Chemical vs Electrical Cardioversion for Emergency Department Patients With Acute Atrial Fibrillation
- Conditions
- Atrial Fibrillation
- Interventions
- Drug: Chemical-firstDrug: Electrical-first
- Registration Number
- NCT01994070
- Lead Sponsor
- University of British Columbia
- Brief Summary
Atrial fibrillation (AF) is the most common type of irregular heartbeat in emergency department (ED) patients. If the irregular heartbeat has been present for less than 48 hours, there is a chance that emergency treatment can convert the heartbeat into normal rhythm.
There are currently two options for accomplishing this; both are widely and safely used in EDs. Each has its advantages and disadvantages. This study will compare the two methods. (1) Patients are given an intravenous medication called procainamide; this converts patients into a normal heart rhythm around 50% of the time. (2) Patients are sedated (put to sleep with a general anesthetic) for about ten minutes, while an electrical current is conducted across the chest; this converts patients into a normal heart rhythm around 90% of the time.
Procainamide can cause low blood pressure in about 10% of patients; this is usually corrected by administering intravenous fluids. Sedation can cause low blood pressure in about 10% of patients, and breathing trouble in about 10% of patients; this is usually corrected by administering intravenous fluids, and administering more oxygen, respectively. In thousands of patients studied around the world, there does not appear to have been a reported stroke or death as a result of these procedures.
A physician will choose one method, but if it fails, will move to the next method. There are thus two options. (1) Chemical conversion, followed by electrical conversion; and (2) Electrical cardioversion, followed by chemical cardioversion. These options both have a 90%+ chance of converting AF into a normal heart rhythm. However, the investigators believe that an electrical-chemical sequence will be faster than a chemical-electrical sequence, while both will be equally safe.
If patients agree to take part in the study, they will be randomized to one of the two options. They will have their breathing, oxygen levels, blood pressure, and heartbeat monitored for their entire ED stay.
The investigators plan to enrol 86 patients at five hospitals over the course of about one year. The primary outcome of ED length-of-stay, as well as secondary outcomes, such as conversion to normal rhythm, and adverse events (such as trouble breathing or low blood pressure) will be documented. In addition, an investigator will contact you at three and thirty days after your visit to make sure that there are no problems. Importantly, although the principal and site investigators will be aware of the primary outcome, attending emergency physicians who actually provide patient care will NOT be aware of the primary outcome--otherwise this could bias patient management.
When the study is finished, the results will be given to the writing committee merely as the "A" and "B" arms, and not specified as either the "chemical-first" or "electrical-first" arms. The writing committee will compose two manuscripts, (1) assuming that "A" is the "chemical-first" arm and "B" the "electrical-first" arm, and (2) assuming that "A" is the "electrical-first"arm, and "B" the "chemical-first" arm. After both manuscripts have been approved by all authors, the blinding will be removed and only the correct manuscript submitted for publication.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 86
- Must have an abnormal heart rhythm diagnosed as AF for less than 48 hours.
- Be eligible for cardioversion (in the judgment of the study doctor).
- Are on the appropriate blood thinner medications.
- Have systolic blood pressure (SBP) above 90 mmHg and less than 160 mmHg and diastolic blood pressure (DBP) less than 95 mmHg at screening and baseline.
- Are adequately hydrated (in the judgment of the study doctor) and have a normal saline intravenous established and it is working properly.
- Must have a body weight between 45 and 136 kg inclusive (99 and 300 lbs).
- Be able and willing to give informed consent.
- Pregnant or nursing a child
- Are diagnosed with any other serious lung, liver, metabolic, kidney, gastrointestinal, central nervous system, or psychiatric disease, infection, having a fever, end stage disease states, or any other diseases that could interfere with the conduct of this study. Your study doctor will confirm this with you.
- Have an infection or fever
- Are allergic to procainamide (the chemical conversion agent) or propofol (the sedative agent)
- Are participating in another drug study or have received an experimental drug within 30 days prior to screening in this study
- Are not currently living in the Vancouver Coastal Health Region
- Are unable or unwilling to be contacted at 30 days by one of the study doctors or study staff to determine 30-day outcomes
- Are unwilling to sign the informed consent form
- Are unable to speak English
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Chemical-first Chemical-first Patients in atrial fibrillation for less than 48 hours will be administered intravenous procainamide (chemical cardioversion) to attempt conversion to normal sinus rhythm. If procainamide is required, physicians will be informed as follows: "50% of patients convert to normal sinus rhythm within one hour and 90% of patients convert within two hours." Physicians can then proceed at their discretion. If this does not succeed, patients will be administered procedural sedation and analgesia and an electrical current applied across their chest (electrical cardioversion) to attempt conversion to normal sinus rhythm. Electrical-first Electrical-first Patients in atrial fibrillation for less than 48 hours will be administered procedural sedation and analgesia and an electrical current applied across their chest (cardioversion) to attempt conversion to normal sinus rhythm. If this does not succeed, they will be given intravenous procainamide (chemical cardioversion). If procainamide is required, physicians will be informed as follows: "50% of patients convert to normal sinus rhythm within one hour and 90% of patients convert within two hours." Physicians can then proceed at their discretion.
- Primary Outcome Measures
Name Time Method Length-of-stay up to 12 hours Length of stay is defined as the time from patient randomization to discharge from the emergency department.
- Secondary Outcome Measures
Name Time Method Adverse events up to 12 hours after randomization * Sentinel risk
* Oxygen desaturation \> 60 seconds or \< 75%
* Apnea \> 60 seconds
* Shock
* Cardiac arrest
* Minor risk
* Oxygen desaturation \< 60 seconds
* Apnea \< 20 seconds
* Airway obstruction
* Failed sedation
* Allergic reaction, no anaphylaxis
* Bradycardia
* Tachycardia
* Hypotension
* Hypertension
* Ventricular arrhythmia
* Seizure
* Minimal risk
* Vomiting / retching
* Subclinical respiratory depression
* Muscle rigidity
* Hypersalivation
* Paradoxical response
* Recovery agitation
* Prolonged recovery
Note: All potential adverse events will be referred to a central safety committee. Members of this committee will be blinded to patient treatment group and blinded to 3- and 30-day outcomes. The central safety committee will determine whether an adverse event occurred and categorize the severity.
Trial Locations
- Locations (1)
St Paul's Hospital
🇨🇦Vancouver, British Columbia, Canada