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Carriers of carbapenem-resistant Enterobacteriaceae (CRE) are often readmitted, exposing patients to CRE cross-transmission.
OBJECTIVE
To identify predictors of persistent CRE carriage upon readmission, directing a risk prediction score.
DESIGN
Retrospective cohort study.
SETTING
University-affiliated general hospital.
PATIENTS
A cohort of 168 CRE carriers with 474 readmissions.
METHODS
The primary and secondary outcomes were CRE carriage status at readmission and length of CRE carriage. Predictors of persistent CRE carriage upon readmission were analyzed using a generalized estimating equations (GEE) multivariable model. Readmissions were randomly divided into derivation and validation sets. A CRE readmission score was derived to predict persistent CRE carriage in 3 risk groups: high, intermediate, and low. The discriminatory ability of the model and the score were expressed as C statistics.
RESULTS
CRE carrier status persisted for 1 year in 33% of CRE carriers. Positive CRE status was detected in 202 of 474 readmissions (42.6%). The following 4 variables were associated with persistent CRE carriage at readmission: readmission within 1 month (odds ratio [OR], 6.95; 95% confidence interval [CI], 2.79–17.30), positive CRE status on preceding admission (OR, 5.46; 95% CI, 3.06–9.75), low Norton score (OR, 3.07; 95% CI, 1.26–7.47), and diabetes mellitus (OR, 1.84; 95% CI, 0.98–3.44). The C statistics were 0.791 and 0.789 for the derivation set (n=322) model and score, respectively, and the C statistic was 0.861 for the validation set of the score (n=152). The rates of CRE carriage at readmissions (validation set) for the groups with low, intermediate, and high scores were 8.6%, 38.9%, and 77.6%, respectively.
CONCLUSIONS
CRE carrier state commonly persists upon readmission, and this risk can be estimated to guide screening policy and infection control measures.
Infect. Control Hosp. Epidemiol. 2016;37(2):188–196
The use of antidepressant drugs in patients with ischaemic heart disease
(IHD) has been debated owing to scarcity of data and conflicting results
regarding the effect of these drugs on mortality.
Aims
To evaluate the association between adherence to antidepressant therapy
and all-cause mortality in a population-based cohort of patients with
IHD.
Method
A total of 63 437 patients with IHD who purchased antidepressants at
least once during the years 2008–2011 were retrospectively followed for
all-cause mortality over 4 years. Adherence was measured as a ratio
between claimed and prescribed durations of medication and modelled as
non-adherence (<20%), poor (20–50%), moderate (50–80%) and good
(>80%). We used multivariable survival analyses adjusted for
demographic and clinical variables that may affect mortality.
Results
The moderate and good adherence groups had significantly reduced adjusted
mortality hazard ratios of 0.83 (95% CI 0.78–0.88) and 0.86 (95% CI
0.82–0.90) respectively, compared with the non-adherence group.
Conclusions
Adherence to antidepressant pharmacotherapy is associated with reduced
all-cause mortality in a population-based large sample cohort of patients
with IHD. Physicians and health policy decision-makers should step up
their efforts to sustain and enhance these patients' adherence to their
antidepressant regimen.
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