Retrospective Study
Copyright ©The Author(s) 2023.
World J Gastrointest Surg. Dec 27, 2023; 15(12): 2765-2773
Published online Dec 27, 2023. doi: 10.4240/wjgs.v15.i12.2765
Table 1 Comparing the two groups’ low anterior resection syndrome scale grades before and following therapy (n = 50)
GroupsBefore treatment
Following 1 wk of treatment
Following 2 wk of treatment
Following 4 wk of treatment
No
Mild
Severe
No
Mild
Severe
No
Mild
Severe
No
Mild
Severe
Observational group06191717691011104
Control group08170916110145812
χ20.3971.2804.2916.472
P value0.5290.5270.1170.039
Table 2 Before and after therapy low anterior resection syndrome scale score comparison of the two groups (points, mean ± SD)
Group
n
Before treatment
Following 1 wk of treatment
Following 2 wk of treatment
Following 4 wk of treatment
Observation group2536.89 ± 3.4530.64 ± 5.23a20.27 ± 2.15a15.21 ± 3.62a
Control group2536.62 ± 3.5933.37 ± 3.67a28.34 ± 1.84a21.84 ± 2.51a
T value0.2712.13614.2597.497
P value0.7560.038< 0.001< 0.001
Table 3 Comparison of the pretreatment and posttreatment scores on the Wexner anal incontinence scale (points, mean ± SD)
Group
n
Before treatment
After 1 wk of treatment
After 2 wk of treatment
After 4 wk of treatment
Observation group2510.45 ± 1.278.33 ± 2.21a5.08 ± 0.89a4.37 ± 0.74a
Control group2510.13 ± 1.489.56 ± 1.84a7.22 ± 0.97a6.52 ± 0.89a
T value0.8202.1398.1289.288
P value0.4160.038< 0.001< 0.001
Table 4 Comparison of Xu Zhongfa’s 5-item, 10-point scale scores in both groups (points, mean ± SD)
Group
n
Before treatment
After 1 wk of treatment
After 2 wk of treatment
After 4 wk of treatment
Observation group256.21 ± 0.887.75 ± 0.67a8.93 ± 0.65a9.12 ± 0.57a
Control group256.05 ± 0.936.94 ± 0.74a8.02 ± 0.73a8.63 ± 0.44a
T value0.6254.0574.6553.402
P value0.5350.709< 0.001< 0.001
Table 5 Comparison of anal pressure indicators between observational and control groups (mmHg, mean ± SD)
GroupnAnal resting pressure
Rectal defecation threshold
Maximum tolerance volume
Before treatment
After 4 wk of treatment
Before treatment
After 4 wk of treatment
Before treatment
After 4 wk of treatment
Observation al group2549.51 ± 3.5359.73 ± 2.12a85.32 ± 3.34115.54 ± 5.62a122.35 ± 9.84134.12 ± 7.82a
Control group2549.34 ± 3.6254.41 ± 2.86a85.09 ± 3.62107.31 ± 6.49a120.18 ± 10.45128.36 ± 11.41a
T value0.1687.4720.2334.7930.7562.082
P value0.8670.0000.8160.0000.4530.043
Table 6 Comparison of the quality of life scores before and after treatment (points, mean ± SD)
Group
n
Before treatment
Following 1 wk of treatment
Following 2 wk of treatment
Following 4 wk of treatment
Observational group2560.52 ± 8.5568.27 ± 8.54a80.81 ± 6.92a85.56 ± 5.26a
Control group2560.23 ± 8.6764.18 ± 7.21a73.35 ± 7.88a78.64 ± 4.33a
T value0.1192.2773.5575.079
P value0.9060.0270.001< 0.001
Table 7 Comparing the occurrence of adverse events between the two groups
Group
n
Local bleeding (cases)
Dizziness (cases)
Fever (cases)
Total incidence (%)
Observation group251108.00
Control group250104.00
χ20.355
P value0.552