Title

Use of Nesiritide (BNP) in Kidney Function in Patients With Congestive Heart Failure (CHF) and Kidney Failure
Efficacy of Intra-renal Infusion of BNP in Enhancing Renal Function in Human CHF With Cardiorenal Syndrome: A Pilot Study
  • Phase

    Phase 1/Phase 2
  • Study Type

    Interventional
  • Intervention/Treatment

    nesiritide ...
  • Study Participants

    4
The objective of this study is to determine the safety and effectiveness of intrarenal administration of brain natriuretic peptide (BNP) in improving renal function as measured by glomerular filtration rate (GFR) and sodium excretion in patients hospitalized with acute congestive heart failure (CHF) and deterioration of kidney function (cardiorenal syndrome).
Study Started
Dec 31
2005
Primary Completion
Mar 31
2010
Study Completion
Mar 31
2010
Results Posted
Oct 17
2012
Estimate
Last Update
Nov 06
2017

Drug Nesiritide

Nesiritide 0.005 ug/kg/min IV for 6 hours, then to 0.01 ug/kg/min for 6 hours then to 0.02ug/kg/min for 6 hours then to 0.03 ug/kg/min for the last 6 hours.

  • Other names: Natrecor, brain natriuretic peptide (BNP)

Nesiritide Experimental

Subjects received an intrarenal infusion of nesiritide at 0.005 microgram/kg/min for 6 hours, 0.01 microgram/kg/min for 6 hours, 0.02 microgram/kg/min for 6 hours, and 0.03 microgram/kg/min for 6 hours.

Criteria

Inclusion Criteria

Age 18 years and older
Clinical diagnosis of class III-IV CHF requiring hospitalization
Current acute CHF decompensation
Systolic BP > 90 mmHg
Stable cardiac rhythm
Estimated creatinine clearance by the Cockcroft-Gault equation of less than or equal to 60 mL/min.
Worsening renal function after greater than or equal to 24 hours of standard therapy as defined by a plasma creatinine concentration greater than their admission of 0.3 mg/dL and a 10% increase from hospital admission creatinine OR creatinine which remains at 0.3 mg/dL and 10% increase from baseline draw done within 4 weeks of hospitalization
Ability to provide informed consent

Exclusion Criteria

Patients needing emergency coronary revascularization or those who may have rapidly changing cardiac function (i.e., patients with acute myocardial infarction or shock)
Peritoneal or hemodialysis within 90 days or anticipation that dialysis or ultrafiltration of any form will be required during the study period
Systolic blood pressure < 90 mmHg or cardiogenic shock
Requirement of pressors for maintenance of blood pressure
Intra-aortic blood pump use
History of significant uncorrected renal artery stenosis as defined by >50% stenosis
Severe aortic or mitral stenosis or significant LV outflow tract obstruction
Pregnant or nursing women
Prisoners
Contraindication to nesiritide
Contraindication to heparin
Cause of acute renal dysfunction can be reasonably ascribed to factors other than heart failure or its treatment
Inability to have NSAID dose held for up to 30 hours, if being treated with these medications
Ongoing treatment with calcineurin inhibitors (cyclosporine or tacrolimus)
Administration of radiocontrast medium within 7 days of enrollment or anticipated use of such agents during the study (other than the minimal contrast required to place the renal infusion catheter)
Known bleeding diathesis
Known condition that would increase the likelihood of vascular perforation or trauma, dissection such as Marfan's syndrome, cystic medial necrosis, abdominal or thoracoabdominal aortic dissection, mycotic aneurysm, abdominal aneurysm, thoracoabdominal aneurysm, renal artery aneurysm, thoracic aneurysm involving the visceral region of the aorta, and severe calcification in the area of the renal arteries
Solitary kidney or solitary functioning kidney
Iodine allergy

Summary

Nesiritide

All Events

Event Type Organ System Event Term Nesiritide

Change in Glomerular Filtration Rate (GFR) at 24 Hours

Kidney function was to be measured by GFR determined by iothalamate clearance. GFR describes the flow rate of filtered fluid through the kidney measured in milliliters per minute per 1.73 m^2 of body surface area. A lower GFR means the kidney is not filtering normally. An estimated GFR of less than 60 mg/min/1.73 m^2 of body surface area is considered to be impaired kidney function.

Nesiritide

Change in Urinary Sodium Excretion at 24 Hours

The fractional excretion of sodium (FENa) measures the percent of filtered sodium that is excreted in the urine. This calculation is widely used to help differentiate prerenal disease (decreased renal perfusion) from acute tubular necrosis (ATN) as the cause of acute kidney injury (AKI, formerly called acute renal failure).

Nesiritide

Age, Categorical

Region of Enrollment

Sex: Female, Male

Overall Study

Nesiritide

Drop/Withdrawal Reasons

Nesiritide