%0 Journal Article %A Hishamshah, Munirah %A Ahmad, Norazah %A Mohd Ibrahim, Hishamshah %A Nur Halim, Nurul Atiqah %A Nawi, Salbiah %A Amran, Fairuz %T Demographic, clinical and laboratory features of leptospirosis and dengue co-infection in Malaysia %D 2018 %J Journal of Medical Microbiology, %V 67 %N 6 %P 806-813 %@ 1473-5644 %R https://doi.org/10.1099/jmm.0.000750 %K co-infection %K leptospirosis %K thrombocytopenia %K dengue %K Malaysia %I Microbiology Society, %X Purpose. In this study, we aim to describe and compare the demographical, clinical and laboratory features of leptospirosis and dengue co-infections (LDCI) against single leptospirosis infections in Malaysia. Methodology. Data of patients admitted to various hospitals in Malaysia from 2011 to 2015 diagnosed with leptospirosis in our laboratory were obtained from their admission records. Co-infection with dengue was determined by collecting dengue serology results. Multivariate analysis and multiple logistic regression were used to differentiate features between single leptospirosis infection and confirmed LDCI. Results/Key findings. Only 602 (29.11 %) out of 2068 leptospira-positive patients were concurrently tested for dengue during their admission in which 44 (7.31 %) patients had positive non-structural protein 1 (confirmed LDCI) while 140 (23.26 %) were positive for dengue IgM (probable LDCI) with the highest number of cases recorded in high-density suburban districts. Myalgia and arthralgia were the only significant distinguishing clinical feature of LDCI while significant laboratory features were thrombocytopenia and high levels of alanine and aspartate transaminases. Only thrombocytopenia displayed a predictive value for LDCI from analysis of multiple logistic regression. Death occurred in 19 (3.16 %) patients in this dataset studied but only three (0.50 %) were attributed to LDCI. Conclusion. There is a considerable prevalence of LDCI in this country of which overlapping demographic, clinical and laboratory presentations pose diagnostic and therapeutic challenges. Efforts to raise awareness regarding LDCI, better access to diagnostic services and further prospective studies are warranted. %U https://www.microbiologyresearch.org/content/journal/jmm/10.1099/jmm.0.000750