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Patient and procedural factors associated with true histology rates in patients undergoing colonoscopy with computer-aided detection of polyps.
Shaukat, Aasma; Lichtenstein, David R; Chung, Daniel C; Seidl, Caitlyn; Wang, Yeli; Navajas, Emma E; Colucci, Daniel R; Baxi, Shrujal; Brugge, William R.
Afiliação
  • Shaukat A; Division of Gastroenterology and Hepatology, Department of Medicine, New York University Grossman School of Medicine, New York, New York, USA. Electronic address: aasma.shaukat@nyulangone.org.
  • Lichtenstein DR; Division of Gastroenterology, Department of Medicine, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Chung DC; Division of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Seidl C; Iterative Health Inc, Cambridge, Massachusetts, USA.
  • Wang Y; Iterative Health Inc, Cambridge, Massachusetts, USA.
  • Navajas EE; Iterative Health Inc, Cambridge, Massachusetts, USA.
  • Colucci DR; Iterative Health Inc, Cambridge, Massachusetts, USA.
  • Baxi S; Iterative Health Inc, Cambridge, Massachusetts, USA.
  • Brugge WR; Division of Gastroenterology, Department of Medicine, Mount Auburn Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Gastrointest Endosc ; 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38964478
ABSTRACT
BACKGROUND AND

AIMS:

Computer-aided detection (CADe) devices have been shown to increase adenoma detection rates and adenomas per colonoscopy compared to standard colonoscopies. Questions remain about whether CADe colonoscopies are mainly increasing the detection of small, nonneoplastic lesions or if they are detecting more pathologically meaningful polyps. In this analysis, we compare the true histology rate (defined as polyps with confirmation of clinically relevant histopathology) of CADe-identified polyps with polyps identified during standard colonoscopies.

METHODS:

Using data from the SKOUT trial, we compared the true histology rate (THR) between CADe and standard colonoscopies. We also conducted a subgroup analysis by patient, procedural, and endoscopist factors. To account for multiple testing of comparisons, we used the false discovery rate.

RESULTS:

A total of 1423 participants were included (CADe, n = 714; standard, n = 709). Overall, THR was similar between the CADe and standard colonoscopy arms for adenomas, sessile serrated lesions, and large hyperplastic polyps. Higher THR with CADe colonoscopy was observed in some subgroups for adenomas. Endoscopists with 11 to 20 years of experience and procedures occurring after 12 pm had significantly higher adenoma THRs in the CADe cohort. Patients younger than 65 years, male patients, and procedures with a withdrawal time of ≥8 minutes had borderline significance in the CADe device adenoma THR subgroup.

CONCLUSIONS:

CADe colonoscopies may hold the key to improving endoscopic quality measures, provided that the polyps identified by the CADe device are those of clinical relevance. Although the benefit and significance in the CADe group were demonstrated in this analysis, further research is warranted to ensure that the true histology is maintained when applied in real-world applications.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article