Escobar Carlos, Malveiro Duarte, Salgado António, Santos Maria Inês, Lameirão Campagnolo João, Cassiano Neves Manuel
Departamento de Pediatria, Hospital Fernando Fonseca, Amadora, Portugal.
Acta Med Port. 2013 Jan-Feb;26(1):5-11. Epub 2013 Apr 24.
INTRODUCTION/AIMS: Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility and osteopenia. Treatment involves a multidisciplinary approach and aims to improve the quality of life. The authors aimed to describe the characteristics of a sample of children with OI, to evaluate the treatment and clinical outcome before and after therapy.
An observational, longitudinal, retrospective and analytic study based on data obtained from the analisys of the clinical files of all patients with OI included in the pamidronate treatment protocol in Dona Estefânia's Hospital. The studied variables were: gender, age at diagnosis, familiar history of OI, age at fracture, fracture location, number of fractures, medical/surgical therapy, age at onset of treatment, number of courses of medical therapy, age at surgical treatment and its complications. A five percent statistics significance level was adopted.
in 21 patients, 61.9% were male and 11 had its OI type registered (five type I, three type III, three type IV). The average age of diagnosis was 20.6 months and there were two diagnostic peaks: the first month - 37%, and 24 months - 26%. On average patients had 0.62 fractures/patient/year, of which 17.4% in the perinatal period and 62% before age three. Most of the fractures occurred in the lower limbs (55.6%). All patients underwent medical treatment, starting at an average of 4.3 years. In follow-up sample (n=14) there was a decrease in the number of fractures after starting treatment with pamidronate (0.76 to 0.35 fractures/patient/year). Intramedullary rods were placed in nine patients (64.3%). In eight patients they were placed in the femur, four unilateral and four bilateral, with no prior history of fracture in three cases. There were no new fractures in the surgically treated bones.
OI is a disease with a wide clinical variability that mainly depends on its type. Despite no cure has been found, medical treatment with biphosphonates and surgical treatment, with intramedullary rods, seems to reduce the incidence of new fracture occurrence.
引言/目的:成骨不全症(OI)是一种以骨脆性增加和骨质减少为特征的遗传性疾病。治疗采用多学科方法,旨在提高生活质量。作者旨在描述一组成骨不全症患儿的特征,评估治疗前后的治疗情况和临床结果。
这是一项基于从埃斯特法尼亚医院帕米膦酸盐治疗方案中纳入的所有成骨不全症患者临床档案分析获得的数据的观察性、纵向、回顾性和分析性研究。研究变量包括:性别、诊断年龄、成骨不全症家族史、骨折年龄、骨折部位、骨折次数、药物/手术治疗、开始治疗年龄、药物治疗疗程数、手术治疗年龄及其并发症。采用5%的统计学显著性水平。
21例患者中,61.9%为男性,11例登记了成骨不全症类型(5例I型,3例III型,3例IV型)。诊断的平均年龄为20.6个月,有两个诊断高峰:第一个月为37%,24个月为26%。患者平均每年骨折0.62次,其中围生期骨折占17.4%,3岁前骨折占62%。大多数骨折发生在下肢(55.6%)。所有患者均接受药物治疗,平均开始治疗年龄为4.3岁。在随访样本(n = 14)中,开始使用帕米膦酸盐治疗后骨折次数减少(从0.76次/患者/年降至0.35次/患者/年)。9例患者(64.3%)植入了髓内钉。8例患者在股骨植入髓内钉,4例单侧,4例双侧,3例既往无骨折史。手术治疗的骨骼未出现新的骨折。
成骨不全症是一种临床变异性很大的疾病,主要取决于其类型。尽管尚未找到治愈方法,但双膦酸盐药物治疗和髓内钉手术治疗似乎可降低新骨折发生的发生率。