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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : -12 مورد

Regimens for treatment of brucellosis (in absence of focal disease due to spondylitis, neurobrucellosis, or endocarditis)

Regimens for treatment of brucellosis (in absence of focal disease due to spondylitis, neurobrucellosis, or endocarditis)
  Regimen Dosing
Nonpregnant adults* Doxycycline 100 mg orally twice daily for 6 weeks
plus
Streptomycin

Weight >65 kg: 1 g IV or IM once daily for the first 14 to 21 days

Weight ≤65 kg: 15 mg/kg IV or IM once daily for the first 14 to 21 days
Doxycycline 100 mg orally twice daily for 6 weeks
plus
Gentamicin 5 mg/kg IV or IM once daily for the first 7 to 10 days
Doxycycline 100 mg orally twice daily for 6 weeks
plus
Rifampin (rifampicin) 600 to 900 mg orally once daily for 6 weeks
Children ≥8 years Doxycycline 4.4 mg/kg per day (maximum 200 mg/day) orally in 2 divided doses for 6 weeks
plus
Rifampin (rifampicin) 15 to 20 mg/kg per day (maximum 900 mg/day) orally once daily or in 2 divided doses for 6 weeks
Doxycycline 4.4 mg/kg per day (maximum 200 mg/day) orally in 2 divided doses for 6 weeks
plus
Streptomycin 15 mg/kg per day (maximum 1 g/day) IV or IM in 1 to 2 doses for the first 14 to 21 days
Doxycycline 4.4 mg/kg per day (maximum 200 mg/day) orally in 2 divided doses for 6 weeks
plus
Gentamicin 5 mg/kg IV or IM once daily for the first 7 to 10 days
Children <8 years Trimethoprim-sulfamethoxazole (TMP-SMX), cotrimoxazole 10 mg/kg (trimethoprim component) per day (maximum 320 mg/day) orally in 2 divided doses for 6 weeks
plus
Rifampin (rifampicin) 15 to 20 mg/kg per day (maximum 900 mg/day) orally once daily or in 2 divided doses for 6 weeks
Pregnant patients <36 weeks gestationΔ TMP-SMX, cotrimoxazole

1 double-strength tablet (160 mg trimethoprim/800 mg sulfamethoxazole) orally 2 daily for 6 weeks

Trimethoprim component is a folic acid antagonist; to assure adequate maternal and fetal levels, we supplement with additional folic acid (eg, 0.8 to 1 mg orally once daily) during the first trimester of pregnancy.
plus
Rifampin (rifampicin) 600 to 900 mg orally once daily for 6 weeks
This table is intended for use in conjunction with UpToDate content on treatment and prevention of brucellosis. The doses listed above are intended for patients with normal kidney function; doses of some of these agents must be adjusted in patients with kidney impairment. For specific adjustments, refer to the drug information monographs included with UpToDate.

IM: intramuscularly; IV: intravenously.

* Preferred regimens for nonpregnant adults are summarized in the table; alternative regimens are discussed in the UpToDate topic on treatment and prevention of brucellosis.

¶ In non-obese, average-weight adult patients, the initial aminoglycoside dose is based on ideal body weight. Kidney function and aminoglycoside serum concentrations should be monitored at least once per week. Dosing listed is recommended for patients with normal kidney function; the initial dose should be adjusted in patients with kidney impairment and as needed to attain target serum concentrations. For further guidance, refer to the UpToDate topic on dosing and administration of parenteral aminoglycosides and the streptomycin and gentamicin drug-specific monographs.

Δ For pregnant women ≥36 weeks gestation, we administer rifampin monotherapy until delivery, given risk of neonatal kernicterus with use of TMP-SMX in the last month of pregnancy. After delivery, we continue combination therapy as in nonpregnant adults; the total duration of treatment is 6 weeks.
Prepared with data from:
  1. American Academy of Pediatrics. Red Book: 2024-2027 Report of the Committee on Infectious Diseases, 33rd ed, Kimberlin DW, Banerjee R, Barnett ED, et al (Eds), American Academy of Pediatrics 2024.
  2. Brucellosis. World Health Organization. https://www.who.int/news-room/fact-sheets/detail/brucellosis (Accessed March 15, 2024).
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