Systems and methods for plasma collection
A plasmapheresis system and a method for operating a plasmapheresis system are provided by which a volume of plasma product (i.e., anticoagulated plasma) so that that the targeted volume of pure plasma in the plasma product is determined based on donor-specific characteristics. In particular, the targeted amount of pure plasma to be collected is based on the weight, or the weight and the height, of the donor. The targeted volume of pure plasma to be collected, TVP, may be a multiple of the donors weight. Alternatively, TVP may be a multiple of the donor's total blood volume, TBV, with the TBV of the donor being determined based on the donor's weight and height. A target volume for the plasma product to be collected, TVPP, is established, and separation of whole blood into a plasma component and a second component continues until the volume of plasma product in a collection container equals TVPP.
1. A system for collecting plasma from a donor comprising:
a) a venipuncture needle for withdrawing whole blood from the donor,
b) a blood separator for separating the whole blood into a plasma product and a second blood component comprising red blood cells;
c) a donor line coupled to the venipuncture needle for introducing whole blood from the donor to the blood separator;
d) a first pump for controlling flow through the donor line;
e) an anticoagulant line coupled to an anticoagulant source for combining anticoagulant with the whole blood;
f) a second pump for controlling flow through the anticoagulant line;
g) a touchscreen is provided for receiving input from an operator; and
h) a programmable controller configured to: determine a target volume of plasma product to be collected (TVPP) based on a weight of the donor, or based on a weight and height of the donor, and a percentage of anticoagulant in the target volume of plasma product to be collected (% AC TVPP ) based on a pre-determined anticoagulant ratio (ACR) and a hematocrit (Hct) of the donor, control the system to operate a draw and return cycle to withdraw whole blood from the donor, add anticoagulant to the whole blood at a pre-determined ratio (ACR), separate the anticoagulated whole blood into the plasma product and the second component and to return the second component to the donor, and stop withdrawing whole blood from the donor and initiate a final return of the second blood component when a measured volume of plasma product in a plasma collection container reaches the target volume for plasma product, TVPP.
2. The system of claim 1 , wherein the controller is further programmed to calculate i) a target volume of pure plasma product to be collected (TVP) from the weight of the donor and ii) the percentage of anticoagulant in the target volume of plasma product to be collected, % AC TVPP , based on the pre-determined anticoagulant ratio, ACR, and the hematocrit, Hct, of the donor, wherein the TVPP=TVP/(1−% AC TVPP ).
3. The system of claim 2 , wherein the controller is further programmed to calculate the target volume of pure plasma to be collected, TVP, as a multiple of the weight of the donor.
4. The system of claim 1 , wherein the controller is further programmed to calculate a total blood volume of the donor (TBV) based on the weight and height of the donor, a target volume of pure plasma product to be collected, TVP, as a percentage of the TBV, and the percentage of anticoagulant in the target volume of plasma product to be collected, % AC TVPP , based on the pre-determined anticoagulant ratio, ACR, and the hematocrit, Hct, of the donor, wherein the TVPP=TVP/(1−% AC TVPP ).
5. The system of claim 4 , wherein the controller is further programmed to calculate the total blood volume of the donor, TBV, based on the weight and height of the donor to calculate a body mass index for the donor (BMI) such that TBV=70/sqrt (BMI/22), where BMI=Wt/Ht 2 .
6. The system of claim 4 , wherein the controller is further programmed to calculate the total blood volume of the donor (TBV) based on the weight (Wt), height (Ht) and sex (Male or Female) of the donor such that TBV=(0.3669*Ht 3 )+(0.03219*Wt)+0.6041 for Males and TBV=(0.3561*Ht 3 )+(0.03308*Wt)+0.1833 for Females, where Ht is in meters and Wt is in kilograms.
7. The system of claim 1 , wherein ACR is the ratio of the amount of whole blood to the amount of anticoagulant (ACR=WB/AC), and the controller is further configured to determine the percent of anticoagulant in the target volume of plasma product, % AC TVPP , such that % AC TVPP =1/(1+ACR (1−Hct)).
8. The system of claim 1 , wherein ACR is the ratio of volume of whole blood plus the volume of anticoagulant to the volume of anticoagulant (ACR=(WB+AC)/AC), and the controller is further configured to determine the percent of anticoagulant in the target volume of plasma product, % AC TVPP , such that % AC TVPP =1/(1+(ACR−1)(1−Hct)).