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Endoscopic Ultrasound for the Diagnosis of Disease and Staging of Cancers in Adult Patients with Gastroenterological or Oncological Disease: A Review of the Clinical Effectiveness, Cost-effectiveness and Safety

Rapid Response Report: Summary with Critical Appraisal

Identification of cancers and gastroenterological diseases can be challenging, as clinicians must ensure the process for identification is accurate while minimizing complications and ensuring sustainability associated with procedures. In addition, for those with cancer, accurate staging is vital for guiding the most appropriate therapy.

There are a number of minimally invasive imaging strategies that may be used for identifying and staging different types of cancers, as well as identifying gastroentological disease. Examples of imaging strategies include computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography (PET), endoscopic retrograde cholangiopancreatography (ERCP), and endoscopic ultrasound (EUS). Each strategy is associated with differing accuracy for different diseases, as well as when comparing diagnosis and staging of illness. In addition, each strategy is associated with other benefits and limitations. For example, EUS is often less expensive and more readily available relative to other imaging modalities like CT, PET and MRI, but CT, PET and MRI allow for visualization of a larger area compared with EUS. Also, the amount of radiation exposure, and need for contrast media, differs between each modality. Lastly, these imaging modalities may be complementary to one another, for example, using EUS to minimize exposure to the more invasive ERCP in people with acute biliary pancreatitis.

The purpose of this review was to evaluate the evidence for clinical effectiveness, safety, and cost effectiveness of EUS compared to other imaging modalities including CT, MRI, PET, or ERCP.

Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list of sources and a summary of the best evidence on the topic that CADTH could identify using all reasonable efforts within the time allowed. Rapid responses should be considered along with other types of information and health care considerations. The information included in this response is not intended to replace professional medical advice, nor should it be construed as a recommendation for or against the use of a particular health technology. Readers are also cautioned that a lack of good quality evidence does not necessarily mean a lack of effectiveness particularly in the case of new and emerging health technologies, for which little information can be found, but which may in future prove to be effective. While CADTH has taken care in the preparation of the report to ensure that its contents are accurate, complete and up to date, CADTH does not make any guarantee to that effect. CADTH is not liable for any loss or damages resulting from use of the information in the report.

Copyright © 2014 Canadian Agency for Drugs and Technologies in Health.

Copyright: This report contains CADTH copyright material. It may be copied and used for non-commercial purposes, provided that attribution is given to CADTH.

Links: This report may contain links to other information available on the websites of third parties on the Internet. CADTH does not have control over the content of such sites. Use of third party sites is governed by the owners’ own terms and conditions.

Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK268809PMID: 25590115

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