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Cholera prevention and control in refugee settings: Successes and continued challenges

  • Kerry Shannon ,

    Contributed equally to this work with: Kerry Shannon, Marisa Hast

    Affiliation Johns Hopkins Medicine, Department of Emergency Medicine, Baltimore, Maryland, United States of America

  • Marisa Hast ,

    Contributed equally to this work with: Kerry Shannon, Marisa Hast

    mhast2@jhu.edu

    Affiliation Johns Hopkins Bloomberg School of Public Health, Department of Epidemiology, Baltimore, Maryland, United States of America

  • Andrew S. Azman,

    Affiliation Johns Hopkins Bloomberg School of Public Health, Department of Epidemiology, Baltimore, Maryland, United States of America

  • Dominique Legros,

    Affiliation World Health Organization, Geneva, Switzerland

  • Heather McKay,

    Affiliation Johns Hopkins Bloomberg School of Public Health, Department of Epidemiology, Baltimore, Maryland, United States of America

  • Justin Lessler

    Affiliation Johns Hopkins Bloomberg School of Public Health, Department of Epidemiology, Baltimore, Maryland, United States of America

Introduction

Cholera has long been viewed as a serious threat for refugee populations [1, 2]. In the 1980s and 90s, refugee camps proliferated in Africa and Asia as a result of large civil wars and environmental disasters. These camps experienced large-scale cholera outbreaks with regularity because of overcrowding, scarce clean water, and poor sanitation and hygiene practices [24]. Death rates were often high because of preexisting malnutrition, comorbidities, and limited access to medical care. With appropriate clinical management, cholera mortality can be well below 1%, but it can be as high as 50%–60% without proper care [3, 57]. During this time, humanitarian organizations developed a variety of guidelines and standards to reduce morbidity and mortality during cholera outbreaks in these populations [8, 9]. Mobilization around these issues was greatly accelerated in 1994, when a particularly massive outbreak occurred among Rwandan refugees in the Lake Kivu region of Zaire (now the Democratic Republic of the Congo), and approximately 42,000 people died [10]. In response to this unprecedented tragedy, the humanitarian community developed and adopted the Sphere standards for the minimum acceptable living conditions and availability of health services in refugee camps and other humanitarian responses [11].

Since this time, the Sphere standards have been updated, and additional coordinating systems have been developed, including the cluster approach to humanitarian response, the Transformative Agenda, and the adaptation of United Nations High Commissioner for Refugees’ (UNHCR) refugee coordination in the context of the Transformative Agenda [1214]. With the recent goal to reduce cholera deaths 90% by 2030 set by the Global Task Force on Cholera Control, there is a renewed urgency to examine successes and address remaining gaps in cholera control [15]. Although refugee camps continue to experience many vulnerabilities, the increased focus on improved camp coordination, preparedness, timely multisectoral response, and adherence to minimum standards has resulted in a notable decrease in the number and size of camp-based cholera outbreaks and associated mortality.

Historical trends in cholera outbreaks in refugee camps

To illustrate these changing trends, we highlight several historic outbreaks in refugee camps as described in the scientific literature. Although it is difficult to directly compare previous refugee populations to modern ones because of sparse data and differences in refugee demography, these illustrative outbreaks provide context for the high cholera morbidity and mortality in camps in these times. We conducted a targeted review of literature published prior to 1994 containing combinations of the keywords “cholera”, “acute diarrhea”, “refugee”, “camp”, and “displaced.” Searches were done on the electronic platforms Google Scholar and PubMed, and approximately 120 articles were reviewed for relevance. There were no formal exclusion criteria. We identified eight outbreaks in refugee camps that occurred between 1971 and 1991 across Africa and Asia (Table 1). Where reported, the proportion of the refugee population affected (attack rate) was 1.8% or greater (4 outbreaks), and the proportion of cases who died (case fatality ratio [CFR]) was as high as 30% (range 1%–30%, 8 outbreaks) [1624].

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Table 1. Sample of cholera outbreaks in refugee camps up to 1994 in published literature.

https://doi.org/10.1371/journal.pntd.0007347.t001

Accounts of these outbreaks consistently describe inadequate water chlorination, a shortage of sanitation facilities, and improper disposal of cholera waste. In most accounts, there were considerable barriers to a timely response, and implementation of cholera control measures was significantly delayed, sometimes for weeks after the outbreak had started. In addition, a lack of cholera-specific training and supplies in health centers was cited as a contributing factor to high CFRs. Some camps fared better than others; a 1988 review found that camps that were planned and/or had an established primary healthcare system saw a more rapid reduction in mortality as compared with unplanned border camps or camps with a consistent influx of new arrivals [25].

In 1994, the largest refugee camp–related outbreak ever reported occurred following the influx of 500,000–800,000 Rwandan refugees into the cholera-endemic North Kivu Province of the Democratic Republic of the Congo [10]. Within a month, 58,000–80,000 cases of cholera occurred in the city of Goma and surrounding refugee camps, with incidence peaking at over 6,000 cases per day. The crude mortality rate was one of the highest ever recorded, at 25–35 deaths per 10,000 people per day [10], vastly exceeding the commonly accepted emergency threshold of one death per 10,000 per day [26, 27]. Numerous factors were identified as contributing to the severity of this outbreak. Because of the rapid relocation of such a large population, sufficient facilities for water and sanitation were not established in advance of refugee arrival. There was only an average of 0.2 liters of clean water per person per day during the first week of the outbreak, and rocky ground limited the ability to dig latrines [28]. These factors in addition to the general poor health of the incoming refugees and endemicity of cholera in North Kivu created ideal conditions for the spread of cholera. Furthermore, overcrowding of medical facilities and lack of training in cholera case management contributed to CFRs that approached 50% in some clinics, and an estimated 24,000 deaths occurred among people who never received care [10, 29].

Based largely on the scale of the humanitarian emergency in this region and the magnitude of mortality seen in Goma, the international community mobilized to develop strong evidence-based standards for refugee health and assistance. In 1997, the Sphere project, a collaboration between 228 humanitarian organizations from 60 countries, developed The Humanitarian Charter, delineating the rights, roles, and duties that should govern the response to humanitarian crises and outlining the core and minimum standards needed to achieve these goals [11]. The Sphere handbook was released in 2000 and was revised in 2004, 2011, and 2018. Though there were previous efforts to set and standardize guidelines for humanitarian response going back to the 1980s [8, 9, 25, 30, 31], the Sphere project helped to set globally applicable evidence-based minimum standards for humanitarian response that were largely accepted as feasible and achievable by the international community [32]. These standards have been widely adopted and endorsed [1, 3335].

The most pertinent Sphere standards for cholera prevention and control are those for water, sanitation, and hygiene (WASH) (Table 2), and for health service delivery. Specific protocols were outlined for cholera preparedness, including pretraining health center staff, stocking sufficient oral rehydration solution and intravenous fluids in advance, improving facilities for sanitation and hygiene, and designating a separate area for cholera treatment centers that minimizes opportunities for transmission [34, 35]. These protocols strongly emphasize the need for surveillance to facilitate prompt diagnosis and rapid medical response. They now play an important role in the design and implementation of refugee camps administered by UNHCR, are incorporated in UNHCR epidemic preparedness and response guidance, and are included in the manuals of numerous other organizations in the humanitarian community, including Médecins Sans Frontières and the International Federation of Red Cross and Red Crescent Societies [36, 37].

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Table 2. Key minimum Sphere standards for water, sanitation, and hygiene.

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Since the adoption of the Sphere standards, additional changes have been made to restructure and improve humanitarian response in ways that further improve cholera outcomes in refugee camps. The Inter-Agency Standing Committee (IASC), a global humanitarian forum, adopted the “cluster approach” in 2005, which designated a global lead for nine sectors of humanitarian response including water and sanitation. The intention of these reforms was to promote partnerships between international humanitarian organizations and to strengthen the capacity of the global humanitarian response in order to increase preparedness, coordination, and accountability in emergencies [12, 38]. In 2011, the IASC implemented the Transformative Agenda, which took additional steps to improve cluster and sector management, accountability, leadership, and coordination in humanitarian response [13]. These changes have led to an organizational infrastructure better prepared and capable of managing cholera outbreaks in refugee settings. Community health programs have been developed using community health workers and hygiene promoters, and case management has improved following the designation of isolated cholera treatment centers and prepositioning of medications and supplies. In some settings, these strategies have been augmented by the use of oral cholera vaccines (OCVs).

Surveillance for cholera in refugee camps has also improved. In coordination with host government ministries of health (MOHs), UNHCR is charged with ensuring that camps are designed and managed to handle cholera outbreaks, including developing appropriate surveillance systems. To this end, suspected cholera cases in refugee camps are immediately reported to UNHCR’s internal health information surveillance system, and appropriate investigation, lab confirmation, and response activities are conducted in collaboration with local MOHs to ensure outbreaks are carefully tracked. This surveillance system, in conjunction with improvements in field and in-country lab capacity, has facilitated both early warning systems and outbreak monitoring.

Recent trends in refugee camp cholera outbreaks

This improved surveillance allows for an in-depth examination of cholera in refugee settings. To examine current trends in cholera in refugee camps, we reviewed all probable and confirmed cholera cases and deaths reported to UNHCR from 2009 to 2016. These data were provided directly from UNHCR’s health information surveillance system under an ongoing data sharing agreement. For this review, data were included from registered refugee camps, settlements, and sites. Urban settings where refugees were integrated into the community were excluded.

For each outbreak, the attack rate and CFR were calculated when possible. The population in each camp was derived from UNHCR outbreak reports if available and from the World Health Organization (WHO) and nongovernmental organizations if not reported by UNHCR (see Table in S1 Table). For cases in which camp population was reported to change over the course of the outbreak, a weighted average of the population was calculated for all available weeks of the outbreak, excluding weeks with zero cases at the beginning or end of an outbreak. If no specific weekly/monthly data were available, yearly population data for camp size were used from the UNHCR population statistics database (http://popstats.unhcr.org/en/demographics). Cases were aggregated by camp and plotted on a map using ArcGIS version 10.2 (ESRI, Redlands, CA, United States of America) and open-source Global Administrative Areas (GADM) shape files to delineate country boundaries [39].

Of the approximately 500 refugee camps and sites required to report to UNHCR, 26 reported confirmed cholera cases between 2009 and 2016. These 26 camps individually reported 38 outbreaks, totaling 8,034 confirmed and suspected cases (range: 1–2,257 cases per outbreak) and 69 deaths (range: 0–14 deaths per outbreak), with an overall CFR of 0.9% (Table 3). Across all outbreaks, CFRs did not exceed 2% in outbreaks with more than 75 cases, and the majority of outbreaks had no mortality due to cholera. For instance, Ifo camps 1, 2, and 3 in Kenya had a combined 485 cases in 2011, and Mae La camp in Thailand had 633 cases in 2010, both with no reported mortality. The median attack rate across outbreaks was 21.4 cases per 10,000 (range: 0.9–451.4 per 10,000). Thirty-three out of the 38 outbreaks occurred in Africa, and 18 were in Kenya alone, largely among subcamps in the Dadaab camp complex (Fig 1). Thailand was the only country outside of Africa that reported cholera in refugee camps. Tanzania had the most documented cases, at 3,620, 97% of which were reported from three camps in 2015 in conjunction with a massive countrywide epidemic [40]. Kenya had the second-highest number of cases (2,908), followed by Thailand (645) and the Republic of the Congo (628).

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Fig 1. Map of reporting UNHCR locations and cumulative reported cholera count, 2009–2016 (created in ArcGIS version 10.2 using GADM shape files found at gadm.org).

GADM, Global Administrative Areas; UNHCR, United Nations High Commissioner for Refugees.

https://doi.org/10.1371/journal.pntd.0007347.g001

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Table 3. Cholera outbreaks in refugee camps (2009–2016).

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Discussion

The dramatic reduction in the size of cholera outbreaks in refugee camps and associated mortality indicates the notable impact of the more systematic approaches to cholera preparedness and control adopted in recent decades. No single camp outbreak had more than 14 deaths, and the overall CFR across outbreaks was below the 1% standard for appropriate clinical management. Cholera-associated mortality in many of these camp settings was lower than outbreaks in nonhumanitarian settings from the same period, including within the same countries [4144]. The CFR in refugee camps across outbreaks was also lower than the overall cholera CFR from the African or Southeast Asian regions at this time [45]. Furthermore, attack rates were below 1% in all but two outbreaks, as compared with attack rates of 2%–10% among camp outbreaks with known population data prior to 1994. These low attack rates are also noteworthy because many of the modern refugee populations originated from or settled in cholera-endemic areas.

These results highlight both the successes and continued importance of enhanced cholera preparedness, response, and multisectoral coordination. Refugee camps remain vulnerable to cholera introductions in part because of the health risks associated with displacement, overcrowding, and inadequate initial water and sanitation conditions among incoming populations. However, as these data indicate, timely and appropriate camp planning, preparedness, coordination with local MOHs, and adherence to minimum WASH standards can greatly reduce the propensity for cholera to spread. Appropriate training and case management can furthermore greatly reduce mortality in the setting of an outbreak, in contrast to prior epidemics in which CFRs were sizable. Adherence to WASH and health standards have furthermore been directly associated with decreased overall mortality and mortality under five years old in refugee camps, particularly in the context of diarrheal disease [33, 46]. In light of the upcoming 2030 goals, these lessons are vitally important for ongoing and expanding policies for cholera preparedness and control.

Despite these overall improvements, significant challenges remain for cholera prevention and control in refugee camps. Although conditions have greatly improved in most refugee settings, there have been situations in which the severity of a crisis has impeded preparedness or timely adherence to minimum standards. In these instances, if cholera is introduced to the camp, there is increased vulnerability to a larger outbreak. For example, a large epidemic of 973 cases occurred following the 2011 famine event in eastern Africa, when more than 200,000 Somalian refugees arrived in the Dadaab camp complex in Kenya [4749]. This outbreak was characterized by large influxes of new arrivals, severe malnutrition, flooding, challenges to clean water access, and security concerns, all of which overwhelmed response efforts [50]. Another example occurred in camps in Tanzania in 2015, when a large countrywide cholera outbreak of nearly 22,000 cases overwhelmed general response efforts and caused 3,504 cases among refugees [51]. In this case, cholera likely did not originate in the refugee population but was associated with the general epidemic in the host country [52, 53]. Of note, the CFR among refugees in Tanzania was 0.5% compared with 1.6% countrywide, indicating the potentially higher degree of cholera preparedness and control within the camps compared with the country as a whole.

A similar population is camps of internally displaced persons (IDPs), who are displaced within the borders of their country of origin. Because of different regulations regarding these populations, UNHCR does not have a general or exclusive mandate over IDPs, and local governments do not always allow humanitarian organizations unrestricted access to these populations [54]. As a result, cholera preparedness and response are not always standardized in IDP camps to the same extent as in refugee camps, potentially leaving them more vulnerable to cholera introductions and outbreaks. Consequently, crude mortality rates in IDP camps have remained higher than refugee camps on average, and large and severe cholera outbreaks continue to occur [26]. Recent noteworthy examples include Yemen, which recorded over 1 million cholera cases among IDPs and other citizens from 2016 to 2018 [55, 56], and South Sudan, which reported more than 6,000 cases in 2014 [57]. The humanitarian community will need to overcome greater political and logistical challenges when serving these communities in order to meet the 2030 goals; however, the successes of cholera control in refugee camps indicate that similar efforts to implement WASH and health standards have the potential to greatly benefit IDP populations and improve cholera outcomes.

For these situations in which crises may overwhelm the capacity to provide appropriate services and the risk of cholera is thought to be high, the use of the OCV is an emerging strategy, endorsed by WHO, to supplement other cholera prevention and control efforts [58]. In 2013, WHO established a global stockpile of OCV, which was first used in an emergency setting in 2014 in two IDP camps in South Sudan [57]. As of July 2017, more than 25 million doses have been deployed from this stockpile, and availability has been increasing each year [59]. Although investment in water, sanitation, and healthcare infrastructure, supplies, and service provision will have the most impact on prevention and control of cholera and other diarrheal diseases, the vaccine is a potentially powerful tool that can be used when minimum standards are challenging to meet in a timely manner because of the severity or complexity of a humanitarian emergency.

There were several limitations to this analysis. Determining accurate population sizes, case counts, and attack rates is challenging in refugee settings, and there were several potential sources of error. Utilizing different sources of population data may introduce biases due to potential variability in data collection methods, which could lead to over- or underestimation of camp populations. Reporting to UNHCR might also have been imperfect, leading to over- or underestimation of cases, particularly in small outbreaks in which cholera may never have been identified. In larger outbreaks, cases might have been double counted because of high mobility of refugees in emergency situations, and cases might have been missed because of overcrowding, lack of presentation to healthcare facilities, or failure to report cases to UNHCR. For these reasons, reported case counts may be higher or lower than reported in other sources.

In addition, only refugees in registered camps, settlements, or sites were included in this analysis. This excludes refugees in urban settings and those integrated into local communities, which is a growing proportion of the refugee population. Furthermore, it is problematic to directly compare modern refugee populations to those in the 1970s and 80s because of drastic changes in disease reporting systems and the changing demographics of refugee populations. For instance, outbreaks represented in the literature from this time might be larger or more severe than the average. Despite these challenges, the available evidence strongly indicates the trends toward decreased cholera transmission and mortality in refugee camps as noted in this paper.

Conclusions

Cholera continues to be a significant problem in humanitarian settings, with recent outbreaks in displaced populations in South Sudan, Yemen, Cameroon, Nigeria, Tanzania, Uganda, Haiti, and Iraq. The success of cholera prevention and control in refugee camps over the past 2 decades highlights the possibility of managing this deadly disease, even in complicated humanitarian crises. Sphere standards and associated control strategies have been shown to be effective in humanitarian crisis settings, dramatically reducing the number and size of outbreaks seen in refugee camps after the North Kivu disaster. Although other vulnerable populations, particularly IDPs, continue to suffer from a substantial cholera burden, application of these strategies in combination with supplementary tools such as OCV have the potential to substantially reduce cholera cases and deaths in line with the 2030 goal of reducing cholera deaths by 90% worldwide.

Supporting information

S1 Table. Sources of refugee camp population data used to calculate attack rates.

https://doi.org/10.1371/journal.pntd.0007347.s001

(DOCX)

Acknowledgments

We would like to acknowledge Allen Gidraf Kahindo Maina, Heiko Hering, Vincent Kahi, Asis K. Das, and Eugene Paik of UNHCR for their cooperation and contributions to this project, including facilitating data sharing agreements, providing and updating health information system data, and reviewing manuscripts for accuracy. We thank Carla Zelaya and Sean Moore for their contributions to the conceptualization of this project, and we thank Carole Deglise of Médecins Sans Frontières, Switzerland, for support regarding cholera in Tanzania.

References

  1. 1. Toole MJ, Waldman RJ. The public health aspects of complex emergencies and refugee situations. Annu Rev Public Health. 1997;18:283–312. Epub 1997/01/01. pmid:9143721.
  2. 2. Connolly MA, Gayer M, Ryan MJ, Salama P, Spiegel P, Heymann DL. Communicable diseases in complex emergencies: impact and challenges. Lancet. 2004;364(9449):1974–83. PubMed PMID: ISI:000225327000036. pmid:15567014
  3. 3. World Health Organization. Cholera Fact Sheet. Geneva: WHO Media Centre; 2015.
  4. 4. Tauxe RV, Mintz ED, Quick RE. Epidemic cholera in the new world: translating field epidemiology into new prevention strategies. Emerg Infect Dis. 1995;1(4):141–6. Epub 1995/10/01. pmid:8903186; PubMed Central PMCID: PMC2626892.
  5. 5. Sack DA, Sack RB, Nair GB, Siddique AK. Cholera. Lancet. 2004;363(9404):223–33. PubMed PMID: ISI:000188243900023. pmid:14738797
  6. 6. World Health Organization. Cholera: global surveillance summary, 2008. Wkly Epidemiol Rec. 2009;84(31):309–24. Epub 2009/08/04. pmid:19645127.
  7. 7. Phelps M, Perner ML, Pitzer VE, Andreasen V, Jensen PKM, Simonsen L. Cholera Epidemics of the Past Offer New Insights Into an Old Enemy. J Infect Dis. 2018;217(4):641–9. Epub 2017/11/23. pmid:29165706; PubMed Central PMCID: PMC5853221.
  8. 8. World Health Organization. Guidelines for Cholera Control. Geneva: World Health Organization; 1993.
  9. 9. Office of the United Nations High Commissioner for Refugees (UNHCR). Handbook for Emergencies: Field Operations. Geneva: United Nations High Commissioner for Refugees; 1982.
  10. 10. Goma Epidemiology Group. Public health impact of Rwandan refugee crisis: what happened in Goma, Zaire, in July, 1994? Goma Epidemiology Group. Lancet. 1995;345(8946):339–44. Epub 1995/02/11. pmid:7646638.
  11. 11. The Sphere Project. Humanitarian Charter and Minimum Standards in Disaster Response,.1st ed. Geneva: Oxfam Publishing; 2000.
  12. 12. Inter-Agency Standing Committee (IASC). Guidance note on using the cluster approach to strengthen humanitarian response. Inter-Agency Standing Committee; 2006 Nov 24 [cited 2017 Oct 18]. Available from: https://interagencystandingcommittee.org/system/files/legacy_files/guidance_note_on_using_the_cluster_approach_to_strengthen_humanitarian_response.pdf.
  13. 13. Inter-Agency Standing Committee (IASC) [Internet]. [cited 2017 Nov 5]. IASC Transformative Agenda. Available from: https://interagencystandingcommittee.org/iasc-transformative-agenda.
  14. 14. United Nations High Commissioner for Refugees (UNHCR) [Internet]. UNHCR Refugee Coordination Model: Adaptation of UNHCR's refugee coordination in the context of the Transformative Agenda. Geneva: United Nations High Commissioner for Regufees; 2017 [cited 2018 Jul 9]. Available from: http://www.unhcr.org/excom/icm/53679e2c9/unhcr-refugee-coordination-model.html.
  15. 15. Global Task Force on Cholera Control. Ending Cholera—A Global Roadmap to 2030. Geneva: World Health Organizaton; 2017.
  16. 16. Mulholland K. Cholera in Sudan: An account of an epidemic in a refugee camp in eastern Sudan, May-June 1985. Disasters. 1985;9(4):247–58. Epub 1985/12/01. pmid:20958607.
  17. 17. Centers for Disease Control. Famine-affected, refugee, and displaced populations: recommendations for public health issues. MMWR Recomm Rep. 1992;41(RR-13):1–76. Epub 1992/07/24. pmid:1326713.
  18. 18. Moren A, Stefanaggi S, Antona D, Bitar D, Etchegorry MG, Tchatchioka M, et al. Practical field epidemiology to investigate a cholera outbreak in a Mozambican refugee camp in Malawi, 1988. J Trop Med Hyg. 1991;94(1):1–7. Epub 1991/02/01. pmid:1995929.
  19. 19. Swerdlow DL, Malenga G, Begkoyian G, Nyangulu D, Toole M, Waldman RJ, et al. Epidemic cholera among refugees in Malawi, Africa: treatment and transmission. Epidemiol Infect. 1997;118(3):207–14. Epub 1997/06/01. pmid:9207730.
  20. 20. Moren A, Bitar D, Navarre I, Etchegorry MG, Brodel A, Lungu G, et al. Epidemiologic Surveillance among Mozambican Refugees in Malawi, 1987–89. Disasters. 1991;15(4):363–72. PubMed PMID: ISI:A1991GU36000006.
  21. 21. Centers for Disease Control. Public Health Consequences of Acute Displacement of Iraqi Citizens—March-May 1991. MMWR Morb Mortal Wkly Rep. 1991;40(26):443–6. pmid:2051974
  22. 22. Mahalanabis D, Choudhuri A, Bagchi N, Bhattacharya A, Simpson T. Oral Fluid Therapy of Cholera among Bangladesh Refugees. The Johns Hopkins Medical Journal. 1973;132(4):197–205. pmid:4698667
  23. 23. Holck S, Preblud S, John B. Cholera in two Kampuchean refugee camps. In: Allegra D, Nieburg P, Grabe M, editors. Emergency Refugee Health-Care—A Chronicle of Experience in the Khmer Assistance Operation 1979–1980. Atlanta, GA: Centers for Disease Control; 1983.
  24. 24. Sorensen E, Dissler K. Practical experience with the management of a cholera outbreak in a refugee camp in eastern Sudan, 1985. Disasters. 1988;12(3):274–81. Epub 1988/09/01. pmid:20958662.
  25. 25. Toole MJ, Waldman RJ. An analysis of mortality trends among refugee populations in Somalia, Sudan, and Thailand. Bull World Health Organ. 1988;66(2):237–47. Epub 1988/01/01. pmid:3260831; PubMed Central PMCID: PMC2491046.
  26. 26. Salama P, Spiegel P, Talley L, Waldman R. Lessons learned from complex emergencies over past decade. Lancet. 2004;364(9447):1801–13. Epub 2004/11/16. doi: S0140673604174059[pii] pmid:15541455.
  27. 27. Toole MJ, Waldman RJ. Prevention of excess mortality in refugee and displaced populations in developing countries. JAMA. 1990;263(24):3296–302. Epub 1990/06/27. pmid:2348541.
  28. 28. Bioforce. Cholera in Goma, July 1994. Rev Epidemiol Sante Publique. 1996;44(4):358–63. Epub 1996/08/01. pmid:8927778.
  29. 29. 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. Epub 1995/02/11. doi: S0140-6736(95)90344-5 [pii]. pmid:7646639.
  30. 30. Shears P, Berry AM, Murphy R, Nabil MA. Epidemiological assessment of the health and nutrition of Ethiopian refugees in emergency camps in Sudan, 1985. Br Med J (Clin Res Ed). 1987;295(6593):314–8. Epub 1987/08/01. pmid:3115429.
  31. 31. United Nations High Commissioner for Refugees (UNHCR). Refugee Health (EC/1995/SC.2/CRP.29). Presented to the 35th meeting of the Sub-Committee on Administrative and Financial Matters of the Executive Committee of the United Nations High Commissioner for Refugees. Geneva: UNHCR; 1995 Sep 11.
  32. 32. Gostelow L. The Sphere Project: the implications of making humanitarian principles and codes work. Disasters. 1999;23(4):316–25. Epub 2000/01/22. pmid:10643108.
  33. 33. Spiegel P, Sheik M, Gotway-Crawford C, Salama P. Health programmes and policies associated with decreased mortality in displaced people in postemergency phase camps: a retrospective study. Lancet. 2002;360(9349):1927–34. Epub 2002/12/21. doi: S0140-6736(02)11915-5 [pii] pmid:12493259.
  34. 34. Medecins Sans Frontieres. Refugee Health: An Approach to Emergency Situations. London, United Kingdom: Macmillan; 1997.
  35. 35. Johns Hopkins Bloomberg School of Public Health, International Federation of Red Cross and Red Crescent Societies. The Johns Hopkins and Red Cross Red Crescent: Public health guide in emergencies. 2nd ed. Geneva: International Federation of Red Cross and Red Crescent Societies; 2008.
  36. 36. United Nations High Commissioner for Refugees (UNHCR). Epidemic Preparedness and Response in Refugee Camp Settings: Guidance for Public Health Officers. Geneva: UNHCR; 2011.
  37. 37. United Nations High Commissioner for Refugees (UNHCR). UNHCR Handbook for Emergencies. 4th ed. Geneva: UNHCR; 2015 [cited 2018 Aug 5]. Available from: https://emergency.unhcr.org/.
  38. 38. Featherstone A. Building a Better Response: Gaps & Good Practice in Training for Humanitarian Reform. Geneva: OCHA & USAID/OFDA; 2012.
  39. 39. Global ADMinistrative Areas (GADM) [Internet]. Global Administrative Areas. c2018 [cited 2018 Jun 8]. Available from: http://gadm.org/country.
  40. 40. Wang A, Hardy C, Rajasingham A, Martinsen A, Templin L, Kamwaga S, et al. Notes from the Field: Chlorination Strategies for Drinking Water During a Cholera Epidemic—Tanzania, 2016. MMWR Morb Mortal Wkly Rep. 2016;65(41):1150–1. Epub 2016/10/21. pmid:27764079.
  41. 41. Loharikar A, Briere E, Ope M, Langat D, Njeru I, Gathigi L, et al. A National Cholera Epidemic With High Case Fatality Rates-Kenya 2009. J Infect Dis. 2013;208:S69–S77. PubMed PMID: ISI:000325766800011. pmid:24101648
  42. 42. Cartwright EJ, Patel MK, Mbopi-Keou FX, Ayers T, Haenke B, Wagenaar BH, et al. Recurrent epidemic cholera with high mortality in Cameroon: persistent challenges 40 years into the seventh pandemic. Epidemiology and Infection. 2013;141(10):2083–93. PubMed PMID: ISI:000323887200010. pmid:23290586
  43. 43. Shikanga OT, Mutonga D, Abade M, Amwayi S, Ope M, Limo H, et al. High Mortality in a Cholera Outbreak in Western Kenya after Post-Election Violence in 2008. American Journal of Tropical Medicine and Hygiene. 2009;81(6):1085–90. PubMed PMID: ISI:000272709600025. pmid:19996441
  44. 44. Ahmed S, Bardhan PK, Iqbal A, Mazumder RN, Khan AI, Islam MS, et al. The 2008 Cholera Epidemic in Zimbabwe: Experience of the icddr,b Team in the Field. J Health Popul Nutr. 2011;29(5):541–6. PubMed PMID: ISI:000296910300015. pmid:22106761
  45. 45. Ali M, Nelson AR, Lopez AL, Sack DA. Updated global burden of cholera in endemic countries. PLoS Negl Trop Dis. 2015;9(6):e0003832. Epub 2015/06/05. pmid:26043000; PubMed Central PMCID: PMC4455997.
  46. 46. Shultz A, Omollo JO, Burke H, Qassim M, Ochieng JB, Weinberg M, et al. Cholera outbreak in Kenyan refugee camp: risk factors for illness and importance of sanitation. Am J Trop Med Hyg. 2009;80(4):640–5. Epub 2009/04/07. doi: 80/4/640 [pii]. pmid:19346392.
  47. 47. United Nations High Commissioner for Regufees (UNHCR). Health and Nutrition Sector Update, Dadaab Refugee Camps, 17th to 23rd of September 2011, Epidemiologic Week 38, Update No. 10. UNHCR: Geneva; 2011.
  48. 48. United Nations High Commissioner for Regufees (UNHCR) [Internet]. UNHCR; Geneva; 2012 Feb 21 [cited 2017 Aug 8]. Dadaab—World's biggest refugee camp 20 years old. Available from: http://www.unhcr.org/4f439dbb9.html.
  49. 49. Medecins Sans Frontieres. Dadaab: The Biggest Refugee Camp in the World is Full. 16 June 2011 [cited 2017 Aug 8]. Available from: https://www.msf.org/overview-biggest-refugee-camp-world-full.
  50. 50. United Nations High Commissioner for Regufees (UNHCR). UNHCR; Geneva; 2011 Nov 15 [cited 2017 Aug 8]. Rainfall, disease, hitting refugee camps in Kenya, Ethiopia. Available from: http://www.unhcr.org/4ec2652b9.html.
  51. 51. Narra R, Maeda JM, Temba H, Mghamba J, Nyanga A, Greiner AL, et al. Notes from the Field: Ongoing Cholera Epidemic—Tanzania, 2015–2016. MMWR Morb Mortal Wkly Rep. 2017;66(6):177–8. Epub 2017/02/17. pmid:28207686; PubMed Central PMCID: PMC5657858.
  52. 52. United Republic of Tanzania, United Nations of Tanzania Office of the Resident Coordinator. Cholera Outbreak 2015 Situation Report No. 2. United Republic of Tanzania: United Nations Resident Coordinators Office; 2015.
  53. 53. United Republic of Tanzania Emergency Operations Center. Cholera Outbreak Situation Update #229. Dodoma, Tanzania: Ministry of Health, Community Development, Gender, Elderly, and Children; 2016.
  54. 54. Griekspoor A, Collins S. Raising standards in emergency relief: how useful are Sphere minimum standards for humanitarian assistance? BMJ. 2001;323(7315):740–2. Epub 2001/09/29. pmid:11576984; PubMed Central PMCID: PMC1121289.
  55. 55. Al-Mekhlafi HM. Yemen in a Time of Cholera: Current Situation and Challenges. Am J Trop Med Hyg. 2018. Epub 2018/03/21. pmid:29557331
  56. 56. Camacho A, Bouhenia M, Alyusfi R, Alkohlani A, Naji MAM, de Radigues X, et al. Cholera epidemic in Yemen, 2016–18: an analysis of surveillance data. Lancet Glob Health. 2018;6(6):e680–e90. Epub 2018/05/08. pmid:29731398; PubMed Central PMCID: PMC5952990.
  57. 57. Abubakar A, Azman AS, Rumunu J, Ciglenecki I, Helderman T, West H, et al. The First Use of the Global Oral Cholera Vaccine Emergency Stockpile: Lessons from South Sudan. PLoS Med. 2015;12(11):e1001901. Epub 2015/11/18. PMEDICINE-D-15-01915 [pii]. pmid:26576044; PubMed Central PMCID: PMC4648513.
  58. 58. Cholera vaccines: WHO position paper—August 2017. Wkly Epidemiol Rec. 2017;92(34):477–98. Epub 2017/08/29. pmid:28845659.
  59. 59. Deployments from the oral cholera vaccine stockpile, 2013–2017. Wkly Epidemiol Rec. 2017;92(32):437–42. Epub 2017/08/12. pmid:28799734.