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3 MATERIAL UND METHODEN

3.3 Methoden

3.3.1 Korrelation von Daten der transkraniellen Magnetstimulation mit der Morphometrie des

3.3.1.2 Durchführung und Auswertung der Magnetresonanztomagraphie

Zur Sicherung der Diagnose und Erhebung pathologischer Befunde der Medulla spinalis wurde bei allen Probanden eine Magnetresonanztomographie des thorakolumbalen Rückenmarks mit einem 3,0 Tesla Magnetresonanztomographen (Philips Achieva MRI scanner; Fa. Philips Medical Systems Nederland, PC Best, Niederlande) durchgeführt. Die Patienten wurden in Rückenlage befindlich unter Verwendung einer 15-Kanal-Wirbelsäulenspule entsprechend dem Standard-Klinikprotokoll in verschiedenen Sequenzen untersucht. Zur Anfertigung der T2-gewichteten sagittalen Bildserien wurden folgende Einstellungen gewählt: Turbo-Spin-Echo (TSE) Sequenz, Pulswiederholzeit (TR) = 3100 ms, Echozeit (TE) = 120 ms, Schichtschnittdicke 1,8 mm mit einem 0,2 mm großen Abstand zwischen den Schnittbildern. Die transversale Schnittebene wurde mit Hilfe der folgenden Parameter bestimmt: TSE Sequenz, TR = 4630,4 bis 8418,8 ms bei einer TE von 120 ms und einer Schichtschnittdicke von 2 mm mit einem Schnittbildintervall von 0,2 mm.

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Neben T2- und T1-gewichteten transversalen und sagittalen Sequenzen wurde im Falle einer Kompression der Medulla spinalis durch Bandscheibenmaterial eine multi-Fast-Field–Echo- (mFFE) Sequenz in transversaler Ebene durchgeführt. Der Nachweis möglicher Blutungen wurde mit Hilfe einer HEMO Sequenz (Blut-Signal-Unterdrückungssequenz) geführt. Für die Diagnose einer möglichen Flüssigkeitsextravasation, welche auf T2-gewichteten Bildern zu einem hyperintensen Signal führt, wurde eine transversale FLAIR (Fluid attenuated inversion recovery) -Sequenz genutzt. In einigen Fällen war der Einsatz einer transversalen SPAIR (Spectral attenuated inversion recovery) -Sequenz zur Unterdrückung des Fettsignals indiziert. Eine Abgrenzung degenerativer von neoplastischen Prozessen wurde im Einzelfall durch die Injektion von Dotarem Godolinum Kontrastmittel (Guerbet GmbH;

Sulzbach/Taunus) und anschließender T1-gewichteter Sequenzen erzielt.

Die Diagnosestellung erfolgte durch die Auswertung von wenigstens der T2- und T1-gewichteten Sequenzen, sowie der mFFE-Bildserien, nach Indikation wurden weitere der oben genannten Sequenzen zur Hilfestellung genutzt. Die Bilddateien wurden im DICOM-Format gespeichert und mit Hilfe der Bildverarbeitungsroutine des Klinikprogramms easyVet (IFS Informationssysteme GmbH, Hannover, Deutschland) ausgewertet.

Im Rahmen dieser Studie wurden morphometrische Parameter erhoben, wie sie zuvor in anderen Veröffentlichungen beschrieben wurden und auch Anwendung in der Humanradiologie finden (Ito et al., 2005; Fehlings et al., 2006; Levine et al., 2009; Boekhoff et al., 2012). Die Beurteilung der Rückenmarksbefunde fand unter Verwendung der T2- und T1-gewichteten Sequenzen, sowie in einigen Fällen der mFFE-Bildserien statt. Mit Hilfe der T2-gewichteten transversalen Bilder wurde die minimale Höhe (mm) des Rückenmarks im Bereich der Kompression durch Bandscheibenmaterial bestimmt. An gleicher Stelle wurde die minimale Höhe (mm) des Rückenmarkkanals, definiert als Abstand zwischen vorgefallenem Bandscheibenmaterial und der gegenüberliegenden Lamina arcus vertebrae, bestimmt. Beide Werte wurden mit Messungen der gleichen Parameter einen Wirbelkörper kranial jedweder Kompression in ein Verhältnis gesetzt (Rückenmarks-Kompressions-Verhältnis bzw. Wirbelkörper-Kompressions-(Rückenmarks-Kompressions-Verhältnis), so dass vergleichbare und körpergrößen-unabhängige Werte erhoben wurden.

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Auf den sagittalen Bildern wurde die Länge (mm) der Kompression mit Hilfe der transversalen Aufnahmen abgetragen und gemessen. Es wurde ein Verhältnis zur Länge des zweiten Lendenwirbelkörpers (KLV = Kompressions-Längen-Verhältnis) gebildet.

Abbildung 4: Messung der Kompression des Rückenmarks

4a: Sagittale T2-gewichtete Sequenz des Rückenmarks eines 3 Jahre alten Mischling-Rüden. Die gelben Pfeile kennzeichnen die Länge des 2. Lendenwirbels (L2), sowie die Länge der Kompression des Rückenmarks.

4b: Korrespondierende transversale T2-gewichtete Sequenz; der weiße Pfeil markiert ein hypointenses Areal, welches vermutlich durch extrudiertes Bandscheibenmaterial hervorgerufen wird.

4c: Der transversalen Position von 4b entsprechende mFFE Sequenz des gleichen Hundes. Das Weichteil-isointense Areal, welches durch den weißen Pfeil markiert wird, kann als Bandscheibenmaterial angesprochen werden und führt zu einer hochgradigen Kompression des Rückenmarks von lateral.

a

c b

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Des Weiteren wurde auf T2-gewichteten sagittalen Sequenzen unter Berücksichtigung der korrespondierenden transversalen Schnittbilder die Länge von Hyperintensitäten gemessen.

Auch diese Werte wurden durch eine Division mit der Länge des zweiten Lendenwirbels normalisiert (HLV = T2-gewichtetes-Hyperintensitäts-Längen-Verhältnis).

Abbildung 5: Messung der intramedullären Hyperintensität

5a: Sagittale T2-gewichtete Sequenz des Rückenmarks eines 12 Jahre alten Shih-Tzu-Rüden. Die gelben Pfeile kennzeichnen die Länge des 2. Lendenwirbels (L2), sowie die Länge der intramedullären Hyperintensität kranial und kaudal der Bandscheibenextrusion.

5b: Korrespondierende transversale T2-gewichtete Sequenz; der weiße Pfeil markiert ein hyperintenses Areal, welches kaudal der Bandscheibenextrusion liegt.

5c: Der weiße Pfeil markiert ein hyperintenses Areal kranial der Bandscheibenextrusion.

a

b c

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36 3.4 Statistische Auswertung

Die statistische Analyse der Daten wurde mit dem kommerziellen Software-Programm SAS® Enterprise-Guide (Version 7.1, Cary, North Carolina, USA) durchgeführt, die graphische Darstellung erfolgte mittels GraphPad Prism ® (Version 5.0 Fa. GraphPad Software, Inc., La Jolla, CA, USA). Alter und Gewicht wurden gemittelt und die Standardabweichung wurde berechnet. Für die Berechnungen der TMMEPs wurden für die Amplituden und Latenzen der Vorder- und Hintergliedmaßen gesondert die Mittelwerte aus den Ergebnissen der Ableitungen rechter und linker Gliedmaßen pro Patient ermittelt. Für die Kalkulationen der TMMEP Parameter Latenz und Amplitude standen bei Hunden mit Paraplegie bei initialer Vorstellung keine Ergebnisse zur Verfügung. Weitere fehlende Ableitungen im Verlauf der Studie wurden für die Berechnungen nicht berücksichtig. Die Berechnung der Entwicklung von Amplituden und Latenzen während des Studienverlaufs war auf die Daten von 11 Hunden mit gepaarten Werten beschränkt. Dazu wurde ein Wilcoxon-Vorzeichen-Rang-Test angewendet. Der Vergleich von KLV und HLV während des Studienverlaufs wurde aufgrund Normalverteilung der Daten ebenfalls mit nicht-parametrischen Methoden unternommen (Wilcoxon-Vorzeichen-Rang-Test, Kruskal-Wallis-Test). Da die Latenzen und Amplituden zum Zeitpunkt wiederkehrender Spontanbewegungen eine Normalverteilung aufwiesen, wurde ein t-Test zur Kalkulation der Assoziation mit den neurologischen Schweregraden durchgeführt. Die Korrelation der Latenzen mit selbigen wurde mit einer (Rang-) Korrelationsanalyse nach Spearman, sowie Pearson untersucht. Die Assoziation von KLV und HLV mit den neurologischen Schweregraden wurde mittels Wilcoxon-Two-Sample-Test und Kruskal-Wallis-Test untersucht. Die Korrelation von KLV und HLV mit den Amplituden und Latenzen zu verschiedenen Zeitpunkten wurde mit Hilfe einer Spearman Korrelation untersucht. Eine statistisch signifikante Differenz lag vor, wenn P

< 0,05.

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37 4 Publikation

4.1 Correlation of transcranial magnetic motor evoked potentials and MRI morphometry in dogs with functional motor recovery after intervertebral disc herniation: A follow-up study

J.S.C.G. Siedenburga, H.-L. Amendta, K. Rohnb, A. Tipolda,c, V.M. Steina*

aDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover

bDepartment of Biometry, Epidemiology and Information Processing, University of Veterinary Medicine Hannover, Hannover, Germany.

cCenter for Systems Neuroscience, Hannover, Germany.

* Corresponding author: Veronika M. Stein +49 511 953 6200 E-mail address: veronika.stein@tiho-hannover.de

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38 Abstract

Functional motor recovery after decompressive surgery in paraplegic dogs with intervertebral disc herniation (IVDH) is crucial for patients and their owners. In this prospective study the hypotheses should be investigated that transcranial magnetic motor evoked potentials (TMMEPs) reliably display the course of motor function improvement in initially paraplegic dogs with thoracolumbar IVDH after decompressive surgery and determine whether there is any association between TMMEP data and severity of neurological signs or correlation with morphometric magnetic resonance imaging (MRI) findings.

At initial presentation TMMEP data including onset latencies and peak-to-peak amplitudes were obtained in 21 paraplegic, sedated dogs from the cranial tibial muscle. Morphometric measurements of MRI of the thoracolumbar spinal cord prior to surgery included L2 normalized ratios of compression length (CLR) and of T2 weighted intramedullary hyperintensities (T2WLR). First follow-up was performed within 1-2 days after first motor function reappearance including neurological examination and TMS. Second follow-up was performed 3 months after first follow-up comprising repeated neurological examination, TMS and MRI.

At initial presentation, TMMEPs could not be recorded from pelvic limbs. However, TMMEPs could be elicited from the cranial tibial muscle in 12/21 dogs at first follow-up and in 20/21 dogs at second follow-up. Comparison of values of these TMMEPs obtained at first and second follow-up showed a significant increase of peak-to-peak amplitudes and significant decrease of onset latencies. A significant association was detected of onset latencies first follow-up and severity of neurological signs at the second follow-up. At second follow-up latencies were significantly associated and correlated with severity of neurological signs. CLR and T2WLR were not significantly correlated with TMMEP data.

In conclusion, TMMEPs reflect motor function recovery after severe spinal cord injury.

Moreover, onset latencies obtained shortly after first reappearance of motor function may provide prognostic information of further motor improvement. However, correlation of TMMEPs with MRI morphometric measurements could not be confirmed.

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Keywords: Intervertebral Disc Herniation; Transcranial Magnetic Motor Evoked Potentials;

Transcranial Magnetic Stimulation, Spinal Cord Injury; Magnetic Resonance Imaging; Dog

Introduction

Spinal cord injury (SCI) in canines is commonly caused by thoracolumbar intervertebral disc herniation (IVDH) resulting in a broad range of clinical signs from paraspinal hyperaesthesia to paraplegia and loss of deep pain perception (DPP) with concomitant impairment of micturition and defecation (Duval et al., 1996; Jeffery and Blakemore, 1999;

Ferreira et al., 2002; Olby et al., 2003; Mayhew et al., 2004; Cerda-Gonzalez and Olby, 2006;

Fluehmann et al., 2006). Transcranial magnetic stimulation (TMS) generates transcranial magnetic motor evoked potentials (TMMEPs), which can be recorded from surface or muscle electrodes (Nollet et al., 2003). These TMMEPs enable a noninvasive and fast evaluation of the functional integrity of descending motor pathways in the brain and spinal cord (Barker et al., 1985). TMS is well established in human medicine, providing information about corticospinal tract damage and lesion location in cervical spinal cord injury (Maertens de Noordhout et al., 1991; Lo et al., 2004; Shields et al., 2006; Kalupahana et al., 2008).

Moreover, it can be of prognostic value in stroke and SCI patients (Clarke et al., 1994;

Pennisi et al., 1999). In veterinary medicine diagnostic applications of TMS have been described in equine and canine species with spinal cord diseases (Sylvestre et al., 1993; Nollet et al., 2002; De Decker et al., 2011). Association of TMMEP data with severity of clinical signs and magnetic resonance imaging (MRI) findings has been described in CSM in Great Danes and Dobermann Pinschers, but was not examined in thoracolumbar IVDH so far (De Decker et al., 2011; Martin-Vaquero and da Costa, 2014).

Prognostic information gained from clinical assessment is widely accepted. In particular, presence or absence of DPP is acknowledged to be the most reliable prognostic indicator for recovery after severe SCI in dogs with plegia and has become a frequently used reference evaluating new prognostic approaches (Duval et al., 1996; Scott and McKee, 1999; Coates, 2000; Davis and Brown, 2002; Jeffery et al., 2013; Jeffery et al., 2016). In the past years a shift of focus towards CSF analysis and diagnostic imaging features revealed several associations with severity of spinal cord injury and correlations with functional outcome (Olby et al., 2003; Ito et al., 2005; Penning et al., 2006; Royal et al., 2009; Srugo et al., 2011;

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Roerig et al., 2013). Among the diagnostic imaging techniques MRI is considered the most accurate identifying characteristics of extruded disc material and parenchymal spinal cord lesions (Bos et al., 2012; Cooper et al., 2014). In previously published studies, MRI morphometric measurements on T2 weighted images were associated with severity of clinical signs and long-term ambulatory outcome after IVDH (Ito et al., 2005; Levine et al., 2009;

Boekhoff et al., 2012).

In this prospective study, the hypotheses should be proven, that a) TMS is a suitable technique for therapy monitoring in initially paraplegic dogs with IVDH after decompressive surgery and b) TMMEP data can reflect different severity of neurological signs. Further objectives were to determine whether c) TMMEP data could provide prognostic estimates about the extent of regeneration of motor function and d) whether a correlation exists between TMMEP data with morphometric MRI findings.

Material and Methods Dogs and study design

Twenty-one client-owned paraplegic dogs admitted to the Department of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Germany, were recruited between May 2013 and May 2015. Prior to study enrollment written owner consent was obtained. The study was conducted in accordance with the guidelines of the Animal Care Committee of the Government of Lower Saxony and national regulations for animal welfare (animal experiment number 33.14-42502-04-13/1277). Dogs had to meet the following inclusion criteria: <20 kg bodyweight, acute to subacute paraplegia (onset < 28 days) with present or absent DPP and spinal cord injury due to IVDH between T3-L3 confirmed by MRI and surgery.

All dogs had a general physical and neurological examination; further clinical examinations included complete blood cell count, routine serum biochemistry and radiographs of the thorax and vertebral column. According to their neurological deficits dogs were assigned to a Sharp and Wheeler (2005) scale (Tab. 1). At initial clinical presentation TMS was performed under deep sedation, as described in previously published studies (Sylvestre et al., 1993; Van Ham et al., 1996; da Costa et al., 2006; Granger et al., 2012; Amendt et al., 2016). Afterwards,

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MRI examinations were performed to definitely localize and characterize the lesion within the spinal cord and subsequently all dogs underwent decompressive surgery. When first motor function reappearance was observed, first follow-up including neurological examination and TMS was performed within 1-2 days later. Second follow-up was performed 3 months after first follow-up comprising repeated neurological examination, TMS and MRI.

TMMEPs

Dogs were sedated with acepromazine (0.02 - 0.05 mg/kg, Vetranquil, CEVA Tiergesundheit GmbH) and levomethadone/fenpipramide (0.2 - 0.4 mg/kg, L-Polamivet, Intervet Deutschland GmbH) intravenously (IV) while heartbeat and body temperature were monitored and TMS performed in lateral recumbency or sternal positioning. TMMEPs were recorded as described in previous studies with minor modifications (Sylvestre et al., 1993; da Costa et al., 2006; Martin-Vaquero and da Costa, 2014; Amendt et al., 2016). A Magstim 200² (Magstim Co Ltd) stimulator, capable of producing a maximum 4.0 Tesla magnetic field (complies with a 100 % intensity) with a 50 mm ring coil was used. The coil was held tangentially to the skull in close contact to the skin with the center of the coil lateral to the vertex to stimulate the motor cortex. The current flow within the coil ran in clockwise direction and four consecutive stimulations were delivered for generation of TMMEPs recorded from each limb. These recordings were obtained after contralateral stimulation by use of an electromyograph (Nicolet™ NicVue 2.9.1, Natus Medical Incorporated). The recording muscle-electrode was positioned in the middle of the muscle belly of the cranial tibial and the extensor carpi radialis muscle, respectively. The reference electrode was positioned subcutaneously one cm distal to the muscle electrode, while the ground electrode was placed subcutaneously on the dorsal midline of the cranial thoracic region and caudal lumbar region, respectively.

To display, adjust and save TMMEP waveforms VikingSelect-Software Version 11.0 (Viasys healthcare, CareFusion) was used. Total recording time was 200 ms following the stimulus;

sensitivity depended on amplitude values and ranged from 0.2 to 10 mV/division for all recordings in the thoracic and pelvic limbs. Onset latency and peak-to-peak amplitude were measured as described by van Ham et al. (1994) by manually directed cursors on the

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oscilloscope. Onset of latencies was measured in milliseconds [ms], being defined as interval between stimulus artifact and first subsequent deflection from the baseline. Peak-to-peak amplitudes were measured in microvolts [mV] and calculated from the peak of the negative wave to the nadir of the first positive wave. Neuronal path length was measured starting at the vertex via the estimated course of nerve fibers to the muscle needle positioned within the cranial tibial and extensor carpi radialis muscle, respectively, contralateral to the stimulation site (Martin-Vaquero and da Costa, 2014).

MRI

To confirm presumptive diagnosis of IVDH the thoracolumbar spinal cord was assessed by MRI. All patients were assessed under general anesthesia using a 3.0 Tesla (T) magnet (Philips Achieva, Philips Medical Systems) with a phased array SENSE (sensitivity encoding)-spine-coil with 15 channels. The thoracolumbar spinal cord was scanned with the following sequences: T2-weighted sequence was a TSE (turbo-spin-echo) sequence with sagittal (TR = 3100 ms, TE = 120 ms, slice thickness 1.8 mm, interslice gap 0.2 mm) and transversal (TR = 8418 ms, TE = 12 ms, slice thickness 1.8 mm, interslice gap 0.2 mm) planes. Images were complemented by transversal planes of T1-weighted (TR = 491 ms, TE = 8 ms, slice thickness 1.8 mm, interslice gap 0.2 mm) and mFFE (multi-echo fast field echo (TR = 21 ms, TE = 7 ms, slice thickness 1.8 mm, interslice gap 0.2 mm) sequences.

MRI data sets of all dogs were evaluated as DICOM formatted images by use of easyVET (IFS GmbH). Evaluation of discernible T2 weighted intramedullary hyperintensities rested upon assessment of sagittal images (Ito et al., 2005; Penning et al., 2006; Levine et al., 2009).

Corresponding transversal T2-weighted images (T2WI) were evaluated for detection of their length expansion (Griffin et al., 2015). T1 weighted sequences were assessed in transversal planes to exclude presence of T1 weighted hyperintensities (Levine et al., 2009). Detection of extruded intervertebral disc material was assessed in sagittal and transversal T2WI, complemented by transversal T1 weighted sequences and mFFE sequences (Levine et al., 2009; Griffin et al., 2015). Quantification of spinal cord compression was achieved by measurements on sagittal T2WI, transversal T1 weighted images were used to confirm longitudinal extent of spinal cord compression-spinal cord (Levine et al., 2009; Griffin et al., 2015). The length of L2 was used to calculate standardized T2 weighted hyperintensity length

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ratio (T2WLR) and spinal cord compression length ratio (CLR), as described before (Ito et al., 2005; Levine et al., 2009; Boekhoff et al., 2012).

Statistical methods

TMMEP variables (latencies and amplitudes) recorded in each dog from the right and left limbs were averaged to give a mean value for each dog and variable, then the means were calculated of all the dogs. At initial presentation in dogs with grades IV-V no TMMEPs could be recorded in pelvic limbs (Tab. 1). Thus, comparison of TMMEP data series was limited to dogs (n = 11) with recordable TMMEPs either at first and second follow-up. Latencies and amplitudes at fist follow-up were normally distributed. Thus, comparison of follow-up TMMEP data was performed by use of parametric tests. Association and correlation between latencies and amplitudes with severity of neurological signs were examined by use of t-test and Spearman correlation, respectively. For comparison of MRI features at initial presentation and at second follow-up, non-parametric methods (Wilcoxon’s signed rank test, Kruskal-Wallis test) were used, since not all data sets were normally distributed. Association between initial CLR, T2WLR and second follow-up TMMEP features with grades of neurological impairment at initial presentation and both follow-up examinations was calculated by use of Wilcoxon two sample test and t-test, respectively. Correlation of CLR and T2WLR obtained at initial presentation with TMMEPs at first follow-up and second follow-up respectively, was calculated with a Pearson and Spearman correlation. Analogously, correlation of MRI features with TMMEPs was calculated with values of second follow-up examinations. P-values of < 0.05 were considered significant. The statistical analyses were performed with a commercially available software program (SAS Enterprise Guide 7.1, SAS Institute Inc.).

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44 Results

Clinical data and neurological status

Twenty-one paraplegic dogs with an IVDH at T3-L3 spinal cord segments were enrolled in this study. Onset of clinical signs was acute to subacute (median: 3 days; range, < 24 hours-23 days). Dogs had a median age of 5.4 years (range, 2.6-13.1 years) and had a median bodyweight of 8.5 kg (range, 3.9-19.6 kg). The study population consisted of 5 sexually intact males, 7 neutered males, 4 sexually intact females and 5 spayed females. The study comprised 7 Dachshunds (33.3 %), 4 mixed breed dogs (19 %), 2 dogs of each of the following chondrodystrophic breeds: French Bulldog, Jack Russell Terrier, Lhasa Apso and Shih Tzu and 1 dog of each of the following breeds: Bolognese, Bolonka Zwetna and Havanese.

16/21 dogs were paraplegic with DPP and therefore classified as grade IV, whereas 5/21 were paraplegic with absent DPP and classified as grade V. All dogs showed reappearance of motor function after decompressive surgery (median 18 days; range, 4-37 days). Overall, 18/21 dogs (85.7 %) became ambulatory during follow-up, whereas 3/21 dogs (14.3 %) with absent DPP prior to surgery remained non-ambulatory (Tab. 1).

TMMEPs and comparison of TMMEPs and neurological status

No TMMEPs could be generated in plegic dogs with grade IV and V at initial presentation. At first follow-up, TMMEPs were recorded in 12/21 dogs. In 6 of these paraparetic dogs (n = 3 with grade II and n= 3 with grade III) TMMEP generation was limited to one pelvic limb. The 9 paraparetic dogs without measurable TMMEPs were all still non-ambulatory (grade III). At the second follow-up examination TMMEPs could be obtained in 19/21 dogs from both

No TMMEPs could be generated in plegic dogs with grade IV and V at initial presentation. At first follow-up, TMMEPs were recorded in 12/21 dogs. In 6 of these paraparetic dogs (n = 3 with grade II and n= 3 with grade III) TMMEP generation was limited to one pelvic limb. The 9 paraparetic dogs without measurable TMMEPs were all still non-ambulatory (grade III). At the second follow-up examination TMMEPs could be obtained in 19/21 dogs from both