Introduction: Carpal tunnel syndrome (CTS) is the most common peripheral nerve entrapment seen within the outpatient orthopaedic clinic; therefore assessment and management of this common condition is of significant importance. Traditionally diagnosis has been made through detailed questioning; clinical examination and nerve conduction studies (NCS). There is however no true consensus as to the gold standard assessment of CTS and the use of NCS can confer additional costs and delay treatment. Previous studies have explored methods of predicting the presence of CTS including the clinician-administered Carpal Tunnel Questionnaire (CTQ) (Kamath and Stothard, 2003). The aim of the present studies is therefore to explore the versatility of the CTQ to see how a novel Patient-completed Version of the CTQ compares to the original Clinican-completed version. Psychometric properties of the questionnaire will be explored together the economic impact of integrating both versions within an orthopaedic care pathway. A further aim is to answer whether the CTQ more effective and cost-effective than NCS for patients referred to an orthopaedic clinic with suspected CTS. Method: 100 patients referred for further investigation of suspected CTS were assessed using parallel patient and clinician-completed versions of the CTQ and results were subsequently compared with those obtained from NCS. Item analysis explored each of the nine constructs of the questionnaire and the original scoring algorithm was validated using binary logistic regression and compared with alternative algorithms. Sensitivity and specificity of the questionnaire when compared to results of NCS was explored using Receiver Operating Characteristic (ROC) analyses. Inter-rater reliability was explored through Pearson’s correlation coefficient. Economic analysis and modelling was carried out to explore potential cost savings of use of the questionnaire rather than NCS for those with suspected CTS. Results demonstrated sensitivity of 92% and specificity of 54.67% (positive predictive value 95.35%) for the patient-completed questionnaire and 96% sensitivity with 70.67% specificity (98.15 positive predictive value) for the clinician-completed questionnaire when used to predict the outcome of NCS. Binary logistic regression confirmed the original scoring algorithm and a revised algorithm did not significantly improve sensitivity. Adoption of the clinician-completed CTQ would have screen out 54% of referrals for NCS, which in the case of the study site would have conferred cost savings of £73,305 per annum (base upon a referral rate of 750 per annum). The patient-completed CTQ in the current sample resulted in 43% of referrals with suspected CTS not requiring NCS to assist in diagnosis with a potential saving of £58,372.5 per annum. There are further considerations of the reduction in waiting times, which are explored further within the analysis. Conclusion: Economic evaluation is complex due to the variety of pathways adopted by different orthopaedic departments. While the results of the Patient-complete version of the CTQ may not be as convincing as the clinician completed the study does provide validation for its use and expands the versatility of this useful adjunct to the assessment of CTS. Both versions could potentially confer significant cost savings and reduce demands on investigative services, reducing waiting times and improving the patient journey in suspected CTS.

O envolvimento do sistema nervoso periférico em diversas doenças auto-imunes é bem estabelecido. No entanto, não existem estudos, com desenho metodológico apropriado, que tenham investigado a relação entre síndrome antifosfolípide primária (SAFP) e neuropatia periférica. Nosso objetivo nesse trabalho foi investigar a ocorrência de neuropatia periférica em pacientes com SAFP. Vinte e seis pacientes com SAFP (critérios de Sapporo) e vinte controles, saudáveis, pareados por sexo e idade, foram recrutados em dois centros de referência. Foram excluídas as causas secundárias de neuropatia periférica e um exame neurológico completo, seguido de estudo de neurocondução, foi realizado em todos os indivíduos. Parestesias foram observadas em oito pacientes (31%). Leve fraqueza distal e anormalidades nos reflexos tendíneos profundos, foram observados em três (11,5%) pacientes. Evidência eletrofisiológica de neuropatia periférica foi observada em nove (35%) pacientes: quatro (15,5%) pacientes apresentaram neuropatia sensitiva ou sensitivo-motora axonal distais (em dois deles, com a superposição de síndrome do túnel do carpo), um (4%) paciente apresentou neuropatia sensitivo-motora, axonal e desmielinizante, acometendo os membros superiores e inferiores, enquanto que em quatro (15,5%) pacientes, observou-se a presença isolada de síndrome do túnel do carpo. As alterações clínicas e sorológicas dos pacientes com SAFP não guardaram qualquer correlação, com as alterações eletrofisiológicas. Em conclusão, neuropatia periférica, em geral assintomática, é comum na SAFP. Estudo de condução nervosa deve ser considerado na avaliação desses pacientes. / The involvement of the peripheral nervous system in diverse autoimmune diseases is well established. However, no appropriately designed studies have been performed in primary antiphospholipid syndrome (PAPS)-related peripheral neuropathy. We aimed to investigate the occurrence of peripheral neuropathy in patients diagnosed with PAPS. Twenty-six consecutive PAPS (Sapporo\'s criteria) patients and twenty age- and gender-matched healthy controls were enrolled at two referral centers. Exclusion criteria were secondary causes of peripheral neuropathy. A complete clinical neurological exam followed by nerve conduction studies (NCSs) were performed. Paresthesias were reported in 8 patients (31%). Objective mild distal weakness and abnormal symmetric deep tendon reflexes were observed in three (11.5%) patients. With regard to the electrophysiological evidence of peripheral neuropathy, nine (35.0%) patients had alterations: four (15.5%) had pure sensory or sensorimotor distal axonal neuropathy (in two of them a carpal tunnel syndrome was also present) and one (4%) had sensorimotor demyelinating and axonal neuropathy involving upper and lower extremities, while four patients (15.5%) showed isolated carpal tunnel syndrome. Clinical and serological results were similar in all PAPS patients, regardless of the presence of electrophysiological alterations. In conclusion, peripheral neuropathy is a common asymptomatic abnormality in PAPS patients. The routine performance of NCS may be considered when evaluating such patients.

O envolvimento do sistema nervoso periférico em diversas doenças auto-imunes é bem estabelecido. No entanto, não existem estudos, com desenho metodológico apropriado, que tenham investigado a relação entre síndrome antifosfolípide primária (SAFP) e neuropatia periférica. Nosso objetivo nesse trabalho foi investigar a ocorrência de neuropatia periférica em pacientes com SAFP. Vinte e seis pacientes com SAFP (critérios de Sapporo) e vinte controles, saudáveis, pareados por sexo e idade, foram recrutados em dois centros de referência. Foram excluídas as causas secundárias de neuropatia periférica e um exame neurológico completo, seguido de estudo de neurocondução, foi realizado em todos os indivíduos. Parestesias foram observadas em oito pacientes (31%). Leve fraqueza distal e anormalidades nos reflexos tendíneos profundos, foram observados em três (11,5%) pacientes. Evidência eletrofisiológica de neuropatia periférica foi observada em nove (35%) pacientes: quatro (15,5%) pacientes apresentaram neuropatia sensitiva ou sensitivo-motora axonal distais (em dois deles, com a superposição de síndrome do túnel do carpo), um (4%) paciente apresentou neuropatia sensitivo-motora, axonal e desmielinizante, acometendo os membros superiores e inferiores, enquanto que em quatro (15,5%) pacientes, observou-se a presença isolada de síndrome do túnel do carpo. As alterações clínicas e sorológicas dos pacientes com SAFP não guardaram qualquer correlação, com as alterações eletrofisiológicas. Em conclusão, neuropatia periférica, em geral assintomática, é comum na SAFP. Estudo de condução nervosa deve ser considerado na avaliação desses pacientes. / The involvement of the peripheral nervous system in diverse autoimmune diseases is well established. However, no appropriately designed studies have been performed in primary antiphospholipid syndrome (PAPS)-related peripheral neuropathy. We aimed to investigate the occurrence of peripheral neuropathy in patients diagnosed with PAPS. Twenty-six consecutive PAPS (Sapporo\'s criteria) patients and twenty age- and gender-matched healthy controls were enrolled at two referral centers. Exclusion criteria were secondary causes of peripheral neuropathy. A complete clinical neurological exam followed by nerve conduction studies (NCSs) were performed. Paresthesias were reported in 8 patients (31%). Objective mild distal weakness and abnormal symmetric deep tendon reflexes were observed in three (11.5%) patients. With regard to the electrophysiological evidence of peripheral neuropathy, nine (35.0%) patients had alterations: four (15.5%) had pure sensory or sensorimotor distal axonal neuropathy (in two of them a carpal tunnel syndrome was also present) and one (4%) had sensorimotor demyelinating and axonal neuropathy involving upper and lower extremities, while four patients (15.5%) showed isolated carpal tunnel syndrome. Clinical and serological results were similar in all PAPS patients, regardless of the presence of electrophysiological alterations. In conclusion, peripheral neuropathy is a common asymptomatic abnormality in PAPS patients. The routine performance of NCS may be considered when evaluating such patients.

Experimental measurements are never perfect, even with sophisticated modern instruments. One of the fundamental problems in signal measurement is distinguishing the noise from the signal. Sometimes the two can be partly distinguished on the basis of frequency components: for example, the signal may contain mostly low-frequency components and the noise may be located at higher frequencies. This is the basis of filtering. This thesis discusses some changes in the experimental protocol such as determining a suitable stimulation site to elicit full compound nerve action potentials (CNAP). The effect of sampling frequency and smoothing techniques to improve the resolution of the conduction velocity distribution (CVD) estimates will also be discussed. A change in stimulation site to elicit the full CNAPs is proposed after realizing that it is relatively difficult to stimulate at the same location to recruit the nerve fibers repeatedly at the elbow. Thus, the stimulation site was changed from elbow to wrist to elicit the full CNAPs. From the simulations it is evident that there was some signal information beyond 2.5 kHz frequency resulting in an increase in the sampling rate from 5 kHz to 10 kHz. The results obtained after employing smoothing techniques improved the CVD resolution. The simulation results were corroborated with the experimental results obtained. Another aspect of this thesis is to check the error tolerance of the EMG decomposition algorithm. Once the muscle electrical activity is recorded, MU trains undergo an automatic decomposition process. Decomposition errors are present in most contractions, thus a human operator has to make changes/correct the values of the motor unit firing times. From the data acquired, false negatives, false positives and false negative-positive errors have been introduced. Different levels of errors to measure the coherence between two motor-unit firing trains from a muscle contraction were also introduced. The firing rate curves are computed for each MU to analyze the interactions between two motor units (MU). The false negatives type of errors was found to be least detrimental. Whereas the false positives and false negative-positive errors affected coherence the most, their error tolerance was only a single error per 5 seconds.

A neuropatia hansênica e a neuropatia hereditária com suscetibilidade à pressão (Hereditary Neuropathy with liability to Pressure Palsies - HNPP) são mononeuropatias múltiplas em que os estudos da condução nervosa (ECN) mostram geralmente alentecimento focal em topografias muito semelhantes. Na ausência de uma história familiar de HNPP e das manifestações na pele típicas da hanseníase, o diagnóstico diferencial entre elas pode ser muito difícil. Procurando identificar características que ajudassem a distinguir essas doenças, revisamos e catalogamos os dados da história clínica e dos ECN de 39 pacientes com HNPP e 78 pacientes com neuropatia hansênica. A manifestação inicial mais frequente na hanseníase foi o déficit sensitivo (43 pacientes-55.1%) e na HNPP foi a fraqueza muscular localizada indolor (24 pacientes-61%). Fraqueza muscular foi significativamente superior na HNPP e déficit sensitivo foi significativamente superior na hanseníase (p<0.001). A evolução clínica foi estável ou progressiva até o tratamento em todos os pacientes com hanseníase e na HNPP dez pacientes (25.6%) tiveram um curso progressivo e 29 (74.4%) uma evolução com flutuações. O padrão predominante ao exame neurológico foi a mononeuropatia múltipla: 66 pacientes (84.6%) na hanseníase e 26 pacientes (66.7%) na HNPP. Espessamento neural foi mais frequente na hanseníase (p=0,001) e déficit sensitivo intradérmico foi observado somente na hanseníase (p<0,001). Episódio prévio ou atual de paralisia aguda de nervo foi referido somente na HNPP (p<0,001). O padrão dos ECN prevalente foi a neuropatia sensitivo-motora assimétrica com alentecimento focal da condução (NSMAAF): 44 pacientes (56.4%) na hanseníase e 31 pacientes (94.0%) na HNPP. Os parâmetros clínicos mais úteis em distinguir as duas doenças foram: a perda sensitiva intradérmica com comprometimento precoce das fibras finas e ocorrência de reação hansênica na hanseníase; o envolvimento motor inicial predominante, episódios de paralisia aguda de nervo e a evolução com flutuações na HNPP. Se o paciente a ser avaliado apresentar mononeuropatia múltipla com alentecimentos focais da velocidade de condução, os seguintes achados neurofisiológicos sugerem hanseníase: a não detecção de potenciais sensitivos ou motores, a redução da amplitude dos potenciais de ação sensitivos dos nervos sural, fibular superficial e radial superficial (< 8,8 ?V), a redução da amplitude do potencial de ação muscular composto dos nervos ulnar e tibial posterior, a redução da velocidade de condução do potencial de ação muscular composto do nervo ulnar motor no segmento do antebraço (< 43 m/s) e a presença de dispersão temporal frequente; enquanto os seguintes achados sugerem HNPP: aumento desproporcional da latência distal do nervo mediano motor e a presença de bloqueio de condução. / The Hansen\'s disease neuropathy (HDN) and the Hereditary Neuropathy with liability to Pressure Palsies (HNPP) are multiple mononeuropathies whose nerve conduction studies (NCS) usually show focal slowing at very similar topographies. In the absence of a family history of HNPP and the typical skin manifestations of HD, the differential diagnosis between them may be very difficult. In order to identify characteristics that may distinguish these diseases, we reviewed the data of 39 patients with HNPP and of 78 patients with HDN. The most frequent presenting sign was a sensory deficit in 43 patients (55.1%) in the HDN and a localized painless muscular weakness in 24 patients (61%) in the HNPP. Muscle weakness was significantly higher in HNPP and sensory deficit was significantly higher in leprosy (p<0.001). The disease was stable or progressive until treatment in all patients with HDN and among HNPP ten patients (25.6%) had a progressive course and 29 (74.4%) an intermittent evolution. Neural thickening was more frequent in leprosy (p=0.001) and intradermal sensory deficit was observed only in leprosy (p<0.001). Previous or current episode of acute nerve palsy was reported only in HNPP (p<0.001). The predominant pattern on neurological examination was the multiple mononeuropathy: 66 patients (84.6%) in the HDN and 26 patients (66.7%) in the HNPP. The most prevalent pattern of NCS was an asymmetric sensorimotor neuropathy with focal slowing (ASMNFS): 44 patients (56.4%) in HDN and 31 patients (94.0%) in HNPP. The most helpful clinical parameters in distinguishing these diseases were the presence of leprosy reaction and the intradermal sensory loss with predominant early involvement of small nerve fibers in HDN; the initial predominant motor involvement, episodes of acute nerve palsies and the intermittent evolution in HNPP. If the patient evaluation show a pattern of multiple mononeuropathy with focal slowing, the following neurophysiological findings suggest HDN: no detection of sensory or motor potentials, amplitude reduction of the sural, superficial fibular and superficial radial (<8.8 ?V) nerves, amplitude reduction of the motor ulnar and posterior tibial nerves, reduction of the conduction velocity of the motor ulnar nerve at the forearm segment (<43 m/s) and the presence of frequent temporal dispersion; while the following findings suggest HNPP: a disproportionate increase in the motor distal latency of the median nerve and the presence of conduction block.

Bakgrund: Nervus medianus är armens mittersta nerv med både efferenta och afferenta nervfibrer. För att undersöka perifera nerver används neurografi. N. medianus sensorik går att undersöka både ortodromt och antidromt där den antidroma metoden framförallt används vid karpaltunnelsyndromfrågeställning. Vanligtvis stimuleras nerven då 7 respektive 14 cm från registreringspunkten på digitorum III, men det finns fördelar med att istället för 7 cm-punkten använda sig av proximal stimulering ovanför armvecket. För denna metod finns dock ont om referensvärden. Syftet med denna studie var därför att samla in referensvärden för latenstider och amplituder.  Metod: Försökspersonerna bestod av 34 personer mellan 22 och 65 år. N. medianus undersöktes sensoriskt med proximal stimulering och registrering på dig III med både 0,1 och 0,2 ms impulsduration.  Resultat: Peaklatenstider varierade mellan 5,94 och 8,7 ms (x̄=7,00 ms) och amplituder varierade mellan 7,2 𝜇V och 72,6 𝜇V (x̄=35,6) vid 0,1 ms impulsduration. Det fanns ett signifikant bidrag av både längd och ålder på både latenstider och amplituder och en signifikant könsskillnad mellan män och kvinnor kunde uppmätas. Det fanns en signifikant, men mycket liten, skillnad i latenstid för impulsduration, men inga skillnader i amplituder. Variationskoefficienten för tre upprepade mätningar varierade mellan 0,9 och 5,3 % för peaklatens och 1,0 och 15,6 % för amplitud.  Slutsats: Hos friska försökspersoner ses en viss variation för amplituder medan latenstider ligger mer samlat. Ålder och längd bör tas med i beräkning av individuella normalvärden och en könsaspekt kan inte heller uteslutas. Impulsduration bör inte ha någon klinisk relevans. Reliabiliteten är bättre för latenstider än amplituder. / Background:. Sensory nerves can be examined both orthodromic and antidromic with nerve conduction studies. In the mixed median nerve is the antidromic method mainly used for evaluation of carpal tunnel syndrome. Usually the nerve is stimulated 7 and 14 cm from the recording at digitorum III, but there are some advantages in changing the 7 cm stimulation point to a more proximal one. The purpose of this study was to collect reference values for peak latency times and amplitudes with a proximal stimulation.  Methods: 34 test subjects in the age of 22-65 years were recruited for the study. Sensory nerve conduction studies of the median nerve with proximal stimulation and recording at digitorum III were performed with both 0,1 and 0,2 ms stimulus duration.  Results: Latency times varied between 5,94 and 8,7 ms (x̄=7,00 ms) and amplitudes varied between 7,2 𝜇V and 72,6 𝜇V (x̄=35,6) when 0,1 ms stimulus duration was used. There was a significant contribution by both length and age on latency times and amplitudes and a significant sex difference. There was a small difference in latency times by stimulus duration, but not in amplitudes. The coefficient of variation varied between 0,9 and 5,3 % for peak latency time and 1,0 and 15,6 % for amplitude.  Conclusion: There was some variation in amplitudes, but the latency times were more gathered together. Age and length have to be taken in consideration while individually reference values are calculated and a sex difference cannot be ruled out. Stimulus duration probably does not have a clinically relevant impact. The reliability is better for latency times than for amplitudes.

Made available in DSpace on 2016-01-26T12:51:22Z (GMT). No. of bitstreams: 1 thiagoguimaraesnaves -dissert.pdf: 396666 bytes, checksum: 322f0d9f8506ec60598fc70d1e33cc6a (MD5) Previous issue date: 2009-10-20 / Objective: To establish electrophysiologic values for CTS diagnosis in the elderly. Casuistic and methods: thirty healthy volunteers with at least 65 years old were selected. Exclusion criteria were: any sensory symptom, peripheral neuropathy, sistemic diseases, alcohol abuse and wrist fracture. The following parameters were calculated: 1. Median sensory distal latency on the segment wrist - digit II, 14 cm (SDL); 2. Median/radial latency difference on the segment wrist - digit I, 10 cm (MRD); 3. Median/ulnar latency difference on the segment wrist - digit IV, 14 cm (MUD4); 4. Median/ulnar mixed latency difference on the segment palm - wrist, 8 cm (MUPD); 5. Combined sensory index (CSI), calculated as the adding of MRD, MUD4 and MUPD; 6. Mixed median palmar latency (PL), 8 cm; 7. Median/ulnar motor latency difference, lumbrical/interossei, 8 cm (LUMB); 8. Median motor distal latency, pulse-APB, 8 cm (DML). Results: Twenty-one volunteers were female and 9 were male. Mean age was 69.9 (range 65-86). The 97.5th upper normal limits suggested were: SDL 3.80 ms, MRD 0.95 ms, MUD4 0.95 ms, MUPD 0.50 ms, PL 2.45 ms, CSI 2.20 ms and DML 4.30 ms. Conclusions: The reference values for MRD, MUD4, MUDP and CSI in elderly are different from youngers. There are quite less differences for DSL and PL and none at all for DML. The use of these new values in elderly will reduce the number of false positives. / Objetivo: determinar parâmetros eletrofisiológicos para diagnóstico da STC em idosos. Casuística e Métodos: Trinta voluntários saudáveis com no mínimo 65 anos de idade foram selecionados. Os critérios de exclusão foram: quaisquer sintomas sensitivos, neuropatia periférica, doenças sistêmicas, abuso alcoólico e antecedente de fratura no pulso. Os seguintes parâmetros foram estudados: 1. Latência distal sensitiva do nervo mediano, segmento pulso-dedo II, 14 cm (LDS); 2. Diferença de latência sensitiva mediano/radial, pulso-dedo I, 10 cm (DMR); 3. Diferença de latência sensitiva mediano/ulnar, pulso-IV dedo, 14 cm (DMU4) ; 4. Diferença de latência mista mediano/ulnar, palma-pulso, 8 cm (DMUP); 5. Índice sensitivo combinado (ISC), calculado pela soma de DMR, DMU4 e DMUP; 6. Latência palmar mista do nervo mediano, 8cm (LP); 7. Diferença de latência motora mediano/ulnar lumbrical-interósseo, 8 cm (LUMB); 8. Latência distal motora do nervo mediano, pulso-APB, 8 cm (LDM). Resultados: Vinte e um voluntários eram mulheres e 9 homens com média de idade de 69,9 anos (variação 65-86). Os limites superiores de normalidade 97,5% sugeridos foram: LDS 3,80 ms, DMR 0,95 ms, DMU4 0,95 ms, DMUP 0,50 ms, LP 2,45 ms, ISC 2,20 ms e LDM 4,30 ms. Conclusões: Os valores de referência para DMR, DMU4, DMUP e ISC em idosos são diferentes em relação aos jovens. As diferenças foram menores para LDS e LP; não houve diferença para LDM. O uso destes novos valores reduzirá o número de exames falso-positivos em idosos.

Made available in DSpace on 2016-06-02T19:22:05Z (GMT). No. of bitstreams: 1 3198.pdf: 3159049 bytes, checksum: 5e8ac93b5a62ff5a959370c795dac4e9 (MD5) Previous issue date: 2010-09-03 / This thesis presents three manuscripts derived of two research projects that were developed during the doctorate program. Project 1. Purpose: To determine the interand intra-rater reliability of nerve conduction studies (NCS) of superficial peroneal, sural and medial plantar nerves. Methods: Two raters performed the bilateral NCS twice in 20 healthy participants (23.5±3.5 years). Reliability was analyzed by the Bland- Altman method and intraclass correlation coefficient (ICC). Results: The Bland-Altman method showed a good level of intra- and inter-rater agreement for all parameters nerves. The amplitude and latency of the medial plantar nerve (rater 1), as well the amplitude of the sural nerve (rater 2) had an intra-rater ICC &#8805;0.75. Inter-rater analysis showed concordance levels between moderate and very low. Project 2. Purposes: a) To compare the effects of three cold modalities on the nerve conduction parameters of the sural (sensory) and tibial (motor) nerves during cooling and post-cooling phases b) To analyze the effect of exercise on recovery of sensory and motor nerve conduction velocity (NCV). Methods: Thirty six healthy young subjects (20.5±1.9 years) were randomly allocated into three groups: ice massage (n=12), ice pack (n=12) and cold water immersion (n=12). Each group received 1 of the 3 cold modalities on the right calf region for 15 minutes. The subjects of each modality group were again randomized to perform a post-cooling activity (30 min rest or walk 15 min followed by rest 15min). Nerve conduction parameters of sural and posterior tibial nerves were evaluated. Results: All 3 modalities reduced amplitude and increased latency and duration of the compound action potential. Ice massage, ice pack, and cold water immersion reduced NCV by 20.4, 16.7, and 22.6 m/s and motor NCV by 2.5, 2.1, and 8.3 m/s, respectively. Cold water immersion, as applied in this study, was the most effective modality in changing nerve conduction parameters. The walk accelerated the recovery of sensory and motor NCV, regardless of the modality previously applied (p<0.0001). Conclusions: The NCS provides quantitative measures that contribute to the objective analysis of neural physiological effects of cryotherapy. All 3 modalities were effective in altering sensory and motor nerve conduction. However, the magnitude and duration of these effects depend on the method applied and the activity after cooling. / Esta tese apresenta três manuscritos derivados de dois projetos de pesquisa que foram desenvolvidos no doutorado. Projeto 1. Objetivo: Avaliar a confiabilidade intra e interavaliador dos testes de condução nervosa (TCN) nos nervos sural, peroneal superficial e plantar medial. Métodos: Dois examinadores realizaram duas vezes os TCN bilaterais em 20 participantes saudáveis (23,5±3,5 anos). A confiabilidade foi analisada pelo método de Bland-Altman e o coeficiente de correlação intraclasse (ICC). Resultados: O método de Bland-Altman indicou um bom nível de concordância intra e inter-avaliador para todos os parâmetros dos TCN. Foram observados ICC intra-avaliador &#8805; 0,75 para amplitude e latência do nervo plantar medial (avaliador 1) e para a amplitude do nervo sural (avaliador 2). A análise inter-avaliador mostrou níveis de concordância entre moderados e muito baixos. Projeto 2. Objetivos: a) Comparar os efeitos de três modalidades de crioterapia sobre os parâmetros de condução dos nervos tibial posterior (motor) e sural (sensorial) durante as fases de resfriamento e pós-resfriamento b) Analisar o efeito do exercício físico na recuperação da velocidade de condução nervosa (VCN) sensorial e motora. Métodos: Trinta e seis sujeitos jovens e saudáveis (20,5±1,9 anos) foram alocados aleatoriamente em três grupos: criomassagem (n=12), pacote de gelo (n=12); imersão em água gelada (n=12). Cada grupo recebeu uma das 3 modalidades de resfriamento na panturrilha direita, durante 15 min. Os sujeitos de cada grupo foram novamente aleatorizados para realizar uma atividade pós-resfriamento (30min de repouso ou 15min de marcha seguido de 15min de repouso). Avaliaram-se os parâmetros de condução nos TCN dos nervos sural e tibial posterior. Resultados. As três modalidades reduziram a amplitude e aumentaram a latência e duração do potencial de ação composto. Criomassagem, pacote de gelo e imersão em água gelada reduziram a VCN sensorial em 20,4, 16,7 e 22,6 m/s, e a VCN motora em apenas 2,5, 2,1 e 8,3 m/s, respectivamente. Imersão em água gelada, como usada neste estudo, foi a modalidade mais eficaz para alterar os parâmetros de condução nervosa. A marcha acelerou a recuperação da VCN sensorial e motora, independente da modalidade previamente aplicada (P<0,0001). Conclusões. Os TCN fornecem medidas quantitativas que subsidiam análises objetivas e úteis na avaliação dos efeitos fisiológicos neurais da crioterapia. As 3 modalidades de resfriamento foram eficazes para alterar a condução sensorial e motora. Contudo, a magnitude e duração desses efeitos dependem do tipo de modalidade usada e da atividade que se realiza após o resfriamento.

Title: Electromyographic and clinical evaluation of vincristine-induced peripheral neuropathy in pediatric patients after treatment of acute lymphoblastic leukemia and correlation with the Bruinkins-Oseretsky Test of Motor Proficiency Second Edition Objectives: The aim of this work was to characterize the neurological consequences of vincristine-induced peripheral neuropathy (VIPN) clinically and electromyographically and to evaluate motor skills of pediatric patients after the end of treatment of acute lymphoblastic leukemia. We also determined the relationship between the results of the clinical and electromyographic evaluation of VIPN and the correlation with the results of motor skills tests. Methods: The study involved 35 probands (19 girls and 16 boys) with a mean age of 10.7 years (SD ± 4.3) and a mean time since the last dose of vincristine of 2.3 years (SD ± 1.2). VIPN was assessed using a clinical pediatric-modified Total Neuropathy Score (ped-mTNS) and nerve conduction studies (NCS). Motor skills were assessed using the Bruinkins-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2). Results: The clinical presence of VIPN, according to ped-mTNS, was found in 20 % of probands. Abnormalities in nerve conduction studies were reported by 60.9 % of probands. Of these, 92.9 % had motor...

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