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先天性膈疝幸存者的随访。

Follow-up of the survivors of congenital diaphragmatic hernia.

机构信息

Department of Pediatrics, Hospital de São João, Porto, Portugal.

出版信息

Early Hum Dev. 2012 Apr;88(4):255-8. doi: 10.1016/j.earlhumdev.2011.08.025. Epub 2011 Sep 23.

Abstract

INTRODUCTION

Survivors of congenital diaphragmatic hernia have increased with the introduction of new treatment modalities and have been reported to experience ongoing medical morbidity until adulthood.

AIM

To describe the long-term functional impact of congenital diaphragmatic repair on the survivors of a single institution cohort of newborns over a 14-year period.

METHODS

The follow up medical charts of 39 congenital diaphragmatic hernia survivors treated at a tertiary neonatal intensive care unit, from January 1997 to December 2010, were analyzed.

RESULTS

The median age at follow up was 70 (4-162) months. Gastrointestinal sequelae were the most common with 12 (30.7%) patients affected by failure to thrive. Chronic lung disease occurred in 5 (12.8%) patients, neurodevelopmental delay in 5 (12.8%), musculoskeletal sequelae in 6 (15.3%), recurrence of hernia in 4 (10.2%) and 2 (7.6%) were deceased.

CONCLUSION

Congenital diaphragmatic hernia survivors are a group of patients that requires long term periodic follow up in a multidisciplinary setting to provide adequate support and improve their quality of life.

摘要

引言

随着新治疗方法的引入,先天性膈疝幸存者的数量有所增加,据报道,他们在成年后仍会持续出现医疗并发症。

目的

描述在 14 年期间,单一机构队列的新生儿先天性膈疝修复对幸存者的长期功能影响。

方法

分析了 1997 年 1 月至 2010 年 12 月在一家三级新生儿重症监护病房接受治疗的 39 名先天性膈疝幸存者的随访医疗记录。

结果

中位随访年龄为 70(4-162)个月。胃肠道后遗症最为常见,有 12 名(30.7%)患者存在生长不良。5 名(12.8%)患者患有慢性肺部疾病,5 名(12.8%)患者存在神经发育迟缓,6 名(15.3%)患者存在肌肉骨骼后遗症,4 名(10.2%)患者出现疝复发,2 名(7.6%)患者死亡。

结论

先天性膈疝幸存者是一组需要在多学科环境中进行长期定期随访的患者,以提供足够的支持并提高他们的生活质量。

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