Aim: To collect real-world data on clinical practice to support healthcare improvement.
Possible methods:
• Digital data-collection tool
• Progressive web applications
• Paper or electronic data-collection forms
• Audits
• Surveys
• Dashboard summaries
Benefits: Quantification of general compliance, product usage data collection, getting customer engagement, capturing real-world practice and real-world evidence, suitable for peer-reviewed publications, and development of product evidence.
Regulatory: Compliance with international data-sovereignty and data-protection regulations. The collection of usage data for EU Medical Device Regulations.
Related work:
- Service evaluation of the impact of capnography on the safety of procedural sedation. Link
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Capnography for monitoring of physician-led procedural sedation procedures at gastrointestinal services (video)
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Clinical practice, monitoring, and patient safety during procedural sedation in five countries. Poster
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Interventions and costs associated with SIVA-defined adverse events during procedural sedation in five countries. Poster
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Patient safety during procedural sedation using capnography monitoring: a systematic review and meta-analysis. Link
- For other related work see our publications page