The current study is approved by the Ethical Committee of Birjand University of Medical Sciences (Ir.bums.REC.1395.194). Also, the study is registered in the Iranian Registry of Clinical Trials (IRCT20140519017756N33). A double-blind clinical trial was used to investigate and compare the analgesic and hemodynamic effects of nitroglycerin-morphine sulfate or morphine sulfate alone. The study was conducted on 60 patients (18 - 50 years old) with the American Society of Anesthesiologists (ASA) 1 and 2. The patients were candidates for simple elective surgery (cholecystectomy, jejunoileostomy, etc.). The flow diagram of the current study is presented in
Figure 1.
The inclusion criteria were being aged 18 to 50 and anesthetic classes 1 and 2 (i.e., the patient did not take any sedative and antiemetic medications and had no history of drug abuse. All abdominal surgeries took less than two hours, bleeding volume was less than 200 mL, and surgical incision length was less than 10 cm. Exclusion criteria were as follows contraindications, nitroglycerin, and morphine drug allergy, severe nausea and side effects (such as hypotension, headache, vomiting, and arrhythmias). Besides, the side effects occurred during the pump usage should be treated, which complicates surgical operations.
In a study performed by Gabriela R and colleagues, initially, the sample size for each group was estimated at 22. However, they increased the sample size to 30 to minimize the impacts of attrition bias and to increase the inaccuracy of results.
Patients were divided into two groups (i.e., case and control groups). For both groups, the following procedures were performed in the operating room: systolic and diastolic blood pressure monitoring, automatic and non-invasive mean arterial blood pressure monitoring, constant measurement of arterial blood oxygen by an oximeter pulse, constant electrocardiogram recording by a 5-lead method, and fluid prescription after the reception.
Surgery was performed using general anesthesia. The anesthesia in both groups was induced equally using propofol, fentanyl, and muscle relaxant with dosages of 2 mg/kg, 3 µg/kg, and 0.5 mg/kg, respectively. All patients were intubated with an endotracheal tube by an anesthesiologist. Bleeding and other outflow parameters were monitored both during and after the surgery. After transferring patients to the recovery room, the Iv PCA with a capacity of 100 ml (adjustable in 2, 4, 6 & 8 mL/h) was filled by an anesthesiologist, and it was kept at the dose of 4 mL per hour. For the control and case groups, morphine sulfate 10 mg/ml (Morphine, Darupakhsh Co., Iran) (0.75 mg/mL) and nitroglycerin-morphine (morphine 0.5 mg/mL + nitroglycerin 10 mg/2mL (Nitral, Caspian Tamin Pharmaceutical Co., Rasht, Iran) 15 μg/mL) infusions were administered. In each group, the remaining part of the pump volume was filled up to 100 ccs with normal saline. A demographic information form (including information on age, sex, anesthesia classification, and vital signs) was completed for all patients. Then, hemodynamic and breathing parameters, nausea and vomiting, and pain were measured based on a VAS Score immediately, 2, 6, 12, and 24 hours after the surgery.
The visual pain scale is a unidimensional measure that contains two ends ranging from 0 to 10. “no pain” on the left (i.e., 0) and “hurt worst” on the right (i.e., 10). Generally, scores in the ranges of 1 - 3, 4 - 7, and 8 - 10 indicate mild, moderate, and severe pain, respectively. Data were analyzed by SPSS version 20 using the t-test (age, pain, hemodynamic parameters of systolic and diastolic blood pressure, heart rate, and breathing rate of the patient) and Mann-Whitney U-test (surgery period and nausea) and the homogeneity was checked by the Kolmogorov-Smirnov test.