DOI: https://doi.org/10.4414/smw.2020.20236
The Quality Assurance Committee of the SSGO (Swiss Society of Gynaecology and Obstetrics) releases guidelines on current topics to ensure quality and the timely implementation of medical innovations. In human medicine, the number of infections caused by antibiotic-resistant bacteria has increased. The urinary tract pathogen Escherichia coli, which is often encountered in general and gynaecological practices, accounts for almost one third of resistant bacteria. Further, new Swiss data confirm that the resistance rate of E. coli to various antibiotics is increasing [1].
As most guidelines on urinary tract infections (UTIs) (table 1) do not specifically consider the treatment of women and do not include the treatment of pregnant women, the Quality Assurance Committee of the SSGO declared an expert recommendation focusing on female UTIs in both pregnant and non-pregnant women to be an urgent need. A guideline was also required in the light of the strategy of the Federal Office of Public Health to reduce antibiotic resistance.
UTIs in men are less frequent, but can be more serious than in women owing to functional and anatomical differences in the urogenital tract. Thus, diagnosis and treatment differ between men and women. UTIs in men are not a topic of this guideline.
Guideline | Country, region | Year of release | Gender |
American Urological Association (AUA)/Canadian Urological Association (CUA)/Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction (SUFU): Guideline on recurrent uncomplicated urinary tract infections in women (2019) [2] | USA, Can | 2019 | Women, not pregnant |
Guideline Harnwegsinfekt (HWI) – Society of Infectious disease [3]Available in German and French | CH | 2020 | Women |
Deutsche Gesellschaft für Allgemeinmedizin und Familienmedizin (DEGAM): " Brennen beim Wasserlassen" [4]. Available in German | D | 2018 | Women, men |
Urinary tract infection (2): antimicrobial prescribing. NICE guideline (NG109) [5] | UK | 2018 | Women, men |
Executive summary of the diagnosis and treatment of urinary tract infection: guidelines of the Spanish Society of Clinical Microbiology and Infectious Diseases (SEIMC) [6] | E | 2018 | Women, men |
European Association of Urology (EAU): Guidelines on urological infections [7] | EU | 2018, update 2019 | Women, men, including prostatitis |
Interdisziplinäre S3 Leitlinie. Epidemiologie, Diagnostik, Therapie, Prävention und Management unkomplizierter, bakterieller, ambulant erworbener Harnwegsinfektionen bei erwachsenen Patienten [8]. Available in German | D, A, CH | 2011, update 2017 | Women, men |
Recurrent urinary tract infection. Urogynaecology Committee; Family Physicians advisory Committee [9] | Can | 2010 | Women, men |
International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases [10] | EU, USA | 2011 | Women |
The American College of Obstetricians and Gynecologists (3): "Treatment of Urinary Tract Infections in Nonpregnant women" [11] | USA | 2008 | Women, not pregnant |
In this guideline on the management of UTIs, we report on the diagnosis and treatment of UTIs and recurrent UTIs in women and during pregnancy, with antibiotic and non-antibiotic options. The guideline also covers antibiotic therapy prior to interventions and operations in gynaecology.
The expert panel comprises members of the SSGO, including gynaecologists, obstetricians and urogynaecologists, and an infectiologist. This guideline meets the following requirements: it addresses UTIs and recurrent UTIs in pregnant and non-pregnant women, it is presented in a compressed, easy-to-understand text form, with practice recommendations for in- and outpatients including evidence-based recommendations (the search strategy is described below), and is regularly updated every 3 to 4 years. The members of the Quality Assurance Committee of the SSGO are gynaecologists working in private practices, in academia, and in regional and teaching hospitals. They have various specialisations and sub-specialisations in obstetrics and gynaecology. In addition, a representative of the Swiss Patient Organisation (SPO) is also a permanent committee member. The expert panel addresses UTIs, a day-to-day problem of Ob/Gyn practitioners nation- and worldwide, in the form of a consensus document and not as a systematic review. The committee discussed the management of UTIs during a series of meetings. A manual literature search was performed to reference statements on diagnostics and treatments where appropriate. A review of the literature, including the Pubmed, Embase and Cochrane Library databases, as well as conference proceedings of the relevant professional societies, was carried out to rate the level of evidence (LoE) and to search existing guidelines. The search for evidence used keywords (MeSH terms) grouped into the following syntax: (urinary tract infection) OR (recurrent urinary tract infection) AND (controlled) AND (randomised controlled trial [Publication Type] OR (randomised AND controlled AND trial [Title / Abstract]). Keywords used alone and/or in combination included the following: women, pregnancy, national, international guidelines, urodynamics, gynaecologic surgery, pelvic floor surgery, antibiotics, phytotherapy, D-mannose, E. coli. The search was restricted to articles in English, German, French, Italian and Spanish that were published up to the end of December 2019. We assessed the LoE according to the recommendations from the Oxford Centre of Evidence-based Medicine (OCEBM, Levels of Evidence working Group. 2011, https://www.cebm.net/2016/05/ocebm-levels-of-evidence/).
The discussions about the recommendations took place in parallel in the Quality Assurance Committee and in the Swiss Working Group of Urogynaecology. The first and the last author of this publication were responsible for finalising the decisions, which were taken by consensus.
All authors declared no conflict of interests; no companies were involved; regular meetings of the members of the SSGO were financed according to the regulations of the society with no extra compensation.
Female acute UTIs are amongst the most common bacterial infections seen by gynaecologists. Half of all women experience UTIs, and at least a quarter of these experience a recurrence. UTIs heal spontaneously at a high rate of 50-70%, and only 0.4-2.6% of uncomplicated UTIs develop into pyelonephritis if left untreated [12, 13].
Urinary tract infections can be categorised in uncomplicated or complicated UTIs or asymptomatic bacteriuria (ASB) (table 2). Recurrent UTIs, at least two infections within 6 months or three infections within a year, can be uncomplicated or complicated. Urine itself is not sterile. Between 1% and 3% of young women and 14-22% of postmenopausal, community-dwelling women have ASB [14].
Uncomplicated UTI | Complicated UTI | Asymptomatic bacteriuria | |
Patients | Women without anatomical or functional abnormalities of the genitourinary tract | Pregnancy, risk factors such as poorly controlled diabetes mellitus, hospital-acquired infections, kidney disease, previous kidney transplant, urolithiasis, anatomical, functional abnormality (genital prolapse), immunosuppressants, indwelling catheter, postoperative (predisposing factors) | Any person, pregnant or non-pregnant |
Clinical signs | UTI (dysuria, pollakiuria, suprapubic pain), pyelonephritis (as UTI with addition of flank or groin pain, fever) | Recurrent UTI with risk factors (see above), previously treated with NSAIDs and/or antibiotics, pyelonephritis. | No clinical signs |
Diagnostics | Not required for first episode of UTI; recommended for pyelonephritis and recurrence: urine analysis, culture. Suspected pyelonephritis: ultrasound | Urine analysis, urine culture. Suspected pyelonephritis: kidney ultrasound, postvoid residual urine, in pregnancy also measure cervical length. Fever >38.3°C and hospitalised patients: blood cultures (2×) | Not required except before urological interventions with risk or probability of vesical mucosa lesions/damage |
Microbiology | E. coli (>80%) (also ESBL), Proteus mirabilis, Klebsiella spp, Staphylococcus saprophyticus, Enterococcus faecalis | E. coli (also ESBL), Enterococcus faecalis, Enterobacterales, Pseudomonas aeruginosa | Any kind of bacteria in an amount of ≥105 bacteria per ml |
ESBL = extended spectrum beta-lactamase; NSAID = nonsteroidal anti-inflammatory drug
Uncomplicated urinary tract infections do not require diagnostic tests. The following tests are available for cases with an unclear clinical presentation:
Midstream urine stix: sensitivity 75%, specificity 82% for leucocyte esterase (proof of leucocytes in urine) [15].
Urine analysis is reliable only if the sample is not contaminated, i.e., <10 squamous cells/high power field. Midstream urine samples, if collected correctly, have a sensitivity of 95% and a specificity of 70% for UTI [16].
Urine cultureis indicated in complicated or recurrent UTI, or if there are strong clinical signs of an infection but antibiotics are not effective [17]. Urine samples collected after bladder catheterisation are considered pathological if a single uropathogen species has ≥102cfu/ml; midstream urine samples are considered to show relevant growth if there are ≥105 cfu/ml.
Imaging: if there are ≥3 UTIs per year, cystoscopy is recommended to rule out intravesical pathology; if there are ≥2 pyelonephritis episodes per year, a kidney computed tomography (CT) scan (contrast CT) is recommended.
At least half of acute uncomplicated UTIs heal spontaneously, although symptoms persist longer than when treated with antibiotics [18]. Requests by the patient for a speedy relief of symptoms are common. In this new treatment guideline, a delay in antibiotic administration for 48 hours is recommended for uncomplicated UTIs and patients under 65 years of age. Pain relief should primarily be by the use of antibiotic-free treatments, such as nonsteroidal anti-inflammatory drugs (NSAIDs) with a phytotherapeutic agent or D-mannose [2, 5, 8]. Uva-ursi extract has been advocated as a phytotherapeutic agent for the relief of symptoms of acute cystitis, although a recent randomised placebo-controlled trial did not show a reduction in antibiotic use [19]. Ibuprofen 3 × 400 mg vs ciprofloxacin 2 × 250 mg for 3 days had an equally good effect on UTI symptoms after 4 days without any significant difference in the rates of recurrence [20]. Both medications are contraindicated in pregnancy.
However, two recent studies challenge the efficacy and safety of NSAIDS. A study from Switzerland reported inferiority of diclofenac to norfloxacin by day 4 and a higher risk of pyelonephritis, even though it reduced antibiotic use in women with an uncomplicated lower UTI [21]. Another recent study from Scandinavia reported that in patients with uncomplicated UTI, ibuprofen 600 mg three times daily was inferior to pivmecillinam, which is not available in Switzerland. All cases of secondary pyelonephritis occurred in the ibuprofen group [22]. Compared with fosfomycin, initial treatment with ibuprofen substantially reduced antibiotic use in women aged 18-65 with mild to moderate symptoms of UTI, but was less effective for symptom relief, and there were more cases of pyelonephritis [23]. Therefore, close clinical observation or follow-up for potential signs of pyelonephritis are indicated if lower UTIs are treated with NSAIDs. In addition, the NSAID treatment regimen should be discussed with women who want to avoid antibiotics or who are open to a delayed prescription.
An antibiotic prescription could be given to specific patients, such as those who plan to travel. Physicians should enquire about allergies.
If symptoms persist after 48 hours, starting an antibiotic is indicated. Also, ascending pain indicates a possible upper urinary infection and calls for the direct administration of antibiotics. Antibiotics may also be promptly prescribed to persons over 65 years of age, because this group of patients is more susceptible to urosepsis or UTI-associated comorbidities. As revealed by a national Danish study, the implementation of the new antibiotics guideline with avoidance of or delayed antibiotic administration led to an increase in pyelonephritis and urosepsis in UTI patients over 65 years of age [24].
Uncomplicated UTIs can be treated empirically. In urgent cases with clear symptoms, pharmacists (in Switzerland) are allowed to provide medication, including antibiotics from the specialty list.
The therapy options for simple UTIs and pyelonephritis are summarised in table3 and for complicated UTIs in table 4 [25], taking into account antibiotic resistance in Switzerland (www.anresis.ch). The Swiss Centre for Antibiotic Resistance provides resistance data obtained by passive surveillance, which overestimates the true resistance rate. The actual resistance patterns of uropathogens in primary care in Switzerland (2019) are reported by Plate et al. [26]. In this study, E. coli showed low resistance rates to the recommended first-line antibiotics. Further, resistance to trimethoprim/sulphamethoxazole was significantly lower than reported by ANRESIS, making trimethoprim/sulfamethoxazole a suitable and cheap alternative for the empirical treatment.
Level of resistance in Switzerland for community-acquired E. coli, www.anresis.ch | Dosage | Duration of treatment | Remarks | |
Uncomplicated UTIs, first choice | ||||
Nitrofurantoin | 1.0% | 2 × 100 mg/day | 5 days | Not effective for pyelonephritits, low tissue absorption. Minimal development of resistance, minimal “collateral damage“. Severe side effects rare (pulmonary fibrosis, liver insufficiency, neuropathy). GFR ≥60ml/min |
Fosfomycin | 1.5% | 1 × 3 g | Single dose | Not effective for pyelonephritits. Administered in the evening 2-3 hours before or after meal. Mainly gastrointestinal side effects |
Trimethoprim/sulfamethoxazole | 23.5% | 2 × 800/160 mg/day | 3–5 days | Side effects: nausea, vomiting, diarrhoea, rare rash (Stevens-Johnson syndrome), jaundice, iatrogenic lupus, leuco- and thrombocytopenia. Lowers levels of oral contraceptives |
Uncomplicated UTIs, second choice | ||||
Ciprofloxacin | 19.0% | 2 × 500 mg/day | 3 days | |
Amoxicillin or amoxicillin/clavulanic acid | 14.2% | 2 × 1 g/day | 7 days | |
Uncomplicated pyelonephritis | ||||
Trimethoprim/sulfamethoxazole | 23.5% | 2 × 800/160 mg/day | (7–)14 days | |
Ciprofloxacin | 19.0% | 2 × 500 mg/day | 7 days | Empirical use only if resistance rate in E. coli <10%. Absorption reduced by milk products |
Ceftriaxone (third generation cephalosporin) | 9.1% | 2 g/day intravenously | 7–14 days | Hospitalisation or outpatient intravenous therapy |
Level of resistance in Switzerland for community-acquired E. coli, www.anresis.ch | Dosage | Duration of treatment | Remarks | |
Amoxicillin/clavulanic acid (first choice) | 14.2% | 2 × 1 g/day or 3 × 625 mg/day | 5–7 days | - |
Cefuroxime (second generation cephalosporin)(Second choice) | 11.7% | 2 × 500 mg | 3–5 days | - |
Trimethoprim/sulfamethoxazole (third choice) | 23.5% | 2 × 800/160 mg/day | 3–5 days | - |
Fosfomycin (third choice) | 1.5% | 1 × 3 g every 2–3 days | 3 cycles | - |
The quinolone resistance rates of E.coli have increased from 1% to 21% in the past 10 years, and its resistance against third and fourth generation cephalosporins has increased from 1% to 9%. The resistance rates of E. coli to fosfomycin and nitrofurantoin remain very low. Therefore, consistent with the guidelines of the Infectious Disease Society of America and the European Society for Microbiology and Infectious Disease from 2011, fosfomycin and nitrofurantoin, as well as cotrimoxazole, can still be recommended as a first choice therapy.
The guideline of the Swiss Society of Infectious Disease dating from February 2020 classified fosfomycin as a second choice drug owing to its lower efficacy compared with nitrofurantoin shown in the study by Huttner et all [27].
The proportion of treatment failures is high and patients should be informed. In a randomised clinical trial that included 513 women with uncomplicated UTIs, clinical resolution at 28 days occurred in 70% of patients treated for 5 days with nitrofurantoin vs 58% of patients who received a single dose of fosfomycin. This is a statistically significant difference; however, nitrofurantoin was given at a dose of 100 mg three times daily, which is not the recommended dosage in Switzerland (100 mg twice daily) [27]. Nevertheless, fosfomycin 3 g, as a single dose, is a convenient, well tolerated and efficient therapy; considering the resistance rate, it is better than trimethoprim/sulfamethoxazole. In clinical practice it is still, in our opinion, a valuable first-choice option. Lopes-Montesinos and Horcajada [28] reviewed the use of oral and intravenous fosfomycin to treat complicated UTIs. Because some bacteria are multidrug-resistant, they evaluated fosfomycin as an antibiotic with enormous potential; randomised studies are under way. Doesschate et al. [29] conducted a double-blind placebo-controlled randomised non-inferiority trial (FORECAST) comparing fosfomycin with ciprofloxacin in complicated UTIs. They demonstrated non-inferiority of oral fosfomyin 3 g every 24 hours compared with oral ciprofloxacin 500 mg every 12 hours for 10 days, both given after at least 48 hours of intravenous treatment. When complicated UTI was treated with multiple-dose fosfomycin, clinical resolution occurred in two of three treatment episodes [30].
A study of the treatment of ASB showed that patients who were not treated had less recurrence than patients treated with antibiotics, and that the resistance rate of the E.coli was lower. In contrast to previous opinions, asymptomatic diabetic patients should not be treated [31]. In cases of acute pyelonephritis, antibiotic therapy for 7 days has proven to be as effective as the 14 days of therapy used previously [32] (LoE Ib). Complicated UTIs should be treated with a 7- to 10-day antibiotic regimen.
As a result of increasing levels of antibiotic resistance, especially to trimethoprim/sulfamethoxazole and quinolones, and increasing awareness of the detrimental effects of antibiotics on the microbiome, antibiotic-free therapies are becoming increasingly important. Alternative options should be recommended to all patients with recurrent infections.
The following recommendations reduce the frequency of recurrence:
The following medications or solutions reduce the frequency of recurrence and can be recommended during the acute phase of a UTI, but not during pregnancy:
In principle, there is an increased risk of pyelonephritis and complications of pregnancy with both symptomatic UTIs and ASB. Pregnant women with ASB are at a 20- to 30-fold greater risk of developing pyelonephritis and possible subsequent complications such as urosepsis, premature birth and SGA (small for gestational age) children [45]. These older and methodologically questionable studies were the background reasoning behind the recommendation for systematic screening for ASB in pregnant women, including antibiotic therapy in cases with positive cultures. Although a new randomised controlled study showed that untreated ASB in pregnant women of a non-risk group (see details below) increases the risk of developing pyelonephritis, there was no increased risk of premature birth or other neonatal or maternal complications. These new data have been taken into consideration in a new meta-analysis and other national guidelines. The benefit of systematically screening all pregnant women for ASB is currently not proven, but bacterial screening following vaginal smears in the first trimester continues to be recommended [46, 47] (LoE 1a). Systematic screening of all pregnant women for ASB can no longer be recommended, with the exception of pregnant women at risk owing to factors such as diabetes mellitus, immunosuppression, functional or structural abnormalities of the urinary tract, previous episodes of pyelonephritis, previous premature births or late pregnancy loss.
Current data show that a single dose of antibiotic, 3 g fosfomycin, is sufficient in pregnancy [31, 48], but is not recommended in cases with an increased risk of premature birth, when more prolonged therapy should be given. Ibuprufen and chinolones like ciprofloxacin are both contraindicated in pregnancy.
Antibiotic therapy for uncomplicated UTI and pyelonephritis during pregnancy and breastfeeding is summarised in table 5.
Level of Resistance in Switzerland for community- acquired E. coli,www.anresis.ch | Dosage | Duration of treatment | Remarks | |
Amoxicillin/clavulanic acid(first choice) | 14.2% | 2–1 g/day or 3–625 mg/day | 5–7 days | Suitable throughout whole pregnancy and breastfeeding period |
Cefuroxime(second generation cephalosporin)(second choice) | 11.7% | 2–500 mg | 3–5 days | Suitable throughout whole pregnancy and breastfeeding period |
Trimethoprim/sulfamethoxazole(third choice) | 23.5% | 2–800/160 mg/day | 3–5 days | Contraindicated in first and third trimester; suitable during breastfeeding |
It is not necessary to routinely screen non-pregnant women for asymptomatic bacteriuria, nor to treat it if incidentally discovered [49]. A study of the treatment of ASB showed that patients who were not treated had fewer recurrences than patients treated with antibiotics and that the resistance rate of E.coli was lower. In contrast to previous opinions, it is now recommended that asymptomatic diabetic patients should not be treated [31]. The study by Kazemier investigated the maternal and neonatal consequences of treated and untreated ASB in pregnancy [50]. The conclusion of the study was that the non-treatment of ASB in pregnant women is an option. As mentioned above, systematic screening for asymptomatic bacteriuria in pregnant women is no longer recommended, with the exception of pregnant women at risk owing to factors such as diabetes mellitus, immunosuppression, functional or structural abnormalities of the urinary tract, previous episodes of pyelonephritis, previous premature births or late pregnancy loss [51].
Testing for and treating of ASB is not recommended except for selected indications (see section below “Antibiotic prophylaxis before a urological procedure”).
Antibiotic prophylaxis is no longer indicated before surgical interventions such as hip or knee prosthesis or gynaecological operations such as hysterectomies [46]. Kidney transplant recipients are a special case [52]. More recent data show that UTIs could significantly impact on graft function and long-term outcomes, and that the prevention and early treatment of UTI is of importance, especially in the first 6 months after transplantation. For information on the dosage for see reference [52].
Pregnancy is another situation where the significance of a prophylactic treatment of ASB is possibly of value. Studies that have a different outcome are discussed above in the sections on “Pregnancy” and “Asymptomatic bacteriuria”.
Prophylactic antibiotics are not indicated before cystoscopy or urodynamic assessment unless the physician responsible makes another decision based on experience and on the individual case. Eradication of ASB is not necessary [53] (LoE IV) except when it comes to mucosal lesions/damage as in, for example, bladder biopsies, for which prophylaxis is indicated. Routine antibiotic prophylaxis should be avoided in urodynamic assessment to investigate urinary stress incontinence in cases of genital prolapse, provided that there is no significant postvoid residual urine (<100 ml). Patients with a cystocele are more likely to have microhaematuria than those without a cystocele, but this is not associated with infection. Important: UTIs must be excluded before any urogynaecology intervention, or treated as necessary (LoE Ib).
Antibiotic prophylaxis before or directly after urodynamic assessment or cystoscopy can be considered in cases where patients have recurrent UTIs, postvoid residual urine >100 ml, neurological bladder dysfunction, age ≥ 70 years, presence of indwelling catheter or immunocompromise. Recommended antibiotics include trimethoprim/sulfamethoxazole 800/160mg or fosfomycin 3 g sachet single dose [54] (LoE IIa).
Single-dose antibiotic prophylaxis with a first generation cephalosporin (cefazolin, 30 minutes before skin incision) is recommended, although according to the latest review from the US Centers for Disease Control and Prevention, there is only moderate evidence supporting this [55] (LoE IIb). Extended antibiotic therapy should not be given if the postoperative recovery is without complications, and also should not be given following mesh operations (sacrocolpopexy, incontinence slings and vaginal meshes) [56]. A published decision analysis model suggests that antibiotic prophylaxis is probably not required before the insertion of mid-urethral slings [57]. Postoperative antibiotic prophylaxis after urogynaecological procedures requiring intermittent self-catheterisation is not indicated [58] (LoE IV).
Postoperative postvoid residual urine, catheterisation for >24 hours or repeated catheterisation, are risk factors for urinary tract infections. Nevertheless, prolonged postoperative prophylactic antibiotic therapy in these situations remains controversial and, based on current evidence, is not recommended [59]. Measuring postvoid residual urine postoperatively using ultrasound is preferable to measuring repeatedly with single-use catheters. If recurrent UTIs occur beyond the immediate postoperative period, it is necessary to establish the cause (fistula, mesh erosion) (LoE Ia).
If it is necessary to drain the bladder long-term postoperatively because of increased postvoid residual urine, suprapubic drainage is preferable to transurethral. No difference is seen in the occurrence of bacteriuria or UTIs with intermittent self-catheterisation using hydrophilic coated single-use catheters or suprapubic catheterisation [60].
For recurrent UTIs there is a distinction between a relapse (UTI due to the same pathogen within two weeks of ending therapy) and a reinfection (new UTI more than 2 weeks after ending therapy, usually due to a different pathogen). Reinfections are twice as frequent and should be treated with the same medication for the same duration as the first infection (LoE Ia). If there are no predisposing factors, it is also possible to treat following a self-diagnosis, which is appreciated by many women. Easy to handle infection-specific Combur®-Strip tests with three fields are available.
In the case of frequent recurrence, antibiotic prophylaxis over a period of 6 months can be considered as a last resort (table 6), either to be taken continuously or only postcoitally if sexual intercourse is the cause. Continuous and postcoital low-dose antibiotic prophylaxis are equally effective in reducing recurrent UTIs.
Dose | Duration | |
Nitrofurantoin | 50–100 mg/day or 3 ×/week | 6 months, then stop. Postcoital: within 30 minutes following sexual intercourse |
Trimethoprim/sulfamethoxazole | 40/200 mg 1 ×/day or 40/2000 mg 3 ×/week | 6 months, then stop. Postcoital: within 30 minutes following sexual intercourse |
Fosfomycin | 3 g every 7–10 days | 6 months, then stop |
Uncomplicated UTIs are ideally treated with antibiotic treatment delayed by 48 hours if symptoms persist. This recommendation is in accordance with recent recommendations of other societies that were published as a reaction to the rise of antibiotic resistance [2, 5, 8].
Our expert opinion emphasises that primarily analgesics such ibuprofen, immunomodulations/vaccines and phytotherapeutics should be used in the treatment of uncomplicated and recurrent UTIs in order to halt antibiotic resistance. The global rise in antibiotic resistance has caused the number of national and international guidelines addressing UTIs to increase in the last 2 years: from 2011 to 2017 no UTI guidelines were published or amended, since 2018 six guidelines have been released, including our gender-specific guideline. The recommendations given in these national and international publications with respect to antibiotic-free therapies should help to contain antibiotic resistance.
Another advantage of the antibiotic-free approach is that it reduces the recurrence rate of UTIs [49]. Similarly, treatment of ASB is obsolete. This also increasingly applies to ASB in pregnancy, although the evidence with respect to this issue is still somewhat weak.
Quinolones should be avoided in uncomplicated UTIs, because they can lead to potentially permanent side effects affecting tendons, muscles, joints, nerves, blood vessels and the central nervous system [62].
Gender-adapted and differentiated UTI treatment algorithms for men and women and pregnant women are required, and will become important in the future.
Recent basic research uses polymerase chain reaction (PCR) in urine cultures to investigate the effect of the bladder microbiome on urinary urge symptoms and UTIs [63, 64]. The bladder microbiome seems to be more complex than previously thought and this begs a reappraisal of our current testing in recurrent UTI. Future research will point out the role of bacterial survival after treatment as well as defects in urothelial barrier function that might contribute to the failure to eradicate UTI.
On a clinical level, large randomised, double-blind studies of alternative approaches to conventional treatment with long follow-up are required.
CB: conception and design, analysis and interpretation of data, drafting and writing of the article, final approval, President of the Swiss Urogynaecological Society. WCA: analysis and interpretation of data, critical examination of the results to extract important information, final approval, Member of the Swiss Society for Infectious Diseases. SB: analysis and interpretation of data, critical examination of the results to extract important information, final approval, Committee Member of the Swiss Urogynaecological Society. DF: analysis and interpretation of data, final approval, Past-president of the Swiss Urogynecological Society. AK: analysis and interpretation of data, final approval, Past-president of the Swiss Urogynecological Society. DS: critically revision of the article for intellectual content, final approval, President of the Quality Assurance Committee of the SSGO (Swiss Society of Gynaecology and Obstetrics). VG: conception and design, analysis and interpretation of data, drafting the article, final approval, Committee Member of the Quality Assurance Committee of the SSGO (Swiss Society of Gynaecology and Obstetrics), Member of the Swiss Urogynaecological Society.
This guideline was approved by the Swiss Society of Gynaecology and Obstetrics and their subcommittees of Urogynaecology and Fetomaternal Medicine.
This study was funded by the Swiss Society of Gynaecology and Obstetrics (SSGO).
This expert panel recommendation has been reviewed by the members of the Quality Assurance Committee of the Swiss Society of Gynaecology and Obstetrics SSGO. The Quality Assurance Committee compiles guidelines and expert letters with utmost care.
The drug manufacturer’s instructions must be observed at all times, in particular the dosage instructions. To the best knowledge of the Committee, guidelines and expert letters correspond to the latest scientific insights at the time of publication. Users must take intervening changes into account.
Ethical approval: This article does not refer to any studies involving human participants or animals carried out by any of the authors.
All authors declare no conflict of interest.
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