What is the reason for complaints after the insertion of a device?

The reason for complaints after the insertion of a device often stems from working or non-working interferences, which can include issues such as incompatibility with the patient's anatomy or the device's failure to function as intended. When a device is implemented, it must interact effectively with the surrounding tissues and systems; any conflict can result in discomfort or dissatisfaction.

In understanding device-related complications, it’s crucial to recognize that patients may report pain, discomfort, or other adverse symptoms if the device interferes with biological processes or if its function is compromised. This interference could be due to various factors, including the positioning of the device, mechanical failure, or the patient's unique biological response to the device.

While other factors such as improper fitting, patient anxiety, and inadequate post-operative care can contribute to complaints, they do not directly address the core issue of how the device interacts with the body or operates during its use. These factors can lead to complications or dissatisfaction but are secondary in this context compared to the direct influence of interferences related to the device itself.