Lindsay Armstrong-Buisseret
Lactic acid gel versus metronidazole for recurrent bacterial vaginosis in women aged 16 years and over: the VITA RCT
Armstrong-Buisseret, Lindsay; Brittain, Clare; Kai, Joe; David, Miruna; Anstey Watkins, Jocelyn; Ozolins, Mara; Jackson, Louise; Abdali, Zainab; Hepburn, Trish; Griffiths, Frances; Montgomery, Alan; Daniels, Jane; Manley, Alice; Dean, Gillian; Ross, Jonathan Dc
Authors
Clare Brittain
Professor JOE KAI joe.kai@nottingham.ac.uk
Professor of Primary Care
Miruna David
Jocelyn Anstey Watkins
Mara Ozolins
Louise Jackson
Zainab Abdali
TRISH HEPBURN Trish.Hepburn@nottingham.ac.uk
Senior Medical Statistician
Frances Griffiths
ALAN MONTGOMERY ALAN.MONTGOMERY@NOTTINGHAM.AC.UK
Director Nottingham Clinical Trials Unit
Professor JANE DANIELS JANE.DANIELS@NOTTINGHAM.AC.UK
Professor of Clinical Trials
Alice Manley
Gillian Dean
Jonathan Dc Ross
Abstract
BACKGROUND: Bacterial vaginosis is a common and distressing condition associated with serious comorbidities. Antibiotic treatment is usually clinically effective in the short term, but recurrence is common and side effects can occur. OBJECTIVES: The objective is to assess whether or not intravaginal lactic acid gel is clinically effective and cost-effective for treating recurrent bacterial vaginosis compared with oral metronidazole (Flagyl, Sanofi). DESIGN: This was an open-label, multicentre, parallel-arm, randomised (1 : 1) controlled trial. SETTING: This took place in one general practice and 19 sexual health centres in the UK. PARTICIPANTS: Women aged ≥ 16 years with bacterial vaginosis symptoms and one or more episode(s) within the past 2 years took part. INTERVENTIONS: The interventions were 5 ml of intravaginal lactic acid gel taken once daily for 7 days (intervention) or 400-mg oral metronidazole tablets taken twice daily for 7 days (control). MAIN OUTCOME MEASURES: The primary outcome was the resolution of bacterial vaginosis symptoms 14 days after randomisation. The secondary outcomes were time to first recurrence of symptoms; number of recurrences and treatment courses over 6 months; microbiological resolution on microscopy of vaginal smears at week 2; time to resolution of symptoms; tolerability, adherence and acceptability of the treatment; prevalence of concurrent sexually transmitted infections; quality of life; and cost-effectiveness. RESULTS: Recruitment stopped prior to reaching the target of 1900 participants on recommendation from the Data Monitoring Committee and Trial Steering Committee after a planned review of the results indicated that the research question had been answered. Overall, 518 participants were randomised and primary outcome data were available for 409 participants (79%; 204 in the metronidazole arm, 205 in the lactic acid gel arm). Participant-reported symptom resolution at week 2 was higher with metronidazole (143/204; 70%) than with lactic acid gel (97/205; 47%) (adjusted risk difference -23.2%, 95% confidence interval -32.3% to -14.0%). Recurrence in 6 months in a subset of participants who had initial resolution and were available for follow-up was similar across arms (metronidazole arm: 51/72, 71%; lactic acid gel arm: 32/46, 70%). A higher incidence of some side effects was reported with metronidazole than with lactic acid gel (nausea 32% vs. 8%; taste changes 18% vs. 1%; diarrhoea 20% vs. 6%, respectively). At week 2, the average cost per participant with resolved symptoms was £86.94 (metronidazole), compared with £147.00 (lactic acid gel). Some participants preferred using lactic acid gel even if they perceived it to be less effective than metronidazole. LIMITATIONS: Loss to follow-up for collection of the primary outcome data was 21% and was similar in both arms. There is a risk of bias owing to missing outcome data at 3 and 6 months post treatment. CONCLUSIONS: A higher initial response was seen with metronidazole than with lactic acid gel, but subsequent treatment failure was common with both. Lactic acid gel was less cost-effective than metronidazole. In general, women disliked taking repeated courses of metronidazole and preferred lactic acid gel, even when they were aware that it was less likely to provide symptom resolution. In the absence of effective curative therapy, further evaluation of non-antibiotic treatments to control the symptoms of recurrent bacterial vaginosis is required to improve quality of life for these patients. Further microbiological analysis of vaginal samples would be useful to identify additional factors affecting response to treatment. TRIAL REGISTRATION: Current Controlled Trials ISRCTN14161293. FUNDING: This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 26, No. 2. See the NIHR Journals Library website for further project information.
Citation
Armstrong-Buisseret, L., Brittain, C., Kai, J., David, M., Anstey Watkins, J., Ozolins, M., …Ross, J. D. (2022). Lactic acid gel versus metronidazole for recurrent bacterial vaginosis in women aged 16 years and over: the VITA RCT. Health Technology Assessment, 26(2), 1-170. https://doi.org/10.3310/ZZKH4176
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 31, 2021 |
Publication Date | Jan 1, 2022 |
Deposit Date | Jan 27, 2022 |
Publicly Available Date | Jan 28, 2022 |
Journal | Health technology assessment (Winchester, England) |
Print ISSN | 1366-5278 |
Electronic ISSN | 2046-4924 |
Publisher | NIHR Journals Library |
Peer Reviewed | Peer Reviewed |
Volume | 26 |
Issue | 2 |
Pages | 1-170 |
DOI | https://doi.org/10.3310/ZZKH4176 |
Public URL | https://nottingham-repository.worktribe.com/output/7342763 |
Publisher URL | https://www.journalslibrary.nihr.ac.uk/hta/ZZKH4176#/abstract |
Additional Information | © Queen’s Printer and Controller of HMSO 2022. This work was produced by Armstrong-Buisseret et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. |
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