Rapid Point-of-Care Testing for COVID-19

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This Canada's Drug Agency Horizon Scan describes how rapid point-of-care screening tests for COVID-19 are being used in Canada and internationally. It also reports on evidence regarding their effectiveness on COVID-19 transmission (no studies identified) and performance. The scan identifies guidance documents that provide suggestions for use in specific settings and populations.

Non-Invasive Ventilation With Helmets for Acute Respiratory Distress Due to COVID-19

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This Health Technology Update newsletter describes patient helmets, also known as “helmet masks,” and their potential use in COVID-19 infection control. These helmets are designed to reduce the risk of COVID-19 transmission from infected patients to health care providers and other patients. The newsletter provides a background to the technology, target populations, cost and availability, current clinical evidence, and potential implications for future research.

COVID-19 Testing: A Summary of Testing Methods

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This report provides an overview of testing methods for COVID-19. A description of published clinical evidence and important considerations related to the potential implementation of these tests are provided. As demands for testing during the pandemic increases, this information may be of interest to health care decision-makers interested in learning more about the availability and variety of testing types and screening methods.

Combined Testing for Severe Acute Respiratory Syndrome Coronavirus 2 and Influenza

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This report looks at the current evidence regarding diagnostic tests that can detect both severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, the virus that causes COVID-19 infection) and seasonal influenza. Combined diagnostic tests can be used to detect both viruses from 1 respiratory sample in a single reaction. The availability of these tests, their cost, and current practice are explored in this Horizon Scan.

Breath Tests for the Detection of Severe Acute Respiratory Syndrome Coronavirus 2

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This Horizon Scan report examines the use of breath tests to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes COVID-19 infections. Breath tests for SARS-CoV-2 work by analyzing the volatile organic compounds (compounds produced by virus-infected cells) present in exhaled breath. Issues related to these tests, such as current practice and cost, are explored in this report.

Point-of-Care Tests for Pancreatitis

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  • Horizon scan reports provide brief summaries of information regarding new and emerging health technologies, which are identified through the Canada's Drug Agency Horizon Scanning Service as topics of potential interest to health care decision-makers in Canada.

An Overview of Pharmacogenomic Testing for Psychiatric Disorders

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Pharmacogenomic testing is a precision medicine technology that examines genetic variation in medication metabolism. Selected for inclusion in the Canada's Drug Agency 2023 Watch List, pharmacogenomic testing has the potential to significantly influence the landscape of health care in Canada over the next 5 years. By analyzing an individual’s unique genetic profile, this testing aims to guide personalized treatment strategies that improve therapeutic outcomes, optimize the medication selection process, and enhance patient experiences.

An Overview of Emerging Trends and Technologies in Ulcerative Colitis

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Key Message

  • This report provides an overview of the evolving therapeutic landscape for moderate to severe ulcerative colitis (UC), including recent changes to clinical practice guidelines, key trends in therapeutic strategies, and new or emerging treatment options, with a focus on biologics and small-molecule therapies.
  • Recent guidelines on the medical management of patients with UC include those of the American Gastroenterological Association (AGA), American College of Gastroenterology (ACG), and European Crohn’s and Colitis Organisation (ECCO), which were published in 2019, 2020, and 2022, respectively. These guidelines provide an accurate reflection of how clinical practice has changed to incorporate newer therapies that have entered the market and newer evidence that has been published since the release of the Canadian guidelines in 2015. The ACG, AGA, and ECCO guidelines all recommend use of a tumour necrosis factor (TNF) antagonist, vedolizumab, or tofacitinib for induction of remission in patients with moderate to severe UC; the AGA and ECCO guidelines also recommend ustekinumab as an option and recommend vedolizumab over adalimumab, whereas the AGA guidelines recommend early use of biologic drugs over a step-up approach after failure of 5-aminosalicylates.
  • Two important trends in therapeutic strategies for UC include changes in the use and definition of treatment targets and recommendations regarding therapeutic drug monitoring (TDM).
    • The 2021 Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE-II) guidelines provide contemporary consensus recommendations for using new and updated targets throughout an individualized treatment timeline in patients with inflammatory bowel disease (IBD). Although histologic remission is not considered a formal UC treatment target in STRIDE-II, it is acknowledged as an adjunctive measure to endoscopic remission to represent a deeper level of healing and is the focus of many current studies.
    • The use of TDM emerged from challenges associated with the use of older biologics (primarily TNF antagonists), which posed difficulties related to immunogenicity and dosing. The relevance of TDM for newer biologics with different mechanisms of action, reduced immunogenicity, and fixed dosing (e.g., vedolizumab and ustekinumab) is a topic of ongoing debate. Although AGA guidelines on TDM in IBD and expert consensus statements support the use of reactive TDM for patients with UC who lose response to a TNF antagonist, evidence gaps remain regarding appropriate use of proactive TDM, utility of TDM for small molecules and biologics outside of the TNF antagonist class, and consistent target concentration thresholds to guide dose changes.
  • There is a substantial pipeline of new and emerging drugs for the treatment of adults with moderate to severe UC, with many in phase IIb or III of clinical development; several notable trends of emerging pharmacotherapies exist, including an increasing number of Janus kinase inhibitors, several therapies with biologic targets that are new in UC (e.g., interleukin-23 antibodies, TNF-like ligand 1A inhibitors), an increasing number of oral therapies, and the first combination of 2 biologic therapies in UC.
  • The Canadian health care system should be prepared to adapt to the rapidly evolving treatment landscape and potential clinical practice changes in moderate to severe UC. Drugs with new mechanisms of action in the treatment area and the new paradigm of combination therapy with multiple biologics of different classes may lead to improved patient outcomes but can also further complicate the treatment decision-making process. Therefore, it is important for health care providers to stay up to date on new and upcoming treatment options, which may require educational initiatives for both providers and patients as well as updates to the Canadian treatment guidelines. Overall, potential changes on the horizon may have substantial implications for the health care system given the prevalence of UC in Canada, the costs of advanced therapies, and the increasing number of available treatment options.

Laser Treatment for Lower Back Pain

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The Canada's Drug Agency Horizon Scanning Service identifies emerging health technologies that may be of potential interest to health care decision-makers in Canada.

Chronic pain, including chronic low back pain, challenges many aspects of people's lives, including social, physical, mental, and professional. Approximately 80% of adults will be affected by chronic lower back pain at least once in their lifetime and seek out multiple treatment options, including drug treatments, psychological treatments, and physical therapies.

ClotChip Portable Blood Clotting Sensor

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This Horizon Scan summarizes the available information regarding an emerging technology, ClotChip, for the identification of blood clotting defects. ClotChip is intended for use at the point of care and uses novel, low-cost technology to perform rapid assessment of the blood's clotting ability. Early evidence has demonstrated the feasibility and utility of ClotChip, which could benefit patients with a variety of bleeding disorders and could potentially save time for health care professionals.