Our goal is to conduct a prospective, national, randomized-controlled, multicenter trial to investigate the effect of handover of anesthesia care on the occurrence of adverse outcomes in the perioperative period.
Intraoperative handover of anesthesia care frequently occurs in clinical routine. Communication between the two anesthesiologists plays a pivotal role for the continuation of anesthesia care. The outgoing clinician must inform the incoming clinician in a short period of time about the important pre- and intraoperative facts and about the surgery while continuing to provide patient care. Contributing factors to inadequate communication during handoffs include insufficient or misleading information, busy and distractive environment, ineffective communication methods, lack of time, lack of standardized procedures, and insufficient staffing. It is estimated that the majority of adverse events in health care involve miscommunication during the handoff between physicians and perhaps other health care practitioners (https://www.jointcommission.org/hot\_topics\_toc/). The goal is to conduct a prospective, national, randomized-controlled, multicenter trial to investigate the effect of handover of anesthesia care on the occurrence of adverse outcomes in the perioperative period. The investigators hypothesizes that handover of anesthesia care does increase the risk for adverse outcomes. The primary outcome parameter is a combined endpoint consisting of all-cause mortality, readmission to any hospital, or major postoperative complications (including prolonged postoperative ventilation ≥ 48 h, major disruption of surgical wound, bleeding, pneumonia, atrial fibrillation, moderate or severe acute kidney injury, new onset of hemodialysis, cardiac arrest, myocardial infarction, sepsis, stroke, pulmonary embolism, deep venous thrombosis, shock, unplanned return to operating room) within 30 days of index surgery. Secondary endpoints are the individual criteria of the primary endpoint, hospital length of stay, ICU admission, and ICU length of stay. As the currently available data on handover of anesthesia care have not been obtained from prospective, randomized controlled trials, the results of the Handicap trial will bring new insights to anesthesia care to improve patients' outcome.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
1,817
There will be one complete handover
University Hospital Aachen
Aachen, Germany
University Hospital Bochum
Bochum, Germany
Kliniken der Stadt Köln gGmbH, Klinik für Anästhesiologie und operative Intensivmedizin
Cologne, Germany
Combined endpoint consisting number of participants with all-cause mortality, readmission to any hospital or major postoperative complications
Time frame: within 30 days of index surgery
Number of participants with all-cause mortality
Time frame: within 30 days of index surgery
Numer of participants with readmission to any hospital
Time frame: within 30 days of index surgery
Number of participants with major postoperative complication
predefined postoperative complication including prolonged postoperative ventilation ≥ 48h, major disruption of surgical wound, bleeding, pneumonia, atrial fibrillation, moderate or severe acute kidney injury, new onset of hemodialysis, cardiac arrest, myocardial infarction, sepsis, stroke, pulmonary embolism, deep venous thrombosis, shock, unplanned return to operating room
Time frame: within 30 days of index surgery
Hospital length of stay
Time frame: within 30 days of index surgery
Number of patients with ICU admission
Time frame: within 30 days of index surgery
ICU length of stay
Time frame: within 30 days of index surgery
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Klinikum Dortmund
Dortmund, Germany
St. Josefs-Hospital Dortmund-Hörde
Dortmund, Germany
Florence-Nightingale-Krankenhaus
Düsseldorf, Germany
Universitätsmedizin Göttingen, Klinik für Anästhesiologie
Göttingen, Germany
University Hospital Heidelberg
Heidelberg, Germany
Kliniken Maria Hilf
Mönchengladbach, Germany
University Hospital Muenster
Münster, Germany
...and 1 more locations