Affiliations 

  • 1 Infectious Disease Division, Respiratory and Enteric Infections Department, International Center for Diarrheal Disease Research, Dhaka, Bangladesh; Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan. Electronic address: hasandmck66@gmail.com
  • 2 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Faculty of Medicine, Al-Azhar University, Cairo, Egypt. Electronic address: khaledelhosiny8@gmail.com
  • 3 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Saigon General Hospital, Ho Chi Minh City, Vietnam; University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam. Electronic address: huuhoai.md@gmail.com
  • 4 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Faculty of Health Sciences, McMaster University, Hamilton, ON. Canada. Electronic address: tieut@mcmaster.ca
  • 5 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; School of Medicine, Faculty of Health and Medical Sciences, Taylor's University, Selangor, Malaysia. Electronic address: soonkhai.low@gmail.com
  • 6 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Saigon General Hospital, Ho Chi Minh City, Vietnam. Electronic address: lehuunhatminh.md@ump.edu.vn
  • 7 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Department of Biomedical Engineering, South Dakota School of Mines and Technology, Rapid City, 57701, United States. Electronic address: banghia0905@gmail.com
  • 8 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Saigon General Hospital, Ho Chi Minh City, Vietnam. Electronic address: lequangloc.md@gmail.com
  • 9 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Department of Chemical and Biological Engineering, South Dakota School of Mines and Technology, Rapid City, 57701, United States. Electronic address: vivianmai1993@gmail.com
  • 10 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Faculty of Medicine, Ain Shams University, Cairo, Egypt. Electronic address: petersamuel86@gmail.com
  • 11 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Institute of Medical Technology, Baghdad, Iraq. Electronic address: drabedmn@gmail.com
  • 12 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Faculty of Medicine, Menoufia University, Yassin Abdel-ghaffar Street, Shebin El-Kom, Menoufia, 32511, Egypt. Electronic address: salma.said56.ss@gmail.com
  • 13 Online Research Club (http://www.onlineresearchclub.org/), Nagasaki, Japan; Faculty of Medicine, Ain Shams University, Cairo, Egypt. Electronic address: dr.gehadmohamed@hotmail.com
  • 14 Evidence Based Medicine Research Group, Ton Duc Thang University, Ho Chi Minh City, 70000, Vietnam; Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, 70000, Vietnam. Electronic address: nguyentienhuy@tdtu.edu.vn
Acta Trop, 2020 Oct;210:105603.
PMID: 32598920 DOI: 10.1016/j.actatropica.2020.105603

Abstract

We aimed to systematically review evidence pertaining to the safety and efficacy of nitazoxanide in treating infectious diarrhea. On September 21, 2017, we identified relevant studies using 12 databases. The estimates of the included studies were pooled as a risk ratio (RR). We conducted a network and pairwise random-effects meta-analysis for both direct and indirect comparisons of different organisms that are known to cause diarrhea. The primary and secondary analysis outcomes were clinical response until cessation of illness, parasitological response and adverse events. We included 18 studies in our analysis. In cryptosporidiosis, the overall estimate favored nitazoxanide in its clinical response in comparison with placebo RR 1.46 [95% CI 1.22-1.74; P-value <0.0001]. Network meta-analysis among patients with Giardia intestinalis showed an increase in the probability of diarrheal cessation and parasitological responses in comparison with placebo, RR 1.69 [95% CI 1.08-2.64, P-score 0.27] and RR 2.91 [95% CI 1.72-4.91, P-score 0.55] respectively. In Clostridium difficile infection, the network meta-analysis revealed a non-significantly superior clinical response effect of nitazoxanide to metronidazole 31 days after treatment RR 1.21 [95% CI 0.87-1.69, P-score 0.26]. In Entamoeba histolytica, the overall estimate significantly favored nitazoxanide in parasitological response with placebo RR 1.80 [95% CI 1.35-2.40, P-value < 0.001]. We highlighted the effectiveness of nitazoxanide in the cessation of diarrhea caused by Cryptosporidium, Giardia intestinalis and Entamoeba histolytica infection. We also found significant superiority of NTZ to metronidazole in improving the clinical response to G. intestinalis, thus it may be a suitable candidate for treating infection-induced diarrhea. To prove the superiority of NTZ during a C. difficile infection may warrant a larger-scale clinical trial since its superiority was deemed insignificant. We recommend nitazoxanide as an appropriate option for treating infectious diarrhea.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.