A Dutch guideline for the treatment of scoliosis in neuromuscular disorders

<p>Abstract</p> <p>Background</p> <p>Children with neuromuscular disorders with a progressive muscle weakness such as Duchenne Muscular Dystrophy and Spinal Muscular Atrophy frequently develop a progressive scoliosis. A severe scoliosis compromises respiratory function and makes sitting more difficult. Spinal surgery is considered the primary treatment option for correcting severe scoliosis in neuromuscular disorders. Surgery in this population requires a multidisciplinary approach, careful planning, dedicated surgical procedures, and specialized after care.</p> <p>Methods</p> <p>The guideline is based on scientific evidence and expert opinions. A multidisciplinary working group representing experts from all relevant specialties performed the research. A literature search was conducted to collect scientific evidence in answer to specific questions posed by the working group. Literature was classified according to the level of evidence.</p> <p>Results</p> <p>For most aspects of the treatment scientific evidence is scarce and only low level cohort studies were found. Nevertheless, a high degree of consensus was reached about the management of patients with scoliosis in neuromuscular disorders. This was translated into a set of recommendations, which are now officially accepted as a general guideline in the Netherlands.</p> <p>Conclusion</p> <p>In order to optimize the treatment for scoliosis in neuromuscular disorders a Dutch guideline has been composed. This evidence-based, multidisciplinary guideline addresses conservative treatment, the preoperative, perioperative, and postoperative care of scoliosis in neuromuscular disorders.</p

Severe restrictive lung disease and vertebral surgery in a pediatric population

The aim of this study is to describe the outcome of surgical treatment for pediatric patients with forced vital capacity (FVC) <40% and severe vertebral deformity. Few studies have examined surgical treatment in these patients, who are considered to be at a high risk because of their pulmonary disease, and in whom preoperative tracheostomy is sometimes recommended. Inclusion criteria include FVC <40%, age <19 years and diagnosis of scoliosis. The retrospective study of 24 patients with severe restrictive lung disease, who underwent spinal surgery. Variables studied were age and gender, pre- and postoperative spirometry (FVC, FEV1, FEV1/FVC), preoperative, postoperative and late use of non-invasive ventilation (BiPAP) or mechanical ventilation, associated multidisciplinary treatment, type and location of the curve, pre- and postoperative curve values, type of vertebral fusion, intra- and postoperative complications, duration of intensive care unit (ICU) stay and length of postoperative hospitalization. Mean age was 13 years (9–19) of which 13 were males and 11 females. Mean follow-up was 32 months (24–45). The etiology was neuromuscular in 17 patients and other etiologies in 7 patients. Mean preoperative FVC was 26% (13–39%). Eight patients had preoperative home BiPAP, 15 preoperative in-hospital BiPAP, and 2 preoperative mechanical ventilation. Nine patients had preoperative nutritional support. Preoperative curve value of the deformity was 88° (40°–129°). Nineteen patients with posterior fusion alone and 5 with anterior and posterior fusion were found. Mean duration of ICU stay was 5 days (1–21). Total postoperative hospital stay was 17 days (7–33). Ventilatory support in the immediate postoperative includes 16 patients requiring BiPAP and 2 volumetric ventilation. None of the patients required a tracheostomy. The intraoperative complications include one death due to acute heart failure; immediate postoperative, four respiratory failures (2 required ICU readmission) and one respiratory infection; and other minor complications occurred in six patients. Overall, 58% of patients had complications. Percentage of angle correction was 56%. After a follow-up of 30 months, FVC was 29% (13–50%). In conclusion, corrective scoliosis surgery in pediatric patients with severe restrictive lung disease is well tolerated, but the management of this population requires extensive experience with the vertebral surgery involved, and a multidisciplinary approach that includes pulmonologists, nutritionists and anesthesiologists. Currently, there is no indication for routine preoperative tracheostomy

Influência da adequação postural em cadeira de rodas na função respiratória de pacientes com distrofia muscular de Duchenne

O objetivo deste estudo foi avaliar a influência da adequação postural em cadeira de rodas na função respiratória de pacientes com distrofia muscular de Duchenne (DMD). Participaram 12 pacientes com diagnóstico de DMD e que possuíam cadeira de rodas adaptada com idade variando de 10 a 22 anos. Cada indivíduo foi avaliado na própria cadeira de rodas e em uma cadeira de rodas padrão, ou seja, sem reclinação ou tilt. As cadeiras dos participantes possuíam adaptações no encosto e no assento, confeccionados de acordo com as especificidades de cada paciente. A avaliação consistiu em mensurar o volume minuto (VM), volume corrente (VC), capacidade vital forçada (CVF), pressões inspiratória (PImax) e expiratória (PEmax) máximas e pico de fluxo expiratório (PFE). Para análise dos dados, foi utilizado o teste t pareado, adotando-se o nível de significância de 0,05. As adaptações resultaram em melhores valores estatisticamente significativos de todos os parâmetros respiratórios: VM (8.963,3 e 10.762,5 mL/min; p=0,028), VC (319,1 e 433,6 mL; p=0,005), CVF (1.476,3 e 1.850 mL; p=0,005), PImax (-41,2 e -51,2 cmH2O; p=0,022), PEmax (29,6 e 36,7 cmH2O; p=0,004) e PFE (162,1 e 185 L/min; p=0,018). Nossos resultados sugerem que a adequação postural em cadeira de rodas influenciou positivamente a função respiratória de pacientes com DMD.The purpose of this study was to determine the influence of wheelchair positioning aids on the respiratory function of patients with Duchenne muscular dystrophy (DMD). Twelve non-ambulatory DMD patients, between 10 to 22 years of age, were evaluated. They were assessed in their adapted wheelchairs and in a standard wheelchair without tilt or reclining. The wheelchairs of the participants possessed adaptations in the backrest and the seat, made according to the specifics of each patient. Minute volume (MV), tidal volume (TV), forced vital capacity (FVC), maximum inspiratory (MIP) and expiratory pressures (MEP) and peak expiratory flow (PEF) were measured. For data analysis we used the paired t-test adopting the significance level of 0.05. The positioning aids resulted in statistically significant better values of all respiratory parameters: MV (8,963.3 and 10,762.5 mL/min; p=0.028), TV (319.1 and 433.6 mL; p=0.005), FVC (1,476.3 and 1,850 mL; p=0.005), MIP (-41.2 and -51.2 cmH2O; p=0.022), MEP (29.6 and 36.7 cmH2O; p=0.004) and PEF (162.1 and 185 L/min; p=0.018). These results may suggest that wheelchair positioning aids can positively influence pulmonary function for non-ambulatory DMD patients