F. M. Y. Fung
University of Hong Kong
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Publication
Featured researches published by F. M. Y. Fung.
Alimentary Pharmacology & Therapeutics | 2003
Wm Wong; Qing Gu; S. K. Lam; F. M. Y. Fung; Kc Lai; Whc Hu; Yuk Kei Yee; C. K. Chan; Hhx Xia; M.-F. Yuen; B. C. Y. Wong
Aim : To test the efficacy of rabeprazole, levofloxacin and rifabutin triple therapy vs. quadruple therapy for the second‐line treatment of Helicobacter pylori infection.
Alimentary Pharmacology & Therapeutics | 2006
Wm Wong; Qing Gu; Kent-Man Chu; Y. K. Yee; F. M. Y. Fung; Teresa Tong; Aoo Chan; Kc Lai; C. K. Chan; B. C. Y. Wong
To test the efficacy of levofloxacin‐based second‐line therapy for resistant Helicobacter pylori infection.
Alimentary Pharmacology & Therapeutics | 2005
B. Xia; Hhx Xia; C. W. Ma; K. W. Wong; F. M. Y. Fung; C.-K. Hui; C. K. Chan; Aoo Chan; Kc Lai; M.-F. Yuen; B. C. Y. Wong
Background: Peptic ulcer disease is mainly caused by Helicobacter pylori infection and the use of non‐steroidal anti‐inflammatory drugs.
Alimentary Pharmacology & Therapeutics | 2001
B. C. Y. Wong; W. H. Wang; Douglas E. Berg; F. M. Y. Fung; K. W. Wong; Wai Man Wong; Kar-Neng Lai; C. H. Cho; Wai Mo Hui; S. K. Lam
Diversity in metronidazole susceptibility and genotypes of Helicobacter pylori have been reported with varying results in different areas.
Alimentary Pharmacology & Therapeutics | 2002
Wai Man Wong; B. C. Y. Wong; H. Lu; Q. Gu; Yan Yin; W. H. Wang; F. M. Y. Fung; Kar-Neng Lai; Hhx Xia; S. D. Xiao; S. K. Lam
To test the efficacy of omeprazole, furazolidone and amoxicillin triple therapy for the treatment of Helicobacter pylori infection after failure of standard first‐line therapy recommended by the Asia‐Pacific Consensus on the management of H. pylori infection.
Alimentary Pharmacology & Therapeutics | 2000
Wai Man Wong; B. C. Y. Wong; K. W. Wong; F. M. Y. Fung; Kar-Neng Lai; Whc Hu; Siu Tsan Yuen; Sy Leung; G. K. K. Lau; Ching-Lung Lai; C. K. Chan; R. Go; Shiu Kum Lam
Conventional 13C‐urea breath testing (13C‐UBT) includes a test meal to delay gastric emptying, which, theoretically, improves the accuracy of the test. Citric acid has been proposed as the best test meal. However, recent studies have suggested that a test meal may not be necessary.
Clinical Infectious Diseases | 2003
Wai Man Wong; Qing Gu; W. H. Wang; F. M. Y. Fung; Douglas E. Berg; Kam Chuen Lai; Harry Hua-Xiang Xia; Wayne H. C. Hu; Chi Kuen Chan; Annie On-On Chan; Man-Fung Yuen; Chee-Kin Hui; Shiu Kum Lam; Benjamin Chun-Yu Wong
The aim of this study was to investigate the effect of metronidazole resistance (MtzR) and clarithromycin resistance (ClaR) on the eradication rate for omeprazole, clarithromycin, and metronidazole triple-therapy regimen and on the development of posttherapy drug resistance in a region of high rates of MtzR. One hundred ninety-six Helicobacter pylori isolates were recovered from patients with duodenal ulcer, gastric ulcer, or nonulcer dyspepsia during upper endoscopy. The prevalences of MtzR, ClaR, and dual resistance were 37.8%, 13.8%, and 8.7%, respectively. The intention-to-treat eradication rates for metronidazole-susceptible (87.2% vs. 67.6%; P=.001) and clarithromycin-susceptible (86.4% vs. 40.7%; P<.001) strains were significantly higher than the rates for resistant strains. Multiple logistic regression analysis implicated younger age (<40 years old), MtzR, ClaR, and the diagnosis of nonulcer dyspepsia as independent factors that predicted treatment failure. The rates of posttreatment MtzR, ClaR, and dual resistance were 88%, 88%, and 75%, respectively. MtxR and ClaR significantly affected the success of eradication therapy. Posttreatment rates of resistance were high and were related to the presence of pretreatment antibiotic resistance.
Alimentary Pharmacology & Therapeutics | 2001
B. C. Y. Wong; Wai Man Wong; W. H. Wang; F. M. Y. Fung; Kar-Neng Lai; Kent-Man Chu; Siu Tsan Yuen; Sy Leung; Whc Hu; M.-F. Yuen; G. K. K. Lau; C. K. Chan; S. K. Lam
To compare 1‐week ranitidine bismuth citrate‐based (RBC) triple therapy vs. omeprazole‐based (O) triple therapy for the eradication of Helicobacter pylori infection in Hong Kong with high prevalence of metronidazole resistance.
Alimentary Pharmacology & Therapeutics | 2002
Hhx Xia; B. C. Y. Wong; Wai Man Wong; Vsy Tang; H. K.-L. Cheung; F. N. F. Sham; F. M. Y. Fung; Kar-Neng Lai; Whc Hu; C. K. Chan; S. K. Lam
Numerous serological tests for the detection of Helicobacter pylori infection have been developed. However, many perform poorly when evaluated in the Chinese population.
Digestion | 2006
Qing Gu; Hhx Xia; Ji De Wang; Wm Wong; Aoo Chan; Kc Lai; C. K. Chan; M.-F. Yuen; F. M. Y. Fung; K. W. Wong; S. K. Lam; B. C. Y. Wong
Aim: To determine the antibiotic susceptibility of Helicobacter pylori and evaluate the efficacy of a clarithromycin-based triple therapy in relation to antibiotic resistance. Methods: Consecutive patients referred for upper endoscopy due to dyspeptic symptoms were recruited. Gastric biopsies were obtained for the CLO test, histology and culture. Antibiotic susceptibility was assessed by the E-test. Patients with H. pylori infection received rabeprazole 20 mg, clarithromycin 500 mg, and amoxicillin 1,000 mg, all twice daily for 7 days. Results: Of 234 patients recruited, 124 were H. pylori-positive and culture was successful in 102 patients. The updated prevalences of resistance to clarithromycin, amoxicillin and metronidazole were 7.8, 0 and 39.2%, respectively. A total of 86 patients received 1-week triple therapy with rabeprazole 20 mg, clarithromycin 500 mg, and amoxicillin 1,000 mg, all twice daily, and 81 patients attended the follow-up test. Eradication rates by per-protocol and intention-to-treat analysis were 92.6 and 87.2%, respectively. The eradication rate by per protocol was significantly higher in patients with clarithromycin-susceptible strains than in those with clarithromycin-resistant strains (98.6 vs. 28.6%, p < 0.001). Conclusion: Clarithromycin resistance reduces the clinical efficacy of clarithromycin-based triple therapy. However, due to the low prevalence of clarithromycin resistance, clarithromycin-based therapy is still the first choice for clinical use.