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The Short- and Long-Term Risk of Mortality in Intracranial Hemorrhage Patients with Tranexamic Acid Treatment in a Population-Based Cohort Study.
Chiu, Chien-Ming; Hu, Sung-Yuan; Liao, Pei-Lun; Huang, Jing-Yang; Chou, Ming-Chih; Yang, Shun-Fa; Yeh, Chao-Bin.
Afiliação
  • Chiu CM; Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
  • Hu SY; Department of Emergency Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
  • Liao PL; Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
  • Huang JY; Department of Emergency Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
  • Chou MC; School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
  • Yang SF; Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung 402, Taiwan.
  • Yeh CB; School of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
J Clin Med ; 13(6)2024 Mar 11.
Article em En | MEDLINE | ID: mdl-38541823
ABSTRACT

Background:

The mortality rate associated with nontraumatic intracranial hemorrhage (NTICrH) remains consistently high under the current care modality. The effectiveness of tranexamic acid (TXA) as a treatment option is still a subject of debate. This study aims to assess the association between TXA administration and both short-term and long-term mortality rates in patients with NTICrH.

Methods:

We conducted a retrospective cohort study using data from the Taiwan National Health Insurance Research Database (NHIRD) spanning from January 2000 to December 2017. The study population consists of NTICrH patients admitted to the ICU, divided into two groups patients who were treated with TXA and those who were not. Propensity score matching (PSM) was conducted to balance the baseline characteristics of the two groups. Cox proportional hazard analysis was conducted to estimate the hazard ratio (HR) for the all-cause mortality. Sensitivity analyses were performed using the inverse probability of treatment-weighted hazard ratio (IPTW-HR). To assess the timing of TXA use, we compared the risk of all-cause mortality within 180 days between patients receiving early TXA treatment and those receiving late TXA treatment.

Results:

There was no significant difference in 180-day all-cause mortality between the groups; the hazard ratio was 1.07 (95% CI 0.96-1.20) in patients treated with TXA compared to those without TXA treatment. Within 7 days of admission, patients treated with TXA had a lower hazard ratio of 0.81 (95% CI 0.74-0.90) for all-cause mortality.

Conclusions:

Lower mortality within the first 7 days was observed in patients with NTICrH who received TXA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article