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Informed consent for gastrointestinal endoscopy: a 2002 ESGE survey
K Triantafyllou1, C Stanciu, A Kruse
1Endoscopy Unit, 2nd Department of Internal Medicine, Athens University, Evangelismos Hospital, Athens, Greece.
Digestive Diseases (Basel, Switzerland)
|February 13, 2003
Summary
Informed consent for endoscopic procedures varies greatly across European countries. Key information, like risks and alternatives, is often inadequately provided, necessitating a review of current practices.
Area of Science:
- Gastroenterology
- Medical Ethics
- Patient Safety
Background:
- Informed consent is mandatory for endoscopic examinations.
- Existing data suggest significant deficiencies in the informed consent process for these procedures.
- The European Society of Gastrointestinal Endoscopy (ESGE) oversees endoscopic practices in member nations.
Purpose of the Study:
- To assess the quality of information provided to patients before endoscopic procedures.
- To evaluate informed consent practices within European Society of Gastrointestinal Endoscopy member countries.
Main Methods:
- A survey was distributed to representatives of national endoscopic societies.
- The survey utilized a structured questionnaire focusing on informed consent quality.
- Data were collected from member countries of the European Society of Gastrointestinal Endoscopy.
Main Results:
- A 59% response rate was achieved from 26 out of 44 surveyed countries.
- Endoscopists are responsible for informed consent in only 23.1% of responding countries.
- While 96% provide procedural information, only 77% allow adequate time for patient questions. Diagnostic/therapeutic alternatives and complication rates are discussed in only 85% and 77% of countries respectively. Procedure-related mortality is disclosed in just 23% of countries.
Conclusions:
- Significant variability exists in the informed consent process for endoscopic procedures across Europe.
- Current practices for obtaining informed consent for endoscopy may require reevaluation and standardization.