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Clinical Trials/NCT01353157
NCT01353157
Completed
N/A

Prediction for Systemic Inflammation With Clinical Scoring Systems and Inflammatory Cytokine Levels in Adult Cardiac and Major Abdominal Surgical Patients

Khon Kaen University1 site in 1 country20 target enrollmentMarch 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Heart; Dysfunction Postoperative, Cardiac Surgery
Sponsor
Khon Kaen University
Enrollment
20
Locations
1
Primary Endpoint
Correlation of clinical scoring systems and inflammatory cytokine levels
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Cardiac surgery with cardiopulmonary bypass (CPB) and hepatic surgery are major operations, associated with a systemic inflammatory response syndrome. The aim of this study is to assess the effectiveness of clinical scoring systems and inflammatory cytokine levels for predicting systemic inflammation. This correlation might identify peri-operative clinical outcomes, then forecast further systemic inflammation in cardiac and hepatic surgical patients.

Detailed Description

Systemic inflammatory response syndrome (SIRS) is commonly found in most major surgery. Early detection of SIRS will lead to early treatment. Serum cytokines levels are reliable markers for SIRS detection but with high cost and inconvenience. Clinical Scoring Systems are commonly used for assessment of patients with SIRS. If they have good correlation with cytokine levels, they might be used to predict peri-operative clinical outcomes.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
December 2010
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • adult patients who had undergone elective cardiac surgery with CPB

Exclusion Criteria

  • under 18 years of age
  • needing emergency surgery
  • needing intra-aortic balloon pump

Outcomes

Primary Outcomes

Correlation of clinical scoring systems and inflammatory cytokine levels

Time Frame: 24 h after CPB

Blood samples were collected sequentially at 0, 0.5, 4, 12, and 24 h after CPB for cytokines \[Interleukin (IL)-6, IL-8, and IL-10\] investigation and leukocyte counts. Clinical scoring systems \[Acute Physiology and Chronic Health Evaluation (APACHE) II, Sequential Organ Failure Assessment (SOFA) and Multi-Organ Dysfunction (MOD)\] were calculated and recorded at each time point. Correlations were assessed.

Study Sites (1)

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