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Population pharmacokinetics of ramipril in patients with chronic heart failure : a real-world longitudinal study
ID
Čvan Trobec, Katja
(
Avtor
),
ID
Grabnar, Iztok
(
Avtor
),
ID
Trontelj, Jurij
(
Avtor
),
ID
Lainščak, Mitja
(
Avtor
),
ID
Kerec Kos, Mojca
(
Avtor
)
PDF - Predstavitvena datoteka,
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(584,02 KB)
MD5: E79603457ADD431E7181B4EFD0F6881C
URL - Izvorni URL, za dostop obiščite
https://acta.pharmaceutica.farmaceut.org/wp-content/uploads/2024/05/31524.pdf
Galerija slik
Izvleček
In patients with chronic heart failure (CHF), the use of angiotensinconverting enzyme inhibitors, including ramipril, is recommended to reduce the risk of heart failure worsening, hospitalisation, and death. Our aim was to investigate the influence of body composition on the pharmacokinetics of ramipril and its active metabolite ramiprilat and to evaluate the changes in pharmacokinetics after prolonged therapy. Twenty-three patients with CHF who were on regular therapy with ramipril participated at the first study visit (median age 77 years, 65 % male, and 70 % New York Heart Association Class II); 19 patients attended the second study visit and the median time between the two visits was 8 months. Pharmacokinetics were assessed using a nonlinear mixed-effects parent-metabolite model comprising two compartments for ramipril and one compartment for ramiprilat. The influence of body size and composition was best described by an allometric relationship with fat-free mass. In addition, ramipril clearance was related to patient age and daily ramipril dose, while clearance of ramiprilat was influenced by glomerular filtration rate and daily ramipril dose. There were no clinically relevant changes in the pharmacokinetics of ramipril and ramiprilat between the study visits. Due to the relatively stable pharmacokinetics of ramipril, regular outpatient visits at 6-month intervals seem appropriate to evaluate ramipril therapy.
Jezik:
Angleški jezik
Ključne besede:
ramipril
,
ramiprilat
,
pharmacokinetics
,
chronic heart failure
,
body composition
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2024
Št. strani:
Str. 315-328
Številčenje:
Vol. 74, no. 2
PID:
20.500.12556/RUL-158260
UDK:
615.015:616.12-008.46
ISSN pri članku:
1846-9558
DOI:
10.2478/acph-2024-0018
COBISS.SI-ID:
194982915
Datum objave v RUL:
31.05.2024
Število ogledov:
279
Število prenosov:
67
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Objavi na:
Gradivo je del revije
Naslov:
Acta pharmaceutica
Skrajšan naslov:
Acta pharm.
Založnik:
Croatian Pharmaceutical Society
ISSN:
1846-9558
COBISS.SI-ID:
3817585
Licence
Licenca:
CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:
Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
farmakokinetika
,
srčno popuščanje
,
ramipril
,
ramiprilat
,
kronično srčno popuščanje
,
telesna sestava
Projekti
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P1-0189
Naslov:
Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih
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