Analysis of Caesarean Section Rate According to the Robson Classification System

Analysis of Caesarean Section Rate According to the 10 Group Robson Classification; A Multicenter Prospective Study in Egypt

A prospective cross- sectional study will be conducted to implement the Robson Classification to assess, analyze and compare Caesarean section rate of the participating hospital over the period of three months. The Robson implementation manual will be used as a tool guide for the study.

Study Overview

Status

Unknown

Detailed Description

Increase rate of unnecessary caesarean sections has been a growing concern in most parts of the world. According to the latest survey one in five women in the world now deliver by caesarean section (CS). The Eastern Mediterranean Region (EMR) with its twenty -two Member States (MSs) as classified by the World Health Organization is of no exception in this respect. Within the EMR, Egypt has the highest CS rate of 54%, with no further improvement to maternal and child mortality rates in Egypt, the association of extremely high CS rate and its potential benefits has been questioned. This may suggest that although the necessary numbers of CSs are performed for the population at risk but the rates higher than the recommended threshold (10-15% according to the WHO) could be the measure of unjustified CSs in healthy populations . However, determining the adequate caesarean section rate at the population level - i.e. the minimum rate for medically indicated caesarean section, while avoiding medically unnecessary operations - is a challenging task. Variations in overall CS rate between different settings or over time are difficult to interpret and compare because of intrinsic differences in hospital factors and infrastructure (primary versus tertiary level), difference in the characteristics of the obstetric population (case mix) served (eg % of women delivered by previous CS) and difference in clinical management protocols. This is seen as one of the barriers in better understanding of CS trends and underlying causes. In order to propose and implement effective measures to achieve optimal CS rates, it is first essential to identify what groups of women are contributing the most towards overall CS rate and investigate the underlying reasons for trends in different settings. Like many developing countries, health care facilities in Egypt have no such standardized internationally accepted classification system in place to monitor and compare facility based CS rates in a consistent and action oriented manner.

Policy makers and health organisations have suggested the need for such classification system that can best monitor and compare CS rates in a standardised, reliable, consistent and action-oriented manner. WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS. It gives an opportunity to evaluate the prevalence of CSs among various groups of women, to compare data between institutions, learn from each other and to create strategies for better results through audit and feed back cycle. This classification is clinically relevant and categorizes women prospectively which in turns allows the implementation and evaluation of interventions targeted to specific groups. Some studies have shown that if this classification is used on a regular basis, it can provide critical assessment to change the practice.

Aim: The study aim is, to assess, analyse and compare CSR of the participating hospital over the period of three months according to the 10 Group Robson classification system

Participating hospitals

1: Ain Shams University Hospital 4: Mataria Teaching Hospital 4: Shatby Alexandria Hospital 5: Benha University Hospital 6: Ahmed Maher Hospital 7: El-Galaa Hospital 8: Alexandria Hospital 9: Behira Hospital 10:Menia Hospital 11: Luxor Hospital 12: Nada Hospital 13: Rofayda Hospital

Study design: A prospective cross- sectional study will be conducted to implement the Robson Classification within the obstetric department of participating hospitals. The Robson implementation manual will be used as a tool guide for the study.

The study population will include all women with live births and stillbirths of at least 28 weeks gestation at from. Two-study investigator from each participating hospital will be assigned who will provide the ongoing support during the study period. Participants will be invited to attend the introductory workshop for the implementation of the Robson Classification by the study coordinators. Variables necessary to categorise women in to Robson groups will be collected through the predesigned proforma. These variables will be used to classify each woman in to Robson groups with the help of a flow diagram. The collected information will be analyzed on the Excel Sheet to finalize the grouping either manually or by an automatic calculator.The results of each group will be statistically analyzed after entering the data in the report and will be sent on a monthly basis by e-mail or fax to study coordinators.

Study Type

Observational

Enrollment (Anticipated)

3000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Cairo, Egypt
        • Recruiting
        • Egyption society of Royal college of obstetricians and gynaecologist
        • Contact:
        • Contact:
        • Principal Investigator:
          • Bismeen Jadoon, MBBS, MRCOG
        • Principal Investigator:
          • Amr El Nouri, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

All women admitted to the labour ward for delivery who are 28 or more weeks of gestation.

Description

Inclusion criteria:

  • Women delivering at ≥ 28 weeks gestation

Exclusion Criteria:

  • Women delivering at < 28 weeks gestation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Robson group 1
Nulliparous women, single cephalic, more than or equal to 37 weeks, in spontaneous labour
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 2
Nulliparous women, single cephalic, more than or equal to 37 weeks, induced or Caesarean section before labour
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 3
Multiparous women with out a previous Caesarean section , with a single cephalic pregnancy, more than or equal 37 weeks gestation in spontaneous labour
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 4
Multiparous women with out a previous Caesarean section , with a single cephalic pregnancy, more or equal 37 weeks gestation who had labour induced or were delivered by Caesarean section before labour
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 5
All Multiparous women with at least one CS with a single cephalic pregnancy, more or equal to 37 weeks gestation
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 6
All nulliparous women with a single breech pregnancy
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 7
Multiparous women with a single breech pregnancy including women with previous Caesarean section
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 8
All women with multiple pregnancies including women with previous Caesarean sections
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 9
All women with a single pregnancy with a transverse or oblique lie, including women with previous Caesarean Section (s)
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.
Robson Group 10
All women with a single cephalic pregnancy less than 37 weeks gestation, including women with previous Caesarean section (s)
WHO proposed the Robson classification system as a global standard for assessing, monitoring and comparing caesarean section rates within healthcare facilities over time, and between facilities. It classifies women in 10 groups based on their obstetric characteristics (parity, previous CS, gestational age, onset of labour, fetal presentation and number of fetuses) without needing the indication for CS.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
caesarean section rate
Time Frame: three months
absolute and relative caesarean section rate
three months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postpartum haemorrhage
Time Frame: from 24 hours to 6 weeks after the delievry
  1. Blood loss of more than 500 mls at vaginal birth
  2. Blood loss of more than 1000 mls at caesarean section
from 24 hours to 6 weeks after the delievry
Maternal morbidity
Time Frame: 7 days after the delivery
Admission to Intensive care unit after the delivery
7 days after the delivery
Neonatal morbidity
Time Frame: 7 days of the delivery
Admission of newborn to Neonatal intensive care unit
7 days of the delivery
Maternal mortality
Time Frame: 42 days after the delivery
maternal death from 24 hours to 42 days after the delivery
42 days after the delivery
Neonatal mortality
Time Frame: 28 days after the delivery
death during the first 28 days of life (0-27 days
28 days after the delivery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 10, 2019

Primary Completion (Anticipated)

August 1, 2019

Study Completion (Anticipated)

August 1, 2019

Study Registration Dates

First Submitted

December 29, 2018

First Submitted That Met QC Criteria

January 3, 2019

First Posted (Actual)

January 4, 2019

Study Record Updates

Last Update Posted (Actual)

July 18, 2019

Last Update Submitted That Met QC Criteria

July 16, 2019

Last Verified

July 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • ERC-RCOG

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Sharing Time Frame

3 months after the study completed

IPD Sharing Supporting Information Type

  • Study Protocol
  • Statistical Analysis Plan (SAP)
  • Informed Consent Form (ICF)
  • Clinical Study Report (CSR)
  • Analytic Code

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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