- Open Access
Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
Malaria Journal volume 13, Article number: 163 (2014)
Malaria in highland areas of Kenya affects children and adults. Local clinicians include symptoms other than fever when screening for malaria because they believe that fever alone does not capture all cases of malaria.
Individuals who presented to dispensaries in a highland Kenya site of low, unstable malaria transmission from 2007–2011 with 1 or more of 11 symptoms were tested by microscopy for malaria. Clinical malaria was defined as asexual Plasmodium falciparum infection on peripheral blood smear in an individual with any screening symptom. Asymptomatic P. falciparum infection was assessed in a cohort at ten time points to determine the extent to which symptomatic episodes with parasitaemia might be attributable to baseline (asymptomatic) parasitaemia in the community.
3,420 individuals were screened for malaria, 634 < 5 years of age and 2,786 ≥ 5 years of age. For the diagnosis of clinical malaria, the symptom of fever had a sensitivity and specificity of 88.9% and15.4% in children <5 years, and 55.8% and 54.4% in children ≥5 years, respectively. Adding the symptom of headache increased sensitivity to 94. 4% in children <5 years and 96.8% in individuals ≥5 years, but decreased specificity to 9.9% and 11.6%, respectively, and increased the number of individuals who would be tested by 6% and 92%, respectively. No combination of symptoms improved upon the presence fever or headache for detection of clinical malaria. In the cohort of asymptomatic individuals, P. falciparum parasitaemia was infrequent (0.1%).
In areas of low, unstable malaria transmission, fever is a sensitive indicator of clinical malaria in children <5 years, but not in older children and adults. Adding headache to fever as screening symptom increases sensitivity of detection in individuals ≥5 years old at the cost of decreased specificity. Screening for symptoms in addition to fever may be required to accurately capture all cases of clinical malaria in individuals ≥5 years old in areas of low malaria transmission.
Fever is the universal screening symptom for malaria in research studies [1–4], but the highland areas of Kenya are unusual in that they have historically had little malaria incidence. Malaria appears to have been introduced by rail and travel of persons from endemic populations to highland areas for tea planting and harvesting in the early 1900s [5, 6]. Thus, families in this area have not had generations of exposure to malaria, as have families in nearby areas, such as Nyanza Province [7, 8]. This is supported by the relative lack of sickle cell trait and G6PD deficiency in individuals in the highland areas as compared to individuals in lowland areas . Thus symptoms and immunity in this population may differ from those in populations with a long history of exposure (e.g. Nyanza Province) and in populations with no exposure for decades (e.g. the United States and Europe). In the highland sites of Kipsamoite and Kapsisiywa, in Nandi North District, Rift Valley Province, Kenya, where our research team has conducted malaria research for the past decade, local clinical officers state that they must inquire about symptoms in addition to fever to capture all cases of malaria.
Kipsamoite and Kapsisiywa experienced an atypical situation in 2007, when widespread indoor residual spraying (IRS) with long-lasting insecticides and introduction of artemisinin combination therapy with artemether-lumefantrine (Coartem©) led to a 14-month period with no clinical cases of malaria and possible interruption of malaria transmission . After this period, asymptomatic parasitaemia has been infrequent in these communities, providing a unique opportunity to study the sensitivity and specificity of fever and other symptoms for P. falciparum parasitaemia, which at this point occur almost exclusively in individuals with symptoms that lead them to seek evaluation and treatment at the health dispensaries on site. Individuals with any of eleven symptoms considered consistent with malaria by study clinical officers were tested for malaria by microscopy. In the present study, sensitivity and specificity of individual symptoms and combinations of symptoms for clinical malaria were assessed, with the primary definition of clinical being P. falciparum parasitaemia in any symptomatic individual. Sensitivity and specificity of individual symptoms and combinations of symptoms for alternate definitions of clinical malaria were also assessed, including: (1) P. falciparum parasitaemia with measured fever (axillary temperature ≥37.5°C), (2) P. falciparum parasitaemia ≥ 1,000 parasites/μL with measured fever, or (3) P. falciparum parasitaemia ≥ 4,000 parasites/μL with measured fever.
Study population and recruitment
The study was conducted in the Kenyan highland sites of Kipsamoite (population ~4,800) and Kapsisiywa (population ~4,000), Nandi County, from 2007 to 2011. Elevation ranges from 1,887 m to 2,132 m at these sites. The area has seasonal, unstable malaria transmission and a history of past malaria epidemics and a recent possible interruption of malaria transmission from April 2007 to May 2008, with no clinical cases of malaria identified in that period . Persons living in these areas are predominantly Nandi, a Kalenjinsub-tribe. Written informed consent for study participation was obtained from heads of households in the area for demographic studies and from individuals (or parents or guardians of persons <15 years of age) for other studies. Ethical approval for the study was obtained from the Kenya Medical Research Institute National Ethical Review Committee and the Institutional Review Board for Human Studies at the University of Minnesota.
Demography and surveillance for clinical malaria and asymptomatic parasitaemia
Demographic surveys and malaria surveillance were performed in these areas. Demography of households was done annually. Surveillance for clinical malaria was conducted at the Kenyan Ministry of Health dispensaries in both sites, which are the only health care facilities within the area. Free malaria diagnosis and treatment were available to all persons within the area. Individuals with symptoms consistent with malaria who did not have a clear alternative diagnosis were tested for Plasmodium species by microscopic examination of blood smears. The symptoms were determined by local clinical officers and included fever, chills, headache, loss of appetite, vomiting, jaundice, diarrhea, backache, joint pains, nausea, and severe malaise. Microscopy was performed as previously described  with2 independent readings and a third reading for slides with discordant results. All persons with positive blood smears for P. falciparum or Plasmodium malariae, the only Plasmodium species documented in this area, were treated with artemether-lumefantrine (Coartem©). In order to determine the extent to which baseline asymptomatic parasitaemia in the community might contribute to parasitaemia detected in symptomatic individuals, ten surveys for asymptomatic P. falciparum parasitaemia were conducted in a cohort of randomly selected individuals from the sites between2007 and 2011.
Since clinical immunity to malaria differs in most populations in children <5 years of age as compared to individuals ≥5 years of age, analyses were done separately for individuals in these two age groups. Frequency of symptoms in individuals with versus without parasitaemia was compared by c2 testing. Logistic regression was conducted to compare odds of having P. falciparum parasitaemia or P. falciparum parasitaemia with a measured temperature ≥37.5°C with a specific symptom. Data were analysed using Stata Version 11 (Stata Corp, College Station, Texas, USA) and R(R Foundation, Wien, Austria).
Sensitivity and specificity of specific symptoms for clinical malaria
During the study period, only 3/3,420 smears done were positive for P. malariae (0.09%), so only the results for individuals positive for P. falciparum were analysed. From 2007 to 2011, 3,420 individuals were screened for malaria, and P. falciparum parasitaemia was detected in 224 individuals (6.5%), including 36/634 children <5 years (5.7%) and 188/786 individuals ≥5 years (6.7%, P = 0.33). The median parasite density was 30,700 (IQR 10,770 - 135390), and did not differ in children <5 years (768 [IQR 295–3202]) compared to individuals ≥5 years (19,420 [IQR 3230–56,920], P = 0.32).
The frequency of individual symptoms for clinical malaria, defined as P. falciparum parasitaemia in a person with any of the eleven symptoms, along with the sensitivity and specificity of each symptom, are presented in Table 1 for children <5 years and in Table 2 for individuals ≥5 years. Findings for clinical malaria defined as symptomatic P. falciparum parasitaemia with measured fever (axillary temperature ≥ 37.5°C) are summarized in Additional files 1 and 2. Negative and positive predictive values are not shown, because the low frequency of P. falciparum parasitaemia in participants seen at these clinics led to high negative predictive values (all >96%) and low positive predictive values (all <16%) for all symptoms assessed.
Symptoms with the greatest specificity lacked sensitivity (e.g. chills in children < 5 years had a specificity 91%, but a sensitivity of only 28%), and those with the greatest sensitivity lacked specificity (e.g. fever in children <5 years had a sensitivity of 89%, but a specificity of only 15%). Of particular interest, fever in individuals ≥ 5 years was neither sensitive (56%) nor specific (54%).
Odds of clinical malaria with specific symptoms
Table 3 summarizes the odds ratios for presence of each symptom for clinical malaria in children <5 years and individuals ≥ 5 years. Individuals <5 years and ≥5 years with P. falciparum parasitaemia were significantly more likely to have headache, malaise, and chills than those without parasitaemia. Individuals ≥5 years with P. falciparum parasitaemia were also significantly more likely to have fever and vomiting, and significantly less likely to have diarrhoea, than those without parasitaemia. Findings for the outcome of P. falciparum parasitaemia with measured fever (axillary temperature ≥37.5°C) were very similar and are summarized in Additional file 3.
Sensitivity and specificity of combinations of symptoms for P. falciparum parasitaemia
To assess whether any combination of symptoms could improve on fever for sensitivity and specificity of detection of clinical malaria, a three-step process was undertaken: (1) candidate subsets of symptoms to consider were selected; (2) for each candidate subset of symptoms, a logistic regression model was fitted including those symptoms; (3) the logistic regression results were used to define rules and estimate their sensitivity and specificity. The results of this assessment are summarized in Table 4 (for individuals <5 years) and Table 5 (for individuals ≥ 5 years).
As documented in Tables 4 and 5, no combination of symptoms had higher sensitivity than presence of fever or headache for detection of clinical malaria, although this combination had poor specificity. Some symptom groupings had improved specificity, but always at the cost of sensitivity. A combination of fever or headache achieved a sensitivity of 94% and 97% for individuals <5 years and ≥5 years respectively (Tables 4 and 5), but at the cost of greatly decreased specificity (6. 5%) in individuals ≥5 years. The addition of headache increased the number of children <5 years who would be tested for P. falciparum infection by only two persons (6%), but increased the number of individuals ≥5 years who would be tested by 1,190 persons (92%).
To assess whether more stringent criteria for a definition of clinical malaria would result in different findings, sensitivity and specificity of symptom combinations was assessed for a number of stricter definitions of clinical malaria, as noted in Tables 4 and 5. Similar patterns were seen for all alternate definitions of clinical malaria. Finally, measured fever was incorporated in the clinic into the “symptom” predictor variable. For the primary definition of clinical malaria (symptomatic P. falciparum parasitaemia), having a history of fever or measured fever in the clinic had a sensitivity and specificity of 94% and 11%, respectively, for children <5 years, and 78% and 44%, respectively, for persons ≥5 years.
Prevalence of asymptomatic parasitaemia
Six hundred and four randomly selected individuals from the site were assessed for presence of asymptomatic parasitaemia in July and November 2007, March, August and October 2008, February, April, August and October 2009, and May 2010. Due to movement of individuals during the study period, different numbers were tested at each time point, but during the three-year period, only five persons out 5,195 tested had asymptomatic parasitaemia (0.1%), with a median parasite density of 240 (interquartile range [IQR], 200–2,560).
Fever is the universal screening tool for clinical malaria in research studies. This is likely appropriate in children <5 years, who constitute the majority of malaria cases in highly endemic areas, because they are more likely to develop fever when they have infection than are older individuals. However in areas such as the highland area of the present study, a substantial proportion of clinical malaria occurs in individuals ≥5 years  and local clinicians state that fever alone does not detect all cases of malaria in these individuals. The present study supports this claim. Almost half of individuals ≥ 5 years who came to the clinic with symptoms of illness and who had P. falciparum parasitaemia would not have been captured as malaria cases had history of fever been the sole screening criterion. A recent study by D’Acremont et al. found that in one area of Tanzania, malaria was a less common cause of fever than other infections, notably respiratory viral infection . The present study answers the inverse question (does fever as a symptom capture all cases of clinical malaria?), and finds that in areas of low malaria transmission, fever alone may not be an adequate screening criterion for malaria.
A history of fever may be absent in individuals ≥5 years with parasitaemia for several reasons. Fever may be less evident in older children and adults than in younger children, whose temperature may be checked or noted by their parent. This is supported by the only modest increase in sensitivity of a history of fever among individuals ≥5 years who had a measured fever at the clinic. In areas of higher transmission, parasitaemia could be incidental rather than causative of symptoms. However in this area, based on the surveys done, one would expect <0.2% of individuals to have asymptomatic parasitaemia, so incidental parasitaemia should account for only a tiny fraction of the parasitaemia in symptomatic individuals seen in the clinic. In addition, history of fever had sensitivity only 65% even for clinical malaria defined as parasitaemia > 4,000 parasites/μL and a measured fever at the clinic, individuals who in this context indisputably have clinical malaria. The Nandi words for each symptom, including fever, were carefully reviewed with our study field assistants, and verified by the clinical officers and the local advisory group, and the symptom of fever was highly sensitive for detection of parasitaemia in young children, so confusion about the term is unlikely. The most likely explanation seems to be that other symptoms precede fever in older individuals. These symptoms bring them to the dispensary, at which time some have measured fever but others remain afebrile. Given the clinical course of malaria, all of these individuals were likely to have a fever eventually, but in a dispensary setting, particularly in an area of low transmission that is working toward elimination, one wants to detect malaria early and accurately. Individuals with malaria who have symptoms other than fever, but are not tested or treated because fever is the sole screening criterion, are likely to go outside the health system, and potentially receive inappropriate treatment.
Unfortunately, no symptom combination emerged that would allow us to detect >90% cases of parasitaemia in individuals ≥5 years without screening many more uninfected individuals. A previous study in highland Uganda found that a history of fever or presence of measured fever at the clinic had a sensitivity of 95.7% and a specificity of 25.5% , but the findings were not separated by age. In the present study, reported or measured fever had a sensitivity and specificity of only 78% and 44%, respectively, for individuals ≥5 years, so reported or measured fever alone would not be adequate for screening in older individuals. The simplest combination of symptoms that achieved approximately 95% sensitivity in individuals ≥ 5 years was fever or headache (sensitivity 96.8%), but screening with these two symptoms increased the number of individuals ≥ 5 years to be screened to almost twice what was required with fever (from 1,290 to 2,480). Headache has been noted in the travel medicine literature to be a frequent complaint in adult travellers with malaria, though most travellers with malaria also have fever . The presence of fever early in travellers, but not in this highland population, may be due to partial immunity from prior exposure in this population, resulting parasitaemia that does not produce immediate fever but does produce other lower-grade symptoms such as headache.
Definitions that relied on more symptoms were more complex, but did not have better sensitivity than asking about fever or headache, so in the present study site, fever or headache will be used as screening symptoms because they are the best single set of screening symptoms that will capture ≥95% individuals with clinical malaria. An alternative would be to wait for individuals to come in for a repeat visit, since malaria likely will eventually result in fever in all individuals, but this would lead to missed chances to diagnose malaria, to prolonged parasitaemia in symptomatic individuals, and potentially to lost confidence in the health dispensary. The findings of the present study may have applicability to other sites of unstable transmission, and in these areas analysis of symptoms should be done to determine if screening for fever alone can detect >95% of individuals who have clinical malaria.
An interesting incidental finding is that the absence of diarrhoea had 96% sensitivity for detection of clinical malaria in individuals ≥5 years. The finding probably reflects a combination of the low incidence of clinical malaria at this site, the frequency of diarrhoea as an illness, the multiple other causes of diarrhoea in this area, and the relatively low frequency of diarrhoea as a symptom of malaria. The study findings contrast with those of Coldren et al., who found a modest association between P. falciparum parasitaemia and a history of diarrhoea in adults from three areas of Kenya with differing malaria transmission intensity . The differences may in part reflect different populations: the present study was restricted to an area of very low endemicity and included children as well as adults.
The present study documents that in a highland area of unstable transmission, where asymptomatic parasitaemia is rare, the symptom of fever alone is adequate for detection of clinical malaria in individuals <5 years but not in individuals ≥5 years. In areas of high malaria transmission, malaria occurs most often in children and is deadliest in children [17–21], so a history of fever, which detects almost all cases of malaria in young children, is a reasonable screening criterion. However, as more areas become areas of low transmission, disease in adults and adolescents may form a larger part of the clinical burden, and additional symptoms may be needed to identify all potential cases. Individuals in areas of unstable, low transmission differ from individuals in areas of high transmission, who have strong clinical immunity, and travellers from non-malaria endemic areas, who have little or no immunity. The intermediate initial presentation of low-grade symptoms, such as headache, may reflect their partial clinical immunity. Studies in other areas of unstable transmission should be conducted to confirm the results of the present study.
Muhe L, Oljira B, Degefu H, Enquesellassie F, Weber MW: Clinical algorithm for malaria during low and high transmission seasons. Arch Dis Child. 1999, 81: 216-220. 10.1136/adc.81.3.216.
Luxemburger C, Nosten F, Kyle DE, Kiricharoen L, Chongsuphajaisiddhi T, White NJ: Clinical features cannot predict a diagnosis of malaria or differentiate the infecting species in children living in an area of low transmission. Trans R Soc Trop Med Hyg. 1998, 92: 45-49. 10.1016/S0035-9203(98)90950-6.
D’Acremont V, Lengeler C, Genton B: Reduction in the proportion of fevers associated with Plasmodium falciparum parasitaemia in Africa: a systematic review. Malar J. 2010, 9: 240-10.1186/1475-2875-9-240.
Chandramohan D, Jaffar S, Greenwood B: Use of clinical algorithms for diagnosing malaria. Trop Med Int Health. 2002, 7: 45-52. 10.1046/j.1365-3156.2002.00827.x.
Matson AT: The history of malaria in Nandi. East Afr Med J. 1957, 34: 431-441.
Campbell JM: Malaria in the Uasin Gishu and the Trans Nzoia, Kenya. East Afr Med J. 1929, 6: 32-43.
Fontaine RE, Najjar AE, Prince JS: The 1958 malaria epidemic in Ethiopia. Am J Trop Med Hyg. 1961, 10: 795-803.
Lindsay SW, Martens W: Malaria in the African highlands: past, present and future. Bull World Health Organ. 1998, 76: 33-45.
Moormann AM, Embury PE, Opondo J, Sumba OP, Ouma JH, Kazura JW, John CC: Frequencies of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency differ in highland and nearby lowland malaria-endemic areas of Kenya. Trans R Soc Trop Med Hyg. 2003, 97: 513-514. 10.1016/S0035-9203(03)80010-X.
John CC, McHugh MM, Moormann AM, Sumba PO, Ofulla AV: Low prevalence of Plasmodium falciparum infection among asymptomatic individuals in a highland area of Kenya. Trans R Soc Trop Med Hyg. 2005, 99: 780-786. 10.1016/j.trstmh.2005.04.012.
John CC, Moormann AM, Pregibon DC, Sumba PO, McHugh MM, Narum DL, Lanar DE, Schluchter MD, Kazura JW: Correlation of high levels of antibodies to multiple pre-erythrocytic Plasmodium falciparum antigens and protection from infection. Am J Trop Med Hyg. 2005, 73: 222-228.
Rolfes MA, McCarra M, Magak NG, Ernst KC, Dent AE, Lindblade KA, John CC: Development of clinical immunity to malaria in highland areas of low and unstable transmission. Am J Trop Med Hyg. 2012, 87: 806-812. 10.4269/ajtmh.2012.11-0530.
D’Acremont V, Kilowoko M, Kyungu E, Philipina S, Sangu W, Kahama-Maro J, Lengeler C, Cherpillod P, Kaiser L, Genton B: Beyond malaria–causes of fever in outpatient Tanzanian children. N Engl J Med. 2014, 370: 809-817. 10.1056/NEJMoa1214482.
Lindblade KA, Katungu I, Wilson ML: Fever and malaria in highland Uganda. Trans R Soc Trop Med Hyg. 2001, 95: 502-503. 10.1016/S0035-9203(01)90018-5.
Pherez FM, Cunha BA: Diagnostic importance of headache as a key symptom in suspecting malaria in adult returning travelers. Travel Med Infect Dis. 2009, 7: 383-384. 10.1016/j.tmaid.2009.09.004.
Coldren RL, Prosser T, Ogolla F, Ofula VO, Adungo N: Literacy and recent history of diarrhoea are predictive of Plasmodium falciparum parasitaemia in Kenyan adults. Malar J. 2006, 5: 96-10.1186/1475-2875-5-96.
Rowe AK, Rowe SY, Snow RW, Korenromp EL, Schellenberg JR, Stein C, Nahlen BL, Bryce J, Black RE, Steketee RW: The burden of malaria mortality among African children in the year 2000. Int J Epidemiol. 2006, 35: 691-704. 10.1093/ije/dyl027.
Kleinschmidt I, Schwabe C, Benavente L, Torrez M, Ridl FC, Segura JL, Ehmer P, Nchama GN: Marked increase in child survival after four years of intensive malaria control. Am J Trop Med Hyg. 2009, 80: 882-888.
Korenromp EL, Williams BG, Gouws E, Dye C, Snow RW: Measurement of trends in childhood malaria mortality in Africa: an assessment of progress toward targets based on verbal autopsy. Lancet Infect Dis. 2003, 3: 349-358. 10.1016/S1473-3099(03)00657-1.
Malaria Fact Sheet. 2013, WHO. 2013. Malaria Fact Sheet. http://www.who.int/mediacentre/factsheets/fs094/en/ (accessed 24/06/2013).
Snow RW, Craig MH, Newton C, Steketee RW: The public health burden of Plasmodium falciparum malaria in Africa. Working Paper 11. Disease Control Priorities Project, Bethesda, Maryland, USA: Fogarty International Center, National Institutes of Health; 2003
We would like to thank the study participants for their participation in the study, Jackson Abuya and the field microscopy team for reading blood smears, study clinical officers for clinical evaluation and study field assistants for site demography. The study was supported by grants U0AI056270 from the National Institutes of Allergy, Immunology, and Infectious Disease; D43TW0080085 from the Fogarty International Center; and a University of Minnesota Department of Pediatrics Amplatz Research award. This paper was published with the permission of the Director, Kenya Medical Research Institute.
The authors declare that they have no competing interests.
ALM conceptualized the study, conducted literature review, performed data analysis and draftedthe manuscript. PC did data cleaning and initial data analysis. GA and WO reviewed the analysis and manuscript and provided key comments on manuscript revision. JSH conducted data analysis and helped to draft the initial and final manuscript. CCJ provided the study design, and oversaw data analysis, programme implementation, drafting of manuscript, and review of the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Plasmodium falciparum parasitaemia with plus a measured axillary temperature ≥37.5°C in children <5 years of age.(DOC 78 KB)
Additional file 2: Plasmodium falciparum parasitaemia plus a measured axillary temperature ≥37.5°C in individuals ≥5 years of age.(DOC 78 KB)
Additional file 3: P. falciparum parasitaemia with a measured axillary temperature ≥37.5°C.(DOC 82 KB)
About this article
Cite this article
Mutanda, A.L., Cheruiyot, P., Hodges, J.S. et al. Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission. Malar J 13, 163 (2014). https://doi.org/10.1186/1475-2875-13-163
- Plasmodium falciparum
- Unstable transmission