Trial record 13 of 204 for:    Open Studies | coronary artery bypass

Risk Factors of Sternal Wound Infection After Coronary Artery Bypass Graft

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by Samsung Medical Center
Sponsor:
Information provided by (Responsible Party):
Sangmin M. Lee, Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT01629030
First received: June 25, 2012
Last updated: July 8, 2014
Last verified: July 2014
  Purpose

The investigators are trying to evaluate the performance of neutrophil and lymphocyte counts as a risk factor of deep sternal wound infection after coronary artery bypass graft surgery.


Condition
Coronary Artery Bypass Graft
Median Sternotomy

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Risk Factors of Sternal Wound Infection After Coronary Artery Bypass Graft

Resource links provided by NLM:


Further study details as provided by Samsung Medical Center:

Primary Outcome Measures:
  • postoperative surgical wound infection [ Time Frame: within first week after the end of coronary artery bypass graft surgery ] [ Designated as safety issue: No ]
    postoperative surgical wound infection within first week after the end of coronary artery bypass graft surgery, classified as a superfical or deep sternal wound infection


Secondary Outcome Measures:
  • preoperative total leukocyte count [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    preoperative total leukocyte count

  • preoperative neutrophil count [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    preoperative neutrophil count

  • preoperative lymphocyte count [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    preoperative lymphocyte count

  • postoperative total leukocyte count [ Time Frame: 2 hour after the end of surgery ] [ Designated as safety issue: No ]
    postoprative total leukocyte count

  • postoperative neutrophil count [ Time Frame: 2 hour after the end of surgery ] [ Designated as safety issue: No ]
    postoperative neutrophil count

  • postoperative lymphocyte count [ Time Frame: 2 hour after the end of surgery ] [ Designated as safety issue: No ]
    postoperative lymphocyte count

  • preoperative NNIS risk index [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    preoperative NNIS risk index

  • preoperative EuroScore [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    preoperative EuroScore

  • Preoperative STS [ Time Frame: 1 day before surgery ] [ Designated as safety issue: No ]
    Preoperative STS (Society of Thoracic Surgeons risk score)

  • the incidence of surgical reopen with surgical wound infection [ Time Frame: within 1 month after surgery ] [ Designated as safety issue: No ]
    the incidence of surgical reopen with surgical wound infection


Estimated Enrollment: 1850
Study Start Date: June 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts
Coronary Artery Bypass Graft Group
Those underwent coronary artery bypass graft surgery with median sternotomy in Samsung Medical Center during the period of January 2008 and December 2011.

Detailed Description:

Deep sternal wound infection after coronary artery bypass graft is a very dangerous complication as it prolongs hospital stay, increase morbidity and mortality, and increase cost of care.

As a risk factor of surgical site infection, risk index reported by NNIS (national nosocomial infection surveillance), Euroscore, or Society of thoracic surgeon risk score are currently used. However, as various performances are reported regarding these index or scoring systems, and many factors are needed for these index or scoring system, there is a need to develop a more simple risk factor with better performance. We focused on the differential blood cell count, as the neutrophil and lymphocyte count are related to the degree of surgical invasion, and inflammatory response. Previous studies reported that the neutrophilia or lymphopenia is related to postoperative infection. Therefore, we are trying to evaluate the performance of preoperative or postoperative the blood cell differential count as a risk factor for sternal wound infection after coronary artery bypass surgery.

  Eligibility

Ages Eligible for Study:   20 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Those underwent coronary artery bypass graft surgery with median sternotomy in Samsung Medical Center during the period of January 2008 and December 2011.

Criteria

Inclusion Criteria:

  • Those underwent coronary artery bypass graft surgery with median sternotomy in Samsung Medical Center during the period of January 2008 and December 2011.

Exclusion Criteria:

  • Those underwent coronary artery bypass graft surgery with mini-thoracotomy
  • Those with insufficient study data recognized by electronic medical record
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01629030

Contacts
Contact: Sangmin M. Lee, MD, PhD 82-2-3410-0362 sangminm.lee@samsung.com
Contact: Won Ho Kim, MD 82-2-3410-1994 bullet57@naver.com

Locations
Korea, Republic of
Samsung Medical Center Recruiting
Seoul, Korea, Republic of, 135-710
Contact: Sangmin M. Lee, MD, PhD    82-2-3410-0362    sangminm.lee@samsung.com   
Contact: Won Ho Kim, MD    82-2-3410-1994    bullet57@naver.com   
Sub-Investigator: Sangmin M. Lee, MD, PhD         
Sub-Investigator: Young Tak Lee, MD, PhD         
Sponsors and Collaborators
Samsung Medical Center
Investigators
Principal Investigator: Sangmin M. Lee, MD, PhD Samsung Medical Center
Principal Investigator: Won Ho Kim, MD, PhD Samsung Medical Center
  More Information

No publications provided

Responsible Party: Sangmin M. Lee, Professor, Samsung Medical Center
ClinicalTrials.gov Identifier: NCT01629030     History of Changes
Other Study ID Numbers: 2012-05-067-001
Study First Received: June 25, 2012
Last Updated: July 8, 2014
Health Authority: South Korea: Institutional Review Board

Keywords provided by Samsung Medical Center:
sternal wound infection
coronary artery bypass graft
risk factor

Additional relevant MeSH terms:
Wound Infection
Infection
Wounds and Injuries

ClinicalTrials.gov processed this record on September 11, 2014