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Cefepime-induced encephalopathy in end-stage renal disease patients.
Nakagawa, Ryo; Sato, Kenichiro; Uesaka, Yoshikazu; Mitsuki, Takashi; Kondo, Kanya; Wake, Atsushi; Ubara, Yoshifumi; Kanzaki, Mami.
Affiliation
  • Nakagawa R; Department of Neurology, Toranomon Hospital, Tokyo, Japan.
  • Sato K; Department of Neurology, Toranomon Hospital, Tokyo, Japan; Okinaka Memorial Institute for Medical Research, Tokyo, Japan. Electronic address: kenisatou-tky@umin.ac.jp.
  • Uesaka Y; Department of Neurology, Toranomon Hospital, Tokyo, Japan; Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
  • Mitsuki T; Department of Hematology, Toranomon Hospital Kajigaya, Kanagawa, Japan.
  • Kondo K; Department of Hematology, Toranomon Hospital Kajigaya, Kanagawa, Japan.
  • Wake A; Department of Hematology, Toranomon Hospital Kajigaya, Kanagawa, Japan.
  • Ubara Y; Nephrology Center, Toranomon Hospital Kajigaya, Kanagawa, Japan.
  • Kanzaki M; Department of Neurology, Toranomon Hospital, Tokyo, Japan; Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
J Neurol Sci ; 376: 123-128, 2017 May 15.
Article in En | MEDLINE | ID: mdl-28431597
ABSTRACT

OBJECTIVES:

Impaired renal function is a risk factor for cefepime (CFPM)-induced encephalopathy (CFPMIE) in patients treated with CFPM; dose-titration to renal function is recommended to prevent CFPMIE. However, available evidence on the incidence of CFPMIE or preventive efficacy of dose adjustment against CFPMIE in end-stage renal disease (ESRD) patients is limited.

METHODS:

Single-centre, retrospective observational study. We reviewed consecutive in-hospital adult patients treated with adjusted-dose of CFPM in the period between September 2012 and September 2016, and assessed the CFPMIE in ESRD patients treated with adjusted-dose of CFPM.

RESULTS:

Out of 422 eligible patients, 6 patients (1.4%) were diagnosed with CFPMIE. The incidence of CFPMIE in ESRD patients was 7.5% (5/67). Among ESRD patients, pre-existing central nervous system (CNS) morbidity was significantly associated with the risk of CFPMIE. CFPMIE occurred in ESRD patients regardless of daily dose, and even with 0.5g/day of CFPM.

CONCLUSIONS:

Pre-existing CNS morbidity may be associated with an increased risk of CFPMIE in ESRD patients. No significant association was observed between CFPM dose and incidence of CFPMIE in ESRD patients, and future investigation on the safer dose-adjustment strategy in ESRD patients is required for achieving balance between successful infectious treatment and reducing CFPMIE.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Cephalosporins / Kidney Failure, Chronic / Anti-Bacterial Agents Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Sci Year: 2017 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Cephalosporins / Kidney Failure, Chronic / Anti-Bacterial Agents Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Sci Year: 2017 Document type: Article Affiliation country: Japón