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dc.contributor.authorEngin, A.
dc.contributor.authorOzkanli, S.
dc.contributor.authorYilmaz-Karadag, F.
dc.contributor.authorCabalak, M.
dc.contributor.authorGencer, S.
dc.contributor.authorPekok, A. Umut
dc.contributor.authorYildirim, D.
dc.contributor.authorSeyman, D.
dc.contributor.authorTeker, B.
dc.contributor.authorYilmaz, H.
dc.contributor.authorYasar, K.
dc.contributor.authorTuran, H.
dc.contributor.authorUguz, M.
dc.contributor.authorKilic, S.
dc.contributor.authorAkkoyunlu, Y.
dc.contributor.authorKaya, S.
dc.contributor.authorErdem, A.
dc.contributor.authorInan, A.
dc.contributor.authorCag, Y.
dc.contributor.authorBolukcu, S.
dc.contributor.authorUlu-Kilic, A.
dc.contributor.authorOzgunes, N.
dc.contributor.authorGorenek, L.
dc.contributor.authorBatirel, A.
dc.contributor.authorAgalar, C.
dc.contributor.authorBalkan, I. Inanc
dc.contributor.authorComoglu, S.
dc.contributor.authorErdem, H.
dc.contributor.authorOzturk-Engin, D.
dc.contributor.authorYesilyurt, M.
dc.contributor.authorKarabay, O.
dc.contributor.authorElaldi, N.
dc.contributor.authorCelebi, G.
dc.contributor.authorKorkmaz, N.
dc.contributor.authorGuven, T.
dc.contributor.authorSumer, S.
dc.contributor.authorTulek, N.
dc.contributor.authorUral, O.
dc.contributor.authorYilmaz, G.
dc.contributor.authorErdinc, S.
dc.contributor.authorNayman-Alpat, S.
dc.contributor.authorSehmen, E.
dc.contributor.authorKader, C.
dc.contributor.authorSari, N.
dc.contributor.authorCicek-Senturk, G.
dc.contributor.authorErtem-Tuncer, G.
dc.contributor.authorGulen, G.
dc.contributor.authorDuygu, F.
dc.contributor.authorOgutlu, A.
dc.contributor.authorAyaslioglu, E.
dc.contributor.authorKaradenizli, A.
dc.contributor.authorMeric, M.
dc.contributor.authorUlug, M.
dc.contributor.authorAtaman-Hatipoglu, C.
dc.contributor.authorSirmatel, F.
dc.contributor.authorCesur, S.
dc.contributor.authorKadanali, A.
dc.contributor.authorKarakas, A.
dc.contributor.authorAsan, A.
dc.contributor.authorGonen, I.
dc.contributor.authorKurtoglu-Gul, Y.
dc.contributor.authorAltin, N.
dc.date.accessioned2021-03-04T09:51:48Z
dc.date.available2021-03-04T09:51:48Z
dc.date.issued2014
dc.identifier.citationErdem H., Ozturk-Engin D., Yesilyurt M., Karabay O., Elaldi N., Celebi G., Korkmaz N., Guven T., Sumer S., Tulek N., et al., "Evaluation of tularaemia courses: a multicentre study from Turkey", CLINICAL MICROBIOLOGY AND INFECTION, cilt.20, sa.12, 2014
dc.identifier.issn1198-743X
dc.identifier.othervv_1032021
dc.identifier.otherav_6a477f67-59dd-41f7-8a66-0c1c3faa5001
dc.identifier.urihttp://hdl.handle.net/20.500.12627/73568
dc.identifier.urihttps://doi.org/10.1111/1469-0691.12741
dc.description.abstractIn this multicentre study, which is the largest case series ever reported, we aimed to describe the features of tularaemia to provide detailed information. We retrospectively included 1034 patients from 41 medical centres. Before the definite diagnosis of tularaemia, tonsillitis (n=653, 63%) and/or pharyngitis (n=146, 14%) were the most frequent preliminary diagnoses. The most frequent clinical presentations were oropharyngeal (n=832, 85.3%), glandular (n=136, 13.1%) and oculoglandular (n=105, 10.1%) forms. In 987 patients (95.5%), the lymph nodes were reported to be enlarged, most frequently at the cervical chain jugular (n=599, 58%), submandibular (n=401, 39%), and periauricular (n=55, 5%). Ultrasound imaging showed hyperechoic and hypoechoic patterns (59% and 25%, respectively). Granulomatous inflammation was the most frequent histological finding (56%). The patients were previously given antibiotics for 1176 episodes, mostly with -lactam/-lactamase inhibitors (n=793, 76%). Antituberculosis medications were provided in seven (2%) cases. The patients were given rational antibiotics for tularaemia after the start of symptoms, with a mean of 26.8 +/- 37.5days. Treatment failure was considered to have occurred in 495 patients (48%). The most frequent reasons for failure were the production of suppuration in the lymph nodes after the start of treatment (n=426, 86.1%), the formation of new lymphadenomegalies under treatment (n=146, 29.5%), and persisting complaints despite 2weeks of treatment (n=77, 15.6%). Fine-needle aspiration was performed in 521 patients (50%) as the most frequent drainage method. In conclusion, tularaemia is a long-lasting but curable disease in this part of the world. However, the treatment strategy still needs optimization.
dc.language.isoeng
dc.subjectBULAŞICI HASTALIKLAR
dc.subjectYaşam Bilimleri
dc.subjectİmmünoloji
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMikrobiyoloji
dc.titleEvaluation of tularaemia courses: a multicentre study from Turkey
dc.typeMakale
dc.relation.journalCLINICAL MICROBIOLOGY AND INFECTION
dc.contributor.departmentGulhane Military Medical Academy , ,
dc.identifier.volume20
dc.identifier.issue12
dc.contributor.firstauthorID219028


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