Computer-Aided Diagnosis for Leaving Colorectal Polyps In Situ : A Systematic Review and Meta-analysis.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
21 May 2024
Historique:
medline: 20 5 2024
pubmed: 20 5 2024
entrez: 20 5 2024
Statut: aheadofprint

Résumé

Computer-aided diagnosis (CADx) allows prediction of polyp histology during colonoscopy, which may reduce unnecessary removal of nonneoplastic polyps. However, the potential benefits and harms of CADx are still unclear. To quantify the benefit and harm of using CADx in colonoscopy for the optical diagnosis of small (≤5-mm) rectosigmoid polyps. Medline, Embase, and Scopus were searched for articles published before 22 December 2023. Histologically verified diagnostic accuracy studies that evaluated the real-time performance of physicians in predicting neoplastic change of small rectosigmoid polyps without or with CADx assistance during colonoscopy. The clinical benefit and harm were estimated on the basis of accuracy values of the endoscopist before and after CADx assistance. The certainty of evidence was assessed using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) framework. The outcome measure for benefit was the proportion of polyps predicted to be nonneoplastic that would avoid removal with the use of CADx. The outcome measure for harm was the proportion of neoplastic polyps that would be not resected and left in situ due to an incorrect diagnosis with the use of CADx. Histology served as the reference standard for both outcomes. Ten studies, including 3620 patients with 4103 small rectosigmoid polyps, were analyzed. The studies that assessed the performance of CADx alone (9 studies; 3237 polyps) showed a sensitivity of 87.3% (95% CI, 79.2% to 92.5%) and specificity of 88.9% (CI, 81.7% to 93.5%) in predicting neoplastic change. In the studies that compared histology prediction performance before versus after CADx assistance (4 studies; 2503 polyps), there was no difference in the proportion of polyps predicted to be nonneoplastic that would avoid removal (55.4% vs. 58.4%; risk ratio [RR], 1.06 [CI, 0.96 to 1.17]; moderate-certainty evidence) or in the proportion of neoplastic polyps that would be erroneously left in situ (8.2% vs. 7.5%; RR, 0.95 [CI, 0.69 to 1.33]; moderate-certainty evidence). The application of optical diagnosis was only simulated, potentially altering the decision-making process of the operator. Computer-aided diagnosis provided no incremental benefit or harm in the management of small rectosigmoid polyps during colonoscopy. European Commission. (PROSPERO: CRD42023402197).

Sections du résumé

BACKGROUND UNASSIGNED
Computer-aided diagnosis (CADx) allows prediction of polyp histology during colonoscopy, which may reduce unnecessary removal of nonneoplastic polyps. However, the potential benefits and harms of CADx are still unclear.
PURPOSE UNASSIGNED
To quantify the benefit and harm of using CADx in colonoscopy for the optical diagnosis of small (≤5-mm) rectosigmoid polyps.
DATA SOURCES UNASSIGNED
Medline, Embase, and Scopus were searched for articles published before 22 December 2023.
STUDY SELECTION UNASSIGNED
Histologically verified diagnostic accuracy studies that evaluated the real-time performance of physicians in predicting neoplastic change of small rectosigmoid polyps without or with CADx assistance during colonoscopy.
DATA EXTRACTION UNASSIGNED
The clinical benefit and harm were estimated on the basis of accuracy values of the endoscopist before and after CADx assistance. The certainty of evidence was assessed using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) framework. The outcome measure for benefit was the proportion of polyps predicted to be nonneoplastic that would avoid removal with the use of CADx. The outcome measure for harm was the proportion of neoplastic polyps that would be not resected and left in situ due to an incorrect diagnosis with the use of CADx. Histology served as the reference standard for both outcomes.
DATA SYNTHESIS UNASSIGNED
Ten studies, including 3620 patients with 4103 small rectosigmoid polyps, were analyzed. The studies that assessed the performance of CADx alone (9 studies; 3237 polyps) showed a sensitivity of 87.3% (95% CI, 79.2% to 92.5%) and specificity of 88.9% (CI, 81.7% to 93.5%) in predicting neoplastic change. In the studies that compared histology prediction performance before versus after CADx assistance (4 studies; 2503 polyps), there was no difference in the proportion of polyps predicted to be nonneoplastic that would avoid removal (55.4% vs. 58.4%; risk ratio [RR], 1.06 [CI, 0.96 to 1.17]; moderate-certainty evidence) or in the proportion of neoplastic polyps that would be erroneously left in situ (8.2% vs. 7.5%; RR, 0.95 [CI, 0.69 to 1.33]; moderate-certainty evidence).
LIMITATION UNASSIGNED
The application of optical diagnosis was only simulated, potentially altering the decision-making process of the operator.
CONCLUSION UNASSIGNED
Computer-aided diagnosis provided no incremental benefit or harm in the management of small rectosigmoid polyps during colonoscopy.
PRIMARY FUNDING SOURCE UNASSIGNED
European Commission. (PROSPERO: CRD42023402197).

Identifiants

pubmed: 38768453
doi: 10.7326/M23-2865
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Roberta Maselli (R)
Silvia Carrara (S)
Alessandro Fugazza (A)
Antonio Capogreco (A)
Maddalena Menini (M)
Davide Massimi (D)
Kazumi Takishima (K)
Kenichi Mochizuki (K)
Yuki Miyata (Y)
Kentaro Mochida (K)
Yoshika Akimoto (Y)
Takanori Kuroki (T)
Yuriko Morita (Y)
Osamu Shiina (O)
Shun Kato (S)
Ishita Barua (I)
Øyvind Holme (Ø)
Paulina Wieszczy (P)
Magnus Løberg (M)
Mette Kalager (M)
Shraddha Gulati (S)
Sophie Williams (S)
Bu Hayee (B)
Mehul Patel (M)
Nishmi Gunasingam (N)
Alexandra Kent (A)
Andrew Emmanuel (A)
Amyn Haji (A)
Hayato Itoh (H)
Kensaku Mori (K)
Tetsuo Nemoto (T)
Carl Munck (C)
Jens Aksel Nilsen (JA)
Stine Astrup Hvattum (SA)
Svein Oskar Frigstad (SO)
Petter Tandberg (P)
Davide Lanza (D)
Giacomo Bonanno (G)

Auteurs

Cesare Hassan (C)

Humanitas University, Department of Biomedical Sciences, Pieve Emanuele, and Humanitas Clinical and Research Center IRCCS, Endoscopy Unit, Rozzano, Italy (C.H., M.S., A.R.).

Masashi Misawa (M)

Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan (M.M., S.K.).

Tommy Rizkala (T)

Humanitas Clinical and Research Center IRCCS, Endoscopy Unit, Rozzano, Italy (T.R., L.C.).

Yuichi Mori (Y)

Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan; University of Oslo, Clinical Effectiveness Research Group; and Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway (Y.M.).

Shahnaz Sultan (S)

Division of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, and VA Health Care System, Minneapolis, Minnesota (S.S.).

Antonio Facciorusso (A)

University of Foggia, Department of Medical Sciences, Section of Gastroenterology, Foggia, Italy (A.F.).

Giulio Antonelli (G)

Gastroenterology and Digestive Endoscopy Unit, Ospedale dei Castelli, Ariccia, and Department of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University of Rome, Rome, Italy (G.A.).

Marco Spadaccini (M)

Humanitas University, Department of Biomedical Sciences, Pieve Emanuele, and Humanitas Clinical and Research Center IRCCS, Endoscopy Unit, Rozzano, Italy (C.H., M.S., A.R.).

Britt B S L Houwen (BBSL)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, the Netherlands (B.B.S.L.H.).

Emanuele Rondonotti (E)

Gastroenterology Unit, Valduce Hospital, Como, Italy (E.R.).

Harsh Patel (H)

Kansas City VA Medical Center, Gastroenterology and Hepatology, Kansas City, Missouri (H.P., P.S.).

Kareem Khalaf (K)

Division of Gastroenterology, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada (K.K.).

James Weiquan Li (JW)

Department of Gastroenterology and Hepatology, Changi General Hospital, Singapore Health Services, and Duke-NUS Academic Medicine Centre, Singapore Health Services, Singapore (J.W.L.).

Gloria M Fernandez (GM)

Endoscopy Unit, Gastroenterology Department, Clinical Institute of Digestive and Metabolic Disease, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain (G.M.F.).

Pradeep Bhandari (P)

Queen Alexandra Hospital, Department of Gastroenterology, Portsmouth, United Kingdom (P.B.).

Evelien Dekker (E)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, and Bergman Clinics Maag and Darm Amsterdam, Amsterdam, the Netherlands (E.D.).

Seth Gross (S)

Department of Gastroenterology, Tisch Hospital, New York University Langone Medical Center, New York, New York (S.G.).

Tyler Berzin (T)

Center for Advanced Endoscopy, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts (T.B.).

Per Olav Vandvik (PO)

Department of Medicine, Lovisenberg Diaconal Hospital, Oslo, Norway (P.O.V.).

Loredana Correale (L)

Humanitas Clinical and Research Center IRCCS, Endoscopy Unit, Rozzano, Italy (T.R., L.C.).

Shin-Ei Kudo (SE)

Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan (M.M., S.K.).

Prateek Sharma (P)

Kansas City VA Medical Center, Gastroenterology and Hepatology, Kansas City, Missouri (H.P., P.S.).

Douglas K Rex (DK)

Indiana University School of Medicine, Division of Gastroenterology, Indianapolis, Indiana (D.K.R.).

Alessandro Repici (A)

Humanitas University, Department of Biomedical Sciences, Pieve Emanuele, and Humanitas Clinical and Research Center IRCCS, Endoscopy Unit, Rozzano, Italy (C.H., M.S., A.R.).

Farid Foroutan (F)

Ted Rogers Centre for Heart Research, University Health Network, Toronto, Ontario, Canada (F.F.).

Classifications MeSH