Page 61 - 林口長庚醫研部電子報-2018年9月刊
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NEWSLETTER                                                                                               NEWSLETTER
 SEPTEMBER                                                                                                 SEPTEMBER

 2018                                                                                                             2018




 It is noted that warfarin group carried a significantly higher annual risk of   Further prospective and randomized controlled validation of our results in

 AKI than the dabigatran group for those with high CHA2DS2-VASc score   a future study is warranted.
 (Figure 2).

 We also tried to evaluate the risk of AKI in NVAF Asians taking other

 DOACs including apixaban, dabigatran, rivaroxaban as compared with

 warfarin. In this nationwide retrospective cohort study, 1,381, 3,863, 6,692

 and 5,038 NVAF patients with CKD and 4,146, 18,007, 23,971, and 22,118

 NVAF patients without CKD taking apixaban, dabigatran, rivaroxaban,

 and warfarin, respectively, from June 1, 2012 to December 31, 2016 were

 enrolled from the Taiwan National Health Insurance Program. Propensity-

 score weighted method was used to balance covariates across study
 groups. Patients were followed until occurrence of AKI or end date of

 study (December 31, 2016). The results also confirmed that three DOACs   ↑ (Figure 1)  ↑ (Figure 2)
            The mechanisms underlying                           Dabigatran was associated with a
 were all associated with a significantly lower risk of AKI compared with   warfarin-related nephropathy (WRN)  lower risk of acute kidney injury than

 warfarin for both CKD-free (hazard ratio (HR): 0.75, 95%CI: 0.69-0.81 for   warfarin among Asians with non-valvular
                                                                atrial fibrillation (NVAF) taking oral
 apixaban; HR: 0.79, 95%CI: 0.74-0.85 for dabigatran; HR: 0.81, 95% CI:       anticoagulants

 0.75-0.87 for rivaroxaban) and CKD cohorts (HR: 0.53, 95%CI: 0.45-0.63

 for apixaban; HR: 0.63, 95%CI: 0.57-0.69 for dabigatran; HR: 0.63, 95%
 CI: 0.58-0.68 for rivaroxaban). No differences in risk of AKI were found

 between any two-paired NOACs. The annual incidence of AKI for all

 NOACs and warfarin increased gradually as the increment of CHA2DS2-

 VASc for both CKD-free and CKD cohorts after propensity score

 weighting (Figure 3).

 Our results were also supported by other studies showing that dabiagtran

 and rivaroxaban were associated with lower risks of several renal

 outcomes including more than 30% decline of eGFR, doubling of serum
                      ↑ (Figure 3)
 creatinine, and the risk of acute kidney injury (Figure 4). In conclusion,   All direct oral anticoagulants (DOACs)
                                                                                 ↑ (Figure 4)
 use of all DOACs (apixaban, dabigatran, and rivaroxaban), provide for   including apixaban, dabigatran, and   Dabigatran and rivaroxaban
      rivaroxaban, were associated with a
 a lower risk of acute kidney injury than warfarin in a large Asian cohort   lower risk of acute kidney injury than   were associated with lower risks

                                                                    of several renal outcomes than
 patients who did or did not have a history of kidney disease.DOACs may   warfarin among Asians with non-valvular   warfarin among patients with non-
 be a safer alternative to warfarin in Asians with NVAF in terms of the risk   atrial fibrillation (NVAF) taking oral   valvular atrial fibrillation (NVAF)
                     anticoagulants
 of anticoagulant-related AKI.                                          taking oral anticoagulants

 59  非經本刊及作者同意,請勿做任何形式之轉載                                                                                          60
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