Prospective Observational Cohort Study of Fetal Atrial Flutter & Supraventricular Tachycardia (FAST Registry)

Edgar Jaeggi

Status: Completed

Conditions: Tachycardia, Supraventricular; Tachycardia, Reciprocating; Tachycardia, Atrial Ectopic; Atrial Flutter; Fetal Hydrops; Tachycardia Atrial; Tachycardia, Paroxysmal; Tachycardia, Atrioventricular Nodal Reentry

Treatments: Other: Prospective observational cohorts

Study type: Observational

Funder types: Other

Identifiers

NCT03376438

1000048953

Details and patient eligibility

About

The FAST Trial Registry is a prospective observational cohort study of fetuses with a new diagnosis of atrial flutter (AF) or supraventricular tachycardia (SVT) that is severe enough to consider prenatal treatment (see eligibility criteria below). Aims of the Registry include to establish a large clinical database to determine and compare the efficacy and safety of different prenatal treatment strategies including observation without immediate treatment, transplacental antiarrhythmic fetal treatment and direct fetal treatment from the time of tachycardia diagnosis to death, neonatal hospital discharge or to a maximum of 30 days after birth.

Full description

Few studies are specifically designed to address health concerns relevant during pregnancy. The consequence is a lack of evidence on best clinical practice. This includes mothers and their babies when pregnancy is complicated by an abnormally fast heart rate up to 300 beats per minute due to supraventricular tachyarrhythmia (SVA) in the unborn baby (fetus). Although fetal SVA, including AF and other forms of SVT, is the most common cause of intended in-utero fetal therapy, our knowledge of drug effects on the baby and the co-treated mother is still limited. The Fetal Atrial Flutter and Supraventricular Tachycardia (FAST) Therapy Trial is a prospective multi-center trial to address this knowledge gap in order to guide future patient management to the best of care.

FAST Trial components include:

1. A prospective Registry (FAST Registry; see this document) as well as
2. Three prospective Randomized Clinical Trials (FAST RCTs; see ClinicalTrials.gov #NCT02624765).

The FAST Registry is a prospective observational cohort study to determine the impact of different prenatal treatment strategies on patients diagnosed with fetal AF without hydrops, AF with hydrops, SVT without hydrops, and SVT with hydrops. All management decisions including the choice of antiarrhythmic medication or the decision to observe without treatment are at the discretion of the treating physician. The primary outcome measure will be the proportion of term deliveries of live-born children with a normal cardiac rhythm. Secondary outcome measures include the efficacy of 1st line, 2nd line, 3rd line, and maintenance drug therapy in controlling the different arrhythmias prior to birth and patient safety.

Participation of a site in the FAST Registry requires experience with the perinatal management of fetal AF and SVT, local REB/IRB approval and an executed legal contract with the Hospital for Sick Children, Toronto.

Participation of a patient in the FAST Registry requires that all inclusion and none of the exclusion criteria are fulfilled (see below). Enrollment is possible within 2 days of the arrhythmia diagnosis and the initial management decision.

Enrollment: 330 patients

Sex: Female

Ages: 16 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Mother has provided written informed consent to participate

2. Fetal AF or SVT with or without hydrops

3. Tachyarrhythmia that is significant enough to justify immediate transplacental pharmacological treatment:

   • Tachycardia ≥ 180 bpm during at least 10% of observation time of 30 minutes or longer
   • Tachycardia ≥ 170 bpm during +100% of time (≤ 30 0/7 weeks of gestation)
   • Tachycardia ≥ 280 bpm (irrespective of SVA duration)
   • SVT with fetal hydrops (irrespective of duration)

4. Gestational age <36 0/7 weeks at time of enrollment

5. Singleton Pregnancy

6. Healthy mother with ± normal pre-treatment cardiovascular findings:

   • ECG within normal range (sinus rhythm; QTc ≤ 0.47; PR ≤ 0.2 sec; QRS: ≤ 0.12 sec; insignificant anomalies; isolated premature beats; isolated complete right bundle
   • Maternal resting heart rate ≥ 50 bpm
   • Maternal systolic BP ≥ 85 mmHg

Exclusion criteria

1. Primary delivery for postnatal cardioversion
2. Antiarrhythmic fetal treatment for more than 2 days at time of enrollment
3. Any maternal-fetal conditions associated with high odds of premature delivery and/or death
4. History of significant maternal heart condition (open heart surgery; sick sinus syndrome; long QT, Brugada syndrome; ventricular tachycardia; WPW syndrome; high-degree heart block; cardiomyopathy)

Trial design

330 participants in 1 patient group

Prospective observational cohorts

Description:

1) Atrial flutter without fetal hydrops; 2) Atrial flutter with fetal hydrops; 3) Supraventricular tachycardia without fetal hydrops; and 4) Supraventricular tachycardia with fetal hydrops

Treatment:

Other: Prospective observational cohorts