Conference Papers

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This collection contains abstracts of conference papers, presented at local and international conferences by the staff of the Faculty of Medicine

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    A diagnostic model for Leptospirosis for use in resource limited settings
    (Sri Lanka Medical Association, 2015) Rajapakse, S.; Weeratunga, P.N.; Rodrigo, C.; Sriharan, S.; Niloofa, M.J.R.; Fernando, N.; de Silva, H.J.; Karunanayake, L.; Premawansa, S.
    INTRODUCTION AND OBJECTIVES: Leptospirosis is a zoonotic infection with significant morbidity and mortality. In this prospective study, we attempted to develop a model for diagnosis of leptospirosis. METHOD: Data was extracted from a prospective multicentre study. All patients with a suspected diagnosis of leptospirosis based on the WHO surveillance criteria were recruited. A derivation cohort and a validation cohort were selected. Positive MAT was used as the gold standard and significant associations in the derivation cohort were selected for construction of a multivariate regression model. Adjusted odds ratios were extracted for significant variables. ROC curves were generated. RESULTS: A total of 592 patients were included with 450 (180 confirmed leptospirosis) in the derivation cohort and 142 (52 confirmed leptospirosis) in the validation cohort. The variables in the final model were: history of exposure to possible source of leptospirosis (OR=2.878;95% Cl=1.527-5.425;p=0.001), serum creatinine>150u.mol/L (OR =2.742; 95% CN1.474-5.101; p=0.001), neutrophil differential percentage (on day 3 of illness) > 82.8% of total WBC count (OR 2.063; 95% Cl = 1.109 - 3.837; p =0.022), serum bilirubin > 27 U/L (OR = 1.767;95%CI 0.968 - 3.226; p=0.050) and platelet count (on day 3 of illness)< 85,000/mm3 (OR=2.350; 95%CI=1.281 -4.313;p=0.006). The Nagelkerke R2 was 0.654. ROC analysis demonstrated a diagnostic model score >14 to have a sensitivity of 80% and a specificity of 60% in the diagnosis of leptospirosis against MAT as the gold standard. CONCLUSION: This proposed diagnostic model for diagnosis of leptospirosis is of potential value to clinicians treating acute febrile illness in areas with limited diagnostic facilities.
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    Clinical and laboratory associations of severity in a Sri Lankan cohort of patients with serologically confirmed Leptospirosis - a prospective study
    (Sri Lanka Medical Association, 2015) Rajapakse, S.; Weeratunga, P.N.; Rodrigo, C.; Sriharan, S.; Niloofa, M.J.R.; Fernando, N.; de Silva, H.J.; Karunanayake, L.; Premawansa, S.; Handunnetti, S.
    INTRODUCTION AND OBJECTIVES: Leptospirosis is a zoonotic infection of significant morbidity and mortality. This study elucidates the markers of severity in a cohort of Sri Lankan patients with serologically confirmed leptospirosis. METHOD: Prospectively recruited patients presenting to three healthcare institutions in the Western province of Sri Lanka with serological confirmation of leptospirosis with the microscopic agglutination test were included. Data regarding the socio-deruographic profile, clinical presentation, complications and biochemical parameters were recorded. Univariate associations and subsequent multivariate logistic regression models were constructed with severity as the dependent variable. RESULTS: A total of 232 patients were included. Majority were male (86.6%). Severe disease was noted in 68.5%. Significant clinical associations of severe disease included fever > 38.8°C on presentation (p=0.008), age>40 yrs; (p = 0.033), muscle tenderness (p=0.04) and tachycardia on admission (p=0.05). Laboratory associations of severe disease were highest white cell count > 12,350/mm3 (p<0.001) and < 7900/mm3 (p = 0.009), highest neutrophil percentage > 84% {p < 0.001). Hemoglobin > 11.2g/dL (p<0.001) and < 10.2 (p<0.001), packed cell volume > 33.8% (p <0.001) and <29.8% (p <0.001), lowest platelet count <63,500/mm3 (p = 0.01), highest ALT > 70 IU/L {p = 0.02) and hyponatremia with sodium <131mEq/L (p=0.004) On multivariate analysis, PCV < 29.8 (P = 0.011; adjusted OR =3.750; Cl = 1.394 - 10.423), ALT >70 P =0.044 adjusted OR =2.639; Cl =1.028-6.774 and hyponatremia< 131 (p=0.019 adjusted OR=6.413; Cl=1.353 -30.388) were found to be independent associations of severe disease. CONCLUSION: Severity associations were demonstrated with both clinical and laboratory parameters.
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    Evidence of leptospira and Hanta virus co-infections amongst patients hospitalised for leptospirosis-like illness
    (Sri Lanka College of Microbiologists, 2003) Sunil-Chandra, N.P.; Premaratna, R.; Somasiri, D.A.D.H.; de Silva, H.J.
    INTRODUCTION: Hantavirus infection and leptospirosis are zoonoses with similar epidemiology and disease forms. Both infections spread to humans from infected rodents. OBJECTIVES: To assess the frequency and clinical manifestations of hantavirus infection in patients hospitalised with leptospirosis-like illness. METHODS: Two groups of patients admitted with leptospirosis-like illness to the University Medical Unit, Ragama, were investigated for evidence of both hantavirus infection and leptospirosis. Demographic data were obtained prospectively from 39 patients (Group 1) (M:F=34:5, mean age 35 yrs) (1996-1997), and retrospectively from 35 patients (Group 2) (M:F=34:1, mean age 30 yrs) who had been admitted to the unit during the previous year (1995-1996). Paired sera from 31/39 patients in Group 1 were tested for IgM antibodies and a single serum sample from 24/35 patients in Group 2 was tested for IgG antibodies to Hantaan and Puumala serotypes of hantavirus using m-capture ELISA separately. The same panels of sera were also tested for the presence of anti-leptospiral IgM (in Group 1) and IgG (in Group 2) antibodies. RESULTS: In Group 1, 9/31 and 25/31 sera were positive for hantavirus and leptospira IgM antibodies respectively. 5/31 were negative for both antibodies. 8/9 hantavirus IgM positive sera were also positive for leptospira IgM antibodies indicating co-infection. 1/9 showed seroconversion to hantavirus only, and 17/31 showed seroconversion to leptospira only. Based on the reactivity of hantavirus IgM antibody positive sera against recombinant hantavirus neucleocapsid proteins by m-capture ELISA, 5/9 had Puumala-like and 2/9 had Hantaan-like predominant antigenic specificities. The other 2/9 showed specificity to Puumala only. In Group 2, 10/24 and 23/24 sera were positive for hantavirus and leptospira IgG antibodies respectively. 1/24 was negative for both. All 10 hantavirus IgG antibody positive sera were also positive for leptospira IgG antibodies. 7 of 10 had specificity to Puumala, 2 of 10 had predominantly Puumala and 1 had predominantly Hantaan antigen specificity. Male predominance, occupations related to agriculture and farming, and exposure to rodents were risk factors associated with leptospirosis-like illness. Anorexia, nausea, and myalgia were features common to all patients More patients with hantavirus infection or with or without leptospirosis than those with leptospira infections only had hepatic (78% Vs. 17%) and renal (56% Vs. 17%) involvement during the course of their illness. Conclusions: In our study, hantavirus infection or co-infection with leptospirosis occurred in about one third of patients with leptospirosis-like illness admitted to hospital. The majority had hepatic and renal involvement. Three hantavirus serotypes, Puumala, Puumala-like and Hantaan-like, were detected.