Eutocic delivery vs. cesarean section: a multicenter retrospective study of factors influencing cesarean rates in Robson groups 1, 2a, 3, and 4a across birth centers
Alessandra Musicco, Gianfranco Sfregola, Vincenzo Dicuonzo, Tatiana Bolgeo, Virginia Milone, Grazia Dicuonzo, Paolo Iovino, Federico Ruta

TL;DR
This study examines factors influencing cesarean section rates among different groups of women in Italy, finding that multiparity and spontaneous labor reduce the likelihood of a C-section.
Contribution
The study provides new insights into how clinical factors like multiparity and labor induction affect cesarean delivery rates across different birth centers.
Findings
Multiparous women are significantly less likely to undergo cesarean section compared to nulliparous women.
Induced labor is associated with a fourfold increased likelihood of cesarean delivery compared to spontaneous labor.
Significant variability in cesarean rates was observed across different birth centers for the same Robson groups.
Abstract
Cesarean deliveries are increasing rapidly worldwide. Although their primary indication is when vaginal delivery is not feasible, there appears to be an overutilization of this procedure, even in the absence of clear medical or obstetric indications. This exposes women to short-term and long-term adverse outcomes. This study aimed to investigate factors associated with cesarean section (CS) in nulliparous and multiparous women undergoing spontaneous and induced labor, focusing on Robson groups 1, 2a, 3, and 4a in birth centers of the Apulia Region (Italy) in 2019. This multicenter retrospective observational study used data from the Delivery Room Registers of 14 facilities in the Apulia Region in 2019, covering 14,331 women. Inclusion criteria were belonging to Robson groups 1, 2a, 3, or 4a. Exclusion criteria were stillbirths and deliveries occurring in ambulances or at home. The…
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| Characteristic | |
|---|---|
| Cesarean delivery | 1,568 (15.7) |
| Robson group | |
| Group 1 | 4,325 (43.3) |
| Group 2a | 1,692 (16.9) |
| Group 3 | 3,416 (34.2) |
| Group 4a | 559 (5.6) |
| Childbirth analgesia | 5,242 (52.5) |
| Operating room | 6,268 (62.7) |
| Physiology-dedicated area | 7,529 (75.4) |
| Labor room availability | 8,718 (87.2) |
| Comparison | OR (95% CI) | |
|---|---|---|
| Group 2a vs. 1 |
| <0.001 |
| Group 3 vs. 1 |
| <0.001 |
| Group 4a vs. 1 |
| 0.013 |
| Group 3 vs. 1 (contrast) |
| <0.001 |
| Group 4a vs. 2a (contrast) |
| <0.001 |
| Groups 2a + 4a vs. 1 + 3 |
| <0.001 |
| Groups 3 + 4a vs. 1 + 2a |
| <0.001 |
| Hospital | Group 1 ( | Group 2a ( | Group 3 ( | Group 4a ( | ||||
|---|---|---|---|---|---|---|---|---|
|
| CD |
| CD |
| CD |
| CD | |
| Mons. Dimiccoli, Barletta | 281 | 25 (8.9%, 6.1–12.8) | 75 | 21 (28.0%, 19.1–39.0) | 273 | 10 (3.7%, 2.0–6.6) | 20 | 0 (0.0%, 0.0–16.1) |
| V. Emanuele II, Bisceglie | 146 | 20 (13.7%, 9.0–20.2) | 76 | 24 (31.6%, 22.2–42.7) | 141 | 2 (1.4%, 0.4–5.0) | 25 | 3 (12.0%, 4.2–30.0) |
| L. Bonomo, Andria | 201 | 21 (10.4%, 6.9–15.4) | 122 |
| 199 | 0 (0.0%, 0.0–1.9) | 40 | 3 (7.5%, 2.6–19.9) |
| D. Camberlingo, F. Fontana | 200 | 44 (22.0%, 16.8–28.2) | 100 |
| 137 | 1 (0.7%, 0.1–4.0) | 27 | 4 (14.8%, 5.9–32.5) |
| Di Summa—Perrino, Brindisi | 432 |
| 37 |
| 225 |
| 18 | 4 (22.2%, 9.0–45.2) |
| Umberto I, Corato | 209 | 49 (23.4%, 18.2–29.6) | 79 |
| 201 | 5 (2.5%, 1.1–5.7) | 40 | 3 (7.5%, 2.6–19.9) |
| San Giacomo, Monopoli | 292 | 37 (12.7%, 9.3–17.0) | 20 |
| 232 | 5 (2.2%, 0.9–5.0) | 3 |
|
| R. Miulli, Acquaviva delle Fonti | 319 | 27 (8.5%, 5.9–12.0) | 436 | 110 (26.6%, 22.6–31.0) | 373 | 61 (16.4%, 13.0–20.5) | 132 | 11 (8.3%, 4.7–14.3) |
| Mater Dei Hospital, Bari | 288 |
| 78 |
| 192 | 12 (6.3%, 3.6–10.8) | 32 | 5 (15.6%, 6.8–31.8) |
| San Paolo, Bari | 194 |
| 45 |
| 173 |
| 25 |
|
| Di Venere, Bari Carbonara | 608 | 93 (15.3%, 12.7–18.4) | 259 | 68 (26.3%, 21.3–32.0) | 347 | 17 (4.9%, 3.1–7.8) | 43 | 1 (2.3%, 0.4–12.0) |
| Occidentale, Castellaneta | 154 | 27 (17.5%, 12.3–24.3) | 41 | 9 (22.0%, 12.0–36.8) | 132 | 8 (6.1%, 3.1–11.5) | 21 | 3 (14.3%, 4.9–35.1) |
| S.S. Annunziata, Taranto | 494 | 31 (6.3%, 4.5–8.9) | 256 | 38 (14.8%, 11.0–19.7) | 401 | 6 (1.5%, 0.7–3.3) | 88 | 7 (8.0%, 3.9–15.7) |
| Teresa M. Mascia, San Severo | 204 | 43 (21.1%, 16.0–27.2) | 44 | 16 (36.4%, 23.4–51.7) | 236 |
| 38 | 6 (15.8%, 7.4–30.5) |
| G. Tatarella, Cerignola | 303 |
| 24 | 12 (50.0%, 31.9–68.1) | 154 | 15 (9.7%, 5.9–15.6) | 7 | 2 (28.6%, 8.2–64.1) |
| Pearson chi-squared test ( | 287.95 (<0.001), 0.069 | 184.67 (<0.001), 0.088 | 76.15 (<0.001), 0.040 | 39.51* (<0.001), 0.071 | ||||
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Taxonomy
TopicsMaternal and Perinatal Health Interventions · Assisted Reproductive Technology and Twin Pregnancy · Maternal and fetal healthcare
Introduction
1
Caesarean section (CS) is a potentially life-saving procedure. However, ensuring timely and safe access to CS remains a major challenge for health systems in countries with high maternal mortality (1). Conversely, in many other settings, women are increasingly undergoing CS without clear, evidence-based indications, contributing to the worldwide secular trend of rising CS rates (2, 3). When performed for medical reasons, CS can prevent severe morbidity and mortality for both mother and infant (4, 5). However, this procedure is also associated with significant short- and long-term risks for the mother–child dyad, underscoring the importance of limiting its use to situations of genuine medical necessity. Reported risks include surgical complications (e.g., inflammatory and neuroendocrine response, organ injury, and fluid and heat loss), procedure-related adverse outcomes (e.g., abdominal pain, bladder or ureteral damage, hysterectomy, and thromboembolic disease), anesthesia-related complications (linked to drugs, techniques, or invasive monitoring), and broader biological effects of childbirth.
Cost-effectiveness is also a crucial consideration when evaluating the use of CS. Across different healthcare systems, vaginal birth has consistently been shown to be less costly than CS, largely due to shorter hospital stays, fewer postoperative complications, and reduced use of medical resources (5). For example, a cost-effectiveness analysis from Colombia demonstrated that spontaneous vaginal delivery was both less expensive and more effective than elective CS for low-risk women, reinforcing the view that vaginal birth is economically preferable and carries important implications for public health policy in middle-income countries (6). Similarly, in Brazil’s private healthcare system, vaginal birth was shown to be less costly and equally or more effective, even in a context where cesarean delivery is often culturally and institutionally favored (7).
Over the past two decades, increasing debate has surrounded the appropriateness of performing CS at maternal request or on the advice of healthcare professionals in the absence of clear medical indications. Issues of safety, cost, women’s rights and preferences, along with both maternal and professional satisfaction, have all been central to this discussion, highlighting the interplay between medical, ethical, and individual considerations (8), which recent literature has further expanded with strategies and ethical advances (9–11).
In recent years, several systematic reviews and institutional statements have emphasized strategies to reduce unnecessary CS, including audit and feedback programs, standardized labor management protocols, and quality-improvement initiatives aimed at primary cesarean births (9, 10). At the same time, multilevel analyses have highlighted how health system drivers and organizational practices contribute to the variability of CS rates (11). Ethical aspects are also increasingly relevant, with women’s autonomy, informed choice, and the balance between maternal preferences and clinical appropriateness gaining prominence in contemporary obstetric care.
The rising global prevalence of CS remains a major public health concern (6, 7). In a setting where CS is available, optimal rates are expected. Recent studies suggest that the ideal CS rate lies between 10 and 20% of all births (12, 13). Nevertheless, despite the introduction of multiple protocols and guidelines for intrapartum care and the publication of official reports comparing CS rates across hospitals, substantial variability persists. This variability has been attributed to inconsistent application of guidelines, lack of uniform regulation regarding maternal requests, defensive medical practices, uneven adherence to standards, and increased surgical activity linked to remuneration mechanisms within the National Health Care System.
Therefore, the purpose of this study was to investigate CS trends in 2019, identifying maternal characteristics associated with a higher risk of undergoing CS, while accounting for institutional and obstetric factors. We also estimated the difference in CS prevalence within the same Robson groups across different inpatient facilities in the Apulia region (Italy). The findings are intended to inform the development of public health benchmarks for maternal and neonatal health programs, guide the design of innovative policies and clinical guidelines, and support risk factor screening and awareness campaigns for pregnant women.
Methods
2
Design
2.1
This was a multicentric retrospective observational study.
Instruments and data collection
2.2
Data collection followed three steps. First, we obtained formal authorization from the Health Management of each participating facility. Next, data were retrieved from 14 facilities in the Apulia Region (Italy). Data were collected in digital format (Microsoft Excel, Microsoft 365) from the Delivery Room Registers (parallel registry and supporting care activity), including Robson classification variables and information on compliance with operational standards. All women meeting the inclusion criteria were considered eligible and included in the analysis; no data extraction or sampling was performed. Subsequently, data were analyzed using descriptive statistics and inferential procedures, including multilevel logistic regression models, chi-squared test, and Fisher’s exact test. The Robson classification, proposed by the World Health Organization in 2015, is a global standard for assessing, monitoring, and comparing CS rates. It categorizes women into 10 mutually exclusive and totally inclusive groups based on obstetric characteristics (14). It has been widely validated, demonstrating high validity (accurately reflecting obstetric risks), reliability (consistent application across settings), and reproducibility (stable results over time). Its high interrater agreement and responsiveness make it an effective tool for monitoring trends and informing both clinical practice and policy decisions.
Ethical considerations
2.3
Patients were not involved in developing the research questions, study design, or participant recruitment. Given the retrospective design, informed consent was not required. All data were fully anonymized prior to analysis; no direct identifiers (e.g., name, surname, and date of birth) and records could not be traced back to individual participants. The use of anonymized data ensured full compliance with ethical and legal standards for data protection.
Sample
2.4
We collected data on 9,992 women from the Delivery Room Registers of birth centers in the Apulia Region (Italy) in 2019. Inclusion criteria were Robson groups 1 (nulliparous, spontaneous labor), 2a (nulliparous, induced labor), 3 (multiparous, spontaneous labor), and 4a (multiparous, induced labor). We excluded women with stillbirths, those with a gestational age of ≤ 28 weeks (as these cases concern fetal intrauterine death management and specific clinical recommendations), and women who delivered in ambulances or at home. We also excluded women belonging to Robson groups 2b, 4b, and 5–10. This choice was adopted as these groups represent absolute maternal and/or fetal clinical recommendations for CS. These groups were excluded because they represented clinical scenarios with absolute maternal and/or fetal indications for CS established based on the woman’s clinical records prior to delivery.
Statistical analysis
2.5
All analyses were performed using STATA^®^ MP 15. Sample characteristics were described as means (SD) for quantitative variables and frequencies (%) for categorical variables. No missing data were present for the variables included in the analysis; therefore, complete case analysis was applied. Because patients were hierarchically nested within 14 healthcare facilities, we applied multilevel binary logistic regression models with a random intercept at the facility level to account for intra-center correlation. This approach adjusts for unobserved heterogeneity across centers while estimating the fixed effects of Robson groups on CS risk. Random slopes were not included, as the objective of the analysis was to assess overall associations between Robson groups and cesarean delivery risk, rather than to model variation in these associations across facilities. The independent variables were the four Robson groups or their combinations, while the dependent variable was dichotomized as 0 = vaginal delivery and 1 = cesarean delivery. We estimated the effects of all four Robson groups individually, group 3 vs. group 1, group 4a vs. group 2a, groups 2a + 4a vs. groups 1 + 3, and groups 3 + 4a vs. groups 1 + 2a. Results are presented as odds ratios (ORs) with 95% confidence intervals (CIs) and p-values. To examine differences in CS distribution across facilities, we used Pearson’s chi-squared test (or Fisher’s exact test when expected cell counts were <5). Because the chi-squared test only indicates overall significance, we performed post-hoc analyses of adjusted standardized residuals to identify specific facility–Robson group combinations contributing to the association. Adjusted residuals follow an approximate standard normal distribution, with values exceeding ±1.96 indicating cells where the observed frequency significantly deviates from expectation under independence. To account for multiple testing, the Bonferroni correction was applied. With four Robson groups analyzed, the adjusted significance threshold was set at a p-value of < 0.013 (0.05/4).
Results
3
Sample characteristics
3.1
Table 1 presents the characteristics of the participants (n = 9,992) and the healthcare settings. Overall, 15.7% of women were delivered by CS, with the largest proportion belonging to Robson group 1 (43.3%). Slightly more than half of the women (52.2%) delivered in hospitals offering pharmacological pain control (analgesia during childbirth). Only 62.7% of the sample had access to a facility with a 24-h operating room available for obstetric emergencies. In addition, approximately 75% of the women delivered in facilities with areas dedicated to the management of physiological/natural labor, and 87.2% were in hospitals where the number of labor-birthing rooms was appropriate to the annual number of births.
Results of the logistic regression
3.2
Table 2 presents the results of the logistic regression comparing different Robson group combinations in relation to cesarean delivery. Compared with group 1 (nulliparous, spontaneous labor), women in group 2a (nulliparous, induced labor) were approximately three times more likely to undergo CS (OR = 3.19, p < 0.001). In contrast, women in groups 3 and 4a (multiparous, spontaneous, and induced labor, respectively) were less likely to have CS. Among women with spontaneous labor, multiparous women (group 3) had 56% lower odds of undergoing CS compared with nulliparous women (group 1) (OR = 0.44, p < 0.001). Similarly, among those with induced labor, multiparous women (group 4a) had 54% lower odds of CS compared with nulliparous women (group 2a) (OR = 0.46, p < 0.001). When considering the full sample, induction of labor was associated with approximately 4-fold higher odds of CS compared with spontaneous labor (OR = 3.87, p < 0.001). Overall, multiparous women were significantly less likely to undergo CS than nulliparous women (OR = 0.18, p < 0.001).
Proportion of cesarean delivery stratified by Robson group and hospital facility
3.3
Table 3 reports the contingency table of CS rates across Robson groups and hospital facilities. For each group, a significant association was observed between facility and type of delivery (all p < 0.001). Specifically, the frequency of CS among women in group 2a was significantly higher than expected in seven hospitals, followed by group 1, where higher-than-expected frequencies were observed in four hospitals. Notably, San Paolo Hospital in Bari showed higher-than-expected CS rates across all Robson groups.
Discussion
4
Interpretation of findings and clinical implications
4.1
This study aimed to investigate delivery patterns in the Apulian Region (Italy), with a particular focus on the prevalence of CS vs. vaginal delivery. Women were analyzed according to their Robson group classification, and the results presented in Tables 2, 3 provide important insights into the factors influencing CS across groups and facilities.
A key finding of this study is the significant difference in CS rates between nulliparous and multiparous women in both spontaneous and induced labor. Specifically, women who had not previously given birth and underwent induction were approximately three times more likely to deliver with CS than those in spontaneous labor. These findings are consistent with previous studies demonstrating that nulliparity and induction of labor are major risk factors for CS. We also found that multiparous women, whether in spontaneous or induced labor, were less likely to undergo CS than their nulliparous counterparts. The protective effect of multiparity on CS has been well documented in previous studies.
In the overall sample, women with induced labor were approximately four times more likely to deliver by CS compared with those in spontaneous labor. This strong association highlights the clinical challenges linked to induction. Our findings are consistent with those of Caughey et al. (15), who, in a study of more than 20,000 women, reported that labor induction was associated with a 2.5-fold higher risk of CS compared with spontaneous labor.
The variation in CS rates across healthcare facilities in the Apulia Region underscores the complex interplay of factors influencing delivery outcomes. Beyond clinical and obstetric factors, the variability in cesarean section rates between hospitals may reflect differences in organizational culture, availability of resources, and professional attitudes toward labor management. Non-clinical determinants, such as physician preferences, institutional protocols, medico-legal pressures, and patient expectations, have been shown to significantly influence the likelihood of cesarean delivery. These considerations provide a broader interpretive framework, supported by the literature, while our empirical findings remain limited to the observed variability across Robson groups and facilities.
The discussion of these results should therefore extend beyond descriptive comparisons. Alternative hypotheses must be considered, including how institutional protocols, professional decision-making styles, and the expectations generated by community norms for childbirth may shape cesarean section rates. Such differences illustrate that variability across facilities is not merely the result of medical indications but also of organizational and cultural dynamics. Addressing this complexity requires the harmonization of clinical pathways, implementation of evidence-based guidelines, and strategies that promote shared decision-making with women and families.
Recent evidence further supports this interpretation. Gupta et al. demonstrated that maternal and institutional factors significantly influence induction success (16). Selin et al. also highlighted population-level predictors of successful induction (17). More recently, Karlsson et al. found that induction of labor was associated with an increased risk of cesarean delivery in nulliparous women (18).
Notable disparities were observed, such as unexpectedly high CS rates in group 2a across seven hospital settings, and in group 1 across four hospitals. These findings suggest that hospital policies, resource allocation, and clinical practices can strongly affect the prevalence of CS, highlighting the need for more individualized and context-sensitive approaches to obstetric care (13, 19, 20).
Research by Betrán et al. (13) highlights the global rise in cesarean delivery rates, with evidence indicating that hospital policies, clinical practices, and resource allocation play a major role in these trends. Practices such as the routine use of CS in certain clinical scenarios and the influence of healthcare infrastructure can contribute to regional variability. Similarly, Vogel et al. (21) emphasize the value of the Robson classification in identifying differences in CS rates across different settings. Within this framework, the classification is particularly useful for comparing local patterns, such as those observed in Apulian hospitals, where institutional and organizational factors may explain part of the heterogeneity in CS prevalence.
Our results suggest that CSs were performed more frequently than expected in our sample, as many women presented with favorable clinical conditions for vaginal delivery. This observation was verified by reviewing clinical records and the data used for the Robson classification, which provided detailed obstetric profiles. These findings are consistent with previous research by Gibbons et al. (19) and Vogel et al. (21), both of which support our observations regarding group 2a. Moreover, Vogel et al. (21) highlighted the influence of hospital-level factors, such as staffing patterns and clinical protocols, on shaping variations in CS rates across facilities. According to the literature, non-clinical factors often play a decisive role in choosing the delivery mode. However, our findings indicate that nulliparity and induction of labor are strong predictors of CS. Finally, the regional and intra-regional variability observed in Apulia appears to reflect differences in care processes affecting women in Robson groups 1, 2a, 3, and 4a.
The implications of our findings extend to both clinical practice and health policy. Effective strategies should aim to align clinical guidelines with institutional capacities to optimize maternal outcomes and reduce unnecessary surgical interventions. Reducing disparities in CS rates requires comprehensive approaches that balance clinical requirements with the principles of patient-centered care (13, 19, 20, 22, 23).
Taken together, these results suggest that differences between facilities may partly be explained by non-clinical drivers, underscoring the importance of considering institutional and cultural contexts when interpreting cesarean section rates (24–27).
The strength of this study is that we collected data from 14 totally different structures of the Apulia Region (Italy), including a relatively large sample, which enhances the generalizability of our findings and reflects real-world practices and outcomes within the regional healthcare system. However, several limitations should be acknowledged. First, although data were extracted from official delivery room registers, there remains the possibility of transcription errors, incomplete reporting, and omissions in diagnostic or procedural coding. These issues are inherent to the use of administrative or registry-based datasets and may have introduced misclassification bias. While quality checks were performed, we cannot fully exclude inaccuracies that could have affected the categorization of Robson groups or the documentation of delivery outcomes. Second, due to the retrospective design and reliance on registry data, we were unable to control for several maternal and neonatal confounders known to influence the likelihood of CS. These include maternal age, pre-pregnancy body mass index, parity history beyond the Robson classification, obstetric comorbidities such as gestational diabetes and hypertension, fetal weight, and fetal presentation. The absence of these variables may have resulted in residual confounding and limited the precision of our effect estimates. Third, we were unable to differentiate between elective and emergency CS, nor to categorize specific indications (e.g., fetal distress, failed induction, or cephalopelvic disproportion). The delivery room register did not include standardized documentation of indications, which limited our ability to directly assess the appropriateness of CS. This represents a key area for improvement in data collection systems, as distinguishing between medical necessity and non-clinical drivers is essential for evaluating adherence to guidelines and informing health policy (28–32).
Future prospective studies should aim to incorporate these variables and ideally link registry data with clinical records to enable more precise categorization of indications and provide a more comprehensive adjustment for both clinical and non-clinical determinants of cesarean delivery (34).
Conclusion and implications for healthcare policies
4.2
The increase in cesarean deliveries reported in the scientific literature is largely influenced by factors beyond clinical guidelines (35, 36). CS is often performed in situations where it may be deemed inappropriate, with appropriateness understood as a dimension of quality of care that encompasses technical and scientific validity, acceptability, and relevance to the individual, specific circumstances, and contexts, in line with current knowledge (37–39). For women in Robson groups 1, 2a, 3, and 4a, the mode of delivery appears to be strongly structure-dependent, as shown by the statistical association between facilities and delivery type. Our findings demonstrate the real possibility of achieving CS rates consistent with those recommended by the World Health Organization (23, 35, 36). Health policies should therefore promote education initiatives targeting both the general population and healthcare professionals, focusing on the dissemination and implementation of evidence-based practices in public and private sectors (37–39).
Based on our findings, several implications for policy and practice can be drawn. At the regional level, systematic use of the Robson classification could support benchmarking and continuous monitoring of CS rates (34–36). At the hospital level, harmonization of intrapartum care protocols and regular audit and feedback may help reduce unwarranted variability (24–27, 33). At the clinical level, promoting evidence-based practices such as VBAC, standardized counseling, and shared decision-making could enhance the appropriateness of delivery mode (22, 23, 35). Future studies are needed to design and validate coordinated interventions aimed at minimizing the influence of non-clinical and structure-dependent factors in determining the mode of delivery (37–39).
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