Renal outcomes related to intraoperative fluid therapy in abdominal hysterectomy
Conditions
Interventions
None listed
Sponsors
University of Health Sciences Istanbul Training and Research Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients aged between 18 and 65 years, classified as ASA physical status I and II, who underwent elective total abdominal hysterectomy under general anesthesia were included in the study.
Exclusion criteria
Exclusion criteria: Patients were excluded from the study if they met any of the following conditions: ASA score III and more, known renal failure, diabetes mellitus, use of diuretics, ischemic heart disease, congestive heart failure, cardiac arrhythmias, severe peripheral arterial disease, estimated blood loss greater than 20 percent of total volume, received blood transfusion, required more than 500 ml of colloid solution, needed vasopressor support, psychiatric conditions that impair ability to give informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome was defined as the measurements of urea, creatinine, eGFR, and urine density in the preoperative, postoperative period, and on the third postoperative day. No secondary outcome was specified. | — |
Countries
Europe
Contacts
Public ContactIREMGUL NALBAT
University of Health Sciences Istanbul Training and Research Hospital Anesthesiology and Reanimation
Outcome results
None listed