How to follow up patients with brachial plexus birth palsy in the long term: a survey of expert opinion.

Stijn G C J de Joode, Martijn G M Schotanus, Lodewijk W van Rhijn, Steven K Samijo
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Abstract

There is no generally accepted diagnostic, treatment and follow-up algorithm for brachial plexus birth palsy in the current literature. This study evaluates the opinion of experts in the field of brachial plexus birth palsy surgery, to provide a follow-up guideline. A total of 35 experts attending an international meeting with a mean of 21.5 years (SD 10.1) of experience in the field filled out a questionnaire to evaluate the following: (1) the surgeons' background; (2) clinical follow-up; (3) radiological follow-up; and (4) International Classification of Functioning, Disability and Health (ICF) domains. A mean of 40 new brachial plexus birth palsy patients were seen per year by each expert, of which 36% needed surgery. In total, 27 experts scheduled a regular follow-up every year and the majority (83%) believed that standardized long-term clinical follow-up is necessary. However, standardized radiological follow-up is not necessary. Only 13 of 34 participants used patient-reported outcome measures to investigate ICF domains.Level of evidence: V.

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如何对臂丛神经出生麻痹患者进行长期随访:专家意见调查。
目前的文献中还没有公认的臂丛神经出生麻痹诊断、治疗和随访算法。本研究评估了臂丛神经出生麻痹手术领域专家的意见,以提供后续治疗指南。共有 35 位专家参加了一次国际会议,他们在该领域的平均经验为 21.5 年(标准差 10.1),他们填写了一份调查问卷,对以下方面进行了评估:(1) 外科医生的背景;(2) 临床随访;(3) 放射学随访;(4) 国际功能、残疾和健康分类 (ICF) 范畴。每位专家每年平均接诊 40 名新的臂丛神经出生麻痹患者,其中 36% 需要手术治疗。共有 27 位专家每年安排定期随访,大多数专家(83%)认为有必要进行标准化的长期临床随访。然而,标准化的放射学随访则没有必要。34 位参与者中只有 13 位使用了患者报告的结果测量方法来调查 ICF 领域:V.
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