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Care-seeking patterns among families that experienced under-five child mortality in rural Rwanda

  • Daniel M. Kagabo ,

    Roles Conceptualization, Formal analysis, Investigation, Project administration, Validation, Writing – original draft

    dankagabo@gmail.com

    Affiliation Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda

  • Catherine M. Kirk,

    Roles Conceptualization, Formal analysis, Supervision, Validation, Writing – original draft

    Affiliation Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda

  • Benjamin Bakundukize,

    Roles Conceptualization, Writing – review & editing

    Affiliation Rwinkwavu District Hospital, Ministry of Health, Rwinkwavu, Rwanda

  • Bethany L. Hedt-Gauthier,

    Roles Conceptualization, Formal analysis, Supervision, Writing – review & editing

    Affiliations Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda, Department of Global Health and Social Medicine, Harvard Medical School, Boston, Massachusetts, United States of America

  • Neil Gupta,

    Roles Supervision, Writing – review & editing

    Affiliations Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda, Division of Global Health Equity, Brigham and Women’s Hospital, Boston, Massachusetts, United States of America

  • Lisa R. Hirschhorn,

    Roles Supervision, Writing – review & editing

    Affiliation Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America

  • Willy C. Ingabire,

    Roles Investigation, Writing – review & editing

    Affiliation Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda

  • Dominique Rouleau,

    Roles Project administration, Writing – review & editing

    Affiliation Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda

  • Fulgence Nkikabahizi,

    Roles Writing – review & editing

    Affiliation Rwinkwavu District Hospital, Ministry of Health, Rwinkwavu, Rwanda

  • Catherine Mugeni,

    Roles Writing – review & editing

    Affiliation Rwanda Biomedical Center, Ministry of Health, Kigali, Rwanda

  • Felix Sayinzoga,

    Roles Writing – original draft

    Affiliation Rwanda Biomedical Center, Ministry of Health, Kigali, Rwanda

  • Cheryl L. Amoroso

    Roles Conceptualization, Formal analysis, Project administration, Supervision, Writing – review & editing

    Affiliation Partners in Health/Inshuti Mu Buzima (PIH/IMB), Rwinkwavu, Rwanda

Abstract

Background

Over half of under-five deaths occur in sub-Saharan Africa and appropriate, timely, quality care is critical for saving children’s lives. This study describes the context surrounding children’s deaths from the time the illness was first noticed, through the care-seeking patterns leading up to the child’s death, and identifies factors associated with care-seeking for these children in rural Rwanda.

Methods

Secondary analysis of a verbal and social autopsy study of caregivers who reported the death of a child between March 2013 to February 2014 that occurred after discharge from the child’s birth facility in southern Kayonza and Kirehe districts in Rwanda. Bivariate analyses using Fisher’s exact tests were conducted to identify child, caregiver, and household factors associated with care-seeking from the formal health system (i.e., community health worker or health facility). Factors significant at α = 0.10 significance level were considered for backwards stepwise multivariate logistic regression, stopping when remaining factors were significantly associated with care-seeking at α = 0.05 significance level.

Results

Among the 516 eligible deaths among children under-five, 22.7% (n = 117) did not seek care from the health system. For those who did, the most common first point of contact was community health workers (45.8%). In multivariate logistic regression, higher maternal education (OR = 3.36, 95% CI: 1.89, 5.98), having diarrhea (OR = 4.21, 95%CI: 1.95, 9.07) or fever (OR = 2.03, 95%CI: 1.11, 3.72), full household insurance coverage (3.48, 95%CI: 1.79, 6.76), and longer duration of illness (OR = 22.19, 95%CI: 8.88, 55.48) were significantly associated with formal care-seeking.

Conclusion

Interventions such as community health workers and insurance promote access to care, however a gap remains as many children had no contact with the health system prior to death and those who sought formal care still died. Further efforts are needed to respond to urgent cases in communities and further understand remaining barriers to accessing appropriate, quality care.

Introduction

Timely and appropriate care-seeking is crucial for good health outcomes, especially among children under five years old [1]. In 2013, more than 6.3 million children died before their fifth birthday, with sub-Saharan Africa accounting for half of these deaths [2]. Integrated Management of Childhood Illness (IMCI) protocols and community case management have improved both access to care and health care workers ability to address under-five illnesses and have reduced child mortality (globally defined as any death occurring before a child’s fifth birthday) [3, 4]. However, in sub-Saharan Africa, limited access to skilled care remains among the significant factors contributing to under-five mortality [5].

Care-seeking for children is defined as actions taken by caregivers of young children in response to a child’s perceived illness. Andersen’s [6] behavioral model identifies three levels of factors that contribute to the decision to seek care or not. Predisposing factors, such as mother’s level of education [7] and the child’s gender [8] have been associated with care-seeking for children. Several enabling resources are also associated with care-seeking in low- and middle-income countries. Distance to the nearest health facility is directly proportional to risk of dying among children [9]. Financial barriers can also hinder access, with transport costs preventing or delaying care-seeking [1, 10], higher socioeconomic status associated with increased likelihood of seeking care [11, 12], and the cost of treatment being a barrier to care-seeking [1315] that can further increase the time between presentation of symptoms and care-seeking [1]. In rural South Africa [16], nearly half of people rely on walking as the primary mode of transport to health facilities [17] and transport costs made up a large proportion of overall healthcare costs [18]. Lastly, there are a number of factors that contributed to the perceived and evaluated need to seek care, including the perception of symptoms as severe or presence of easily identifiable symptoms have been shown to prompt care-seeking for sick infants and children [7, 8, 11]. In addition, preference for seeking informal care, such as self-medication or traditional healers can also delay seeking formal care [15].

Rwanda has made tremendous progress in reducing child mortality, with one of the most rapid declines of child mortality ever recorded [19] from 152 under-five deaths per 1,000 live births in 2005 to 50 in 2015 [20]. This reduction has been attributed to a number of initiatives in the health sector, including improving geographic access by increasing the number of primary healthcare facilities [21] and reducing financial barriers through the community-based health insurance [22]. Further, specific health promotion interventions in Rwanda included insecticide-treated mosquito bed net distribution, high childhood vaccination and vitamin A supplementation coverage, implementation of community- and facility-based IMCI protocols [16], and the near-elimination of infant HIV infections [23].

Despite these gains, Rwanda has an under-five mortality rate that remains seven times higher than developed nations [20, 24]. Accessing professional healthcare plays a large role in the reduction of mortality during acute illness. However, little is known about the determinants and patterns of care-seeking prior to a child’s death in Rwanda. To continue the reduction of under-five mortality, better understanding the predictors of care-seeking behaviors among caregivers of young children in Rwanda is needed. This can inform patient-centered interventions that address factors related to delayed access to healthcare for sick children. To this end, the aim of this study is to describe the socio-demographic characteristics associated with care-seeking among families that experienced an under-five death in two rural districts in Rwanda. By focusing on care-seeking behaviors and the context around children whose illness led to the worst possible outcome of death, we hope to identify critical interventions to prevent future child mortality.

Materials and methods

Study design and setting

This study is a secondary analysis of data that the authors collected for a verbal and social autopsy study, which interviewed primary caregivers that experienced the death of a child under-five years of age between March 2013 to February 2014 in the Kirehe District Hospital and Rwinkwavu District Hospital catchment areas, in Kirehe and southern Kayonza Districts, respectively. In these two catchment areas, there are three levels of healthcare delivered by the Ministry of Health (MOH) with support from Partners In Health/Inshuti Mu Buzima (PIH/IMB). At the community level, there are three community health workers for each village and two of them (called “binomes”) provide services for children under-five, including the diagnosis and treatment of pneumonia, malaria, and diarrhea through community IMCI. Health centers (15 in Kirehe District and 8 in southern Kayonza District) provide mainly outpatient primary healthcare. District hospitals provide secondary care, mostly to patients referred from health centers. The most complicated cases are referred to tertiary hospitals [25], which are primarily based in the capital city of Kigali. The terrain in rural Rwanda is hilly and the average walking distance from households to the nearest health facility in Kirehe is 92.4 minutes and 64.2 minutes in Kayonza [26]. The most common forms of transportation in these districts are walking and fee-per-use methods such as bicycles, minibuses, and motorcycle taxis. The STROBE checklist (S1 File) is available in the supplementary materials.

Participants and data collection

The original data collection aimed to have a census of all under-five deaths during the study period. For the main verbal and social autopsy study, all under-five deaths during the study period were identified from community and health facility records by triangulating existing MOH reporting systems and the Monitoring of Vital Events using Information Technology (MoVe-IT) program. MoVe-IT was introduced in the two districts in 2012 to complement existing reporting systems, and consisted of text message reporting by community health workers of all vital events among mothers and under-five children [27]. Families that experienced an under-five death were located in the community with the help of community health workers. For this secondary analysis, all children under-five that died and were captured in the original data collection were included unless they met the exclusion criteria for our secondary analysis: neonatal deaths that occurred before discharge from the facility where they were born and children whose caregivers did not report on care-seeking were excluded. Those born outside of a facility were included if the caregivers reported on care-seeking.

Data was collected through household interviews with caregivers of the deceased child. Caregivers were asked to report on demographic characteristics, and the symptoms and care-seeking patterns prior to the child’s death using a structured interview questionnaire adapted from the World Health Organization’s (WHO) verbal autopsy tool [28]. The WHO’s verbal autopsy tool contains a series of questions about specific symptoms the child experienced during the illness that resulted in the child’s death, such as presence of a fever or diarrhea, the duration of the illness prior to death, as well as contextual factors such as whether the child was involved in an accident, distance of the household to a health facility, and caregiver perception of illness severity. The questionnaire also included a subset of questions from the MOH’s Death Audit Tool (i.e, place of birth, places where care was sought, reasons for not seeking care, time spent in health facilities, perceived quality of care, status of mother and father, household religion, household occupation, and health insurance coverage) and the 2010 Rwanda Demographic and Health Survey (i.e., household assets and housing materials). Variables were grouped into predisposing factors, enabling factors, and perceived and evaluated need based on the Andersen framework for care-seeking (Fig 1).[6]

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Fig 1. Behavioral model of predictors of care-seeking behavior.

https://doi.org/10.1371/journal.pone.0190739.g001

No personal identifiers were stored on the data collection form; instead, caregivers’ identifiers were stored in a separate file in a secure location with matching study IDs for data cleaning and validation. Initial data were collected on paper with double entry for data quality control but the majority of data were collected using Android tablets.

Analysis

The primary outcome of interest in this study was formal care-seeking prior to the child’s death, which was defined as seeking care from the formal health system through community health workers or health facilities (health posts, health centers, hospitals, or private clinics). Taking a child to traditional healers or seeking self-treatment from a pharmacy or from neighbors were all categorized as not seeking formal care.

We describe child, caregiver and household variables and test for their associations with care-seeking using a Fisher’s exact test. All variables associated with care-seeking at α = 0.10 significance level in the bivariate analyses were entered into a full logistic regression model. We used backwards stepwise regression to identify predictors and risk factors associated with seeking care upon noticing the child’s illness among children under-five, stopping when all remaining variables were significant at the α = 0.05 significance level. All analyses were completed in Stata version 13 (StataCorp 2011. College Station, TX).

Ethical approval

This study was approved by Rwanda National Ethics Committee (RNEC) and the Partners Institutional Review Board in Boston, Massachusetts under the Population Health Implementation and Training (PHIT) program, a partnership between PIH/IMB, the University of Rwanda and the Rwanda MOH. All caregivers who participated provided written informed consent. Given the sensitive nature of the questionnaire, all data collectors were trained to be considerate of and sensitive to the caregiver’s needs such as giving time to respond, ensuring caregivers understood that all answers were voluntary, providing comfort in any instance where a caregiver may have become upset, and postponing or ending the interview if preferred by the caregivers.

Results

In the original verbal and social autopsy study, 618 out of 650 households with an under five death between March 2013 to February 2014 were visited; 5% of families were not interviewed due to caregiver refusal, relocation or being unable to be found based on the information contained in facility, community, and MoVe-IT death records (n = 29, see Fig 2). Of the 618 under-five children whose caregivers were interviewed, 97 died before discharge from the health facility where they were born, leaving 521 deaths available for this study. Of these, the respondent was unsure whether care was sought for five children (1.0%) and these children were excluded, leaving 516 in the final sample.

Half of children who died were above one year of age (50.2%; n = 259), while 35.1% (n = 181) were infants aged 28 days to 1 year, and 14.7% (n = 76) were neonates (Table 1). Fifty-five percent of the children were male (54.5%, n = 281). The most common symptoms for children in our sample were fever (63.3%, n = 322), breathing problems (55.2%, n = 284), vomiting (45.0%, n = 232) and diarrhea (32.8%, n = 168). Less common symptoms were convulsions (20.6%, n = 105/510) or unconsciousness (16.2%, n = 77/475). A small number (4.3%, n = 22) experienced an accident or injury that led to their death. For nearly all children (97.5%, n = 499/512), both parents were still alive at the time of death. Duration of the child’s illness prior to death varied with 28.9% (n = 149) of the children ill for over one week, 32.6% (n = 168) ill between three to seven days, 21.1%, (n = 109) ill for 12 hours to two days, and 17.4% (n = 90) were ill for less than 12 hours.

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Table 1. Descriptive characteristics of the child, caregivers, and household.

https://doi.org/10.1371/journal.pone.0190739.t001

The majority of children’s parents were living together (77.0%, n = 384/499) and 94.7% of mothers (n = 484/511) and 86.6% of fathers (n = 433/500) worked in agriculture. For the 492 mothers with age recorded, most were aged 20–29 (42.1%, n = 207) or 30–39 (41.3%, n = 203). For the 384 fathers with age recorded, 28.9% (n = 111) were 20–29, 38.8% (n = 149) were age 30–39, 22.1% (n = 85) were age 40–49 and 10.2% (n = 39) were over age 50. A third of mothers (30.6%, n = 150/491) and a quarter of fathers (26.5%, n = 103/389) reported having no formal education. The majority of families (87.8%, n = 453) had unfinished exterior walls (walls that were not cemented) and lacked access to electricity in their households (92.8%, n = 478/515). Two-thirds of families (66.0%, n = 334/506) had insurance for all family members, and 20.5% had no insured family members (n = 104/506). Over one-third of households (37.6%, n = 193/514) reported living more than two hours walking distance from the nearest health facility. When asked what factors pose problems for the household when seeking healthcare in general, the most common responses were getting money to pay for treatment (57.6%, n = 297) and distance to the nearest health facility (41.7%, n = 215).

Overall, in 22.7% (n = 117) of the under-five deaths, the caregiver did not seek any formal healthcare prior to the child’s death (Table 2). Of caregivers who sought formal care prior to the child’s death, 45.8% (n = 182) reported that the first point of care was community health workers and 42.5% (n = 168) reported going first to a health center or other outpatient clinic.

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Table 2. Formal and informal care seeking prior to the child’s death.

https://doi.org/10.1371/journal.pone.0190739.t002

Thirty-four (8.9%) caregivers who eventually sought formal care first pursued self-treatment from a traditional healer (7.9%, n = 31) or pharmacy (1.0%, n = 3). Over half of caregivers that sought formal care went to a community health worker at some point during the illness (58.4%, n = 233), nearly all visited a health center or other outpatient clinic (84.0%, n = 335), and a third went to a hospital (33.6%, n = 134). Of caregivers that did not seek any formal care, 19.7% (n = 23/117) visited a traditional healer or sought self-treatment from a pharmacy. Caregivers who did not seek formal care prior to the child’s death were asked to report reasons for not seeking care upon noticing the child’s illness. The most commonly reported reason for not seeking formal care was the perception that the child fell ill and died quickly (45.3%, n = 53). Only 17.1% (n = 20) of the caregivers reported finances being a barrier and 18.0% (n = 21) reported not thinking the illness was serious.

Care-seeking patterns were significantly different depending on the child’s age (p = 0.04, Table 3). Children with fever (p<0.001), breathing problems (p<0.001), diarrhea (p<0.001), vomiting (p<0.001) and unconsciousness (p = 0.023) were more likely to have sought formal care. Children with three or more symptoms nearly always had formal care (90.9%, n = 249/274) compared to 38.6% (n = 22/274) of children who did not exhibit one of the six most common symptoms (p<0.001). Significantly more children involved in an accident or injury that led to their death received no formal care (54.5%, n = 12/22) compared to those not involved in an accident or injury (21.3%, n = 105/494, p = 0.001). Children with symptoms lasting less than 12 hours were less likely to have formal care (64.4%, n = 58/90) compared to those with symptoms lasting over a week (6.7%, n = 10/149, p<0.001). A third of mothers with no education did not seek formal care for their children (35.3%, n = 53/150) compared to 17.3% (n = 59/341) among those with primary education or higher (p<0.001). A higher portion of young fathers aged 20–29 sought formal care (85.6%, n = 95/111) compared older fathers (p = 0.036). Households with all members insured were significantly more likely to seek care with 82.9% (n = 277/334) as compared to 66.3% (n = 69/104) of those with no insurance sought care (p<0.001). Households that were over two hours from the nearest health facility were less likely to seek formal care (27.5%, n = 53/193) as compared to those who lived closer (19.6%, n = 63/231, p = 0.050). Self-reported barriers to care such as getting money to pay, distance, not wanting to go alone, and getting permission were not associated with ultimately seeking care prior to child’s death.

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Table 3. Bivariate associations between care-seeking and child, caregiver, and household characteristics.

https://doi.org/10.1371/journal.pone.0190739.t003

In the final multivariate model (Table 4), caregivers were more likely to seek care if the child presented with a fever (Odds Ratio [OR] = 2.03, 95% Confidence Interval [CI]: 1.11, 3.72, p = 0.022), diarrhea (OR = 4.21, 95% CI: 1.95, 9.07, p<0.001), had an illness duration of greater than 12 hours (ill from 12 hours to 48 hours, OR = 4.51, 95% CI: 2.16, 9.42, p<0.001; from three to seven days, OR = 13.70, 95% CI: 6.04, 31.07, p<0.001; and over one week, OR = 22.19, 95% CI: 8.88, 55.48, p<0.001 compared to illness duration less than 12 hours), had a higher level of maternal education (OR = 3.36, 95% CI: 1.89, 5.98, p<0.001), and if the household was fully insured (OR = 3.48, 95% CI: 1.79, 6.76, p<0.001).

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Table 4. Multivariate logistic regression of care-seeking predictors.

https://doi.org/10.1371/journal.pone.0190739.t004

Discussion

In our study, we found that nearly a quarter of children under-five that died in Kirehe and southern Kayonza Districts during the study period had no care during their final illness. While the majority of children did access the formal health system, the care received was not able to prevent the child’s death. For those who sought formal care, Rwanda’s large network of community health workers was an important resource and the most common first point of care. Factors at all levels of Andersen’s care-seeking model predicted whether a child ultimately had contact with the formal health care system prior to death—the predisposing factor of maternal education, the enabling factor of household health insurance coverage, and several factors related to the severity of the child’s illness and symptoms [6]. It is vital to understand care-seeking behavior prior to death in order to identify facilitating factors and barriers to accessing timely and appropriate care in rural parts of Rwanda and develop interventions to prevent unnecessary child deaths in the future.

In our study, longer duration of illness was a strong predictor of care-seeking; for caregivers who did not seek care, the caregiver reporting the death occurred quickly was the main reason provided for not seeking care. There are several factors identified in other studies that could contribute to this finding including lack of awareness of the severity of the child’s illness [29], first attempting traditional medicines or self-treatment [30], as well as lack of access to timely transportation when an illness occurs quickly. A number of barriers may create challenges for accessing care when a death occurs quickly, such as incidents of injuries, drowning, or other accidents. This may also be associated with caregivers’ preferring to seek care during the day due to safety concerns at night [31] or limited accessibility of nighttime travel. Additionally, limited access to emergency transportation poses challenges for quick, affordable access to care [32]. In Rwanda, ambulance use is limited for responding to community emergencies; ambulances are primarily used for inter-health facilities transfers or traffic accidents [33]. Interventions which might address these challenges could include having the one male community health worker in the “binome” pair accompany caregivers for night time emergencies to help ensure safety of the child and caregiver while also increasing access to care during this critical period. Further, strengthening the emergency transport system to facilitate urgent transfers from the community to a health facility is needed.

We also found that the symptoms related to the child’s illness were important factors for whether or not formal care was sought. Similar to a study in Tanzania [34], we found that caregivers were significantly more likely to seek care if a child had fever or diarrhea. This may be due in part to the contribution of community health workers who, under the national community health program, have sensitized parents about danger signs and the importance of seeking care whenever children present with these noticeable symptoms [30]. Further, community health workers are trained in IMCI to detect, treat and provide referrals as appropriate for common childhood illnesses [16]. It is noted however that signs of respiratory distress were not associated with care-seeking, and further investigation is required to determine if the messaging to families about when to seek care when these symptoms are present can be improved. In addition to helping with the early identification of common symptoms, community health workers need to emphasize the importance of timely care-seeking by caregivers before their children’s health becomes critical.

While household wealth was not directly measured, we believe that the majority of households in this study were likely to be of lower socioeconomic status, with limited access to electricity and homes primarily constructed with unfinished walls. These findings indicate slightly lower socioeconomic standing of the households in our study than a national, population survey which found in the Eastern Province that 15.3% of households have electricity and 63.4% of individuals were living in houses with unfinished walls [35]. However, and perhaps surprisingly given that associated costs are often a barrier for care-seeking [36], none of these indicators of poor socioeconomic status were associated with care-seeking in our results and for those who did not seek care, very few indicated limited finances as a barrier. This may be explained by the focus of Rwanda’s health policies on reducing social inequity [37] or that there is limited variability in socioeconomic status in this study population. Community-based health insurance, called mutuelle de santé, has increased care-seeking by reducing financial barriers to care, with enrolled families having twice the healthcare utilization rates compared to uninsured families [38]. In 2010, household enrollment in mutuelle de santé peaked at 90% [14], and later decreased to 73% household enrollment in 2014 [39]. Rwanda’s community-based health insurance system may increase access to care by preventing catastrophic out of the pocket payment whenever family members are sick [22], and this insurance is subsidized with co-payment exemptions for the poorest households [40]. The possibility that subsidized insurance for the poorest households reduces the impact of poverty on care-seeking behavior is also supported by the finding that households with all family members were covered by health insurance were significantly more likely to take the child for care when ill. Additionally, cost barriers may be difficult for families to discuss, given that the ultimate outcome was the child’s death.

Limitations of this study should be noted. Information about what occurred during the time leading up to the child’s death was based on caregiver’s recall of specific symptoms and health care-seeking patterns. However, we aimed to minimize recall bias by interviewing caregivers within twelve months after the child’s death. Further, there was the potential for desirability bias, where individuals may not be fully forthcoming about their child’s death, wanting to shield themselves from blame. However, only assessing care-seeking behaviors for children who died should minimize the bias as we are not comparing them to children who survived a similar illness. Finally, it is noted that this study only includes care-seeking behaviors among families that experienced an under-five death. While this may not be generalizable to all families with children under-five, it is still important because its sheds light on scarcely researched care-seeking patterns in rural Rwanda and challenges faced by caregivers in critical time of an under-five child.

Conclusions

As we reflect on the commendable achievement in improved health in Rwanda, these findings highlight that barriers remain to timely care-seeking for critically ill children in rural Rwanda with nearly a quarter of children who died having no contact with the formal health system prior to death. With the majority of the deceased children having accessed the formal health system, further research should explore the care experiences and quality of care services received. Efforts to decentralize primary health care, and to promote integrated community case management and health insurance have contributed to reducing child mortality, but more must be done to maintain this momentum and ensure all children have access to potentially lifesaving services. Community health workers remain a vital first point-of-care for families and in creating awareness of childhood illness danger signs and also in encouraging timely care-seeking. Another significant point-of-care is primary health centers. Nevertheless, this study highlights important challenges with responding to urgent cases in rural communities and further assessment is needed to determine feasibility and efficiency of enhanced expanded emergency response systems and improve the quality of care to save lives.

Supporting information

Acknowledgments

This study was developed under the Partners In Health/Inshuti Mu Buzima Intermediate Operational Research Training Program, developed and facilitated by Bethany Hedt-Gauthier and Neil Gupta. We would like to thank Adeline Uwonkunda, Pilar Kandamage, Chantal Niyirema, Alice Mukahirwa, Peter Barebwanuwe, Marie Paul Nisingizwe, and Hari S. Iyer for their contribution to this work. We appreciate the community health workers for their support in locating families. Most importantly, we are immensely grateful to the mothers, fathers and other primary caregivers who shared their experiences of losing their child.

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