Abstract
Objective
To analyse caesarean section (CS) using Robson 10-group classification system in an Ethiopian university hospital.
Design
Cross-sectional study.
Setting
A university hospital in eastern, Ethiopia.
Participants
980 women who underwent CS from January 2016 to April 2017.
Main outcome
Robson groups (1–10—based on gestational age, fetal presentation, number of fetus, onset of labour and history of CS) and indications for CS.
Results
Robson group 3 (multiparous women with single cephalic full-term pregnancy in spontaneous labour with no history of CS), group 5 (multiparous women with single cephalic full-term pregnancy with history of CS) and group 1 (single cephalic nulliparous women full-term pregnancy in spontaneous labour) were the major contributors to the overall CS at 21.4%, 21.1% and 19.3%, respectively. The three major indications for CS were fetal compromise (mainly fetal distress), obstructed labour (mainly cephalopelvic disproportion) and previous CS.
Conclusion
Robson groups 3, 5 and 1 were the major contributors to the overall CS rate. Fetal compromise, obstructed labour and previous CS were the underlying indications for performing CS. Further study is required to assess the appropriateness of the indications and to reduce CS among the low-risk groups (groups 1 and 3).
Keywords: caesarean section, ethiopia, maternal health, robson classification, audit
Strengths and limitations of this study.
Conducted in a university hospital with large catchment population.
Analysed caesarean section over 16 months to avoid seasonal variations.
Because of retrospective design, some relevant information might be missing.
Most of the women were referred cases with underlying complications and may not be generalised to general population.
Single-hospital (with large burden of referred cases) study, might be less generalisable.
Introduction
Over the last few decades, the global caesarean section (CS) rate has significantly increased and reached an unprecedented level.1 Although there is no specific rate of recommended CS rate,2 no improvement in maternal and neonatal outcomes was observed in CS rates above 10%.3 4 CS is performed when vaginal delivery is not possible or contraindicated.5 In such cases, not performing a CS could endanger the life of the mother and the fetus. However, CS is also performed without medical reasons or with imprecise indications such as obstructed labour, with intact membranes.6 This potentially life-saving procedure is not without risk and might become life-threatening in the index or future pregnancies for both the mother and child. Immediate and long-term complications of CS including increased risk of maternal mortality and morbidity, increased need for blood transfusion, longer hospitalisation, postpartum infections, retained placenta, stillbirths and postpartum haemorrhage were reported.7–9
Although the national population-based CS rate of Ethiopia is still one of the lowest in the world (2%),10 a national review conducted in 2011 indicated a high CS rate in facilities (15% in public facilities vs 46.1% in for-profit centres),11 which is expected to be higher now because of the general increase in the CS rate. A study conducted in eastern Ethiopia indicated a CS rate of 34.3% (26.6% in public facilities and 58.7% in private hospitals).12 The population-based study, from the Demographic and Health Survey, is low since many women in need of CS do never reach facilities (institutional delivery rate of 26%).10 This indicates that some women might be exposed to unnecessary CS while others do not get the CS they need.6 For example, CS is highest among women with at least secondary education, living in urban areas or are rich compared with their counterparts.13 14 In urban settings and among the rich, there is a concern, in many countries, that the intervention is being over utilised and unnecessary interventions are done. In rural settings, however, lack of access to adequately staffed and equipped health institutions for providing essential obstetric surgery is contributing largely to maternal mortality and complications.15
The challenge is to keep CS rates low while maintaining safe outcomes for the mother and infant. This requires continuous auditing of CS. Three different classifications—based on primary clinical indications, the degree of urgency or absolute need for caesarean delivery, and Robson classification—have been reported as a framework for auditing CS.16 A systematic review comparing different classifications concluded that the Robson classification is optimal for monitoring CS17 and the WHO recommended Robson classification as a global standard tool for monitoring CS.2 The Robson classification also called the Ten Group Classification System (TGCS), classifies CS into 10 mutually exclusive and exhaustive groups based on the category of the pregnancy, the previous obstetric record of the woman, the course of labour and delivery, and the gestational age of the pregnancy.18 Although the application of the TGCS and its importance for targeting population and reducing CS rates has been previously noted,19–21 there is no study in Ethiopia and contribution of different groups to the overall CS is unknown. In Ethiopia, where most facilities are situated in urban centres and high CS rate in referral hospitals is registered,12 22 an audit of CS deliveries using the TGCS is important to know which groups of women are mainly contributing to the increase in CS rate. The aim of this study was to analyse CSs using the TGCS and identify indications for CS in Hiwot Fana Specialized University Hospital in eastern Ethiopia.
Methods
Study design and participants
This study was conducted as part of a PhD study on severe maternal morbidity and mortality in eastern Ethiopia. We conducted a cross-sectional study to analyse all CS performed from January 2016 to April 2017 at the department of obstetrics of Hiwot Fana Specialised University Hospital (HFSUH) Harar, eastern Ethiopia. The study population included all women who underwent CS in the hospital during the specified period. Laparotomy for uterine rupture and files with missing information were excluded. The identity of women who underwent CS was obtained from the delivery logbook, admission and discharge register and operation logbook. The admission and discharge register and delivery logbook contain information about all women who delivered in the hospital regardless of mode of delivery (vaginal, CS) while the operation logbook contains only information about women who underwent CS. Using the medical registration number of each woman, we accessed all CS files performed during the study period.
Study setting
HFSUH is a tertiary referral hospital affiliated with the College of Health and Medical Sciences, Haramaya University, Ethiopia where around 3500 deliveries took place annually. The hospital serves both referred complicated cases and self-referred uncomplicated births. During the study period, the department of obstetrics was run by seven consultants, eight residents and 16 (nurse) midwives. The department has its operation theatre for obstetric cases.
Variables
For each CS case, we collected data on maternal characteristics (age, history of CS, parity and gravidity), pregnancy-related information (gestational age, fetal presentation, number of fetus and onset of labour) and maternal and fetal outcomes at discharge (complications, fifth minute APGAR score, birth weight, fetal and maternal status). Maternal complications included presence of a potentially life-threatening conditions (severe postpartum haemorrhage, severe pre-eclampsia, eclampsia, ruptured uterus, sepsis or severe systemic infections); admission to the intensive care unit other than for routine postoperative recovery; or receiving blood products. Presence of any life-threatening complication (including maternal near miss or deaths) was assessed at discharge. Maternal near miss refers to a woman who nearly died (developed organ dysfunction) but survived the complication, based on the WHO definition.23 The dependent variable was the Robson classification group. The 10 groups and their characteristics are shown in box 1. Fetal presentations were classified as cephalic, breech or transverse/oblique. Gestational age was categorised as a term (≥37 weeks) or preterm (<37 weeks). Gestational age is assessed using early prenatal ultrasound or last menstrual period. In case of no early ultrasound and unknown last menstrual period, a combination of physical examination, third trimester ultrasound and estimated fetal weight is used for estimation of gestational age. For cases with undocumented gestational age, we used a birth weight of ≥2500 gm as a proxy to term pregnancy. The course of pregnancy was categorised as spontaneous and induced/CS before labour. Number of parity was classified as nulliparous or multiparous. The number of fetuses was categorised as singleton or multiple pregnancies.
Box 1. Robson’s 10-group classification.
Description
Nulliparous, single cephalic, ≥37 weeks, in spontaneous labour.
Nulliparous, single cephalic, ≥37 weeks, induced or caesarean section (CS) before labour.
Multiparous (excluding previous CS), single cephalic, ≥37 weeks, in spontaneous labour.
Multiparous (excluding previous CS), single cephalic, >37 weeks, induced or CS before labour.
Previous CS, single cephalic, ≥ 37 weeks.
All nulliparous breeches.
All multiparous breeches (including previous CS).
All multiple pregnancies (including previous CS).
All abnormal lies (including previous CS).
All single cephalic, <37 weeks (including previous CS).
Data collection
Data were collected by medical students (OP, MM, MC, IK) from University of Groningen, the Netherlands. Data collectors were trained and supervised by the first author (AKT). All data quality, indications and eligibility of cases were confirmed by a senior obstetrician (TG). All CSs during the study period were retrieved from the operation register and were double checked with delivery logbook and admission and discharge registers. Completeness of data was checked by the first author (AKT).
Data processing and analysis
All completed data were entered using EpiData V.3.1(http://www.epidata.dk) and analysed using SPSS V.23. Descriptive statistics of study participants and variables was conducted. The Robson group was assigned based on four obstetric concepts (with their parameters)—category of the pregnancy, previous obstetric history, course of labour and gestational age.18 Missing files in the archive room and cases with incomplete information were excluded. All reported indications were classified as absolute maternal and non-absolute indications using the recommendations by Stanton et al.16 Absolute maternal indications included obstructed labour, major antepartum haemorrhage (APH), malpresentation (transverse, oblique and brow) and uterine rupture in hierarchical order. Non-absolute indications include fetal compromise, previous CS, failure to progress, breech, severe pre-eclampsia and eclampsia (with no hierarchy). Results were presented as frequencies, percentages, means and SD.
Results
During the study period, there were 4758 deliveries, of which 1224 (25.7%) were CS. After excluding incomplete cases (n=96) and missing files (148), 980 cases were included in the final analysis (figure 1). The mean age of participants was 26.3 (±5.7) years. Mean duration of hospitalisation was 6.3 (±3.9) days. A quarter of study participants (25%) had a potentially life-threatening condition, including 2.8% women with maternal near miss and nine maternal deaths. The mean gestational age was 37.7 (±2.2) weeks. Sociodemographic characteristics and obstetric conditions are summarised in table 1.
Table 1.
Variables | n | % |
Age (years) | ||
<20 | 78 | 7.9 |
20–35 | 850 | 86.7 |
> 35 | 53 | 5.4 |
Duration of hospitalisation | ||
1–7 days | 674 | 70.8 |
>7 days | 278 | 29.2 |
Type of CS | ||
Elective/planned | 72 | 7.4 |
Emergency | 908 | 92.6 |
Gravidity | ||
1 | 305 | 31.1 |
2–4 | 421 | 43.0 |
>4 | 254 | 25.9 |
Parity | ||
0 | 319 | 32.5 |
1–4 | 473 | 48.3 |
> 4 | 188 | 19.2 |
Gestational age | ||
Preterm (≤36 weeks) | 111 | 11.3 |
Term (37–42 weeks) | 863 | 88.1 |
Post-term (>42 weeks) | 4 | 0.6 |
Onset of labour | ||
Spontaneous | 728 | 74.4 |
Induced/CS before labour | 251 | 25.6 |
Fetal presentation | ||
Cephalic | 808 | 82.4 |
Breech | 135 | 13.8 |
Transverse/oblique/brow/others | 37 | 3.8 |
Fetal status at birth | ||
Alive | 924 | 94.3 |
Stillbirths | 56 | 5.7 |
Apgar score at 5 min | ||
<7 | 89 | 9.5 |
>7 | 836 | 90.5 |
Birth weight (g) | ||
<2500 | 157 | 16.1 |
2500–4000 | 779 | 80.1 |
>4000 | 37 | 3.8 |
Potential life-threatening conditions (n=245) | ||
Severe postpartum hemorrhage | 18 | 1.8 |
Severe pre-eclampsia | 122 | 12.4 |
Eclampsia | 62 | 6.3 |
Ruptured uterus | 6 | 0.6 |
Sepsis | 14 | 1.4 |
Transfusion of blood (>1 unit RBC) | 107 | 10.9 |
Maternal status at discharge | ||
Alive | 971 | 99.1 |
Dead | 9 | 0.9 |
CS, caesarean section; RBC, red blood cells.
Robson TGCS
In our study, single cephalic multiparous women at term in spontaneous labour with no previous history of CS (group 3) were the highest contributors to the overall CS rate, contributing 21.4% of all CS. The second highest contributors were women with a single cephalic presentation at term and previous CS (group 5) contributing 21.1% to the overall CS. The third highest contributors were single cephalic nulliparous women at term and in spontaneous labour (group 1) with 19.3%. All women with breech, transverse or oblique presentation (groups 6, 7, and 9 combined) contributed 13.8% to the overall CS. All single cephalic women in preterm (group 10) contributed 6.2% of all the CS (figure 2).
Indications for performing CS
As shown in figure 3, the main indications for performing CS were fetal compromise (fetal distress, cord prolapse or intrauterine growth retardation), obstructed labour (cephalopelvic disproportion, fetal macrosomia or unspecified disproportions) and previous CS. Indications per Robson group are shown in table 2. Absolute maternal indications (obstructed labour, major APH, malpresentation or uterine rupture) were the leading indications only in three groups: group 3 (obstructed labour), group 9 (malpresentation) and group 10 (major APH). In the other groups, non-absolute indications were the leading indications for performing CS—group 1 (fetal compromise), groups 2 and 4 (failure to progress), group 5 (previous CS), groups 6,7 and 8 (breech presentation). In general, CS was performed for absolute maternal indications in 36.6% (359/980) of cases (table 2). Diagrammatic representation of contribution of each indication within the groups is presented in figure 4.
Table 2.
Indications | Group 1 | Group 2 | Group 3 | Group 4 | Group 5 | Group 6 | Group 7 | Group 8 | Group 9 | Group 10 | Total n (%) |
Absolute maternal indications | 359 (36.6) | ||||||||||
Obstructed labour* | 73 (38.6) | 4 (7.0) | 74 (35.2) | 6 (9.7) | 29 (14.0) | 3 (8.8) | 8 (11.8) | 0 (0.0) | 5 (15.6) | 2 (3.3) | 204 (20.8) |
Major APH | 1 (0.5) | 1 (1.8) | 32 (15.2) | 17 (27.4) | 11 (5.3) | 2 (5.9) | 6 (8.8) | 6 (10.0) | 2 (6.3) | 21 (34.4) | 99 (10.1) |
Malpresentation† | 5 (2.7) | 0 (0.0) | 16 (7.6) | 0 (0.0) | 4 (1.9) | 0 (0.0) | 0 (0.0) | 3 (5.0) | 23 (71.8) | 0 (0.0) | 51 (5.2) |
Uterine rupture | 1 (0.5) | 0 (0.0) | 1 (0.5) | 1 (1.6) | 2 (1.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 5 (0.5) |
Non-absolute indications | 621 (63.4) | ||||||||||
Fetal compromise‡ | 101 (53.5) | 13 (22.8) | 65 (31.0) | 11 (17.7) | 20 (9.7) | 6 (17.6) | 8 (11.8) | 5 (8.3) | 2 (6.3) | 7 (11.5) | 238 (24.3) |
Previous CS | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 136 (65.7) | 0 (0.0) | 18 (26.5) | 5 (8.3) | 0 (0.0) | 7 (11.5) | 166 (16.9) |
Failure to progress§ | 6 (3.2) | 32 (56.1) | 5 (2.4) | 21 (33.9) | 3 (1.4) | 7 (20.6) | 9 (13.2) | 3 (5.0) | 0 (0.0) | 10 (16.4) | 96 (9.8) |
Breech presentation | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 16 (47.1) | 19 (27.9) | 21 (35.0) | 0 (0.0) | 0 (0.0) | 56 (5.7) |
(Severe pre-) eclampsia | 1 (0.5) | 2 (3.5) | 3 (1.4) | 2 (3.2) | 0 (0.0) | 0 (0.0) | 0 (0.00 | 12 (20.0) | 0 (0.0) | 13 (21.3) | 33 (3.4) |
Others | 1 (0.5) | 5 (8.8) | 14 (6.7) | 4 (6.5) | 2 (1.0) | 0 (0.0) | 0 (0.0) | 5 (8.3) | 0 (0.0) | 1 (1.6) | 32 (3.3) |
Total n (%) | 189 (100) | 57 (100) | 210 (100) | 62 (100) | 207 (100) | 34 (100) | 68 (100) | 60 (100) | 32 (100) | 61 (100) | 980 (100) |
*Cephalopelvic disproportion, macrosomia and unspecified disproportions.
†Transverse, oblique or brow.
‡Fetal distress, cord prolapse and intrauterine growth restriction.
§Prolonged labour, cervical arrest and failed induction.
APH, antepartum haemorrhage; CS, caesarean section.
Discussion
Our study showed that groups 3, 5, and 1 were the major contributors to the overall CS rate. This indicates high CS rate both in primary (groups 1 and 3) and secondary (group 5) CS. The study also showed that only one-third (36.6%) of the CS were performed for absolute maternal indications. A quarter of the women had a potentially life-threatening condition (including nine maternal deaths), resulting in admission for more than 7 days in 29.2% of the women. Since a majority of births in Ethiopia are occurring at home,10 most births in the hospital are among women with complications or women living in the urban areas nearby the hospital.
Our findings are in line with a classification applied in hospitals from Tanzania and South Africa24 25 where the three major groups (1, 3 and 5) were the same, though in a different order. In South Africa, groups 1, 5 and 3 while in Tanzania groups 1, 3 and 5 were the leading contributors. This may be related to variations in population demographics and overall CS rates.26 The contribution of group 3 could be justifiable in our study since the majority of the CS were performed for absolute maternal indications (obstructed labour and major antepartum haemorrhage).
In a study from a university hospital in Cote d’Ivoire, however, the most common groups were groups 1, 2 and 3.27 The importance of group 2 (nulliparous single cephalic term pregnancy, induced or caesarean before labour) in the study from Cote d’Ivoire could be explained by variations in indications for inductions of vaginal birth or CS in the two settings. In most high-income settings, groups 5, 2 and 1 are the major contributors to overall CS rate unlike the studies from low-income settings.28–31 The variations between high-income settings and our study may be related to fertility trends and, therefore, stronger presentation of groups 1 and 2 in high-income settings, compared with stronger presentation of multiparous women (group 3) in our low-resource setting with high fertility rates.10 26 Induction of labour (group 2) is more frequently practised in high-income settings ranging from 8.3% in Latvia to 33% in Wallonia (Belgium) compared with 4.4% in Africa.32 33 Risk selection in antenatal care is better developed, which leads to more frequently indicating induction of labour.34 Barriers for induction of labour in low-resource settings might be the unavailability of facilities to perform CS in case of failed induction.35 The fact that group 5 women were one of the major contributors both in high-income and low-income settings indicates the importance of preventing primary caesarean if a meaningful reduction in overall CS rate is to be achieved. In a study from Tanzania both primary and secondary CS were rising overtime.24
The strength of this study is the inclusion of all CS performed over 16 months in a referral hospital covering large catchment area. Although the hospital is serving both uncomplicated births and women with complications, the majority of the cases were cases of women referred with already existing complications and may be less generalisable. Accessing all CS files was difficult due to non-digital archiving of hospital files. Incompleteness of information (history of previous CS, fetal presentation) and incorrect recording of medical registration numbers on logbooks were the reasons for exclusion. We feel that incompleteness of information and inability to locate medical records were not related to any outcomes, and therefore, would not introduce systematic bias. Although the core variables for Robson classification (parity, history of CS, onset of labour, number of fetus, gestational age and fetal lie and presentation) are part of routine obstetric assessment,26 the retrospective design of our study may have affected our results because of the incompleteness of the records. We were unable to compute relative size of each Robson groups, and therefore, we cannot say anything about the relative size of each group and are unable to compare women who underwent CS with women who gave birth vaginally.
The performance of CS among low-risk groups (groups 1, 2, 3 and 4) for non-absolute medical indications—fetal compromise and failure to progress—should be further examined. In the majority of facilities, and HFSUH is not an exception, birth monitoring is minimal with a low recording of fetal heart rate on partograph.36 37 Inadequate facilities for monitoring fetal heart rate and lack of close monitoring are challenges to relying on such indications.38 Opportunities for instrumental delivery and training staff to increase its uptake are warranted to decrease primary caesarean among low-risk groups. Limiting the CS rate in low-risk pregnancies is key to lowering the trend of increased CS.39 Since TGCS is not an audit of the appropriateness of indications for CS,40 a continuous audit of indications for CS should be designed to achieve an optimum level of appropriate CS rates. Possible reasons for the increase in CS among groups 1 and 3 should be explored to decrease overall CS rate and repeat caesarean in the future (group 5). A prospective study consisting both women who delivered vaginally and through CS is necessary to understand the proportion of CS within each Robson group.
Supplementary Material
Acknowledgments
We want to thank the hospital managers for creating a conducive environment for conducting this study. We want to extend our thanks to supportive staffs in the maternity unit and card archive room for their support in relocating women’s medical files.
Footnotes
OP, MM, MC and IK contributed equally.
Contributors: AKT and JS conceived the study and wrote the original draft of the manuscript. OP, MdeM, MS and IK collected data. AKT, TG and JS did the supervision and provided mentorship. Analysis was done by AKT. All authors contributed to the writing and reviewed the article and approved the final version of the manuscript to be published.
Funding: AKT received a PhD grant from the Dutch Organisation for Internationalization in Education (NUFFIC).
Disclaimer: The funding organisation has no role in the design, execution or decision to publish the study.
Competing interests: None declared.
Patient consent: Not required.
Ethics approval: This study was approved by the institutional health research ethics review committee of College of Health and Medical Sciences, Haramaya University in Ethiopia (ref no: C/A/R/D/01/1681/16).
Provenance and peer review: Not commissioned; externally peer reviewed.
Data sharing statement: Data essential for conclusion are included in this manuscript. Additional data can be obtained from the corresponding author on reasonable request.
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