pulmonary edema
Conditions
Interventions
Phenylephrine group (P Group) :During the operation, the experimental drug was pumped continuously, the initial dose was 10ml/h, and the infusion speed of the experimental drug was adjusted to maintai
Control group:During the operation, 10ml/h of normal saline was pumped continuously
Sponsors
Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: (1) Patients undergoing elective hysteroscopic type 2 or type 3 hysteromyomectomy under general anesthesia; (2) Age 18-60; (3) ASA I-II level; (4) The expected operation time is more than 30 minutes.
Exclusion criteria
Exclusion criteria: (1) Patients with BMI greater than 35kg/m2; (2) Pregnant or lactating patients; (3) Patients with a history of abnormal surgical anesthesia; (4) Patients with cardiovascular and cerebrovascular diseases, such as hypertension, coronary heart disease or cerebrovascular malformations; (5) The patient refuses the participant; (6) Patients with height less than 150cm; (7) Patients with body weight less than 45kg; (8) Patients with cardiopulmonary insufficiency.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of pulmonary edema; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pulmonary ultrasound B line score;Hemodynamic parameters of TEB;Loss of Distention fluid;Electrolytes, Hemoglobin and HCT in blood gas analysis;Surgical visual field clarity score;Blood loss;Adverse event; | — |
Countries
China
Contacts
Public ContactJiawei Chen
Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed