SIRS in Cyanotic and Acyanotic Children in Cardiac Surgery
NCT ID: NCT04254744
Last Updated: 2021-03-15
Study Results
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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COMPLETED
197 participants
OBSERVATIONAL
2020-02-04
2021-02-04
Brief Summary
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Detailed Description
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Children with congenital cyanotic heart disease (CCHD) have complex changes in all blood values and clotting profiles due to chronic hypoxemia. Increased erythrocyte count decreases plasma and coagulation factors, platelet count and function. Therefore, blood and blood products transfusion may increase during intraoperative and postoperative periods. In addition, durations of cardiopulmonary bypass may prolong due to the complex defects of children with CCHD. Previous studies have reported that the duration of CPB and the amount of fresh frozen plasma transfusion increase SIRS formation.
The aim of this study is to investigate postoperative SIRS rates and risk factors in cyanotic and acyanotic children undergoing open heart surgery for congenital heart disease.
Patients aged between 0-16 years and undergoing open heart surgery for cyanotic and acyanotic congenital heart disease will be included in the study. Patients with preoperative renal failure or hepatic disease will be excluded. Patient's age, weight, comorbidities, details of previous operation will be recorded. Preoperative hematocrit value, white blood cell and platelet counts, biochemical parameters (blood urea nitrogen, creatinine, electrolyte values), diagnosis of CCHD, RACHS1 (risk adjustment for surgery for congenital heart disease) will be recorded. In intraoperative period; operation time, CPB time, aortic cross-clamp time, circulatory arrest time, body temperature and lowest body temperature reached during CPB, cardioplegia amount, The ACT (activated coagulation time), urine amount will be recorded. Intraoperative blood gas values, lactate, mean arterial pressure, glucose values will be recorded at 30 min intervals. The amount of crystalloid and colloid, erythrocyte, fresh frozen plasma, platelet and cryoprecipitate used in intraoperative period will be recorded. Heparin and protamine doses administered will be recorded. Vasoactive agents (dopamine, dobutamine, adrenaline, nitroglycerine) used in intraoperative period will be recorded.
During the postoperative intensive care period; arterial blood gases and lactate, hematocrit, liquid (crystalloid and colloid) and blood products administered will be monitored at 6th, 24th and 48th hours. The vasoactive agents used, the inotropic score, the amount of urine and the use of diuretics will be recorded. Length of stay ICU, duration of mechanical ventilation, length of stay hospital will be recorded.
Diagnosis of SIRS; in the postoperative period, the age-specific SIRS criteria determined by the International Pediatric Sepsis Consensus Conference will be used. Patients will be evaluated for the diagnosis of SIRS at postoperative 6th, 12th, 24th and 48th hours. SIRS rates and risk factors in cyanotic and acyanotic patients will be determined.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Acyanotic children
Acyanotic children undergoing cardiac surgery due to congenital heart disease
Sevoflurane
Sevoflurane inhalation for anesthesia
Cyanotic children
Cyanotic children undergoing cardiac surgery due to congenital heart disease
Sevoflurane
Sevoflurane inhalation for anesthesia
Interventions
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Sevoflurane
Sevoflurane inhalation for anesthesia
Eligibility Criteria
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Inclusion Criteria
* undergoing open heart surgery for cyanotic and acyanotic congenital heart disease
Exclusion Criteria
* Patients with preoperative hepatic disease
* Patients with preoperative inflammatory disease
* Patients using anti-inflammatory drug
1 Month
16 Years
ALL
No
Sponsors
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Cukurova University
OTHER
Responsible Party
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Feride Karacaer
Associated professor
Locations
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Cukurova University
Adana, , Turkey (Türkiye)
Countries
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Other Identifiers
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SIRS, cardiac surgery
Identifier Type: -
Identifier Source: org_study_id
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