This study was extracted from a larger randomized, controlled clinical trial. Part of the data obtained for this research is reported in a published paper (
39). Another part of the collected data aimed to examine the effect of Olea ointment on episiotomy wound healing has been reported in this present study. This research project included primiparous women who had normal vaginal delivery with episiotomy. According to Jahdi et al.'s (
40) study, the sample size was estimated using the confidence interval of 95% and the test power of 90%. Accordingly, at least 36 women should have been allocated to each group; however, given the possibility of 15% dropouts, 41 women were assigned to each of the intervention and control groups. Accordingly, 82 primiparous women who met the inclusion criteria were selected using the purposive sampling method. Next, they were randomly divided into two groups [intervention (n = 41) and control (n = 41)] by drawing cards A or B. The required data was collected from December 2017 to May 2018. Inclusion criteria were as follows: Iranian nationality, primiparous, age between 18 - 35 years, reading and writing literacy, willingness to participate in the study, live term singleton pregnancy with vertex presentation, mediolateral episiotomy with no rupture, no chronic systemic diseases hindering wound healing (e.g., cardiac, renal, pulmonary, and coagulation disorders, diabetes, anemia, mental illness, and malnutrition), no history of previous injury, surgery, and visible lesions in perineum (genital warts, hemorrhoids), persistent constipation according to the patient's self-reports, no premature rupture of the membrane for more than 18 hours, duration of the first, second, and third stages of delivery < 14 hours, 2 hours, and half an hour respectively, no manual removal of placenta, no postpartum hemorrhage (PPH), no perineal hematoma, infant weight between 2500 - 4000 g, and non-hospitalization of newborn or neonatal anomalies. On the other hand, exclusion criteria were reluctance to further participate in the study, use of other supplements for wound healing during the study, incorrect usage of the ointment for more than two nights, sensitivity to the Olea ointment, failure to refer to the hospital on Days 5 and 10 postpartum, sexual contacts within the first five days postpartum, and the manipulation of perineum after wound healing. In general, nine women were excluded from the study (four women having approximation and five women not referring back to the center) (
Figure 1).
The required data were collected using demographic forms addressing age, level of education, occupation, and income as well as reproductive information forms with items on gestational age, gravida, abortion rate, gender and weight of newborn, newborn head circumference, and duration of the 1st, 2nd, and 3rd delivery stages. Moreover, perineal healing was assessed using the REEDA scale, which dealt with redness, edema, ecchymosis, discharge, and approximation. The REEDA scale is an international instrument developed by Davidson in 1974 (
41). The scale is scored based on the 4-point Likert, with a higher score indicating the presence of the concerned subscale. The minimum and maximum scores were 0 and 15, representing the degree of wound healing. In this scale, the scores 0, 1 - 5, 6 - 10, and 11 - 15 indicate complete, moderate, poor, and no wound healing, respectively. Sheikhan et al. and Pazandeh and Savadzadeh used this scale in their studies and confirmed its validity and reliability (
42,
43). In this study, the face and content validity of the demographic, obstetrics, and delivery information forms were confirmed.
The data were extracted from interviews, patients' medical files, observation, and examination, with the direct participation of researchers. Both groups were trained on how to care for the perineal region and episiotomy, personal hygiene, nutrition, and physical mobility using the face-to-face method and pamphlets. Prior to the intervention, the wound status was assessed in terms of redness, edema, ecchymosis, discharge, and approximation in each group using the REEDA scale.
Olea ointments were ordered in 30 g tubes, containing the same portions of olive oil, Sesame oil, and honey from Farateb Yazd Company, Yazd, Iran, and were delivered via post. The first intervention was performed 4 hours post-episiotomy. The intervention group were asked to place ointment on the suture after washing and drying the perineum region and to cover it using a clean, sanitary pad after 1 - 2 minutes. They were also requested to repeat this procedure every other 8 hours until the Day 10 after childbirth. Note that the researchers did the first intervention, while the women themselves performed the next interventions.
Meanwhile, the women in the Olea ointment group were persuaded to use normal saline (twice per day until Day 10) to wash the perineal region accompanied by Olea at home. The second group received only routine hospital care as washing with normal saline twice per day until Day 10 postpartum. A bottle of normal saline 0.9% (1000 cc) and one tube of Olea ointment were used for each woman in the Olea group. The second group members also used a bottle of normal saline 0.9% (1000 cc). The researchers assessed the episiotomy status 2 and 24 hours after the first intervention and on Days 5 and 10 postpartum. If episiotomy was not healed, it was re-assessed by the researchers on Day 14 after childbirth. Furthermore, the patient were asked to contact the researchers in the case of any difficulties such as fever, chills, burning, itching, and allergy to Olea ointment, scarring, pain, and swelling in the wound area.
Statistical analysis was then performed using the SPSS software version 16. To this end, statistical tests (namely frequency, central indices, standard deviation, Mann-Whitney U test, Fisher’s exact test, independent-sample t-test, repeated-measure test, Friedman test, and chi-square) were used. P < 0.05 was also set as the significance level.