Modeling of Amiodarone Effect on Heart Rate Control in Critically Ill Patients With Atrial Tachyarrhythmias
NCT ID: NCT03413150
Last Updated: 2019-09-26
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
COMPLETED
Total Enrollment
80 participants
Study Classification
OBSERVATIONAL
Study Start Date
2007-01-31
Study Completion Date
2012-04-30
Brief Summary
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Aims Amiodarone is the gold-standard medication to control heart rate in critically ill patients with atrial tachyarrhythmias (ATs); however, effective doses and covariates influencing its efficacy remain unknown. The investigators therefore performed pharmacodynamic modeling of heart rate reduction induced by amiodarone in these patients. Methods and Results This observational study included 80 consecutive severely ill patients receiving amiodarone to treat ATs. A total of 1348 time-heart rate observations with 361 amiodarone dose administrations were analyzed during a period of up to 6 days after hospital treatment initiation using a nonlinear mixed-effect model. Pretreatment with amiodarone before intensive care administration, paroxysmal versus persistent AT, catecholamine infusion, and fluid and magnesium loading were among the covariates assessed in the model. In case of paroxysmal AT in a patient not pretreated with amiodarone, a 300 mg intravenous loading dose combined with an 800 mg oral dose on the first day, followed by 800 mg/day orally for 4 days was effective in achieving a heart rate between 80 and 115 bpm within the first day, and to maintain it during the next 4 days. Corresponding doses were twice as high in patients with persistent AT. Use of intravenous magnesium (p\\0.02) and fluid loading (p\\0.02) was associated with an earlier and greater heart rate decrease, while use of dobutamine had an opposite influence (p\\0.05). Conclusions In critically ill patients with AT, the dose of amiodarone required to control heart rate is influenced by the type of AT and by other easily measurable conditions which may allow better individualization of amiodarone dosing.
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Detailed Description
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Conditions
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Atrial Fibrillation
Atrial Tachycardia
Study Design
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Observational Model Type
COHORT
Study Time Perspective
RETROSPECTIVE
Study Groups
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severely ill patients receiving amiodarone for ATs
cohort study was conducted from January 2007 to April 2012 in the 18-bed medical ICU of a tertiary teaching hospital.Data were extracted from the files of 80 consecutive critically ill patients who had received at least one dose of amiodarone to treat or prevent atrial tachycardia during their hospitalization in the ICU.
Amiodarone
Intervention Type
DRUG
Data were extracted from the files of 80 consecutive critically ill patients who had received at least one dose of amiodarone to treat or prevent AT during their hospitalization in the ICU.
Interventions
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Amiodarone
Data were extracted from the files of 80 consecutive critically ill patients who had received at least one dose of amiodarone to treat or prevent AT during their hospitalization in the ICU.
Intervention Type
DRUG
Eligibility Criteria
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Inclusion Criteria
* critically ill patients who had received at least one dose of amiodarone to treat or prevent AT during their hospitalization in the ICU.
Exclusion Criteria
* Patients with paced rhythm or incomplete charts were excluded
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Groupe Hospitalier Pitie-Salpetriere
OTHER
Sponsor Role
lead
Responsible Party
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Joe Elie Salem
MD
Responsibility Role
PRINCIPAL_INVESTIGATOR
References
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Other Identifiers
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CIC1421-17-13
Identifier Type: -
Identifier Source: org_study_id
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