Commentary

The SR by Martin-Cabezas et al. addressed a focused clinical question ‘What is the short-term clinical influence of probiotic as an adjunctive therapy to SRP, in terms of PPD reduction and CAL gain, when compared with SRP alone or in combination with placebo in the treatment of CP in humans?’ The authors adhered to PRISMA guidelines3, 4 for preparing this systematic review. Overall, the study has been conducted and reported well. The authors searched multiple databases, journals and bibliography of included articles and review articles. However, they did not include grey literature. They appropriately restricted their included studies to four randomised controlled trials. All studies were assessed to have low risk of bias. Only three studies were included in meta-analysis because two studies were performed in same institution and a subgroup of patients overlapped between these studies5,6 The probiotic tested in all studies was ‘L. reuteri (strains DSM17938 and L. reuteri ATCC PTA529; Prodentis; BioGaia, Lund, Sweden)’ which was taken as two lozenges twice daily for three weeks in two studies; for 12 weeks in one study, and for three weeks, starting at 21 days after SRP. Differences in drug regimen, definition of CP, quadrant or full mouth SRP, parallel or split-mouth study design and follow-up period (42-360 days) contributed to significant heterogeneity among the included studies. All studies were funded by BioGaia® (Sweden), a probiotic company. The authors rightfully acknowledge the limitations of the evidence due to heterogeneity, small number of studies and short-term follow-up period. However, the authors' discussion on the effect of probiotics as similar to other adjuncts (systemic antibiotics, sub-antimicrobial-dose doxycycline and chlorhexidine chips) used along with SRP described in the recent meta-analysis and clinical practice guideline by Smiley et al.1, 2 is premature. Multiple RCTs were available for the majority of adjuncts analysed in Smiley et al. prior to publication of clinical practice guidelines. With very limited studies on probiotics and the fact that all four included studies only tested L. reuteri, the comparative effectiveness of probiotics to already recommended adjuncts needs to wait until robust RCTs are published.

Practice point

  • Significant heterogeneity among the few studies limits the strength of conclusions regarding the efficacy of probiotics as an adjunct in the treatment of CP.

  • Using probiotics as an adjunct to SRP in deep periodontal pockets can be considered given a trend towards clinical benefit as well as low cost or harm.