Analysis of Malfunctions of Implanted Electronic Devices in Patients Undergoing Radiotherapy

The study investigates how often malfunctions occur in pacemakers and other implanted electronic devices in patients treated with radiotherapy.

In patients with implanted electronic devices, such as pacemakers or defibrillators, radiotherapy may affect device function. Malfunctions may be temporary or permanent and may affect patient safety. The study aims to better understand how often such malfunctions occur and which factors influence them.

A better understanding of these risks will help improve patient safety during radiotherapy and adapt treatment approaches.

Purpose of the study

The purpose of the study is to determine the frequency and characteristics of malfunctions of implanted electronic devices in patients undergoing radiotherapy and to identify factors that influence their occurrence.

Study procedure

The study is carried out as part of standard radiotherapy treatment.

If the patient decides to participate, researchers will monitor the function of implanted electronic devices during and after radiotherapy. They will collect data on the course of treatment, the radiotherapy techniques used and any changes in device function.

The study does not interfere with treatment itself; it only monitors it.

Who can take part?

Adult patients with implanted electronic devices, such as a pacemaker or defibrillator, who are referred for radiotherapy.

How to apply?

Patients will be informed about the possibility of participation before the start of treatment. The decision to participate is confirmed by signing an informed consent form. Participation is voluntary and may be withdrawn at any time without affecting further treatment.

The study does not pose an additional risk, as it involves only monitoring of treatment. By participating, patients help improve the safety and methods of future treatment.