When we analyzed the distribution of the participant women in terms of problems experienced during the 6 week postpartum period, it was seen that women of control group had nearly two times more abundant and dark lochia than the women of intervention group on the 2nd postpartum day (RR: 0.48). Similarly, women of control group had 1.5 times more pain- sensitivity-redness in the incision area than the women of intervention group on the 2nd postpartum day (RR: 0.84) and 15th postpartum day (RR: 0.73). Also, 14.3% of the control group and one woman of intervention group had yellowish and green discharge in the incision area on the 42nd postpartum day. When we analyzed the distribution of breast problems of the women of both groups, it was found out that women of control group had 2.3 times more engorgement, pain and sensitivity on the 2nd postpartum day (RR: 0.44) and 6.3 times more engorgement, pain and sensitivity on the 15th postpartum day than women of intervention group. Also, on the 42nd postpartum day, nearly half of the control group (42.9%) had engorgement, pain and sensitivity symptoms in breasts whereas only two women of intervention women suffered the same problems. Additionally, poor breastfeeding was seen among the women of both groups on the 2nd postpartum day at similar levels (Intervention Group: 25.7%, Control Group: 28.6 %). Also, it was found out according to the findings that women of control group had poorer breastfeeding compared to the women of intervention group on the 15th postpartum day (Intervention Group: 7.1%, Control Group: 42.9%) and on the 42nd postpartum day (Intervention Group: 2.9%, Control Group: 28.6%) (see Table 3).
When we analyzed the distribution of the participant women in terms of problems experienced during the 6 week postpartum period, it was seen that women of control group had nearly two times more abundant and dark lochia than the women of intervention group on the 2nd postpartum day (RR: 0.48). Similarly, women of control group had 1.5 times more pain- sensitivity-redness in the incision area than the women of intervention group on the 2nd postpartum day (RR: 0.84) and 15th postpartum day (RR: 0.73). Also, 14.3% of the control group and one woman of intervention group had yellowish and green discharge in the incision area on the 42nd postpartum day. When we analyzed the distribution of breast problems of the women of both groups, it was found out that women of control group had 2.3 times more engorgement, pain and sensitivity on the 2nd postpartum day (RR: 0.44) and 6.3 times more engorgement, pain and sensitivity on the 15th postpartum day than women of intervention group. Also, on the 42nd postpartum day, nearly half of the control group (42.9%) had engorgement, pain and sensitivity symptoms in breasts whereas only two women of intervention women suffered the same problems. Additionally, poor breastfeeding was seen among the women of both groups on the 2nd postpartum day at similar levels (Intervention Group: 25.7%, Control Group: 28.6 %). Also, it was found out according to the findings that women of control group had poorer breastfeeding compared to the women of intervention group on the 15th postpartum day (Intervention Group: 7.1%, Control Group: 42.9%) and on the 42nd postpartum day (Intervention Group: 2.9%, Control Group: 28.6%) (see Table 3).
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