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

Author:

de Joode Stijn G. C. J.123ORCID,Schotanus Martijn G. M.124,van Rhijn Lodewijk W.245,Samijo Steven K.1,

Affiliation:

1. Department of Orthopedic Surgery and Traumatology, Zuyderland Medical Center, Sittard-Geleen and Heerlen, The Netherlands

2. School of Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht, The Netherlands

3. Department of Orthopedic Surgery and Traumatology, Spital Nidwalden, Stans, Switzerland

4. Department of Orthopedic Surgery and Traumatology, Maastricht University Medical Center, Maastricht, The Netherlands

5. Department of Orthopedic Surgery, UMC Utrecht, The Netherlands

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

Publisher

SAGE Publications

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