MANAGEMENT OF VASCULAR ACCESS IN EUROPE:
PART 2 - A MULTI CENTRE STUDY OF RELATED COMPLICATIONS
MedIQal® was used. After random selection of patients, the proj-
ect installation software was sent to the participating centre. For
all selected patients a standard data set was filled in at baseline,
after six months and after 12 months. The standard data set includ-
ed information concerning the type of VA, puncture techniques
used, function of the VA and medication used. Throughout the
one-year study period, VA related complications requiring inter-
vention were registered as well as details concerning related
interventions and hospitalisation.
Haemodialysis patients included
Age median (range)
n=1380
64 years (15-90)
56%
Sex (% males)
Duration of treatment for ESRD median (range)
Age of vascular access in use median (range)
Previous permanent VA used
No previous
37 months (6-370)
30 months (0-300)
59.2%
22.9%
17.9%
One
More than one
Table 1: Description of study population.
| STATISTICAL ANALYSIS |
patients matching the inclusion criteria (see below) to the coor-
dinating centre in Antwerp, Belgium. The list included patients’
initials, birth date and sex. In the coordinating centre, a cohort
of 30 patients was randomly selected from this list. If the total
number of patients in a centre was below 30, all eligible patients
were included.
Basic statistical techniques were used to describe the types of VA
used, complications observed and hygienic handling applied.
Students’ t-test was used for comparison of continuous vari-
ables and chi-square test for comparison of percentages, con-
sidering a p-value of p < 0.05 as the significance level. For com-
plications, in-depth analysis was only performed on complications
occurring frequently: thrombosis, stenosis, infection, bleeding and
flow problems. Per patient, each reported complication was only
counted once, also when it occurred more than one time dur-
ing the study period. Differences in complication rates were relat-
ed to patient characteristics, type of VA and puncture techniques
used. Complication rates were also related to centre character-
istics and hygiene policies, questioned during the first, centre based
part of the study. Risk ratios for complications were calculated using
logistic regression analysis enabling control for confounding fac-
tors.
| SELECTION CRITERIA |
All adult patients who started a chronic haemodialysis programme
at least six months prior the start of the study were included for
at random selection. Children of less than 15 years and patients
on haemodialysis for less than six months were excluded.
| DATA COLLECTION |
Centres started the study in the period 1998-1999. For data
Distribution of vascular access
Other
RESULTS
The questionnaire was distributed to 108 centres and 81 of them
sent their patients’ list to the coordinating centre enabling a
random selection of 30 patients. Finally, 47 centres out of 16
European countries completed the study. Participating centres were
mainly from United Kingdom (n=11), Belgium (n=9) and Germany
(n=6). In the remaining countries (Austria, Cyprus, Denmark,
Finland, France, Greece, Italy, Malta, the Netherlands, Norway,
Slovenia, Spain and Switzerland) less than four centres participated.
0.7%
Catheter
13.0%
Graft
9.6%
| PATIENT CHARACTERISTICS |
A total of 1380 patients were included. Median age was 64
with 56% male. Patients were on chronic haemodialysis therapy
for a median of 37 months (Table 1). During the one year study
period 15.5% of patients died, 6.4% were transplanted, 0.7%
switched to PD and 4.5% were lost to follow-up.
AV Fistula
76.7%
collection, a computer-based questionnaire developed by
Figure 1: Types of vascular access at baseline.
| DESCRIPTION OF VA IN USE AT BASELINE |
The category 'other' included 12 patients treated with a
combination of an AV fistula and a catheter.
At start of the observation period, 77% of patients had a native
AV fistula, 10% had an AV graft and 13% a catheter. AV grafts
46 EDTNA|ERCA JOURNAL 2003 XXIX1