Skip to content


  • Research
  • Open Access

The prognostic value of schizontaemia in imported Plasmodium falciparum malaria

  • 1,
  • 1, 2,
  • 1,
  • 3,
  • 3, 4 and
  • 1, 2Email author
Malaria Journal201211:301

  • Received: 23 May 2012
  • Accepted: 23 August 2012
  • Published:



In Plasmodium falciparum infection, peripheral parasite counts do not always correlate well with the sequestered parasite burden. As erythrocytes parasitized with mature trophozoites and schizonts have a high tendency to adhere to the microvascular endothelium, they are often absent in peripheral blood samples. The appearance of schizonts in peripheral blood smears is thought to be a marker of high sequestered parasite burden and severe disease. In the present study, the value of schizontaemia as an early marker for severe disease in non-immune individuals with imported malaria was evaluated.


All patients in the Rotterdam Malaria Cohort diagnosed with P. falciparum malaria between 1 January 1999 and 1 January 2012 were included. Thick and thin blood films were examined for the presence of schizontaemia. The occurrence of WHO defined severe malaria was the primary endpoint. The diagnostic performance of schizontaemia was compared with previously evaluated biomarkers C-reactive protein and lactate.


Schizonts were present on admission in 49 of 401 (12.2%) patients. Patients with schizontaemia were more likely to present with severe malaria, a more complicated course and had longer duration of admission in hospital. Schizontaemia had a specificity of 0.95, a sensitivity of 0.53, a negative predictive value of 0.92 and a positive predictive value of 0.67 for severe malaria. The presence of schizonts was an independent predictor for severe malaria.


Absence of schizonts was found to be a specific marker for exclusion of severe malaria. Presence of schizonts on admission was associated with a high positive predictive value for severe malaria. This may be of help to identify patients who are at risk of a more severe course than would be expected when considering peripheral parasitaemia alone.


  • Schizont
  • Prognosis
  • Malaria
  • Falciparum
  • Import
  • Severe


Sequestration of infected erythrocytes in the microvasculature is one of the main pathological features of severe Plasmodium falciparum infection [14]. Particularly, erythrocytes parasitized with mature trophozoites and schizonts have a high tendency to adhere to the microvascular endothelium and are therefore often absent in collected peripheral blood samples. However, the appearance of schizonts in peripheral blood smears is thought to reflect a high sequestered parasite burden and was recognized as a sign of severe disease already in early field studies on malaria [5]. The predominance of mature parasites on peripheral smears was found to reflect more severe disease by Silamut and White [6], but only a few other studies on the performance of schizontaemia as a predictor for severe disease have been done [79]. In addition, data is only available from studies in areas with malaria endemicity where many inhabitants are believed to have some degree of immunity toward malaria (so-called semi-immunity). Data in non-immune individuals are lacking.

Although it is stated in the current WHO malaria guidelines that the presence of schizontaemia may be associated with a poor outcome in P. falciparum malaria, presence of schizonts is currently not a well-established WHO criterion for severe disease [9, 10]. To further explore the value of schizontaemia as an early marker for severe disease in non-immune individuals with imported malaria, the prognostic value of schizontaemia was assessed in a large cohort of travellers with P. falciparum malaria.



The Harbour Hospital is a 161-bed general hospital located in Rotterdam, The Netherlands. It comprises the Institute for Tropical Diseases, which serves as a national referral centre. All patients in the Rotterdam Malaria Cohort diagnosed with P. falciparum malaria between 1 January 1999 and 1 January 2012 were included in this observational study. Of all patients identified, demographic, clinical and laboratory data were collected using a standardized form and stored in an electronic database. Patients with a mixed infection of P. falciparum with another Plasmodium species were included in this study, but pure non-falciparum Plasmodium infections were excluded. Multiple malaria episodes in a single patient were only regarded as separate cases if caused by true re-infection; recrudescent infections of P. falciparum were excluded.

Laboratory investigations

Available laboratory examinations included red and white blood cell counts, haematocrit, platelet counts, C-reactive protein, serum electrolytes, total bilirubin, serum creatinine and urea, sodium, potassium, liver enzymes, blood glucose and venous plasma lactate.

Detection of Plasmodium parasites

The standard procedure to diagnose malaria comprised a quantitative buffy coat (QBC) analysis, a rapid diagnostic test (RDT) for malaria antigens Binax NOW® Malaria Test (Binax, Inc, Maine, USA), and thick and thin blood smears using freshly collected blood specimens from finger pricks. The malaria rapid test and the QBC analysis were performed according to the manufacturer’s instructions. QBC capillaries were examined independently by two technicians by microscopic analysis of two complete rows of the region between the bottom of the capillary and the polynuclear leukocyte layer using an Olympus BX-60 fluorescence microscope equipped UV-filter and 50x objective and 12.5x oculars (total magnification 625x). These two lanes represented about 100 microscopic fields (at 625x magnification) and took an average examination time of 5 min. Subsequently, the polynuclear and mononuclear cell layer was screened for schizonts, gametocytes, malaria pigment and elderly trophozoites of Plasmodium vivax and Plasmodium ovale.

Thick blood smears were stained with Field’s stain (Brunschwig Chemie, Amsterdam, The Netherlands) and thin smears with Diff Quick stain (Medion Diagnostics, Düdingen, Switzerland). Both staining procedures had been optimized for optimal staining of Plasmodium parasites as well as Schüffner’s dots and Maurer’s clefts in infected erythrocytes. Thick and thin smears were examined with regular light microscopes at a total magnification of 1,250x. The Plasmodium species was identified on morphological characteristics in the thin and thick blood smears. Since a real-time quantitative PCR became available several years ago, a substantial proportion of the samples were additionally confirmed by PCR (without discrepant findings compared to classic light microscopy).

Parasite counting and identification of Plasmodium falciparum schizonts

Parasitaemia was determined by parasite counting as described before [11]. Plasmodium falciparum schizonts were defined as clustered malaria pigment adjacent to two or more nuclei of P. falciparum in thick blood smears or QBC capillaries. Compared to thin and thick blood smears QBC analysis is the most sensitive test to detect Plasmodium parasites. Plasmodium falciparum schizonts can be identified in the erythrocyte layer in the QBC capillary, but identification within the leukocyte layer is difficult due to the intense fluorescent signal of the leukocyte nuclei. For this reason, this layer is also screened for quenched fluorescence by malaria pigment. If malaria pigment was detected in the leukocyte layer of the QBC capillary, the thick and thin blood smears were thoroughly examined for the presence of schizonts by analysis of at least 200 microscopic fields at 625x magnification.


Severe malaria

Patients were classified as having severe malaria if they met one or more of the WHO criteria for severe malaria, as published [9], either on presentation or later during hospital admission.


Schizontaemia was defined as presence of one or more P. falciparum schizonts identified in QBC and/or blood smear examinations from a blood sample taken on admission.

Immunity to malaria

The degree of immunity to malaria was estimated as previously described [12]. In brief, adult immigrants from a malaria-endemic country living in The Netherlands were considered partially immune. Immigrant patients who had been living in a malaria-endemic area for at least two years at the time of diagnosis were presumed semi-immune. Tourists from non-endemic countries who travelled to malaria-endemic regions were considered non-immune.

Statistical analysis

All data were not normally distributed (Kolmogorov-Smirnov test) and are therefore presented as medians and range. Univariate comparisons were performed using the Mann–Whitney U test and the Fisher’s Exact test. Trends between categorical variables were done with the Chi square test for Trend. Odds ratios were calculated using the approximation of Woolf. For clinical reference, the diagnostic performance of schizontaemia for severe disease was compared to that of the classic biomarkers serum C-reactive protein and plasma lactate [1315]. Binary logistic regression analysis was used to analyse if schizontaemia was independently associated with malaria severity. Malaria severity was entered as the dependent variable. To test its independence from parasite load and the previously evaluated markers lactate and C-reactive protein, these were entered as co-variants. As parasite load was a highly skewed continuous variable with a logarithmic distribution, the data were transformed to log-parasitaemia to make them suitable for logistic regression analysis.


Patient characteristics

Between 1 January 1999 and 1 January 2012, a total of 562 cases of imported malaria were seen. Of these cases, 161 cases were caused by non-falciparum Plasmodium species; 401 infections were caused P. falciparum infections including three patients who had a mixed infection (two with P. falciparum and P. ovale, one with P. falciparum and P. vivax, respectively). No patient with a mixed P. falciparum infection presented with schizontaemia on admission. These 401 patients with either a pure P. falciparum infection or a mixed Plasmodium infection with P. falciparum were included in this study.


Schizonts were present on admission in 49 of 401 (12.2%) patients. The general characteristics of the patients with presence and absence of schizonts on admission are shown in Table 1. Males were less likely to present with schizontaemia than female patients (Odds ratio 0.37 (95% confidence interval 0.20-0.67), p = 0.0018). Although the number of patients who acquired P. falciparum malaria outside of Africa was relatively low (n = 26), these patients tended to present with schizontaemia more frequently than patients who contracted malaria in Africa (Odds ratio 0.26 (95% CI 0.086-0.79), p = 0.0259). There were no differences between patients presenting with and without schizontaemia with regard to their immune status, ethnic background and use of malaria chemoprophylaxis, nor did they differ in duration of symptomatology. As detailed in Table 1, patients with schizontaemia presented more ill on admission: they had higher pulse rates, were more likely to have impaired consciousness and laboratory parameters were compatible with more severe degree of liver and kidney injury as well as more compromised tissue perfusion given the higher plasma lactate levels. Other laboratory parameters revealed that patients with schizontaemia also presented with significantly higher parasite loads, higher leucocyte counts, higher C-reactive protein levels and significantly lower platelet counts. When the WHO severity criteria for malaria [9] were assessed in both patient groups, patients with schizontaemia were more likely to present with or develop severe and complicated disease and they had to stay significantly longer in hospital than patients without demonstrable schizontaemia on admission (Table 2). Death occurred in two of 401 malaria patients, one with and one without schizontaemia on admission. Presence of schizontaemia on admission significantly increased with increasing parasite loads on admission (Chi square test for Trend, p < 0.0001), as shown in Figure 1.
Table 1

General characteristics of patients with imported Plasmodium falciparum malaria grouped by presence or absence of schizontaemia on admission


All patients


No schizontaemia

P value


n = 401

n = 49

n = 352


Demographic s


 Age, years

39 (4–78)

41 (4–70)

39 (5–78)


 Male, female, n (%)

292 (72.8), 109 (27.2)

26 (53.1), 23 (46.9)

266 (75.6), 86 (24.4)


Continent of acquisition


 Africa, n (%)

360 (89.8)

38 (77.6)

322 (91.5)


 Asia, n (%)

16 (4.0)

5 (10.2)

11 (3.1)


 South and Central America, n (%)

10 (2.5)

3 (6.1)

7 (2.0)


 Unknown, n (%)

15 (3.7)

3 (6.1)

12 (3.4)


Duration of signs/symptoms


 <8 days, n (%)

259 (64.6)

30 (61.2)

229 (65.1)


 8-14 days, n (%)

74 (18.5)

15 (30.6)

59 (16.8)


 15-28 days, n (%)

27 (6.7)

0 (0)

27 (7.7)


 >28 days, n (%)

8 (2.0)

0 (0)

8 (2.3)


 Unknown, n (%)

33 (8.2)

4 (8.2)

29 (8.2)


Use of malaria chemoprophylaxis


 No chemoprophylaxis, n (%)

272 (67.8)

35 (71.4)

237 (67.3)


 Inadequate use, n (%)

72 (18.0)

6 (12.2)

66 (18.8)


 Adequate use, n (%)

39 (9.7)

6 (12.2)

33 (9.4)


 Unknown, n (%)

18 (4.5)

2 (4.1)

16 (4.5)


Vital signs on admission


 Body temperature, °C

38.5 (35.5-41.2)

38.7 (35.7-41.2)

38.5 (35.5-41.0)


 Pulse rate, beats per minute

95 (45–150)

105 (68–150)

92 (45–150)


 Systolic blood pressure, mm Hg

120 (64–190)

118 (64–160)

120 (73–190)


 Impaired consciousness (GCS < 15), n (%)

9 (2.2)

5 (10.2)

4 (1.1)


 Cerebral malaria (GCS ≤ 11), n (%)

5 (1.2)

2 (4.1)

3 (0.9)


Laboratory data on admission


 Haemoglobin, mmol/L

8.3 (2.5-11.1)

7.8 (3.8-10.9)

8.4 (2.5-11.1)


 Leucocyte count, x 109/L

5.1 (1.3-18.5)

6.1 (2.5-18.5)

5.0 (1.3-13.4)


 Thrombocytes, x 109/L

86 (2–385)

38 (10–164)

94 (2–385)


 C-reactive protein, mg/L

98 (5–476)

166 (22–476)

87 (5–373)


 Serum creatinine, μmol/L

95 (39–1,081)

110 (39–1,081)

95 (47–871)


 Serum sodium, mmol/L

135 (115–146)

132 (115–142)

135 (119–146)


 Lactate dehydrogenase, U/L

275 (118–2,297)

435 (135–2,038)

262 (118–2,297)


 Total bilirubin, μmol/L

24 (4–416)

44 (9–269)

23 (4–416)


 Plasma lactate, mmol/L

1.6 (0.5-6.2)

2.7 (0.6-6.2)

1.5 (0.5-4.7)


Parasite count


P. falciparum load (asexual parasites/μL)

8,400 (2–1,380,600)

162,000 (144–1,380,600)

5,430 (2–860,000)


 Gametocytes, presence, absence, n (%)

64 (16.0), 337 (84.0)

11 (22.4), 38 (77.6)

53 (15.1), 299 (84.9)


Table 2

Outcome measures of patients with imported Plasmodium falciparum malaria, grouped by presence or absence of schizontaemia on admission


All patients (n = 401)

Schizontaemia (n = 49)

No schizontaemia (n = 352)


Odds ratio (95% CI)

Case-fatalities, n (%)

2 (0.5)

1 (2.0)

1 (0.3)



Severe malaria, n (%)

62 (15.5)

33 (67.3)

29 (8.2)


23.0 (11.3-46.6)

ICU admission, n (%)

92 (22.9)

38 (77.6)

54 (15.3)


19.1 (9.2-39.6)

Exchange transfusion, n (%)

40 (10.0)

26 (53.1)

14 (4.0)


27.3 (12.6-59.2)

Renal replacement therapy, n (%)

7 (1.7)

4 (8.2)

3 (0.9)


10.3 (2.2-47.7)

Mechanical ventilation, n (%)

4 (1.0)

3 (6.5)

1 (0.3)


22.9 (2.3-224.8)

Time in hospital, days (range)

5 (0–56)

7 (0–56)

5 (0–19)


Figure 1
Figure 1

The percentage of patients with schizontaemia on admission, stratified by peripheral parasite count.

The diagnostic accuracy of schizontaemia as a predictor for severe malaria was characterized by a high specificity, negative predictive value and an acceptable positive predictive value. When compared to the performance of plasma lactate, schizontaemia had a lower sensitivity but a higher specificity and positive predictive value for severe disease. When compared to the performance of C-reactive protein, schizontaemia had a higher specificity and positive predictive value for severe disease (Table 3). Using binary logistic regression analysis, schizontaemia was found to be an independent predictor for severe malaria with odds ratios substantially exceeding that found for C-reactive protein and lactate but not that found for parasite load (Table 4).
Table 3

Descriptive statistics of schizontaemia, lactate and C-reactive protein as predictors for severe malaria


Schizontaemia (presence)

Plasma lactate (mmol/L)

C-reactive protein






Median (range)


1.6 (0.5-6.2)

98 (5–476)





Standard deviation




Optimal cut-off





0.53 (0.40-0.66)

0.80 (0.67-0.89)

0.76 (0.63-0.86)


0.95 (0.92-0.97)

0.63 (0.55-0.70)

0.75 (0.70-0.80)

Youden’s index





0.67 (0.52-0.80)

0.39 (0.30-0.49)

0.35 (0.27-0.45)


0.92 (0.88-0.94)

0.91 (0.85-0.95)

0.95 (0.91-0.97)

Table 4

Results of binary logistic regression analysis of explanatory variables for severe malaria



S.E. β

Wald’s χ


P value

Odds ratio (95% CI)

C-reactive protein






1.01 (1.00-1.02)

Log parasitaemia






14.13 (4.71-42.38)

Plasma lactate






1.52 (0.89-2.57)







6.52 (1.92-22.13)









Sequestration of parasitized erythrocytes in the microvasculature of vital organs is a cardinal feature of P. falciparum malaria and is a cause of major pathology in severe disease [14]. Maturing P. falciparum parasites disappear from the peripheral blood after 24–26 hours to complete the asexual life cycle in the microvasculature, as the tendency to adhere to the endothelial wall increases during the maturation process [6]. This process of sequestration accounts for the fact that peripheral parasite counts do not always correlate well with the sequestered parasite burden. This discrepancy was noted soon after the use of the peripheral parasitaemia to predict the outcome of P. falciparum infection became common practice in the 1930s [5].

In the microvasculature, rupturing schizonts release up to 32 merozoites [7, 16], causing an exponential rise in parasitaemia. A high schizont count is therefore likely to precede a rise in parasitaemia and might be an early marker for severe disease. The presence of schizontaemia may also be relevant to guide selection of parenteral treatment. As compared to quinine, artemisinin derivatives like artesunate have an anti-malarial efficacy to the broadest spectrum of parasite stages, including the generally less drug-sensitive schizonts [1, 7]. This may provide another argument to treat patients with schizontaemia with artemisinin derivatives given the convincing proof of past studies in regions of malaria endemicity showing that artesunate was superior over quinine for treatment of severe malaria in both children and adult patients [17, 18], not only in terms of reduction of mortality and parasite clearance but also in ease of use. Recent studies in non-endemic industrialized regions confirmed that in non-immune travellers with imported malaria, treatment with artesunate results in a comparable rapid parasite clearance to that observed in semi-immune individuals [19, 20].

In the present study schizontaemia was found to be a useful marker for severe malaria. Although schizontaemia was more frequently seen in patients with high-grade parasitaemia, the predictive power appeared to be independent of parasitaemia. In the study by Silamut and White [6] in adult Thai patients and children from The Gambia, it was demonstrated that a predominance of mature parasite forms in the peripheral blood reflect a greater sequestered parasite mass and the presence of >10 4 mature trophozoites and schizonts per μL of peripheral blood was found to have a high sensitivity (90%) and specificity (70%) for fatal outcome. The data of the present study confirm the prognostic value of schizontaemia for severe disease in predominantly non-immune travellers, comparable to that observed in semi-immune patients in region of malaria endemicity. However, it should be noted that besides differences in presumed immunity towards malaria, the current study also differed in its design with regard to outcome. In many studies in malaria-endemic regions, the primary outcome measure is usually survival or death and studies are restricted to these severe cases using the WHO severity criteria as an entry criterion. Since case fatalities are less common in the western non-endemic, resource-rich setting [12] and malaria is only seen as a sporadic imported disease, the present study in patients with imported malaria focused on severe malaria as the primary outcome, using the WHO criteria to define disease severity.

Unfortunately, for the present study quantitative counts of the different parasite stages were not available. Although quantification would likely have resulted in a more precise estimation of its prognostic value, the specificity of schizontaemia was found to be a useful tool for exclusion of severe disease. The negative predictive value of schizontaemia is high, and comparable to that of C-reactive protein and lactate. Moreover, unlike C-reactive protein and lactate [1315] schizontaemia on admission was also associated with a high positive predictive value. This may provide the clinician with a helpful tool for decision making in the acute care setting by allowing an early identification of those malaria patients who are at risk of a more severe and complicated course than would normally be expected when considering peripheral parasitaemia alone.


Absence of schizonts on admission in travellers with imported P. falciparum malaria was found to be a specific marker for exclusion of severe disease; in contrast, presence of schizonts had a high positive predictive value for presence of severe disease and can thus help to identify patients that may be candidates in need of intensive monitoring and timely administration of preferably (parenteral) artemisinin derivatives.



Ms Corine Stuij is acknowledged for secretarial assistance. The Port of Rotterdam is thanked for their unconditional financial grant.

Authors’ Affiliations

Department of Internal Medicine, Harbour Hospital, Rotterdam, The Netherlands
Institute for Tropical Diseases, Harbour Hospital, Haringvliet 72, 3011, TG, Rotterdam, The Netherlands
Laboratory of Parasitology, Harbour Hospital and Institute for Tropical Diseases, Rotterdam, The Netherlands
Department of Medical Microbiology and Infectious Diseases, Erasmus Medical Centre, Rotterdam, The Netherlands


  1. White NJ, Ho M: The pathophysiology of malaria. Adv Parasitol. 1992, 31: 83-173.View ArticlePubMedGoogle Scholar
  2. Mackintosh CL, Beeson JG, Marsh K: Clinical features and pathogenesis of severe malaria. Trends Parasitol. 2004, 20: 597-603. 10.1016/ ArticlePubMedGoogle Scholar
  3. Miller LH, Baruch DI, Marsh K, Doumbo OK: The pathogenic basis of malaria. Nature. 2002, 415: 673-679. 10.1038/415673a.View ArticlePubMedGoogle Scholar
  4. Franke-Fayard B, Fonager J, Braks A, Khan SM, Janse CJ: Sequestration and tissue accumulation of human malaria parasites: can we learn anything from rodent models of malaria?. PLoS Pathog. 2010, 6: e1001032-10.1371/journal.ppat.1001032.PubMed CentralView ArticlePubMedGoogle Scholar
  5. Field JW: Blood examination and prognosis in acute falciparum malaria. Trans R Soc Trop Med Hyg. 1949, 43: 33-48. 10.1016/0035-9203(49)90022-X.View ArticlePubMedGoogle Scholar
  6. Silamut K, White NJ: Relation of the stage of parasite development in the peripheral blood to prognosis in severe falciparum malaria. Trans R Soc Trop Med Hyg. 1993, 87: 436-443. 10.1016/0035-9203(93)90028-O.View ArticlePubMedGoogle Scholar
  7. Lwin KM, Ashley EA, Proux S, Silamut K, Nosten F, McGready R: Clinically uncomplicated Plasmodium falciparum malaria with high schizontaemia: a case report. Malar J. 2008, 7: 57-10.1186/1475-2875-7-57.PubMed CentralView ArticlePubMedGoogle Scholar
  8. Young MD: The prognostic value of finding schizonts of Plasmodium falciparum in the peripheral blood. Trans R Soc Trop Med Hyg. 1995, 89: 237-View ArticlePubMedGoogle Scholar
  9. World Health Organization: Guidelines for the treatment of malaria. 2010,, second editionthGoogle Scholar
  10. World Health Organization: Communicable Diseases Cluster: Severe falciparum malaria. Trans R Soc Trop Med Hyg. 2000, 94 (Suppl 1): S1-S90.View ArticleGoogle Scholar
  11. van Gool T, van Wolfswinkel ME, Koelewijn R, van Thiel PP, Jacobs J, van Hellemond JJ, van Genderen PJ: A simple and fast method to exclude high Plasmodium falciparum parasitaemia in travellers with imported malaria. Malar J. 2011, 10: 300-10.1186/1475-2875-10-300.PubMed CentralView ArticlePubMedGoogle Scholar
  12. van Genderen PJ, Hesselink DA, Bezemer JM, Wismans PJ, Overbosch D: Efficacy and safety of exchange transfusion as an adjunct therapy for severe Plasmodium falciparum malaria in nonimmune travelers: a 10-year single-center experience with a standardized treatment protocol. Transfusion. 2010, 50: 787-794. 10.1111/j.1537-2995.2009.02488.x.View ArticlePubMedGoogle Scholar
  13. van Wolfswinkel ME, Hesselink DA, Zietse R, Hoorn EJ, van Genderen PJ: Hyponatraemia in imported malaria is common and associated with disease severity. Malar J. 2010, 25: 140-View ArticleGoogle Scholar
  14. Van Genderen PJ, van der Meer IM, Consten J, Petit PLC, van Gool T, Overbosch D: Evaluation of plasma lactate as a parameter for disease severity on admission in travelers with Plasmodium falciparum malaria. J Travel Med. 2005, 12: 261-264.View ArticlePubMedGoogle Scholar
  15. van Wolfswinkel ME, Hesselink DA, Hoorn EJ, de Rijke YB, Koelewijn R, van Hellemond JJ, van Genderen PJ: Copeptin does not accurately predict disease severity in imported malaria. Malar J. 2012, 5: 11-16.Google Scholar
  16. Lew VL: Malaria: endless fascination with merozoite release. Curr Biol. 2005, 15: R760-R761. 10.1016/j.cub.2005.08.059.View ArticlePubMedGoogle Scholar
  17. Dondorp A, Nosten F, Stepniewska K, Day N, White N: South East Asian Quinine Artesunate Malaria Trial (SEAQUAMAT) group: Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial. Lancet. 2005, 366: 717-725.View ArticlePubMedGoogle Scholar
  18. Dondorp AM, Fanello CI, Hendriksen IC, Gomes E, Seni A, Chhaganlal KD, Bojang K, Olaosebikan R, Anunobi N, Maitland K, Kivaya E, Agbenyega T, Nguah SB, Evans J, Gesase S, Kahabuka C, Mtove G, Nadjm B, Deen J, Mwanga-Amumpaire J, Nansumba M, Karema C, Umulisa N, Uwimana A, Mokuolu OA, Adedoyin OT, Johnson WB, Tshefu AK, Onyamboko MA, Sakulthaew T, Ngum WP, Silamut K, Stepniewska K, Woodrow CJ, Bethell D, Wills B, Oneko M, Peto TE, von Seidlein L, Day NP, White NJ, AQUAMAT group: Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet. 2010, 376: 1647-1657. 10.1016/S0140-6736(10)61924-1.PubMed CentralView ArticlePubMedGoogle Scholar
  19. Zoller T, Junghanss T, Kapaun A, Gjorup I, Richter J, Hugo-Persson M, Mørch K, Foroutan B, Suttorp N, Yürek S, Flick H: Intravenous artesunate for severe malaria in travelers, Europe. Emerg Infect Dis. 2011, 17: 771-777. 10.3201/eid1705.101229.PubMed CentralView ArticlePubMedGoogle Scholar
  20. Kreeftmeijer-Vegter AR, van Genderen PJ, Visser LG, Bierman WF, Clerinx J, van Veldhuizen CK, de Vries PJ: Treatment outcome of intravenous artesunate in patients with severe malaria in the Netherlands and Belgium. Malar J. 2012, 11: 102-10.1186/1475-2875-11-102.PubMed CentralView ArticlePubMedGoogle Scholar


© van Wolfswinkel et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Please note that comments may be removed without notice if they are flagged by another user or do not comply with our community guidelines.