What type of order would typically not require a signed consent form for administration?

Routine lab orders do not typically require a signed consent form for administration because they are considered standard diagnostic procedures that do not pose significant risk to the patient. These orders are part of regular clinical practice aimed at assessing a patient's health status or monitoring specific conditions. Consent for routine labs is generally implied by the patient's agreement to receive care and is often included in the consent for treatment that patients provide upon admission to a healthcare facility.

In contrast, blood administration orders generally necessitate informed consent due to the risks associated with blood transfusions, such as allergic reactions or transfusion-related infections. Emergency intervention orders also typically require consent when time permits, to ensure that patients are aware of and agree to the procedures being performed, as they may have significant implications for their health. Medication orders may require consent in specific scenarios, particularly for high-risk medications or off-label uses. Thus, compared to these other types of orders, routine lab orders are the least likely to require a signed consent form.