Skip to main content

Identifying transferable lessons from cholera epidemic responses by Médecins Sans Frontières in Mozambique, Malawi and the Democratic Republic of Congo, 2015–2018: a scoping review

Abstract

Background

Cholera epidemics occur frequently in low-income countries affected by concurrent humanitarian crises. Evaluations of these epidemic response remains largely unpublished and there is a need to generate evidence on response efforts to inform future programmes. This review of MSF cholera epidemic responses aimed to describe the main characteristics of the cholera epidemics and related responses in these three countries, to identify challenges to different intervention strategies based on available data; and to make recommendations for epidemic prevention and control practice and policy.

Methods

Case studies from the Democratic Republic of Congo, Malawi and Mozambique were purposively selected by MSF for this review due to the documented burden of cholera in each country, frequency of cholera outbreaks, and risk of humanitarian crises. Data were extracted on the characteristics of the epidemics; time between alert and response; and, the delivery of health and water, sanitation and hygiene interventions. A Theory of Change for cholera response programmes was built to assess factors that affected implementation of the responses.

Results and conclusions

20 epidemic response reports were identified, 15 in DRC, one in Malawi and four in Mozambique. All contexts experienced concurrent humanitarian crises, either armed conflict or natural disasters. Across the settings, median time between the date of alert and date of the start of the response by MSF was 23 days (IQR 14–41). Almost all responses targeted interventions community-wide, and all responses implemented in-patient treatment of suspected cholera cases in either established health care facilities (HCFs) or temporary cholera treatment units (CTUs). In three responses, interventions were delivered as case-area targeted interventions (CATI) and four responses targeted households of admitted suspected cholera cases. CATI or delivery of interventions to households of admitted suspected cases occurred from 2017 onwards only. Overall, 74 factors affecting implementation were identified including delayed supplies of materials, insufficient quantities of materials and limited or lack of coordination with local government or other agencies. Based on this review, the following recommendations are made to improve cholera prevention and control efforts: explore improved models for epidemic preparedness, including rapid mobilisation of supplies and deployment of trained staff; invest in and strengthen partnerships with national and local government and other agencies; and to standardise reporting templates that allow for rigorous and structured evaluations within and across countries to provide consistent and accessible data.

Introduction

Across Sub-Saharan Africa, an estimated 430 million people are at risk of cholera [1]. Annually, there are an estimated 1.3–4.0 million cases of cholera worldwide resulting in between 21,000 and 143,000 deaths [1]. Many of the largest epidemics on the continent have occurred concurrently with armed conflict and ongoing humanitarian crises [2,3,4,5]. Cholera epidemics can evolve rapidly and most often occur in settings with limited surveillance systems to detect the outbreak’s onset.

By 2030, the Global Task Force on Cholera Control (GTFCC) has set a target to reduce cholera mortality by 90% and eliminate cholera in 20 out of 47 countries by 2030 [6]. The renewed focus on cholera provides a framework for synchronising the efforts of countries, donors, implementing agencies and support coordinated multisectoral implementation of cholera control measures [7]. The strategy has three axes: (1) to focus on cholera hotspots in endemic countries with well targeted interventions; (2) to reinforce early detection and response to contain epidemics quickly; and (3) to provide an effective mechanism for coordinated technical support, financing and resources at the global and country level [8]. There are five pillars of the GTFCC including surveillance, case management, oral cholera vaccination (OCV), water, sanitation and hygiene (WASH), and community engagement. All pillars interact and play an integral role in multisector responses in short-term, emergency responses and for longer term sustainable elimination of the disease.

Progress towards this target set by the GTCC may benefit from critical review of past responses, particularly as low- and middle-income country (LMIC) governments, including Democratic Republic of Congo (DRC), Malawi and Mozambique, develop multisectoral National Cholera Plans (NCPs) to address cholera within their contexts [9]. Typically, interventions to prevent and control cholera epidemics have varied between mass, community-wide campaigns, in which multisector interventions are aligned to other WASH-related disease control efforts and aim to prevent the recurrence of outbreaks [10], to household-level or case-area targeted interventions (CATIs), in which services are delivered to a defined area surrounding a case to take advantage of the natural clustering of cases within a given radius, so as to contain or extinguish the outbreaks [11,12,13,14,15]. Whilst cholera responses will always be specific to the geographical and social context, it is important that the operational constraints for delivering timely interventions are documented and evaluated. Previous reviews have shown a dearth of evaluations of epidemic responses, depriving governmental and other response actors of an evidence base for improving practice and a baseline against which to track progress [16, 17]. In particular, delayed detection, confirmation and response can considerably dampen the impact of CATI-like approaches, with delays of > 2 weeks expected to result in spill-over beyond the initial outbreak cluster [18]; interventions that seek to contain outbreaks before they propagate widely, including case-based or localised distribution of hygiene kits [19] and vaccination [20, 21] are particularly dependent on early response, as is case management of cholera cases [22, 23].

Over the last five decades, the international non-governmental organisation (NGO), Médecins Sans Frontières (MSF) has intervened in multiple cholera epidemics in crisis-affected Sub-Saharan African settings. In this review, we present three countries (DRC; Malawi; and Mozambique) as case studies of MSF’s response to cholera epidemics during the period 2015–2018. The aim of this study was to describe the main characteristics of the cholera epidemics and related responses in these three countries, to identify challenges of different intervention strategies based on available data; and to make recommendations for epidemic prevention and control practice and policy.

Methods

Study design, inclusion and exclusion criteria

This review analysed cholera response reports by MSF. Intervention reports were eligible for inclusion if they were finalised during 2015–2018 and described or evaluated the organisation’s intervention during a cholera outbreak. Mozambique, Malawi and DRC were purposively selected due to the documented burden of cholera in each of the countries [6], frequency of cholera outbreaks [5]; and risk of humanitarian crises [3, 4, 24]. World Health Organization (WHO) definitions for a cholera alert were used in both the responses and this analysis [25]. The review is reported according to the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses extension for Scoping Reviews (PRISMA-ScR) guidelines [26] (Additional file 1). The review was not pre-registered prior to publication.

Theory of change

To guide the review, we developed a Theory of Change (ToC) diagram to identify requirements for implementing a cholera epidemic response, and pathways whereby the intended effects on cholera transmission and disease burden (Impact) may be achieved and/or influenced by common challenges (Fig. 1). ToC models can be useful to create alongside evaluations of programmes as they can provide insights into the key bottlenecks and constraints of programme implementation [27,28,29]. This ToC was developed with inputs from the study team and acts as a framework by which we can understand the barriers within the past responses. The ToC Inputs are (1) national and local emergency preparedness supplies, the supply of interventions to the intervention site and national and local surveillance systems that can detect the outbreak; these determine (2) adequate health promotion and timely provision of the interventions to the target population (Activities); which in turn lead to (3) the target population understanding the health promotion and intending to accept or utilise the interventions (Outputs); (4) intervention recipients that are motivated and have the ability to practice the target behaviour/s or access cholera control services (Outputs); and, finally to (5) a reduction in transmission of Vibrio cholerae and mortality of cholera cases (Outcomes and Impact).

Fig. 1
figure 1

Theory of Change of cholera response programmes, with challenges identified in the case studies in DRC, Mozambique and Malawi, 2015–2018

Data extraction and analysis

Documents were shared by MSF’s operational desks overseeing programmes in the three countries, and were transferred to Endnote X9 (Clarivate Analytics, Boston, USA). Reports were screened according to the inclusion criteria described and data extracted by two reviewers into an MS Excel (Microsoft, Redmond, VA, USA) sheet. Data extraction was reviewed by two co-authors (LDG and ER) and any disagreements agreed by consensus.

Qualitative operational factors that affected the response were extracted from reports and analysis was conducted in MS Excel (Microsoft, Redmond, VA, USA). Based on thematic content analysis [30, 31], common challenges were identified and coded deductively according to pathways to the ToC. These have been mapped to Fig. 1 to show the key challenges affecting an effective cholera response programme.

Data were extracted on the following, as available:

  1. 1.

    Description of the outbreak (e.g., country, geographical setting, transmission, and number of cases and deaths);

  2. 2.

    Time lag from alert (i.e., through formal or informal surveillance systems) or onset (i.e., report of a suspected cholera case meeting the WHO definition) to response (i.e., initiation of health and/or WASH interventions for prevention and control of cholera, as specified in Table 1);

  3. 3.

    Specific health and WASH interventions implemented (Table 1);

  4. 4.

    Population targeted by interventions (e.g., community-wide interventions, CATI, households of cases or only cases treated at health care facilities, HCF);

  5. 5.

    Operational factors mentioned in the report that affected the response, organised thematically based on a Theory of Change (ToC) of cholera responses (see below and Fig. 1).

Table 1 Categories and definitions of cholera prevention and control interventions included in the review

Results

Description of outbreaks and intervention sites

Twenty outbreak response reports, of the 35 provided by MSF, met the inclusion criteria. Of the 15 reports that were excluded from the analysis, eight were incomplete and did not provide enough data for extraction and seven were duplicative reports from the same outbreak but written by another person. There were 15 included reports from DRC, four from Mozambique and one from Malawi. Twelve outbreaks were in rural settings, seven in urban and one in both. All contexts experienced concurrent humanitarian crises, either armed conflict or natural disasters. In Mozambique, all outbreaks were among populations affected by armed conflict with one outbreak among a population affected by armed conflict and a natural disaster (flooding and cyclones). In Malawi, the outbreak started among displaced populations, and, in DRC, all outbreaks were in areas with ongoing medium-intensity conflict. All 20 reports reported the date of the initial outbreak alert, but no report detailed the date of onset of symptoms in the first identified cases. Alerts came through both formal surveillance systems (70%, n = 14) and informal sources (30%, n = 6), and all were additionally investigated by MSF. Formal surveillance systems included routine health surveillance systems and sentinel sites. Informal sources included community-based reporting from community health workers (CHWs) to a local HCF, typically based on report of a person with suspected symptoms of cholera. Two of the alerts were confirmed by culture (10%, n = 2), half were reported as confirmed but the authors did not specify if this was by culture (50%, n = 10) and in two instances the alerts reported the use of RDTs, but it was unclear if this was for confirmation of the alert or for general monitoring of the outbreak (10%, n = 2). Other characteristics of the outbreaks such as previous MSF operations, locations and/or distances to HCFs, or length of the outbreaks were not included in any of the reports. Characteristics of the outbreaks including cumulative cases, cumulative deaths and case fatality rate (CFR) are reported in Table 2.

Table 2 Description of outbreaks in the Democratic Republic of Congo, Malawi and Mozambique between 2015 and 2018

Time from alert to response

Across the three countries, median time from the date of the alert to date of case confirmation was 10 days (IQR 3–28). The median time between the date of alert and date of the start of the response by MSF was 23 days (IQR 14–41). Among the eight reports that also reported when WASH interventions started, there was a further median delay of 8 days (IQR 6–12) from the launch of a response to the launch of any WASH intervention. Median time from alert to response overall and by country are reported in Table 3.

Table 3 Median delays (with interquartile range (IQR) and range) between cholera alerts, confirmation, response and launch of water, sanitation and hygiene (WASH) interventions in the Democratic Republic of Congo, Malawi and Mozambique, 2015–2018

Delivery of health and WASH interventions

Almost all responses targeted interventions community-wide, and all responses implemented in-patient treatment of suspected cholera cases in either established HCFs or temporary cholera treatment units (CTUs). In three responses, interventions were delivered as CATI and four responses targeted households of admitted suspected cholera cases. CATI responses or delivery of interventions to households of admitted suspected cases occurred from 2017 onwards only (Table 4).

Table 4 Implementation of cholera responses in the Democratic Republic of Congo, Malawi and Mozambique, 2015–2018

Among the 20 responses, OCV was deployed only twice (both in DRC) and no response across the three countries included antibiotic chemoprophylaxis. WASH interventions deployed across responses varied between years and contexts, but the most widely implemented interventions were distribution of point-of-use (POU) water treatment, distribution of non-food items (NFIs) and behaviour change interventions that promoted hand washing with soap (Table 4).

Common challenges affecting cholera responses

For each outbreak, challenges that delayed the response and affected the implementation of programme activities were extracted from reports and mapped to the ToC (Fig. 1). Overall, 74 challenges were identified across reports: 33 from DRC, 29 from Mozambique and 12 from Malawi (Table 5). Among the Inputs for programme delivery, delayed supplies of materials (c) and hiring or availability of health promotion staff (g and i) were frequently cited as challenges. In addition to delays, insufficient quantities of materials were delivered for effective programme delivery (d) and an insufficient number of key staff hired, particularly staff for infection, prevention and control (IPC) in the HCFs (h). The most widely reported challenge affecting Activities was the limited or lack of coordination with local government or other agencies (a), which is likely related to the second most commonly mentioned challenge of incomplete or inaccurate epidemiological data collection during the response (b), which could have affected timeliness of response initiation, the appropriateness of the response strategy and real-time adaptation of the response. Activities were also affected by the distances between households and HCFs and the ability to reach the population during bad weather or insecurity (j, k and n). Among Outputs, adequate case management was constrained by staff inexperience with cholera case management protocols (e) and in some cases, the response was affected by stigma and fear of cholera among the population (f). Other aspects of programme delivery that were frequently reported as challenging included limited water supply available to the population (l), which may affect their ability to adopt hygiene behaviours, and the inadequate medical waste management in HCFs, which could pose a nosocomial transmission risk (m).

Table 5 Common challenges found in implementing cholera responses, by country

Discussion

Responses to cholera epidemics among populations affected by humanitarian crises can be complex, comprising multiple interacting components, and are often applied in both urban and rural contexts. The case studies included in this review relate to largescale responses by one major humanitarian agency to cholera epidemics in three countries. The package of interventions mobilised for each response varied but common challenges were identified. The findings from this review are discussed in relation to three key areas: (1) characteristics of the included cholera epidemics; (2) time from alerts to response experienced by MSF; and (3) delivery of interventions and factors affecting implementation.

Characteristics of included cholera epidemics

All epidemics reviewed here occurred in identified cholera hotpots in Sub-Saharan Africa [21], which have documented weak surveillance systems [34], low coverage of WASH services [35] and high global acute malnutrition (GAM) prevalence (2.7%, 6.1%, and 8.10% in Malawi, Mozambique and DRC, respectively [36]), which all increase risk and severity of outbreaks. Additionally, presence of armed conflict and population displacement likely exacerbated V. cholerae transmissibility and case fatality among symptomatic cases, as demonstrated by other research documenting the overlap between crises and cholera epidemics [37,38,39,40]. CFR was high in DRC compared to Mozambique and Malawi; however, any comparison may be erroneous as it does not reflect data from individual treatment centres, and varying levels of misclassification and under-ascertainment may apply to both the numerators and denominators to calculate CFRs. Additional efforts to estimate overall CFR need to be undertaken during and after outbreaks to identify the circumstances where cholera cases are dying and to develop strategies to prevent those deaths.

Time from alert to response

Overall, from 2015 to 2018, median time from epidemic alert to confirmation, by national surveillance systems, was 10 days. Between alert and response by MSF, median time was 22.5 days. In Malawi, DRC and Mozambique, up to 31, 78 and 126 days were observed from alert to response by MSF, respectively. Epidemic detection and time to response in our review of MSF data were comparatively longer compared to a recently published review by Ratnayake et al. [18], which found delays of 5 days between alert and confirmation and 10 days between alert and response, but similar to a review by Bruckner and Checchi [41] of other infectious disease outbreaks in fragile states which showed median delays of 29 days between alert and confirmation or 55 days from alert to response. In most case studies described here, epidemics were confirmed but the methods were not specified. Additionally, our data indicated that epidemiological data were often inaccurate or incomplete: reliance on under-resourced surveillance systems may have led to the data delays in the alert, delayed confirmation and delays to the resulting response [34].

Delivery of interventions and factors affecting implementation

Delivery of interventions to case-households and/or through CATI was only identified in seven case studies from MSF, all from 2017 onwards. The majority of responses implemented interventions community-wide. Although community-wide interventions are a theoretically equitable approach to intervention delivery, cholera control in outbreaks needs to focus on the dominant transmission pathways between cases and non-cases [10]. Cholera clusters in both space and time within case-households and the areas surrounding case households (~ 150–200 m radius around case households [42]) due to short incubation periods [43], bacterial shedding from both symptomatic and asymptomatic cases [44] and shared WASH risk factors and behaviours [45].

OCV has been recommended since 2010 for epidemic response and in humanitarian crises [46] since 2013, and made available for deployment from a global OCV stockpile, funded by GAVI (the Vaccine Alliance) since 2016. In a recent summary of the 83 deployments and 104 OCV campaigns globally between 2013 and 2018, there were 14 instances where Malawi deployed OCV to the population and 1–3 in DRC [47]. However, only two responses included in this review included vaccination. In both instances in DRC, OCV was provided to MSF through the national government to use leftover and expiring supplies and not as the main intervention strategy. Reports provided little to no information on what factors affected delivery of vaccination in the two instances it was available in DRC. Although OCV is available for deployment, our review highlights that there may still be barriers to humanitarian agencies such as MSF accessing or using those stockpiles and further work is required to understand these challenges. Antibiotic chemoprophylaxis was also not employed in any of the responses, despite being a potentially cost-effective option for cholera control [48].

Among the WASH interventions deployed across the 20 cholera epidemics, the most commonly implemented interventions were the distribution of POU water treatment products, NFIs and behaviour change interventions to promote handwashing with soap. There is considerable evidence to support the effectiveness of these interventions especially when delivered to case-households or areas surrounding suspected cholera cases [49,50,51], though high coverage needs to be accompanied by efforts to promote and facilitate their use [19]. Generally, the heterogeneity in interventions and the need to come up with a context appropriate response package suggests problems with structured decision-making on the most locally appropriate intervention package. Although guidance for outbreak response has been provided by many agencies [25, 32, 52,53,54,55,56,57], there is currently no standard package of WASH interventions for cholera outbreaks in humanitarian contexts and there is disagreement between guidelines on intervention strategies [10].

By the time interventions were implemented, it is likely that their potential effects were reduced as some of the reports stated themselves. Limited coordination is not new in outbreak response nor public health, but the frequency in which this challenge was cited across reports indicates that more attention to partnership with local governments and other actors is required both to enhance the ability to detect outbreaks but also to maximise efficiency [6]. Similarly, epidemic preparedness, whereby supplies are pre-positioned or ready to distribute, has been noted as a challenge previously and remains a consistent barrier to feasible and effective cholera control [10]. Supply chain challenges will diminish the effectiveness of any intervention, underscoring the importance of strengthened national and local supply chains [14, 19, 21]. Both supply of materials and human resources were challenges across these case studies and the development of operational models for scaling up both staffing capacity and the supply of materials is an area that could be explored further.

Of immediate concern across the case studies was the reported inexperience of staff with cholera case management protocols and/or lack of training they received if they had little to no experience in cholera case management. Inadequate care was potentially provided to admitted cases, and this will not only affect the CFR among the population [44] but will likely affect the population’s perception and uptake of the intervention [58, 59]. Treatment of cholera cases relies on a strong supply chain of essential medicines and both training and supervision of health care providers on site. Additionally, medical waste management in HCFs needs to be monitored due to both the occupational hazard it poses to both patients and staff and also to avert nosocomial transmission.

Limitations

This review is based on the retrospective review of programmatic data of only one humanitarian agency’s cholera responses in three Sub-Saharan African countries. Thus the generalisability of our findings may be limited as we only have limited data from one agency and three countries. The data were neither publicly available nor in a prescribed format for this analysis. The review relied on the manual compilation of reports from the MSF archives in each target country and what was available at the time of request. There is no compilation of cholera responses or cholera data internally in MSF or globally. We therefore expect to have unintentionally excluded some reports in our data harvest from the organisation. The information presented across the reports may reflect biases of the report authors, or areas of emphasis typical of MSF’s organisational culture, to an unquantifiable level. Reports are written subjectively, did not follow a set format nor allow implementers to capture challenges or compare responses against one another. For example, the dates of programme delivery and activities may not be collected systematically, nor the dates recorded accurately. As noted in the search strategy, many of the initial reports retrieved were duplicative as they were from the same outbreaks but written by different authors. This questions if the numerous reports written from one outbreak are an efficient use of human resources, and that there could potentially be other ways of writing to support capturing lessons from outbreak responses [16, 17, 60]. The lack of a systematic structure reduces the utility of the reports to capture useful accounts of responses.

There are many more reports available from DRC than either Malawi or Mozambique. This could potentially skew the results and challenges extracted from these outbreak responses. Whilst DRC has frequent outbreaks and can provide transferable lessons to the sub-Saharan African region, further retrospective reviews of outbreak responses would need to cover a broader geographical range and time frame to draw out generalisable recommendations. Interviews with individuals from operational agencies could also prove useful to further elucidate challenges.

Lastly, whilst our analysis draws out common challenges cited in the reports, it does not take into account the contextual constraints of these countries. The response may have been affected by the under-resourced national public health systems in these three countries, concurrent crises or the epidemiology of the settings, such as previous outbreaks, previous vaccination campaigns or the timing of the epidemics, which could all affect both the epidemic propagation and response efforts.

Conclusions and recommendations

Documentation and evaluation of cholera responses are limited and heterogenous. The case studies included in this review show that responses to cholera epidemics by MSF have varied in implementation strategy, selection of interventions and have incurred considerable delays from alert to response.

Based on this review, we can make a number of recommendations to improve the development of evidence-based, rapid epidemic cholera control efforts:

  • Explore improved models for epidemic preparedness, including rapid mobilisation of supplies and deployment of trained staff;

  • Focus on the competencies and processes required to rapidly take decisions on the appropriate package of interventions and modality (e.g., community-based interventions versus CATI delivery);

  • Invest in and strengthen partnerships with national and local government and other agencies as part of epidemic preparedness activities and invest in coordination mechanisms;

  • Dedicate time and staff to training and supervising health care providers to provide adequate case management to admitted cholera patients;

  • Conduct rigorous and structured evaluations of cholera response programmes to understand factors for delays, the interlink between health and WASH interventions and provide evidence-based guidance to programmes;

  • Standardise reporting templates within and across countries, and across international humanitarian agencies, to provide consistent and accessible data by internal and external staff and collate learnings.

Availability of data and materials

The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CHW:

Community Health Worker

CTC:

Cholera Treatment Centre

CTU:

Cholera Treatment Unit

DRC:

Democratic Republic of Congo

HCF:

Health Care Facility

IPC:

Infection, Prevention and Control

MSF:

Médecins Sans Frontières

MoH:

Ministry of Health

NGO:

Non-Governmental Organisation

OCV:

Oral Cholera Vaccination

ORP:

Oral Rehydration Point

PNECHOL-MD:

Programme National d’Elimination du Choléra et de lutte contre les autres Maladies Diarrhéiques

POU:

Point of use

RDT:

Rapid Diagnostic Test

WASH:

Water, sanitation and hygiene

References

  1. Ali M, Nelson AR, Lopez AL, Sack DA. Updated global burden of cholera in endemic countries. PLoS Negl Trop Dis. 2015;9(6):e0003832.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  2. WHO. Cholera 2017. Wkly Epidemiol Rec. 2018;38(93):489–500.

    Google Scholar 

  3. World Bank. Fragile and conflict-affected situations lists from FY06 to FY20. 2020. https://pubdocs.worldbank.org/en/176001594407411053/FCSList-FY06toFY20.pdf.

  4. CRED. The International Disaster Database 1990 to present. http://www.emdat.be/.

  5. WHO. Weekly epidemiological record: cholera articles. https://www.who.int/cholera/statistics/en/.

  6. Global Task Force on Cholera Control. Ending cholera: a global roadmap to 2030. 2017.

  7. Lancet T. Cholera: ending a 50-year pandemic. Lancet. 2017;390:1623.

    Article  Google Scholar 

  8. Legros D. Global cholera epidemiology: opportunities to reduce the burden of cholera by 2030. J Infect Dis. 2018;218(suppl_3):S137–40.

    Article  PubMed  PubMed Central  Google Scholar 

  9. GTFCC. Interim guiding document to support countries for the development of their national cholera plan. 2020.

  10. D’Mello-Guyett L, Gallandat K, Van den Bergh R, Taylor D, Bulit G, Legros D, et al. Prevention and control of cholera with household and community water, sanitation and hygiene (WASH) interventions: a scoping review of current international guidelines. PLoS ONE. 2020;15(1):e0226549.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Rebaudet S, Bulit G, Gaudart J, Michel E, Gazin P, Evers C, et al. The case-area targeted rapid response strategy to control cholera in Haiti: a four-year implementation study. PLoS Negl Trop Dis. 2019;13(4):e0007263.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Roskosky M, Acharya B, Shakya G, Karki K, Sekine K, Bajracharya D, et al. Feasibility of a comprehensive targeted cholera intervention in the Kathmandu Valley, Nepal. Am J Trop Med Hyg. 2019;100(5):1088–97.

    Article  PubMed  PubMed Central  Google Scholar 

  13. von Seidlein L, Deen JL. Preventing cholera outbreaks through early targeted interventions. PLoS Med. 2018;15(2):e1002510.

    Article  Google Scholar 

  14. Finger F, Bertuzzo E, Luquero FJ, Naibei N, Touré B, Allan M, et al. The potential impact of case-area targeted interventions in response to cholera outbreaks: a modeling study. PLOS Med. 2018;15(2):e1002509.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Ratnayake R, Finger F, Azman AS, Lantagne D, Funk S, Edmunds WJ, et al. Highly targeted spatiotemporal interventions against cholera epidemics, 2000–19: a scoping review. Lancet Infect Dis. 2020;21:e37–48.

    Article  PubMed  Google Scholar 

  16. Warsame A, Murray J, Gimma A, Checchi F. The practice of evaluating epidemic response in humanitarian and low-income settings: a systematic review. BMC Med. 2020;18(1):315.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Warsame A, Blanchet K, Checchi F. Towards systematic evaluation of epidemic responses during humanitarian crises: a scoping review of existing public health evaluation frameworks. BMJ Glob Health. 2020;5(1):e002109.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Ratnayake R, Finger F, Edmunds WJ, Checchi F. Early detection of cholera epidemics to support control in fragile states: estimation of delays and potential epidemic sizes. BMC Med. 2020;18(1):397.

    Article  PubMed  PubMed Central  Google Scholar 

  19. D’Mello-Guyett L, Greenland K, Bonneville S, D’Hondt R, Mashako M, Gorski A, et al. Distribution of hygiene kits during a cholera outbreak in Kasai-Oriental, Democratic Republic of Congo: a process evaluation. Confl Health. 2020;14:51.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Pezzoli L. Global oral cholera vaccine use, 2013–2018. Vaccine. 2020;38(Suppl 1):A132–40.

    Article  PubMed  Google Scholar 

  21. Lessler J, Moore SM, Luquero FJ, McKay HS, Grais R, Henkens M, et al. Mapping the burden of cholera in sub-Saharan Africa and implications for control: an analysis of data across geographical scales. Lancet. 2018;391:1908–15.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Siddique AK, Salam A, Islam MS, Akram K, Majumdar RN, Zaman K, et al. Why treatment centres failed to prevent cholera deaths among Rwandan refugees in Goma, Zaire. Lancet. 1995;345(8946):359–61.

    Article  CAS  PubMed  Google Scholar 

  23. Roberts L, Toole MJ. Cholera deaths in Goma. Lancet. 1995;346(8987):1431.

    Article  CAS  PubMed  Google Scholar 

  24. CRED. Complex Emergency Database 2003 to present. http://www.cedat.be/.

  25. MSF. Management of a cholera epidemic. Médecins Sans Frontières; 2017.

    Google Scholar 

  26. 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.

    PubMed  Google Scholar 

  27. Brand SL, Quinn C, Pearson M, Lennox C, Owens C, Kirkpatrick T, et al. Building programme theory to develop more adaptable and scalable complex interventions: realist formative process evaluation prior to full trial. Evaluation. 2018;25(2):149–70.

    Article  Google Scholar 

  28. Bonell C, Prost A, Melendez-Torres GJ, Davey C, Hargreaves JR. Will it work here? A realist approach to local decisions about implementing interventions evaluated as effective elsewhere. J Epidemiol Community Health. 2021;75(1):46.

    PubMed  Google Scholar 

  29. De Silva MJ, Breuer E, Lee LA, Asher L, Chowdhary N, Lund C, et al. Theory of change: a theory-driven approach to enhance the Medicial Research Council’s framework for complex interventions. Trials. 2014;15:267.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Flemming K, Booth A, Garside R, Tuncalp O, Noyes J. Qualitative evidence synthesis for complex interventions and guideline development: clarification of the purpose, designs and relevant methods. BMJ Glob Health. 2019;4(Suppl 1):e000882.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Booth A, Noyes J, Flemming K, Moore G, Tuncalp O, Shakibazadeh E. Formulating questions to explore complex interventions within qualitative evidence synthesis. BMJ Glob Health. 2019;4(Suppl 1):e001107.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Global Task Force on Cholera Control. Cholera outbreak response: field manual. WHO; 2019.

    Google Scholar 

  33. WHO. Cholera vaccines: WHO position paper—August 2017. Wkly Epidemiol Rec. 2017;34(92):477–500.

    Google Scholar 

  34. Ratnayake R, Tammaro M, Tiffany A, Kongelf A, Polonsky JA, McClelland A. People-centred surveillance: a narrative review of community-based surveillance among crisis-affected populations. Lancet Planet Health. 2020;4(10):e483–95.

    Article  PubMed  PubMed Central  Google Scholar 

  35. DHS. Democratic Republic of Congo. 2014.

  36. Our World in Data. Prevalence of wasting, weight for height (% of children under 5). 2017. https://ourworldindata.org/hunger-and-undernourishment#too-little-weight-for-height-wasting.

  37. Shannon K, Hast M, Azman AS, Legros D, McKay H, Lessler J. Cholera prevention and control in refugee settings: successes and continued challenges. PLoS Negl Trop Dis. 2019;13(6):e0007347.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Richterman A, Azman AS, Constant G, Ivers LC. The inverse relationship between national food security and annual cholera incidence: a 30-country analysis. BMJ Glob Health. 2019;4(5):e001755.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Talisuna AO, Okiro EA, Yahaya AA, Stephen M, Bonkoungou B, Musa EO, et al. Spatial and temporal distribution of infectious disease epidemics, disasters and other potential public health emergencies in the World Health Organisation Africa region, 2016–2018. Glob Health. 2020;16(1):9.

    Article  Google Scholar 

  40. Spiegel PB, Le P, Ververs MT, Salama P. Occurrence and overlap of natural disasters, complex emergencies and epidemics during the past decade (1995–2004). Confl Health. 2007;1:2.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Bruckner C, Checchi F. Detection of infectious disease outbreaks in twenty-two fragile states, 2000–2010: a systematic review. Confl Health. 2011;5:13.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Debes AK, Ali M, Azman AS, Yunus M, Sack DA. Cholera cases cluster in time and space in Matlab, Bangladesh: implications for targeted preventive interventions. Int J Epidemiol. 2016;45:2134–9.

    PubMed  Google Scholar 

  43. Azman AS, Rudolph KE, Cummings DA, Lessler J. The incubation period of cholera: a systematic review. J Infect. 2013;66(5):432–8.

    Article  PubMed  Google Scholar 

  44. Harris JB, LaRocque RC, Qadri F, Ryan ET, Calderwood SB. Cholera. Lancet. 2012;379(9835):2466–76.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Richterman A, Sainvilien DR, Eberly L, Ivers LC. Individual and Household Risk Factors for Symptomatic Cholera Infection: A Systematic Review and Meta-analysis. J Infect Dis. 2018;218(suppl_3):S154–64.

    Article  PubMed  PubMed Central  Google Scholar 

  46. WHO. Cholera vaccines: WHO position paper. Wkly Epidemiol Rec. 2010;13(85):117–28.

    Google Scholar 

  47. Pezzoli L, Oral Cholera Vaccine Working Group of the Global Task Force on Cholera C. Global oral cholera vaccine use, 2013–2018. Vaccine. 2019;38:A132–40.

    Article  PubMed  Google Scholar 

  48. Reveiz L, Chapman E, Ramon-Pardo P, Koehlmoos TP, Cuervo LG, Aldighieri S, et al. Chemoprophylaxis in contacts of patients with cholera: systematic review and meta-analysis. PLoS ONE. 2011;6(11):e27060.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Taylor DL, Kahawita TM, Cairncross S, Ensink JH. The impact of water, sanitation and hygiene interventions to control cholera: a systematic review. PLoS ONE. 2015;10(8):e0135676.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  50. George CM, Monira S, Sack DA, Rashid MU, Saif-Ur-Rahman KM, Mahmud T, et al. Randomized controlled trial of hospital-based hygiene and water treatment intervention (CHoBI7) to reduce cholera. Emerg Infect Dis. 2016;22(2):233–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Lantagne D, Yates T. Household water treatment and cholera control. J Infect Dis. 2018;218(suppl_3):S147–53.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Sphere. The Sphere project: humanitarian charter and minimum standards in humanitarian response. Sphere; 2018.

    Google Scholar 

  53. ICDDR’B. COTS program 2.0. ICDDR’B; 2018.

    Google Scholar 

  54. UNICEF. Cholera toolkit. United Nations Children’s Fund; 2013.

    Google Scholar 

  55. ACF. Manuel Pratique: Eau, Assainissement, Hygiène dans la Lutte Contre le Choléra. Action Contre la Faim; 2013.

    Google Scholar 

  56. Oxfam. Cholera outbreak guidelines: preparedness, prevention and control. Oxfam; 2012.

    Google Scholar 

  57. WHO. Cholera outbreak, assessing the outbreak response and improving preparedness. World Health Organisation; 2004.

    Google Scholar 

  58. Mahadik VJ, Mbomena J. Impact of health education programme on knowledge, attitude and practice (KAP) of people in cholera affected areas of Luapula Province-Zambia. Med J Zamb. 1983;17(2):32–8.

    CAS  Google Scholar 

  59. Guillaume Y, Jerome GJ, Ternier R, Ivers LC, Raymond M. “It was a ravage!”: lived experiences of epidemic cholera in rural Haiti. BMJ Glob Health. 2019;4(6):e001834.

    Article  PubMed  PubMed Central  Google Scholar 

  60. Abdelmagid N, Checchi F, Garry S, Warsame A. Defining, measuring and interpreting the appropriateness of humanitarian assistance. J Int Humanit Action. 2019;4(1):1–13.

    Article  Google Scholar 

Download references

Acknowledgements

We are grateful to the support of several colleagues who have engaged in the practical and academic aspects of this scoping review both in DRC, Mozambique, Malawi, Belgium and the UK. We also thank Ahmed Abd-Elrahman, Emmanuel Lampaert and Catherine Van Overloop from MSF Brussels; and to Katie Greenland and Ruwan Ratnayake at LSHTM. Last but by no means least, we thank the communities of DRC, Mozambique and Malawi in which these responses were conducted.

Disclaimer

The findings and conclusions in this report are those of the author(s) and do not necessarily represent the official position of the individuals involved or funding agency.

Funding

This study was funded by Médecins Sans Frontières. The ethics committee of MSF reviewed the study reviewed the study protocol but had no role in study design, data analysis or decision to publish.

Author information

Authors and Affiliations

Authors

Contributions

LDG conceived and designed the study, with input from OC, RD, RVDB, PM and FC. LDG and ER extracted the data, LDG analysed the data with input from FC and OC. LDG drafted the manuscript and all co-authors contributed revisions to the manuscript. LDG had final responsibility for the decision to submit for publication. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Lauren D’Mello-Guyett.

Ethics declarations

Ethics approval and consent to participate

No individual patient data were used in this study. All study procedures were approved by the Research Ethics Committee of the London School of Hygiene and Tropical Medicine (No. 17994) and received an ethics exemption from the International Ethics Board of Médecins Sans Frontières.

Consent for publication

Not applicable.

Competing interests

On behalf of all authors, there are no competing interests to declare that could be construed to have influenced the work. The authors alone are responsible for their views expressed in this article and they do not represent the views, decisions or policies of the institutions with which they are associated. Authors from MSF (RD, EM, MM, RVDB), UNICEF (PM) and respective Ministries of Health (PW) contributed independently in their own rights as individuals.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Preferred Reporting Items for Systematic Reviews and Meta Analyses extension for Scoping Reviews (PRISMA-ScR) checklist.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, 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 changes were made. 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

D’Mello-Guyett, L., Cumming, O., Rogers, E. et al. Identifying transferable lessons from cholera epidemic responses by Médecins Sans Frontières in Mozambique, Malawi and the Democratic Republic of Congo, 2015–2018: a scoping review. Confl Health 16, 12 (2022). https://doi.org/10.1186/s13031-022-00445-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13031-022-00445-1

Keywords