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Systematic review of techniques used to validate the registration of augmented-reality images using a head-mounted device to navigate surgery

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Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.bjoms.2022.08.007

Keywords

Augmented reality; Surgery

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This review examines validation studies on augmented-reality head-mounted devices (HMD) used for surgical navigation. The majority of studies used HoloLens devices with different registration methods and software. The mean registration error calculated in this study can be considered as a minimum acceptable standard.
Augmented-reality (AR) head-mounted devices (HMD) allow the wearer to have digital images superposed on to their field of vision. They are being used to superpose annotations on to the surgical field akin to a navigation system. This review examines published validation studies on HMD-AR systems, their reported protocols, and outcomes. The aim was to establish commonalities and an acceptable registration outcome. Multiple databases were systematically searched for relevant articles between January 2015 and January 2021. Studies that exam-ined the registration of AR content using a HMD to guide surgery were eligible for inclusion. The country of origin, year of publication, medical specialty, HMD device, software, and method of registration, were recorded. A meta-analysis of the mean registration error was conducted. A total of 4784 papers were identified, of which 23 met the inclusion criteria. They included studies using HoloLens (Microsoft) (n = 22) and nVisor ST60 (NVIS Inc) (n = 1). Sixty-six per cent of studies were in hard tissue specialties. Eleven studies reported registration errors using pattern markers (mean (SD) 2.6 (1.8) mm), and four reported registration errors using surface markers (mean (SD) 3.8 (3.7) mm). Three studies reported registration errors using manual alignment (mean (SD) 2.2 (1.3) mm). The majority of studies in this review used in-house software with a variety of registration methods and reported errors. The mean registration error calculated in this study can be con-sidered as a minimum acceptable standard. It should be taken into consideration when procedural applications are selected.(c) 2022 Published by Elsevier Ltd on behalf of The British Association of Oral and Maxillofacial Surgeons.

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