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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05172479
Other study ID # ACH-2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 12, 2021
Est. completion date September 11, 2023

Study information

Verified date September 2023
Source Aseer Central Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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).


Description:

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).


Recruitment information / eligibility

Status Completed
Enrollment 3274
Est. completion date September 11, 2023
Est. primary completion date September 11, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
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.
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.
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.
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.
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.

Locations

Country Name City State
Bahrain Bahrain Defence Force Hospital Ar Rifa' Southern Governorate
Bahrain King Hamad University Hospital Muharraq
Kuwait Amiri Hospital Kuwait
Oman Armed Forces Hospital Oman Muscat
Qatar Hamad Medical Corporation Doha
Saudi Arabia Aseer Central Hospital (ACH) Abha Aseer Province
Saudi Arabia North Medical Tower Arar Northern Borders Province
Saudi Arabia King Fahad Specialist Hospital Dammam Eastern Province
Saudi Arabia Johns Hopkins Aramco Healthcare Dhahran Eastern Province
Saudi Arabia King Abdulaziz University Hospital Jeddah Makkah Al Mukarramah Province
Saudi Arabia King Fahd Armed Forces Hospital Jeddah Makkah Al Mukarramah Province
Saudi Arabia Royal Commission Hospital in Jubail Jubail Eastern Province
Saudi Arabia Armed Force Hospital Southern Region-Khamis Mushayt (AFHSR-KM) Khamis Mushait Aseer Province
Saudi Arabia King Abdullah bin Abdulaziz University Hospital (KAAUH) Riyadh Riyadh Province
Saudi Arabia King Fahad Medical City (KFMC) Riyadh Riyadh Province
Saudi Arabia King Saud Medical City (KSMC) Riyadh Riyadh Province
Saudi Arabia Sulaiman Al-Habib Hospital Riyadh
Turkey Kocaeli University Hospital Kocaeli
United Arab Emirates Sheikh Shakhbout Medical City Abu Dhabi
United Arab Emirates Rashid Hospital Dubai

Sponsors (3)

Lead Sponsor Collaborator
Aseer Central Hospital Armed Force Hospital Southern Region-Khamis Mushayt (AFHSR-KM), King Khalid University (KKU)

Countries where clinical trial is conducted

Bahrain,  Kuwait,  Oman,  Qatar,  Saudi Arabia,  Turkey,  United Arab Emirates, 

References & Publications (1)

Algarni AM, Alfaifi MS, Bshabshe AAA, et al. 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): protocol for an international multicentre prospective external validation cohort study. medRxiv. 2022.2019.22272537.

Outcome

Type Measure Description Time frame Safety issue
Primary In-hospital mortality Mortality rate during hospitalization of patient 30 days
Secondary Intensive care unit admission Number of participants admitted to an intensive care unit 30 days
Secondary Length of stay in the intensive care unit Stay in intensive care unit >72 hours 30 days
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