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Position-cortical coherence as a marker for somatosensory integrity early post-stroke, a prospective cohort study

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Programme and Proceedings Book

From Science to Evidence-based Practice

22-23-24 May 2019 | The Netherlands

Third congress on

NeuroRehabilitation

and Neural Repair

Deutsche Gesellschaft für Neurotraumatologie und klinische Neuro-rehabilitation e.V. DGNKN

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88

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Position-cortical coherence as a marker for somatosensory

integrity early post-stroke, a prospective cohort study.

S. Zandvliet1, E. van Wegen1, S. Campfens2, H. van der Kooij2, G. Kwakkel1,

C. Meskers1

1Rehabilitation Medicine, Amsterdam UMC, Amsterdam, Netherlands 2Biomechanical Engineering, University of Twente, Enschede, Netherlands

Introduction: Neurophysiological assessments in addition to clinical scales can

potentially elucidate the role of somatosensory function in post-stroke motor recovery.

Main objective:To investigate the longitudinal construct validity of

position-cortical coherence (PCC), the agreement between evoked wrist perturbations and EEG, as a measure of afferent integrity, with respect to longitudinal recovery of sensorimotor function.

Methods: PCC was measured serially in 48 patients after a fi rst-ever ischemic

stroke, in addition to Fugl-Meyer motor assessment of the upper extremity (FM-UE) and Erasmus modifi cation of the Nottingham Sensory Assessment (EmNSA), within 3, 5, 12 and 26 weeks post-stroke. Change in PCC over time represented by: percentage presence of PCC (%PCC), mean amplitude of PCC over the affected hemisphere (Amp-A) were addressed as well as their association with FM-UE and EmNSA. Patients were classifi ed into: expected-fi tters (FM-UE-baseline=18 points), unexpected-expected-fi tters (FM-UE-baseline<18 points) and non-fi tters (FM-UE-baseline<18 points), to the proportional recovery model.

Results and discussion: %PCC increased from baseline to 12 weeks post-stroke

(ß:1.6%, CI:0.32-2.86%, P=0.01), which was no longer signifi cant after adjusting for EmNSA and FM-UE. A signifi cant positive association was found between %PCC, Amp-A and EmNSA. Unexpected fi tters (N=8) showed longitudinally signifi cantly higher %PCC than those expected to fi t the proportional recovery model (N=23).

Conclusion: We demonstrated the longitudinal construct validity of %PCC and

Amp-A as a measure of afferent pathway integrity. A high %PCC in unexpected fi tters suggests that this marker contains information above afferent integrity, i.e. cortical excitability. More work is needed to improve clinical prediction models for functional outcome post-stroke.

Acknowledgments: We received fi nancial support from the Hersenstichting and

ERC. Thur sda y 23 M ay 20 19

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