Abstract
Background
The incidence and overuse of caesarean section, an adverse pregnancy outcome closely associated with pregnancy complications, is markedly high globally. However, previous research has predominantly examined individual complications in isolation, leaving a need for a comprehensive evaluation of multimorbidity patterns. We aimed to explore the associations between caesarean sections and adverse pregnancy outcomes in a Chinese population.
Methods
We retrieved data from the National Maternal Near Miss Surveillance System in Jilin Province in China from 2021 to 2023. We summarised them using descriptive statistics and used the Rao-Scott χ2 test to compare the differences between spontaneous labour and caesarean section. Then, we used latent class analysis (LCA) to cluster pregnancy complications and logistic regression to examine their association with modes of delivery.
Results
We included 85 446 pregnant women, of whom 53 916 (63.1%) had undergone caesarean sections and 31 530 (36.9%) had experience spontaneous labour. There were significant differences in terms of pregnancy complications between pregnant women who underwent spontaneous labour and those who had caesarean sections. We then clustered pregnancy complication symptoms into six classes using LCA and fitted three models. After adjusting for potential confounders, the incidence of caesarean sections was significantly higher in pregnant women with diabetes and hypothyroidism (odds ratio (OR) = 1.177; 95% confidence interval (CI) = 1.105–1.253), hyperthyroidism and kidney disease (OR = 2.078; 95% CI = 1.391–3.106), with hypertension and hypothyroidism (OR = 3.613; 95% CI = 3.217–4.058), and hypertension, diabetes, and anaemia (OR = 3.365; 95% CI = 2.997–3.779) when compared to pregnant women with a lower incidence of pregnancy complications.
Conclusions
Caesarean sections occur frequently among pregnant women in China and are significantly associated with specific pregnancy complication clusters, particularly those involving hypertension, diabetes, anaemia, and thyroid dysfunction. These findings suggest that women with multimorbidity profiles should receive enhanced antenatal surveillance and individualised delivery planning to optimise maternal outcomes.
Pregnancy complications, such as hypertension, diabetes, and anaemia, occur frequently worldwide and can result in maternal and neonatal mortality and morbidity [1–3]. They often vary across contexts and depend on factors such as demographics and prior experiences of pregnancy [3,4]. They are also closely associated with caesarean sections which, despite being a life-saving intervention, have not shown to lower mortality rates in cases where population-level caesarean section rates exceed 16% [5,6]. In fact, some studies have indicated that caesarean section had short- and long-term adverse effects both on women and their infant [7]. This paradox is particularly acute in Chinese population, where the national caesarean rate far surpasses the WHO-recommended threshold of 15%, with an incidence rate of over 30% [8,9]. However, robust evidence characterising the relationship between specific complication profiles and delivery mode in this population remains scarce.
A fundamental challenge in addressing this overuse is that pregnancy complications rarely occur in isolation [10]. Multiple conditions often co-exist, sharing risk factors or pathophysiological pathways [11]. However, conventional analyses typically examine individual complications separately, potentially obscuring the burden of multimorbidity on clinical decision-making. Latent class analysis (LCA) models offer a methodologically rigorous approach to this problem, as they operate on the premise that the observed distribution of variables results from a finite latent mixture of underlying distributions [12] and are regarded as more statistically robust than usual cluster analyses [13]. Specifically, the approach could be employed to identify homogeneous subgroups within the heterogeneous population of pregnant women with comorbidities. This would allow for the characterisation of distinct multimorbidity patterns and their differential associations with caesarean section utilisation.
Despite the recognised association between caesarean section and pregnancy complications, several gaps remain in our understanding of these conditions in China, where the overall caesarean section rate exceeds the WHO-recommended thresholds [14]. Nevertheless, robust evidence from large-scale Chinese cohorts characterising these associations remains scarce. Secondly, research has predominantly concentrated on medically indicated caesarean sections [8], thereby resulting in an insufficient quantification of the risks associated with non-medically indicated procedures. Thirdly, most prior studies have examined individual adverse outcomes in isolation. With these gaps in mind, we sought to ascertain the prevalence of pregnancy complications in the population of Chinese pregnant women and to examine the associations between various pregnancy complications and the incidence of caesarean sections.
METHODS
Data source and participants
We retrieved our study data from the National Maternal Near Miss Surveillance System established by the National Health Commission in China in 2010 to capture annual data from municipal, provincial, and national hospitals onto an online system [15]. Here we used data from 13 hospitals in Jilin Province, spanning the period from 1 January 2021 to 31 December 2023. Our study adheres to the Journal of Global Health’s GRABDROP guidelines.
We included women aged 15–49 years (i.e. in their reproductive years) with singleton pregnancies, and excluded those who were continuing their pregnancy after leaving hospital; duplicate records; those with missing age; cases of miscarriage; pregnancies at less than 28 weeks’ gestation. The ethics committee of School of Public Health, Jilin University (2024-08-10) approved this study.
Variables
We considered demographic characteristics (age, marital status, and education) and reported experiences of pregnancies (number of pregnancies, delivery history, caesarean section history, and delivery season that might be associated with method of delivery).
Pregnancy complications included hypertension disorder (defined as systolic blood pressure ≥140 mm Hg and/or diastolic blood pressure ≥90 mm Hg), including pre-existing hypertension, gestational hypertension, preeclampsia, and unclassified hypertension; diabetes (including type 1 and type 2 diabetes, and gestational diabetes); anaemia (haemoglobin concentration of <110 g/L); heart disease; liver disease; kidney disease; hypothyroidism; and hyperthyroidism. Pregnancy complications were diagnosed by clinical doctors identified using ICD-10 codes. Method of delivery encompassed spontaneous labour and caesarean section.
Statistical analysis
We descriptively summarised the participants’ characteristics and pregnancy complications and used the Rao-Scott χ2 test to compare the spontaneous labor and caesarean section groups. We imputed missing values using the K-Nearest Neighbor algorithm.
In the context of pregnancy complications, LCA could help extend the usual binary categorisation of pregnant women as ‘diseased’ and ‘not diseased’ and expand analyses of complications beyond a single condition. Here, we utilised LCA to cluster the pregnancy complications, establishing models by setting the global maximum of the log-likelihood function with a maximum of 1000 iterations. The number of assumed latent classes ranged from two to 10, with five fitted models. We also considered the Akaike information criterion, Bayesian information criterion, and χ2 goodness of fit when evaluating model fit. Finally, each class is labelled with an understandable name to enable easier interpretation.
We used logistic regression to examine the associations between pregnancy complications clustered by LCA and method of delivery, fitting three models. Model 1 was a univariate and examined the association between pregnancy complications and caesarean section. Model 2 was multivariate and included significant demographic characteristics for pregnant women as covariates, while model 3 further incorporated important pregnancy complications. A multicollinearity test on independent variables included in the models showed no multicollinearity (variance inflation factor <10).
We used SPSS, version 24.0 (Armonk, New York, USA) and R, version 4.2.2 (R Foundation for Statistical Computing, Vienna, Austria) software with ‘poLCA’ [16], ‘ggplot2’ [17], and ‘DMwR2 [18] packages. A two-sided P-value <0.05 indicated significance.
RESULTS
Participants’ demographic characteristics
We retrieved data on 94674 pregnant women and included 85 446 in our analysis (Figure 1). Of these, 53 916 (63.1%) underwent caesarean section to delivery, 71 122 (83.2%) were aged 20–34 years, 78 540 (91.9%) were married, and 48207 (56.4%) had a college education and above. Only 41 881(49%) were pregnant for the first time, 26 401 (30.9%) had previous deliveries, and 12 397 (14.5%) had undergone a caesarean section. The number of pregnant women delivered varied in different seasons, with 24399 (28.6%) in spring and 18264 (21.4%) in autumn. The spontaneous labour and caesarean section groups differed in age (P < 0.001), marital status (P < 0.001), education (P < 0.001), number of pregnancies (P < 0.001), delivery history (P < 0.001), caesarean section history (P < 0.001), and delivery season (P < 0.001) (Table 1). There were no significant differences in basic characteristics and pregnancy complications between all and included pregnant women with caesarean section and between pregnant women with and without missing values (Tables S1 and S2 in the Online Supplementary Document).
Figure 1.
Flowchart of participants selection.
Table 1.
Descriptive statistics of participants
| Overall (n = 85 446) | Spontaneous labour (n = 31 530) | Caesarean section (n = 53 916) | P-value* | |
|---|---|---|---|---|
|
Age in years
|
|
|
|
<0.001 |
| 15–19 |
514 (0.6) |
307 (59.7) |
207 (40.3) |
|
| 20–34 |
71 122 (83.2) |
27 965 (39.3) |
43 157 (60.7) |
|
| 35–49 |
13 810 (16.2) |
3258 (23.6) |
10 552 (76.4) |
|
|
Marital status
|
|
|
|
<0.001 |
| Not married |
6906 (8.1) |
1079 (15.6) |
5827 (84.4) |
|
| Married |
78 540 (91.9) |
30 451 (38.8) |
480 89 (61.2) |
|
|
Education
|
|
|
|
<0.001 |
| Primary school and below |
777 (0.9) |
269 (34.6) |
508 (65.4) |
|
| Junior middle school |
11 176 (13.1) |
4007 (35.9) |
7169 (64.1) |
|
| Senior middle school |
25 286 (29.6) |
10 018 (39.6) |
15 268 (60.4) |
|
| College degree and above |
48 207 (56.4) |
17 236 (35.8) |
30 971 (64.2) |
|
|
Number of pregnancies
|
|
|
|
<0.001 |
| 1 |
41 881 (49.0) |
15 661 (37.4) |
26 220 (62.6) |
|
| 2 |
23 325 (27.3) |
9084 (38.9) |
14 241 (61.1) |
|
| 3 |
12 174 (14.2) |
4295 (35.3) |
7879 (64.7) |
|
| ≥4 |
8066 (9.4) |
2490 (30.9) |
5576 (69.1) |
|
|
Delivery history
|
|
|
|
<0.001 |
| No |
59 045 (69.1) |
21 448 (36.3) |
37 597 (63.7) |
|
| Yes |
26 401 (30.9) |
10 082 (38.2) |
16 319 (61.8) |
|
|
Caesarean section history
|
|
|
<0.001 | |
| No |
73 049 (85.5) |
31 058 (42.5) |
41 991 (57.5) |
|
| Yes |
12 397 (14.5) |
472 (3.8) |
11 925 (96.2) |
|
|
Delivery season
|
|
|
|
<0.001 |
| Spring |
24 399 (28.6) |
9097 (37.3) |
15 302 (62.7) |
|
| Summer |
22 257 (26.0) |
8228 (37.0) |
14 029 (63.0) |
|
| Autumn |
18 264 (21.4) |
6497 (35.6) |
11 767 (64.4) |
|
| Winter |
20 526 (24.0) |
7708 (37.6) |
12 818 (62.4) |
|
|
Pregnancy with hypertension
|
|
|
|
<0.001 |
| No |
80 583 (94.3) |
30 803 (38.2) |
49 780 (61.8) |
|
| Yes |
4863 (5.7) |
727 (14.9) |
4136 (85.1) |
|
|
Pregnancy with diabetes
|
|
|
|
<0.001 |
| No |
67 653 (79.2) |
25 758 (38.1) |
41 895 (61.9) |
|
| Yes |
17 793 (20.8) |
5772 (32.4) |
12 021 (67.6) |
|
|
Pregnancy with anaemia
|
|
|
|
<0.001 |
| No |
63 914 (74.8) |
22 548 (35.3) |
41 366 (64.7) |
|
| Yes |
21 532 (25.2) |
8982 (41.7) |
12 550 (58.3) |
|
|
Pregnancy with heart disease
|
|
|
|
<0.001 |
| No |
85 304 (99.8) |
31 512 (36.9) |
53 792 (63.1) |
|
| Yes |
142 (0.2) |
18 (12.7) |
124 (87.3) |
|
|
Pregnancy with liver disease
|
|
|
|
0.623 |
| No |
84 892 (99.4) |
31 320 (36.9) |
53 572 (63.1) |
|
| Yes |
554 (0.6) |
210 (37.9) |
344 (62.1) |
|
|
Pregnancy with kidney disease
|
|
|
|
0.024 |
| No |
85 402 (99.9) |
31 521 (36.9) |
53 881 (63.1) |
|
| Yes |
44 (0.1) |
9 (20.5) |
35 (79.5) |
|
|
Pregnancy with hypothyroidism
|
|
|
|
<0.001 |
| No |
79 559 (93.1) |
29 639 (37.3) |
49 920 (62.7) |
|
| Yes |
5887 (6.9) |
1891 (32.1) |
3996 (67.9) |
|
|
Pregnancy with hyperthyroidism
|
|
|
|
<0.001 |
| No |
85 205 (99.7) |
31 472 (36.9) |
53 733 (63.1) |
|
| Yes | 241 (0.3) | 58 (24.1) | 183 (75.9) | |
*Rao-Scott χ2 test.
Prevalence of pregnancy complications
A total of 40705 pregnant women had pregnancy complications, including 4863 (5.7%) with hypertension, 17 793 (20.8%) with diabetes, 21532 (25.2%) with anaemia, 142 (0.2%) with heart disease, 554 (0.6%) with liver disease, 44 (0.1%) with kidney disease, 5887 (6.9%) with hypothyroidism, and 241 (0.3%) with hyperthyroidism. There were significant differences of pregnancy complications (except for liver and kidney disease) between spontaneous labour and caesarean section groups (Table 1; Table S3 in the Online Supplementary Document).
LCA of pregnant women
We clustered pregnancy complication symptoms into six classes using LCA, labelling them based on prevalence (Table S4 in the Online Supplementary Document) as class 1 (pregnancy with lower incidence of complications, meaning below the average in terms of prevalence), class 2 (pregnancy with anaemia and liver disease), class 3 (pregnancy with diabetes and hypothyroidism), class 4 (pregnancy with hyperthyroidism and kidney disease), class 5 (pregnancy with hypertension and hypothyroidism), and class 6 (pregnancy with hypertension, diabetes and anaemia). The highest incidence of caesarean section was in class 5, and the incidence of caesarean section was over 80% in both classes 5 and 6 (Figure 2; Figure S1 and Table S5 in the Online Supplementary Document).
Figure 2.
Prevalence of the pregnancy complications in six classes. Class 1: pregnancy with lower incidence of complications. Class 2: pregnancy with anaemia and liver disease. Class 3: pregnancy with diabetes and hypothyroidism. Class 4: pregnancy with hyperthyroidism and kidney disease. Class 5: pregnancy with hypertension and hypothyroidism. Class 6: pregnancy with hypertension, diabetes, and anaemia
Results of logistic regression analysis
We used pregnancies with a lower incidence of complications as the reference for all classes in the logistic regression analyses. In all models, compared with pregnancy with lower incidence of complications, all classes except pregnancy with anaemia and liver disease were significantly associated with caesarean sections. In model 1, pregnancy with diabetes and hypothyroidism (OR = 1.241; 95% CI = 1.171–1.315), pregnancy with hyperthyroidism and kidney disease (OR = 2.208; 95% CI = 1.516–3.215), pregnancy with hypertension and hypothyroidism (OR = 3.581; 95% CI = 3.210–3.994), and pregnancy with hypertension, diabetes, and anaemia (OR = 3.197; 95% CI = 2.869–3.563) were significantly associated with caesarean sections. In model 2, pregnancy with diabetes and hypothyroidism (OR = 1.185; 95% CI = 1.112–1.262), pregnancy with hyperthyroidism and kidney disease (OR = 2.177; 95% CI = 1.456–3.255), pregnancy with hypertension and hypothyroidism (OR = 3.742; 95% CI = 3.334–4.199), and pregnancy with hypertension, diabetes and anaemia (OR=3.335; 95% CI=2.947–3.738) were significantly associated with caesarean sections.
In model 2, pregnancy with diabetes and hypothyroidism (OR = 1.198; 95% CI = 1.130–1.271), pregnancy with hyperthyroidism and kidney disease (OR = 2.193; 95% CI = 1.502–3.203), pregnancy with hypertension and hypothyroidism (OR = 3.506; 95% CI = 3.140–3.914), and pregnancy with hypertension, diabetes, and anaemia (OR = 3.082; 95% CI = 2.763–3.438) were significantly associated with caesarean sections. In model 3, caesarean sections were associated with pregnancy with diabetes and hypothyroidism (OR = 1.177; 95% CI = 1.105–1.253), pregnancy with hyperthyroidism and kidney disease (OR = 2.078; 95% CI = 1.391–3.106), pregnancy with hypertension and hypothyroidism (OR = 3.613; 95% CI = 3.217–4.058), pregnancy with hypertension, diabetes, and anaemia (OR = 3.365; 95% CI = 2.997–3.779), but not with pregnancy with anaemia and liver disease (OR = 0.894; 95% CI = 0.704–1.134) (Figure 3). = =
Figure 3.
Associations between pregnancy complications and caesarean section. Model 1 was a univariable logistic regression analysis. Model 2 was a multivariable logistic regression analysis adjusting for all significant demographic characteristics, while model 3 further added pregnancy complications significant in model 2. Reference: pregnancy with lower incidence of complications. OR – odds ratio.
DISCUSSION
We observed a high incidence of caesarean sections in a population of pregnant women from China, with some variations in terms of demographic characteristics and experience of pregnancy. We also found the associations between various pregnancy complications and caesarean sections. Among the pregnancy complication classes, pregnant women with hypertension and hypothyroidism; with hypertension, diabetes, and anaemia; with hyperthyroidism and kidney disease; and with diabetes and hypothyroidism had a higher risk of caesarean section compared to those with a lower incidence of complications. Previous studies have predominantly concentrated on the influence of single pregnancy complications on adverse pregnancy outcomes [3,5]. To address this, we analysed the association between pregnant women with multiple pregnancy complications and caesarean sections.
The rate of caesarean sections in pregnant women was 63.1% in our study, which is higher than reported in countries or regions such as Brazil (55.7%) and Germany (30.5%) [9]. Previous research showed that caesarean section use was markedly high in China among low obstetric risk births [14]. Women’s family and community environment, for example, were found to be associated with factors such as the decision for caesarean section and the outcomes of postpartum care [19]. Fear of labour pain and previous psychological trauma were also found to be significant factors associated with pregnant women’s decision to undergo a caesarean section, with those who used this delivery method tending to believe it was safer [20]. In some cases, women selected the optimal time for the birth of their babies [19]. Our findings indicate a correlation between delivery season and the incidence of caesarean sections. This may be attributable to the varying climatic conditions across different seasons, thereby underscoring the environmental impact on the selection of delivery methods [21]. Previous studies have also found delivery seasons to be associated with the incidence of postpartum depression [22].
Our results also show pregnant women to be susceptible to hypertension, diabetes, and other pregnancy complications, with the combined complications being associated with elevated risks of caesarean section. This phenomenon may be ascribed to the inclination among obstetricians to perform the caesarean section surgery on pregnant women with pregnancy complications [23]. Consequently, we recommended that greater emphasis be placed on the utilisation of caesarean section in pregnant women with pregnancy complications and argue for a reduction in the use of caesarean section without indications in general.
In prior studies, pregnant women with anaemia primarily had iron deficiency anaemia [24]. Hepcidin, a peptide hormone predominantly produced by the liver and is key in regulating iron absorption and homeostasis, controls the balance of homeostatic systems [24]. We observed no significant association between the incidence of caesarean section and pregnancy with anaemia and liver disease. The reason may be that severe anaemia increases perioperative risks, including postpartum haemorrhage, transfusion, and infection, which may theoretically deter clinicians from recommending surgical delivery [25]. Furthermore, anaemia is independently closely related to other adverse pregnancy outcomes, such as an increased risk of placental abruption, maternal shock, and even intensive care unit admission and maternal death [26], highlighting the clinical complexity of managing this high-risk population.
Pregnant women with hypothyroidism and diabetes in our sample had an increased risk of undergoing caesarean sections, which is consistent with previous research [27]. A previous study observed a close association between thyroid dysfunction and diabetes. The prevalence of diabetes in patients with hypothyroidism is higher than that in the general population, and vice versa [28]. Requirements for thyroid hormones and daily iodine intake increase during pregnancy, leading to a higher risk of thyroid hormone deficiency [29]. Thyroid diseases are prevalent among pregnant women, with significant implications for maternal and infant health [30]. Thyroid hormones affect early growth and development of the foetus; abnormal thyroid function, for example, is closely associated with adverse developmental outcomes in the foetus [30]. Thyroid dysfunction is associated with various adverse pregnancy outcomes [31]. All other forms of overt hyperthyroidism in pregnancy, except for gestational transient thyrotoxicosis, must be treated to reduce the risks of adverse outcomes, including preeclampsia, low birth weight, miscarriage, and preterm delivery [32]. Furthermore, pregnancy with diabetes has consistently been shown to heighten the probability of caesarean section [5]. Research has also found gestational diabetes mellitus to be associated with an increased risk of preterm delivery, low one-minute Apgar score, macrosomia, and infant born large for gestational age [33]. Consequently, international guidelines advocate preconception counselling for women with pre-existing diabetes mellitus (type 1 or type 2) or obesity [34]. We recommended that they consult with medical experts or nutritionists to develop appropriate nutrition plans and reduce weight in a reasonable manner, and that women with gestational diabetes pay attention to glycaemic control and choose appropriate medication regimens.
A meta-analysis has shown that pregnant women suffering from chronic kidney disease are more likely to undergo caesarean sections [35]. We similarly noted that pregnant women with hyperthyroidism and kidney disease had a higher risk of undergoing caesarean sections. Clinical hyperthyroidism affects between 0.1% and 0.4% of pregnancies [36]; it affects kidney function directly and indirectly through systemic hemodynamic, metabolic, and cardiovascular effects, leading to kidney injury in severe cases [37]. Additionally, kidney diseases, including glomerular diseases, tubulointerstitial disease, and chronic kidney disease, might also be causative factors in hyperthyroidism [38]. Previous studies have demonstrated that the incidence of caesarean section was higher in pregnant women with hyperthyroidism and those with kidney disease [23,39]. The beta subunit of human chorionic gonadotropin, which rises rapidly in early pregnancy, shares structural homology with the thyroid stimulating hormone. This molecular similarity enables human chorionic gonadotropin to exert weak thyrotropic activity at the thyroid stimulating hormone receptor, potentially contributing to gestational thyroid dysfunction [36]. The high incidence of caesarean section in pregnancy with chronic kidney disease might be attributable to the high rate of maternal indications for induction [40]. The presence of chronic kidney disease, in conjunction with hypertension or diabetes, has been demonstrated to increase the probability of adverse pregnancy outcomes, including caesarean sections [41].
Our findings suggest that pregnant women experiencing pregnancy with hypertension and hypothyroidism have a higher probability of undergoing caesarean section. Pregnancy with hypertension was seen to be associated with the occurrence of caesarean sections in previous studies [42] and has been identified as a contributing factor to several adverse pregnancy outcomes such as congenital malformations, intrauterine growth retardation, and even perinatal and foetal death [43]. The incidence of hypertension during pregnancy, including cases complicated by chronic hypertension, is relatively high (5–10%) [44]. In our study, the incidence of pregnancy with hypertension was 5.7%, while the incidence of pregnancy with hypothyroidism was 6.9%.
Pregnancies with hypertension, diabetes, and anaemia, as the three most common complications, were related to one another. Pregnant women with anaemia were more likely to be diagnosed with hypertension and diabetes [45]. Diabetes has previously been identified as a risk factor for hypertension [46]. For noncommunicable diseases such as hypertension, diabetes, and anaemia, a set of assessment measures can be carried out before pregnancy and appropriate preconceptional care can be taken to reduce the incidence of pregnancy-related diseases in women [47]. In addition, pregnancy is now regarded as a physiological stress test that may reveal predispositions to future cardiovascular and endocrine disease [48]. It is therefore necessary that sensitive and reliable early screening and diagnostic tools be developed, and that early treatment be carried out in order to mitigate both immediate pregnancy risks and long-term maternal health burdens.
This study has several strengths. We based our analysis on large-scale provincial monitoring data from a three-year period and used LCA, a robust statistical approach, to classify multiple pregnancy complications. However, we note several limitations, as well. First, we only described associations between various pregnancy complications and caesarean section and could not establish inferences, which would necessitate a different study design. Second, the classes of pregnancy complications in this study were limited, while the combination of pregnancy complications is diverse in reality, meaning we were unable to consider all possible combinations of pregnancy complications.
CONCLUSIONS
In this retrospective cohort study, we used data from 85 446 pregnant women in China collected between 1 January 2021 and 31 December 2023 using a national surveillance system. We noted a high incidence of caesarean section (63.1%) and found that pregnant women with multiple simultaneous pregnancy complications had a higher incidence of caesarean sections compared to those with fewer complications. These findings suggest that implementing comprehensive, multidisciplinary antenatal clinics for women with ≥2 complications, selecting appropriate delivery methods with the objective of improving the utilisation of caesarean sections.
Additional material
Acknowledgements
We would like to extend our gratitude to all those who took part in this project.
Ethics statement: This study has been approved by ethics committee of School of Public Health, Jilin University (2024-08-10), and followed the tenets of the Declaration of Helsinki.
Data availability: All data included in this study, along with the statistical code used for the analyses, are available from the corresponding author upon reasonable request.
Footnotes
Funding: This work was supported by grants from the Jilin Province Health Science and Technology Capability Enhancement Project (grant no. 2021GL007).
Authorship contributions: TJ, GY and LY conceptualised the study. TJ and CK were responsible for the study methodology. GY, YL and YM did the formal analysis. TJ, GY, WL and LW wrote the original draft, and CK, LY and WB reviewed and edited the manuscript. WB supervised the study, and LY acquired the funding. All authors have read and agreed to the published version of the manuscript.
Disclosure of interest: The authors completed the ICMJE Disclosure of Interest Form (available upon request from the corresponding author) and disclose no relevant interests
REFERENCES
- 1.Hirshberg A, Srinivas SK.Epidemiology of maternal morbidity and mortality. Semin Perinatol. 2017;41:332–7. 10.1053/j.semperi.2017.07.007 [DOI] [PubMed] [Google Scholar]
- 2.Sun L, Yue H, Sun B, Han L, Tian Z, Qi M, et al. Estimation of high risk pregnancy contributing to perinatal morbidity and mortality from a birth population-based regional survey in 2010 in China. BMC Pregnancy Childbirth. 2014;14:338. 10.1186/1471-2393-14-338 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Duley L.The global impact of pre-eclampsia and eclampsia. Semin Perinatol. 2009;33:130–7. 10.1053/j.semperi.2009.02.010 [DOI] [PubMed] [Google Scholar]
- 4.Huang Y, Xu J, Peng B, Zhang W.Risk factors for adverse pregnancy outcomes in Chinese women: a meta-analysis. PeerJ. 2023;11:e15965. 10.7717/peerj.15965 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Alexopoulos AS, Blair R, Peters AL.Management of Preexisting Diabetes in Pregnancy: A Review. JAMA. 2019;321:1811–9. 10.1001/jama.2019.4981 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Betran AP, Torloni MR, Zhang J, Ye J, Mikolajczyk R, Deneux-Tharaux C, et al. What is the optimal rate of caesarean section at population level? A systematic review of ecologic studies. Reprod Health. 2015;12:57. 10.1186/s12978-015-0043-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Sandall J, Tribe RM, Avery L, Mola G, Visser GH, Homer CS, et al. Short-term and long-term effects of caesarean section on the health of women and children. Lancet. 2018;392:1349–57. 10.1016/S0140-6736(18)31930-5 [DOI] [PubMed] [Google Scholar]
- 8.Betran AP, Torloni MR, Zhang JJ, Gülmezoglu AM.WHO Statement on Caesarean Section Rates. BJOG. 2016;123:667–70. 10.1111/1471-0528.13526 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Wu ML, Nichols PM, Cormick G, Betran AP, Gibbons L, Belizan JM.Global inequities in cesarean section deliveries and required resources persist. Eur J Obstet Gynecol Reprod Biol. 2023;285:31–40. 10.1016/j.ejogrb.2023.03.036 [DOI] [PubMed] [Google Scholar]
- 10.Brown HK, Fung K, Cohen E, Dennis CL, Grandi SM, Rosella LC, et al. Patterns of multiple chronic conditions in pregnancy: Population-based study using latent class analysis. Paediatr Perinat Epidemiol. 2024;38:111–20. 10.1111/ppe.13016 [DOI] [PubMed] [Google Scholar]
- 11.Jiang L, Tang K, Magee LA, von Dadelszen P, Ekeroma A, Li X, et al. A global view of hypertensive disorders and diabetes mellitus during pregnancy. Nat Rev Endocrinol. 2022;18:760–75. 10.1038/s41574-022-00734-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Weller B, Bowen N, Faubert S.Latent Class Analysis: A Guide to Best Practice. J Black Psychol. 2020;46:287–311. 10.1177/0095798420930932 [DOI] [Google Scholar]
- 13.Sinha P, Calfee CS, Delucchi KL.Practitioner’s Guide to Latent Class Analysis: Methodological Considerations and Common Pitfalls. Crit Care Med. 2021;49:e63–79. 10.1097/CCM.0000000000004710 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Boerma T, Ronsmans C, Melesse DY, Barros AJD, Barros FC, Juan L, et al. Global epidemiology of use of and disparities in caesarean sections. Lancet. 2018;392:1341–8. 10.1016/S0140-6736(18)31928-7 [DOI] [PubMed] [Google Scholar]
- 15.Mu Y, Wang X, Li X, Liu Z, Li M, Wang Y, et al. The national maternal near miss surveillance in China: A facility-based surveillance system covered 30 provinces. Medicine (Baltimore). 2019;98:e17679. 10.1097/MD.0000000000017679 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Linzer DA, Lewis JB.poLCA: An R Package for Polytomous Variable Latent Class Analysis. J Stat Softw. 2011;42:1–29. 10.18637/jss.v042.i10 [DOI] [Google Scholar]
- 17.Wickham H. ggplot2: Elegant Graphics for Data Analysis. Cham, Switzerland: Springer Cham; 2016. [Google Scholar]
- 18.Torgo L. DMwR2: Functions and Data for the Second Edition of “Data Mining with R”. Available: https://search.r-project.org/CRAN/refmans/DMwR2/html/00Index.html. Accessed: 25 February 2026.
- 19.Kirby RS, Hanlon-Lundberg KM.Cesarean delivery: improving on nature? Birth. 1999;26:259–62. 10.1046/j.1523-536x.1999.00259.x [DOI] [PubMed] [Google Scholar]
- 20.Lavender T, Hofmeyr GJ, Neilson JP, Kingdon C, Gyte GM.Caesarean section for non-medical reasons at term. Cochrane Database Syst Rev. 2012;2012:CD004660. 10.1002/14651858.CD004660.pub3 [DOI] [PubMed] [Google Scholar]
- 21.Osei E, Agbemefle I, Kye-Duodu G, Binka FN.Linear trends and seasonality of births and perinatal outcomes in Upper East Region, Ghana from 2010 to 2014. BMC Pregnancy Childbirth. 2016;16:48. 10.1186/s12884-016-0835-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Yang SN, Shen LJ, Ping T, Wang YC, Chien CW.The delivery mode and seasonal variation are associated with the development of postpartum depression. J Affect Disord. 2011;132:158–64. 10.1016/j.jad.2011.02.009 [DOI] [PubMed] [Google Scholar]
- 23.Pillar N, Levy A, Holcberg G, Sheiner E.Pregnancy and perinatal outcome in women with hyperthyroidism. Int J Gynaecol Obstet. 2010;108:61–4. 10.1016/j.ijgo.2009.08.006 [DOI] [PubMed] [Google Scholar]
- 24.Percy L, Mansour D, Fraser I.Iron deficiency and iron deficiency anaemia in women. Best Pract Res Clin Obstet Gynaecol. 2017;40:55–67. 10.1016/j.bpobgyn.2016.09.007 [DOI] [PubMed] [Google Scholar]
- 25.Ferguson MT, Dennis AT.Defining peri-operative anaemia in pregnant women - challenging the status quo. Anaesthesia. 2019;74:237–45. 10.1111/anae.14468 [DOI] [PubMed] [Google Scholar]
- 26.Shi H, Chen L, Wang Y, Sun M, Guo Y, Ma S, et al. Severity of Anemia During Pregnancy and Adverse Maternal and Fetal Outcomes. JAMA Netw Open. 2022;5:e2147046. 10.1001/jamanetworkopen.2021.47046 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Tirosh D, Benshalom-Tirosh N, Novack L, Press F, Beer-Weisel R, Wiznitzer A, et al. Hypothyroidism and diabetes mellitus - a risky dual gestational endocrinopathy. PeerJ. 2013;1:e52. 10.7717/peerj.52 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Rong F, Dai H, Wu Y, Li J, Liu G, Chen H, et al. Association between thyroid dysfunction and type 2 diabetes: a meta-analysis of prospective observational studies. BMC Med. 2021;19:257. 10.1186/s12916-021-02121-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Biondi B, Kahaly GJ, Robertson RP.Thyroid Dysfunction and Diabetes Mellitus: Two Closely Associated Disorders. Endocr Rev. 2019;40:789–824. 10.1210/er.2018-00163 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Becks GP, Burrow GN.Thyroid disease and pregnancy. Med Clin North Am. 1991;75:121–50. 10.1016/S0025-7125(16)30475-8 [DOI] [PubMed] [Google Scholar]
- 31.van den Boogaard E, Vissenberg R, Land JA, van Wely M, van der Post JA, Goddijn M, et al. Significance of (sub)clinical thyroid dysfunction and thyroid autoimmunity before conception and in early pregnancy: a systematic review. Hum Reprod Update. 2011;17:605–19. 10.1093/humupd/dmr024 [DOI] [PubMed] [Google Scholar]
- 32.Lee SY, Pearce EN.Hyperthyroidism: A Review. JAMA. 2023;330:1472–83. 10.1001/jama.2023.19052 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Ye W, Luo C, Huang J, Li C, Liu Z, Liu F.Gestational diabetes mellitus and adverse pregnancy outcomes: systematic review and meta-analysis. BMJ. 2022;377:e067946. 10.1136/bmj-2021-067946 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.American Diabetes Association Professional Practice Committee for Diabetes 15. Management of Diabetes in Pregnancy: Standards of Care in Diabetes-2026. Diabetes Care. 2026;49 Supplement_1:S321–38. 10.2337/dc26-S015 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Al Khalaf S, Bodunde E, Maher GM, O’Reilly ÉJ, McCarthy FP, O’Shaughnessy MM, et al. Chronic kidney disease and adverse pregnancy outcomes: a systematic review and meta-analysis. Am J Obstet Gynecol. 2022;226:656–70.e32. 10.1016/j.ajog.2021.10.037 [DOI] [PubMed] [Google Scholar]
- 36.Kobaly K, Mandel SJ.Hyperthyroidism and Pregnancy. Endocrinol Metab Clin North Am. 2019;48:533–45. 10.1016/j.ecl.2019.05.002 [DOI] [PubMed] [Google Scholar]
- 37.Yamaguchi Y, Uchimura K, Takahashi K, Ishii T, Hanai S, Furuya F.Hyperthyroidism exacerbates ischemic reperfusion injury in the kidney. Endocr J. 2022;69:263–72. 10.1507/endocrj.EJ21-0395 [DOI] [PubMed] [Google Scholar]
- 38.Iglesias P, Bajo MA, Selgas R, Díez JJ.Thyroid dysfunction and kidney disease: An update. Rev Endocr Metab Disord. 2017;18:131–44. 10.1007/s11154-016-9395-7 [DOI] [PubMed] [Google Scholar]
- 39.Fink JC, Schwartz SM, Benedetti TJ, Stehman-Breen CO.Increased risk of adverse maternal and infant outcomes among women with renal disease. Paediatr Perinat Epidemiol. 1998;12:277–87. 10.1046/j.1365-3016.1998.00129.x [DOI] [PubMed] [Google Scholar]
- 40.Bharti J, Vatsa R, Singhal S, Roy KK, Kumar S, Perumal V, et al. Pregnancy with chronic kidney disease: maternal and fetal outcome. Eur J Obstet Gynecol Reprod Biol. 2016;204:83–7. 10.1016/j.ejogrb.2016.07.512 [DOI] [PubMed] [Google Scholar]
- 41.Al Khalaf SY, O'Reilly É J, McCarthy FP, Kublickas M, Kublickiene K, Khashan AS.Pregnancy outcomes in women with chronic kidney disease and chronic hypertension: a National cohort study. Am J Obstet Gynecol. 2021;225:298.e1–.e20. 10.1016/j.ajog.2021.03.045 [DOI] [PubMed] [Google Scholar]
- 42.Hagans MJ, Stanhope KK, Boulet SL, Jamieson DJ, Platner MH.Delivery outcomes after induction of labor among women with hypertensive disorders of pregnancy. J Matern Fetal Neonatal Med. 2022;35:9215–21. 10.1080/14767058.2021.2022645 [DOI] [PubMed] [Google Scholar]
- 43.Li F, Wang T, Chen L, Zhang S, Chen L, Qin J.Adverse pregnancy outcomes among mothers with hypertensive disorders in pregnancy: A meta-analysis of cohort studies. Pregnancy Hypertens. 2021;24:107–17. 10.1016/j.preghy.2021.03.001 [DOI] [PubMed] [Google Scholar]
- 44.Agrawal A, Wenger NK.Hypertension During Pregnancy. Curr Hypertens Rep. 2020;22:64. 10.1007/s11906-020-01070-0 [DOI] [PubMed] [Google Scholar]
- 45.Beckert RH, Baer RJ, Anderson JG, Jelliffe-Pawlowski LL, Rogers EE.Maternal anemia and pregnancy outcomes: a population-based study. J Perinatol. 2019;39:911–9. 10.1038/s41372-019-0375-0 [DOI] [PubMed] [Google Scholar]
- 46.Umesawa M, Kobashi G.Epidemiology of hypertensive disorders in pregnancy: prevalence, risk factors, predictors and prognosis. Hypertens Res. 2017;40:213–20. 10.1038/hr.2016.126 [DOI] [PubMed] [Google Scholar]
- 47.Hadar E, Ashwal E, Hod M.The preconceptional period as an opportunity for prediction and prevention of noncommunicable disease. Best Pract Res Clin Obstet Gynaecol. 2015;29:54–62. 10.1016/j.bpobgyn.2014.05.011 [DOI] [PubMed] [Google Scholar]
- 48.McNestry C, Killeen SL, Crowley RK, McAuliffe FM.Pregnancy complications and later life women’s health. Acta Obstet Gynecol Scand. 2023;102:523–31. 10.1111/aogs.14523 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.



