|Year : 2016 | Volume
| Issue : 2 | Page : 61-67
|Role of serum lactate and malarial retinopathy in prognosis and outcome of falciparum and vivax cerebral Malaria: A prospective cohort study in adult assamese tribes
Kaustubh Suresh Chaudhari1, Sahil Prashant Uttarwar2, Nikhil Narayan Tambe3, Rohan S Sharma4, Anant Arunrao Takalkar5
1 Department of Internal Medicine and Infectious Disease, Vanvasi Kalyan Ashram, Kokrajhar, Assam, India
2 Department of Internal Medicine, Primary Health Center, Rajur, India
3 Department of Internal Medicine, M.G.M. Medical College, Navi Mumbai, India
4 Department of Internal Medicine, Dr. V. M. Government Medical College, Solapur, Maharashtra, India
5 Department of Preventive and Social Medicine, Navodaya Medical College, Raichur, Karnataka, India
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|Date of Web Publication||10-May-2016|
| Abstract|| |
Introduction: There is no comprehensive data or studies relating to clinical presentation and prognosis of cerebral malaria (CM) in the tribal settlements of Assam. High rates of transmission and deaths from complicated malaria guided us to conduct a prospective observational cohort study to evaluate the factors associated with poor outcome and prognosis in patients of CM. Materials and Methods: We admitted 112 patients to the Bandarpara and Damodarpur Tribal Health Centers (THCs) between 2011 and 2013 with a strict diagnosis of CM. We assessed the role of clinical, fundoscopy and laboratory findings (mainly lactic acid) in the immediate outcome in terms of death and recovery, duration of hospitalization, neurocognitive impairment, cranial nerve palsies and focal neurological deficit. Results: The case fatality rate of CM was 33.03% and the prevalence of residual neurological sequelae at discharge was 16.07%. These are significantly higher than the previous studies. The mortality rate and neurological complications rate in patients with retinal whitening was 38.46% and 23.07%, with vessel changes was 25% and 18.75%, with retinal hemorrhage was 55.55% and 11.11% and with hyperlactatemia was 53.85% and 18.46%, respectively. Three patients of papilledema alone died. Conclusion: Our study suggests a strong correlation between hyperlactatemia, retinal changes (whitening, vessel changes and hemorrhage) and depth and duration of coma with longer duration of hospitalization, increased mortality, neurological sequelae and death. Plasmodium vivax mono-infection as a cause of CM has been confirmed. Prognostic evaluation of CM is useful for judicious allocation of resources in the THC.
Keywords: Assam tribes, cerebral malaria, falciparum, lactic acid, papilledema, prognosis, retinopathy, vivax
|How to cite this article:|
Chaudhari KS, Uttarwar SP, Tambe NN, Sharma RS, Takalkar AA. Role of serum lactate and malarial retinopathy in prognosis and outcome of falciparum and vivax cerebral Malaria: A prospective cohort study in adult assamese tribes. J Global Infect Dis 2016;8:61-7
|How to cite this URL:|
Chaudhari KS, Uttarwar SP, Tambe NN, Sharma RS, Takalkar AA. Role of serum lactate and malarial retinopathy in prognosis and outcome of falciparum and vivax cerebral Malaria: A prospective cohort study in adult assamese tribes. J Global Infect Dis [serial online] 2016 [cited 2017 Mar 27];8:61-7. Available from: http://www.jgid.org/text.asp?2016/8/2/61/177524
| Introduction|| |
Malaria constitutes a significant public health problem in India and contributes 77% of the total malaria in Southeast Asia. In 2012 alone, the National Vector Borne Disease Control Program(NVBDCP) detected and treated 1.06 million cases, out of which, around 50% were due to Plasmodium falciparum. About 80% of the cases were restricted to a small indigenous population residing in remote, mountainous regions. About 30-40% of Assamese population is at a high risk of malaria. 
Assam contributes to more than 5% of malaria cases in India. Mosquitoes breed aggressively in the hot and humid climate with prolonged rainfall, periodic floods and vast forest ranges present in Assam. Lack of health care workers in tribal settings, far-off locations of tertiary health centers, paucity of referral services and transportation facilities, migration of population from high endemic areas and emergence of resistant parasites are important factors responsible for persistence of malaria in tribal zones of Assam. Of the total burden of malaria in India, North Eastern states contribute 10% malaria, 11% P. falciparum cases and 20% malaria deaths. 
Cerebral malaria (CM) is a major cause of malaria-related deaths. Most studies in CM have been done in Africa. There is a paucity of studies conducted in India. Adult CM in India has poor prognosis, high mortality and a relatively greater number of Plasmodium vivax positivity. ,,
In this cohort study, we intend to evaluate the various clinical and biochemical factors that correlate with the prognosis and immediate outcome of an admitted adult patient of CM. Predicting a CM with poor prognosis will salvage both resources and time in these resource-deprived forests.
| Materials and methods|| |
The prospective observational cohort study was conducted in the Tribal Health Center (THC) in Kokrajhar's tropical rain forest in the Northeastern part of Assam. The forests receive an annual rainfall of 2300-2500 mm and have temperatures peaking to 86-88°F during summer and falling as low as 50-55°F during winter. The flood prone rivers intersecting the hills and a relative humidity of 75-85% make the overall environment conducive for intense all-year round transmission of malaria.  The deaths occurred mostly in the rainy season (April-September) and among all age groups of both sexes. 
Health services in the area include two THCs assisted by 6 tribal outreach ambulatory clinics which serve 16 tribal settlements in the Chakrashila forest. The referral hospital was the Rup Nath Brahma Civil Hospital that served the entire Kokrajhar district and also the adjoining forests.
The THC is a 12-bedded indoor facility equipped with all major intravenous (i.v.), intramuscular (i.m.) medications and basic resuscitation facilities. Of all, 38 patients requiring advanced ventilatory support were transported to the Rup Nath Brahma Civil Hospital for critical care and data was followed up through discharge summaries and hospital records. All anti-malarial medications were available at the aforesaid hospital.
A total of 112 adults (>12 years) were included in the study. They comprised of 73 males and 39 females with CM admitted to the Bandarpara and Damodarpur THCs between March 2011 and November 2013. Patients were either detected in comb operations in the forest settlements or enrolled directly to the THC.
Cerebral malaria was taken to be the admission criteria according to the WHO definition : a0 person with coma persisting for more than 30 min after a generalized convulsion and with confirmed P. falciparum asexual parasitemia.  However, cases of P. vivax with altered sensorium were also included in the study due to recent reports of rise in vivaxcerebral malaria.  All other causes of the altered sensorium viz., meningitis, encephalitis and postictal state were diagnosed clinically and with lab tests and excluded from the study.
On admission, the demographic characteristics, symptoms, previous medical history and results of physical examinations were recorded. To quantify the depth of coma, Glasgow coma scale (GCS) score of <9 was taken to be coma and 5 or less was taken to be deep coma. Neurological and detailed fundoscopic examinations were done at admission and during discharge.
A sample of 5 ml of blood was drawn for examination using IV cannula. The diagnostic methods used to detect malarial parasites were conventional thick and thin peripheral blood smears stained with Giemsa. The slide was considered negative when there were no parasites in a 100 high-power field. The parasite density was calculated against 200 white blood cells (WBCs) using the formula: Parasite density (parasite/μL of whole blood) = (Number of parasites counted/WBC counted) × WBC count/μL.
PCR studies targeted against the 18S ribosomal RNA gene were done only on the 38 patients referred to higher centers for identifying the exact genus of infecting plasmodia. The primer sequences were modified for this study: 59-ATCAGCTTTTGATGTTAGGGT ATT-39, genus-specific; 59-TAACAAGGACTTCCAAGC-39, P. vivax-specific; and 59-GCTCAAAGATACAAATATAAGC-39, P. falciparum-specific. Each sample was subjected to a minimum of four rounds of PCR.
Using on admission values, severe anemia was indicated by a hemoglobin (Hb) <5 g/dl, acute renal failure by a serum creatinine >3 mg/dl, jaundice by a serum bilirubin >3 mg/dl, hypoglycemia by a blood glucose level <40 mg/dl and lactic acid was taken as significant above 45 mg/dl.
The retinal findings were documented by direct ophthalmoscopy, performed shortly after admission on administration of a topical mydriatic [Figure 1]. Retinal whitening, vessel changes and retinal hemorrhage are diagnostic of malaria. Papilledema was noted; however, taken alone it is not diagnostic of CM. Retinal whitening occurs as less bright mosaic patterns found specifically in central temporal macula and fovea. Vessel changes are commonly seen in peripheral fundus esp. branch points and involve orange or white discoloration of the vessels instead of red. White-centered intraretinal blot hemorrhages similar to Roth spots are found in CM.
|Figure 1: Fundoscopy of a patient showing retinal whitening and hemorrhage and cotton wool spots and solitary hemorrhage near macula in a cerebral malaria patient|
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Mortality and discharge summaries were documented.
The patients were treated with quinine. It was initially given intravenously and then orally, once the patients regained the ability to swallow. For the IV treatment, a loading dose (quinine 20 mg/kg, diluted in 10 ml/kg 5% dextrose) given over a period of 4 h followed by maintenance doses (quinine 10 mg/kg, diluted in 10 ml/kg 5% dextrose), each given over a period of 4 h, every 8 h. Subsequently, oral quinine (10 mg quinine sulfate/kg) was given every 8 h, to complete a 7-day course of treatment.
Data entry was carried out in MS excel sheet and analysis was done using SPSS 19.0 version. Tests such as Chi-Square and independent sample t-test were performed as test of significance. P value < 0.05 shall be considered as significant. Logistic regression model was used to find the prediction of death among subjects.
| Results|| |
Out of 112 patients of CM, 65% were male; with ages ranging from 15 to 77 years. The age groups comprised of 13-20 (8%), 21-40 (38%), 41-60 (36%) and >60 years (18%). The patients belonged to the following tribes - Bodo (63%), Dimasa (10%), Sonowal (15%) and Turung (12%).
Of all patients, 50% presented with vomiting, 56% with visual disturbances, 34% with headache, 38% with jaundice and 31% with prior seizures. About 47% had hypotension along with signs of circulatory failure and 38% had profound coma with GCS <5 [Table 1]. Coma lasted from 2 to 32 h before recovery or death. Patients with coma <3 h recovered or were alive with neurological deficit In 35% patients coma lasted for more than 8 h and they developed some form of neurological sequelae or died. About 21% of CM patients had hepatomegaly, 28% had splenomegaly and 29% of patients had meningeal irritation in the form of neck stiffness.
|Table 1: Distribution of study subjects according to clinical signs at the time of admission|
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Malarial retinopathy is the most sensitive indicator of CM. Retinopathy presents as retinal whitening, vessel aberrations, or retinal hemorrhage. These findings can present together with papilledema. Of all, 51% had normal fundoscopy finding, 12% had papilledema alone, 16% had only retinal hemorrhage and 17% had both papilledema and retinal hemorrhage.
In the laboratory work-up, 26% of CM patients were severely anemic (Hb <5), 13% had severe thrombocytopenia (platelets < 50,000/μL), 58% of patients had elevated serum lactate (>45 mg/dl), 28% had serum bilirubin >3 mg/dl and 27% had serum creatinine >3 mg/dl [Table 2].
Parasite density had statistically significant association with CM and case fatality. We found that 46% of CM patients had parasite density of >500,000/μL with case fatality rate of 59.62%. CM is commonly associated with P. falciparum. Our study also found few cases suffering from CM due to P. vivax exclusively. 78% had CM due to P. falciparum and 22% due to P. vivax. Mortality was 33% in P. falciparum and 32% in P. vivax. In P. falciparum CM, neurological sequelae were observed in 51% and full recovery in 16%. In P. vivax CM, neurological sequelae were observed in 16% and full recovery in 52%.
The mortality rate and neurological complications rate in patients with retinal whitening was 38.46% and 23.07%, with vessel changes was 25% and 18.75%, with retinal hemorrhage was 55.55% and 11.11%, and with hyperlactatemia was 53.85% and 18.46% respectively [Table 3]. There were three deaths observed in patients with papilledema alone. Patients with combined papilledema and hemorrhage were admitted for a period of 5-10 days whereas those with retinal hemorrhage alone were admitted for 9-12 days. Papilledema in CM was found to be independent of the other signs of malaria retinopathy in predicting death. Our study suggests that this malarial retinopathy can be used to identify prognosis of adult CM, as has already been established in children.
About 54% of patients with serum lactate >45 mg/dl died, 18% developed neurological defects and 28% fully recovered. Our study corroborates the important prognostic significance of serum lactate with high mortality in CM.
Case fatality rate of our study is (37/112) 33.03%. Out of 112 patients, 16.07% (18) developed neurological sequelae and 50.89% (57) fully recovered without neurological defects. Correlation of independent findings with outcomes is summarized in [Table 4].
| Discussion|| |
Malaria has been researched extensively, but scant research has been done with regards to adult CM in tribal population. Moreover, CM due to P. vivax (which is rare to find) has been studied. Considering the huge chunk of tribal population living in highly malaria-endemic areas and the scarcity of resources available to treat fatal complications such as CM, we conducted a research study to help determine the prognosis of such patients and allow for efficient allocation of resources to tackle them as timely and specific therapy can be lifesaving. ,,,
Our study focuses on the prognostic significance of serum lactate, malarial retinopathy and parasite density in CM. The study provides data about P. falciparum and P. vivax CM in the tribal areas of Kokrajhar, Assam. The case fatality rate of CM has been determined in the tribal setup. The prognosis and outcome in terms of duration of hospitalization, depth of coma, neurological sequelae, full recovery and death has been studied in depth. The neurocognitive outcomes could not be studied due to lack of questionnaires in the local tribal languages.
The incidence of fever and vomiting in the patient population was comparable to previous studies. There was a higher incidence of headache, jaundice, hypotension with circulatory failure, deep coma (GCS <5) and lesser incidence of splenomegaly compared to previous studies. ,
The case fatality rate of CM (33.03%) of our study was significantly higher than previously reported studies which were around 13-22%. ,, The reasons include late reporting of the patients, paucity of advanced treatment options for critically ill patients, poor connectivity to the tertiary care center, problems with transportation facilities and socio-cultural inhibition toward contemporary medical practices.
There has been proven evidence from studies in Gambia and Malawi of serum lactate as a prognostic indicator of CM in pediatric population. , Our study supports this finding in adult CM. Lactic acidosis (lactate >45 mg/dl) is associated with anemia, respiratory distress and is indirectly responsible for raised mortality. , Serum lactate can be increased due to high parasite density or metabolic acidosis due to hypoxia in host tissues. The major contribution is due to hypoxia caused by obstruction of microvasculature by adhering parasitized red blood cells (RBCs).  Other contributing factor for raised lactate can be raised catabolism in muscle after seizure activity in some patients or decreased oxygen carrying capacity of the blood due to hemolytic anemia. 
Lactic acidosis is believed to lead directly to a fatal outcome by the following processes impairment of cardiac output and other vital cellular functions;  inhibition of uptake of antimalarial drugs by infected erythrocytes  and increased cytoadherence of infected erythrocytes to capillary endothelium. 
Cerebral malaria is a diagnosis of exclusion. Fundoscopy is a good tool to diagnose malarial retinopathy. Retinal whitening, retinal hemorrhage and retinal vessel changes are specific to CM due to vasculopathy. Papilledema may or may not be associated retinal finding. Presence of papilledema suggests poor prognosis.  Our study corroborates the use of malarial retinopathy as a diagnostic tool for adult CM as well as the use of associated papilledema for assessment of prognosis. It has been suggested that 2 pathways may predict poor outcome in CM: Increased intracranial pressure manifesting as papilledema and retinal edema and vessel abnormalities (probably related to glucose levels, hematocrit and lactate levels).  The unique white and pale orange retinal vessels seen in CM can be explained by the sequestration of late-stage parasitized RBCs with reduced amounts of Hb.  The mortality in patients having both retinal hemorrhage and papilledema was 66.6% as compared to 55.5% patients with retinal hemorrhage alone. This supports the results from Malawian study of pediatric CM which had 18% case fatality with malarial retinopathy alone and 36% combined with papilledema. ,,,
Our study substantiates the evidence of high parasite density associated with CM.  We also conclude that the case fatality rate is higher in patients with raised parasite density (more than 500,000/uL). This can be explained by increased amount of cytoadherence by parasitized erythrocytes, which results in raised lactate and higher mortality due to vascular pathology.
Clinical data provided by Kochar et al. indicates that P. vivax can cause both sequestration-related and nonsequestration related complications of severe malaria, all of which are commonly associated with P. falciparum infections.  Of the 38 patients referred to the higher center for critical care, 12 had P. vivax mono-infection, 21 had P. falciparum mono-infection and 5 had mixed infection. This is the highest number P. vivax CM cases reported in any study from India till now in adult cases. Kochar et al. reported 14 cases of CM out of 154 pediatric cases admitted for P. vivax malaria. Our study validates the previous study and hence shows that P. vivax can be responsible for adult CM. This demonstrates the need for change in the WHO definition of CM which concentrates only on asexual stage of P. falciparum (and not P. vivax) in blood smear.
Our study was undertaken with the intent of initiating more clinical research in tribal setting in Assam. The data will help in learning the shortcomings of health care set up and using serum lactate and retinopathy findings for determining the prognosis of patients. It will also help in using the limited supply of antimalarials and referral services judiciously. Our study addresses major hurdles while doing research in tribal areas such as geography, language barrier, resource limitation and lack of intensive care facility.
We recommend further randomized case-control studies to evaluate these prognostic factors. Retinopathy subsets such as whitening, vessel changes, hemorrhage and lactic acid levels should be studied in depth to create a prognostic classification. Since neurocognitive outcome could not be evaluated due to lack of questionnaires in local tribal language, further studies are recommended in this accord.
Our study demonstrates a strong correlation between retinal changes (whitening, vessel changes and hemorrhage) and a poor outcome of CM. Combinations of high parasite index, severe hypoglycemia, hyperlactatemia, retinal findings and longer duration of deep coma can be used to identify the prognosis in terms of neurological sequelae, duration of hospitalization and those with higher risk of death. Role of P. vivax mono-infection as a rising causal factor for CM needs to be further evaluated in view of significant number of deaths due to complicated vivax malaria.
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Conflicts of interest
There are no conflicts of interest.
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Kaustubh Suresh Chaudhari
Department of Internal Medicine and Infectious Disease, Vanvasi Kalyan Ashram, Kokrajhar, Assam
Source of Support: None, Conflict of Interest: None
[Table 1], [Table 2], [Table 3], [Table 4]
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