vascular access the kidneycare audit. the challenge of vascular access – renal national service...
TRANSCRIPT
Vascular access
The KidneyCare Audit
The challenge of vascular access –Renal National Service Framework
Standard 3“All children, young people and adults with established renal failure are to have timely and appropriate surgery for permanent vascular or peritoneal dialysis access, which is monitored and maintained to achieve its maximum longevity.”
Overall 13,343 (77%) of prevalent patients were having dialysis therapy delivered by definitive access.Centres varied from 52% to 95%.For HD patients only, definitive access was used in 69%, range from 44% to 94%.
Renal Registry Vascular access survey – incident cohort
Patient survival, HD starters, by access type
0%
20%
40%
60%
80%
100%
0 50 100 150 200 250 300 350 400Days
Su
rviv
al p
rob
ab
lity
AVF+AVG
Temp line + Tunnel line
Infection: aetiology
Morbidity and mortality
Causes of death in dialysis patients
USRDS 1996 Annual Data Report
10.2%16.9%
16.1%5.5%
12.6%
3.5% 15.6%
19.6%
Venous catheters and morbidityVenous catheters and morbidityUK Vascular access survey 2005UK Vascular access survey 2005
No of venous access vs Staph aureus episodes
R2 = 0.4035
0
20
40
60
80
100
120
0 50 100 150 200
Total venous access (n)
No of venous access vs Inpatients
R2 = 0.5193
0
10
20
30
40
50
60
0 50 100 150 200Total venous access (n)
Year 2004: 1547 Staph. Aureus infections (462 (29%) related to MRSA)in haemodialysis population
One third of bed days in HD population related to catheter related problemsCost of a single episode of bacteraemia: £6209
Infection pathways and access
Further information
• www.ic.nhs.uk• [email protected]
The National Kidney Care AuditThe National Kidney Care Audit
Audit Question Standard/Best Practice Reference Associated Measures Impact of non-achievement
Does the proportion of patients starting haemodialysis with functioning permanent access meet the Renal Association and Vascular Society
Guidelines for permanent vascular access?
No patient on dialysis, including those patients who present late, should wait more than four weeks for fistula construction
(Clinical Practice Guidelines for Haemodialysis, UK Renal Association, 4th Edition, 2006)
Number of days spent in hospital to establish first functioning permanent vascular access
At risk of infection especially MRSA
Number of operations and other interventions (eg. angioplasty, revision surgery) to establish first functioning permanent
access.
No time to prepare or make informed choice, educate and empower
A proxy for failure to pre-emptively transplant list and
therefore long await time for transplantation
Patients should undergo fistula creation between 6 and 12 months before haemodialysis is expected to start to allow time
for adequate maturation of the fistula or time for a revision procedure if the fistula fails or is inadequate for use (source as
above)
Percentage of catheter starters who have functioning permanent access established within three and twelve months
Repeated admissions for percutaneous lines
Increased crash landing
At least 65% of patients presenting more than three months before initiation of dialysis should start HD with a usable native
Arteriovenous fistula (source as above).
Percentage of Haemodialysis patients starting with permanent access
Inadequate dose of dialysis delivered
Percentage of Haemodialysis patients starting with catheter access
Poor correction of metabolic abnormalities - legacy of poor care impact on long term adaptation to dialysis and adverse
clinical outcomes
Checksum of these two measures should equal 100%
Percentage of Haemodialysis patients starting with temporary access due to late referral (known to the renal service for less
than 3 months before starting dialysis)
Higher ESA (erythropoietin stimulating agent) requirements
Worse transplant outcomes
What are the hospital-acquired infection rates associated with vascular access in the maintenance of the haemodialysis population and how
does this compare with the national average and the best performance?
No avoidable HCAI in dialysis patients and an overall reduction in MRSA by 50 % by 2008 (Department of Health)
Percentage of RRT patients diagnosed with hospital acquired infection including complications relating to vascular access,
eg. line-related sepsis, clotted graft
The number of Staphylococcal systemic infections per annum varies from 2.3 to 33.8, average 13, the figures for
MRSA alone being from 0 to 21.5, average 4.
ContentContent
• Patient Transport• Vascular access
– Stream 1 Prevalent Patient Access Data– Stream 2 Comorbidity
• In patient utilisation• Infection
– Stream 3• Process measures (based on NRDS)
Part 1:Prevalent recordingPart 1:Prevalent recording
April 07 – Mar 08 196 (4.4) 188 (4.2) 4438
o Not shared 29 (15) 29 (15)
o Shared, not completed 78 (40) 70 (38)
o Shared & completed 89 (45) 89 (47)
MESS data England
Modality
Modality of dialysis No. (%) MRSA bacteraemia
Haemofiltration 3 (3.4)
Haemodialysis 84 (94.4)
Unknown 2 (2.2)
All 89 (100)
Table 2: Modality of dialysis in patients in established renal failure where record shared and completed
Access type
Renal access type No. (%) MRSA bacteraemia
AV- simple 23 (26)
AVG 3 (3.4)
Non-tunnelled – femoral 6 (6.8)
Non-tunnelled - jugular 4 (4.5)
Tunnelled – femoral 5 (4.7)
Tunnelled - Jugular 47 (53)
All 89 (101.9)
Table 3: Type of renal access in patients in established renal failure where record shared and completed
0
2
4
6
8
10
12
14
16
Que
en
Eliz
abet
h H
ospi
tal (
Birm
ingh
am)
St
Jam
es'
s U
niv
ersi
ty H
ospi
tal (
Leed
s)
Roy
al P
rest
on
Ho
spita
l
Jam
es C
ook
Un
iver
sity
Ho
spita
l (M
iddl
esb
roug
h)
Leic
este
r G
ener
al H
osp
ital
Ba
rts
and
the
Lon
don
Hos
pita
l
Ham
me
rsm
ith &
Cha
ring
Cro
ss H
osp
ital
Roy
al S
usse
x C
ount
y H
ospi
tal
So
uth
me
ad H
osp
ital (
Bris
tol)
St
Luke
s H
osp
ital (
Bra
dfo
rd)
Kin
g's
Col
leg
e H
osp
ital
Nor
folk
& N
orw
ich
Uni
vers
ity H
ospi
tal
Wa
lsgr
ave
Ho
spita
l (C
ove
ntry
)
Guy
's a
nd S
t T
hom
as'
s H
osp
ital
List
er H
osp
ital
Roy
al F
ree
& M
iddl
esex
Hos
pita
l
St
Hel
ier
Hos
pita
l
Ad
den
broo
kes
Ho
spita
l (C
am
brid
ge)
Der
rifo
rd H
ospi
tal
Ke
nt &
Can
terb
ury
Hos
pita
l
Roy
al C
ornw
all
Ho
spita
l (T
relis
ke)
Roy
al L
ive
rpoo
l Un
iver
sity
Hos
pita
l
Su
nde
rlan
d R
oyal
Hos
pita
l
Col
ches
ter
Ge
nera
l Ho
spita
l
Hea
rtla
nds
Hos
pita
l (B
irm
ingh
am)
Hop
e H
ospi
tal (
Sa
lford
)
Ipsw
ich
Hos
pita
l
Que
en
Ale
xan
dra
Hos
pita
l (P
orts
mou
th)
Roy
al S
hre
wsb
ury
Hos
pita
l
Uni
vers
ity H
ospi
tal A
intr
ee
Uni
vers
ity H
ospi
tal o
f N
orth
Sta
ffo
rdsh
ire
Bri
sto
l Ro
yal H
osp
ital f
or C
hild
ren
Cou
nte
ss o
f C
hest
er H
ospi
tal
Cum
berla
nd
Infir
ma
ry
Fre
eman
Hos
pita
l & R
oyal
Vic
toria
Inf
irmar
y
Hul
l Roy
al I
nfirm
ary
Not
tingh
am
City
Hos
pita
l
Oxf
ord
Rad
cliff
e H
ospi
tal
Roy
al I
nfir
mar
y M
anch
est
er
AVF - simple AVG Non-tunnelled venous catheter - Femoral/other
Non-tunnelled venous catheter - J/SC Tunnelled venous catheter - Femoral/other Tunnelled venous catheter - J/SC
Not completed
Linkage with Renal Registry
Infection• Bacteraemia
– Staph. Aureus– ?CDT
In patient stats• Bed utilisation• Admissions by code
– Bacteraemia– Pneumonia– Endocarditis– Spinal Abscess
Arteriovenous fistula
Date of AVF The date that the arteriovenous fistula was constructed
To monitor use of arterio-venous fistula Date format
Side of AVF The side of the body used for construction of an arteriovenous fistula
To identify the site used for arteriovenous fistula construction
n
01 Right 02 Left
Site of AVF The artery and vein used for construction of arteriovenous fistula
To identify the site used for arteriovenous fistula construction
n
01 Snuff box 02 Radiocephalic 03 Brachiocephalic 04 Brachiobasilic 05 Ulnacephalic 06 Radioulnar 07 Popliteal to long saphenous 08 Other
Drugs used to prevent thrombosis
The drugs prescribed to prevent thrombosis To monitor use of arteriovenous fistula n
01 Aspirin 02 Dipyridamole 03 Clopidogrel 04 Warfarin 05 Other
Blood pump speed The rate of blood flow through the dialyser during average dialysis
To determine whether there is adequate flow n
01 <100 ml/min
02 100-200 ml/min
03 200-300 ml/min
04 300-400 ml/min
04 >400 ml/min
Procedure
Recurrent dataComplication date Date of development of a complication of
arteriovenous fistulaTo monitor morbidity arising from AVF formation
Date format
Complications Comlications of arteriovenous fistula To monitor morbidity arising fom AVF formation
n
01 AVF stenosis 02 AVF infection 03 AVF aneurysm 04 AVF pseudoaneurysm 05 AVF rupture 06 AVF thrombosis 07 Steal syndrome 08 Heart failure
Surveillance date Surveillance of AVF with one of a number of techniques
To monitor arteriovenous fistula Date format
Surveillance technique Method used to monitor AVF To monitor arteriovenous fistula n
01 Clinical examination 02 Reduction in dialysis adequacy 03 Static venous pressure measurement 04 Blood flow rate assessment 05 Recirculation measurement 06 Duplex ultrasonography 07 Fistulography 08 Other
AVF revision Date of revision of arteriovenous fistula To monitor need for revision of arteriovenous fistula
Date format
AVF revision Type of revision of arteriovenous fistula To monitor revision of arteriovenous fistula n
RADIOLOGICALa. To Fistula 01 Angioplasty 02 Angioplasty with cutting balloon 03 Angioplasty with stent 04 Thrombolysis 05 Otherb. To central veins 06 Angioplasty 07 Angioplasty with cutting balloon 08 Angioplasty with stent 09 Thrombolysis 10 OtherSURGICAL 11 Surgical corection with jump graft 12 Surgical correction with vein patch 13 Banding of arteriovenous fistula 14 Thrombolysis of arteriovenous fistula 15 Ligation of arteriovenous fistula 16 Evacuation of haematoma 17 Pseudoaneurysm repair 18 Refashioning of arteriovenous fistula 19 Drill procedure for STEAL syndrome 20 Other
Start recurring group (for AVF revision)
Start recurring group (for surveillance)
End recurring group (for surveillance)
Start recurring group (for complication of AVF)
End recurring group (for complication of AVF)
What is needed from units
• Prevalent dataset– Electronic coding of access type at each session– Target 80% of units
• Comorbidity datset– HES and HPA linkage
• Process measures– Pilot sites– Use NRD (all ready finished a small pilot)