Prognostic Accuracy of qSOFA, SIRS, and EWSs for In-hospital Mortality in Emergency Department

NCT ID: NCT05172479

Last Updated: 2023-09-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

3274 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-12-12

Study Completion Date

2023-09-11

Brief Summary

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Early identification of a patient with infection who may develop sepsis is of utmost importance. Unfortunately, this remains elusive because no single clinical measure or test can reflect complex pathophysiological changes in patients with sepsis. However, multiple clinical and laboratory parameters indicate impending sepsis and organ dysfunction. Screening tools using these parameters can help identify the condition, such as SIRS, quick SOFA (qSOFA), National Early Warning Score (NEWS), or Modified Early Warning Score (MEWS). The 2016 SCCM/ESICM task force recommended using qSOFA, while the 2021 Surviving Sepsis Campaign strongly recommended against its use compared with SIRS, NEWS, or MEWS as a single screening tool for sepsis or septic shock. We hypothesised that qSOFA has greater prognostic accuracy than SIRS and EWS (NEWS/NEWS2/MEWS).

Detailed Description

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Over the past decade, medical advances in sepsis continued to focus on sepsis as a prevalent condition that accounts for 10% of admissions to intensive care units (ICUs) and is associated with a 10-20% in-hospital mortality rate. Standardised protocols and physician awareness have significantly improved survival, but mortality rates remain between 20% and 36%, with \~270,000 deaths annually in the United States. However, of patients with sepsis, 80% are treated in an emergency department (ED), and the remainder develops sepsis during hospitalisation with other conditions. In 2016, the Society of Critical Care Medicine/European Society of Intensive Care Medicine (SCCM/ESICM) task force redefined sepsis based on organ dysfunction and mortality prediction. Sepsis now is defined as life-threatening organ dysfunction caused by dysregulated host response to infection. This definition emphasises the complexity of the disease that cannot be explained by infection or body response to it. Acute change in Sequential Organ Failure Assessment (SOFA) score ≥2 indicates sepsis-related organ dysfunction, a predictor of excess in-hospital mortality. Systemic Inflammatory Response Syndrome (SIRS) and "severe sepsis" terms were omitted from the most recent definition. SIRS has been criticised for its poor specificity, while "severe sepsis" may underestimate sepsis's seriousness. A subset of patients may develop septic shock with underlying profound organ dysfunction and excess mortality. Clinically, septic shock is defined as persistent hypotension requiring vasopressors to maintain mean arterial pressure (MAP) ≥ 65 mm Hg and serum lactate level ≥ 2 mmol/L (18 mg/dL) despite adequate volume resuscitation. Early identification of a patient with infection who may develop sepsis is of utmost importance. Unfortunately, this remains elusive because no single clinical measure or test can reflect complex pathophysiological changes in patients with sepsis. However, multiple clinical and laboratory parameters indicate impending sepsis and organ dysfunction. Screening tools using these parameters can help identify the condition, such as SIRS, quick SOFA (qSOFA), National Early Warning Score (NEWS), or Modified Early Warning Score (MEWS). The 2016 SCCM/ESICM task force recommended using qSOFA, while the 2021 Surviving Sepsis Campaign strongly recommended against its use compared with SIRS, NEWS, or MEWS as a single screening tool for sepsis or septic shock. We hypothesised that qSOFA has greater prognostic accuracy than SIRS and EWS (NEWS/NEWS2/MEWS).

Conditions

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Sepsis Septic Shock

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Positive qSOFA

Adult patients with suspected infection and a qSOFA score ≥ 2 at the triage in the ED who are planned for hospitalization

Measurement of qSOFA score

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's qSOFA score.

Negative qSOFA

Adult patients with suspected infection and a qSOFA score \< 2 at the triage in the ED who are planned for hospitalization

Measurement of qSOFA score

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's qSOFA score.

Positive SIRS

Adult patients with suspected infection and a SIRS criteria ≥ 2 at the triage in the ED who are planned for hospitalization

Measurement of SIRS criteria

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's SIRS criteria.

Negative SIRS

Adult patients with suspected infection and a SIRS criteria \< 2 at the triage in the ED who are planned for hospitalization

Measurement of SIRS criteria

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's SIRS criteria.

Positive NEWS

Adult patients with suspected infection and a NEWS ≥ 5 or red score (i.e., a score of 3 in any one parameter) at the triage in the ED who are planned for hospitalization

Measurement of NEWS

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS.

Negative NEWS

Adult patients with suspected infection and a NEWS \< 5 at the triage in the ED who are planned for hospitalization

Measurement of NEWS

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS.

Positive NEWS2

Adult patients with suspected infection and a NEWS2 ≥ 5 or red score (i.e., a score of 3 in any one parameter) at the triage in the ED who are planned for hospitalization

Measurement of NEWS2

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS2.

Negative NEWS2

Adult patients with suspected infection and a NEWS2 \< 5 at the triage in the ED who are planned for hospitalization

Measurement of NEWS2

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS2.

Positive MEWS

Adult patients with suspected infection and a MEWS ≥ 5 at the triage in the ED who are planned for hospitalization

Measurement of MEWS

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's MEWS.

Negative MEWS

Adult patients with suspected infection and a MEWS \< 5 at the triage in the ED who are planned for hospitalization

Measurement of MEWS

Intervention Type DIAGNOSTIC_TEST

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's MEWS.

Interventions

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Measurement of qSOFA score

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's qSOFA score.

Intervention Type DIAGNOSTIC_TEST

Measurement of SIRS criteria

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's SIRS criteria.

Intervention Type DIAGNOSTIC_TEST

Measurement of NEWS

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS.

Intervention Type DIAGNOSTIC_TEST

Measurement of NEWS2

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's NEWS2.

Intervention Type DIAGNOSTIC_TEST

Measurement of MEWS

At the patient's arrival to the ED triage, the nurse will enter the patient's vital signs data into electronic data capture (EDC) system that will calculate the patient's MEWS.

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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quick Sequential Organ Failure Assessment (qSOFA) Systemic inflammatory response syndrome (SIRS) National Early Warning Score (NEWS) National Early Warning Score 2 (NEWS2) Modified Early Warning Score (MEWS)

Eligibility Criteria

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Inclusion Criteria

1. Adult patients (age ≥18 years),
2. Suspected infection (based on the opinion of the emergency physician),
3. Planned for hospitalization,
4. Willing to give oral informed consent (if required by recruiting center's IRB).

Exclusion Criteria

1. Presentation to ED is not due to infection (e.g., autoimmune diseases, myocardial infarction, stroke, venous thromboembolism, trauma, intoxication … etc.),
2. Pregnancy,
3. Transferred from another hospitals,
4. Code status is "Do-Not-Resuscitate" (DNR)
5. Elective admission through ED
6. Initial diagnosis of infection in the ED was not confirmed after finishing of the recruitment and follow-up phase.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Armed Force Hospital Southern Region-Khamis Mushayt (AFHSR-KM)

UNKNOWN

Sponsor Role collaborator

King Khalid University (KKU)

UNKNOWN

Sponsor Role collaborator

Aseer Central Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Abdullah M Algarni

Family medicine consultant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abdullah M Algarni, MBBS

Role: PRINCIPAL_INVESTIGATOR

Aseer Central Hospital (ACH)

Locations

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Bahrain Defence Force Hospital

Riffa, Southern Governorate, Bahrain

Site Status

King Hamad University Hospital

Al Muharraq, , Bahrain

Site Status

Amiri Hospital

Kuwait City, , Kuwait

Site Status

Armed Forces Hospital Oman

Muscat, , Oman

Site Status

Hamad Medical Corporation

Doha, , Qatar

Site Status

Aseer Central Hospital (ACH)

Abhā, Aseer Province, Saudi Arabia

Site Status

Armed Force Hospital Southern Region-Khamis Mushayt (AFHSR-KM)

Khamis Mushait, Aseer Province, Saudi Arabia

Site Status

King Fahad Specialist Hospital

Dammam, Eastern Province, Saudi Arabia

Site Status

Johns Hopkins Aramco Healthcare

Dhahran, Eastern Province, Saudi Arabia

Site Status

Royal Commission Hospital in Jubail

Jubail, Eastern Province, Saudi Arabia

Site Status

King Abdulaziz University Hospital

Jeddah, Makkah Al Mukarramah Province, Saudi Arabia

Site Status

King Fahd Armed Forces Hospital

Jeddah, Makkah Al Mukarramah Province, Saudi Arabia

Site Status

North Medical Tower

Arar, Northern Borders Province, Saudi Arabia

Site Status

King Abdullah bin Abdulaziz University Hospital (KAAUH)

Riyadh, Riyadh Region, Saudi Arabia

Site Status

King Fahad Medical City (KFMC)

Riyadh, Riyadh Region, Saudi Arabia

Site Status

King Saud Medical City (KSMC)

Riyadh, Riyadh Region, Saudi Arabia

Site Status

Sulaiman Al-Habib Hospital

Riyadh, , Saudi Arabia

Site Status

Kocaeli University Hospital

Kocaeli, , Turkey (Türkiye)

Site Status

Sheikh Shakhbout Medical City

Abu Dhabi, , United Arab Emirates

Site Status

Rashid Hospital

Dubai, , United Arab Emirates

Site Status

Countries

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Bahrain Kuwait Oman Qatar Saudi Arabia Turkey (Türkiye) United Arab Emirates

References

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Algarni AM, Alfaifi MS, Al Bshabshe AA, Omair OM, Alsultan MA, Alzahrani HM, Alali HE, Alsabaani AA, Alqarni AM, Alghanem SA, Al Mufareh BS, Almemari AM, Sindi AA, Ozturan IU, Alhadhira AA, Shujaa AS, Alotaibi AH, Awladthani MM, Alsaad AA, Almarshed AA, AlQahtani AM, Harris TR, Alyahya BA, Assiri SA, Abuzeyad FH, Kazim SN, Al-Fares AA, Almazroua FY, Marzook NT, Basri AA, Elsafti AM, Alalshaikh AS, Ozturan CA, Alawad YI, AlOmari A, Alkhateeb MA, Farooq MM, AlMutairi LA, Alasfour MM, Al Haber MI, Umar UA, Bokhary NH, Alqahtani SF, Almutairi A, Alyahya HF, Alzahrani WS, Alsalmi F, Omair AM, Alasmari FM, Alfifi SY, Al-Nujimi MS, Foroutan F. Prognostic accuracy of qSOFA score, SIRS criteria, and EWSs for in-hospital mortality among adult patients presenting with suspected infection to the emergency department (PASSEM) Multicenter prospective external validation cohort study protocol. PLoS One. 2024 Jan 17;19(1):e0281208. doi: 10.1371/journal.pone.0281208. eCollection 2024.

Reference Type BACKGROUND
PMID: 38232095 (View on PubMed)

Related Links

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Other Identifiers

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ACH-2

Identifier Type: -

Identifier Source: org_study_id

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