RESUMEN
ABSTRACT Objective: to evaluate the application of a noninvasive intervention consisting of a postural modification using personalized models and osteopathy in people with occipital neuralgia. Method: retrospective study of the intervention performed in adult population with occipital neuralgia, consisting of postural modification using personalized plantar orthoses and osteopathy, in a study period of four years. The observed variables were: persistence of headache, alignment of the axes, plantar support, center of gravity and center of mass; medical interview data, visual analogue scale, Win-Track gait analysis system and Kinovea software for video analysis (clinical assessment instruments used). Results: a total of 34 records of people with occipital neuralgia were studied. A fraction of 58.8% of the patients reported improvement after the intervention. The visual analogue scale data were provided for 64.7% of the records and significant differences (p <0.001) between the means before (8.4 ± 1.7) and after the intervention (2.6 ± 2.7) were found. Conclusion: postural modification using personalized orthoses and osteopathy substantially improves the symptomatology of patients with occipital neuralgia.
RESUMO Objetivo: avaliar a aplicação de uma intervenção não invasiva que consiste em uma modificação postural usando modelos personalizados e osteopatia em pessoas com neuralgia occipital. Método: estudo retrospectivo da intervenção realizada em população adulta com neuralgia occipital que consiste de modificação postural empregando órteses plantares personalizadas e osteopatia, em um período de estudo de quatro anos. As variáveis observadas foram: persistência de cefaleia, alinhamento dos eixos, apoio plantar, centro de gravidade e centro de massa; dados da entrevista médica, escala visual analógica, sistema de análise de marcha Win-Track e o software Kinovea para análise de vídeo (instrumentos de avaliação clínica utilizados). Resultados: foram estudados no total 34 registros de pessoas com neuralgia occipital. Uma fração de 58,8% dos pacientes informou apresentar melhoria após a intervenção. Os dados da escala visual analógica foram fornecidos para 64,7% dos registros, encontrando diferenças significativas (p<0,001) entre as médias antes (8,4±1,7) e depois da intervenção (2,6±2,7). Conclusão: a modificação postural empregando órteses personalizadas e osteopatia melhora substancialmente a sintomatologia dos pacientes com neuralgia occipital.
RESUMEN Objetivo: evaluar la aplicación de una intervención no invasiva consistente en una modificación postural empleando plantillas personalizadas y osteopatía en personas con neuralgia occipital. Método: estudio retrospectivo de la intervención llevada a cabo en población adulta con neuralgia occipital, de modificación postural empleando órtesis plantares personalizadas y osteopatía, en un período de estudio de cuatro años. Las variables observadas fueron: persistencia de cefalea, alineación de los ejes, apoyo plantar, centro de gravedad y centro de masa; datos de la entrevista médica, la escala visual análoga, el sistema de análisis de la marcha Win-Track y el software Kinovea para análisis de vídeo (instrumentos de valoración clínica utilizados). Resultados: un total de 34 registros de personas con neuralgia occipital fueron estudiados. Un 58,8% refería presentar mejoría tras la intervención. Los datos de la escala visual análoga eran proporcionados un 64,7% de los registros, encontrándose diferencias significativas (p<0,001) entre las medias previas a la intervención (8,4±1,7) y aquellas posteriores (2,6±2,7). Conclusión: la modificación postural empleando órtesis personalizadas y osteopatía mejora sustancialmente la sintomatología de los pacientes con neuralgia occipital.
Asunto(s)
Humanos , Postura/fisiología , Dimensión del Dolor/clasificación , Osteopatía/métodos , Neuralgia/fisiopatología , Neuralgia/terapia , Estudios Retrospectivos , Lóbulo OccipitalRESUMEN
Introduction Systematic reviews report intraperitoneal local anesthetic (IPLA) effective in adults but until now no review has addressed IPLA in children. The objective of this review was to answer the question, does IPLA compared with control reduce pain after pediatric abdominal surgery. Materials and Methods Data sources: MEDLINE, EMBASE, Cochrane databases, trials registries, ProQuest, Web of Science, Google Scholar, and Open Gray. STUDY SELECTION: Independent duplicate searching for randomized controlled trials of IPLA versus no IPLA/placebo in children ≤ 18 years of age, reporting pain, or opioid use outcomes. DATA EXTRACTION: Independent duplicate data extraction and quality assessment using standardized fields. Results The selection process uncovered three eligible published trials and one unpublished study, all in laparoscopy surgery. Qualitative synthesis suggested that IPLA may reduce pain scores, opioid use, time to first opioid, and the need for rescue analgesia, with no effect on hospital stay. Risk of bias was significant. Conclusions IPLA appears promising in pediatric surgery. The high absorptive capacity of the peritoneum and high peritoneal surface area to volume ratio in children presents a dose limitation. In comparison to adult surgery, IPLA has been understudied in pediatric surgery.
Asunto(s)
Anestesia Local/métodos , Anestésicos Locales/administración & dosificación , Dimensión del Dolor/clasificación , Dolor Postoperatorio/tratamiento farmacológico , Abdomen/cirugía , Adolescente , Adulto , Analgésicos Opioides/administración & dosificación , Niño , Preescolar , Humanos , Inyecciones Intraperitoneales/métodos , Laparoscopía , Dolor Postoperatorio/prevención & control , Peritoneo/cirugía , Ensayos Clínicos Controlados Aleatorios como AsuntoRESUMEN
OBJECTIVE: The self-report Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS) and Douleur Neuropathique 4 Questions (DN4) neuropathic pain screening tools have been shown to be reliable, valid, and able to differentiate neuropathic pain from inflammatory or mixed pain syndromes. However, no studies have compared these tools to determine whether their outcomes are similar. This study evaluated agreement and correlation between the S-LANSS and DN4 in the identification of neuropathic pain in subjects with low back-related leg pain. METHODS: This observational study compared S-LANSS and DN4 scores in 45 patients with low back-related leg pain. The S-LANSS and DN4 cutoff scores of 12 and 4, respectively, were used to classify subjects as positive or negative for the presence of neuropathic pain for each screening tool. The κ statistic was used to determine whether there was agreement in classification of neuropathic pain between the 2 screening tools. Pearson correlation coefficient was used to determine correlation between scores of the 2 screening tools. RESULTS: Neuropathic pain was identified in 15 subjects (33%) using the S-LANSS and in 19 subjects (42%) using the DN4. Agreement on neuropathic pain classification was fair, with a κ value of 0.34. There was moderate to good correlation (r = 0.62; P < .001) between scores obtained from the 2 tools. CONCLUSIONS: The finding of fair agreement suggests that despite the moderate to good correlation between scores, the cutoff points for the classification of neuropathic pain of the 2 tools may not be congruent.
Asunto(s)
Dolor de la Región Lumbar/diagnóstico , Neuralgia/diagnóstico , Dimensión del Dolor/instrumentación , Autoinforme , Encuestas y Cuestionarios , Adulto , Anciano , Enfermedad Crónica , Intervalos de Confianza , Evaluación de la Discapacidad , Femenino , Humanos , Irlanda , Modelos Logísticos , Estudios Longitudinales , Dolor de la Región Lumbar/clasificación , Dolor de la Región Lumbar/epidemiología , Extremidad Inferior/fisiopatología , Masculino , Tamizaje Masivo/métodos , Persona de Mediana Edad , Neuralgia/clasificación , Neuralgia/epidemiología , Dimensión del Dolor/clasificación , Pronóstico , Reproducibilidad de los Resultados , Índice de Severidad de la EnfermedadRESUMEN
OBJECTIVES: To evaluate pain severity and distribution in relation to sleep difficulty in older adults. DESIGN: Population-based cross-sectional study. SETTING: Community within a 5-mile radius of the study center at the Institute for Aging Research, Hebrew SeniorLife (HSL), Boston. PARTICIPANTS: Seven hundred sixty-five participants of the Maintenance of Balance, Independent Living, Intellect, and Zest in the Elderly (MOBILIZE) Boston Study aged 64 and older. MEASUREMENTS: Pain severity was measured using the Brief Pain Inventory (BPI) Pain Severity Subscale. Musculoskeletal pain distribution was grouped according to no pain, single site, two or more sites, and widespread pain (upper and lower extremities and back pain). Three aspects of sleep difficulty were measured using items from the Center for Epidemiologic Studies Depression Scale, Revised (trouble getting to sleep, sleep more than usual, and restless sleep). RESULTS: Prevalence of trouble getting to sleep according to BPI severity was 17.8%, 19.7%, 32.0%, and 37.0% for the lowest to highest pain severity quartiles, respectively. Similar relationships between pain and sleep were observed across sleep measures according to pain severity and distribution. Adjusted for sociodemographic characteristics, chronic conditions, and health behaviors, chronic pain was strongly associated with trouble sleeping (≥ 1 d/wk) (single-site pain, odds ratio (OR)=1.77, 95% confidence interval (CI)=1.10-2.87; multisite pain, OR=2.38, 95% CI=1.48-3.83; widespread pain, OR=2.55, 95% CI=1.43-4.54, each compared with no pain). Similar associations were observed for restless sleep and sleeping more than usual. For specific pain sites alone or in combination with other sites of pain, only modest associations were observed with sleep problems. CONCLUSION: Widespread or other multisite pain and moderate to severe pain are strongly associated with sleep difficulty in older adults. Further research is needed to better understand the burden and consequences of pain-related sleep problems in older adults.
Asunto(s)
Actividades Cotidianas/psicología , Demencia/epidemiología , Demencia/fisiopatología , Dolor/epidemiología , Dolor/fisiopatología , Equilibrio Postural/fisiología , Qi , Trastornos del Inicio y del Mantenimiento del Sueño/epidemiología , Trastornos del Inicio y del Mantenimiento del Sueño/fisiopatología , Anciano , Anciano de 80 o más Años , Arteriopatías Oclusivas/epidemiología , Arteriopatías Oclusivas/fisiopatología , Arteriopatías Oclusivas/psicología , Boston , Enfermedad Crónica , Comorbilidad , Estudios Transversales , Demencia/psicología , Diabetes Mellitus/epidemiología , Diabetes Mellitus/fisiopatología , Diabetes Mellitus/psicología , Femenino , Evaluación Geriátrica , Encuestas Epidemiológicas , Cardiopatías/epidemiología , Cardiopatías/fisiopatología , Cardiopatías/psicología , Humanos , Degeneración del Disco Intervertebral/epidemiología , Degeneración del Disco Intervertebral/fisiopatología , Degeneración del Disco Intervertebral/psicología , Desplazamiento del Disco Intervertebral/epidemiología , Desplazamiento del Disco Intervertebral/fisiopatología , Desplazamiento del Disco Intervertebral/psicología , Enfermedades Pulmonares/epidemiología , Enfermedades Pulmonares/fisiopatología , Enfermedades Pulmonares/psicología , Masculino , Osteoartritis/epidemiología , Osteoartritis/fisiopatología , Osteoartritis/psicología , Dolor/psicología , Dimensión del Dolor/clasificación , Dimensión del Dolor/psicología , Enfermedades del Sistema Nervioso Periférico/epidemiología , Enfermedades del Sistema Nervioso Periférico/fisiopatología , Enfermedades del Sistema Nervioso Periférico/psicología , Trastornos del Inicio y del Mantenimiento del Sueño/psicología , Estenosis Espinal/epidemiología , Estenosis Espinal/fisiopatología , Estenosis Espinal/psicologíaRESUMEN
The aim of the study is the effectiveness of a multi-week inpatient rehabilitation treatment with holistic complex conservative therapy for cervical present complaints using the Lawlis scores. A major part of the conservative treatment is represented by physical, physical therapy and sports therapy exercise programs. 77 patients with cervical spine disorders were treated 01-10-2006 to 30-09-2009 in rehabilitation clinic with a complex conservative treatment measures. The analysis was performed using a questionnaire, a clinical investigation, and a radiological examination of the cervical spine. At the beginning and end of the intervention subjective scores for symptoms complaints NRS scale and assessment of treatment results by the doctor after a 4-point rating scale were collected. The average age was 53.7 years at the time of treatment. Of these, 43 patients (56%) females and 34 (44%) were male. Of 77 patients 27 (35%) patients were the results excellent, 31 (40%) patients good, 8 (11%) patients satisfactory, 11 (14%) patients bad. Of 77 patients 66 (85.7%) patients were satisfied with rehabilitation treatment, 11 (14.3%) patients dissatisfied. The subjective assessment of the complaints numerical rating scale (NRS scale) improved significantly (p<0.001) from 8.5 to 2.4 points after treatment. An objective evaluation by the attending physician based on various clinical parameters was assessed in 75% of the cases as good or very good. Conservative treatment of cervical disorders included a variety of treatments available. A major part of the conservative treatment is represented by physical, physical therapy and sports therapy exercise programs. The primary goal of treatment is to eliminate pain or pain reduction. This can be achieved inter alia through Root detumescence and promotion of the venous flow. The success of each treatment varies from patient to patient. The study shows that the complex described here, conservative therapy, is a very good method for the treatment of cervical spine disorders in post-traumatic, degenerative and disc-related spinal disorders. The primary goal of treatment is to achieve freedom from pain was achieved as easily as the subjective assessment of the complaints proved using the NRS scale. Also the high patient satisfaction (86%) suggests that the complex conservative therapy can be a satisfactory choice as a treatment method.
Asunto(s)
Vértebras Cervicales/patología , Dimensión del Dolor/clasificación , Enfermedades de la Columna Vertebral/fisiopatología , Enfermedades de la Columna Vertebral/rehabilitación , Terapia por Ejercicio , Femenino , Humanos , Masculino , Persona de Mediana Edad , Modalidades de Fisioterapia , Encuestas y Cuestionarios , Resultado del Tratamiento , Rayos XAsunto(s)
Manejo del Dolor , Dimensión del Dolor , Enfermedades de la Piel/fisiopatología , Factores de Edad , Analgésicos/efectos adversos , Analgésicos/uso terapéutico , Analgésicos Opioides/uso terapéutico , Anestesia Local , Anestésicos Combinados , Anestésicos Locales , Ansiolíticos/uso terapéutico , Biopsia , Niño , Preescolar , Terapia Combinada , Procedimientos Quirúrgicos Dermatologicos , Humanos , Lactante , Recién Nacido , Dolor/diagnóstico , Dolor/cirugía , Dimensión del Dolor/clasificación , Piel/patología , Enfermedades de la Piel/patologíaRESUMEN
OBJECTIVE: To evaluate the effect of acupuncture combined with physiotherapy in comparison with acupuncture and physiotherapy performed alone in different parameters; pain intensity, muscle tension, functional disability and muscle strength in the treatment of tension neck syndrome (TNS). DESIGN: A prospective, comparative clinical trial. SETTING: Acupuncture and Rehabilitation Department. BACKGROUND: TNS can occur in computer users. Acupuncture has been one alternative treatment in physiotherapeutic rehabilitation of musculoskeletal disorders. SUBJECTS: Forty-six patients with TNS. INTERVENTIONS: Patients were allocated into three groups: Group-1 received physiotherapy (therapeutic exercises) combined with acupuncture; Group-2, acupuncture alone, and Group-3, physiotherapy alone; over a period of 10 weeks, with one or two sessions weekly. OUTCOME ASSESSMENT: All patients had completed the protocols and were assessed using a visual analogue scale for pain intensity (VASpain) and muscle tension (VASmt), the Neck Disability Index: Brazilian Portuguese version for functional disability, and the cranio-cervical Flexion Test for isometric neck muscle strength (INMS); in the periods before treatment (baseline), after 10 weeks of treatment, and after 6 months of follow-up. RESULTS: All groups showed significant improvement (p < 0.001) in these parameters after 10 weeks of treatment and after 6 months of follow-up. Group-1 was superior to Group-3 in pain and functional disability improvements (p<0.05); and Group-1 was superior to both Group-2 (p < 0.01) and Group-3 (p < 0.05) in INMS. After 6 months of follow-up, the improvements of all groups were maintained (p < 0.05). CONCLUSION: The data suggested that acupuncture effect may facilitate and/or enhance physiotherapy performance in musculoskeletal rehabilitation for tension neck syndrome.