Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f3eef6c65e258fe7aab0db05e116b2db |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M2205-3393 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M2205-3331 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M2205-3334 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3431 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3458 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3675 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3609 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-1611 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3441 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-36224 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-36225 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-341 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3672 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3437 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61M1-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61M1-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61M1-34 |
filingDate |
2019-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7aacb942b3595040be5565998b6e886b |
publicationDate |
2021-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
EP-3842084-A1 |
titleOfInvention |
Apparatus for extracorporeal blood treatment |
abstract |
A CRRT apparatus comprising a filtration unit (2), a blood circuit (17), a blood pump (21), a dialysate line (13) and one or more lines (8; 51; 57; 58; 63; 69; 67; 74) to transfer a respective solution into blood; a fluid source for each of said one or more lines, wherein said solution comprises at least one buffer agent in the form of bicarbonate or bicarbonate precursor. A control unit (12) is configured to receive a patient prescription and to determine a parameter (J<sub>buffer_load</sub>/BW) indicative of a steady state acid-base balance in the blood of the patient who has to undergo a CRRT blood treatment, wherein said parameter is determined as a function of the concentration of said buffer agent in said fluid source and as a function of the estimated or calculated patient systemic steady state concentration of bicarbonate and/or bicarbonate precursors. |
priorityDate |
2019-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |