Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 17, Number 7—July 2011

Severe Plasmodium knowlesi Malaria in a Tertiary Care Hospital, Sabah, Malaysia

Timothy William, Jayaram Menon, Giri S. Rajahram, Leslie Chan, Gordon Ma, Samantha Donaldson, Serena Khoo, Charlie Fredrick, Jenarun Jelip, Nicholas M. Anstey, and Tsin Wen YeoComments to Author 
Author affiliations: Author affiliations: Queen Elizabeth Hospital, Kota Kinabalu, Sabah, Malaysian Borneo (T. William, J. Menon, G. Rajahram, L. Chan, G. Ma, S. Donaldson, S. Khoo, C. Fredrick); Department of Health, Kota Kinabalu, Malaysia (J. Jelip); Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia (N.M. Anstey, T.W. Yeo); Royal Darwin Hospital, Darwin (N.M. Anstey, T.W. Yeo)

Cite This Article


The simian parasite Plasmodium knowlesi causes severe human malaria; the optimal treatment remains unknown. We describe the clinical features, disease spectrum, and response to antimalarial chemotherapy, including artemether-lumefantrine and artesunate, in patients with P. knowlesi malaria diagnosed by PCR during December 2007–November 2009 at a tertiary care hospital in Sabah, Malaysia. Fifty-six patients had PCR-confirmed P. knowlesi monoinfection and clinical records available for review. Twenty-two (39%) had severe malaria; of these, 6 (27%) died. Thirteen (59%) had respiratory distress; 12 (55%), acute renal failure; and 12, shock. None experienced coma. Patients with uncomplicated disease received chloroquine, quinine, or artemether-lumefantrine, and those with severe disease received intravenous quinine or artesunate. Parasite clearance times were 1–2 days shorter with either artemether-lumefantrine or artesunate treatment. P. knowlesi is a major cause of severe and fatal malaria in Sabah. Artemisinin derivatives rapidly clear parasitemia and are efficacious in treating uncomplicated and severe knowlesi malaria.

The simian parasite Plasmodium knowlesi has recently been found to be a major cause of human malaria in Malaysian Borneo (1,2), with the disease also reported from southern and eastern Asia (3). To our knowledge, the only large epidemiologic and clinical studies have been from Sarawak State, Malaysian Borneo, with case series or reports from persons or returning travelers from Myanmar (4), Thailand (5,6), Vietnam (7), Philippines (8,9), Singapore (10), Sarawak (11), western Malaysia (12), and Indonesia (13).

The potential for P. knowlesi to cause severe disease has been suggested by experimental simian and human infections (1416). The first description of naturally acquired severe human P. knowlesi infection was a retrospective study from Sarawak that detailed 4 fatal cases with multiorgan failure (17). Subsequently, a prospective study from the Kapit District Hospital in Sarawak enrolled 107 persons with P. knowlesi monoinfection and demonstrated that 10 patients had severe disease as defined by World Health Organization (WHO) criteria, resulting in 2 deaths (2).

The disease spectrum and clinical features of large numbers of patients infected with P. knowlesi have not been described outside Sarawak. To reliably differentiate P. malariae from P. knowlesi infections by using only microscopy is difficult (18); such differentiation requires molecular methods (1). In a random survey from several districts in Sabah, the state that borders Sarawak, 44 of 49 cases of microscopy-diagnosed P. malariae infection were confirmed by PCR to be P. knowlesi, indicating that knowlesi malaria was not confined to isolated areas (17). In recent years at Queen Elizabeth Hospital (QEH), a tertiary care referral hospital in Kota Kinabalu, Sabah State, patients with severe malaria by WHO criteria had received a diagnosis by microscopy as P. malariae infection, but P. knowlesi was suspected as the etiologic agent. We conducted a retrospective review of the clinical spectrum of all case-patients with P. malariae malaria who were admitted to QEH during December 2007–November 2009 and confirmed the diagnosis of P. malariae or P. knowlesi infection by molecular methods.

The optimal management of knowlesi malaria is not known. P. knowlesi infection has been successfully treated with chloroquine (2) and quinine (2); however, the therapeutic efficacy of other antimalarial agents is not known. Artemisinin-derivative combination therapy is now the WHO treatment of choice for uncomplicated falciparum malaria (19) and is increasingly recommended for nonfalciparum malaria (20); its efficacy in knowlesi malaria is unknown. Similarly, intravenous artesunate is now the treatment of choice for severe falciparum malaria in adults (19,21), but the therapeutic response to this regimen in severe knowlesi malaria is unknown. As part of our study, we documented the therapeutic responses in uncomplicated and severe knowlesi malaria treated with artemisinin derivatives.


Study Site

QEH serves as a tertiary care hospital for the Malaysian state of Sabah, which has an estimated population of 3 million. It has a modern well-equipped intensive care unit with facilities for invasive ventilation, hemodynamic support, and renal replacement therapy.

Retrospective Case Review

All patients with microscopy-diagnosed malaria during December 2007–November 2009 were recorded from a prospective laboratory register, and those with P. malariae monoinfection or mixed infections were identified. Additional patients, for whom conditions had been diagnosed by microscopy as caused by other Plasmodium species but were identified as P. knowlesi infections by PCR, were also included. Case records were reviewed, and clinical information was entered into a standardized data collection form. Severe disease was classified on the basis of WHO criteria for severe falciparum malaria (22). National policy recommends that all patients with microscopy-diagnosed malaria be hospitalized until negative blood smears are obtained on 2 consecutive examinations. The study was approved by the Medical Research Ethics Sub-Committee of the Malaysian Ministry of Health and the Menzies School of Health Research, Australia.

Laboratory Procedures

Blood films were examined by experienced laboratory microscopists, and the parasite count was classified on a scale of 1 to 4 (1= 4–40 parasites/µL, 2 = 41–400 parasites/µL, 3 = 401–4,000 parasites/µL, 4 = >4,000 parasites/µL). Hematologic results (Sysmex XT1800 [Sysmex Corp., Mundelein, IL, USA] and CELL-DYN Sapphire [Abbott Diagnostics, Abbot Park, IL, USA]) and prothrombin and partial thromboplastin times (STA Compact Hemostasis Analyzer [Diagnostica Stago, Asnières sur Seine, France]) were obtained on site. Serum sodium, potassium, glucose, creatinine, bilirubin, albumin (Roche/Hitachi Modular Analytics EVO, Roche, Basel, Switzerland), and arterial blood gas levels (Radiometer ABL520, Radiometer, Brønchøj, Denmark) were also assayed on site. Blood cultures were performed with an automated system (Becton Dickinson, Franklin Lakes, NJ, USA) and dengue serology by ELISA (PanBio, Brisbane, Australia). In accordance with QEH policy, all slides indicating P. malariae monoinfection or mixed infections were sent for molecular testing at the Sabah State Reference Laboratory, along with ≈15% of other species. Parasite DNA was extracted, and nested PCR was performed for P. falciparum, P. vivax, P. malariae, P. ovale, and P. knowlesi by methods previously published (1,17).

Statistical Analysis

Data were analyzed by using STATA version 9.2 (StataCorp LP, College Station, TX, USA). For continuous variables, intergroup differences were compared by Student t test or Mann-Whitney U test. For categorical outcome variables, intergroup differences were compared by using the χ2 test or Fisher exact test. Logistic regression was used to determine the association between binary outcomes and other variables. A 2-sided value of p<0.05 was considered significant.


Baseline Characteristics


Thumbnail of Flowchart of microscopy and PCR results of Plasmodium malariae or P. knowlesi infections by severity, Sabah, Malaysia, 2007–2009.

Figure. Flowchart of microscopy and PCR results of Plasmodium malariae or P. knowlesi infections by severity, Sabah, Malaysia, 2007–2009.

Included in the final analysis were 56 patients with PCR-confirmed P. knowlesi malaria. On the basis of WHO severity criteria (22), 22 (39%) had severe malaria, and 34 (61%) had uncomplicated disease (Figure). These patients were identified from a group of 74 patients with documented P. malariae malaria listed in the laboratory microscopy register: 54 had P. knowlesi monoinfection shown by PCR and medical records available for review (Figure). In addition, another 2 patients received a diagnosis by microscopy as being infected with other Plasmodium sp. but were found to have P. knowlesi monoinfections on PCR testing (Figure). All 24 patients with severe malaria had PCR performed; of these, 22 had P. knowlesi monoinfection (Figure). In the group with uncomplicated infection, 41 had PCR; 34/41 had only P. knowlesi monofection; 4 cases were mixed with P. knowlesi and other species; 2 cases were non–P. knowlesi, and no Plasmodium sp. was detected in 1 patient (Figure).

The baseline demographics and clinical symptoms of both groups with PCR-confirmed P. knowlesi monoinfections are detailed in Table 1. The mean age of the patients with severe malaria (57 years; 95% confidence interval [CI] 50–64 years) was significantly older than that of the uncomplicated group (37 years; 95% CI 34–42 years) (p<0.001); however, the proportion with chronic coexisting conditions did not differ significantly between groups (Table 1). In severe disease, the proportion of female patients (36%) was significantly higher than that in uncomplicated malaria (8.8%) (odds ratio [OR] 5.9, 95% CI 1.4–25.6; p = 0.02). Overall, 8 of 11 female patients had severe disease. Two women were pregnant; 1 had severe malaria, and the other had uncomplicated malaria. Two male patients had second uncomplicated infections during the study period; 1 became infected 10 months after the first, and the other had a mixed P. vivax/P. knowlesi infection 6 weeks after initial infection. Both patients had received chloroquine for the first P. knowlesi infection. One patient with uncomplicated disease also had HIV infection.

Almost all patients with severe and uncomplicated disease had a history of fever, and no significant difference was found in duration of fever or other clinical symptoms before the patient sought treatment (Table 1). However, patients with severe complications had a lower mean arterial pressure and an increased respiratory rate. Of those not already intubated on transfer or admission to QEH, patients with severe disease also had lower oxygen saturation at room air than did those with uncomplicated disease (Table 1).

Laboratory and Radiologic Investigations

In patients with severe disease, hemoglobin concentrations and platelet counts were significantly lower, and leukocyte counts, prothrombin time, and partial thromboplastin time were elevated, compared with results for patients with uncomplicated malaria (Table 2). Sodium and albumin concentrations were also significantly decreased, and creatinine and total bilirubin levels increased in patients with severe disease (Table 2). Parasite counts were significantly higher in severe disease (Table 2). Blood cultures, performed in 12/34 patients with uncomplicated disease, were all negative. Dengue serologic testing was performed on admission for 11 patients with uncomplicated disease; 10 were negative for immunoglobulin (Ig) M and IgG, and 1 patient was positive for IgM. Blood cultures were performed for 17 patients with severe disease; 1 patient had Enterobacter cloacae bacteremia, 5 had coagulase-negative Staphylococcus infection (attributed to contamination), and samples from the remainder were negative. Dengue serologic tests for 10 patients with severe disease were all negative. Chest radiographs were obtained on admission for 30 patients (8 with uncomplicated disease, 17 with severe disease); none with uncomplicated disease were reported to have infiltrates, compared with 8/17 with severe disease (p = 0.01); all of those with severe disease had acute respiratory distress syndrome (ARDS) with hypoxemia.

Severe Malaria

Of patients with severe disease, 17 were referred from district hospitals and 5 were directly admitted. Twenty-one of these patients had complications on admission, and in 1 patient with acute renal failure, respiratory distress developed 3 days after the start of therapy. During the hospital course, 7 patients each had 1 WHO criterion for severity, and 15 each had >2 severity criteria (2, n = 6; 3, n = 5; 4, n = 1; 5, n = 1; and 6, n = 2) (Table 3). The mean age of the 6 patients who died was 64 years (95% CI 49–78 years), and the mean age of the 16 survivors (was 53 years (95% CI 45–61 years; p = 0.1). Decreased Glasgow Coma Scores (GCS 14 and 11) on initial hospital visit were seen in 2 patients who died, but other signs and symptoms did not satisfy WHO criteria for cerebral malaria. No cases of severe anemia (<6 g/dL) were found. Acute respiratory distress (n = 13), acute renal failure (n = 12), shock (n = 12), and hyperbilirubinemia (n = 9) were the most common manifestation of severe disease (Table 3). Seven patients had acidosis (on the basis of arterial blood gas analysis) (Table 3). Seven (32%) patients had significant elevations of the prothrombin and partial thromboplastin times, although none were reported to have clinically important bleeding. In patients with acute respiratory distress, the ratio of the partial pressure of oxygen to the fraction of inspired oxygen (PaO2:FiO2) was available for 11/13 patients. In this group, the mean ratio was 165 (range 101–250), with 10 meeting the criteria for ARDS (PaO2:FiO2 <200). Eight patients had cardiac function evaluated by transthoracic echocardiogram, and all had normal results, except for a 76-year-old woman with a left ventricular ejection fraction of 30%.

Seventeen patients required intensive care unit management, 12 received inotrope support, 11 required hemodialysis, and 10 received mechanical ventilation (Table 3). The median duration of intensive care stay was 6 days (range 1–11 days); for hemodialysis, 3 days (range 1–6); and for mechanical ventilation, 3 days (range 1–9). Eleven patients were transfused with erythrocytes, 2 with fresh frozen plasma, and 4 with platelets (Table 3).

Malarial and Antimicrobial Drug Therapy

Of 34 patients with confirmed, uncomplicated P. knowlesi malaria, 15 received oral chloroquine, 11 received oral quinine, and 8 received artemether-lumefantrine. Two patients from the quinine group received intravenous quinine for ≈24 hours before treatment was changed to oral therapy. Daily peripheral blood films were available for 10 patients who received chloroquine (mean admission parasitemia 2+), for 8 who received quinine (mean admission parasitemia 3+), and for 6 who received artemether-lumefantrine (mean admission parasitemia 2+). When we excluded patients who received intravenous therapy initially, the difference was significant in median parasite clearance times between those who received artemether-lumefantrine (1 day; range 0–3) and those who received chloroquine (2.5 days; range 1–3) or quinine (2.5 days; range 1–3); p = 0.01. The proportion with negative results for parasitemia by day 1 was 4/6, 3/10, and 1/8 for artemether-lumefantrine, chloroquine, and quinine, respectively (p = 0.1), and 5/6, 5/10, and 4/8 for each group on day 2 (p = 0.2). Among patients with uncomplicated disease, 11/34 patients received doxycycline, and 7/34 received other antimicrobial drugs during their hospitalization.

In December 2008, hospital policy changed, and the recommendation was made that patients receive intravenous artesunate, when available, rather than quinine for treatment of severe malaria. Of the 22 patients with severe P. knowlesi malaria, 16 received intravenous quinine, and 6 received intravenous artesunate. Daily peripheral blood films were available for 11 of the patients in the quinine group (mean admission parasitemia 3+) and 4 of the artesunate group patients (mean admission parasitemia 3+), with median parasite clearance time significantly shorter with artesunate (2 days; range 1–3) than with quinine (4 days; range 2–7) (p = 0.02). Of the 6 patients who died, 5 received quinine (median severity criteria 2; case-fatality rate 31%), and 1 received artesunate (median severity criteria 2.5; case-fatality rate 16.6%). Of patients with severe malaria, 13/22 received doxycycline, and 16/22 received other antimicrobial drugs during their hospital course.


Six (27%) of the 22 patients with severe malaria died; mean time from admission to QEH and death was 2.5 days (range 0–4). Of these, all had >3 severity criteria; 6 had ARDS, 5 had acute renal failure, and 4 had shock. All patients who died had a parasitemia level of 4+; survivors had a median level of 3+. None of the patients with uncomplicated disease died. The mean duration of hospital stay was 8.4 days (95% CI 6.3–10.5) for those with severe disease and 5.3 days (95% CI 4.1–7.4) for those with uncomplicated malaria.


Studies from Sarawak have shown that P. knowlesi infections can result in severe and fatal disease (2,17). The present 2-year case series from Sabah indicates that in a tertiary referral hospital setting, the proportion of severe P. knowlesi malaria is higher than reported previously, with 39% of patients having severe malaria according to WHO criteria. The increased frequency of severe disease likely reflects referral bias because a large proportion of patients were referred from surrounding district hospitals. The case-fatality rate for severe malaria of 27% in this study is comparable to that of a previous study (2) and at least as high as that seen with P. falciparum malaria (21). The main demographic factors for severe malaria were increasing age (mean 57 years) and female gender. The former is consistent with a study of falciparum malaria where age was an independent risk factor for development of severe disease and death (23). The reason(s) for the large proportion of severe disease in female patients, noted previously in knowlesi malaria (2) and vivax malaria (24), remain unclear.

For 12 of the 13 patients with respiratory distress, the diagnosis was confirmed by a low arterial partial pressure of oxygen and decreased oxygen saturation with a need for mechanical ventilation. One patient with an increased respiratory rate alone had metabolic acidosis; the 4 other patients had ARDS and hypoxemia. This finding suggests that hypoxemia from acute lung injury is the major cause of respiratory distress in P. knowlesi malaria, although metabolic acidosis can also contribute. Shock occurred in more than half of patients who had severe malaria; however, repeated blood cultures showed clinically significant bacteremia in <10% of patients, which suggests that in most cases of severe knowlesi malaria, concurrent bacteremia does not contribute to hypotension. A previous report with smaller numbers of severe knowlesi malaria found metabolic acidosis in only 10% (2), compared with 30% of severe patients in this study for whom arterial blood gas results showed clear metabolic acidosis. The cause in 6 of 7 patients with acidosis may have been shock and hypoxemia; only 1 patient had neither. Although 30% of patients with severe disease had elevated prothrombin time or partial thromboplastin time, no clinically notable bleeding episodes were observed.

The susceptibility of pregnant women to severe disease in falciparum malaria (22) may also be the case in knowlesi malaria; 18% of women admitted with P. knowlesi malaria were pregnant. One patient in the third trimester of pregnancy survived acute renal failure and shock, but the fetus died.

The multiorgan failure experienced by patients with severe knowlesi malaria is similar to that reported in adults with severe falciparum malaria in areas where the transmission rate is low and unstable (22). However, as seen in a smaller series of severe knowlesi malaria, the ≈50% proportion with ARDS and shock is higher than that reported in series of severe falciparum malaria (22,23,2529). Furthermore, 2 of the major clinical syndromes of severe falciparum malaria—unarousable coma and severe anemia—were absent (2). The absence of severe anemia may reflect the lower malaria transmission rate, the relatively short duration of illness, and the exclusion from this adult referral hospital of children, an age group prone to this complication in falciparum malaria (23). Severe anemia has been described in knowlesi malaria in children elsewhere in Sabah (30). The reasons for the lack of coma are less clear and may reflect differences in pathophysiology between knowlesi and falciparum malaria. In the only detailed autopsy study of fatal knowlesi malaria, widespread microvascular parasite accumulation was found, including within the brain, but no features to suggest cytoadherence of parasitized red cells to endothelial cells, a hallmark of the pathophysiology of severe falciparum malaria (31). Additional causes of impaired microvascular flow and organ dysfunction in falciparum malaria include dysregulated immune responses (32), endothelial activation with elevated angiopoietin-2 and von Willebrand factor (33,34), and decreased vascular nitric oxide bioavailability (25) and red cell deformability (35), but their roles in knowlesi malaria remain unknown.

Thrombocytopenia is nearly universal in P. knowlesi infections; platelet counts are lowest in cases of severe disease when no evidence suggests concurrent dengue. In contrast to platelet counts, leukocyte counts were higher in severe malaria than in uncomplicated malaria. Secondary bacterial infection was uncommon, which suggests that severe P. knowlesi infection itself may account for the neutrophilia.

The optimal management of knowlesi malaria is not known, and the 2010 WHO Malaria Treatment Guidelines do not provide recommendations for its treatment (19). Artemisinin-derivative combination therapy is recommended as first-line treatment of falciparum malaria in Africa and Asia, but there are no reports of artemisinin-derivative combination therapy efficacy in knowlesi malaria. In previous reports, uncomplicated P. knowlesi malaria was treated with chloroquine and primaquine (2,36), whereas severe disease was treated with intravenous quinine (1,2,17). Past studies in Sarawak have shown that although most patients with microscopy-diagnosed P. malariae infection had P. knowlesi, ≈10% were actually infected with P. falciparum (17). In settings such as Malaysia, with a high prevalence of chloroquine-resistant falciparum malaria (37,38), inadvertent use of chloroquine for misdiagnosed falciparum malaria may have deleterious consequences. In uncomplicated knowlesi malaria, we found that chloroquine, quinine, and artemether-lumefantrine were all efficacious, and although comparisons were uncontrolled, those receiving artemether-lumefantrine had faster parasite clearance times. The 1-day median parasite clearance time after using artemether-lumefantrine in our hospitalized patients was similar to that seen in a community study in which chloroquine was used (2), though parasite densities may not have been comparable.

Intravenous artesunate (compared with quinine) reduces the proportion of deaths in severe falciparum malaria (21), but its efficacy is unknown in severe knowlesi malaria. In our study, artesunate-treated patients had faster parasite clearance, and the case-fatality rate (17%) was lower than for those who received quinine (31%). However, the retrospective design and small number of severe cases and deaths do not enable us to assess a possible survival benefit. Current treatment policy at QEH for uncomplicated knowlesi malaria is oral artemether-lumefantrine and for severe knowlesi malaria, intravenous artesunate.

Our study has several limitations. The main ones are the retrospective design and inability to review 10% of the charts. Although samples from most P. malariae patients were sent for molecular confirmation, 8% of the results were unavailable. Several cases microscopically diagnosed as falciparum or vivax malaria were PCR-positive for P. knowlesi. Because only ≈15% of non–P. malariae slides are sent for PCR, we may have underestimated the true proportion of patients hospitalized with knowlesi malaria. Because QEH is a hospital for adults, we were unable to describe the disease spectrum in children.

Our study further highlights the public health implications of P. knowlesi. A high proportion of knowlesi malaria patients admitted to a tertiary care referral hospital in a malaria-endemic area had severe and fatal disease characterized by multiorgan failure, a high proportion with ARDS and shock, and a notable absence of coma. The pathogenic mechanisms underlying this disease spectrum remain unknown. Artemisinin derivatives result in rapid parasite clearance and are efficacious in both uncomplicated and severe knowlesi malaria. Prospective studies to further define the epidemiology, pathogenesis, and optimal treatment for knowlesi malaria are needed.

Dr William is an infectious diseases physician at QEH, Kota Kinabalu, Sabah, Malaysia. His research interests include the clinical spectrum, diagnosis, pathophysiology, and treatment of knowlesi malaria.



We thank Frederick Andreos, Joseph Benedict, Damica Kunsiong, and Juhanah Gimboh for their help in the study. We also thank the Director General of Health (Malaysia) for permission to publish this article.

N.M.A. and T.W.Y. are supported by Australian National Health and Medical Research Council Fellowships



  1. Singh  B, Lee  K, Matusop  A, Radhakrishnan  A, Shamsul  S, Cox-Singh  J, A large focus of naturally acquired Plasmodium knowlesi infections in human beings. Lancet. 2004;363:101724. DOIPubMedGoogle Scholar
  2. Daneshvar  C, Davis  TM, Cox-Singh  J, Rafa'ee  MZ, Zakaria  SK, Divis  PC, Clinical and laboratory features of human Plasmodium knowlesi infection. Clin Infect Dis. 2009;49:85260. DOIPubMedGoogle Scholar
  3. Baird  JK. Malaria zoonoses. Travel Med Infect Dis. 2009;7:26977. DOIPubMedGoogle Scholar
  4. Zhu  HM, Li  J, Zheng  H. Human natural infection of Plasmodium knowlesi [in Chinese]. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2006;24:701.PubMedGoogle Scholar
  5. Jongwutiwes  S, Putaporntip  C, Iwasaki  T, Sata  T, Kanbara  H. Naturally acquired Plasmodium knowlesi malaria in human, Thailand. Emerg Infect Dis. 2004;10:22113.PubMedGoogle Scholar
  6. Putaporntip  C, Hongsrimuang  T, Seethamchai  S, Kobasa  T, Limkittikul  K, Cui  L, Differential prevalence of Plasmodium infections and cryptic Plasmodium knowlesi malaria in humans in Thailand. J Infect Dis. 2009;199:114350. DOIPubMedGoogle Scholar
  7. Van den Eede  P, Van  HN, Van Overmeir  C, Vythilingam  I, Duc  TN, Hung le X, et al. Human Plasmodium knowlesi infections in young children in central Vietnam. Malar J. 2009;8:249. DOIPubMedGoogle Scholar
  8. Luchavez  J, Espino  F, Curameng  P, Espina  R, Bell  D, Chiodini  P, Human infections with Plasmodium knowlesi, the Philippines. Emerg Infect Dis. 2008;14:8113. DOIPubMedGoogle Scholar
  9. Centers for Disease Control and Prevention. Simian malaria in a U.S. traveler—New York, 2008. MMWR Morb Mortal Wkly Rep. 2009;58:22932.PubMedGoogle Scholar
  10. Ng  OT, Ooi  EE, Lee  CC, Lee  PJ, Ng  LC, Pei  SW, Naturally acquired human Plasmodium knowlesi infection, Singapore. Emerg Infect Dis. 2008;14:8146. DOIPubMedGoogle Scholar
  11. Bronner  U, Divis  PC, Farnert  A, Singh  B. Swedish traveller with Plasmodium knowlesi malaria after visiting Malaysian Borneo. Malar J. 2009;8:15. DOIPubMedGoogle Scholar
  12. Cox-Singh  J, Singh  B. Knowlesi malaria: newly emergent and of public health importance? Trends Parasitol. 2008;24:40610. DOIPubMedGoogle Scholar
  13. Figtree  M, Lee  R, Bain  L, Kennedy  T, Mackertich  S, Urban  M, Plasmodium knowlesi in human, Indonesian Borneo. Emerg Infect Dis. 2010;16:6724.PubMedGoogle Scholar
  14. Ibiwoye  MO, Howard  CV, Sibbons  P, Hasan  M, van Velzen  D. Cerebral malaria in the rhesus monkey (Macaca mulatta): observations on host pathology. J Comp Pathol. 1993;108:30310. DOIPubMedGoogle Scholar
  15. Chin  W, Contacos  PG, Collins  WE, Jeter  MH, Alpert  E. Experimental mosquito-transmission of Plasmodium knowlesi to man and monkey. Am J Trop Med Hyg. 1968;17:3558.PubMedGoogle Scholar
  16. White  NJ. Plasmodium knowlesi: the fifth human malaria parasite. Clin Infect Dis. 2008;46:1723. DOIPubMedGoogle Scholar
  17. Cox-Singh  J, Davis  TM, Lee  KS, Shamsul  SS, Matusop  A, Ratnam  S, Plasmodium knowlsei malaria in humans is widely distributed and potentially life threatening. Clin Infect Dis. 2008;46:16571. DOIPubMedGoogle Scholar
  18. Lee  KS, Cox-Singh  J, Singh  B. Morphological features and differential counts of Plasmodium knowlesi parasites in naturally acquired human infections. Malar J. 2009;8:73. DOIPubMedGoogle Scholar
  19. World Health Organization. Guidelines for the treatment of malaria, 2nd ed. Geneva: The Organization; 2010.
  20. Douglas  NM, Anstey  NM, Angus  BJ, Nosten  F, Price  RN. Artemisinin combination therapy for vivax malaria. Lancet Infect Dis. 2010;10:40516. DOIPubMedGoogle Scholar
  21. 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;366:71725.PubMedGoogle Scholar
  22. World Health Organization. Severe falciparum malaria. Trans R Soc Trop Med Hyg. 2000;94(Suppl 1):S190. DOIPubMedGoogle Scholar
  23. Dondorp  AM, Lee  SJ, Faiz  MA, Mishra  S, Price  R, Tjitra  E, The relationship between age and the manifestations of and mortality associated with severe malaria. Clin Infect Dis. 2008;47:1517. DOIPubMedGoogle Scholar
  24. Tjitra  E, Anstey  NM, Sugiarto  P, Wariker  N, Kenangalem  E, Karyana  M, Multidrug-resistant Plasmodium vivax associated with severe and fatal malaria: a prospective study in Papua, Indonesia. PLoS Med. 2008;5:e128. DOIPubMedGoogle Scholar
  25. Yeo  TW, Lampah  DA, Gitawati  R, Tjitra  E, Kenangalem  E, McNeil  YR, Impaired nitric oxide bioavailability and L-arginine reversible endothelial dysfunction in adults with falciparum malaria. J Exp Med. 2007;204:2693704. DOIPubMedGoogle Scholar
  26. Krishnan  A, Karnad  DR. Severe falciparum malaria: an important cause of multiple organ failure in Indian intensive care unit patients. Crit Care Med. 2003;31:227884. DOIPubMedGoogle Scholar
  27. Lichtman  AR, Mohrcken  S, Engelbrecht  M, Bigalke  M. Pathophysiology of severe forms of falciparum malaria. Crit Care Med. 1990;18:6668. DOIPubMedGoogle Scholar
  28. Aursudkij  B, Wilairatana  P, Vannaphan  S, Walsh  DS, Gordeux  VR, Looareesuwan  S. Pulmonary edema in cerebral malaria patients in Thailand. Southeast Asian J Trop Med Public Health. 1998;29:5415.PubMedGoogle Scholar
  29. Bruneel  F, Hocqueloux  L, Alberti  C, Wolff  M, Chevret  S, Bedos  JP, The clinical spectrum of severe imported falciparum malaria in the intensive care unit: report of 188 cases in adults. Am J Respir Crit Care Med. 2003;167:6849. DOIPubMedGoogle Scholar
  30. Barber  BE, William  T, Jikal  M, Jilip  J, Prabakaran  D, Menon  J, Plasmodium knowlesi malaria in children. Emerg Infect Dis. 2011;17:81420.PubMedGoogle Scholar
  31. Cox-Singh  J, Hiu  J, Lucas  SB, Divis  PC, Zulkarnaen  M, Chandran  P, Severe malaria—a case of fatal Plasmodium knowlesi infection with post-mortem findings: a case report. Malar J. 2010;9:10. DOIPubMedGoogle Scholar
  32. Schofield  L, Grau  GE. Immunological processes in malaria pathogenesis. Nat Rev Immunol. 2005;5:72235. DOIPubMedGoogle Scholar
  33. Löwenberg  EC, Charunwatthana  P, Cohen  S, van den Born  BJ, Meijers  JC, Yunus  EB, Severe malaria is associated with a deficiency of von Willebrand factor cleaving protease, ADAMTS13. Thromb Haemost. 2010;103:1817. DOIPubMedGoogle Scholar
  34. Yeo  TW, Lampah  DA, Gitawati  R, Tjitra  E, Kenangalem  E, Piera  K, Angiopoietin-2 is associated with decreased endothelial nitric oxide and poor clinical outcome in severe falciparum malaria. Proc Natl Acad Sci U S A. 2008;105:17097102. DOIPubMedGoogle Scholar
  35. Dondorp  AM, Nyanoti  M, Kager  PA, Mithwani  S, Vreeken  J, Marsh  K. The role of reduced red cell deformability in the pathogenesis of severe falciparum malaria and its restoration by blood transfusion. Trans R Soc Trop Med Hyg. 2002;96:2826. DOIPubMedGoogle Scholar
  36. Daneshvar  C, Davis  TM, Cox-Singh  J, Rafa'ee  MZ, Zakaria  SK, Divis  PC, Clinical and parasitological response to oral chloroquine and primaquine in uncomplicated human Plasmodium knowlesi infections. Malar J. 2010;9:238. DOIPubMedGoogle Scholar
  37. Lokman Hakim  S, Sharifah Roohi  SW, Zurkurnai  Y, Noor Rain  A, Mansor  SM, Palmer  K, Plasmodium falciparum: increased proportion of severe resistance (RII and RIII) to chloroquine and high rate of resistance to sulfadoxine-pyrimethamine in Peninsular Malaysia after two decades. Trans R Soc Trop Med Hyg. 1996;90:2947. DOIPubMedGoogle Scholar
  38. Maqsudur Rahman  KM. Study of Plasmodium falciparum resistance to 4-aminoquinolines (chloroquine) in Sabah, Malaysia. J Trop Med Hyg. 1980;83:25964.PubMedGoogle Scholar




Cite This Article

DOI: 10.3201/eid1707.101017

Table of Contents – Volume 17, Number 7—July 2011

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.



Please use the form below to submit correspondence to the authors or contact them at the following address:

Tsin Wen Yeo, Global Health Division, Menzies School of Health Research, PO Box 41096, Casuarina, Darwin, NT 0811, Australia

Send To

10000 character(s) remaining.


Page created: August 15, 2011
Page updated: August 15, 2011
Page reviewed: August 15, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.