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Impact of Influenza/RSV PCR Point-of-care Testing in the Emergency Medical Service.

Not Applicable
Conditions
Influenza
Interventions
Diagnostic Test: Rapid diagnosis of influenza in the emergency medical service
Registration Number
NCT04048369
Lead Sponsor
University Hospital, Clermont-Ferrand
Brief Summary

The purpose of the study is to compare Emergency Department patients who undergo influenza and RSV PCR testing using an FDA-approved point-of-care device (Cepheid Xpert® Xpress Flu/RSV) located in the ED, to patients who undergo influenza and RSV PCR testing at the core laboratory.

The principal purpose is to determine if the time spent in the ED is different in the group undergoing POC influenza testing compared to those undergoing laboratory-based influenza testing.

Detailed Description

* This study will be conducted during the influenza's epidemic season. The start and the end of this study will be determined using national epidemic bases (national reference center for inluenza in Lyon).

* Collection of consent of eligible patients after medical information by a senior emergency physician

* Sampling = nasopharyngeal swabbing for all patients using usual testing or point-of-care testing

* first arm : performing the test at the adult emergency department 24h/24

* second arm : sending the test to the virology laboratory and realization during working hours

* Collection of clinical data : a specific standardized questionnaire is used, as soon as the patient is included and until he leaves the emergency medical service, to collect clinical data and the time taken to take care of the patient

In order to reduce the bias of this study, it has been established :

After verification of the eligibility criteria and obtaining the written consent of the patient, a randomization procedure will be initiated for the patient. Randomization will be centralized at the DRCI of Clermont-Ferrand University Hospital. Patients will be randomly assigned to one of the study groups by means of individual block randomization. A document describing the randomization procedure will be kept confidentially in the DRCI of Clermont-Ferrand University Hospital;

- The collection of data will be prospective.

A listing of patients opposing to the study's participation to verify that their characteristics are homogeneous to the general population The choice of the Genexpert® automaton used in the "point of care testing" arm whose principle of operation requires a minimum of manipulations (\<2 minutes) and does not generate inter-operator variability Statistical analyzes will be performed with the Stata software (version 13, StataCorp, College Station). All statistical tests will be carried out at the risk of error of the first species α of 5%. Part of the analysis of the secondary endpoints should be primarily exploratory in nature. As discussed by Feise in 2002 (Feise RJ, Do 2: 8), the adjustment of the risk of error of 1st species will not be proposed systematically, but case by case in view of clinical considerations and not just statistical ones.

Continuous variables will be presented as mean and standard deviation, subject to the normality of their distribution (Shapiro-Wilk test if necessary). In case of non-normality, they will be presented as median, quartiles, and extreme values. The qualitative variables will be expressed in numbers and percentages associated. Graphic representations will be associated with these analyzes as much as possible.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
431
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Point-of-care testing armRapid diagnosis of influenza in the emergency medical servicefor patients randomized to the Point-of-care testing arm, nurse will perform influenza and RSV testing using an FDA-approved point-of-care device (Cepheid Xpert® Xpress Flu/RSV) in the ED, 24/24, 7/7.
Core Lab testing armRapid diagnosis of influenza in the emergency medical servicefor patients randomized to the Core lab testing arm, influenza/RSV PCR will be performed in the core virology laboratory using Simplexa Flu A/B and RSV direct (r) assay (Diasorin), during working hours (8 am-6pm Monday to Friday, 8 am-5pm the Saturday)
Primary Outcome Measures
NameTimeMethod
Time of care in the adult emergency departmentthrough study completion, an average of 1 week

Emergency care time, calculated from the time of first medical-care contact to the time of release of the adults emergency department.

This time will be calculated from the data collected on the standardized questionnaire

Secondary Outcome Measures
NameTimeMethod
Prescription of antibiotics initiated at the adults emergency departmentwithin 72 hours after taking care of the patient

nature of antibiotics

Costs of the prescription of imaging tests at the adults emergency departmentwithin 72 hours after taking care of the patient

Costs of examinations related to the patient respiratory pathology (euros)

Number of prescription of biology examinationswithin 72 hours after taking care of the patient

Number of laboratory examinations related to respiratory pathology

Duration of the prescription of antibiotics initiated at the adults emergency departmentwithin 72 hours after taking care of the patient

duration of treatment (day)

Costs of antibiotics initiated at the adults emergency departmentwithin 72 hours after taking care of the patient

associated costs (euros)

Prescription of antiviral initiated in adults emergency departmentwithin 72 hours after taking care of the patient

nature of antiviral prescription

Duration of the specific antiviral prescription initiated in adults emergency departmentwithin 72 hours after taking care of the patient

duration of treatment (day)

Costs of specific antiviral prescription initiated in adults emergency departmentwithin 72 hours after taking care of the patient

associated costs (euros)

Posology of antibiotics initiated at the adults emergency departmentwithin 72 hours after taking care of the patient

posology (mg)

Type of prescription of imaging tests at the adults emergency departmentwithin 72 hours after taking care of the patient

type of examinations related to the patient respiratory pathology

Number of prescription of imaging tests at the adults emergency departmentwithin 72 hours after taking care of the patient

Number of examinations related to the patient respiratory pathology

Costs of prescription of biology examinationswithin 72 hours after taking care of the patient

Costs of laboratory examinations related to respiratory pathology (euros)

Type of prescription of biology examinationswithin 72 hours after taking care of the patient

type of laboratory examinations related to respiratory pathology

Trial Locations

Locations (1)

CHU de Clermont-Ferrand

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Clermont-Ferrand, Auvergne, France

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