RESUMO
BACKGROUND: Foot deformities have been frequently reported in cerebral palsy (CP), and numerous diagnostic modalities and treatment options have recently been developed to achieve a better level of management for children with CP. METHODS: A thorough search of the English literature, published between January 2013 and March 2016, was performed. A summary of the new findings that had not previously described was reported. The review included recent advances regarding clinical and gait evaluation, orthotic management, botulinum toxin A treatment, and surgical correction. RESULTS: The review summarized new findings reported in 46 articles and abstracts that were published between January 2013 and March 2016. Older articles were included and cited when an original description was mentioned, or when a change or development of some findings was discussed. CONCLUSIONS: Foot deformity forms an essential part of evaluating children with CP. Dramatic advances have been achieved in gait assessment, conservative management, and surgical correction. Promising results have been reported with the goal to reach a higher level of orthopaedic care and optimize the functional potentials for children with CP. LEVEL OF EVIDENCE: Level IV-literature review.
Assuntos
Paralisia Cerebral/complicações , Deformidades do Pé/terapia , Toxinas Botulínicas Tipo A/uso terapêutico , Criança , Deformidades do Pé/complicações , Humanos , Fármacos Neuromusculares/uso terapêutico , Ortopedia/tendências , Modalidades de FisioterapiaRESUMO
Falls in the elderly are a significant problem both in and out of the hospital. The Deficit Reduction Act of 2005 and the Fiscal Year 2009 Inpatient Prospective Payment System Final Rule, as outlined by the Centers for Medicare & Medicaid Services, placed on hospitals the financial burden of fall prevention for falls (ie, hospital-acquired conditions) that could have been prevented by following evidence-based guidelines. Multifaceted and individualized programs have been created to prevent falls in the elderly. Many of these interventions are based on expert opinion and statistical trends. Our review of the literature revealed that the risk of fall is only slightly greater in the hospital environment than in the home and that there is no medical evidence that evidence-based guidelines are effective in fall prevention.
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Acidentes por Quedas/prevenção & controle , Serviços de Assistência Domiciliar , Hospitais , Medicaid/economia , Medicare/economia , Sistema de Pagamento Prospectivo/economia , Mecanismo de Reembolso/economia , Acidentes por Quedas/economia , Idoso , Humanos , Incidência , Estados Unidos/epidemiologiaRESUMO
Scoliosis, hip dysplasia, and other lower extremity deformities are common musculoskeletal pathology found in patients with cerebral palsy. Imaging studies allow for an improved identification of patients with these issues, help to understand the pathology, and aid in planning treatment strategies. Most of these deformities are visualized using plain radiographic techniques. Occasionally, as in the case of preoperative planning, advanced imaging, such as computerized topography and MRI, can be used for additional information. This article provides insight into the various imaging techniques for these musculoskeletal issues and aids in better care for patients with cerebral palsy.
Assuntos
Paralisia Cerebral/diagnóstico por imagem , Doenças Musculoesqueléticas/diagnóstico por imagem , Paralisia Cerebral/fisiopatologia , Humanos , Doenças Musculoesqueléticas/fisiopatologia , RadiografiaRESUMO
BACKGROUND: Scoliosis is a common complication of severe neuromuscular diseases. The aim of this study is to determine the impact of posterior spinal fusion on pulmonary function parameters in patients with severe neuromuscular disease at our medical center. METHODS: Retrospective chart review of all patients with severe neuromuscular disease who had posterior spinal fusion between 2012 and 2017 at Texas Children's Hospital. Patients with growing rods, brain injury or malformation, and/or spina bifida were excluded. Pulmonary function measures before and after spinal surgery were determined. RESULTS: A total of 20 eligible patients were identified, 7 with Duchenne muscular dystrophy, 6 with spinal muscular atrophy, 3 with merosin deficient muscular dystrophy, 2 with Charcot-Marie-Tooth, 1 with central core disease, and 1 with dystroglycanopathy. The mean change in vital capacity from pre- to postspine surgery was a loss of 0.63 L for the spinal muscular atrophy patients, a loss of 0.36 L for the Duchenne muscular dystrophy patients, and a gain of 0.23 L for the merosin deficient patients. The difference between spinal muscular atrophy and merosin deficient patients was statistically significant (P = .02) CONCLUSION: In this single-center retrospective study, we found that after spine surgery for scoliosis, all patients with spinal muscular atrophy and most patients with Duchenne muscular dystrophy lost vital capacity, while the patients with merosin deficient muscular dystrophy gained vital capacity. These differences were not associated with differences is respiratory strength, body mass index, or surgical outcomes.
Assuntos
Pulmão/fisiopatologia , Escoliose/cirurgia , Adolescente , Criança , Feminino , Humanos , Masculino , Atrofia Muscular Espinal/fisiopatologia , Distrofia Muscular de Duchenne/fisiopatologia , Estudos Retrospectivos , Fusão Vertebral/efeitos adversos , Capacidade VitalRESUMO
STUDY DESIGN: Retrospective cross-sectional, longitudinal radiographic analysis. OBJECTIVE: To report the natural history of spinopelvic parameters in achondroplasia. SUMMARY OF BACKGROUND DATA: Sagittal spinal deformity is common in children with achondroplasia. However, few data exist on their normative spinal parameters. METHODS: Lateral standing spine radiographs of children with achondroplasia were reviewed. Measurements included thoracic kyphosis, lumbar lordosis (LL), thoracolumbar kyphosis (TLK), pelvic incidence (PI), T1 pelvic angle (TPA), and sagittal balance (SVA). Comparison between age groups and longitudinal analysis of children with minimum five-year radiographic evaluation was performed; evolution of radiographic measurements was assessed. Children who underwent surgical correction of TLK were studied separately to describe changes of sagittal spinal parameters associated with TLK surgical correction. RESULTS: In cross-sectional analysis, 745 radiographs (282 children) were measured. During the first three years, TLK decreased and LL and sacral slope increased significantly. After age 3 years, TLK decreased gradually until age 10. Afterwards, TLK decrease became non-significant. PI increased gradually after age 10. In the longitudinal group, 81 children were followed an average of 8.7 (5-19) years between age 4.4 and 13.1 years. TLK decreased; LL and PI increased significantly. TPA and SVA remained within the normal range although changes with growth were statistically significant. In the surgical group, 19 children underwent surgical TLK correction. Apart from TLK correction, no sagittal parameters changed significantly after surgery. These 19 children had higher TLK and lower LL compared with a nonsurgical group at similar average age. CONCLUSION: In children with achondroplasia, TLK improvement occurs primarily before age 3 years; hyperlordosis at the lumbosacral level is the compensatory mechanism. Significant changes in the sagittal spinal parameters occur early in life, suggesting the importance of attention to sagittal malalignment to prevent any possible clinical sequelae of severe hyperlordosis. LEVEL OF EVIDENCE: Level III, prognostic study.
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Acondroplasia/diagnóstico por imagem , Vértebras Lombares/diagnóstico por imagem , Ossos Pélvicos/diagnóstico por imagem , Vértebras Torácicas/diagnóstico por imagem , Acondroplasia/complicações , Adolescente , Criança , Pré-Escolar , Estudos Transversais , Feminino , Humanos , Cifose/diagnóstico por imagem , Cifose/etiologia , Estudos Longitudinais , Lordose/diagnóstico por imagem , Lordose/etiologia , Masculino , Radiografia , Estudos Retrospectivos , Sacro/diagnóstico por imagem , Posição OrtostáticaRESUMO
OBJECTIVES: Iliosacral screw pathways in the first (S1) and second (S2) sacral segments are commonly used for adult pelvic ring stabilization. We hypothesize that radiographically "safe" pathways exist in pediatric patients. SETTING: Academic level I Trauma Center. PATIENTS: All patients between ages 2 and 16 years with a computed tomography scan including the pelvis obtained over a 6-week period (174 children, mean age 10.8 ± 3.9 years; 90 boys, 84 girls). INTERVENTION: The width and height at the "constriction point" in 3 safe screw pathways were measured bilaterally by 3 orthopaedists (resident, trauma fellow, trauma attending). Pathways corresponding to: (1) an "iliosacral" screw at S1, a "trans-sacral trans-iliac" (TSTI) screw at S1, and a TSTI screw at S2. MAIN OUTCOME MEASUREMENTS: (1) Mean width and height of pathways, (2) interrater reliability coefficient, (3) availability of pathways greater than 7 mm, (4) growth of pathways with age, (5) sacral morphology. RESULTS: The interrater reliability coefficient was above 0.917 for all measurements. Radiographically safe pathways were available for 99%, 51%, and 89% of children for iliosacral screws at S1 (width 16.4 ± 2.8 mm, height 15.1 ± 3.3 mm), TSTI screws at S1 (width 7.2 ± 4.9 mm, height 8.3 ± 5.6 mm), and TSTI at S2 (width 9.3 ± 2.2 mm, height 11.5 ± 2.7 mm), respectively. CONCLUSIONS: Contrary to our hypothesis, almost all children aged 2-16 had a radiographically safe screw pathway for an iliosacral screw at S1, and most of the children had an available pathway for a TSTI screw at S2. However, only 51% had a pathway for a TSTI screw at S1.