1. Baseline Characteristics
A total of 203 primiparous women were included in the study, with 163 in the vaginal delivery group and 40 in the cesarean section group. The baseline characteristics of the study participants are listed in Table 1.
Table 1: Baseline characteristics of participants
|
cesarean section
(n=40)
|
vaginal delivery
(n=163)
|
X2/t/z
|
P
|
age(year)
|
29(27,32)
|
28(26,31)
|
-1.620
|
0.105
|
height
|
159.5(156,162)
|
160(157,163)
|
-1.435
|
0.151
|
weight
|
65(58.5,73.5)
|
67(62,74)
|
-1.107
|
0.268
|
BMI(kg/m2)
|
26.81±4.57
|
26.67±3.38
|
0.172
|
0.864
|
Gestational weeks(weeks)
|
39.71(39.21,40.5)
|
39.86(39.14,40.43)
|
-0.149
|
0.882
|
diabetes(%)
|
|
|
0.02
|
0.887
|
no
|
33(82.50)
|
136(83.44)
|
|
|
yes
|
7(17.50)
|
27(16.56)
|
|
|
hypertension(%)
|
|
|
0.000
|
1.000
|
no
|
39(97.50)
|
157(96.32)
|
|
|
yes
|
1(2.50)
|
6(3.68)
|
|
|
hypothyroidism(%)
|
|
|
0.21
|
0.647
|
no
|
35(87.50)
|
149(91.41)
|
|
|
yes
|
5(12.50)
|
14(8.59)
|
|
|
estimated fetal weigh(EFW)
|
3484.5(3220.5,3626.5)
|
3339(3157,3567)
|
-1.284
|
0.199
|
biparietal diameter(BPD)
|
9.40±0.37
|
9.41±0.33
|
-0.164
|
0.870
|
headcir cumferenceHC
|
33.19±1.27
|
33.12±0.92
|
0.407
|
0.685
|
epidural analgesia(%)
|
|
|
8.923
|
0.003
|
no
|
6(15.00)
|
5(3.07)
|
|
|
yes
|
34(85.00)
|
158(96.93)
|
|
|
fetal presentation(%)
|
|
|
8.705
|
0.013
|
OA
|
12(30.00)
|
89(54.60)
|
|
|
OP
|
10(25.00)
|
20(12.27)
|
|
|
OT
|
18(45.00)
|
54(33.13)
|
|
|
AOP(°)
|
124.35±14.67
|
140.00±15.36
|
-5.825
|
0.000
|
MLA(°)
|
81.80±44.76
|
64.91±41.98
|
2.251
|
0.025
|
HPD(mm)
|
40.68±9.14
|
33.20±7.80
|
5.246
|
0.000
|
PD(mm)
|
42.20±16.06
|
52.85±15.3
|
-3.906
|
0.000
|
Maternal age, height, weight, gestational age, estimated fetal weight (EFW), maternal gestational diabetes, and maternal preeclampsia were not statistically different between the two groups (P > 0.05). However, significant differences were observed in epidural analgesia, fetal presentation, AOP, MLA, HPD, and PD (P < 0.05).
2. Logistic Regression Analysis
Multiple logistic regression analysis was performed to identify the independent influencing factors for predicting the delivery mode in primiparous women. The results are listed in Table 2.
Table 2: Logistic regression analysis of influencing factors
|
B
|
S.E.
|
Wald
|
P
|
OR
|
95%CI
|
VIF
|
下限
|
上限
|
epidural analgesia
|
1.606
|
0.777
|
4.271
|
0.031
|
4.983
|
1.086
|
22.853
|
1.011
|
fetal presentation
|
|
|
|
|
|
|
|
2.002
|
OA
|
|
|
|
|
1.000
|
|
|
|
OP
|
-3.236
|
1.527
|
4.495
|
0.031
|
0.039
|
0.002
|
0.783
|
|
OT
|
-1.308
|
0.934
|
1.959
|
0.155
|
0.270
|
0.043
|
1.688
|
|
AOP
|
0.052
|
0.024
|
4.773
|
0.004
|
1.053
|
1.005
|
1.103
|
2.795
|
MLA
|
0.025
|
0.013
|
3.414
|
0.052
|
1.025
|
0.998
|
1.053
|
1.860
|
HPD
|
-0.067
|
0.034
|
3.969
|
0.027
|
0.935
|
0.875
|
0.999
|
2.299
|
PD
|
-0.006
|
0.020
|
0.097
|
0.312
|
0.994
|
0.956
|
1.033
|
2.308
|
The analysis revealed that epidural analgesia (odds ratio [OR], 6.762; 95% confidence interval [CI]: 1.196-38.217), fetal presentation (OR, 1.281; 95% CI: 0.047-2.427), AOP (OR, 1.071; 95% CI: 1.022-1.123), and HPD (OR, 0.928; 95% CI: 0.869-0.991) were independent factors influencing vaginal delivery.
3. Construction and Validation of the Nomogram
Based on the results of the logistic regression analysis, a nomogram was constructed to predict the probability of vaginal delivery in primiparous women (Figure 7).
To use the nomogram, the value for each variable was located on the corresponding axis, and a line was drawn upward to determine the number of points for each variable. The total points were calculated by summing the points for all variables and locating the total points on the "Total Points" axis. A downward line was drawn to determine the probability of vaginal delivery.
The internal validation of the nomogram prediction model was performed using the Bootstrap method with 1000 repetitions of sampling, and the calibration curve showed good consistency between the actual observations and the nomogram predictions, with an absolute error of 0.024, indicating a high calibration degree of the model, as seen in Figure 8.The nomogram exhibited good discrimination, with a sensitivity of 74.2%, a specificity of 77.5%, and an AUC of 0.808 (95% CI: 0.729-0.886) (Figure 9).
4.External validation of the model
Sixty-one primiparas from Anxi County Maternal and Child Health Hospital were randomly selected for external validation of the model.The baseline characteristics of the two study participants are listed in Table 3.
Table 3: Baseline characteristics of participants in both groups
|
Internal data(n=203)
|
External data
(n=61)
|
X2/t/z
|
P
|
age(year)
|
29(27,31)
|
27(25,31)
|
-1.69
|
0.091
|
weight(kg)
|
67(62,74)
|
66.7(62,71)
|
-0.679
|
0.497
|
Gestational weeks(weeks)
|
39.86(39.14,40.43)
|
39.57(38.86,40.14)
|
-1.887
|
0.059
|
estimated fetal weigh(EFW)
|
3347(3164,3587)
|
3350(3100,3600)
|
-0.281
|
0.779
|
AOP(°)
|
136.92±16.42
|
135.48±20.99
|
0.562
|
0.575
|
HPD(mm)
|
34.67±8.59
|
35.84±8.56
|
-0.928
|
0.354
|
Outcomes(%)
|
|
|
0.679
|
0.410
|
cesarean section
|
40(19.70)
|
15(24.59)
|
|
|
vaginal delivery
|
163(80.30)
|
46(75.41)
|
|
|
epidural analgesia(%)
|
|
|
0.241
|
0.623
|
no
|
11(5.42)
|
5(8.20)
|
|
|
yes
|
192(94.58)
|
56(91.80)
|
|
|
fetal presentation(%)
|
|
|
2.390
|
0.303
|
OA
|
101(49.75)
|
26(42.62)
|
|
|
OP
|
30(14.78)
|
14(22.95)
|
|
|
OT
|
72(35.47)
|
21(34.43)
|
|
|
The comparison of clinical data between the two groups showed no statistically significant differences in maternal age, weight, gestational week, estimated fetal weight (EFW), amniotic fluid volume (AOP), maternal-fetal distance (HPD), fetal position, and the use of epidural anesthesia for pain relief, among other factors (P > 0.05).
A bootstrap method was used to resample 1000 times for external validation of the nomogram prediction model.The calibration curve graph shows that there is good consistency between the actual observations and the predictions of the nomogram, with an absolute error of 0.033, indicating a high calibration degree of the model. See Figure 10. The nomogram exhibited good discrimination, with a sensitivity of 78.3%, a specificity of 80.0%, and an AUC of 0.839(95% CI: 0.717-0.961).(Figure 11)