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Cilostazol May Improve Maturation Rates and Durability of Vascular Access for Hemodialysis
Todd E Russell1, Gregory C Kasper1, Andrew J Seiwert1
11 Jobst Vascular Institute, The Toledo Hospital, Toledo, OH, USA.
Insights
Cilostazol therapy significantly improved arteriovenous fistula maturation and durability for hemodialysis patients. This treatment reduced complications and extended access lifespan, offering a potential benefit for dialysis access management.
Area of Science:
- Nephrology
- Vascular Surgery
- Pharmacology
Background:
- Arteriovenous access is crucial for hemodialysis.
- Access maturation and durability are significant challenges.
- Pathophysiological pathways of access failure are not fully understood.
Purpose of the Study:
- To evaluate the efficacy of cilostazol in improving vascular access maturation rates.
- To assess the impact of cilostazol on the durability and complication rates of dialysis access.
- To determine if preoperative and postoperative cilostazol therapy benefits hemodialysis patients.
Main Methods:
- A case-control study comparing cilostazol treatment group (33 patients) with a control group (116 patients).
- Treatment group received cilostazol pre- and post-surgery for dialysis access creation.
- Outcomes included fistula maturation, time to failure, and complication rates.
Main Results:
- Cilostazol group showed a 3.8 times higher likelihood of fistula maturation (88% vs 66%).
- Fewer complications and longer time to first complication were observed in the cilostazol group.
- Access failure time was significantly longer in the cilostazol group (903.7 vs 381.6 days).
Conclusions:
- Preoperative and postoperative cilostazol therapy may enhance dialysis access maturation and longevity.
- Cilostazol demonstrates potential as an adjunct therapy for improving hemodialysis access outcomes.
- Further randomized trials are warranted to confirm these findings and clinical impact.
Abstract:
Cilostazol is effective in controlling pathophysiological pathways similar or identical to those involved in nonmaturation and failure of the arteriovenous access. This case-control study examined whether cilostazol would improve maturation rates and durability of vascular access for hemodialysis. The treatment group included 33 patients who received cilostazol for ≥30 days prior to creation of a dialysis access and continued with cilostazol therapy for ≥60 days after surgery. The matched (gender, age, race, diabetes, and the year of surgery) control group included 116 patients who underwent the same procedure but did not receive cilostazol prior to and at least 3 months after surgery. Primary outcomes were maturation and, for those that matured, time of functioning access, defined as the time from the first use to irreparable failure of the access. Secondary outcomes were time to maturation, complications, and time to first complication. Study group patients were 3.8 times more likely to experience fistula maturation compared to the controls (88% vs 66%, RR = 3.8, 95% confidence interval: 1.3-11.6, P = .016). Fewer patients in the study group had complications (76% vs 92%, P = .025), and the time from construction of the fistula to the first complication was longer (345.6 ± 441 days vs 198.3 ± 185.0 days, P = .025). Time to maturation was similar in both groups (119.3 ± 62.9 days vs 100.2 ± 61.7 days, P = .2). However, once matured, time to failure was significantly longer in the treatment group (903.7 ± 543.6 vs 381.6 ± 317.2 days, P = .001). Multivariate analysis confirmed that the likelihood of maturation was significantly higher in the treatment group patients. These results suggest that dialysis access patients may benefit from preoperative and postoperative cilostazol therapy. If confirmed by a randomized trial, this treatment will have a major beneficial impact on patients dependent on a well-functioning access for their hemodialysis.
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