Pectus Arcuatum Definitions, Diagnostics, and Surgical Guidelines: A Systematic Review.

IF 15.7 1区 医学 Q1 SURGERY
Rawan M Zeineddine,Ahmed E Khedr,Juan M Farina,Nour B Odeh,Abdulrahman Senjab,J Asher Jenkins,Dawn E Jaroszewski
{"title":"Pectus Arcuatum Definitions, Diagnostics, and Surgical Guidelines: A Systematic Review.","authors":"Rawan M Zeineddine,Ahmed E Khedr,Juan M Farina,Nour B Odeh,Abdulrahman Senjab,J Asher Jenkins,Dawn E Jaroszewski","doi":"10.1001/jamasurg.2025.2365","DOIUrl":null,"url":null,"abstract":"Importance\r\nPectus arcuatum is a rare anterior chest wall deformity that is often confused with excavatum, carinatum, or a mixed deformity. A complete understanding of its clinical and physiological basis will improve diagnostic accuracy and allow for standardized management.\r\n\r\nObjectives\r\nTo gain a comprehensive understanding of pectus arcuatum, focusing on its nomenclatures, epidemiology, classification, pathophysiology, preoperative presentation and assessments, management options, and surgical outcomes.\r\n\r\nEvidence Review\r\nPubMed, Google Scholar, and subsequent reference searches were used to extract original studies addressing pectus arcuatum fully or partially. The searches were performed on February 2, 2025. Two independent reviewers screened articles based on preestablished inclusion and exclusion criteria. Quality assessment was performed, but given the rarity of arcuatum and the limited, heterogeneous nature of available literature, none of the studies were excluded based on the level of evidence or quality assessments. Using a standardized data extraction form, results were synthesized and presented as a review with recommendations to guide clinical decision-making.\r\n\r\nFindings\r\nA total of 65 studies were included in the final review. Of those, 37 (56.9%) were cohort studies, 18 (27.7%) were case reports, 8 (12.3%) were case series, and 2 (3.1%) were technical reports. A total of 455 cases of pectus arcuatum were represented. Heterogeneity was found in nomenclature, epidemiology, associated conditions, assessments, management, and outcomes. An open surgical approach and, more recently, hybrid open and minimally invasive technique are reported for surgical repair. Postoperative outcomes were good in most surgical series, with no significant difference when compared with the repair of other pectus deformities.\r\n\r\nConclusions and Relevance\r\nResults of this systematic review reveal that pectus arcuatum is a rare variant of pectus deformities that is distinct from carinatum and excavatum. Unified terminology and standardized diagnostic criteria are important to facilitate proper management. Minimally invasive hybrid approaches continue to refine outcomes, balancing invasiveness with efficacy.","PeriodicalId":14690,"journal":{"name":"JAMA surgery","volume":"13 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAMA surgery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1001/jamasurg.2025.2365","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

Abstract

Importance Pectus arcuatum is a rare anterior chest wall deformity that is often confused with excavatum, carinatum, or a mixed deformity. A complete understanding of its clinical and physiological basis will improve diagnostic accuracy and allow for standardized management. Objectives To gain a comprehensive understanding of pectus arcuatum, focusing on its nomenclatures, epidemiology, classification, pathophysiology, preoperative presentation and assessments, management options, and surgical outcomes. Evidence Review PubMed, Google Scholar, and subsequent reference searches were used to extract original studies addressing pectus arcuatum fully or partially. The searches were performed on February 2, 2025. Two independent reviewers screened articles based on preestablished inclusion and exclusion criteria. Quality assessment was performed, but given the rarity of arcuatum and the limited, heterogeneous nature of available literature, none of the studies were excluded based on the level of evidence or quality assessments. Using a standardized data extraction form, results were synthesized and presented as a review with recommendations to guide clinical decision-making. Findings A total of 65 studies were included in the final review. Of those, 37 (56.9%) were cohort studies, 18 (27.7%) were case reports, 8 (12.3%) were case series, and 2 (3.1%) were technical reports. A total of 455 cases of pectus arcuatum were represented. Heterogeneity was found in nomenclature, epidemiology, associated conditions, assessments, management, and outcomes. An open surgical approach and, more recently, hybrid open and minimally invasive technique are reported for surgical repair. Postoperative outcomes were good in most surgical series, with no significant difference when compared with the repair of other pectus deformities. Conclusions and Relevance Results of this systematic review reveal that pectus arcuatum is a rare variant of pectus deformities that is distinct from carinatum and excavatum. Unified terminology and standardized diagnostic criteria are important to facilitate proper management. Minimally invasive hybrid approaches continue to refine outcomes, balancing invasiveness with efficacy.
弓胸肌的定义、诊断和手术指南:系统回顾。
重要性弓形直肌是一种罕见的前胸壁畸形,常与凹状畸形、凸状畸形或混合畸形相混淆。全面了解其临床和生理基础将提高诊断的准确性,并允许规范化管理。目的全面了解弓胸肌的命名、流行病学、分类、病理生理学、术前表现和评估、治疗选择和手术结果。pubmed、谷歌Scholar和随后的参考文献检索用于提取全部或部分涉及弓胸肌的原始研究。搜寻工作于2025年2月2日进行。两名独立审稿人根据预先确定的纳入和排除标准筛选文章。进行了质量评估,但鉴于弓形瘤的罕见性和现有文献的有限、异质性,没有一项研究根据证据水平或质量评估被排除在外。使用标准化的数据提取表格,将结果综合起来,并作为一项综述提出建议,以指导临床决策。最后的综述共纳入了65项研究。其中,37篇(56.9%)为队列研究,18篇(27.7%)为病例报告,8篇(12.3%)为病例系列,2篇(3.1%)为技术报告。本文共报道了455例弓突胸。在命名法、流行病学、相关条件、评估、管理和结果方面发现异质性。开放手术入路和最近的开放微创混合技术被报道用于外科修复。在大多数手术系列中,术后结果良好,与其他胸骨畸形的修复相比无显著差异。结论与相关性本系统综述的结果表明,弓形胸是一种罕见的胸骨畸形,不同于隆突和凹突。统一的术语和标准化的诊断标准对于促进适当的管理很重要。微创混合入路继续改善结果,平衡侵入性和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
JAMA surgery
JAMA surgery SURGERY-
CiteScore
20.80
自引率
3.60%
发文量
400
期刊介绍: JAMA Surgery, an international peer-reviewed journal established in 1920, is the official publication of the Association of VA Surgeons, the Pacific Coast Surgical Association, and the Surgical Outcomes Club.It is a proud member of the JAMA Network, a consortium of peer-reviewed general medical and specialty publications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信