Effect of C-Reactive Protein-Guided Antibiotic Treatment Duration, 7-Day Treatment, or 14-Day Treatment on 30-Day Clinical Failure Rate in Patients With Uncomplicated Gram-Negative Bacteremia: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
02 06 2020
Historique:
entrez: 3 6 2020
pubmed: 3 6 2020
medline: 24 6 2020
Statut: ppublish

Résumé

Antibiotic overuse drives antibiotic resistance. Gram-negative bacteremia is a common infection that results in substantial antibiotic use. To compare the clinical effectiveness of C-reactive protein (CRP)-guided, 7-day, and 14-day antibiotic durations 30, 60, and 90 days after treatment initiation. Multicenter, noninferiority, point-of-care randomized clinical trial including adults hospitalized with gram-negative bacteremia conducted in 3 Swiss tertiary care hospitals between April 2017 and May 2019, with follow-up until August 2019. Patients and physicians were blinded between randomization and antibiotic discontinuation. Adults (aged ≥18 years) were eligible for randomization on day 5 (±1 d) of microbiologically efficacious therapy for fermenting, gram-negative bacteria in blood culture(s) if they were afebrile for 24 hours without evidence for complicated infection (eg, abscess) or severe immunosuppression. Randomization in a 1:1:1 ratio to an individualized CRP-guided antibiotic treatment duration (discontinuation once CRP declined by 75% from peak; n = 170), fixed 7-day treatment duration (n = 169), or fixed 14-day treatment duration (n = 165). The primary outcome was the clinical failure rate at day 30, defined as the presence of at least 1 of the following, with a non-inferiority margin of 10%: recurrent bacteremia, local suppurative complication, distant complication (growth of the same organism causing the initial bacteremia), restarting gram-negative-directed antibiotic therapy due to clinical worsening suspected to be due to the initial organism, or death due to any cause. Secondary outcomes included the clinical failure rate on day 90 of follow-up. Among 504 patients randomized (median [interquartile range] age, 79 [68-86] years; 306 of 503 [61%] were women), 493 (98%) completed 30-day follow-up and 448 (89%) completed 90-day follow-up. Median antibiotic duration in the CRP group was 7 (interquartile range, 6-10; range, 5-28) days; 34 of the 164 patients (21%) who completed the 30-day follow-up had protocol violations related to treatment assignment. The primary outcome occurred in 4 of 164 (2.4%) patients in the CRP group, 11 of 166 (6.6%) in the 7-day group, and 9 of 163 (5.5%) in the 14-day group (difference in CRP vs 14-day group, -3.1% [1-sided 97.5% CI, -∞ to 1.1]; P < .001; difference in 7-day vs 14-day group, 1.1% [1-sided 97.5% CI, -∞ to 6.3]; P < .001). By day 90, clinical failure occurred in 10 of 143 patients (7.0%) in the CRP group, 16 of 151 (10.6%) in the 7-day group, and 16 of 153 (10.5%) in the 14-day group. Among adults with uncomplicated gram-negative bacteremia, 30-day rates of clinical failure for CRP-guided antibiotic treatment duration and fixed 7-day treatment were noninferior to fixed 14-day treatment. However, interpretation is limited by the large noninferiority margin compared with the low observed event rate, as well as low adherence and wide range of treatment durations in the CRP-guided group. ClinicalTrials.gov Identifier: NCT03101072.

Identifiants

pubmed: 32484534
pii: 2766635
doi: 10.1001/jama.2020.6348
pmc: PMC7267846
doi:

Substances chimiques

Anti-Bacterial Agents 0
C-Reactive Protein 9007-41-4

Banques de données

ClinicalTrials.gov
['NCT03101072']

Types de publication

Comparative Study Equivalence Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2160-2169

Subventions

Organisme : Swiss National Science Foundation
Pays : Switzerland

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Auteurs

Elodie von Dach (E)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.
Faculty of Medicine, Clinical Research Center, Geneva University Hospitals, Geneva, Switzerland.

Werner C Albrich (WC)

Division of Infectious Diseases and Hospital Epidemiology, Cantonal Hospital St Gallen, St Gallen, Switzerland.

Anne-Sophie Brunel (AS)

Infectious Diseases Service, University Hospital, University of Lausanne, Lausanne, Switzerland.

Virginie Prendki (V)

Faculty of Medicine, Division of Internal Medicine of the Aged, Geneva University Hospitals, Geneva, Switzerland.

Clémence Cuvelier (C)

Faculty of Medicine, Division of Internal Medicine of the Aged, Geneva University Hospitals, Geneva, Switzerland.

Domenica Flury (D)

Division of Infectious Diseases and Hospital Epidemiology, Cantonal Hospital St Gallen, St Gallen, Switzerland.

Angèle Gayet-Ageron (A)

Faculty of Medicine, Clinical Research Center, Geneva University Hospitals, Geneva, Switzerland.
Division of Clinical Epidemiology, Department of Health and Community Medicine, Geneva University Hospitals, Geneva, Switzerland.

Benedikt Huttner (B)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Philipp Kohler (P)

Division of Infectious Diseases and Hospital Epidemiology, Cantonal Hospital St Gallen, St Gallen, Switzerland.

Eva Lemmenmeier (E)

Division of Infectious Diseases and Hospital Epidemiology, Cantonal Hospital St Gallen, St Gallen, Switzerland.

Shawna McCallin (S)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Anne Rossel (A)

Department of Internal Medicine, Geneva University Hospitals, Geneva, Switzerland.

Stephan Harbarth (S)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Laurent Kaiser (L)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Pierre-Yves Bochud (PY)

Infectious Diseases Service, University Hospital, University of Lausanne, Lausanne, Switzerland.

Angela Huttner (A)

Faculty of Medicine, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

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