Raman Spectroscopy for Instant Bladder Tumor Diagnosis: System Development and In Vivo Proof-Of-Principle Study in Accordance with the European Medical Device Regulation (MDR2017/745)
This work reports on an in vivo Raman-based endoscopy system, invaScope, enabling Raman measurements of healthy and tumor bladder tissue during an endoscopic procedure in the operating theatre. The presented study outlines the progression from the initial concept (validated through previously perfor...
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Veröffentlicht in: | Cancers 2024-09, Vol.16 (18), p.3238 |
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description | This work reports on an in vivo Raman-based endoscopy system, invaScope, enabling Raman measurements of healthy and tumor bladder tissue during an endoscopic procedure in the operating theatre. The presented study outlines the progression from the initial concept (validated through previously performed ex vivo studies) to the approval and implementation of a clinical investigational device according to the requirement within the framework of the European Medical Device Regulation (MDR2017/745). The study's primary objective was to employ the invaScope Raman system within the bladder, capturing in vivo spectroscopic Raman data followed by standard histo- and cytopathological examinations of urological tissue (considered the gold standard). The collected data were analyzed and correlated with histopathological findings post-procedure. Additionally, the study aimed to assess the feasibility of using diagnostic equipment, probes, and software for application in a clinical setting, evaluating usability aspects that are important during surgical procedures. This research represents a pivotal step toward advancing Raman spectroscopy for routine clinical use in characterizing bladder lesions. |
doi_str_mv | 10.3390/cancers16183238 |
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The presented study outlines the progression from the initial concept (validated through previously performed ex vivo studies) to the approval and implementation of a clinical investigational device according to the requirement within the framework of the European Medical Device Regulation (MDR2017/745). The study's primary objective was to employ the invaScope Raman system within the bladder, capturing in vivo spectroscopic Raman data followed by standard histo- and cytopathological examinations of urological tissue (considered the gold standard). The collected data were analyzed and correlated with histopathological findings post-procedure. Additionally, the study aimed to assess the feasibility of using diagnostic equipment, probes, and software for application in a clinical setting, evaluating usability aspects that are important during surgical procedures. This research represents a pivotal step toward advancing Raman spectroscopy for routine clinical use in characterizing bladder lesions.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers16183238</identifier><identifier>PMID: 39335209</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Biocompatibility ; Biopsy ; Bladder cancer ; Classification ; Clinical outcomes ; Compliance ; Design ; Diagnosis ; Endoscopy ; Feasibility studies ; Health care expenditures ; Healthcare industry software ; Laboratories ; Lasers ; Medical equipment ; Medical prognosis ; Medical research ; Medical technology ; Medicine, Experimental ; Patient safety ; Physiological apparatus ; Product development ; Raman spectroscopy ; Regulation ; Software ; Spectrum analysis ; Tumors ; Usability</subject><ispartof>Cancers, 2024-09, Vol.16 (18), p.3238</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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The presented study outlines the progression from the initial concept (validated through previously performed ex vivo studies) to the approval and implementation of a clinical investigational device according to the requirement within the framework of the European Medical Device Regulation (MDR2017/745). The study's primary objective was to employ the invaScope Raman system within the bladder, capturing in vivo spectroscopic Raman data followed by standard histo- and cytopathological examinations of urological tissue (considered the gold standard). The collected data were analyzed and correlated with histopathological findings post-procedure. Additionally, the study aimed to assess the feasibility of using diagnostic equipment, probes, and software for application in a clinical setting, evaluating usability aspects that are important during surgical procedures. This research represents a pivotal step toward advancing Raman spectroscopy for routine clinical use in characterizing bladder lesions.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39335209</pmid><doi>10.3390/cancers16183238</doi><orcidid>https://orcid.org/0000-0003-4257-593X</orcidid><orcidid>https://orcid.org/0009-0001-9367-6207</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biocompatibility Biopsy Bladder cancer Classification Clinical outcomes Compliance Design Diagnosis Endoscopy Feasibility studies Health care expenditures Healthcare industry software Laboratories Lasers Medical equipment Medical prognosis Medical research Medical technology Medicine, Experimental Patient safety Physiological apparatus Product development Raman spectroscopy Regulation Software Spectrum analysis Tumors Usability |
title | Raman Spectroscopy for Instant Bladder Tumor Diagnosis: System Development and In Vivo Proof-Of-Principle Study in Accordance with the European Medical Device Regulation (MDR2017/745) |
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