| Literature DB >> 32648089 |
Garyphallia Poulakou1, Saad Nseir2,3, George L Daikos4.
Abstract
Entities:
Mesh:
Year: 2020 PMID: 32648089 PMCID: PMC7343898 DOI: 10.1007/s00134-020-06173-5
Source DB: PubMed Journal: Intensive Care Med ISSN: 0342-4642 Impact factor: 17.440
Contemporary studies delivering the message “less contact isolation in the ICU is more”
| Author, Year | Setting design | Study Size | Target organisms | Intervention | Main outcomes |
|---|---|---|---|---|---|
Huskins WC et al., 2011 [ | Cluster-randomized trial, Three periods: Baseline (April through November 2005), Randomization and implementation (December 2005 through February 2006), and Intervention (March through August 2006) | 5434 admissions to 10 intervention ICUs 3705 admissions to eight control ICUs | MRSA VRE | Surveillance cultures were obtained for MRSA and CRE colonization from patients in all participating ICUs; the results were reported only to ICUs assigned to the intervention In intervention ICUs, patients who were colonized or infected with MRSA or VRE were assigned to care with contact precautions; all the other patients were assigned to care with universal gloving | The intervention was not effective in reducing the transmission of MRSA or VRE The use of barrier precautions by providers was less than what was required The turnaround time for reporting a positive result on a surveillance culture was prolonged |
Cepeda JA, et al., 2005 [ | Multicenter, 1-year Prospective Study conducted in 3 ICUs (Medical and Surgical) | Admitted Patients Included | MRSA | Nose or groin swabs obtained within 24 h of admission, once a week and at discharge In the middle 6 months, MRSA-positive patients were not moved to a single room or cohort nursed unless they were carrying other MDROs | Transfer of MRSA-colonised or infected patients into single rooms or cohorting did not reduce cross-infection |
Derde LPD, et al 2014 [ | Multicenter (conducted in 13 ICUs), interrupted time series study (phase 2), followed by a cluster randomized trial (phase 3) A 6-month baseline period was performed before phase 2 (phase 1 | 1st phase Screened Analyzed At Risk for MDR colonization: 1688 2nd phase Screened Analyzed At Risk for MDR colonization: 1681 3rd phase Screened Analyzed At Risk for MDR colonization: 2029 3rd phase (rapid screening) Screened Analyzed At Risk for MDR colonization: 2007 | HRE VRE MRSA | Chromogenic screening for HRE, MRSA and VRE (conventional screening) PCR screening for MRSA, VRE (rapid screening) ICUs were randomly assigned to either conventional screening or rapid screening [PCR testing for MRSA and VRE and chromogenic screening for highly resistant Enterobacteriaceae (HRE)]; with contact precautions for identified carriers | Mean hand hygiene compliance improved from 52% in phase 1 to 69% in phase 2, and 77% in phase 3 A decrease in trend of acquisition of antimicrobial-resistant bacteria in phase 2 was largely caused by changes in acquisition of MRSA In the context of a sustained high level of compliance to hand hygiene and chlorhexidine bathings, screening and isolation of carriers did not reduce acquisition rates of multidrug-resistant bacteria, whether or not screening is done with rapid testing or conventional testing |
Ledoux G, et al 2016 [ | Prospective, before-after study, conducted in a mixed ICU, during two 12-month periods 1-month ‘wash-out’ period interval | 1st period 2nd period | Ceftazidime or Imipenem-resistant ESBL-GNB MRSA VRE | Nasal and Rectal swabs, Tracheal Aspirate in intubated or tracheostomized patients obtained on admission and once a week During 1st period: systematic isolation performed in all patients at ICU admission During 2nd period: patient isolation performed when at least one risk factor for MDRO was met | Targeted isolation of patients at ICU admission was not inferior to systematic isolation, regarding the percentage of patients with ICU-acquired infections related to MDR bacteria [85 of 585 (14.5%) vs. 84 of 636 (13.2%) patients, risk difference,− 1.3%, 95% confidence interval (− 5.2 to 2.6%)] |
Djibré M, et al 2017 [ | Single-Center, Observational Study performed in patients admitted to MICU and SICU during 2 consecutive 6-month periods | 1st period Screened Included 2nd period Screened Included | CRE ESBL (very low infection rate of MRSA and VRE in this Unit) | Rectal swabs were obtained on admission and once a week Universal screening for MDRO carriage and ACPs during the first 6-month period During the second 6-month period screening was maintained, but ACP were enforced in the presence of at least 1 defined risk factor for MDRO | The rate of acquired MDRO (positive screening or clinical specimen) was similar during both periods (10% [ A targeted isolation screening policy on ICU admission was safe compared with universal screening and isolation regarding the rate of ICU acquired MDRO colonization or infection |
Zahar JR, et al 2013 [ | Based on the database of Iatroref III (a multicenter cluster-randomized clinical trial, testing the effects of MFSP, NCT00461461) Two centers included | Screened Included Isolated patients: 170 Non- isolated patients: 980 | GNB MRSA VRE | A subdistribution hazard regression model with careful adjustment on confounding factors was used to assess the effect of patient isolation on the occurrence of medical errors and adverse events | After adjustment of confounders, errors in anticoagulant prescription [subdistribution hazard ratio (sHR) = 1.7, |
Searcy R.J., et al 2018 [ | Single-Center, Retrospective Chart Review of patient on MV receiving MRSA nasal screening and sedated within 24–48 h of ICU admission | Screened Included MRSA-positive: 114 MRSA negative:112 | MRSA | Nasal PCR assay Calculation of rate of inappropriate sedation, length of ICU stay, length of time on MV, and incidence of ventilator-associated complications | Patients placed on CI spent longer in the ICU (10.4 vs. 6.8 days, |
Sypsa V et al., 2012 [ | Prospective observational study conducted in a surgical unit of a tertiary-care hospital Surveillance culture for CPKP were obtained from all patients upon admission and weekly thereafter | Screened | Carbapenemase-producing Klebsiella pneumoniae | The Ross-Macdonald model for vector-borne diseases was applied to obtain estimates for the basic reproduction number R0 (average number of secondary cases per primary case in the absence of infection control) and assess the impact of infection control measures on CPKP containment in endemic and hyperendemic settings | The use of surveillance culture on admission and subsequent separation (mostly cohorted, less often in single room CI) of carriers from non-carriers coupled with improved hand hygiene compliance and contact precautions may attain maximum containment of CPKP in endemic and hyperendemic settings; it was estimated that in periods where R0 is 2, hand hygiene compliance should exceed 50% in order to attain an effective reproduction number below unity |
| Dhar S et al., 2014 [ | Prospective cohort study Eleven teaching hospitals | 1013 observations conducted on HCP | Not applicable | Compliance with individual components of contact isolation precautions and overall compliance (all five measures together) during varying burdens of isolation | Compliance with all components was 28.9%. As the burden of isolation increased (20% or less to greater than 60%), a decrease in compliance with hand hygiene (43.6–4.9%) and with all five components (31.5–6.5%) was observed |
ACP additional contact precautions, CI contact isolation, CRE carbapenem-resistant enterobacteriaceae, ESBL extended spectrum beta-lactamase, GNB gram-negative bacilli, HCP health-care personnel, HRE highly resistant enterobacteriaceae, ICU intensive care unit, MDRO multi-drug resistant organism, MFSP multifaceted safety programs, MICU medical intensive care unit, MV mechanical ventilation, MRSA methicillin-resistant Staphylococcus aureus, NICU neonatal intensive care unit, SICU surgical intensive care unit, VRE vancomycin-resistant enterococci