Development and validation of a multivariable model predicting the required catheter dwell time among mechanically ventilated critically ill patients in three randomized trials.

Catheter dwell time Central venous catheters Critical care Intensive care unit Predictive score

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
16 Jan 2023
Historique:
received: 19 10 2022
accepted: 03 01 2023
entrez: 16 1 2023
pubmed: 17 1 2023
medline: 17 1 2023
Statut: epublish

Résumé

The anatomic site for central venous catheter insertion influences the risk of central venous catheter-related intravascular complications. We developed and validated a predictive score of required catheter dwell time to identify critically ill patients at higher risk of intravascular complications. We retrospectively conducted a cohort study from three multicenter randomized controlled trials enrolling consecutive patients requiring central venous catheterization. The primary outcome was the required catheter dwell time, defined as the period between the first catheter insertion and removal of the last catheter for absence of utility. Predictors were identified in the training cohort (3SITES trial; 2336 patients) through multivariable analyses based on the subdistribution hazard function accounting for death as a competing event. Internal validation was performed in the training cohort by 500 bootstraps to derive the CVC-IN score from robust risk factors. External validation of the CVC-IN score were performed in the testing cohort (CLEAN, and DRESSING2; 2371 patients). The analysis was restricted to patients requiring mechanical ventilation to comply with model assumptions. Immunosuppression (2 points), high creatinine > 100 micromol/L (2 points), use of vasopressor (1 point), obesity (1 point) and older age (40-59, 1 point; ≥ 60, 2 points) were independently associated with the required catheter dwell time. At day 28, area under the ROC curve for the CVC-IN score was 0.69, 95% confidence interval (CI) [0.66-0.72] in the training cohort and 0.64, 95% CI [0.61-0.66] in the testing cohort. Patients with a CVC-IN score ≥ 4 in the overall cohort had a median required catheter dwell time of 24 days (versus 11 days for CVC-IN score < 4 points). The positive predictive value of a CVC-IN score ≥ 4 was 76.9% for > 7 days required catheter dwell time in the testing cohort. The CVC-IN score, which can be used for the first catheter, had a modest ability to discriminate required catheter dwell time. Nevertheless, preference of the subclavian site may contribute to limit the risk of intravascular complications, in particular among ventilated patients with high CVC-IN score. Trials Registration NCT01479153, NCT01629550, NCT01189682.

Sections du résumé

BACKGROUND BACKGROUND
The anatomic site for central venous catheter insertion influences the risk of central venous catheter-related intravascular complications. We developed and validated a predictive score of required catheter dwell time to identify critically ill patients at higher risk of intravascular complications.
METHODS METHODS
We retrospectively conducted a cohort study from three multicenter randomized controlled trials enrolling consecutive patients requiring central venous catheterization. The primary outcome was the required catheter dwell time, defined as the period between the first catheter insertion and removal of the last catheter for absence of utility. Predictors were identified in the training cohort (3SITES trial; 2336 patients) through multivariable analyses based on the subdistribution hazard function accounting for death as a competing event. Internal validation was performed in the training cohort by 500 bootstraps to derive the CVC-IN score from robust risk factors. External validation of the CVC-IN score were performed in the testing cohort (CLEAN, and DRESSING2; 2371 patients).
RESULTS RESULTS
The analysis was restricted to patients requiring mechanical ventilation to comply with model assumptions. Immunosuppression (2 points), high creatinine > 100 micromol/L (2 points), use of vasopressor (1 point), obesity (1 point) and older age (40-59, 1 point; ≥ 60, 2 points) were independently associated with the required catheter dwell time. At day 28, area under the ROC curve for the CVC-IN score was 0.69, 95% confidence interval (CI) [0.66-0.72] in the training cohort and 0.64, 95% CI [0.61-0.66] in the testing cohort. Patients with a CVC-IN score ≥ 4 in the overall cohort had a median required catheter dwell time of 24 days (versus 11 days for CVC-IN score < 4 points). The positive predictive value of a CVC-IN score ≥ 4 was 76.9% for > 7 days required catheter dwell time in the testing cohort.
CONCLUSION CONCLUSIONS
The CVC-IN score, which can be used for the first catheter, had a modest ability to discriminate required catheter dwell time. Nevertheless, preference of the subclavian site may contribute to limit the risk of intravascular complications, in particular among ventilated patients with high CVC-IN score. Trials Registration NCT01479153, NCT01629550, NCT01189682.

Identifiants

pubmed: 36645531
doi: 10.1186/s13613-023-01099-9
pii: 10.1186/s13613-023-01099-9
pmc: PMC9842826
doi:

Banques de données

ClinicalTrials.gov
['NCT01479153', 'NCT01189682', 'NCT01629550', 'NCT01479153']

Types de publication

Journal Article

Langues

eng

Pagination

5

Informations de copyright

© 2023. The Author(s).

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Auteurs

Jeanne Iachkine (J)

Department of Clinical Research and Biostatistics, Caen University Hospital and Caen Normandy University, Caen, France.
INSERM U1311 DYNAMICURE, Caen Normandy University, Caen, France.

Niccolò Buetti (N)

Infection Control Program and World Health Organization Collaborating Center on Patient Safety, Hospitals and Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Harm-Jan de Grooth (HJ)

Department of Intensive Care, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.

Anaïs R Briant (AR)

Department of Clinical Research and Biostatistics, Caen University Hospital and Caen Normandy University, Caen, France.

Olivier Mimoz (O)

Inserm U1070, Poitiers University, Poitiers, France.
Poitiers University Hospital, 86021, Poitiers, France.

Bruno Mégarbane (B)

Medical and Toxicological Intensive Care Unit, Lariboisière Hospital, AP-HP, INSERM, UMRS-1144, Paris University, Paris, France.

Jean-Paul Mira (JP)

Medical ICU, Cochin Hospital, AP-HP, 75014, Paris, France.

Xavier Valette (X)

Department of Medical Intensive Care, Caen University Hospital, 14000, Caen, France.

Cédric Daubin (C)

Department of Medical Intensive Care, Caen University Hospital, 14000, Caen, France.

Damien du Cheyron (D)

Department of Medical Intensive Care, Caen University Hospital, 14000, Caen, France.

Leonard A Mermel (LA)

Department of Epidemiology and Infection Prevention, Lifespan Hospital System, Providence, RI, USA.
Department of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.

Jean-François Timsit (JF)

Medical and Infectious Diseases ICU (MI2), Bichat Hospital, AP-HP, University of Paris, IAME, INSERM U1137, Paris, France.

Jean-Jacques Parienti (JJ)

Department of Clinical Research and Biostatistics, Caen University Hospital and Caen Normandy University, Caen, France. parienti-jj@chu-caen.fr.
INSERM U1311 DYNAMICURE, Caen Normandy University, Caen, France. parienti-jj@chu-caen.fr.

Classifications MeSH