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杜氏肌营养不良症患者的存活率。

Survival of patients with Duchenne muscular dystrophy.

作者信息

San Martín P Pamela, Solis F Fresia, Cavada Ch Gabriel

机构信息

Dirección de Investigación y Desarrollo, Teletón, Chile.

Escuela de Salud Pública, Facultad de Medicina, Universidad de Chile, Chile.

出版信息

Rev Chil Pediatr. 2018 Aug;89(4):477-483. doi: 10.4067/S0370-41062018005000704.

Abstract

INTRODUCTION

Duchenne muscular dystrophy (DMD) leads to a progressive deterioration of the mus cle function and premature death. There are no longitudinal studies on the course of this pathology in Chile.

OBJECTIVE

To determine survival between the years 1993-2013, divided into two periods (1993-2002 and 2003-2013), and the effect of social determinants in patients with DMD admitted in Teleton Institutes of Chile (TI).

PATIENTS AND METHOD

Prospective follow-up study in a clinical series of 462 patients with DMD. The information was obtained by searching for patients with DMD in OLAP cube (Online Analytical Processing). From the clinical records of the TI of Santiago, the variables corresponding to the diagnostic method, stage of DMD described in terms of muscle de terioration and function according to Swinyard classification were recorded; existence and type of tests that conclude the diagnosis and, in the cases reported, the existence of family history. Kaplan Meier survival analysis was applied, where global survival was defined between birth and age of death. The determinant factors analyzed were estimated through the Cox-Snell's proportional risk model.

RESULTS

Survival at 20 years of age from TI entry was 51.7% (CI95%: 45.1-57.8), 48.5% in the period 1993-2002 and 72.8% between 2003-2013. The percentage of survival at the same age according to socioeconomic status (SES) was 82% in high SES, 67% in middle SES, and 42% in low SES, with a statistically significant difference between high and middle SES in relation to extreme poverty. Ac cording to country areas, the survival was close to 75 % at 17 years of age.

CONCLUSIONS

The survival information from patients with DMD from childhood to adult life is valuable for predicting the clinical course of the disease with the current medical care. There is evidence of improvement in the probability of survival at the age of 20 and marked inequity according to the socioeconomic variable.

摘要

引言

杜氏肌营养不良症(DMD)会导致肌肉功能逐渐衰退并过早死亡。智利尚无关于这种病症病程的纵向研究。

目的

确定1993年至2013年期间的生存率,分为两个阶段(1993 - 2002年和2003 - 2013年),以及社会决定因素对智利特莱顿研究所(TI)收治的DMD患者的影响。

患者与方法

对462例DMD患者的临床系列进行前瞻性随访研究。通过在OLAP多维数据集(在线分析处理)中搜索DMD患者来获取信息。从圣地亚哥TI的临床记录中,记录与诊断方法、根据斯温亚德分类法描述的DMD肌肉退化和功能阶段相关的变量;确诊的检查项目及类型,以及在报告病例中的家族病史。应用Kaplan - Meier生存分析,总体生存定义为从出生到死亡年龄之间。通过Cox - Snell比例风险模型估计分析的决定因素。

结果

从进入TI起20岁时的生存率为51.7%(95%置信区间:45.1 - 57.8),1993 - 2002年期间为48.5%,2003 - 2013年期间为72.8%。根据社会经济地位(SES),同一年龄的生存率在高SES组为82%,中SES组为67%,低SES组为42%,高SES与中SES相比,相对于极端贫困有统计学显著差异。根据国家地区,17岁时的生存率接近75%。

结论

DMD患者从儿童期到成年期的生存信息对于预测当前医疗护理下该疾病的临床病程很有价值。有证据表明20岁时的生存概率有所提高,并且根据社会经济变量存在明显的不平等。

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