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Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial
INTRODUCTION: Cervical hybrid surgery (HS) combines anterior cervical discectomy and fusion (ACDF) and cervical disc arthroplasty (CDA) to establish an individualized surgical plan for patients with multiple cervical disc degenerative diseases. In order to maintain the stability of the spine after H...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273717/ https://www.ncbi.nlm.nih.gov/pubmed/37328785 http://dx.doi.org/10.1186/s13063-023-07409-7 |
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author | He, Junbo Liu, Qingyu Yang, Zijiao Liu, Hao Wu, Tingkui Ding, Chen Huang, Kangkang Wang, Beiyu |
author_facet | He, Junbo Liu, Qingyu Yang, Zijiao Liu, Hao Wu, Tingkui Ding, Chen Huang, Kangkang Wang, Beiyu |
author_sort | He, Junbo |
collection | PubMed |
description | INTRODUCTION: Cervical hybrid surgery (HS) combines anterior cervical discectomy and fusion (ACDF) and cervical disc arthroplasty (CDA) to establish an individualized surgical plan for patients with multiple cervical disc degenerative diseases. In order to maintain the stability of the spine after HS, an external cervical collar is often used. However, there is still controversy regarding the importance of a cervical collar following surgery. This study aims to determine whether the cervical collar is effective and how long it should be worn after surgery. METHODS: This is a randomized, single-center, prospective, parallel-controlled trial. Eligible participants will be selected according to the inclusion and exclusion criteria. The primary outcome is the neck disability index, which will be evaluated before surgery and at one week, 3 weeks, 6 weeks, 3 months, 6 months, and 12 months following surgery. The secondary outcomes consist of the Japanese Orthopedic Association Scores, MOS 36-item short-form health survey (SF-36), visual analog scale, Pittsburgh Sleep Quality Index (PSQI), Bazaz dysphagia scoring system, Falls Efficacy Scale, cervical collar satisfaction score, neck soft tissue assessment, and Braden Scale, as well as radiologic assessments for cervical lordosis, disc height of the operative levels, fusion rate, range of motion (ROM), and complications including anterior bone loss, prosthesis migration, and heterotopic ossification. The clinical and radiologic examinations were performed by investigators with no therapeutic relationship with the individual patient. All radiographs were examined by one independent radiologist. ETHICS AND DISSEMINATION: The results of this study will be published in peer-reviewed journals and presented at conferences. Upon completion of this trial, our findings could provide an appropriate cervical collar-wearing guideline for patients receiving HS. TRIAL REGISTRATION: ChiCTR.org.cn ChiCTR2000033002. Registered on 2020–05-17. |
format | Online Article Text |
id | pubmed-10273717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102737172023-06-17 Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial He, Junbo Liu, Qingyu Yang, Zijiao Liu, Hao Wu, Tingkui Ding, Chen Huang, Kangkang Wang, Beiyu Trials Study Protocol INTRODUCTION: Cervical hybrid surgery (HS) combines anterior cervical discectomy and fusion (ACDF) and cervical disc arthroplasty (CDA) to establish an individualized surgical plan for patients with multiple cervical disc degenerative diseases. In order to maintain the stability of the spine after HS, an external cervical collar is often used. However, there is still controversy regarding the importance of a cervical collar following surgery. This study aims to determine whether the cervical collar is effective and how long it should be worn after surgery. METHODS: This is a randomized, single-center, prospective, parallel-controlled trial. Eligible participants will be selected according to the inclusion and exclusion criteria. The primary outcome is the neck disability index, which will be evaluated before surgery and at one week, 3 weeks, 6 weeks, 3 months, 6 months, and 12 months following surgery. The secondary outcomes consist of the Japanese Orthopedic Association Scores, MOS 36-item short-form health survey (SF-36), visual analog scale, Pittsburgh Sleep Quality Index (PSQI), Bazaz dysphagia scoring system, Falls Efficacy Scale, cervical collar satisfaction score, neck soft tissue assessment, and Braden Scale, as well as radiologic assessments for cervical lordosis, disc height of the operative levels, fusion rate, range of motion (ROM), and complications including anterior bone loss, prosthesis migration, and heterotopic ossification. The clinical and radiologic examinations were performed by investigators with no therapeutic relationship with the individual patient. All radiographs were examined by one independent radiologist. ETHICS AND DISSEMINATION: The results of this study will be published in peer-reviewed journals and presented at conferences. Upon completion of this trial, our findings could provide an appropriate cervical collar-wearing guideline for patients receiving HS. TRIAL REGISTRATION: ChiCTR.org.cn ChiCTR2000033002. Registered on 2020–05-17. BioMed Central 2023-06-16 /pmc/articles/PMC10273717/ /pubmed/37328785 http://dx.doi.org/10.1186/s13063-023-07409-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol He, Junbo Liu, Qingyu Yang, Zijiao Liu, Hao Wu, Tingkui Ding, Chen Huang, Kangkang Wang, Beiyu Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title | Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title_full | Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title_fullStr | Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title_full_unstemmed | Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title_short | Cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
title_sort | cervical collar use following anterior cervical hybrid surgery: protocol for a prospective randomized, time-controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273717/ https://www.ncbi.nlm.nih.gov/pubmed/37328785 http://dx.doi.org/10.1186/s13063-023-07409-7 |
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