Dengue often presents with non-specific clinical signs, and given the current paucity of accurate, rapid diagnostic laboratory tests, identifying easily obtainable bedside markers of dengue remains a priority. Previous studies in febrile Asian children have suggested that the combination of a positive tourniquet test (TT) and leucopenia can distinguish dengue from other febrile illnesses, but little data exists on the usefulness of these tests in adults or in the Americas. We evaluated the diagnostic accuracy of the TT and leucopenia (white blood cell count <5000/mm3) in identifying dengue as part of an acute febrile illness (AFI) surveillance study conducted in the Emergency Department of Saint Luke's Hospital in Ponce, Puerto Rico. From September to December 2009, 284 patients presenting to the ED with fever for 2–7 days and no identified source were enrolled. Participants were tested for influenza, dengue, leptospirosis and enteroviruses. Thirty-three (12%) patients were confirmed as having dengue; 2 had dengue co-infection with influenza and leptospirosis, respectively. An infectious etiology was determined for 141 others (136 influenza, 3 enterovirus, 2 urinary tract infections), and 110 patients had no infectious etiology identified. Fifty-two percent of laboratory-positive dengue cases had a positive TT versus 18% of patients without dengue (P<0.001), 87% of dengue cases compared to 28% of non-dengue cases had leucopenia (P<0.001). The presence of either a positive TT or leucopenia correctly identified 94% of dengue patients. The specificity and positive predictive values of these tests was significantly higher in the subset of patients without pandemic influenza A H1N1, suggesting improved discriminatory performance of these tests in the absence of concurrent dengue and influenza outbreaks. However, even during simultaneous AFI outbreaks, the absence of leucopenia combined with a negative tourniquet test may be useful to rule out dengue.
In the Americas, the incidence and severity of dengue cases has increased dramatically in the past 30 years. Early diagnosis and initiation of appropriate therapy can substantially reduce dengue morbidity and mortality. However the absence of a point-of-care diagnostic test and the non-specific clinical signs and symptoms in early disease make differentiating dengue from other acute febrile illnesses challenging. Identifying dengue during an outbreak of another disease is especially difficult. The combination of a simple bedside test, the tourniquet test (TT), and a readily available laboratory test, the white blood cell count, has been reported to be a useful triage tool for identifying children with dengue in Asia, but little information exists on the performance of these tests in the Americas or among adults. We evaluated the utility of these tests in the setting of a concurrent influenza epidemic in Puerto Rico in 2009. A positive TT or leucopenia (white blood cell count <5000) was present in 94% of patients with laboratory proven dengue. Patients without either of these findings rarely had dengue. Our study indicates that a combination of two rapid, widely available tests can assist clinicians in distinguishing dengue from other illnesses with similar signs and symptoms.
Citation: Gregory CJ, Lorenzi OD, Colón L, Sepúlveda García A, Santiago LM, Cruz Rivera R, et al. (2011) Utility of the Tourniquet Test and the White Blood Cell Count to Differentiate Dengue among Acute Febrile Illnesses in the Emergency Room. PLoS Negl Trop Dis 5(12): e1400. https://doi.org/10.1371/journal.pntd.0001400
Editor: Aravinda M. de Silva, University of North Carolina at Chapel Hill, United States of America
Received: July 7, 2011; Accepted: October 3, 2011; Published: December 6, 2011
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Funding: This study was funded by the Centers for Disease Control and Prevention (CDC). CDC scientists participated in the study design, data collection and analysis, decision to publish, and preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Dengue, the disease caused by four related but distinct dengue viruses (DENV), is now considered the most important arthropod-borne disease worldwide. It is transmitted through the bite of an infected mosquito, usually Aedes aegypti or Aedes albopictus , and is endemic to tropical and subtropical regions. Dengue affects 50–100 million people each year. In 2007, more than 890,000 dengue cases were reported in the Americas. Globally, 500,000 patients with dengue, mostly children, require hospitalization and at least 12,500 die each year . There is significant year-to-year variation in the incidence of dengue, with large outbreaks typically occurring in 3- to 5-year cycles.
Island-wide epidemics of dengue have been identified in Puerto Rico since 1915  but similar to other countries in the Western Hemisphere, dengue epidemics have increased in frequency and severity over the past 20 years . During the last large island-wide dengue outbreak in 2007, disease appeared to be more severe than in previous large outbreaks, with more hospitalizations and cases of dengue hemorrhage fever (DHF), and a high proportion of cases with hemorrhagic manifestations . In 2007, a total of 10,508 suspected dengue cases were reported to the passive dengue surveillance system (PDSS) in Puerto Rico; 53% were hospitalized, 32% had hemorrhage and less than 1% died. One lesson learned from this outbreak was that most of the laboratory-confirmed fatal cases had a delay in diagnosis and treatment initiation, highlighting the importance of timely dengue diagnosis .
While morbidity and mortality has been linked to delayed provision of supportive treatment , case fatality rates for severe dengue infections, including DHF and dengue shock syndrome (DSS), can be reduced from 10% to 20% to less than 1% with early diagnosis and proper treatment –. However, there is no rapid, point-of-care diagnostic test available, and the clinical diagnosis of dengue may be challenging, as it usually presents with non-specific symptoms, including fever, headache and myalgia. Therefore, dengue is difficult to distinguish from other AFIs, such as influenza, leptospirosis, and enteroviral infections. In 2007, a simultaneous outbreak of acute gastroenteritis and dengue at the height of the dengue outbreak made recognition of dengue difficult, especially among those with warning signs for severe dengue such as persistent vomiting and abdominal pain. The concurrent outbreaks threatened to overwhelm the emergency and inpatient capacity of many Puerto Rican hospitals. In addition, simultaneous outbreaks of dengue and leptospirosis , dengue and measles , and dengue and influenza  in Puerto Rico caused similar difficulties with the clinical recognition, diagnosis, and management of dengue in the past.
The tourniquet test (TT) has been recommended as a tool to differentiate dengue from other AFIs . Studies from Thailand found that a positive TT in combination with leucopenia could distinguish dengue from other AFI in children –. The aim of our study was to evaluate the accuracy and usefulness of the TT and leucopenia (white blood cell count <5,000/mm3) in identifying dengue among patients with AFI in a setting with a large number of adult cases and during concurrent dengue and influenza outbreaks.
Materials and Methods
The study design and consent process was approved by the Institutional Review Boards (IRB) at the Centers for Disease Control and Prevention (CDC protocol # 5638) and Ponce University School of Medicine. Written consent was not required by the IRB as data was analyzed anonymously, the project was considered enhanced public health surveillance and the risk to the patient was considered minimal to none. Data was stripped of personal identifiers for analysis purposes and the database did not include any information that could link back to individual patients. Dengue is reportable by law in Puerto Rico and this project used the same reporting form used in the PDSS and no additional blood specimens were obtained in this project beyond what are normally collected for routine surveillance. Verbal consent was obtained for performing nasopharyngeal testing for influenza and for conducting the tourniquet test, a standard non-invasive dengue diagnostic test. A patient information sheet in Spanish written at an elementary-school level explaining the purpose of the study and the rationale and nature of these tests was read to and given to the patient. Verbal consent for performance of the influenza testing was documented by recording the results of the rapid influenza test on a separate sheet. The bottom half of the sheet, with explanation of test results in Spanish, was given to the patient and the top half was kept in a locked cabinet inside a secure CDC facility with access available only to study investigators.
The PDSS in Puerto Rico has been in operation for more than 30 years as previously described . In 2009, the PDSS at the Saint Luke's Episcopal Hospital, in Ponce, Puerto Rico, was augmented to include surveillance for all AFI. Children and adults presenting to the emergency department (ED) were eligible for enrollment if they met the following case definition of AFI: documented fever of ≥38.0°C at presentation to the ED or history of fever that persists for 2 to 7 days without identified source of fever. Those with an identifiable source of fever, including but not limited to diagnoses of otitis media, sinusitis, pneumonia, cellulitis, impetigo, wound infection, pyelonephritis, osteomyelitis or varicella were excluded. Saint Luke's Episcopal Hospital is a 425 bed tertiary care hospital that serves more than 54,000 patients in their ED each year. The Saint Luke's Episcopal Hospital is one of the largest hospitals outside of the San Juan metropolitan area and serves as the primary referral hospital for a population of more than 500,000 people in southern Puerto Rico .
The surveillance period was from September 29, 2009 through December 18, 2009. All patients presenting for medical care at the ED of Saint Luke's Episcopal Hospital who met the case definition above were enrolled in the surveillance system. At the time of enrollment, study personnel explained the purpose of the surveillance project and obtained verbal consent for participation. Participants were interviewed to collect demographic data included on the standard PDSS data collection form, including age, sex, place of residence, and days from symptom onset to specimen collection. Clinical data that were recorded included the duration of fever, the presence or absence of headache, eye pain, myalgia, arthralgia, rash, nausea and vomiting, and hemorrhagic manifestations, including positive TT. Laboratory data recorded on the form include white blood cell count, platelet count, and highest and lowest hematocrit values. Performance of a white blood cell count, blood and urine cultures and other laboratory tests were at the discretion of the attending physician in the course of routine patient care but were not part of the study protocol. For all patients, a blood sample and two nasopharyngeal samples were collected for diagnostic testing.
A TT was performed by trained study personnel. The standard TT was performed by inflating a blood pressure (BP) cuff on the upper arm of the patient to a point mid way between their systolic and diastolic pressure for 5 minutes, and then counting the number of petechiae in a 2.5 cm2 area on the volar aspect of the forearm just distal to the antecubital fossa 2 minutes after releasing the BP cuff. The TT was considered positive if 10 or more petechiae were identified. Leucopenia was defined as a total white blood cell count of <5,000/mm3, in keeping with previously published criteria from Asia and the Americas , .
Two nasopharyngeal samples were obtained. The first sample was tested onsite by using the QuikVue Influenza A + B rapid influenza test (Quidel Corporation, San Diego, CA), and the second sample placed in viral transport media and refrigerated until transport to the CDC's Dengue Branch for confirmatory influenza testing by polymerase chain reaction (PCR) testing. A 5–10 ml venous blood sample was collected, immediately refrigerated at 4°C, centrifuged on site, and transported on ice within 3 days to the Dengue Branch for further testing. Samples were initially tested for the presence of DENV via serotype-specific reverse-transcriptase PCR (RT-PCR) –, DENV-specific non-structural protein-1 assay (NS-1) , and an anti-DENV IgM enzyme-linked immunosorbent assay (MAC-ELISA) . Samples with sufficient quantity of serum remaining were subsequently transported on ice to the Bacterial Zoonosis Branch of the CDC in Atlanta for testing for leptospirosis. Specimens were screened for IgM antibodies to leptospirosis by using the rapid dipstick ELISA ImmunoDOT kit (GenBio, Inc., San Diego, CA). Specimens with positive or borderline results with the ImmunoDOT kit were further tested by using the microscopic agglutination test (MAT) . Patient sera were serially diluted in the MAT and mixed with a panel of 20 Leptospira reference antigens that represented 17 serogroups. Resulting agglutination titers were read by using darkfield microscopy, and the final titer was expressed as the reciprocal of the last well that agglutinates 50% of the antigen. Samples from patients with illness of <3 days duration and with sufficient sera remaining were shipped at −70°C to the Picornavirus Laboratory at CDC and tested for enteroviruses by a pan-enterovirus real-time RT-PCR by using primers and probe targeting the 5′ non-translated region . In PCR-positive specimens, the enterovirus type was identified by semi-nested PCR amplification and sequencing of a portion of the region encoding the VP1 capsid protein, as previously described . All personnel performing laboratory testing were unaware of the clinical condition of the patient including TT and WBC count results.
Data was initially entered into a Microsoft Access database (Access 2007; Redmond WA) and exported to SAS version 9.2 (SAS Institute, Cary, NC). We calculated the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of leucopenia and a positive TT, both in isolation and in combination, to differentiate dengue from other AFI. Proportions were compared using test or Fisher's exact test as appropriate. For each test, statistical significance was considered to be a P value≤0.05.
A total of 284 patients with AFI were enrolled. Thirty-one (11%) patients were laboratory confirmed as having dengue, 136 (48%) influenza and 3 (1%) were diagnosed with enterovirus. Dual infections were confirmed in two additional patients; one patient had influenza and dengue and the other had influenza and leptospirosis. These two patients were excluded from data analysis. Urinary tract infections were found in two patients (Escherichia coli and Staphlococcus saprophyticus). None of the patients had a positive blood culture. No etiology was identified among the remaining 110 enrolled patients. Serotype information was available by PCR from 20/31 laboratory-confirmed pure dengue infections, 18 were DENV-4 and 1 each were DENV-1 and DENV-2.
A TT was performed on 247 (88%) patients, of whom 54 (22%) had a positive result (Table 1). No patient had an adverse event from performance of the TT or was unable to tolerate the procedure. Half (52%) of the patients with laboratory-confirmed dengue had a positive TT while 18% of patients with influenza and 17% of patients with other AFI had a positive TT. WBC results were available for 276 (98%) patients. Dengue patients were also significantly more likely to have leucopenia (87%) than influenza patients (44%, P<0.001) and patients with other AFI (12%, P<0.001). Forty five percent of dengue patients had a positive TT and leucopenia, whereas <10% of patients with either influenza (7%, P<0.0001) or another AFI (5%, P<0.0001) had both a positive TT and leucopenia. Almost all (94%) dengue patients had either a positive TT or leucopenia compared with 57% of influenza patients and 26% of patients with other AFI.
When compared by age group, a positive TT was more common among laboratory-confirmed dengue patients aged ≤15 years than dengue patients >15 years old (67% vs. 46%), but this difference was not statistically significant (P = 0.43) (Table 2). Among patients aged ≤15 years, dengue patients were more likely to have a positive TT (67%) than patients with influenza (18%) or other AFI (17%). However, dengue patients were not more likely to have leucopenia when compared with influenza patients in this age group (67% vs. 54%, respectively, P = 0.98). Among patients >15 years old, a higher proportion of patients with dengue had leucopenia (96%) when compared with influenza patients (33%) and patients with other AFI (11%) (P<0.001). The proportion of dengue patients who presented with both a positive TT and leucopenia was similar for both age groups (44% vs. 46%). A higher proportion of dengue patients were positive for both tests either alone or in combination when compared with patients with influenza and patients with other AFI regardless of the patient's age. However, the difference was only statistically significant among patients in the older age group.
The TT used alone correctly identified half (sensitivity 52%) of the patients who had dengue (Table 3). The TT performed better in identifying patients who did not have dengue (specificity 82%), and a negative TT was highly associated with the absence of disease (NPV 92%). Neither the specificity nor the NPV of the TT changed significantly when influenza patients were excluded. In contrast, the presence of leucopenia alone identified most laboratory-confirmed dengue cases (sensitivity 87%). However, the specificity of leucopenia was less than that of the TT (specificity 72% vs. 82%, respectively), and it was highly affected by the presence of influenza patients. The combination of a negative TT and normal white cell count correctly identified most patients who did not have dengue (94% specificity), whereas having either a positive TT or leucopenia correctly identified a similar proportion of patients with dengue (94% sensitivity).
The relationship between TT results and platelet count, a marker of disease severity in dengue, is shown in Table 4. A positive TT was associated with laboratory-confirmed dengue in patients with a platelet count greater than 100,000 (P = 0.0001) but not in patients with a platelet count below this level. For patients without dengue, no association was seen between the platelet level and a positive TT.
Our study sought to evaluate the usefulness of a positive TT and leucopenia alone and in combination in identifying patients with dengue among children and adults with AFI in an ED of a dengue endemic area. Previous studies examining the use of one or both of these tests have primarily been performed in Asia among children suspected to have dengue and who required hospital admission –, –. While direct comparisons with the results of Asian studies are difficult because of differences in disease epidemiology and study design, our study supports the findings of previous studies conducted in Thailand , , which found that the presence of either leucopenia, a positive TT, or both is helpful in distinguishing between patients with and without dengue. In our study and others , , , leucopenia alone was found to be an especially good indicator of dengue among adults. Future studies examining the predictive value of the tourniquet test for the diagnosis of dengue in adults should evaluate a positive TT in combination with leucopenia.
As described in previous studies, we found that a positive TT alone was specific but not sensitive in distinguishing dengue from other AFI , –. This is especially true when the WHO cut-off of 20 or more petechiae per 2.5 cm2 is used. As in other studies, we chose to maximize detection of positive dengue cases (or the sensitivity of the tourniquet test) by using the cut-off of 10 or more petechiae per 2.5 cm2 , , . The presence of either a positive TT or leucopenia correctly identified 94% of patients who had dengue, and the absence of a positive TT or leucopenia was highly predictive of the absence of disease with a NPV >98%. That is, less than 2% of enrolled patients with neither a positive TT nor leucopenia had dengue.
Compared with the data reported from Thailand on the combined performance of the TT and leucopenia in identifying dengue patients, our results showed a lower sensitivity (45% vs.74%) and PPV (52% vs.73%–83%) but similar specificity (94% vs. 86%) –. Our finding of lower sensitivity most likely reflects differences in study design. These previous studies primarily enrolled hospitalized patients who then received daily TTs until the day of defervescence. Our study participants had a single TT performed at initial presentation to the ED. Previous research has demonstrated that the sensitivity of the TT depends on repeated testing and the timing of the test with respect to the day of illness with sensitivity increasing as a patient nears defervescence , . Most (68%) of our participants were enrolled within three days of symptom onset so that the sensitivity of the TT found in our study corresponds to the day −4/day −3 values found in the study from Thailand (52% versus 46%–56%) . We feel that using values solely from the time of initial patient contact is more useful, as it uses only information that is available to physicians at the time of initial triage.
Given that the study was performed in the setting of a concomitant influenza pandemic (CDC, unpublished data) and we did not restrict enrollment to suspected dengue cases that required hospitalization, our study also provides data on the performance of these triage criteria for dengue during periods of high influenza transmission. The lower PPV in our study largely reflects the effect of the study being conducted among patients with AFI (versus only those suspected of having dengue) at the time of a major outbreak of another AFI. While the specificity and PPV of the combination of tests was lower when cases with pandemic influenza A H1N1 were included, overall performance was still good. Reanalyzing the data after excluding influenza cases resulted in a PPV for the combination of leucopenia and positive TT of 74%, similar to previously published estimates , . As only 12% of patients without dengue or influenza had leucopenia in our study, there was only a minor decrease in the NPV upon excluding influenza patients for the combination of leucopenia and positive TT (92% vs 84%).
Our study has some important limitations. It was performed at an ED in a tertiary-level referral hospital with a large catchment area, and patients seeking care at this facility are more likely to have severe disease than patients who seek care at lower-level facilities. Thus, dengue cases in our study were likely not representative of the whole spectrum of dengue occurring in Puerto Rico. Data were missing on TT and white blood cell count results for approximately 12% and 2% percent of patients, respectively. The 35 participants who did not have a TT performed did not differ significantly from those who did have a TT performed in terms of sex or median age. No cases of dengue were diagnosed among the patients who did not have a TT performed. In most cases, only one serum specimen was available for dengue testing, leading to the possibility that some true dengue cases were not detected and misclassified as dengue negative. A comprehensive testing strategy, including a highly sensitive, single-plex anti-DENV RT-PCR, a NS-1 assay, and a MAC ELISA, was used to try to limit the amount of this misclassification bias.
The effects of dengue serotype and immunological status (primary versus secondary dengue infection) on the incidence of a positive TT or leucopenia have not yet been sufficiently investigated. Few studies have examined the role of these variables on the performance of these tests and these studies have usually been relatively small. Even fewer studies have had an adequate number of cases with both virological confirmation and immunological data to look at both variables simultaneously and stratify serotype specific results by immunological status, an important potential confounder. A positive TT was more frequently seen in children with dengue in Nicaragua when DENV-1 was the predominant serotype compared to an era when DENV-2 was circulating widely . However this difference was not evident in the sub-group of virologically confirmed cases and the study did not stratify between primary and secondary infections. No difference in white blood cell count was seen between 385 adults with DENV-2 or DENV-3 infection in Taiwan , but significantly more DENV-3 patients had secondary infections making accurate comparisons between groups difficult. No differences were seen in the proportion of European travelers with a positive TT between patients with a primary or secondary immune response , but the small number of patients with a secondary immune response limited the power of the study. No significant differences for TT positivity or leukocyte count in primary and secondary infections were seen among 89 hospitalized DENV-1 patients in Fiji .
Overall our study indicates that a combination of two rapid, widely available tests can assist clinicians in distinguishing dengue from other AFIs that have similar clinical signs and symptoms. Previous investigators have reported that the combination of the TT and leucopenia is more accurate in identifying patients with dengue than the World Health Organization's 1997 clinical case definition , and our data supports the contention that few patients with dengue are likely to be missed when these criteria are used. Twenty-nine of the 31 laboratory-positive dengue patients had either a positive TT or leucopenia. The two dengue patients that were not detected by these two tests were thrombocytopenic.
Our study and others  suggest that the TT may be useful in identifying dengue patients before a major decrease in platelet count, a group for whom dengue is often overlooked as a diagnostic possibility in Puerto Rico. Patients in our study population with AFI who had a negative TT and normal WBC appear to be at low risk of having dengue, and patients with both leucopenia and a positive TT have a high likelihood of having dengue, even in the setting of an outbreak of another clinically similar illness. Increased emphasis should be placed on determining the usefulness of the TT in combination with white blood cell count in identifying patients with dengue in Puerto Rico and elsewhere in the Americas. Further exploration of the sensitivity, specificity and predictive value of these tests by day of illness would be of particular benefit for clinical decision making. Additional larger studies should also be conducted to explore the effect of dengue serotype and immune status on the diagnostic performance of these tests.
STARD Flowchart for tourniquet test.
We express gratitude to Dr. Jenaro Scarano (Saint Luke's Medical Director), Dr. Carlos Garcia, Dr. Ivonne Galarza and Dr. Edna Hernández for their collaboration and support. We also thank the physicians, nurses and clinical laboratory staff of Saint Luke's Episcopal Hospital who were involved in the study.
Conceived and designed the experiments: CJG KMT. Performed the experiments: CJG ODL LC ASG RCR LJCB FOB DVA KMT JG LA. Analyzed the data: CJG ODL LMS. Wrote the paper: CJG ODL KMT.
- 1. Halstead S (1988) Pathogenesis of dengue: challenges to molecular biology. Science 239: 476–81.S. Halstead1988Pathogenesis of dengue: challenges to molecular biology.Science23947681
- 2. World Health Organization. Dengue and Dengue Haemorrhagic fever. World Health Organization. Dengue and Dengue Haemorrhagic fever.Available at: http://www.who.int/mediacentre/factsheets/fs117/en/print.html. Accessed October 6, 2010. Available at: http://www.who.int/mediacentre/factsheets/fs117/en/print.html. Accessed October 6, 2010.
- 3. King WW (1917) The epidemic of dengue in Porto Rico (sic), 1915. New Orleans Med Surg J 69: 564–71.WW King1917The epidemic of dengue in Porto Rico (sic), 1915.New Orleans Med Surg J6956471
- 4. San Martín JL, Brathwaite O, Zambrano B, Solórzano JO, Bouckenooghe A, et al. (2010) The epidemiology of dengue in the Americas over the last three decades: a worrisome reality. Am J Trop Med Hyg 82: 128–35.JL San MartínO. BrathwaiteB. ZambranoJO SolórzanoA. Bouckenooghe2010The epidemiology of dengue in the Americas over the last three decades: a worrisome reality.Am J Trop Med Hyg8212835
- 5. Tomashek K, Rivera A, Muñoz-Jordan J, Hunsperger E, Santiago L, et al. (2009) Description of a large island-wide outbreak of dengue in Puerto Rico, 2007. Am J Trop Med Hyg 81: 467–74.K. TomashekA. RiveraJ. Muñoz-JordanE. HunspergerL. Santiago2009Description of a large island-wide outbreak of dengue in Puerto Rico, 2007.Am J Trop Med Hyg8146774
- 6. Malavige GN, Fernendo S, Fernando DJ, Seneviratne SL (2004) Dengue viral infections. Postgrad Med J 80: 588–601.GN MalavigeS. FernendoDJ FernandoSL Seneviratne2004Dengue viral infections.Postgrad Med J80588601
- 7. Kittigul L, Pitakarnjanakul P, Sujirarat D, Siripanichgon K (2007) The differences of clinical manifestations and laboratory findings in children and adults with dengue virus infection. J Clin Virol 39: 76–81.L. KittigulP. PitakarnjanakulD. SujiraratK. Siripanichgon2007The differences of clinical manifestations and laboratory findings in children and adults with dengue virus infection.J Clin Virol397681
- 8. Nimmannitya S Dengue Hemorrhagic fever: diagnosis and management. In: Gubler DJ, Kuno G, editors. Dengue and Dengue Hemorrhagic Fever. Cambridge: CAB International. pp. 133–145.S. NimmannityaDengue Hemorrhagic fever: diagnosis and management.DJ GublerG. KunoDengue and Dengue Hemorrhagic FeverCambridgeCAB International133145
- 9. Ellis T, Imrie A, Katz AR, Effler PV (2008) Underrecognition of leptospirosis during a dengue fever outbreak in Hawaii, 2001–2002. Vector-Borne and Zoonotic Dis 8: 541–8.T. EllisA. ImrieAR KatzPV Effler2008Underrecognition of leptospirosis during a dengue fever outbreak in Hawaii, 2001–2002.Vector-Borne and Zoonotic Dis85418
- 10. Dietz VJ, Nieburg P, Gubler DJ, Gomez I (1992) Diagnosis of measles by clinical case definition in dengue-endemic areas: implication for measles surveillance and control. Bull World Health Organ 70: 745–50.VJ DietzP. NieburgDJ GublerI. Gomez1992Diagnosis of measles by clinical case definition in dengue-endemic areas: implication for measles surveillance and control.Bull World Health Organ7074550
- 11. Morens DM, Rigau-Perez JG, Lopez-Correa RH, Moore CG, Ruiz-Tiben EE, et al. (1986) Dengue in Puerto Rico, 1977: public health response to characterize and control an epidemic of multiple serotypes. Am J Trop Med Hyg 35: 197–211.DM MorensJG Rigau-PerezRH Lopez-CorreaCG MooreEE Ruiz-Tiben1986Dengue in Puerto Rico, 1977: public health response to characterize and control an epidemic of multiple serotypes.Am J Trop Med Hyg35197211
- 12. WHO (1997) Dengue hemorrhagic fever: diagnosis, treatment, prevention, and control. Geneva: World Health Organization. WHO1997Dengue hemorrhagic fever: diagnosis, treatment, prevention, and controlGenevaWorld Health Organization
- 13. Kalayanarooj S, Vaughn DW, Nimmannitya S, Green S, Suntayakorn S, et al. (1997) Early clinical and laboratory indicators of acute dengue illness. J Infect Dis 176: 313–21.S. KalayanaroojDW VaughnS. NimmannityaS. GreenS. Suntayakorn1997Early clinical and laboratory indicators of acute dengue illness.J Infect Dis17631321
- 14. Kalayanarooj S, Nimmannitya S, Suntayakorn S, Vaughn DW, Nisalak A, et al. (1999) Can doctors make an accurate diagnosis of dengue infections at an early stage? Dengue Bulletin 23: 1–5.S. KalayanaroojS. NimmannityaS. SuntayakornDW VaughnA. Nisalak1999Can doctors make an accurate diagnosis of dengue infections at an early stage?Dengue Bulletin2315
- 15. Sawasdivorn S, Vibulvattanakit S, Sasavatpakdee M, Iamsirithavorn S (2001) Efficacy of clinical diagnosis of dengue fever in paediatric age groups as determined by WHO case definition 1997 in Thailand. Dengue Bulletin 25: 56–64.S. SawasdivornS. VibulvattanakitM. SasavatpakdeeS. Iamsirithavorn2001Efficacy of clinical diagnosis of dengue fever in paediatric age groups as determined by WHO case definition 1997 in Thailand.Dengue Bulletin255664
- 16. Caribbean Business (2010, May 27) Puerto Rico's Largest Private Hospitals. Caribbean Business2010, May 27Puerto Rico's Largest Private Hospitals.Retrieved from http://www.caribbeanbusinesspr.com. Retrieved from http://www.caribbeanbusinesspr.com.
- 17. Gregory CJ, Santiago LM, Arguello DF, Hunsperger E, Tomashek K (2010) Clinical and Laboratory Features that differentiate Dengue from Other Febrile Illness in an Endemic Area-Puerto Rico, 2007–2008. Am J Trop Med Hyg 82: 922–29.CJ GregoryLM SantiagoDF ArguelloE. HunspergerK. Tomashek2010Clinical and Laboratory Features that differentiate Dengue from Other Febrile Illness in an Endemic Area-Puerto Rico, 2007–2008.Am J Trop Med Hyg8292229
- 18. Chien LJ, Liao TL, Shu PY, Huang JH, Gubler DJ, et al. (2006) Development of real-time reverse transcriptase PCR assays to detect and serotype dengue viruses. J Clin Microbiol 44: 1295–304.LJ ChienTL LiaoPY ShuJH HuangDJ Gubler2006Development of real-time reverse transcriptase PCR assays to detect and serotype dengue viruses.J Clin Microbiol441295304
- 19. Johnson BW, Russell BJ, Lanciotti RS (2005) Serotype-specific detection of dengue viruses in a fourplex real-time reverse transcriptase PCR assay. J Clin Microbiol 43: 4977–83.BW JohnsonBJ RussellRS Lanciotti2005Serotype-specific detection of dengue viruses in a fourplex real-time reverse transcriptase PCR assay.J Clin Microbiol43497783
- 20. Bessoff K, Phoutrides E, Delorey M, Acosta LN, Hunsperger E (2010) Defining the utility of a commercial NS1 antigen capture kit as a Dengue Virus (DENV) diagnostic test. Clin Vaccine Immunol 17: 949–53.K. BessoffE. PhoutridesM. DeloreyLN AcostaE. Hunsperger2010Defining the utility of a commercial NS1 antigen capture kit as a Dengue Virus (DENV) diagnostic test.Clin Vaccine Immunol1794953
- 21. Martin DA, Biggerstaff BJ, Allen B, Johnson AJ, Lanciotti RS, et al. (2002) Use of immunoglobulin M cross-reactions in differential diagnosis of human flaviviral encephalitis infections in the United States. Clin Diagn Lab Immunol 9: 544–9.DA MartinBJ BiggerstaffB. AllenAJ JohnsonRS Lanciotti2002Use of immunoglobulin M cross-reactions in differential diagnosis of human flaviviral encephalitis infections in the United States.Clin Diagn Lab Immunol95449
- 22. Dikken H, Kmety E (1978) Serological typing methods of leptospires. In: Bergan T, Norris JR, editors. Methods in Microbiology. London: Academic Press. pp. 259–307.H. DikkenE. Kmety1978Serological typing methods of leptospires.T. BerganJR NorrisMethods in MicrobiologyLondonAcademic Press259307
- 23. Kilpatrick DR, Yang C-F, Ching K, Vincent A, Iber J, et al. (2009) Rapid group serotype, and vaccine strain-specific identification of poliovirus isolates by real-time reverse transcription-PCR using degenerate primers and probes containing deoxyinosine residues. J Clin Microbiol 47: 1939–41.DR KilpatrickC-F YangK. ChingA. VincentJ. Iber2009Rapid group serotype, and vaccine strain-specific identification of poliovirus isolates by real-time reverse transcription-PCR using degenerate primers and probes containing deoxyinosine residues.J Clin Microbiol47193941
- 24. Nix WA, Oberste MS, Pallansch MA (2006) Sensitive, seminested PCR amplification of VP1 sequences for direct identification of all enterovirus serotypes from original clinical specimens. J Clin Microbiol 44: 2698–704.WA NixMS ObersteMA Pallansch2006Sensitive, seminested PCR amplification of VP1 sequences for direct identification of all enterovirus serotypes from original clinical specimens.J Clin Microbiol442698704
- 25. Phuong CXT, Nhan NT, Wills B, Kneen R, Ha NTT, et al. (2002) Evaluation of the World Health Organization standard tourniquet test and a modified tourniquet test in the diagnosis of dengue infection in Viet Nam. Trop Med Int Health 7: 125–132.CXT PhuongNT NhanB. WillsR. KneenNTT Ha2002Evaluation of the World Health Organization standard tourniquet test and a modified tourniquet test in the diagnosis of dengue infection in Viet Nam.Trop Med Int Health7125132
- 26. Norlijah O, Nor Khamisah A, Kamarul A, Mangalam S (2006) Repeated tourniquet testing as a diagnostic tool in dengue infection. Med J Malaysia 61: 22–7.O. NorlijahA. Nor KhamisahA. KamarulS. Mangalam2006Repeated tourniquet testing as a diagnostic tool in dengue infection.Med J Malaysia61227
- 27. Srikiatkhachorn A, Gibbons R, Green S, Libraty DH, Thomas S, et al. (2010) Dengue Hemorrhagic Fever: The Sensitivity and Specificity of the World Health Organization Definition for Identification of Severe Cases of Dengue in Thailand, 1994–2005. CID 50: 1135–1143.A. SrikiatkhachornR. GibbonsS. GreenDH LibratyS. Thomas2010Dengue Hemorrhagic Fever: The Sensitivity and Specificity of the World Health Organization Definition for Identification of Severe Cases of Dengue in Thailand, 1994–2005.CID5011351143
- 28. Mayxay M, Phetsouvanh R, Moore CE, Chansamouth V, Vongsouvath M, et al. (2011) Predictive value of the tourniquet test for the diagnosis of dengue infection in adults. Trop Med Int Health 16: 127–133.M. MayxayR. PhetsouvanhCE MooreV. ChansamouthM. Vongsouvath2011Predictive value of the tourniquet test for the diagnosis of dengue infection in adults.Trop Med Int Health16127133
- 29. Hammond SN, Balmaseda A, Perez L, Tellez Y, Indira S, et al. (2005) Differences in dengue severity in infants, children, and adults in a 3-year hospital-based study in Nicaragua. Am J Trop Med Hyg 73: 1063–1070.SN HammondA. BalmasedaL. PerezY. TellezS. Indira2005Differences in dengue severity in infants, children, and adults in a 3-year hospital-based study in Nicaragua.Am J Trop Med Hyg7310631070
- 30. Chairulfatah A, Setiabudi D, Ridad A, Colebunders R (1995) Clinical manifestations of dengue haemorrhagic fever in children in Bandung, Indonesia. Annales de la Societe Belge de Medecine Tropicale 5: 291–295.A. ChairulfatahD. SetiabudiA. RidadR. Colebunders1995Clinical manifestations of dengue haemorrhagic fever in children in Bandung, Indonesia.Annales de la Societe Belge de Medecine Tropicale5291295
- 31. Balmaseda A, Hammond SN, Pérez L, Tellez Y, Indira S, et al. (2006) Serotype-specific differences in clinical manifestations of dengue. Am J Trop Med Hyg 74: 449–456.A. BalmasedaSN HammondL. PérezY. TellezS. Indira2006Serotype-specific differences in clinical manifestations of dengue.Am J Trop Med Hyg74449456
- 32. Chan K-S, Chang J-S, Chang K, Lin C-C, Huang J-H, et al. (2009) Effect of serotypes on clinical manifestation of dengue fever in adults. J Microbiol Immunol Infect 42: 471–478.K-S ChanJ-S ChangK. ChangC-C LinJ-H Huang2009Effect of serotypes on clinical manifestation of dengue fever in adults.J Microbiol Immunol Infect42471478
- 33. Wichmann O, Gascon J, Schunk M, Puente S, Siikamaki H, et al. (2007) Severe dengue virus infection in travelers: risk factors and laboratory indicators. JID 195: 1089–1096.O. WichmannJ. GasconM. SchunkS. PuenteH. Siikamaki2007Severe dengue virus infection in travelers: risk factors and laboratory indicators.JID19510891096
- 34. Kuberski T, Rosen L, Reed D, Mataika J (1977) Clinical and laboratory observations on patients with primary and secondary dengue type 1 infections with hemorrhagic manifestations in Fiji. Am J Trop Med Hyg 26: 775–783.T. KuberskiL. RosenD. ReedJ. Mataika1977Clinical and laboratory observations on patients with primary and secondary dengue type 1 infections with hemorrhagic manifestations in Fiji.Am J Trop Med Hyg26775783