Efficacy and Safety of Oral Anticoagulants Among Thai Octogenarians With Nonvalvular Atrial Fibrillation

Sponsor
Mahidol University (Other)
Overall Status
Completed
CT.gov ID
NCT04047654
Collaborator
(none)
327
1
8.3
39.3

Study Details

Study Description

Brief Summary

A retrospective cohort study of Thai octogenarians with nonvalvular atrial fibrillation (NVAF) initiating apixaban, dabigatran, rivaroxaban or warfarin was conducted in medical school hospital in Thailand. Patients were recruited from January 1, 2013, to December 31, 2018. The efficacy outcome was early recurrence of stroke or transient ischemic attack (TIA) in 90 days after initiation of oral anticoagulants (OACs). The safety outcome were major bleeding and clinically relevant non-major bleeding complications in 180 days. Continuous variables were compared using independent t test and MannWhitney U test, and categorical variables were compared using chi-square test or Fisher's exact test. Furthermore, hazard ratios and P values were calculated by the use of multivariable Cox's regression analysis.

Condition or Disease Intervention/Treatment Phase
  • Drug: Non vitamin K oral anticoagulants

Detailed Description

This is a retrospective cohort study of Thai octogenarians with NVAF. Patients who were prescribed with apixaban, dabigatran, edoxaban, rivaroxaban or warfarin from January 1, 2013, to December 31, 2018 were recruited. The primary efficacy was recurrent ischemic stroke or TIA in 90 days after initiating OACs. The secondary efficacy were recurrent ischemic stroke or TIA in 180 days after initiating OACs. While any bleeding complications were defied as primary safety outcomes. Continuous variables were compared using independent t test and MannWhitney U test, and categorical variables were compared using chi-square test or Fisher's exact test.

Study Design

Study Type:
Observational
Actual Enrollment :
327 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Efficacy and Safety of Oral Anticoagulants Among Thai Octogenarians With Nonvalvular Atrial Fibrillation : A Retrospective Study
Actual Study Start Date :
Apr 22, 2019
Actual Primary Completion Date :
Dec 31, 2019
Actual Study Completion Date :
Dec 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Non vitamin K oral anticoagulants (NOACs)

Patients who were prescribed with apixaban, dabigatran, edoxaban, or rivaroxaban for stroke secondary prevention.

Drug: Non vitamin K oral anticoagulants
Non vitamin K oral anticoagulants are apixaban, dabigatran, rivaroxaban, and edoxaban

Warfarin

Patients who were prescribed with warfarin for stroke secondary prevention.

Outcome Measures

Primary Outcome Measures

  1. Rate recurrence of stroke or TIA in 90 days [90 days after initiation of OACs]

    Rate recurrence of stroke or TIA in 90 days after initiation of OACs

Secondary Outcome Measures

  1. Rate recurrence of stroke or TIA in 180 days [180 days after initiation of OACs]

    Rate recurrence of stroke or TIA in 180 days after initiation of OACs

  2. Rate of major bleeding [180 days after initiation of OACs]

    Rate of major bleeding in 90 days and 180 days after initiation of OACs

  3. Rate of clinically relevant non-major bleeding [180 days after initiation of OACs]

    Rate of clinically relevant non-major bleeding in 90 days and 180 days after initiation of OACs

  4. Patients's baseline characteristics associated with recurrence of stroke or TIA as assessed by multivariate cohort analysis [180 days after initiation of OACs]

    Patients's baseline characteristics associated with recurrence of stroke or TIA in 180 days after initiation of OACs as assessed by multivariate cohort analysis

  5. Patients's baseline characteristics associated with major bleeding and clinically relevant non-major bleeding as assessed by multivariate cohort analysis [180 days after initiation of OACs]

    Patients's baseline characteristics associated with major bleeding and clinically relevant non-major bleeding in 180 days as assessed by multivariate cohort analysis

Eligibility Criteria

Criteria

Ages Eligible for Study:
80 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age more than 80 years old

  • Patients who were diagnosed with I48, I63 or G45 from International Classification of Diseases 10th version (ICD-10). Patients who were diagnosed atrial fibrillation and flutter, cerebral infarction or transient cerebral ischemic attacks (TIA) and related syndromes)

  • Patients were prescribed apixaban, dabigatran, edoxaban, rivaroxaban, or warfarin

Exclusion Criteria:
  • Patients were prescribed oral anticoagulants for other indications
  1. Prophylaxis thromboembolic events in valvular atrial fibrillation

  2. Treatment of venous thromboembolism

  3. Prophylaxis thromboembolic events in hip or knee replacement

  • Patients who had contraindication to oral anticoagulants
  1. Creatinine clearance calculated from Cockcroft-Gault equation 1.1 Creatinine clearance less than 30 mL/min (for patients who receiving Dabigatran) 1.2 Creatinine clearance less than 15 (mL/min (for patients who receiving Apixaban, Edoxaban, Rivaroxaban)

  2. Patients were diagnosed acute hepatitis, chronic active hepatitis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Siriraj Hospital, Phramongkutklao Hospital Bangkok Thailand 10700

Sponsors and Collaborators

  • Mahidol University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mahidol University
ClinicalTrials.gov Identifier:
NCT04047654
Other Study ID Numbers:
  • NOACs in Thai Octogenarians
First Posted:
Aug 7, 2019
Last Update Posted:
Feb 21, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mahidol University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2020