Author:
Erdem Hakan,Ulu-Kilic Ayşegül,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 Saygın,Bosilkovski Mile,Inan Dilara,Saltoglu Nese,Abdel-Baky Laila,Adeva-Bartolome Maria Teresa,Ceylan Bahadır,Sacar Suzan,Turhan Vedat,Yılmaz Emel,Elaldi Nazif,Kocak-Tufan Zeliha,Uğurlu Kenan,Dokuzoğuz Başak,Yılmaz 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
Abstract
ABSTRACTNo 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%] versusn= 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.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology