NICE will consider the issues raised in the report through its prioritisation board to determine if guidance should be developed in this area; decisions will be published on the NICE website. (AI summary)
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In terms of screening for these conditions in relatives of people with inherited thrombophilia, this is also not straightforward, as there are advantages and disadvantages. There are some situations where knowing that a child has an inherited defect may improve medical decision- making, and may give an opportunity to educate about signs and symptoms of VTE, which could lead to earlier diagnosis (as in this case); or to provide targeted thromboprophylaxis in clinical situations where the risk of VTE is increased; and to promote lifestyle modifications to avoid other prothrombotic risk factors (eg, sedentary lifestyle, overweight/obesity, and smoking). Conversely, inherited thrombophilia testing during childhood may be inappropriate, given the low risk of a thrombotic event; interpretation of screening tests can be challenging and may result in misdiagnosis. There are also ethical concerns about testing in those who may not have the maturity or understanding to make an informed decision. Screening is also problematic in situations where there is no clear medical benefit to the individual being screened. Nevertheless, NICE will consider the issues raised in your report through our recently implemented organisation-wide approach to prioritisation and topic selection. This is overseen by a single prioritisation board that guides the selection and coordination of our guidance development. We will ask our prioritisation board to consider if guidance should be developed in this area. In line with our usual practice, decisions made by the prioritisation board will be published on the NICE website. I hope this response has helped outline our role and the reasoning behind our lack of guidance in this specific area and would like to reiterate my sincere condolences to Lilly’s family.