Analysis of Adenosine on Sinus and Atrioventricular Nodal Conduction in the Pediatric Transplanted Heart
Information source: Columbia University
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Sinus Bradycardia; Atrioventricular Block
Intervention: Adenosine (Drug); Cardiac catheterization (Procedure)
Phase: Phase 1
Status: Not yet recruiting
Sponsored by: Columbia University Official(s) and/or principal investigator(s): Eric S Silver, MD, Principal Investigator, Affiliation: Columbia University
Overall contact: Eric S Silver, MD, Phone: 212-342-0525, Email: es2301@columbia.edu
Summary
Heart transplants save the lives of nearly 500 children in heart failure per year. Columbia
is one of the largest pediatric heart transplant centers in the world, averaging 25
transplants per year, and providing ongoing care to nearly 250 children with transplanted
hearts. After transplant, children are at increased risk to develop sudden onset of
abnormally fast heart rates. This research project will study adenosine, a medication that
is routinely used to slow fast heart rates in non-transplanted children (i. e. normal
hearts), and its effects on the transplanted heart. Adenosine is often not used in patients
with transplanted hearts because, based on prior limited research in adult patients, the
standard adult dose may have a longer medication effect, producing a slower heart rate for
an undesirable period of time. However, the current alternatives to adenosine treatment are
either inappropriate for the pediatric age range, or have increased risk of unwanted side
effects. This research project will answer two questions: is adenosine safe to give a child
who has had a heart transplant, and will it be effective in treating the fast heart rate?
All pediatric heart transplant patients undergo regular heart testing, known as a cardiac
catheterization, one or more times per year. Three days before testing, participants will
be asked to stop a regular medication, dipyridamole, because it slows the breakdown of
adenosine in the body, and may increase its effects. (Of note, all patients that are on
dipyridamole are also on aspirin, which gives a second line of heart protection, and will
not be stopped.) After regular cardiac catheterization, all patients will already have
intravenous (IV) access to give medication. Also, this setting allows the opportunity to
have a back-up pacing catheter in the heart, ensuring that there will not be a longer than
desired effect from the medication. Adenosine will be given per a low-dose protocol until
either the medication effect is seen or the maximum dose is reached. There will be no
difference in procedure recovery period time, and patients will resume regular home
medications after finishing the test. As Columbia is one of largest pediatric heart
transplant centers in the world, studying the effects of adenosine at low doses will benefit
the investigators population greatly, either to find a new recommended medication dose, or
to provide evidence that this medication is truly inadvisable for the investigators
patients.
Clinical Details
Official title: Prospective Analysis of Low-Dose Adenosine on Sinus and Atrioventricular Nodal Conduction in the Pediatric Transplanted Heart
Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Incidence of sinus bradycardia or atrioventricular block with low-dose adenosine administration that is greater than 12 seconds and requires hemodynamic intervention (ventricular escape pacing).
Secondary outcome: Prevalence of inducing atrioventricular block (defined as a single non-conducted P wave) at adenosine doses lower than suggested starting dose (100µg/kg) in PALS algorithm.
Detailed description:
After cardiac catheterization, the study protocol will begin with 12. 5µg/kg of adenosine
(one eighth the recommended starting clinical dose), and will double to 25µg/kg, 50µg/kg,
100µg/kg and finally 200µg/kg (not to surpass the total maximum dose of 12mg). A pacing
catheter will be placed within the right ventricle prior to medication administration.
Escalating doses will stop if ventricular pacing is required due to a ventricular pause
greater than 12 seconds or if atrioventricular block is demonstrated with a ventricular
pause less than 12 seconds. If there is no prolonged pause requiring pacing and no
demonstration of medication effect the subsequent dose will be given.
Progression to the next dose of the adenosine will depend on both the primary and secondary
study outcomes. If the adenosine dose produces clinically significant bradycardia (> 12
seconds), ventricular pacing will be used to maintain cardiac output, and the dose will be
considered unsafe to use clinically and testing will end for that patient. If the adenosine
dose produces atrioventricular block but with a pause of less than 12 seconds (thus does not
require pacing), the dose will be considered effective and the study will terminate as well.
However, if the adenosine dose does not produce atrioventricular block or require pacing
intervention, the dose will be considered safe but ineffective and the study will progress
to the next higher dose. Before dose progression, the study will pause for additional 30
seconds to ensure complete adenosine metabolism, as the half-life of adenosine is less than
10 seconds and does not exhibit cumulative effects. The subsequent dose will then be
administered and the ECG observed for clinically significant bradycardia and
atrioventricular block. This will be repeated until clinically significant bradycardia
and/or atrioventricular block is observed, or up to the final 200μg/kg (not to surpass the
total maximum of 12mg) dose.
Eligibility
Minimum age: 6 Months.
Maximum age: 25 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patients who have undergone a heart transplantation and who receive their routine
care at the Morgan Stanley Children's Hospital of New York, Columbia University
Medical Center
Exclusion Criteria:
- Patients admitted to the inpatient heart failure team
- Patients present for their first outpatient catheterization after new transplant
- Abnormal hemodynamics concerning for acute rejection
- Patients present for follow up of rejection (last biopsy positive)
- Ingested methylxanthine-containing foods that day
- Patients taking oral dipyridamole and did not discontinue it 3 days prior to testing
- Prior transplant history of coronary artery vasculopathy with this allograft or
concern for abnormal coronary vasculature by angiography on the day of the
catheterization
- Patients taking carbamazepine (may potentiate adenosine effect)
- Patients with known conduction disease (first, second or third degree
atrioventricular block) and/or with pre-existing sinus node dysfunction (based on
pre-existing ECG, Holter or inpatient telemetry)
- Patients/guardians unable to give consent in English
Locations and Contacts
Eric S Silver, MD, Phone: 212-342-0525, Email: es2301@columbia.edu Additional Information
Starting date: July 2015
Last updated: June 3, 2015
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