Skip to main content Skip to main navigation menu Skip to site footer

open access & Peer Reviewed

Probiotics for Diarrhea in Children

Anirban Mandal, Puneet Kaur Sahi

Downloads

Download data is not yet available.

Abstract

Diarrhea remains the second leading cause of death in children below 5 years of age; in addition it is also the reason for a considerable morbidity in children of all ages throughout the globe. Apart from oral rehydration solution, continued feeding, oral zinc and antibiotics for diarrhea of bacterial etiology, there have been no other proven measures for diarrheal illnesses in children. Probiotics are non-pathogenic live microorganisms. When ingested, probiotics can survive passage through the stomach and small bowel. Probiotics are supposed to have preventive as well as curative effects on several types of diarrhea of different etiologies.

Keywords: Gastroenteritis, Saccharomyces, Bifidobacterium, Functional food.

Introduction

Diarrheal disease is responsible for a huge burden on human society. Even with improvements in the case management, diarrhea is responsible for 1.5 million deaths annually, or 1% of deaths in children under 5 years. Although the majority of these deaths occur in the developing world, it is a common reason for medical consultation and hospital admission in Western societies and exacts an enormous social toll in terms of loss of productivity among affected individuals and their caregivers [1].

Probiotics, commonly known as “good bacteria” can offer health benefits in a number of ways when consumed. The use of probiotic microorganisms for the prevention or therapy of gastrointestinal disorders is an obvious measure and perhaps the most usual application of probiotics because most health effects attributed to them are related directly or indirectly to the gastrointestinal tract [2]. In this review, we summarize the available evidence on the use of probiotics for diarrheal diseases in children.

History

The health benefits of bacteria consumed in food have been known since ages; records dating back to as early as the Persian version of the Old Testament. Noble laureate Elie Metchnikoff in 1908 suggested that products of proteolytic bacterial action on protein resulted in “intestinal autointoxication”. He presented a hypothesis that consumption of yogurt containing Lactobacillus lead to reduced number of toxin-producing bacteria in the intestine and thus contributed to the long life of Bulgarian peasants [3]. The concept of probiotic is derived from the Greek word meaning “for life” and the term came into practice in 1965 [4]. Since then the interest in probiotics has grown many folds and currently, the market for probiotics has reached to over 60 billion USD [5].

Definition and properties of probiotics

The FAO/ WHO defines probiotic as a “live microorganism which, when administered in adequate amounts, confer a health benefit to the host” [6]. Following this, the International Life Science Institute (ILSI) [7] and the European Food and Feed Cultures Association (EFFCA) [8] have given similar definitions for probiotic: “a live microbial food ingredient that, when consumed in adequate amounts, confers health benefits on the consumers”. The properties of an ideal probiotic should be [9]:

  1. of human origin

  2. nonpathogenic

  3. contains sufficient number of viable cells

  4. unaffected to destruction by technical processing

  5. unaffected to destruction by gastric acid and bile

  6. adhere to intestinal epithelium

  7. able to inhabit the gastrointestinal tract, even if for a short time

  8. producing antimicrobial substances

  9. modulating immune responses

  10. influencing human metabolic activities (i.e. cholesterol assimilation, vitamin production) and

  11. undergone in vivo and in-vitro trials to prove any attributed probiotic effect and documented a clinical benefit

Common probiotic strains

Various organisms (bacteria and fungus) have been identified as meeting the diagnostic criteria for probiotics. The common ones are presented in (table 1).

Table 1 Common probiotic strains
Bifidobacterium spp Lactobacillus spp Saccharomyces spp
B. bifidum L. acidophilus S. boulardii
B. breve L. casei (rhamnosus)
B. lactis L. fermentum
B. longum L. gasseri
B. infantis L. johnsonii
B. adolescents L. lactis
B. paracasei
B. plantarum
B. reuteri

The indigenous intestinal flora

There are an estimated 1014 cells in human body, and out of this only 10% are not bacteria. The gastrointestinal tract of mammals is a complex, dynamic and diverse ecosystem comprising of interactions between aerobic and anaerobic, nonpathogenic bacteria. There are 400 separate species in this complex yet stable colony. The majority of the gut organisms, which represent 40% of the fecal weight, are accounted for by luminal flora; nevertheless, the organisms present in the fecal matter do not necessarily signify the important host-microbial symbiosis of the mucosal bound flora [10]. Within first few days after birth, the newborn’s gut is colonized with bacteria. A diverse range of bacteria inoculates the gut initially; this includes Bifidobacteria, Enterobacteria, Bacteroids, Clostridia, and Gram-positive cocci. Later on, there are swift changes in the flora depending on the mode of delivery, gestational age, and diet (breastfeeding/ formula feeding). Vaginally delivered breastfed infants have similar colonization to vaginally born formula-fed infants at 48 hours of life, indicating a similar “inoculums”. However, by 7 days, only 22% of breastfed infants are colonized with B. fragilis, as compared to 61% of those fed on formula [11]. Interestingly, there is a minimal role of diet in the composition of fecal flora in the older child and adult [12].

Fungi are present in the stools of up to 65% of individuals, Candida being the predominant genus. It appears that pathogenic colonization by yeast, under normal circumstances, is inhibited by the normal bacterial flora. However, alteration or destruction of the fecal flora by antibiotics would lead to yeast multiplying in great numbers [13].

Mechanism of action of probiotics in diarrhea

Although animal and molecular studies have generated a great deal of data, most theories remain speculative and confirmation of findings in vivo and in human clinical trials have been lacking. Almost certainly multiple mechanisms operate together and it is clear that single strains may act using different mechanisms in different disease processes [14].

Many probiotic organisms elaborate ‘bacteriocins’, restricting the growth or pathogenicity of non-homologous strains. Other probiotic activities including the production of lactic acid, short chain fatty acids and hydrogen peroxide lower intraluminal pH and contribute to a hostile environment for other potentially pathogenic species. Some probiotic products, such as proteases produced by Saccharomyces boulardii have been shown to degrade toxins produced by pathogens such as Clostridium deficile, Vibrio cholera or pathogenic Escherichia coli [15]. Additionally, probiotics metabolic activity may have useful nutritional or clinical activity. It has long been appreciated that the enzyme ß-galactosidase produced by lactobacilli may be useful in preventing diarrhea in individuals with acquired deficiency of this enzyme [16].

Some probiotic agents are able to bind directly to invasive species or to otherwise disrupt their ability to interact with or bind to endothelial receptors. Probiotics including several species of Lactobacillus have been shown to upregulate goblet cell production of mucins and protective ‘trefoil factors’. They also stimulate crypt located Paneth cells in the production of ‘defensins’, cationic proteins which are able to insert themselves into microbial membranes to form destructive pores. In addition, probiotics may also influence proteins controlling tight junctions between enterocytes, reducing the potential for the absorption of harmful macromolecules and the ability of luminal pathogens to translocate into the submucosal space [17].

Submucosal: Critical to the development of innate immunity is the system for recognizing microbe-associated molecular patterns (MAMPs)-conserved regions comprising motifs or repeating units from a wide range of molecules including lipopolysaccharides, peptidoglycans, and nucleic acids found more frequently on the surface of microbial species than on host cells. These pattern recognition receptors (PRRs) including the toll-like receptors (TLR) on the surface of host cells (including dendritic cells in the gut) are key determinants of detection and host interaction directing subsequent effector response [18]. Adaptive immune responses have also been shown to be influenced by the presence of probiotic organisms, some of which are able to stimulate immunoglobulin (particularly secretory IgA) production and to modulate the development and activity of regulatory T-lymphocytes. Similarly, probiotics are known to influence the pattern of cytokine release as well.

It is likely that host-microbe signaling takes place continuously rather than awaiting recruitment at the time of disease. The potential for probiotics to influence this series of interactions through the activation of NF-ĸß, thereby controlling DNA transcription, the inflammatory response and the balance of TH1/TH2 activation, hold exciting promise for the ability of these agents to influence chronic inflammatory processes [19]. Such effects are also likely to be important in modulating the immune response to acute infection within the gastrointestinal tract.

The molecular interactions between host and microbiota have been shown to have an influence on the enteric nervous and endocrine systems. Experimental work has identified the activity of certain probiotic species in inducing opioid and cannabinoid receptors in the gastrointestinal tract as well [20].

Probiotics Uses

Probiotics for diarrhea of viral origin

Viral agents are responsible for acute diarrheal episodes in children throughout the world with Rotavirus being the most important agent. A Cochrane database of systematic review compiled pooled estimates of benefit for Lactobacillus in acute rotavirus diarrhea [Allen SJ 21] and found a reduction in the duration of diarrhea of 29 hours (95% CI 16-42 hours), a reduction in stool frequency on day 2 following the intervention of 1.25 stools per day (95% CI 0.4-2.1). Grandy et al [22] studied S. boulardii alone or in combination with three other probiotics including two strains of Lactobacillus in rotavirus diarrhea. Both products seemed to be associated with a reduction in the duration of diarrhea. However, a Turkish study found benefit in terms of reduced duration of diarrhea for one of only four intervention groups given S. boulardii [23].

Although a number of treatment studies have reported the detection of other (i.e. non-rotavirus) viral agents [24, 25], individual isolates have been few in number and no studies have reported primary or secondary outcomes for probiotics administered for acute diarrheal episodes attributable to specific viral etiologies other than rotavirus.

Similarly, studies of prevention of diarrheal disease have generally failed to provide evidence of protection against specific viral agents. A Peruvian study in the prevention of diarrhea in children aged 6-29 months reported a reduction in the detection of adenovirus from stool specimens in a cohort supplemented with Lactobacillus GG [26]. But, on the other hand, Sur et al. have found no difference in recovery rates for adenovirus, rotavirus, norovirus, or astrovirus for children from a deprived urban setting of India, receiving L. casei Shirota compared with a control cohort [27].

Children with HIV (Human immunodeficiency virus) infection comprise a special population which is susceptible to diarrheal illnesses due to a host of infections. The published studies on the efficacy of probiotics in the treatment of diarrhea in this population have come to disparate conclusions; some [28, 29] but not others [30, 31], finding efficacy. In a large study of Malawian children with severe acute malnutrition [32], over 40% of whom were HIV positive, were randomized to receive a multicomponent probiotic containing lactobacilli or placebo. The study did not find an improvement in rates of diarrhea for probiotic recipients.

Probiotics for bacterial diarrhea

Two studies of Lactobacillus rhamnosus GG found no evidence of protection for the 15-20% of children with ‘invasive’ pathogens, principally Salmonella or Shigella [33]. In the only study specifically addressing bacterial disease, there was an earlier resolution of diarrhea for LGG (co-treated with trimethoprim-sulfamethoxazole) during an outbreak of Shigella dysentery in Estonia [34]. Hwe et al [35] described an improvement in stool consistency for 20 children with pathogenic E. coli cultured from the stool. However, a three-species probiotic mixture including Escherichia faecium was not found to significantly reduce the duration of diarrhea due to Salmonella or Campylobacter in Taiwan [25]. Several studies using combination probiotic products (S. boulardii or E. coli Nissle 1917) in middle-income countries report overall efficacy for groups with significant (10-20%) contributions from pathogenic species but sufficient data is not provided to assess efficacy by diarrheal pathogen [36, 37, 38, 39].

A large community prevention study from India [27] documented a reduction of diarrheal disease with Aeromonas and Cryptosporidium species in Lactobacillus casei Shirota recipients; though other bacteria (including pathogenic E. coli), viral and protozoal species were recovered at equivalent rates. Another study from urban India reported protection against dysentery (defined by a parental history of bloody diarrhea), although no impact was seen on the overall incidence of diarrhea [40].

Probiotics for parasitic diarrhea

A Cuban study in children with persistent diarrhea (35 out of 40 having giardial cysts in stool) improved with administration of S. boulardii [41]. In cases of amoebic dysentery, reduced duration of bloody diarrhea and a lower rate of cyst excretion on day 5 are reported in 25 Turkish children receiving Saccharomyces [41]. A randomized trial in 48 symptomatic children with Blastocystis hominis demonstrated higher rates of clinical cure and disappearance of cysts from the stool with probiotics [43].

Probiotics for Clostridium defficile associated diarrhea (CDAD)

Although a meta-analysis performed by McFarland for the treatment of CDAD found evidence in favor of treatment with S. boulardii [44], the Cochrane group and other reviewers [45, 46, 47] have conclude that despite holding promise, currently data are not sufficient to make a recommendation for the use of Saccharomyces or other Probiotics for the treatment of primary or relapsing CDAD.

Five published studies of the use of Saccharomyces in the prevention of antibiotic-associated diarrhea (AAD) have provided secondary outcome measures for CDAD. Reviewers [45, 48, 49] have concluded that inadequate evidence currently exists in order to make a recommendation concerning the role of S. boulardii or other Probiotics in the primary prevention of CDAD.

Probiotics for antibiotic associated diarrhea (AAD)

There have been no published RCT investigating the effect of Probiotics for the treatment of non-Clostridium defficile AAD in children; thus, their use cannot be recommended at this time.

A Cochrane meta-analysis of probiotic use of children to prevent or ameliorate (i.e. shorten duration and/ or severity) AAD [50] documents that probiotics produced a statistically significant reduction in the incidence of AAD (RR 0.52; 95% CI 0.38-0.72) with the number needed to prevent one case of AAD being 7. Analysis of secondary outcomes revealed that probiotics decreased the mean duration of diarrhea by three-quarters of a day. The difference in mean stool frequency was not statistically significant. Analysis by probiotic strain revealed a significant effect for LG and Lactobacillus sporogenes but not for boulardii.

Probiotics for traveler’s diarrhea

Several studies using lactobacilli have suggested benefit in protecting travelers from diarrhea, but in only one study using a mixture of strains (containing Lactobacillus acidophilus, Lactobacillus bulgaricus, Bifidobacterum bifidum and Streptococcus thermophilus) was the reduction in the overall incidence of diarrhea statistically significant [51]. Travelers to a variety of destinations including North Africa, South America, India and Turkey derived some measure of protection from S. boulardii [52]. Several attempts have been made to conduct meta-analysis from these data, estimating risk ratios marginally in favor of probiotics (RR estimates between 0.85 and 0.93) but with confidence intervals close to or encompassing the point of equivalence [53, 54, 55].

Probiotics for diarrhea in children attending day care centers

One RCT documented that a daily administration of L. reuteri for 3 months in 336 otherwise healthy, Mexican children attending day care centers a significant reduction in the number of episodes of diarrhoea, episodes of diarrhoea per child, mean duration of diarrhoea episodes and days with diarrhea per child both during the intervention and for the next 3-month follow-up period compared to the placebo group [56]. Another RCT carried out in malnourished Indonesian children found that the consumption of regular calcium milk with L. reuteri compared with regular calcium milk alone reduced the risk of diarrhoeal disease [57]. A double-blind RCT from Croatia in 210 children attending daycare centers found that that B. animalis subsp. lactis BB-12 given for months had no effect on the prevention of gastrointestinal [58].

Probiotics for persistent diarrhea

A Cochrane review of probiotics for persistent diarrhea [59] yielded a pooled estimate for reduction in the mean duration of diarrhea from 9 to 4 days, with significantly fewer stools on day 5 (a reduction from a mean of 5 to fewer than 2 stools per day).

Probiotics for acute diarrhea of undetermined etiology

A 2010 Cochrane database of systematic review provides a meta-analysis of 63 studies of probiotic agents involving more than 8000 participants, mostly children, conducted in a variety of geographical and social settings [21]. Overall conclusions suggest that probiotics shorten the duration of diarrhea by 24 hours {95% confidence interval (CI) 16-33 hours} and for a mean difference in stool frequency on day 2 of 0.8 (95% CI 0.4-1.1), with a relative risk of continuing diarrhea on day 4 of 0.4 (95% CI 0.3-0.5). No adverse effects were attributed in these studies to the administration of the probiotic.

There is still clearly much to learn about how best to use probiotics in acute diarrheal disease. Only a few studies have directly compared probiotic products [60-63] or ranged doses [64, 65]. The Cochrane review [21] found similar pooled estimates of efficacy for studies conducted in countries categorized by high or low mortality, nevertheless, a preponderance of negative studies [66, 67, 68, 69, 70, 71] have been reported from resource-limited settings where infectious agents and the intestinal microbiota might be expected to be different from those of Western societies. Other little-explored influences on treatment include the role of prebiotic nutritional supplements, breastfeeding [26] or other dietary practices, the effects of accompanying or recent antibiotic treatment, the availability of clean water and adequate sanitation and other currently ill-defined influences on the resident microbiota.

Uncertainties aside, majority of reviewers and expert committees [65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76], including American Academy of Pediatrics [77] and European Society of Pediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) [78] have concluded that preparations containing probiotics (of the specific strains studied in these trials) both shorten the duration and reduce the severity of acute diarrhea in children.

Safety of probiotics

Probiotics are considered ‘generally recognized as safe’ (GRAS) and well tolerated in humans but case reports have described bacteremia and fungemia secondary to probiotics. For example, there is a report of a 1-year-old immunocompetent child developing fungemia after receiving S. boulardii for gastroenteritis [79]. The Mayo Clinic reported eight immunocompromised patients post-liver transplant having positive blood culture for Lactobacillus [80]. Furthermore, two infants with short bowel syndrome were found to be bacteremic withprobiotic strains of Lactobacillus GG [81]. Long-term use of probiotics under antibiotic selection pressure could cause antibiotic resistance, and the resistance gene could be transferred to other bacteria [82]. The committee on Nutrition of the European Society of Pediatric Gastroenterology, Hepatology and Nutrition concluded that more studies are required to establish the safety and efficacy of probiotics in children. Till date safety of probiotics is established in healthy infants and children. Caution should be exercised when using these in immunocompromised patients or those with indwelling central venous catheters. It is out of the purview of The American Food and Drug Administration to establish a formal regulatory category for functional foods that includes probiotics. Variations in products do exist and some studies have even found that certain preparations contain no viable bacteria.

Conclusion

A low-cost probiotic intervention capable of reducing the risks of diarrhea in the early years of life, even with modest efficacy, would have an enormous impact on the developing world. Assuming that efficacy is confirmed for prevention and treatment of childhood diarrhea in these settings, a great deal of work will be needed for its broad implementation.

References

  1. Walker CL, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, et al. Global burden of childhood pneumonia and diarrhoea. Lancet. 2013;381(9875):1405-16. View Article Google Scholar
  2. De-Vrese M, Marteau PR. Probiotics and prebiotics: effects on diarrhea. J Nutr. 2007;137(S3):803S-11S. View Article Google Scholar
  3. Metchnikoff II. The prolongation of life: optimistic studies. The prolongation of life: optimistic studies. 2004;:-. View Article Google Scholar
  4. Lilly DM, Stillwell RH. Probiotics: growth-promoting factors produced by microorganisms. Science. 1965;147(3659):747-8. View Article Google Scholar
  5. Probiotic Ingredients Market by Function (Regular, Preventative, Therapy), Application (Food & Beverage, Dietary Supplements, & Animal Feed), End Use (Human & Animal Probiotics), Ingredient (Bacteria & Yeast), and by Region - Global Trends & Forecast to 2020. . . View Article
  6. Joint FAO/WHO Working Group, Joint FAO/WHO Working Group. Guidelines for the evaluation of probiotics in food.London: World Health Organization, ON, Canada: Food and Agriculture Organization; 2002. View Article
  7. Roberfroid MB. Concepts In Functional Foods. Nutrition Today. 1999;34(4):162-65. View Article Google Scholar
  8. Bourdichon F, Casaregola S, Farrokh C, Frisvad JC, Gerds ML, Hammes WP, Harnett J, Huys G, Laulund S, Ouwehand A, Powell IB. Food fermentations: microorganisms with technological beneficial use. International journal of food microbiology 2012 Mar. 15;154(3):87-97. View Article Google Scholar
  9. Borchers AT, Selmi C, Meyers FJ, Keen CL, Gershwin ME. Probiotics and immunity. J Gastroenterol. 2009;44(1):26-46. View Article Google Scholar
  10. Teitelbaum JE, Wyllie R, Hyams JS. Indigenous flora. Pediatric Gastrointestinal and Liver Disease, 4th Edition. Philadelphia: Elsevier Inc. 2011;28-38. . . View Article
  11. Long S, Swenson R. Development of anaerobic fecal flora in healthy newborn infants. J Pediatr. 1977;91:298-301. View Article Google Scholar
  12. Simon G, Gorbach S. The human intestine microflora. Dig Dis Sci. 1986;31:127-62. View Article Google Scholar
  13. Eckburg PB, Bik EM, Bernstein CN, Purdom E, Dethlefsen L, Sargent M, et al. Diversity of the human intestinal microbial flora. Science. 2005;308(5728):1635-8. View Article Google Scholar
  14. Cruchet S, Furnes R, Maruy A, Hebel E, Palacios J, Medina F, at al. The use of probiotics in pediatric gastroenterology: a review of the literature and recommendations by Latin-American experts. Paediatr Drugs. 2015;17(3):199-216. View Article Google Scholar
  15. Castagliuolo I, Riegler MF, Valenick L, LaMont JT, Pothoulakis C. Saccharomyces boulardii protease inhibits the effects of Clostridium difficile toxins A and B in human colonic mucosa. Infect Immun. 1999;67(1):302-7. View Article Google Scholar
  16. de Vrese M, Stegelmann A, Richter B, Fenselau S, Laue C, Schrezenmeir J. Probiotics compensation for lactase insufficiency. Am J Clin Nutr. 2001;73(Suppl 2):421S-429S. View Article Google Scholar
  17. Hill C, Guarner F, Reid G, Gibson GR, Merenstein DJ, Pot B, et al. Expert consensus document. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic Nat Rev Gastroenterol Hepatol. 2014;11(8):506-14. View Article Google Scholar
  18. Lebeer S, Vanderleyden J, De Keersmaecker SC. Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens. Nat Rev Microbiol. 2010;8(3):171-84. View Article Google Scholar
  19. Sherman PM, Ossa JC, Johnson-Henry K. Unraveling mechanisms of action of probiotics. Nutr Clin Pract. 2009;24(1):10-4. View Article Google Scholar
  20. Yan F, Polk DB. Probiotics as functional food in the treatment of diarrhea. Curr Opin Clin Nutr Metab Care. 2006;9(6):717-21. View Article Google Scholar
  21. Allen SJ, Martinez EG, Gregorio GV, Dans LF. Probiotics for treating acute infectious diarrhoea. Cochrane Database Syst Rev. 2010;(11):CD003048-. View Article Google Scholar
  22. Grandy G, Medina M, Soria R, Terán CG, Araya M. Probiotics in the treatment of acute rotavirus diarrhoea. A randomized, double-blind, controlled trial using two different probiotic preparations in Bolivian children BMC Infect Dis. 2010;10:253-. View Article Google Scholar
  23. Dalgic N, Sancar M, Bayraktar B, Pullu M, Hasim O. Probiotic, zinc and lactose-free formula in children with rotavirus diarrhea: are they effective? Pediatr Int. . 2011;53(5):677-82. View Article Google Scholar
  24. Szymański H, Pejcz J, Jawień M, Chmielarczyk A, Strus M, Heczko PB. Treatment of acute infectious diarrhoea in infants and children with a mixture of three Lactobacillus rhamnosus strains--a randomized, double-blind, placebo-controlled trial. Aliment Pharmacol Ther 2006. 15;23(2):247-53. View Article Google Scholar
  25. Chen CC, Kong MS, Lai MW, Chao HC, Chang KW, Chen SY, et al. Probiotics have clinical, microbiologic, and immunologic efficacy in acute infectious diarrhea. Pediatr Infect Dis J. 2010;29(2):135-8. View Article Google Scholar
  26. Oberhelman RA, Gilman RH, Sheen P, Taylor DN, Black RE, Cabrera L, et al. A placebo-controlled trial of Lactobacillus GG to prevent diarrhea in undernourished Peruvian children. J Pediatr. 1999;134(1):15-20. View Article Google Scholar
  27. Sur D, Manna B, Niyogi SK, Ramamurthy T, Palit A, Nomoto K, et al. Role of probiotic in preventing acute diarrhoea in children: a community-based, randomized, double-blind placebo-controlled field trial in an urban slum. Epidemiol Infect. 2011;139(6):919-26. View Article Google Scholar
  28. Heiser CR, Ernst JA, Barrett JT, French N, Schutz M, Dube MP. Probiotics, soluble fiber, and L-Glutamine (GLN) reduce nelfinavir (NFV)- or lopinavir/ritonavir (LPV/r)-related diarrhea. J Int Assoc Physicians AIDS Care (Chic). 2004;3(4):121-9. View Article Google Scholar
  29. Anukam KC, Osazuwa EO, Osadolor HB, Bruce AW, Reid G. Yogurt containing probiotic Lactobacillus rhamnosus GR-1 and L. reuteri RC-14 helps resolve moderate diarrhea and increases CD4 count in HIV/AIDS patients J Clin Gastroenterol. 2008;42(3):239-43. View Article Google Scholar
  30. Salminen MK, Tynkkynen S, Rautelin H, Poussa T, Saxelin M, Ristola M, et al. The efficacy and safety of probiotic Lactobacillus rhamnosus GG on prolonged, noninfectious diarrhea in HIV Patients on antiretroviral therapy: a randomized, placebo-controlled, crossover study. HIV Clin Trials. 2004;5(4):183-91. View Article Google Scholar
  31. Trois L, Cardoso EM, Miura E. Use of probiotics in HIV-infected children: a randomized double-blind controlled study. J Trop Pediatr. 2008;54(1):19-24. View Article Google Scholar
  32. Kerac M, Bunn J, Seal A, Thindwa M, Tomkins A, Sadler K, et al. Probiotics and prebiotics for severe acute malnutrition (PRONUT study): a double-blind efficacy randomised controlled trial in Malawi. Lancet. 2009;374(9684):136-44. View Article Google Scholar
  33. Shornikova AV, Isolauri E, Burkanova L, Lukovnikova S, Vesikari T. A trial in the Karelian Republic of oral rehydration and Lactobacillus GG for treatment of acute diarrhoea. Acta Paediatr. 1997;86(5):460-5. View Article Google Scholar
  34. Sepp E, Tamm E, Torm S, Lutsar I, Mikelsaar M, Salminen S. Impact of a Lactobacillus probiotic on the fecal microflora in children with Shigellosis. Microecol Ther. 1999;23(1):74-80. View Article Google Scholar
  35. Htwe K, Yee KS, Tin M, Vandenplas Y. Effect of Saccharomyces boulardii in the treatment of acute watery diarrhea in Myanmar children: a randomized controlled study. Am J Trop Med Hyg. 2008;78(2):214-6. View Article Google Scholar
  36. Kurugöl Z, Koturoğlu G. Effects of Saccharomyces boulardii in children with acute diarrhoea. Acta Paediatr. 2005;94(1):44-7. View Article Google Scholar
  37. Henker J, Laass M, Blokhin BM, Bolbot YK, Maydannik VG, Elze M, et al. The probiotic Escherichia coli strain Nissle 1917 (EcN) stops acute diarrhoea in infants and toddlers. Eur J Pediatr. 2007;166(4):311-8. View Article Google Scholar
  38. Henker J, Laass MW, Blokhin BM, Maydannik VG, Bolbot YK, Elze M, et al. Probiotic Escherichia coli Nissle 1917 versus placebo for treating diarrhea of greater than 4 days duration in infants and toddlers. Pediatr Infect Dis J. 2008;27(6):494-9. View Article Google Scholar
  39. Vivatvakin B, Kowitdamrong E. Randomized control trial of live Lactobacillus acidophilus plus Bifidobacterium infantis in treatment of infantile acute watery diarrhea. J Med Assoc Thai. 2006;89(Suppl 3):S126-33. View Article Google Scholar
  40. Sazawal S, Dhingra U, Hiremath G, Sarkar A, Dhingra P, Dutta A, et al. Prebiotic and probiotic fortified milk in prevention of morbidities among children: community-based, randomized, double-blind, controlled trial. PLoS One. 2010;5(8):e12164-. View Article Google Scholar
  41. Castaneda C, Garcia E, Santa Cruz M, Fernandez M, Monterrey P. Effects of Saccharomyces boulardii in children with chronic diarrhea, especially cases due to giardiasis. Rev Mex Pueric Pediatr. 1995;2:12-16. Google Scholar
  42. Mansour-Ghanaei F, Dehbashi N, Yazdanparast K, Shafaghi A. Efficacy of saccharomyces boulardii with antibiotics in acute amoebiasis. World J Gastroenterol. 2003;9(8):1832-3. View Article Google Scholar
  43. Dinleyici EC, Eren M, Dogan N, Reyhanioglu S, Yargic ZA, Vandenplas Y. Clinical efficacy of Saccharomyces boulardii or metronidazole in symptomatic children with Blastocystis hominis infection. Parasitol Res. 2011;108(3):541-5. View Article Google Scholar
  44. McFarland LV. Meta-analysis of probiotics for the prevention of antibiotic associated diarrhea and the treatment of Clostridium difficile disease. Am J Gastroenterol. 2006;101(4):812-22. View Article Google Scholar
  45. Dendukuri N, Costa V, McGregor M, Brophy JM. Probiotic therapy for the prevention and treatment of Clostridium difficile-associated diarrhea: a systematic review. CMAJ. 2005;173(2):167-70. View Article Google Scholar
  46. Pillai A, Nelson R. Probiotics for treatment of Clostridium difficile-associated colitis in adults. Cochrane Database Syst Rev. 2008;(1):CD004611-. View Article Google Scholar
  47. Miller K, Fraser T. Q: What is the role of probiotics in the treatment of acute Clostridium difficile-associated diarrhea? Cleve Clin J Med. . 2009;76(7):391-2. View Article Google Scholar
  48. Hsu J, Abad C, Dinh M, Safdar N. Prevention of endemic healthcare-associated Clostridium difficile infection: reviewing the evidence. Am J Gastroenterol. 2010;105(11):817-2327-39. View Article Google Scholar
  49. Tung JM, Dolovich LR, Lee CH. Prevention of Clostridium difficile infection with Saccharomyces boulardii: a systematic review. Can J Gastroenterol. 2009;23(12):817-21. View Article Google Scholar
  50. Goldenberg JZ, Lytvyn L, Steurich J, Parkin P, Mahant S, Johnston BC. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev. 2015;(12):CD004827-. View Article Google Scholar
  51. Black F, Anderson P, Orskov J, Gaarlev K, Laulund S. Prophylactic efficacy of Lactobacili on traveller’s diarrhea. Travel Med. 1989;7:333-5. View Article Google Scholar
  52. Kollaritsch H, Kremsner P, Weidermann G, Scheiner O. Prevention of traveler’s diarrhea: comparison of different non-antibiotic preparations. Travel Med Int. 1989;6:9-17. View Article Google Scholar
  53. Sazawal S, Hiremath G, Dhingra U, Malik P, Deb S, Black RE. Efficacy of probiotics in prevention of acute diarrhoea: a meta-analysis of masked, randomised, placebo-controlled trials. Lancet Infect Dis. 2006;6(6):374-82. View Article Google Scholar
  54. McFarland LV. Meta-analysis of probiotics for the prevention of traveler's diarrhea. Travel Med Infect Dis. 2007;5(2):97-105. View Article Google Scholar
  55. Takahashi O, Noguchi Y, Omata F, Tokuda Y, Fukui T. Probiotics in the prevention of traveler's diarrhea: meta-analysis. J Clin Gastroenterol. 2007;41(3):336-7. View Article Google Scholar
  56. Gutierrez-Castrellon P, Lopez-Velazquez G, Diaz-Garcia L, Jimenez-Gutierrez C, Mancilla-Ramirez J, Estevez-Jimenez J, et al. Diarrhea in preschool children and Lactobacillus reuteri: a randomized controlled trial. Pediatrics. 2014;133(4):e904-9. View Article Google Scholar
  57. Agustina R, Kok FJ, van de Rest O, Fahmida U, Firmansyah A, Lukito W, et al. Randomized trial of probiotics and calcium on diarrhea and respiratory tract infections in Indonesian children. Pediatrics. 2012;129(5):e1155-64. View Article Google Scholar
  58. Hojsak I, Močić Pavić A, Kos T, Dumančić J, Kolaček S. Bifidobacterium animalis subsp. lactis in prevention of common infections in healthy children attending day care centers - Randomized, double blind, placebo-controlled study Clin Nutr. 2016;35(3):587-91. View Article Google Scholar
  59. Bernaola Aponte G, Bada Mancilla CA, Carreazo NY, Rojas Galarza RA. Probiotics for treating persistent diarrhoea in children. Cochrane Database Syst Rev. 2013;(8):CD007401-. View Article Google Scholar
  60. Canani RB, Cirillo P, Terrin G, Cesarano L, Spagnuolo MI, De Vincenzo A, et al. Probiotics for treatment of acute diarrhoea in children: randomised clinical trial of five different preparations. BMJ. 2007;335(7615):340-. View Article Google Scholar
  61. Majamaa H, Isolauri E, Saxelin M, Vesikari T. Lactic acid bacteria in the treatment of acute rotavirus gastroenteritis. J Pediatr Gastroenterol Nutr. 1995;20(3):333-8. View Article Google Scholar
  62. Grossi E, Buresta R, Abbiati R, Cerutti R; Pro-DIA study group. Clinical trial on the efficacy of a new symbiotic formulation, Flortec, in patients with acute diarrhea: a multicenter, randomized study in primary care. J Clin Gastroenterol. 2010;44(Suppl.1):S35-41. View Article Google Scholar
  63. Grandy G, Medina M, Soria R, Terán CG, Araya M. Probiotics in the treatment of acute rotavirus diarrhoea. A randomized, double-blind, controlled trial using two different probiotic preparations in Bolivian children BMC Infect Dis. 2010;10:253-. View Article Google Scholar
  64. Jasinski C, Tanji MN, Schelotto F, et al. Efficacy of lactobacillus GG in oral rehydration solution. Pediatrika. 2002;22(7):231-43. View Article Google Scholar
  65. Guandalini S. Probiotics for children with diarrhea: an update. J Clin Gastroenterol. 2008;42(S2):S53-7. View Article Google Scholar
  66. Basu S, Chatterjee M, Ganguly S, Chandra PK. Efficacy of Lactobacillus rhamnosus GG in acute watery diarrhoea of Indian children: a randomised controlled trial. J Paediatr Child Health. 2007;43(12):837-42. View Article Google Scholar
  67. Khanna V, Alam S, Malik A, Malik A. Efficacy of tyndalized Lactobacillus acidophilus in acute diarrhea. Indian J Pediatr. 2005;72(11):935-8. View Article Google Scholar
  68. Costa-Ribeiro H, Ribeiro TC, Mattos AP, Valois SS, Neri DA, Almeida P, et al. Limitations of probiotic therapy in acute, severe dehydrating diarrhea. J Pediatr Gastroenterol Nutr. 2003;36(1):112-5. View Article Google Scholar
  69. Mao M, Yu T, Xiong Y, Wang Z, Liu H, Gotteland M, et al. Effect of a lactose-free milk formula supplemented with bifidobacteria and streptococci on the recovery from acute diarrhoea. Asia Pac J Clin Nutr. 2008;17(1):30-4. View Article Google Scholar
  70. Ritchie BK, Brewster DR, Tran CD, Davidson GP, McNeil Y, Butler RN. Efficacy of Lactobacillus GG in aboriginal children with acute diarrhoeal disease: a randomised clinical trial. J Pediatr Gastroenterol Nutr. 2010;50(6):619-24. View Article Google Scholar
  71. Sarker SA, Sultana S, Fuchs GJ, Alam NH, Azim T, Brüssow H, et al. Lactobacillus paracasei strain ST11 has no effect on rotavirus but ameliorates the outcome of nonrotavirus diarrhea in children from Bangladesh. Pediatrics. 2005;116(2):e221-8. View Article Google Scholar
  72. Szajewska H, Setty M, Mrukowicz J, Guandalini S. Probiotics in gastrointestinal diseases in children: hard and not-so-hard evidence of efficacy. J Pediatr Gastroenterol Nutr. 2006;42(5):454-75. View Article Google Scholar
  73. Vandenplas Y, Salvatore S, Vieira M, Devreker T, Hauser B. Probiotics in infectious diarrhoea in children: are they indicated? Eur J Pediatr. . 2007;166(12):1211-8. View Article Google Scholar
  74. Floch MH, Walker WA, Sanders ME, Nieuwdorp M, Kim AS, Brenner DA, et al. Recommendations for Probiotic Use-2015 Update: Proceedings and Consensus Opinion. J Clin Gastroenterol. 2015;49(S3):S69-73. View Article Google Scholar
  75. Gupta V, Garg R. Probiotics. Indian J Med Microbiol. 2009;27(3):202-9. View Article Google Scholar
  76. Guarino A, Lo Vecchio A, Canani RB. Probiotics as prevention and treatment for diarrhea. Curr Opin Gastroenterol. 2009;25(1):18-23. View Article Google Scholar
  77. Thomas DW, Greer FR; American Academy of Pediatrics Committee on Nutrition; American Academy of Pediatrics Section on Gastroenterology, and Nutrition. Probiotics and prebiotics in pediatrics. Pediatrics. 2010;126(6):1217-31. View Article Google Scholar
  78. Guarino A, Albano F, Ashkenazi S, Gendrel D, Hoekstra JH, Shamir R, et al. Paediatric Infectious Diseases evidence-based guidelines for the management of acute gastroenteritis in children in Europe. J Pediatr Gastroenterol Nutr. 2008;48(S2):S81-122. View Article Google Scholar
  79. Platincx M, Legein J, Vandenplas Y. Fungemia with Saccharomyces boulardii in a 1-year-old girl with protracted diarrhea. J Pediatr Gastroenterol Nutr. 1995;21:113-5. View Article Google Scholar
  80. Patel R, Cockeril FR, Porayko MK, et al. Lactobacillemia in liver transplant patients. Clin Infect Dis. 1994;18:207-12. View Article Google Scholar
  81. Kunz A, Noel J, Fairchol M. Two cases of Lactobacillus bacteremia during probiotic treatment of short gut syndrome. J Pediatr Gastroenterol Nutr. 2004;38:557-8. View Article Google Scholar
  82. Dai M, Lu J, Wang Y, Liu Z, Yuan Z. In vitro development and transfer of resistance to chlortetracycline in Bacillus subtilis. J Microbiol. 2012;50(5):807-12. View Article Google Scholar
Author's Affiliation
Article Details

Issue: Vol 1 No 2 (2017)
Page No.: AV5-AV12
Published online: May 7, 2017
Section: Review Article
DOI: https://doi.org/10.5281/zenodo.574854

Copyright Info

Creative Commons License

Copyright: The Authors. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
How to Cite
Mandal, A., & Sahi, P. (2017). Probiotics for Diarrhea in Children. Journal Of Medical Research And Innovation, 1(2), AV5-AV12. doi:10.5281/zenodo.574854
Downloading options
Article Statistics
HTML viewed = 436 times
PDF viewed = 34 times
XML viewed = 29 times