A systematic review of non-antibiotic measures for the prevention of urinary tract infections in pregnancy

Background

Urinary tract infections (UTIs) are common in pregnancy and account for the highest proportion of primary care antibiotic prescriptions issued to pregnant women in the UK. It is well known that antibiotic use is associated with increased antimicrobial resistance and therefore measures to minimise antibiotic use for UTI prevention have been studied. The efficacy and safety of these measures in pregnancy have not been addressed and therefore the aim of this study was to systematically review the literature to identify and evaluate potential measures to prevent UTIs in pregnant women.

Methods

Ten databases (EMBASE, AMED, BNI, CINAHL, Medline, PubMed, PsycINFO, Cochrane Trials, Scopus and Science Direct) were systematically searched in July 2017 for studies reporting non-antibiotic measures to prevent UTIs in pregnancy. The terms (“urinary tract infection” or UTI or bacteriuria or cystitis) AND (prevention) AND (pregnan*) were used. The quality of the publications was appraised using the Critical Appraisal Skills Programme (CASP) checklists for cohort study, case-control study and randomised controlled trial. The results were synthesised using a textual narrative approach.

Results

Search results yielded 3276 publications and after reviewing titles and removing duplicates, 57 full text articles were assessed for eligibility and eight were included in the review. Five different approaches (hygiene measures, cranberry juice, immunisation, ascorbic acid and Canephron® N) have been identified, all of which are reported to be safe in pregnancy.

Conclusion

The quality of the evidence varied considerably and only hygiene measures were supported by evidence to be recommended in practice. Future work needs to concentrate on strengthening the evidence base through improved design and reporting of studies with a focus on immunisation, ascorbic acid and Canephron® N.

Urinary tract infections (UTIs) account for the highest proportion of primary care antibiotic prescriptions issued to pregnant women in the UK [1]. Pregnant women have an increased susceptibility to UTIs because of physiological changes. The growing uterus can result in urinary retention which predisposes the woman to infection. In addition, hormonal fluctuations relax the ureteral muscle and cause accumulation of urine in the bladder which also increases the chance of developing a UTI [2].

Treatment of UTIs is recommended in pregnancy if bacteria are detected in the urine even if there are no accompanying symptoms i.e. in asymptomatic bacteriuria (ASB) [3]. Both ASB and symptomatic UTIs in pregnancy are risk factors for the development of pyelonephritis which can result in severe maternal morbidity [4]. It is estimated that 20–30% of women with bacteriuria in the first trimester go on to develop pyelonephritis in later trimesters [5]. Therefore, although ASB on its own is not treated in the general population, guidelines published by the European Urological Association (EAU) [3] and Scottish Intercollegiate Guidelines Network (SIGN) [6] recommend screening and treating bacteriuria with or without symptoms. The current management strategy according to these guidelines is to use a short course of antibiotics.

Whilst antibiotics are vital in eradication of UTIs, antimicrobial resistance due to their use is a global health threat [7, 8]. Antimicrobial resistance means that bacteria can survive antibiotic treatment and cause serious or life threatening infections. Use of antibiotics is strongly associated with increasing emergence of resistant bacteria and subsequent redundancy of antibiotics i.e. previously effective antibiotics are losing their efficacy [8, 9]. Unlike the general population, the choice of safe antibiotics in pregnancy is limited because of teratogenic potential e.g. quinolones should be avoided in pregnancy because of a risk of joint malformations in the foetus. Therefore antibiotics becoming ineffective due to antimicrobial resistance is a particular concern in pregnancy as it further limits the range of drugs available to treat infections safely [10]. An example of this in practice is the replacement of trimethoprim with nitrofurantoin as the first line antibiotic to treat UTIs [11] because of an increase in resistance due to its widespread use in the UK [12]. Use of antibiotics can also result in carriage of resistant bacteria by individuals for a period of several months to a year after completing a course of antibiotics [13]. The resistant bacteria can transfer to close physical contacts and may colonise and infect subsequent hosts. This is especially of concern in pregnancy as women can pass on resistant bacteria to the neonate during birth, which is when they are most vulnerable to infection. An example of resistance specific to obstetric practice is the increase in ampicillin resistant neonatal infections due to maternal use of ampicillin [14, 15].

As well as contributing to antimicrobial resistance, antibiotic use in pregnancy also carries the risk of being harmful to the foetus. Recently, a study has found a link between antibiotic use and increased risk of spontaneous miscarriages [16]. Another study assessing the effects of nitrofurantoin, trimethoprim-sulfamethoxazole and cephalosporins which are used to treat UTIS, found an increased risk of birth defects such as oral clefts, oesophageal and anorectal abnormalities in the offspring [17]. In addition, research has also found an association with antibiotic use in pregnancy and functional impairment in children later on in life [18].

In light of the risks, it is essential that the use of antibiotics in pregnancy is carefully considered with a balance struck between the risks and benefits of these drugs. The UK’s 5 year antimicrobial resistance strategy [19] developed by the Department of Health (DH) and Department for Environment Food and Rural Affairs (Defra) identifies seven key areas where action is needed to tackle antimicrobial resistance. One of these key areas is ‘improving infection prevention and control practices’ which will lead to a reduction in the use of antibiotics as infection rates will be minimised. Improving infection prevention is also one of the main recommendations of ‘The Review on Antimicrobial Resistance’ (2016), chaired by economist Jim O’Neill [8]. Non-antibiotic measures to minimise antibiotic use for UTI prevention have been studied but the efficacy and safety of these measures in pregnancy have not been addressed [20]. Therefore, the aim of this systematic review is to identify alternate measures reported in scientific literature which may be used to prevent UTIs in pregnancy. The benefits of non-antibiotic measures to prevent UTIs in pregnancy are two-fold. Firstly, the reduced use of antibiotics will mean that they remain effective for longer, and secondly, medication which is potentially harmful in pregnancy can be avoided.

Ten databases (EMBASE, AMED, BNI, CINAHL, Medline, PubMed, PycINFO, Cochrane Trials, Scopus and Science Direct) were searched and the final search string was conducted in July 2017. The inclusion criteria according to PICOS (see Table 1) consisted of studies reporting non-antibiotic measures for the prevention of UTIs in pregnant women.

Studies conducted exclusively in non-pregnant groups or in conditions such as diabetes or spinal cord injury were excluded. Search terms were; P: (pregnan*), I: (prevention or control or management), O: (“urinary tract infection” or UTI or bacteriuria or cystitis) as shown in Table 2.

The search terms ‘control’ or ‘management’ were initially used but these terms did not yield relevant results therefore this paper focuses on prevention only. The final search strategy is available in Additional file 1.

A manual search of references from included studies was also conducted. The quality of the publications was appraised using the Critical Appraisal Skills Programme (CASP) checklists for cohort study, case-control study and randomised controlled trial [21,22,23]. The results were analysed and discussed using a narrative synthesis approach.

Search results yielded 3276 publications and after reviewing titles and removing duplicates, 56 full text articles and one conference abstract were assessed for eligibility by FG and eight were included in the review as shown in Fig. 1. The results identified five different measures (hygiene behaviour, cranberry juice, immunisation, ascorbic acid and Canephron® N) which can be used for the prevention of UTIs in pregnancy. Quality appraisal of the included publications using the CASP checklists is shown in Tables 3, Table 4 and Table 5. The characteristics of the publications are included in Table 6.

Identification of publications

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Hygiene behaviour

Three observational studies were identified which investigated the association between sexual and genital hygiene behaviours of pregnant women and the incidence of asymptomatic bacteriuria (defined as > 10⁵ colony forming units/ml of urine) or symptomatic UTIs. One study by Badran et al. [24] was not included in the review due to repetition of results from a previously conducted study.

The study by Amiri et al. [25] was a case-control study which included 100 cases matched to 150 controls i.e. total of 250 pregnant women. The two groups were compared in terms of differences in genital hygiene or sexual activity. The study by Elzayat et al. [26] was an observational cohort study that included 170 pregnant women between the ages of 18–41. Participants in this study were administered a questionnaire about their hygiene behaviours and a urine sample was tested to determine the prevalence of bacteriuria. Both studies show that hygiene behaviours are associated with the incidence of UTIs.

Cranberry juice

There were two studies that assessed the effectiveness of cranberry juice in preventing UTIs during pregnancy. Wing et al. [27] conducted a randomised controlled trial with 188 pregnant women under 16 weeks of pregnancy and compared the efficacy of cranberry juice with a placebo. There was a 57% reduction in bacteriuria and 41% reduction in all UTIs reported in this trial. Essadi et al. [28] conducted a randomised controlled trial that compared cranberry juice with water in 760 pregnant women. They also reported positive results for the effectiveness of cranberry juice and 70.5% of the participants who drank cranberry juice showed a significant reduction in UTIs compared to 32.16% of women who drank water.

Immunisation

Immunisation as a means of preventing UTIs in pregnancy was assessed by two studies. Baertschi et al. [29] conducted a before-after study using a bacterial extract in 62 women who were 16–28 weeks pregnant. Use of the extract significantly reduced the incidence of UTIs and recurrence rates fell from 52.5% prior to using the extract to 19.4% after women started using the extract. Grischke and Ruttgers [30] investigated the effectiveness of an intramuscular vaccine in an open randomised trial. A total of 400 women were included in the trial and a significant difference was seen in the incidence of UTIs in the trial (28 infections) and control groups (84 infections) suggesting a beneficial effect of the vaccine.

Ascorbic acid

Ochoa-Brust et al. [31] conducted a RCT to evaluate whether daily intake of ascorbic acid (100 mg) prevented UTIs in pregnancy. There was a total of 110 pregnant women, 55 in the trial group and 55 in the control group. The infection percentage was 12.7% in women who were given daily ascorbic acid compared with 29.1% in women who received the comparator.

Canephron® N

Ordzhonikidze et al. [32] conducted a cohort study in 300 pregnant women using Canephron® N which is a herbal product. Women were divided into two groups, those who had a current UTI and those who suffered with chronic urinary tract problems but did not have a current exacerbation. The results show that the frequency of pyelonephritis was 1.5 times less in the first group and 1.3 times less in the second group due to use of this product.

The five different measures (hygiene behaviour, cranberry juice, immunisation, ascorbic acid and Canephron® N) highlighted in the review vary in the evidence supporting their use for the prevention of UTIs in pregnancy.

Hygiene behaviour

The EAU guideline for urological infections states that studies investigating hygiene behaviours have not found any association with the incidence of UTIs [3]. The two observational studies included in this review, however, provide evidence that hygiene behaviours are associated with the incidence of UTIs. Results show that increased sexual activity of greater than two or three times a week was linked to a high frequency of UTIs. However, washing the genital area and voiding the bladder after intercourse had a protective effect. The direction of wiping the genital area after voiding the bladder was also found to be important and women who wiped from back to front had a higher incidence of UTIs according to both studies. Lastly, Amiri et al. [25] also found that drinking inadequate amounts of fluid and delaying voiding of the bladder also increased the likelihood of UTIs.

The overall evidence from these studies supports the adoption of protective hygiene behaviours, which may seem intuitive, as good hygiene is well known to protect against all types of infections. Women should be provided with specific recommendations because they may get upset if they get advised to ‘just keep clean’ as evidenced by a qualitative study conducted by Flower et al. [33].

Cranberry juice

Both RCTs [27, 28] assessing the efficacy of cranberry juice to prevent UTIs in pregnancy concluded that it has the potential to be effective. However, both studies had limitations which shed doubt on the effectiveness of this intervention. The study by Wing et al. [27] was underpowered with a small sample size (188 women). Essadi et al. [28] had a larger cohort (760 women) but compared cranberry juice to water which led to inadequate blinding giving rise to a risk of performance bias i.e. systemic differences between the groups. In addition, it is not clear if they used intention-to-treat analysis which may have distorted the results in favour of cranberry juice. A point to note with regards to Essadi et al. [28] is that it was published as a conference poster and full details were not available but it was included because the abstract reported data in sufficient detail to determine the significance of the results.

A limitation of cranberry juice seen in both studies was the high volume of juice that needed to be ingested (240 ml [27] and 250 ml [28]). Both trials had a high withdrawal rate mostly due to gastrointestinal disturbances which can limit its use on grounds of acceptability to women. These results point to a need to investigate a standardised content of cranberries in alternative formulations such as tablets and capsules which may help with improving adherence and tolerability of this intervention.

Both these trials view cranberry juice as potentially effective at preventing UTIs in pregnancy but a Cochrane review by Jepson et al. [34] included both these studies in a meta-analysis and found cranberries to be ineffective in preventing UTIs in pregnancy. Thus, although there has been interest in using cranberries for UTI prevention, the evidence does not support its efficacy. It can still be used as a self-care option, if preferred by women, because of its known safety in pregnancy [35, 36].

Immunisation

Both studies investigating the role of immunisation to safely reduce the recurrence of UTIs in pregnancy found favourable results, however both had significant limitations. Baertschi et al. [29] used a bacterial extract consisting of different strains of Escherichia coli (E.coli), which is the most common uropathogen [37], however this vaccine would not be effective against any other type of bacteria. Furthermore it was an open pilot study and did not have a control group to compare the effectiveness of the vaccine. Therefore, the results need to be confirmed by a RCT, as noted by the authors themselves. Grischke and Ruttgers [30] conducted their study in a sample where 68 pregnant women were given the intramuscular vaccine but the number of pregnant women in the control group was not specified. Blinding was not clearly described either and so there is an unclear risk of bias. Therefore, immunisation as an approach to prevent UTIs in pregnancy needs further exploration to assess its feasibility in practice.

Ascorbic acid

Ochoa-Brust et al. [31] concluded that daily ascorbic acid was beneficial especially in areas with a high incidence of UTIs and antimicrobial resistance. This is a promising result but requires additional trials to strengthen the evidence before it can be recommended. It is not clear whether the authors used intention-to-treat analysis because they did not specify the withdrawal rate and there was a selection bias as they excluded women who were non-adherent or had ‘serious side effects’ from the medication. Excluding these results from analysis may distort the results in favour of ascorbic acid. It is worth noting, however, that no harmful effects were observed in the offspring of women who ingested ascorbic acid daily.

Canephron® N

Canephron® N is a phytotherapeutic medicine with antibacterial properties and contains three herbs namely rosemary, lovage and centaury [38]. It is manufactured by a German company, Bionorica®, which focuses on researching and developing plant-based medicines. Ordzhonikidze et al. [32] conducted a study with pregnant women using this product, to optimise management of urinary tract diseases including ASB and pyelonephritis, which concluded that it could be recommended for prevention of urinary tract complications in pregnancy. The reporting of results was not comprehensive so it was not possible to determine how the study was conducted in sufficient detail (see Table 3). A review by Naber et al. [38] assessing the efficacy of Canephron® N suggests that there might be some benefit from its use in pregnant women because it included evidence from additional studies which have not been discussed here as they were conducted in pregnant women with co-morbidities and so did not meet the inclusion criteria of this review. It is worth noting that the safety of Canephron® N in pregnancy has been established [39, 40] but in order to make an evidence based recommendation, its efficacy needs to be confirmed by a randomised controlled trial.

A total of ten databases were searched and search terms were mutually agreed by the authors and an independent colleague to ensure a comprehensive process. The studies included in the review were assessed independently by the authors using CASP checklists. Any disagreement was resolved by meeting and discussing the relevant studies. A limitation of this review is that only English language publications were included therefore there might be options which have not been identified. The results of this review have been discussed using a narrative synthesis approach due to the heterogeneous design of the included studies and the differing nature of the interventions identified.

All the approaches identified in this review are reported to be safe and effective. However apart from hygiene behaviours, the evidence behind these approaches is not robust enough to be recommended in practice. Future work needs to focus on strengthening the evidence base through improved design and reporting of clinical trials, in particular for the use of immunisation, ascorbic acid and Canephron® N. It is important that evidence based non-antibiotic measures to prevent UTIs in pregnancy are discovered to combat the danger that antimicrobial resistance poses to the health of this vulnerable patient group as well as the wider population.

ASB:

Asymptomatic bacteriuria

Defra:

Department for Environment Food and Rural Affairs

DH:

Department of Health

EAU:

European Association of Urology

RCT:

Randomised control trial

SIGN:

Scottish Intercollegiate Guidelines Network

UTI:

Urinary tract infection

We would like to thank all the authors of the original studies, and Tim Chapman, the pharmacy division’s liaison librarian at the University of Reading, for his support with conducting the literature search.

Funding

This work was supported by the University of Reading as a PhD studentship for F.G.

Affiliations

1. School of Pharmacy, University of Reading, PO Box 226, Whiteknights, Reading, RG6 6AP, UK

   • Flavia Ghouri
   • , Amelia Hollywood
   •  & Kath Ryan

Contributions

FG conducted the literature search and screened the papers for eligibility for this review. All authors (FG, AH and KR) screened the publications for quality assessment. The final manuscript was prepared by FG, then edited and approved by AH and KR.

Corresponding author

Correspondence to Amelia Hollywood.

Ethics approval and consent to participate

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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