Scheduled removal of central venous catheters (CVC) to prevent CVC-related bloodstream infections in patients with hematological disease or autologous stem cell transplantation: a registry-based randomized simulation-study.
Jens Peter PanseDaniela TölleEva FiegleJan-Hendrik NaendrupMartin Schmidt-HieberBoris BöllMarcus Ulrich HentrichDaniel TeschnerEnrico SchalkPublished in: Annals of hematology (2022)
Although not generally recommended, scheduled central venous catheter (CVC) removal is sometimes carried out in order to reduce the CVC-related bloodstream infection (CRBSI) incidence. We conducted a simulation for scheduled CVC removal within the multicenter CRBSI registry (SECRECY). Non-tunneled jugular and subclavian CVC in patients with hematological disease or with germ cell tumors (including patients receiving autologous stem cell transplantation [SCT]) were included. Cases were randomized in a 1:1:1:1 ratio to either a simulated, scheduled CVC removal after 7, 14, and 21 days, or to non-simulated, unscheduled CVC removal (control group). The primary endpoint was definitive CRBSI incidence for a scheduled CVC removal after 14 days (dCRBSI-D14 rmv ). Among other, secondary endpoints were definite CRBSI incidence for a scheduled removal after 7 days (dCRBSI-D7 rmv ) and 21 days (dCRBSI-D21 rmv ). Data on 2984 CVC were included. Patients' median age was 59 (range 16-95) years, 58.8% being male. The vast majority (98.4%) were patients with hematological malignancies. Jugular veins were the main insertion site (93.2%). dCRBSI-D14 rmv was 3.10/1000 CVC days as compared to 4.15/1000 CVC days in the control group (p = 0.23). There was a significant difference between dCRBSI-D7 rmv (0.86/1000 CVC days) and controls (p < 0.001), but not between dCRBSI-D21 rmv (4.10/1000 CVC days) and controls (p = 0.96). Our data suggest that in patients with hematological diseases or autologous SCT recipients scheduled CVC removal after 14 days does not result in a lower CRBSI incidence compared to unscheduled removal.Trial registration: DRKS00006551, 2014/09/29, retrospectively registered.
Keyphrases
- stem cell transplantation
- high dose
- clinical trial
- phase iii
- bone marrow
- open label
- double blind
- end stage renal disease
- randomized controlled trial
- squamous cell carcinoma
- low dose
- newly diagnosed
- radiation therapy
- mesenchymal stem cells
- big data
- peritoneal dialysis
- germ cell
- ultrasound guided
- cross sectional
- locally advanced