The purpose of this HTA is to inform the policy questions through an assessment of the clinical effectiveness and safety, cost-effectiveness, patients’ perspectives and experiences, ethical issues, and implementation issues of minimally invasive glaucoma surgery devices and procedures for adults with glaucoma.
Dr. Cindy Hutnik has received funding from Allergan for research and for being on a user’s group panel, and from Medicus for writing articles or editorials and being on an expert panel on glaucoma management. The other authors declared no conflicts of interest relevant to this report.
Disclaimer: This report is prepared by the Canadian Agency for Drugs and Technologies in Health (CADTH). This report contains a comprehensive review of existing public literature, studies, materials, and other information and documentation (collectively the “source documentation”) available to CADTH at the time it was prepared, and it was guided by expert input and advice throughout its preparation.
The information in this report is intended to help health care decision-makers, patients, health care professionals, health systems leaders, and policy-makers make well-informed decisions and thereby improve the quality of health care services. The information in this report should not be used as a substitute for the application of clinical judgment in respect to the care of a particular patient or other professional judgment in any decision-making process, nor is it intended to replace professional medical advice. While CADTH has taken care in the preparation of this 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 responsible for any errors or omissions or injury, loss, or damage arising from or as a result of the use (or misuse) of any information contained in or implied by the information in this report
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