Arteriovenous fistula or graft dysfunction more likely in ADPKD patients in the long run

24 Feb 2020
Arteriovenous fistula or graft dysfunction more likely in ADPKD patients in the long run

Patients with autosomal dominant polycystic kidney disease (ADPKD) are at a lower risk of arteriovenous fistula or graft (AVF/AVG) dysfunction in the short term, but suffer from an excess risk in the long-term, a recent study has found.

Researchers enrolled 557 ADPKD patients (mean age, 56.0±12.6 years; 50.6 percent male) from the National Health Insurance Research Database of Taiwan. Participants were followed for the development of the primary outcome of AVF/AVG dysfunction; major adverse cardiovascular events (MACEs) were designated as a second outcome. A parallel group of 1,671 non-ADPKD participants (mean age, 55.0±14.7 years; 50.1 percent male) were also included as controls.

After propensity score matching, the incidence of AVF/AVG dysfunction was nominally lower in those with vs without ADPKD during the first 90 days (38.83 vs 48.99 per 100 person-years). This corresponded to a nonsignificantly lower risk in those with the kidney disease (subdistribution hazard ratio [SHR], 0.79 95 percent confidence interval [CI], 0.58–1.08; p=0.137).

This trend persisted until 180 days (45.85 vs 51.31 per 100 person-years; SHR, 0.90, 95 percent CI, 0.73–1.10; p=0.300). Beyond this point, however, the pattern flipped, with ADPKD patients seeing a greater incidence and risk of AVF/AVG dysfunction at 1 year (44.2 vs 41.0 per 100 person-years; SHR, 1.08, 95 percent CI, 0.92–1.27; p=0.361) and within 5 years (27.38 vs 24.69 per 100 person-years; SHR, 1.09, 95 percent CI, 0.96–1.23; p=0.168).

Notably, by 10 years, the excess in incidence in ADPKD patients was substantial enough that it achieved statistical significance (17.5 vs 13.8 per 100 person-years; SHR, 1.19, 95 percent CI, 1.00–1.41; p=0.045).

Sci Rep 2020;10:1985