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  4. Efficacy and tolerability of antibiotic combinations in neurobrucellosis: results of the Istanbul study
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Efficacy and tolerability of antibiotic combinations in neurobrucellosis: results of the Istanbul study

Journal
Antimicrobial agents and chemotherapy
Date Issued
2012-03
Author(s)
Erdem, Hakan
Ulu-Kilic, Aysegül
Kilic, Selim
Karahocagil, Mustafa
Shehata, Ghaydaa
Eren-Tulek, Necla
Yetkin, Funda
Celen, Mustafa Kemal
Ceran, Nurgul
Gul, Hanefi Cem
Mert, Gurkan
Tekin-Koruk, Suda
Dizbay, Murat
Inal, Ayse Seza
Nayman-Alpat, Saygin
Inan, Dilara
Saltoglu, Nese
Abdel-Baky, Laila
Adeva-Bartolome, Maria Teresa
Ceylan, Bahadir
Sacar, Suzan
Turhan, Vedat
Yilmaz, Emel
Elaldi, Nazif
Kocak-Tufan, Zeliha
Ugurlu, Kenan
Dokuzoguz, Basak
Yilmaz, Hava
Gundes, Sibel
Guner, Rahmet
Ozgunes, Nail
Ulcay, Asim
Unal, Serhat
Dayan, Saim
Gorenek, Levent
Karakas, Ahmet
Tasova, Yesim
Usluer, Gaye
Bayindir, Yasar
Kurtaran, Behice
Sipahi, Oguz Resat
Leblebicioglu, Hakan
DOI
10.1128/AAC.05974-11
Abstract
No data on whether brucellar meningitis or meningoencephalitis can be treated with oral antibiotics or whether an intravenous extended-spectrum cephalosporin, namely, ceftriaxone, which does not accumulate in phagocytes, should be added to the regimen exist in the literature. The aim of a study conducted in Istanbul, Turkey, was to compare the efficacy and tolerability of ceftriaxone-based antibiotic treatment regimens with those of an oral treatment protocol in patients with these conditions. This retrospective study enrolled 215 adult patients in 28 health care institutions from four different countries. The first protocol (P1) comprised ceftriaxone, rifampin, and doxycycline. The second protocol (P2) consisted of trimethoprim-sulfamethoxazole, rifampin, and doxycycline. In the third protocol (P3), the patients started with P1 and transferred to P2 when ceftriaxone was stopped. The treatment period was shorter with the regimens which included ceftriaxone (4.40 ± 2.47 months in P1, 6.52 ± 4.15 months in P2, and 5.18 ± 2.27 months in P3) (P = 0.002). In seven patients, therapy was modified due to antibiotic side effects. When these cases were excluded, therapeutic failure did not differ significantly between ceftriaxone-based regimens (n = 5/166, 3.0%) and the oral therapy (n = 4/42, 9.5%) (P = 0.084). The efficacy of the ceftriaxone-based regimens was found to be better (n = 6/166 [3.6%] versus n = 6/42 [14.3%]; P = 0.017) when a composite negative outcome (CNO; relapse plus therapeutic failure) was considered. Accordingly, CNO was greatest in P2 (14.3%, n = 6/42) compared to P1 (2.6%, n = 3/117) and P3 (6.1%, n = 3/49) (P = 0.020). Seemingly, ceftriaxone-based regimens are more successful and require shorter therapy than the oral treatment protocol.
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