Background
Thrombocytopenia is an early and consistent feature of malaria [
1-
4], but its pathogenesis remains incompletely understood. In falciparum malaria there is increased platelet consumption as evidenced by shortened survival of radiolabelled platelets [
5] and the finding of plentiful megakaryocytes in patients’ bone marrow [
6] and appropriately elevated plasma thrombopoietin levels [
7]. Both systemic microvascular sequestration [
8] and endothelial activation [
9,
10] may play a pathophysiological role, a hypothesis supported by the observation that the radiolabelled platelets of patients with falciparum malaria are diffusely sequestered, rather than pooling in the liver or spleen [
5]. Yet while thrombocytopenia is a ubiquitous laboratory finding, it had been thought to have limited clinical significance, as major bleeding is relatively uncommon in the disease [
11].
Recently it has been suggested that thrombocytopenia may have important implications for patient triage. Population studies have shown an association between thrombocytopenia and outcome [
12] and a recent study from India proposed that thrombocytopenia should be added to the World Health Organization (WHO) criteria for the definition of severe malaria [
13]. To clarify this issue, data from adults with severe falciparum malaria prospectively enrolled in clinical studies of severe malaria were analysed to determine if the platelet count could assist in clinical decision-making and whether the degree of thrombocytopenia has predictive utility independent of current clinical and laboratory prognostic indices. Measures of microvascular sequestration and endothelial activation and their relationship with the platelet count were examined to further explore the pathogenesis of the thrombocytopaenia seen in the disease.
Methods
Two datasets were combined for this analysis. The first (n = 560) was compiled prospectively at the Centre for Tropical Diseases in Ho Chi Minh City, Vietnam, between 1991 and 1996 in a study that compared the efficacy of artemether and quinine in adults with severe falciparum malaria [
14]. The second comprised data collected prospectively in studies assessing a range of adjunctive therapies in severe falciparum malaria at Chittagong Medical College Hospital, Bangladesh, and Ispat General Hospital, Rourkela, India, between 2004 and 2011 [
15-
18].
Malaria transmission was low and seasonal at all sites. Falciparum malaria was diagnosed if a blood film showed asexual forms of Plasmodium falciparum. When expert microscopy was not available immediately, patients were enrolled if an immunochromatographic rapid diagnostic test (Paracheck Pf, Orchid Biomedical Systems, Goa, India) was positive; P. falciparum infection was confirmed later by microscopy of a simultaneously collected blood slide.
All patients satisfied a strict definition of severe falciparum malaria that used modified WHO criteria [
19], including cerebral malaria (Glasgow Coma Scale (GCS) <11); severe anaemia (haematocrit <20% with a parasite count > l00,000/mm
3); renal failure (blood urea nitrogen ≥21.4 mmol/L or plasma creatinine level ≥265 μmol/L); pulmonary oedema (oxygen saturation <90% and bibasal crepitations); generalized convulsions; acidosis (venous bicarbonate <15 mmol/L); hyperparasitaemia (peripheral parasitaemia >10%); hyperlactataemia (venous lactate >4 mmol/L); jaundice (bilirubin >43 μmol/L and a parasite count > l00,000/mm
3); hypoglycaemia (glucose <2.2 mmol/L); and spontaneous bleeding or shock (systolic blood pressure <80 mmHg with cool extremities). Patients were excluded if they were <14 years of age or if they had received parenteral anti-malarial treatment for >48 hours before enrolment. Disease severity was defined by the number of these criteria that a patient satisfied. The independent prognostic utility of the admission platelet count was compared with the widely validated RCAM score [
20-
22] calculated from the patients’ respiratory rate and GCS on admission (Table
1). Major bleeding was defined as bleeding which resulted in death or necessitated blood transfusion.
Table 1
Calculation of the RCAM score
Glasgow coma scale | 15 | 11 to 14 | ≤10 |
Respiratory rate | <20 | 20 to 39 | ≥40 |
On enrolment, a history was taken, a physical examination performed and venous blood collected. In Vietnam, patients were randomized to receive intramuscular quinine (n = 271) or intramuscular artemether (n = 279); all the Bangladeshi and Indian patients received intravenous artesunate. Patients received supportive care as per contemporary WHO treatment guidelines [
11,
23,
24]. Access to mechanical ventilation was limited in Vietnam; access to both mechanical ventilation and renal replacement therapy was limited in Bangladesh. Platelet transfusion was not available at any of the sites. The peripheral parasite count (parasites/μL) on admission was calculated from the thin film using the formula: parasite count/1,000 red blood cells × 125.6 × haematocrit (%); or from the thick film using the formula: parasite count/200 white blood cells × 40. In Vietnam haematological indices were manually determined in the hospital laboratory; in Bangladesh and India they were measured with an automated analyser in local private laboratories.
In Vietnam the hospital laboratory performed most biochemical analysis, but plasma glucose and lactate were measured on the ward using dedicated online analysers (Analox, Middlesborough, United Kingdom). Biochemical indices were measured in Bangladesh and India using portable handheld analysers (i-Stat, Abbott, Princeton, New Jersey, USA). Plasma was processed and stored at −80°C for analysis of other laboratory parameters: plasma
Plasmodium falciparum histidine rich protein 2 (
PfHRP2), a measure of parasite biomass, was measured in Bangkok, Thailand, using ELISA (Cellabs, Sydney, New South Wales, Australia), according to the manufacturer’s instructions with minor modifications [
25]; angiopoietin-2 (Ang-2), a measure of endothelial activation, was measured in Darwin, Australia, using ELISA (R&D Systems, Minneapolis, Minnesota, USA) [
26].
In the Bangladeshi and Indian patients video recordings of blood flow in the microcirculation were collected with an orthogonal polarizing spectral (OPS) imaging device (either Cytoscan from Cytometrics, Heathpark Honiton, Devon, United Kingdom or Microscan from Microvision Medical, Amsterdam, the Netherlands) and quantified using image analysis software (Open Lab 3.1.5, Improvision, Waltham, Massachusetts, USA) as described previously [
17].
Statistics
Data were analysed using statistical software (Stata version 10, StataCorp, College Station, Texas, USA). Correlation coefficients were determined using Spearman’s method. Groups were analysed using the Kruskal-Wallis test and the chi-squared test. Logistic regression was performed where necessary and to control for any influence of the study site or the administered anti-malarial therapy.
Ethics review
All of the studies received prospective ethical approval from OXTREC (Oxford Tropical Research Ethics Committee) and local ethics review bodies. The ethics and scientific-review committee of The Center for Tropical Diseases in Ho Chi Minh City approved the Vietnamese study, the Bangladeshi Medical Research Council approved the Bangladeshi studies and the institutional ethical board of Ispat General Hospital approved the Indian studies.
Discussion
In this multi-centre study of adults with severe falciparum malaria, the platelet count on admission correlated with disease severity and outcome, but had limited independent prognostic utility when considered with other laboratory indices. Knowledge of the platelet count offered no significant prognostic advantage over determination of the respiratory rate and GCS. The platelet count on admission was lower in patients who went on to develop major bleeding, but was unable to identify this population reliably.
Thrombocytopenia was more frequent in this series than in previous studies of adults with falciparum malaria [
2,
3,
27], presumably as a result of a strict case definition leading to the enrolment of patients with more severe disease. The increased mean platelet volume, although available in few patients, suggests the presence of young, functional platelets, and likely explains the relatively low incidence of major bleeding - despite the profound thrombocytopenia - seen in the study. This low incidence of major bleeding and the significant challenges associated with the delivery of blood products in the resource-poor setting [
28] argues strongly against the routine use of platelet transfusions in these patients. The prompt and spontaneous recovery seen in the platelet counts of this patient population provides additional support for this clinical approach [
29].
After an association between thrombocytopenia and outcome was demonstrated in a large Indonesian population-based study of malaria, it was suggested that a platelet count of less than 20 × 10
9/L should be used as a severity criterion in malaria and that the platelet count might have use in patient triage [
12]. An Indian hospital-based study reached similar conclusions [
13]. A platelet count has the virtue of being easier to measure than some other recognized laboratory predictors of mortality, such as plasma lactate and base deficit. Our series confirms that profound thrombocytopenia should alert clinicians managing patients with malaria - patients with a platelet count below 20 × 10
9/L were five times more likely to die than patients with a higher platelet count. However, if clinicians in this series had used the platelet count to triage patients, it would not have resulted in significant changes in their management. None of the patients who would later die despite being classified as low-risk with the simple bedside RCAM score had an admission platelet count below 20 × 10
9/L. Thus, whilst there is an association between the presence of profound thrombocytopenia and the likelihood of a complicated course, the addition of another severity criterion to the already complex definition of severe falciparum malaria [
30] may not assist clinicians substantially.
OPS imaging has been used to demonstrate microvascular obstruction
in vivo in adults with falciparum malaria [
15]. The correlation seen in this series between microvascular obstruction and the circulating platelet count may represent the diffuse sequestration of radiolabelled platelets seen in thrombocytopenic patients with falciparum malaria [
5]. Certainly platelets have been implicated in the pathogenesis of two of the processes (auto-agglutination [
31] and cytoadherence [
32]) that contribute to microvascular obstruction, and increased numbers of platelets and platelet-fibrin thrombi have been reported in the cerebral microcirculation of paediatric cases of fatal falciparum malaria [
8]. However, platelets are notable by their absence from the microcirculation in adult post-mortem series [
33,
34]. Furthermore thrombocytopenia is also frequent in
Plasmodium vivax malaria [
12,
27], a disease in which significant sequestration is absent [
35]. Although severe thrombocytopenia is less frequent in vivax malaria, there are many shared findings, including increased mean platelet volumes and a correlation with the circulating parasite count [
36], suggesting that there are common pathways in the pathogenesis of the thrombocytopenia in the two infections.
One of these common pathways is likely to be endothelial activation [
34,
37]. During endothelial activation, activated high-multimeric von Willebrand Factor (vWF) is released from specialized secretory vesicles in endothelial cells known as Weibel-Palade bodies (WPBs) [
38]. Once in the circulation, vWF aggregates platelets, resulting in their clearance from the circulation. Studies performed in both falciparum and vivax malaria demonstrate an inverse association between the circulating platelet count and plasma concentrations and activity of vWF [
9,
10]. Falls in the plasma concentrations of ADAMTS13, a regulating enzyme that catabolizes vWF multimers, are also seen in infections with both species [
9,
10]. Although vWF and ADAMTS13 were not determined in this series, plasma concentrations of Ang-2 were markedly elevated, suggesting the presence of pronounced systemic endothelial activation. Indeed, Ang-2 is stored in WPBs and is released with vWF during WPB exocytosis.
An interaction between microvascular obstruction and endothelial activation may explain the association between the OPS findings and the circulating platelet count seen in this series [
34]. The resting, un-activated endothelium constitutively releases nitric oxide, which helps maintain endothelial quiescence and also directly inhibits platelet aggregation [
39,
40]. The shear stress of normally flowing blood is the principal signal for this nitric oxide release [
40] and it would therefore be expected that microvascular obstruction could lead to endothelial activation via this mechanism. Microvascular obstruction also leads to tissue hypoperfusion and hypoxia - another potent stimulus for endothelial activation. Endothelial activation facilitates further cytoadherence through the upregulation of endothelial receptors that act as ligands for parasitized erythrocytes [
34], resulting in further microvascular obstruction and potentially precipitating a vicious cycle.
The study has other noteworthy haematological findings. Erythropoiesis was significantly depressed with a reticulocyte production index of less than 1 in almost 90% of the patients. Accordingly, most patients were anaemic but severe anaemia (haematocrit <20%) was relatively infrequent, a finding that may reflect the fact that this study was performed exclusively in adults [
41]. It suggests that prognostic tools that use the platelet count and haemoglobin concentration may have limited utility in the adult population [
12]. The median white blood cell count was greater in this cohort than in outpatients with malaria in whom mild leucopenia is typical [
42]. The admission white cell count was significantly higher in the patients who died than in survivors, an association that has been recognized previously [
13,
43].
Our study had significant limitations. Its retrospective design precluded complete data collection. Measurements of vWF and ADAMTS13 concentrations and activity would have defined the extent of this pathway’s contribution to the pathogenesis of thrombocytopenia. Coagulation studies would have defined the contribution of coagulopathy to bleeding complications, although disseminated intravascular coagulation was rarely suspected clinically. The study assessed the prognostic utility of the admission platelet count, but sequential measurement may have improved its ability to predict bleeding complications, in particular. The dataset consisted of patients who had already satisfied a definition of severe malaria; the prognostic utility of the platelet count may be different outside of a study setting. Because the studies only enrolled adults, the findings cannot necessarily be generalized to children.
Acknowledgements
We thank the directors and staff of the trial hospitals and the doctors, research nurses and research assistants for their help; in particular Dr Sophia Lam, Dr Sam Douthwaite and Dr Sophie Cohen, who collected and collated data in Bangladesh and India. We also thank Dr Gareth Turner (MORU) and Professor Nick Anstey for valuable and constructive advice during the preparation of the manuscript and Dr Kamolrat Silamut, Dr Kesinee Chotinavich, Dr Charlie Woodrow (all MORU) and Kim Piera (Menzies), who provided valuable laboratory support. JH is supported by the National Health and Medical Research Council of Australia. RNP is supported by the Wellcome Trust. NJW, NPJD and AMD are supported by the Wellcome Trust as part of the Wellcome Trust-Mahidol University-Oxford Tropical Medicine Research Programme.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
JH cared for patients in Bangladesh and India, performed the statistical analysis and wrote the first draft of the manuscript. NHP and TTH cared for patients and supervised the study in Vietnam. PC, KP, RJM, PP and HWFK cared for patients in Bangladesh. MUH and MAF supervised the study in Bangladesh. SKM and SM supervised the study in India. RNP revised the manuscript. AMD cared for patients in Bangladesh and supervised the studies in Bangladesh and India. NJW and NJD cared for patients in Vietnam, supervised all of the studies and revised the manuscript. All authors read and approved the final manuscript.