Skip to main content
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America logoLink to Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
. 2014 Jul 1;59(1):v–vi. doi: 10.1093/cid/ciu281

Crossing Borders: One World, Global Health

Clive M Brown, Martin S Cetron
PMCID: PMC4305156  PMID: 25551839

Abstract

The section listed above, written by members of the CDC's Division of Global Migration and Quarantine and focusing on globally mobile populations and infectious disease outbreaks, is freely available online only, in this issue of Clinical Infectious Diseases at (http://cid.oxfordjournals.org).

Rotavirus Enteritis in Dadaab Refugee Camps: Implications for Immunization Programs in Kenya and Resettlement Countries

Maurice Ope, Steve B. Ochieng, Collins Tabu, Nina Marano.

Dadaab refugee camp, established in Kenya in 1991, is host to >500 000 refugees, most of whom are Somali in origin [1]. Annually, the United States resettles approximately 11 000 refugees from Africa, 4000 of them from Kenya. Although substantial progress has been made to provide safe water and improve sanitation in Dadaab, diarrheal disease remains among the leading causes of morbidity and mortality. Several disease outbreaks, including hepatitis E virus [2], cholera [3], and wild poliovirus [4], have been attributed to poor sanitation in the camps.

Rotavirus enteritis is an acute viral infection that is transmitted by the fecal–oral route and affects nonimmune people, particularly children <5 years old [5, 6]. Rotavirus causes severe diarrhea in young children, particularly in developing countries, and contributes to high childhood mortality [5]. Rotavirus infects nearly every child by the age of 3–5 years. Severe rotavirus enteritis is, however, preventable through vaccination early in life. To date, 53 countries have implemented routine vaccination against rotavirus, including 12 in Africa (Botswana, Burkina Faso, Burundi, Ethiopia, The Gambia, Ghana, Malawi, Mali, Rwanda, South Africa, Tanzania, and Zambia) [7]. The role of rotavirus as a cause of diarrhea in refugee settings has not been well established, and such data are vital to inform policy on use of rotavirus vaccines in these settings. We therefore sought to determine the relative contribution of rotavirus to diarrheal illness among children <5 years old in a refugee camp.

Surveillance among refugee populations is an important part of controlling diseases in Kenya and in countries where active resettlement is occurring. The Kenya Medical Research Institute and the Centers for Disease Control and Prevention established a respiratory disease surveillance program in Dadaab refugee camp in 2006. Diarrheal disease surveillance was initiated in 2011 to assess infectious causes of illness. To determine the relative contribution of rotavirus to diarrheal illness among children in Dadaab refugee camps, stool samples were collected from all children <5 years old with acute diarrhea (defined as ≥3 loose stools in 24 hours) at the health facilities (1 hospital and 4 health posts) in Dadaab's Hagadera refugee camp from January to December 2011. Patients whose parents did not consent and children <1 week old were excluded. The stool samples were transported to the laboratory at 4°C–8°C within 4–6 hours of collection and were tested for rotavirus by Premier Rotaclone enzyme immunoassay.

Of 424 children tested, 98 (23.1%) were confirmed to be infected with rotavirus. Rotavirus infection was more common among hospitalized children (89.8%; 95% confidence interval [CI], 83.8%–95.8%) than among those treated as outpatients (10.2%; 95% CI, 4.2%–16.2%). Rotavirus equally affected boys (49%) and girls (51%). The median age of children infected with rotavirus was 10 months (range, 2–48 months). Rotavirus positivity was most common in the 16-week to 16-month age group (n = 67 [68%], P < .01). Even though we could not establish seasonality due to the limited duration of surveillance, we found that rotavirus was circulating throughout the year.

Although poor sanitation and hygiene are generally thought to be responsible for most diarrheal illness in refugee camps [8, 9], our surveillance showed that rotavirus is an important cause of severe endemic diarrheal disease among Somali children in Dadaab refugee camp. Our surveillance also showed that rotavirus was circulating throughout the year, unlike in temperate climates, where it is associated with winter [5]. Further studies are required to determine the genotype of the circulating rotavirus strains in Dadaab refugee camp, particularly to establish if unusual strains may be imported to resettlement countries [10].

The finding of rotavirus as a major cause of severe endemic diarrheal illness among children in Dadaab refugee camp has important implications for vaccine policymakers and healthcare providers, particularly those serving refugees in resettlement countries and in Kenya. Because vaccination in camp settings can be challenging, the feasibility and effectiveness of providing vaccine through campaigns need further evaluation.

Editorial comment (C. B.). Millennium developmental goal 4 (MDG4) calls for a two-thirds reduction in childhood mortality from the 1990 baseline by 2015. While many factors contribute to mortality in children under 5, among infectious causes respiratory and diarrheal diseases are important. Thus, strategies that reduce deaths from diarrhea in children are essential for attaining MDG4 goals.

Rotavirus vaccine is effective in reducing severe rotavirus-associated diarrhea and child mortality [11]. The World Health Organization (WHO) recommends that rotavirus vaccine be included in national immunization programs as part of a diarrheal disease control strategy [12]. Because most rotavirus infections occur early in life, timely administration of the vaccine is necessary before a large target population is naturally infected. WHO recommends rotavirus vaccine administration along with the vaccines for diphtheria, pertussis, and tetanus (DPT1, DPT2, and DPT3) at 6, 10, and 14 weeks of age [5]. Kenya plans to introduce rotavirus vaccination (Rotarix) in the routine immunization schedule in July 2014 [13].

Along with the provision of safe water and ensuring proper sanitation and hygiene, important strategies for the control of diarrheal diseases (depending on age) include breastfeeding, using oral rehydration solution, and, if diarrhea is moderate to severe, intravenous fluids, zinc supplementation, and immunization with rotavirus vaccine. Overall, rotavirus vaccine has been shown to be 30% effective against all-cause severe gastroenteritis, and 51%–93% protective against rotavirus gastroenteritis [1416]. In addition to recommending rotavirus vaccine inclusion in national immunization programs, for countries where diarrheal deaths account for ≥10% of mortality among children aged <5 years, WHO strongly recommends introduction of the vaccine. The prevalence in this refugee camp was twice that value; thus, evaluating rotavirus vaccine as a childhood vaccine in refugee camps will provide important information for its efficacy in this setting and potentially support attaining MDG4 goals.

Notes

Acknowledgments. The authors acknowledge Umesh Parashar, Jacqueline Tate, and Steve Bowen of the Centers for Disease Control and Prevention for their contributions to this manuscript.

Potential conflicts of interest. All authors: No reported conflicts.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

References

  • 1.United Nations High Commissioner for Refugees. UNHCR statistical yearbook. 2012. 53.
  • 2.Ahmed JA, Moturi E, Spiegel P, et al. Hepatitis E outbreak, Dadaab refugee camp, Kenya, 2012. Emerg Infect Dis. 2013;19:1010–2. doi: 10.3201/eid1906.130275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Mutonga D, Langat D, Mwangi D, et al. National surveillance data on the epidemiology of cholera in Kenya, 1997–2010. J Infect Dis. 2013;208(suppl 1):S55–61. doi: 10.1093/infdis/jit201. [DOI] [PubMed] [Google Scholar]
  • 4.Centers for Disease Control and Prevention. U.S.-incurred costs of wild poliovirus infections in a camp with U.S.-bound refugees—Kenya, 2006. MMWR Morbid Mortal Wkly Rep. 2008;57:232–5. [PubMed] [Google Scholar]
  • 5.World Health Organization. Rotavirus vaccines. WHO position paper—January 2013. Wkly Epidemiol Rec. 2013;88:49–64. [PubMed] [Google Scholar]
  • 6.World Health Organization. Polio vaccines and polio immunization in the pre-eradication era: WHO position paper. Wkly Epidemiol Rec. 2010;85:213–28. [PubMed] [Google Scholar]
  • 7.PATH. Country introductions of rotavirus vaccines. Maps and list. Available at: http://sites.path.org/rotavirusvaccine/rotavirus-advocacy-and-communications-toolkit/country-introduction-maps-and-list/ Accessed 6 March 2014.
  • 8.Shultz A, Omollo JO, Burke H, et al. Cholera outbreak in Kenyan refugee camp: risk factors for illness and importance of sanitation. Am J Trop Med Hyg. 2009;80:640–5. [PubMed] [Google Scholar]
  • 9.Mahamud AS, Ahmed JA, Nyoka R, et al. Epidemic cholera in Kakuma Refugee Camp, Kenya, 2009: the importance of sanitation and soap. J Infect Dev Ctries. 2012;6:234–41. doi: 10.3855/jidc.1966. [DOI] [PubMed] [Google Scholar]
  • 10.Weinberg GA, Payne DC, Teel EN, et al. First reports of human rotavirus G8P[4] gastroenteritis in the United States. J Clin Microbiol. 2012;50:1118–21. doi: 10.1128/JCM.05743-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Neuzil KM, Parashar UD, Steele AD. Rotavirus vaccines for children in developing countries: understanding the science, maximizing the impact, and sustaining the effort. Vaccine. 2012;30(suppl 1):A1–2. doi: 10.1016/j.vaccine.2011.10.108. [DOI] [PubMed] [Google Scholar]
  • 12.Kiulia NM, Nyaga MM, Seheri ML, et al. Rotavirus G and P types circulating in the eastern region of Kenya: predominance of G9 and emergence of G12 genotypes. Pediatr Infect Dis J. 2014;33(suppl 1):S85–8. doi: 10.1097/INF.0000000000000059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Ministry of Health, Kenya. Kenya Division of Vaccine and Immmunization comprehensive multi-year plan 2013–2018. Nairobi: Division of Vaccines and Immunization.
  • 14.Parashar UD, Hummelman EG, Bresee JS, et al. Global illness and deaths caused by rotavirus disease in children. Emerg Infect Dis. 2003;9:565–72. doi: 10.3201/eid0905.020562. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lopman B, Vicuña Y, Salazar F, et al. Household transmission of rotavirus in a community with rotavirus vaccination in Quininde, Ecuador. PLoS One. 2013;8:e67763. doi: 10.1371/journal.pone.0067763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Lopman B, Vicuña Y, Salazar F. Correction: household transmission of rotavirus in a community with rotavirus vaccination in Quininde, Ecuador. PLoS One. 2013;8 doi: 10.1371/journal.pone.0067763. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America are provided here courtesy of Oxford University Press

RESOURCES