TY - JOUR
T1 - Blood culture differential time to positivity enables safe catheter retention in suspected catheter-related bloodstream infection: A randomized controlled trial
AU - Sabatier, Caroline
AU - García, Xaime
AU - Ferrer, Ricard
AU - Duarte, Montserrat
AU - Colomina, Montserrat
AU - Alcaráz, Dolores
AU - Fontanals, Dionisia
AU - Vallés, Jordi
PY - 2015/4/1
Y1 - 2015/4/1
N2 - © 2013 Elsevier España, S.L.U. and SEMICYUC. Objective: To evaluate the clinical usefulness and safety of the differential-time-to-positivity (DTP) method for managing the suspicion of catheter-related bloodstream infection (CR-BSI) in comparison with a standard method that includes catheter removal in critically ill patients. Methods-Design: A prospective randomized study was carried out. Setting: A 16-bed clinical-surgical ICU (July 2007-February 2009). Interventions: Patients were randomly assigned to one of two groups at the time CR-BSI was suspected. In the standard group, a standard strategy requiring catheter withdrawal was used to confirm or rule out CR-BSI. In the DTP group, DTP without catheter withdrawal was used to confirm or rule out CR-BSI. Measurements: clinical and microbiological data, CR-BSI rates, unnecessary catheter removals, and complications due to new puncture or to delays in catheter removal. Results: Twenty-six patients were analyzed in each group. In the standard group, 6 of 37 suspected episodes of CR-BSI were confirmed and 5 colonizations were diagnosed. In the DTP group, 5 of 26 suspected episodes of CR-BSI were confirmed and four colonizations were diagnosed. In the standard group, all catheters (58/58, 100%) were removed at the time CR-BSA was suspected, whereas in the DTP group, only 13 catheters (13/41, 32%) were removed at diagnosis, and 10 due to persistent septic signs (10/41, 24%). In cases of confirmed CR-BSI, there were no differences between the two groups in the evolution of inflammatory parameters during the 48. hours following the suspicion of CR-BSI. Conclusions: In critically ill patients with suspected CR-BSI, the DTP method makes it possible to keep the central venous catheter in place safely.
AB - © 2013 Elsevier España, S.L.U. and SEMICYUC. Objective: To evaluate the clinical usefulness and safety of the differential-time-to-positivity (DTP) method for managing the suspicion of catheter-related bloodstream infection (CR-BSI) in comparison with a standard method that includes catheter removal in critically ill patients. Methods-Design: A prospective randomized study was carried out. Setting: A 16-bed clinical-surgical ICU (July 2007-February 2009). Interventions: Patients were randomly assigned to one of two groups at the time CR-BSI was suspected. In the standard group, a standard strategy requiring catheter withdrawal was used to confirm or rule out CR-BSI. In the DTP group, DTP without catheter withdrawal was used to confirm or rule out CR-BSI. Measurements: clinical and microbiological data, CR-BSI rates, unnecessary catheter removals, and complications due to new puncture or to delays in catheter removal. Results: Twenty-six patients were analyzed in each group. In the standard group, 6 of 37 suspected episodes of CR-BSI were confirmed and 5 colonizations were diagnosed. In the DTP group, 5 of 26 suspected episodes of CR-BSI were confirmed and four colonizations were diagnosed. In the standard group, all catheters (58/58, 100%) were removed at the time CR-BSA was suspected, whereas in the DTP group, only 13 catheters (13/41, 32%) were removed at diagnosis, and 10 due to persistent septic signs (10/41, 24%). In cases of confirmed CR-BSI, there were no differences between the two groups in the evolution of inflammatory parameters during the 48. hours following the suspicion of CR-BSI. Conclusions: In critically ill patients with suspected CR-BSI, the DTP method makes it possible to keep the central venous catheter in place safely.
KW - Catheter-related infections
KW - Central venous catheter
KW - Critical care
KW - Diagnosis
U2 - 10.1016/j.medin.2013.12.012
DO - 10.1016/j.medin.2013.12.012
M3 - Article
SN - 0210-5691
VL - 39
SP - 135
EP - 141
JO - Medicina Intensiva
JF - Medicina Intensiva
IS - 3
ER -