How long do people need to be monitored after fainting?
For the first time, physicians in the emergency department (ED) have evidence-based recommendations on how best to catch the life-threatening conditions that make some people faint. New research published in Circulation suggests that low-risk patients can be safely sent home by a physician after spending two hours in the ED, and medium and high-risk patients can be sent home after six hours if no danger signals are detected.
Most of the time fainting is harmless, but a small percentage of people faint due to serious medical conditions, such as an irregular heartbeat, or arrhythmia. These arrhythmias usually come and go quickly, and the person’s heart rhythm returns to normal by the time the ambulance arrives or they reach the ED. Fear of these arrhythmias coming back have led to patients being kept in the ED for eight to 12 hours. Approximately half of all patients who are hospitalized for fainting across Canada are admitted so their heart rhythm can be monitored. However, only a small proportion of patients will experience a dangerous irregular heartbeat, heart attack or death within a month of fainting.
“Before this study we didn’t know which fainting patients needed to be monitored in the Emergency Department, and how long they needed to be monitored. We didn’t know who needed to be hospitalized in order to catch life-threatening conditions. Now we have answers to these questions that will help improve patient care, and potentially reduce ED wait times and hospital admissions,” said lead author Dr. Venkatesh Thiruganasambandamoorthy, an associate professor at the University of Ottawa and an emergency physician and scientist at The Ottawa Hospital.
Dr. Thiruganasambandamoorthy’s team previously created a simple tool to help emergency physicians identify those fainting patients who are at greater risk of adverse events. In this observational study, they used the tool to rank 5,581 patients from six EDs across Canada as low (0.4 percent risk of an arrhythmia within 30 days), medium (8.7 percent) or high risk (25.3 percent).
Out of the 5,581 people, 74 percent were classified as low-risk, 19 percent as medium-risk and 7 percent as high-risk. One month after fainting, 3.7% percent of individuals (207) suffered an arrhythmia.
The team found that one half of the arrhythmias were identified within the first two hours of arrival at the ED for low-risk patients, and within six hours for the medium and high-risk patients. They also found that 92 percent of the underlying arrhythmias were identified within 15-days among the medium and high-risk patients.
“We learned that irregular heartbeat called arrhythmias usually happen soon after fainting,” said Dr. Thiruganasambandamoorthy. “This means we can catch most of these events in those first few hours in the emergency department, where we can quickly give people the treatment they need. The types of arrhythmias that medium-risk patients suffer are important but non-life threatening, so these patients can be monitored from the comfort of their homes. A few days in hospital can be considered for high-risk patients”
Low-risk patients, the majority of fainting patients, can be discharged home after two hours without further heart rhythm monitoring. After six hours have passed for medium and high-risk patients, a physician can decide whether to admit them to hospital while considering their overall health, ability to cope at home, injuries and need for further monitoring. The research team found that medium and high-risk patients benefit from home heart rhythm monitoring for 15 days, which should ideally start when they leave the ED.
“Our study suggests that three quarters of the 200,000 fainting patients who come to Canadian emergency departments every year are at low risk of adverse events. They can safely be sent home once they’ve been in the ED two hours and a physician sees them,” said Dr. Thiruganasambandamoorthy.
Researchers at The Ottawa Hospital are known around the world for creating decision rules that improve patient care.
This article was reprinted with the permission of the Ottawa Hospital Research Institute.