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Published on: July 11, 2015
Long-term follow up of childhood tuberculous meningitis
1Department of Paediatrics and Child Health, Tygerberg Children's Hospital, South Africa. jfs@gerga.sun.ac.za
Insights
Long-term treatment with modern antituberculosis drugs in children resulted in significant long-term disabilities, including cognitive impairment and poor scholastic progress, impacting future prospects. Early suspicion of tuberculous meningitis (TBM) is crucial in high-incidence areas to prevent such morbidity.
Area of Science:
- Pediatrics
- Infectious Diseases
- Neurology
Background:
- Tuberculous meningitis (TBM) is a severe infection in children, often leading to long-term neurological sequelae.
- Modern antituberculosis drugs are standard treatment, but their long-term impact on childhood TBM outcomes requires ongoing evaluation.
Purpose of the Study:
- To determine the long-term functional outcomes in children treated for tuberculous meningitis (TBM) with contemporary antituberculosis chemotherapy.
Main Methods:
- A cohort of 76 children treated with a 6-month regimen of isoniazid, rifampicin, ethionamide, and pyrazinamide was followed up to a median age of 9 years.
- Management of raised intracranial pressure included ventriculo-peritoneal shunts for non-communicating hydrocephalus and medical management (acetazolamide, furosemide) for communicating hydrocephalus.
Main Results:
- Only 20% of children achieved complete functional normality at follow-up.
- Major deficits included cognitive impairment (80%), poor scholastic progress (43%), and emotional disturbance (40%).
- Motor impairment affected 25%, with most able to walk, but 6% unable to run. Visual impairment occurred in one child; no sensori-neural deafness was reported.
Conclusions:
- Children treated for TBM experience significant long-term disabilities, affecting social, academic, and career trajectories, particularly those from deprived socioeconomic backgrounds.
- A high index of suspicion for TBM in high-incidence regions is essential to mitigate long-term morbidity.
Abstract:
The purpose of the present study was to determine the long-term outcome of 76 children (40 females and 36 males) diagnosed and treated with modern antituberculosis drugs. The median age of the children on admission was 29.5 months and on follow-up 9 years. Antituberculosis therapy consisted of daily isoniazid (20 mg/kg), rifampicin (20 mg/kg), ethionamide (20 mg/kg), and pyrazinamide (40 mg/kg) for 6 months. Twenty-three children received daily prednisone (2-4 mg/kg) for the first month of treatment. Raised intracranial pressure was actively monitored and treated. Patients with non-communicating hydrocephalus received ventriculo-peritoneal shunts shortly after admission while communicating hydrocephalus was treated with oral acetazolamide (100 mg/kg/day) and furosemide (1 mg/kg/day) in 3-4 divided doses. Communicating hydrocephalus that did not respond to this regimen within the first month of treatment also underwent ventriculo-peritoneal shunting. Only 20% of children were functionally completely normal at follow-up. Main areas of functional deficit were cognitive impairment (80%), poor scholastic progress (43%), and emotional disturbance (40%). Twenty-five per cent of children had evidence of motor impairment, but all could walk and only 5 of 76 children (6% of total) were unable to run. One child was blind but no child had sensori-neural deafness. It was concluded that these disabilities in children from mainly deprived socioeconomic backgrounds have serious implications for their future social, academic, and career prospects. A high index of suspicion of TBM in high tuberculosis incidence communities will help prevent the morbidity documented in this study.
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