eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Salmonella Infection: Treatment & Medication

Author: Archana Chatterjee, MD, PhD, Professor of Pediatrics, Medical Microbiology and Immunology, and Pharmacy, Division of Pediatric Infectious Diseases, Chief of Division of Pediatric Infectious Diseases, Creighton University School of Medicine; Hospital Epidemiologist and Medical Director of Infection Control, Children's Hospital
Coauthor(s): Catherine O'Keefe, DNP, APRN, Assistant Professor of Nursing, Pediatric Nurse Practitioner, Pediatric Infectious Diseases, Creighton University School of Nursing; Meera Varman, MD, Assistant Professor, Department of Pediatrics, Section of Pediatric Infectious Diseases, Creighton University School of Medicine
Contributor Information and Disclosures

Updated: Jan 9, 2009

Treatment

Medical Care

  • Salmonella gastroenteritis
    • For uncomplicated gastroenteritis caused by nontyphoidal Salmonella species, antimicrobial therapy is not indicated because it does not shorten the duration of illness and may prolong the duration of fecal excretion.
    • Treatment involves monitoring hydration status and intravenous (IV) therapy to correct electrolyte imbalance or restore intravascular volume.
    • Antidiarrheal agents may actually prolong GI transit time and the illness.
    • Antimicrobial agents and hospital admission may be recommended in Salmonella gastroenteritis in infants younger than 3 months, infants younger than 12 months with temperatures of more than 39°C and unknown blood culture results, and patients with hemoglobinopathies, human immunodeficiency virus (HIV) infection or other causes of immunosuppression, neoplasms, or chronic GI illnesses.
    • The recommended antibiotics for individuals at high risk for invasive disease include ampicillin, amoxicillin, and trimethoprim-sulfamethoxazole (TMP-SMZ). In areas with multidrug resistance, cefotaxime or ceftriaxone are recommended.
  • Treatment of invasive Salmonella disease (bacteremia, extraintestinal manifestations)
    • Empiric antimicrobial therapy should include a broad-spectrum cephalosporin (cefotaxime or ceftriaxone). Once susceptibilities are available, narrow-spectrum therapy includes ampicillin, amoxicillin, cefotaxime, ceftriaxone, chloramphenicol, TMP-SMZ, or a fluoroquinolone.
    • A 14-day course of antibiotics is recommended for patients with bacteremia.
    • Patients with localized infection, such as osteomyelitis or an abscess, or patients with bacteremia and HIV infections should receive 4-6 weeks of therapy.
    • For Salmonella meningitis, ceftriaxone or cefotaxime is recommended for 4 weeks or longer.
  • Enteric fever caused by S typhi infection
    • For S typhi infection, initial empiric therapy with ceftriaxone is recommended due to widespread resistance. If susceptible, chloramphenicol, ampicillin, or TMP-SMZ may be used. Duration of therapy should be 14 days.   
    • In severe infection, parenteral therapy is indicated.
    • Use antipyretics with caution or not at all because they may cause precipitous drops in temperature and shock. Fever may last 5-7 days, even with appropriate therapy. 
    • Relapse is common (£ 15%), and patients must be re-treated.
    • A short course of high dose-corticosteroids may be involved in treatment of patients with life-threatening neurologic complications of enteric fever.
    • High-dose ampicillin or high-dose amoxicillin plus probenecid for 4-6 weeks has cured many chronic carriers. Ciprofloxacin is the drug of choice for adult carriers.1
  • Multidrug resistance
    • As many as 40% of nontyphoidal Salmonella (NTS) isolates in the United States are multidrug resistant, with increasing resistance to all Salmonella strains worldwide.3 In particular parts of the world (ie, India, Pakistan, Egypt), multiply antibiotic-resistant strains of S typhi are reported. Travelers from these regions should be treated with a 7-day to 10-day course of ceftriaxone or 5-day to 7-day course of ciprofloxacin or ofloxacin.
    • Decreased ciprofloxacin susceptibility and ceftriaxone resistance has been reported in developing countries.17,18,19

Surgical Care

  • Cholecystectomy may be curative in carriers with chronic gallbladder disease.
  • Focal abscesses may require drainage.3

Consultations

  • Consider consultation with a pediatric infectious disease specialist if the appropriate antibiotic for treatment or the length of treatment are questioned in patients with documented Salmonella infection.
  • Consider surgical consultation for patients with enteric fever who appear to have complications such as intestinal perforation, splenic rupture, or pancreatitis.

Diet

  • Restrict initial oral intake to electrolyte solutions, such as Pedialyte or clear liquids.
  • Add solid foods only when the diarrhea appears to be improving and dehydration is not present.
  • Initially, children can be started on a BRAT diet (ie, bananas, rice, applesauce, toast) and then slowly advanced to a regular diet as tolerated.

Medication

In most simple gastroenteritis, antibiotics are not necessary and, in fact, can prolong the duration of illness.

Antibiotics

Patients who are susceptible to invasive disease, those with invasive Salmonella, and those with enteric fever require treatment with antimicrobials.


Amoxicillin (Amoxil, Polymox, Trimox)

Interferes with cell wall synthesis. High-dose amoxicillin can be used if treatment with parenteral therapy not necessary.

Adult

4-6 g/d PO divided tid

Pediatric

100 mg/kg/d PO divided q6h

Coadministration with allopurinol may increase risk of rash

Pregnancy

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

Precautions

Adjust dose in patients with known renal failure


Ampicillin (Marcillin, Omnipen, Polycillin, Principen)

Demonstrated effectiveness in treatment of gastroenteritis, invasive disease, and enteric fever.

Adult

500-3000 mg IV q4-6h; not to exceed 12 g/d

Pediatric

200-300 mg/kg/d IV divided q6h; not to exceed 12 g/d

Coadministration with allopurinol may increase risk of rash

Pregnancy

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

Precautions

Adjust dose in renal failure; breastfeeding infants may have bowel flora modification, allergic response, and interference of culture results for fever workup


Ceftriaxone (Rocephin)

Third-generation cephalosporin with broad gram-negative coverage and CNS penetration. Ceftriaxone or cefotaxime is considered DOC for Salmonella meningitis.

Adult

1-4 g/d IV/IM divided q12-24h

Pediatric

Meningitis: 100 mg/kg/d IV divided q12-24h; not to exceed 4 g/24h
Nonmeningitic dosage: 50-75 mg/kg/d IV divided q12-24h

Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, or aminoglycosides may increase nephrotoxicity

Pregnancy

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

Precautions

Caution with penicillin-allergic patients secondary to cross-reactivity with penicillins; caution with renal impairment; may cause reversible cholelithiasis, sludging in gallbladder, and jaundice; use with caution in neonates and continuous dosing because of risk of hyperbilirubinemia


Cefotaxime (Claforan)

Third-generation cephalosporin. Cefotaxime or ceftriaxone considered DOC for treatment of Salmonella meningitis.

Adult

1-2 g/dose IV q6-8h

Pediatric

Meningitis: 200 mg/kg/d IV divided q6h
Nonmeningitic dosage: 100-200 mg/kg/d IV divided q6-8h

Probenecid may increase cefotaxime levels; coadministration with furosemide or aminoglycosides may increase nephrotoxicity

Pregnancy

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

Precautions

Caution with hypersensitivity to penicillin; adjust dosage in patients with renal impairment; may cause neutropenia, thrombocytopenia, eosinophilia, positive Coombs test, and elevated BUN, creatinine, and liver enzymes


Chloramphenicol (Chloromycetin)

Considered by many to be DOC for treatment of enteric fever. PO chloramphenicol no longer available in United States.

Adult

50-100 mg/kg/d IV divided q6h; not to exceed 4 g/24h

Pediatric

<2 weeks: 25 mg/kg/d IV divided q6h
>2 weeks: 50-100 mg/kg/d IV divided q6h; not to exceed 4 g/24h

Concomitant use of phenobarbital and rifampin may lower serum levels; phenytoin may increase serum levels; may increase phenytoin levels, reduce metabolism of oral anticoagulants, and decrease absorption of vitamin B-12

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

Caution in G-6-PD deficiency, renal and hepatic dysfunction, and neonates; monitoring of serum levels in neonates and infants is essential; may cause idiosyncratic marrow suppression known as gray baby syndrome


Trimethoprim-sulfamethoxazole (TMP-SMZ, Septra, Bactrim)

Sulfonamide derivative. Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid.

Adult

160 mg/dose PO bid (based on TMP component)

Pediatric

<2 months: Contraindicated
>2 months: 8-10 mg/kg/d PO divided bid (based on TMP component)

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 thrombocytopenic purpura in elderly patients; 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; age <2 mo

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

May cause kernicterus in newborns; may cause blood dyscrasias, crystalluria, glossitis, renal or hepatic injury, GI irritation, or Stevens-Johnson syndrome; may cause hemolysis in patients with G-6-PD deficiency; should not be used at term in pregnancy; reduce dose in renal impairment


Ciprofloxacin (Cipro)

Quinolone antibiotic considered DOC for adult chronic carriers with S typhi infection.

Adult

500 mg PO bid for 14 d

Pediatric

20-30 mg/kg/d PO divided q12h; must be used with caution in patients <18 y; benefits of treatment with drug must outweigh risks

Antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after taking fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; ciprofloxacin reduces therapeutic effects of phenytoin; probenecid may increase ciprofloxacin serum concentrations
May increase toxicity of theophylline, caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT)

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

Has caused arthropathy in immature animals; adjust dose in patients with renal failure

Glucocorticoids

Glucocorticoids have been demonstrated to have some benefit in patients with severe neurologic complications of enteric fever.


Dexamethasone (Decadron)

Demonstrated some potential benefits in patients with obtundation, shock, stupor, or coma from enteric fever.

Adult

3 mg/kg IV for 1 dose, followed by 1 mg/kg IV q6h for total duration of 48h

Pediatric

Administer as in adults

Barbiturates, carbamazepine, phenytoin, rifampin, and INH may reduce effects; estrogens may enhance effects

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

Adverse effects may include mood changes, seizures, hyperglycemia, diarrhea, GI bleeding, Cushingoid effect, and cataracts with prolonged use; must taper drug and monitor for adrenal axis suppression

More on Salmonella Infection

Overview: Salmonella Infection
Differential Diagnoses & Workup: Salmonella Infection
Treatment & Medication: Salmonella Infection
Follow-up: Salmonella Infection
References

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Further Reading

Keywords

Salmonella infection, bacterial gastroenteritis, infectious colitis, Salmonella typhi, S typhi, enteric fever, typhoid fever, Salmonella enteritidis, S enteritidis, nontyphoidal Salmonella, NTS, bacteremia, meningitis, food-borne gastroenteritis, osteomyelitis, cell disease, AIDS, neoplasms, appendicitis, hepatosplenomegaly, bradycardia

Contributor Information and Disclosures

Author

Archana Chatterjee, MD, PhD, Professor of Pediatrics, Medical Microbiology and Immunology, and Pharmacy, Division of Pediatric Infectious Diseases, Chief of Division of Pediatric Infectious Diseases, Creighton University School of Medicine; Hospital Epidemiologist and Medical Director of Infection Control, Children's Hospital
Archana Chatterjee, MD, PhD is a member of the following medical societies: American Academy of Pediatrics, American Society for Microbiology, International Society for Infectious Diseases, Pediatric Infectious Diseases Society, and Society for Pediatric Research
Disclosure: GlaxosmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Sanofi-Pasteur Honoraria Speaking and teaching; Wyeth Honoraria Speaking and teaching; GlaxoSmithKline Grant/research funds Other; MedImmune  Other; Merck Grant/research funds Other; Novartis Grant/research funds Other; Sanofi-Pasteur Grant/research funds Other

Coauthor(s)

Catherine O'Keefe, DNP, APRN, Assistant Professor of Nursing, Pediatric Nurse Practitioner, Pediatric Infectious Diseases, Creighton University School of Nursing
Catherine O'Keefe, DNP, APRN is a member of the following medical societies: American Academy of Nurse Practitioners, National Association of Pediatric Nurse Practitioners, and Nebraska Nurse Practitioners
Disclosure: Nothing to disclose.

Meera Varman, MD, Assistant Professor, Department of Pediatrics, Section of Pediatric Infectious Diseases, Creighton University School of Medicine
Meera Varman, MD is a member of the following medical societies: American Academy of Pediatrics, Infectious Diseases Society of America, and Pediatric Infectious Diseases Society
Disclosure: phamaceutical companies Honoraria Speaking and teaching; phamaceutical companies Grant/research funds clinical trials

Medical Editor

José Rafael Romero, MD, Director of Pediatric Infectious Diseases Fellowship Program, Associate Professor, Department of Pediatrics, Combined Division of Pediatric Infectious Diseases, Creighton University/University of Nebraska Medical Center
José Rafael Romero, MD is a member of the following medical societies: American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, New York Academy of Sciences, and Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Larry I Lutwick, MD, Professor of Medicine, State University of New York, Downstate Medical School; Director, Infectious Diseases, Veterans Affairs New York Harbor Health Care System, Brooklyn Campus
Larry I Lutwick, MD is a member of the following medical societies: American College of Physicians and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Consulting; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Novartis Honoraria Speaking and teaching; sanofi pasteur Grant/research funds Unrestricted research grant; sanofi pasteur  Consulting; sanofi pasteur Honoraria Speaking and teaching; Tap Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching

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: None None None

 
 
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