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Clinical impact of a change in antibiotics or the addition of glycopeptide antibiotics for persistent febrile neutropenia after autologous stem cell transplantation.
Yoshino, Nozomu; Kimura, Shun-Ichi; Kawamura, Koji; Nakata, Yuya; Matsuoka, Akari; Ishikawa, Takuto; Meno, Tomohiro; Nakamura, Yuhei; Kawamura, Masakatsu; Kawamura, Shunto; Takeshita, Junko; Misaki, Yukiko; Yoshimura, Kazuki; Gomyo, Ayumi; Okada, Yosuke; Tamaki, Masaharu; Kusuda, Machiko; Kameda, Kazuaki; Akahoshi, Yu; Sato, Miki; Tanihara, Aki; Nakasone, Hideki; Kako, Shinichi; Kanda, Yoshinobu.
Affiliation
  • Yoshino N; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kimura SI; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kawamura K; Division of Clinical Laboratory Medicine, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan.
  • Nakata Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Matsuoka A; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Ishikawa T; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Meno T; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Nakamura Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kawamura M; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kawamura S; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Takeshita J; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Misaki Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Yoshimura K; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Gomyo A; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Okada Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Tamaki M; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kusuda M; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kameda K; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Akahoshi Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Sato M; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Tanihara A; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Nakasone H; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kako S; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Kanda Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan. Electronic address: ycanda-tky@umin.ac.jp.
J Infect Chemother ; 2024 Jun 24.
Article in En | MEDLINE | ID: mdl-38925426
ABSTRACT

BACKGROUND:

A change in empirical antibiotics or the addition of glycopeptide antibiotics is often applied in cases of persistent febrile neutropenia (FN) despite the administration of broad-spectrum antibiotics. However, the clinical benefit of these approaches remains unclear.

METHODS:

We conducted a retrospective study to evaluate the effectiveness of a change in antibiotics or the addition of glycopeptide antibiotics for persistent FN after autologous hematopoietic cell transplantation (auto-HCT). We retrospectively reviewed the records of 208 patients who received auto-HCT at our institution between 2007 and 2019. FN that lasted for 4 days or longer was defined as persistent FN. We compared the time to defervescence between patients whose initial antibiotics were changed and/or who additionally received glycopeptide antibiotics, and those without these antibiotic modifications.

RESULTS:

Among patients who fulfilled the criteria of persistent FN (n = 125), changes in antibiotics were not significantly associated with the time to defervescence in a multivariate analysis (hazard ratio [HR] 0.72, p = 0.27). On the other hand, the addition of glycopeptide antibiotics was paradoxically associated with a delay in defervescence (HR 0.56, p = 0.033).

CONCLUSIONS:

Although there may be differences in patient backgrounds, no significant differences were observed in either a univariate or multivariate analysis. Since neither a change in antibiotics nor the addition of glycopeptide antibiotics was associated with earlier defervescence in persistent FN after auto-HCT, routine antibiotic modifications might not be necessary in this setting.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Infect Chemother Journal subject: MICROBIOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: Japón Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Infect Chemother Journal subject: MICROBIOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: Japón Country of publication: Países Bajos