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Biocompatibility parameters with standard and increased dose of citrate in hemodialysis : a randomized trial
ID
Orsag, Aleša
(
Avtor
),
ID
Božič, Mojca
(
Avtor
),
ID
Hudoklin, Samo
(
Avtor
),
ID
Simčič, Saša
(
Avtor
),
ID
Gubenšek, Jakob
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(2,10 MB)
MD5: 07AC5A2E877C16DFBF70FB978A94329B
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/2077-0383/10/13/2987
Galerija slik
Izvleček
Background: The dose of citrate needed in regional citrate anticoagulation (RCA) to achieve optimal biocompatibility is unknown. We performed a randomized trial comparing two doses (ACTRN12613001340729). Methods: In 30 patients a single hemodialysis with either standard (2.7 mmol/L) or increased dose of citrate (4 mmol/L) was performed. C5a-desArg, myeloperoxidase (MPO), thrombin-antithrombin complex (TAT), and platelet factor 4 (PF4) were measured and the inner surface of the dialyzer fibers was evaluated with scanning electron microscopy (SEM). Results: A good separation of anticoagulation effect was achieved (post-filter ionized calcium 0.20 vs. 0.31 mmol/L, p < 0.05). There was no effect of citrate dose on any of the biocompatibility parameters; transient and parallel increase in PF4 after 30 min and parallel increase in TAT after 4 h were observed. There were no visually detected clotting problems within the circuit and no significant hypocalcemia in either group. SEM clotting score was excellent and comparable in both groups (p = 0.59). Conclusions: Given the excellent results in both groups, absence of between group differences and inability of the increased dose of citrate to completely blunt the small residual increase in PF4 and TAT, we conclude that the standard dose of citrate seems sufficient in RCA for chronic hemodialysis.
Jezik:
Angleški jezik
Ključne besede:
biocompatibility
,
complement system
,
hemodialysis
,
myeloperoxidase
,
platelet factor 4
,
regional citrate anticoagulation
,
thrombin–antithrombin complex
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2021
Št. strani:
11 str.
Številčenje:
Vol. 10, iss. 13, art. 2987
PID:
20.500.12556/RUL-135718
UDK:
616.1
ISSN pri članku:
2077-0383
DOI:
10.3390/jcm10132987
COBISS.SI-ID:
69247491
Datum objave v RUL:
29.03.2022
Število ogledov:
1674
Število prenosov:
127
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Journal of clinical medicine
Skrajšan naslov:
J. clin. med.
Založnik:
MDPI
ISSN:
2077-0383
COBISS.SI-ID:
5405759
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
04.07.2021
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
biokompatibilnost
,
hemodializa
,
mieloperoksidaza
,
antikoagulacija
,
trombin-antitrombin kompleks
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0323
Naslov:
Ledvične bolezni in nadomestna zdravljenja
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
University Medical Center Ljubljana
Številka projekta:
20180054
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