Impact of Interventions on Admissional SOFA Score on Clinical Outcomes of Critically Ill Patients

April 17, 2024 updated by: José Raimundo Araujo de Azevedo, Hospital Sao Domingos

Introduction: The SOFA score (Sequential Organ Function Assessment) and its derived measures, such as the Delta SOFA, are used worldwide to determine the severity and prognosis of critically ill patients.

Objectives: The primary objective of this study was to assess the impact of standardized interventions on the six organ dysfunctions of SOFA score on outcomes of critically ill patients through the 48-hour delta SOFA with evaluation of the effectiveness of the interventions performed. Result will be correlated with the 28-day mortality.

The secondary outcome measures comprised the evaluation of standardized interventions on ICU and hospital length of stay; vasopressor-free and ventilator-free days within the 28 days following ICU admission, through the effectiveness of interventions performed Uni and multivariate statistical analysis will be used to determine organ failures associated to outcome.

Study Overview

Status

Completed

Detailed Description

This prospective, observational cohort study will include patients admitted to a medical ICU (12 beds), a surgical ICU (13 beds), and a high complexity surgical and trauma ICU (12 beds). of a tertiary hospital from August 01, 2023 to January31, 2024. The trial will include all patients aged above 18 years, admitted to the ICU for at least 3 days. Patients will be excluded for the following reasons: if they are pregnant, moribund and patients readmitted to the ICU in the same hospital admission.

For the patients who met the inclusion criteria, we will collect the demographic data regarding the age, gender, the admission category (medical or surgical), the primary admission diagnosis, the simplified acute physiology score III (SAPS 3), admission sequential organ failure assessment (SOFA) and 48-hour SOFA.

Whenever the admission SOFA score is ≥ 2, the result will be presented to the attending physician who will establish in the therapeutic plan the interventions for each of the dysfunctions identified according to a standardized intervention protocol (Table 1). After 48 hours, a new SOFA score is determined, while the prospective clinical surveillance team simultaneously identify if the interventions proposed by the protocol for each of the organ dysfunctions were effectively implemented.

Three groups of patients will be identified based on their SOFA scores at admission and the 48-hour delta SOFA values: those with an admission SOFA score < 2 (Group1), those with an admission SOFA score ≥ 2 whose delta SOFA reflected improvement at the end of 48 hours after admission (SOFA after 48 hours < SOFA on admission) (Group 2, n= ) and finally, those with an admission SOFA score ≥ 2 whose SOFA score increased or remained unchanged at the end of 48 hours postadmission (SOFA after 48 hours ≥ admission SOFA) (Group 3, n= ). The effectiveness of the interventions on organic disfunction will be evaluated in the groups 2 and 3 through the formula:

Number of patients with an organic disfunction and effective intervention / Number of patients with that organic dysfunction X 100

Results will be correlated with 28-day mortality.

Table 1. SOFA standardized protocol

  1. Respiratory Protective mechanical ventilation; mechanical power < 16 NIV Prevention of P-SILI: ROX and HACOR index
  2. Hemodynamic SOSD protocol; Pressoric target; Lactate clearance
  3. Neurologic Image; EEG; Sedation goals
  4. Hematologic Basic disease approach; drugs; DDAVP use; platelet transfusion
  5. Renal Avoid nephrotoxicity; Avoid hypotension
  6. Hepatic Avoid hepatotoxic drugs; basic disease approach.

NIV, Non-invasive ventilation; P-SILI, patient self-inflicted lung injury; ROX, ratio of oxygen saturation index; HACOR, Heart rate, acidosis, consciousness oxygenatrion and respiratory rate; SOSD, salvage, optimization, stabilization and de-escalation; DDAVP, 1-desamino-8-d-arginine-vasopresssin.

Study Type

Observational

Enrollment (Actual)

849

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

    • MA
      • Sao Luis, MA, Brazil, 65060-000
        • Hospital São Domingos

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

Sampling Method

Probability Sample

Study Population

Adult patients admitted to a medical ICU, a Surgical ICU and a High complexity surgical and trauma ICU in the period from April 01, 2023 to March 31, 2024 and lenght of stay of at least 3 days.

Description

Inclusion Criteria:

  • Patients aged above 18 years,
  • Lenght of ICU stay of at least 3 days.

Exclusion Criteria:

  • Pregnant patients
  • End-of-life
  • Patients readmitted to the ICU in the same hospitalization

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group 1
Patients with SOFA score < 2 at admission. No intervention
Group 2

Patients with SOFA score equal to or > 2 on admission and who improved after 48 hours of treatment.

Intervention focused on identified organ dysfunction(s)

Standardized interventions according organ dysfunction
Group 3

Patients with SOFA score equal to or > 2 on admission and who did not improve after 48 hours of treatment.

Intervention focused on identified organ dysfunction(s)

Standardized interventions according organ dysfunction

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of standardized interventions in respiratory dysfunction on 48-hour delta SOFA with evaluation of the effectiveness of the interventions performed.
Time Frame: 48 hours

Lung protective ventilation: Tidal volume = 6 ml/kg; Plateau pressure < 28 mmHg; driving pressue < 16 cm H2O; Mechanical power < 16 Joules/min; Prevention of self-inflicted lung injury (P-SILI): ROX index > 4.8 and HACOR < 5. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with respiratory dysfunction and effective intervention / Number of patients with respiratory dysfunction X 100

48 hours
Impact of standardized interventions in hemodinamic dysfunction on 48-hour delta SOFA
Time Frame: 48 hour

SOSD (salvage, optimization, stabilization and de-escalation ) protocol; mean arterial pressoric taget of at least 65 mm Hg, Lactate serum level < 19 mg/dL. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hemodinamic dysfunction and effective intervention / Number of patients with hemodinamica dysfunction X 100

48 hour
Impact of standardized interventions in neurologic dysfunction on 48-hour delta SOFA
Time Frame: 48 hour

Image: cranial CT; Electroencephalografic monitoring and RASS Score between -1 and +1 The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with neurologic dysfunction and effective intervention / Number of patients with neurologic dysfunction X 100

48 hour
Impact of standardized interventions in hematologic dysfunction on 48-hour delta SOFA
Time Frame: 48 hour

Basic disease approach; avoid drugs that interfere with coagulation; Platelet transfusion in case of hemohhage; DDAVP when indicated. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hematologic dysfunction and effective intervention / Number of patients with hematologic dysfunction X 100

48 hour
Impact of standardized interventions iin renal dysfunction on 48-hour delta SOFA
Time Frame: 48 hour

Avoid nephotoxic drugs; Mantain mean arterial blood pressure > 65 mmHg The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with renal dysfunction and effective intervention / Number of patients with renal dysfunction X 100

48 hour
Impact of standardized interventions in hepatic dysfunction on 48-hour delta SOFA
Time Frame: 48 hour

Avoid hepatotoxic drugs;basic disease approach The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hepatic dysfunction and effective intervention / Number of patients with hepatic dysfunction X 100

48 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of standardized interventions in respiratory dysfunction on ICU length of stay
Time Frame: 28 days

Lung protective ventilation: Tidal volume 6 ml/kg; Pateau pressure < 28 mmHg; driving pressue < 16 cm H2O; Mechanical power < 16 Joules/min; Prevention of self-inflicted lung injury (P-SILI): ROX index > 4.8 and HACOR < 5. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with respiratory dysfunction and effective intervention / Number of patients with respiratory dysfunction X 100

28 days
Impact of standardized interventions in hemodinamic dysfuction on ICU length of stay
Time Frame: 28 days

SOSD (salvage, optimization, stabilixation and de-escalation ) protocol; mean arterial pressoric taget of at least 65 mm Hg, Lactate serum level < 19 mg/dL. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hemodinamic dysfunction and effective intervention / Number of patients with hemodinamic dysfunction X 100

28 days
Impact of standardized interventions in neurologic dysfunction on ICU length of stay
Time Frame: 28 days

Image: cranial CT; Electroencephalografic monitoring and RASS Score between -1 and +1 The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with neurologic dysfunction and effective intervention / Number of patients with neurologic dysfunction X 100

28 days
Impact of standardized interventions in hematologic dysfunction on ICU length of stay
Time Frame: 28 days

Basic disease approach; avoid drugs that interfere with coagulation; Platelet transfusion in case of hemohhage; DDAVP when indicated. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hematologic dysfunction and effective intervention / Number of patients with hematologic dysfunction X 100

28 days
Impact of standardized interventions iin renal dysfunction on ICU length of stay
Time Frame: 28 days

Avoid nephotoxic drugs; Mantain mean arterial blood pressure > 65 mmHg The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with renal dysfunction and effective intervention / Number of patients with renal dysfunction X 100

28 days
Impact of standardized interventions in hepatic dysfunction on ICU length of stay
Time Frame: 28 days

Avoid hepatotoxic drugs;basic disease approach The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hepatic dysfunction and effective intervention / Number of patients with hepatic dysfunction X 100

28 days
Impact of standardized interventions in respiratory dysfunction on vasopressor-free days
Time Frame: 28 days

Lung protective ventilation: Tidal volume 6 ml/kg; Pateau pressure < 28 mmHg; driving pressue < 16 cm H2O; Mechanical power < 16 Joules/min; Prevention of self-inflicted lung injury (P-SILI): ROX index > 4.8 and HACOR < 5. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with respiratory dysfunction and effective intervention / Number of patients with respiratory dysfunction X 100

28 days
Impact of standardized interventions in hemodinamic dysfuction on vasopressor-free days
Time Frame: 28 days

SOSD (salvage, optimization, stabilixation and de-escalation ) protocol; mean arterial pressoric taget of at least 65 mm Hg, Lactate serum level < 19 mg/dL. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hemodinamic dysfunction and effective intervention / Number of patients with hemodinamic dysfunction X 100

28 days
Impact of standardized interventions in neurologic dysfunction on vasopressor-free days
Time Frame: 28 days

Image: cranial CT; Electroencephalografic monitoring and RASS Score between -1 and +1 The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with neurologic dysfunction and effective intervention / Number of patients with neurologic dysfunction X 100

28 days
Impact of standardized interventions in hematologic dysfunction on vasopressor-free days
Time Frame: 28 days

Basic disease approach; avoid drugs that interfere with coagulation; Platelet transfusion in case of hemohhage; DDAVP when indicated. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hematologic dysfunction and effective intervention / Number of patients with hematologic dysfunction X 100

28 days
Impact of standardized interventions iin renal dysfunction on vasopressor-free days
Time Frame: 28 days

Avoid nephotoxic drugs; Mantain mean arterial blood pressure > 65 mmHg The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with renal dysfunction and effective intervention / Number of patients with renal dysfunction X 100

28 days
Impact of standardized interventions in hepatic dysfunction on vasopressor-free days
Time Frame: 28 days

Avoid hepatotoxic drugs;basic disease approach The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hepatic dysfunction and effective intervention / Number of patients with hepatic dysfunction X 100

28 days
Impact of standardized interventions in respiratory dysfunction on ventilator-free days
Time Frame: 28 days

Lung protective ventilation: Tidal volume 6 ml/kg; Pateau pressure < 28 mmHg; driving pressue < 16 cm H2O; Mechanical power < 16 Joules/min; Prevention of self-inflicted lung injury (P-SILI): ROX index > 4.8 and HACOR < 5. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with respiratory dysfunction and effective intervention / Number of patients with respiratory dysfunction X 100

28 days
Impact of standardized interventions in hemodinamic dysfuction on ventilator-free days
Time Frame: 28 days

SOSD (salvage, optimization, stabilixation and de-escalation ) protocol; mean arterial pressoric taget of at least 65 mm Hg, Lactate serum level < 19 mg/dL. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hemodinamic dysfunction and effective intervention / Number of patients with hemodinamic dysfunction X 100

28 days
Impact of standardized interventions in neurologic dysfunction on ventilator-free days
Time Frame: 28 days

Image: cranial CT; Electroencephalografic monitoring and RASS Score between -1 and +1 The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with neurologic dysfunction and effective intervention / Number of patients with neurologic dysfunction X 100

28 days
Impact of standardized interventions in hematologic dysfunction on ventilator-free days
Time Frame: 28 days

Basic disease approach; avoid drugs that interfere with coagulation; Platelet transfusion in case of hemohhage; DDAVP when indicated. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hematologic dysfunction and effective intervention / Number of patients with hematologic dysfunction X 100

28 days
Impact of standardized interventions iin renal dysfunction on ventilator-free days
Time Frame: 28 days

Avoid nephotoxic drugs; Mantain mean arterial blood pressure > 65 mmHg The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with renal dysfunction and effective intervention / Number of patients with renal dysfunction X 100

28 days
Impact of standardized interventions in hepatic dysfunction on ventilator-free days
Time Frame: 28 days

Avoid hepatotoxic drugs;basic disease approach The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hepatic dysfunction and effective intervention / Number of patients with hepatic dysfunction X 100

28 days
Impact of standardized interventions in respiratory dysfunction on hospital length of stay
Time Frame: 60 days

Lung protective ventilation: Tidal volume 6 ml/kg; Pateau pressure < 28 mmHg; driving pressue < 16 cm H2O; Mechanical power < 16 Joules/min; Prevention of self-inflicted lung injury (P-SILI): ROX index > 4.8 and HACOR < 5. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with respiratory dysfunction and effective intervention / Number of patients with respiratory dysfunction X 100

60 days
Impact of standardized interventions in hemodinamic dysfuction on hospital length of stay
Time Frame: 60 days

SOSD (salvage, optimization, stabilixation and de-escalation ) protocol; mean arterial pressoric taget of at least 65 mm Hg, Lactate serum level < 19 mg/dL. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hemodinamic dysfunction and effective intervention / Number of patients with hemodinamic dysfunction X 100

60 days
Impact of standardized interventions in neurologic dysfunction on hospital length of stay
Time Frame: 60 days

Image: cranial CT; Electroencephalografic monitoring and RASS Score between -1 and +1 The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with neurologic dysfunction and effective intervention / Number of patients with neurologic dysfunction X 100

60 days
Impact of standardized interventions in hematologic dysfunction on hospital length of stay
Time Frame: 60 days

Basic disease approach; avoid drugs that interfere with coagulation; Platelet transfusion in case of hemohhage; DDAVP when indicated. The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hematologic dysfunction and effective intervention / Number of patients with hematologic dysfunction X 100

60 days
Impact of standardized interventions in renal dysfunction on hospital length of stay
Time Frame: 60 days

Avoid nephotoxic drugs; Mantain mean arterial blood pressure > 65 mmHg The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with renal dysfunction and effective intervention / Number of patients with renal dysfunction X 100

60 days
Impact of standardized interventions in hepatic dysfunction on hospital length of stay
Time Frame: 60 days

Avoid hepatotoxic drugs;basic disease approach The effectiveness of the interventions on organic disfunction will be evaluated through the formula:

Number of patients with hepatic dysfunction and effective intervention / Number of patients with hepatic dysfunction X 100

60 days

Collaborators and Investigators

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

Investigators

  • Study Director: JOSE R AZEVEDO, MD, PhD, Hospital São Domingos
  • Principal Investigator: BARBARA L RIBEIRO, MD, Hospital São Domingos

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

August 1, 2023

Primary Completion (Actual)

January 30, 2024

Study Completion (Actual)

March 31, 2024

Study Registration Dates

First Submitted

February 21, 2023

First Submitted That Met QC Criteria

March 16, 2023

First Posted (Actual)

March 30, 2023

Study Record Updates

Last Update Posted (Actual)

April 19, 2024

Last Update Submitted That Met QC Criteria

April 17, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • HSD 2023 1

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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