eMedicine Specialties > Nephrology > Tubulointerstitial Diseases of the Kidney

Pyelonephritis, Chronic: Treatment & Medication

Author: Anupama Gowda, MBBS, MD, Consulting Staff, Atlanta Nephrology Associates, PC
Coauthor(s): Chike Magnus Nzerue, MD, Associate Dean for Clinical Affairs, Meharry Medical College
Contributor Information and Disclosures

Updated: Sep 15, 2008

Treatment

Medical Care

  • Stages I and II VUR
    • This is reflux of urine to the ureter or renal pelvis without ureteral dilatation.
    • Medical therapy with antibiotics, such as amoxicillin, trimethoprim/sulfamethoxazole (Bactrim), trimethoprim alone, or nitrofurantoin, is usually sufficient.
    • Continue antibiotic therapy until puberty or until reflux resolves.
    • The rule in these cases is spontaneous resolution; surgery is not indicated.
  • Stages III and IV VUR (severe reflux)
    • Data from the Birmingham Reflux Study (international reflux study in children) show that medical and surgical therapies for reflux are equally effective.
    • Surgery for severe reflux involves reimplantation of the ureters.
    • The indications for surgery include the following: (1) medical noncompliance with formation of new scars, and (2) reflux persisting after puberty in women (should be surgically treated to prevent possible complications, eg, pyelonephritis, abortions in pregnancy).

Surgical Care

  • The following are indications for surgical therapy:
    • Failure to comply with medical regimen
    • Breakthrough infections occurring in patients who are compliant
    • Women of childbearing age who prefer surgical therapy
  • Surgery entails the reimplantation of the ureters with the creation of an adequate submucosal tunnel and detrusor support.

Diet

  • Progressive renal injury can be reduced by restricting dietary protein intake.

Medication

The penicillins (amoxicillin) and first-generation cephalosporins are the drugs of choice because of good activity against gram-negative rods and good oral bioavailability. In infants, the choice of antibiotics is either amoxicillin or a first-generation cephalosporin. In patients aged 3-6 months, therapy can be changed to sulfamethoxazole or nitrofurantoin. Older children and adults may be treated with trimethoprim-sulfamethoxazole (Bactrim). Once one antibiotic is chosen, frequent changes in the antibiotic regimen are discouraged to help prevent the development of resistance.

Antibiotics

Therapy must be comprehensive and cover all likely pathogens in the context of this clinical setting.


Amoxicillin (Amoxil)

Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria.

Adult

500 mg PO q8h

Pediatric

125 mg PO q8h

Reduces efficacy of oral contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment; may enhance chance of candidiasis


Cephalexin (Keflex)

First-generation cephalosporin arrests bacterial growth by inhibiting bacterial cell wall synthesis. Bactericidal activity against rapidly growing organisms.

Adult

500 mg PO qid

Pediatric

25-50 mg/kg/d PO divided qid; not to exceed 4 g/d

Coadministration with aminoglycosides increase nephrotoxic potential

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment


Trimethoprim and sulfamethoxazole (Bactrim DS, Septra DS)

Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid. Antibacterial activity includes common urinary tract pathogens, except Pseudomonas aeruginosa.

Adult

1 DS tab (TMP 160 mg/SMZ 800 mg) PO bid

Pediatric

8-12 mg/kg/d (TMP component) PO divided bid

May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly persons; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine

Documented hypersensitivity; megaloblastic anemia due to folate deficiency

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBC counts frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; prolonged IV infusions or high doses may cause bone marrow depression (if signs occur, administer 5-15 mg/d of leucovorin)
Caution in folate deficiency (eg, chronic alcoholism, elderly, anticonvulsant therapy, malabsorption syndrome); hemolysis may occur in G-6-PD deficiency; patients with AIDS may not tolerate or respond to TMP/SMZ; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation


Nitrofurantoin (Furadantin, Macrodantin)

Synthetic nitrofuran that interferes with bacterial carbohydrate metabolism by inhibiting acetylcoenzyme A. Bacteriostatic at low concentrations (5-10 mcg/mL) and bactericidal at higher concentrations.

Adult

50-100 mg PO hs

Pediatric

Not established

Anticholinergics may delay gastric emptying and increase absorption, increasing nitrofurantoin bioavailability; antacids made of magnesium salts may decrease effects, decreasing absorption; high doses of concurrent probenecid decrease renal clearance and increase toxicity

Documented hypersensitivity; renal insufficiency

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

May cause severe and irreversible peripheral neuropathy that can be fatal; renal impairment, diabetes, electrolyte imbalance, anemia, and vitamin B deficiency increase risk for adverse effects; prolonged use may result in fungal or bacterial overgrowth of resistant or nonsusceptible organisms

More on Pyelonephritis, Chronic

Overview: Pyelonephritis, Chronic
Differential Diagnoses & Workup: Pyelonephritis, Chronic
Treatment & Medication: Pyelonephritis, Chronic
Follow-up: Pyelonephritis, Chronic
References

References

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Further Reading

Keywords

chronic pyelonephritis, reflux nephropathy, kidney disease, renal injury, renal disease, kidney infection, renal infection, urinary tract obstruction, struvite calculi, renal dysplasia, vesicoureteral reflux, VUR, UTI, urinary tract infection, renal scar, renal scarring, flaccid bladder, end-stage renal disease, ESRD, end-stage kidney disease, intrarenal reflux, intra-renal reflux, progressive renal scarring, proteinuria, hypertension, focal glomerulosclerosis, FGS, xanthogranulomatous pyelonephritis, XPN, failure to thrive, Proteus, Escherichia coli, E coli, azotemia

Contributor Information and Disclosures

Author

Anupama Gowda, MBBS, MD, Consulting Staff, Atlanta Nephrology Associates, PC
Disclosure: Nothing to disclose.

Coauthor(s)

Chike Magnus Nzerue, MD, Associate Dean for Clinical Affairs, Meharry Medical College
Chike Magnus Nzerue, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American College of Physicians-American Society of Internal Medicine, American Society of Nephrology, and National Kidney Foundation
Disclosure: Nothing to disclose.

Medical Editor

Richard A Santucci, MD, FACS, Chief of Urology, Detroit Receiving Hospital; Specialist-in-Chief of Urology, Detroit Medical Center; Chief of Urologic Trauma Surgery, Sinai Grace Hospital; Director, The Center for Urologic Reconstruction; Clinical Professor of Urology, Michigan State College of Medicine
Richard A Santucci, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, and Société Internationale d'Urologie (International Society of Urology)
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

CME Editor

Rebecca J Schmidt, DO, FACP, FASN, Professor of Medicine, Section Chief, Department of Medicine, Section of Nephrology, West Virginia University School of Medicine
Rebecca J Schmidt, DO, FACP, FASN is a member of the following medical societies: American College of Osteopathic Internists, American College of Physicians, American Medical Association, American Society of Nephrology, International Society of Nephrology, National Kidney Foundation, Renal Physicians Association, and West Virginia State Medical Association
Disclosure: Abbott Grant/research funds Speaking and teaching; Genzyme Honoraria Consulting; Roche Honoraria Consulting

Chief Editor

Vecihi Batuman, MD, FACP, FASN, Professor of Medicine, Section of Nephrology-Hypertension, Tulane University School of Medicine; Chief, Medicine Service, Southeast Louisiana Veterans Health Care System
Vecihi Batuman, MD, FACP, FASN is a member of the following medical societies: American College of Physicians, American Society of Hypertension, American Society of Nephrology, and International Society of Nephrology
Disclosure: Nothing to disclose.

 
 
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