BACKGROUND: Japanese encephalitis (JE) is associated with high mortality and neurological sequelae. The unpredictable course and lack of specific treatment pose major challenges in management. The tropical climate and paddy ecosystem in Nepal provide a suitable setting. AIMS: To determine the aetiology of febrile encephalopathy and describe the clinico-laboratory profile and outcome of JE in Nepali children. METHODS: A hospital-based prospective and observational study was conducted over a 1-year period (2000-2001). Children aged from >1 month to 14 years with fever >38 degrees C for <2 weeks and altered sensorium were recruited. JE was confirmed by anti-JE IgM in cerebrospinal fluid and/or serum. RESULTS: Of 117 consecutively enrolled patients, 58 had JE. Ten patients had concomitant infections, four with malaria and six with bacterial meningitis, and were excluded from analysis. Clinical findings were as follows: boys, 69%; age 4-14 years, 71%; presentation during summer and autumn, 83%; fever >3 days, 69%; altered sensorium <2 days, 50%; Glasgow coma score 8-12, 63%; seizures, 58%. Four (8.3%) died. At discharge, neurological sequelae were detected in 24 (50%) and hemiparesis was the most common form. Longer duration of vomiting, altered sensorium and focal neurological deficit on admission were independently associated with sequelae at discharge. Sequelae persisted in nine (18.8%) at 6 weeks follow-up. Long duration of altered sensorium (beta co-efficient 0.35, odds ratio 1.4, p=0.042) and presence of focal neurological deficit on admission (beta co-efficient 1.6, odds ratio 5.2, p=0.049) were independent predictors of sequelae at 6 weeks. CONCLUSION: JE was the commonest cause of febrile encephalopathy. Neurological sequelae were common but resolved in two-thirds of cases.
BACKGROUND:Japanese encephalitis (JE) is associated with high mortality and neurological sequelae. The unpredictable course and lack of specific treatment pose major challenges in management. The tropical climate and paddy ecosystem in Nepal provide a suitable setting. AIMS: To determine the aetiology of febrile encephalopathy and describe the clinico-laboratory profile and outcome of JE in Nepali children. METHODS: A hospital-based prospective and observational study was conducted over a 1-year period (2000-2001). Children aged from >1 month to 14 years with fever >38 degrees C for <2 weeks and altered sensorium were recruited. JE was confirmed by anti-JE IgM in cerebrospinal fluid and/or serum. RESULTS: Of 117 consecutively enrolled patients, 58 had JE. Ten patients had concomitant infections, four with malaria and six with bacterial meningitis, and were excluded from analysis. Clinical findings were as follows: boys, 69%; age 4-14 years, 71%; presentation during summer and autumn, 83%; fever >3 days, 69%; altered sensorium <2 days, 50%; Glasgow coma score 8-12, 63%; seizures, 58%. Four (8.3%) died. At discharge, neurological sequelae were detected in 24 (50%) and hemiparesis was the most common form. Longer duration of vomiting, altered sensorium and focal neurological deficit on admission were independently associated with sequelae at discharge. Sequelae persisted in nine (18.8%) at 6 weeks follow-up. Long duration of altered sensorium (beta co-efficient 0.35, odds ratio 1.4, p=0.042) and presence of focal neurological deficit on admission (beta co-efficient 1.6, odds ratio 5.2, p=0.049) were independent predictors of sequelae at 6 weeks. CONCLUSION:JE was the commonest cause of febrile encephalopathy. Neurological sequelae were common but resolved in two-thirds of cases.
Authors: P Gunasekaran; K Kaveri; Kavita Arunagiri; S Mohana; R Kiruba; V Senthil Kumar; P Padmapriya; B V Suresh Babu; A Khaleefathullah Sheriff Journal: Indian J Med Res Date: 2012-05 Impact factor: 2.375
Authors: Ajit Rayamajhi; Imran Ansari; Elizabeth Ledger; Krishna P Bista; Daniel E Impoinvil; Sam Nightingale; Rajendra Kumar; Chandeshwor Mahaseth; Tom Solomon; Michael J Griffiths Journal: BMC Infect Dis Date: 2011-10-28 Impact factor: 3.090
Authors: Ajit Rayamajhi; Sam Nightingale; Nisha Keshary Bhatta; Rupa Singh; Rachel Kneen; Elizabeth Ledger; Krishna Prasad Bista; Penny Lewthwaite; Chandeshwar Mahaseth; Lance Turtle; Jaimie Sue Robinson; Sareen Elizabeth Galbraith; Malgorzata Wnek; Barbara Wilmot Johnson; Brian Faragher; Michael John Griffiths; Tom Solomon Journal: PLoS One Date: 2015-04-17 Impact factor: 3.240
Authors: Martin Ludlow; Jeroen Kortekaas; Christiane Herden; Bernd Hoffmann; Dennis Tappe; Corinna Trebst; Diane E Griffin; Hannah E Brindle; Tom Solomon; Alan S Brown; Debby van Riel; Katja C Wolthers; Dasja Pajkrt; Peter Wohlsein; Byron E E Martina; Wolfgang Baumgärtner; Georges M Verjans; Albert D M E Osterhaus Journal: Acta Neuropathol Date: 2015-12-10 Impact factor: 17.088