Journal of the College of Physicians and Surgeons Pakistan
ISSN: 1022-386X (PRINT)
ISSN: 1681-7168 (ONLINE)
Affiliations
doi: 10.29271/jcpsp.2026.03.310ABSTRACT
Objective: To identify the factors associated with postoperative ileus (POI) following Caesarean section.
Study Design: A descriptive study.
Place and Duration of the Study: Department of Obstetrics and Gynaecology, Zeynep Kamil Women's and Children's Diseases Training and Research Hospital, Istanbul, Turkiye, between April 2021 and February 2025.
Methodology: A total of 293 women who underwent Caesarean section were evaluated postoperatively. POI was defined as the absence of the first flatus within 24 hours after surgery. Demographic and obstetric characteristics, as well as factors associated with POI, were compared between patients with and without POI.
Results: POI developed in 33 patients (11.3%). Multivariate binary logistic regression showed an increased risk of POI with each 1-unit decrease in preoperative haemoglobin level (RR 1.357, 95% CI = 1.029-1.791, p = 0.031) and with intraoperative drain placement (RR 6.433, 95% CI = 2.326-17.792, p <0.001).
Conclusion: POI can delay postpartum recovery. Preoperative anaemia, history of POI, and intraoperative drain placement are significant risk factors for POI after Caesarean section.
Key Words: Caesarean section, Ileus, Maternal health, Postoperative complications, Postpartum women.
INTRODUCTION
Postoperative ileus (POI) is a temporary, non-mechanical gastrointestinal dysfunction that develops after surgery and is caused by loss of peristalsis. It presents clinically with abdominal distension, abdominal tenderness, and decreased bowel sounds.1
POI after Caesarean section, the most common obstetric procedure, may result in a prolonged hospital stay, delayed recovery for both mother and child, and increased medical costs. Bleeding greater than 1,000 ml during Caesarean section, multiple pregnancy, corporeal uterine incision, use of topical haemostatic agents, and advanced maternal age have been reported as risk factors for this complication.2 A diagnosis of pre-eclampsia, exposure to general anaes- thesia, estimated blood loss >1 L, and transfusion of blood products were identified as potential risk factors for postcesarean ileus.3
Precautions and practices in the postoperative period for the management of this condition have been frequently studied. It has been reported that a preoperative low-residue diet reduces ileus and pain after Caesarean section.4 Early oral feeding within two hours following Caesarean section has been found to speed the restoration to normal bowel function.5 Chewing gum within the first hour postoperatively has also been shown to enhance recovery.6
The postpartum period is an emotional and challenging time in which the mother, in addition to other post-surgical periods, also undertakes the care of the newborn baby. This study aimed to identify risk factors associated with prolonged time to first flatus in women undergoing Caesa-rean section.
METHODOLOGY
This descriptive study was conducted at the Department of Obstetrics and Gynaecology, Zeynep Kamil Women's and Children's Diseases Training and Research Hospital, Istanbul, Turkiye, between April 2021 and February 2025. Ethical approval was obtained from the Clinical Research Ethics Committee of Zeynep Kamil Women's and Children's Diseases Training and Research Hospital, Istanbul, Turkiye (No. 54; date: 3rd March 2021). The sample size was calculated using the Open-Epi. For a study with a 95% confidence interval and 80% power, a minimum of 260 participants was required.
Women aged 18-45 years who gave birth via Caesarean section at this hospital were included in the study. Women declining participation and those diagnosed with a psychiatric disease or gastrointestinal disease were excluded from the study. Patients were informed about the study and assigned to it on days when the research team was on duty in the maternity ward. A total of 293 postpartum women were included. Patients were evaluated on the first and second postoperative days. The patient’s age was confirmed from official records. Weight and height were measured by the midwife within 1–48 hours of hospitalisation, and these measurements were used to calculate the body mass index (BMI) before surgery. Past medical history and obstetric history were recorded based on the patients’ statements. Data on surgery and anaesthesia were obtained from the surgery and anaesthesia records. Previous abdominal surgery included all intra-abdominal procedures, including Caesarean section. Flatus complications related to previous surgeries were only evaluated in those who had surgery. In the postoperative period following Caesarean section, an independent nurse or physician working on the ward and not involved in the research asked patients to report the time of first passage of flatus. The time to first flatus was obtained from these records and documented accordingly. Postpartum women who did not have their first flatus by the end of the 24th hour were defined as having POI. Laboratory and other clinical follow-up data were obtained from printed and electronic patient files. Smokers were defined as those who continued smoking during pregnancy.
The distribution of data across groups was evaluated with the Kolmogorov-Smirnov test. Quantitative variables were analysed with the Student’s t-test for data that were normally distributed and with the Mann-Whitney U test for data that were not normally distributed. Categorical variables were analysed using the Pearson chi-square test, and odds ratios (OR) with 95% confidence intervals (CIs) for those found significant between the two groups were also reported. A p-value <0.05 was considered to be statistically significant. Quantitative variables were reported as mean ± standard deviation (SD). Categorical variables were reported as numbers and percentages. The binary logistic regression was performed using the Backward LR method. All of the statistical analyses were performed using IBM SPSS Statistics 17 (IBM SPSS, Turkiye).
RESULTSA total of 311 eligible patients were invited to the study. Seven patients declined to participate in the study, and five were excluded due to high Postpartum Edinburgh Depression Scale scores. Additionally, six patients were excluded because of a history of gastrointestinal disease. A total of 293 postpartum women were included in the study. Thirty-three (11.3%) developed POI. No differences were observed in age, gravida, parity, number of previous Caesarean sections, maternal weight before pregnancy and before surgery, height, maternal BMI before pregnancy and before surgery, gestational age at birth, fasting time before Caesarean section, operation time, or laboratory variables, except for preoperative and postoperative haemoglobin levels which were significantly lower in patients who developed POI (p = 0.009 and p = 0.029, respectively; Table I).
Univariate analyses revealed that patients who had experienced POI after previous abdominal surgery were significantly more likely to develop POI (p = 0.013). The prevalence of smoking was 12.5% in the POI group and 13.1% in the group without POI. The two groups were statistically similar. Intraoperative and postoperative conditions related to the current Caesarean section were also analysed. Drain placement was associated with a significantly increased risk of POI (p <0.001). Haemorrhage greater than 1,000 cc was observed in 12.1% and 4.6% of the groups with and without POI, respectively.
Table I: Demographic and postoperative characteristics of patients with and without POI.|
Variables |
Cases with POI (n = 33) |
Cases without POI (n = 260) |
p-values |
||
|
Age* (year) |
31.4 |
±6.5 |
30.0 |
±5.9 |
0.216a |
|
Gravida** |
3 |
2-4 |
2 |
1-3 |
0.293b |
|
Parity** |
2 |
1-3 |
1 |
0-2 |
0.010b |
|
Number of CS** |
1 |
1-2 |
1 |
0-2 |
0.103b |
|
Pre-pregnancy weight (kg)** |
70 |
63.5-82.0 |
68 |
60-80 |
0.461b |
|
Weight before surgery** |
80 |
72.5-88.5 |
80 |
70-90 |
0.815b |
|
Pre-pregnancy BMI (kg/m2)** |
27.3 |
24.9-29.1 |
26.3 |
22.9-30.2 |
0.370b |
|
BMI before surgery (kg/m2)** |
31.8 |
±4.6 |
31.0 |
±5.0 |
0.704a |
|
Gestational age at birth** |
266 |
249-273 |
266 |
259-273 |
0.684b |
|
Fasting time before CS (hours)** |
8 |
6-12.0 |
8 |
6-12 |
0.674b |
|
Operation time (minute)** |
60 |
45-65.0 |
55 |
45-60 |
0.285b |
|
Preoperative Hgb (g/dL)** |
10.8 |
±1.3 |
11.5 |
±1.4 |
0.009a |
|
Postoperative Hgb (g/dL)** |
9.7 |
8.9-10.8 |
10.4 |
9.4-11.3 |
0.029b |
|
Creatinine (mg/dL)** |
0.55 |
0.50-0.64 |
0.52 |
0.46-0.59 |
0.225b |
|
*Mean ± standard deviation, **Median (IQR), a Independent Student’s t-test, b Mann-Whitney U test, BMI: Body mass index; CS: Caesarean section, Hgb: Haemo-globin level; POI: Postoperative ileus. |
|||||
Table II: Medical history, Caesarean section operation, and postoperative characteristics of patients with and without POI.
|
Variables |
Cases with POI (n = 33) |
Cases without POI (n = 260) |
p-values |
|||
|
n |
% |
n |
% |
|
||
|
Previous abdominal surgery |
Yes |
20 |
60.6 |
143 |
55.0 |
0.541 |
|
No |
13 |
39.4 |
117 |
45.0 |
|
|
|
POI in previous abdominal surgery* |
Yes |
5 |
15.2 |
7 |
3.5 |
0.013a |
|
No |
28 |
84.8 |
251 |
96.5 |
|
|
|
Hypertensive diseases of pregnancy |
Yes |
5 |
15.2 |
38 |
14.6 |
0.935 |
|
No |
28 |
84.8 |
222 |
85.6 |
|
|
|
Diabetes
|
Yes |
5 |
15.2 |
51 |
19.6 |
0.539 |
|
No |
28 |
84.8 |
209 |
80.4 |
|
|
|
Smoking
|
Yes |
4 |
12.5 |
29 |
13.1 |
1.000 |
|
No |
28 |
87.5 |
192 |
86.9 |
|
|
|
Indication for CS
|
Urgent |
18 |
54.5 |
118 |
45.2 |
0.320 |
|
Elective |
15 |
45.5 |
142 |
54.8 |
|
|
|
Anesthesia method |
General |
9 |
27.3 |
57 |
21.9 |
0.488 |
|
Spinal |
24 |
72.7 |
203 |
78.1 |
|
|
|
Incision type |
Kerr incision |
33 |
100.0 |
255 |
98.1 |
1.000a |
|
T or J incision |
0 |
0.0 |
5 |
1.9 |
|
|
|
Complicated uterine incision** |
Yes |
3 |
9.1 |
7 |
2.7 |
0.090a |
|
No |
30 |
90.9 |
253 |
97.3 |
|
|
|
Intra-abdominal adhesion
|
Present |
8 |
24.2 |
45 |
17.3 |
0.330 |
|
Absent |
25 |
75.8 |
215 |
82.7 |
|
|
|
Urinary tract injury |
Present |
2 |
6.1 |
2 |
0.8 |
0.064a |
|
Absent |
31 |
93.9 |
258 |
99.2 |
|
|
|
Bowel injury |
Present |
0 |
0.0 |
1 |
0.4 |
1.000a |
|
Absent |
33 |
100.0 |
259 |
99.6 |
|
|
|
>1,000 cc haemorrhage |
Yes |
4 |
12.1 |
12 |
4.6 |
0.091a |
|
No |
29 |
87.9 |
248 |
95.4 |
|
|
|
Uterine atony |
Yes |
3 |
9.1 |
10 |
3.8 |
0.170a |
|
No |
30 |
90.9 |
250 |
96.2 |
|
|
|
Surgical intervention for atony |
Yes |
2 |
6.1 |
8 |
3.1 |
0.313a |
|
No |
31 |
93.9 |
252 |
96.9 |
|
|
|
Drain placement |
Yes |
9 |
27.3 |
13 |
5.0 |
<0.00a |
|
No |
24 |
72.7 |
247 |
95.0 |
|
|
|
Blood product transfusion |
Yes |
4 |
12.1 |
5 |
1.9 |
0.011a |
|
No |
29 |
87.9 |
255 |
98.1 |
|
|
|
Postoperative fever
|
Yes |
0 |
0.0 |
3 |
1.2 |
1.000a |
|
No |
33 |
100.0 |
257 |
98.8 |
|
|
|
Oliguria in the first 6 hours postoperatively |
Yes |
1 |
3.0 |
8 |
3.1 |
1.000a |
|
No |
32 |
97.2 |
252 |
96.9 |
|
|
|
Fluid balance |
In balance |
0 |
0.0 |
15 |
5.8 |
0.199 |
|
Plus |
29 |
87.9 |
196 |
75.4 |
|
|
|
Minus |
4 |
12.1 |
49 |
18.8 |
|
|
|
Follow-up in ICU |
Yes |
9 |
27.3 |
46 |
17.7 |
0.184 |
|
No |
24 |
72.7 |
214 |
82.3 |
|
|
|
aFisher’s exact test, *Cases that had previously undergone surgery were included. **Complicated uterine incision: The situation where the uterine incision extends to the vagina. ICU: Intensive care unit; POI: Postoperative ileus. |
||||||
Table III: Multivariate binary logistic regression analysis of all cases, including age, BMI before delivery, and any parameter with a p <0.2 in univariate analysis.
|
Variables |
RR |
95% CI |
p-values |
|
All cases regression analysis |
|
|
|
|
Preoperative Hgb (g/dL) |
1.357 |
1.029-1.791 |
0.031 |
|
Blood product transfusion |
5.769 |
1.227-27.120 |
0.026 |
|
Drain placement |
6.433 |
2.326-17.793 |
<0.001 |
|
Cases that have undergone surgery before |
|
|
|
|
POI in previous abdominal surgery |
11.931 |
2.598-54.796 |
<0.001 |
|
Postoperative Hgb (g/dL) |
1.844 |
1.197-2.842 |
0.006 |
|
Drain placement |
9.777 |
2.441-39.136 |
0.001 |
|
Hgb: Haemoglobin level. |
|||
No statistically significant difference was found between the two groups. The need for blood product transfusion was 12.1% in the group with POI and 1.9% in the group without POI, demonstrating a statistically significant difference (p = 0.011; Table II).
Multivariate binary logistic regression analysis showed that, when all cases were evaluated, the relative risk (RR) for the development of POI was 1.357 (95% CI = 1.029-1.791, p = 0.031) for a 1-unit decrease in preoperative haemoglobin level. The RR for the development of POI associated with drain placement and with the need for blood product transfusion during the current operation were 6.433 (95% CI = 2.326-17.793, p <0.001) and 5.769 (95% CI = 1.227-27.120, p = 0.026), respectively.
In the multivariate binary logistic regression analysis including only patients who had previously undergone abdominal surgery, a history of POI in the previous surgery was found to be a significant predictor of POI in the current operation (RR = 11.931, 95% CI = 2.598-54.796; p <0.001). Postoperative Hgb decrease was associated with an RR of 1.844 (p = 0.006), while drain placement was associated with an RR of 13.924 (p <0.001; Table III).
DISCUSSION
This study aimed to determine the risk factors that are effective in prolonging the postoperative flatus time in women who gave birth by Caesarean section. Low preoperative and postoperative haemoglobin levels, history of gastrointestinal disease, and drain placement were determined as factors that increase the risk of POI.
The importance of nutritional interventions in preventing postoperative complications in general surgery cases has been reported. In a clinical nutrition in surgery guideline, some recommendations are as follows: in cases that are scheduled for surgery and not at risk of aspiration, fluid intake may be allowed up to two hours, and solid intake may be allowed up to six hours before surgery. Oral intake can be resumed two hours after surgery.7 In Caesarean section cases, it has been reported that practices such as preoperative low-residue diet, early feeding within 2 hours in the postoperative period, and chewing gum after Caesarean section are beneficial in preventing POI.4,5,8 At the study centre, except in emergencies, Caesarean section is performed after 6 hours of preoperative fasting, and it is not desired to extend this period. Feeding begins 4-6 hours postoperatively. The present study group was not suitable for comparing nutritional practices and fasting duration, and no difference was found between the two groups. In a retrospective case-control study comparing patient-controlled analgesia with intramuscular analgesia after Caesarean section, the incidence of moderate-to-severe adynamic ileus was reported to be higher in the patient-controlled analgesia group (21.8% vs. 13.5%).9 Intramuscular analgesia was preferred in all cases included in the study.
In a comparative animal study, it was shown that in rats exposed to haemorrhagic shock, there was impaired smooth muscle contraction and, therefore, intestinal contractility following the inflammatory response.10 A retrospective cohort study evaluating women who had undergone Caesarean section over six years reported that intraoperative bleeding >1,000 mL was the most significant risk factor associated with postoperative paralytic ileus in multivariate analyses.11 Potential risk factors for the development of ileus following Caesarean section were identified in a retrospective case-control study in cases with and without paralytic ileus within six weeks following cWQWWaesarean section. These factors included the use of magnesium sulphate, general anaesthesia, estimated blooWd loss greater than one litre, and blood product transfusion.3 Severe preoperative anaemia was found to be a risk factor for POI development [OR 2.7 (1.5–5.0), p = 0.001].12 In the present study, although blood transfusion was significant in univariate analysis, no difference was found in multivariate analysis. However, preoperative haemoglobin level was a risk factor for the development of POI in all cases. Preventing anaemia in pregnancy, which creates a burden of disease, is important for reducing maternal and foetal morbidity and mortality. The World Health Organization (WHO) recommends 30-60 mg/day elemental iron supplementation during pregnancy.13 Considering this study, preoperative anaemia is a condition that should be taken into consideration and can be prevented with safe antenatal care.
There are limited studies evaluating the risk of POI occurring in subsequent abdominal surgery. In a 3-stage abdominal surgery performed in ulcerative colitis cases, it has been reported that the development of POI in the first stage does not pose an increased risk for developing POI in the subsequent surgical stage.14 In the current study, the frequency of experiencing flatus problems in the previous operation was higher in patients who had POI in the last Caesarean section. Studies have focused on the effects of nicotine, a component of cigarettes, on gastrointestinal system motility rather than on the effects of smoking on gastrointestinal motility. Smoking is the most common source of nicotine exposure. Transdermal nicotine administration has been reported to shorten total colonic transit time.15 Smoking status was assessed in the current study; however, no significant difference was observed between the groups.
Drain placements are used to monitor the discharge of blood, pus, and ascites from body cavities.16 In a prospective controlled study of gastric cancer patients who underwent total gastrectomy, prophylactic drain placement was shown to delay healing and be associated with delayed bowel movements.17 In a clinical review on abdominal drains, it was reported that abdominal drain placements may be associated with intestinal obstruction. The importance of removing the drain at the appropriate time in preventing complications was reported.18 Drains are generally removed without complications, but in rare cases, herniation, evisceration, and knotting of the drain tube may occur.19,20 Consistent with these studies, drain placement was found to pose a risk in terms of POI development in our study. As a result, it is critical to carefully assess the indications for drain placement, not to extend the follow-up period with the drain beyond what is essential, and to be aware of the problems that may arise during drain placement and removal.
Clinical algorithms in the clinic where the study was con- ducted propose conventional preoperative and postoperative care, as well as precautions to avoid POI. The strength of this study lies in its ability to represent this patient group.
A study evaluating mobilisation within 48 hours postoperatively in major elective surgery cases reported a significant improvement in the composite outcome for every four-minute increase in mobilisation.21 Although all of the patients in the current study were mobilised within 4-6 hours after surgery, the intensity of mobilisation within the first 24 hours was not assessed. The present study was not sufficient to evaluate the risk of POI that may be related to the type of anaesthetic method. These are the limitations of the study.
CONCLUSION
POI in postpartum patients can cause delays in recovery, difficulties with activities such as breastfeeding and caring for the newborn, and the development of psychological and social issues. This study determined that preoperative anaemia, history of POI in previous abdominal surgeries, and surgical drain placement are risk factors for the development of POI.
ETHICAL APPROVAL:
Ethical approval was obtained from the Clinical Research Ethics Committee of the Zeynep Kamil Women and Children's Diseases Training and Research Hospital, Istanbul, Turkiye (No. 54; date: 3rd March 2021). The study was conducted in accordance with the Declaration of Helsinki.
PATIENTS’ CONSENT:
Informed consent was obtained from each patient.
COMPETING INTEREST:
The authors declared no conflict of interest.
AUTHORS’ CONTRIBUTION:
NUT: Conception, acquisition, analysis of data, drafting, and revision of the manuscript.
HE, MY: Acquisition of data and revision of the manuscript.
HAT: Analysis of data, drafting, and revision of the manuscript.
All authors approved the final version of the manuscript to be published.
REFERENCES