DIAGNOSis of Infection in Emergency Department (DIAGNOSED)

Comparison of the Performance Indicators (Sensitivity and Specificity) of qSOFA, SIRS, NEWS, and RETTS Scores, for Diagnosis of the Infected Patient at the Emergency Department Triage

Septic pathology is an extremely frequent reason for consultation in our emergency services, with an annual incidence of severe forms between 50 to 95 cases per 100,000 inhabitants and a constant increase estimated at 9% per year. Diagnosing these patients early and precisely is a major challenge for the clinician, as this diagnosis will lead to more or less aggressive medical management.

The criteria of S.I.R.S, used to define and to sort patients in sepsis according to the old definition, were completely abandoned in the last recommendations for lack of specificity but also of sensitivity. The latest recommendations suggest using another score, the "Quick Sepsis Related Organ Failure Assesment (qSOFA) score", in order to early detect septic patients at risk of poor progress. However, the recent literature highlights a very low sensitivity of the qSOFA score for the screening of septic patients, ranging from 30 to 60% according to the studies. In addition to qSOFA, other scores are described in the literature with apparently higher sensitivity, and thus seem more suitable for our daily practice. Among them is the NEWS score or the RETTS score.

Each of these scores is again based upon the values of vital signs recorded as soon as the patient arrives in the emergency department. To date, very few studies have been interested, in a prospective way, in the sensitivity and the specificity of these different scores to diagnose the "infected" patients in the emergency departments.

Therefore a non-interventional, prospective, multicenter cohort study is carried out here, in order to be able to compare, on the same cohort of patients admitted into emergency services, the diagnostic performance of these different scores with respect to the presence or absence of an infection.

The aim of this study is to define the best clinical score to use in emergency medicine to quickly diagnose the infected patients, and offer them the best medical care.

Study Overview

Detailed Description

Septic pathology is an extremely frequent reason for consultation in our emergency services, with an annual incidence of severe forms between 50 to 95 cases per 100,000 inhabitants and a constant increase estimated at 9% per year. Diagnosing these patients early and precisely is a major challenge for the clinician, as this diagnosis will lead to more or less aggressive medical management with direct repercussions on the patient's morbidity and mortality.

The latest publications of March 2017 have completely changed the definition of the septic patient, in particular by eliminating the concept of "severe sepsis". Today the patient can be classified as either an "infected" or "sepsis" patient when there is associated organ failure, or as "septic shock" when it is necessary to use a cathecholaminergic support to maintain a sufficient blood pressure. There is a real nosological continuum between these three diagnostic entities and each of them is tainted by a growing intra-hospital mortality. One in ten patients will progress from infection to sepsis during their hospitalization and 3% of sepsis will progress to septic shock, making it easy to understand the value of screening these patients quickly in order to stop the progression of the infection. The triage of these patients, as soon as they arrive in an emergency service is therefore essential.

The criteria of S.I.R.S, used to define and to sort patients in sepsis according to the old definition, were completely abandoned in the last recommendations for lack of specificity but also of sensitivity. Indeed, a large number of non-septic patients presenting to the emergency department, has at least two SIRS criteria from the initial phase of their care, making it difficult to use this score as a reliable diagnostic tool.

The latest recommendations suggest using another score, the "Quick Sepsis Related Organ Failure Assesment (qSOFA) score", in order to early detect septic patients at risk of poor progress. This score is easily usable because it takes into account only three criteria that are: (i) the respiratory rate ≥ 22 / min, (ii) the systolic blood pressure ≤ 100 mmHg, (iii) and the level of vigilance of the patient to evaluate by the Glasgow score <15. Each criterion is weighted by 1 point if it is present. A score of qSOFA ≥2 is considered positive, and in this case the patient must be managed quickly with optimization of its volemia and implementation of a suitable antibiotic treatment within one hour.

However, the recent literature highlights a very low sensitivity of the qSOFA score for the screening of septic patients, ranging from 30 to 60% according to the studies. Such sensitivity values seem insufficient to properly screen septic patients in an emergency department. Some authors even report similar AUCs for qSOFA and SIRS at 0.72 and 0.73, respectively, to screen for the severe septic patient, concluding that the decision to abandon SIRS for qSOFA may be a little premature.

In addition to qSOFA, other scores are described in the literature with apparently higher sensitivity, and thus seem more suitable for our daily practice. Among them is the NEWS score or the RETTS score.

Each of these scores is again based upon the values of vital signs recorded as soon as the patient arrives in the emergency department, such as the respiratory rate, the heart rate, the oxygen saturation, the temperature, the blood pressure or the level of patient's vigilance.

A prospective cohort study of 1535 patients in emergency departments have compared the RETTS score to the qSOFA score showing a much better sensitivity of the RETTS score with a value of 85% against only 32% for qSOFA, for the screening of patients with severe sepsis according to the "SEPSIS-2" definition.

A recent study published in April 2017, compared qSOFA, SIRS, and NEWS to predict mortality or hospitalizations into intensive care units for septic patients in emergencies. Once again the qSOFA score showed a low sensitivity at 54% versus 67% for a NEWS score ≥ 8.

To date, several studies have compared the prognostic contribution of these different scores and their ability to predict mortality or even hospitalization in intensive care units, but very few studies have been interested, in a prospective way, in the sensitivity and the specificity of these different scores to diagnose the "infected" patients in the emergency departments. Whereas this first step seems essential in order to implement the most appropriate therapeutic strategy, today, if we stick to the recommendations, the diagnosis of the infected patient is based solely on the physician clinical feeling.

Therefore it seemed interesting to carry out a prospective, multicenter cohort study, in order to be able to compare, on the same cohort of patients admitted into emergency services, the diagnostic performance of these different scores (qSOFA, SIRS, NEWS, and RETTS ) with respect to the presence or absence of an infection.

Study Type

Observational

Enrollment (Actual)

759

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alpes Maritimes
      • Antibes, Alpes Maritimes, France, 06600
        • Centre Hospitalier d'Antibes
      • Grasse, Alpes Maritimes, France, 06130
        • Centre hospitalier de Grasse
      • Nice, Alpes Maritimes, France, 06001
        • Centre Hospitalier Universitaire de Nice
    • Bouches Du Rhône
      • Marseille, Bouches Du Rhône, France, 13005
        • Hopital de La Timone
      • Marseille, Bouches Du Rhône, France, 13005
        • Hopital Nord
    • Var
      • Toulon, Var, France, 83000
        • Hopital Saint Anne
      • Toulon, Var, France, 83000
        • Hôpital Sainte Musse

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

-Patients meeting the eligibility criteria from all participating investigational centers during the study period

Description

Inclusion Criteria:

  • Patient of 18 years old or more
  • Patients consulting in the emergency department
  • Verbal agrement to participate

Exclusion Criteria:

  • Patients consulting for an isolated traumatologic reason
  • Patients under legal protection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Initial vital signs upon arrival at ED triage to evaluate the qSOFA score
Time Frame: Timepoint 0 (ED triage)
  • Respiratory rate (movements per minute)
  • Systolic blood pressure (Hg mm)
  • Glasgow coma score (number from 0 to 15)

will be assessed to evaluate the qSOFA score (number from 0 to 3)

Timepoint 0 (ED triage)
Initial vital signs upon arrival at ED triage to evaluate the NEWS score
Time Frame: Timepoint 0 (ED triage)
  • Respiratory rate (movements per minute)
  • Pulsed SpO2 (%) with oxygen therapy (if applicable) and without oxygen therapy
  • Oxygen therapy (yes ou no)
  • Tympanic temperature (°C)
  • Systolic blood pressure (Hg mm)
  • Heart rate (beats per minute)
  • Glasgow coma score (number from 0 to 15)

will be assessed to evaluate the NEWS score (number from 0 to 20)

Timepoint 0 (ED triage)
Initial vital signs upon arrival at ED triage to evaluate the RETTS score
Time Frame: Timepoint 0 (ED triage)
  • Blocked airway or stridor (yes or no)
  • Respiratory rate (movements per minute)
  • Pulsed SpO2 (%) without oxygen therapy
  • Heart rate (beats per minute)
  • Level of conciousness (alert, accute disorientation, somnolence, Glasgow<9)
  • Tympanic temperature (°C)

will be assessed to evaluate the RETTS score (4 classes from "green" to "red")

Timepoint 0 (ED triage)
Initial vital signs upon arrival at ED triage and blood count to evaluate the SIRS score
Time Frame: Timepoint 0 (ED triage) and timepoint of blood sampling upon medical examination (average of 30 minutes after Timepoint 0)
  • Tympanic temperature (°C)
  • Heart rate (beats per minute)
  • Respiratory rate (movements per minute)
  • Leucocytemia (cells per mm³)

will be assessed to evaluate the SIRS score (number from 0 to 4)

Timepoint 0 (ED triage) and timepoint of blood sampling upon medical examination (average of 30 minutes after Timepoint 0)
Antibiotic therapy instauration by the physician either during the emergency care managment or when leaving the emergency department (antibiotic therapy mentionned in the exit prescrition)
Time Frame: from patient arrival in the ED, to his leaving (from 1 hour to 24 hours)
The prescription of an antibiotic therapy will define the presence of an infection
from patient arrival in the ED, to his leaving (from 1 hour to 24 hours)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Presence of a SOFA score value of 2 or greater
Time Frame: from patient arrival in the ED, to his leaving (from 1 hour to 24 hours)

The occurence of a SOFA score value of 2 or greater will define the presence of sepsis according to the last recommandations.

Vital signs to be recorded for the SOFA score evaluation:

  • Thrombocytemia (10^9/L)
  • Bilirubinemia (µmol/l)
  • Creatininemia (µmol/l)
  • Glasgow coma score
  • Average blood pressure (Hg mm)
  • Cathecholamine usage
  • Pa02/FiO2 ratio
from patient arrival in the ED, to his leaving (from 1 hour to 24 hours)
Overall survival at Day 28
Time Frame: Day 1 to Day 28 (from patient arrival in the ED, to the 28th day after)
Patient status will be collected in the patient file. Every patient leaving the hospital before Day 28 will be considered alive at Day 28.
Day 1 to Day 28 (from patient arrival in the ED, to the 28th day after)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 9, 2018

Primary Completion (Actual)

April 13, 2018

Study Completion (Actual)

September 1, 2018

Study Registration Dates

First Submitted

April 19, 2018

First Submitted That Met QC Criteria

October 12, 2018

First Posted (Actual)

October 17, 2018

Study Record Updates

Last Update Posted (Actual)

October 17, 2018

Last Update Submitted That Met QC Criteria

October 12, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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