Use of Phenoxybenzamine [PBZ] IV to Assist High Flow Low Pressure Perfusion [HFLPP] on Cardio-pulmonary Bypass

Use of Phenoxybenzamine [PBZ] IV to Assist High Flow Low Pressure Perfusion [HFLPP] on Cardio-pulmonary Bypass in Infants and Children With Congenital Heart Disease and to Assist Steady State Alfa-blockade in the Intensive Care Phase

Cardiopulmonary bypass [CPB] in small size bodies can result in decreased peripheral perfusion. This results in anaerobic metabolism as evidenced by lactic acidosis. High flow perfusion results in systemic hypertension which is accentuated by moderate hypothermia commonly used during cardiopulmonary bypass. Phenoxybenzamine [PBZ] is an arteriolar vasodilator that acts by irreversibly blocking the alpha adrenergic receptors. It causes vasodilatation allowing high flow, low pressure CPB. It has been used extensively outside US in Canada, Europe and Australia. In the US oral PBZ is FDA approved, whereas intravenous PBZ is only available as an investigational drug

Study Overview

• Status: Terminated
• Conditions: Cardiopulmonary Bypass; Congenital Heart Surgery
• Intervention / Treatment: Drug: Phenoxybenzamine

Detailed Description

Background Cardiopulmonary bypass [CPB] in small size bodies can result in decreased peripheral perfusion. This results in anaerobic metabolism as evidenced by lactic acidosis. High flow results in systemic hypertension which is accentuated by moderate hypothermia commonly used during cardiopulmonary bypass. Phenoxybenzamine [PBZ] is an arteriolar vasodilator that acts by irreversibly blocking the alpha adrenergic receptors. It causes vasodilatation allowing high flow, low pressure CPB. It has been used extensively outside US in Canada, Europe and Australia. In the US oral PBZ is FDA approved, whereas intravenous PBZ is only available as an investigational drug. At the Cleveland Clinic this medication has been used under this protocol since 1994 in >1000 without any significant or serious adverse outcome. The drug is also used at Texas Children's Hospital, Hospital for Sick Children in Toronto, Children's Hospital of Wisconsin and a number of centers throughout Europe, Australia and Asia. The drug has helped reduce the mortality of children undergoing cardiopulmonary bypass.

The theoretic benefit of PBZ in this patient population is uniform and smooth reduction fo systemic vascular resistance in the perioperative period. This uniform systemic vasodilation allows low pressure, high flow systemic perfusion on cardiopulmonary bypass. We feel that this ins in part responsible for improved outcome after cardiopulmonary bypass, including less end-organ edema formation and dysfunction. Due to experience in this and other centers we strongly believe that the use of PBZ in the bypass management protocol of these patients represents the state-of-the-art and not an experimental investigation. Since in the US the drug is not available except as an investigational drug, we have been required to use it as an investigational new drug [IND] PBZ[oral] is currently used in the US for the management of pheochromocytoma. It has a proven track record and known to be safe. Use in a large number of patients worldwide has shown no serious side-effects except hypotension [which is an effect indeed] requiring norepinephrine [an alpha agonist commonly used after cardiopulmonary bypass in these patients anyway].

Patients

The following patients are candidates for receiving PBZ for HFLPP. These include:

1. All patients under 16 kg.
2. Those patients between 16-18 kg whose pre bypass hemoglobin is <16 g/dl
3. All patients are less than 18 years of age.

Use of Phenoxybenzamine:

Loading dose given at the time of going on CPB:

• For patients with obstructing lesions on systemic side:

  • 0.25 mg/kg dose in the bypass circuit
  • None intravenous

• For patients without obstructing left sided lesions:

  • 0.5 mg/kg in the bypass circuit
  • 0.5 mg/kg I.V. at cannulation

Maintenance dose given in the post-operative period:

• 0.3 mg/kg I.V. every 8 hours till oral intake is started or for first 48 hours
• 0.3 mg/kg P.O. every 8 hours for next 24 hours
• 0.15 mg/kg P.O. every 8 hours for next 24 hours and then stop
• Hold PBZ if the patient is on norepinephrine infusion or the mean arterial pressure is lower than that allowed for the age group

• Do not use maintenance dose in the following patients unless they are on maximum dose of sodium nitroprusside infusion and still hypertensive:

  • Norwood patients
  • Fontan patients
  • Patients with residual left ventricular obstructive lesions - don't use at all in the post operative period

Data collected and monitored for the purpose of this study only:

Demographic information, side effects and mortality data would be recorded and kept in a password protected computer in a secure-access-only physician office. Only composite data without individual identifiers will be reported to the IRB and FDA. No publication is planned from this study and no follow-up will be done after the patient is discharged from the hospital.

Side effects to be monitored:

• Hypotension requiring norepinephrine in excess of usual dose [0.2 micrograms/kg/min]
• Death from such hypotension in the absence of other causes [such as bleeding, sepsis]
• Effects occuring within 12 hours of I.V. dose administration or within 24 hours of P.O. dose administration
• Any unanticipated or unusual side effects [none noted since 1994] Consent Informed consent would be obtained from the parents/guardians of all patients. Assent will be obtained from children of >7 years age.

• Study Type: Interventional
• Enrollment (Actual): 87
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: No older than 18 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

Patients

The following patients are candidates for receiving PBZ for HFLPP. These include:

1. All patients under 16 kg.
2. Those patients between 16-18 kg whose pre bypass hemoglobin is <16 g/dl
3. All patients are less than 18 years of age

Exclusion Criteria:

1. Those with bloodless prime in Cardiopulmonary bypass circuit
2. Age > 18years
3. Wt. >16 kg

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: 1; Treatment Group

Drug: Phenoxybenzamine; Use of Phenoxybenzamine: Loading dose given at the time of going on CPB: For patients with obstructing lesions on systemic side:0.25 mg/kg dose in the bypass circuitNone intravenous; For patients without obstructing left sided lesions:0.5 mg/kg in the bypass circuit0.5 mg/kg I.V. at cannulation Maintenance dose given in the post-operative period: 0.3 mg/kg I.V. every 8 hours till oral intake is started or for first 48 hours; 0.3 mg/kg P.O. every 8 hours for next 24 hours; 0.15 mg/kg P.O. every 8 hours for next 24 hours and then stop; Hold PBZ if the patient is on norepinephrine infusion or the mean arterial pressure is lower than that allowed for the age group; Other Names: Dibenzyline

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants Achieving High Flow Low Pressure on Cardiopulmonary Bypass	Percentage of patients who achieved high flow, low pressure on cardiopulmonary bypass	From time of cardiopulmonary bypass initiation until the time that high flow, low pressure on cardiopulmonary bypass was achieved, assessed up to 1 hour

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mortality	Percentage of patients who died within 30 days of the procedure	30 days

Collaborators and Investigators

• Sponsor: The Cleveland Clinic
• Investigators: Principal Investigator: Muhammad A Mumtaz, MD, The Cleveland Clinic

Study record dates

Study Major Dates

• Study Start: June 1, 2006
• Primary Completion (Actual): February 1, 2009
• Study Completion (Actual): February 1, 2009

Study Registration Dates

• First Submitted: February 11, 2008
• First Submitted That Met QC Criteria: February 11, 2008
• First Posted (Estimate): February 22, 2008

Study Record Updates

• Last Update Posted (Actual): December 19, 2017
• Last Update Submitted That Met QC Criteria: November 20, 2017
• Last Verified: November 1, 2017

More Information

Terms related to this study

• Keywords: Cardiopulmonary bypass; Phenoxybenzamine; Congenital heart surgery
• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Adrenergic Antagonists; Adrenergic Agents; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Antihypertensive Agents; Vasodilator Agents; Adrenergic alpha-Antagonists; Phenoxybenzamine
• Other Study ID Numbers: CCF IRB # 06-494