Hemodialysis Access:
General Considerations
THOMAS S. HUBER
Based on a chapter in the seventh edition by Robyn A. Macsata and Anton N. Sidawy
160
120
Incident
Original projection: 136,882 (2015)
New projection: 150,772 (2020)
Actual: 110,854 (2006)
80
40
0
800
600
1083
Prevalent
Original projection: 713,531 (2015)
New projection: 784,613 (2020)
Actual: 506,256 (2006)
200
80
84
88
92
96
04
08
12
16
20
Cost
The Medicare costs associated with ESRD are staggering.
Although ESRD accounts for only 1.3% of the general Medicare population, it accounted for 7.5% ($25.7 billion) of the
general Medicare costs in 2010.1 Notably, Medicare is the
primary payer for patients with ESRD in the United States
and is responsible for more than 80% of the patients.1 The
Medicare expenditure per patient with ESRD in 2006 was
greatest for patients on hemodialysis (hemodialysis $71,889,
peritoneal dialysis $53,327, transplant $24,951).2 Among
those patients undergoing hemodialysis, the expenditure
(patient per year) was greatest for those with catheters (catheters $77,093, grafts $71,616, stulae $53,470).2
BOX 73-1
00
Year
1084
goals, and the management of complications. These guidelines emphasize autogenous AV access, as might be suspected
by the overarching goals, with the generic recommendations
that autogenous access should be used before prosthetic
access and that dialysis catheters should be avoided. The
expert panel dened the autogenous radial-cephalic, brachialcephalic, and brachial-basilic AV accesses as preferred and
stated that the prosthetic AV access was acceptable. The
latest version of the KDOQI guidelines established a 65%
goal for autogenous access among prevalent dialysis patients
with a catheter rate of less than 10% in the absence of a
maturing autogenous access. The expert panel stated that the
patency rate for autogenous access should be more than 3
years by life-table analysis with thrombosis and infectious
rates of less than 0.25 episodes/patient-year at risk and less
than 1% over the lifetime of the access, respectively. Similarly, the patency rates for prosthetic accesses should be more
than 2 years with a thrombosis rate of less than 0.5 episodes/
patient-year and an infection rate of less than 10% over the
lifetime of the access.
BOX 73-2
AVFs placed
AVFs in use
AV Grafts
All CVCs
CVCs >90 days
50%
40%
30%
20%
10%
0%
2003 2004 2005 2006 2007 2008 2009 2010 2011
Figure 73-2 The prevalent rates for the various vascular access congurations in the United States are shown for the time period from
7/2003 to 12/2011. Note the dramatic increase in the autogenous
[arteriovenous (AV) accesses] (AVFs [AV stulae] in use) and the corresponding decrease in the rates of prosthetic AV accesses (AV Grafts).
The rates of the patients dialyzing with a dialysis catheter have
remained relatively stable. CVCs, Central venous catheters. (From the
Fistula First: National Vascular Access Improvement Initiative website,
http://www.stularst.org/AboutFistulaFirst/FFBIData.aspx.)
1085
Patency
Improved patency has been cited as a major justication for
the preferential use of autogenous access. The patency rates
for upper extremity autogenous and prosthetic AV accesses
in adults were dened by Huber et al14 in their systematic
review of the literature (Fig. 73-3). Although the primary and
secondary patency rates for the autogenous access were superior, the quality of the underlying evidence was limited and
likely included a selection and publication bias. Notably, the
reported patency rates for both the autogenous and prosthetic
accessess were signicantly less than the outcome measures
dened by KDOQI. Disbrow et al15 compared the patency
rates between autogenous and prosthetic AV accesses among
incident dialysis patients with suitable veins for autogenous
access. The investigators concluded that the patency and
intervention rates for the two access types were comparable
although the patients with autogenous accesses required the
use of a tunneled catheter for a longer period. Schild et al16
reported that the long-term patency rates for prosthetic and
autogenous AV accesses were comparable, concluding that
prosthetic access should be placed in patients who were not
candidates for autogenous access. The secondary patency
80
Auto 2
60
PTFE 2
Auto 1
40
PTFE 1
20
0
0
12
15
18
21
24
27
Months
Figure 73-3 The patency rates for the autogenous (Auto) and prosthetic (PTFE) upper extremity arteriovenous (AV) accesses are plotted
against time (months) with the positive standard error bars. Both the
primary (Auto 1, PTFE 1) and secondary (Auto 2, PTFE 2) patency rates
for the two access types are shown. The patency rates for the autogenous accesses were better than their corresponding prosthetic counterparts with the one exception of the initial (1.5-mo) time point for
the primary patency comparison. PTFE, Polytetrauoroethylene. (From
Huber TS, et al: Patency of autogenous and PTFE upper extremity arteriovenous hemodialysis accesses: a systematic review. J Vasc Surg 38:10051011, 2003.)
100
Percent Patent
1086
Patient-Specic Considerations
The goal for the individual patient is to establish the most
functional access with good long-term patency and minimal
complications. As outlined previously, this is an autogenous
AV access for most patients. However, a variety of concerns
should be addressed in this complex decision process about
the most appropriate access for a specic patient, including
age, gender, life expectancy, anatomy, comorbidities, likelihood of success (i.e., autogenous maturation rate, long-term
prosthetic access patency), urgency of dialysis, and patient
preference. In most cases, the question about the most appropriate access can be distilled down to whether the patient is
suitable for an autogenous AV access and whether the access
is likely to be successful. The important distinction between
the emphasis on a functional access and an autogenous access
is illustrated by the prospective, longitudinal study by Solesky
et al,22 who tracked outcome after access creation. They were
able to achieve the national target rate for autogenous access
of 66%, but a signicant portion of the dialysis support over
the study period was provided by catheters, with a 27% catheter prevalence rate. This experience led them to conclude
that the current algorithms are problematic and rely heavily
on catheters.
radial-cephalic conguration.31-34 Indeed, it has been suggested that the national initiatives may need to be reevaluated for elderly patients.35 Advanced age and life expectancy
are interrelated in terms of access choice because the improved
long-term patency attributed to autogenous accesses may not
be as relevant for elderly patients, particularly if one considers
that the obligatory period from access creation to cannulation can be prolonged. Vachharajani et al36 examined the role
of the Fistula First Initiative in octogenarians and emphasized
that life expectancy and functional status should be considered, given the poor long-term outcome, high mortality, and
high discharge rate to a chronic care facility of the patients
in the study. Tunneled dialysis catheters may be a reasonable
option in some elderly patients.
Decision Making
The critical question remains as to how individual predictors
can or should be incorporated into the selection of the most
appropriate access choice for an individual patient. Such a
choice incorporates some potentially modiable (e.g.,
smoking, specic choice of artery/vein, obesity) and nonmodiable (e.g., age, gender, presence of peripheral vascular
disease) factors. Lok et al57 have developed a scoring system
to predict autogenous access maturation. They identied age
greater than 65 years (2 pts), peripheral vascular disease
(3 pts), coronary artery disease (2.5 pts), and white race
(3 pts) as signicant predictors. In their model, patients
were given 3 points as a baseline and then the individual
scores for the various comorbidities were summed. Successful
maturation was found to correlate with the point total, in
that patients in the highest-scoring group, with a score higher
than 9, had a failure rate of 69% (Fig. 73-4). Notably, a
70-year-old African-American woman (age 2 pts, race 0,
baseline 3 pts) with an above-knee amputation (peripheral
veno-occlusive disease 3 pts) and coronary artery disease
(CAD 2.5 pts) would have a score of 10.5, corresponding to
a 31% successful maturation rate. Interestingly, Lilly et al58
used data from the Centers for Medicare and Medicaid Services to examine the Lok model and concluded that the
model was not all that predictive, emphasizing that many
1087
1088
80
70
P0.0001
Percentage (%)
60
50
69
40
30
50
20
34
10
24
0
N = 88
N = 169
N = 161
N = 11
Risk categories
Table 73-1
Clinical scenarios
favoring autogenous
success
Clinical scenarios
favoring prosthetic
access
Potential
autogenous access
No potential
autogenous access
Autogenous access
Adjuncts for
autogenous access
Serial assessment
Remedial imaging/
intervention
Mature access
Preoperative Evaluation
Early Referral
The KDOQI recommendations outline the preoperative
evaluation for patients requiring permanent hemodialysis
access.6 Ideally, patients should initiate dialysis with a functional autogenous access, albeit rarely achieved. This goal
requires early referral to an access surgeon and access placement well in advance of the target date so that the access
(autogenous or prosthetic) is suitable for cannulation when
required, allowing for the requisite time for maturation and
remedial interventions. Accordingly, the KDOQI panel recommends that patients with a glomerular ltration rate lower
than 30 mL/min/1.73 m2 (chronic kidney disease stage 4)
1089
1090
on non-dialysis days if possible, given the logistics of coordinating both procedures (i.e., dialysis, access procedure)
and the fact that most patients are physically tired after
dialysis.
Noninvasive Imaging
Noninvasive imaging in the diagnostic vascular laboratory is
the cornerstone of our approach to permanent dialysis access.
It is also recommended by the KDOQI and likely represents
the current standard of care. Numerous studies have documented that preoperative noninvasive imaging increases
the percentage of patients undergoing autogenous access,
although whether it results in a higher autogenous access
maturation rate has been less clear.52,63-65 Notably, Ferring
et al66 performed a randomized, controlled trial and reported
that preoperative noninvasive imaging was associated with a
lower initial failure rate for autogenous access, improved
primary assisted patency at 1 year, but no difference in primary
patency at the same time point.
The noninvasive imaging in our practice includes the
evaluation of both the arterial and venous circulation. Specically, pressure measurements in the brachial, radial, ulnar,
and digital arteries are taken, and the corresponding Doppler
waveforms of all but the digital vessels are recorded. The
Allens test is repeated, and the diameters of both the radial
(at the wrist) and brachial (at the antecubital fossa) arteries
are measured. The cephalic and basilic veins are interrogated
with ultrasound from the wrist to the axilla, complete with
diameter measurements similar to the preoperative vein
survey obtained prior to infrainguinal arterial revascularization. The upper extremity central veins are also examined for
the presence of deep venous thrombosis, although the interrogation of the veins within the thoracic cavity is limited.
Notably, there is some variation in the vein diameter measurements, likely secondary to the variations in the patients
general state of hydration related to their dialysis cycle.67
This variation justies repeating the peripheral vein imaging
if the basilic and cephalic veins are deemed too small on the
initial study.
The preoperative noninvasive venous imaging has been
widely accepted, but the arterial imaging has not been as
widely adopted. We would contend that the arterial imaging
is equally important, given the high incidence of occlusive
disease in both the forearm and inow (i.e., subclavian, axillary, proximal brachial) vessels and the signicant anatomic
variants that can compromise the access choice and maturation rate.47,48,68-70
Access Conguration
A preliminary operative plan can usually be generated on the
basis of the results of the history, physical examination, and
noninvasive imaging. Our criteria for an adequate artery
include no hemodynamically signicant arterial inow stenoses and a diameter greater than 2 mm, and those for the vein
include no outow stenoses and a peripheral vein segment of
suitable length and diameter (>3 mm).53 Although these
criteria have been validated for autogenous access, they are
BOX 73-3
also likely appropriate for patients being evaluated for a prosthetic access.
The possible access congurations are shown in Box 73-3,
as listed by the nomenclature recommended by the Society
for Vascular Surgery Reporting Standards.71 This exhaustive
list can be distilled down to autogenous radial-cephalic, other
forearm autogenous, autogenous brachial-cephalic, autogenous brachial-basilic, other upper arm autogenous, forearm
prosthetic, and upper arm prosthetic. Notably, this list reects
our preferences in descending order and is consistent with
the KDOQI guidelines (preferred: autogenous radial-cephalic,
brachial-cephalic, transposed brachial-basilic; acceptable:
forearm prosthetic, upper arm).
Distal Radial-Cephalic Autogenous Arteriovenous Access.
The autogenous radial-cephalic AV access at the wrist was
the earliest autogenous accesses described and can be an
excellent option for certain patients. Unfortunately, it is
Upper Arm Autogenous Arteriovenous Access. The brachialcephalic and brachial-basilic are the traditional or common
upper arm autogenous access options and are associated with
better patency rates than the forearm autogenous AV accesses
as already noted. The proximal radial artery can be used as
an alternative to the brachial artery at the antecubital fossa,
and essentially all the same access congurations can be constructed. Access procedures based on the proximal radial
artery may have a lower incidence of access-related ischemia,
commonly referred to as steal syndrome (see Chapter 78),
than the brachial artery, although the obvious tradeoffs are
the absolute size of the artery and the quantity of arterial
inow. Both a randomized, controlled trial89 and a metaanalysis90 have reported that the autogenous brachial-basilic
access is superior to an upper arm prosthetic AV access in
terms of patency and reintervention rates. The basilic vein is
an attractive choice for an autogenous access because it is
relatively thick walled, large in diameter, and well preserved
in terms of cannulation for venipunctures and intravenous
catheters due to its relatively deep course. The transposed
brachial-basilic AV access can be performed as either a singleor a two-stage procedure (i.e., anastomosis/transposition or
anastomosis with subsequent transposition). El Mallah91
reported that the patency rates were superior for the twostage approach in a small, randomized trial, but the results
from other retrospective series have been contradictory.92,93
The two-stage procedure affords the obvious advantage that
the transposition is not performed unless that vein has
matured or dilated sufcient for cannulation, thus avoiding a
more complicated procedure (and the potential wound complications) unless there is some assurance that the access will
be successful. It has also been our anecdotal impression that
the maturation rate for the basilic vein is higher for the
two-stage approach.
The other autogenous AV access options in the upper
arm include the brachial-brachial and brachial-median antecubital AV accesses. The published experience with the
brachial-brachial conguration is somewhat limited and
contradictory.94-96 However, it is another autogenous option
for patients with a large brachial vein or paired brachial
veins. These veins are often intimately attached to the
brachial artery and have multiple communicating branches
that can complicate the dissection. The brachial-brachial
autogenous access can be constructed in two stages, as outlined previously for the brachial-basilic conguration, and
the same advantages apply. The brachialmedian antecubital
access (i.e., Gracz) can be an attractive option in patients
with CKD whose veins are somewhat diminutive and in
whom dialysis is not imminent.97 The cephalic or basilic
veins, which have diminutive outow, may ultimately dilate
enough to be suitable for cannulation.
Prosthetic Arteriovenous Access. The increased emphasis
on autogenous access by the KDOQI guidelines and the other
national initiatives has gradually decreased the number of
prosthetic AV accesses, although they play a signicant role
and may be a better access choice for some patients, as
1091
1092
Additional Imaging
The access conguration chosen on the basis of the noninvasive imaging may be conrmed with additional imaging.
We have traditionally used catheter-based venography and
arteriography, although they have partially been replaced by
computed tomography (CT)based alternatives. Notably, the
techniques for the CT venogram and arteriogram are somewhat different, and specic protocols should be developed
with the radiology team to ensure that the vessels of interest
are adequately imaged. The potential indications for arteriography are the presence of peripheral arterial occlusive
disease, diabetes, complex access procedures, multiple
failed access procedures, abnormal noninvasive studies, and
prior episodes of access-related hand ischemia. The potential
indications for venography include arm edema, multiple
venous collaterals, pacemakers, multiple central venous
catheters, multiple prior access procedures, and complex
reconstructions.
We have reported a 40% incidence of some type of abnormality on catheter-based arteriography and venography
during the prospective validation of our access algorithm,
with the ndings affecting the operative plan in up to half
the cases.53 Our ndings are likely not particularly surprising,
given the presence of forearm arterial occlusive disease in
the diabetic population and the high incidence of central
vein problems reported with central venous catheters, PICC
lines, and pacemakers. Iodinated contrast agents are nephrotoxic and relatively contraindicated in patients with CKD,
although the associated risk can be reduced with a combination of hydration, acetylcysteine, and sodium bicarbonate.
Operative Technique
The generic operative technique for hemodialysis access is
identical to that for all vascular surgical procedures, but
several points merit further comment. First, the choice of
anesthesia is based primarily on surgeon and patient preference, the various local, regional, and general approaches all
being acceptable. There is some suggestion that regional
anesthesia may lead to dilatation of both the peripheral veins
Autogenous Brachial-Cephalic
Arteriovenous Access
End to end
anastomosis
1093
1094
Cephalic
vein
Brachial
artery
End to end
anastomosis
Axillary
vein
Basilic
vein
Brachial
artery
End to end
anastomosis
Median
antecubital
vein
Brachial
artery
6 mm
PTFE graft
Separate
incision
1095
1096
Postoperative Care
General
Autogenous accesses that fail to mature sufciently for cannulation are evaluated further to identify the underlying,
potentially correctable, problem. In our practice, we usually
obtain a duplex ultrasound examination at one of the early,
monthly postoperative follow-up visits, with the timing dictated by the clinical progression of the access and the patients
status, delaying further investigation somewhat in patients
with CKD and no immediate need for dialysis. Remedial
imaging and intervention are dictated by the presumed
underlying cause of the failure to mature, with the common
problems including focal stenosis in the outow vein, diffuse
stenosis in the outow vein, inadequate arterial inow, central
vein stenosis/occlusion, accessory veins, and inaccessibility
due to the access depth relative to the skin (i.e., obesity). A
stulogram with central vein runoff is usually obtained for
patients with presumed problems in the outow or central
Axillary
vein
6 mm
PTFE
graft
Brachial
artery
End to end
anastomosis
Balloon Angioplasty Maturation. Balloon angioplasty maturation (BAM) likely represents the most aggressive treatment
algorithm to facilitate access maturation.118,119 In the technique outline by De Marco Garcia et al,118 angioplasty was
performed on the vein selected for the autogenous access
through its spatulated end prior to the construction of the
stula, and then remedial angioplasty procedures were performed at 2, 4, and 6 weeks postoperatively with sequentially
larger balloons. The investigators reported that 85% of the
veins were ultimately used for dialysis and that the 12-month
secondary patency rates were also approximately 85%.
1097
1098
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83. Cavatorta F, et al: Ulno-basilic arteriovenous stulae: indications and
surgical technique. J Vasc Access 9:7380, 2008.
84. Bourquelot P, et al: Placement of wrist ulnar-basilic autogenous arteriovenous access for hemodialysis in adults and children using microsurgery. J Vasc Surg 53:12981302, 2011.
85. Capurro F, et al: The middle arm arteriovenous stula is an additional
option to expand autogenous hemodialysis access. J Vasc Access
13:208214, 2012.
86. Bonforte G, et al: The middle-arm stula as a valuable surgical approach
in patients with end-stage renal disease. J Vasc Surg 52:15511556,
2010.
87. Jennings WC: Creating arteriovenous stulas in 132 consecutive
patients: exploiting the proximal radial artery arteriovenous stula:
reliable, safe, and simple forearm and upper arm hemodialysis access.
Arch Surg 141:2732, 2006.
88. Gefen JY, et al: The transposed forearm loop arteriovenous stula: a
valuable option for primary hemodialysis access in diabetic patients.
Ann Vasc Surg 16:8994, 2002.
89. Keuter XH, et al: A randomized multicenter study of the outcome of
brachial-basilic arteriovenous stula and prosthetic brachial-antecubital forearm loop as vascular access for hemodialysis. J Vasc Surg 47:395
401, 2008.
90. Lazarides MK, et al: Transposed brachial-basilic arteriovenous stulas
versus prosthetic upper limb grafts: a meta-analysis. Eur J Vasc Endovasc
Surg 36:597601, 2008.
91. El Mallah S: Staged basilic vein transposition for dialysis angioaccess.
Int Angiol 17:6568, 1998.
92. Syed FA, et al: Comparison of outcomes of one-stage basilic vein
transpositions and two-stage basilic vein transpositions. Ann Vasc Surg
26:852857, 2012.
93. Reynolds TS, et al: A comparison between one- and two-stage brachiobasilic arteriovenous stulas. J Vasc Surg 53:16321638, 2011.
94. Greenberg JI, et al: The brachial artery-brachial vein stula: expanding
the possibilities for autogenous stulae. J Vasc Surg 48:12451250,
1250, 2008.
95. Torina PJ, et al: Brachial vein transposition arteriovenous stula: is it
an acceptable option for chronic dialysis vascular access? J Vasc Access
9:3944, 2008.
96. Lioupis C, et al: Autogenous brachial-brachial stula for vein access:
haemodynamic factors predicting outcome and 1 year clinical data. Eur
J Vasc Endovasc Surg 38:770776, 2009.
97. Bender MH, et al: The Gracz arteriovenous stula evaluated: results of
the brachiocephalic elbow stula in haemodialysis angio-access. Eur J
Vasc Endovasc Surg 10:294297, 1995.
98. Curi MA, et al: Hemodialysis access: inuence of the human immunodeciency virus on patency and infection rates. J Vasc Surg 29:608616,
1999.
99. Brock JS, et al: The inuence of human immunodeciency virus infection and intravenous drug abuse on complications of hemodialysis
access surgery. J Vasc Surg 16:904910, 1992.
100. Gorski TF, et al: Complications of hemodialysis access in HIV-positive
patients. Am Surg 68:11041106, 2002.
101. Barnard KJ, et al: Accessible autogenous vascular access for hemodialysis in obese individuals using lipectomy. Am J Surg 200:798802, 2010.
102. Zanow J, et al: Proximalization of the arterial inow: a new technique
to treat access-related ischemia. J Vasc Surg 43:12161221, 2006.
103. Huber TS, et al: Midterm outcome after the distal revascularization
and interval ligation (DRIL) procedure. J Vasc Surg 48:926932, 2008.
104. Cavatorta F, et al: Subclavian vein stenosis: a potentially serious complication in chronic hemodialysis patients with permanent cardiac
pacemakers. Int J Artif Organs 20:316318, 1997.
105. Asif A, et al: Patency rates for angioplasty in the treatment of pacemaker-induced central venous stenosis in hemodialysis patients: results
of a multi-center study. Semin Dial 22:671676, 2009.
106. Reynolds TS, et al: Pre-operative regional block anesthesia enhances
operative strategy for arteriovenous stula creation. J Vasc Access
12:336340, 2011.
107. Sahin L, et al: Ultrasound-guided infraclavicular brachial plexus block
enhances postoperative blood ow in arteriovenous stulas. J Vasc Surg
54:749753, 2011.
108. Elsharawy MA, et al: Does regional anesthesia inuence early outcome
of upper arm arteriovenous stula? Saudi J Kidney Dis Transpl 21:1048
1052, 2010.
109. Schenk WG, III: Improving dialysis access: regional anesthesia
improves arteriovenous stula prevalence. Am Surg 76:938942, 2010.
110. DAyala M, et al: The effect of systemic anticoagulation in patients
undergoing angioaccess surgery. Ann Vasc Surg 22:1115, 2008.
111. Schild AF, et al: Preliminary prospective randomized experience with
vascular clips in the creation of arteriovenous stulae for hemodialysis.
Am J Surg 178:3337, 1999.
112. Wixon CL, et al: Understanding strategies for the treatment of ischemic steal syndrome after hemodialysis access. J Am Coll Surg 191:301
310, 2000.
113. Lee T, et al: Needle inltration of arteriovenous stulae in hemodialysis: risk factors and consequences. Am J Kidney Dis 47:10201026,
2006.
114. Ayez N, et al: Secondary interventions in patients with autologous
arteriovenous stulas strongly improve patency rates. J Vasc Surg
54:10951099, 2011.
115. Berman SS, et al: Impact of secondary procedures in autogenous arteriovenous stula maturation and maintenance. J Vasc Surg 34:866871,
2001.
116. Hingorani A, et al: Impact of reintervention for failing upper-extremity
arteriovenous autogenous access for hemodialysis. J Vasc Surg 34:1004
1009, 2001.
117. Lee T, et al: Decreased cumulative access survival in arteriovenous
stulas requiring interventions to promote maturation. Clin J Am Soc
Nephrol 6:575581, 2011.
118. De Marco Garcia LP, et al: Primary balloon angioplasty plus balloon
angioplasty maturation to upgrade small-caliber veins (<3 mm) for
arteriovenous stulas. J Vasc Surg 52:139144, 2010.
119. Samett EJ, et al: Augmented balloon-assisted maturation (aBAM) for
nonmaturing dialysis arteriovenous stula. J Vasc Access 12:912, 2011.
120. Stoikes N, et al: Salvage of inaccessible arteriovenous stulas in obese
patients: a review of 132 brachiocephalic stulas. Am Surg 75:705709,
2009.
121. Faiyaz R, et al: Salvage of poorly developed arteriovenous stulae with
percutaneous ligation of accessory veins. Am J Kidney Dis 39:824827,
2002.
122. Levit RD, et al: Asymptomatic central venous stenosis in hemodialysis
patients. Radiology 238:10511056, 2006.
123. Renaud CJ, et al: Comparative outcomes of treated symptomatic versus
non-treated asymptomatic high-grade central vein stenoses in the
outow of predominantly dialysis stulas. Nephrol Dial Transplant
27:16311638, 2012.
CHAPTER 74
Hemodialysis Access:
Dialysis Catheters
KAREN WOO / VINCENT L. ROWE
INDICATIONS
The tunneled hemodialysis catheter serves a valuable role in
the treatment of patients with end-stage renal disease and has
distinct advantages over autogenous (arteriovenous stula
[AVF]) and prosthetic (arteriovenous graft [AVG]) arteriovenous hemodialysis access. The benets of tunneled hemodialysis catheters include immediate use for hemodialysis,
uncomplicated and needle-free connection to the dialysis
circuit, elimination of cannulation site complications, and
simple insertion technique that can be performed by many
different interventional specialists.2
The most common indication for placement of a tunneled
hemodialysis catheter is for urgent hemodialysis while the
patient is waiting for an AVF to be created or to mature.
Hemodialysis through a mature AVF represents the most
optimal form of hemodialysis access, and ideally patients
should be referred for placement of permanent access long
before the need for hemodialysis. In this way, patients have
an adequate amount of time for AVF maturation, and the
requirement for a tunneled hemodialysis catheter is eliminated altogether. Unfortunately, demise of renal function is
not a linear estimation. At the same time, care before endstage renal disease is often inadequate, resulting in late referral to a nephrologist and to an access surgeon.
TYPES OF CATHETERS
The feasibility of using a felt cuffed catheter for prolonged
hemodialysis was rst described in 1988.3 The authors documented a median catheter survival of 8 weeks for a tunneled
hemodialysis catheter placed in the subclavian vein. Since
this initial report, catheter design and preferred anatomic
position for placement have evolved. Early cuffed catheters
were straight in conguration and stiff. These have been
largely supplanted by precurved exible catheters with various
tip designs.
Design Characteristics
Catheter designs aim to achieve one main goal: adequate
dialysis clearance at a relatively high ow rate. Currently used
hemodialysis machines maintain ow rates of 300 to 350 mL/
min through indwelling catheters to provide reasonable
clearance times for the patients.4 To support the high-ow
demand, some manufacturers have increased the catheter
lumen size up to 16F. In addition, the phenomenon of recirculation must be minimized to ensure adequate clearance.
The arterial lumen of the catheter is the outow to the
dialysis machine from the patient; the venous lumen is
dened as the inow from the machine back to the patient.
Access recirculation is the reentry of dialyzed blood from the
venous lumen directly into the arterial lumen, thus bypassing
the systemic circulation and leading to inefcient dialysis.5
Design Categories
Numerous manufacturer modications exist in an effort to
satisfy the requirements of high ow rates and minimal
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A
B
Figure 74-2
catheter is inserted into the internal jugular vein and tunneled over the clavicle. Newer polyurethane catheters have
a stiffer construct and higher tensile strength and thereby
allow thinner walled catheters with smaller outer diameters.
Numerous reviews directly compare performance of individual tunneled hemodialysis catheters with specic outcome
variables of ow rate, recirculation time, and patency. Unfortunately, despite isolated benecial characteristics of a particular catheter, no universal signicant benet has been
demonstrated by one catheter over the competitors.2,4,5,7
PREOPERATIVE EVALUATION
History and Physical Examination
As with any clinical assessment, the proper preoperative
evaluation of a patient begins with a detailed history and
physical examination. Specic inquiries should include
details such as prior long-term central line placement, prior
AVF or AVG placement, prior tunneled hemodialysis catheter infections, history of a coagulation disorder, and history
of a pacemaker. Physical examination of the neck and chest
is critical in the evaluation of the hemodialysis patient. Evidence of a previously placed tunneled hemodialysis catheter,
previous permanent accesses, upper extremity or facial edema,
and ipsilateral venous distention with visible venous collaterals should alert the clinician to the possibility of central
veno-occlusive disease.
Numerous specialists have acquired the skill set to properly place a tunneled hemodialysis catheter. However, there
is a signicant advantage in terms of continuity of care when
the same practitioner places the tunneled hemodialysis catheter and the permanent access or when a team approach
coordinates these procedures. There are a nite number of
access sites available for both tunneled catheter and permanent access placement. Therefore, a comprehensive plan that
embraces all forms of hemodialysis access may provide
maximum benet of each crucial access site.
CATHETER INSERTION
Site Selection
Numerous venous access sites exist for insertion of a tunneled
hemodialysis catheter. However, the right internal jugular
vein is the preferred access site because it has the best patency,
presumably owing to less kinking. In a prospective evaluation, factors affecting long-term survival of tunneled hemodialysis catheters were analyzed in a cohort of 812 catheters
in 492 patients.2 Factors that were associated with immediate
failure of the tunneled hemodialysis catheter were malposition and kinking. A tunneled hemodialysis catheter placed
in the right internal jugular vein demonstrated signicantly
longer survival compared with one placed in the left internal
jugular vein. Tunneled hemodialysis catheters placed in the
femoral vein had the worst long-term survival. The subclavian vein should be avoided if possible to prevent catheterinduced subclavian stenosis, which would negatively affect
the future placement of ipsilateral permanent access.2,4
A tunneled hemodialysis catheter from the right internal
jugular vein should be 17 to 19 cm in length; catheters from
the left are slightly longer. When femoral access is used, long
catheters (24 to 31 cm) should be placed so that the tip
can reach into the inferior vena cava to produce the best
ow rates.
Technique
Tunneled hemodialysis catheter insertion should be performed in a procedure room under uoroscopic guidance.
Bedside placement is discouraged because of the need for
proper sterility, the possibility of additional endovascular
procedures (such as venography and venoplasty), and the
requirement for uoroscopy. The procedure is usually performed under local anesthesia with conscious sedation.
Patients who have had numerous prior catheters have an
increased risk of central venous stenoses or occlusions that
may increase the complexity of the procedure. In such
cases, general anesthesia is preferred. Preoperative antibiotic
prophylaxis directed at gram-positive bacterial strains is
administered before skin incision in each case. The skin
is then prepared with isopropyl alcohol and chlorhexidine
solutions.
Ultrasound evaluation with a sterile covered transducer
conrms access vein patency. The site of vein cannulation
should be 3 to 4 cm cephalad to the clavicle. Real-time ultrasound guidance is used to access the vein. The puncture is
performed with a micropuncture 21-gauge needle, 0.018-inch
guide wire, and 5F coaxial catheter (Fig. 74-3). After successful vein cannulation with the micropuncture needle, the introducer and 0.018-inch wire are removed and exchanged for
a 0.035-inch wire. In preparation for the large-bore hemodialysis catheter, a 1-cm skin incision is made surrounding the
wire entry site (Fig. 74-4, short arrow). Fluoroscopic imaging
should be used during all wire maneuvers to conrm wire
position.
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Antegrade Placement
A small incision is made on the anterior chest where the
tunneled hemodialysis catheter is to exit the subcutaneous
tunnel (Fig. 74-4, long arrow). The exit site of the tunneled
hemodialysis catheter should be inferior and lateral to the
vein entry site in location. The exit site should also be positioned such that the felt cuff on the catheter shaft is 1 cm
Figure 74-4 Placement of the tunneled hemodialysis catheter alongside the anticipated catheter course to determine where to position
the exit site. Internal jugular vein puncture site (short arrow); upper
chest catheter exit site (long arrow).
proximal to the exit site. Placement of the tunneled hemodialysis catheter alongside the anticipated catheter course is
useful in determining where the exit site should be positioned. The tunneled hemodialysis catheter is then attached
to the tunneling device and passed subcutaneously from the
chest incision up through the vein entry site incision in the
neck, traversing anterior to the clavicle en route (Fig. 74-5).
The track of the wire is sequentially dilated, and the nal
introducer and peel-away sheath unit is inserted until the
sheath is hubbed at the skin (Fig. 74-6). The introducer
and wire are removed, and the tunneled hemodialysis catheter is inserted through the peel-away sheath (Fig. 74-7).
Once the tunneled hemodialysis catheter is fully inserted, the
peel-away sheath is withdrawn.
Each lumen of the catheter is aspirated and ushed with
dilute heparin (100 units of heparin sulfate per milliliter of
normal saline). Both of these actions should be easily accomplished without resistance. If resistance is encountered, the
tunneled hemodialysis catheter should be examined under
uoroscopy to rule out a kink in the path of the catheter
or malpositioning of the tip. Ideally, the most distal tip of
the catheter should be in the distal superior vena cava/
proximal right atrium border. This preferred position corresponds to the shadow of the right mainstem bronchus
(Fig. 74-8).
The chest wall and vein entry site incisions are closed
with absorbable sutures, and the tunneled hemodialysis
Figure 74-6
1103
Retrograde Placement
Pneumothorax
Figure 74-8 Chest radiograph demonstrating proper position of the
tip of the tunneled hemodialysis catheter (arrow) at the level of the
right mainstem bronchus.
An end-expiratory upright chest radiograph should be performed after placement of a tunneled hemodialysis catheter
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Hemothorax
Placement of tunneled hemodialysis catheters may be complicated by the development of a hemothorax when the back
wall of either a vein or artery and the parietal pleura are
perforated by an advancing needle tip, dilator, or sheath.17
The subclavian vein or artery, the innominate vein, or even
the superior vena cava may be involved. The lack of effective
tamponade combined with negative respiratory pressure may
result in a large blood loss through a small puncture. Clinically, patients may develop respiratory compromise accompanied by dullness to percussion and decreased breath sounds
on the affected side. A decreased hematocrit and evidence of
uid in the pleural cavity on the chest radiograph strongly
support the diagnosis. Drainage of the pleural space with a
tube thoracostomy is generally adequate therapy and should
be performed for signicant hemothorax to prevent entrapment of the lung. Rarely, bleeding must be controlled surgically or, if possible, percutaneously with the use of covered
stents.
Subcutaneous Hematoma
Subcutaneous hematoma can occur when vessels in the cervical and clavicular area are lacerated. Prolonged compression
(15 minutes or more), with or without catheter removal,
usually controls the bleeding unless there is a major vascular
Wire Embolism
Wire embolism occurs when control of the wire is lost during
the procedure or the guide wire is sheared off by the access
needle as it is withdrawn. If resistance to wire removal is
encountered, uoroscopic imaging should be used, and
removal of the wire and needle together as a unit may be
required. Fortunately, most foreign bodies, including segments of guide wires, can usually be removed in the angiography suite with use of a wire snare retrieval system.19
Cardiac Arrhythmia
Cardiac complications related to central venous catheterization are rare. Arrhythmia during placement of a tunneled
hemodialysis catheter is associated with the guide wires irritating the myocardium. Patients who have a history of a
cardiac arrhythmia or those with altered plasma electrolytes
are at a higher risk. The problem can be minimized by use of
guide wires that have distance markings and uoroscopy to
visualize the location of the tip of guide wires and catheters.
If cardiac arrhythmias develop after the placement of a tunneled hemodialysis catheter, the catheter position should be
checked uoroscopically or with a chest radiograph and the
catheter tip should be withdrawn if the tip is near or traversing the tricuspid valve. Rarely, patients will have arrhythmias
that require chemical or electrical cardioversion. In a series
of 300 patients who underwent central venous catheterization, the incidence of cardioversion for a procedure-associated
arrhythmia was 0.9%.20
Cardiac Perforation
The soft, exible hemodialysis catheters that are currently
used are unlikely to perforate the heart. More common causes
of cardiac perforation are guide wires, dilators, and rigid introducers. Cardiac perforation may result in acute pericardial
tamponade from bleeding or uid infusion into the pericardial
space. Signs and symptoms of pericardial tamponade can
develop rapidly and include shock and cyanosis with marked
cervical venous distention. Tachycardia and mufed heart
sounds are generally present, and a large globular cardiac
silhouette may be present on a chest radiograph. Any intraluminal catheter devices should be removed and pericardiocentesis or a pericardial window created. If the tamponade
recurs after pericardiocentesis or creation of a window, median
sternotomy with formal cardiac repair may be necessary.
Nerve Injuries
Catheter Misplacement
In a prospective study of 1619 patients, the incidence of
catheter tip malposition, dened as extrathoracic or ventricular positioning, was 3.3%.24 The use of uoroscopy during
catheter placement should eliminate the occurrence of catheter tip malposition. If there is a question as to the location
of the tip of the catheter during placement, contrast material
can be injected through the catheter under uoroscopic guidance to help dene the anatomy.
Venous
If the catheter tip is left in the subclavian, axillary, jugular,
or hepatic vein, the catheter tip or pressure generated during
hemodialysis frequently causes intimal injury, which leads to
thrombosis of the vein.25 Stiff catheters or introducers left
abutting the wall of the superior vena cava or more peripheral
veins can also erode through the vessel wall and produce a
hemomediastinum or hydromediastinum.
Arterial
Catheters may be inadvertently placed into the subclavian or
carotid artery without the practitioners recognizing the
problem. This is more common in a hypotensive or poorly
oxygenated patient who may not have return of bright red,
pressurized blood when an artery is punctured. As tunneled
hemodialysis catheters are generally placed on an elective
basis, arterial placement is rare. If there is a question of arterial placement, the pressure can be transduced through the
catheter to see if the waveform is arterial or venous. A sample
from the catheter can also be sent for a blood gas analysis to
Air Embolism
Air embolism is a rare but potentially lethal complication of
central venous catheterization that can be either an acute or
a late complication.17 In its late form, air embolism generally
occurs when air enters the catheter either before attachment
of the tubing or when the tubing becomes disconnected.28,29
Air embolization can also occur through cracks in the catheter or its hub as well as through the catheter track after the
removal of a central venous catheter.30 Patients should be
instructed that in the event the catheter becomes disconnected or uncapped, a critical complication could result.
Patients should be instructed to cap the open catheter with
a thumb or nger and to call for help immediately. An occlusive dressing should be placed over the skin puncture site
when the catheter is removed to allow adequate sealing of
the track.
If sudden cardiorespiratory collapse develops in a patient
with a tunneled hemodialysis catheter, air embolism must be
strongly considered. Further embolization must be prevented
by capping or clamping of the catheter while the patient is
simultaneously placed in the Trendelenburg and left lateral
decubitus position (Durant maneuver).31 This position displaces air away from the pulmonic valve, which relieves the
right ventricular outow obstruction. The catheter can be
advanced into the heart to aspirate the air.32
The brachial plexus is the nerve structure that is most vulnerable during percutaneous catheterization by virtue of its large
size and proximity to the subclavian vein and artery.21,22
Acute upper extremity pain referred along a neural anatomic
pathway suggests impingement on the brachial plexus and
necessitates immediate withdrawal of needles or catheters.
Permanent injury is rare. The vagus, recurrent laryngeal, and
phrenic nerves are also in proximity to the internal jugular
vein. However, these are small nerves and are infrequently
injured. The development of hoarseness after catheter placement suggests injury to the vagus or recurrent laryngeal nerve.
Phrenic nerve injuries are generally asymptomatic and are
incidentally identied on radiographic examination when an
elevated hemidiaphragm is seen.23 The development of
Horners syndrome has also been reported by inadvertent
trauma to the stellate ganglion during percutaneous cannulation of the internal jugular vein.
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Catheter Embolism
Fractures can develop in the material of chronically indwelling catheters. This usually occurs at sites of stress, such as the
thoracic inlet.33,34 Fractures can result in breaking off and
embolization of the distal aspect of the catheter. Catheter
embolism is diagnosed when an incomplete catheter is
removed from a patient. The retained catheter segment can
typically be removed in the angiography suite with use of a
wire snare retrieval system.35
Catheter Occlusion
Catheter occlusion occurs in 30% to 40% of patients with
tunneled hemodialysis catheters.36 Occlusion of the catheter
generally is a consequence of the development of a brin
sleeve or plug at the catheter tip. The ability to infuse uid
into the catheter but the inability to withdraw blood often
indicates impending occlusion.
Prevention
A randomized controlled trial of the use of low-dose warfarin
to prevent catheter thrombosis demonstrated lack of efcacy.37 Another randomized trial was performed with three
arms: aspirin 325 mg/day, warfarin titrated to an international normalized ratio of 2 to 3, and control group. This
study found that whereas both aspirin and warfarin were
equally effective at increasing catheter patency, there was a
signicant increase in the risk of gastrointestinal bleeding in
both treatment groups.38 As such, use of antiplatelet agents
or systemic anticoagulation is not recommended to prevent
thrombosis. However, a randomized trial of patients assigned
to a catheter-locking regimen of heparin (5000 units/mL)
three times a week or recombinant tissue plasminogen activator (1 mg in each lumen) substituted for heparin one session
a week did demonstrate a twofold decrease in the risk of
catheter malfunction in patients treated with recombinant
tissue plasminogen activator once a week with no increase in
the risk of bleeding.39
Treatment
Local infusion of brinolytic agents has been used in the
salvage of occluded central venous catheters.40,41 Currently,
alteplase is the only brinolytic agent that is approved for
treatment of occluded central venous catheters. Most commonly, 2 mg of brinolytic agent in 2 mL of solution is
injected and allowed to dwell in the catheter for 2 to 3 hours.
The catheter is then irrigated and ushed, with removal of
any residual clot. This process can be repeated until patency
is restored. However, use of this technique may result in only
a limited number of additional dialysis sessions before the
treatment must be repeated. A study of 570 catheters during
a 2.5-year period demonstrated a median of ve to seven
additional dialysis sessions after each treatment.42 Guide
wires should never be passed through catheters in an effort
to relieve an obstruction because of the risk of dislodging part
or all of the occlusion and causing an embolic event.
internal jugular vein catheter, 42% of patients in the subclavian group had a stenosis versus 10% in the jugular group.52
As such, cannulation of the subclavian vein for hemodialysis
access should be avoided if at all possible. Catheter-associated
central vein stenosis can also involve the brachiocephalic
vein as well as the superior vena cava.
Presentation
Central vein stenosis can be completely asymptomatic.
Often, an ipsilateral upper extremity access is created without
knowledge of a central vein stenosis, which results in the
rapid development of symptoms, the most common of which
is arm edema. Patients with brachiocephalic vein stenosis
can also present with facial edema. Other manifestations of
central vein stenosis are aneurysmal dilatation of the extremity veins and the ipsilateral AVF, thrombosis of the access,
inadequate dialysis, prolonged bleeding after use of the access,
and superior vena cava syndrome.49
Treatment
Catheter-Related Infection
There are three categories of catheter-related infection: exit
site infection, tunnel infection, and bacteremia.1 The NKF
KDOQI guidelines dene an exit site infection as inammation conned to the area surrounding the catheter exit site,
not extending superiorly beyond the cuff if the catheter is
tunneled, with exudate culture conrmed to be positive. A
tunnel infection is dened as the catheter tunnel superior to
the cuff is inamed, painful, and may have drainage through
the exit site that is culture positive. Finally, catheter-related
bacteremia is dened as blood cultures are positive for the
presence of bacteria with or without the accompanying
symptom of fever. The incidence of catheter-related bacteremia ranges from 0.6 to 6.5 episodes per 1000 catheter days.54
Bacteriology
The predominant organism isolated from infected lines is
gram-positive (52%-84%), with Staphylococcus aureus making
up 21% to 43%.54 Methicillin-resistant S. aureus is reported
in 12% to 38% of cases.54 Gram-negative bacilli, including
Treatment
Ideally, the management of an infected hemodialysis catheter
includes removal of the catheter.54 Initial empirical antibiotic
therapy should include broad-spectrum coverage of potentially resistant strains of gram-positive organisms as well as
gram-negative organisms.57 This coverage should be adjusted
to a focused regimen when culture results become available.
Amphotericin B or caspofungin, which has a more favorable
toxicity prole, should be used if there is evidence of disseminated fungal infection or if patients demonstrate persistent
fungemia after catheter removal.47 Uncomplicated S. aureus
catheter-related bacteremia is generally treated with 4 to 6
weeks of antibiotic therapy; gram-negative bacilli or enterococcus bacteremia is usually treated with 7 to 14 days of
therapy. Bacteremia with Candida is usually treated with a
minimum of 14 days of antibiotic therapy. Complicated bacteremia with septic thrombophlebitis or endocarditis is
usually treated for 4 to 6 weeks and osteomyelitis for 6 to
8 weeks.57
Catheter exit site infections alone can usually be salvaged
with topical and systemic antibiotics without the need for
catheter replacement.57 Presence of a tunnel infection or
catheter-related bacteremia requires catheter removal with
delayed placement of a permanent access. The NKF KDOQI
Work Group recommends delay of placement of a new permanent access until culture results have been negative for
at least 48 hours after cessation of antibiotic therapy.1
Depending on the length of antibiotic therapy, this may
or may not be reasonable. Strategies for catheter salvage
include exchange over a wire and catheter salvage with or
without antibiotic lock. Whereas catheter salvage has been
described, it is associated with failure rates greater than
65%.54 As such, the safest course of action is most often to
remove the catheter.
Elevation and compression of the upper extremity can occasionally be enough to relieve the edema associated with
central venous stenosis but is unlikely to be effective if there
is an access on the ipsilateral extremity. NKF KDOQI guidelines recommend percutaneous transluminal angioplasty with
or without stent placement as the preferred treatment for
central venous stenosis.1 In a small randomized study of percutaneous transluminal angioplasty and stent placement,
1-year primary patency in both groups was dismal at 12% and
11%, respectively.53 However, the secondary patency at 1 year
was 100% for percutaneous transluminal angioplasty and
78% for stenting. This marked difference in primary and
secondary patency underscores the fact that multiple procedures are usually needed to maintain patency after endovascular management of central venous stenoses.
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