Cooke and his co-workers 1 reported three cases of aneurysmal dilation (one with fatal rupture) in Dacron aortic prosthetic grafts. The authors noted that, although similar instances of Dacron prosthesis failure in peripheral arteries had been reported, they could find no previous record of dilation of an aortic prosthesis. Two of the dilated prostheses were recovered, but, despite extensive testing, reasons for graft failure were not identified. In editorial comment on the report by Cooke et al, Deterling 2 stated that when using manufactured devices for human spare parts, one must commit himself to a followup of such a patient for his remaining life. Only by this means will the safety and effectiveness of the spare part become known. Deterling concluded with a plea for reporting all graft failures, preferably with identifying details of material and construction and an attempt to evaluate factors responsible for failure. In the current issue