Yue Yang

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Name: 杨悦
Organization: Shenyang Pharmaceutical University , China
Department:
Title: Professor(PhD)
Co-reporter:Ting Ting Guo;Yang Song;Yu Ren;Zhi Xin Liu;Gang Cheng
Journal of Digestive Diseases 2016 Volume 17( Issue 1) pp:11-19
Publication Date(Web):
DOI:10.1111/1751-2980.12304

Objective

Midodrine has been reported to improve systemic and renal hemodynamics in patients with cirrhotic ascites. However, the results of clinical trials are conflicting. The aim of this study is to evaluate the effects of midodrine on cirrhotic ascites through a meta-analysis and systematic review.

Methods

We searched PubMed (January 1966–December 2014), EMBASE (January 1966–December 2014), the Cochrane Library (Issue 11, 2014), ScienceDirect (January 1966–December 2014), and the China National Knowledge Infrastructure (January 1979–December 2014) databases using the terms ‘midodrine’ AND ‘cirrhosis’ AND ‘ascites’ AND ‘paracentesis’ for all relevant randomized controlled trials using midodrine for treatment of cirrhotic ascites.

Results

In all, 10 trials with a total of 462 patients were included. As a novel therapy for cirrhotic ascites, midodrine was not found to improve survival [odds ratio (OR) 0.81, 95% confidence interval (CI) 0.23–2.91]; although it might improve response rates (OR 3.36, 95% CI 1.47–7.69) and reduce plasma renin activity (MD −3.10, 95% CI −5.37 to −0.84). When midodrine was used as an alternative to albumin in large-volume paracentesis, the mortality was higher for midodrine than for albumin (OR 10.76, 95% CI 1.35–85.97). However, there was no statistically significant difference in the development of paracentesis-induced circulatory dysfunction between midodrine group and albumin group (OR 1.69, 95% CI 0.43–6.72).

Conclusions

Midodrine may have treatment effects on cirrhotic ascites. Better powered and well-designed trials are required to assess the extent of the efficacy of midodrine in specifically targeted patients.

Co-reporter:Xin Mao, Yue Yang
Journal of Pharmaceutical Sciences (February 2017) Volume 106(Issue 2) pp:652-659
Publication Date(Web):1 February 2017
DOI:10.1016/j.xphs.2016.09.023
The study aims to explore the challenges and the gaps faced by Chinese Drug Control Institutes in achieving the standards of World Health Organization (WHO) Medicine Prequalification. The study was undertaken with 6 Provincial Drug Control Institutes in China from November 2012 to November 2013. The study assessed key elements required to comply with WHO Good Practices for Pharmaceutical Quality Control Laboratories (GPPQCL). For GPPQCL, the study found gaps in quality management system, control of documentation, data-processing equipment, premises and equipment, contracts, reagents (water), reference substances and reference materials, calibration, verification of performance and qualification of equipment, instruments and other devices, analytical worksheet, evaluation of test results, personnel, and validation of analytical procedures. The study indicates that gaps are attributed to differences between the standards of Chinese Accreditation Standards and WHO-GPPQCL.
Renin
Propanedial
FORSYTHIN
ACETONITRILE
MIDODRINE