lung cancer
Conditions
Interventions
Conventional liquid therapy group:conventional fluid therapy
Target oriented liquid therapy group:Targeted liquid therapy guided by dynamic monitoring of ? SV using TEE
Sponsors
Xuzhou Central Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Age>18 years old; 2. ASA grades I-III; 3. BMI 15~30 kg/m^2.
Exclusion criteria
Exclusion criteria: 1. Individuals with contraindications for TEE; 2. Individuals with severe cardiovascular, brain, lung, liver, and kidney diseases; 3. Surgical duration<1 hour; 4. Refuse to participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative Recovery Quality Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Arterial blood lactate, aLac;Centrol venous-to-arterial carbon dioxided tension difference, Pcv-aCO2;Centrol venous oxygen saturation, ScvO2;Oxygen delivery index, DO2I;heart rate;blood pressure;Incidence of postoperative cognitive impairment;VAS scores;Postoperative complications;Inflammatory factor levels;Infusion volume;Liquid output;Number of cases of vasoactive drug use;Pull out time;PACU stay time;First exhaust time after surgery;Removal time of drainage tube;Postoperative hospitalization days; | — |
Countries
China
Contacts
Public ContactMeng Xiangdi
Xuzhou Central Hospital
Outcome results
None listed