Somalia, ravaged by conflict since 1991, has areas endemic for visceral leishmaniasis (VL), a deadly parasitic disease affecting the rural poor, internally displaced, and pastoralists. Very little is known about VL burden in Somalia, where the protracted crisis hampers access to health care. We reviewed evidence about VL epidemiology in Somalia and appraised control options within the context of this fragile state’s health system. VL has been reported in Somalia since 1934 and has persisted ever since in foci in the southern parts of the country. The only feasible VL control option is early diagnosis and treatment, currently mostly provided by nonstate actors. The availability of VL care in Somalia is limited and insufficient at best, both in coverage and quality. Precarious security remains a major obstacle to reach VL patients in the endemic areas, and the true VL burden and its impact remain unknown. Locally adjusted, innovative approaches in VL care provision should be explored, without undermining ongoing health system development in Somalia. Ensuring VL care is accessible is a moral imperative, and the limitations of the current VL diagnostic and treatment tools in Somalia and other endemic settings affected by conflict should be overcome.
Citation: Sunyoto T, Potet J, Boelaert M (2017) Visceral leishmaniasis in Somalia: A review of epidemiology and access to care. PLoS Negl Trop Dis 11(3): e0005231. doi:10.1371/journal.pntd.0005231
Editor: Abhay R. Satoskar, Ohio State University, UNITED STATES
Published: March 9, 2017
Copyright: © 2017 Sunyoto et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The project leading to this research has received funding from the European Union’s Horizon2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement ° 642609. TS is the author receiving the grant under the Euroleish project (see www.euroleish.net). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The global burden of visceral leishmaniasis (VL) is estimated at 0.2 to 0.4 million cases, resulting in 50,000 deaths every year . Eastern Africa is the second-highest-burdened region, after the Indian subcontinent . VL suppresses the immune response, and epidemics in populations affected by malnutrition or displacement can be severe [3,4]. This deadly parasitic disease has been mainly reported in parts of southern Somalia [5,6], though data from Somalia are scarce and the true magnitude of the VL burden remains unknown.
Somalia was conflict-ridden even before the state implosion in 1991, and its health indicators are among the worst in the world [7,8]. With a high burden of infectious disease [9,10] and weak surveillance systems, outbreaks are commonplace . The United Nations–backed government is still struggling to exert control beyond the capital (Mogadishu) and urban towns, while most of the VL-endemic areas in southern Somalia are controlled by al Shabaab, an al Qaeda-affiliated Islamist movement hostile to international agencies . Health care in these areas is mostly provided by multiple nonstate actors that face great difficulty in accessing those in need [13,14].
Prompt diagnosis plus adequate VL treatment is lifesaving, and in anthroponotic foci, it is the cornerstone of VL control. However, providing VL care is difficult to enact in a fragmented health system . With the establishment of a federal government in 2013, the health system-strengthening agenda has been gaining momentum [16,17], and many unmet needs have been identified [18–20]. In this paper, we review the evidence on the current burden of VL and availability of care in Somalia, from which we derive recommendations for VL control. Our aim is to draw attention to the neglected tropical diseases (NTDs) agenda in fragile state such as Somalia, and hopefully, our recommendations prove useful in similar settings affected by protracted conflict.
We searched the MEDLINE (via Pubmed) online database for articles with leishmaniasis and Somalia in the title with no date limit and published up to 31 March 2016 without language restriction. Additional search terms used in Medical Subject Headings (MeSH) were “leishmaniasis, visceral”; “kala-azar”; and “Somalia”. We searched reference lists from these articles by hand to identify other relevant publications. In addition, we searched documents and reports from agencies, institutions, and organizations with projects in or related to Somalia and contacted the authors of this grey literature for additional information. An experience from a VL control project managed by Médecins Sans Frontières (MSF), a private international humanitarian medical non-governmental organization (NGO), was described.
Ethics Statement: All sources/key informants give consent for the article. The study is exempted from ethical review by MSF Institutional Review Board (IRB).
The literature search yielded 12 papers, all of which were retrieved in full-text and included in the analysis (see Table 1).
VL epidemiology in Somalia
The parasite species causing VL in the east-African region belongs to the Leishmania donovani complex, and the same species was confirmed in Somalia in 2000–2001 . The presence of sand fly vectors in this region is generally associated with cracks in black cotton clay soil, Acacia and Balanites woodland, and termite mounds . Semi-arid regions, where the sand fly Phlebotomus orientalis is the vector , contrast with the savannah and forested areas, where P. martini and P. celiae have been incriminated . Exposure to bites mainly happens outdoors—male persons are more at risk because of their cultural roles of herding cattle or forest traversing [25,26]. Women and children are usually infected in and around the house, leading to clusters around VL cases and household contacts [27,28].
In the Bakool region of southwestern Somalia, an entomological assessment identified mainly P. martini and P. vansomerenae as potential vectors. These sand flies have their optimal breeding and resting in the ventilation shafts of termite mounds, which are ubiquitous in Somalia[24,29]. Being in the vicinity of termite hills (the eroded or pinnacle type) are thought to lead to exposure . The vector microhabitat in these Macrotermes termite mounds is also influenced by various factors, such as moisture, humidity, temperature, and rainfall, all of which are highly variable in different parts of Somalia.
The ecological situation in the endemic foci of VL in the south has yet to be described in depth, as these areas differ from the higher-altitude northern zones. Somalia has a generally arid and semi-arid climate with two seasonal rainfalls. Its southern part is a rugged plateau, crossed by two major rivers, the Jubba and Shabelle (from Ethiopia highlands), with fertile inter-riverine areas. Seasonality of VL vectors (abundance after rainy season) are well established elsewhere , but in Somalia, no information exists to date.
There have been no studies on local determinants, risk factors for VL, transmission dynamics, or vector control in Somalia, but the transmission cycle is supposedly human to human, similar to that in Uganda, Sudan, South Sudan, and Kenya [28,32,33]. Though several animals have been suggested as reservoir hosts (dogs, wild mammals such as the Nile rat, mice, gerbils, servals), their role in transmission in the region is unclear [34,35]. Climatic change has led to frequent floods and droughts in the eastern Africa region, which is thought to influence the transmission or epidemic cycle of vector-borne diseases, including that of VL [36,37]. In Somalia, changes in land use, such as agriculture and deforestation, may lead to desertification and provide habitats for VL vectors.
Contrasting with Sudan, where VL was already described in 1904 , in Somalia, it was first reported by Penso in 1934 , then followed by a case series in 1955 . In the 1960s, Cahill [41,42] and Baruffa  mapped the origin of patients. The coastal areas in Lower Juba and Middle Shabelle River were considered endemic [44,45], with the most recent case report coming from Baidoa region  (see Fig 1). Few epidemiological surveys were carried out, such as the one in Giohar district, Middle Shabelle showing 26% positivity with the leishmanin skin test (LST)—an intradermal test of the delayed-type hypersensitivity response—and 11% with serology . There are no recent population-based estimates of VL incidence or prevalence in Somalia. An LST survey conducted in 2001 among displaced people in camps around Xuddur, Bakool region revealed a 15% positivity rate, indicating previous exposure to Leishmania infection . Different methods, such as immunofluorescence, ELISA, and direct agglutination test (DAT) , were used to measure circulating antibodies to provide baseline data and to explore which methods would be the most suitable for diagnosis or for epidemiological population studies in Somalia [48,49].
Adapted from Worldsofmaps.net (under Creative Commons license).
To date, there have been no reports of VL from the northern parts of Somalia (Somaliland and Puntland zones). There is also no information available in the literature about it, as highlighted in this review. It is clear that the knowledge on VL foci in Somalia is constrained by the country’s emergency situation, which does not allow large epidemiological studies and exhaustive disease mapping to take place. The predictions made by spatial risk maps  are consistent, with a significant VL presence in southern Somalia and much less of a presence along the coastal areas of northern Somalia.
VL affects the most marginalised: the rural poor and those lacking access to health services, such as the pastoralists and agropastoralists, who comprise approximately 60% of the population in the south-central zones of Somalia . The socioeconomic impact of VL in a country where almost half the population lives in extreme poverty  is not known. In 2000, the confirmation of a VL outbreak among Somalian refugees living in camps in north-eastern Kenya triggered concern about the VL situation inside Somalia [21,53]. From May 2000 to August 2001, 904 VL cases were diagnosed in Kenya, originating from southern Somalia, north-eastern Kenya, and south-eastern Ethiopia. Unusual rainfall patterns, malnutrition, and migration of a population seeking food and security were likely major factors in the outbreak . In this context, an endemic focus was recognized as it was unfolding in parallel in the Bakool region in Somalia, where it was discovered that the “fever and big belly” syndrome that corresponded with the main symptoms of VL had been long known locally . The disease mainly affected children, which had also been observed in Mogadishu hospitals in the early 1990s .
MSF VL control project in Xuddur, Bakool region, 2002–2009
The MSF project in Xuddur started in 2000 as a nutrition program and gradually expanded to a 290-bed health centre by 2008. The VL component commenced when an unusual number of malnourished children did not improve despite proper nutritional support. At first, tuberculosis was suspected as the underlying problem, but VL was later confirmed, as described by Marlet et al. [21,22]. In an 11-month period, 59% of patients presenting a history of fever of at least 1 month, splenomegaly, and wasting tested positive on the DAT and were treated for VL.
A total of 1,671 patients were treated from 2002 to 2006, with a steep increase of cases in late 2005, which later peaked in 2006 with 1,002 new cases and then decreased to 715 and 833 cases in 2007 and 2008, respectively. These numbers do not necessarily reflect the real incidence trend at the population level. The treatment used was injections of sodium stibogluconate (SSG) dosed at 20 mg/kg/day for 30 days. Program data shows an overall case fatality rate (CFR) of 4.5%, while 88% were cured during the period between 2002 and 2008. The defaulter rate improved after the rk39 rapid diagnostic test (RDT) was introduced in 2004, as fewer patients had to wait for DAT tests that had to be performed abroad. Health education on adherence was emphasized, and meals for the caretakers were provided. Better awareness among the population about treatment availability was thought to lead to a shorter duration of sickness before seeking treatment.
The programme was negatively affected by the reigning insecurity, which led to repeated evacuations and forced MSF to deploy a remote management approach, in which no presence of international staff could be maintained on the ground anymore. Evaluating the risk after a serious security incident, MSF decided to close the project in Xuddur in 2009 while remaining in other areas of Somalia until the organization pulled out of the country by August 2014 .
Current availability of VL care in Somalia
VL-endemic areas are located in parts of southern Somalia continually mired in conflict. Since al Shabaab rose to prominence in 2008, access to care has been extremely problematic in these areas. At present, there are three facilities able to diagnose and treat VL: two in the Bakool region (Xuddur and Tijeglow) and one in the Bay region (Baidoa). The coverage of these three health centres is not known, as baseline prevalence and population data are missing. The officially reported number of VL cases from the country remains consistent at 400 to 1,000 per year [55,56]. In 2014, an incidence rate of 4.35 per 10,000 inhabitants was estimated by WHO, with an estimated 2–4 underreporting ratio .
Adherence to the prolonged VL SSG treatment regimen is a challenge. In the clinic in Baidoa, care is provided on an outpatient basis, and patients who travel from far away have to stay with relatives in town. There is no further referral level for complicated cases beyond the Baidoa clinic. Structured referral is nonexistent. As the VL clinic also provides general health services, its doctors and nurses face a huge workload. It is not uncommon that suspected VL patients travel by their own means to hospitals in Mogadishu to seek care, only to find that no diagnosis tests or drugs for VL are available (M. Dakane, personal communication). In such a context, people tend to use the informal sector, largely composed of privately organized initiatives—pharmacy retailers, traditional healers, and Islamic charities[58,59]. One example is the many children with splenomegaly—one of VL’s main symptoms—who demonstrate burn marks on their stomachs, indicating traditional care-seeking pathways followed before reaching the hospital (G. Elders, personal communication).
Despite the issuance of a 2012 National Guideline for VL in Somalia with support from WHO and various NGOs , there is no national control programme in place yet. The precarious security situation remains the stumbling block for active case finding or outreach activity; thus, VL care is in practice restricted to patients who are able to reach treatment centres. Wider community sensitisation on VL prevention and treatment is practically nonexistent. The unstable context also affects procurement and supply of VL diagnostic kits and drugs and the possibility of implementation of vector control measures. Since 2011, WHO has supported the implementing partners with procurement alongside on-the-job training in neighbouring countries (J. A. Ruiz-Postigo, WHO, personal communication).
What is known about VL in Somalia is very limited, as evidenced from our review of the medical literature. Recent global attention to NTDs  has not benefited Somalia, where the overall context appears to be a deterrent for action. With the shift from an emergency service delivery approach towards health system building, life-threatening condition like VL are at risk of being further neglected due to emerging, competing priorities in the health sector [62,63].
Understanding the health system context
The health system in Somalia is a diverse, heterogeneous landscape, mirroring its context [12,64,65]. Apart from al Shabaab’s outright ban on Western agencies [66,67], other factors, such as donors’ counterterrorism legislation and difficulties in negotiating access, have led to cessation or limitation of activity by many NGOs [15,68]. The political economy of aid, subject to politicisation or clan rivalry [69,70], should be well understood in any planning of a health care programme. Thriving private sectors, a weak regulatory environment, urban–rural discrepancies, and the limited reach of state health authorities are features that need to be taken into account.
The Somali social fabric, abiding to customary and Islamic law , whereby clans and extended family influence the decision to seek care for illnesses such as VL , is important to understand. The cost of health care is almost always borne by households through out-of-pocket expenditure . Although a kinship transfer system—from remittances of Somali diaspora or clan mobilisation—perhaps provides a partial safety net , the most vulnerable groups, such as less powerful subclans or nomadic peoples, may not benefit. Additionally, there is urban bias in care provision , with the remote, rural areas where VL is endemic being underserved.
VL is unamenable to mass preventive chemotherapy or vaccination; case detection and management is, therefore, crucial. Service delivery through the health system would be the generic mantra in most contexts, but for Somalia, we advocate for exploring nonconservative approaches to mitigate the impact of VL. Local, small-scale, indigenous solutions (rather than nationwide goals) may work better in Somalia, with more focus on local (region or district level) priorities and action.
VL care provision cannot wait until peace returns; with the current climate-related famine threat in the Horn of Africa, alertness and preparedness for another VL outbreak is important for the whole region [50,73]. A mobile team strategy has been implemented successfully in South Sudan (M. den Boer, personal communication)—recruited from local tribes, their tasks include training, health education, bringing drugs and diagnostics, and going to places where there are outbreak rumours to provide immediate assistance. Innovative thinking in improving care would also benefit VL patients. Examples include disease risk mapping using a spatially referenced population database in Somalia [74,75] or use of technical support platforms, such as telemedicine, encompassing teleconsultation and telementoring. The latter has already been deployed in Somalia in paediatric and tuberculosis (TB) services, with encouraging results [76–78]. Surveillance, using up-to-date geographical information on the distribution of VL, can assist in targeting the villages where most patients come from to carry out a more active approach if and when circumstances allow. In a complex, protracted conflict like the one in Somalia, the surveillance system suffers from the breakdown in health services and routine data collection, and without a functional governmental health system, the classical approach to epidemiological surveillance as a centrally operated public sector information management system is not obvious. Therefore, innovative approaches to VL surveillance should be explored, starting with improved coordination of various stakeholders (WHO, NGOs, the community) and proactively building on innovative approaches and new technologies. A few examples that can be considered are using crowdsourced information, event-based or community-based surveillance, and exploiting the digital potential of the Somali community, who are using cell phones and internet on a large scale. WHO has paved the way in this case by proposing the online DHIS2 platform as a uniform and flexible platform that allows various stakeholders to participate in the surveillance endeavour in this complex context. Improving the spread of information and awareness about the disease could be done simultaneously thanks to technological advances in communication tools.
Qualified health cadres are lacking at all levels in Somalia [8,81], and local initiatives to bring care closer to the community should therefore be supported. To deal with VL, these capacity-building efforts could be better targeted, with basic in-service skills being provided to the local workers, as opposed to formal qualification. The plan to recruit and train female community health workers [17,81], if rolled out in endemic areas of southern Somalia, could include detection of suspect VL cases. Increasing awareness of VL among the population and availability of care are as important as improving the quality of curative service itself. Working with various actors in the complex backdrop of health care provision is labour-intensive, but it may provide better outcomes than what has been implemented in Somalia in the last decades. Commitment from the local communities, through their own structure, would be crucial in ensuring access to care for this deadly disease.
Looking at the local dynamics through a different lens would help in adapting how care should be organized and delivered. However, there are technical obstacles: the existing tools to diagnose and treat VL in the eastern African region are imperfect and extremely difficult to use in conflict settings with scarcity of health staff. The current treatment option of 30 days’ daily SSG injections or 17 days’ combination of SSG and Paromomycin [56,82] are far from ideal, as not all patients are able to travel to the treatment centres or to afford prolonged in-patient care. A short-course oral treatment for self-administration at home would be a breakthrough in such settings. Likewise, better RDTs with improved accuracy and that differentiate between past and present infections are needed, as current treatment cannot be justified to be given empirically without diagnosis confirmation. Clinical diagnosis by community workers would still require certain training and supervision and should be in conjunction with RDT use. There is a clear gap in the current research and development landscape to invest in user-friendly tools that are easier to roll out in unstable contexts such as Somalia. The operational challenges in conflict-ridden areas like parts of Somalia or South Sudan should also be considered when formulating global research portfolios as well as resource allocations (see Table 2 for complete recommendations).
To ignore the burden of neglected diseases in conflict-affected areas is not only detrimental to public health, but also to our morals . VL in Somalia should not be left as just another neglected disease in a neglected conflict. Existing tools for VL control—albeit imperfect—should be deployed, their outcomes monitored, and efforts continued to develop better control tools. Innovative strategies—adapted to the stateless context—without undermining the health-system-building process are needed. Addressing VL in Somalia is a moral imperative, as it means averting avoidable deaths for the most vulnerable: the rural poor, internally displaced, and nomadic populations.
Key learning points
- Visceral leishmaniasis (VL), fatal without treatment, is known to be endemic in parts of southern Somalia, with outbreaks reported in the past.
- Information on VL in Somalia in the literature is scarce and the only currently feasible control option is provision of diagnosis and treatment.
- Due to the ongoing conflict and difficulty in accessing the people in need, availability of VL care within the country is limited.
- There is a need to stop the neglect of VL in Somalia through innovative strategies and improve emergency preparedness.
- Further research is needed to improve existing diagnosis and treatment tools to be more adapted to be used in such a context.
Five key papers in the field
- Chappuis F, Sundar S, Hailu A, Ghalib H, Rijal S, Peeling RW, et al. Visceral leishmaniasis: what are the needs for diagnosis, treatment and control? NatRevMicrobiol. 2007;5(1740–1534 (Electronic)):873–82.
- Alvar J, Vélez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis Worldwide and Global Estimates of Its Incidence. PLoS ONE. 2012;7(5):e35671.
- Murray HW, Berman JD, Davies CR, Saravia NG. Advances in leishmaniasis. Lancet. 2005;366(9496):1561–77.
- Marlet MVL, Sang DK, Ritmeijer K, Muga RO, Onsongo J, Davidson RN. Emergence or re-emergence of visceral leishmaniasis in areas of Somalia, north-eastern Kenya, and south-eastern Ethiopia in 2000–01. Trans R Soc Trop Med Hyg. 2003;97(5):515–8.
- Raguenaud M-E, Jansson A, Vanlerberghe V, Van der Auwera G, Deborggraeve S, Dujardin J-C, et al. Epidemiology and clinical features of patients with visceral leishmaniasis treated by an MSF clinic in Bakool region, Somalia, 2004–2006. PLoS Negl Trop Dis. 2007;1(1):e85.
This article is dedicated to the memory of Dr. Karel Keiluhu and Philippe Havet of MSF, who lost their lives in Somalia in December 2011. We acknowledge the tremendous efforts of all the health care staff working to tackle VL in Somalia and other countries in the region, with special thoughts to the late Ibrahim Ahmed. The author is grateful to the many scholars, researchers, activists, and citizens of Somalia and the Horn of Africa whose support and insights have informed this paper in one way or another. Special thanks go to Dr. Koert Ritmeijer, Margriet den Boer, and Dr. J. A. Ruiz-Postigo for critical reading of the manuscript. Many thanks go to Dr. Said Mohamed Jimale from the Somalia Neglected Tropical Disease Control Initiative (SNTDCI) and Dr. Mohammed Dakane and Dr. Sharif Mohamed from SOS Hospital, SOS Children’s Villages Somalia. Sarah Venis (MSF UK) provided editing assistance. The views expressed in this paper are those of the authors; the authors alone are responsible for their opinions or assertions in this publication. TS worked for MSF projects in Somalia as a physician and a medical coordinator between 2008 and 2012.
- 1. Alvar J, Vélez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis Worldwide and Global Estimates of Its Incidence. PLoS ONE. 2012;7: e35671. doi: 10.1371/journal.pone.0035671. pmid:22693548
- 2. Hailu A, Dagne DA, Boelaert M. Leishmaniasis. In: Gyapong J, Boatin B, editors. Neglected Tropical Diseases—Sub-Saharan Africa. Cham: Springer International Publishing; 2016. pp. 87–112.
- 3. 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: 862–871. pmid:8921468
- 4. Collin SM, Coleman PG, Ritmeijer K, Davidson RN. Unseen Kala-azar deaths in south Sudan (1999–2002). Trop Med Int Health. 2006;11: 509–12. doi: 10.1111/j.1365-3156.2006.01589.x. pmid:16553934
- 5. Postigo JAR. Leishmaniasis in the World Health Organization Eastern Mediterranean Region. Int J Antimicrob Agents. 2010;36.
- 6. Malaria Consortium. Leishmaniasis control in eastern Africa: Past and present efforts and future needs. Situation and gap analysis. 2010.
- 7. World Health Organization. Child Health in Somalia: A Situation Analysis [Internet]. 2012. http://www.emro.who.int/images/stories/somalia/documents/layout_childhealth_9mar.pdf?ua=1
- 8. WHO. Strategic review of the Somali health sector: Challenges and Prioritized actions. 2015. p. 44.
- 9. Heppner G, Magill AJ, Gasse RA O C. The Threat of Infectious Disease in Somalia. N Engl J Med. 1993;329: 2002–12.
- 10. Laughlin LW, Legters LJ. Disease threats in Somalia. Am J Trop Med Hyg. 1993;48.
- 11. Bruckner C, Checchi F. Detection of infectious disease outbreaks in twenty-two fragile states, 2000–2010: a systematic review. Confl Health. 2011;5: 1–10.
- 12. Pavignani E. The Somali healthcare arena. A (still incomplete) mosaic. A report for School of Population Health, University of Queensland, Australia. 2012.
- 13. Burki TK. Somalia: a gathering storm? Lancet. 2013;382: 1237–1238. pmid:24137794
- 14. Guha-Sapir D, Ratnayake R. Consequences of Ongoing Civil Conflict in Somalia: Evidence for Public Health Responses. PLoS Med. 2009;6: e1000108. doi: 10.1371/journal.pmed.1000108. pmid:19668357
- 15. Hammond L, Vaughan-Lee H. Humanitarian space in Somalia: a scarce commodity. Humanit Policy Gr Work Pap. 2012; 1–16. http://www.odi.org.uk/resources/details.asp?id=6430&title=humanitarian-space-somalia-aid-workers-principles
- 16. Warsame A. Opportunity for health systems strengthening in Somalia. Lancet Glob Heal. 2014;2: e197–e198.
- 17. Ministry of Health Somalia Federal Government. Somalia Health Sector Strategic Plan January 2013 –December 2016. 2013.
- 18. Somalia Ministries of Health and Health Sector Partners. Somali Health Sector: A Call for life saving health programmes especially for women and children. 2015.
- 19. Elkheir N, Sharma A, Cherian M, Saleh OA, Everard M, Popal GR, et al. A cross-sectional survey of essential surgical capacity in Somalia. BMJ Open. 2014;4: e004360. doi: 10.1136/bmjopen-2013-004360. pmid:24812189
- 20. Kohler JC, Pavignani E, Michael M, Ovtcharenko N, Murru M, Hill PS. An examination of pharmaceutical systems in severely disrupted countries. BMC Int Health Hum Rights. 2012;12: 34. doi: 10.1186/1472-698X-12-34. pmid:23217184
- 21. Marlet MVL, Sang DK, Ritmeijer K, Muga RO, Onsongo J, Davidson RN. Emergence or re-emergence of visceral leishmaniasis in areas of Somalia, north-eastern Kenya, and south-eastern Ethiopia in 2000–01. Trans R Soc Trop Med Hyg. 2003;97: 515–8. pmid:15307414
- 22. Marlet MVL, Wuillaume F, Jacquet D, Quispe KW, Dujardin JC, Boelaert M. A neglected disease of humans: A new focus of visceral leishmaniasis in Bakool,Somalia. Trans R Soc Trop Med Hyg. 2003;97: 667–671. http://dx.doi.org/10.1016/S0035-9203(03)80099-8 pmid:16117959
- 23. Schorscher J, Goris M. Incrimination of Phlebotomus (Larroussius) orientalis as a vector of visceral leishmaniasis in western Upper Nile Province, southern Sudan. Trans R Soc Trop Med Hyg. 1992;86: 622–3. pmid:1287918
- 24. Gebre-Michael T, Lane R. The roles of Phlebotomus martini and P.celiae (Diptera: Phlebotominae) as vectors of visceral leishmaniasis in the Aba Roba focus, southern Ethiopia. Med Vet Entomol. 1996;10: 53–62. pmid:8834743
- 25. Gerstl S, Amsalu R, Ritmeijer K. Accessibility of diagnostic and treatment centres for visceral leishmaniasis in Gedaref State, northern Sudan. Trop Med Int Heal. 2006;11: 167–175.
- 26. Bucheton B, Kheir MM, el-Safi SH, Hammad A, Mergani A, Mary C et al. The interplay between environmental and host factors during an outbreak of visceral leishmaniasis in eastern Sudan. Microbes Infect. 2002;4: 1449–57. pmid:12475635
- 27. Schaefer KU, Kurtzhals JA, Kager PA, Gachihi GS, Gramiccia M, Kagai JM et al. S. Studies on the prevalence of leishmanin skin test positivity in the Baringo District, Rift Valley, Kenya. Am J Trop Med Hyg. 1994;50: 78–84. pmid:8304576
- 28. Schaefer KU, Kurtzhals JA, Gachihi GS, Muller AS K P. A prospective sero-epidemiological study of visceral leishmaniasis in Baringo District, Rift Valley Province, Kenya. Trans R Soc Trop Med Hyg. 1995;89: 471–5. pmid:8560511
- 29. Gebre-Michael T, Malone JB, Balkew M, Ali A, Berhe N, Hailu A, et al. Mapping the potential distribution of Phlebotomus martini and P. orientalis (Diptera: Psychodidae), vectors of kala-azar in East Africa by use of geographic information systems. Acta Trop. 2004;90: 73–86. pmid:14739026
- 30. Raguenaud M-E, Jansson A, Vanlerberghe V, Van der Auwera G, Deborggraeve S, Dujardin J-C, et al. Epidemiology and clinical features of patients with visceral leishmaniasis treated by an MSF clinic in Bakool region, Somalia, 2004–2006. PLoS Negl Trop Dis. 2007;1: e85. doi: 10.1371/journal.pntd.0000085. pmid:17989791
- 31. Elnaiem DEA. Ecology and control of the sand fly vectors of Leishmania donovani in East Africa, with special emphasis on Phlebotomus orientalis. J Vector Ecol. 2011;36: 23–31.
- 32. Kolaczinski JH, Worku DT, Chappuis F, Reithinger R, Kabatereine N, Onapa A, et al. Kala-azar control, Uganda. Emerg Infect Dis. 2007;13: 507–9. doi: 10.3201/eid1303.060706. pmid:17552117
- 33. Reithinger R, Brooker S, Kolaczinski JH. Visceral leishmaniasis in eastern Africa—current status. Trans R Soc Trop Med Hyg. 2007;101: 1169–70. doi: 10.1016/j.trstmh.2007.06.001. pmid:17632193
- 34. Dereure J, el-Safi SH, Bucheton B, Boni M, Kheir MM, Davoust B et al. Visceral leishmaniasis in eastern Sudan: parasite identification in humans and dogs; host-parasite relationships. Microbes Infect. 2003;5: 1103–8. pmid:14554251
- 35. Ibrahim ME, Lambson B, Yousif a O, Deifalla NS, Alnaiem D a, Ismail A, et al. Kala-azar in a high transmission focus: an ethnic and geographic dimension. Am J Trop Med Hyg. 1999;61: 941–4. pmid:10674674
- 36. Abubakar A, Ruiz-Postigo JA, Pita J, Lado M, Ben-Ismail R, Argaw D, et al. Visceral Leishmaniasis Outbreak in South Sudan 2009–2012: Epidemiological Assessment and Impact of a Multisectoral Response. PLoS Negl Trop Dis. 2014;8: e2720. doi: 10.1371/journal.pntd.0002720. pmid:24675573
- 37. Dhimal M, Ahrens B, Kuch U. Climate change and spatiotemporal distributions of vector-borne diseases in Nepal—A systematic synthesis of literature. PLoS ONE. 2015;10: 1–31.
- 38. Zijlstra EE, El-Hassan a M. Leishmaniasis in Sudan. Mucosal leishmaniasis. Trans R Soc Trop Med Hyg. 2001;95 Suppl 1: S27–S58.
- 39. Penso G. Il kala azar nella Somalia Italiana. Bollettini e Atti di Ric Accad Medica Roma,. 1934;60: 292–3.
- 40. Moise R. A proposito dei casi di kala azar finora segnalati. Ann Med Nav Trop. 1955;68: 481–501.
- 41. Cahill KM. Clinical and epidemiological patterns of leishmaniasis in Africa. Trop Geogr Med. 1968;20: 109–17. pmid:4871799
- 42. Cahill K. Studies in Somalia. Trans R Soc Trop Med Hyg. 1971;65: 28–42. pmid:5092427
- 43. Baruffa G. The problem of kala-azar in Somalia. Riv Parassitol. 1966;27: 1–14. pmid:5940035
- 44. Shiddo SA, Aden MA, Akuffo HO, Mohamud KA, Herzi AA, Herzi MH et al. 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 1. 1995;89: 361–5.
- 45. Shiddo SA, Akuffo HO, Mohamed AA, Huldt G, Nilsson LA, Ouchterlony O et al. Visceral leishmaniasis in Somalia: prevalence of leishmanin-positive and seropositive inhabitants in an endemic area. Trans R Soc Trop Med Hyg. 1995;89: 21–4. pmid:7747298
- 46. Woolhead A. A recent case of visceral leishmaniasis in Somalia. Ann Trop Med Parasitol. 1995;89: 687–8. pmid:8745944
- 47. Harith AE, Kolk AHJ, Kager PA, Leeuwenburg J, Muigai R, Kiugu S, et al. A simple and economical direct agglutination test for serodiagnosis and sero-epidemiological studies of visceral leishmaniasis. Trans R Soc Trop Med Hyg. 1986;80: 583–586. pmid:3101241
- 48. Shiddo SA, Mohamed AA, Huldt G, Loftenius A, Nilsson L, Jonsson J, Ouchterlony O T R. Visceral leishmaniasis in Somalia. Circulating antibodies as measured by DAT, immunofluorescence and ELISA. Trop Geogr Med. 1995;47: 68–73. pmid:8592766
- 49. Shiddo S, Huldt G, Nilsson L, Ouchterlony O, Thorstensson R. Visceral leishmaniasis in Somalia. Significance of IgG subclasses and of IgE response. Immunol Lett. 1996;50: 87–93. pmid:8793564
- 50. Pigott DM, Bhatt S, Golding N, Duda K a, Battle KE, Brady OJ, et al. Global distribution maps of the leishmaniases. Elife. 2014;3: 1–21.
- 51. Qayad MG. Health Care Services in Transitional Somalia: Challenges and Recommendations. Bild An Int J Somali Stud. 2007;7: 190–210.
- 52. World Bank. Somalia—Socioeconomic survey 2002. Somalia Watching Brief; no. 1. [Internet]. Washington City; 2003. http://documents.worldbank.org/curated/en/2003/01/6762297/somalia-socioeconomic-survey-2002
- 53. 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. 2001;7: 603–4. doi: 10.3201/eid0707.010746. pmid:11485683
- 54. Karunakara U. Why MSF decided to leave Somalia | Médecins Sans Frontières (MSF) International [Internet]. [cited 2 Mar 2016]. http://www.msf.org/article/why-msf-decided-leave-somalia
- 55. WHO. WHO Global Health Observatory [Internet]. [cited 3 Apr 2016]. http://www.who.int/gho/neglected_diseases/leishmaniasis/en/
- 56. World Health Organization. Visceral leishmaniasis: control strategies and epidemiological situation update in East Africa: report of a WHO bi-regional consultation Addis Ababa, Ethiopia, 9–11 March 2015—See more at: [Internet]. World Health Organization; 2015. http://apps.who.int/iris/handle/10665/190168#sthash.98Q1mye7.dpuf
- 57. WHO. Leishmaniasis in high-burden countries: an epidemiological update based on data reported in 2014. Wkly Epidemiol Rec. 2016; 287–296. pmid:27263128
- 58. Unicef. Health Care Seeking Behaviour in Somalia: A Literature Review. 2008; 1–48.
- 59. Buckley J, O’Neill L, Aden A. Somalia private sector assessment [Internet]. Oxford Policy Management. 2015. http://www.opml.co.uk/sites/default/files/Somalia Private Sector Assessment.pdf
- 60. Fuje MM, Ruiz Postigo JA EM& B-IR. SCALING UP THE CONTROL OF VISCERAL LEISHMANIASIS IN SOMALIA. 2011. p. Poster presented at 7th European Congress of Tropi.
- 61. Hotez PJ, Kamath A. Neglected tropical diseases in sub-Saharan Africa: Review of their prevalence, distribution, and disease burden. PLoS Negl Trop Dis. 2009;3: 2–11.
- 62. Somalia Health Advisory Board. Prioritization of Health Policy Actions in Somali Health Sector. 2014.
- 63. Warsame A, Handuleh J, Patel P. Prioritization in Somali health system strengthening: a qualitative study. Int Heal. 2016;8: 204–10. Epub 2015 Sep 29.
- 64. Pavignani E, Michael M, Murru M, Beesley ME, Hill PS. Making sense of apparent chaos: health-care provision in six country case studies. Int Rev Red Cross. 2013;95: 41–60.
- 65. Hill PS, Pavignani E, Michael M, Murru M, Beesley ME. The “empty void” is a crowded space: health service provision at the margins of fragile and conflict affected states. Confl Health. 2014;8: 20. doi: 10.1186/1752-1505-8-20. pmid:25349625
- 66. IRIN. Al-Shabab ban on agencies threatens aid. In: October 2011 [Internet]. [cited 25 Mar 2016]. http://www.irinnews.org/report/94321/somalia-al-shabab-ban-agencies-threatens-aid
- 67. Seal A, Bailey R. The 2011 Famine in Somalia: lessons learnt from a failed response? Confl Health. 2013;7: 22. doi: 10.1186/1752-1505-7-22. pmid:24171715
- 68. Svoboda E, Zyck SA, Osman D, Hashi A. Islamic humanitarianism? The evolving role of the Organisation for Islamic Cooperation in Somalia and beyond. 2015.
- 69. Capobianco E, Naidu V, World Bank. A review of health sector aid financing to Somalia (Inglés) [Internet]. World Bank working paper. 2008. http://www-wds.worldbank.org/external/default/WDSContentServer/WDSP/IB/2008/05/30/000333037_20080530022142/Rendered/PDF/439750PUB0Box310only109780821375174.pdf
- 70. Leduc B, Neuman M. Somalia: Everything is Open to Negotiations in: Humanitarian Negotiations Revealed. In: MAGONE C, NEUMAN M, WEISSMAN F, editors. London: C. Hurst & Co. (Publishers) Ltd., 41 Great Russell Street, London, WC1B 3PL; 2011. pp. 77–94.
- 71. Menkhaus K. Governance without Government in Somalia. Int Secur. 2006;31: 74–106.
- 72. Helander B. Getting the most out of it: nomadic health care seeking and the state in southern Somalia. Nomadic Peoples. 1990. pp. 122–132.
- 73. Burki T. East African countries struggle with visceral leishmaniasis. Lancet. 2009;374: 371–372. pmid:19655434
- 74. Linard C, Alegana V a, Noor AM, Snow RW, Tatem AJ. A high resolution spatial population database of Somalia for disease risk mapping. Int J Health Geogr. 2010;9: 45. doi: 10.1186/1476-072X-9-45. pmid:20840751
- 75. Anyamba A, Chretien J-P, Small J, Tucker CJ, Formenty PB, Richardson JH, et al. Prediction of a Rift Valley fever outbreak. Proc Natl Acad Sci U S A. 2009;106: 955–9. doi: 10.1073/pnas.0806490106. pmid:19144928
- 76. Zachariah R, Bienvenue B, Ayada L, Manzi M, Maalim A, Engy E, et al. Practicing medicine without borders: Tele-consultations and tele-mentoring for improving paediatric care in a conflict setting in Somalia? Trop Med Int Heal. 2012;17: 1156–1162.
- 77. Maalim AM, Zachariah R, Khogali M, Van griensven J, Van den bergh R, Tayler-Smith K, et al. Supporting “medicine at a distance” for delivery of hospital services in war-torn somalia: How well are we doing? Int Health. 2014;6: 70–73. doi: 10.1093/inthealth/iht035. pmid:24431137
- 78. Liddle KF, Elema R, Thi SS, Greig J, Venis S. TB treatment in a chronic complex emergency: Treatment outcomes and experiences in Somalia. Trans R Soc Trop Med Hyg. 2013;107: 690–698. doi: 10.1093/trstmh/trt090. pmid:24080739
- 79. WHO. WHO to implement online epidemiological surveillance for leishmaniasis [Internet]. 2016 [cited 2 Nov 2016]. http://www.who.int/neglected_diseases/news/WHO_implement_epidemiological_surveillance_leishmaniasis/en/
- 80. Canada: Immigration and Refugee Board of Canada. Somalia: Prevalence of cell phones and Internet cafes in Mogadishu, including the ability to use cell phones for financial transfers (2012-February 2015) [Internet]. [cited 8 Jun 2016]. http://www.refworld.org/docid/550c35904.html
- 81. Somalia Ministry of Health. Human Resources for Health Strategic Plan for Central and South Somalia 2014–2018. 2014.
- 82. Control of the leishmaniases: Report of a WHO expert committee. World Health Organization—Technical Report Series. 1990. pp. 9–131.
- 83. Beyrer C, Villar JC, Suwanvanichkij V, Singh S, Baral SD, Mills EJ. Neglected diseases, civil conflicts, and the right to health. Lancet. 2007;370: 619–627. doi: 10.1016/S0140-6736(07)61301-4. pmid:17707757