The Effects of the Thai Traditional Medicine of Abdominal Massage on Defecation in Post Lumbar Laminectomy Patients

Objective: This prospective study examined the defecation enhancement effects in post-lumbar laminectomy patients who received Thai traditional medicine of abdominal massage (TTMAM) in combination with standard nursing care, compared with patients receiving only standard nursing care. Methods: This prospective, randomized, controlled trial was conducted at Siriraj Hospital between 2011 and 2015. Eighty-eight patients with spinal stenosis scheduled for lumbar laminectomy with or without fusion were enrolled. The patients were randomly assigned to two groups: the first group underwent standard nursing care combined with TTMAM (the TTMAM group), and the second group underwent standard nursing care (the non-TTMAM group). The clinical outcomes regarding the first defecation within 3 days after surgery, abdominal distension, and patient satisfaction with defecation care were evaluated. Results: When comparing the first defecation within 3 days after surgery, no significant differences were found in the number of patients between the two groups. The number of the patients who had their first defecation within 3 days after surgery was higher in the TTMAM group (46.5%) than the non-TTMAM group (27.3%). There was significantly less abdominal distension on the third day after surgery in the TTMAM group than in the non-TTMAM group. Moreover, the mean score of patient satisfaction of the TTMAM group was higher than that of the non-TTMAM group. Conclusion: Thai traditional medicine of abdominal massage tends to help defecation in post-lumbar laminectomy patients as it relieves abdominal distension and increases satisfaction with defecation care. Therefore, the use of TTMAM with other bowel care methods could provide additional benefit for lumbar laminectomy patients

The Effects of the Thai Traditional Medicine of Abdominal Massage on Defecation in Post Lumbar Laminectomy Patients

Objective: This prospective study examined the defecation enhancement effects in post-lumbar laminectomy patients who received Thai traditional medicine of abdominal massage (TTMAM) in combination with standard nursing care, compared with patients receiving only standard nursing care. Methods: This prospective, randomized, controlled trial was conducted at Siriraj Hospital between 2011 and 2015. Eighty-eight patients with spinal stenosis scheduled for lumbar laminectomy with or without fusion were enrolled. The patients were randomly assigned to two groups: the first group underwent standard nursing care combined with TTMAM (the TTMAM group), and the second group underwent standard nursing care (the non-TTMAM group). The clinical outcomes regarding the first defecation within 3 days after surgery, abdominal distension, and patient satisfaction with defecation care were evaluated. Results: When comparing the first defecation within 3 days after surgery, no significant differences were found in the number of patients between the two groups. The number of the patients who had their first defecation within 3 days after surgery was higher in the TTMAM group (46.5%) than the non-TTMAM group (27.3%). There was significantly less abdominal distension on the third day after surgery in the TTMAM group than in the non-TTMAM group. Moreover, the mean score of patient satisfaction of the TTMAM group was higher than that of the non-TTMAM group. Conclusion: Thai traditional medicine of abdominal massage tends to help defecation in post-lumbar laminectomy patients as it relieves abdominal distension and increases satisfaction with defecation care. Therefore, the use of TTMAM with other bowel care methods could provide additional benefit for lumbar laminectomy patients

The Efficacy of Thai Herbal Prasaplai Formula for Treatment of Primary Dysmenorrhea: A Short-Term Randomized Controlled Trial

This study aims to compare the efficacy of pain relief between a specific Thai herbal Prasaplai formula (PPF) and placebo in patients with primary dysmenorrhea. Forty women with primary dysmenorrhea symptoms were randomized into two groups. The experimental group received PPF capsules 1000 mg orally three times per day before meals for three days starting from the first day of menstruation. The placebo group received placebo as the same dose and time. Average pain intensity from the first day to the third day of cycle significantly decreased in both groups ( < 0.001), but with no statistically significant difference between groups. Using a pre-and posttreatment difference in NRS of at least 2, a greater proportion of patients in PPF group experienced pain relief compared to placebo during the first and second day of period. A greater proportion of PPF group also experienced no pain compared to the placebo group on day 1 and day 3 by using multidimensional scoring. The PPF demonstrates pain relief activity when used during menstruation in primary dysmenorrhea patients, with no adverse effects. However, further studies are needed in order to assess the value of PPF as a long-term prophylaxis for primary dysmenorrhea

The Efficacy of Thai Herbal Prasaplai Formula for Treatment of Primary Dysmenorrhea: A Short-Term Randomized Controlled Trial

This study aims to compare the efficacy of pain relief between a specific Thai herbal Prasaplai formula (PPF) and placebo in patients with primary dysmenorrhea. Forty women with primary dysmenorrhea symptoms were randomized into two groups. The experimental group received PPF capsules 1000 mg orally three times per day before meals for three days starting from the first day of menstruation. The placebo group received placebo as the same dose and time. Average pain intensity from the first day to the third day of cycle significantly decreased in both groups (p<0.001), but with no statistically significant difference between groups. Using a pre- and posttreatment difference in NRS of at least 2, a greater proportion of patients in PPF group experienced pain relief compared to placebo during the first and second day of period. A greater proportion of PPF group also experienced no pain compared to the placebo group on day 1 and day 3 by using multidimensional scoring. The PPF demonstrates pain relief activity when used during menstruation in primary dysmenorrhea patients, with no adverse effects. However, further studies are needed in order to assess the value of PPF as a long-term prophylaxis for primary dysmenorrhea