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Method for stabilizing blood pressure in hemodialysis subjects

a hemodialysis and blood pressure technology, applied in the direction of biocide, plant growth regulators, cyclic peptide ingredients, etc., can solve the problems of reducing the efficiency of fluid removal during treatment, affecting the effect of hemodialysis, and avoiding the abandonment of one of the principal objectives of hemodialysis, so as to reduce excess extracellular fluid, maintain blood pressure, and facilitate the effect of reducing excess extracellular fluid

Inactive Publication Date: 2007-09-13
INTRADIALYTIC PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015] The present invention provides a rational method for reducing excess extracellular fluid in a subject undergoing hemodialysis by administering a vasopressin receptor agonist (e.g., a V-1 receptor agonist, e.g., a V1a receptor agonist) to the subject in an effective amount and thereby maintaining blood pressure during hemodialysis in order to facilitate reducing excess extracellular fluid in the subject.

Problems solved by technology

In addition, hypotensive events impede the efficiency of fluid removal during the treatment.
Although hypotension is a frequent complication on hemodialysis, hypertension is frequent between dialysis treatments.
However, this solution abandons one of the principal objectives of hemodialysis, the removal of excess water ingested between treatments.
When AVP fails to be secreted by bororeflex-mediated stimulation, hypotension and inappropriate vasodilation ensue.
As baroreflex-mediated secretion requires intact autonomic afferent pathways, many patients on hemodialysis may have insufficient AVP release in response to decreased circulating blood volume.

Method used

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  • Method for stabilizing blood pressure in hemodialysis subjects
  • Method for stabilizing blood pressure in hemodialysis subjects
  • Method for stabilizing blood pressure in hemodialysis subjects

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0054] This Example describes the procedure to utilize vasopressin to stabilize blood pressure during hemodialysis and facilitate removal of excess extracellular fluid.

[0055] Description of Study Procedures

[0056] Healthy controls and patients with end-stage renal disease (e.g. defined as creatinine clearance of less than 10 min) were studied. The studies were conducted on regularly scheduled hemodialysis days. The duration of hemodialysis remained the same as that prescribed prior to the study period. AVP or placebo (normal saline) was administered at a constant rate of 0.15, 0.3 or o.6 mU / kg / min through a venous line (controls) or through the venous limb of the dialysis circuit (hemodialysis patients). The patient's hemodialysis prescription remained unchanged except for the administration of AVP or placebo. Intradialytic hypotension was treated in the customary manner with the infusion of isotonic and hypertonic fluids.

[0057] Serum AVP levels were determined by a radioimmunoass...

example 2

[0090] This Example describes a procedure to test that long term administration of vasopressin during hemodialysis results in an improvement of patient's hypertension.

[0091] Experimental Methods and Design

[0092] Data Collection

[0093] This is a randomized, double-blinded, placebo-controlled trial to determine the effect of AVP administration during dialysis on blood pressure.

[0094] Eligible patients are stratified for purposes of randomization into high blood pressure (systolic blood pressure or SBP 140-170) and very high blood pressure (SBP>170) groups, as well as diabetic and non-diabetic groups.

[0095] Patients are randomized to receive normal saline with AVP (treatment) or normal saline alone (placebo) during dialysis. A randomization protocol is used to determine whether the drug or placebo is to be administered. The identity of the substance being administered remains unknown to both the clinical staff and the patient. To insure that the nursing personnel does not become bi...

example 3

[0104] Methods

[0105] Patients. Studies were performed at the Acute Dialysis Unit of the New York Presbyterian Hospital and at the Columbia University Dialysis Center, both located at Columbia Presbyterian Medical Center. All patients gave informed consent to participate in the study, which was approved by the Institutional Review Board of Columbia University.

[0106] All patients were studied at regularly scheduled dialysis sessions. Patients underwent conventional hemodialysis with hollow fiber high flux polysulfone dialyzers on volumetric dialysis machines (Cobe Centrysystem 3, Gambro Renal Care Products, Inc., Lakewood, Colo.). Dialysis times were 3.5-4.5 hours. Blood flow was 300-400 mL / min and dialysate was delivered at 600 mL / min. The dialysis bath contained potassium, 2 mEq / L; calcium, 2.5 mEq / L; magnesium, 0.75 mEq / L; and bicarbonate, 40 mEq / L. In those patients who were prescribed dialysate sodium modeling and / or reduced dialysate temperature (35-37° C.) prior to the study,...

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Abstract

The present invention provides a method for regulating blood pressure in a hemodialysis subject using a vasopressin receptor agonist, so as to facilitate removal of excessive extracellular fluid in the subject.

Description

[0001] This patent application claims the benefit of the filing date of U.S. Ser. No. 60 / 450,609, filed Feb. 26, 2003, the contents of all of the foregoing application are incorporated by reference in their entireties into the present patent application. [0002] Throughout this application various publications are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains.FIELD OF THE INVENTION [0003] The present invention provides methods for stabilizing blood pressure, e.g., high blood pressure, in a hemodialysis subject using a vasopressin receptor agonist, e.g., a V-1 receptor agonist. BACKGROUND OF THE INVENTION [0004] Hypertension is the leading cause of cardiovascular disease in patients on hemodialysis. A major contributor to hypertension in these patients is chronic volume expansion. Hemodialysis is often inadequate to re...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/08A61K31/00A61FA61K38/17
CPCA61K38/11A61K38/095
Inventor LANDRY, DONALD W.OLIVER, JUAN A.
Owner INTRADIALYTIC PHARMA
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