A new subcutaneous device (Dialock(TM); Biolink Corp., Middleboro, MA)
provides vascular access to patients who currently require hemodialys
is (HD). The device consists of a port-like valve, implanted subcutane
ously below the clavicle, which provides a linear flow passage to two
catheters placed in the right atrium via the jugular vein. The valve i
s accessed percutaneously with needle-cannulas that functionally conve
rt the device to twin catheters for connecting the patient to the HD l
ines. Interdialytic patency is maintained using a standard heparin loc
k. The device has been implanted in 10 outpatients under local anesthe
sia, with almost immediate use for HD (median, 3 days) and has functio
ned successfully for more than 6 months (mean +/- SD, 4.0 +/- 1.7; > 4
00 dialysis sessions). Blood flows over 300 ml/min were consistently a
chieved (average, 320 +/- 50) with venous and arterial pressures of 19
7 +/- 42 mmHg and -241 +/- 31 mmHg, respectively. After 40 patient-mon
ths, condition of the needle puncture sites remains satisfactory. Four
systemic infections have occurred in three patients; all have resolve
d without the need for device removal. There have been no infections a
t the puncture sites. One patient whose heparin lock was not changed f
or 23 days (for reasons unrelated to the device) required fibrin sheat
h stripping of his catheters. Patient and nurse acceptance has been ex
cellent. The device may offer substantial improvement over conventiona
l devices for HD access.