- Open Access
Plasma leakage in dengue: a systematic review of prospective observational studies
BMC Infectious Diseases volume 21, Article number: 1082 (2021)
Plasma leakage is a precursor to life-threatening complications of dengue, but this group is poorly defined and not often reported in literature. Patients with Dengue haemorrhagic fever (DHF) as defined in the 1997 World Health Organization classification are often reported, and they all have plasma leakage, but some patients with plasma leakage do not meet the definition of DHF. The study aims to estimate the frequency of plasma leakage and DHF (as a surrogate of plasma leakage) in dengue and its variations based on virus serotype, geography, patient gender and pre-existing immunity to dengue. PUBMED, Scopus, EMBASE, CINAHL and Web of Science were searched for prospective observational studies reporting on plasma leakage or DHF. Quality of data was assessed using the NIH quality assessment tool for cohort studies. Forty-three studies that recruited 15,794 confirmed dengue patients were eligible. Cumulative frequency of plasma leakage was 36.8% (15 studies, 1642/4462, 95% CI 35.4–38.2%), but surprisingly the estimated cumulative frequency of DHF was higher (45.7%, 32 studies, 4758/10417, 95% CI 44.7–46.6%), indicating that current medical literature over-reports DHF or under-reports plasma leakage. Therefore, a reliable estimate for the proportion of dengue patients developing plasma leakage cannot be derived from existing medical literature even after applying rigorous inclusion criteria to select homogenous studies. Plasma leakage is an important marker of “at-risk” dengue patients and standardizing its definition, diagnosis and reporting should be a priority in research and global policy.
An estimated 96 million symptomatic cases of dengue occur annually in 129 countries where the disease transmission is endemic [1, 2]. Burden of dengue is high in low–middle income countries where the health system comes under strain at times of seasonal epidemics [3, 4]. Nowadays, patient management and classification are standardised by guidelines published by the World Health Organization (WHO) or health departments in each country. The WHO guidelines published in 1997 classified the clinical spectrum of dengue as dengue fever and dengue haemorrhagic fever (DHF) with four different grades of DHF (I–IV) of increasing severity . In a revised guideline published in 2009, this classification was changed as dengue fever and severe dengue . Both classifications are currently used as one did not replace the other.
A typical case of dengue starts with a febrile phase characterised by fever, anorexia, headache, arthralgia, myalgia, or retro-orbital pain. Some patients progress to a subsequent critical phase characterised by increased capillary permeability and extravasation of fluid into interstitial space (plasma leakage), which occurs around day 5–7 of fever, and lasts for 48–72 h . This is usually accompanied or preceded (by approximately 24–48 h) by a thrombocytopaenia. A progressive rise in haematocrit (evidence of haemoconcentration) or demonstration of extravasated fluid in pleural, peritoneal cavity by ultrasonography (or clinically) is used to establish the diagnosis of plasma leakage. Failure to recognise the onset of plasma leakage may lead to shock, multi-organ dysfunction syndrome and death. Alternatively, overenthusiastic fluid replacement during plasma leakage may lead to pulmonary oedema and its complications once this phase ends. Nevertheless, identification of this stage in illness is a critical for a favourable outcome. After the critical phase, patient enters a recovery phase characterised by resolution of symptoms and plasma leakage. Some patients move directly from febrile phase to recovery phase without a critical phase. As most complications in dengue stem from plasma leakage (except for a minority who can have abnormal bleeding and organ dysfunction without plasma leakage), identifying the proportion of patients progressing from febrile phase to critical phase is important for triaging at-risk patients for close monitoring either in an in- or outpatient basis, when all patients cannot be offered the same intense monitoring. Currently there is no reliable estimate for this proportion of patients, except for highly variable results reported from individual studies.
Both WHO classifications do not entirely capture the subgroup with plasma leakage, though the DHF category (in the 1997 classification) is a close approximation. Plasma leakage is an essential criterion to define DHF, but it is only one out of four such criteria (others being thrombocytopaenia, fever and haemorrhagic tendency) which must all be fulfilled to designate a patient as having DHF . Therefore, all DHF patients have plasma leakage, but the converse is not true. While this classification is useful to identify patients before complications, waiting for all four criteria to be fulfilled leaves some people with plasma leakage at risk of being unattended. The 2009 WHO classification categories do not have a good overlap with the plasma leakage subgroup, though one criterion to define severe dengue in this classification is “severe plasma leakage”, while other criteria are “severe bleeding” and evidence of organ dysfunction. However, from a clinical point of view this is problematic as the options for clinicians are limited once these complications develop. Identifying all with plasma leakage is ideal to prevent complications, but this is ignored in this classification. Unfortunately, as most dengue cohorts report results according to WHO classifications, the proportion of patients developing plasma leakage (or critical phase in illness) is unknown. The objective of this systematic review is to fill this gap by estimating the proportion of patients developing plasma leakage in dengue from prospective observational studies, and to see variations of this estimate based on geographical origin, infecting serotype, gender, and pre-existing immunity against dengue.
A systematic search was used to identify relevant studies published on or after 1997 (year of WHO publication that introduced the first major clinical classification on dengue), and indexed in PUBMED, Scopus, Web of Science, CINAHL and EMBASE databases using keywords “dengue” and (“plasma leakage” OR “critical phase” OR hemorrhag*), and (“prospective” OR “trial” OR “observational” OR “cohort”), without language restrictions. The last date of search was 15th April 2021. Full search strategy and the number of hits from each database is shown in Additional file 4: Table S1. Only prospective studies were included as for reliable reporting, the criteria for diagnosis of plasma leakage needs to be uniformly applied for all patients and this cannot be guaranteed in cross-sectional or retrospective study designs. Clinical trials were excluded as their interventions may influence the natural history of disease and case control studies were excluded as the sample size of patients with and without plasma leakage were pre-defined. Prospective observational cohorts with following characteristics were also deemed ineligible to preserve the quality of evidence; unconfirmed dengue diagnosis, reporting on ascites and pleural effusion separately (risk of counting same patient twice), sample size < 100 (arbitrary limit to exclude small cohorts to reduce variability), recruiting patients from some severity categories only (e.g., dengue shock syndrome) or exclusively from settings where a disproportionate number of severely ill patients are likely to be recruited (e.g. intensive care units). We included studies that recruited both children and adults, from any geographic region and regardless of whether recruitment was hospital or community based (but analysed separately). Anticipating that most eligible studies would not report on plasma leakage alone, an a priori decision was made to include DHF as a surrogate outcome when classification was done according to WHO 1997 criteria. Calculating DHF frequency is useful to validate the reliability of results as the percentage of patients with DHF must be lower than that for plasma leakage. Studies that used the WHO 2009 classification were included only if they reported the total number of patients with plasma leakage. Bibliography of included studies were manually searched for missed eligible studies.
After removing duplicates in search results, all abstracts were independently screened by CR and CS and any disagreements were resolved by consensus of all authors. Full text articles were examined for all results identified during screening and conference abstracts were excluded (Fig. 1). From the final list of eligible studies, following data items were extracted; time window of recruitment, country of origin, method of dengue diagnosis, WHO classification system used in the study (or its variations), definition of plasma leakage, total sample size, total number of patients with plasma leakage (or DHF, if reported), number of deaths, distribution of plasma leakage or DHF in serotype, gender or pre-existing immunity-based subgroups (Tables 1, 2 and Additional file 4: Table S2). Only published data were considered. The quality of included studies were assessed with a modified NIH quality assessment tool  for observational cohort studies, and were categorized to a two tiered system with “Tier 1” having better quality evidence than “Tier 2” (Additional file 1). Summary estimates for proportion of patients with plasma leakage and DHF (and 95% confidence intervals) were calculated and comparisons were made across subgroups based on geographical origin, gender, infecting serotype, primary vs. secondary dengue infection and study quality (tier 1 studies vs. all included studies) to identify statistically significant differences, using Z test for proportions. A p value < 0.05 was considered as statistically significant. There is no published protocol for this review.
Forty-three studies met the inclusion criteria [8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50] which included 40 hospital based and 3 community based cohorts that collectively recruited 15,794 patients (Table 1). Another ten studies [51,52,53,54,55,56,57,58,59,60] initially considered as eligible, were later excluded due to a high probability of reporting on same cohorts in the included studies. When two or more papers described the same cohort (e.g., interim analysis), the one that had a larger sample size was selected. Most included studies started recruitment after 1997, but three studies [33, 34, 60] had a recruitment time window straddling 1997, and one of these was a re-analysis of a prospective cohort that was active between 1995 and 1999.  Eighteen studies [10,11,12,13, 15, 21, 23, 25, 26, 28, 29, 31, 33,34,35, 38, 59, 60] included children only while others included both adults and children or adults only. The definition of children varied from those under 12 years (e.g., Sri Lanka) to less than 18 years of age (e.g., Philippines). Two studies [9, 28] were done in multiple countries while others reported from a single country and altogether 18 countries/territories were represented in included studies. Twenty-seven studies used the WHO 1997 criteria to classify patients, five used WHO 2009 criteria, and seven used both. One study  reported the primary data which formed the basis of the WHO 2009 clinical classification. Based on the quality assessment, seventeen studies were categorised as “Tier 2” studies, [12, 14, 16, 20, 22, 23, 26, 27, 29, 30, 35,36,37, 39, 42, 45, 48] and the rest as “Tier 1” studies (Additional file 2). Some studies reported on symptomatic hospitalised patients while others reported on all symptomatic patients regardless of hospitalisation, and one reported on asymptomatic patients in the community. These were analysed separately (Table 2) since hospitalised patients are more likely to be ill, have DHF or plasma leakage, and hence lumping all together in the analysis may create an artefact in the observed percentages. A comprehensive summary of characteristics of included studies (including the method of laboratory confirmation of dengue), is provided in Table 1. The PRISMA checklist for this review is provided as additional file 3.
Fifteen studies reported the proportion of patients with plasma leakage out of all symptomatic and hospitalised patients (Table 2), but the method of diagnosis was inconsistent. Six studies predominantly relied on ultrasonography [8, 20, 32, 36, 41, 42] while the remainder used chest X-ray alone,  chest X-ray with ultrasonography,  ultrasonography and a rise in haematocrit > 20%, [43, 49] a rise in haematocrit (> 20% or > 15%) with clinical examination [18, 45, 50] or clinical examination alone . One study did not mention the method of diagnosis . With this variability, the cumulative percentage of plasma leakage in symptomatic, hospitalised dengue patients was 36.8% (1642/4462, 95% CI 35.4–38.2%) (Table 2). Only one study reported that some patients with plasma leakage were managed as outpatients, and in this study the percentage with plasma leakage was 51.4% out of all symptomatic patients (126/245), regardless of hospitalisation. None of the studies recruited non-hospitalised asymptomatic patients in the community so there is no data on the proportion of plasma leakage out of all dengue patients (symptomatic and asymptomatic).
The number of studies reporting on the breakdown of patients with plasma leakage across the subgroups of interest (gender, infecting serotypes, primary vs. secondary infection and geographical origin) were too few (n ≤ 3) for a meaningful analysis (Additional file 4: Table S2). Regarding the quality of studies, when only “Tier 1” studies were considered, the frequency of plasma leakage among symptomatic and hospitalised patients increased to 39.4% (1224/3104, 95% CI 37.7–41.2%) and this was a statistically significant increase (p < 0.0001).
Dengue haemorrhagic fever
Thirty-two studies reported on the number of patients with DHF out of all symptomatic and hospitalised patients [Cumulative percentage: 45.7% (4758/10417), 95% CI 44.7–46.6%] (Table 2). Eight studies reported the number of DHF cases out of all symptomatic patients (whether hospitalised or not) and with this denominator, the cumulative percentage decreased to 28.6% (1304/4566, 95% CI 27.2–29.9%). One study  reported on both symptomatic and asymptomatic patients and in that study, the percentage with DHF was 6.3% of all dengue patients (36/569).
In the subgroup analysis (Additional file 4: Table S2), gender breakdown for DHF patients was available in 10 studies, breakdown by infecting serotype in 5–6 studies and breakdown as primary vs. secondary infection in 16 studies. DENV serotypes 2 or 3 infections were associated with a higher percentage of DHF compared to DENV 1 infection (p < 0.001). Secondary infection was more likely to result in DHF than in primary infection (p < 0.001). Regarding the geographical origin, cohorts from Asia (from South and Southeast Asia, n = 27) reported a significantly higher DHF percentage than those from Latin America and the Caribbean (collectively referred to as Americas, n = 5) (p < 0.001). Regarding the quality of studies, when only “Tier 1” studies were considered, the DHF percentage among hospitalised symptomatic patients increased to 47.7% (4098/8585, 95% CI 46.7–48.8%), and this was a statistically significant increment (p = 0.005).
Of all studies reporting on plasma leakage, six [8, 12, 14, 20, 32, 49] specifically mentioned no deaths, one (this study mentions a haematocrit rise > 20% rather than a “plasma leakage”) reported eight deaths , while the others did not confirm the presence or absence of deaths. Of all studies reporting on DHF, 26 reported on deaths (9 studies reported 60 deaths, [9, 15, 16, 18, 19, 21, 22, 30, 43] and 17 studies reported no deaths [8, 10,11,12, 14, 20, 23, 27,28,29, 32, 33, 37,38,39, 44, 49]). Thirty-five deaths occurred in DHF patients while for 24, it was not mentioned if they had DHF. Only one death was confirmed in a non-DHF patient. Overall, the dengue specific mortality was 0.6% (68/11,339).
This systematic review which assessed 43 prospective observational studies, that collectively recruited 15,794 laboratory confirmed dengue patients, could not resolve a reliable estimate for the number of patients developing plasma leakage in dengue. This unreliability stems from the observed higher frequency for DHF (compared to plasma leakage), as this cannot be true since patients with DHF are a subgroup of patients with plasma leakage. Either DHF is over-reported, or plasma leakage is under-reported, or both these scenarios may be true. The discussion will focus on few theories to explain this discrepancy. Also, almost all existing data refers to hospitalised symptomatic dengue patients with hardly any data on plasma leakage or DHF frequency among all dengue patients (symptomatic or asymptomatic, regardless of hospitalisation); This has a significant bias to inflate the proportion of patients with plasma leakage or DHF as hospitalised patients are closely monitored. There is also no data to compare the number of deaths across patient groups that had or did not have plasma leakage.
Plasma leakage is an important outcome in dengue to put on record as most complications occur within this group. Unlike plasma leakage, which is a biological phenomenon related to disease pathogenesis, [11, 61,62,63,64,65] other identifiers of “at-risk” patients such as shock may be confounded by medical mismanagement or patient driven factors such as oral fluid intake (in addition to disease pathogenesis). Definition and setting standards for diagnosing plasma leakage has been long neglected and as this review highlights, even after using rigorous inclusion criteria (prospective cohorts of confirmed dengue patients), the observed estimates for the proportion of patients with plasma leakage were highly variable across studies and led to an unreliable cumulative estimate when compared against the surrogate measure of DHF (which was more frequently reported, as it is part of the clinical classification in 1997 WHO guidelines).
The main reason for under-reporting plasma leakage is probably the lack of global standards to diagnose it. The studies we reviewed collectively used many methods to define plasma leakage, but each individual study mostly used only one of these methods. In this regard, recent studies mostly rely on ultrasonography while old studies relied on demonstrating a progressive increase of haematocrit from baseline. Some studies have relied on less sensitive methods such as clinical examination or chest radiographs to record this outcome. In our opinion, ultrasonography and haemoconcentration are both important to define plasma leakage while clinical examination or chest radiographs are unreliable and should not be used. Ultrasonography directly visualises fluid in third space, but interpretation is subject to operator expertise. Furthermore, at times of epidemics, the demand for scans is high and access is limited in resource limited settings. Haemoconcentration, as demonstrated by a 20% rise in haematocrit compared to baseline, is inexpensive and less time consuming, but establishing a baseline value may be difficult in a patient presenting late in illness. Given these reasons, there will always be a proportion of patients diagnosed by one of these methods but not the other, and if both methods are not used, the total number of patients will be under-reported. A working group comprising of public health experts and researchers in several countries recently attempted to define internationally acceptable endpoints in the clinical syndrome dengue, and the final consensus on what was defined as “moderate plasma leakage” is very similar to what is mentioned above except that a haematocrit cut-off of 15% is recommended, instead of 20% . However, it may not be possible to capture asymptomatic patients or non-hospitalised patients with these outcomes as this will require evaluation in a clinical setting. A prospective cohort study conducted by us recently, out of 426 patients, 129 (30.3%) had plasma leakage confirmed by ultrasonography, 146 (34.8%) by a haematocrit rise > 20%, and 200 (46.7%) by either one of these methods . While being positive by one method significantly increased the odds of being positive by the other, the non-overlap across the groups diagnosed by either method was also large (> 15% haematocrit rise may be a better cut-off). The final estimate for plasma leakage in this study is closer to and higher than the cumulative DHF frequency calculated in this systematic review and in our opinion, this is probably a closer observation to reality for symptomatic and hospitalised patients.
It is also possible that the frequency of DHF is overestimated in some of the included studies in this review. The local guidelines in some countries may not strictly adhere to the WHO criteria to define DHF (but still report it as DHF). For example, in our experience as clinicians in Sri Lanka, a diagnosis of DHF is synonymous with plasma leakage with less weighting given to other criteria such as thrombocytopaenia or bleeding. This will create a discrepancy in reporting against others who strictly rely on all four criteria to make designate a diagnosis of DHF. On top of that, the variation imposed by the diagnostic method for plasma leakage highlighted above, also affects the reported number of DHF patients.
Given these issues affecting the reliability of data, we have low confidence in the results observed for the subgroup analysis (Additional file 4: Table S2) and will not discuss it further. In our opinion, the chance of some of these results (associations with gender, infecting serotype and geographical origin) being outdated with more robust and reliable data reporting in future, are high. Having said that, the observed higher risk of DHF with secondary dengue infection is an expected finding given the current understanding of immunopathology of the disease . There is also conflicting evidence that some serotypes cause more severe disease than others [67,68,69,70,71]. However, statistical power to compare multiple serotypes against disease severity is limited in a single centre study because typically a dengue epidemic is dominated by one serotype. To overcome this, long-term studies covering multiple epidemics in one place or meta-analyses as reported here will be needed, but with more robust data. Finally there is some anecdotal evidence that dengue in South and Southeast Asia leads to more adverse outcomes compared to the Americas as the age standardised incidence rates, age standardised death rates and disability adjusted life years (DALYs) lost, are higher in the former group of countries collectively, than in the latter . However, this observation may also be influenced by a higher overall dengue incidence in Asia, discrepancies in access to healthcare and policy differences in each country affecting outcome definitions, clinical management and reporting (Additional files 2, 3).
Finally, due to variations in the definition of paediatric age group in different countries (12–18 years), it is not possible to estimate a cumulative plasma leakage (and DHF) frequency for adults and children from current medical literature using a systematic review as most studies will not agree with an arbitrary age limit used in a systematic review to define paediatric patients. However, data from individual studies suggest that DHF and plasma leakage frequencies may differ between adults and children. This is another issue which needs to be addressed by a global consensus.
This systematic review has several limitations and the main one as discussed above is the inability to reach a conclusion with current data. However, this is a limitation of the data rather than the method of the review. Regarding the methods, we did not further subgroup studies based on how they defined plasma leakage for two reasons; (a) not all studies mentioned this and (b) the number of studies in each subgroup will be few given the varying methods and their combinations used. We also removed studies with a sample size less than 100 with the intention of reducing variability introduced by small studies. This limit was arbitrary.
In conclusion, the proportion of dengue patients that have plasma leakage (or a critical phase in their illness) cannot be estimated from medical literature, which is a concern given how clinically important this subgroup is. This essentially prevents us from understanding how this outcome differs between adults and children, infections with different dengue serotypes, patient gender and geographical location. In dengue, patients at-risk must be identified before complications occur and defining this “at-risk” group as those with plasma leakage is a feasible, safer, and practical approach. This group will include most patients who would develop complications except for a minority with abnormal bleeding and organ dysfunction without plasma leakage. However, setting global standards to define this subgroup has long been neglected. We recommend that standardisation of diagnosis and reporting of plasma leakage in dengue should be a priority in research, and once a consensus is reached it should be applied globally. As a first-step, prospective dengue cohorts in future should report the number of patients with plasma leakage (and the method of diagnosis) in addition to the data routinely reported according to WHO clinical classifications.
Availability of data and materials
All data generated or analysed during this study are included in this published article and its Additional information files.
Dengue haemorrhagic fever
World Health Organization (WHO)
Disability adjusted life years
Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, et al. The global distribution and burden of dengue. Nature. 2013;496(7446):504–7.
Stanaway JD, Shepard DS, Undurraga EA, Halasa YA, Coffeng LE, Brady OJ, et al. The global burden of dengue: an analysis from the Global Burden of Disease Study 2013. Lancet Infect Dis. 2016;16(6):712–23.
Tissera HA, Jayamanne BDW, Raut R, Janaki SMD, Tozan Y, Samaraweera PC, et al. Severe dengue epidemic, Sri Lanka, 2017. Emerg Infect Dis. 2020;26(4):682–91.
Zeng Z, Zhan J, Chen L, Chen H, Cheng S. Global, regional, and national dengue burden from 1990 to 2017: a systematic analysis based on the global burden of disease study 2017. EClinicalMedicine.
World Health Organization. Dengue haemorrhagic fever: diagnosis, treatment and control. Geneva: WHO; 1997.
World Health Organization. Dengue guidelines for diagnosis, treatment, prevention and control. New Delhi: WHO; 2009.
National Institutes of Health. Study Quality Assessment Tools: National Heart, Lung and Blood Institute; 2020. https://www.nhlbi.nih.gov/health-topics/study-quality-assessment-tools.
Adil B, Rabbani A, Ahmed S, Arshad I Sr, Khalid MA. Gall bladder wall thickening in dengue fever—aid in labelling dengue hemorrhagic fever and a marker of severity. Cureus. 2020;12(11):e11331.
Alexander N, Balmaseda A, Coelho ICB, Dimaano E, Hien TT, Hung NT, et al. Multicentre prospective study on dengue classification in four South-east Asian and three Latin American countries. Trop Med Int Health. 2011;16(8):936–48.
Anderson KB, Gibbons RV, Thomas SJ, Rothman AL, Nisalak A, Berkelman RL, et al. Preexisting Japanese encephalitis virus neutralizing antibodies and increased symptomatic dengue illness in a School-Based cohort in Thailand. PLoS Negl Trop Dis. 2011;5(10).
Avirutnan P, Punyadee N, Noisakran S, Komoltri C, Thiemmeca S, Auethavornanan K, et al. Vascular leakage in severe dengue virus infections: a potential role for the nonstructural viral protein NS1 and complement. J Infect Dis. 2006;193(8):1078–88.
Basuki PS, Budiyanto, Puspitasari D, Husada D, Darmowandowo W, Ismoedijanto, et al. Application of revised dengue classification criteria as a severity marker of dengue viral infection in Indonesia. Southeast Asian J Trop Med Public Health. 2010;41(5):1088–94.
Biswas HH, Gordon A, Nunez A, Perez MA, Balmaseda A, Harris E. Lower low-density lipoprotein cholesterol levels are associated with severe dengue outcome. PLoS Negl Trop Dis. 2015;9(9):19.
Bodinayake CK, Tillekeratne LG, Nagahawatte A, Devasiri V, Arachchi WK, Strouse JJ, et al. Evaluation of the WHO 2009 classification for diagnosis of acute dengue in a large cohort of adults and children in Sri Lanka during a dengue-1 epidemic. PLoS Negl Trop Dis. 2018;12(2):15.
Capeding MR, L’Azou M, Manalaysay M, Vince-Woo CR, Rivera RG, Kristy Sy A, et al. Laboratory-confirmed dengue in children in three regional hospitals in the Philippines in 2009–2010. Pediatr Infect Dis J. 2015;34(11):1145–51.
Chatterjee SS, Sharma A, Choudhury S, Chumber SK, Bage R, Parkhe N, et al. Dengue fever in a south Asian metropolis: a report on 219 cases. Iranian J Microbiol. 2017;9(3):174–85.
Cordeiro MT, Silva AM, Brito CAA, Nascimento EJM, Magalhaes MCF, Guimaraes GF, et al. Characterization of a dengiie patient cohort in Recife, Brazil. Am J Trop Med Hyg. 2007;77(6):1128–34.
Fariz-Safhan MN, Tee HP, Abu Dzarr GA, Sapari S, Lee YY. Bleeding outcome during a dengue outbreak in 2005 in the East-coast region of Peninsular Malaysia: a prospective study. Trop Biomed. 2014;31(2):270–80.
Guilarde AO, Turchi MD, Siqueira JB Jr, Feres VC, Rocha B, Levi JE, et al. Dengue and dengue hemorrhagic fever among adults: clinical outcomes related to viremia, serotypes, and antibody response. J Infect Dis. 2008;197(6):817–24.
Herath H, Udeshika WAE, Samarawickrama SSM, Yogendranathan N, Jayamali WD, Kulatunga A, et al. Prediction of plasma leakage phase of dengue in resource limited settings. Clin Epidemiol Global Health. 2019;7(3):279–82.
Jagadishkumar K, Jain P, Manjunath VG, Umesh L. Hepatic involvement in dengue fever in children. Iran J Pediatr. 2012;22(2):231–6.
Jain S, Mittal A, Sharma SK, Upadhyay AD, Pandey RM, Sinha S, et al. Predictors of dengue-related mortality and disease severity in a tertiary care center in north India. Open Forum Infect Dis. 2017;4(2).
Kirawittaya T, Yoon IK, Wichit S, Green S, Ennis FA, Gibbons RV, et al. Evaluation of cardiac involvement in children with dengue by serial echocardiographic studies. PLoS Negl Trop Dis. 2015;9(7).
Kittigul L, Pitakarnjanakul P, Sujirarat D, Siripanichgon K. The differences of clinical manifestations and laboratory findings in children and adults with dengue virus infection. J Clin Virol. 2007;39(2):76–81.
Kularatnam GAM, Jasinge E, Gunasena S, Samaranayake D, Senanayake MP, Wickramasinghe VP. Evaluation of biochemical and haematological changes in dengue fever and dengue hemorrhagic fever in Sri Lankan children: a prospective follow up study. BMC Pediatrics. 2019;19(1).
Kulasinghe S, Ediriweera R, Kumara P. Association of abnormal coagulation tests with dengue virus infection and their significance as early predictors of fluid leakage and bleeding. SriLanka J Child Health. 2016;45(3):184–8.
Laul A, Laul P, Merugumala V, Pathak R, Miglani U, Saxena P. Clinical profiles of dengue infection during an outbreak in northern India. J Trop Med. 2016;2016:5917934.
L’Azou M, Moureau A, Sarti E, Nealon J, Zambrano B, Wartel TA, et al. Symptomatic dengue in children in 10 Asian and Latin American Countries. N Engl J Med. 2016;374(12):1155–66.
Malavige GN, Ranatunga PK, Velathanthiri VGNS, Fernando S, Karunatilaka DH, Aaskov J, et al. Patterns of disease in Sri Lankan dengue patients. Arch Dis Child. 2006;91(5):396–400.
Malavige GN, Velathanthiri VGNS, Wijewickrama ES, Fernando S, Jayaratne SD, Aaskov J, et al. Patterns of disease among adults hospitalized with dengue infections. QJM Mon J Assoc Phys. 2006;99(5):299–305.
Manamperi M, Jayamanne BDW, Somaratne T, Perera N, Fernando L. Predictive value of persistent NS1 antigen positivity beyond 3rd day for dengue haemorrhagic fever in Sri Lankan children. BMC Res Notes. 2019;12(1).
Pham TB, Matheus S, Vu TQH, Deparis X, Marechal V. Early clinical and biological features of severe clinical manifestations of dengue in Vietnamese adults. J Clin Virol. 2009;45(4):276–80.
Phuong CX, Nhan NT, Kneen R, Thuy PT, van Thien C, Nga NT, et al. Clinical diagnosis and assessment of severity of confirmed dengue infections in Vietnamese children: is the world health organization classification system helpful? Am J Trop Med Hyg. 2004;70(2):172–9.
Poeranto S, Sutaryo S, Josef HK, Juffrie M. A relationship between dengue virus serotype and the clinical severity in paediatric patients from Gondokusuman region, Yogyakarta between 1995 and 1999. Pediatr Med Rodzinna. 2016;12(3):318–25.
Prasad D, Bhriguvanshi A. Clinical profile, liver dysfunction and outcome of dengue infection in children: a prospective observational study. Pediatr Infect Dis J. 2020;39(2):97–101.
Premaratna R, Ragupathy A, Miththinda JK, de Silva HJ. Timing, predictors, and progress of third space fluid accumulation during preliminary phase fluid resuscitation in adult patients with dengue. Int J Infect Dis. 2013;17(7):e505–9.
Raman MH, Alam AYMS, Rahman AM, Khan MS, Shapla NR, Aleem MA. Presentation, management and outcome of dengue fever—a study of 200 cases. J Med. 2013;14(1):18–22.
Sabchareon A, Sirivichayakul C, Limkittikul K, Chanthavanich P, Suvannadabba S, Jiwariyavej V, et al. Dengue infection in children in Ratchaburi, Thailand: a cohort study. I. Epidemiology of symptomatic acute dengue infection in children, 2006–2009. PLoS Negl Trop Dis. 2012;6(7).
Seet RCS, Quek AML, Lim ECH. Post-infectious fatigue syndrome in dengue infection. J Clin Virol. 2007;38(1):1–6.
Senaratne T, Wimalaratne H, Alahakoon DGS, Gunawardane N, Carr J, Noordeen F. Characterization of dengue virus infections in a sample of patients suggests unique clinical, immunological, and virological profiles that impact on the diagnosis of dengue and dengue hemorrhagic fever. J Med Virol. 2016;88(10):1703–10.
Suwarto S, Nainggolan L, Sinto R, Effendi B, Ibrahim E, Suryamin M, et al. Dengue score: a proposed diagnostic predictor for pleural effusion and/or ascites in adults with dengue infection. BMC Infect Dis. 2016;16(1).
Taylor WR, Fox A, Pham KT, Le HNM, Tran NTH, Tran GV, et al. Dengue in adults admitted to a referral hospital in Hanoi, Vietnam. Am J Trop Med Hygiene. 2015;92(6):1141–9.
Thomas L, Moravie V, Besnier F, Valentino R, Kaidomar S, Coquet LV, et al. Clinical presentation of dengue among patients admitted to the adult emergency department of a tertiary care hospital in martinique: implications for triage, management, and reporting. Ann Emerg Med. 2012;59(1):42–50.
Vasanwala FF, Thein TL, Leo YS, Gan VC, Hao Y, Lee LK, et al. Predictive value of proteinuria in adult dengue severity. PLoS Negl Trop Dis. 2014;8(2).
Yacoub S, Lam PK, Huynh TT, Ho HHN, Thi HTD, Van NT, et al. Endothelial nitric oxide pathways in the pathophysiology of dengue: a prospective observational study. Clin Infect Dis. 2017;65(9):1453–61.
Yung CF, Lee KS, Thein TL, Tan LK, Gan VC, Wong JGX, et al. Dengue serotype-specific differences in clinical manifestation, laboratory parameters and risk of severe disease in adults, Singapore. AM J TROP MED HYG. 2015;92(5):999–1005.
Potts JA, Gibbons RV, Rothman AL, Srikiatkhachorn A, Thomas SJ, Supradish PO, et al. Prediction of dengue disease severity among pediatric Thai patients using early clinical laboratory indicators. PLoS Negl Trop Dis. 2010;4(8).
Tang Y, Kou Z, Tang X, Zhang F, Yao X, Liu S, et al. Unique impacts of HBV co-infection on clinical and laboratory findings in a recent dengue outbreak in China. Am J Trop Med Hyg. 2008;79(2):154–8.
Sigera PC, Weeratunga P, Deepika Fernando S, Lakshitha De Silva N, Rodrigo C, Rajapakse S. Rational use of ultrasonography with triaging of patients to detect dengue plasma leakage in resource limited settings: a prospective cohort study. Trop Med Int Health. 2021.
Trung DT, le Thao TT, Dung NM, Ngoc TV, Hien TT, Chau NV, et al. Clinical features of dengue in a large Vietnamese cohort: intrinsically lower platelet counts and greater risk for bleeding in adults than children. PLoS Negl Trop Dis. 2012;6(6):e1679.
Oliveira RAS, da Silva MMC, Calzavara-Silva CE, Silva AM, Cordeiro MT, de Moura PMMF, et al. Primary dengue haemorrhagic fever in patients from northeast of Brazil is associated with high levels of interferon-β during acute phase. Mem Inst Oswaldo Cruz. 2016;111(6):378–84.
Kalayanarooj S, Vaughn DW, Nimmannitya S, Green S, Suntayakorn S, Kunentrasai N, et al. Early clinical and laboratory indicators of acute dengue illness. J Infect Dis. 1997;176(2):313–21.
Sirivichayakul C, Limkittikul K, Chanthavanich P, Jiwariyavej V, Chokejindachai W, Pengsaa K, et al. Dengue infection in children in Ratchaburi, Thailand: a cohort study. ii. Clinical manifestations. PLoS Negl Trop Dis. 2012;6(2).
Thomas L, Brouste Y, Najioullah F, Hochedez P, Hatchuel Y, Moravie V, et al. Prospective and descriptive study of adult dengue cases in an emergency department. Martinique Medecine et Maladies Infectieuses. 2010;40(8):480–9.
Vaughn DW, Green S, Kalayanarooj S, Innis BL, Nimmannitya S, Suntayakorn S, et al. Dengue viremia titer, antibody response pattern, and virus serotype correlate with disease severity. J Infect Dis. 2000;181(1):2–9.
Xavier Eurico De Alencar L, De Mendonca Braga-Neto U, Jose Moura Do Nascimento E, Tenorio Cordeiro M, Maria Silva A, Alexandre Antunes De Brito C, et al. HLA-B*44 is associated with dengue severity caused by DENV-3 in a brazilian population. J Trop Med. 2013:648475.
Yacoub S, Lam PK, le Vu HM, Le TL, Ha NT, Toan TT, et al. Association of microvascular function and endothelial biomarkers with clinical outcome in dengue: an observational study. J Infect Dis. 2016;214(5):697–706.
Suwarto S, Sasmono RT, Sinto R, Ibrahim E, Suryamin M. Association of endothelial glycocalyx and tight and adherens junctions with severity of plasma leakage in dengue infection. J Infect Dis. 2017;215(6):992–9.
Kalayanarooj S, Gibbons RV, Vaughn D, Green S, Nisalak A, Jarman RG, et al. Blood group AB is associated with increased risk for severe dengue disease in secondary infections. J Infect Dis. 2007;195(7):1014–7.
Srikiatkhachorn A, Gibbons RV, Green S, Libraty DH, Thomas SJ, Endy TP, et al. Dengue hemorrhagic fever: the sensitivity and specificity of the world health organization definition for identification of severe cases of dengue in Thailand, 1994–2005. Clin Infect Dis. 2010;50(8):1135–43.
Srikiatkhachorn A. Plasma leakage in dengue haemorrhagic fever. Thromb Haemost. 2009;102(6):1042–9.
Rathore AP, Mantri CK, Aman SA, Syenina A, Ooi J, Jagaraj CJ, et al. Dengue virus-elicited tryptase induces endothelial permeability and shock. J Clin Investig. 2019;129(10):4180–93.
Rathore APS, Senanayake M, Athapathu AS, Gunasena S, Karunaratna I, Leong WY, et al. Serum chymase levels correlate with severe dengue warning signs and clinical fluid accumulation in hospitalized pediatric patients. Sci Rep. 2020;10(1):11856.
Halstead SB. Neutralization and antibody-dependent enhancement of dengue viruses. Adv Virus Res. 2003;60:421–67.
Durbin AP. Dengue vascular leak syndrome: insights into potentially new treatment modalities. J Clin Investig. 2019;129(10):4072–3.
Tomashek KM, Wills B, Lum LCS, Thomas L, Durbin A, Leo YS, et al. Development of standard clinical endpoints for use in dengue interventional trials. PLoS Negl Trop Dis. 2018;12(10):21.
Vicente CR, Herbinger K-H, Fröschl G, Malta Romano C, de Souza Areias Cabidelle A, Cerutti Junior C. Serotype influences on dengue severity: a cross-sectional study on 485 confirmed dengue cases in Vitória Brazil. BMC Infect Dis. 2016;16:320.
Thein TL, Wong JG, Tan LK, Yung CF, Gan V, Ooi EE, et al. Dengue serotypes and disease severity in Singapore. Int J Infect Dis. 2012;16:e114.
Sigera PC, Amarasekara R, Rodrigo C, Rajapakse S, Weeratunga P, De Silva NL, et al. Risk prediction for severe disease and better diagnostic accuracy in early dengue infection; the Colombo dengue study. BMC Infect Dis. 2019;19(1):680.
Soo K-M, Khalid B, Ching S-M, Chee H-Y. Meta-analysis of dengue severity during infection by different dengue virus serotypes in primary and secondary infections. PLoS ONE. 2016;11(5):e0154760.
Guo C, Zhou Z, Wen Z, Liu Y, Zeng C, Xiao D, et al. Global epidemiology of dengue outbreaks in 1990–2015: a systematic review and meta-analysis. 2017;7(317).
CR is supported by an NHMRC (Australia) investigator Grant (no. 1173666). The funding body has no influence for the design of the study and collection, analysis and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests. Chaturaka Rodrigo is an associate editor for BMC Infectious Diseases.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Modified study quality assessment tool.
Quality assessment of each included study.
PRISMA checklist for a systematic review.
Search strategy and results. Table S2. Subgroup analysis of plasma leakage and dengue haemorrhagic fever (DHF) frequency.
About this article
Cite this article
Rodrigo, C., Sigera, C., Fernando, D. et al. Plasma leakage in dengue: a systematic review of prospective observational studies. BMC Infect Dis 21, 1082 (2021). https://doi.org/10.1186/s12879-021-06793-2
- Plasma leakage
- Critical phase
- Systematic review