Prophylactic antibiotics for children with recurrent urinary tract infections

The Canadian Paediatric Society gives permission to print single copies of this document from our website. For permission to reprint or reproduce multiple copies, please see our copyright policy.

Urinary tract infections (UTIs) are a common cause of acute illness in infants and young children, occurring in an estimated 8% of girls and 2% of boys by seven years of age, with a recurrence rate of 10% to 30%.^[1] Guidelines and recommendations for diagnosing UTIs were recently updated by the Canadian Paediatric Society and should be consulted for how to sample and test urine, how to interpret results and for treatment strategies.^[2] The present position statement examines published data regarding the efficacy of prophylaxis following a UTI in infants and young children.

Is prophylaxis ever indicated?

The premise of antibiotic prophylaxis for UTIs is that it can prevent UTIs and long-term sequelae (eg, hypertension and renal failure).^[3] Traditional thinking is that infants and young children who are diagnosed with vesicoureteral reflux (VUR) of any grade are at increased risk for recurrent UTIs and, therefore, require antibiotic prophylaxis.^[4] However, many older studies investigating antibiotic prophylaxis were small and of poor quality.^[5] Also, because a stringent definition of UTI was not used, they tended to overestimate the efficacy of prophylaxis.^[6] Even if prophylaxis is effective, there is increasing doubt that recurrent UTIs in children with normal kidneys lead to long-term sequelae, even when such infections result in renal scarring.^[7]

The American Academy of Pediatrics Subcommittee on Urinary Tract Infection published updated clinical practice guidelines in 2011. Their meta-analysis of six studies that included children <24 months of age did not show a significant benefit of antibiotic prophylaxis, either in infants without VUR or in those with grades I to IV VUR. The sample size was small for some subgroups in these studies.^[6] However, a Cochrane meta-analysis of 12 studies that included children in varying age groups indicated that if the largest and best-designed studies (Montini et al,^[8] published in 2008, and the Prevention of Recurrent urinary tract Infection in children with Vesicoureteric Reflux and Normal Renal Tracts [PRIVENT] trial,^[9] published in 2009) were combined, there was a small but significant decrease in recurrent UTIs in the prophylaxis group, independent of VUR.^[10]

Recently, the results of the Randomized Intervention for Children with Vesicoureteral Reflux (RIVUR) trial were published.^[11] Table 1 summarizes the details of this trial along with results from the two previously completed large trials (Montini et al^[8] and the PRIVENT trial^[9]) including a total of 1521 enrolled children with ≥1 previous UTIs. The RIVUR trial^[11] enrolled only children with VUR and followed them for two years, while the other two trials enrolled children with or without VUR (including some children who were never assessed for VUR) and followed them for one year. Montini et al^[8] excluded children with proven grades IV or V VUR. The PRIVENT trial enrolled children of all ages, while the age limit for the other two trials was seven years (Montini et al) and 71 months (RIVUR). There was a striking predominance of girls in the RIVUR trial (92%). Montini et al used bagged urines for children who were not toilet trained and required two samples suggestive of a UTI, while the two other trials required a single catheter or suprapubic specimen for such children. The definitions of UTI in the three studies also varied. Only Montini et al required fever, and only the PRIVENT trial did not require pyuria. The Montini et al trial was not blinded and did not include a placebo, while the other two did both. The primary outcome in all three trials was a single recurrent UTI.

Given the heterogeneity in study design, it is not surprising that the results of the trials differ (Table 1). The efficacy of antibiotic prophylaxis was very low in the Montini et al trial.^[8] The other two trials demonstrated higher efficacy, but if it is assumed that patients lost to follow-up did not have UTIs, antibiotics would have to be prescribed for one year for 17 children with UTI with or without VUR (PRIVENT^[9]) or for two years for nine children with VUR (RIVUR^[11]) to prevent recurrent UTIs in one child. As expected, the Montini et al and RIVUR trials described a much higher rate of recurrences among children with grade III or higher VUR than in other children. The relationship between VUR and recurrences was not reported in the PRIVENT trial. The sample size of the studies was too small to demonstrate whether the efficacy of prophylaxis is the same with all grades of reflux. All three trials found a similar low rate of worsening of renal scarring in both cases and controls. The median time to recurrence in both groups in the Montini trial was 113 days. One-half of the recurrences in the placebo group in the PRIVENT study occurred within three months and three-quarters occurred within six months.

Minor adverse drug reactions were reported in 7% of children on prophylaxis in the Montini et al^[8] trial. It was not clear whether medication was then stopped. Medication was stopped in 1.4% of cases and 3.5% of controls in the PRIVENT trial^[9], and in 2.3% of cases and 2.0% of controls in the RIVUR trial^[11] for suspected adverse drug reactions, suggesting that trimethoprim-sulfamethoxazole was well tolerated. Few children were lost to follow-up (approximately 8% in Montini et al, 2% in PRIVENT and 6% in RIVUR). However, noncompliance was suspected in approximately 25% of cases in all three trials. This occurred almost equally in cases and controls in the PRIVENT and RIVUR studies, and suggests that compliance with long-term antibiotic prophylaxis outside of a study setting is likely to be suboptimal, further limiting efficacy.

None of the studies referenced in the present statement were powered to compare the efficacy or safety of different prophylactic antibiotics. Some studies suggest that treating with nitrofurantoin may prevent more UTIs than trimethoprim-sulfamethoxazole, but this drug is associated with gastrointestinal side effects.^[10] Developing local resistance to the antibiotic prescribed was a common finding in studies in which this was assessed.^[8][10][11]

Summary

The vast majority of children receiving UTI prophylaxis do not benefit. There is no evidence that prophylaxis prevents renal scarring or other long-term sequelae. Moreover, there is increasing evidence that recurrent UTIs do not contribute to chronic renal failure in children with no structural renal anomaly.^[7] Therefore, more harm than benefit may result from prophylaxis. Long-term antibiotics may cause adverse events as well as promote resistance to all available oral antibiotics. Managing constipation appropriately may be helpful for decreasing UTI recurrences.^[12] It is important for clinicians to inform the parents of a child who has had a UTI about the risk and signs or symptoms of a recurrence, and urge them to seek prompt diagnosis and therapy when suspicions arise.

Recommendations

• Antibiotic prophylaxis is no longer routinely recommended after a UTI but may still be considered when a child is known to have a grade IV or V VUR, or a significant urological anomaly. A large number of children must be treated to prevent one UTI, although this number may be smaller for children with grade IV or V VUR, or a significant urological anomaly. An increasing risk for antibiotic resistance may soon negate the benefits of prophylaxis even in these cases.
• For cases in which prophylaxis is still used, it should generally last for no longer than three to six months. If the abnormality persists, prophylaxis should be reassessed. Antibiotic resistance increases with prolonged prophylaxis.
• If the decision is made to offer prophylaxis to children with grade IV or V VUR, or a major urological anomaly, the risks and benefits should be discussed with parents.
• Trimethoprim/sulfamethoxazole or nitrofurantoin are the usual choices for prophylaxis, unless contraindicated or the child has already had urinary isolates test positive for resistance to these drugs. These antibiotics are inexpensive, generally well tolerated and disrupt bowel flora less than most others. Nitrofurantoin is no longer commercially available as a suspension and parents will need to be referred to a compounding pharmacy to obtain it. They can also be advised to crush the pills and mix the powder with yogurt or apple sauce. There is insufficient evidence to recommend a specific dose; however, traditionally, one-quarter to one-third of the daily total treatment dose is given once per day. There are no data on the efficacy of the practice of alternating prophylactic antibiotics on a monthly basis.
• Prophylaxis should be stopped or changed if an organism that is resistant to the prophylactic antibiotic is identified in a urine culture, even when the culture is believed to be contaminated. That antibiotic is highly likely to be ineffective in preventing UTIs and continuing to use it will promote development of further resistance. If a child has a urinary isolate that is resistant to both trimethoprim/sulfamethoxazole and nitrofurantoin, consider discontinuing prophylaxis. Experience suggests that using broader-spectrum agents for prophylaxis (such as cefixime or ciprofloxacin) often results in a UTI with an organism that is resistant to any remaining oral options for therapy.
• Cases with grade IV or V VUR, or another significant urological anomaly, should be discussed with or seen by a paediatric nephrologist or urologist.
• Parents of a child who has had a UTI need to be informed of the signs and symptoms of a recurrence. The threshold should be low for testing for a UTI in such children.

Addendum

A recent randomized controlled trial (RCT) following 392 infants with Grade 3 to 5 vesicoureteral reflux who received antibiotic prophylaxis or no intervention showed a small but statistically significant benefit in preventing a first UTI (21% versus 35.6%). However, results showed no difference in incidence of renal scars or renal function at age 2 years^[13]. The study did report significantly more non-E. coli pathogens in the prophylaxis arm. Notably, all UTIs caused by Pseudomonas species occurred in the prophylaxis arm. This trial, coupled with a systematic review (seven RCTs following a total of 1427 children) showed no influence of antibiotic prophylaxis in preventing renal scarring, even in children with VUR^[14]. This finding has the downside of favouring breakthrough infections with non-E. coli pathogens that are potentially resistant to usual prophylaxis, which further supports a ‘watchful waiting’ approach for otherwise healthy children with a first UTI, even when they have VUR.

CPS INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE (2015)

Members: Robert Bortolussi (past Chair); Natalie A Bridger MD; Jane C Finlay MD (past member); Susanna Martin MD (Board Representative); Jane C McDonald MD; Heather Onyett MD; Joan L Robinson MD (Chair); Marina Salvadori MD (past member); Otto G Vanderkooi MD
Consultant: Noni E MacDonald MD
Liaisons: Upton D Allen MBBS, Canadian Pediatric AIDS Research Group; Carrie Byington MD, Committee on Infectious Diseases, American Academy of Pediatrics; Nancy Scott-Thomas MD, College of Family Physicians of Canada; Charles PS Hui MD, Committee to Advise on Tropical Medicine and Travel (CATMAT), Public Health Agency of Canada; Nicole Le Saux MD, Immunization Monitoring Program, ACTive (IMPACT); Dorothy L Moore MD, National Advisory Committee on Immunization (NACI); John S Spika MD, Public Health Agency of Canada

CPS COMMUNITY PAEDIATRICS COMMITTEE (2015)

Members: Carl Cummings MD (Chair); Sarah Gander MD; Ruth B Grimes MD; Barbara Grueger MD (past member); Mia Eileen Lang MD (past member); Larry B Pancer MD; Anne Rowan-Legg MD; Ellen P Wood MD (Board Representative)
Liaisons: Fabian P Gorodzinsky MD, CPS Community Paediatrics Section

Updated by:  Michelle Barton-Forbes MD, Ari Bitnun MD

References

Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. Internet addresses are current at time of publication.