The 90-day treatment was also associated with an approximately 60 percent reduction in the incidence of reported pharyngitis in the six-month period following use of the product. 5 pgs.15 Masdea L, Kulik EM, Hauser-Gerspach I, Ramseier AM, Filippi A, Waltimo T. Antimicrobial activity of Streptococcus salivarius K12 on bacteria involved in oral malodour.
7 Di Pierro F, Donato G, Fomia F, Adami T, Careddu D, Cassandro C, Albera R. Preliminary pediatric clinical evaluation of the oral probiotic Streptococcus salivarius K12 in preventing recurrent pharyngitis and/or tonsillitis caused by Streptococcus pyogenes and recurrent acute otitis media. You can find "kits" of this halitosis medication at your drug store or pharmacy. In Martin DR, Tagg JR (Eds.) Unpublished, internal report. In Martin DR, Tagg JR (Eds.) 4 pgs. In addition, a six-month follow-up was included (without supplementation) to evaluate the potential for any long-term protective role that BLIS K12 might offer. They also experienced a statistically significant reduction in tracheitis (bacterial infection of the trachea), viral pharyngitis, rhinitis, flu, laryngitis, acute otitis media, enteritis and stomatitis (inflammation of the mucous membrane of the mouth, e.g. 2005;11 Suppl 1:29-31. Thirty-one of them were treated daily for 90 days with a slowly dissolving BLIS K12 tablet. 9 Di Pierro F, Colombo M, Zanvit A, Risso P, Rottoli AS. This includes the oral cavity (i.e. “Test tube” research15 has shown that BLIS K12 is effective against several bacteria involved in causing halitosis. Arch Oral Biol.
This includes the oral cavity (i.e. While probiotics certainly reside in the intestines, there are other areas of the body where they also reside. rotten egg smell) levels one week after treatment showed that 85 percent of the BLIS K12-treated group and 30 percent of the placebo group (mouthwash only) had substantial reductions.
Well, only partially right. BLIS K12 has solid science behind it for helping to prevent streptococcal pharyngitis and/or tonsillitis, ear infections (otitis media) and to help treat halitosis. The next controlled study10 examined the effects of BLIS K12 vs. placebo in 130 children with recurrent, tonsillitis caused by bacteria known group A beta-hemolytic streptococci (GABHS). Well, this was the verdict from a study looking at the Oral Malodour Parameters on a group of chronic bad breath sufferers. In a controlled, 90-day study,6 researchers tested the Streptococcus salivarius K12 strain (hereafter referred to as BLIS K12) for its potential effect in preventing streptococcal pharyngitis and/or tonsillitis in 40 adults with a diagnosis of recurrent oral streptococcal pharyngitis. Halitosis, commonly referred to as bad breath, is a noticeably unpleasant odor on the exhaled breath. The discovery of the special K12 strain makes an interesting story. Int J Gen Med. a few minutes) so that colonization in the oral cavity can take place.
In New Zealand, the home of K12, these kits are named These bad breath products all contain the same K12 strain. Oral Microbiol Immunol. All Content Copyright © 2007-2019 Probiotics-LoveThatBug. BLIS K-12 STREPTOCOCCUS SALIVARIUS- prevents recurring infections in mouth and throat in children & adults, antimicrobial, supports upper respiratory health and prevents bad breath, may reduce strep infectionsBLIS M-18 STREPTOCOCCUS SALIVARIUS- reduces halitosis because it eradicates the odor causing S. mutans, boosts the immune system protecting against infections in the ear, nose and throat.
No probiotic supplement was given to the remaining 54 children who served as controls. 'nuff said. 2008 Dec;27(12):1261-3.13 Di Pierro F, Donato G, Fomia F, Adami T, Careddu D, Cassandro C, Albera R. Preliminary pediatric clinical evaluation of the oral probiotic Streptococcus salivarius K12 in preventing recurrent pharyngitis and/or tonsillitis caused by Streptococcus pyogenes and recurrent acute otitis media. Streptococci and Streptococcal Diseases: Entering the new Millennium. VR1 FAO/WHO.
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Testing showed that BLIS K12 suppressed the growth of black-pigmented bacteria in saliva samples and also in various strains of bacteria implicated in halitosis. 5 pgs.
2016 Jan 19;12:87-92. No probiotic supplement was given to the remaining 54 children who served as controls.
Furthermore, the research has shown that BLIS K12 has benefit for adults and children alike. The results showed that in two children, the use of BLIS K12 colonized the oral cavity. 2016 Nov 21;8:77-81.12 Power DA, Burton JP, Chilcott CN, Dawes PJ, Tagg JR. Furthermore, the research has shown that BLIS K12 has benefit for adults and children alike.
2013 Mar;13(3):339-43. In the six-month follow-up during which there was no further supplementation, the incidence of ear infections was reduced by about 65 percent.In another study,14 children who were prone to recurrent otitis media were supplemented with one billion CFU daily of BLIS K12, or placebo, to examine the effect on the rate of infection recurrence. The BLIS K12 group also showed a significant 80 percent decrease in the incidence of oral viral infections. XIV Lancefield International Symposium on Streptococci and Streptococcal Diseases. In addition, children treated with BLIS K12 needed less antibiotic therapy, less medication for reducing fevers and missed fewer days of school because of related illness. The K12 strain has been researched thoroughly and with particular attention to its safety.And the conclusion: "demonstrating the absence of adverse reactions in subjects actively ingesting S salivarius K12" and continues "indicate that it have very low pathogenic potential and is unlikely to cause disease in healthy humans".Professor Tagg summed up his research: "This is how bacteria have developed the weaponry to take on competing bacteria. 4 pgs.9 Di Pierro F, Colombo M, Zanvit A, Risso P, Rottoli AS. Health and Nutritional Properties of Probiotics in Food including Powder Milk with Live Lactic Acid Bacteria. Results showed that even nine months after the use of BLIS K12 had been stopped, the probability of new GABHS infections was significantly lower (P>0.001) when compared to the period before dosing commenced. 2012;5:991-7.14 Burton JP, Chilcott CN, Power DA, Dawes PJ, Tagg JR.
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