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Effects and Safety of an Oral Adsorbent on Chronic Kidney Disease Progression: A Systematic Review and Meta-Analysis.
Chen, Ying-Chun; Wu, Mei-Yi; Hu, Ping-Jen; Chen, Tzu-Ting; Shen, Wan-Chen; Chang, Wei-Chiao; Wu, Mai-Szu.
Afiliação
  • Chen YC; Department of Pharmacy, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan. 12556@s.tmu.edu.tw.
  • Wu MY; Division of Nephrology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan. e220121@gmail.com.
  • Hu PJ; Division of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan. e220121@gmail.com.
  • Chen TT; Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei 10617, Taiwan. e220121@gmail.com.
  • Shen WC; Department of Primary Care Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan. e220121@gmail.com.
  • Chang WC; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taitung MacKay Memorial Hospital, Taitung 95054, Taiwan. a801891@hotmail.com.
  • Wu MS; Division of Gastroenterology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan. a801891@hotmail.com.
J Clin Med ; 8(10)2019 Oct 17.
Article em En | MEDLINE | ID: mdl-31627462
ABSTRACT

BACKGROUND:

AST-120 (Kremezin), which is an oral spherical carbon adsorbent, has been reported to have the potential for retarding disease progression in patients with chronic kidney disease. We aimed to evaluate its efficacy and safety in this study.

METHODS:

We systematically searched for randomized controlled trials published in PubMed, Embase, and Cochrane databases. The primary outcomes were the renal outcome and all-cause mortality, and the change in serum indoxyl sulfate (IS) levels. The safety outcome was also evaluated in terms of reported major adverse events. A random-effects model was used when heterogeneity was expected.

RESULTS:

Eight studies providing data for 3349 patients were included in the meta-analysis. The risk ratio of renal outcome and all-cause mortality were 0.97 (95% CI 0.88-1.07; 6 trials) and 0.94 (0.73-1.20; 5 trials), respectively. Furthermore, the weighted mean change in IS levels from baseline to the end of the study was -0.28 mg/dL (95% CI -0.46 to -0.11; 4 trials).

CONCLUSIONS:

This study provides evidence that AST-120 can effectively lower IS levels but still controversial in terms of slowing disease progression and all-cause mortality. Except for dermatological events, the incidence of adverse events did not differ significantly between the AST-120 and placebo groups.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Idioma: En Revista: J Clin Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Idioma: En Revista: J Clin Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Taiwan