Inflammation Indıces and Mortality in Adult Crush Syndrome
The Association of Systemic Inflammation-Based Hematological Indices With APACHE II, SOFA and 28-Day Mortality in Adult Crush Syndrome: A Retrospective Cohort Study
1 other identifier
observational
325
1 country
1
Brief Summary
This retrospective observational cohort study aims to evaluate the prognostic value of inflammatory hematological indices, including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), and pan-immune-inflammation value (PIV), in predicting 28-day mortality in adult patients with crush syndrome admitted to the intensive care unit (ICU). Patients aged 18 years and older diagnosed with crush syndrome between January 1, 2018, and September 30, 2025, were included. The primary outcome is 28-day mortality. Secondary outcomes include ICU mortality and in-hospital mortality. The predictive performance of inflammatory indices will be compared with established severity scores such as APACHE II and SOFA.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 28, 2025
CompletedFirst Submitted
Initial submission to the registry
February 19, 2026
CompletedFirst Posted
Study publicly available on registry
February 25, 2026
CompletedFebruary 25, 2026
February 1, 2026
7.8 years
February 19, 2026
February 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
28-day All-Cause Mortality
All-cause mortality occurring within 28 days after intensive care unit (ICU) admission in adult patients diagnosed with crush syndrome.
28 Days
Secondary Outcomes (2)
ICU Mortality
During ICU stay (up to 28 days)
In-Hospital Mortality
During hospital stay (up to 90 days)
Eligibility Criteria
Adult patients diagnosed with crush syndrome and admitted to the intensive care unit of Ataturk University Hospital between January 2018 and September 2025.
You may qualify if:
- Age ≥18 years
- Diagnosis of crush syndrome based on clinical and laboratory findings
- Admission to the intensive care unit (ICU) between January 1, 2018 and September 30, 2025
- Availability of complete blood count parameters within the first 24 hours of ICU admission
You may not qualify if:
- Age \<18 years
- Incomplete medical records
- Missing laboratory data required for calculation of inflammatory indices
- Patients discharged or transferred within 24 hours of ICU admission
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ataturk University Research Hospital
Erzurum, 20100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Anesthesiology and Reanimation
Study Record Dates
First Submitted
February 19, 2026
First Posted
February 25, 2026
Study Start
January 1, 2018
Primary Completion
October 28, 2025
Study Completion
October 28, 2025
Last Updated
February 25, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share