Blood Levels of Sevoflurane and Desflurane
Study Details
Study Description
Brief Summary
16 patients with American Society of AnesthesioIogy (ASA) physical status I-III will recruited to this study. Patients will divided to the 2 groups. %1.5 Sevoflurane will apply in Group S and %6 Desflurane will apply in Group D. Each groups will divide 2 subgroups. Two lung ventilation will be performed to Group Sa and Group Da, one lung ventilation will be performed to Group Sb and Group Db. At the time point 40.minutes first blood sample will given from patients. Blood sample will be taken at intervals of 10 minutes from groups of two lung ventilation. In groups of one lung ventilation, blood samples will be taken at the time interval of 10 minutes after one lung ventilation started. All blood samples will be assess in Gas Chromatography.
Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
Investigator aimed to assess blood level of sevoflurane and desflurane during two lung ventilation and one lung ventilation. The investigators will use Gas Chromatography for define drugs levels. 16 patients with ASA I-III patients who undergo thoracotomy and abdominal surgery will be recruited to this study. Patients will divided in to the 2 groups. %1.5 Sevoflurane will apply in Group S and %6 Desflurane will apply in Group D during anesthesia maintenance. Each groups will divide 2 subgroups which are one lung ventilation groups and two lung ventilation groups. Two lung ventilation will be performed to Group Sa and Group Da, one lung ventilation will be performed to Group Sb and Group Db. Sequential blood samples will be taken from both arterial and central venous canula at the same time point. First blood samples will be taken at 40. minutes of anesthesia. Sequential samples will be taken at interval of 10 minutes during two lung ventilation. In one lung ventilation second blood samples will be taken at the 10. minutes of one lung ventilation. After than at the interval of 10 minutes, collection of blood samples both arterial and central venous will be continue.
All collection will assess with gas chromatography.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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two lung ventilation of Sevoflurane In GroupSa, 1,5 % sevoflurane will be apply continuously and blood samples will be taken at intervals of 10 minutes starting from the 40th minute. |
Drug: Sevoflurane
Measurement of blood desflurane level during one lung ventilation
Other Names:
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one lung ventilation of Sevoflurane In GroupSa, 1,5 % sevoflurane will be apply continuously and first samples will taken at the 40. minutes and collection of blood samples will be continue at intervals of 10 minutes after one lung ventilation started. |
Drug: Sevoflurane
Measurement of blood desflurane level during one lung ventilation
Other Names:
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two lung ventilation of Desflurane In GroupSa, 6 % desflurane will be apply continuously and blood samples will be taken at intervals of 10 minutes starting from the 40th minute. |
Drug: Desflurane
Measurement of blood desflurane level during one lung ventilation
Other Names:
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one lung ventilation of desflurane In GroupSa, 6 % desflurane will be apply continuously and first samples will taken at the 40. minutes and collection of blood samples will be continue at intervals of 10 minutes after one lung ventilation started. |
Drug: Desflurane
Measurement of blood desflurane level during one lung ventilation
Other Names:
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Outcome Measures
Primary Outcome Measures
- Measurement of blood levels of Sevoflurane and Desflurane [from 40th minute to the end of the operation]
Data collections will be ensured from arterial and venous blood sample and than samples will be assessed with gas chromatography and blood sevoflurane and desflurane level will be measured. Blood samples will take every 10 minutes. Only blood levels of sevoflurane and desflurane will be assessed.
Secondary Outcome Measures
- determine of ventilation-perfusion mismatch with p(A-a)O2 [from 40th minute to the end of the one lung ventilation]
During one lung ventilation, p(a-A)O2 will be assessed with arterial blood analyses
Eligibility Criteria
Criteria
Inclusion Criteria: ASA I-II patients
- Who undergo thoracotomy or abdominal surgery
Exclusion Criteria:
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ASA IV and up patients
-
Patients who taken inotropic agent
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Ebru Biricik | Adana | In The USA Or Canada, Please Select... | Turkey | 01380 |
Sponsors and Collaborators
- Cukurova University
Investigators
- Principal Investigator: Ebru Biricik, MD, Cukurova University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- One lung ventilation