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Correction of thrombocytopenia caused by linezolid with scheduled sequential tedizolid use in patients with vertebral osteomyelitis by antibiotic resistant Gram-positive organisms.
Ueda, Takashi; Nakajima, Kazuhiko; Ichiki, Kaoru; Ishikawa, Kaori; Yamada, Kumiko; Tsuchida, Toshie; Otani, Naruhito; Takahashi, Yoshiko; Ishihara, Mika; Takubo, Shingo; Iijima, Kosuke; Ikeuchi, Hiroki; Uchino, Motoi; Kimura, Takeshi; Takesue, Yoshio.
Afiliación
  • Ueda T; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: taka76@hyo-med.ac.jp.
  • Nakajima K; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: nakajima@hyo-med.ac.jp.
  • Ichiki K; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: ichiki@hyo-med.ac.jp.
  • Ishikawa K; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: i-kaori@hyo-med.ac.jp.
  • Yamada K; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan; Department of Clinical Technology, Hyogo College of Medicine, Hyogo, Japan. Electronic address: yamakumi@hyo-med.ac.jp.
  • Tsuchida T; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: tsuchida@huhs.ac.jp.
  • Otani N; Department of Public Health, Hyogo College of Medicine, Nishinomiya, Nishinomiya, Hyogo, Japan. Electronic address: n-otani@hyo-med.ac.jp.
  • Takahashi Y; Department of Pharmacy, Hyogo College of Medicine Hospital, Nishinomiya, Hyogo, Japan. Electronic address: yktabu@hyo-med.ac.jp.
  • Ishihara M; Department of Pharmacy, Hyogo College of Medicine Hospital, Nishinomiya, Hyogo, Japan. Electronic address: ykkura@hyo-med.ac.jp.
  • Takubo S; Department of Pharmacy, Hyogo College of Medicine Hospital, Nishinomiya, Hyogo, Japan. Electronic address: stakubo@hyo-med.ac.jp.
  • Iijima K; Department of Clinical Technology, Hyogo College of Medicine, Hyogo, Japan. Electronic address: ko-iizima@hyo-med.ac.jp.
  • Ikeuchi H; Department of Inflammatory Bowel Disease, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: ikeuci2s@hyo-med.ac.jp.
  • Uchino M; Department of Inflammatory Bowel Disease, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan. Electronic address: uchino2s@hyo-med.ac.jp.
  • Kimura T; Department of Pharmacy, Hyogo College of Medicine Hospital, Nishinomiya, Hyogo, Japan. Electronic address: t-kimura@hyo-med.ac.jp.
  • Takesue Y; Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan; Department of Clinical Infectious Diseases, Tokoname City Hospital, Tokoname, Aichi, Japan. Electronic address: takesuey@hyo-med.ac.jp.
J Infect Chemother ; 28(7): 1023-1028, 2022 Jul.
Article en En | MEDLINE | ID: mdl-35477667
ABSTRACT

INTRODUCTION:

Because of thrombocytopenia, linezolid treatment tends to be stopped before the completion of therapy for complicated infections that require prolonged antimicrobial administration. In contrast, tedizolid shows a favorable hematologic profile. The primary end-point of this study was to evaluate the efficacy of switching treatment to tedizolid in patients who developed thrombocytopenia during linezolid therapy.

METHODS:

This retrospective study was conducted in patients with vertebral osteomyelitis (VO) caused by antibiotic-resistant Gram-positive bacteria. Treatment failure was defined as the reappearance of infection signs within 2 weeks after stopping tedizolid and discontinuation of tedizolid because of continued thrombocytopenia or other adverse effects.

RESULTS:

Eight patients with native VO (n = 3) and postoperative VO (n = 5) were included in the study. The causative organisms were MRSA in all patients except one. Platelet counts decreased from 35.2 ± 11.5 × 104/mm3 to 17.8 ± 6.2 × 104/mm3 during linezolid therapy and improved without washout period in all patients after switching to tedizolid on days 5-7 (28.6 ± 4.9 × 104/mm3, p = 0.002). Tedizolid therapy was completed and treatment failure was not observed in any patient. The duration of treatment was 20.0 ± 11.2 days for linezolid and 30.3 ± 9.5 days for tedizolid (total, 50.3 ± 10.7 days). One patient died because of underlying disease, and there was no recurrence in the remaining 7 patients (median follow-up 501 days).

CONCLUSIONS:

Switching therapy to tedizolid improved thrombocytopenia that occurred during linezolid therapy, and it enabled the completion of therapy for VO patients.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: J Infect Chemother Asunto de la revista: MICROBIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: J Infect Chemother Asunto de la revista: MICROBIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2022 Tipo del documento: Article