3.8 Article

Implementing a Neurotrauma Registry in Latin America and the Caribbean

Journal

JOURNAL OF NEUROSCIENCES IN RURAL PRACTICE
Volume 13, Issue 3, Pages 525-528

Publisher

SCIENTIFIC SCHOLAR LLC
DOI: 10.1055/s-0042-1745816

Keywords

Caribbean region; Latin America; LMICs; neurotrauma; traumatic brain injury; trauma registry

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This study aims to ascertain the interest of Latin America and the Caribbean (LAC) nations in establishing a shared neurotrauma registry. A descriptive review was conducted on the interests of LAC nations, and it was found that all representatives agreed to adopt the registry for tracking the burden of traumatic brain injury (TBI) and associated pathologies within the region. The study suggests that implementing a neurotrauma registry can benefit the region through a shared database to track disease, improve outcomes, build research, and influence policy.
Background Traumatic brain injury (TBI) has a disproportionately greater impact in low- and middle-income countries (LMICs). One strategy to reduce the burden of disease in LMICs is through the implementation of a trauma registry that standardizes the assessment of each patient's management of care. Objective This study aims to ascertain the interest of Latin America and the Caribbean (LAC) nations in establishing a shared neurotrauma registry in the regional block, based on an existing framework for collaboration. Methods A descriptive review was performed regarding the interests of LAC nations in implementing a shared neurotrauma registry in their region. We convened a meeting with seven Caribbean and five Latin American nations. Results One hundred percent (n = 12) of the LAC representatives including neurosurgeons, neurointensivists, ministers of health, and chief medical officers/emergency medical technicians (EMTs) agreed to adopt the registry for tracking the burden of TBI and associated pathologies within the region. Conclusion The implementation of a neurotrauma registry can benefit the region through a shared database to track disease, improve outcomes, build research, and ultimately influence policy.

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