Impact of the Sensitivity to Empiric Antibiotics on Clinical Outcomes after Biliary Drainage for Acute Cholangitis.


Journal

Gut and liver
ISSN: 2005-1212
Titre abrégé: Gut Liver
Pays: Korea (South)
ID NLM: 101316452

Informations de publication

Date de publication:
15 11 2020
Historique:
received: 18 05 2019
revised: 20 10 2019
accepted: 03 11 2019
pubmed: 14 2 2020
medline: 26 8 2021
entrez: 14 2 2020
Statut: ppublish

Résumé

Empiric antibiotics are given in combination with biliary drainage for acute cholangitis but sometimes turn out to be insensitive to microorganisms in blood and bile. Clinical outcomes were compared according to sensitivity to microorganisms detected in blood and bile culture to evaluate the impact of sensitivity to empiric antibiotics in cholangitis. Consecutive patients who underwent biliary drainage for acute cholangitis were retrospectively studied. Clinical outcomes such as 30-day mortality, length of hospital stay and high care unit stay, organ dysfunction and duration of fever were compared in three groups: group A (sensitive to both blood and bile culture), group B (sensitive to blood culture alone) and group C (insensitive to both blood and bile culture). Eighty episodes of cholangitis were classified according to sensitivity results: 42, 32 and six in groups A, B and C. Escherichia coli and Klebsiella were two major pathogens. There were no significant differences in 30-day mortality rate (7%, 0%, and 0%, p=0.244), length of hospital stay (28.5, 21.0, and 20.5 days, p=0.369), organ dysfunction rate (14%, 25%, and 17%, p=0.500), duration of fever (4.3, 3.2, and 3.5 days, p=0.921) and length of high care unit stay (1.4, 1.2, and 1.7 days, p=0.070) in groups A, B and C. Empiric antibiotics were changed in 11 episodes but clinical outcomes appeared to be non-inferior even in 31 episodes of cholangitis who were on inadequate antibiotics throughout the course. Sensitivity of empiric antibiotics was not associated with clinical outcomes in acute cholangitis.

Sections du résumé

Background/Aims
Empiric antibiotics are given in combination with biliary drainage for acute cholangitis but sometimes turn out to be insensitive to microorganisms in blood and bile. Clinical outcomes were compared according to sensitivity to microorganisms detected in blood and bile culture to evaluate the impact of sensitivity to empiric antibiotics in cholangitis.
Methods
Consecutive patients who underwent biliary drainage for acute cholangitis were retrospectively studied. Clinical outcomes such as 30-day mortality, length of hospital stay and high care unit stay, organ dysfunction and duration of fever were compared in three groups: group A (sensitive to both blood and bile culture), group B (sensitive to blood culture alone) and group C (insensitive to both blood and bile culture).
Results
Eighty episodes of cholangitis were classified according to sensitivity results: 42, 32 and six in groups A, B and C. Escherichia coli and Klebsiella were two major pathogens. There were no significant differences in 30-day mortality rate (7%, 0%, and 0%, p=0.244), length of hospital stay (28.5, 21.0, and 20.5 days, p=0.369), organ dysfunction rate (14%, 25%, and 17%, p=0.500), duration of fever (4.3, 3.2, and 3.5 days, p=0.921) and length of high care unit stay (1.4, 1.2, and 1.7 days, p=0.070) in groups A, B and C. Empiric antibiotics were changed in 11 episodes but clinical outcomes appeared to be non-inferior even in 31 episodes of cholangitis who were on inadequate antibiotics throughout the course.
Conclusions
Sensitivity of empiric antibiotics was not associated with clinical outcomes in acute cholangitis.

Identifiants

pubmed: 32050314
pii: gnl19248
doi: 10.5009/gnl19248
pmc: PMC7667925
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

842-849

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Auteurs

Satoshi Kawamura (S)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Yuki Karasawa (Y)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Nobuo Toda (N)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Yousuke Nakai (Y)

Department of Gastroenterology, University of Tokyo Hospital, Tokyo, Japan.

Chikako Shibata (C)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Ken Kurokawa (K)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Junya Arai (J)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Kazuyoshi Funato (K)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Shigeyuki Kurosaki (S)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Shuya Maeshima (S)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Mayuko Kondo (M)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Kentaro Kojima (K)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Takamasa Ohki (T)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Michiharu Seki (M)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

Kazuhiko Koike (K)

Department of Gastroenterology, University of Tokyo Hospital, Tokyo, Japan.

Kazumi Tagawa (K)

Department of Gastroenterology, Mitsui Memorial Hospital, Tokyo, Japan.

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