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Treatment of Chronic Q Fever: Clinical Efficacy and Toxicity of Antibiotic Regimens.
van Roeden, Sonja E; Bleeker-Rovers, Chantal P; de Regt, Marieke J A; Kampschreur, Linda M; Hoepelman, Andy I M; Wever, Peter C; Oosterheert, Jan Jelrik.
Afiliação
  • van Roeden SE; Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht.
  • Bleeker-Rovers CP; Department of Internal Medicine, Division of Infectious Diseases and Radboud Expert Centre for Q Fever, Radboud University Medical Center, Nijmegen.
  • de Regt MJA; Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht.
  • Kampschreur LM; Department of Internal Medicine and Infectious Diseases, Medical Centre Leeuwarden.
  • Hoepelman AIM; Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht.
  • Wever PC; Department of Medical Microbiology and Infection Control, Jeroen Bosch Hospital,'s-Hertogenbosch, the Netherlands.
  • Oosterheert JJ; Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht.
Clin Infect Dis ; 66(5): 719-726, 2018 02 10.
Article em En | MEDLINE | ID: mdl-29040457
ABSTRACT

Background:

Evidence on the effectiveness of first-line treatment for chronic Q fever, tetracyclines (TET) plus hydroxychloroquine (HCQ), and potential alternatives is scarce.

Methods:

We performed a retrospective, observational cohort study to assess efficacy of treatment with TET plus quinolones (QNL), TET plus QNL plus HCQ, QNL monotherapy, or TET monotherapy compared to TET plus HCQ in chronic Q fever patients. We used a time-dependent Cox proportional hazards model to assess our primary (all-cause mortality) and secondary outcomes (first disease-related event and therapy failure).

Results:

We assessed 322 chronic Q fever patients; 276 (86%) received antibiotics. Compared to TET plus HCQ (n = 254; 92%), treatment with TET plus QNL (n = 49; 17%), TET plus QNL plus HCQ (n = 29, 10%), QNL monotherapy (n = 93; 34%), or TET monotherapy (n = 54; 20%) were not associated with primary or secondary outcomes. QNL and TET monotherapies were frequently discontinued due to insufficient clinical response (n = 27, 29% and n = 32, 59%). TET plus HCQ, TET plus QNL, and TET plus QNL plus HCQ were most frequently discontinued due to side effects (n = 110, 43%; n = 13, 27%; and n = 12, 41%).

Conclusions:

Treatment of chronic Q fever with TET plus QNL appears to be a safe alternative for TET plus HCQ, for example, if TET plus HCQ cannot be tolerated due to side effects. Treatment with TET plus QNL plus HCQ was not superior to treatment with TET plus HCQ, although this may be caused by confounding by indication. Treatment with TET or QNL monotherapy should be avoided; switches due to subjective, insufficient clinical response were frequently observed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre Q / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre Q / Antibacterianos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2018 Tipo de documento: Article