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Volume 7, Number 7—June 2001

Letter

Visceral Leishmaniasis (Kala-Azar) Outbreak in Somali Refugees and Kenyan Shepherds, Kenya

Suggested citation for this article

To the Editor: A sharp increase in suspected visceral leishmaniasis (VL or kala-azar) cases was reported in April through May 2000 in three Kenyan refugee camps (Ifo, Dagahaley, and Hagadera). Located around Dadaab town in Northeastern Province, the three camps house an estimated 125,000 Somali refugees. VL outbreaks have been well documented in five distinct foci in Kenya (1,2), but until this outbreak, VL was only sporadically seen in the refugee camps or the province.

We investigated a possible outbreak in the refugee sites. Before April 2000, doctors would request a formol-gel test (FGT) in case of suspected VL and treat an FGT-positive case with antimonials. Although the FGT is of uncertain validity, it is still used in district hospitals in Kenya for lack of alternative diagnostic tests. We considered a clinician's request of an FGT as a proxy for "clinical VL suspicion" and assessed the number of FGTs done from January 1999 to March 31, 2000. The first suspected VL patient was traced back to August 1999; this 40-year-old male Somali refugee had been ill for 8 months and sought treatment at Dagahaley camp. He responded well to antimonial treatment. From that date to April 1, 2000, an FGT was requested for five more patients; results were positive for two.

Specific surveillance for VL was set up by the refugee health services in April 2000. Suspected patients or their caretakers were interviewed. Finger-prick blood was collected on filter paper and analyzed by direct agglutination test (DAT) (3). In August 2000, splenic aspirates were performed on eight patients for direct microscopic examination, and parasite culture was attempted for three specimens. In vitro isolation and gp63 polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) molecular typing was done at the Protozoology Unit of the Prince Leopold Institute of Tropical Medicine in Antwerp, Belgium. Serologically or parasitologically confirmed cases were given stibogluconate (Pentostam), 20 mg/kg/day, for 28 days.

We reviewed surveillance data for the period April 1-August 31, 2000, and interviewed the health staff. For case classification, a probable case of VL was illness in a patient with 1) a fever of >2 weeks' duration 2) splenomegaly or wasting, and 3) positive DAT serology. A confirmed case had these clinical signs, as well as a positive parasitology smear or culture. From April 2000 and August 31, 2000, 26 probable (DAT-positive) VL cases were observed and 8 others were confirmed parasitologically. Gp63 PCR-RFLP molecular typing showed Leishmania donovani in one specimen. The case-fatality rate was 10 (29.4%) of 34 patients in the group of probable and confirmed VL cases. Six deaths occurred before treatment could be started, and one was a complication of the diagnostic procedure (spleen aspirate).

Thirty-two interviews were completed in the group of 34 probable or confirmed VL patients. Median age was 15 years, and 8 (25) of the 32 were female. Median delay between onset of symptoms and date of diagnosis was 8 months. Six were Kenyan citizens, five of them shepherds who were grazing their cattle in the area around Dadaab. Of the Somali refugees, seven had been living for >2 years in the refugee camp when their symptoms began. (Five had been born in the camps.) However, 16 (61.5%) of 26 patients arrived in the camps after the onset of their symptoms. Most of them were Ogadeni shepherds, who reportedly grazed their cattle in the Lower Juba region.

Other evidence points to a serious problem inside Somalia as well. Médecins sans Frontières reported 48 VL cases from July 28 and September 21, 2000, in Hudur, Bakol region. Other nongovernmental organizations reported cases from several towns in Gedo region. The distribution of VL in Somalia before the war is poorly documented, but the disease was known to be endemic in Giohar district, north of Mogadishu (4). In 1994, Woolhead reported VL in a woman from Baidoa and warned of potential outbreaks because of the war (5). Although several of the 34 patients reported here may have been infected in Somalia, local transmission in Kenya cannot be excluded, since some of the refugees denied having left camp and six were Kenyan citizens.

This outbreak is reason for concern in the context of the deteriorating nutritional situation in drought-affected northeastern Kenya. Malnutrition is a known risk factor for the development of clinical VL in infected persons (6). In southern Sudan, deaths caused by VL were attributed to malnutrition in a famine- and war-stricken population (7). The current nutritional status of the Somali refugees in the Dadaab camps is precarious. After the 1996 food scarcity problem (8), food rations for refugees were maintained at the recommended 2,100 kcal/person/day. In February 2000, however, the ration was again reduced below the vital minimum. A cross-sectional random cluster survey on August 29-31, 2000, showed rising malnutrition levels in <5-year-old refugee children (Médecins sans Frontières, unpub. data).

Immediate outbreak control measures have been taken by refugee camp health authorities, the surveillance system was strengthened (including initiation of active case-finding measures), and diagnostic and therapeutic facilities were upgraded. Six-month peridomestic spraying of the refugee shelters with lambda-cyhalothrin (ICON) is a routine vector control measure in the camps. Special attention needs to be paid, however, to the food security for the refugees in the light of the current outbreak. Our observations on 16 imported cases also raise concerns about VL transmission inside Somalia, where access to health care is virtually nonexistent in many areas and a VL outbreak might go undetected.

Günter Boussery*, Marleen Boelaert†, Joke Van Peteghem*, Philip Ejikon‡, and Koen Henckaerts*
Author affiliations: *Médecins sans Frontières, Brussels, Belgium; †Institute of Tropical Medicine, Antwerp, Belgium; ‡Médecins sans Frontières, Nairobi, Kenya

Acknowledgment

We thank the doctors and nurses in the Dadaab refugee health services for data collection and J.C. Dujardin for species identification.

References

  1. Schaefer KU, Kurtzhals JA, Sherwood JA, Githure JI, Kager PA, Muller AS. Epidemiology and clinical manifestations of visceral and cutaneous leishmaniasis in Baringo District, Rift Valley, Kenya. A literature review. Trop Geogr Med. 1994;46:12933.PubMed
  2. World Health Organization. Control of the leishmaniases. Report of a WHO Expert Committee. World Health Organ Tech Rep Ser. 1990;793:1158.PubMed
  3. El Harith A, Kolk AH, Kager PA, Leeuwenburg J, Muigai R, Kiugu S, A simple and economical direct agglutination test for serodiagnosis and sero-epidemiological studies of visceral leishmaniasis. Trans R Soc Trop Med Hyg. 1986;80:5837. DOIPubMed
  4. Shiddo SA, Aden Mohamed A, Akuffo HO, Mohamud KA, Herzi AA, Herzi Mohamed H, Visceral leishmaniasis in Somalia: prevalence of markers of infection and disease manifestations in a village in an endemic area. Trans R Soc Trop Med Hyg. 1995;89:3615. DOIPubMed
  5. Woolhead A. A recent case of visceral leishmaniasis in Somalia. Ann Trop Med Parasitol. 1995;89:6878.PubMed
  6. Cerf BJ, Jones TC, Badaro R, Sampaio D, Teixeira R, Johnson WD Jr. Malnutrition as a risk factor for severe visceral leishmaniasis. J Infect Dis. 1987;156:10303. DOIPubMed
  7. Seaman J, Mercer AJ, Sondorp E. The epidemic of visceral leishmaniasis in western Upper Nile, southern Sudan: course and impact from 1984 to 1994. Int J Epidemiol. 1996;25:86271. DOIPubMed
  8. Boelaert M, Englebert M, Hanquet G, Van Damme W, Van der Stuyft P. Refugee relief rations. Lancet. 1997;349:1775. DOIPubMed

Suggested Citation for this article: Boussery G, Boelaert M, Van Peteghem J, Ejikon P, Henckaerts K. Visceral Leishmaniasis (Kala-Azar) Outbreak in Somali Refugees and Kenyan Shepherds, Kenya. Emerg Infect Dis [serial on the Internet]. 2001, Jun [date cited]. http://dx.doi.org/10.3201/eid0707.017746

DOI: 10.3201/eid0707.017746

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