Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI

Abstract Challenges remain for clinicians over balancing the efficacy of active antithrombotic therapy and simultaneous bleeding reduction in patients. The clinical data of 347 patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) were retrospectively analyz...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yong-zhe Guo, Zi-wen Zhao, Shu-mei Li, Liang-long Chen
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/c428ba58c6174d438a65548fa754bc3d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c428ba58c6174d438a65548fa754bc3d
record_format dspace
spelling oai:doaj.org-article:c428ba58c6174d438a65548fa754bc3d2021-12-02T15:09:06ZClinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI10.1038/s41598-021-96606-y2045-2322https://doaj.org/article/c428ba58c6174d438a65548fa754bc3d2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-96606-yhttps://doaj.org/toc/2045-2322Abstract Challenges remain for clinicians over balancing the efficacy of active antithrombotic therapy and simultaneous bleeding reduction in patients. The clinical data of 347 patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) were retrospectively analyzed. On the basis of the given tirofiban, the patients were assigned into three different dose groups: high dose group (group H), medium dose group (group M), and low dose group (group L). The tirofiban efficacy was evaluated in terms of major adverse cardiovascular event (MACE) parameters and lab endpoints, including platelet count and function. The tirofiban safety was assessed by the occurrence of bleeding events. The patients were followed up for 1 month after the PCI. No significant difference in MACE events was evident among these groups (p > 0.05). Groups H and M reported an obvious reduction in platelet count (p < 0.05 for both) and an increased platelet inhibition rate (p < 0.05 for both). Group H showed a higher rate of total bleeding events than the other groups (Group H vs. Group M: 34.4% vs. 16.5%; Group H vs. Group L: 34.4% vs. 10.3%; p < 0.05 for both). A proper administration of a low dose of tirofiban may be a superior alternative in treating ACS patients, which can produce a similar favorable clinical outcome and a decrease in bleeding complication.Yong-zhe GuoZi-wen ZhaoShu-mei LiLiang-long ChenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yong-zhe Guo
Zi-wen Zhao
Shu-mei Li
Liang-long Chen
Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
description Abstract Challenges remain for clinicians over balancing the efficacy of active antithrombotic therapy and simultaneous bleeding reduction in patients. The clinical data of 347 patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) were retrospectively analyzed. On the basis of the given tirofiban, the patients were assigned into three different dose groups: high dose group (group H), medium dose group (group M), and low dose group (group L). The tirofiban efficacy was evaluated in terms of major adverse cardiovascular event (MACE) parameters and lab endpoints, including platelet count and function. The tirofiban safety was assessed by the occurrence of bleeding events. The patients were followed up for 1 month after the PCI. No significant difference in MACE events was evident among these groups (p > 0.05). Groups H and M reported an obvious reduction in platelet count (p < 0.05 for both) and an increased platelet inhibition rate (p < 0.05 for both). Group H showed a higher rate of total bleeding events than the other groups (Group H vs. Group M: 34.4% vs. 16.5%; Group H vs. Group L: 34.4% vs. 10.3%; p < 0.05 for both). A proper administration of a low dose of tirofiban may be a superior alternative in treating ACS patients, which can produce a similar favorable clinical outcome and a decrease in bleeding complication.
format article
author Yong-zhe Guo
Zi-wen Zhao
Shu-mei Li
Liang-long Chen
author_facet Yong-zhe Guo
Zi-wen Zhao
Shu-mei Li
Liang-long Chen
author_sort Yong-zhe Guo
title Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
title_short Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
title_full Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
title_fullStr Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
title_full_unstemmed Clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in ACS patients undergoing PCI
title_sort clinical efficacy and safety of tirofiban combined with conventional dual antiplatelet therapy in acs patients undergoing pci
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c428ba58c6174d438a65548fa754bc3d
work_keys_str_mv AT yongzheguo clinicalefficacyandsafetyoftirofibancombinedwithconventionaldualantiplatelettherapyinacspatientsundergoingpci
AT ziwenzhao clinicalefficacyandsafetyoftirofibancombinedwithconventionaldualantiplatelettherapyinacspatientsundergoingpci
AT shumeili clinicalefficacyandsafetyoftirofibancombinedwithconventionaldualantiplatelettherapyinacspatientsundergoingpci
AT lianglongchen clinicalefficacyandsafetyoftirofibancombinedwithconventionaldualantiplatelettherapyinacspatientsundergoingpci
_version_ 1718387900640395264