
Methods: This was an IRB-approved, pretest-posttest quasiexperiment at an 802-bed hospital in Detroit MI. Inpatients ≥18 years of age with solid organ and bone marrow transplant, or those with immunocompromising conditions in the intensive care unit (ICU) were included. Collection periods were RV season 1 (RVS1), Oct. 2014—Mar. 2015 (send-out testing), and RV season 2 (RVS2), Oct. 2015—Apr. 2016 (in-house testing). TAT was measured from specimen collection to result; time to intervention (TTI) was measured from specimen collection to change in drug therapy. RVS1 and RVS2 were compared using bivariate tests.
Results: 131 patients were included, 56 RVS1, 75 RVS2. 61.1% of patients were clinically diagnosed with pneumonia, 27.5% of which was microbiologically confirmed. The in-house panel reduced TAT and TTI, and had more positive testing (Table 1). Most common pathogens were influenza (8 in RVS1, 5 in RVS2), coronavirus (0 and 11), and rhinovirus (1 and 7). Differences were not observed between groups for frequency or type of intervention or outcome.
Conclusion: Diagnostic yield and TTI were improved by in-house RV testing, but this did not impact length of stay (LOS), duration of therapy (DOT), or frequency of drug-related interventions. The majority of interventions were discontinuation of oseltamivir, with minimal impact on antibacterial use.
Outcome |
RVS1 (n=56) |
RVS2 (n=75) |
P |
Positive test, n (%) |
11 (19.6) |
32 (42.7) |
< 0.01 |
TAT, median hrs (IQR) |
47 (11—61) |
6 (3.5—11) |
< 0.001 |
TTI, median hrs (IQR) |
52 (38—69) |
14( 9—30) |
< 0.001 |
DOT, median days (IQR) |
4 (2—7) |
4 (2—7) |
0.958 |
LOS, median days (IQR) |
8 (4—14) |
6 (3—13.5) |
0.491 |
Intervention, n (%) |
20 (35.7) |
23 (30.6) |
0.543 |
Start antiviral |
3 (5.4) |
7 (9.3) |
0.515 |
Discontinue oseltamivir |
14 (25.0) |
13 (17.3) |
0.283 |
Discontinue antibiotic |
2 (3.6) |
4 (5.3) |
0.633 |
Adjust immunosuppression |
1 (1.8) |
2 (2.7) |
0.739 |

N. Mercuro,
None
R. Tibbetts, None
L. Samuel, None
S. L. Davis, None