Does Acupressure Affect Gastrointestinal Function, Pain and Anxiety?
Gastrointestinal Dysfunction, Anxiety, Pain, Postoperative
About this trial
This is an interventional supportive care trial for Gastrointestinal Dysfunction focused on measuring Acupressure, Gastrointestinal Dysfunction, Anxiety, Pain
Eligibility Criteria
Inclusion Criteria:
- Age 18-75 years
- Able to understand the information given
- Willing to receive acupressure
- No lesions or wounds in the areas where acupressure was to be applied
- Operated on under general anaesthesia pulse, blood pressure, body temperature and oxygen saturation values within normal range during the operation
- No failure or disorder developing intraoperatively or postoperatively related to fluid-electrolyte balance, acid-base balance, or tissue perfusion.
Exclusion Criteria:
- American Society of Anaesthesiologists (ASA) physical status IV
- A requirement for simultaneous combined surgery,
- A need for postoperative fasting according to the preoperative evaluation or intraoperative findings (eg, panperitonitis with intraperitoneal abscess)
- Patients with a cardiac pacemaker
- A history of syncope or seizures
- Pregnant or lactating women
- The presence of any disease related to bleeding or a clotting disorder
- Patients who were unwilling to participate in the research.
Sites / Locations
- Di̇lek Soylu
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Placebo group
Experimental group
Since acupressure administration was reported to have placebo effects, a placebo group was used to investigate the true effect of acupressure use. The application of placebo may consist of moderate pressure on an incorrect acupuncture point or a light touch on a real acupuncture point. This will allow us to determine the contribution of the placebo effect resulting from direct human contact and interaction in the light touch group. At postoperative 0, 4, and 8 hours, a light touch was applied to the ST25 (Stomach Meridian 25th point), CV12 (Conception Vessel Meridian 12th point), TH6 (Triple Heater Meridian 6th point) and HT7 (Shenmen point points) for one second. No patients experienced pain or a feeling of pressure.
As invasive acupuncture may cause hematoma and the wristband method of non-invasive acupressure may cause patient discomfort, itching, swelling of the wrist, and skin destruction, manual acupressure was applied in this study to reduce the risk of complications to a minimum. The frequency and duration of the application of acupressure was decided from a scan of literature and expert opinion. The first acupressure session was applied in the first postoperative hour immediately after routine treatment and care of the patients who came to the ward from the recovery unit. Acupressure by applying pressure with the thumbs for a total of 12 mins, as 3 mins at each of the ST25, CV12, TH6 and HT7 acupuncture points, was performed at 0, 4 and 8 hours postoperatively. The acupuncture points were determined using the measurements of the patient's own fingers.