Effective Feedback to Improve Primary Care Prescribing Safety
NCT01602705
Complications of Surgical and Medical Care: General Terms
Edinburgh, United Kingdom
View Trial DetailsNCT Number: NCT01354197
The study observed the 28 days mortality of 9 participated University base surgical intensive care unit (SICU) as well as the occurrence of adverse events in SICU.
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Notify Me18 year and older
All sexes
Observational
Department of Anesthesiology, Faculty of Medicine, Chulalongkorn hospital, Bangkok, Thailand
The adverse events included pulmonary aspiration, pulmonary emboli, drug error, new stroke, symptomatic deep vein thrombosis, pneumothorax, unplanned extubation, upper GI hemorrhage, myocardial infarction, abdominal hypertension, acute lung injury(ALI)/acute respiratory distress syndrome (ARDS), re-intubation within 72 hours, delirium, cardiac arrest, new arrhythmia, acute kidney injury, sepsis
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 28 days
Number of Participants who Did Not Survive up to 28 days after surgical ICU admission
Time frame: 3 days
Number of Participants with Readmission to ICU up to 3 days (72 hours) after discharge from ICU
Royal College of Anesthesiologists of Thailand
Other
Multicenter Study of Outcome and Adverse Events in Surgical Intensive Care Unit of Thai University Hospital
Acronym: THAI-SICU
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