IP Library Granted Patent US 7,758,900
Granted Patent B2
US 7,758,900 · App. 11/678,525 · Granted Jul 20, 2010

Multi-part substitution infusion fluids and matching anticoagulants

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Quick Facts
Patent No.
US 7,758,900
App. No.
11/678,525
Granted
Jul 20, 2010
Kind
B2
Abstract

A multi-part substitution infusion fluid for an extracorporeal blood treatment and methods for using same are provided. Generally, the multi-part substitution fluid comprises a first solution composed of electrolites but without divalent cations and a second solution comprising divalent cations. Another embodiment includes a third solution comprising a matching citrate/citric acid anticoagulant. The described methods of using the multi-part substitution infusion fluids significantly reduce risks associated with various extracorporeal blood treatments.

Claims (13)

1. A three part system for extracorporeal blood treatment comprising:

a first aqueous infusion fluid comprising sodium ion, potassium ion, chloride ion and phosphate ion;

a second aqueous infusion fluid comprising calcium ion and from about 2.5 mmol/L to about 20 mmol/L of magnesium ion; and

a citrate anticoagulant solution comprising from about 19 mmol/L to about 135 mmol/L of citric acid and from about 80 mmol/L to about 550 mmol/L of trisodium citrate.

2. The three part system for extracorporeal blood treatment according to claim 1 , wherein the second aqueous infusion fluid has from about 10 mmol/L to about 35 mmol/L of the calcium ion.

3. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid has from about 70 mmol/L to about 130 mmol/L of the sodium ion.

4. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid has from about 0.01 mmol/L to about 5 mmol/L of the potassium ion.

5. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid has from about 100 mmol/L to about 150 mmol/L of the chloride ion.

6. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid has from about 0.01 mmol/L to about 1.5 mmol/L of the phosphate ion.

7. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid further comprises from about 2 mmol/L to about 11.5 mmol/L of glucose.

8. The three part system for extracorporeal blood treatment according to claim 7 , wherein the second aqueous infusion fluid further comprises from about 30 mmol/L to about 100 mmol/L selected from a group consisting of sulphate, gluconate, glubionate and chloride ion.

9. The three part system for extracorporeal blood treatment according to claim 1 , wherein the first aqueous infusion fluid further comprises amino acids and/or trace elements.

10. The three part system for extracorporeal blood treatment according to claim 1 further comprising ions selected from a group consisting of iron, zinc, copper and manganese.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2014
From: BAXTER HEALTHCARE SA; BAXTER INTERNATIONAL INC.
To: NIKKISO CO., LTD.
Reel/Frame 032210/0629 →
CHANGE OF ASSIGNEE ADDRESS Recorded Jun 14, 2010
From: BAXTER HEALTHCARE S.A.
To: BAXTER HEALTHCARE S.A.
Reel/Frame 024532/0126 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2009
From: EDWARDS LIFESCIENCES CORPORATION
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE S.A.
Reel/Frame 023660/0315 →