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One way to speed up clinical trials: Skip right to the data with electronic medical records
In health care crises, researchers can avoid waiting for clinical trial results by using data from health care systems to analyze the effectiveness of treatments for COVID-19 and other illnesses. Scientific knowledge, as measured by numbers of papers published, has been estimated to double every 17.3 years. However, it takes an average of about 17 years for health and medical research – going from basic lab studies on cell cultures and animals to clinical trials in people – to result in actual changes patients see in the clinic. The typical process of medical research is generally not well equipped to respond effectively to quickly evolving pandemics. This has been especially evident for the COVID-19 pandemic, in part because the virus the causes COVID-19 mutates frequently. Scientists and public health officials are often left continually scrambling to develop and test new treatments to match emerging variants.
Medigy Insights
Health care crises can benefit from the use of health care system data to analyze treatment effectiveness for COVID-19 and other illnesses, avoiding the wait for clinical trial results. However, the standard medical research timeline of 17 years from basic laboratory studies to clinical trials and patient outcomes is not well-suited for rapidly evolving pandemics like COVID-19. This is exacerbated by the virus's frequent mutations, which require scientists and public health officials to continually develop and test new treatments for emerging variants.
Continue reading at theconversation.com
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