A pulmonary embolism is a blood clot that blocks and stops blood flow to an artery in the lung. In most cases, the blood clot starts in a deep vein in the leg and travels to the lung. Rarely, the clot forms in a vein in another part of the body. When a blood clot forms in one or more of the deep veins in the body, it's called a deep vein thrombosis (DVT). Because one or more clots block blood flow to the lungs, pulmonary embolism can be life-threatening. However, prompt treatment greatly reduces the risk of death. Taking measures to prevent blood clots in your legs will help protect you against pulmonary embolism. The design and implementation of CDS tools should not only include careful consideration of their content and purpose, but their method of monitoring for success in terms of outcomes, functionality, and how they fit in the context of other CDS tools that are currently in place (see Section 5 for further details). However, formalized support and regulation for CDS is not abundantly common. In 2018, the US Food and Drug Administration offered a draft set of recommendations for CDS software (Food and Drug Administration 2018). Although not enacted into law, this type of oversight only proposes to cover certain types of CDS, but it is not yet fully defined what it would cover. Organizations such as the Health Information and Management Systems Society (HIMSS) and the American Medical Informatics Association (AMIA) have made comments on this draft, making apparent the need for further clarification by the FDA on what types of CDS will be effected. Due to a lack of current formalized regulation, CDS developers and implementers must be conscientious in assuring these tools are in fact functioning as intended and not unintentionally causing patient harm. Referring to the 5 rights and GUIDE checklist may be helpful.