Plantar heel pain is commonly encountered by clinicians. Various conditions, such as plantar fasciopathy, myofascial syndrome and entrapment of the tibial, plantar and calcaneal nerves at the tarsal tunnel can cause plantar heel pain. This diversity in aetiology makes the diagnosis and treatment challenging. There are limited studies on pain mechanisms in patients with planter heel pain. There is no gold criterion standard for the diagnosis. Although various interventions have been reported, no specific treatment approach has yet been identified as being most effective. The first aim of this thesis was to critically appraise the literature on plantar heel pain of neural origin. Various databases were searched for peer-reviewed articles that predominantly focused on neurogenic plantar heel pain or that discussed relevant biomechanics of the tibial, plantar and calcaneal nerves. This review revealed inconsistency in the literature regarding the diagnosis and treatment of neurogenic plantar heel pain. There also was a lack of evidence for treatment approaches although the majority of patients with plantar heel pain are reported to improve with conservative treatment. The second aim of this thesis was to examine the biomechanical effects of clinical tests and combination of movements on various structures associated with plantar heel pain. This aim was achieved through cadaver studies (Study 1–3), in which strain in the plantar fascia and the nerves of the lower limb, and excursion of the nerves were measured during various movements and positions of the lower limb. Study 1 examined the Dorsiflexion-eversion test used to diagnose tarsal tunnel syndrome (TTS) and the Windlass test for plantar fasciopathy given the similarity between both tests. Both the Dorsiflexion-eversion and Windlass tests significantly increased strain in the structures that are commonly associated with plantar heel pain (the tibial and plantar nerves and plantar fascia). This suggests that the usefulness of the Dorsiflexion-eversion and Windlass tests in the differential diagnosis of plantar heel pain might be limited. Study 2 investigated the influence of different positions in adjacent joints on nerve biomechanics during ankle and toe movement. Increased strain in the tibial nerve at the ankle and plantar nerves associated with ankle and toe movement was significantly higher when the nervous system was pre-tensioned at a more proximal joint. Strain was even higher when the nerve bed was pre-tensioned at two joints. Study 3 examined a modified straight leg raising (SLR) test in which ankle dorsiflexion is performed before hip flexion. This test has been suggested to diagnose distal neuropathies such as TTS. During the modified SLR, the excursion and strain in the sciatic nerve associated with hip flexion were transmitted distally along the nerve from the hip to the foot. As a result, the strain in the nerves around the foot and ankle increased significantly during hip flexion. This movement did not affect plantar fascia strain. Consequently, the modified SLR may be a useful test to differentially diagnose plantar heel pain. This test warrants future research to evaluate its clinical use in patients with neurogenic plantar heel pain. The third aim of this thesis was to determine the reliability of high-resolution ultrasound for measuring the cross-sectional area of the tibial nerve at the tarsal tunnel and to compare the tibial nerve size between people with and without plantar heel pain. Study 4 investigated intra and intertester reliability in 10 participants without plantar heel pain by calculating intraclass correlation coefficients, measurement error and smallest detectable difference (SDD). Intra and intertester reliability were excellent, with very small measurement error and SDD. Tibial nerve enlargement in an individual patient by as little as 1.8 mm2 can be detected reliably with high-resolution ultrasound. The use of average value of three scans is recommended to compare between the involved and uninvolved side. Differences in the nerve size between 26 patients with plantar heel pain and 20 control participants were also analysed. There was no significant difference in tibial nerve size between both groups. Future research is needed to investigate the tibial nerve size in patients with proven TTS using ultrasonography. The fourth aim of this thesis was to investigate the characteristics of plantar heel pain through Study 5 for the same group of patients and control participants as in Study 4. Several self-report measures on pain and quality of life were used. Clinical tests and quantitative sensory tests (QST) were performed at local and remote sites on the involved and uninvolved side in the patients and on one side in the control participants. In the patients, mechanical hyperalgesia was the main finding as demonstrated by changes in palpation and pressure pain threshold. Other findings were changes in current thresholds, vibration threshold and thermal perception thresholds. These results suggest the existence of sensory changes that likely indicates change in peripheral and central pain processing. It is recommended to utilise a multidimensional pain assessment for patients with plantar heel pain. The findings in this thesis are important for the diagnosis and treatment of plantar heel pain. For future research, the results suggest to use fresh cadavers when investigating biomechanics of the clinical tests and nerve gliding exercises that are used for patients with plantar heel pain. It is also suggested to evaluate the cross-sectional area of the tibial nerve at the tarsal tunnel, the QSTs and all other diagnostic measurements in this thesis in patients with neurogenic plantar heel pain or patients with TTS.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / A hanseníase, uma doença conhecida por suas lesões de pele anestésicas, é a principal causa de neuropatia periférica nos países endêmicos. Os episódios reacionais são classicamente conhecidos por promover piora da função nervosa através das chamadas neurites que variam de quadros exuberantes a assintomáticos. Estas características da neuropatia tornam o diagnóstico precoce excepcionalmente desafiador assim como a necessidade de se intervir para se prevenir lesões permanentes nos nervos. Este estudo clínico, prospectivo, foi realizado selecionando-se pacientes com hanseníase, independente da forma clínica, no Ambulatório Souza Araujo, Fiocruz, Rio de Janeiro, que apresentavam episódios reacionais. O objetivo foi estudar o perfil neurológico clínico, eletroneurofisiológico e por imagem do nervo antes e após o tratamento das reações. Foram avaliados vinte e cinco pacientes levando-se em conta: exame neurológico, avaliação fisioterápica, estudo de condução nervosa, avaliação de espessura e ecogenicidade nervosa pelo método ultrassonográfico, fluxometria por laser Doppler e teste quantitativo da sensibilidade durante e um ano após o tratamento da reação. Estes pacientes foram divididos em três grupos: oito pacientes com neurite aguda, nove pacientes com neurite silenciosa e oito pacientes com reação cutânea sem neurite. Nos pacientes com episódios reacionais, observou-se predomínio do sexo masculino (60%), do grupo multibacilar (80%) e da forma clínica borderline-lepromatosa (36%). A neurite isolada foi o tipo de reação mais frequente, seguida de neurite associada à reação do tipo1, seguida da neurite associada à reação do tipo 2. O nervo motor mais acometido por neurite foi o fibular seguido pelo ulnar, enquanto o nervo sensitivo mais acometido foi o sural. O padrão eletroneuromiográfico característico dos episódios reacionais foi a mononeurite múltipla. A ultrassonografia, a fluxometria por laser Doppler e o teste quantitativo de sensibilidade, associados à clínica e ao estudo da condução nervosa, foram tidos como exames úteis para avaliação inicial e para acompanhar o tratamento dos episódios reacionais. Após o tratamento, foi constatada melhora nos parâmetros referentes à função motora, mas o mesmo não ocorreu para sensibilidade. Com esse estudo, observa-se a necessidade de acompanhamento multidiciplinar com exames especializados para os pacientes com hanseníase a fim de diagnóstico de reação e tratamento precoce evitando sequelas neurológicas. / Leprosy, a disease known for its characteristic insensitive skin patches, is the main cause of peripheral neuropathy in endemic countries. Leprosy reactions are well-known for promoting nerve function impairment by neuritis which range from asymptomatic to exuberant clinical pictures. These neuropathy characteristics make early diagnosis exceptionally challenging as the need to intervene in order to prevent permanent nerve damage. This prospective clinical study was done selecting leprosy patients regardless their clinical form, who had presented leprosy reaction at the Souza Araújo Out-patient clinic, FIOCRUZ, Rio de Janeiro. The objective was to study the neurologic, the neurophysiological, and the nerve image pattern before and after the treatment of leprosy reactions.Twenty five patients at the time of leprosy reactions and one year after the reaction treatment had been evaluated by means of neurologic examination, physiotherapyc examination, nerve conduction study, evaluation of thickness and echogenicity of the committed nerves through the use of ultrasound, Laser Doppler fluxometry, and also by the quantitative sensory test. The patients were divided in three groups: eight patients had acute neuritis, nine had silent neuritis, and eight had skin reaction without neuritis.This study was approved by the ethics committee of the Oswaldo Cruz Foundation.In the evaluated patients presenting reactional episodes there had been a male predominance (60%), a multibacillary group predominance (80%) and a borderline-lepromatosus (36%) clinic form predominance. The isolated neuritis was the most frequent leprosy reaction, followed by neuritis associated with type 1 reaction, and by neuritis associated with type 2 reaction. The most common motor nerve affected by neuritis was peroneal, followed by ulnar nerve whereas most common sensory nerve affected was sural.The characteristic electroneuromyography pattern of leprosy reactions was multiplex mononeuropathy. The ultrasound, Laser Doppler fluxometry, and the quantitative sensory test together with the clinical examination and with the nerve conduction study were helpful exams for initial evaluation and follow-up treatment of leprosy reaction. A motor function improvement had been observed after the treatment but the same didnt occur regarding the sensory function.Throughout these studies it had been observed a need of a multidiscipline follow up for leprosy patients with specialized exams in order to have reaction diagnoses and early treatment avoiding neurological sequelae

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / A hanseníase, uma doença conhecida por suas lesões de pele anestésicas, é a principal causa de neuropatia periférica nos países endêmicos. Os episódios reacionais são classicamente conhecidos por promover piora da função nervosa através das chamadas neurites que variam de quadros exuberantes a assintomáticos. Estas características da neuropatia tornam o diagnóstico precoce excepcionalmente desafiador assim como a necessidade de se intervir para se prevenir lesões permanentes nos nervos. Este estudo clínico, prospectivo, foi realizado selecionando-se pacientes com hanseníase, independente da forma clínica, no Ambulatório Souza Araujo, Fiocruz, Rio de Janeiro, que apresentavam episódios reacionais. O objetivo foi estudar o perfil neurológico clínico, eletroneurofisiológico e por imagem do nervo antes e após o tratamento das reações. Foram avaliados vinte e cinco pacientes levando-se em conta: exame neurológico, avaliação fisioterápica, estudo de condução nervosa, avaliação de espessura e ecogenicidade nervosa pelo método ultrassonográfico, fluxometria por laser Doppler e teste quantitativo da sensibilidade durante e um ano após o tratamento da reação. Estes pacientes foram divididos em três grupos: oito pacientes com neurite aguda, nove pacientes com neurite silenciosa e oito pacientes com reação cutânea sem neurite. Nos pacientes com episódios reacionais, observou-se predomínio do sexo masculino (60%), do grupo multibacilar (80%) e da forma clínica borderline-lepromatosa (36%). A neurite isolada foi o tipo de reação mais frequente, seguida de neurite associada à reação do tipo1, seguida da neurite associada à reação do tipo 2. O nervo motor mais acometido por neurite foi o fibular seguido pelo ulnar, enquanto o nervo sensitivo mais acometido foi o sural. O padrão eletroneuromiográfico característico dos episódios reacionais foi a mononeurite múltipla. A ultrassonografia, a fluxometria por laser Doppler e o teste quantitativo de sensibilidade, associados à clínica e ao estudo da condução nervosa, foram tidos como exames úteis para avaliação inicial e para acompanhar o tratamento dos episódios reacionais. Após o tratamento, foi constatada melhora nos parâmetros referentes à função motora, mas o mesmo não ocorreu para sensibilidade. Com esse estudo, observa-se a necessidade de acompanhamento multidiciplinar com exames especializados para os pacientes com hanseníase a fim de diagnóstico de reação e tratamento precoce evitando sequelas neurológicas. / Leprosy, a disease known for its characteristic insensitive skin patches, is the main cause of peripheral neuropathy in endemic countries. Leprosy reactions are well-known for promoting nerve function impairment by neuritis which range from asymptomatic to exuberant clinical pictures. These neuropathy characteristics make early diagnosis exceptionally challenging as the need to intervene in order to prevent permanent nerve damage. This prospective clinical study was done selecting leprosy patients regardless their clinical form, who had presented leprosy reaction at the Souza Araújo Out-patient clinic, FIOCRUZ, Rio de Janeiro. The objective was to study the neurologic, the neurophysiological, and the nerve image pattern before and after the treatment of leprosy reactions.Twenty five patients at the time of leprosy reactions and one year after the reaction treatment had been evaluated by means of neurologic examination, physiotherapyc examination, nerve conduction study, evaluation of thickness and echogenicity of the committed nerves through the use of ultrasound, Laser Doppler fluxometry, and also by the quantitative sensory test. The patients were divided in three groups: eight patients had acute neuritis, nine had silent neuritis, and eight had skin reaction without neuritis.This study was approved by the ethics committee of the Oswaldo Cruz Foundation.In the evaluated patients presenting reactional episodes there had been a male predominance (60%), a multibacillary group predominance (80%) and a borderline-lepromatosus (36%) clinic form predominance. The isolated neuritis was the most frequent leprosy reaction, followed by neuritis associated with type 1 reaction, and by neuritis associated with type 2 reaction. The most common motor nerve affected by neuritis was peroneal, followed by ulnar nerve whereas most common sensory nerve affected was sural.The characteristic electroneuromyography pattern of leprosy reactions was multiplex mononeuropathy. The ultrasound, Laser Doppler fluxometry, and the quantitative sensory test together with the clinical examination and with the nerve conduction study were helpful exams for initial evaluation and follow-up treatment of leprosy reaction. A motor function improvement had been observed after the treatment but the same didnt occur regarding the sensory function.Throughout these studies it had been observed a need of a multidiscipline follow up for leprosy patients with specialized exams in order to have reaction diagnoses and early treatment avoiding neurological sequelae

Doenças do neurônio motor (DNM) representam um grupo de doenças que cursam com fraqueza muscular progressiva e inexorável, e o manejo clínico é baseado no controle dos sintomas. Estes doentes sofrem de acometimentos motores e não motores intensos e de evolução progressiva. Entretanto, além dos sintomas motores, de humor e de déficits cognitivos, uma caracterização mais profunda de sintomas não- motores nesses doentes raramente foi relatada. Este estudo transversal objetivou descrever os sintomas não motores na DMN e seu impacto na qualidade de vida e no estado funcional, com foco na dor e alterações sensoriais. Oitenta doentes (31 mulheres, 55,7 ± 12,9 anos) com DNM foram submetidos a exame clínico extenso, avaliação de dor (questionário de dor McGill, Inventário breve de dor, questionário douleur neuropathique-4), avaliação psicofísica [teste quantitativo da sensibilidade (TQS) e modulação condicionada da dor (MCD)], avaliações de humor e catastrofismo, e foram comparados com controles saudáveis (CS) pareados por sexo e idade. Dor crônica (presente a maior parte dos dias por mais de três meses) foi presente em 46% dos doentes (escala numérica da dor = 5,18 ± 2,0). A dor de origem musculo- esquelética ocorreu em 40,5% e foi localizada principalmente na região da cabeça/pescoço (51%) e da região lombar (35%). A dor neuropática não presente nesta amostra. Comparado aos CS, os doentes com DNM apresentaram menor limiar de detecção de frio (p < 0,002) e valores de MCD significativamente menores (4,9 ± 0,2% vs. 22,1 ± 0,2%, p = 0,012). Os resultados do TQS/MCD não diferiram entre os doentes com DNM com e sem dor. A intensidade da dor foi correlacionada estatisticamente com ansiedade, depressão e catastrofismo, e os escores de espasticidade foram correlacionados inversamente com a MCD (rho = -0,30, p = 0,026). A dor é um sintoma frequentemente relatado por doentes com DNM. Alterações somatossensoriais e de MCD existem em DNM e podem estar relacionadas com a natureza neurodegenerativa da doença. Estudos adicionais devem investigar formas de melhor quantificar estas alterações e explorar estratégias de tratamento mais apropriadas para o seu controle / Motor neuron disorders (MNDs) represent a group of diseases that curse with inexorable muscle weakness and medical management is based on symptom control. These patients suffer from intense motor and non-motor progressive symptoms. However, apart from motor symptoms, mood and cognitive impairments, deeper characterization of non-motor symptoms in these patients have been rarely reported. This cross-sectional study aimed to describe non-motor symptoms in MND and their impact on quality of life and functional status, with a focus on clinical pain and sensory changes. Eighty patients (31 females, 55.7±12.9 years old) with MND underwent a extensive clinical examination, pain (McGill pain questionnaire, brief pain inventory, douleur neuropathique-4), psychophysics [quantitative sensory testing (QST) and conditioned pain modulation (CPM)], mood and catastrophizing assessments, and were compared to sex- and age-matched healthy controls (HC). Chronic pain (present on most days for more than three months) was present in 46% of patients (numerical visual scale=5.18±2.0). Pain of musculoskeletal origin occurred in 40.5% and was mainly located in the head/neck (51%) and lower back (35%). Neuropathic pain was not present in this sample. Compared to HC, MND patients had a lower cold detection threshold (p < 0.002), and significantly lower CPM scores (4.9±0.2% vs. 22.1±0.2%, p=0.012). QST/CPM results did not differ between MND patients with and without pain. Pain intensity was statistically correlated with anxiety, depression, and catastrophism, and spasticity scores were inversely correlated with CPM (rho=-0.30, p=0.026). Pain is frequently reported by patients with MNDs. Somatosensory and CPM changes exist in MNDs and may be related to the neurodegenerative nature of the disease. Further studies should investigate ways to better quantify these changes and explore the treatment strategies most appropriated for their control

Doenças do neurônio motor (DNM) representam um grupo de doenças que cursam com fraqueza muscular progressiva e inexorável, e o manejo clínico é baseado no controle dos sintomas. Estes doentes sofrem de acometimentos motores e não motores intensos e de evolução progressiva. Entretanto, além dos sintomas motores, de humor e de déficits cognitivos, uma caracterização mais profunda de sintomas não- motores nesses doentes raramente foi relatada. Este estudo transversal objetivou descrever os sintomas não motores na DMN e seu impacto na qualidade de vida e no estado funcional, com foco na dor e alterações sensoriais. Oitenta doentes (31 mulheres, 55,7 ± 12,9 anos) com DNM foram submetidos a exame clínico extenso, avaliação de dor (questionário de dor McGill, Inventário breve de dor, questionário douleur neuropathique-4), avaliação psicofísica [teste quantitativo da sensibilidade (TQS) e modulação condicionada da dor (MCD)], avaliações de humor e catastrofismo, e foram comparados com controles saudáveis (CS) pareados por sexo e idade. Dor crônica (presente a maior parte dos dias por mais de três meses) foi presente em 46% dos doentes (escala numérica da dor = 5,18 ± 2,0). A dor de origem musculo- esquelética ocorreu em 40,5% e foi localizada principalmente na região da cabeça/pescoço (51%) e da região lombar (35%). A dor neuropática não presente nesta amostra. Comparado aos CS, os doentes com DNM apresentaram menor limiar de detecção de frio (p < 0,002) e valores de MCD significativamente menores (4,9 ± 0,2% vs. 22,1 ± 0,2%, p = 0,012). Os resultados do TQS/MCD não diferiram entre os doentes com DNM com e sem dor. A intensidade da dor foi correlacionada estatisticamente com ansiedade, depressão e catastrofismo, e os escores de espasticidade foram correlacionados inversamente com a MCD (rho = -0,30, p = 0,026). A dor é um sintoma frequentemente relatado por doentes com DNM. Alterações somatossensoriais e de MCD existem em DNM e podem estar relacionadas com a natureza neurodegenerativa da doença. Estudos adicionais devem investigar formas de melhor quantificar estas alterações e explorar estratégias de tratamento mais apropriadas para o seu controle / Motor neuron disorders (MNDs) represent a group of diseases that curse with inexorable muscle weakness and medical management is based on symptom control. These patients suffer from intense motor and non-motor progressive symptoms. However, apart from motor symptoms, mood and cognitive impairments, deeper characterization of non-motor symptoms in these patients have been rarely reported. This cross-sectional study aimed to describe non-motor symptoms in MND and their impact on quality of life and functional status, with a focus on clinical pain and sensory changes. Eighty patients (31 females, 55.7±12.9 years old) with MND underwent a extensive clinical examination, pain (McGill pain questionnaire, brief pain inventory, douleur neuropathique-4), psychophysics [quantitative sensory testing (QST) and conditioned pain modulation (CPM)], mood and catastrophizing assessments, and were compared to sex- and age-matched healthy controls (HC). Chronic pain (present on most days for more than three months) was present in 46% of patients (numerical visual scale=5.18±2.0). Pain of musculoskeletal origin occurred in 40.5% and was mainly located in the head/neck (51%) and lower back (35%). Neuropathic pain was not present in this sample. Compared to HC, MND patients had a lower cold detection threshold (p < 0.002), and significantly lower CPM scores (4.9±0.2% vs. 22.1±0.2%, p=0.012). QST/CPM results did not differ between MND patients with and without pain. Pain intensity was statistically correlated with anxiety, depression, and catastrophism, and spasticity scores were inversely correlated with CPM (rho=-0.30, p=0.026). Pain is frequently reported by patients with MNDs. Somatosensory and CPM changes exist in MNDs and may be related to the neurodegenerative nature of the disease. Further studies should investigate ways to better quantify these changes and explore the treatment strategies most appropriated for their control