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1.
J Spinal Cord Med ; 43(3): 331-338, 2020 05.
Article in English | MEDLINE | ID: mdl-30207875

ABSTRACT

Objective: The objective of the present work was to determine the prognostic validity of the trunk control test for walking and independence in individuals with SCI.Design: A cohort, prospective study was carried out in all individuals with sub-acute SCI.Setting: All inpatients at the Mexico City based National Rehabilitation Institute (INR).Participants: Ninety individuals with a clinical diagnosis of sub-acute SCI, American Spinal Injury Association Impairment Scale (AIS) A-D, and that have not participated in a rehabilitation program were included. Thirty-five individuals had good initial trunk control and the remaining 55 had poor trunk control. All individuals participated in a standard rehabilitation program subsequently.Interventions: N/AOutcome Measures: The trunk control test was performed at baseline. At 1, 3, 6, 9 and 12 months after the first evaluation, walking and independence were assessed.Results: Survival Analysis revealed that 62.5% and 100% individuals with good trunk control at baseline assessment were respectively walking and independent in ADL at 12 months and 14% and 48% individuals with poor trunk control were walking and independent in ADL. Cox regression analysis revealed that individuals with good trunk control were 4.6 times more likely to walk independently at 12 months and 2.9 times more likely to be independent in activities of daily living.Conclusion: The present study revealed that the trunk control test is useful for providing a prognosis of independence and walking at 1 year in individuals with SCI, independently of the neurologic level and the severity of the injury.


Subject(s)
Outcome Assessment, Health Care/standards , Recovery of Function/physiology , Spinal Cord Injuries/diagnosis , Spinal Cord Injuries/physiopathology , Torso/physiopathology , Walking/physiology , Activities of Daily Living , Adult , Female , Humans , Male , Mexico , Middle Aged , Prognosis , Prospective Studies , Reproducibility of Results , Severity of Illness Index , Spinal Cord Injuries/rehabilitation
2.
Clin Neuropharmacol ; 40(3): 131-139, 2017.
Article in English | MEDLINE | ID: mdl-28471767

ABSTRACT

INTRODUCTION: Brain injuries are one of the leading causes of disability worldwide. It is estimated that nearly half of patients who develop severe sequelae will continue with a chronic severe disability despite having received an appropriate rehabilitation program. For more than 3 decades, there has been a worldwide effort to investigate the possibility of pharmacologically stimulating the neuroplasticity process for enhancing the recovery of these patients. OBJECTIVE: The objective of this article is to make a critical and updated review of the available evidence that supports the positive effect of different drugs on the recovery from brain injury. METHOD: To date, there have been several clinical trials that tested different drugs that act on different neurotransmitter systems: catecholaminergic, cholinergic, serotonergic, and glutamatergic. There is both basic and clinical evidence that may support some positive effect of these drugs on motor, cognitive, and language skills; however, only few of the available studies are of sufficient methodological quality (placebo controlled, randomized, blinded, multicenter, etc) to make solid conclusions about their beneficial effects. CONCLUSIONS: Currently, the pharmacological stimulation of neuroplasticity still does not have enough scientific evidence to make a systematic therapeutic recommendation for all patients, but it certainly is a feasible and very promising field for future research.


Subject(s)
Brain Injuries/drug therapy , Drugs, Investigational/therapeutic use , Evidence-Based Medicine , Neuronal Plasticity/drug effects , Amantadine/therapeutic use , Animals , Brain Injuries/etiology , Brain Injuries/rehabilitation , Brain Injuries, Traumatic/drug therapy , Brain Injuries, Traumatic/rehabilitation , Combined Modality Therapy , Disease Models, Animal , Dopamine Agents/therapeutic use , Humans , Memantine/therapeutic use , Stroke/physiopathology
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