
==== Front
NPJ Womens Health
NPJ Womens Health
Npj Women's Health
2948-1716
Nature Publishing Group UK London

31
10.1038/s44294-024-00031-1
Article
Incidence of postpartum depression among women with postpartum haemorrhage in Kano, northern Nigeria
Tsiga-Ahmed Fatimah Isma’il fitsiga.cmed@buk.edu.ng

12
Umar Musa Usman 34
Adamu Aishatu Lawal 12
Sulaiman Sahabi Kabir 5
Gboluwaga Amole Taiwo 126
Jalo Rabiu Ibrahim 12
Ibrahim Usman Muhammad 7
Ayaba Aminatu Kwaku 2
Ahmed Zainab Datti 8
Sunusi Surayya Murtala 2
Abdullahi Nafisat Tijjjani 2
Kabir Hajara Shehu 4
Abu Stephen Mohammed 5
Galadanci Hadiza Shehu 6
1 https://ror.org/049pzty39 grid.411585.c 0000 0001 2288 989X Department of Community Medicine, Bayero University, Kano, Nigeria
2 https://ror.org/05wqbqy84 grid.413710.0 0000 0004 1795 3115 Department of Community Medicine, Aminu Kano Teaching Hospital, Kano, Nigeria
3 https://ror.org/049pzty39 grid.411585.c 0000 0001 2288 989X Department of Psychiatry, Bayero University, Kano, Nigeria
4 https://ror.org/05wqbqy84 grid.413710.0 0000 0004 1795 3115 Department of Psychiatry, Aminu Kano Teaching Hospital, Kano, Nigeria
5 https://ror.org/005ywxj74 grid.442527.2 0000 0000 9365 7327 Department of Medicine, Yobe State University Teaching Hospital, Damaturu, Nigeria
6 grid.411585.c 0000 0001 2288 989X Africa Centre of Excellence for Population Health and Policy, BUK, Kano, Nigeria
7 https://ror.org/0278jft56 0000 0004 4660 0618 Department of Community Medicine, Federal University, Dutse, Jigawa Nigeria
8 https://ror.org/05wqbqy84 grid.413710.0 0000 0004 1795 3115 Department of Obstetrics & Gynaecology, Bayero University/Aminu Kano Teaching Hospital Kano, Kano, Nigeria
10 9 2024
10 9 2024
2024
2 1 322 4 2024
9 8 2024
© The Author(s) 2024
2024
https://creativecommons.org/licenses/by-nc-nd/4.0/ Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
The burden of postpartum depression (PPD), an important but largely neglected cause of maternal morbidity, is often increased by the presence of common co-morbidities, such as postpartum haemorrhage (PPH). Additionally, stress and the absence of social support can amplify PPD risk. Understanding the relationship between these conditions will help identify at-risk women and allow prompt intervention. Using a prospective cohort design, we recruited 72 women who had experienced PPH and another 72 women who had not within 24 h of delivery to assess the risk of PPD among them. The cumulative incidence of PPD among all participants was 15.3% (19/124). There was insufficient evidence to suggest that women with PPH have a higher risk of PPH than women without PPH (OR: 1.32; 95% CI: 0.55–3.13). Poor social support and high perceived stress increased the risk of PPD. We recommend screening for PPD among women with high perceived stress and low social support.

Subject terms

Diseases
Health care
Institutional-based research grant, TETFund grantTETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1 Fogarty International Center (FIC) and the National Institute on Alcohol Abuse and Alcoholism (NIAAA) of the U.S. National Institutes of Health1D43TW011544 1D43TW011544 issue-copyright-statement© Springer Nature Limited 2024
==== Body
pmcIntroduction

Postpartum depression (PPD) is a mood disorder that manifests as a feeling of melancholy and disinterest, which occurs within the first four weeks of delivery and may last up to a year after childbirth1,2. PPD affects approximately 1 in 7 new mothers globally, with an estimated prevalence of 17.7% in the first year following delivery1,3. The frequency of PPD varies between African countries, albeit higher than values found in high-income settings. In Nigeria, rates ranging from 10.7% to 44.39% have been documented in various sub-geographical regions2. PPD has been linked to suicide in the mother, impaired mother-infant bonding, as well as a negative influence on the child’s emotional and cognitive development4,5. Akin to PPD, postpartum haemorrhage (PPH) is a worldwide public health priority, resulting in over 70,000 annual maternal deaths globally6,7. Globally, about 14 million people experience PPH annually6, and it is the leading preventable cause of maternal mortality and morbidity, globally. In sub-Saharan Africa, PPH is responsible for between 30% and 50% of maternal deaths8, and in Nigeria, PPH is estimated to account for nearly a quarter (23%) of maternal deaths9.

In addition to the potentially fatal outcomes, PPH has also been linked with increased maternal morbidity, particularly due to improved survival associated with improving maternal health services. Notably among these PPH-related consequences are mental illnesses, including anxiety, post-traumatic stress disorder and postpartum depression (PPD)10. A recent review and metanalysis involving nine studies reported that PPH was strongly linked to a higher risk of developing postpartum depression. More specifically, compared to women without PPH, the risk of PPD was raised by 27% in women with PPH5. Similarly, a population-based longitudinal study from the United Kingdom found a substantial correlation between PPH and a higher incidence of postnatal depression and posttraumatic stress disorder (PTSD) in the first year after delivery. The prevalence of PND was 5.34%, and that of PTSD was 0.20% among women who had PPH11. Several other studies have documented a similar relationship between PPH and PPD12–16.

The development of PPD is linked to the physiological changes of the postpartum period, characterised by profound changes in placental and maternal hypothalamic hormones, a decline in circulating blood volume, and alterations in metabolism17,18. PPH is a pathologically stressful event that can in addition to reducing blood volume, also lead to endocrine imbalance, a documented aetiologic factor for PPD18. The most common consequences of PPH are anaemia and trauma. Furthermore, clinical symptoms of PPH, such as fatigue, reduced cognitive abilities, and emotional instability, can lead to increased stress levels that alter the hypothalamic–pituitary–adrenal (HPA) axis function, leading to increased vulnerability to mood disorders18. Consistent with a role for HPA axis dysfunction in PPD, levels of the stress hormones are altered in patients with PPD.

Postpartum haemorrhage and postpartum depression are common and serious public health problems associated with maternal and child distress5. Although PPD is the most common psychiatric disorder during the 5 years after delivery19, the relationship between this disorder and the traumatic experience of postpartum haemorrhage is under-studied, in developing countries like Nigeria. Most studies exploring the relationship between PPH and PPD are from high-income settings. Given the prevalence of PPH and over 7 million births occurring in Nigeria annually20, over a million women will experience PPH, and many will suffer its health sequelae. Therefore, there is a need to investigate this relationship further. This study aimed to recruit women with and without PPH within 24 h of delivery and follow them up to estimate the incidence of PPD at 6, 10 and 14 weeks postpartum and to evaluate the effect of social support and perceived stress on the risk of PPD.

Results

At the end of the study period, complete data on 124 women was analysed, giving a response rate of 82.7%. Eleven women from the PPH group and thirteen from the comparative group were excluded because they either did not fulfil the inclusion criteria or had incomplete data. There were 63 women who had PPH and 61 women without PPH, the majority of whom were from Gwale LGA (26.2% non-PPH and 28.6% PPH respondents). The respondent’s ages ranged from 18 to 44 years, with a mean and standard deviation (SD) of 27 ± 5 years. All but two women (98.39%, n = 122) were married, 76.61% (n = 95) were from a monogamous setting, and 30.65% (n = 38) had post-secondary education. The husbands’ mean age ± SD was 39 ± 7 years, and 52.83% (n = 65) were educated up to tertiary level.

Among respondents who had PPH, the quantity of blood loss ranged from 500 to 1500 mls (IQR 500,1000 mls). Approximately a third of the respondents (31.75% < n = 20) were transfused after PPH, and only one woman (1.59% < n = 1) had a hysterectomy secondary to PPH. Among all respondents, a sizeable number had strong social support (62.90%, n = 78), and the majority of the respondents reported experiencing moderate levels of perceived stress (59.68%, n = 74). Baseline characteristics are presented in Table 1Table 1 Baseline characteristics of 124 women with and without postpartum haemorrhage who delivered at the study facilities

Characteristic	Total	PPH n = 63	Non-PPH n = 61	P-value	
Age (years)	
<25	41 (33.06%)	21 (33.33%)	20 (32.79%)	0.751	
≥25	83 (66.94%)	42 (66.67%)	41 (67.21%)		
Family structure	
Monogamous	95 (76.61%)	48 (76.19)	48 (77.05%)	0.910	
Polygamous	29 (23.39%)	15 (23.81%)	14 (22.95%)		
Highest educational level	
Post-secondary	38 (30.65%)	17 (26.98%)	21 (34.43%)	0.760	
Secondary	71 (57.26%)	39 (61.90%)	32 (52.46%)		
Primary	11 (8.87%)	5 (7.94%)	6 (9.84%)		
Non-formal	4 (3.23%)	2 (3.17%)	2 (3.28%)		
Husband’s highest education	
Tertiary	65 (52.83%)	34 (55.74%)	31 (39.21)	0.379	
Secondary	45 (36.29%)	27 (42.86%)	18 (29.51%)		
Primary	4 (3.23%)	2 (3.17%)	2 (3.28%)		
Non-formal	10 (8.06%)	3 (4.76%)	5 (11.48%)		
Parity	
1	14 (11.29%)	7 (11.11%)	7 (11.48%)	0.455	
2–3	71 (68.85%)	33 (52.38%)	38 (62.30%)		
≥5	39 (31.45%)	23 (36.41%)	16 (26.23%)		
Had unplanned pregnancy	
No	27 (21.77%)	15 (23.81%)	12 (19.67%)	0.577	
Yes	97(78.13%)	48 (76.19%)	49 (80.33%)		
Have pre-existing medical conditions	
Yes	14 (11.29%)	6 (9.52%)	8 (13.11%)	0.528	
No	110(88.71%)	57 (90.48%)	53 (86.89%)		
Gestational age at delivery	
Pre-term	15 (12.20%)	8 (12.7%)	7 (11.67%)	0.835	
Term	108 (87.80%)	55 (87.30%)	53 (88.33%)		
Perceived stress	
Low	14 (11.29%)	4 (6.35%)	10 (16.39%)	0.034	
Moderate	74 (59.68%)	35 (59.68%)	39(63.93%)		
High	36 (29.03%)	36 (29.03%)	24 (38.10%)		
Social support	
Poor	12 (9.68%)	8 (12.70%)	4 (6.56%)	0.402	
Moderate	34 (27.42%)	15 (23.81%)	19(31.15%)		
Strong	78 (62.90%)	40 (63.49%)	38 (62.30%)		

At the conclusion of follow-up, the overall cumulative incidence of postpartum depression among all respondents was 15.32% (n = 19); 17.46% (n = 11) among women who had PPH and 13.11% (n = 8) among women who did not have PPH. The incidence was highest in both groups on the first visit, despite insufficient evidence to support a difference between the groups (Table 2).Table 2 Incidence of PPD among 124 women who had PPH and those who didn’t

Time of diagnosis	Total	Postpartum depression	
	Frequency (proportion)	PPH frequency (proportion)	NON-PPH frequency (proportion)	P-value	
At 6 weeks	12 (9.7%)	8 (12.7%)	4 (6.56%)	0.248	
At 10 weeks	4 (3.3%)	2 (3.57%)	2 (3.51%)	0.986	
At 14 weeks	3 (2.8%)	1 (1.85%)	2 (3.63%)	0.517	
Cumulative total	19 (15.3%)	11 (17.46%)	8 (13.11%)	0.467	

The distribution of PPD by baseline characteristics and risk factors for PPD is presented in Table 3. Among all respondents, the incidence of PPD was higher among respondents who were less than 25 years (84.21%) and from monogamous households (78.95%). There was insufficient evidence of a difference in the incidence of PPD between women who had PPH and those who did not, and this relationship was maintained even after adjusting for the effects of age, parity, perceived stress and social support. Nonetheless, perceived stress and social support were found to be independent risk factors for PPD after adjusting for these variables. Compared to women who had low perceived stress, the odds of PPD were approximately three times in those who had moderate stress [AOR: 2.60, 95% CI: 1.10–13.20] and 4 times among those with high perceived stress [AOR: 4.20, 95% CI: 1.04–18.55]. Similarly, respondents with strong [AOR: 11.68, 95% CI: 4.03–18.74] and moderate social support [AOR: 6.20, 95% CI: 1.22–13.60] had higher odds of PPD compared to those with poor support.Table 3 Multivariable logistic regression model for risk factors of PPD among 124 women with and without postpartum haemorrhage who delivered at the study facilities

Characteristic	Total n = 124	PPD n = 19	Non-PPD	Crude OR 95% CI	Adjusted OR*	
PPH status	
Non-PPH	61 (49.19%)	8 (42.11%)	53 (50.48%)	Reference	Reference	
PPH	63 (50.81%)	11 (57.89%)	52 (49.52%)	1.40 (0.52–3.78)	1.32 (0.55–3.13)	
Age (years)	
<25	41 (33.06%)	16 (84.21%)	25 (23.81%)	Reference		
≥25	83 (66.94%)	3 (15.79%%)	80 (76.19%)	0.49 (0.18–1.31)	0.77 (0.22–1.91)	
Family structure	
Monogamous	95 (76.61%)	15 (78.95%)	80 (76.19%)	Reference		
Polygamous	29 (23.39%)	4 (21.05%)	25 (23.89%)	0.32 (0.10–1.49)		
Parity	
1	14 (11.29%)	1 (5.26%)	13 (12.38%)	Reference		
2–4	71 (68.85%)	13 (68.42%)	58 (55.24%)	1.34 (0.27–6.75)	1.60 (0.19–4.89)	
≥5	39 (31.45%)	5 (26.32%)	34 (32.38%)	0.69 (0.11–4.23)	0.90 (0.45–5.11)	
Had unplanned pregnancy	
Yes	27 (21.77%)	5 (26.32%)	22 (20.94%)	Reference		
No	97(78.13%)	14 (73.68%)	83 (79.05%)	1.00 (0.30–3.34)		
Have pre-existing medical conditions	
Yes	14 (11.29%)	3 (15.79%)	11(10.48%)	Reference		
No	110(88.71%)	16 (84.21%)	94 (89.52%)	2.53 (0.70–9.12)		
Gestational age at delivery	
Pre-term	15 (12.10%)	1 (5.26%)	14 (13.33%)	Reference		
Term	109 (87.80%)	18 (94.74%)	91 (86.67%)	2.78 (0.34–22.41)		
Perceived stress	
Low	14 (11.29%)	2 (10.53%)	12 (11.43%)	Reference	Reference	
Moderate	74 (59.68%)	5 (26.32%)	69 (65.71%)	1.8 (0.21–15.45)	2.60 (1.10–13.20)	
High	36 (29.03%)	12 (63.16%)	24 (22.86%)	4.33 (0.50–37.92)	4.20 (1.04–18.55)	
Social Support	
Strong	78 (62.90%)	3 (15.79%)	75 (71.43%)	Reference	Reference	
Moderate	34 (27.42%)	6 (31.58%)	28 (26.67%)	6.48 (1.56–14.87)	6.20 (1.22–13.60)	
Poor	12 (9.68%)	10 (52.63%)	2 (1.90%)	12.00 (4.13–18.70)	11.68 (4.03–18.74)	
*Adjusted for age, parity, perceived stress and social support.

On stratified analysis, we did not observe evidence of effect modification of both perceived stress (P = 0.266) and social support (0.601) on the relationship between PPH and PPD (Table 4)Table 4 Interaction effects of social support and perceived stress on the relationship between PPH and PPD

Variable	OR (95% CI)	P-value	Mantel–Haenszel OR (95% CI)	P-value	
Social support	
Poor	–				
Moderate	0.93 (0.35–10.86)	0.442	0.15 (0.34–3.89)	0.266	
Strong	0.95 (0.17–12.87)	0.589			
Perceived stress	
Low	–				
Moderate	1.88 (0.21–3.60)	0.855	1.14 (0.39–3.31)	0.601	
High	2.05 (0.34–12.41)	0.420			

Discussion

This is a prospective cohort study of women with and without PPH who were followed up until 14 weeks postpartum in order to evaluate the incidence of PPD. The findings of our study show that the overall cumulative 14-week incidence of PPD for all respondents was 15.32%(17.46%, and 13.11% for women with PPH and without PPH respectively).

The incidence of PPD was not significantly different between women who had PPH and those who didn’t, and this lack of association persisted even after controlling for age, parity, perceived stress and social support. After controlling for these confounders, the only independent risk factors for PPD were perceived stress and social support. Social support and perceived stress, however, did not modify the relationship between PPH and PPD.

Our findings reveal that approximately 1 in 5 women who had postpartum haemorrhage in Kano develop PPD, a value higher than the 13.11% risk of PPD obtained from women who did not have PPH. The risk of PPD among both groups of women obtained in this study is akin to findings from China, where puerperal women with PPH were more likely to screen positive for postpartum depressive symptoms than those without PPH (16.4% vs 11.7%)13. Values from around the world, however differing from ours, also showed higher rates of PPD among women who had PPH as opposed to those who did not; from France (35% vs 15%)21, from Sweden (2.0% vs 1.9%)14. and from the UK (5.34% as opposed to 4.75%).11. Even though these results were consistent, the variances seen could have been caused by different inclusion criteria and methodological variations. For instance, one study defined PPD as having a value of EDPS score of 11 or above21, another defined PPH as losing >1000 mls13, while the third study limited its study group to term births with a non-anomalous pregnancy14. Two recent metanalyses revealed pooled evidence which showed that women with PPH are at increased risk of PPD compared with women without PPH5,22.

Over a third of the women who experienced PPH in this study reported high perceived stress relative to those who did not. Additionally, having high perceived stress was associated with increased odds of PPD. Epidemiological data has linked the occurrence of traumatic birth events, including PPH to higher stress levels10,23–25. Our results are in keeping with a review which reported a pooled incidence of PTSD after traumatic childbirth of 19.4% (95% CI 11.9–26.5%)26. Postpartum haemorrhage can have a profound psychological impact on mothers leading to feelings of fear, anxiety, helplessness, and loss of control. Witnessing or experiencing a life-threatening event during childbirth can trigger symptoms of post-traumatic stress disorder (PTSD) or contribute to general feelings of distress12. These psychological factors are closely linked to the development of postpartum depression. Thus, it is unsurprising that more than half of the PPD cases among women who experienced PPH were those with high perceived stress. The physical consequences of PPH, such as fatigue, weakness, anaemia, and the need for medical interventions like blood transfusions or surgery, can contribute to postpartum physical recovery challenges. This physical trauma and stress can exacerbate feelings of emotional distress and increase the risk of developing postpartum depression, pre-term deliveries and a pre-existing medical condition prior to pregnancy.

Our findings revealed an inverse relationship between social support and PPD. A significant number of our study participants among both groups had strong social support, however, there were more women with poor social support among those who had PPD. In line with our discovery, strong social support has been seen to positively influence the occurrence of PPD in African communities2,27,28. Social support plays a crucial role in promoting individual well-being, resilience, and community cohesion. In Africa, social support encompasses a rich tapestry of familial, communal, religious, and cultural practices that contribute to individual and collective well-being. African communities often exhibit strong bonds of solidarity and reciprocity, where neighbours, friends, and community members come together to support one another. In addition, family is central to social support in Africa, with strong kinship ties serving as the primary source of support. Extended family networks provide emotional, financial, and practical assistance to mothers after childbirth. This may further explain why women from monogamous homes in this study had a higher risk of PPD.

A major strength of this study is its prospective design. The prospective design allowed us to correctly estimate blood loss during delivery, a major flaw identified from previous studies, disentangle the temporal direction of association between PPH and PPD and assess the risk of PPD over time at three follow-up periods postpartum. Our study had some limitations, and the results must therefore be interpreted with caution. While all measures were put in place to reduce bias due to loss of follow-up, a negligible number of respondents could not be located after assessing the baseline information. A major source of potential bias in cohort studies arises from the degree of accuracy with which subjects have been classified with the outcome status. To avoid this, all staff collecting information underwent rigorous training with continuous supportive supervision. We also measured both PPH and PPD objectively using standardised tools.

We investigated the risk of PPD among women with and without PPH. Our findings showed insufficient evidence to suggest that women with PPH have a higher risk of PPH than women without PPH. However, perceived stress and social support were significantly associated with the development of PPD. We recommend the provision of holistic postpartum care that addresses both physical and emotional recovery needs as well as integrating mental health screening and support services into routine postpartum visits, alongside medical assessments.

Methods

This study is a multicenter prospective cohort study carried out in two tertiary hospitals (Aminu Kano Teaching Hospital and Murtala Muhammad Specialist Hospital) and one secondary hospital (Sabo Bakin Zuwo Maternity Hospital) within Kano, northern Nigeria. Kano state is one of the most populous states in Nigeria, with an estimated population of >14 million in 2022. Kano State is also among the states with poor maternal and child health indices, with a maternal mortality ratio of 1025 deaths per 100,000 live births (compared to the National figure of 576 per 100,000)29, and a high total fertility rate of over 6.5 births per woman30.

Aminu Kano Teaching Hospital (AKTH) and Murtala Muhammad Specialist Hospital (MMSH) serve as referral centres serving people from Kano and neighbouring states, while Sabo Bakin Zuwo Maternity Hospital (SBZMH) mainly serves people from within the Kano metropolis. The average number of annual births is 3800, 14,000 and 4000 in AKTH, MMSH and SBZMH, respectively.

The study population included women who gave birth in the three designated hospitals between April 13th 2023, and July 30th 2023, irrespective of parity and age. The study only comprised eligible women who were Kano residents, had a live birth, and received prenatal care in these facilities. In addition, women who had undergone a caesarean section, had a severe illness or had a history of mood disorders were excluded.

Prior data indicate that the incidence of PPD is 16% in Kano2. We hypothesise an absolute difference of 20% between our two study groups, based on observed difference of 20% found in a similar study21. Thus, a sample size of 75 for each group (total sample of 150), will achieve a power of 80% to observe a difference in incidence risk of 20% between women with and without PPH at 5% level of significance.

Baseline sociodemographic data, medical and obstetric history were obtained using a structured interviewer-administered questionnaire and other clinical data were obtained from the hospital records.

A Hausa-translated version of the Edinburgh postnatal depression scale (EDPS) was used to screen for PPD31. The EDPS is a 10-item, widely used, efficient and easy-to-use scale for identifying women at risk of postpartum depression32. Responses are scored between 0 and 3 based on the severity of the symptom, and the sum of the points for the 10 elements determines the final score, which can reach a maximum of 30. The EPDS is not a diagnostic tool but rather a means to identify the presence of a depressive symptom. The validity of EDPS has been tested in different settings, including Nigeria33,34, and has also been translated into several languages, including the Hausa Language31,33,35.

This study employed the Mini International Neuropsychiatric Interview (MINI) version 7.0.2 for DSM-5 to diagnose depressive disorders among the participants36. MINI is a short, standardised, structured instrument of choice often used for quick psychiatric evaluation in clinical and research settings. It covers a range of psychiatric disorders, including mood disorders, anxiety disorders, psychotic disorders, substance use disorders, and more. Studies have confirmed the validity and reliability of MINI37. Adopted by mental health practitioners and health organisations in over 100 countries, the MINI is the most extensively used psychiatric structured diagnostic interview instrument globally and has been verified and translated into more than 70 languages36. The scoring of the MINI entails determining whether or not specific criteria for a range of psychiatric disorders are present. Usually, responses are categorised as “Yes”, denoting the presence of symptoms or “No”, denoting their absence.

Social support was evaluated using the Oslo Social Support Scale (OSSS-3). The OSSS-3 is a brief measure designed to assess perceived social support, especially in population-based surveys and clinical contexts and has been recommended as a tool to assess social support in Nigeria38,39. Respondents score each of the three items on a Likert scale, which captures various facets of social support. The scores for each item are typically summed, with higher scores indicating greater perceived social support.

Perceived stress was measured using the Perceived Stress Scale. The Perceived Stress Scale (PSS-10) is a 10-item widely used psychological instrument for measuring the perception of stress in individuals over the past month. The PSS-10 covers various aspects of stress, including unpredictability, lack of control, and coping ability. Respondents rate their answers on a Likert scale, typically ranging from 0 (never) to 4 (very often). The PSS can be self-administered, making it appropriate for surveys. The total score can range from 0 to 4, with higher scores on the PSS indicating a higher level of perceived stress40.

The primary outcome, postnatal depression, was evaluated at 6, 10 and 14 weeks using the Edinburgh postnatal depression scale and the Mini International Neuropsychiatric Interview version 7.0.2 for DSM-5. Initial screening was conducted using the EDPS, and as recommended, a score of 9 or higher on the EDPS was the threshold for administering the MINI to establish the diagnosis of postpartum depression31. Confirmation of a major depressive disorder, as well as categorisation into current, past or recurrent, was made using the elements A1 to A6 on the A module of the MINI version 7.0.2.

The primary exposure, primary postpartum haemorrhage, was defined using the WHO description i.e. excess bleeding from the uterine cavity associated with childbirth in the quantity of 500 mls or more within 24 h of delivery41.

Other exposures included were social support classified as poor social support (score of 3–8), moderate social support (9–11) and strong social support (12–14) and perceived stress defined as low perceived stress (scores from 0 to 13), moderate stress (14 to 26), and high stress (scores from 27 to 40).

Explanatory variables were sociodemographic characteristics of the respondents, past medical history, obstetric history, and information regarding the most recent birth, including clinical findings, were also included as explanatory variables.

Selection of exposed group began with midwives in the delivery rooms of the three facilities being trained on how to quantify the volume of blood loss within 24 h of delivery. Under-buttock plastic calibrated drapes were used immediately after a woman delivered to collect blood around delivery time. Subsequently, sanitary towels were collected and weighed and specially formulated charts were used to calculate blood loss based on weight. Two nurses (research assistants) visited the delivery unit daily to identify women who had lost more than 500 mls within 24 h using the blood loss chart. Any woman who met the inclusion criteria was then enrolled as a participant in the exposed group. For each woman recruited into the exposed group, one woman who fulfilled the inclusion criteria but had not lost up to 500 mls of blood within 24 h was selected using a random sampling technique for recruitment into the unexposed group. This was done using randomly generated numbers from a tablet form within the list of the women without PPH who delivered that day.

Upon recruitment, baseline information was collected from participants of both groups. Clinical data and information on perceived stress and social support were also obtained.

All respondents were followed up for 14 weeks and the time for data collection was made to coincide with the second, third and fourth immunisation visits, which are at 6, 10 and 14 weeks. Index date of follow up was the date of the delivery. For participants who did not show up, phone calls were made, and they were visited in their homes.

Two nurses at the well-child clinic where women come for routine childhood immunisation collected data on the outcome (PPD). The EPDS was administered to each participant during the first visit, and those with a score of 9 and above were further evaluated using the MINI. Participants with scores less than 9 had the EPDS re-administered during the next visit, and the procedure was repeated until the last visit (at 14 weeks).

We utilised STATA version 15.0 (StataCorp LLC, College Station, TX, USA) for data analysis. Background characteristics were presented using frequencies and proportions as well as means and their corresponding standard deviations (SD) or median and interquartile range as appropriate. We estimated the cumulative incidence of PPD as the total number of PPD cases at the end of follow-up divided by the number of respondents followed up from the beginning of the study. We fitted logistic regression models to report the crude odds ratio (OR) and 95% confidence interval (CI) for the factors associated with PPD among all respondents and then employed a multivariable logistic regression modelling to report the adjusted odds ratio (aOR) and CI for the independent risk factors for PPD. We adopted a backward selection approach to modelling, beginning with a complete model that included all relevant variables and sequentially removing variables with a p-value > 0.20 and no established theoretical relevance. The likelihood ratio test was used to identify better models. The final model included our primary exposure to PPH status, age, parity, perceived stress and social support. We employed Mantel Haenszel (MH) odds to stratify the effect of PPH on PPD by perceived stress and social support and presented the ORs and CIs for each category.

Ethical approval for this study was obtained from the Health Research Ethics Committees of the Kano State Ministry of Health (SHREC/2022/3366) and Aminu Kano Teaching Hospital (NHREC/28/01/2020/AKTH/EC/3355). Permission to conduct the study was sought from the management of the three hospitals. Every respondent provided signed informed consent, and the provisions of the Helsinki declarations were adhered to.

Acknowledgements

The project was supported by an institutional-based research grant, TETFund grant TETF/DR&D/CE/UNIV/KANO/INR/2020/V0L1, and the Fogarty International Centre (FIC) and the National Institute on Alcohol Abuse and Alcoholism (NIAAA) of the U.S. National Institutes of Health (NIH) award number 1D43TW011544. The findings and conclusions are those of the authors and do not necessarily represent the official position of the FIC, NIAAA, NIH, the Department of Health and Human Services, or the government of the United States of America.

Author contributions

F.I.T., U.M.U., A.T.G., Z.D.A. and H.S.G. conceived and designed the study. F.I.T., S.M.A., S.M.S., N.T.A. and H.K.S. collected data. R.I.J., A.A.K., S.M.A. and S.K.S. performed a literature search. F.I.T., A.L.A. and R.I.J. performed the statistical analysis. F.I.T., U.M.I., A.T.G. and A.L.A. drafted the paper. Z.D.A., U.M.U. and S.K.S. assisted with data interpretation and critically reviewed the paper for intellectual content. A.A.K., S.M.S. and N.T.A. revised the paper. All authors contributed to and approved the paper.

Competing interests

The authors declare no competing interests.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
==== Refs
References

1. Lim G Perinatal depression Curr. Opin. Anaesthesiol. 2021 34 233 237 10.1097/ACO.0000000000000998 33935170
Lim, G. Perinatal depression. Curr. Opin. Anaesthesiol. 34, 233–237 (2021).33935170 10.1097/ACO.0000000000000998
2. Abba AH A prospective study on the incidence and predictors of postpartum depression among pregnant women attending an antenatal clinic in Kano, Northern Nigeria Open J. Psychiatry 2023 13 207 220 10.4236/ojpsych.2023.133017
Abba, A. H. et al. A prospective study on the incidence and predictors of postpartum depression among pregnant women attending an antenatal clinic in Kano, Northern Nigeria. Open J. Psychiatry 13, 207–220 (2023).10.4236/ojpsych.2023.133017
3. Grisbrook MA Associations among caesarean section birth, post-traumatic stress, and postpartum depression symptoms Int. J. Environ. Res. Public Health 2022 19 4900 10.3390/ijerph19084900 35457767
Grisbrook, M. A. et al. Associations among caesarean section birth, post-traumatic stress, and postpartum depression symptoms. Int. J. Environ. Res. Public Health 19, 4900 (2022).35457767 10.3390/ijerph19084900
4. Slomian J Honvo G Emonts P Reginster JY Bruyère O Consequences of maternal postpartum depression: a systematic review of maternal and infant outcomes Women’s Health (Lond.) 2019 15 1745506519844044 31035856
Slomian, J., Honvo, G., Emonts, P., Reginster, J. Y. & Bruyère, O. Consequences of maternal postpartum depression: a systematic review of maternal and infant outcomes. Women’s Health (Lond.) 15, 1745506519844044 (2019).31035856
5. Schoretsanitis, G. et al. Postpartum hemorrhage and postpartum depression: a systematic review and meta‐analysis of observational studies. Acta Psychiatr. Scand. 1–10 10.1111/acps.1358310 (2023).
6. WHO. Postpartum Haemorrhage (PPH) SUMMIT [Internet]. Bill and Melinda Gates Foundation, MSD for Mothers, and HRP. 2023 [cited 9th January 2024]. Available from: https://www.who.int/publications/m/item/who-postpartum-haemorrhage-(pph)-summit.
7. Bienstock JL Eke AC Hueppchen NA Postpartum hemorrhage N. Engl. J. Med. 2021 384 1635 1645 10.1056/NEJMra1513247 33913640
Bienstock, J. L., Eke, A. C. & Hueppchen, N. A. Postpartum hemorrhage. N. Engl. J. Med. 384, 1635–1645 (2021).33913640 10.1056/NEJMra1513247
8. Forbes G Factors influencing postpartum haemorrhage detection and management and the implementation of a new postpartum haemorrhage care bundle (E-MOTIVE) in Kenya, Nigeria, and South Africa Implement. Sci. 2023 18 1 10.1186/s13012-022-01253-0 36631821
Forbes, G. et al. Factors influencing postpartum haemorrhage detection and management and the implementation of a new postpartum haemorrhage care bundle (E-MOTIVE) in Kenya, Nigeria, and South Africa. Implement. Sci. 18, 1 (2023).36631821 10.1186/s13012-022-01253-0
9. Prata N Ejembi C Fraser A Shittu O Minkler M Community mobilization to reduce postpartum hemorrhage in home births in northern Nigeria. Social Sci. Med. 2012 74 1288 1296 10.1016/j.socscimed.2011.11.035
Prata, N., Ejembi, C., Fraser, A., Shittu, O. & Minkler, M. Community mobilization to reduce postpartum hemorrhage in home births in northern Nigeria. Social. Sci. Med. 74, 1288–1296 (2012).10.1016/j.socscimed.2011.11.035
10. Carroll M Daly D Begley CM The prevalence of women’s emotional and physical health problems following a postpartum haemorrhage: a systematic review BMC Pregnancy Childbirth 2016 16 261 10.1186/s12884-016-1054-1 27596720
Carroll, M., Daly, D. & Begley, C. M. The prevalence of women’s emotional and physical health problems following a postpartum haemorrhage: a systematic review. BMC Pregnancy Childbirth 16, 261 (2016).27596720 10.1186/s12884-016-1054-1
11. Parry-Smith W Postpartum haemorrhage and risk of mental ill health: a population-based longitudinal study using linked primary and secondary care databases J. Psychiatr. Res. 2021 137 419 425 10.1016/j.jpsychires.2021.03.022 33774536
Parry-Smith, W. et al. Postpartum haemorrhage and risk of mental ill health: a population-based longitudinal study using linked primary and secondary care databases. J. Psychiatr. Res. 137, 419–425 (2021).33774536 10.1016/j.jpsychires.2021.03.022
12. Kountanis JA Relationship between postpartum mood disorder and birth experience: a prospective observational study Int. J. Obstet. Anesth. 2020 44 90 99 10.1016/j.ijoa.2020.07.008 32861082
Kountanis, J. A. et al. Relationship between postpartum mood disorder and birth experience: a prospective observational study. Int. J. Obstet. Anesth. 44, 90–99 (2020).32861082 10.1016/j.ijoa.2020.07.008
13. Wang K Postpartum hemorrhage and postpartum depressive symptoms: a retrospective cohort study Depress. Anxiety 2022 39 246 253 10.1002/da.23245 35167153
Wang, K. et al. Postpartum hemorrhage and postpartum depressive symptoms: a retrospective cohort study. Depress. Anxiety 39, 246–253 (2022).35167153 10.1002/da.23245
14. Liu C The association between postpartum hemorrhage and postpartum depression: a Swedish national register-based study PloS ONE 2021 16 e0255938 10.1371/journal.pone.0255938 34379698
Liu, C. et al. The association between postpartum hemorrhage and postpartum depression: a Swedish national register-based study. PloS ONE 16, e0255938 (2021).34379698 10.1371/journal.pone.0255938
15. Tebeka S Prevalence and incidence of postpartum depression and environmental factors: the IGEDEPP cohort J. Psychiatr. Res. 2021 138 366 374 10.1016/j.jpsychires.2021.04.004 33932643
Tebeka, S. et al. Prevalence and incidence of postpartum depression and environmental factors: the IGEDEPP cohort. J. Psychiatr. Res. 138, 366–374 (2021).33932643 10.1016/j.jpsychires.2021.04.004
16. Meltzer-Brody S Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women Psychol. Med. 2017 47 1427 1441 10.1017/S0033291716003020 28112056
Meltzer-Brody, S. et al. Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women. Psychol. Med. 47, 1427–1441 (2017).28112056 10.1017/S0033291716003020
17. Baktygalikyzy, K. D., Tlekovna, A. M., Nurkozhakyzy, A. S., Rakhimzhanovna, K. S. editors. Postpartum Depression Is The Central Problem Of Our Century. The 15th International scientific and practical conference “Distance education as the main problem of young people” (December 26–29, 2023) Madrid, Spain International Science Group 2023 345 p; 2023.
18. Hantsoo L The role of the hypothalamic-pituitary-adrenal axis in depression across the female reproductive lifecycle: current knowledge and future directions Front. Endocrinol. (Lausanne) 2023 14 1295261 10.3389/fendo.2023.1295261 38149098
Hantsoo, L. et al. The role of the hypothalamic-pituitary-adrenal axis in depression across the female reproductive lifecycle: current knowledge and future directions. Front. Endocrinol. (Lausanne) 14, 1295261 (2023).38149098 10.3389/fendo.2023.1295261
19. Albacar G An association between plasma ferritin concentrations measured 48 h after delivery and postpartum depression J. Affect. Disord. 2011 131 136 142 10.1016/j.jad.2010.11.006 21130499
Albacar, G. et al. An association between plasma ferritin concentrations measured 48 h after delivery and postpartum depression. J. Affect. Disord. 131, 136–142 (2011).21130499 10.1016/j.jad.2010.11.006
20. UNICEF. Situation of women and children in Nigeria: Challenges faced by women and children in Nigeria [Internet]. 2021 [cited 10th January 2024]. Available from: https://www.unicef.org/nigeria/situation-women-and-children-nigeria#:~:text=According%20to%20data%2C%20Nigeria%20is,7%20million%20babies%20are%20born.
21. Ricbourg A Emotional impact of severe post-partum haemorrhage on women and their partners: an observational, case-matched, prospective, single-centre pilot study Eur. J. Obstet. Gynecol. Reprod. Biol. 2015 193 140 143 10.1016/j.ejogrb.2015.07.020 26298809
Ricbourg, A. et al. Emotional impact of severe post-partum haemorrhage on women and their partners: an observational, case-matched, prospective, single-centre pilot study. Eur. J. Obstet. Gynecol. Reprod. Biol. 193, 140–143 (2015).26298809 10.1016/j.ejogrb.2015.07.020
22. Sheng B Jiang G Ni J Association between postpartum depression and postpartum hemorrhage: a systematic review and meta-analysis Acta Obstetr. Gynecol. Scand. 2024 103 1263 1270 10.1111/aogs.14795
Sheng, B., Jiang, G. & Ni, J. Association between postpartum depression and postpartum hemorrhage: a systematic review and meta-analysis. Acta Obstetr. Gynecol. Scand. 103, 1263–1270 (2024).10.1111/aogs.14795
23. Scheepstra, K. W., Van Steijn, M. E., Dijksman, L. M. & van Pampus, M. G. Post-traumatic stress disorder in women and their partners, following severe post-partum hemorrhage: A study protocol for a prospective cohort study. Cogent Med. 4, 10.1080/2331205X.2017.1278840 (2017).
24. Van Steijn ME Severe postpartum hemorrhage increases risk of posttraumatic stress disorder: a prospective cohort study J. Psychosom. Obstet. Gynecol. 2021 42 335 345 10.1080/0167482X.2020.1735343
Van Steijn, M. E. et al. Severe postpartum hemorrhage increases risk of posttraumatic stress disorder: a prospective cohort study. J. Psychosom. Obstet. Gynecol. 42, 335–345 (2021).10.1080/0167482X.2020.1735343
25. Latt SM Primary postpartum haemorrhage and longer-term physical, psychological, and psychosocial health outcomes for women and their partners in high income countries: a mixed-methods systematic review PLoS ONE 2023 18 e0274041 10.1371/journal.pone.0274041 37315027
Latt, S. M. et al. Primary postpartum haemorrhage and longer-term physical, psychological, and psychosocial health outcomes for women and their partners in high income countries: a mixed-methods systematic review. PLoS ONE 18, e0274041 (2023).37315027 10.1371/journal.pone.0274041
26. Lai X The incidence of post‐traumatic stress disorder following traumatic childbirth: a systematic review and meta‐analysis Int. J. Gynecol. Obstet. 2023 162 211 221 10.1002/ijgo.14643
Lai, X. et al. The incidence of post‐traumatic stress disorder following traumatic childbirth: a systematic review and meta‐analysis. Int. J. Gynecol. Obstet. 162, 211–221 (2023).10.1002/ijgo.14643
27. Desta M Postpartum depression and its association with intimate partner violence and inadequate social support in Ethiopia: a systematic review and meta-analysis J. Affect. Disord. 2021 279 737 748 10.1016/j.jad.2020.11.053 33234282
Desta, M. et al. Postpartum depression and its association with intimate partner violence and inadequate social support in Ethiopia: a systematic review and meta-analysis. J. Affect. Disord. 279, 737–748 (2021).33234282 10.1016/j.jad.2020.11.053
28. Dlamini LP Mahanya S Dlamini SD Shongwe MC Prevalence and factors associated with postpartum depression at a primary healthcare facility in Eswatini South Afr. J. Psychiatry 2019 25 1 7
Dlamini, L. P., Mahanya, S., Dlamini, S. D. & Shongwe, M. C. Prevalence and factors associated with postpartum depression at a primary healthcare facility in Eswatini. South Afr. J. Psychiatry 25, 1–7 (2019).
29. MNCH2 and UKaid. Our work in Kano [Internet]. [cited 16th January 2024]. Available from: https://www.mnch2.com/kano-state/ (2024).
30. National Population Commission (NPC) [Nigeria] and ICF. Nigeria Demographic and Health Survey 2018. Abuja, Nigeria, and Rockville, Maryland, USA: NPC and ICF (2019).
31. Tungchama FP Relationship between quality of life and postpartum depression among women in North-Central, Nigeria Highl. Med. Res. J. 2017 17 11 18
Tungchama, F. P. et al. Relationship between quality of life and postpartum depression among women in North-Central, Nigeria. Highl. Med. Res. J. 17, 11–18 (2017).
32. Cox JL Holden JM Sagovsky R Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale Br. J. Psychiatry 1987 150 782 10.1192/bjp.150.6.782 3651732
Cox, J. L., Holden, J. M. & Sagovsky, R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br. J. Psychiatry 150, 782 (1987).3651732 10.1192/bjp.150.6.782
33. Adewuya AO Ola BA Dada AO Fasoto OO Validation of the Edinburgh Postnatal Depression Scale as a screening tool for depression in late pregnancy among Nigerian women J. Psychosom. Obstet. Gynaecol. 2006 27 267 272 10.1080/01674820600915478 17225628
Adewuya, A. O., Ola, B. A., Dada, A. O. & Fasoto, O. O. Validation of the Edinburgh Postnatal Depression Scale as a screening tool for depression in late pregnancy among Nigerian women. J. Psychosom. Obstet. Gynaecol. 27, 267–272 (2006).17225628 10.1080/01674820600915478
34. Obindo T Omigbodun O The validation of Edinburgh postpartum depression scale I North Central, Nigeria J. Med. Trop. 2007 9 29 40
Obindo, T. & Omigbodun, O. The validation of Edinburgh postpartum depression scale I North Central, Nigeria. J. Med. Trop. 9, 29–40 (2007).
35. Cox J Thirty years with the Edinburgh Postnatal Depression Scale: voices from the past and recommendations for the future Br. J. Psychiatry 2019 214 127 129 10.1192/bjp.2018.245 30774059
Cox, J. Thirty years with the Edinburgh Postnatal Depression Scale: voices from the past and recommendations for the future. Br. J. Psychiatry 214, 127–129 (2019).30774059 10.1192/bjp.2018.245
36. Sheehan DV The Mini-International Neuropsychiatric Interview (MINI): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10 J. Clin. Psychiatry 1998 59 22 33 9881538
Sheehan, D. V. et al. The Mini-International Neuropsychiatric Interview (MINI): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J. Clin. Psychiatry 59, 22–33 (1998).9881538
37. Mostafa Abdel Monhem, A. & Magdy Hassan Hussein, B. Minor psychiatric morbidity in young Saudi mothers using mini international neuropsychiatric interview [MINI]. (2010).
38. Kocalevent R-D Social support in the general population: standardization of the Oslo social support scale (OSSS-3) BMC Psychol. 2018 6 31 10.1186/s40359-018-0249-9 30016997
Kocalevent, R.-D. et al. Social support in the general population: standardization of the Oslo social support scale (OSSS-3). BMC Psychol. 6, 31 (2018).30016997 10.1186/s40359-018-0249-9
39. Abiola T Udofia O Zakari M Psychometric properties of the 3-item Oslo Social Support Scale among Clinical Students of Bayero University Kano, Nigeria Malays. J. Psychiatry 2013 22 32 41
Abiola, T., Udofia, O. & Zakari, M. Psychometric properties of the 3-item Oslo Social Support Scale among Clinical Students of Bayero University Kano, Nigeria. Malays. J. Psychiatry 22, 32–41 (2013).
40. Cohen, S., Kamarck, T. & Mermelstein, R. Perceived Stress Scale. Measuring Stress: A Guide for Health and Social Scientists p 235–283 (Mind Garden Inc., 1994).
41. Vogel JP Williams M Gallos I Althabe F Oladapo OT WHO recommendations on uterotonics for postpartum haemorrhage prevention: what works, and which one? BMJ Glob. Health 2019 4 e001466 10.1136/bmjgh-2019-001466 31139461
Vogel, J. P., Williams, M., Gallos, I., Althabe, F. & Oladapo, O. T. WHO recommendations on uterotonics for postpartum haemorrhage prevention: what works, and which one? BMJ Glob. Health 4, e001466 (2019).31139461 10.1136/bmjgh-2019-001466
