Probiotics for the Prevention of Vaginal Infections: A Systematic Review (2024)

  • Journal List
  • Cureus
  • v.16(7); 2024 Jul
  • PMC11318795

As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsement of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice

Probiotics for the Prevention of Vaginal Infections: A Systematic Review (1)

Link to Publisher's site

Cureus. 2024 Jul; 16(7): e64473.

Published online 2024 Jul 13. doi:10.7759/cureus.64473

PMCID: PMC11318795

PMID: 39135840

Monitoring Editor: Alexander Muacevic and John R Adler

Andrea M Zuñiga VinuezaProbiotics for the Prevention of Vaginal Infections: A Systematic Review (2)1

Author information Article notes Copyright and License information PMC Disclaimer

Abstract

Probiotics, particularly Lactobacillus strains, have been proposed as an alternative or adjunct therapy for bacterial vaginosis (BV) and vulvovaginal candidiasis (VVC) due to their potential to restore a healthy vaginal microbiota. This systematic review evaluated 11 randomized controlled trials with a Jadad score greater than three, indicating high-quality studies based on criteria such as randomization, blinding, and dropout rates. The review demonstrated significant improvements in clinical outcomes and vaginal microbiota restoration. However, variability in results highlights the need for further research.

Keywords: systematic review, randomized controlled trials, vulvovaginal candidiasis, bacterial vaginosis, vaginal health, probiotics

Introduction and background

Bacterial vaginosis (BV) and vulvovaginal candidiasis (VVC) are the two most prevalent types of vaginal infection [1-5]. Each presents with a distinct set of clinical symptoms, and they are considered distinct entities with distinct etiologies and pathogenesis [1]. Mixed infections involving simultaneous BV and VVC are rare, with limited understanding of their relationship and interactions. A study of women in Argentina with recurrent vulvovaginal candidiasis (RVVC) found that 35% were associated with BV, and 33.2% had an intermediate vaginal microbiota[1].

Bacterial vaginosis, marked by a reduction in Lactobacillus spp. and overgrowth of anaerobic bacteria, affects 20%-50% of women globally [2]. Vulvovaginal candidiasis, primarily caused by Candida albicans, affects approximately 75% of women at least once in their lifetime, with 40%-50% experiencing recurrent episodes [3]. Conventional treatments for BV and VVC, including antibiotics and antifungals, often fail to prevent recurrence owing to persistent biofilms and emerging drug resistance [4]. Probiotics, particularly Lactobacillus strains, have been proposed as a promising alternative or adjunct therapy for BV and VVC because of their ability to restore and maintain healthy vaginal microbiota [5]. In Ecuador, probiotics are primarily available as oral, over-the-counter medications. This highlights the necessity of reviewing the availability of new formulations and alternative uses to enhance their effectiveness in different populations and conditions.

Previous studies have examined the use of probiotics to treat or alleviate BV and VVC through oral and vaginal administration. Although these findings appear promising, the effectiveness and mechanisms of probiotics in this context remain largely unexplored and inconsistent. A systematic review is necessary to consolidate the evidence, identify gaps, and clarify the role of probiotics in managing BV and VVC. This review aimed to evaluate the effectiveness of probiotics in preventing BV and VVC, to identify the most effective strains and administration methods, and to provide evidence-based clinical recommendations. Given the high prevalence and recurrence of these infections, understanding the potential of probiotics could enhance management strategies and improve women's reproductive health outcomes [1-5].

Review

Materials and methods

Study Design

This systematic review was designed to evaluate the effectiveness of probiotics used solely as an intervention to prevent infections in various clinical trials. The inclusion criteria for this review mandated that the studies focus on infection prevention rather than treatment and provide comprehensive methodological details for quality assessment using the Jadad scale.

Search Strategy

A comprehensive literature review was carried out in June 2024 by utilizing the PubMed and Web of Science (WOS) databases, incorporating the keywords "probiotics," "bacterial vaginosis," and "candidiasis, vulvovaginal." The search results were further refined by applying filters to only publications with free full text, randomized controlled trials (RCTs), and those published within the past five years in either English or Spanish. This approach was taken to ensure that the most current and relevant studies were included, reflecting current research trends and advancements in the field. The reference lists of relevant articles were also examined to identify additional studies. The decision to limit the search to the past five years was made to guarantee that the studies included were the most recent and relevant, reflecting current research trends and advancements in the field.

A total of 114 studies were retrieved through the comprehensive search: 23 articles from PubMed and 91 from WOS. The abstracts and titles of these articles were reviewed for eligibility based on the inclusion and exclusion criteria following the PRISMA guidelines.

Inclusion and Exclusion Criteria

The inclusion and exclusion criteria are presented in Table ​Table11.

Table 1

Inclusion and exclusion criteria

RCTs:randomized controlled trials

Criteria TypeCriterion
InclusionStudies published in English or Spanish
InclusionRCTs that assessed the preventive effects of probiotics
InclusionConducted on human participants
InclusionProbiotics used alone without adjunctive antimicrobial therapy
ExclusionStudies that focused on treatment rather than prevention
ExclusionNon-randomized or observational studies
ExclusionStudies that did not provide clear data on probiotic strains and dosages
ExclusionPhase 1 or Phase 2 studies, study protocols, and studies not providing outcome data

Open in a separate window

Data Extraction

The information extracted from eligible studies included the following: title, authors, publication year, study design, sample size, population characteristics, and inclusion and exclusion criteria. Two reviewers independently extracted the information. Intervention details, including the type of probiotics used, dosage, and duration of the intervention, were also extracted. Outcomes were categorized as primary and secondary outcomes, and documented results and conclusions were included (Figure ​(Figure11).

Figure 1

Open in a separate window

A PRISMA flow diagram outlining the study selection process

This flow diagram details the selection process for the systematic review, including the identification, screening, eligibility, and inclusion of studies. The initial search yielded 114 records from PubMed and the Web of Science (WOS). After removing duplicates, 102 records were screened for relevance, and 74 were excluded. Full-text assessments were conducted on 28 articles, resulting in 11 studies meeting the inclusion criteria for the final review.

*Sources: PubMed and Web of Science

**Exclusion reasons: Protocol studies, Phase 1 or 2 studies, studies focusing on or using antimicrobial agents or other drugs.

PRISMA:Preferred Reporting Items for Systematic Reviews and Meta-Analyses

Quality Assessment

In addition to the Jadad scale, which evaluates randomization, blinding, and withdrawals, several other quality aspects are crucial for the comprehensive assessment of study reliability. These aspects include allocation concealment, adherence to intervention protocols, and handling of missing data [6, 7].

The Jadad scale, also known as the Oxford quality scoring system, consists of three items: randomization, blinding, and withdrawals/dropouts. Each component earned a score from 0 to two, resulting in a maximum score of five. A total score of 0 to two indicates low quality, while three to five indicates high quality [6].

Adhering to intervention protocols is crucial for maintaining consistency with the study design, which involves monitoring and documenting participants' compliance with the probiotic regimen and any deviations [7]. Handling the missing data is critical. Effective strategies include intention-to-treat analysis, imputation methods, and thorough documentation of reasons for dropout or non-compliance, ensuring robust study conclusions [7].

Data Synthesis

Research articles that fulfilled the inclusion criteria and attained a minimum score of three on the Jadad scale were considered for qualitative synthesis. A narrative synthesis strategy was utilized to summarize the results, concentrating on the effectiveness of probiotics in preventing infections and unfavorable occurrences.

Results

In the systematic review process, a comprehensive search was conducted across multiple databases. The search strategy yielded 23 articles from PubMed, 91 articles from the WOS, and 0 articles from the Cochrane database. After applying the inclusion and exclusion criteria, 11 studies met the criteria for inclusion in the systematic review. These studies were selected because they specifically focused on the preventive effects of probiotics without the adjunctive use of antibiotics or other pharmaceuticals. The studies included were all RCTs with a Jadad score of three or higher, ensuring high methodological quality (Table ​(Table22).

Table 2

Characteristics of the included studies on probiotics for vaginal health

RCT: randomized controlled trial; BV: bacterial vaginosis; VVC: vulvovaginal candidiasis; PPROM: preterm pre-labor rupture of membranes; PROM: pre-labor rupture of membranes; IL: interleukin; VAS: visual analog scale; VT: vaginal tablets

AuthorsYearMethodsInterventions and comparatorsMain resultsConclusionsRandomizationRandomization methodDouble-blindDouble-blind methodWithdrawals and dropoutsJadad score
Mändar R, et al. [8]2023RCT, 182 women (89 BV, 93 VVC)Probiotics (oral/vaginal) vs. placeboSignificant improvement in BV and VVC symptoms, increase in LactobacillusProbiotics effective for BV and VVC, administrable orally and vaginallyYesDouble-blind randomizationYesIndistinguishable placeboNot specified4
Yang S, et al. [9]2020RCT, 86 pregnant womenProbiotics vs. placeboNo difference in vaginal microbiota diversity between groupsProbiotics do not adversely affect vaginal microbiota during pregnancyYesDouble-blind randomizationYesIndistinguishable placeboNot specified4
Ang XY, et al. [10]2023RCT, 78 pregnant womenProbiotics (SynForU-HerCare) vs. placeboImprovement in vaginal and gastrointestinal microbiota in the probiotics groupProbiotics prevent adverse changes in microbiota during VCYesDouble-blind randomizationYesIndistinguishable placeboNot specified4
Park SH, et al. [11]2023RCT, 101 womenMED-01 vs. placeboSignificant reduction in the Nugent score in the probiotics groupMED-01 is effective for treating BV, improves vaginal microbiotaYesDouble-blind randomizationYesIndistinguishable placeboNot specified4
Jepsen IE, et al. [12]2022RCT, 74 womenLactobacillus vs. placeboNo significant improvement in vaginal microbiota with probioticsProbiotics do not significantly modulate vaginal microbiota before fertility treatmentsYesDouble-blind randomizationYesIndistinguishable placeboNot specified4
Armstrong, Eric; et al. [13]2022Randomized, placebo-controlled, double-blind trialLACTIN-V vs. placeboLower concentrations of IL-1 alpha and soluble E-cadherinLACTIN-V reduced genital inflammation and epithelial barrier disruptionYesDescribed and appropriateYesDescribed and appropriateYes5
Bangar, Sampada; et al. [14]2023Randomized, placebo-controlled, double-blind trialLactobacillusVT vs. placeboNo significant difference in BV recurrence between groupsLactobacillusVT was acceptable and safe but did not show additional benefit over metronidazoleYesDescribed and appropriateYesDescribed and appropriateYes5
Koirala, Ranjan; et al. [15]2023Randomized, placebo-controlled, double-blind crossover trialLactobacillus paracasei LPC-S01 vs. placeboReduction in the relative abundance of Gardnerella spp.Potential positive effect on the vaginal microbial ecosystemYesDescribed and appropriateYesDescribed and appropriateYes5
Vaccalluzzo, Amanda; et al. [16]2023Randomized, placebo-controlled, double-blind trialLacticaseibacillus rhamnosus TOM 22.8 vs. placeboRestoration of the physiological pH and reduction of potentially pathogenic bacteriaEffective strategy for the treatment of vaginal dysbiosisYesDescribed and appropriateYesDescribed and appropriateYes5
Vanda, Raziyeh, et al. [17]2023Randomized, placebo-controlled, double-blind trialOral probiotic vs. placeboReduction in PPROM and PROMOral probiotics can reduce complications such as PPROM and PROMYesDescribed and appropriateYesDescribed and appropriateYes5
Vivekanandan et al. [18]2023Randomized, placebo-controlled, double-blind trialVagiBIOM suppository vs. placeboImprovement in vaginal pH, VAS itching score, total Nugent score, and vaginal health indexEffective in improving vaginal Lactobacillus diversity and overall vaginal healthYesDescribed and appropriateYesDescribed and appropriateYes5

Open in a separate window

Bias and Limitations

This systematic review faces several limitations that could affect its comprehensiveness and reliability. Potential selection bias exists, as relevant studies may have been inadvertently overlooked despite extensive search efforts. Limiting the search to English and Spanish publications also excluded studies in other languages, potentially narrowing the scope of the review. Publication bias is another concern, with studies showing positive results being more likely to be published, which can skew the findings and overestimate the effectiveness of probiotics.

The included studies exhibit considerable heterogeneity in probiotic strains, dosages, intervention durations, and population characteristics, complicating direct comparisons and generalizability. Variations in study design, sample size, and outcome measures further contribute to this inconsistency. Additionally, while the Jadad scale was used for quality assessment, it primarily focused on randomization, blinding, and withdrawals without thoroughly evaluating other crucial quality aspects such as allocation concealment, adherence to intervention protocols, and handling of missing data.

Most studies had short follow-up periods, insufficient to capture the long-term effects of probiotics on preventing vulvovaginal infections. Longer-term studies are necessary to assess sustained impacts. Confounding factors such as adherence to the probiotic regimen, concurrent medication use, and variations in diet and lifestyle were not consistently controlled, which could influence outcomes and limit attributing effects solely to the probiotic interventions.

Discussion

These studies collectively emphasize the potential advantages of probiotics in controlling BV and VVC, highlighting substantial improvements in clinical results and the restoration of the vaginal microbiota. Nonetheless, the results exhibited some inconsistencies in effectiveness, underscoring the necessity for additional exploration.

Several studies, including those by Mändar et al. [8] and Park et al. [11], have demonstrated that probiotics significantly improve BV and VVC symptoms and reduce recurrence rates. Mändar et al. [8] reported that probiotics, administered both orally and vaginally, resulted in significant symptom relief and an increase in Lactobacillus spp., supporting the therapeutic potential of probiotics in managing these infections effectively. Similarly, Park et al. [11] found that the MED-01 probiotic formulation significantly reduced the Nugent scores, indicating improved vaginal microbiota and effective BV treatment. In contrast, Yang et al. [9] and Jepsen et al. [12] reported no significant differences in vaginal microbiota diversity or improvement in symptoms with probiotic use compared with placebo. These discrepancies may stem from differences in the study populations, probiotic strains, dosages, and duration of treatment. The impact of probiotics on the restoration of a healthy vaginal microbiota has been highlighted in multiple studies. Ang et al. [10] and Koirala et al. [15] found that probiotics led to significant improvements in both the vaginal and gastrointestinal microbiota. Ang et al. [10] noted that probiotics prevented adverse microbiota changes during vaginal infections, while Koirala et al. [15] observed a reduction in the relative abundance of Gardnerella spp., a common pathogen associated with BV. These findings suggest that probiotics play a crucial role in maintaining vaginal health by promoting beneficial bacterial growth. Armstrong et al. [13] investigated the anti-inflammatory effects of the Lactobacillus crispatus CTV-05 probiotic, finding reduced concentrations of IL-1 alpha and soluble E-cadherin, which are markers of genital inflammation and epithelial barrier disruption. This study indicates that probiotics may not only address microbial imbalances but also enhance the integrity of the vaginal epithelial barrier, offering additional protective benefits.

Studies by Bangar et al. [14] and Vaccalluzzo et al. [16] confirmed the safety and feasibility of probiotics. Bangar et al. [14] reported that Lactobacillus vaginal tablets (VTs) were well-tolerated, although they did not show any added benefits over metronidazole in reducing BV recurrence. Vaccalluzzo et al. [16] highlighted the effectiveness of Lacticaseibacillus rhamnosus in restoring physiological pH and reducing pathogenic bacteria. Bacterial vaginosis and VVC endanger pregnant women by increasing the risk of preterm birth (PTB) and premature rupture of membranes (PROM) through adverse effects on the vaginal microbiota and host immunity. Bacterial vaginosis results from the overgrowth of anaerobic bacteria and a reduction in Lactobacillus species, which is crucial for a healthy vaginal environment. Pathogenic bacteria in BV cause inflammation and weaken fetal membranes, increasing the risk of PROM and PPROM. Lactobacillus species, including L. acidophilus, L. fermentum, L. crispatus, and L. jensenii, enhance vaginal health by producing lactic acid and hydrogen peroxide, which lower pH and inhibit pathogenic bacteria. A higher presence of Lactobacillus species in the vaginal microbiota correlates with a reduced risk of BV and urinary tract infections, both associated with adverse pregnancy outcomes such as PTB and PROM [17].

Vanda et al. [17] provide significant insights into oral probiotics' role in preventing complications like PPROM and PROM. This randomized placebo-controlled double-blind trial showed that administering oral probiotics significantly reduced the incidence of PPROM and PROM in pregnant women. These findings emphasize the potential of probiotics to maintain or restore vaginal health, which is crucial for preventing serious pregnancy-related complications. Probiotics positively influence the vaginal microbiome, potentially reducing the risk of infection and inflammation, leading to PPROM and PROM. This study highlights the importance of incorporating probiotics in prenatal care to enhance maternal and neonatal health outcomes. However, larger, long-term studies are necessary to validate these findings and establish comprehensive clinical guidelines for probiotic use.

Vivekanandan et al. [18] conducted a thorough study evaluating the Lactobacillus vaginal suppository's efficacy in enhancing vaginal health. This randomized, double-blind, placebo-controlled trial showed significant improvements in vaginal pH balance, reduced itching, improved Nugent scores, and overall improved vaginal health index scores in women using probiotics. These findings support the Lactobacillus suppository as an effective intervention for increasing the diversity and abundance of beneficial Lactobacillus species, which is vital for preventing and managing conditions such as BV and VVC. These results suggest that probiotic suppositories could be a valuable alternative or complement to conventional antimicrobial therapies, offering a non-antibiotic approach to maintaining vaginal health. Future research should compare different probiotic formulations and delivery methods to optimize clinical applications and enhance patient adherence and satisfaction.

Biases and Limitations

This systematic review encountered several constraints that affected its comprehensiveness and dependability. One of the limitations is the potential for selection bias, as pertinent studies may have been overlooked despite a thorough search. By limiting the search to English and Spanish publications, studies in other languages were excluded, which may have narrowed the scope of the review. Publication bias is also a concern, as studies with positive outcomes are more likely to be published, which could skew the findings and overestimate the effectiveness of probiotics. The studies included in the review displayed disparities in probiotic strains, dosages, duration of intervention, and characteristics of the study population, which complicates direct comparisons and generalizability. Variations in the study design, sample size, and outcome measures added to the inconsistency. The Jadad scale, which was employed for quality assessment, primarily focused on randomization, blinding, and withdrawals without providing a thorough evaluation of other quality aspects, such as allocation concealment, adherence to the intervention protocols, and handling of missing data. Most studies had short follow-up periods, which were insufficient for capturing the long-term effects of probiotics on preventing vulvovaginal infections, necessitating long-term studies to assess sustained impacts. Confounding factors, such as adherence to the probiotic regimen, concurrent medication use, and variations in diet and lifestyle, were not consistently controlled, which could have influenced the outcomes and limited the attribution of effects solely to probiotic interventions.

Conclusions

The selected studies collectively underscore the potential benefits of probiotics in managing BV and VVC. The evidence indicates significant improvements in clinical outcomes and the restoration of the vaginal microbiota, although the efficacy varies. Probiotics have shown promise in alleviating symptoms, reducing recurrence rates, and promoting the growth of beneficial bacteria while reducing pathogenic species. They also appear to provide additional benefits, such as reducing genital inflammation and maintaining the integrity of the vaginal epithelial barrier.

Probiotics have been shown to be safe and well-tolerated, with some studies suggesting their use as a valuable alternative or adjunct to conventional antimicrobial therapies. Furthermore, the potential role of probiotics in prenatal care, particularly in preventing complications such as PPROM and PROM, highlights their broader clinical significance. Most studies included in this review have relatively short follow-up periods. Longer-term studies are essential to assess the sustained impact of probiotic interventions on preventing vulvovaginal infections. These studies should aim to evaluate the long-term safety, efficacy, and potential for recurrence reduction over extended periods, providing more comprehensive evidence for clinical practice.

However, the variability in study results highlights the need for further research. Future studies should focus on standardizing probiotic strains, dosages, and treatment durations and exploring different delivery methods to optimize clinical applications and enhance patient adherence and satisfaction. Establishing comprehensive clinical guidelines based on large-scale, long-term studies is crucial for integrating probiotics effectively into the management and prevention of BV and VVC.

The evidence underscores the potential of probiotics in managing BV and VVC, with specific strains like Lactobacillus rhamnosus and Lactobacillus paracasei showing promise. Probiotics can alleviate symptoms, reduce recurrence rates, and promote beneficial bacterial growth while minimizing pathogenic species. Despite these positive outcomes, variability in study results necessitates the standardization of probiotic formulations, dosages, and treatment protocols. Long-term studies are crucial to validate these findings and establish comprehensive clinical guidelines, ensuring the effective integration of probiotics into the management and prevention of BV and VVC.

Disclosures

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:

Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.

Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.

Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Author Contributions

Concept and design: Andrea M. Zuñiga Vinueza

Acquisition, analysis, or interpretation of data: Andrea M. Zuñiga Vinueza

Drafting of the manuscript: Andrea M. Zuñiga Vinueza

Critical review of the manuscript for important intellectual content: Andrea M. Zuñiga Vinueza

Supervision: Andrea M. Zuñiga Vinueza

References

1. Bacterial vaginosis and vulvovaginal candidiasis pathophysiologic interrelationship. Sobel JD, Vempati YS. Microorganisms. 2024;12:108. [PMC free article] [PubMed] [Google Scholar]

2. Prevalence of bacterial vaginosis and its association with risk factors among nonpregnant women: a hospital based study. Ranjit E, Raghubanshi BR, Maskey S, Parajuli P. Int J Microbiol. 2018;2018:8349601. [PMC free article] [PubMed] [Google Scholar]

3. Recurrent vulvovaginal candidiasis: an immunological perspective. Rosati D, Bruno M, Jaeger M, Ten Oever J, Netea MG. Microorganisms. 2020;8:144. [PMC free article] [PubMed] [Google Scholar]

4. Pathogenesis and virulence of Candida albicans. Lopes JP, Lionakis MS. Virulence. 2022;13:89–121. [PMC free article] [PubMed] [Google Scholar]

5. Bacterial vaginosis- a brief synopsis of the literature. Coudray MS, Madhivanan P. Eur J Obstet Gynecol Reprod Biol. 2020;245:143–148. [PMC free article] [PubMed] [Google Scholar]

6. Quality assessment and relevant clinical impact of randomized controlled trials of varicocele: next step to good-quality randomized controlled trial of varicocele treatment. Kim KS, Chung JH, Park HJ, Shin WJ, Lee BH, Lee SW. World J Mens Health. 2022;40:290–298. [PMC free article] [PubMed] [Google Scholar]

7. A general framework for the evaluation of clinical trial quality. Berger VW, Alperson SY. Rev Recent Clin Trials. 2009;4:79–88. [PMC free article] [PubMed] [Google Scholar]

8. Impact of Lactobacillus crispatus-containing oral and vaginal probiotics on vaginal health: a randomised double-blind placebo controlled clinical trial. Mändar R, Sõerunurk G, Štšepetova J, et al. Benef Microbes. 2023;14:143–152. [PubMed] [Google Scholar]

9. Effect of oral probiotic Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 on the vaginal microbiota, cytokines and chemokines in pregnant women. Yang S, Reid G, Challis JR, et al. Nutrients. 2020;12:368. [PMC free article] [PubMed] [Google Scholar]

10. Lactobacillus probiotics restore vaginal and gut microbiota of pregnant women with vaginal candidiasis. Ang XY, Roslan NS, Ahmad N, et al. Benef Microbes. 2023;14:421–431. [PubMed] [Google Scholar]

11. Efficacy and safety of Med-01 probiotics on vaginal health: a 12-week, multicenter, randomized, double-blind, placebo-controlled clinical trial. Park SH, Lee ES, Park ST, et al. Nutrients. 2023;15:331. [PMC free article] [PubMed] [Google Scholar]

12. Probiotic treatment with specific lactobacilli does not improve an unfavorable vaginal microbiota prior to fertility treatment-a randomized, double-blinded, placebo-controlled trial. Jepsen IE, Saxtorph MH, Englund AL, Petersen KB, Wissing ML, Hviid TV, Macklon N. Front Endocrinol (Lausanne) 2022;13:1057022. [PMC free article] [PubMed] [Google Scholar]

13. Sustained effect of LACTIN-V (Lactobacillus crispatus CTV-05) on genital immunology following standard bacterial vaginosis treatment: results from a randomised, placebo-controlled trial. Armstrong E, Hemmerling A, Miller S, et al. Lancet Microbe. 2022;3:0–42. [PMC free article] [PubMed] [Google Scholar]

14. Prevention of recurrence of bacterial vaginosis using lactobacilli-containing vaginal tablets among women with HIV: a randomized, placebo-controlled, double-blinded phase IV trial. Bangar S, Sonar P, Mane A, et al. Int J Infect Dis. 2023;129:197–204. [PubMed] [Google Scholar]

15. Effect of oral consumption of capsules containing Lactobacillus paracasei LPC-S01 on the vaginal microbiota of healthy adult women: a randomized, placebo-controlled, double-blind crossover study. Koirala R, Gargari G, Arioli S, et al. FEMS Microbiol Ecol. 2020;96:0. [PMC free article] [PubMed] [Google Scholar]

16. Lacticaseibacillus rhamnosus TOM 22.8 (DSM 33500) is an effective strategy for managing vaginal dysbiosis, rising the lactobacilli population. Vaccalluzzo A, Pino A, Grimaldi RL, Caggia C, Cianci S, Randazzo CL. J Appl Microbiol. 2024;135:110. [PubMed] [Google Scholar]

17. Pregnancy outcomes in pregnant women taking oral probiotic undergoing cerclage compared to placebo: two blinded randomized controlled trial. Vanda R, Dastani T, Taghavi SA, Sadeghi H, Lambert N, Bazarganipour F. BMC Pregnancy Childbirth. 2024;24:311. [PMC free article] [PubMed] [Google Scholar]

18. VagiBIOM Lactobacillus suppository improves vaginal health index in perimenopausal women with bacterial vaginosis: a randomized control trial. Vivekanandan V, Khan ZH, Venugopal G, et al. Sci Rep. 2024;14:3317. [PMC free article] [PubMed] [Google Scholar]

Articles from Cureus are provided here courtesy of Cureus Inc.

Probiotics for the Prevention of Vaginal Infections: A Systematic Review (2024)
Top Articles
Latest Posts
Recommended Articles
Article information

Author: Moshe Kshlerin

Last Updated:

Views: 6230

Rating: 4.7 / 5 (77 voted)

Reviews: 92% of readers found this page helpful

Author information

Name: Moshe Kshlerin

Birthday: 1994-01-25

Address: Suite 609 315 Lupita Unions, Ronnieburgh, MI 62697

Phone: +2424755286529

Job: District Education Designer

Hobby: Yoga, Gunsmithing, Singing, 3D printing, Nordic skating, Soapmaking, Juggling

Introduction: My name is Moshe Kshlerin, I am a gleaming, attractive, outstanding, pleasant, delightful, outstanding, famous person who loves writing and wants to share my knowledge and understanding with you.