Which complication is NOT typically included in a patient's informed consent?

The patient's previous health history is generally not included in an informed consent discussion as a complication. Informed consent typically focuses on the specific procedure or treatment being proposed, highlighting the associated risks, benefits, and alternative options that the patient may have. The essential elements included in informed consent are intended to inform the patient about the current procedure and its immediate implications.

Informed consent involves discussing the side effects of medication, risks associated with the procedure, and potential complications during recovery. These elements are crucial as they directly relate to the patient's decision-making process regarding the treatment. However, the patient's past health history serves more as foundational information for assessing the appropriateness of the treatment rather than as a complication that might be covered in the consent process. It informs the healthcare provider about the patient's overall health but does not constitute a risk or complication of the current procedure being performed.