Journal of Global Infectious Diseases

ORIGINAL ARTICLE
Year
: 2020  |  Volume : 12  |  Issue : 3  |  Page : 135--140

Risk factors of inpatients mortality of visceral leishmaniasis, Khartoum State, Sudan


Omaima Abdel Majeed Mohamed Salih1, Abdelsalam M Nail2, Gad Allah Modawe3, Mohamed Osman Swar4, Mohamed H Ahmed5, Atif Khalil6, Abdelsalam Basheir Satti7, Nadir Abuzeid7,  
1 Department of Pediatrics and Child Health, Faculty of Medicine and Health Sciences, Omdurman Islamic University, Sudan
2 Department of Internal Medicine, Faculty of Medicine and Health Sciences, Omdurman Islamic University, Sudan
3 Department of Biochemistry, Faculty of Medicine and Health Sciences, Omdurman Islamic University, Sudan
4 Department of Pediatrics and Child Health, School of Medicine, Ahfad University for Women, Sudan
5 Department of Medicine, Milton Keynes University Hospital NHS Foundation Trust, Milton Keynes, Buckinghamshire, UK
6 Department of Nephrology, Noble Hospital, Isle of Man, UK
7 Department of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Omdurman, Sudan

Correspondence Address:
Dr. Omaima Abdel Majeed Mohamed Salih
Department of Pediatrics and Child Health, Faculty of Medicine and Health Sciences, Omdurman Islamic University, Omdurman
Sudan

Abstract

Background: Visceral leishmaniasis (VL) is one of the common infections in Sudan and can be associated with an increase in morbidity and mortality. The aim of this study was to assess the risk factors associated with mortality and morbidity with VL. Materials and Methods: This is a cross-sectional hospital-based study that recruited 150 patients with VL from two centers in Khartoum. Secondary data were extracted from the patient records, and data were analyzed using SPSS version 24.0. Results: The study included 2.5% of infants, 39.4% children, and 58% of adults. Male represents 77.3% of the cohort, and total mortality was 16%. Among the death reported 12.5% in infants, 16.7% were children, and 70.8% were in adults. Laboratory parameters significantly associated with mortality in univariate analysis were low white cell count, low platelets, high creatinine, and high liver enzymes. While risk factors such as infant, male, acquired infection from Eastern Sudan or White Nile, weight loss, morbid diseases, and concomitant bacterial infections were also associated with significant mortality in univariate analysis. Importantly, logistic regression analysis revealed significant association with infant (P = 0.02), concomitant bacterial infections (P = 0.003), comorbid disease (P = 0.001), low total blood cell count (P = 0.018), low platelets (P = 0.013), and high aspartate transaminase/alanine aminotransferase (P = 0.013). Conclusion: Health education and awareness are needed in terms of prevention and control, especially with high mortality seen in the infant. Treatment of underlying co-morbid diseases and bacterial infections are important to enhance survival. Patients with Leishmania are vulnerable; therefore, regular routine blood tests are an essential part of management to manage complications such as renal, hepatic failure, or severe anemia.



How to cite this article:
Salih OA, Nail AM, Modawe GA, Swar MO, Ahmed MH, Khalil A, Satti AB, Abuzeid N. Risk factors of inpatients mortality of visceral leishmaniasis, Khartoum State, Sudan.J Global Infect Dis 2020;12:135-140


How to cite this URL:
Salih OA, Nail AM, Modawe GA, Swar MO, Ahmed MH, Khalil A, Satti AB, Abuzeid N. Risk factors of inpatients mortality of visceral leishmaniasis, Khartoum State, Sudan. J Global Infect Dis [serial online] 2020 [cited 2020 Oct 28 ];12:135-140
Available from: https://www.jgid.org/text.asp?2020/12/3/135/293800


Full Text



 Introduction



Leishmaniasis is a serious challenge for health authorities in a big country like Sudan. This can be attributed to the fact that its transmitted by female sand-fly, leading to an intracellular protozoa parasite. Depending on the immune system of the host, the disease may not show any clinical presentation and lead to self-resolving. Unfortunately, leishmaniasis can be associated with cutaneous ulcer localized or disseminated and mutilating mucocutaneous disease. Death can occur as a result of infection of the reticulo-endothelial system and lethal systemic illness.[1] Many factors lead to an increase in infection with leishmaniasis within recent years. For instance, human immunodeficiency virus (HIV) and tuberculosis (TB) are associated with leishmaniasis. The disease affects globally around 12 million people, with 900,000–1.3 million new cases each year. This increase in infection rate was attributed in part to an increase in global travel.[2] Several environmental, social, and economic reasons also lead to an increase in the prevalence of leishmaniasis. For instance, leishmaniasis is the disease of the poor populations who also suffer from malnutrition. Environmental factors such as mining, dam building, and large irrigation schemes with road construction in developing countries may all lead to an increase in the number of sand fly and hence leishmaniasis.[3] It worth mentioning that in 1996 in Kabul, the capital of Afghanistan, the resurgence of visceral leishmaniasis (VL) has occurred because of deficiencies in the control of the vector (sand-fly) and lack of access to medical treatment due to the cost and increasing drug resistance to first-line treatment.[4] Because HIV/AID increases susceptibility to infections with leishmaniasis approximately by 100–1000, one challenge for African countries will be how to deal with an increase in the number of individuals who suffer from leishmaniasis and HIV infection.[4] Children are at greater risk than adults in endemic areas. Incomplete therapy of the initial disease is also another important risk factor for recurrence.[1],[2],[3],[4]

Sudan has the highest number of reported cases of leishmaniasis in East Africa[5] where the disease is endemic since the early 1900s, in particular in eastern and central regions.[6] Due to lack of or no access to medical facilities in rural areas in Sudan, the diagnosis of VL can be late or when complications were diagnosed.[6] The objective of this study was to investigate the risk factors associated with VL that lead to an increase in morbidity and mortality in hospital patients in Khartoum state, Sudan.

 Materials and Methods



Data collection

This a descriptive cross-sectional hospital-based study. The study is conducted in Tropical Medicine teaching Hospital in Omdurman and Jaafar Ibn Auf Pediatric teaching Hospital (both are known centers for the treatment of visceral leishmania), from January 2016 to December 2017. Record of all patients admitted to both hospitals during the study period were included in the study. Secondary Data was extracted from the patient's records and then re-entered into a predesigned data collection form, cleaned and analyzed using SPSS version 24. 24 (SPSS Inc., Chicago, IL, USA).

Statistical analysis

Descriptive statistics in terms of frequency tables with percentages were classified each row by total population column (Survival vs. Death) using cross-tabulation. Furthermore, analysis to determine the associations between the main outcome variable (inpatients' mortality due to VL) was the dependent variable, and the other relevant factors as the independent variable with Chi-square test (for categorical variables) and logistic regression analysis univariate and multivariate were used for analysis odds ratio (OR) with a 95% confidence interval (CI) was calculated and statistical significance was defined as P < 0.05.

Ethical clearance and approval

Ethical clearance and approval for conducting this research were obtained from the Khartoum state Ministry of the health research department.

 Results



The study included 150 patients, 2.5% (4) were infants, 39.4% (59) were children, and 58% (87) were adults. Male represents 77.3% of the cohort. Areas of acquisition of the disease were Kordofan 34%, East of Sudan 24%, White Nile 14%, South Sudan 8.7%, Dar four 8%, Blue Nile 6%, and Khartoum 4.7%. Among the death reported, 12.5% were among infants, 16.7% of children, and 70.8 were in adults. Importantly, 41.7% of death noted were among those who acquired the disease in Eastern Sudan and 20.8% among those in Kordofan [Table 1].{Table 1}

[Table 2] shows the clinical presentations and laboratory investigations of participants and percentages of survival and mortality with VL. The highest percentage of survival and death was seen with a disease duration between 1 and 6 months. Weight loss, edema, bleeding, bleeding, jaundice, and cough were observed in 78.7%, 15.3%, 15.3%, 22.7%, and 7.3%, respectively. Spleen size >8 cm was seen 31.3%, primary infection with VL was encountered in 88%. HIV and TB were reported in 7.3%, 7.3, respectively. Secondary bacterial infections were observed in 41.3%. Laboratory investigations were noted to be also in the abnormal range in the large number of patients. For instance, abnormal hemoglobin, white cell count, platelets, high creatinine, high liver enzymes, and low albumin were observed in 89.3%, 79.3%, 69.3%, 14.7, 57.3%, and 44.7%, respectively.{Table 2}

Univariate analysis showed that there was the statistical association with mortality and risk factors such as being infant, male, acquired infection from Eastern Sudan or White Nile, weight loss, morbid diseases, and concomitant bacterial infections. Investigations that significantly associated with mortality in univariate analysis were total white blood cell count (TWBC), low platelets, high creatinine, and high liver enzymes [Table 3]. Importantly, logistic regression analysis, which rely on dependent variable survival versus mortality for univariate and multivariate risk factors, revealed significant statistically association with infants (P = 0.02), concomitant bacterial infections (P = 0.003), comorbid disease (P = 0.001), low WBC (P = 0.018), low platelets (P = 0.013) and high aspartate transaminase/alanine aminotransferase (P = 0.013). However, univariate analysis showed a significant association with risk factors such as males, residency in Eastern Sudan, residency in White Nile, and weight loss. However, other risk factors did not show significant effect [Table 3].{Table 3}

 Discussion



VL is the world's second-deadliest parasitic disease after malaria, and one of the most important health problems in Sudan, without treatment, VL is nearly always fatal.[7],[8] The present study shows that most of the patients were males (77.3%) with higher mortality. This inline with the finding of the largest report of a 14-years registry (2002–2015) about cumulative cases and mortality of visceral leishmaniasis done in Eastern Sudan.[7] The high prevalence of VL among males in the study can be attributed to the greater exposure of males than females to the sand fly vector due to differences in occupations.[8],[9],[10],[11],[12],[13],[14] The mortality rate (16.0%) observed in the present study is higher than that reported by Nail et al., 2013, which was 5.6%,[14] and less than the fatality reported in 1998.[13] Importantly, several studies showed leishmaniasis in children is associated with a higher rate of morbidity and mortality (especially those <1 year).[14],[15],[16],[17],[18] Our study showed that the age of the patient is a strong indicator of the poor clinical course of VL as infants shows 17.9 risk of mortality compared to another age group. This can be attributed in part to the immaturity of the immune system in infants and children.[19],[20] Furthermore, children exhibit increased interleukin-10 levels and L-arginine secretion, which are factors associated with parasite persistence and greater VL severity. These parameters, coupled with the immaturity of the immune system, could explain the poor prognosis for this age group.[21],[22],[23],[24],[25],[26],[27]

Patients who acquire the disease from Eastern Sudan in our study showed 2.74 higher risk of mortality when compared with patients coming from other VL foci. Furthermore, patients from Eastern Sudan in our study were noticed to have the more complicated clinical presentation. For instance, VL was associated with an increased incidence of other comorbid diseases and renal impairment (P = 0.018–0.002, respectively). This may explain the higher mortality among patients from Eastern Sudan compared to White Nile patients and patients from other regions. Nail, also noticed that mortality is higher in Eastern Sudan in comparison with other regions of Sudan.[28]

Importantly, it was shown in meta-analysis that thrombocytopenia was the second most important predictor of VL-induced death after bleeding and jaundice, especially when the platelet count is below 50 × 109/l.[17] In this study, low platelet count is associated with 1.39 higher risk of mortality. Although it is not possible to state with certainty the cause of thrombocytopenia in VL patients, splenic sequestration of platelets is possibly the main cause of a low platelet count.[17],[29] Thus, detection of bleeding regardless of the cause at the first diagnosis or during treatment is crucial in the identification of severity and reduction of mortality from VL. Ministry of Health of Brazil[30] recommends platelet transfusion for VL patients presented with counts lower than 10 × 109/l. and individuals presenting with hemoglobin levels <7 g/Dl would receive transfusions of packed red cells.

Secondary bacterial infections are known to be an important cause of death among VL-infected individuals.[17] Many studies showed that the presence of coinfections was a strong predictor of adverse evolution.[16],[17],[20],[21],[29] This per se emphasis the importance of treating and preventing general infections. In this study, we have shown secondary bacterial infection was associated with 2.8 time's higher mortality. Another indicator that secondary bacterial infection was an important risk factor for hospital death from VL, the present study showed that patients with low TWBCs count have a statistically significant higher mortality compared with patients with normal WBCs (OR = 2.00 P = 0.000). Several studies showed a similar association between TWBCs and high mortality.[16],[17],[18],[31] Therefore, proper septic screening, use of antibiotics and the constant monitoring of WBCs are mandatory steps throughout treatment.

Even though several studies showed that HIV/TB co-infection were associated with a poor prognosis,[17],[18],[31],[32],[33],[34] the present study showed that HIV/TB co-infection were not associated with increased risk of mortality.[16],[17],[18],[35],[36]

It worth mentioning that renal impairment in the present study was also associated with increased mortality. Daher et al. showed an increase in serum creatinine was associated with increased morbidity and mortality.[37] Hence, early identification of these clinical and laboratory characteristics, at the time when patients are first attended, is extremely important for reducing mortality through instituting efficient therapeutic and prophylactic measures.

The study is not without limitations. The cross-sectional design of the study may not allow for the temporal relationship. The study recircuited patients from two centers in Khartoum in limited duration; therefore, the outcome of this study cannot be generalized for all Sudan. Despite these limitations, the study is novel and able to determine factors that associated with increase in mortality and morbidity with VL.

 Conclusion



The main demographic features that affect mortality are the age of the patients mainly being infant, and acquisition of VL from Eastern Sudan compared to patients who acquire the disease from other VL foci in Sudan and South Sudan. The main clinical features that result in a higher risk of in-hospital death from VL are secondary bacterial infection and the presence of comorbid disease. HIV/VL and TB/VL co-infection did not increase the risk of in-hospital death from VL among our study participants. The main laboratory investigation that predicts adverse outcome are low platelet count, low WBCs, elevated liver enzymes, and renal impairment.

Research Quality and Ethics Statement

The authors of this manuscript declare that this scientific work complies with reporting quality, formatting, and reproducibility guidelines set forth by the EQUATOR Network. The authors also attest that this clinical investigation was determined to require the Institutional Review Board/Ethics Committee review and the corresponding protocol/approval issued on 1/2/2019 by the Ministry of Health, state of Khartoum, Sudan. We also certify that we have not plagiarized the contents in this submission and have done a Plagiarism Check.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1World Health Organization. Leishmaniasis: The Disease and its Epidemiology. Available from: http://www.who.int/leishmaniasis/disease_epidemiology/en/. [Last accessed on 2014 Apr 10].
2Centers for Disease Control and Prevention. Parasites Home: Leishmaniasis. Epidemiology & Risk Factors. Available from: http://www.cdc.gov/parasites/leishmaniasis/epi.html. [Last accessed on 2014 Apr 11].
3Coleman RE, Burkett DA, Putnam JL, Sherwood V, Caci JB, Jennings BT, et al. Impact of phlebotomine sand flies on U.S. military operations at Tallil Air Base, Iraq: 1. background, military situation, and development of a “Leishmaniasis Control Program”. J Med Entomol 2006;43:647-62.
4Myles O, Wortmann GW, Cummings JF, Barthel RV, Patel S, Crum-Cianflone NF, et al. Visceral leishmaniasis: Clinical observations in 4 US army soldiers deployed to Afghanistan or Iraq, 2002-2004. Arch Intern Med 2007;167:1899-901.
5Alvar 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.
6Zijlstra EE, el-Hassan AM. Leishmaniasis in Sudan. Visceral leishmaniasis. Trans R Soc Trop Med Hyg 2001;95 Suppl 1:S27-58.
7World Health Organization. Control of Neglected Tropical Diseases (NTD). Report; World Health Organization; 2015.
8WHO. Control of the Leishmaniases. Report of a Meeting of the WHO Expert Committee on the Control of the Leishmaniases. WHO Technical Report Series 949. Geneva: WHO; 22-26 March, 2010. Available from: http://apps.who.int/iris/bitstream/10665/44412/1/WHO_TRS_949_eng.pdf.[Last accessed on 2019 Dec 12].
9Adam GK, Ali KM, Abdella YH, Omar SM, Ahmed MA, Abdalla TM, et al. Trend in cumulative cases and mortality rate among visceral leishmaniasis patients in Eastern Sudan: A 14-year registry, 2002–2015. Int J Infect Dis 2016;51:81-4.
10Gadisa E, Custodio E, Cañavate C, Sordo L, Abebe Z, Nieto J, et al. Usefulness of the rK39-immunochromatographic test, direct agglutination test, and leishmanin skin test for detecting asymptomatic Leishmania infection in children in a new visceral leishmaniasis focus in Amhara State, Ethiopia. Am J Trop Med Hyg 2012;86:792-8.
11Perry D, Dixon K, Garlapati R, Gendernalik A, Poché D, Poché R. Visceral leishmaniasis prevalence and associated risk factors in the Saran district of Bihar, India, from 2009 to July of 2011. Am J Trop Med Hyg 2013;88:778-84.
12Rijal S, Koirala S, Van der Stuyft P, Boelaert M. The economic burden of visceral leishmaniasis for households in Nepal. Trans R Soc Trop Med Hyg 2006;100:838-41.
13Majeed B, Sobel J, Nawar A, Badri S, Muslim H. The persisting burden of visceral leishmaniasis in Iraq: Data of the National Surveillance System, 1990-2009. Epidemiol Infect 2013;141:443-6.
14Nail AM, Imam AM. Visceral leishmaniasis: Clinical and demographic features in an African population. Pak J Med Sci 2013;29:485-9.
15Zijlstra EE, el-Hassan AM, Ismael A, Ghalib HW. Endemic Kala-Azar in Eastern Sudan: A longitudinal study on the incidence of clinical and subclinical infection and post-Kala-Azar dermal leishmaniasis. Am J Trop Med Hyg 1994;51:826-36.
16Driemeier M, de Oliveira PA, Druzian AF, Lopes Brum LF, Pontes ER, Dorval ME, et al. Late diagnosis: A factor associated with death from visceral leishmaniasis in elderly patients. Pathog Glob Health 2015;109:283-9.
17de Queiroz Sampaio MJ, Cavalcanti NV, Bezerra Alves JG, Fernandes Filho MJ, Correia JB. Risk factors for death in children with visceral leishmaniasis. PLoS Negl Trop Dis 2010;4:e877.
18Coura-Vital W, Araújo VE, Reis IA, Amancio FF, Reis AB, Carneiro M. Prognostic factors and scoring system for death from visceral leishmaniasis: An historical cohort study in Brazil. PLoS Negl Trop Dis 2014;8:e3374.
19Belo VS, Struchiner CJ, Barbosa DS, Nascimento BW, Horta MA, da Silva ES, et al. Risk factors for adverse prognosis and death in American visceral leishmaniasis: A meta-analysis. PLoS Negl Trop Dis 2014;8:e2982.
20Abongomera C, Ritmeijer K, Vogt F, Buyze J, Mekonnen Z, Admassu H, et al. Development and external validation of a clinical prognostic score for death in visceral leishmaniasis patients in a high HIV co-infection burden area in Ethiopia. PLoS One 2017;12:e0178996.
21Mueller Y, Mbulamberi DB, Odermatt P, Hoffmann A, Loutan L, Chappuis F. Risk factors for in-hospital mortality of visceral leishmaniasis patients in eastern Uganda. Trop Med Int Health 2009;14:910-7.
22de Araújo VE, Morais MH, Reis IA, Rabello A, Carneiro M. Early clinical manifestations associated with death from visceral leishmaniasis. PLoS Negl Trop Dis 2012;6:e1511.
23Costa DL, Rocha RL, Carvalho RM, Lima-Neto AS, Harhay MO, Costa CH, et al. Serum cytokines associated with severity and complications of kala-azar. Pathog Glob Health 2013;107:78-87.
24Groux H, Cottrez F, Rouleau M, Mauze S, Antonenko S, Hurst S, et al. A transgenic model to analyze the immunoregulatory role of IL-10 secreted by antigen-presenting cells. J Immunol 1999;162:1723-9.
25Slatter MA, Gennery AR. Clinical immunology review series: An approach to the patient with recurrent infections in childhood. Clin Exp Immunol 2008;152:389-96.
26Munder M. Arginase: An emerging key player in the mammalian immune system. Br J Pharmacol 2009;158:638-51.
27Müller I, Hailu A, Choi BS, Abebe T, Fuentes JM, Munder M, et al. Age-related alteration of arginase activity impacts on severity of leishmaniasis. PLoS Negl Trop Dis 2008;2:e235.
28Nail AM. Visceral leishmaniasis: A comparative analysis of clinical and demographic in two foci from Sudan. Aljouf Med J 2014;1:9-13.
29Varma N, Naseem S Hematologic changes in visceral leishmaniasis/kalaazar. Indian J Hematol Blood Transfus 2010;26:78-82.
30Bezerra JMT, de Araújo VEM, Barbosa DS, Martins-Melo FR, Werneck GL, Carneiro M. Burden of leishmaniasis in Brazil and federated units, 1990-2016: Findings from Global Burden of Disease Study 2016. PLoS Negl Trop Dis 2018;12(9):e0006697. doi: 10.1371/journal.pntd. 0006697. eCollection 2018 Sep.
31Werneck GL, Batista MS, Gomes JR, Costa DL, Costa CH. Prognostic factors for death from visceral leishmaniasis in Teresina, Brazil. Infection 2003;31:174-7.
32Olivier M, Badaró R, Medrano FJ, Moreno J. The pathogenesis of Leishmania/HIV co-infection: Cellular and immunological mechanisms. Ann Trop Med Parasitol 2003;97 Suppl 1:79-98.
33Cruz I, Nieto J, Moreno J, Cañavate C, Desjeux P, Alvar J. Leishmania/HIV co-infections in the second decade. Indian J Med Res 2006;123:357-88.
34Alvar J, Aparicio P, Aseffa A, Den Boer M, Cañavate C, Dedet JP, et al. The relationship between leishmaniasis and AIDS: The second 10 years. Clin Microbiol Rev 2008;21:334-59.
35Okwor I, Uzonna JE. The immunology of leishmania/HIV co-infection. Immunol Res 2013;56:163-71.
36Druzian AF, de Souza AS, de Campos DN, Croda J, Higa MG Jr., Dorval ME, et al. Risk factors for death from visceral leishmaniasis in an urban area of Brazil. PLoS Negl Trop Dis 2015;9:e0003982.
37Daher EF, Evangelista LF, Silva Júnior GB, Lima RS, Aragão EB, Arruda GA, et al. Clinical presentation and renal evaluation of human visceral leishmaniasis (kala-azar): A retrospective study of 57 patients in Brazil. Braz J Infect Dis 2008;12:329-32.