Objective—To establish the reference ranges for motor evoked potential (MEP) latency and amplitude in clinically normal Doberman Pinschers, compare the MEPs of Doberman Pinschers with and without clinical signs of cervical spondylomyelopathy (CSM; wobbler syndrome), and determine whether MEP data correlate with neurologic or magnetic resonance imaging (MRI) findings.
Animals—16 clinically normal and 16 CSM-affected Doberman Pinschers.
Procedures—Dogs were classified according to their neurologic deficits. After sedation with acepromazine and hydromorphone, transcranial magnetic MEPs were assessed in each dog; latencies and amplitudes were recorded from the extensor carpi radialis and cranial tibial muscles. Magnetic resonance imaging was performed to evaluate the presence and severity of spinal cord compression.
Results—Significant differences in cranial tibial muscle MEP latencies and amplitudes were detected between clinically normal and CSM-affected dogs. No differences in the extensor carpi radialis MEP were detected between groups. There was a significant correlation (r = 0.776) between the cranial tibial muscle MEP latencies and neurologic findings. Significant correlations were also found between MRI findings and the cranial tibial muscle MEP latencies (r = 0.757) and amplitudes (r = −0.453).
Conclusions and Clinical Relevance—Results provided a reference range for MEPs in clinically normal Doberman Pinschers and indicated that cranial tibial muscle MEP latencies correlated well with both MRI and neurologic findings. Because of the high correlation between cranial tibial muscle MEP data and neurologic and MRI findings, MEP assessment could be considered as a screening tool in the management of dogs with spinal cord disease.
Objective—To evaluate use of transcranial magnetic
motor evoked potentials for assessment of the functional
integrity of the cervical spinal cord in largebreed
dogs with cervical spinal cord disease.
Design—Randomized, controlled, masked study.
Animals—10 healthy large-breed control dogs and 25
large-breed dogs with cervical spinal cord diseases.
Procedure—Affected dogs were allocated to 3
groups on the basis of neurologic status: signs of
neck pain alone, ambulatory with ataxia in all limbs, or
nonambulatory. Transcranial magnetic stimulation
was performed on each dog with the same standard
technique. Motor evoked potentials (MEP) were
recorded from electrodes inserted in the tibialis cranialis
muscle. Following the procedure, each dog was
anesthetized and cervical radiography, CSF analysis,
and cervical myelography were performed. The MEP
latencies and amplitudes were correlated with neurologic
status of the dogs after correction for neuronal
Results—Mean MEP latencies and amplitudes were
significantly different between control dogs and dogs
in each of the 3 neurologic categories, but were not
significantly different among dogs in the 3 neurologic
categories. A linear association was evident between
MEP latencies and amplitudes and severity of neurologic
deficits; the more severe the neurologic deficits,
the more prolonged the latencies and the more
decreased the amplitudes.
Conclusions and Clinical Relevance—Transcranial
magnetic MEP are useful to assess severity of cervical
spinal cord disease in large-breed dogs.
Impairment of the functional integrity of the cervical
spinal cord was found even in dogs with neck pain
alone. (J Am Vet Med Assoc 2002;221:60–64)
Objective—To determine accuracy, intermethod agreement, and inter-reviewer agreement for multisequence magnetic resonance imaging (MRI) and 2-view orthogonal myelography in small-breed dogs with first-time intervertebral disk (IVD) extrusion.
Design—Prospective evaluation study.
Animals—24 dogs with thoracolumbar IVD extrusion.
Procedures—Each dog underwent MRI and myelography. Images obtained with each modality were independently evaluated and assigned standardized scores in a blinded manner by 3 reviewers. Results were compared with surgical findings. Inter-reviewer and intermethod agreements were assessed via κ statistics. Accuracy was assessed as the percentage of dogs for which ≥ 2 of 3 reviewers recorded findings identical to those determined surgically.
Results—Inter-reviewer agreement was substantial for site (κ = 0.70) and side of IVD extrusion (κ = 0.62) in T2-weighted magnetic resonance images and was substantial for site (κ = 0.72) and fair for side of extrusion (κ = 0.37) in myelographic images. Agreement for site between each modality and surgical findings was near perfect (κ = 0.94 and 0.88 for MRI and myelography, respectively). Intermethod agreement was substantial for site (κ = 0.71) and moderate for side of extrusion (κ = 0.40). Accuracy of MRI for site and side was 100% when results for T1-weighted, T2-weighted, and contrast-enhanced T1-weighted sequences were combined. Accuracy of myelography was 90.9% and 54.5% for site and side, respectively.
Conclusions and Clinical Relevance—Agreement between imaging results and surgical findings for identification of IVD extrusion sites in small-breed dogs was similar for MRI and myelography. However, MRI appeared to be more accurate than myelography and allowed evaluation of extradural compressive mass composition.
Objective—To compare electroencephalography (EEG) artifact associated with use of the subdermal wire electrode (SWE), gold cup electrode (GCE), and subdermal needle electrode (SNE) over an 8-hour period in sedated and awake dogs.
Animals—6 healthy dogs.
Procedures—8 EEG channels were recorded during 20-minute video-EEG recording sessions (intermittently at 0.5, 2, 4, 6, and 8 hours) with and without chlorpromazine sedation. Nonphysiologic artifacts were identified. Duration of artifact was summed for each channel. Number of unaffected channels (NUC) was determined.
Results—NUC was significantly affected by electrode type and sedation over time; median for SWE (2.80 channels; 95% confidence interval [CI], 0.84 to 5.70 channels) was significantly different from medians for GCE (7.87 channels; 95% CI, 7.44 to 7.94 channels) and SNE (7.60 channels; 95% CI, 6.61 to 7.89 channels). After 4 hours, NUC decreased in awake dogs, regardless of electrode type. In awake dogs, duration of artifact differed significantly between SWE and GCE or SNE; medians at 8 hours were 61.55 seconds (95% CI, 21.81 to 173.65 seconds), 1.33 seconds (95% CI, 0.47 to 3.75 seconds), and 21.01 seconds (95% CI, 6.85 to 64.42 seconds), respectively.
Conclusions and Clinical Relevance—The SWE had a significant duration of artifact during recording periods > 2 hours, compared with results for the GCE and SNE, in awake dogs. The GCE, SNE, and sedation resulted in significantly more channels unaffected by artifact. For longer recordings, caution should be exercised in selecting EEG electrodes and sedation state, although differences among electrodes may not be clinically relevant.
Objective—To evaluate the effects of various combinations of Paco2 and Pao2 values on brain morphometrics.
Animals—6 healthy adult dogs.
Procedures—A modified Latin square design for randomization was used. Dogs were anesthetized with propofol (6 to 8 mg/kg, IV), and anesthesia was maintained with isoflurane (1.7%) and atracurium (0.2 mg/kg, IV, q 30 min). Three targeted values of Paco2 (20, 40, and 80 mm Hg) and 2 values of Pao2 (100 and 500 mm Hg) were achieved in each dog, yielding 6 combinations during a single magnetic resonance (MR) imaging session. When the endpoints were reached, dogs were given at least 5 minutes for physiologic variables to stabilize before T1-weighted MR images were obtained. Total brain volume (TBV) and lateral ventricular volume (LVV) were calculated from manually drawn contours of areas of interest by use of a software program, with each dog serving as its own control animal. Three blinded investigators subjectively evaluated the lateral ventricular size (LVS) and the cerebral sulci width (CSW). Brain morphometric values were compared among the target blood gas states.
Results—No significant differences in TBV were found among target states. The LVV was significantly greater during hypocapnia, compared with hypercapnia at the same Pao2 value. With regard to the subjective evaluations, there were no significant differences among evaluators or among combinations of Pao2 and Paco2 values.
Conclusions and Clinical Relevance—The changes observed in LVV during hypocapnia and hypercapnia may serve as a potential confounding factor when neuromorphometric evaluations are performed in anesthetized dogs. (Am J Vet Res 2010;71:1011–1018)
Objective—To assess the effects of alterations in PaCO2 and PaO2 on blood oxygenation level–dependent (BOLD) signal intensity determined by use of susceptibility-weighted magnetic resonance imaging in brains of isoflurane-anesthetized dogs.
Animals—6 healthy dogs.
Procedures—In each dog, anesthesia was induced with propofol (6 to 8 mg/kg, IV) and maintained with isoflurane (1.7%) and atracurium (0.2 mg/kg, IV, q 30 min). During 1 magnetic resonance imaging session in each dog, targeted values of PaCO2 (20, 40, or 80 mm Hg) and PaO2 (100 or 500 mm Hg) were combined to establish 6 experimental conditions, including a control condition (PaCO2, 40 mm Hg; PaO2, 100 mm Hg). Dogs were randomly assigned to different sequences of conditions. Each condition was established for a period of ≥ 5 minutes before susceptibility-weighted imaging was performed. Signal intensity was measured in 6 regions of interest in the brain, and data were analyzed by use of an ANCOVA and post hoc Tukey-Kramer adjustments.
Results—Compared with control condition findings, BOLD signal intensity did not differ significantly in any region of interest. However, signal intensities in the thalamus and diencephalic gray matter decreased significantly during both hypocapnic conditions, compared with all other conditions except for the control condition.
Conclusions and Clinical Relevance—In isoflurane-anesthetized dogs, certain regions of gray matter appeared to have greater cerebrovascular responses to changes in PaCO2 and PaO2 than did others. Both PaO2 and PaCO2 should be controlled during magnetic resonance imaging procedures that involve BOLD signaling and taken into account when interpreting findings.