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Trend analysis of malaria prevalence in Halaba special district, Southern Ethiopia
BMC Research Notes volume 12, Article number: 190 (2019)
The study aimed to determine the prevalence of malaria in Halaba special district, Southern Ethiopia, from 2013 to 2017.
Of a total 583,668 malaria suspected cases examined during the study period, 55,252 (9.5%) were microscopically confirmed to be positive for malaria, at the rate of 27,712 (50.2%) females and 27,540 (49.8%) males (P = 0.95). The highest prevalence of 8454 (15.3%) malaria cases were observed in Halaba health center, followed by Halaba district hospital, at 7290 (13.2%), while the lowest cases, 1765 (3.2%), were confirmed in Wejago health center. The highest prevalence of malaria, 25,716 (46.5%), was registered among the age group ≥ 15 year old (P = 0.006). Plasmodium vivax and Plasmodium falciparum were the two major malaria parasites detected in this study, with the prevalence of 33,855 (62.3%) and 21,397 (38.7%), respectively (P = 0.0001). The detected high prevalence of P. vivax in this study may clearly indicate that more attention has been given to control P. falciparum strains in the study area. This may be a great challenge for the achievement of malaria elimination goals. Therefore, all concerned bodies should act collaboratively to combat the high prevalence of P. vivax from the study district.
Malaria is major public health problems worldwide with an estimated 3.3 billion people is at risk of being infected with malaria and develop the disease and 1.2 billion are at high risk [1, 2]. Its burden is more concerning in poorest, children and pregnant women. Globally, an estimated 198 million cases and 584,000 deaths occurred due to malaria in 2013 . This figure is showing a decrease in malaria case incidence by 30% and mortality rates by 47% since 2000 . However, yet malaria remains a major public health problem in the world with significant medical, economic and social implications especially in sub-Saharan Africa countries . Malaria is a major public health concern in Ethiopia. About 75% of the country’s landmass is malarious and 60% of the population is at risk of developing the disease . Its prevalence and transmission in Ethiopia relay on altitude and rainfall . In Ethiopia, most malaria cases occur at altitude < 2000 m above sea levels . Its prevention and control strategies such as the use of insecticide treated bed-nets (ITNs), prompt and effective treatment of clinical cases, intermittent preventive treatment for pregnant women and under-five children, indoor residual spraying(IRS) are now being widely adopted across Ethiopia, with increasing amounts of coverage achieved . However, the coexistence of both Plasmodium falciparum and Plasmodium vivax malaria parasites create a challenge in prevention, control and elimination of the disease [10,11,12,13,14,15].
Halaba special district is the known malaria endemic area in Ethiopia . Unlike the national prevalence, the proportion of P. vivax and P. falciparum malaria parasites was 70% and 30% in the study district. In addition, the existence of anti-malaria drug-resistant P. falciparum strains was also reported from the same study area . Hence, despite few studies have been conducted in Halaba special district, as the knowledge level of the investigators, there has not been studied report in the last 5 years to show the trend of malaria prevalence. Therefore, this study was aimed to investigate the trend analysis of malaria prevalence in Halaba special district, Southern Ethiopia, from 2013 to 2017.
Materials and methods
Study setting and period
This study was conducted in Halaba special district, Southern Ethiopia. Halaba special district is located in Southern Nation, Nationalities and Peoples Region (SNNPR), at the distance of 85 km from Hawassa town and 310 km from Addis Ababa, the capital city of Ethiopia (Fig. 1). The study site is found within an altitude ranging from 1554 to 2149 m above sea level, and an astronomic location of 38°7′0″E longitude and 7°18′0″N latitude. Halaba special district is generally characterized by dry climatic condition with about 86% mid-land (Weinadega) and 14% law-land (Kola) zones. The mean annual rainfall of the study area is ranging from 857 to 1085 mm, while the mean annual temperature varies from 17 to 20 °C with a mean value of 18 °C. The district has a total population of 259,810, which encompasses 129,893 males and 129,917 females . The study was conducted between March to May 2018.
Retrospective blood film malaria reports from Halaba special district hospital and health centers between September 2013 to August 2017 were carefully analyzed.
The study population and data collection
The study population was all malaria blood film tested individuals at Halaba special district hospital and health centers during the study period. To assess the participants’ condition, socio-demographic and laboratory data were collected from patients’ registration book. The meteorological data were collected from the nearby meteorological agency.
The data was entered into excel Microsoft and analyzed by using statistical package for social sciences software SPSS version 20.0. Pearson correlation analysis was used to evaluate the association between dependent and independent variables. In all cases P value < 0.05 was considered as statistically significant.
This study was conducted after obtaining the ethical clearance from the College of Natural and Computational Sciences, Addis Ababa University. Permission letter was also obtained from Halaba special district Health office to use the described retrospective malaria morbidity data.
During the last 5 years period, from September 2013 to August 2017, a total of 583,668, blood smears were prepared and examined from malaria-suspected patients at Halaba special district health centers and hospitals for detection of the malaria parasite. Of these, 55,252 (9.5%) were microscopically confirmed malaria cases. Demographically, 27,540 (49.8%) of the patients were males and 27,712 (50.2%) were females. With regard to area, Halaba health center holed the highest (15.3%) malaria prevalence followed by Halaba district hospital (13.2%) and Guba health center (12.8%) while the lowest malaria cases were reported from Wejago health center (3.2%). There was a statistically significant variation (P = 0.002) in malaria prevalence among the areas (Fig. 2).
The highest malaria case was reported 41.2% in 2013 while the lowest case 5.1% was reported in 2017. However, the prevalence of P. vivax was seen increased, the lowest prevalence was 56.5% in 2013 and the highest prevalence was 67.2% in 2017, while the P. falciparum was observed decreased from 43.5% in 2013 to 5.1% in 2017. Overall, the prevalence of P. falciparum was 38.7% whereas that of P. vivax was 61.3% (Table 1).
With regard to meteorological data, at 1 month lag of rainfall, the prevalence of malaria was seen increased. There was a statistically significant variation (P = 0.0001) between malaria distribution and meteorological data (Table 1). There were no reported mixed infections during the study period. P. vivax was consistently more prevalent than P. falciparum irrespective of season.
Malaria was detected in all age groups in the study district but the age group ≥ 15 years were highly affected, with the prevalence rate of 25,716 (46.5%), followed by ≤ 4 year olds and 5–14 year olds with the prevalence rates of 17,231 (31.2%) and 12,305 (22.3%), respectively. There was statistical significant variation (P = 0.006) in malaria prevalence among the age groups. In all age groups P. vivax was seen predominant species. With regard to the sex, prevalence of 27,540 (49.8%) was reported for males and 27,712 (50.2%) for females. There was no statistical significant variation (P = 0.95) in malaria distribution among sex.
Malaria is a major public health concern in Ethiopia. About 75% of the country’s landmass is malarious and 60% of the population is at risk of developing the disease . This retrospective study was aimed at evaluating 5-year trends of malaria prevalence in Halaba special district, Southern Ethiopia, from 2013 to 2017.
In the present study, the highest prevalence of malaria was treated in Halaba health center followed by Halaba district hospital and Guba health center whereas the lowest cases were confirmed in Wejago health center. The findings were higher than the previous report from the same study site by . The climatic change and laboratory capacity to detect the parasite might be contributed to the existing variation.
The declining trend of malaria prevalence observed in the study district onwards 2013 was attributed to the existing better malaria prevention and control strategies . The same trend has also been reported from different parts of the world including Eritrea , Zanzibar , Kenya  and South Africa  where proper usage of insecticide treated bed nets (ITNs) and indoor residual spraying (IRS) have reduced malaria prevalence. In agreement with the previous study  reported from Halaba, the prevalence of malaria, in the current study was slightly higher among females than males. In contrast, [6, 24] reported a higher malaria infection rate among males in northwest Ethiopia. The variation was may be due to a demographically large number of females in the current study area.
In the present study, malaria was detected in all age groups although the age group ≥ 15 years were highly affected, with the prevalence rate of 51,432 (46.5%), followed by ≤ 4-year-olds and 5–14-year-olds with the prevalence rates of 34,462 (31.2%) and 25,610 (22.3%), respectively. The finding was in agreement to what was recorded in Butajira area  and Halaba district  where a high prevalence of malaria in the age group 0–4 years and ≥ 15 years reported, respectively. This could be due to low immune status and less self-protection from vector among children and frequent outdoor spending of adults.
In the current study, the highest peak of malaria prevalence was registered in the months between (Sept–Dec) with the lowest reported prevalence in Jan, Feb, Jun, and Jul. This finding is in agreement with the studies reported from Ethiopia [10, 26], from China , and from India , where the positive correlation was observed between monthly rainfall and malaria parasite incidence. This may be because climatic and environmental factors other than rainfall could also determine the occurrence of malaria.
Plasmodium falciparum and P. vivax were the two species of malaria parasites detected in the current study. This was in line with the national profile of Plasmodium species . However, the proportion of P. falciparum 38.7% and P. vivax 61.3% was quite different from the national prevalence of 60% and 40% for P. falciparum and P. vivax, respectively. In agreement with this, several studies  from Wonago  from Butajira  from South-central, Ethiopia  from Butajira  from China and  from India, reported a high prevalence of P. vivax in their studies. In contrast with this finding , from Gondar,  form Bahirdar  from Serbo town and  from Southwest Ethiopia reported a high prevalence of P. falciparum. This could be due to the difference in the study area, study period, climate, malaria control, and prevention strategies and laboratory capacities.
In this study, the overall malaria prevalence was dominated by P. vivax. The spread of chloroquine-resistant P. vivax may be one possible reason for the dominance of P. vivax in the study area [8, 38, 39]. The existence of chloroquine-resistant P. vivax has also been reported from the study district by different authors [40, 41]. Moreover, the high prevalence of P. vivax in the present study may also be an indication of the presence of people that are negative for Duffy antigen expression in Ethiopia (.
Overall, the observed declining trend of malaria prevalence in Halaba special district onwards 2013 is suggestive for the existence of possible malaria control and prevention measures. But the existence of high prevalence P. vivax in the study district indicating that, much attention has been given to control P. falciparum. This could be a great challenge for the success of ongoing malaria elimination programme in Ethiopia. Therefore, concerned bodies should act aggressively in order to control the high prevalence of P. vivax in Halaba special district, Southern Ethiopia. Further detailed investigation emphasizing P. vivax chloroquine resistance pattern should also be needed.
Since this study was conducted using secondary data obtained from patients’ health record, being as any secondary data it is liable to disadvantages but we are familiar with the data set and critical analysis which the data was subjected to make the conclusion valid.
in-door residual spraying
insecticide treated bed-nets
Southern Nation, Nationalities and Peoples Region
WHO. World Health Organization: World malaria report 2011. Geneva.
Iwuafor AA, Egwuatu CC, Nnachi AU, Akujobi CN, Ita IO, Ogban GI, Egwuatu TO. Malaria related febrile illness and the use of insecticide-treated nets (INTs) for malaria control amongst under-5 year old children in Calabar, Nigeria. BMC J Inf Dis. 2016;16:151.
WHO. World Health organization: World malaria report 2013. Geneva.
WHO. World Health Organization: World malaria report 2014. Geneva.
Isah AY, Amanabo MA, Ekele BA. Prevalence of malaria parasitaemia amongst asymptomatic pregnant women attending a Nigerian hospital. Ann Afr Med. 2011;10(2):171–4.
Alemu A, Muluye D, Mihiret M, Adugna M, Gebeyaw M. Ten year trend analysis of malaria prevalence in Kola Diba, North Gondar, Northwest, Ethiopia. Parasites Vectors. 2012;5(173):1–6.
Deressa W, Ali A, Enqusellassie F. Self-treatment of malaria in rural communities, Butajira, southern Ethiopia. Bull World Health Organ. 2003;81:261–8.
Ketema T, Getahun K, Bacha K. Therapeutic efficacy of chloroquine for treatment of Plasmodium vivax malaria cases in Halaba district, South Ethiopia. Parasites Vectors. 2009;4:46.
Yewhalaw D, Wassie F, Steurbaut W, Spanoghe P, Bortel VW, Denis L, et al. Multiple insecticide resistance: an impediment to insecticide based malaria vector control program. PLoS ONE. 2011;6(1):e16066.
Alemu A, Abebe G, Tsegaye W, Golassa L. Climatic variables and malaria transmission dynamics in Jimma town, South West Ethiopia. Parasites Vectors. 2011;4:30.
FMoH. Federal Ministry of Health of Ethiopia: National strategic plan for malaria prevention, control and elimination in Ethiopia, 2011–2015. Ethiopia: Addis Ababa; 2010.
WHO. World Health Organization: World malaria report 2016. Geneva.
WHO. World Health Organization report: guidelines for the treatment of malaria. 3rd ed. Geneva: World Health Organization; 2015.
World Bank. World Development Indicator: Poverty rate at international poverty lines. http://wdi.worldbank.org/table/28.2014. Accessed 24 Nov 2018.
SNNPR. Southern Nations, Nationalities and People’s Region Health Bureau Malaria Annual Report (EFY 2007), Hawassa, Ethiopia. 2015.
Ketema T, Getahun K, Bacha K. Therapeutic efficacy of chloroquine for treatment of Plasmodium vivax malaria cases in Halaba district, South Ethiopia. Parasites Vectors. 2011;4:46.
Abeku TA, Helinski ME, Kirby MJ, Kefyalew T, Awano T, Batisso E, et al. Changes in malaria epidemiology and effectiveness of interventions in Ethiopia and Uganda: beyond Garki project baseline survey. Malar J. 2015;14:337.
Nyarango PM, Gebremeskel T, Mebrahtu G, Mufunda J, Abdulmumini U, Ogbamariam A, et al. A steep decline of malaria morbidity and mortality trends in Eritrea between 2000 and 2004: the effect of combination of control methods. Malar J. 2006;5:33.
Bhattarai A, Ali AS, Kachur SP, Martensson A, Abbas AK, Khatib R, et al. Impact of artemisinin-based combination therapy and insecticide-treated nets on malaria burden in Zanzibar. PLoS Med. 2007;4(11):e309.
Fegan GW, Noor AM, Akhwale WS, Cousens S, Snow RW. Effect of expanded insecticide-treated bednet coverage on child survival in rural Kenya: a longitudinal study. Lancet. 2007;370(9592):1035–9.
Kleinschmidt BL, Streat I, Maharaj E, Barnes R, Durrheim KI, et al. Seven years of regional malaria control collaboration–Mozambique, South Africa, and Swaziland. Am J Trop Med Hyg. 2007;76(1):42–7.
Tefera G. Prevalence of malaria and associated factors among patients attending at Hallaba Health Centre, Southern Ethiopia. Immunol Infect Dis. 2014;2:25–9.
Ferede G, Worku A, Getaneh A, Ahmed A, Haile T, Abdu Y, et al. Prevalence of malaria from blood smears examination: a seven-year retrospective study from Metema hospital, Northwest Ethiopia. Malar Res Treat. 2013;2013:704–30.
Tesfaye S, Belyhun Y, Teklu T, Medhin G, Mengesha T, Petros B. Malaria pattern observed in the highland fringe of Butajira, Southern Ethiopia: a ten-year retrospective analysis from parasitological and metrological data. MWJ. 2012;3(5):1–8.
Gebretsadik D, Getacher Feleke D, Fiseha M. Eight-year trend analysis of malaria prevalence in Kombolcha, South Wollo, North-central Ethiopia: a retrospective study. Parasites Vectors. 2018;11(55):2–6.
Xiao D, Long Y, Wang S, Fang L, et al. Spatiotemporal distribution of malaria and the association between its epidemic and climate factors in Hainan, China. Malar J. 2010;9:185.
Pemola DN, Jauhari RK. Climatic variables and malaria incidence in Dehradun, Uttaranchal, India. J Vect Borne Dis. 2006;43:21–8.
Tadesse F, Fogarty AW, Deressa W. Prevalence and associated risk factors of malaria among adults in East Shewa Zone of Oromia Regional State, Ethiopia: a cross-sectional study. BMC Public Health. 2018;18(25):1–8.
Molla E, Bedane A. Malaria prevalence and its associated risk factors among patients attending Chichu and Wonago health centers, South Ethiopia. JRHS. 2016;16(4):185–9.
Dedgeba S, Mamo H. Malaria trends in Silt’i district from 2009–2015 and current childhood malaria in K’ibbet hospital, south-central Ethiopia. MWJ. 2017;8(22):1–5.
Woyessa A, Deressa W, Ali A, Lindtjørn B. Prevalence of malaria infection in Butajira area, south-central Ethiopia. Malar J. 2012;11:84.
Wange X, Yang L, Jiang T, Zhang B, Wang S, Wu Z, et al. Effects of a malaria elimination program: a retrospective study of 623 cases from 2008 to 2013 in a Chinese county hospital near the China–Myanmar border. Emerg Microb Inf. 2016;5:e6. https://doi.org/10.1038/emi.2016.6.
Nidhish G, Pushpalatha E, Anju Viswan K. Incidence and prevalence of malaria in Thrissur district, kerala: a time series analysis. J Commun Dis. 2018;50(1):16–21.
Yimer M, Hailu T, Mulu W, Abera B, Ayalew W. A 5 year trend analysis of malaria prevalence within the catchment areas of Feleghiwot referral Hospital, Bahir Dar city, northwest-Ethiopia: a retrospective study. BMC Res Notes. 2017;10(239):1–4.
Karunamoorthi K, Bekele M. Changes in malaria indices in an ethiopian health centre: a five year retrospective analysis. Health Scope. 2012;1(3):118–26.
Sena L. Analysis of spatiotemporal dynamics and associ lectric dam and control villages, Jimma zone, Southwest Ethiopia. Ph.D. Dissertation, Addis Ababa, Ethiopia. 2015.
Teka H, Petros B, Yamuah L, Tesfaye G, et al. Chloroquineresistant Plasmodium vivax malaria in Debre zeit, Ethiopia. Malar. J. 2008;7:220.
Carrara VI, Sirilak S, Thonglairuam J, Rojanawatsirivet C, et al. Deployment of early diagnosis and mefloquineartesunate treatment of falciparum malaria in Thailand: the Tak Malaria Initiative. PLoS Med. 2006;3:e183.
Ketema T, Bacha K, Birhanu T, Petros B. Chloroquine resistant Plasmodium vivax malaria in Serbo town, Jimma zone, South-west Ethiopia. Malar J. 2013;8:177.
Getachew S, To S, Trimarsanto H, Thriemer K, Clark TG, Petros B, et al. Variationin complexity of infection and transmission stability between neighbouring populations of Plasmodium vivax in southern Ethiopia. PLoSONE. 2015;10(10):e0140780.
Woldearegai TG, Kremsner PG, Kun JF, Mordmüller B. Plasmodium vivax malaria in Duffy-negative individuals from Ethiopia. Trans R Soc Trop Med Hyg. 2013;107(5):328–31.
Mbanefo CE, Ahmed MA, Titouna A, Elmaraezy A, Trang TN, Long PN, et al. Association of glucose-6-phosphate dehydrogenase deficiency and malaria: a systematic review and meta-analysis. Sci Rep. 2017;7:45963.
TS conceptualized, designed the study, collected, analyzed and interpreted data, and wrote the manuscript; BP reviewed content and edited the whole part of the manuscript. Both authors read and approved the final manuscript.
The authors would very grateful to all staff members of Halaba special district health office, health centers and hospitals, Southern Ethiopia for their timely help by retrieving the case notes to carry out this study. Our heartfelt thanks also go to the National Meteorology Agency for providing us valuable meteorological data of Halaba district. The authors would also like to thank Addis Ababa University, College of Natural and Computational Sciences, for the provision of the ethical clearance to conduct the study.
The authors declare that they have no competing interests.
Availability of data and materials
All available data which served for the drawing of conclusion was included in the result section of the manuscript.
Consent for publication
Not applicable, because the manuscript does not include any individual personal data.
Ethics approval and consent to participate
Ethical approval for the study was granted by Addis Ababa University, College of Natural and Computational Sciences Institutional Review Board (CNS-IRB) Committee with Minute No. IBR/032/2018 & Ref. No. CNSDO/463/10/2018. Following official permission, support letters written by the university were submitted to the concerned bodies in the study district. Official permission letters were also granted from health offices of the study district prior to the actual data collection.
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Shamebo, T., Petros, B. Trend analysis of malaria prevalence in Halaba special district, Southern Ethiopia. BMC Res Notes 12, 190 (2019) doi:10.1186/s13104-019-4215-2
- Malaria prevalence
- Plasmodium spp.