Nausea and vomiting, post operative period, laparoscopic Cholecystectomy, women
Conditions
Interventions
80 female adult, between 18 and 70 years old, with Body Mass Index under 35, who belong to classification 1 and 2 of the American Society of Anesthesiology will be included, 40 patients by group.
kidney, located at the top of the cymba and below the antihelix bifurcation
sympathetic,between the inferior branch of the antihelix and the helix
stomach, which is at the area where the root of the helix ends
occipital, located in the upper back corner of the lateral side of the antitragus. Patients of control group will not be treated No treatment).
Anesthesia will be induced and maintained in both goups
Procedure/surgery
E02.190.044.133
Sponsors
Faculda de Ciências Médicas Universidade de Pernambuco
Faculda de Ciências Médicas Universidade de Pernambuco
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: adult females between; 18 and 70 years old; with Body Mass Index under 35; who belong to classification 1 and 2 of the American Society of Anaesthesiology; submitted to uncomplicated Laparoscopic cholecystectomy.
Exclusion criteria
Exclusion criteria: Laparoscopic cholecystectomy with surgical or anesthetic complications; operation time longer than 90 minutes; nausea and vomiting on the immediate preoperative time; patient ASA 3 or more; use of antiemetic 12 hours before the procedure; continuous use of analgesic or corticoids; abusive history of alcohol and drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1. Reduction in the number of vomiting episodes in the first six postoperative hours in the intervention group (AA), verifying through direct observation compared to the control group, with a significance of 5%. Events will be registered immediately after postanesthesia care unit admission and at the second, fourth, and sixth hours after the surgery. ;Expected outcome 2. Decreased intensity of nausea in the intervention group (AA) in relation to the control group, verified by visual analogue scale every two hours in the first six postoperative hours, with a significance of 5%. Events will be registered immediately after postanesthesia care unit admission and at the second, fourth, and sixth hours after the surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 3. Decreased demand for use of antiemetic drugs in the first six postoperative hours, verified by the direct observation of the researcher, upon spontaneous request of the patient. It is expected a decreased demand for drugs in the intervention group (AA) with a significance level of 5%. Events will be registered immediately after postanesthesia care unit admission and at the second, fourth, and sixth hours after the surgery. | — |
Countries
Brazil
Contacts
Public Contactluiz miranda
Faculda de Ciências Médicas Universidade de Pernambuco
Outcome results
None listed