
Methods: A third follow-up survey of MRSA, VRE, ESBLs, CREs and CDI was done in adult inpatients in Canadian hospitals with ≥ 50 beds in Feb 2016. Data describing the participating hospitals and the patient cases were obtained at each participating site using standard criteria and case definitions.
Results: 159 hospitals with 34 510 inpatients participated in the follow-up survey with representation from 9 provinces. Routine universal or targeted admission screening for VRE decreased from 99% in 2010 to 90% in 2012 and to 77% in 2016. 105 hospitals participated in all 3 surveys; median prevalence rates in these hospitals are summarized in the Table. The prevalence of MRSA, CDI, ESBL and CRE did not significantly change over time. The prevalence of VRE also did not significantly change from 2012 to 2016, even if only centres that screened for VRE at the time of the survey were included in the analysis. The median prevalence of CRE was lower in centres that screened for VRE (p=0.01). Although not statistically significant, centres that did not screen for VRE in 2016 tended to have higher prevalence of MRSA and ESBL. In 2016, CREs were reported from 24 hospitals (15%) compared to 10 hospitals (7%) in 2012.
|
Median prevalence per 100 inpatients (range) |
||
|
2010 |
2012 |
2016 |
MRSA |
4.2 (0-14.8) |
4.0 (0-13.9) |
4.1 (0-18.5) |
VRE |
0.5 (0-13.0) |
1.3 (0-12.7) |
0.8 (0-18.5) |
CDI |
0.8 (0-4.3) |
1.0 (0-5.5) |
1.1 (0-4.5) |
ESBL |
|
0.5 (0-8.5) |
0.3 (0-10.9) |
CRE |
|
0 (0-1.3) |
0 (0-1.6) |
Conclusion: These data provide national prevalence rates for MRSA, VRE, ESBLs, CREs, and CDI among adult inpatients in Canadian hospitals. There was no significant change in the prevalence of any of the organisms from 2012 to 2016. CREs were identified in more hospitals in 2016 than in 2012, but remain infrequently identified in Canadian hospitals. There has been a substantial decrease in the number of hospitals that screen patients for VRE; this change in practice might lead to changes in the prevalence of other antibiotic resistant organisms.

P. Martin,
None
K. Bush, None
M. Dyck, None
Z. Hirji, None
O. E. Larios, None
A. Mcgeer, None
C. Moore, None
K. Weiss, None
A. E. Simor, None