Introduction
Addressing Maternal Anaemia through Evidence and Innovation
Anaemia is a widespread global health challenge, particularly affecting pregnant women and young children. It has profound consequences on health, development, and economic productivity. According to the World Health Organization (WHO), anaemia affects 37% of women of reproductive age globally, with over 32 million women experiencing anaemia during pregnancy.
Postpartum anaemia is equally concerning—up to 80% of women may be anaemic within 48 hours after delivery. The leading cause is iron deficiency, which accounts for over 60% of anaemia cases globally. In sub-Saharan Africa, where the burden is especially high, up to 44% of pregnant women are anaemic, and between 20% and 37% continue to experience iron deficiency after childbirth.
The health risks of maternal anaemia are significant. Iron Deficiency Anaemia (IDA) is associated with poor pregnancy outcomes such as premature birth, low birth weight, intrauterine growth restriction, stillbirth, and even maternal death. The consequences extend into the postpartum period, affecting both maternal recovery and infant health.
Current global recommendations advise the use of 60mg of elemental iron daily during pregnancy until haemoglobin (Hb) reaches normal levels. While oral iron is widely used and affordable, it often causes gastrointestinal side effects like diarrhoea and abdominal discomfort, which limit adherence. Intravenous (IV) iron—especially Ferric Carboxymaltose (FCM)—has emerged as a more effective alternative, offering rapid correction of anaemia with fewer side effects.
Evidence from studies conducted in Nigeria, including the IVON trial, has shown that FCM is both safe and effective. It significantly reduced iron deficiency and IDA during pregnancy by 73% and 78%, respectively, compared to oral iron. Its single-dose administration, high bioavailability, and ease of use make it particularly well-suited for health systems with limited capacity.
In many Nigerian health facilities, anaemia in pregnancy is still managed primarily through iron and folic acid (IFA) supplements. However, moderate to severe anaemia often goes undiagnosed, and mild anaemia—which can progress into more severe forms—is frequently overlooked due to limited screening capacity.
Alongside FCM, Multiple Micronutrient Supplementation (MMS) is another promising intervention. MMS provides a combination of essential vitamins and minerals, including iron and folic acid, and has been shown to reduce the risk of low birth weight, preterm births, small-for-gestational-age babies, and stillbirths. Although MMS contains a lower dose of iron than IFA, its broader nutritional benefits offer significant advantages for maternal health, especially in resource-limited settings.
Building on evidence from IVON, IVON-PP, and IVON-IS, the CAPREMAN study will scale these interventions across a wider range of states and facilities in Nigeria. Key gaps identified—such as unclear treatment pathways, weak postpartum follow-up, and lack of standardized screening protocols—will be directly addressed.
By co-designing a comprehensive, evidence-based guideline that integrates Hemocue point-of-care testing, FCM, and MMS, CAPREMAN seeks to create a robust, scalable framework for preventing and managing maternal anaemia in Nigeria. This initiative has the potential to transform maternal health services and reduce anaemia-related complications across the country.
Aim
This project aims to develop, implement, and test a comprehensive guideline for maternal anaemia prevention and management within health facilities in Nigeria.
Objectives
Study Outcomes
The CAPREMAN study is designed to assess the real-world impact of a co-designed, guideline-based approach to anaemia prevention and management in pregnant and postpartum women across Nigeria.
Primary Outcome
The primary outcomes for this study will include:
Secondary Outcomes
The secondary outcomes for this study will include:
To reduce marked variations in sociodemographic and biological attributes, as well as potential confounders, enrolled patients will be encouraged to continue their care at the hospital of enrolment. Efforts will also be made by designated research staff to trace participants who drop out at any point during the study
Methodology
Design: Mixed-methods implementation study combining co-design of a guideline, its implementation, and evaluation.
Study location: Three Nigerian states – Lagos (South-West), Kano and Kaduna (North-West).
Facilities: Seven (7) healthcare facilities per state. This includeS:
Selection criteria for facilities:
Study population: All pregnant and postpartum women attending selected facilities.
Data collection: Baseline and follow-up data from health facilities to assess clinical and implementation outcomes.
Implementation strategy: Co-designed guideline introduced using Plan-Do-Study-Act (PDSA) quality improvement cycles, evaluated through process and outcome metrics.
Ethical Considerations
The CAPREMAN study has received ethical approval from the National Health Research Ethics Committee of Nigeria, the Health Research Ethics Committee of Lagos University Teaching Hospital, and the ethics committees of the participating states. Our research is guided by core ethical principles — respect for autonomy, non-maleficence, beneficence, and justice — to ensure the highest standards of participant care and protection.
Participation in the study is entirely voluntary. Before joining, all eligible women will be fully informed about the study’s purpose and procedures and asked to provide written consent. Young women aged 15 to 18 years are allowed to consent for themselves, in accordance with national guidelines. Participants have the right to withdraw from the study at any time without affecting their access to usual healthcare.
We are committed to protecting the privacy and confidentiality of all participants. Personal information and data collected will be securely stored and accessible only to authorised study staff. No participant will bear any cost related to the study, and reasonable incentives will be offered to encourage participation without exerting undue influence.
Ethical Approvals
S/N | STATE/SITES | IRB APPROVAL NUMBER |
1 | NHREC | NHREC/01/01/2007 |
2 | LUTH HREC | ADM/DSCST/HREC/APP/7143 |
3 | FMC Ebute Metta HREC | HREC 25-08 |
4 | LSMOH Social Approval | LSMH/8238/I/59 |
5 | Alimosho GH, MCC Amuwo-Odofin, MCC Eti-Osa & PHCs | LSMH/8238/I/60 |
6 | LSPHCB HREC (Rauf Aregbesola and Festac PHC) | LS/PHCB/MS/1128/VOL.XIV/95 |
7 | AKTH HREC | NHREC/28/01/2020/AKTH/EC/3991 AKTH/MAC/SUB/12A/P-3/VI/4091 |
8 | Kano State MoH HREC | NHREC/17/03/2018 SHREC/2025/6004 |
9 | Kaduna State MoH HREC | MOH/ADM/744/VOL.1/1110020 |
10 | ABUTH HREC | ABUTHZ/HREC/B23/2025 |
CAPREMAN PROJECT INVESTIGATORS
CAPREMAN, a multi-site implementation project, is being conducted in three Nigerian states: Kano, Kaduna, and Lagos.
Chief Investigator
Prof Bosede Afolabi FAS, MBChB, DM(Notts), FRCOG, FWACS, FMCOG
Professor of Obstetrics and Gynaecology, Department of Obstetrics and Gynaecology, Faculty of Clinical Sciences, College of Medicine, University of Lagos/Lagos University Teaching Hospital (LUTH).
Co-Principal Investigator
Dr. Mobolanle Balogun: Professor, Department of Community Health and Primary Care, College of Medicine, University of Lagos (CMUL), and a consultant public health physician in Lagos University Teaching Hospital (LUTH).
Co-investigators
Prof. Titilope Adeyemo: Professor, Department of Hematology and Blood Transfusion, College of Medicine, University of Lagos/ Lagos University Teaching Hospital (LUTH).
Prof. Arinola E. Joda: Associate Professor, Faculty of Pharmacy, College of Medicine, University of Lagos.
Dr. Onikepe Owolabi: Research and Strategy Director, Maternal Reproductive Health Collective (MRHC).
Dr Aduragbemi Banke-Thomas: Associate Professor of Maternal and Newborn Health at the London School of Hygiene and Tropical Medicine, United Kingdom. He is also Visiting Professor on the Erasmus Mundus Europubhealth programme and at the University of Greenwich.
Dr Opeyemi Akinajo: Consultant Obstetrician and Gynecologist, Department of Obstetrics and Gynecology, Lagos University Teaching Hospital (LUTH).
Dr Gbenga Olorunfemi: Obstetrician and Gynaecologist, a biostatistics and research methods consultant at the Pan African University, Ibadan, Nigeria, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria and University of Witwatersrand, Johannesburg, South Africa.
Dr Rabi’at Aliyu Muhammad: Senior Lecturer with Ahmadu Bello University Zaria and Consultant Obstetrician-Gynaecologist working in the Materno-Fetal Medicine unit at the Ahmadu Bello University Teaching Hospital Zaria.
Dr. Aminatu A. Kwaku: Consultant Community Health Physician, Aminu Kano Teaching Hospital, Honorary Senior Lecturer, Bayero University, Kano
The study sites include:
S/N | Site/Institution Name | State |
1. | Aminu Kano Teaching Hospital |
|
2. | Sheikh Jiddah General Hospital |
Kano |
3. | Waziri Gidado General Hospital | |
4. | Sabo Bakin Zuwo General Hospital | |
5. | Sharada PHC | |
6. | Kabuga PHC | |
7. | Khadija Memorial Hospital | |
8. | Ahmadu Bello University Teaching Hospital |
Kaduna |
9. | Hajiya Gambo Sawaba General Hospital | |
10. | Major Ibrahim Bellow Abdullahi | |
11. | Yusuf Dantsoho Memorial Hospital | |
12. | Babban Dodo PHC | |
13. | Sabo Tasha PHC | |
14. | Muslim Specialists’ Hospital | |
15. | Federal Medical Centre, Ebute-Metta |
Lagos |
16. | Alimosho General Hospital | |
17. | Mother and Child Clinic (MCC) Eti-Osa | |
18. | Mother and Child Clinic (MCC), Amuwo Odofin | |
19. | Rauf Aragbesola PHC | |
20. | FESTAC PHC | |
21. | Havana Specialist Hospital |
We are working with antenatal and postnatal clinics in Lagos, Kano, and Kaduna States. If you are pregnant or recently delivered and receive care at any of our partner health facilities, you may be eligible to join the study.