Serious adverse events were defined as events
that were fatal or life-threatening, that resulted
in clinically significant or persistent disability,
that required or prolonged a hospitalization, or
that were judged by the investigator to represent
a clinically significant hazard or harm to the
participant that might require medical or surgical
intervention to prevent one of the other events
listed above.30,31 A short list of monitored conditions were reported as adverse events if they were
evaluated in an emergency department: hypotension, syncope, injurious falls, electrolyte abnormalities, and bradycardia. We also monitored occurrences of acute kidney injury or acute renal
failure if they were noted on admission or occurred during a hospitalization and were reported in the hospital discharge summary as a
primary or main secondary diagnosis. The Medical Dictionary for Regulatory Activities was used to
classify the safety events. Coding was performed
at the coordinating center, and up to three codes
were assigned to each safety event. The relationship of serious adverse events to the intervention
was assessed by the trial safety officer and reviewed monthly by the safety committee.
Serious adverse events were defined as events that were fatal or life-threatening, that resulted in clinically significant or persistent disability, that required or prolonged a hospitalization, or that were judged by the investigator to represent a clinically significant hazard or harm to the participant that might require medical or surgical intervention to prevent one of the other events listed above.30,31 A short list of monitored conditions were reported as adverse events if they were evaluated in an emergency department: hypotension, syncope, injurious falls, electrolyte abnormalities, and bradycardia. We also monitored occurrences of acute kidney injury or acute renal failure if they were noted on admission or occurred during a hospitalization and were reported in the hospital discharge summary as a primary or main secondary diagnosis. The Medical Dictionary for Regulatory Activities was used to classify the safety events. Coding was performed at the coordinating center, and up to three codes were assigned to each safety event. The relationship of serious adverse events to the intervention was assessed by the trial safety officer and reviewed monthly by the safety committee.
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