2025, Volume 18, Issue 10, pp 967 – 975

Tailoring BoNT A treatment and assessment across recovery stages after stroke: a report of four clinical cases

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Authors and Affiliations

* Corresponding author Miruna Săndulescu, Department of Physical and Rehabilitation Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania; E-mail: [email protected]

Abstract

Achieving effective spasticity management in post-stroke patients remains a significant therapeutic challenge. It requires the anticipation and management of multiple potential complications through a complex, individualized therapeutic approach. The therapeutic goals in stroke-related spasticity vary considerably depending on the intensity and duration of spasticity, as well as the degree of motor control in the affected limb segments. This study presents four clinical case reports involving patients with post-stroke spasticity ranging from grade 1+ to 4 on the Modified Ashworth Scale (MAS), each exhibiting a distinct temporal profile of symptom progression and levels of motor control in affected limbs. All patients received conservative rehabilitation therapy in conjunction with botulinum toxin (BoNT-A) administration. Spasticity assessment is essential for evaluating treatment efficacy and for planning and refining rehabilitation strategies. Employing case-appropriate functional clinical scales facilitates dynamic assessment and quantification of motor deficits, thereby enabling precise definition and ongoing monitoring of therapeutic goals. Given the heterogeneous functional status of patients with post-stroke spasticity, therapeutic objectives and evaluation strategies must be tailored accordingly. BoNT-A therapy necessitates a patient-specific approach concerning dosing and injection intervals. Repeated BoNT-A treatment in cases of severe spasticity produced sustained reductions in limb pain and mitigated periarticular tissue damage. In patients with mild spasticity and preserved motor function, functionality reached substantial recovery, as reflected in outcomes from appropriately selected functional measures, with injections spaced at intervals exceeding three months and employing progressively lower doses.

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About this article

PMC ID: 
PubMed ID: 10.25122/jml-2025-0151
DOI: JMedLife-18-967

Article Publishing Date (print):
Available Online: 

Journal information

ISSN Printing: 1844-122X
ISSN Online: 1844-3117
Journal Title: Journal of Medicine and Life

Copyright License: Open Access

This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.

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