoin 4′‐hydroxylase (CYP2C19).


Digestive Diseases and Sciences | 2005

The Efficacy of High- and Low-Dose Intravenous Omeprazole in Preventing Rebleeding for Patients with Bleeding Peptic Ulcers and Comorbid Illnesses

Hsiu Chi Cheng; Ai-Wen Kao; Chiao-Hsiung Chuang; Bor-Shyang Sheu

This study sought to determine if high-dose omeprazole infusion could improve the control of rebleeding in patients with comorbid illnesses and bleeding peptic ulcers. After achieving hemostasis by endoscopy, 105 patients were randomized into high-dose (n = 52) and low-dose (n = 53) groups, receiving 200 and 80 mg/day omeprazole, respectively, as a continuous infusion for 3 days.Thereafter, oral omeprazole, 20 mg/day, was given. The cumulative rebleeding rates comparatively rose in both groups (high-dose vs. low-dose group), beginning on day 3 (15.4% vs. 11.3%), day 7 (19.6% vs. 20%), and day 14 (32.7% vs. 28.9%), until day 28 (35.4% vs. 33.3%), and were not significantly different between the two groups (P > 0.50). Multiple logistic regression confirmed that a serum albumin level < 3 g/dL was an independent factor associated with rebleeding (P = 0.002). For patients with comorbidities, 3-day omeprazole infusion, despite increasing the daily dose from 80 to 200 mg, was not adequate to control peptic ulcer rebleeding.


Alimentary Pharmacology & Therapeutics | 2002

Impact of intravenous omeprazole on Helicobacter pylori eradication by triple therapy in patients with peptic ulcer bleeding

Bor-Shyang Sheu; Chih Hsien Chi; Chao Ching Huang; Ai-Wen Kao; Y.-L. Wang; Hsiao Bai Yang

To test the impact of intravenous omeprazole on Helicobacter pylori eradication for bleeding peptic ulcers.


The American Journal of Gastroenterology | 2007

The Impact of Body Mass Index on the Application of On-Demand Therapy for Los Angeles Grades A and B Reflux Esophagitis

Bor-Shyang Sheu; Hsiu Chi Cheng; Wei Lun Chang; Wei-Ying Chen; Ai-Wen Kao

BACKGROUND AND AIMS:Patients with Los Angeles grade A or B reflux esophagitis (RE-AB) can potentially be switched from active-phase therapy to on-demand esomeprazole as maintenance therapy. Body mass index (BMI) correlates significantly with reflux symptoms. We investigated whether BMI affects the efficacy of esomeprazole in active-phase or subsequent on-demand therapy.METHODS:Three hundred fifty patients with RE-AB were prospectively enrolled to receive an 8-wk course of esomeprazole (40 mg/day) as active-phase therapy. Based on the daily severity of acid regurgitation and heartburn, the cumulative proportions of patients with sustained symptomatic response (SSR), defined as free from symptoms for the last 7 days, were compared among different BMI groups (control: BMI <25 kg/m2, overweight: BMI 25–30 kg/m2, obese: BMI >30 kg/m2). In patients who had achieved SSR by week 8, on-demand therapy for 2 months was started. The number of 40-mg esomeprazole tablets used per 4-wk period was recorded.RESULTS:SSR rates were lower in both the overweight and obese groups than in the control group (P < 0.001). During on-demand therapy, the mean number of tablets used per 4-wk period was lower in the control group than in either the overweight or the obese group (13.2 vs 15.3 or 16.2, P < 0.05). The failure rate of on-demand therapy increased with increasing BMI—2.4%, 5.3%, and 14.2%, respectively, for the control, overweight, and obese groups (P = 0.002).CONCLUSION:For RE-AB, a higher BMI decreases the rate of SSR after 8-wk of esomeprazole therapy, and increases the need for medication and the failure rate of on-demand therapy.


Helicobacter | 2004

The rdxA Gene Plays A More Major Role Than frxA Gene Mutation in High‐level Metronidazole Resistance of Helicobacter pylori in Taiwan

Yao Jong Yang; Jiunn-Jong Wu; Bor-Shyang Sheu; Ai-Wen Kao; Ay-Huey Huang

Background.  Metronidazole‐resistant H. pylori associating with mutations of rdxA or frxA is still a debated topic. This study investigates whether rdxA and frxA mutations of H. pylori accounted for the high MIC value (≥ 64 µg/ml) of metronidazole (Mtz).


Helicobacter | 2002

Stool Antigen Assay to Screen H. pylori Infection and to Assess the Success of 3-Day and 7-Day Eradication Therapy in the Patients with Partial Gastrectomy

Bor-Shyang Sheu; Hsiao-Bai Yang; Yen-Lin Wang; Ai-Wen Kao; Chiao-Hsiung Chuang; Pin Wen Lin; Yuh-Chung Chang

Background. Even after partial gastrectomy, Helicobacter pylori may persist in the residual stomach but be less abundant in the bacterial load. H. pylori stool antigen is a reliable noninvasive tool to detect H. pylori infection in patients without gastrectomy. We thus test whether [ 1 ] the course of H. pylori eradication therapy could be diminished [ 2 ]; stool antigen can effectively detect H. pylori infection for the patients with gastrectomy.


Journal of Gastroenterology and Hepatology | 2004

Hypergastrinemia after Helicobacter pylori infection is associated with bacterial load and related inflammation of the oxyntic corpus mucosa

Chiao-Hsiung Chuang; Bor-Shyang Sheu; Hsiao-Bai Yang; Ai-Wen Kao; Hsiu Chi Cheng; Wei-Jen Yao

Background and Aim:  Helicobacter pylori infection causes hypergastrinemia. This study aimed to determine the association between serum gastrin and the severity of H. pylori‐related gastric histology.


Journal of General Internal Medicine | 2005

Posttreatment 13C-Urea Breath Test Is Predictive of Antimicrobial Resistance to H. pylori After Failed Therapy

Ai-Wen Kao; Hsiu Chi Cheng; Bor-Shyang Sheu; Ching-Yih Lin; Ming-Jen Sheu; Hsiao-Bai Yang; Jiunn-Jong Wu

AbstractOBJECTIVE: We tested whether a 13C-urea breath test can predict antimicrobial resistance of Helicobacter pylori (H. pylori). METHODS: Seventy patients who had failed triple eradication therapy and 108 untreated H. pylori-infected patients were given a 13C-urea breath test, endoscopy for culture of H. pylori, and assessment of clarithromycin resistance. The patients who had failed triple therapy then received 1 week of quadruple therapy to eradicate residual H. pylori. RESULTS: The posttreatment value of the 13C-urea breath test expressed as excessive δ13CO2 per ml (ECR) was higher in patients with residual H. pylori with clarithromycin resistance than in those without (23.8 vs 10.6; P<.0001). With a cutoff of ECR >or<-15, the 13C-urea breath test was 88.6% sensitive and 88.9% specific in predicting clarithromycin resistance of residual H. pylori. The H. pylori eradication rate of the rescue regimen was higher for patients with a posttreatment ECR of the 13C-urea breath test≤15 than for those with a value >15 (93.8% vs 73.3%; P<.05). In contrast, in treatment-naive H. pylori-infected patients, the pretreatment value of the 13C-urea breath test did not differ between patients infected with clarithromycin-resistant or-sensitive isolates (P>.05). CONCLUSION: The posttreatment value of the 13C-urea breath test is predictive of clarithromycin resistance in residual H. pylori after failed triple therapy and predicts efficacy of the rescue regimen. The value of the noninvasive test is promising for primary care physicians who need to select a rescue regimen without invasive H. pylori culture.


Journal of The Formosan Medical Association | 2003

On-Demand Therapy for Los Angeles Grade A and B Reflux Esophagitis: Esomeprazole Versus Omeprazole

Ai-Wen Kao; Bor-Shyang Sheu; Ming-Jen Sheu; Ye-Mei Chang; Shu-Feng Huang; Chiao-Hsiung Chuang; Yung-Ling Lai; Yeh-Heuy Kao

BACKGROUND AND PURPOSE Reflux esophagitis of Los Angeles grade A or B is more common than grades C and D disease among Taiwanese. This study compared the efficacy of esomeprazole 40 mg and omeprazole 20 mg for starting on-demand therapy for grade A and B reflux esophagitis. METHODS 100 patients with grade A and B reflux esophagitis were randomized to receive either esomeprazole 40 mg once daily (n = 50) or omeprazole 20 mg once daily (n = 50) for the first 4 weeks. Sustained symptomatic response (SSR) was defined as freedom from symptoms for the last 7 days of the 4-week treatment duration. On-demand therapy was used for the next 4 weeks in patients with SSR; patients without SSR continued with the same proton pump inhibitor regimen. Patients were asked to record their daily severity of acid regurgitation (AR) and heartburn (HB). Medication usage during on-demand therapy was recorded. RESULTS Forty six patients in the esomeprazole group and 45 patients in the omeprazole group completed the study protocol. The rate of SSR was higher in the esomeprazole group than in the omeprazole group (per-protocol: 73.9% vs 51.1%, p < 0.05; intent-to-treat: 68% vs 46%, p < 0.05). The symptomatic scores for AR and HB were similar between patients taking medication continuously and those taking medication on-demand with both esomeprazole and omeprazole. For patients starting on-demand therapy, the total number of tablets used during 4 weeks was lower in the esomeprazole group than in the omeprazole group (13.5 vs 18.5, p < 0.05). CONCLUSIONS In patients with grade A and B reflux esophagitis, esomeprazole 40 mg was more effective than omeprazole 20 mg for the initiation of on-demand therapy.


Alimentary Pharmacology & Therapeutics | 2005

The efficacy of Helicobacter pylori eradication related to CYP2C19 metabolism: Author's reply

Bor-Shyang Sheu; Ai-Wen Kao; Hui Chuan Cheng; S.-F. Hunag; T.-W. Chen; Cheng Chang Lu; Jiunn-Jong Wu

random mating and without factors that change allelic frequency (selection, genetic drift, gene flow and mutation), the Hardy–Weinberg genotypic proportions will not change over time. For a system of two codominant alleles with dominant, heterozygous, or recessive types like the CYP2C19, chi-square could be used to test their genotypic proportions and should show no statistically significant differences. We found that there are significant differences between observed and expected proportions in the CYP2C19 genotypes, reflecting the possibility of selection bias of their study, which means the generalization of their results is questionable (Table 1). The proportion of their genotypic distribution is also different from many other studies 4 and our data (Table 1). The results of Sheu et al. showed that the CYP2C19 genotypes can influence the therapeutic effect of different proton-pump inhibitors in the anti-Helicobacter treatment. However, the extensive metabolizer genotypes must be known first for the drug selection. The genotypic distribution of their study may not represent the general population of Taiwan.

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Bor-Shyang Sheu

National Cheng Kung University

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Chiao-Hsiung Chuang

National Cheng Kung University

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Jiunn-Jong Wu

National Cheng Kung University

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Hsiu Chi Cheng

National Cheng Kung University

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Hsiao-Bai Yang

National Cheng Kung University

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Hui Chuan Cheng

National Cheng Kung University

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S.-F. Hunag

National Cheng Kung University

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T.-W. Chen

National Cheng Kung University

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Wei Lun Chang

National Cheng Kung University

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Yao Jong Yang

National Cheng Kung University

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