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Showing papers by "Long H. Nguyen published in 2017"


Journal ArticleDOI
16 Mar 2017-Gut
TL;DR: Long-term antibiotic use in early-to-middle adulthood was associated with increased risk of colorectal adenoma, and recent antibiotic use within the past four years was not associated with risk.
Abstract: Objective Recent evidence suggests that antibiotic use, which alters the gut microbiome, is associated with an increased risk of colorectal cancer. However, the association between antibiotic use and risk of colorectal adenoma, the precursor for the majority of colorectal cancers, has not been investigated. Design We prospectively evaluated the association between antibiotic use at age 20–39 and 40–59 (assessed in 2004) and recent antibiotic use (assessed in 2008) with risk of subsequent colorectal adenoma among 16 642 women aged ≥60 enrolled in the Nurses9 Health Study who underwent at least one colonoscopy through 2010. We used multivariate logistic regression to calculate ORs and 95% CIs. Results We documented 1195 cases of adenoma. Increasing duration of antibiotic use at age 20–39 (p trend =0.002) and 40–59 (p trend =0.001) was significantly associated with an increased risk of colorectal adenoma. Compared with non-users, women who used antibiotics for ≥2 months between age 20 and 39 had a multivariable OR of 1.36 (95% CI 1.03 to 1.79). Women who used ≥2 months of antibiotics between age 40 and 59 had a multivariable OR of 1.69 (95% CI 1.24 to 2.31). The associations were similar for low-risk versus high-risk adenomas (size ≥1 cm, or with tubulovillous/villous histology, or ≥3 detected lesions), but appeared modestly stronger for proximal compared with distal adenomas. In contrast, recent antibiotic use within the past four years was not associated with risk of adenoma (p trend =0.44). Conclusions Long-term antibiotic use in early-to-middle adulthood was associated with increased risk of colorectal adenoma.

138 citations


Journal ArticleDOI
TL;DR: The data do not support the suggestion that PPI use increases dementia risk, and associations for H2 receptor antagonists (H2RAs) are examined as a secondary aim.

62 citations


Journal ArticleDOI
TL;DR: The primary and secondary prevention of spontaneous bacterial peritonitis is recommended in high‐risk patients with cirrhosis and rifaximin has the potential advantage of preventing bacterial overgrowth and translocation without the systemic side effects of broad‐spectrum antibiotics.
Abstract: SummaryBackground The primary and secondary prevention of spontaneous bacterial peritonitis (SBP) is recommended in high-risk patients with cirrhosis. Several studies evaluating the efficacy of rifaximin for SBP prophylaxis have yielded conflicting results. Rifaximin has the potential advantage of preventing bacterial overgrowth and translocation without the systemic side effects of broad-spectrum antibiotics. Aim To evaluate the efficacy of rifaximin in the primary and secondary prevention of SBP. Methods A literature search using five databases was performed to identify studies on the association between rifaximin and SBP. We performed two meta-analyses: (1) rifaximin compared to systemic antibiotics and (2) rifaximin compared to no antibiotics. Random-effect modelling was conducted to determine overall pooled estimates and 95% confidence intervals (CIs). Results Five studies with 555 patients (295 rifaximin, 260 systemic antibiotics) compared rifaximin with systemic antibiotics. The pooled odds ratio (OR) for SBP was 0.45 (95% CI 0.16-1.27; P = .13) in patients receiving rifaximin and strengthened on sensitivity analysis (OR 0.38, 95% CI 0.19-0.76, P = .01). In the analysis comparing rifaximin with no antibiotics, there were five studies with 784 patients (186 rifaximin, 598 no antibiotics). The OR for SBP was 0.34 (95% CI 0.11-0.99; P < .05) in patients receiving rifaximin. In subgroup analysis, rifaximin reduced the risk of SBP by 47% compared to no antibiotics for primary prophylaxis and by 74% compared to systemic antibiotics for secondary prophylaxis. Conclusion Rifaximin may be effective in preventing SBP in patients with cirrhosis and ascites compared to systemically absorbed antibiotics and compared to placebo.

56 citations