Cystitis

Earn CME/CE in your profession:


Continuing Education Activity

Cystitis refers to infection of the lower urinary tract, or more specifically, the urinary bladder. It may be broadly categorized as either uncomplicated or complicated. Uncomplicated cystitis refers to lower urinary tract infection (UTI) in either men or non-pregnant women who are otherwise healthy. Acute cystitis is typically caused by a bacterial infection of the urinary bladder. Complicated cystitis, on the other hand, is associated with risk factors that increase the virulence of the infection or the potential of failing antibiotic therapy. Acute cystitis is typically caused by a bacterial infection of the urinary bladder. Women are particularly susceptible due to the proximity of the rectum to the urethral meatus as well as the relatively short urethral length in females. This activity reviews the evaluation and treatment of cystitis and describes the role of the interprofessional team in the care of patients with this condition.

Objectives:

  • Identify the causes of cystitis.
  • Describe the presentation of cystitis.
  • Summarize the treatment of cystitis.
  • Explain modalities to improve care coordination among interprofessional team members to improve outcomes for patients affected by cystitis.

Introduction

Cystitis refers to infection of the lower urinary tract, or more specifically, the urinary bladder.[1][2] It may be broadly categorized as either complicated or uncomplicated (simple). Uncomplicated cystitis refers to a lower urinary tract infection (UTI) in either men or non-pregnant women who are otherwise healthy. On the other hand, complicated cystitis is associated with risk factors that increase the likelihood and danger of the infection or the chances of failing antibiotic therapy. 

Etiology

Acute cystitis is typically caused by a bacterial infection of the urinary bladder. Women are particularly susceptible due to the close proximity of the rectum to the urethral meatus as well as the relatively short urethral length in females. Accounting for approximately 75% to 95% of cases, Escherichia coli is the most common etiologic agent in uncomplicated UTIs in women, followed by Klebsiella.[3] Other common etiologic pathogens include species of the Enterobacteriaceae family, such as Proteus mirabilis, and other bacteria, such as Staphylococcus saprophyticus and enterococcus. Other bacterial species very rarely cause UTIs and usually represent contamination when isolated from the urine culture of an otherwise healthy person. These include bacteria such as Group B streptococci, Lactobacillus, and other coagulase-negative staphylococci other than S. saprophyticus.[4][5][6]

Escherichia coli is also the most common cause of complicated cystitis, but the spectrum of microbial pathogens that may cause a complicated UTI is much broader and includes organisms such as Enterobacter, Citrobacter, Serratia, Pseudomonas, enterococci, staphylococci, and even fungi. The incidence of antimicrobial resistance in complicated infections is also significantly higher. Notable resistant organisms include the extended-spectrum beta-lactamase (ESBL) producing bacteria, as well as carbapenem-resistant and fluoroquinolone-resistant organisms, particularly E. coli.[7][8] 

Epidemiology

Approximately one-third of women will have had a UTI by age 24 and one-half by age 32. The incidence of UTI is 12% in women based on self-reported annual incidence. A university cohort study estimates the annual incidence of UTI at 0.5 to 0.7 UTIs per person-year in sexually active women. Factors that increase the risk for uncomplicated cystitis include sexual intercourse, spermicide use, new sex partner within the past year, previous UTI, strong family history of UTI in a first-degree female relative, and post-menopausal state. Acute cystitis is much more common than pyelonephritis, with an estimated ratio of 18 to 28 cystitis episodes for every episode of pyelonephritis.[9]

Depending on the underlying condition, there is wide variation in the incidence of complicated UTIs. The estimated prevalence of asymptomatic bacteriuria in women with diabetes is 26% compared to 6% in non-diabetic females. Patients with diabetes are also at increased risk of developing both acute cystitis and pyelonephritis. UTIs are common in patients who had renal transplantation, with retrospective cohort studies showing an incidence between 47% and 75%.[10]

The risk is highest in the first year post-transplantation. Approximately 2.3% of pregnant women develop a symptomatic UTI. Other risk factors for developing a complicated UTI include nephrolithiasis, immunocompromised status, the presence of foreign bodies such as a urinary catheter, urinary tract instrumentation, renal insufficiency, functional or anatomic abnormality of the urinary tract, urinary stents, strictures, and obstructive uropathy.[11] 

The incidence of simple cystitis in men is relatively low. It is estimated to be fewer than 10 cases per year per 10,000 men under age 65.[12] Symptoms of a simple UTI in men are the same as in women; dysuria, urinary frequency, urgency, and suprapubic pain. Recurrent symptoms or reinfections after treatment, fever and pelvic or perineal pain suggest prostatitis. Fever, chills, flank pain, or any signs of a systemic illness suggest a complicated urinary tract infection.[11] 

Pathophysiology

Cystitis usually develops due to the colonization of the periurethral mucosa by bacteria from the fecal or vaginal flora and the ascension of such pathogens to the urinary bladder. Uropathogens may have microbial virulence factors that allow them to escape host defenses and invade tissues in the urinary tract. UTIs in males are much less common due to the longer anatomic urethra, the drier periurethral environment, and the antibacterial defenses provided by the prostatic fluid. Traditionally, all UTIs in males were considered complicated. However, uncomplicated UTIs may occasionally occur, especially in males between 15 and 50, especially in those who are sexually active, are uncircumcised, or do anal intercourse, as long as they do not have any risk factors for complicated UTIs such as urologic abnormalities, bladder outlet obstruction, urolithiasis or recent urinary tract instrumentation.[13]

The underlying host factors largely determine the pathogenesis of complicated UTIs. Impairment of the immune system and voiding dysfunction from autonomic neuropathy may predispose patients with diabetes to develop UTIs. In renal insufficiency, accumulation of uremic toxins may reduce host defenses, and decreased renal blood flow may impair antimicrobial clearance. Kidney stones may cause an obstruction and provide a potential nidus of infection. In the setting of urinary catheterization, internal and external biofilms may form on the catheter, and pathogens may persist in retained pools of urine in the urinary bladder.[14]

The overwhelming identifiable bacteria causing most cases of cystitis is Escherichia coli (from 75% to 95% of cases). Other organisms causing cystitis include Klebsiella pneumoniae and Proteus mirabilis. (Klebsiella is the most common cause of UTIs after E. coli.) Patients with recent hospitalizations or prior treatment for a UTI may present with Pseudomonas, enterococci, and staphylococci, such as S. saprophyticus. Many other organisms, such as lactobacilli, Group B streptococci, and coagulase-negative staphylococci, are generally considered contaminants unless there are very high numbers of a single organism where an actual infection is possible.[15]

History and Physical

Acute cystitis often presents urinary symptoms, including dysuria, urinary frequency, urgency, suprapubic pain or tenderness, and occasionally hematuria. Based on a systematic review examining the history and examination findings of women with uncomplicated UTI, the combination of dysuria and urinary frequency in the absence of vaginal discharge or irritation is highly predictive of uncomplicated cystitis (90% correlation).[16] Symptoms may be subtle or atypical in the very young and the very old. Urine cloudiness or a "foul odor" in the absence of other signs or symptoms is generally insufficient to justify a diagnosis of cystitis.[17]

Patients with complicated acute cystitis will often present similarly to uncomplicated cystitis. Specific patient populations with complicated cystitis may have atypical symptoms. For example, patients with multiple sclerosis occasionally present with acute neurologic deterioration, while those with a spinal cord injury may present with autonomic dysfunction or increased spasticity.

Cystitis may be differentiated from pyelonephritis by the absence of systemic findings such as fever, chills, or sepsis. Findings such as flank pain, costovertebral angle tenderness, nausea, and vomiting indicate upper UTI or pyelonephritis.

When evaluating a patient with symptoms of UTI, it is important to obtain a history of any previous episode of UTI, any recent antibiotic use, or any other risk factors that may predispose one to complicated infection such as diabetes, immunocompromised status, recent urologic procedures or instrumentation, renal transplantation, history of kidney stones, anatomical or functional urinary tract abnormalities, or pregnancy.

A pelvic examination is important in evaluating women with cystitis, especially if they have recurrent urinary tract infections. Recurrent infections are defined as two documented UTIs within six months or three in one year. Management of recurrent urinary infections is discussed elsewhere, particularly in the American Urological Association Guidelines on Recurrent Urinary Tract Infections.[18] Recurrent infections with the identical organism (called a relapsing infection) suggest a urinary stone. In men, recurrent infections may also indicate chronic bacterial prostatitis. Positive urine cultures are necessary to make a definitive diagnosis of recurrent or relapsing UTIs. 

In frail and debilitated patients, many general symptoms, such as a change of mental or functional status, fevers, chills, and falls, are associated with a presumptive diagnosis of UTI. Recent evidence suggests that only urinary changes (color changes, odor, gross hematuria) and acute dysuria were reliably associated with documented UTIs.[17] Changes in urinary odor and color alone suggest bacteriuria, but the evidence is lacking that antibiotic treatment is warranted until or unless other symptoms, such as fever, develop. Recommended treatment for changes in mental status is hydration (for possible dehydration), observation, and assessment for other causes.[19] Mental status changes may or may not suggest a UTI in these patients, as studies are conflicting.[17][20]

Evaluation

The diagnosis of acute cystitis is usually made clinically in a patient with signs and symptoms consistent with a lower UTI in combination with laboratory evidence of pyuria and/or nitrites. Physical examination findings are often not necessary for the diagnosis of cystitis but may be more important for patients with pyelonephritis or vaginitis. Often in young, non-pregnant women with typical cystitis symptoms, especially in the absence of vaginal discharge or irritation, clinical suspicion may be sufficient in making the diagnosis and initiating treatment without laboratory confirmation.[1][21][22][23] However, it is highly recommended that a urinalysis and a urine culture be obtained prior to starting antibiotic treatment. If the patient does not improve on the initial antibiotic, there will be inadequate clinical information to optimally manage changes in treatment. 

Urinalysis, when indicated, is the most important laboratory test in diagnosing a UTI. A clean catch sample is usually sufficient, but if an uncontaminated specimen with few epithelial cells cannot otherwise be obtained, as in some morbidly obese women, a quick urethral catheterization should be considered. The risk of UTI from a single urethral catheterization in previously uninfected women is only about 1%.[24]

The visual appearance of the urine is notoriously unreliable when diagnosing a UTI. Clear urine may be grossly infected, and cloudy urine may be sterile with the "cloudiness" caused by calcium phosphate debris or protein. One simple test is to add a few drops of glacial acetic acid to a test tube of the cloudy urine specimen. If this causes the "cloudiness" to disappear, the urine is most likely full of calcium phosphate debris.

Pyuria, which is the presence of at least 10 white blood cells (WBCs)/HPF or leukocytes in an unspun midstream urine specimen, is almost always present. The absence of pyuria is suggestive of an alternative diagnosis.

Urinary dipsticks may also be used in the diagnosis of UTI. They detect the presence of leukocyte esterase, an enzyme produced by leukocytes, and nitrites, which indicate the presence of Enterobacteriaceae. (Nitrates are broken down to nitrites only in the presence of bacteria, so a positive nitrite test indicates or is strongly suggestive of bacteriuria).[24] Only Acinetobacter, Pseudomonas, and Enterococcus typically fail to convert nitrates to nitrites.[25] A positive dipstick test for leukocyte esterase or nitrites is helpful and confirmatory in patients with typical symptoms of acute cystitis. A negative dipstick test, however, does not reliably rule out a diagnosis of UTI.[6][26][27] 

It is reasonable to treat patients with UTI symptoms with antibiotics based on positive nitrites, but other diagnoses should be considered if the leukocyte esterase is negative.[28] The positive predictive value of having both a positive leukocyte esterase and nitrites is quite high at 85%, with an equally high negative predictive value of 92%.[28]

A urine culture is beneficial for identifying etiologic pathogens and for determining antimicrobial susceptibility profiles. Greater than or equal to 100,000 CFU (colony forming units)/mL indicates clinically relevant bacteriuria, but the growth of greater than or equal to 1,000 CFU is considered significant in men and from samples obtained through straight catheterization of the bladder. Less than 100,000 CFU/mL does not rule out a urinary tract infection.[15][29] In cases of acute uncomplicated cystitis, however, urine cultures are often considered unnecessary and not routinely done, although they can be very helpful in patients with persistent symptoms and presumed treatment failures, especially in view of the increasing rates of antibiotic resistance.[24]

Urinalyses and urine cultures must be performed prior to antibiotic therapy in all men with acute cystitis symptoms and women with risk factors for complicated UTIs. They are also indicated in patients with atypical symptoms, those who do not respond to treatment, and where symptoms recur within 2 to 4 weeks.[11] A pregnancy test should be done on women of childbearing age.

Men who have recurrent episodes of cystitis should undergo an evaluation for prostatitis. In young men who are sexually active with a single episode of cystitis, urologic evaluation may not be indicated. Risk factors for a complicated UTI should prompt a urologic evaluation and workup. 

Multiple drug-resistant organisms are becoming an increasingly difficult problem. They are defined as bacteria resistant to three or more different categories of antibiotics. Antibiotic drug resistance is a primary reason to obtain urine cultures in any potentially complicated or difficult infection and in all high-risk patients with urinary infections. 

Patients with complicated cystitis who do not respond after 48 to 72 hours of appropriate antimicrobial treatment will require further evaluation through radiographic imaging of the upper urinary tract.[11] This may be in the form of computed tomography (CT) or ultrasonography. CT imaging is usually the test of choice and is more sensitive in detecting abnormal processes that may interfere with treatment response, such as urinary obstruction, stones, diverticula, or abscess formation. Ultrasound of the kidneys, especially when combined with a KUB (short for kidneys, ureters, and bladder: i.e., a flat plate of the abdomen), may be adequate in patients who should minimize radiation exposure or otherwise avoid CT imaging.[11] A cystoscopy may optionally be done as well. 

Treatment / Management

Acute cystitis is treated with antibiotic therapy. The selection of an antimicrobial agent depends on a patient’s risk factors for infection with multiple drug-resistant organisms. Patients who are at low risk for resistant etiologic organisms are treated with one of the first-line or preferred antimicrobial agents, which include:

  • Nitrofurantoin 100 mg twice a day for 5 to 7 days
  • Sulfamethoxazole-trimethoprim (SMX-TMP) double-strength twice a day for three days (if local antibiotic resistance is <20%)
  • Fosfomycin 3 gm as a single oral dose
  • Pivmecillinam 400 mg twice a day for 5 to 7 days (not approved in the US)[30]

Nitrofurantoin is generally the first choice antibiotic for simple cystitis. It does not promote resistance or yeast overgrowth, has a high clinical cure rate of 79% to 92%, and can be safely used even in older patients as long as their glomerular filtration rate is >60 ml/min. It has little tissue penetration and therefore is inappropriate for patients with fevers, pyelonephritis, or other evidence of systemic illness.[31][32] Nitrofurantoin is less active against organisms in the Proteeae group (Proteus, Morganella, and Providencia) which produce urease that raises the urinary pH. It has been shown that nitrofurantoin is less effective in UTIs where the urine pH is 8 or higher.[33] Nitrofurantoin is a bacteriostatic rather than a bacteriocidal drug. Therefore, it should not be given for less than five days.[24]

Sulfamethoxazole-Trimethoprim (SMX-TMP) is recommended when local resistance to the antibiotic is <20%. It has good tissue penetration, including into the prostate. The overall clinical cure rate is reported as 79% to 100%.[34][35] Trimethoprim can be used alone with similar efficacy in patients with a sulfa allergy.[36] Unfortunately, resistance to SMX-TMP tends to develop relatively rapidly.[37]

Fosfomycin has a similar overall clinical cure rate as nitrofurantoin.[38] It is often not included in urine culture results and is therefore not used frequently in the US. However, it retains activity against many drug-resistant organisms, including E. coli and Enterococcus; therefore, it is not recommended for routine use initially. It can be used for both Gram-negative and Gram-positive organisms, including vancomycin-resistant strains. It is less effective against Klebsiella and Pseudomonas. Also, it is inappropriate for use in real or suspected pyelonephritis due to insufficient renal tissue levels. It is a bacteriocidal drug that is generally underutilized.

It works by interfering with bacterial cell wall synthesis but in a manner distinct from beta-lactams. It is a unique antibiotic with relatively little resistance despite being available since 1969. It has been used off-label for prostatitis and has been shown to increase the immune response. It also penetrates biofilms well. While the usual dose is a single 3-gram packet, up to 3 doses can be used 2-3 days apart in complex situations.[39] Fosfomycin can safely be used in pregnancy (FDA category B), where its single-dosing schedule is advantageous.[40] Recent studies have suggested that fosfomycin can also be useful in complicated UTIs and pyelonephritis, but additional studies are needed for confirmation before this can be generally recommended.[40][41][42]

Pivmecillinam is not available in the US but is used elsewhere, particularly in Nordic countries, due to its very low reported bacterial resistance.[43] It is a penicillin with an extended spectrum that is useful only in the urinary tract. Like nitrofurantoin, it does not significantly promote antibiotic resistance but is also not useful in pyelonephritis or systemic infections due to poor tissue penetration.[44] 

Complicated infections are generally treated with 10 to 14 days of antibiotics. People with diabetes will be at increased risk for yeast infections during and immediately following antibiotic treatment, so appropriate steps should be taken. 

Antimicrobial selection should be individualized based on patient factors, including allergies, adverse effects, tolerability, local bacterial resistance patterns, potential drug interactions, cost and insurance coverage, renal function, compliance history, and recent use of a specific antimicrobial agent within the preceding three months. Nitrofurantoin should not be used in patients with creatinine clearance or a glomerular filtration rate (GFR) of less than 60 mL per minute, while SMX-TMP should be avoided in places where regional resistance is greater than 20%, as well as in patients with allergies to sulfa. Risk factors for such resistance include recent prior contact with healthcare, use of SMX-TMP within the previous six months, and travel, especially internationally. The suspicion of pyelonephritis or a complicated UTI also precludes the use of nitrofurantoin, fosfomycin, norfloxacin, pivmecillinam, and possibly fosfomycin because of their poor penetration into renal tissues.[6][45]

Alternative or second-line antimicrobial agents are used in acute cystitis patients with factors or circumstances that prevent using the first-line agents. A 5 to 7-day course of an oral beta-lactam such as amoxicillin-clavulanate 500 mg twice daily, cefpodoxime 100 mg twice daily, cefdinir 300 mg twice daily, cefadroxil 500 mg twice daily, or cephalexin 500 mg twice daily (although this agent is less well-studied) is usually preferred. If beta-lactam agents are contraindicated, doxycycline (a tetracycline) or a fluoroquinolone such as ciprofloxacin, norfloxacin, or levofloxacin for three days (simple UTIs) or 7 to 14 days (complicated UTIs) may be used. Global resistance to SMX-TMP and amoxicillin are approaching or exceeding 20%, making these agents less useful in many geographical areas. 

Another approach is to start patients initially on a single dose of an IV parenteral agent while in the office or ER, such as ceftriaxone 1 gram, ertapenem 1 gram, or gentamycin/tobramycin 5 mg/kg. (Of these, ceftriaxone is preferred, and the aminoglycosides are reserved for those who cannot be safely given either of the other choices.) This is followed by 10 to 14 days of an oral antibiotic depending on the final urine culture results. 

Gentamicin bladder instillations can also be used to help treat UTIs, but this requires catheterization so it is generally not preferred except for selected patients, usually those with neurogenic bladders or on self-catheterization programs.[11][46][47] The suggested dosage is 30 to 60 cc of 480 mg of gentamicin/liter of normal saline or 80 mg of gentamicin in 50 to 60 mL of normal saline.[11] Tobramycin at the same dosage or neomycin/bacitracin/polymixin B (40 mg/mL) may also be used, but gentamicin has been the most studied for this purpose. Chlorhexidine and povidone-iodine bladder instillations have also been effective in reducing bacteriuria and UTIs, but not neomycin/bacitracin/polymixin B.[11][48] Bladder instillation therapy can be a reasonable option for patients already on self-intermittent catheterization with recurrent or intractable UTIs.[48]

Mandelamine can be a useful prophylactic agent, especially for recurrent multi-drug resistant infections.[11][49] Given twice daily (1,000 mg BID), mandelamine is converted to formaldehyde in the bladder if the urine is acidic (5.5 or less).[50] It is usually given together with 500 to 1,000 mg of vitamin C to maintain urinary acidity.[11] Mandelamine should not be used if the glomerular filtration rate (GFR) is <10 mL/min or if the urinary pH cannot be maintained at 5.5 or less. It also is not recommended for use together with sulfonamides due to potential precipitation.[11]

D-mannose has also been used with some success as a non-antibiotic-based UTI prophylactic agent, with some studies and meta-analyses suggesting equivalence with antibiotic prophylaxis.[51][52][53] It is well tolerated with few side effects but is not appropriate for treating an active UTI. The suggested dosage is 2 grams daily. While it seems to be generally helpful as a prophylactic agent, the available data and studies are far from conclusive.[51][52][53][54]

Urine culture and sensitivity testing are required to guide antimicrobial regimens in patients at risk for multiple drug-resistant (MDR) organisms. Risk factors include a previous MDR isolate (resistant to three or more antimicrobial classes), recent stay in a healthcare facility, recent travel to areas with a high prevalence of MDR organisms, or use of broad-spectrum antimicrobial agents in the previous three months. The appropriate empiric regimen includes nitrofurantoin, SMX-TMP, fosfomycin, and pivmecillinam (if available). An alternative approach would be to defer treatment until culture and susceptibility results are available, especially if the use of any of the above first-line agents is precluded for any reason.

Symptomatic treatment with analgesics may be used in patients with severe dysuria. Phenazopyridine is a urinary analgesic used in the short-term treatment of urinary dysuria or discomfort, but it is not therapeutic and will not affect the clinical course of an infection.

Cystitis in men is relatively uncommon and not very well studied. In a healthy man without any risk factors for a complicated UTI or any symptoms suggestive of infection outside the bladder, the treatment approach should be the same as in women with a complicated UTI. For men with severe symptoms, anatomical or urologic abnormalities, or suspicion of prostate involvement, fluoroquinolones have been recommended for initial use as empiric therapy, pending culture and susceptibility testing results and local quinolone resistance patterns. Quinolones are preferred initial agents, when possible, due to their broad spectrum of activity and high tissue penetration levels. Doxycycline, SMX-TMP, and cephalosporins may also be used initially, which help minimize quinolone resistance. All men with clearly diagnosed UTIs have generally been considered complicated infections and are at risk for developing chronic prostatitis, which may not become clinically apparent for weeks or even months after the initial infection. For this reason, some recommend using prostate-penetrating antibiotics (doxycycline, SMX-TMP, quinolones) in all men with UTIs for at least four to six weeks to allow for the buildup of adequate antibiotic concentrations inside the prostate and reduce the likelihood of developing subsequent chronic prostatitis.[11] 

Patients who do not respond to an appropriate antimicrobial regimen after 48 to 72 hours or who have a recurrence of symptoms within a few weeks will require further evaluation, including consideration of other potential causes or infection with resistant organisms. Urine culture and susceptibility testing should be obtained, and patients must be treated with a different empiric antimicrobial agent with subsequent tailoring of the regimen based on susceptibility results.[6][11] 

Differential Diagnosis

In female patients with dysuria, differential diagnoses include vaginitis and urethritis. Vaginitis is usually associated with vaginal discharge, dyspareunia, and pruritus. Its causes include bacterial vaginosis, trichomoniasis, or yeast infection. Painful bladder syndrome may be considered in patients with persistent symptoms of bladder discomfort but with no evidence of infectious etiology. This is, however, a diagnosis of exclusion. Prostatitis must be ruled out in men with lower UTI symptoms, especially when associated with fever, malaise, perineal pain, or obstructive urinary symptoms. Recurrent UTIs in male patients should heighten suspicion of chronic bacterial prostatitis.

  • Painful bladder syndrome - No evidence of infection (pyuria, bacteriuria, positive urine cultures) but symptoms of frequency, urgency, and dysuria.; it is usually a diagnosis of exclusion. 
  • Pelvic inflammatory disease - This is associated with pelvic and lower abdominal pain, fever, and possible cervical discharge.
  • Prostatitis - May present with ejaculatory pain and/or vague pelvic discomfort along with a soft, boggy, tender prostate on rectal exam. Urinalysis is usually negative.
  • Vaginitis - Usually associated with vaginal discharge, itching, odor, dyspareunia, and possibly dysuria. Typically no urinary urgency or frequency.
  • Vaginitis, atrophic (hormonal) - This condition presents in post-menopausal women and is associated with vaginal dryness, dyspareunia, vaginal discharge (thin, watery), pale labia, and vaginal lining.
  • Urethritis - White cells (pyuria) present on urinalysis but no bacteriuria. Sexually active women are at high risk. 

Prognosis

Patients with uncomplicated cystitis typically have an improvement in symptoms within three days after initiation of antibiotic therapy. Recurrent cystitis occurs in 25% of women within six months after their first UTI, and the rate increases in women with more than one prior UTI. Complications are rare, especially in patients who are appropriately treated. Bacteremia and sepsis from uncomplicated cystitis are uncommon.

Emphysematous cystitis is a rare but serious complication of a lower urinary tract infection. It is associated with gas formation in the bladder wall and is potentially fatal if not properly managed. Emphysematous cystitis is more likely to cause abdominal pain (80%) than simple cystitis (50%); pneumaturia will likely be present in about 70% of patients, and half will have bacteremia. The diagnosis is most reliably made with a CT scan. The primary risk factor is diabetes which is present in about 2/3 of affected patients. Other risk factors include female gender, immunocompromised conditions, urinary abnormalities, urinary obstruction or retention, indwelling urinary catheter, age over 60, and chronic UTIs.[55][56] 

Treatment is primarily medical with antibiotics, but catheter drainage should be used in cases of retention, incomplete bladder emptying, or significant hematuria. About 10% of patients will develop a necrotizing infection of the bladder wall and will require surgical intervention involving partial or complete resection.[56]

Complications

  • Pyelonephritis
  • Renal or perinephric abscess formation
  • Renal vein thrombosis
  • Sepsis
  • Acute renal failure
  • Emphysematous pyelonephritis
  • Prostatitis

Deterrence and Patient Education

Patients with cystitis should be made aware of the importance of adherence to their prescribed antibiotic regimen. Increasing oral fluid intake should also be encouraged. In sexually active patients, post-intercourse voiding may help to reduce recurrent infection. Patients should be advised to follow up if their symptoms worsen or do not improve after treatment with an antibiotic has started.

Pearls and Other Issues

Consider bladder instillation therapy for patients on dialysis and those performing regular intermittent self-catheterization.

Mandelamine with vitamin C or D-mannose is a reasonable option for UTI prevention in selected patients, although more studies are needed to confirm their effectiveness.

Gepotidacin is a new antibiotic in a novel chemical class called triazaacenaphthylene.[57] It selectively binds and inhibits bacterial topoisomerase IV and DNA gyrase, preventing or significantly slowing bacterial DNA replication.[58][59] Unlike fluoroquinolones, gepotidacin contains no fluorine, appears not to cause any arthropathy, and utilizes a unique mechanism of action.[58][59] It is effective against many target organisms like E. coli and Neisseria gonorrhea that are resistant to current antibiotics.[57][60] If approved by the FDA, it would be the first new antibiotic for UTIs in over 20 years. The initial indication is likely for simple UTIs as its potential clinical application in complicated urinary tract infections, prostatitis, and urinary sepsis is still to be determined.

Investigationally, initial attempts to make vaccines to help prevent urinary tract infections have only been marginally successful, but research in this area is continuing.[61][62][63] Some are made from whole bacterial cells, while others are based on E. coli bioconjugates or E.coli type 1 fimbrial adhesive protein.[64][65] Another approach to an experimental vaccine targets four outer membrane receptors involved in E. coli iron absorption (IreA, FyuA, IutA, and Hma), which are critical to the survival of the pathogen.[66] In Europe, an oral immune system stimulant is currently available and has demonstrated a 95% reduction in E. coli recurrences.[67] 

Improving personal hygiene for many women appears to be helpful. Optimal personal hygiene suggestions include:

  • Wash hands before wiping after voiding.
  • Use adult or baby wipes instead of plain toilet paper.
  • Wiping just once, from front to back, after voiding.
  • Use showers instead of baths.
  • Use a non-toxic liquid soap with minimal chemicals or perfumes to clean the vaginal area. Any liquid soap or shampoo safe for babies is likely to be acceptable.
  • Use soft cotton or microfiber washcloths rather than hands, nylon, or luffa pads for soap application while washing.
  • Wash the vaginal opening first to avoid contamination or movement of bacteria to this critical area.

Enhancing Healthcare Team Outcomes

Cystitis is a commonly encountered disorder by primary care clinicians. The diagnosis and management are relatively straightforward in most patients. However, there are other patients with structural abnormalities, diabetes, and patients with spinal cord problems who are more difficult to manage due to the risk of recurrent cystitis. Hence, an interprofessional team approach is necessary to improve outcomes.

An interprofessional healthcare team approach is essential in managing cystitis. Patient education is the key, and all clinicians who manage patients with cystitis should encourage an increase in fluid intake. Several studies show that increased fluid intake reduces the risk of recurrent infections. The pharmacist should educate the patient on medication compliance, verify all drugs are appropriately dosed and perform medication reconciliation to preclude any drug-drug interactions. The nurse should educate sexually active women to void after sexual intercourse as this has been shown to lessen the risk of a bacterial infection. Patients with recurrent infections should be referred to a urologist for a more extensive workup. Only with open communication between members of the interprofessional team can the morbidity of cystitis be lowered; therefore, it is incumbent on any team member who notices an issue or a change in the patient's status to document their findings and reach out to the appropriate team members for corrective action. [Level 5]

Outcomes

Patients with uncomplicated cystitis typically have an improvement in symptoms within three days after initiation of antibiotic therapy. However, recurrent cystitis occurs in 25% of women within six months after the first UTI, and the rate increases in women with more than one prior UTI. Complications are rare, especially in patients who are appropriately treated. When males present with a first-time episode, a referral to a urologist should be made to ensure no structural or functional abnormality. Immunosuppressed individuals or those with diabetes who require chronic catheterization or take steroids regularly have a greater potential to develop sepsis. They should be closely monitored and managed by an infectious disease specialist.[68]


Details

Author

Raymund Li

Updated:

5/30/2023 3:57:44 PM

References


[1]

Goldman JD,Julian K, Urinary tract infections in solid organ transplant recipients: Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice. Clinical transplantation. 2019 Sep     [PubMed PMID: 30793386]


[2]

Duane S,Vellinga A,Murphy AW,Cormican M,Smyth A,Healy P,Moore M,Little P,Devane D, COSUTI: a protocol for the development of a core outcome set (COS) for interventions for the treatment of uncomplicated urinary tract infection (UTI) in adults. Trials. 2019 Feb 7     [PubMed PMID: 30732617]


[3]

Behzadi P,Behzadi E,Yazdanbod H,Aghapour R,Akbari Cheshmeh M,Salehian Omran D, A survey on urinary tract infections associated with the three most common uropathogenic bacteria. Maedica. 2010 Apr;     [PubMed PMID: 21977133]

Level 3 (low-level) evidence

[4]

Byron JK, Urinary Tract Infection. The Veterinary clinics of North America. Small animal practice. 2019 Mar     [PubMed PMID: 30591189]

Level 3 (low-level) evidence

[5]

Karamali M,Shafabakhsh R,Ghanbari Z,Eftekhar T,Asemi Z, Molecular pathogenesis of interstitial cystitis/bladder pain syndrome based on gene expression. Journal of cellular physiology. 2019 Jan 4;     [PubMed PMID: 30609029]


[6]

Rank EL,Lodise T,Avery L,Bankert E,Dobson E,Dumyati G,Hassett S,Keller M,Pearsall M,Lubowski T,Carreno JJ, Antimicrobial Susceptibility Trends Observed in Urinary Pathogens Obtained From New York State. Open forum infectious diseases. 2018 Nov;     [PubMed PMID: 30539040]


[7]

Talan DA,Takhar SS,Krishnadasan A,Abrahamian FM,Mower WR,Moran GJ,EMERGEncy ID Net Study Group., Fluoroquinolone-Resistant and Extended-Spectrum β-Lactamase-Producing Escherichia coli Infections in Patients with Pyelonephritis, United States(1). Emerging infectious diseases. 2016 Sep     [PubMed PMID: 27532362]


[8]

Colpan A, Johnston B, Porter S, Clabots C, Anway R, Thao L, Kuskowski MA, Tchesnokova V, Sokurenko EV, Johnson JR, VICTORY (Veterans Influence of Clonal Types on Resistance: Year 2011) Investigators. Escherichia coli sequence type 131 (ST131) subclone H30 as an emergent multidrug-resistant pathogen among US veterans. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2013 Nov:57(9):1256-65. doi: 10.1093/cid/cit503. Epub 2013 Aug 6     [PubMed PMID: 23926176]


[9]

Kranz J,Schmidt S,Lebert C,Schneidewind L,Mandraka F,Kunze M,Helbig S,Vahlensieck W,Naber K,Schmiemann G,Wagenlehner FM, The 2017 Update of the German Clinical Guideline on Epidemiology, Diagnostics, Therapy, Prevention, and Management of Uncomplicated Urinary Tract Infections in Adult Patients. Part II: Therapy and Prevention. Urologia internationalis. 2018;     [PubMed PMID: 29539622]


[10]

Suárez Fernández ML,Ridao Cano N,Álvarez Santamarta L,Gago Fraile M,Blake O,Díaz Corte C, A Current Review of the Etiology, Clinical Features, and Diagnosis of Urinary Tract Infection in Renal Transplant Patients. Diagnostics (Basel, Switzerland). 2021 Aug 12     [PubMed PMID: 34441390]


[11]

Sabih A, Leslie SW. Complicated Urinary Tract Infections. StatPearls. 2024 Jan:():     [PubMed PMID: 28613784]


[12]

Krieger JN,Ross SO,Simonsen JM, Urinary tract infections in healthy university men. The Journal of urology. 1993 May     [PubMed PMID: 8483206]


[13]

Tyagi P, Moon CH, Janicki J, Kaufman J, Chancellor M, Yoshimura N, Chermansky C. Recent advances in imaging and understanding interstitial cystitis. F1000Research. 2018:7():. pii: F1000 Faculty Rev-1771. doi: 10.12688/f1000research.16096.1. Epub 2018 Nov 9     [PubMed PMID: 30473772]

Level 3 (low-level) evidence

[14]

Pinto H,Simões M,Borges A, Prevalence and Impact of Biofilms on Bloodstream and Urinary Tract Infections: A Systematic Review and Meta-Analysis. Antibiotics (Basel, Switzerland). 2021 Jul 8     [PubMed PMID: 34356749]

Level 1 (high-level) evidence

[15]

Hooton TM, Roberts PL, Cox ME, Stapleton AE. Voided midstream urine culture and acute cystitis in premenopausal women. The New England journal of medicine. 2013 Nov 14:369(20):1883-91. doi: 10.1056/NEJMoa1302186. Epub     [PubMed PMID: 24224622]


[16]

Bent S, Nallamothu BK, Simel DL, Fihn SD, Saint S. Does this woman have an acute uncomplicated urinary tract infection? JAMA. 2002 May 22-29:287(20):2701-10     [PubMed PMID: 12020306]


[17]

Juthani-Mehta M, Quagliarello V, Perrelli E, Towle V, Van Ness PH, Tinetti M. Clinical features to identify urinary tract infection in nursing home residents: a cohort study. Journal of the American Geriatrics Society. 2009 Jun:57(6):963-70. doi: 10.1111/j.1532-5415.2009.02227.x. Epub     [PubMed PMID: 19490243]


[18]

Anger J, Lee U, Ackerman AL, Chou R, Chughtai B, Clemens JQ, Hickling D, Kapoor A, Kenton KS, Kaufman MR, Rondanina MA, Stapleton A, Stothers L, Chai TC. Recurrent Uncomplicated Urinary Tract Infections in Women: AUA/CUA/SUFU Guideline. The Journal of urology. 2019 Aug:202(2):282-289. doi: 10.1097/JU.0000000000000296. Epub 2019 Jul 8     [PubMed PMID: 31042112]


[19]

Nace DA,Drinka PJ,Crnich CJ, Clinical uncertainties in the approach to long term care residents with possible urinary tract infection. Journal of the American Medical Directors Association. 2014 Feb     [PubMed PMID: 24461240]


[20]

Sundvall PD, Ulleryd P, Gunnarsson RK. Urine culture doubtful in determining etiology of diffuse symptoms among elderly individuals: a cross-sectional study of 32 nursing homes. BMC family practice. 2011 May 19:12():36. doi: 10.1186/1471-2296-12-36. Epub 2011 May 19     [PubMed PMID: 21592413]

Level 2 (mid-level) evidence

[21]

Pouwels KB,Hopkins S,Llewelyn MJ,Walker AS,McNulty CA,Robotham JV, Duration of antibiotic treatment for common infections in English primary care: cross sectional analysis and comparison with guidelines. BMJ (Clinical research ed.). 2019 Feb 27     [PubMed PMID: 30814052]


[22]

Kulchavenya EV,Neymark AI,Borisenko DV,Kapsargin FP, [Acute uncomplicated cysititis: do we follow the guidelines?] Urologiia (Moscow, Russia : 1999). 2018 Dec     [PubMed PMID: 30742380]


[23]

Phamnguyen TJ,Murphy G,Hashem F, Single centre observational study on antibiotic prescribing adherence to clinical practice guidelines for treatment of uncomplicated urinary tract infection. Infection, disease & health. 2019 May     [PubMed PMID: 30598405]

Level 2 (mid-level) evidence

[24]

Bono MJ, Leslie SW, Reygaert WC, Doerr C. Uncomplicated Urinary Tract Infections (Nursing). StatPearls. 2024 Jan:():     [PubMed PMID: 33760460]


[25]

Bono MJ, Leslie SW, Reygaert WC. Uncomplicated Urinary Tract Infections. StatPearls. 2024 Jan:():     [PubMed PMID: 29261874]


[26]

Swamy S, Kupelian AS, Khasriya R, Dharmasena D, Toteva H, Dehpour T, Collins L, Rohn JL, Malone-Lee J. Cross-over data supporting long-term antibiotic treatment in patients with painful lower urinary tract symptoms, pyuria and negative urinalysis. International urogynecology journal. 2019 Mar:30(3):409-414. doi: 10.1007/s00192-018-3846-5. Epub 2018 Dec 18     [PubMed PMID: 30564872]


[27]

May M,Schostak M,Lebentrau S, Guidelines for patients with acute uncomplicated cystitis may not be a paper tiger: a call for its implementation in clinical routine. International urogynecology journal. 2019 Feb;     [PubMed PMID: 30564871]


[28]

Bellazreg F, Abid M, Lasfar NB, Hattab Z, Hachfi W, Letaief A. Diagnostic value of dipstick test in adult symptomatic urinary tract infections: results of a cross-sectional Tunisian study. The Pan African medical journal. 2019:33():131. doi: 10.11604/pamj.2019.33.131.17190. Epub 2019 Jun 21     [PubMed PMID: 31558930]

Level 2 (mid-level) evidence

[29]

Wilson ML, Gaido L. Laboratory diagnosis of urinary tract infections in adult patients. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2004 Apr 15:38(8):1150-8     [PubMed PMID: 15095222]


[30]

Lee RA, Centor RM, Humphrey LL, Jokela JA, Andrews R, Qaseem A, Scientific Medical Policy Committee of the American College of Physicians, Akl EA, Bledsoe TA, Forciea MA, Haeme R, Kansagara DL, Marcucci M, Miller MC, Obley AJ. Appropriate Use of Short-Course Antibiotics in Common Infections: Best Practice Advice From the American College of Physicians. Annals of internal medicine. 2021 Jun:174(6):822-827. doi: 10.7326/M20-7355. Epub 2021 Apr 6     [PubMed PMID: 33819054]


[31]

McKinnell JA,Stollenwerk NS,Jung CW,Miller LG, Nitrofurantoin compares favorably to recommended agents as empirical treatment of uncomplicated urinary tract infections in a decision and cost analysis. Mayo Clinic proceedings. 2011 Jun     [PubMed PMID: 21576512]


[32]

Huttner A,Verhaegh EM,Harbarth S,Muller AE,Theuretzbacher U,Mouton JW, Nitrofurantoin revisited: a systematic review and meta-analysis of controlled trials. The Journal of antimicrobial chemotherapy. 2015 Sep     [PubMed PMID: 26066581]

Level 1 (high-level) evidence

[33]

Sheele JM,Libertin CR,Fink I,Jensen T,Dasalla N,Lyon TD, Alkaline Urine in the Emergency Department Predicts Nitrofurantoin Resistance. The Journal of emergency medicine. 2022 Jan 6;     [PubMed PMID: 35000812]


[34]

Iravani A,Klimberg I,Briefer C,Munera C,Kowalsky SF,Echols RM, A trial comparing low-dose, short-course ciprofloxacin and standard 7 day therapy with co-trimoxazole or nitrofurantoin in the treatment of uncomplicated urinary tract infection. The Journal of antimicrobial chemotherapy. 1999 Mar     [PubMed PMID: 10225575]


[35]

Kavatha D,Giamarellou H,Alexiou Z,Vlachogiannis N,Pentea S,Gozadinos T,Poulakou G,Hatzipapas A,Koratzanis G, Cefpodoxime-proxetil versus trimethoprim-sulfamethoxazole for short-term therapy of uncomplicated acute cystitis in women. Antimicrobial agents and chemotherapy. 2003 Mar;     [PubMed PMID: 12604518]


[36]

Warren JW,Abrutyn E,Hebel JR,Johnson JR,Schaeffer AJ,Stamm WE, Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America (IDSA). Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 1999 Oct;     [PubMed PMID: 10589881]


[37]

Nicolle LE, Harding GK, Thomson M, Kennedy J, Urias B, Ronald AR. Efficacy of five years of continuous, low-dose trimethoprim-sulfamethoxazole prophylaxis for urinary tract infection. The Journal of infectious diseases. 1988 Jun:157(6):1239-42     [PubMed PMID: 3259613]


[38]

Stein GE, Comparison of single-dose fosfomycin and a 7-day course of nitrofurantoin in female patients with uncomplicated urinary tract infection. Clinical therapeutics. 1999 Nov     [PubMed PMID: 10890258]


[39]

Falagas ME,Vouloumanou EK,Samonis G,Vardakas KZ, Fosfomycin. Clinical microbiology reviews. 2016 Apr;     [PubMed PMID: 26960938]


[40]

Schulz GS,Schütz F,Spielmann FVJ,Uglione da Ros L,de Almeida JS,Lopes Ramos JG, iSingle Dose Antibiotic Therapy for Urinary Infections during Pregnancy: A Systematic Review and Meta-Analysis of Randomized Clinical Trials. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics. 2022 Jan 7;     [PubMed PMID: 34995367]

Level 1 (high-level) evidence

[41]

Hatlen TJ, Flor R, Nguyen MH, Lee GH, Miller LG. Oral fosfomycin use for pyelonephritis and complicated urinary tract infections: a 1 year review of outcomes and prescribing habits in a large municipal healthcare system. The Journal of antimicrobial chemotherapy. 2020 Jul 1:75(7):1993-1997. doi: 10.1093/jac/dkaa126. Epub     [PubMed PMID: 32303061]


[42]

Wald-Dickler N, Lee TC, Tangpraphaphorn S, Butler-Wu SM, Wang N, Degener T, Kan C, Phillips MC, Cho E, Canamar C, Holtom P, Spellberg B. Fosfomycin vs Ertapenem for Outpatient Treatment of Complicated Urinary Tract Infections: A Multicenter, Retrospective Cohort Study. Open forum infectious diseases. 2022 Jan:9(1):ofab620. doi: 10.1093/ofid/ofab620. Epub 2021 Dec 23     [PubMed PMID: 35036466]

Level 2 (mid-level) evidence

[43]

Graninger W. Pivmecillinam--therapy of choice for lower urinary tract infection. International journal of antimicrobial agents. 2003 Oct:22 Suppl 2():73-8     [PubMed PMID: 14527775]


[44]

Nicolle LE,Madsen KS,Debeeck GO,Blochlinger E,Borrild N,Bru JP,Mckinnon C,O'Doherty B,Spiegel W,Van Balen FA,Menday P, Three days of pivmecillinam or norfloxacin for treatment of acute uncomplicated urinary infection in women. Scandinavian journal of infectious diseases. 2002;     [PubMed PMID: 12195873]


[45]

Nace DA,Perera SK,Hanlon JT,Saracco S,Anderson G,Schweon SJ,Klein-Fedyshin M,Wessel CB,Mulligan M,Drinka PJ,Crnich CJ, The Improving Outcomes of UTI Management in Long-Term Care Project (IOU) Consensus Guidelines for the Diagnosis of Uncomplicated Cystitis in Nursing Home Residents. Journal of the American Medical Directors Association. 2018 Sep;     [PubMed PMID: 30037743]

Level 3 (low-level) evidence

[46]

Cox L,He C,Bevins J,Clemens JQ,Stoffel JT,Cameron AP, Gentamicin bladder instillations decrease symptomatic urinary tract infections in neurogenic bladder patients on intermittent catheterization. Canadian Urological Association journal = Journal de l'Association des urologues du Canada. 2017 Sep;     [PubMed PMID: 29382457]


[47]

Lala V,Leslie SW,Minter DA, Acute Cystitis StatPearls. 2022 Jan;     [PubMed PMID: 29083726]


[48]

Ziadeh T,Chebel R,Labaki C,Saliba G,Helou EE, Bladder instillation for urinary tract infection prevention in neurogenic bladder patients practicing clean intermittent catheterization: A systematic review. Urologia. 2022 May;     [PubMed PMID: 34612750]

Level 1 (high-level) evidence

[49]

Lo TS,Hammer KD,Zegarra M,Cho WC, Methenamine: a forgotten drug for preventing recurrent urinary tract infection in a multidrug resistance era. Expert review of anti-infective therapy. 2014 May;     [PubMed PMID: 24689705]


[50]

Kevorkian CG,Merritt JL,Ilstrup DM, Methenamine mandelate with acidification: an effective urinary antiseptic in patients with neurogenic bladder. Mayo Clinic proceedings. 1984 Aug;     [PubMed PMID: 6379319]


[51]

Kranjčec B,Papeš D,Altarac S, D-mannose powder for prophylaxis of recurrent urinary tract infections in women: a randomized clinical trial. World journal of urology. 2014 Feb;     [PubMed PMID: 23633128]

Level 1 (high-level) evidence

[52]

Kyriakides R,Jones P,Somani BK, Role of D-Mannose in the Prevention of Recurrent Urinary Tract Infections: Evidence from a Systematic Review of the Literature. European urology focus. 2021 Sep;     [PubMed PMID: 32972899]

Level 1 (high-level) evidence

[53]

Lenger SM,Bradley MS,Thomas DA,Bertolet MH,Lowder JL,Sutcliffe S, D-mannose vs other agents for recurrent urinary tract infection prevention in adult women: a systematic review and meta-analysis. American journal of obstetrics and gynecology. 2020 Aug;     [PubMed PMID: 32497610]

Level 1 (high-level) evidence

[54]

De Nunzio C,Bartoletti R,Tubaro A,Simonato A,Ficarra V, Role of D-Mannose in the Prevention of Recurrent Uncomplicated Cystitis: State of the Art and Future Perspectives. Antibiotics (Basel, Switzerland). 2021 Apr 1;     [PubMed PMID: 33915821]

Level 3 (low-level) evidence

[55]

Grupper M, Kravtsov A, Potasman I. Emphysematous cystitis: illustrative case report and review of the literature. Medicine. 2007 Jan:86(1):47-53. doi: 10.1097/MD.0b013e3180307c3a. Epub     [PubMed PMID: 17220755]

Level 3 (low-level) evidence

[56]

Thomas AA,Lane BR,Thomas AZ,Remer EM,Campbell SC,Shoskes DA, Emphysematous cystitis: a review of 135 cases. BJU international. 2007 Jul     [PubMed PMID: 17506870]

Level 3 (low-level) evidence

[57]

Perry C,Hossain M,Powell M,Raychaudhuri A,Scangarella-Oman N,Tiffany C,Xu S,Dumont E,Janmohamed S, Design of Two Phase III, Randomized, Multicenter Studies Comparing Gepotidacin with Nitrofurantoin for the Treatment of Uncomplicated Urinary Tract Infection in Female Participants. Infectious diseases and therapy. 2022 Dec     [PubMed PMID: 36271314]

Level 1 (high-level) evidence

[58]

Fishman C,Caverly Rae JM,Posobiec LM,Laffan SB,Lerman SA,Pearson N,Janmohamed S,Dumont E,Nunn-Floyd D,Stanislaus DJ, Novel Bacterial Topoisomerase Inhibitor Gepotidacin Demonstrates Absence of Fluoroquinolone-Like Arthropathy in Juvenile Rats. Antimicrobial agents and chemotherapy. 2022 Nov 15     [PubMed PMID: 36255258]


[59]

Tiffany C,Dumont EF,Hossain M,Srinivasan M,Swift B, Pharmacokinetics, safety, and tolerability of gepotidacin administered as single or repeat ascending doses, in healthy adults and elderly subjects. Clinical and translational science. 2022 Sep     [PubMed PMID: 35769034]


[60]

Biedenbach DJ,Bouchillon SK,Hackel M,Miller LA,Scangarella-Oman NE,Jakielaszek C,Sahm DF, In Vitro Activity of Gepotidacin, a Novel Triazaacenaphthylene Bacterial Topoisomerase Inhibitor, against a Broad Spectrum of Bacterial Pathogens. Antimicrobial agents and chemotherapy. 2016 Jan 4;     [PubMed PMID: 26729499]


[61]

Uehling DT, Hopkins WJ, Balish E, Xing Y, Heisey DM. Vaginal mucosal immunization for recurrent urinary tract infection: phase II clinical trial. The Journal of urology. 1997 Jun:157(6):2049-52     [PubMed PMID: 9146577]

Level 1 (high-level) evidence

[62]

Uehling DT, Hopkins WJ, Elkahwaji JE, Schmidt DM, Leverson GE. Phase 2 clinical trial of a vaginal mucosal vaccine for urinary tract infections. The Journal of urology. 2003 Sep:170(3):867-9     [PubMed PMID: 12913718]

Level 1 (high-level) evidence

[63]

Hopkins WJ, Elkahwaji J, Beierle LM, Leverson GE, Uehling DT. Vaginal mucosal vaccine for recurrent urinary tract infections in women: results of a phase 2 clinical trial. The Journal of urology. 2007 Apr:177(4):1349-53; quiz 1591     [PubMed PMID: 17382730]

Level 1 (high-level) evidence

[64]

Eldridge GR, Hughey H, Rosenberger L, Martin SM, Shapiro AM, D'Antonio E, Krejci KG, Shore N, Peterson J, Lukes AS, Starks CM. Safety and immunogenicity of an adjuvanted Escherichia coli adhesin vaccine in healthy women with and without histories of recurrent urinary tract infections: results from a first-in-human phase 1 study. Human vaccines & immunotherapeutics. 2021 May 4:17(5):1262-1270. doi: 10.1080/21645515.2020.1834807. Epub 2020 Dec 16     [PubMed PMID: 33325785]


[65]

Langermann S, Palaszynski S, Barnhart M, Auguste G, Pinkner JS, Burlein J, Barren P, Koenig S, Leath S, Jones CH, Hultgren SJ. Prevention of mucosal Escherichia coli infection by FimH-adhesin-based systemic vaccination. Science (New York, N.Y.). 1997 Apr 25:276(5312):607-11     [PubMed PMID: 9110982]


[66]

Forsyth VS,Himpsl SD,Smith SN,Sarkissian CA,Mike LA,Stocki JA,Sintsova A,Alteri CJ,Mobley HLT, Optimization of an Experimental Vaccine To Prevent Escherichia coli Urinary Tract Infection. mBio. 2020 Apr 28     [PubMed PMID: 32345645]


[67]

Beerepoot MA, Geerlings SE, van Haarst EP, van Charante NM, ter Riet G. Nonantibiotic prophylaxis for recurrent urinary tract infections: a systematic review and meta-analysis of randomized controlled trials. The Journal of urology. 2013 Dec:190(6):1981-9. doi: 10.1016/j.juro.2013.04.142. Epub 2013 Jul 15     [PubMed PMID: 23867306]

Level 1 (high-level) evidence

[68]

Wang Q,Sun M,Ma C,Lv H,Lu P,Wang Q,Liu G,Hu Z,Gao Y, Emphysematous pyelonephritis and cystitis in a patient with uremia and anuria: A case report and literature review. Medicine. 2018 Nov     [PubMed PMID: 30407278]

Level 3 (low-level) evidence