2017
DOI: 10.1016/j.tvjl.2017.01.015
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Correlation between severity of clinical signs and transcranial magnetic motor evoked potentials in dogs with intervertebral disc herniation

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Cited by 5 publications
(6 citation statements)
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“…At 2nd follow‐up, onset latencies were significantly longer in non‐ambulatory compared to ambulatory dogs. However, the number of dogs with Grade III in comparison to Grade II and I at 2nd follow‐up was very low, thus the high impact of single values could bias this analysis, as these findings are in conflict with recently published data . The normalization of onset latencies in the present study, eliminating the effect of differing body size between patients could explain the differing results of these 2 studies as well.…”
Section: Discussioncontrasting
confidence: 79%
See 1 more Smart Citation
“…At 2nd follow‐up, onset latencies were significantly longer in non‐ambulatory compared to ambulatory dogs. However, the number of dogs with Grade III in comparison to Grade II and I at 2nd follow‐up was very low, thus the high impact of single values could bias this analysis, as these findings are in conflict with recently published data . The normalization of onset latencies in the present study, eliminating the effect of differing body size between patients could explain the differing results of these 2 studies as well.…”
Section: Discussioncontrasting
confidence: 79%
“…The low number of dogs that could be included for calculation could be a reason for non-significant differences and over-estimation of differences between these groups at the same time, limiting validity of these calculations.At 2nd follow-up, onset latencies were significantly longer in nonambulatory compared to ambulatory dogs. However, the number of dogs with Grade III in comparison to Grade II and I at 2nd follow-up was very low, thus the high impact of single values could bias this analysis, as these findings are in conflict with recently published data 53. The normalization of onset latencies in the present study, eliminating the effect of differing body size between patients could explain the differing results of these 2 studies as well.TMMEP amplitudes did not differ significantly between ambulatory and non-ambulatory dogs during follow-up.…”
contrasting
confidence: 80%
“…Transcranial magnetic motor evoked potentials (TMMEP) can be elicited reliably in dogs under sedation (92,93). However, they are extremely sensitive to spinal cord injury and are lost completely in dogs that are paraplegic (94,95). With less severe injuries, latency increases and amplitude decreases, but these values do not discriminate initial severity as well as clinical assessment and evaluation of MEPs at time of presentation does not provide prognostic information (94,95).…”
Section: Motor Evoked Potentialsmentioning
confidence: 99%
“…While a variety of factors have been associated with the development of ambulation in dogs with absent pain perception, no predictors in the acute or subacute stage of its subsequent development have yet been established. Considerations worthy of further investigation include clinical parameters such as the onset of spasticity, imaging biomarkers such as DTI indices and tractography, electrodiagnostic evaluation of descending motor tract function or motor neuron pool excitability and serum and cerebrospinal fluid biomarkers of inflammation or structural spinal cord proteins (5,68,77,(89)(90)(91)(92)(93)(94)(95)(96)(97)(98). While specific markers in serum and cerebrospinal fluid have not been evaluated to predict spinal walking, serum glial fibrillary acidic protein (GFAP) and phosphorylated neurofilament heavy chain (pNFH) have been reported to be useful among deep pain negative dogs in predicting outcome and the development of progressive myelomalacia (96)(97)(98).…”
Section: Prediction and Facilitation Of Spinal Walkingmentioning
confidence: 99%