SYSTEMATIC REVIEW article

Front. Glob. Women’s Health, 22 May 2025

Sec. Sex and Gender Differences in Disease

Volume 6 - 2025 | https://doi.org/10.3389/fgwh.2025.1523901

Through a gender lens: a scoping review of gendered experiences of AMR causes, burden and workforce in Nigeria


Ayodele Oluwakemi Majekodunmi
Ayodele Oluwakemi Majekodunmi1*Mabel Kamweli AworhMabel Kamweli Aworh2Esteller MbadiweEsteller Mbadiwe3Kikiope Oluwafikemi OluwaroreKikiope Oluwafikemi Oluwarore4Mwapu Dika NdahiMwapu Dika Ndahi5Dooshima Kwange
Dooshima Kwange6
  • 1Food and Agriculture Organisation of the United Nations, Abuja, Nigeria
  • 2Department of Biological and Forensic Sciences, Fayetteville State University, Fayetteville, NC, United States
  • 3Ducit Blue Solutions, Abuja, Nigeria
  • 4One Health Development Initiative, Abuja, Nigeria
  • 5Department of Veterinary and Pest Control Services, Federal Ministry of Agriculture and Food Security, Abuja, Nigeria
  • 6Tesedona Foundation for Animal Health, Abuja, Nigeria

Background: Nigeria is among the countries with the top 10 highest burdens of infectious and zoonotic diseases worldwide. There is a correspondingly high rate of antimicrobial use and misuse in humans and animals, leading to antimicrobial resistance (AMR). Antimicrobial Resistance has a very high impact on women and girls as they form the majority of health workers at community level as well as being the main care givers and livestock custodians in the home, most likely to prescribe, purchase or administer antibiotics. However, there is very little information about gendered aspects of AMR in Nigeria. This paper undertakes a scoping review of antimicrobial resistance in Nigeria through a gender lens, looking at how sex and gender interact with antimicrobial resistance and efforts to mitigate its negative effects.

Methods: A PRISMA scoping review was conducted for peer-reviewed articles published from the year 2000, describing studies in Nigeria on AMR, infectious disease treatment (including treatment seeking behaviour) and access and experiences of healthcare, which either take an explicit gender approach or include sex/gender as a key variable.

Results: Studies show clear gender differences in levels of disease risk/resistance, health-seeking behaviour and patterns of access to healthcare (including antimicrobials). Despite the fact that these patterns are clearly recognised across multiple publications in different settings, we did not find evidence of a corresponding analysis of how gender might reinforce these vulnerabilities.

Conclusions: Gendered aspects of infectious diseases, antimicrobial access and resistance are documented in Nigeria, albeit often incidentally. This data should be taken into account when considering the AMR problem and in the design of various interventions and the design of various interventions towards improving AMR and One Health in Nigeria.

Introduction

Antimicrobial resistance is a global health issue with significant health, financial and societal impacts, including increased morbidity, mortality, healthcare costs and productivity losses. Over 750,000 deaths annually occur as a consequence of drug-resistant bacteria and if no action is taken, this could increase to 10 million by 2050, with∼4.1 million deaths from Africa alone (1). Nigeria is among the countries with the top 10 highest burdens of infectious and zoonotic diseases worldwide (2). There is a correspondingly high rate of antimicrobial use and misuse in humans and animals, leading to antimicrobial resistance (AMR) (3, 4).

Several factors contribute to AMR in LMICs including easy access to antimicrobials without prescriptions (both medical and veterinary), low health care worker (HCW) to population ratios, and over-prescription of antimicrobials by professionals, routine use as livestock growth promoters, and poor waste management are some of the drivers of AMR in LMICs (57).

High levels of antimicrobial-resistant infections are recorded in humans, especially in sepsis, respiratory, and diarrheal infections (3, 8). High levels of AMR, including several patterns of MDR have also been recorded in food animal species and the environment. High levels of AM residues have also been found in food products, especially in poultry, eggs and fish (9). Resistance to over 20 commonly used disinfectants and antiseptics have also been isolated from humans, food animals and the environment (912). Several antimicrobials banned for use in animals in Nigeria (chloramphenicol, nitrofuran) or on the WHO or OIE critical lists (Colistin, Vancomycin, second & third generation fluoroquinolones) are routinely used in food producing animals in Nigeria (9, 1316).

Antimicrobials are the bedrock of modern medicine. They are also vital for livestock production and husbandry. Thus, AMR threatens food production at a global level and creates enhanced potential for zoonotic disease emergence or re-emergence. People working in healthcare, agriculture and food production will also become more vulnerable, as they are increasingly exposed to resistant bacteria at work. The effects of AMR are far reaching, a threat not just to Sustainable Development Goals 2 (no hunger) and 3 (good health), but also to SDGs 1 (no poverty) 5 (gender equality) and 10 (reduced inequalities). LMICs are more susceptible to infection and are increasingly exposed to antibiotic resistant bacteria. Thus, “antibiotic resistance can breed poverty, while poverty feeds the problem of antibiotic resistance” (17).

A significant barrier to action is that AMR affects the most vulnerable people, who suffer greater impacts on their health and food systems, in addition to other development issues. Since AMR has the potential to increase existing inequalities, including gender inequality, meaningful efforts to combat AMR should take these into account.

Agriculture in Nigeria is dominated by smallholder farmers and contributes 21% to GDP, 36% to employment and 60% to non-oil export value (18). A large proportion of smallholder livestock farmers are women and girls. They are the primary care givers in homes and health facilities, also responsible for food purchase and preparation. Thus, they are affected by or fuel AMR through contact with sick people and animals, self-prescribing and dispensing of AMs, making decisions on observance of withdrawals periods and use of animal products as well as economic losses from untreatable infections.

In Nigeria, gender plays a significant role in antimicrobial resistance (AMR), particularly due to women's responsibilities in healthcare, agriculture, and informal medicine distribution. Many women, especially in rural areas, self-prescribe antibiotics for family members due to limited healthcare access while traditional birth attendants routinely administer antibiotics during childbirth without proper dosage control, contributing to resistance (19, 20). Female smallholder farmers, who dominate poultry and aquaculture, frequently misuse antibiotics to prevent livestock diseases, leading to high antimicrobial residues in food products (9). Economic losses from resistant infections disproportionately impact these women, as they rely on livestock for household income. Additionally, cultural barriers limit women's access to formal healthcare, pushing them to rely on unregulated patent medicine vendors, many of whom often women themselves sell antibiotics without prescriptions (21, 22). As primary caregivers, women also bear the burden of treating resistant infections in their families, increasing their unpaid labour and economic strain (23). Despite their critical roles, women remain underrepresented in AMR policymaking and research.

A wealth of literature examines the relationships between gender, power relations, health and infectious disease. It shows strong links between gender, poverty and women's poorer health outcomes, clearly identifying gender as one of many social determinants of health. In Nigeria, gender plays a key role in disease risk, levels and patterns of antimicrobial access, use and resistance, access to healthcare and health seeking behaviour.

Despite its position as a high priority global health issue, there is a paucity of literature that explicitly addresses sex, gender and antimicrobial resistance. In 2018, the WHO recognized the need for a focus on gender and equity issues in national AMR strategies to “understand and acknowledge how men, women and different groups in society” were differently exposed to the risk of, or affected by, antibiotic resistance” (24). This gap in evidence is mirrored in Nigeria, thus the need for a scoping review to systematically map the research done in this area and identify any existing gaps in knowledge. The specific research question is: What is known from the literature about how sex and gender interact with antimicrobial resistance to produce different experiences and perspectives of AMR.

This paper is divided into two sections. The first reviews the evidence for gendered experiences of AMR in Nigeria while the second highlights the contributions of women and women-led initiatives to mitigating AMR in Nigeria.

Methods

This scoping review was conducted according to the PRISMA extension for scoping reviews guideline (25). To gain perspectives on gender within the AMR research, prevention and control space, expert consultations amongst female STEM professionals working in AMR across public, private and not-profit sectors were conducted.

Eligibility criteria

Papers included in the review were selected according to the following criteria: those with a focus on or assessment of gender differences in any aspect of AMR: levels and patterns of awareness; antimicrobial access, use and stewardship; infection prevention and control.

Peer-reviewed journal papers were included if they were: published during or after 2000, written in English, based in Nigeria, described studies on AMR, infectious disease treatment (including treatment seeking behaviour) and access and experiences of healthcare, which either take an explicit gender approach or include sex/gender as a key variable. Quantitative, qualitative and mixed-method studies were included in order to consider different aspects of gender in AMR. As this is a scoping review, an inclusive approach has been used, considering all types of peer-reviewed articles as eligible, to ensure that all available data on this topic was captured.

Papers were excluded if they did not fit into the conceptual framework of the study, were based outside Nigeria, did not include sex/gender as a key variable or found no significant differences by gender.

Search strategy

To identify potentially relevant documents, the following bibliographic databases were searched from 2000 to date: PUBMED, Web of Science, and African Journals Online (AJOL) The search strategies were drafted and further refined by initial results.

Data screening

A systematic screening process was conducted following PRISMA guidelines. A total of 114 studies were initially identified by the search strategy. After removing 29 duplicate studies, 85 unique studies remained for further evaluation. During the screening phase, 38 studies were excluded due to irrelevance, leaving 47 full-text articles for eligibility assessment. All 47 studies met the inclusion criteria, and none were excluded at this stage. Consequently, 47 studies were included in the final review, as shown in Figure 1 and Table 1.

Figure 1
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Figure 1. PRISMA flow diagram.

Table 1
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Table 1. Summary of articles reviewed.

Search strategy key words:

1. Antimicrobial Resistance

2. Antibiotic resistance/

3. Antibiotic prescription/

4. Antimicrobial Stewardship/

5. Women/

6. Gender/

7. Sex/

8. Female/

9. Male/

10. Treatment seeking behavior/

11. Health$ access/

12. Antimicrobial access/

13. Antibiotic access/

14. Urinary tract infection

15. Tuberculosis/

16. Sexually Transmitted infections

17. Infectious disease treatment

Results

Data was extracted on article characteristics, area of AMR focus and results of gender. Studies were then grouped by condition/infectious disease under study, area of AMR, and study design, along with the measures used and broad findings. We did not identify any previous reviews (systematic or otherwise) of this topic in the literature.

After duplicates were removed, a total of 85 citations were identified from searches of electronic databases. Based on the title and the abstract, 38 were excluded as irrelevant, with 47 full text articles to be retrieved and assessed for eligibility. Upon full text review, all 47 were found to be eligible and no exclusions were made.

Of these 47 studies, 19 had an explicit gender approach in their design whereas 27 merely included gender as a variable. The majority were cross-sectional studies (16), followed by cohort studies (12) and Randomised (8) and non-randomised control trials (2). The frequency of publications increased over time as shown in Table 2. Mycobacterial infections (tuberculosis, leprosy) were well represented, as well as sexually transmitted infections (including HIV) and urinary tract infections.

Table 2
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Table 2. Distribution of article types covering gender in AMR.

Gender differences in risk of infection and AMR

There are gender differences in risk of infection and AMR for different infections. Women have a 7 times higher risk of UTI for biological/anatomical reasons, accounting for 60% of UTI infections. Women also experience more severe antimicrobial resistance, with 30% vancomycin-resistant Staph aureaus in women with UTI, compared to just 8% in men (26, 27). On the other hand, men are more likely to be infected with TB and less likely to comply with treatment guidelines for both TB and leprosy (2830). The major risk factors for infection also differ by sex—HIV co-infection for women and urban residence for men (41).

Nigeria has one of the highest maternal mortality rates in the world, accounting for 19% of global maternal deaths. Yet overwhelmingly, men retain the power to make decisions about contraceptive use which are implemented by women (22, 31). Women's experiences associated with pregnancy, abortion and childbirth may put them at increased risk of antibiotic resistance. These include harmful practices by health care workers that can result in infection for example Oduenyi et al. (31) report >30% women experienced unnecessary routine episiotomies, manual exploration or lavage of the uterus during childbirth.

Inherent gender discrimination in health service delivery further affects women's health seeking behaviour through sub-standard levels of care: 65% of women reported physical and/or verbal abuse from HCWs at facilities (31). This expectation of poor treatment by HCWs is the reason 11%–20% women choose not to attend health facilities when ill (20, 32). Workplace violence and gender discrimination experienced by healthcare workers themselves serves to normalize and reinforce these behaviours—8% report violent incidents including rape, sexual assault and beatings (31). Women comprise the majority of the healthcare workforce but the majority of supervisors are male (31, 33).

Gender inequality

Gender inequality limits women's access, choice, agency and autonomy in accessing healthcare services. Low agency in decision making and financial dependence on male partners results in reduced attendance at health facilities for women, lower immunization rates in children and unmet needs for contraception in Nigeria (22, 31, 34, 35). 15%–36% of women did not attend health facilities when ill or pregnant because they did not have permission from their spouse (20, 32). Female-headed households spent a higher proportion of their income on healthcare (and education) than male-headed households, but also reported 2.5 times higher untreated morbidity due to cost, compared to male-headed households.

Patterns of health seeking behaviour also differ by gender in different settings across the country: women were more likely than men to seek treatment from formal healthcare facilities where they mostly provide maternal & child health services and are perceived as being “for women” (32, 34). In other settings, men were twice as likely to seek healthcare when ill and 20 times more likely to use the formal sector than women due to their sole control of household resources; women were more likely to patronize PPMVs (21, 36).

Despite comparable levels of knowledge on HIV & STIs, men were twice as likely to seek treatment compared to women due to higher stigmatization and fear of spouses' finding out (40% young women in the study were married compared to just 17% of young men) (34). This is reflected in a 2011 study of people self-reporting STIs where 86% of men based their report on a medical diagnosis compared to just 6% of women. Women were also less likely to inform their partners of their status (37).

Discussion

Results show clear gender differences in all aspects of AMR in Nigeria, including the burden of AMR, the behavioural patterns that promote it, and the lived experiences of healthcare workers. These are clearly well-recognized patterns, yet such recognition often occurs without a corresponding analysis of how gender might reinforce these vulnerabilities (38). In Nigeria, where 98% of HCWs believe men should be involved in family planning (and 60% believe women cannot take these decisions without their spouse) only 10% encourage women to bring their partners along to consultations (31).

Studies and interventions on AMR rarely show these gendered nuances, despite the strong evidence for gender as a social determinant of health. More attention is required to how gender perspectives in awareness of AMR, antimicrobial consumption and stewardship, health care, livestock production affect our ability to reduce and prevent antimicrobial resistance. More attention is also required to increase the number of women working on AMR and STEM in general and improve the supporting enabling environment for them to thrive.

Nigeria has quite significant representation of women and women-led initiatives working in AMR research and control at all levels, across the public, private and non-profit sectors. Expert consultations among this target group investigate the gendered aspects of women working in STEM, AMR research and control, specific challenges. They also offer recommendations to better understand gender aspects of AMR in Nigeria and leverage on them to accelerate the fight against this priority health threat.

There are both positive and negative aspects of being a female STEM professional working in AMR. In line with the workplace norms in Nigeria (39), tokenism, being overlooked or taken less seriously than male colleagues, being subjected to inappropriate comments by male colleagues and then made to feel this is culturally acceptable were commonly cited instances, both in professional life, and during education and STEM training.

On the other hand, supporting and being supported by other women in the workplace and mentorship by accomplished female scientists locally and globally, have been very positive.

It has been clearly demonstrated that having a close network of supportive women is key to career success for women (40). This is particularly important to encourage continued participation of women in in STEM careers and AMR. The One Health approach and multisectoral nature of the AMR space in Nigeria has also provided beneficial opportunities to build bridges and share experiences with colleagues in other sectors (including other women).

On the other hand, some of the barriers and negative experiences mean that women must still work harder to prove their value in the fight against AMR.

The following are recommended to address the low consideration of gender and inclusivity in AMR in Nigeria:

Equality, diversity and inclusion in AMR behavioural change

Awareness and behavioural change communication is key in the fight against AMR. To make this more effective, messaging should be tailored to different groups within the general public audience, including men, women and youths. Efforts should be made to increase women and youth inclusion opportunities in all areas of behavioural change, including innovation, research and development. Messaging also needs to be localised and evidence-based, delivering, context—specific messages and scenarios in local languages, which take gender differences into account.

There is a need to identify diverse AMR champions to give this often silent, abstract problem a human face by sharing their personal stories to encourage behavioural change. AMR can be difficult to conceptualise hence the need to be able to connect to the stories of others to appreciate the looming dangers.

Governance

Comprehensive mapping of projects, programmes, expertise and resources for AMR is necessary to clearly determine levels of gender sensitivity and plan for improvement of same. Increased political commitment is also important to guarantee implementation the National Action Plan on AMR at subnational and community levels where gender considerations are most significant. Finally, inclusion of gender considerations in design, implementation, evaluation and reporting of AMR interventions must be improved for gender mainstreaming.

Inclusivity in AMR prevention and control

To improve inclusivity in AMR interventions, gender-sensitive stakeholder mapping is very useful, to strengthen the ecosystem of women in STEM & AMR. Women in this field need more opportunities to connect and support each other. Mentorship and networking amongst women should be promoted both nationally and globally. In terms of impact, existing programs and organizations should be supported to reach more women, especially in areas with significant barriers to girls' educations and women's workforce participation. Investments in gender equality in access to and experiences of STEM education from the basic educational levels (primary and secondary) to advance level promote participation of girls. All relevant institutions and workplaces should establish and implement equality, diversity and equity policies to improve workplace experiences for women. This will lead to increased participation of qualified women can be employed and supported to remain productive at their at all stages of their lives.

Conclusion

There is clear but limited evidence of the gender differences within the root causes and burden of AMR in Nigeria, as well as within the workforce responsible for preventing and controlling it. Allocating resources to improve the inclusion of gender and inclusivity in the study and practice of AMR prevention and control is key. Together with the recommendations proffered here, this will produce much needed evidence and guidance to more effectively combat this priority health problem.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author contributions

AM: Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft, Writing – review & editing. MA: Writing – original draft, Writing – review & editing. EM: Writing – original draft, Writing – review & editing. KO: Writing – original draft, Writing – review & editing. MN: Writing – original draft, Writing – review & editing. DK: Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. O’Neill J. (2014). Antimicrobial Resistance: Tackling a Crisis for the Health and Wealth of Nations. Available at: https://amr-review.org/sites/default/files/AMR%20Review%20Paper%20-%20Tackling%20a%20crisis%20for%20the%20health%20and%20wealth%20of%20nations_1.pdf (Accessed June 01, 2024).

Google Scholar

2. Allen T, Murray KA, Zambrana-Torrelio C, Morse SS, Rondinini C, Di Marco M, et al. Global hotspots and correlates of emerging zoonotic diseases. Nat Commun. (2017) 8(1):1124. doi: 10.1038/s41467-017-00923-8

PubMed Abstract | Crossref Full Text | Google Scholar

3. Egwuenu A, Obasanya J, Okeke I, Aboderin O, Olayinka A, Kwange D, et al. Antimicrobial use and resistance in Nigeria : situation analysis and recommendations, 2017. Pan Afr Med J Conf Proc. (2018) 2. doi: 10.11604/pamj.cp.2018.8.2.701

Crossref Full Text | Google Scholar

4. Iheanacho CO, Eze UIH. Antimicrobial resistance in Nigeria : challenges and charting the way forward. Eur J Hosp Pharm. (2022) 29(2):119. doi: 10.1136/ejhpharm-2021-002762

PubMed Abstract | Crossref Full Text | Google Scholar

5. Ayukekbong JA, Ntemgwa M, Atabe AN. The threat of antimicrobial resistance in developing countries : causes and control strategies. Antimicrob Resist Infect Control. (2017) 6(1):47. doi: 10.1186/s13756-017-0208-x

PubMed Abstract | Crossref Full Text | Google Scholar

6. Sakeena MHF, Bennett AA, McLachlan AJ. Non-prescription sales of antimicrobial agents at community pharmacies in developing countries : a systematic review. Int J Antimicrob Agents. (2018) 52(6):771–82. doi: 10.1016/j.ijantimicag.2018.09.022

PubMed Abstract | Crossref Full Text | Google Scholar

7. Otaigbe II, Elikwu CJ. Drivers of inappropriate antibiotic use in low- and middle-income countries. JAC Antimicrob Resist. (2023) 5(3):dlad062. doi: 10.1093/jacamr/dlad062

PubMed Abstract | Crossref Full Text | Google Scholar

8. Federal Ministries of Agriculture Environment and Health. Antimicrobial Use and Resistance in Nigeria: Situation Analysis and Recommendations. Abuja: Federal Republic of Nigeria (2017).

Google Scholar

9. Oloso NO, Fagbo S, Garbati M, Olonitola SO, Awosanya EJ, Aworh MK, et al. Antimicrobial resistance in food animals and the environment in Nigeria: a review. Int J Environ Res Public Health. (2018) 15(6):1284. doi: 10.3390/ijerph15061284

PubMed Abstract | Crossref Full Text | Google Scholar

10. Adelowo OO, Fagade OE, Oke AJ. Prevalence of co-resistance to disinfectants and clinically relevant antibiotics in bacterial isolates from three hospital laboratory wastewaters in Southwestern Nigeria. World J Microbiol Biotechnol. (2008) 24(9):1993–7. doi: 10.1007/s11274-008-9697-3

Crossref Full Text | Google Scholar

11. Alabi OS, Sanusi EA. Efficacy of three disinfectant formulations against multidrug resistant nosocomial agents. Afr J Clin Exp Microbiol. (2012) 13(3):178–82. doi: 10.4314/ajcem.v13i3.8

Crossref Full Text | Google Scholar

12. Olusoga OD, Terry AO, Abolore YR, Sunday OA, Webber Mark A. Variable efficacy of clinically important biocides against common bacterial pathogens isolated from tertiary hospitals in Nigeria. Int J Trop Dis Health. (2018) 31:1–8. doi: 10.9734/IJTDH/2018/41707

Crossref Full Text | Google Scholar

13. OIE. List of Antimicrobial Agents of Veterinary Importance. Paris: World Organization for Animal Health (2015).

Google Scholar

14. OIE. Terrestrial Animal Health Code. Paris: World Organization for Animal Health (2017).

Google Scholar

15. WHO. Critically Important Antimicrobials for Human Medicine—ranking of Medically Important Antimicrobials for Risk Management of Antimicrobial Resistance Due to Non-Human Use. Geneva: World Health Organization (2017).

Google Scholar

16. Kwange D, Mwapu N. Antimicrobial Use Data Collection and Report to OIE—nigeria. Abuja, Nigeria: Department of Veterinary and Pest Control Services, Federal Ministry of Agriculture and Rural Development (2019).

Google Scholar

17. Van der Heijden M, Sandgren A, Pränting M, Karvanen M, Aagaard H, Zorzet A, et al. When the Drugs Don’t Work: Antibiotic Resistance as a Global Development Problem. Uppsala, Sweden: ReAct (2019).

Google Scholar

18. FAO. The future of livestock in Nigeria. Opportunities and challenges in the face of uncertainty. Rome (2019).

Google Scholar

19. Odetola TD. Health care utilization among rural women of child-bearing age: a Nigerian experience. Pan Afr Med J. (2015) 20(1):151. doi: 10.11604/pamj.2015.20.151.5845

PubMed Abstract | Crossref Full Text | Google Scholar

20. Okonofua F, Ntoimo L, Ogungbangbe J, Anjorin S, Imongan W, Yaya S. Predictors of women’s utilization of primary health care for skilled pregnancy care in rural Nigeria. BMC Pregnancy Childbirth. (2018) 18(1):106. doi: 10.1186/s12884-018-1730-4

PubMed Abstract | Crossref Full Text | Google Scholar

21. Onah MN, Govender V. Out-of-pocket payments, health care access and utilisation in south-eastern Nigeria: a gender perspective. PLoS One. (2014) 9(4):e93887. doi: 10.1371/journal.pone.0093887

PubMed Abstract | Crossref Full Text | Google Scholar

22. Yaya S, Okonofua F, Ntoimo L, Udenige O, Bishwajit G. Gender inequity as a barrier to women’s access to skilled pregnancy care in rural Nigeria: a qualitative study. Int Health. (2019) 11(6):551–60. doi: 10.1093/inthealth/ihz019

PubMed Abstract | Crossref Full Text | Google Scholar

23. Yusuf A. Women’s Empowerment and Sexual Reproductive Health in Africa (Doctoral dissertation, Texas A&M University). (2020).

Google Scholar

24. World Health Organization. Tackling Antimicrobial Resistance (AMR) Together. Working Paper 5.0: Enhancing the Focus on Gender and Equity. Geneva: WHO (2018).

Google Scholar

25. Tricco AC, Lillie E, Zarin W, O'Brien KK, Colquhoun H, Levac D, et al. PRISMA Extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med. (2018) 169(7):467–73. doi: 10.7326/M18-0850

PubMed Abstract | Crossref Full Text | Google Scholar

26. Anucha JC, Morikwe UC, Ikegbunam MN. Age and gender-based antibiotic susceptibility patterns of Staphylococcus aureus among HIV patients in some selected hospitals in anambra central, Nigeria. Genet Mol Med. (2021) 3(2):1–5. doi: 10.33425/2689-1077.1011

Crossref Full Text | Google Scholar

27. Oladeinde BH, Omoregie R, Olley M, Anunibe JA. Urinary tract infection in a rural community of Nigeria. N Am J Med Sci. (2011) 3 (2):75–7. doi: 10.4297/najms.2011.375

PubMed Abstract | Crossref Full Text | Google Scholar

28. Nwankwo IU. Public perception on gender issues and women’s HealthCare concerns related to leprosy: implications for leprosy control program in southeast Nigeria. In: Kronenfeld JJ, editor. Underserved and Socially Disadvantaged Groups and Linkages with Health and Health Care Differentials. Bingley, United Kingdom: Emerald Publishing Limited (2019). p. 165–87.

Google Scholar

29. Oshi SN, Alobu I, Ukwaja KN, Oshi DC. Investigating gender disparities in the profile and treatment outcomes of tuberculosis in Ebonyi state, Nigeria. Epidemiol Infect. (2015) 143(5):932–42. doi: 10.1017/S095026881400291X

PubMed Abstract | Crossref Full Text | Google Scholar

30. Ukwaja KN, Alobu I, Nweke CO, Onyenwe EC. Healthcare-seeking behavior, treatment delays and its determinants among pulmonary tuberculosis patients in rural Nigeria: a cross-sectional study. BMC Health Serv Res. (2013) 13(1):25. doi: 10.1186/1472-6963-13-25

PubMed Abstract | Crossref Full Text | Google Scholar

31. Oduenyi C, Banerjee J, Adetiloye O, Rawlins B, Okoli U, Orji B, et al. Gender discrimination as a barrier to high-quality maternal and newborn health care in Nigeria: findings from a cross-sectional quality of care assessment. BMC Health Serv Res. (2021) 21(1):198. doi: 10.1186/s12913-021-06204-x

PubMed Abstract | Crossref Full Text | Google Scholar

32. Okoronkwo IL, Onwujekwe OE, Ani FO. The long walk to universal health coverage: patterns of inequities in the use of primary healthcare services in Enugu, Southeast Nigeria. BMC Health Serv Res. (2014) 14(1):132. doi: 10.1186/1472-6963-14-132

PubMed Abstract | Crossref Full Text | Google Scholar

33. Osazuwa-Peters N, Azodo CC, Ehizele AO, Obuekwe ON. Gender differences in characteristics, occupational exposure, and infection control practices among dental professionals in Edo State, Nigeria: original research. S Afr J Epidemiol Infect. (2012) 27(2):61–5. doi: 10.10520/EJC122392

Crossref Full Text | Google Scholar

34. Mmari KN, Oseni O, Fatusi AO. STI Treatment-seeking behaviors among youth in Nigeria: are there gender differences? Int Perspectives Sex Reprod Health. (2010) 36(2):72–9. doi: 10.1363/3607210

Crossref Full Text | Google Scholar

35. Antai D. Gender inequities, relationship power, and childhood immunization uptake in Nigeria: a population-based cross-sectional study. Int J Infect Dis. (2012) 16(2):e136–45. doi: 10.1016/j.ijid.2011.11.004

PubMed Abstract | Crossref Full Text | Google Scholar

36. Onah MN, Horton S. Male-female differences in households’ resource allocation and decision to seek healthcare in south-eastern Nigeria: results from a mixed methods study. Soc Sci Med. (2018) 204:84–91. doi: 10.1016/j.socscimed.2018.03.033

PubMed Abstract | Crossref Full Text | Google Scholar

37. Adeyemi EO. Gender inequities in sexually transmitted infections: implications for HIV infection and control in Lagos State, Nigeria. Infect Dis Rep. (2011) 3(1):e7–e7. doi: 10.4081/idr.2011.e7

PubMed Abstract | Crossref Full Text | Google Scholar

38. ReAct. Scoping the Significance of Gender for Antibiotic Resistance React. Upsalla: ReAct (2020).

Google Scholar

39. Phillips Consulting. (2019). Gender Equality in the Nigerian Workplace Available at: https://phillipsconsulting.net/reports_post/gender-equality-in-the-nigerian-workplace/ (Accessed June 01, 2024).

Google Scholar

40. Yang Y, Chawla NV, Uzzi B. A network’s gender composition and communication pattern predict women’s leadership success. Proc Natl Acad Sci USA. (2019) 116(6):2033–8. doi: 10.1073/pnas.1721438116

PubMed Abstract | Crossref Full Text | Google Scholar

41. Oshi DC, Oshi SN, Alobu IN, Ukwaja KN. Gender-related factors influencing women’s health seeking for tuberculosis care in Ebonyi state, Nigeria. J Biosoc Sci. (2016) 48(1):37–50. doi: 10.1017/S0021932014000534

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: antimicrobial resistance (AMR), gender, inequity, infectious diseases, Nigeria

Citation: Majekodunmi AO, Aworh MK, Mbadiwe E, Oluwarore KO, Ndahi MD and Kwange D (2025) Through a gender lens: a scoping review of gendered experiences of AMR causes, burden and workforce in Nigeria. Front. Glob. Women's Health 6:1523901. doi: 10.3389/fgwh.2025.1523901

Received: 6 November 2024; Accepted: 27 March 2025;
Published: 22 May 2025.

Edited by:

Stephen Opoku, University of Alabama at Birmingham, United States

Reviewed by:

Ebenezer Senu, Kwame Nkrumah University of Science and Technology, Ghana
Simeon Babarinde, The Scripps Research Institute, United States

Copyright: © 2025 Majekodunmi, Aworh, Mbadiwe, Oluwarore, Ndahi and Kwange. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ayodele Oluwakemi Majekodunmi, YXlvZGVsZUBhamlzZWZpaS5vcmc=

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