Severe vivax malaria: a systematic review and meta-analysis of clinical studies since 1900
© Rahimi et al.; licensee BioMed Central. 2015
Received: 20 June 2014
Accepted: 29 October 2014
Published: 8 December 2014
Malaria caused by Plasmodium vivax was long considered to have a low mortality, but recent reports from some geographical areas suggest that severe and complicated vivax malaria may be more common than previously thought.
The primary objective of this systematic review and meta-analysis was to describe the reported clinical characteristics and the geographical variation in prevalence of reported severe vivax malaria and its change over time derived from English-language articles published since 1900. Medline and Scopus databases were searched for original papers on severe vivax malaria, using as inclusion criteria modified 2010 WHO criteria for the diagnosis of severe falciparum malaria. Articles before 1949 were identified through reference lists in journals, textbooks, and personal collections of colleagues.
A total of 77 studies with reported severe vivax malaria and 63 studies with no reported severe vivax malaria (totaling 46,411 and 6,753 vivax malaria patients, respectively) were included. The 77 studies with reported severe vivax malaria were mainly from India (n = 33), USA (n = 8), Indonesia (n = 6), and Pakistan (n = 6). Vivax endemic countries not reporting severe vivax malaria beyond individual case reports included: the Greater Mekong Sub-region, China, North Korea, Bangladesh, Afghanistan, Middle East (except Qatar), the horn of Africa, and Madagascar. Only 17/77 reports were from before 2000. Vivax mono-infection was confirmed by PCR in 14 studies and co-morbidities were ruled out in 23 studies. Among the 77 studies reporting severe vivax malaria, severe thrombocytopenia (<50,000/mm3) was the most common “severe” manifestation (888/45,775 with pooled prevalence of 8.6%). The case fatality was 0.3% (353/46,411). Severity syndromes varied widely between different geographical areas, with severe anaemia being most prominent in areas of high transmission and chloroquine resistance.
Plasmodium vivax can cause severe and even fatal disease, but there is a recent increase in reports over the past 15 years with larger series restricted to a limited number of geographical areas. The biological basis of these variations is currently not known. More detailed epidemiological studies are needed which dissociate causation from association to refine the definition and estimate the prevalence of severe vivax malaria.
KeywordsPlasmodium vivax Severe Malaria Complication Prevalence Systematic review Meta-analysis
Of the five Plasmodium species causing disease in humans, Plasmodium falciparum is the main cause of severe and fatal disease. Traditionally Plasmodium vivax has been considered relatively benign, except for occasional severe manifestations notably severe anaemia and the acute respiratory distress syndrome . Although death in P. vivax infections has been recognized for over a century, the last decade has seen a remarkable increase in case reports, series and studies describing severe and fatal vivax malaria. An estimated 2.8 billion people globally live in one of the 95 countries endemic for P. vivax[2–5]. In general, in P. vivax endemic areas transmission is low and seasonal (Central, West, South, and South-East Asia), the Americas, and the horn of Africa (and Madagascar); whereas the rest of Africa is relatively spared because of the absence of the Duffy blood group which mediates parasite invasion . In contrast transmission is substantially higher on the island of New Guinea. India contributes nearly half (46%) , China 19%, while Indonesia and Pakistan together contribute 12% of the global population at risk . India has the majority of clinical cases.
Occasional fatalities in vivax malaria have been reported since the species was first recognized, particularly in already debilitated patients, and significant mortality has been attributed to vivax malaria in the first and second world wars although details of speciation are often scanty. Plasmodium vivax was associated with a 7.7% mortality in the malariatherapy of neurosyphilis, but this was attributed in part to the debilitated condition of the patients and mortality in Plasmodium malariae infections was even higher . Early publications reporting severe vivax malaria include case reports [7–9] and small case series [10, 11], but in recent years, larger studies conducted in India, Indonesian Papua, and Papua New Guinea suggest a stronger association between P. vivax infection, severe disease and death than recognized previously [12–16]. A systematic review and meta-analysis was conducted from all identifiable English-language articles published since 1900 reporting human cases of severe P. vivax infection. The primary objective was to describe the geographical variation in prevalence of severe vivax malaria and the different presenting syndromes and characteristics, as well as to analyse the changes in reporting over time.
Search engines, terms, and strategies
Eligible studies on severe vivax malaria since 1949 were identified in Medline (via PubMed) and Scopus (via Scopus). The final search and updates in both databases were carried out on January 28, 2014. Articles before 1949 (Pre-PubMed era) were mainly searched through other sources including reference lists of published journal articles and (old) textbooks and through gifts of personal collections of colleagues. Details on variables, search terms, and search strategies are explained in Additional file 1.
All literature in English describing clinical studies in human vivax malaria was considered, recognizing that there is also a substantial literature in other languages. Malaria was diagnosed by peripheral blood smear (PBS) and in recent years by rapid diagnostic test (RDT) or polymerase chain reaction (PCR). Since severity criteria for severe vivax malaria have not been specified yet, modified criteria defined in the 2010 WHO supplement on severe falciparum malaria were used as the outcome of interest used for inclusion, with the addition of thrombocytopenia as this has been used as a severity criterion in several publications (<50,000/mm3)  [see Additional file 2]. It should be noted that thrombocytopenia is not a severity criterion for falciparum malaria, and has never been validated as an independent severity measure in vivax malaria. Only articles reporting P. vivax mono-infection were selected. Studies included those where the denominators were both inpatients and outpatients with vivax malaria and studies reporting only inpatients with vivax malaria patients. Exclusion criteria included duplicate reporting, mixed infections (P. vivax with any other Plasmodium species), and insufficient data for extraction. All types of study designs with primary data (having patients of either gender or any age) were eligible, but case reports and case series were not included in pooled calculations of prevalence because the denominator was uncertain. The complete selected articles were analysed and data were coded into a data extraction form (DEF).
Bias assessment and quality assurance
Eligibility for inclusion of every article was reviewed by independent reviewers (Bilal Ahmad Rahimi, Wali Mohammad Wyar, and Arjen M. Dondorp). Disagreements between reviewers were resolved by discussion, and extracted data were validated by an independent person (Watcharee Chokejindachai).
where = Pooled prevalence of the severity signs among vivax malaria patients;
pi = Prevalence of the severity sign in each study;
wi =1/var (pi), which was the weight of each study.
where n = Total number of patients with a specific severity sign due to vivax malaria; freq = Total number of patients with vivax malaria in the study.
A subgroup analysis was performed in order to compare prevalence of severity signs before and after 2000 and between different WHO regions (Africa [AFRO], Americas [AMRO], Eastern-Mediterranean [EMRO], Europe [EURO], South-East Asia [SEARO], and Western Pacific [WPRO]) and countries, using Chi2 test. Software STATA version 12 (Stata Corp LP, Texas USA) was used for statistical analysis.
Characteristics of studies reporting severe vivax malaria
Characteristics of the 77 studies with severe vivax malaria patients are explained in Additional file 3. Among them, 36 were retrospective hospital-based studies (RHBS) and 41 were prospective hospital-based studies (PHBS). Regarding their geographical origin, 42 (54.5%), 17 (22.1%), 10 (13%), and 8 (10.4%) were from SEARO, AMRO, EMRO, and WPRO, respectively. Specified by country, 33 (42.9%), 8 (10.39%), 6 (7.8%), and 6 (7.8%) studies were reported from India, USA, Pakistan, and Indonesia, respectively.
Pooled prevalence of severity signs from 140 studies reporting on both severe and uncomplicated vivax malaria
Overall 77 studies reported patients with severe vivax malaria patients while 63 studies did not report any patients as having severe vivax malaria.
Pooled prevalence of the various severity signs in studies with and without reported severe vivax malaria patients (140 studies)
Total patients with severity sign
Pooled prevalence, %
95% CI, %
Pooled prevalence of severity signs from 77 studies reporting on severe vivax malaria only
Pooled prevalence of severity signs among reported severe vivax malaria patients (77 studies)
Total patients with severity sign
Pooled prevalence, %
95% CI, %
Comparisons with falciparum malaria
In Indonesian Papua, coma associated with PCR-confirmed P. vivax mono-infection (and without overt co-morbidities) occurred 23 times less frequently than that seen with falciparum malaria and was estimated as occurring in one in 29,500 infections . In Thailand, the risk of hospitalization with impaired consciousness with microscopy-diagnosed P. vivax (not PCR-confirmed) was one in 858 infections, with the risk being 15.2 fold less than that with P. falciparum. Mortality was 0.22% in children hospitalized in Eastern Thailand with vivax malaria (concomitant falciparum malaria excluded by microscopy only) .
Pooled prevalence of severity signs in vivax malaria from 62 studies reporting on both inpatients and outpatients
Among 77 studies with severe vivax malaria patients, 62 studies reported severity signs in both inpatients and outpatients of vivax malaria. In these studies, 31 reported cerebral malaria, six generalized seizures, 14 renal dysfunction, 19 respiratory dysfunction, 31 hepatic dysfunction, 17 abnormal bleeding/DIC, seven haemoglobinuria, eight hypoglycaemia, four metabolic acidosis, six circulatory collapse/shock, 23 severe anaemia, 21 severe thrombocytopenia, and 28 studies reported fatal cases [see Additional files 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17].
Pooled prevalence of severity signs in vivax malaria from 15 studies reporting on inpatients only
Among 77 studies with severe vivax malaria patients, 15 studies described severity signs only in inpatients vivax malaria. In these studies, 11 reported cerebral malaria, 5 repeated generalized seizures, 6 renal dysfunction, 8 respiratory dysfunction, 12 hepatic dysfunction, 7 abnormal bleeding/DIC, 3 haemoglobinuria, 6 hypoglycaemia, 4 metabolic acidosis, 5 circulatory collapse/shock, 10 severe anaemia, 6 severe thrombocytopenia, and 9 studies reported deaths [see Additional files 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 and 31].
Comparison of severity signs between vivax and falciparum malaria
There is substantial variation in the reported geographic distribution and the incidence of severe manifestations of vivax malaria. This analysis also shows a large increase since the year 2000 in the number of studies and numbers of patients reported with severe P. vivax infections, (which in most studies was confirmed as mono-infection by PCR). Of these 33 (42.9%) studies came from India. In contrast, a large number of endemic countries do not report severe vivax malaria, including the Greater Mekong Sub-region, North-east China, North-Korea, Bangladesh, Afghanistan, Middle East (except Qatar), Somalia, and Madagascar. There are two general presentations reported; severe anaemia in young children from the island of New Guinea where transmission is high, and vital organ dysfunction usually in adults from low transmission settings. A large variation in organ involvement was observed in the latter group. Vivax malaria was reported as an important cause of hospital admission in endemic areas, but a major problem in determining the true incidence and prevalence of severe vivax malaria is that severe disease has been considered relatively unusual in vivax malaria, and so its absence from a clinical series has not been considered noteworthy. For example in over 1,000 patients with severe malaria admitted to a centre in Ho Chi Minh city, Vietnam, specializing in its management there was one case of severe vivax (cerebral) malaria and no cases of vivax malaria associated acute renal failure (TT Hien & NP Phu: personal communication), but this paucity of severe disease was not considered noteworthy and so not reported. This contrasts with a prevalence of severe disease amongst admitted cases of over 30% in some series. Thus estimating incidence and prevalence from series which do report severe vivax malaria provides overestimates. Furthermore the most prevalent severity sign reported was thrombocytopenia <50,000/μL (26.1%), which is not regarded as a severity sign in falciparum malaria, and has not been validated as an independent severity measure in vivax malaria. The least prevalent manifestation was haemoglobinuria (0.1%). In studies with only inpatients of vivax malaria, thrombocytopenia (35.9%) was the most commonly reported severity sign, while least prevalent severity sign was respiratory dysfunction (1%). Mortality in studies with only inpatients of vivax malaria was 28.2%, compared to 0.2% in groups with both inpatients and outpatients of vivax malaria.
How can the sharp increase in reported cases of severe vivax malaria, the geographical heterogeneity, and the different severe manifestations be explained?
It seems unlikely that underreporting can explain the scarcity of cases in the last century, although there are only few data to support this. A study in American and Allied soldiers in India reported in 1944, described cerebral malaria in 5/1,375 cases (0.4%) with P. vivax, compared to 93/2664 (3.5%) with P. falciparum or mixed infection . An Indian study from 1982 reported severe malaria in 4/178 (2.2%) patients with P. vivax compared to 64/382 (17%) with P. falciparum or mixed infection . A more recent Indian study showed a substantially higher proportion of patients (50/338 (15%)) having severe vivax malaria . One contributor to this discrepancy is the inclusion of thrombocytopenia as a severity criterion in recent series.
The geographical heterogeneity is more substantiated by data; a study from the Thai-Myanmar border from 1997 describes a very low incidence of patients with severe P. vivax malaria (3 out of 2573 patients) . A case of P. vivax-related pulmonary oedema has been reported from this area .
Can the increase in chloroquine resistance account for the observed geographical differences?
Chloroquine resistance has been well documented on the Island of New Guinea (Papua New Guinea  and Indonesian Papua [25, 26] and more recently in Amazonas . All these regions report severe vivax malaria. On the other hand, chloroquine resistance has not been clearly described in other areas also reporting severe cases, including India [28–31] and Pakistan [32, 33], although study methodology was not optimal. Chloroquine resistance in settings where chloroquine is still widely used will extend the duration of illness considerably, and recurrent infection is expected to result in an increase in patients presenting with severe anaemia. Indeed, severe anaemia is by far the most common presentation in PNG and Indonesia (a high transmission setting where children are affected predominantly), but less so in Amazonia (a low transmission setting where adults are affected predominantly). Compounding factors to severe anaemia include falciparum malaria, intestinal helminths and nutritional deficiencies [34, 35]. A retrospective study in Indonesian Papua reported similar adjusted odd ratios of death associated with severe anaemia (Hb <5 g/dl) of 4.43 and 5.93 for P. vivax and P. falciparum, respectively. In the same population patients with both falciparum and vivax malaria and thrombocytopenia <50,000/mm3 had an increased mortality, although as not all the other clinical and laboratory measures used to assess disease severity were recorded it is unclear whether thrombocytopenia was an independent risk factor or not . In a study by Limaye and colleagues in Mumbai, India, the most common severe manifestation causing death was ARDS (six out of six patients) .
Can the heterogeneity be explained by differences in background P. vivax parasitaemia, resulting in misdiagnosis of severe febrile illnesses with coincidental P. vivax parasitaemia, analogous to the overdiagnosis of falciparum malaria as a cause of illness in parasitaemic African children?
There are few data available, but in Bikaner (India) where many of the Indian reports on severe malaria originate, the population prevalence of vivax malaria is only around 1% (Maude RE, personal communication). In contrast, the population prevalence is higher in endemic regions Myanmar [37, 38], which does not report severe vivax. In this review, 23/77 (29.9%) studies attempted to rule out possible co-morbidities as confounders. One possibility is that other severe febrile illnesses could reactivate hepatic hypnozoites resulting in relapse. High vivax relapse rates, up to over 40%, have been observed following P. falciparum infection [39–41]. Of the reported studies, only 11 (18.6%) studies used PCR for confirmation of P. vivax mono-infection, but even this would not rule out recently cleared falciparum infection. Typhoid fever, relapsing fever, trench fever, epidemic typhus, and brucellosis have been incriminated as activating P. vivax hypnozoites . In many of the published studies there were only limited efforts to rule out other diseases, including falciparum malaria, bacterial diseases, and viral diseases [13, 43, 44]. Regions could also vary in prevalence of other severe chronic illnesses .
Further detailed study of the reported severe manifestations might shed some light on pathogenesis. In Bikaner, where severe vivax malaria is commonly reported, high rates of acute kidney injury are reported in severe vivax malaria in children aged 0–5 years (8/41: 19.5%), an age group in whom acute tubular necrosis (the pathology implicated in falciparum malaria associated renal failure) is rare. Acidosis was reported in 7/65 children with vivax malaria (mean arterial pH 7.1) but its aetiology was unclear. In falciparum malaria acidosis is associated with a high lactate-pyruvate ratio indicating an anoxic pathogenesis, whereas in sepsis lactic pyruvate rations are not elevated. There is clearly a need for more in-depth prospective epidemiological studies, where background age-stratified population P. vivax parasitaemia prevalence is documented and there is proper evaluation of other concomitant illnesses. One such study from Papua, Indonesia, comparing population prevalence with coma in hospitalized patients estimated the incidence of cerebral malaria as 1:29,486 in P. vivax compared to 1:1,276 in P. falciparum infections. This suggested that P. vivax-associated coma is 23 times less common than P. falciparum-associated coma .
Are P. vivax strains associated with severe disease intrinsically more pathogenic?
Epidemics of severe vivax malaria were reported from the USSR over fifty years ago. Changes in strain virulence could explain the recent and geographical restricted increase in reported cases, although there are no hard data available to support this hypothesis. Vivax strains clearly do differ between regions, which is most evident in the observed relapse patterns. Pathophysiological studies exploring difference in parasite virulence could reveal whether more virulent strains of this parasite with a once benign reputation have appeared.
An earlier systematic review on complicated vivax malaria in South America was reported by Lacerda and colleagues in 2012 . In this review, most of the information derived from non-peer reviewed sources (including masters’ dissertations, doctoral theses, and national congresses’ abstracts) and all data came from the Brazilian literature . A recent review by Baird included all published literature on all types of studies, including case reports (since 1990) and case series .
This analysis had several limitations. The pooled prevalence estimates of severe manifestations are based only on reported studies which include cases of severe vivax malaria and this provides a selection bias. Absence of severe disease amongst patients with vivax malaria appears much less likely to be reported. Assessing the pooled prevalence of severe vivax malaria against the general population or all vivax malaria cases as denominator is not feasible with the current data. Nearly all the estimated worldwide 390 million clinical cases of vivax malaria/year  are not reported in the studies. Except for one community-based study , all of the studies included in this systematic review are hospital-based, excluding case reports or small case series. As a consequence, the estimated pooled prevalence of the different severity manifestations represents proportions amongst patients considered sufficiently ill to warrant hospital admission. In addition, no definite criteria for the diagnosis of severe vivax malaria currently exist (they are “borrowed” from falciparum malaria except for the addition of thrombocytopenia, which has been inadequately justified), and many of the studies did not exclude possible co-morbidities or possible mixed Plasmodium infection. Another shortcoming is that we only selected English language articles, whereas there is a significant literature in other languages, e.g. reports from Amazonia are often in Portuguese.
In summary, there has been a marked increase in reported cases of severe vivax in certain geographical regions of the P. vivax endemic world, which cannot be explained with the current understanding of the disease and warrants further study into its aetiology. The use of thrombocytopenia as an independent severity criterion requires justification. In addition, more detailed epidemiological studies are needed, which adequately exclude co-morbidities, and take into account transmission intensity and anti-malarial drug susceptibility. As for severe P. falciparum malaria, P. vivax- specific criteria for defining severe disease are necessary to facilitate comparison between studies and establish its true prevalence.
Disseminated intravascular coagulation
Peripheral blood smear
Rapid diagnostic test.
We are grateful to Kandahar University, Afghanistan Ministry of Higher Education, and World Bank. We are thankful of Jeanne Packer from Oxford University for her kind help in access to the full articles.
- Anstey NM, Russell B, Yeo TW, Price RN: The pathophysiology of vivax malaria. Trends Parasitol. 2009, 25: 220-227. 10.1016/j.pt.2009.02.003.View ArticlePubMedGoogle Scholar
- Guerra CA, Howes RE, Patil AP, Gething PW, Van Boeckel TP, Temperley WH, Kabaria CW, Tatem AJ, Manh BH, Elyazar IR, Baird JK, Snow RW, Hay SI: The international limits and population at risk of Plasmodium vivax transmission in 2009. PLoS Negl Trop Dis. 2010, 4: e774-10.1371/journal.pntd.0000774.PubMed CentralView ArticlePubMedGoogle Scholar
- Galinski MR, Barnwell JW: Plasmodium vivax: who cares?. Malar J. 2008, 7: S9-10.1186/1475-2875-7-S1-S9.PubMed CentralView ArticlePubMedGoogle Scholar
- Price RN, Tjitra E, Guerra CA, Yeung S, White NJ, Anstey NM: Vivax malaria: neglected and not benign. Am J Trop Med Hyg. 2007, 77: 79-87.PubMed CentralPubMedGoogle Scholar
- Gething PW, Elyazar IRF, Moyes CL, Smith DL, Battle KE, Guerra CA, Patil AP, Tatem AJ, Howes RE, Myers MF, George DB, Horby P, Wertheim HF, Price RN, Jueller I, Baird JK, Hay SI: A long neglected world malaria map: Plasmodium vivax endemicity in 2010. PLoS Negl Trop Dis. 2012, 6: e1814-10.1371/journal.pntd.0001814.PubMed CentralView ArticlePubMedGoogle Scholar
- Swellengrebel NH, Buck A: Malaria in the Netherlands. 1938, Amsterdam: Scheltema & Holkema ltdGoogle Scholar
- Billings F, Post WE: Fatal malaria due to the tertian parasite. Trans Chicago Pathological Soc. 1915, 9: 209-215.Google Scholar
- Boshes B: Neuropsychiatric manifestations during the course of malaria; experiences in the Mediterranean Theater in World War II. Arch Neurol Psychiatry. 1947, 58: 14-27. 10.1001/archneurpsyc.1947.02300300024003.View ArticlePubMedGoogle Scholar
- Verma KC, Magotra ML: Vivax cerebral malaria in Jammu. Indian Pediatr. 1976, 13: 229-231.PubMedGoogle Scholar
- Price JP: Pernicious malaria in children: a report of 24 cases. South Med J. 1937, 30: 901-10.1097/00007611-193709000-00008.View ArticleGoogle Scholar
- Dhayagude RG, Purandare NM: Autopsy study of cerebral malaria with reference to malarial granuloma. Arch Pathol. 1943, 36: 550-558.Google Scholar
- Barcus MJ, Basri H, Picarima H, Manyakori C, Sekartuti , Elyazar I, Bangs MJ, Maguire JD, Baird JK: Demographic risk factors for severe and fatal vivax and falciparum malaria among hospital admissions in northeastern Indonesian Papua. Am J Trop Med Hyg. 2007, 77: 984-991.PubMedGoogle Scholar
- Tjitra E, Anstey NM, Sugiarto P, Warikar N, Kenangalem E, Karyana M, Lampah DA, Price RN: Multidrug-resistant Plasmodium vivax associated with severe and fatal malaria: a prospective study in Papua, Indonesia. PLoS Med. 2008, 5: e128-10.1371/journal.pmed.0050128.PubMed CentralView ArticlePubMedGoogle Scholar
- Genton B, D’Acremont V, Rare L, Baea K, Reeder JC, Alpers MP, Muller I: Plasmodium vivax and mixed infections are associated with severe malaria in children: a prospective cohort study from Papua New Guinea. PLoS Med. 2008, 5: e127-10.1371/journal.pmed.0050127.PubMed CentralView ArticlePubMedGoogle Scholar
- Naha K, Dasari S, Prabhu M: Spectrum of complications associated with Plasmodium vivax infection in a tertiary hospital in South-Western India. Asian Pac J Trop Med. 2012, 5: 79-82. 10.1016/S1995-7645(11)60251-4.View ArticlePubMedGoogle Scholar
- Limaye CS, Londhey VA, Nabar ST: The study of complications of vivax malaria in comparison with falciparum malaria in Mumbai. J Assoc Physicians India. 2012, 60: 15-18.PubMedGoogle Scholar
- WHO: Guidelines for the Treatment of Malaria. 2010, Geneva: World Health Organization, 2Google Scholar
- Lampah DA, Yeo TW, Hardianto SO, Tjitra E, Kenangalem E, Sugiarto P, Price RN, Anstey NM: Coma associated with microscopy-diagnosed Plasmodium vivax: a prospective study in Papua, Indonesia. PLoS Negl Trop Dis. 2011, 5: e1032-10.1371/journal.pntd.0001032.PubMed CentralView ArticlePubMedGoogle Scholar
- Luxemburger C, Ricci F, Nosten F, Raimond D, Bathet S, White NJ: The epidemiology of severe malaria in an area of low transmission in Thailand. Trans R Soc Trop Med Hyg. 1997, 91: 256-262. 10.1016/S0035-9203(97)90066-3.View ArticlePubMedGoogle Scholar
- Wattanagoon Y, Srivilairit S, Looareesuwan S, White NJ: Convulsions in childhood malaria. Trans R Soc Trop Med Hyg. 1994, 88: 426-428. 10.1016/0035-9203(94)90415-4.View ArticlePubMedGoogle Scholar
- Fitz-Hugh T, Pepper DS, Hopkins HO: The cerebral form of malaria. Bull US Army Med. 1944, 83: 39-48.Google Scholar
- Gopinathan VP, Subramanian AR: Pernicious syndromes in Plasmodium infections. Med J Aust. 1982, 2: 568-572.PubMedGoogle Scholar
- Pukrittayakamee S, Chantra A, Vanijanonta S, White NJ: Pulmonary oedema in vivax malaria. Trans R Soc Trop Med Hyg. 1998, 92: 421-422. 10.1016/S0035-9203(98)91075-6.View ArticlePubMedGoogle Scholar
- Rieckmann KH, Davis DR, Hutton DC: Plasmodium vivax resistance to chloroquine?. Lancet. 1989, 2: 1183-1184.View ArticlePubMedGoogle Scholar
- Baird JK, Basri H, Purnomo , Bangs MJ, Subianto B, Patchen LC, Hoffman SL: Resistance to chloroquine by Plasmodium vivax in Irian Jaya, Indonesia. Am J Trop Med Hyg. 1991, 44: 547-552.PubMedGoogle Scholar
- Schuurkamp GJ, Spicer PE, Kereu RK, Bulungol PK, Rieckmann KH: Chloroquine-resistant Plasmodium vivax in Papua New Guinea. Trans R Soc Trop Med Hyg. 1992, 86: 121-122. 10.1016/0035-9203(92)90531-G.View ArticlePubMedGoogle Scholar
- de Santana Filho FS, Arcanjo AR, Chehuan YM, Costa MR, Martinez-Espinosa FE, Vieira JL, Barbosa M, Alecrim WD, Alecrim M: Chloroquine-resistant Plasmodium vivax, Brazilian Amazon. Emerg Infect Dis. 2007, 13: 1125-1126. 10.3201/eid1307.061386.PubMed CentralView ArticlePubMedGoogle Scholar
- Valecha N, Joshi H, Eapen A, Ravinderan J, Kumar A, Prajapati SK, Ringwald P: Therapeutic efficacy of chloroquine in Plasmodium vivax from areas with different epidemiological patterns in India and their Pvdhfr gene mutation pattern. Trans R Soc Trop Med Hyg. 2006, 100: 831-837. 10.1016/j.trstmh.2005.11.012.View ArticlePubMedGoogle Scholar
- Garg M, Gopinathan N, Bodhe P, Kshirsagar NA: Vivax malaria resistant to chloroquine: case reports from Bombay. Trans R Soc Trop Med Hyg. 1995, 89: 656-657. 10.1016/0035-9203(95)90432-8.View ArticlePubMedGoogle Scholar
- Mishra N, Singh JP, Srivastava B, Arora U, Shah NK, Ghosh SK, Bhatt RM, Sharma SK, Das MK, Kumar A, Anvikar AR, Kaitholia K, Gupta R, Sonal GS, Dhariwal AC, Valecha N: Monitoring antimalarial drug resistance in India via sentinel sites: outcomes and risk factors for treatment failure, 2009–2010. Bull World Health Organ. 2012, 90: 895-904.PubMed CentralPubMedGoogle Scholar
- Baird JK: Chloroquine resistance in Plasmodium vivax. Antimicrob Agents Chemother. 2004, 48: 4075-4083. 10.1128/AAC.48.11.4075-4083.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- Beg MA, Sani N, Mehraj V, Jafri W, Khan MA, Malik A, Menezes E, Hussain R, Smego R: Comparative features and outcomes of malaria at a tertiary care hospital in Karachi, Pakistan. Int J Infect Dis. 2008, 12: 37-42. 10.1016/j.ijid.2007.04.006.View ArticlePubMedGoogle Scholar
- Leslie T, Mayan MI, Hasan MA, Safi MH, Klinkenberg E, Whitty CJ, Rowland M: Sulfadoxine-pyrimethamine, chlorproguanil-dapsone, or chloroquine for the treatment of Plasmodium vivax malaria in Afghanistan and Pakistan: a randomized controlled trial. JAMA. 2007, 297: 2201-2209. 10.1001/jama.297.20.2201.View ArticlePubMedGoogle Scholar
- Melo GC, Reyes-Lecca RC, Vitor-Silva S, Monteiro WM, Martins M, Benzecry SG, Alecrim MG, Lacerda MV: Concurrent helminthic infection protects schoolchildren with Plasmodium vivax from anemia. PLoS One. 2010, 5: e11206-10.1371/journal.pone.0011206.PubMed CentralView ArticlePubMedGoogle Scholar
- Boel M, Carrara VI, Rijken M, Proux S, Nacher M, Pimanpanarak M, Paw MK, Moo O, Gay H, Bailey W, Singhasivanon P, White NJ, Nosten F, McGready R: Complex Interactions between soil-transmitted helminths and malaria in pregnant women on the Thai-Burmese border. PLoS Negl Trop Dis. 2010, 4: e887-10.1371/journal.pntd.0000887.PubMed CentralView ArticlePubMedGoogle Scholar
- Lampah DA, Yeo TW, Malloy M, Kenangalem E, Douglas NM, Ronaldo D, Sugiarto P, Simpson JA, Peospoprodjo JR, Anstey NM, Price RN:Severe thrombocytopenia: A risk factor for mortality in Papua, Indonesia. J Infect Dis. 2014, jiu487v1-jiu487 [Epub ahead of print],Google Scholar
- Moon SU, Lee HW, Kim JY, Na BK, Cho SH, Lin K, Sohn WM, Kim TS: High frequency of genetic diversity of Plasmodium vivax field isolates in Myanmar. Acta Trop. 2009, 109: 30-36. 10.1016/j.actatropica.2008.09.006.View ArticlePubMedGoogle Scholar
- Zhong D, Bonizzoni M, Zhou G, Wang G, Chen B, Vardo-Zalik A, Cui L, Yan G, Zheng B: Genetic diversity of Plasmodium vivax malaria in China and Myanmar. Infect Genet Evol. 2011, 11: 1419-1425. 10.1016/j.meegid.2011.05.009.PubMed CentralView ArticlePubMedGoogle Scholar
- Looareesuwan S, White NJ, Chittamas S, Bunnag D, Harinasuta T: High rate of Plasmodium vivax relapse following treatment of falciparum malaria in Thailand. Lancet. 1987, 2: 1052-1055.View ArticlePubMedGoogle Scholar
- Mayxay M, Pukrittayakamee S, Newton PN, White NJ: Mixed-species malaria infections in humans. Trends Parasitol. 2004, 20: 233-240. 10.1016/j.pt.2004.03.006.View ArticlePubMedGoogle Scholar
- Douglas NM, Nosten F, Ashley EA, Phaiphun L, van Vugt M, Singhasivanon P, White NJ, Price RN: Plasmodium vivax recurrence following falciparum and mixed species malaria: risk factors and effect of antimalarial kinetics. Clin Infect Dis. 2011, 52: 612-620. 10.1093/cid/ciq249.PubMed CentralView ArticlePubMedGoogle Scholar
- Shanks GD, White NJ: The activation of vivax malaria hypnozoites by infectious diseases. Lancet Infect Dis. 2013, 13: 900-906. 10.1016/S1473-3099(13)70095-1.View ArticlePubMedGoogle Scholar
- Sharma A, Khanduri U: How benign is benign tertian malaria?. J Vector Borne Dis. 2009, 46: 141-144.PubMedGoogle Scholar
- Mehmood A, Ejaz K, Ahmed T: Severity of Plasmodium vivax malaria in Karachi: a cross-sectional study. J Infect Dev Ctries. 2012, 6: 664-670.View ArticlePubMedGoogle Scholar
- Manning L, Laman M, Rosanas-Urgell A, Michon P, Aipit S, Bona C, Siba P, Mueller I, Davis TM: Severe anemia in papua new guinean children from a malaria-endemic area: a case–control etiologic study. PLoS Negl Trop Dis. 2012, 6: e1972-10.1371/journal.pntd.0001972.PubMed CentralView ArticlePubMedGoogle Scholar
- Lacerda MV, Mourao MP, Alexandre MA, Siqueira AM, Magalhaes BM, Martinez-Espinosa FE, Santana Filho FS, Brasil P, Ventura AM, Tada MS, Couto VS, Silva AR, Silva RS, Alecrim MG: Understanding the clinical spectrum of complicated Plasmodium vivax malaria: a systematic review on the contributions of the Brazilian literature. Malar J. 2012, 11: 12-10.1186/1475-2875-11-12.PubMed CentralView ArticlePubMedGoogle Scholar
- Baird JK: Evidence and implications of mortality associated with acute Plasmodium vivax malaria. Clin Microbiol Rev. 2013, 26: 36-57. 10.1128/CMR.00074-12.PubMed CentralView ArticlePubMedGoogle Scholar
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