Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24719
Title: Efficacy and tolerability of antibiotic combinations in Neurobrucellosis: Results of the Istanbul study
Authors: Erdem, Hakan
Kılıç, Ayşegül Ulu
Kılıç, Selim
Karahocagil, Mustafa
Shehata, Ghaydaa
Tülek, Necla Eren
Yetkin, Funda
Çelen, Mustafa Kemal
Ceran, Nurgül
Gül, Hanefi Cem
Mert, Gürkan
Koruk, Suda Tekin
Dizbay, Murat
İnal, Ayşe Seza
Alpat, Saygın Nayman
Bosilkovski, Mile
İnan, Dilara
Saltoğlu, Neşe
Abdel-Baky, Laila
Adeva-Bartolome, Maria Teresa
Ceylan, Bahadır
Saçar, Suzan
Turhan, Vedat
Elaldı, Nazif
Tufan, Zeliha Koçak
Uğurlu, Kenan
Dokuzoğuz, Başak
Yılmaz, Hava
Gündeş, Sibel
Güner, Rahmet
Özgüneş, Nail
Ulçay, Asım
Ünal, Serhat
Dayan, Saim
Görenek, Levent
Karakaş, Ahmet
Tasova, Yeşim
Usluer, Gaye
Bayındır, Yaşar
Kurtaran, Behice
Sipahi, Oğuz Reşat
Leblebicioğlu, Hakan
Uludağ Üniversitesi/Tıp Fakültesi/Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Anabilim Dalı.
Yılmaz, Emel
22037135100
Keywords: Microbiology
Pharmacology & pharmacy
Nervous-system brucellosis
Bacterial-meningitis
Therapeutic features
Management
Diagnosis
Turkey
Issue Date: Mar-2012
Publisher: American Society of Microbiology
Citation: Erdem, H. vd. (2012). "Efficacy and tolerability of antibiotic combinations in Neurobrucellosis: Results of the Istanbul study". Antimicrobial Agents and Chemotherapy, 56(3), 1523-1528.
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.
URI: https://doi.org/10.1128/AAC.05974-11
https://journals.asm.org/doi/10.1128/AAC.05974-11
http://hdl.handle.net/11452/24719
ISSN: 0066-4804
1098-6596
Appears in Collections:Scopus
Web of Science

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