eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Brucellosis: Treatment & Medication

Author: Nicholas John Bennett, MBBCh, PhD, Staff Physician, Department of Pediatrics, State University of New York Upstate Medical University
Coauthor(s): Joseph Domachowske, MD, Associate Professor, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University; Walid Abuhammour, MD, FAAP, Associate Professor of Pediatrics, Michigan State University; Director of Pediatric Infectious Disease, Department of Pediatrics, Hurley Medical Center; Khaled Nashar, MD, Instructor of Clinical Internal Medicine, Section of Hospitalist Medicine, Division of General Internal Medicine, Department of Medicine, University of Pittsburgh Medical Center
Contributor Information and Disclosures

Updated: Jan 25, 2008

Treatment

See Medication.

Surgical Care

Surgical intervention may be required to drain pyogenic joint effusions or rare paraspinal abscesses. Valve replacement surgery is often recommended in addition to a prolonged course of antibiotics.

Consultations

  • Infectious disease specialist: Consult an infectious disease specialist regarding treatment in patients with brucellosis.
  • Surgeon: Consult with a surgeon, if indicated.

Medication

Antibiotics

Despite extensive studies, optimal antibiotic therapy for brucellosis remains under dispute. For acute brucellosis in adults and children older than 8 years, World Health Organization (WHO) guidelines recommend rifampin (600-900 mg) and doxycycline (200 mg) daily for a minimum of 6 weeks. Treatment in children younger than 8 years requires rifampin and cotrimoxazole.9,10 Treatment of meningoencephalitis or endocarditis requires combination therapy with rifampin, a tetracycline, and an aminoglycoside.

Table 2. Age-related Dosing of Antimicrobial Agents in Brucellosis

Open table in new window

Table
AgeAntimicrobial AgentsDose
Patients >8 yDoxycycline plus streptomycin or doxycycline plus gentamicinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 6 wk; not to exceed 200 mg/d Streptomycin: 1 g/d IM for 2 wk Gentamicin: 3-5 mg/kg/d IM/IV divided q8h for 1 wk
Alternative in patients >8 yDoxycycline plus rifampinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 6 wk; not to exceed 200 mg/d Rifampin: 15-20 mg/kg/d PO for 6 wk; not to exceed 600-900 mg/d
Patients <8 yTrimethoprim-sulfamethoxazole (TMP-SMZ) plus rifampinTMP-SMZ: 8-10 mg (based on TMP component)/kg/d for 45 d; not to exceed 2 double-strength tab/d Rifampin: 15-20 mg/kg/d PO for 45 d; not to exceed 600-900 mg/d
Patients >8 y with meningitis,* endocarditis, or osteomyelitisDoxycycline plus streptomycin or doxycycline plus gentamicinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 4-6 mo; not to exceed 200 mg/d Streptomycin: 20 mg/kg/d IM for 1-2 wk; not to exceed 1 g/d Gentamicin: 3-5 mg/kg/d IM/IV divided q8h for 1-2 mo
Patients <8 y with meningitis,* endocarditis, or osteomyelitisTMP-SMZ plus rifampinTMP-SMZ: 8-10 mg (based on TMP component)/kg/d PO divided bid for 4-6 mo Rifampin: 15-20 mg/kg/d PO for 4-6 mo; not to exceed 600-900 mg/d
AgeAntimicrobial AgentsDose
Patients >8 yDoxycycline plus streptomycin or doxycycline plus gentamicinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 6 wk; not to exceed 200 mg/d Streptomycin: 1 g/d IM for 2 wk Gentamicin: 3-5 mg/kg/d IM/IV divided q8h for 1 wk
Alternative in patients >8 yDoxycycline plus rifampinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 6 wk; not to exceed 200 mg/d Rifampin: 15-20 mg/kg/d PO for 6 wk; not to exceed 600-900 mg/d
Patients <8 yTrimethoprim-sulfamethoxazole (TMP-SMZ) plus rifampinTMP-SMZ: 8-10 mg (based on TMP component)/kg/d for 45 d; not to exceed 2 double-strength tab/d Rifampin: 15-20 mg/kg/d PO for 45 d; not to exceed 600-900 mg/d
Patients >8 y with meningitis,* endocarditis, or osteomyelitisDoxycycline plus streptomycin or doxycycline plus gentamicinDoxycycline: 2-4 mg/kg/d PO qd or divided bid for 4-6 mo; not to exceed 200 mg/d Streptomycin: 20 mg/kg/d IM for 1-2 wk; not to exceed 1 g/d Gentamicin: 3-5 mg/kg/d IM/IV divided q8h for 1-2 mo
Patients <8 y with meningitis,* endocarditis, or osteomyelitisTMP-SMZ plus rifampinTMP-SMZ: 8-10 mg (based on TMP component)/kg/d PO divided bid for 4-6 mo Rifampin: 15-20 mg/kg/d PO for 4-6 mo; not to exceed 600-900 mg/d

*The use of corticosteroids as adjunctive therapy to antibiotics may be beneficial in culture-proven meningitis.


Doxycycline (Bio-Tab, Doxy, Vibramycin)

Bacteriostatic agent that reversibly binds to the 30S and 50S bacterial ribosomes.

Adult

200 mg/d PO qd or divided bid

Pediatric

<8 years: Not recommended
>8 years: 2-4 mg/kg/d PO qd or divided bid; not to exceed 200 mg/d

Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of PO contraceptives, causing breakthrough bleeding and increased risk of pregnancy

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider testing drug serum levels in prolonged therapy; tetracycline use during tooth development (last one half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines


Trimethoprim and sulfamethoxazole (Cotrim, Septra, Bactrim)

Commonly termed cotrimoxazole. Produces a sequential blockade in folic acid synthesis. This effect is frequently synergistic and bactericidal.

Adult

160 mg (based on TMP component)/800 mg (sulfamethoxazole component) PO q12h (ie, 1 double-strength tab PO bid)

Pediatric

8-10 mg (based on TMP component)/kg/d 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

Do not use near term in pregnancy because of risk of kernicterus in newborns; discontinue at first appearance of rash or sign of adverse reaction; frequently obtain CBC counts; discontinue if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; caution in folate deficiency (eg, chronic alcoholism or patients who are elderly, are receiving anticonvulsant therapy, or have malabsorption syndrome); hemolysis may occur in G-6-PD deficiency; patients with AIDS may not tolerate or respond; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation


Rifampin (Rifadin, Rimactane)

Bacteriostatic or bacteriocidal agent, depending on concentration of the drug at the site of infection. Suppresses initiation of chain formation for RNA synthesis.

Adult

600-900 mg/d PO/IV

Pediatric

15-20 mg/kg/d PO/IV qd or divided q12h; not to exceed 600-900 mg/d

Induces microsomal enzymes, which may decrease effects of acetaminophen, PO anticoagulants, barbiturates, benzodiazepines, beta-blockers, chloramphenicol, PO contraceptives, corticosteroids, mexiletine, cyclosporine, digitoxin, disopyramide, estrogens, hydantoins, methadone, clofibrate, quinidine, dapsone, tazobactam, sulfonylureas, theophyllines, tocainide, and digoxin; blood pressure may increase with coadministration of enalapril; coadministration with isoniazid may result in higher rate of hepatotoxicity than with either agent alone (discontinue one or both agents if alterations occur in LFTs)

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

Obtain CBC counts and baseline clinical chemistry panels prior to and throughout therapy; weigh benefits against risk of further liver damage in patients with liver disease; interruption of therapy and high-dose intermittent therapy are associated with thrombocytopenia that is reversible if therapy is discontinued as soon as purpura occurs; if treatment is continued or resumed after appearance of purpura, cerebral hemorrhage or death may occur


Streptomycin

Bacteriostatic by means of inhibiting protein synthesis by binding to 30S ribosomal subunit.

Adult

1 g/d IM

Pediatric

20 mg/kg/d IM; not to exceed 1 g/d

Nephrotoxicity may be increased with aminoglycosides, cephalosporins, penicillins, amphotericin B, vancomycin, and loop diuretics; increased potential for neuromuscular blockade with concomitant administration of magnesium, curarizing agents, colimycin, or chloramphenicol

Documented hypersensitivity; non–dialysis-dependent renal insufficiency

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Ototoxicity and nephrotoxicity may occur; risk factors for ototoxicity include excessive doses, preexisting renal disease, excessive serum peak concentration, and concurrent use of loop diuretics or vancomycin; can cause reversible neuromuscular blockade when administered with anesthetic agents or neuromuscular relaxants or in patients with myasthenia gravis or infant botulism


Gentamicin (Garamycin)

Bacteriostatic by means of inhibiting protein synthesis by binding to 30S ribosomal subunit.
Dosing regimens are numerous; adjust dose based on CrCl and changes in volume of distribution. May be administered IV/IM.

Adult

1-1.5 mg/kg IV q8h

Pediatric

3-5 mg/kg/d IV divided q8h

Coadministration with other aminoglycosides, cephalosporins, penicillins, and amphotericin B may increase nephrotoxicity; aminoglycosides enhance effects of neuromuscular blocking agents, thus, prolonged respiratory depression may occur; coadministration with loop diuretics may increase auditory toxicity of aminoglycosides; possible irreversible hearing loss of varying degrees may occur (monitor regularly)

Documented hypersensitivity; non–dialysis-dependent renal insufficiency

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Narrow therapeutic index (not intended for long-term therapy); caution in renal failure (not on dialysis), myasthenia gravis, hypocalcemia, and conditions that depress neuromuscular transmission; adjust dose in renal impairment

More on Brucellosis

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

References

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  8. Young EJ, Tarry A, Genta RM, et al. Thrombocytopenic purpura associated with brucellosis: report of 2 cases and literature review. Clin Infect Dis. Oct 2000;31(4):904-9. [Medline].

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Further Reading

Keywords

brucellosis, Brucella abortus, Brucella melitensis, Brucella suis, Brucella canis, Brucella infection, zoonosis, Mediterranean fever, Malta fever, gastric remittent fever, undulant fever, sarcoidosis, endocarditis, sacroiliitis, epididymoorchitis, meningitis, papilledema, optic neuropathy, radiculopathy, stroke, intracranial hemorrhage, neurobrucellosis, hepatic abscess, splenic abscess, thyroid abscess, epidural abscess, pneumonitis, pleural empyema, uveitis, peritonitis, food-borne brucellosis, failure to thrive, chronic fatigue syndrome, hepatosplenomegaly, lymphadenopathy, arthritis, osteomyelitis

Contributor Information and Disclosures

Author

Nicholas John Bennett, MBBCh, PhD, Staff Physician, Department of Pediatrics, State University of New York Upstate Medical University
Nicholas John Bennett, MBBCh, PhD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Coauthor(s)

Joseph Domachowske, MD, Associate Professor, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University
Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa
Disclosure: Nothing to disclose.

Walid Abuhammour, MD, FAAP, Associate Professor of Pediatrics, Michigan State University; Director of Pediatric Infectious Disease, Department of Pediatrics, Hurley Medical Center
Walid Abuhammour, MD, FAAP is a member of the following medical societies: American Medical Association and Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

Khaled Nashar, MD, Instructor of Clinical Internal Medicine, Section of Hospitalist Medicine, Division of General Internal Medicine, Department of Medicine, University of Pittsburgh Medical Center
Khaled Nashar, MD is a member of the following medical societies: American College of Physicians, American Medical Association, and American Society of Hypertension
Disclosure: Nothing to disclose.

Medical Editor

Itzhak Brook, MD, MSc, Professor, Department of Pediatrics, Georgetown University School of Medicine
Itzhak Brook, MD, MSc is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians-American Society of Internal Medicine, American Federation for Clinical Research, American Medical Association, American Society for Microbiology, Armed Forces Infectious Diseases Society, Association of Military Surgeons of the US, Infectious Diseases Society of America, International Immunocompromised Host Society, International Society for Infectious Diseases, Medical Society of the District of Columbia, New York Academy of Sciences, Pediatric Infectious Diseases Society, Society for Ear, Nose and Throat Advances in Children, Society for Experimental Biology and Medicine, Society for Pediatric Research, Southern Medical Association, and Surgical Infection 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.com, Inc
Disclosure: Pfizer Inc Stock Investment from broker recommendation; Avanir Pharma Stock Investment from broker recommendation

Managing Editor

Mark R Schleiss, MD, American Legion Chair of Pediatrics, Professor of Pediatrics, Division Director, Division of Infectious Diseases and Immunology, Department of Pediatrics, University of Minnesota School of Medicine
Mark R Schleiss, MD is a member of the following medical societies: American Pediatric Society, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Society for Pediatric Research
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief 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

Chief Editor

Russell W Steele, MD, Professor and Vice Chairman, Department of Pediatrics, Head, Division of Infectious Diseases, Louisiana State University Health Sciences Center
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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