Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2334-13-498
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dc.titleUtility of warning signs in guiding admission and predicting severe disease in adult dengue
dc.contributor.authorLeo, Y.-S
dc.contributor.authorGan, V.C
dc.contributor.authorNg, E.-L
dc.contributor.authorHao, Y
dc.contributor.authorNg, L.-C
dc.contributor.authorPok, K.-Y
dc.contributor.authorDimatatac, F
dc.contributor.authorGo, C.-J
dc.contributor.authorLye, D.C
dc.date.accessioned2020-10-27T11:15:17Z
dc.date.available2020-10-27T11:15:17Z
dc.date.issued2013
dc.identifier.citationLeo, Y.-S, Gan, V.C, Ng, E.-L, Hao, Y, Ng, L.-C, Pok, K.-Y, Dimatatac, F, Go, C.-J, Lye, D.C (2013). Utility of warning signs in guiding admission and predicting severe disease in adult dengue. BMC Infectious Diseases 13 (1) : 498. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2334-13-498
dc.identifier.issn14712334
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181543
dc.description.abstractBackground: The recommendation from the 2009 World Health Organization guidelines for managing dengue suggests that patients with any warning sign can be hospitalized for observation and management. We evaluated the utility of using warning signs to guide hospital admission and predict disease progression in adults.Methods: We conducted a prospective cohort study from January 2010 to September 2012. Daily demographic, clinical and laboratory data were collected from adult dengue patients. Warning signs were recorded. The proportion of admitted patients using current admission criteria and warning signs was compared. The sensitivity, specificity, positive and negative predictive values of warning signs in predicting disease progression were also evaluated.Results: Four hundred and ninety-nine patients with confirmed dengue were analyzed. Using warning signs instead of the current admission criteria will lead to a 44% and 31% increase in admission for DHF II-IV and SD cases respectively. The proportion of non-severe dengue cases which were admitted also increased by 32% for non DHF II-IV and 33% for non-SD cases. Absence of any warning signs had a NPV of 91%, 100% and 100% for DHF I-IV, DHF II-IV and SD. Of those who progressed to severe illness, 16.3% had warning signs on the same day while 51.3% had warning signs the day before developing severe illness, respectively.Conclusions: Our findings demonstrated that patients without any warning signs can be managed safely with ambulatory care to reduce hospital resource burden. No single warning sign can independently predict disease progression. The window from onset of warning sign to severe illness in most cases was within one day. © 2013 Leo et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectabdominal pain
dc.subjectadult
dc.subjectarticle
dc.subjectclinical evaluation
dc.subjectclinical feature
dc.subjectcohort analysis
dc.subjectconsensus development
dc.subjectcontrolled study
dc.subjectdengue
dc.subjectdiagnostic test accuracy study
dc.subjectdisease classification
dc.subjectdisease course
dc.subjectdisease severity
dc.subjectfemale
dc.subjecthematocrit
dc.subjecthepatomegaly
dc.subjecthospital admission
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmucosal bleeding
dc.subjectpatient safety
dc.subjectpractice guideline
dc.subjectpredictive value
dc.subjectprognosis
dc.subjectsensitivity and specificity
dc.subjectthrombocyte count
dc.subjectvomiting
dc.subjectdengue
dc.subjecthospitalization
dc.subjectmiddle aged
dc.subjectprospective study
dc.subjectyoung adult
dc.subjectAdult
dc.subjectCohort Studies
dc.subjectDengue
dc.subjectDisease Progression
dc.subjectFemale
dc.subjectHospitalization
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectProspective Studies
dc.subjectSensitivity and Specificity
dc.subjectYoung Adult
dc.typeArticle
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.contributor.departmentMEDICINE
dc.description.doi10.1186/1471-2334-13-498
dc.description.sourcetitleBMC Infectious Diseases
dc.description.volume13
dc.description.issue1
dc.description.page498
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