Evaluation of rod breakage after three-column osteotomy / Avaliação da quebra de haste após realização de osteotomia das três colunas / Evaluación de la rotura de varilla después de realización de osteotomía de las tres columnas

ABSTRACT Objective To identify the incidence and possible risk factors associated with rod breakage in patients who underwent vertebral column resection (VCR) or pedicle subtraction osteotomy (PSO) to treat complex deformities of the spine. Methods Retrospective analysis of a series of 32 patients operated from 2014 to 2018 in a single center. The patients were analyzed for demographic (sex, age), biometric (BMI), radiographical (pre- and postoperative angular variations), and surgical (arthrodesed and osteotomized levels) characteristics. Descriptive analyses were performed for the numerical variables (mean, standard deviation, maximum, median, and minimum) and frequency analysis was performed for the categorical variables. Logistic regression analysis was performed for the dependent variable "rod breakage", using a stepwise technique to select the variables for the best model, assuming statistical significance of 0.05. Results Of the 32 patients selected, rod breakage occurred in 34.4%. Mean age was 36.6 years (± 19.8), ranging from 10 to 74 years, and the mean BMI was 25.1 (±6.0). Most patients were subjected to VCR (75.0%), were males (56.2%) and did not smoke (90.6%). Logistic regression analysis showed that "arthrodesed levels" were was positively associated with rod breakage (OR 1.72; CI95%: 1.13-3.10; p<0.05). The other factors were not associated with breakage. Conclusion Rod breakage is a frequent complication after three-column osteotomy, especially in long constructions. Level of evidence III; Retrospective Study.

RESUMO Objetivos Identificar a incidência e possíveis fatores de risco relacionados à quebra de hastes em pacientes submetidos à ressecção colunar vertebral (RCV) ou osteotomia de subtração pedicular (OSP) para o tratamento cirúrgico de doenças complexas da coluna vertebral. Métodos Análise retrospectiva de uma série de 32 pacientes operados de 2014 a 2018, em um único centro. Os pacientes foram avaliados quanto às características demográficas (sexo, idade), biométricas (IMC), radiológicas (variação angular antes e após a correção) e cirúrgicas (níveis artrodesados, níveis osteotomizados). As análises descritivas foram realizadas para as variáveis numéricas (média, desvio-padrão, máximo, mediana e mínimo) e, para as variáveis categóricas foi realizada a análise da frequência. Realizou-se análise de regressão logística para a variável dependente "quebra", utilizando a técnica stepwise para seleção das variáveis que compõem o melhor modelo, considerando o nível de significância de 0,05. Resultados Foram selecionados 32 pacientes; a proporção de quebra foi de 34,4%. Observou-se que a média de idade foi de 36,6 anos (± 19,8 anos), distribuindo-se entre 10 e 74 anos, e o IMC médio foi 25,1 (± 6,0). Verificou-se que a maior parte dos indivíduos foi submetida a técnica RCV (75,0%), era do sexo masculino (56,2%) e não fumava (90,6%). Na análise de regressão logística, "níveis artrodesados" associou-se positivamente à quebra (OR 1,72; IC95%; 1,13-3,10; p < 0,05). Os outros fatores não se associaram à quebra. Conclusão A quebra de hastes é uma complicação frequente das osteotomias das três colunas, principalmente, em construções longas. Nível de evidência III; Estudo Retrospectivo.

RESUMEN Objetivos Identificar la incidencia y los posibles factores de riesgo relacionados a la rotura de varillas en pacientes sometidos a resección de la columna vertebral (RCV) u osteotomía de sustracción pedicular (OSP) para el tratamiento quirúrgico de enfermedades complejas de la columna vertebral. Métodos Análisis retrospectivo de una serie de 32 pacientes operados desde 2014 hasta 2018, en un único centro. Los pacientes fueron evaluados cuanto a las características demográficas (sexo, edad), biométricas (IMC), radiológicas (variación angular antes y después de la corrección) y quirúrgicas (niveles artrodesados, niveles osteotomizados). Los análisis descriptivos fueron realizados para las variables numéricas (promedio, desviación estándar, máximo, mediana y mínimo) y, para las variables categóricas fue realizado el análisis de frecuencia. Se realizó análisis de regresión logística para la variable dependiente «rotura¼, utilizando la técnica stepwise para selección de las variables que componen el mejor modelo, considerando el nivel de significancia de 0.05. Resultados Fueron seleccionados 32 pacientes; la proporción de rotura fue de 34,4%. Se observó que el promedio de edad fue de 36,6 años (± 19,8 años), distribuyéndose entre 10 a 74 años, y el IMC promedio fue de 25,1 (± 6,0). Se verificó que la mayor parte de los individuos fue sometida a la técnica RCV (75,0%), era del sexo masculino (56,2%) y no fumaba (90,6%). En el análisis de regresión logística, los "niveles artrodesados" se asociaron positivamente a la rotura (OR 1,72; IC 95%; 1,13-3,10; p <0,05). Los otros factores no se asociaron a la rotura. Conclusión La rotura de varillas es una complicación frecuente de las osteotomías de tres columnas, principalmente en construcciones largas. Nivel de evidencia III; Estudio Retrospectivo.

Valoración de la lordosis lumbar y diámetro foraminal utilizando el Soporte de Cirugía Espinal / Evaluation of lumbar lordosis and foraminal diameter using a Spinal Surgery Table

Introducción Tenemos como objetivo, cuantificar los cambios de la lordosis fisiológica en las distintas posiciones, de pie y en decúbito ventral, sobre el Soporte de Cirugía Espinal (SCE) y evaluar indirectamente los cambios de diámetro de los distintos forámenes, midiendo la distancia interpedicular. Materiales y métodos 20 pacientes de 20 a 40 años. Se tomaron radiografías, en posición de pie y sobre el SCE. Se midió la lordosis lumbar en radiografías de pié, y sobre el SCE en dos posiciones (baja/alta) así como la distancia interpedicular de los forámenes de cada segmento. Resultados Se constata una pérdida de la lordosis en la primera posición de 21,65° (37,00%) y en la segunda posición de 28,75° (49,14%). Encontramos un aumento de la distancia interpedicular en todos los niveles tanto en la posición baja como alta del SCE. Los forámenes que presentaron mayor apertura fueron los segmentos de L4-L5, seguidos por L5-S1. Conclusiones Se encontró una pérdida promedio de la lordosis fisiológica del 37,00% y del 49,14% con la utilización del SCE en las dos posiciones utilizadas. En todos los casos existió un aumento de la distancia interpedicular, que vario entre un 10 y un 15%. Los forámenes que mayor apertura presentaron en las distintas posiciones fueron los segmentos L4-L5 seguido por L5-S1. La cifotización de los segmentos móviles permitirían una mejor liberación sacorradicular al aumentar el diámetro del canal y los forámenes. Nivel de Evidencia: IV

Background The aim of this study is to quantify the changes of the physiological lordosis in the different positions, standing and in ventral decubitus, on a Spinal Surgery Table (SST), and indirectly evaluate the changes in diameter of the different foramina, and measuring the interpedicular distance. Methods The study included 20 patients from 20 to 40 years old. X-rays were taken in standing position and on the SST. Lumbar lordosis was measured using the X-rays in the standing position, and on the SST in two positions (low/high), as well as the interpedicular distance of the foramina of each segment. Results A loss of lordosis was found in the first position of 22.65° (37.00%) and in the second position of 28.75° (49.14%). An increase was found in the interpedicular distance at all levels in both the low and high position of the SST. The foramina with the greatest opening were the L4-L5 segments, followed by L5-S1. Discussion A mean loss of 37.00% and 49.14%, respectively, was found in the physiological lordosis with the use the SST in the two positions used. In all cases there was an increase in the interpedicular distance, which varied between 10% and 15%. The foramina with the greatest openness in the different positions were segments L4-L5 followed by L5-S1. The kyphotisation of the mobile segments would allow a better sacrum-radicular release when increasing the diameter of the channel and the foramina. Evidence Level: IV

Dolor crónico post cirugía de columna lumbar: magnitud del problema y opciones terapéuticas / Chronic pain after lumbar spine surgery: magnitude of the problem and therapeutic options

El dolor crónico postoperatorio de cirugía de columna lumbar tiene una incidencia entre un 10-50 por ciento de los pacientes postoperados, siendo de difícil manejo. Se ha denominado síndrome de fracaso de cirugía espinal lumbar (FBSS) a aquellos pacientes que han sido beneficiarios de una cirugía del raquis lumbosacro y en quienes no se logra una mejoría de manera satisfactoria, presentando dolor crónico lumbar, siendo su incidencia de alrededor de un 20 por ciento, y debido a una mala evolución del proceso de recuperación que puede ocasionar fibrosis en el canal medular. Existen diversas alternativas terapéuticas para afrontar este problema, donde destacan el tratamiento farmacológico, medicina física y el abordaje intervencionista no quirúrgico y quirúrgico implementados últimamente, con el fin de disminuir de manera efectiva el dolor en este grupo de pacientes. Sin embargo, a pesar de las terapias combinadas, existe un grupo de pacientes que debe ser sometido a una nueva intervención quirúrgica con resultados poco promisorios.

Chronic postoperative pain of lumbar spine surgery has an incidence between 10-50 percent of postoperative patients, being difficult to manage. The Failed Back Surgery Syndrome (FBSS) has been referred to those patients who have been beneficiaries of lumbosacral spinal surgery and who do not achieve a satisfactory improvement, presenting chronic lumbar pain with an incidence around 20 percent and due to a poor evolution of the recovery process that can cause fibrosis in the medullary canal. There are several therapeutic alternatives to address this problem, which highlights the pharmacological treatment, physical medicine and the non-surgical and surgical intervention approach recently implemented, in order to effectively reduce pain in this group of patients. However, despite the combination therapies, there is a group of patients that must undergo a new surgical intervention with little promising results.

Perioperative Factors Associated with Severe Pain in Post-Anesthesia Care Unit after Thoracolumbar Spine Surgery: A Retrospective Case-Control Study

STUDY DESIGN: A retrospective case-control study. PURPOSE: To evaluate the effect of nitrous oxide and anesthetic and operative factors associated with severe pain in the early postoperative period after thoracolumbar spine surgery. OVERVIEW OF LITERATURE: Thoracolumbar spine surgery is the most common procedure in spine surgery, and up to 50% of the patients suffer from moderate to severe pain. Nitrous oxide has analgesic, anxiolytic, and anesthetic effects; nevertheless, its benefits for early postoperative pain control and opioid consumption remain to be established. METHODS: The medical records of eligible participants who underwent thoracolumbar spine surgery between July 2016 and February 2017 were reviewed. Enrolment was performed consecutively until reaching 90 patients for the case (severe pain) group (patients with a pain score of >7 out of 10 at least once during the post-anesthesia care unit [PACU] admission), and 90 patients for the control (mild-to-moderate pain) group (patients with a pain score of <7 in every PACU assessment). The data collected comprised patient factors, anesthetic factors, surgical factors, PACU pain score, and PACU pain management. RESULTS: A total of 197 patients underwent thoracolumbar spine surgery with an incidence of early postoperative severe pain of 53.3%. The case-control study revealed no differences in the factors related to pain intensity. A subgroup analysis was performed for failed back surgery syndrome (FBSS), spinal stenosis, and spondylolisthesis. After multivariate analyses, only the age group of 19–65 years and the baseline Oswestry Disability Index (ODI) were found to be significant risk factors for early postoperative severe pain in the PACU (odds ratio [OR], 2.86; 95% confidence interval [CI], 1.32–6.25; OR, 1.03; 95% CI, 1.01–1.05, respectively). CONCLUSIONS: Nitrous oxide, anesthetic agents, and surgical techniques did not affect the early postoperative pain severity. Age under 66 years and the baseline ODI were the significant risk factors for pain intensity during the early postoperative period of the FBSS, spinal stenosis, and spondylolisthesis subgroups.

Spinal cord stimulation for fail back surgery syndrome: literature review and clinical study / Estimulación de la médula espinal para el síndrome de cirugía de espalda fallida: revisión de la literatura y estudio clínico / Estimulação da medula espinhal para síndrome de cirurgia de retorno: revisão da literatura e estudo clínico

ABSTRACT Objective: Fail back surgery syndrome (FBSS) is a common cause of pain following spine surgery, and is associated with persistent or recurrent pain despite anatomically correct intervention. Spinal cord stimulation (SCS) is regarded as one of the most effective methods of treatment for fail back surgery syndrome. Methods: We studied 34 patients who underwent test stimulation and chronic SCS for FBSS. Results: Six months postoperatively, mean improvement by the visual analog scale (VAS) of average and maximum daily pain, and the painDETECT score, were 54.4%, 50.7% and 57.3%, respectively. This meets the criteria for effectiveness of the method, according to the literature. Most of patients reported significant improvements in life quality and less need for analgesics. Complications were seen in nine patients (26.4%) and included: intraoperative dura injury (one patient, 2.9%), wound infection (one patient, 2.9%), and electrode displacement (seven patients, 20.5%). No cases of postoperative neurological deterioration were seen. Conclusions: SCS is safe and effective for the treatment of neuropathic pain caused by FBSS. Level of Evidence IV; Case series.

RESUMO Objetivos: A síndrome da cirurgia de falência reversa (SAF) é uma causa comum de dor após cirurgia de coluna e associada a dor persistente ou recorrente, apesar da intervenção anatomicamente correta. Estimulação da medula espinhal (SCS) é considerado como um dos métodos mais eficazes de tratamento para a síndrome de cirurgia de retorno. Métodos: Foram estudados 34 pacientes submetidos a estimulação de teste e SCS crônica para FBSS. Resultados: 6 meses de pós-operatório melhora a média de dor diária média e máxima diária na escala análoga visual (VAS), bem como a pontuação do PainDetect foram de 54,4%, 50,7% e 57,3%, respectivamente. Ele atende aos critérios de eficácia do método, de acordo com a literatura. A maioria dos pacientes relatou melhora significativa da qualidade de vida e menor necessidade de analgésicos. As complicações foram observadas em nove pacientes (26,4%) e incluíram: lesão da dura-máter intraoperatória (um paciente, 2,9%), infecção da ferida (um paciente, 2,9%), deslocamento do eletrodo (sete pacientes, 20,5%). Não houve casos de deterioração neurológica no pós-operatório. Conclusões: A SCS é segura e eficaz para o tratamento da dor neuropática causada pela FBSS. Nível de Evidência IV; Séries de casos.

RESUMEN Objetivo: El síndrome de cirugía de espalda fallida (FBSS) es una razón común para el dolor después de la cirugía de la columna vertebral y se asocia con dolor persistente o recurrente a pesar de la intervención anatómicamente correcta. La estimulación de la médula espinal (SCS) se considera uno de los métodos de tratamiento más eficaces para el síndrome de cirugía de espalda fallida. Métodos: Se estudiaron 34 pacientes que se sometieron a estimulación de prueba y SCS crónica para FBSS. Resultados: A los seis meses la mejora promedio postoperatoria por la escala visual análoga (EVA) del dolor diario promedio y máximo diario, así como el puntaje de painDETECT fueron 54,4%, 50,7% y 57,3%, respectivamente. Esto cumple con los criterios de efectividad del método, según la literatura. La mayoría de los pacientes informaron una mejoría significativa de la calidad de vida y una menor necesidad de analgésicos. Las complicaciones se observaron en nueve pacientes (26,4%) e incluyeron: lesión duramadre intraoperatoria (uno paciente, 2,9%), infección de la herida (uno paciente, 2,9%), desplazamiento del electrodo (siete pacientes, 20,5%). No se observaron casos de deterioro neurológico postoperatorio. Conclusiones: SCS es seguro y efectivo para el tratamiento del dolor neuropático causado por FBSS. Nivel de Evidencia IV; Series de casos.

Failed Back Surgery Syndrome: A Review Article

Postsurgical spine syndrome is becoming an increasingly common challenge for clinicians who deal with spinal disorders owing to the expanding indications for spinal surgery and the aging world population. A multidisciplinary approach is most appropriate for patients who are unlikely to benefit from further formal surgical intervention. Anticonvulsant medications are effective in managing neuropathic pain after surgery, whereas opioids are rarely beneficial. Neuromodulation via a surgically implanted dorsal column neurostimulator is gaining popularity owing to its substantial superiority over conventional medical management and/or further surgical intervention. However, considering that prevention is always better than cure, spinal surgeons need to be well aware of the many poor prognostic indicators for spinal surgery, particularly psychosocial overlay.

Etiology, Evaluation, and Treatment of Failed Back Surgery Syndrome

The study aimed to review the etiology of failed back surgery syndrome (FBSS) and to propose a treatment algorithm based on a systematic review of the current literature and individual experience. FBSS is a term that groups the conditions with recurring low back pain after spine surgery with or without a radicular component. Since the information on FBSS incidence is limited, data needs to be retrieved from old studies. It is generally accepted that its incidence ranges between 10% and 40% after lumbar laminectomy with or without fusion. Although the etiology of FBSS is not completely understood, it is possibly multifactorial, and the causative factors may be categorized into preoperative, operative, and postoperative factors. The evaluation of patients with FBSS symptoms should ideally initiate with reviewing the patients' clinical history (observing “red flags”), followed by a detailed clinical examination and imaging (whole-body X-ray, magnetic resonance imaging, and computed tomography). FBSS is a complex and difficult pathology, and its accurate diagnosis is of utmost importance. Its management should be multidisciplinary, and special attention should be provided to cases of recurrent disc herniation and postoperative spinal imbalance.

Undiagnosed Peripheral Nerve Disease in Patients with Failed Lumbar Disc Surgery

STUDY DESIGN: Retrospective study (level of evidence=3). PURPOSE: We examine the relationship between residual symptoms after discectomy for lumbar disc herniation and peripheral nerve (PN) neuropathy. OVERVIEW OF LITERATURE: Patients may report persistent or recurrent symptoms after lumbar disc herniation surgery; others fail to respond to a variety of treatments. Some PN neuropathies elicit symptoms similar to those of lumbar spine disease. METHODS: We retrospectively analyzed data for 13 patients treated for persistent (n=2) or recurrent (n=11) low back pain (LBP) and/or leg pain after primary lumbar discectomy. RESULTS: Lumbar re-operation was required for four patients (three with recurrent lumbar disc herniation and one with lumbar canal stenosis). Superior cluneal nerve (SCN) entrapment neuropathy (EN) was noted in 12 patients; SCN block improved the symptoms for eight of these patients. In total, nine patients underwent PN surgery (SCN-EN, n=4; peroneal nerve EN, n=3; tarsal tunnel syndrome, n=1). Their symptoms improved significantly. CONCLUSIONS: Concomitant PN disease should be considered for patients with failed back surgery syndrome manifesting as persistent or recurrent LBP.

Complication of epiduroscopy: a brief review and case report

Epiduroscopy is defined as a percutaneous, minimally invasive endoscopic investigation of the epidural space. Periduroscopy is currently used mainly as a diagnostic tool to directly visualize epidural adhesions in patients with failed back surgery syndrome (FBSS), and as a therapeutic action in patients with low back pain by accurately administering drugs, releasing inflammation, washing the epidural space, and mechanically releasing the scars displayed. Considering epiduroscopy a minimally invasive technique should not lead to underestimating its potential complications. The purpose of this review is to summarize and explain the mechanisms of the side effects strictly related to the technique itself, leaving aside complications considered typical for any kind of extradural procedure (e.g. adverse reactions due to the administration of drugs or bleeding) and not fitting the usual concept of epiduroscopy for which the data on its real usefulness are still lacking. The most frequent complications and side effects of epiduroscopy can be summarized as non-persistent post-procedural low back and/or leg discomfort/pain, transient neurological symptoms (headache, hearing impairment, paresthesia), dural puncture with or without post dural puncture headache (PDPH), post-procedural visual impairment with retinal hemorrhage, encephalopathy resulting in rhabdomyolysis due to a dural tear, intradural cyst, as well as neurogenic bladder and seizures. We also report for first time, to our knowledge, a case of symptomatic pneumocephalus after epiduroscopy, and try to explain the reason for this event and the precautions to avoid this complication.

Current strategy for chronic pain after spinal surgery

Failed back surgery syndrome was recently renamed, as chronic pain after spinal surgery (CPSS) by international classification of disease-11. CPSS is a challenging clinical condition. It has a variety of causes associated with preoperative, intraoperative and postoperative periods. Also, psychosocial factors should be considered. Diagnostic tools must be used differently, for each patient. Imaging and interventional nerve block for diagnosis, should be used properly. Strategy of management requires a multidisciplinary approach. The effect of conservative management (medication, interventional management) and invasive procedure (spinal cord stimulator, intrathecal drug delivery system) has been studied by many researchers. However, an evidence-based guide on management of CPSS, remains necessary, and further research is needed. This review focuses on understanding and clinical approaches for CPSS.

Effects of ozone on the pain and disability in patients with failed back surgery syndrome / Efeitos do ozônio na dor e na incapacidade em pacientes com síndrome dolorosa pós-laminectomia

Summary Introduction: Low back pain is one of the painful disorders of higher prevalence. It has several etiologies and surgery may be indicated in the presence of neurological deficits or compression syndromes. However, in up to 40% of cases, patients develop worsening of pain and failed back surgery syndrome (FBSS), which is an important cause of chronic pain with high morbidity and disability. In the last two decades, ozone has been shown to be a new therapeutic option for FBSS due to its analgesic and anti-inflammatory properties. Objective: To evaluate the effect of ozone therapy on pain and disability in patients with failed back surgery syndrome. Method: We selected 19 patients undergoing epiduroscopy and injection of ozone. Patients were evaluated preoperatively and 21 days after the procedure, using the following instruments: Visual Analogue Scale (VAS), Brief Pain Inventory, Roland-Morris Questionnaire Disability, Oswestry Disability Index (ODI), Neuropathic Pain Symptom Inventory and Douleur Neuropathique 4. Results: The patients showed significant pain relief, but no improvement was observed in the functional scales. Conclusion: Our results suggest that epidural ozone therapy can be a treatment option in FBSS to reduce the intensity of the pain.

Resumo Introdução: A dor lombar é um dos distúrbios dolorosos de maior prevalência. Tem diversas etiologias e, na presença de déficits neurológicos ou síndromes compressivas, pode ser indicada cirurgia. Entretanto, em até 40% dos casos os pacientes podem evoluir com piora da dor e síndrome dolorosa pós-laminectomia (SDPL), que se constitui em uma importante causa de dor crônica com grande morbidade e incapacidade. Nas últimas duas décadas, o ozônio tem se mostrado uma nova opção terapêutica para a SDPL em virtude das suas propriedades analgésicas e anti-inflamatórias. Objetivo: Avaliar o efeito da ozonioterapia na dor e na incapacidade de pacientes com SDPL. Método: Foram selecionados 19 pacientes, submetidos a epiduroscopia e aplicação de ozônio. Os pacientes foram avaliados no pré-operatório e 21 dias após o procedimento, por meio de Escala Visual Analógica, Inventário Breve de Dor, Questionário Roland-Morris de Incapacidade, Oswestry Disability Scale, Inventário de Sintomas de Dor Neuropática e Questionário de Dor Neuropática. Resultados: Os pacientes apresentaram redução significante nos escores das escalas de avaliação de dor; porém, essa redução não foi observada na avaliação da incapacidade funcional. Conclusão: Os dados obtidos sugerem que a ozonioterapia epidural pode ser uma opção de manejo da SDPL na diminuição da intensidade da dor.

Effectiveness of an interdisciplinary program in patients with failed back surgery syndrome / Eficácia de um programa interdisciplinar em pacientes com síndrome pós-laminectomia / Eficacia de un programa interdisciplinario en pacientes con síndrome postlaminectomía

ABSTRACT Objective: To evaluate the results of an interdisciplinary program administered to patients with failed back surgery syndrome, aiming at functional improvement, modulation of pain, reduction of anxiety symptoms and depression, and improvement of quality of life. Method: This is a non-randomized prospective study with a sample of patients with failed back surgery pain syndrome diagnosed with persistent or recurrent pain after surgery to the lumbar spine (laminectomy and arthrodesis) referred to liaison in the Pain Clinic (n= 26). The instruments used were Brief Pain Inventory, Roland-Morris Questionnaire and Beck Anxiety and Depression Inventories. The generic WHOQOL-bref13 questionnaire was used to evaluate the quality of life and the fear of moving was assessed by the Tampa Scale for Kinesiophobia. Results: There was a predominance of females, the mean age was 42.3 ± 5.8 years, 43% were married and average schooling was 7 ± 4.5 years. The mean time of pain reported was 8 ± 6.8 months in addition to high levels of anxiety, depression and kinesiophobia. After the intervention, there was a significant improvement in the perception of quality of life and of all parameters evaluated (p<0.05), with functional gains as well as decreased pain threshold. Conclusion: The interdisciplinary intervention in patients with failed back surgery syndrome provides better functional performance, decreases the intensity of pain, anxiety and depression symptoms, and improves quality of life. The inclusion of this intervention associated with drug therapy may the patient develop an active and independent lifestyle.

RESUMO Objetivo: Avaliar os resultados de um programa interdisciplinar aplicado a pacientes com síndrome pós-laminectomia, visando melhora funcional, modulação da dor, redução de sintomas de ansiedade e depressão e aumento da qualidade de vida. Método: Trata-se de um estudo prospectivo não randomizado, com amostra constituída por um grupo de pacientes com síndrome dolorosa pós-laminectomia diagnosticados com dor persistente ou recorrente após cirurgias da coluna lombar (laminectomia e artrodese) encaminhados para interconsultas na Clínica da Dor (n= 26). Os instrumentos utilizados foram: Inventário Breve de Dor, Questionário Roland-Morris e Inventários Beck de ansiedade e depressão. Para avaliar a qualidade de vida, foi utilizado Questionário Genérico Whoqol-bref13 e o medo de se movimentar foi avaliado pela Escala Tampa para Cinesiofobia. Resultados: Houve predomínio de mulheres, a média de idade foi 42,3 ± 5,8 anos, 43% eram casados e a média de escolaridade foi de 7 ± 4,5 anos. O tempo médio de dor relatado foi de 8 ± 6,8 meses, além de níveis altos de ansiedade, depressão e cinesiofobia. Após a intervenção houve melhora significativa na percepção da qualidade de vida e de todos os parâmetros avaliados (p < 0,05) observando-se ganhos funcionais, assim como a diminuição do limiar de dor. Conclusão: A intervenção interdisciplinar nos pacientes com síndrome pós-laminectomia proporciona melhor desempenho funcional, diminui a intensidade da dor, os sintomas de ansiedade e depressão, melhorando a qualidade de vida. A inclusão desta intervenção associada ao tratamento farmacológico pode desenvolver um estilo de vida ativo e independente.

RESUMEN Objetivo: Evaluar los resultados de un programa interdisciplinario subministrado a pacientes con síndrome postlaminectomía que busca la mejora funcional, la modulación del dolor, la reducción de los síntomas de ansiedad y depresión y calidad de vida. Método: Se trata de un estudio prospectivo no aleatorio de una muestra compuesta por un grupo de pacientes con síndrome doloroso postlaminectomía diagnosticados con dolor persistente o recurrente después de la cirugía de la columna lumbar (laminectomía y fusión) referidos a interconsultas en la Clínica del Dolor (n= 26). Los instrumentos utilizados fueron: Cuestionario breve del dolor, Cuestionario Roland-Morris e inventarios de ansiedad y depresión de Beck. Para evaluar la calidad de vida se utilizó el cuestionario genérico WHOQOL-BREF13 y el miedo de moverse fue evaluado por la Escala de Tampa de Kinesiofobia. Resultados: Hubo un predominio de mujeres, la edad promedio fue de 42,3 ± 5,8 años, 43% eran casados y la educación promedio fue de 7 ± 4,5 años. Se reportó una duración promedio del dolor de 8 ± 6,8 meses, además de altos niveles de ansiedad, depresión y kinesiofobia. Después de la intervención se observó una mejoría significativa en la percepción de la calidad de vida y de todos los parámetros (p < 0,05), siguiendo las ganancias funcionales, así como la disminución del umbral del dolor. Conclusión: La intervención interdisciplinaria en pacientes con síndrome postlaminectomía mejora la funcionalidad, disminuye la intensidad del dolor, los síntomas de ansiedad y depresión y mejora la calidad de vida. La inclusión de esta intervención asociada con el tratamiento farmacológico puede proporcionar una vida activa e independiente.

Response to: Clinical Use, Quality of Life and Cost-Effectiveness of Spinal Cord Stimulation Used to Treat Failed Back Surgery Syndrome

No abstract available.

Letter to the editor: Clinical Use, Quality of Life and Cost-Effectiveness of Spinal Cord Stimulation Used to Treat Patients with Failed Back Surgery Syndrome

No abstract available.

Neuropathic Pain after Spinal Surgery

Neuropathic pain after spinal surgery, the so-called failed back surgery syndrome (FBSS), is a frequently observed troublesome disease entity. Although medications may be effective to some degree, many patients continue experiencing intolerable pain and functional disability. Only gabapentin has been proven effective in patients with FBSS. No relevant studies regarding manipulation or physiotherapy for FBSS have been published. Spinal cord stimulation (SCS) has been widely investigated as a treatment option for chronic neuropathic pain, including FBSS. SCS was generally accepted to improve chronic back and leg pain, physical function, and sleep quality. Although the cost effectiveness of SCS has been proved in many studies, its routine application is limited considering that it is invasive and is associated with safety issues. Percutaneous epidural adhesiolysis has also shown good clinical outcomes; however, its effects persisted for only a short period. Because none of the current methods provide absolute superiority in terms of clinical outcomes, a multidisciplinary approach is required to manage this complex disease. Further studies concerning the etiology, diagnosis, treatment, and cost effectiveness of FBSS are warranted to deepen our understanding of this condition.

The Usefulness of Selective Nerve Root Block for Failed Back Surgery Syndrome / 대한정형외과학회잡지

PURPOSE: To retrospectively evaluate the improvement of symptoms and diagnosis using selective nerve root block (SNRB) for radiating pain after spine surgery. MATERIALS AND METHODS: From October 2012 to October 2013, 112 patients with failed back surgery syndrome (41 male and 71 female, with the mean age of 62.4 years and range of 35 to 78 years), who were admitted and underwent SNRB, were included. All patients were followed-up for more than 12 months. Three groups were classified: Group 1 included patients with no improvement or aggravation of symptoms, group 2 included those with improvement of radiating pain, and group 3 included those with recurrence of radiating. RESULTS: Among the 112 patients, there were 15 patients in group 1, 59 patients in group 2, and 38 patients in group 3. Laminectomy was the highest surgical procedure, inducing failed back surgery syndrome. In group 2, the occurrence of failed back surgery syndrome was higher in case that radiating pain was complained more than 1 year before the first surgery. There is statistically significant symptom improvement in accordance with the visual analogue scale and Korean version of Oswestry disability index on every group after SNRB (p<0.05). CONCLUSION: It is considered that SNRB is expected to improve the symptoms and to find the cause of symptoms as a diagnostic value even after spine surgery.

Spinal Cord Stimulation in Failed Back Surgery Syndrome: Review of Clinical Use, Quality of Life and Cost-Effectiveness

Failed back surgery syndrome (FBSS) is complex and recurrent chronic pain after spinal surgery. Several important patient and surgery related risk factors play roles in development of FBSS. Inadequate selection of the candidates for the spinal surgeries is one of the most crucial causes. The guidelines suggest that conservative management featuring pharmacologic approaches and rehabilitation should be introduced first. For therapy-refractory FBSS, spinal cord stimulation (SCS) is recommended in selected patients. Treatment efficacy for FBSS has increased over the years with the majority of patients experiencing pain relief and reduced medicinal load. Improved quality of life can also be achieved using SCS. Cost-effectiveness of SCS still remains unclear. However evidence for SCS role in FBSS is controversial, SCS can be beneficial for carefully classified patients.

Epidural neuroplasty/epidural adhesiolysis

Epidural neuroplasty is a treatment modality for back pain and/or radiating pain caused by mechanical compression or neural inflammation of intra-spinal neural structures. Since epidural neuroplasty was first introduced as a treatment for pain caused by epidural adhesion such as failed back surgery syndrome (FBSS), it has been performed as a treatment for many kinds of pain of spinal origin including acute/chronic herniation of intervertebral disc, radiculopathy, spinal stenosis, FBSS, epidural adhesion, vertebral compression fracture, vertebral metastasis, resistant multilevel degenerative arthritis, epidural scar pain by infection or meningitis, and whiplash injury. Epidural neuroplasty is a catheterization technique used to treat back pain and/or radiating pain by injecting therapeutic drugs into lesions of epidural space shown as a filling defect in epidurogram. Usually, normal saline, local anesthetics, and steroid are used as therapeutic drugs. The exact mechanisms of action of the procedure are unknown but include 2 postulated mechanisms of action for pain relief. i.e., mechanical adhesiolysis by volume effect and chemical adhesiolysis by injected drugs. Relative large volumes of normal saline injection resolve adhesions and wash out accumulated pain substances; local anesthetics are used for stabilization and analgesia of flaring neural structures and for pain management for procedure related pain; and steroid is used for the treatment of inflammation of neural and peri-neural structures. The resolution of filling defect can be verified by post-procedure epidurogram. The key point of epidural neuroplasty for good results, is the exact localization of the epidural catheter into the epidural lesion.

Interrater Reliability of the Postoperative Epidural Fibrosis Classification: A Histopathologic Study in the Rat Model

STUDY DESIGN: Agreement study. PURPOSE: To validate the interrater reliability of the histopathological classification of the post-laminectomy epidural fibrosis in an animal model. OVERVIEW OF LITERATURE: Epidural fibrosis is a common cause of failed back surgery syndrome. Many animal experiments have been developed to investigate the prevention of epidural fibrosis. One of the common outcome measurements is the epidural fibrous adherence grading, but the classification has not yet been validated. METHODS: Five identical sets of histopathological digital files of L5-L6 laminectomized adult Sprague-Dawley rats, representing various degrees of postoperative epidural fibrous adherence were randomized and evaluated by five independent assessors masked to the study processes. Epidural fibrosis was rated as grade 0 (no fibrosis), grade 1 (thin fibrous band), grade 2 (continuous fibrous adherence for less than two-thirds of the laminectomy area), or grade 3 (large fibrotic tissue for more than two-thirds of the laminectomy area). A statistical analysis was performed. RESULTS: Four hundred slides were independently evaluated by each assessor. The percent agreement and intraclass correlation coefficient (ICC) between each pair of assessors varied from 73.5% to 81.3% and from 0.81 to 0.86, respectively. The overall ICC was 0.83 (95% confidence interval, 0.81-0.86). CONCLUSIONS: The postoperative epidural fibrosis classification showed almost perfect agreement among the assessors. This classification can be used in research involving the histopathology of postoperative epidural fibrosis; for example, for the development of preventions of postoperative epidural fibrosis or treatment in an animal model.

Jiawei shentong zhuyu decoction prevented the occurrence of failed back surgery syndrome and its effect on serum TNF-alpha a clinical study / 中国中西医结合杂志

<p><b>OBJECTIVE</b>To explore the clinical roles of Jiawei Shentong Zhuyu Decoction (JSZD) in preventing the occurrence of failed back surgery syndrome (FBSS), and to observe its effect on serum tumor necrosis factor-alpha (TNF-alpha).</p><p><b>METHODS</b>Totally 100 patients prepared for surgical operation due to lumbar intervertebral disc herniation were randomly assigned to the treatment group and the control group according to random number table, 50 cases in each group. Patients in the treatment group additionally took JSZD, one dose per day, taken in two portions, once in the morning and once in the evening. Those in the control group took Celecoxib Capsule (200 mg each time, once per day) and Mecobalamin Tablet (0.5 mg each time, 3 times per day). They only took Mecobalamin Tablet from the 11th day. All patients were treated for 30 days. Japanese Orthopaedic Association (JOA) score was performed before treatment, at week 1, after treatment, at 6 months of followed-ups, and at 12 months of followed-ups. And the levels of TNF-alpha in the peripheral blood were observed before treatment and at one month after treatment.</p><p><b>RESULTS</b>Totally 93 patients completed the followed-up study. The JOA scores were improved after treatment, at 6 and 12 months of followed-ups (P < 0.05, P < 0.01). The JOA score at 6 months of followed-ups was superior in the treatment group to that of the control group (P < 0.05). Five patients (accounting for 10.6%) suffered from FBSS in the treatment group, while 9 (accounting for 19.6%) suffered from FBSS in the control group. The treatment group was superior to the control group (P < 0.05). The TNFalpha level was improved after treatment in the two groups. Of them, the improvement of TNF-alpha in the treatment group was better than that of the control group (P < 0.05).</p><p><b>CONCLUSION</b>The application of JSZD was effective for preventing the occurrence of FBSS, and improved the serum TNF-alpha level.</p>