Pediatric Urinary Tract Infection Medication

  • Author: Donna J Fisher, MD; Chief Editor: Russell W Steele, MD   more...
 
Updated: Feb 16, 2012
 

Medication Summary

Antibiotics are used to treat urinary tract infection (UTI) and to prevent its recurrence. Avoid nephrotoxic drugs whenever possible. On occasion, analgesic therapy may be used to provide relief because of voiding symptoms.

Start antibiotics after urinalysis and culture are obtained in patients with UTI. A 10-day course of antibiotics is recommended, even for an uncomplicated infection. Typical short-course treatments should be reserved for nontoxic-appearing adolescent females with UTI. Be aware of increasing rates of antibiotic resistance and the need to choose antibiotic therapy accordingly.

If the urinalysis is positive for nitrites, the bacterium responsible for the infection is exceedingly likely to be sensitive to a third-generation cephalosporin. However, the 8+% resistance of nitrite-positive organisms to first-generation oral cephalosporins limits their use.[36]

Empiric antibiotics should be chosen for coverage of the most common uropathogens; namely, E coli and Enterococcus, Proteus, and Klebsiella species. For suspected pyelonephritis, parenteral antibiotics are recommended.

Evidence indicates that oral antibiotics are adequate therapy for febrile UTIs in young infants and children; short-term (fever) and long-term (renal scarring) outcomes are comparable to those that occur with parenteral therapy.

The possibility of antibiotic resistance must be considered when choosing empiric therapy, especially with ampicillin. Knowledge of the local antibiotic resistance helps in guiding antibiotic choice.

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Antibiotic agents

Class Summary

Antibiotics are used to treat bacterial infections of the urinary tract. Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.

Ceftriaxone (Rocephin)

 

This agent is used for initial parenteral therapy for complicated pyelonephritis in pediatric patients beyond the neonatal period. It is indicated for urinary tract infections caused by E coli, Proteus mirabilis, Morganella morganii, P vulgaris, or K pneumoniae.

Cefotaxime (Claforan)

 

Cefotaxime is used as the initial parenteral therapy for pediatric patients with acute complicated pyelonephritis. It may be used for neonates or jaundiced patients. In infants, a 2- to 8-week regimen also includes ampicillin. A dose every 6-8 hours is required.

Ampicillin (Marcillin, Omnipen, Polycillin)

 

Ampicillin is a parenteral therapy for the initial treatment of patients with acute pyelonephritis or with gram-positive cocci in urinary sediment or when no organisms are observed. It is indicated for urinary tract infections caused by E coli and P mirabilis.

Amoxicillin and clavulanate (Augmentin)

 

This is an oral therapy for completion of initial treatment of infection with a susceptible organism. Amoxicillin inhibits bacterial cell-wall synthesis by binding to penicillin-binding proteins. The addition of clavulanate inhibits beta-lactamase producing bacteria.

This is a good alternative antibiotic for patients who are allergic or have an intolerance to the macrolide class. It is usually well tolerated and provides good coverage against most infectious agents. It is not effective against Mycoplasma and Legionella species. The half-life of the oral dosage form is 1-1.3 hours. This treatment has good tissue penetration but does not enter the cerebrospinal fluid (CSF).

For patients over age 3 months, base the dosing protocol on the amoxicillin content. Because of different amoxicillin-clavulanic acid ratios in the 250mg tablet (250-125) versus the 250mg chewable tablet (250-62.5), do not use the 250mg tablet until the child weighs over 40kg. The amoxicillin and clavulanate combination is also available as an oral suspension for children.

Gentamicin (Garamycin)

 

This is the initial parenteral therapy for patients with bacterial pyelonephritis who are allergic to cephalosporins. For complicated UTIs, it is sometimes used in combination with a cephalosporin.

Sulfamethoxazole and trimethoprim (Bactrim, Cotrim, Septra)

 

This is an oral treatment for bacterial urinary tract infection and for prevention of reinfection. It is available in oral tablet or suspension form.

Cephalexin (Biocef, Cefanex, Keflex)

 

Cephalexin is a first-generation cephalosporin. This is an oral treatment for bacterial UTI and for prevention of infection in infants younger than 6-8 weeks.

Cefixime (Suprax)

 

Cefixime is a third-generation cephalosporin. It is an oral treatment for acute bacterial urinary tract infection. By binding to 1 or more penicillin-binding proteins, it arrests bacterial cell-wall synthesis and inhibits bacterial growth.

Cefpodoxime (Vantin)

 

Cefpodoxime is a third-generation cephalosporin. It is an oral treatment for acute bacterial UTI. It is indicated for the management of infections caused by susceptible mixed aerobic-anaerobic microorganisms.

Nitrofurantoin (Furadantin, Macrobid, Macrodantin)

 

This is an oral treatment for bacterial lower UTI (cystitis) and for the prevention of reinfection. Nitrofurantoin is a synthetic nitrofuran that interferes with bacterial carbohydrate metabolism by inhibiting acetylcoenzyme A. It is bacteriostatic at low concentrations (5-10 mcg/mL) and is bactericidal at higher concentrations.

Trimethoprim (Proloprim, Trimpex)

 

Trimethoprim is an oral antibiotic used for the prevention of UTI. It is a dihydrofolate reductase inhibitor that prevents the production of tetrahydrofolic acid in bacteria. It is active in vitro against a broad range of gram-positive and gram-negative bacteria, including uropathogens; eg, Enterobacteriaceae and Staphylococcus saprophyticus.

Resistance is usually mediated by decreased cell permeability or by alterations in the structure or amount of dihydrofolate reductase. Trimethoprim demonstrates synergy with sulfonamides, potentiating inhibition of bacterial tetrahydrofolate production.

Ciprofloxacin (Cipro, Cipro XR)

 

This is a fluoroquinolone that inhibits bacterial deoxyribonucleic acid (DNA) synthesis and, consequently, growth by inhibiting DNA gyrase and topoisomerases, which are required for replication, transcription, and translation of genetic material. Quinolones have broad activity against gram-positive and gram-negative aerobic organisms. Ciprofloxacin has no activity against anaerobes. Continue treatment for at least 2 days (7-14d typical) after signs and symptoms have disappeared.

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Analgesics

Class Summary

These agents are used to provide relief from voiding symptoms due to urinary tract infection.

Acetaminophen (Tylenol, Panadol, Tempra)

 

Acetaminophen is a nonopioid, systemic analgesic used for moderate voiding discomfort caused by urinary tract infection.

Ibuprofen (Motrin, Advil)

 

Ibuprofen is a nonsteroidal anti-inflammatory agent that is used to provide symptomatic relief of dysuria.

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Urinary bladder analgesics

Class Summary

These agents are used to relieve burning, spasticity, and pain during voiding due to urinary tract infection.

Phenazopyridine (Azo-Standard, Pyridium, Urodine)

 

Phenazopyridine exerts local, topical anesthetic or analgesic action on urinary mucosa. It is used for symptomatic relief of pain, burning, urgency, frequency, and other discomforts arising from irritation of the lower urinary tract mucosa caused by infection, trauma, surgery, endoscopic procedures, passage of sound, or catheters. Analgesic action may reduce or eliminate the need for systemic analgesics.

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Contributor Information and Disclosures
Author

Donna J Fisher, MD  Assistant Professor of Pediatrics, Tufts University School of Medicine; Interim Chief, Division of Pediatric Infectious Diseases, Baystate Children's Hospital

Donna J Fisher, MD is a member of the following medical societies: American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Society for Healthcare Epidemiology of America

Disclosure: Nothing to disclose.

Chief Editor

Russell W Steele, MD  Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine

Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association

Disclosure: Nothing to disclose.

Additional Contributors

Leslie L Barton, MD Professor Emerita of Pediatrics, University of Arizona College of Medicine

Leslie L Barton, MD is a member of the following medical societies: American Academy of Pediatrics, Association of Pediatric Program Directors, Infectious Diseases Society of America, and Pediatric Infectious Diseases Society

Disclosure: Nothing to disclose.

Ann G Egland, MD Consulting Staff, Department of Operational and Emergency Medicine, Walter Reed Army Medical Center

Ann G Egland, MD is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Association of Military Surgeons of the US, Medical Society of Virginia, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Terrance K Egland, MD Director, Business Planning and Development, Bureau of Medicine and Surgery

Disclosure: Nothing to disclose.

Stanley Hellerstein, MD (Retired) Pediatric Nephrologist, Children's Mercy Hospital of Kansas City; (Retired) Ernest L Glasscock, MD Chair in Pediatric Research, Professor of Pediatrics, University of Missouri School of Medicine at Kansas City

Disclosure: Nothing to disclose.

David S Howes, MD Professor of Medicine and Pediatrics, Section Chief and Emergency Medicine Residency Program Director, University of Chicago Division of the Biological Sciences, The Pritzker School of Medicine

David S Howes, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Physicians-American Society of Internal Medicine, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Stephen L Thornton, MD Assistant Professor of Emergency Medicine, University of Kansas Hospital

Stephen L Thornton, MD is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Grace M Young, MD Associate Professor, Department of Pediatrics, University of Maryland Medical Center

Grace M Young, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Emergency Physicians

Disclosure: Nothing to disclose.

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Application of low-risk criteria and approach for the febrile infant. A reasonable approach for treating febrile infants younger than 3 months who have a temperature of greater than 38°C.
Table 1. Urinalysis for Presumptive Diagnosis of Urinary Tract Infection*
Method Findings
Bright-field or phase-contrast microscopy of centrifuged urinary sedimentBacteria
Gram stain of uncentrifuged or centrifuged urinary sedimentBacteria
Nitrite and leukocyte esterase testPositive = UTI likely
Nitrite testPositive = UTI probable
Leukocyte esterase testPositive = Nonspecific
*Negative microscopic findings for bacteria do not rule out a UTI, nor do negative results of dipstick testing for nitrite and leukocyte esterase.
Table 2. Quantitative Urine Culture for the Diagnosis of Urinary Tract Infection*
Method Finding
Suprapubic aspirationIf a UTI is present, bacteria are likely to be proliferating in bladder urine, with growth of any organism except 2000-3000 CFU/mL coagulase-negative staphylococci.
Catheterization in a girl or midstream, clean-void collection in a circumcised boyFebrile infants and children with UTI usually have >50,000 CFU/mL of a single urinary pathogen; however, UTI may be present with 10,000-50,000 CFU/mL of a single organism.*
Midstream, clean-void collection in a girl or uncircumcised boyUTI is indicated when >100,000 CFU/mL of a single urinary pathogen is present in a symptomatic patient. Pyuria usually present. A UTI may be present with 10,000-50,000 CFU/mL of a single bacterium.*
Any method in a girl or boyIf the patient is asymptomatic, bacterial growth is usually >100,000 CFU/mL of the same organism on different days. If pyuria is absent, this result probably indicates colonization rather than infection.
*Patients with urinary frequency (ie, decreased bladder incubation time) are those most likely to have bacteria proliferating in the urinary bladder in the presence of low colony counts.
Table 3. Antibiotic Agents for Parenteral Treatment of a Urinary Tract Infection
Drug Dosage and Route Comment
Ceftriaxone50-75 mg/kg/day IV/IM as a single dose or divided q12hDo not use in infants < 6wk of age; parenteral antibiotic with long half-life; may displace bilirubin from albumin
Cefotaxime150 mg/kg/day IV/IM divided q6-8hSafe to use in infants < 6wk of age; used with ampicillin in infants aged 2-8wk
Ampicillin100 mg/kg/day IV/IM divided q8hUsed with gentamicin in neonates < 2wk of age; for enterococci and patients allergic to cephalosporins
GentamicinTerm neonates < 7 days: 3.5-5 mg/kg/dose IV q24h



Infants and children < 5y: 2.5 mg/kg/dose IV q8h or single daily dosing with normal renal function of 5-7.5 mg/kg/dose IV q24h



Children =5y: 2-2.5 mg/kg/dose IV q8h or single daily dosing with normal renal function of 5-7.5 mg/kg/dose IV q24h



Monitor blood levels and kidney function if therapy extends >48 h
Note: IM = intramuscular; IV = intravenous; q = every.
Table 4. Antibiotic Agents for the Oral Treatment of Urinary Tract Infection
Antibacterial Agent Daily Dosage
Sulfisoxazole120-150 mg/kg divided q4-6h
Sulfamethoxazole and trimethoprim6-12 mg/kg TMP, 30-60 mg/kg SMZ divided q12h
Amoxicillin and clavulanic acid20-40 mg/kg divided q8h
Cephalexin20-50 mg/kg divided q6h
Cefixime8 mg/kg divided q12-24h
Cefpodoxime10 mg/kg divided q12h
Nitrofurantoin*5-7 mg/kg divided q6h
*Nitrofurantoin may be used to treat lower UTIs. However, because of its limited tissue penetration, nitrofurantoin is not suitable for the treatment of kidney infection.
Table 5. Antibiotic Agents to Prevent Reinfection
Agent Single Daily Dose
Nitrofurantoin*1-2 mg/kg PO
Sulfamethoxazole and trimethoprim*1-2 mg/kg TMP, 5-10 mg/kg SMZ PO
Trimethoprim1-2 mg/kg PO
*Do not use nitrofurantoin or sulfa drugs in infants younger than 6 weeks. Reduced doses of an oral, first-generation cephalosporin, such as cephalexin at 10 mg/kg, may be used until the child reaches age 6 weeks. Ampicillin or amoxicillin are not recommended, because of the high incidence of resistant E coli.
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