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Prolonged Cardiopulmonary Bypass Time as Predictive Factor for in Hospital Infection

NCT ID: NCT04548167

Last Updated: 2021-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

7064 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-09-01

Study Completion Date

2021-10-22

Brief Summary

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This study is to analyse the demographics and microbiological factors concerning patients undergoing cardio surgical intervention using CPB complicated with bloodstream infection (BSI) postoperatively.

Detailed Description

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Infectious complications after cardiovascular surgery, especially in operations that use cardiopulmonary bypass (CPB), is associated with significant morbidity and increase in peri-operative mortality. Prolonged CPB usage could be predictive for early bloodstream infection following cardia surgery. This study is to analyse the demographics and microbiological factors concerning patients undergoing cardio surgical intervention using CPB complicated with bloodstream infection (BSI) postoperatively.

Conditions

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Bloodstream Infection (BSI)

Keywords

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cardiovascular surgery cardiopulmonary bypass (CPB) nosocomial infection early bloodstream infection postoperative septicaemia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* adult patients undergoing cardiac surgery

Exclusion Criteria

* patients having active or previous endocarditis
* patients whose causative microorganism of postoperative BSI was identical to that isolated from preoperative or intraoperative samples
* patients with common skin colonized microorganisms, such as coagulase-negative Staphylococci, Viridans group Streptococci, Corynebacterium species, Bacillus species, Propionibacterium species, and Aerococcus species or Micrococcus species, which were isolated from only a single blood sample and without evidence of clinical sepsis, because contamination was considered.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Basel, Switzerland

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Denis Berdajs, Prof. Dr. med.

Role: PRINCIPAL_INVESTIGATOR

Klinik für Herzchirurgie, University Hospital Basel

Locations

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Klinik für Herzchirurgie, University Hospital Basel

Basel, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2020-00210; ch20Berdajs2

Identifier Type: -

Identifier Source: org_study_id