Core Curriculum

Essentials of anticoagulation in
hemodialysis
Karl-Georg FISCHER
Department of Medicine, Division of Nephrology and General Medicine, University Hospital Freiburg,
Freiburg, Germany
Abstract
Numerous acquired hemostatic abnormalities have been identied in renal insufciency. Hemodial-
ysis procedures add to these disturbances as they repetitively imply turbulent blood ow, high shear
stress, and contact of blood to articial surfaces. This nonphysiological environment leads to acti-
vation of platelets, leukocytes, and the coagulation cascade, resulting in fouling of the membrane
and ultimately in clotting of bers and the whole hemodialyzer. Anticoagulation in hemodialysis is
targeted to prevent this activation of coagulation during the procedure. Most agents inhibit the
plasmatic coagulation cascade. Still commonly used is unfractionated heparin, followed by low-mo-
lecular-weight heparin preparations with distinct advantages. Immune-mediated heparin-induced
thrombocytopenia constitutes a potentially life-threatening complication of heparin therapy requir-
ing immediate switch to nonheparin alternative anticoagulants. Danaparoid, lepirudin, and argatro-
ban are currently being used for alternative anticoagulation, all of which possess both advantages
and limitations. In the past, empirical strategies reducing or avoiding heparin were applied for
patients at bleeding risk, whereas nowadays regional citrate anticoagulation is increasingly used
to prevent bleeding by allowing procedures without any systemic anticoagulation. Avoidance of
clotting within the whole hemodialyzer circuit is not granted. Specific knowledge of the mechanisms
of coagulation, the targets of the anticoagulants in use, and their respective characteristics
constitutes the basis for individualized anticoagulation aimed at achieving full patency of the
circuit throughout the procedure. Patency of the circuit is an important prerequisite for optimal
hemodialysis quality.
Key words: Hemodialysis, coagulation, heparins, danaparoid, argatroban, lepirudin
INTRODUCTION
Adequate anticoagulation in hemodialysis procedures re-
lies on knowledge of the basic principles of hemostasis
and notably the clotting cascade. Hemostatic abnormal-
ities in renal insufciency as well as activation of clotting
on articial surfaces further require attention. These as-
pects are discussed in the rst part of this review, fol-
lowed by the second part, which focuses on the principles
of anticoagulation and the currently available main anti-
coagulants used in routine hemodialysis procedures.
PRINCIPLES OF COAGULATION
Hemostasis can be dened as a process of brin clot for-
mation to seal a site of vascular injury without resulting in
total occlusion of the vessel. To this end, a complex array
of multiple processes including both cellular elements
and numerous plasma factors with enzymatic activity
is arranged (1) to activate clotting rapidly, (2) to limit
Correspondence to: K.-G. Fischer, MD, PhD, Department of
Medicine, Division of Nephrology and General Medicine,
University Hospital Freiburg, Freiburg Medical School,
Hugstetter Strasse 55, D-79106 Freiburg, Germany.
E-mail: [email protected]
Hemodialysis International 2007; 11:178189
r 2007 The Authors. Journal compilation r 2007 International Society for Hemodialysis 178
and subsequently terminate this activation, and (3) to re-
move the clot by brinolysis in the end.
The initial hemostatic response to stop bleeding is the
formation of a platelet plug at the site of vessel wall injury.
Platelets are activated by a multitude of stimuli, the most
potent of which are thrombin and collagen. Upon acti-
vation, platelets adhere to the subendothelial matrix,
aggregate, secrete their granule content, and expose pro-
coagulant phospholipids such as phosphatidylserine.
Platelet-derived membrane microvesicles markedly in-
crease the phospholipid surface on which coagulation
factors form multimolecular enzyme complexes with pro-
coagulant activity. Hence, platelet activation also leads to
propagation of plasmatic coagulation.
The coagulation process has long been viewed as a
cascade of proteolytic reactions ultimately resulting in
brin clot formation.
1,2
In this, 2 different mechanisms to
initiate clotting, i.e., the extrinsic and intrinsic pathway,
were dened, ultimately leading to a common pathway of
coagulation. Whereas this concept ts well with the
screening laboratory tests prothrombin time and activat-
ed partial thromboplastin time (aPTT), it does not suf-
ciently explain certain clinical observations, which
challenge the view of 2 independent pathways of activa-
tion in vivo. Here, a model of cell-based hemostasis was
proposed comprising of 3 overlapping stages of initiation
on tissue-factor (TF)-bearing cells, amplication on plate-
lets, and propagation on the activated platelet surface.
3,4
For didactic purposes, the process of plasmatic brin
generation is described based on the classical concept of a
coagulation cascade, which comprises the sequential and
often overlapping activation of proenzymes or zymogens
to active enzymes, resulting in a stepwise amplication.
Its activation occurs by initiation of the extrinsic or the
intrinsic pathway (Figure 1). The extrinsic pathway is ini-
tiated by expression of TF, e.g., due to endothelial dam-
age. Tissue factor is a cofactor for the production of
activated factor VII (FVIIa). The TFFVIIa complex (the
extrinsic X-ase or tenase) activates factor X and factor
IX. In vivo, clotting is primarily initiated by this TF path-
way.
5
The intrinsic pathway, also termed the contact
activation pathway, is thought to be prominently involved
in activation of clotting on articial surfaces such as
hemodialysis membranes, but recent data challenge this
assumption.
6
Here, contact with negatively charged
surfaces leads to activation of high-molecular-weight
kininogen (HMWH), prekallikrein, and factor XII in an
ordered fashion (Figure 1). Activated factor XII (FXIIa)
activates FXI and FXIa activates factor IX. Factor IXa and
factor VIIIa form the intrinsic X-ase enzyme complex,
which activates factor X to FXa. Therefore, the exogenous
and contact activation pathway both converge in produc-
tion of FXa, which is the central activator of the subse-
quent common pathway. The FXa and FVa form the
prothrombinase complex, which converts prothrombin
(FII) to the active protease thrombin (FIIa) with enor-
mous efciency. Finally, thrombin converts the soluble
brinogen into insoluble brin, which is then stabilized
by FXIIIa to form stable clots. Assembly and function of
the aforementioned enzyme complexes require anionic
phospholipid surfaces and calcium ions.
The coagulation process is terminated by the circulat-
ing enzyme inhibitors antithrombin and TF pathway
inhibitor. Upon clot formation, thrombin binds to throm-
bomodulin. Owing to the subsequent conformational
change, the substrate specicity of thrombin no longer
allows for activation of platelets or cleavage of thrombin.
Instead, thrombin then activates the anticoagulant protein
C pathway, thus terminating its own production and
activation. Concerning brinolysis, the reader is referred
to current textbooks on hemostaseology.
HEMOSTATIC ABNORMALITIES IN
RENAL INSUFFICIENCY
The accumulation of uremic toxins causes complex dis-
turbances of the coagulation system. Uremia can lead
to an increased bleeding tendency, e.g., due to platelet
dysfunction,
7
which is further enhanced with use of anti-
coagulants during extracorporeal blood purication pro-
cedures. In contrast, clot formation and development of
Figure 1 Plasmatic coagulation cascade. Extrinsic and in-
trinsic pathway of activation converge, as both result in en-
zyme complexes converting factor X to Xa. Factor Xa is part
of the prothrombinase complex, which activates prothrom-
bin to thrombin. Thrombin is the nal key enzyme convert-
ing soluble brinogen to insoluble brin.
Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 179
thrombosis can also occur at increased rates in dialysis
patients: pulmonary embolism is more frequent in dialy-
sis patients than in age-matched controls.
8
Patients on
chronic intermittent hemodialysis frequently suffer from
vascular access thrombosis,
9
the risk of which is in-
creased in polytetrauoroethylene grafts compared with
arteriovenous stulas.
10
Further, numerous hemostatic
abnormalities have been found, which may account for
the increased risk of thrombosis in end-stage renal dis-
ease (ESRD) patients, a few of which are subsequently
mentioned: Patients with chronic renal failure have a high
prevalence of systemic inammation and diffuse endo-
thelial damage that may cause hypercoagulability.
11,12
Activation of platelets and monocytes has also been de-
tected.
13
Uremic patients with thrombotic events show
significantly higher platelet-derived microparticle counts
than patients without thrombotic events.
14
Antithrombin
levels as well as antithrombin activity can be reduced.
15,16
In patients with ESRD, deciencies of the anticoagulant
proteins C and S have been observed.
9,15,16
Activated
protein C resistance can occur
9
or activity of the antico-
agulant protein C can be decreased by inhibitors.
9,17
Ac-
tivation of the TF coagulation pathway has been found.
13
These complex hemostatic abnormalities have been
linked not only to thrombosis but also to progres-
sive atherosclerosis, a frequent condition in ESRD pa-
tients.
12,15
Hypercoagulability increases as renal function
declines.
12
Recently, in 16 subjects on maintenance HD,
deciencies in protein C, protein S, antithrombin, and
activated protein C resistance were completely corrected
within months after renal transplantation.
9
Hypercoagu-
lability in ESRD patients therefore essentially represents
an acquired and reversible condition. During the hemo-
dialysis treatment, markers of a procoagulant state in-
crease further despite the use of anticoagulants.
12,15,18
Although the clinical relevance of this subclinical throm-
bus formation is unclear, some authors suggest that an
increase in heparin dose by 50% compared with standard
recommendations may be warranted.
18
For further details
on thrombogenesis in hemodialysis patients, the reader is
referred to a recent review.
19
ACTIVATION OF THE COAGULATION
CASCADE IN THE EXTRACORPOREAL
CIRCUIT
Hemodialysis causes turbulent blood ow and high shear
rates.
20
Turbulent blood ow and high shear stress acti-
vate platelets directly. Shear is one major pathway of
platelet-induced hemostasis and thrombosis.
21
At slow
blood ow, platelets can bind to brinogen adherent to
the articial surface via their GPIIb/IIIa receptor. Receptor
binding and thrombin formation due to contact activation
result in the release of platelet secretion products, platelet
aggregation, and activation of the coagulation cascade. In
HD leukocytes and platelets coaggregate,
22,23
an effect
that in part appears to be membrane-dependent.
24
Co-
aggregation is followed by activation of both cell types.
On adhesion to articial surfaces, granulocytes release the
contents of their granules.
25
Granulocytes and monocytes
express TF, a potent activator of the coagulation cascade.
In addition to cellular activation, contact of blood with
articial surfaces induces profound activation of plasmat-
ic coagulation.
26
Clotting on articial surfaces is thought
to mainly occur via the intrinsic (contact activation) path-
way described above. The degree to which the coagula-
tion cascade is activated is determined by the blood ow
and the local concentration of factor XIIa. In addition to
the intrinsic pathway, extracorporeal blood purication
procedures also activate the extrinsic (TF) pathway of
coagulation.
6
Within the extracorporeal circuit, not only the dialyzer
but also other components are thrombogenic. The nee-
dles or catheters used for vascular access, the tubing, and
the arterial and venous bubble traps all contribute to
thrombogenesis. The arterial and venous bubble traps are
very thrombogenic, because blood ow is slower and in
some areas even stasis of blood may be present. In addi-
tion, the interface of air and blood and the turbulences in
the bubble trap are known inductors of the coagulation
cascade. Further risk factors for premature occlusion of
the extracorporeal circuit are slow blood ow, high hema-
tocrit, and blood transfusions into the extracorporeal
circuit.
STANDARD ANTICOAGULATION IN
HEMODIALYSIS
Routine anticoagulation for extracorporeal blood puri-
cation procedures is performed by agents interfering with
the plasmatic clotting cascade. Knowledge of the specific
characteristics of the agents in use is a prerequisite of
adequately tailoring the anticoagulant prescription to the
patients clinical condition and the setting in which
hemodialysis treatment is required.
According to their specific characteristics, anticoagu-
lants for hemodialysis procedures can be divided into
different subgroups. Here, 3 major features should be
known: (1) Anticoagulants may differ by their chemical
composition. For example, heparins and danaparoid are
glycosaminoglycans, the direct thrombin inhibitor lepiru-
din is a large polypeptide, and the small direct thrombin
Fischer
Hemodialysis International 2007; 11:178189 180
inhibitor argatroban is a synthetic derivative of arginin.
(2) Anticoagulants may exert their inhibition of the clot-
ting cascade indirectly by binding to physiological anti-
coagulants. This is the case for the heparins and
danaparoid, whose action mainly depends on the pres-
ence of antithrombin. In contrast, the direct thrombin
inhibitors do not require natural cofactors for their ac-
tion. (3) Anticoagulants may differ in their targets within
the clotting cascade or may exert different inhibitory po-
tency for the same target. For example, by definition, un-
fractionated heparin (UFH) inhibits FXa and FIIa with
equal potency, whereas danaparoid predominantly inhib-
its FXa. Figure 2 depicts the targets of selected anticoag-
ulants within the clotting cascade.
The subsequent sections can only give a short overview
on each anticoagulant agent or strategy. The information
provided therein does not allow for proper use of the re-
spective anticoagulant. Careful evaluation of the infor-
mation provided by the manufacturer and the dose rec-
ommendations given is a prerequisite for their use. For
further details on anticoagulation for hemodialysis pro-
cedures, the reader is referred to an overview published
recently.
19
Unfractionated heparin
Unfractionated heparin preparations constitute a mixture
of anionic glucosaminoglycans of varying molecular size
(540, mean 15 kDa). The main action of heparin on the
coagulation system is indirect due to the binding to an-
tithrombin (heparin-binding factor I). Heparin enhan-
ces the activity of this natural anticoagulant protein 1000
to 4000-fold. Antithrombin inactivates thrombin, factor
Xa, and to a lesser extent factors IXa, XIa, and XIIa. At
high doses, heparin also binds to heparin-binding factor
II. Heparin is ineffective against thrombin or factor Xa if
they are located in a thrombus or bound to brin or to
activated platelets. Because UFH has a narrow therapeutic
window of adequate anticoagulation without bleeding,
laboratory testing (aPTT or as bedside test activated clot-
ting time, ACT) of its effect is required. In addition to
increasing the bleeding risk, other side effects of heparin
are worsening of osteoporosis and lipid status, allergic
reactions such as pruritus, and thrombocytopenia.
Immune-mediated heparin-induced thrombocytopenia
(HIT) is a rare but life-threatening complication of hep-
arin therapy.
27,28
Application of heparin during hemodialysis requires an
initial loading dose, followed by a maintenance dose: as
an initial loading dose, the European best-practice guide-
lines for HD recommend administering 50 IU/kg UFH
into the arterial access needle.
29
The maintenance dose of
heparin is 500 to 1500 IU of UFH/hr, given via constant
infusion into the arterial line using an infusion pump.
29
Alternatively, the maintenance dose can be given as re-
peated bolus injection. During intermittent HD, the pa-
tient is systemically anticoagulated. The ACT is adjusted
to 80% above the baseline value. Because the hemodial-
ysis patient is systemically anticoagulated for at least 4 hr,
aPTT should be checked before surgical procedures after
dialysis. Heparin requirements during HD are determined
by patient-related factors, the amount of heparin adsorp-
tion to the membrane of the dialyzer, and the thrombo-
genicity of components of the extracorporeal circuit.
Table 1 lists the dose recommendations for use of UFH
for intermittent HD. The recommendations should be
considered as guidelines and not followed uncritically in
any individual patient.
Low-molecular-weight heparin (LMWH)
Low-molecular-weight heparin preparations comprise a
mixture of anionic glucosaminoglycans with a smaller
size (molecular weight: 48 kDa) compared with UFH.
The LMWH also bind to antithrombin. However, because
of the short chain length of LMWH, antithrombin/LMWH
complexes have less afnity to thrombin, resulting in a
reduced inhibition of thrombin compared with UFH. The
inhibitory effect on factor Xa vs. thrombin is 1:1 for UFH
but 2.5:1 or 3:1 in LMWH, depending on the individual
Figure 2 Targets of selected anticoagulants within the co-
agulation cascade. Antithrombin and heparin cofactor II in-
hibit key factors in the clotting cascade. Unfractionated
heparin (UFH), low-molecular-weight heparin (LMWH),
and danaparoid are indirect agents increasing the activity
of the natural inhibitors. Direct thrombin inhibitors block
thrombin. Citrate chelates calcium and thereby inhibits all
steps of the coagulation cascade.
Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 181
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Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 183
LMWH preparation. Several LMWH preparations have
been marketed, which differ in their chemical and phar-
macokinetic properties. Despite not being interchange-
able, LMWH preparations share the following common
features: (1) The anticoagulant effect (anti-Xa activity) of
LMWH in patients with normal renal function is highly
correlated with body weight, allowing use of a xed dose
per kilogram body weight. Laboratory monitoring is not
necessary in patients with normal renal function. (2) In
renal failure, dosing has to be reduced. (3) If monitoring
is performed, anti-factor Xa activity needs to be meas-
ured, while aPTTand ACTare not reliable.
30,31
Recently, a
modied Xa-ACT has been demonstrated to measure re-
liably the anticoagulant effect of LMWH preparations
within a point-of-care setup.
31
If anti-factor Xa activity
is measured, a level of 40.5 IU/mL is recommended in
the venous line of the extracorporeal circulation. In pa-
tients at high risk of bleeding, a lower anti-Xa activity may
be sufcient to prevent clotting of the dialysis circuit. (4)
LMWH are much less likely to induce HIT type II. A more
detailed description of common features of LMWH has
been given elsewhere.
19
Table 1 lists dose recommendations for use of LMWH
for intermittent HD as provided by the manufacturers.
The recommendations should be considered as guidelines
and not followed uncritically in any individual patient.
ALTERNATIVE ANTICOAGULATION IN
HIT
A moderate decline in platelet count is frequently ob-
served after commencing HD. However, thrombocytope-
nia during heparin therapy may hint at immune-mediated
HIT, which constitutes a potentially life-threatening com-
plication. This requires immediate diagnostic and appro-
priate therapeutic measures.
27,28
Heparin-induced thrombocytopenia type I
Within the rst 2 to 3 days of heparin therapy, a modest
reduction in platelet count (o100,000/mL) is frequently
seen. This is not due to an immunologic reaction but is
caused by a direct heparin-induced degranulation of
platelets. This type of thrombocytopenia (HIT type I) is
regarded as harmless. Platelet count increases even
though heparin therapy is continued.
Heparin-induced thrombocytopenia type II
From 4 to 10 days after initiating heparin therapy, HIT
type II may develop, which is an immune-mediated dis-
ease (now commonly referred to as HIT and likewise in
the consecutive sections in this review). Antibody forma-
tion against the complex of heparin and platelet factor 4
(HIT antibodies) is the cause of this devastating disease.
If HIT is suspected, immediate action has to be taken and
all heparin application has to be stopped, even before
laboratory test results are available conrming the pres-
ence of antibodies. Occasionally, HIT manifests immedi-
ately on start of heparin therapy, if the patient had
previous contact with heparin. In HIT, thrombocytope-
nia (420,000/mL, mean 60,000/mL) indicates platelet
consumption owing to the disease process. Here, low
platelet count is not associated with bleeding complica-
tions; instead, venous and arterial thromboembolism may
occur. Among the procoagulant abnormalities of the co-
agulation system, HIT presents with the highest rate of
clot formation (50% within 30 days).
32
HIT is also called
the white clot syndrome, because characteristic platelet-
rich, white arterial thrombi are formed. These may mani-
fest in a dramatic clinical picture with ischemia of one or
several limbs and a high mortality rate due to cerebral or
myocardial infarctions. However, the majority of thrombi
are formed in the venous system including the lungs. The
venous manifestations are frequently overlooked or not
interpreted as a manifestation of HIT.
Anticoagulation in hemodialysis patients
with HIT
If HIT is likely to be present, all applications of heparin
have to be stopped, including heparin ointments to the
skin or heparin-coated catheters. A heparin-free dialysis
must not use heparin for initial rinsing. LMWH prepar-
ations must also be avoided. Although LMWH induce
HITantibodies less frequently than UFH, they have a high
rate of cross-reactivity once UFH has induced HIT anti-
body formation. As long as the platelet count is low in
active HIT, systemic anticoagulation is mandatory to re-
duce the risk of life-threatening thrombus formation.
During this time, it is not sufcient to use, e.g., regional
citrate anticoagulation that merely prevents clot forma-
tion in the extracorporeal circulation. Established system-
ic alternative anticoagulation in patients with HIT is
performed with danaparoid, lepirudin, or argatroban.
Additionally, fondaparinux may become an additional
alternative option.
The subsequent sections only can give a short overview
on each anticoagulant agent. The information provided
therein does not allow for proper use of the respective
anticoagulant. Careful evaluation of the information pro-
vided by the manufacturer and the dose recommendations
Fischer
Hemodialysis International 2007; 11:178189 184
given is a prerequisite for their use. For further details on
alternative anticoagulation for hemodialysis procedures in
HIT patients including the numerous caveats, the reader is
referred to a detailed review published recently.
28
Danaparoid
Danaparoid is a heparinoid of low molecular weight
(5.5 kDa) consisting of heparan sulfate (83%), dermatan
sulfate, and chondroitin sulfate. Danaparoid constitutes
the alternative anticoagulant that was most widely used
for management of HD in patients with HIT.
33
In 2002,
danaparoid was withdrawn by the manufacturer from the
U.S. market, whereas it is still available in Canada and the
European Community.
The main anticoagulant effect of danaparoid depends
on binding to antithrombin and heparin cofactor II. Fac-
tor Xa is more selectively inhibited than with the use of
LMWH. The activity ratio for factor Xa to thrombin
inhibition is 22:1 (compared with 3:1 with LMWH).
Danaparoid has a low rate of cross-reactivity against
HIT antibodies. During danaparoid treatment, HIT anti-
bodies can be detected in vitro in 10% of cases. In 6.5%
of patients with HIT, persistent or repeated thrombocy-
topenia was observed with use of danaparoid.
34
As posi-
tive in vitro cross-reactivity is of uncertain clinical
significance, attention should focus on platelet count
monitoring after starting danaparoid application. A fur-
ther decline in platelet count, or new brin deposits and
clot formation within the extracorporeal circuit after ap-
plication of danaparoid, may indicate clinically relevant
cross-reactivity. For monitoring of danaparoid therapy
anti-Xa activity has to be measured, and aPTT is not
helpful. The half-life of the anti-Xa activity of danaparoid
is 25 hr in patients with normal renal function and is
further prolonged in uremia. An antidote is not available.
Table 1 lists the dose recommendations for use of
danaparoid for intermittent HD as provided by the manu-
facturer. The recommendations should be considered as
guidelines and not followed uncritically in any individual
patient. If applied with appropriate care, danaparoid pro-
vides adequate anticoagulation for HD of HIT patients
with a favorable benet/risk ratio, even during long-term
use. Before invasive procedures, appropriate (repetitive)
laboratory measurements have to be carried out in he-
modialysis patients on danaparoid treatment.
Direct thrombin inhibitors
Direct thrombin inhibitors do not require natural cofac-
tors to inhibit the clotting cascade. Instead, they directly
bind to and block thrombin, the nal key enzyme within
the coagulation process inducing the conversion of solu-
ble brinogen to insoluble brin. From the different
thrombin inhibitors currently available, lepirudin and
argatroban are approved for alternative anticoagulation
in HIT (in the United States and a number of other coun-
tries).
Hirudin
Lepirudin is a recombinant hirudin preparation approved
for the treatment of HIT in patients. Lepirudin is difcult
to use in patients with renal failure or on dialysis.
35,36
Because it is mainly eliminated by the kidneys, its half-life
is markedly prolonged in renal failure.
37
After a single
loading dose, the patient may be therapeutically antico-
agulated for 1 week or longer. Therefore, bleeding risk is
increased especially when interventions or surgery cannot
be circumvented. In this regard, adequate hirudin dosing
is essential.
35
Hirudin dose requirements in critically ill
patients on continuous HD are minimal, especially in the
case of anuria.
38
Bleeding risk can be reduced by applying
hirudin as a bolus rather than continuous infusion. In
case of bleeding complications, there is no antidote avail-
able to antagonize the anticoagulant effect of hirudin.
High-volume hemoltration, but not HD, is effective in
reducing hirudin plasma levels.
39,40
An ultraltrate vol-
ume of 15% of body weight reduces hirudin plasma levels
by 50%.
39
Hirudin constitutes a polypeptide and does not show
cross-reactivity to HIT antibodies. Yet, up to 74% of pa-
tients treated with hirudin for more than 5 days develop
anti-hirudin antibodies (aHAb).
41,42
The presence of
aHAb often requires dose adjustments.
41,43
Recent in
vivo studies clearly show that hirudin action is marked-
ly prolonged because aHAb delay its renal clearance even
without renal impairment.
44
In the presence of aHAb,
hemoltration no longer constitutes a rescue measure to
reduce hirudin plasma levels rapidly.
44
This aim may be
achieved only by plasmapheresis.
Monitoring of therapy is frequently performed by
measuring aPTT (target range 1.52.5 of normal). Acti-
vated partial thromboplastin time is not ideal for moni-
toring lepirudin therapy, because it does not linearly
increase with lepirudin blood levels and effect; thus, high
aPTT levels may correspond to very high lepirudin lev-
els.
45
Lepirudin levels are more reliably assessed by ecarin
clotting time or chromogenic substrate assays.
45
Table 1 lists the dosing recommendations for use of
lepirudin for intermittent HD. The recommendations
should be considered as guidelines and not followed
Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 185
uncritically in any individual patient. Hirudin is a valid
alternative anticoagulant for HD procedures in HIT
patients, but it should be used with caution and care-
ful monitoring. Especially before invasive procedures,
appropriate (repetitive) laboratory measurements have
to be carried out in hemodialysis patients on lepirudin
treatment.
Argatroban
Argatroban is a potent arginine-derived, synthetic, cata-
lytic site-directed thrombin inhibitor being approved as
an alternative anticoagulant for HIT in the United States,
Canada, and a number of European countries. It does not
cross-react with HIT antibodies. In contrast to hirudin,
argatroban is metabolized primarily by the liver, and its
half-life is only moderately extended in patients with re-
nal insufciency.
46
In a retrospective analysis of 47 HIT patients requiring
renal replacement therapy, argatroban provided effective
anticoagulation with an acceptable safety prole.
47
A pro-
spective cross-over study of 12 maintenance HD patients
showed different argatroban dosing regimens to be safe
and well tolerated.
48
There are conicting data concerning the necessity of
dose adjustments of argatroban in renal failure.
4951
In
ICU patients suffering from overt renal and additionally
from occult liver insufciency, dose reductions may be
frequently necessary (unpublished observations of the
author). Based on this experience, in ICU patients, in
our center we start argatroban at a reduced dose, provid-
ed there is no acute thrombosis. Careful monitoring and
dosing is required. Similar experiences have also been
reported by others.
50
Periodic monitoring of the antico-
agulant activity of argatroban is recommended using for
example the aPTT, the ECT, or the activated clotting time
(ACT).
48,49
Argatroban appears to be at least as well suited as le-
pirudin for anticoagulation of HIT patients requiring HD.
Its predominant hepatic elimination favors argatroban for
alternative anticoagulation in chronic renal failure. Its role
and dosing in ICU patients suffering from acute renal
failure remain to be dened.
Table 1 lists the dosing recommendations for use of
argatroban for HD. The recommendations should be con-
sidered as guidelines and not followed uncritically in any
individual patient. In particular, ICU patients often do
not require full-dose argatroban. Before invasive proce-
dures, appropriate (repetitive) laboratory measurements
have to be carried out in hemodialysis patients on arg-
atroban treatment.
Other agentsfondaparinux
Fondaparinux is a fully synthetic pentasaccharide derived
from the minimal binding region of heparin to the anti-
thrombin molecule and exerts high anti-Xa activity.
52
Despite not being formally approved, fondaparinux has
occasionally been used for alternative anticoagulation in
HIT patients. The half-life is longer than with LMWH
preparations and is further prolonged in renal failure.
Therefore, its dose is to be reduced for anticoagulation in
patients with renal insufciency and for HD procedures.
Recently, successful anticoagulation with fondaparinux
has been described in a maintenance HD patient with
symptomatic HIT.
53
The role of fondaparinux for antico-
agulation in HD procedures of HIT patients requires fur-
ther evaluation.
Role of regional citrate anticoagulation
in HIT
Regional citrate anticoagulation (for details see below) al-
lows the use of heparin-free HD without systemic anti-
coagulation. As long as platelet count is decreased in HIT
or other laboratory or clinical signs of active disease with
thromboembolism are present, extracorporeal anticoagu-
lation alone is insufcient and systemic anticoagulation
using hirudin, danaparoid, or argatroban is mandatory. If
systemic anticoagulation is no longer indicated, but re-
peated heparin use should be avoided for a prolonged
period of time, regional citrate anticoagulation is an ex-
cellent choice to prevent recurrence of HIT.
Alternative anticoagulation in HIT
Low-dose UFH
Even in patients at high risk for bleeding complications,
UFH still is the most frequently used agent for anticoag-
ulation during HD, although at a reduced dose. In low
heparin intermittent HD, the system is rinsed with 2500
to 5000 IU of heparin and subsequently with at least 2 L
saline solution to remove the anticoagulant that has not
bound to the surface of the articial polymers. The fol-
lowing hemodialysis treatment uses a low-maintenance
dose of heparin in order to maintain the systemic ACT no
higher than 40% above baseline.
Heparin-free hemodialysis
If the bleeding risk is extremely high (e.g., in patients
at risk for intracranial bleeding), maintenance heparin
is completely avoided. This is possible if dialysis
Fischer
Hemodialysis International 2007; 11:178189 186
membranes with low thrombogenicity (e.g., polysulfone),
a short treatment time (23 hr), and a high blood ow
(4250 mL/min) are used. It may be helpful to rinse the
extracorporeal system repeatedly with saline (25150 mL
injected into the arterial line every 1530 min). This
treatment without maintenance dosing is frequently
called heparin-free dialysis. However, with commence-
ment of the treatment the patient receives a small dose of
heparin as the extracorporeal circuit is connected to the
patients circulation. In addition, during the treatment,
adsorbed heparin can be released from the articial poly-
mers and reach the patient. The amount of heparin is very
low and does not elevate aPTT or ACT. However, if the
patient has developed HIT antibodies even a small
amount of the substance is sufcient to trigger the im-
munologic process again. Therefore, in case of HIT the
so-called heparin-free dialysis (applying heparin for re-
circulation into the tubing system, followed by saline
washout) must not be used. Even heparin-coated cath-
eters or dialyzers are not allowed.
Regional citrate anticoagulation
Regional citrate anticoagulation is an interesting alterna-
tive method compared with heparin in patients with a
high bleeding risk. Citrate infused into the arterial line
chelates calcium and magnesium, and thus inhibits the
coagulation cascade in the extracorporeal circulation. The
deficit in ionized calcium is present only locally in the
extracorporeal circulation because, before blood reinfu-
sion, calcium is substituted into the venous line to target
normal ionized calcium. Some aspects of citrate antico-
agulation necessitate a modication of the dialysis pre-
scription: (1) Citrate is metabolized in the liver to form
bicarbonate, and may induce metabolic alkalosis. To com-
pensate for this bicarbonate production, bicarbonate con-
centration in the dialysate needs to be reduced to avoid
metabolic alkalosis. (2) Trisodium citrate may induce
hypernatremia. To compensate for sodium infusion, the
sodium concentration in the dialysate should be reduced.
(3) Dependent on the respective ionized calcium concen-
tration, both the citrate and calcium infusion are to be
modied: (a) If in the venous line (before calcium substi-
tution) the concentration of ionized calcium is not low
enough, or ACT is too short, the citrate infusion rate
should be increased. (b) If ionized calcium in the arterial
line (before citrate infusion) is too low, calcium infusion
has to be increased to avoid systemic hypocalcemia.
Development of alkalosis is usually not a problem in
intermittent HD, as citrate anticoagulation is used for only
a few hours per week. In addition, many of the citrate
calcium complexes are removed into the dialysate and are
not infused into the patient.
It has been demonstrated that bleeding complications
are reduced compared with low-dose heparin.
53
Citrate
anticoagulation also improves biocompatibility and re-
duces deposition of blood components on the dialysis
membrane compared with UFH or LMWH.
54,55
A sim-
plied treatment protocol has recently been published
and may help to promote this valuable option in HD
therapy.
56
Manuscript received January 2007; revised January 2007.
REFERENCES
1 Davie EW, Ratnoff OD. Waterfall sequence for intrinsic
blood clotting. Science. 1964; 145:13101312.
2 MacFarlane RG. An enzyme cascade in the blood clotting
mechanism, and its function as a biological amplier.
Nature. 1964; 202:498499.
3 Hoffman M, Monroe DM. A cell-based model of hemo-
stasis. Thromb Haemost. 2001; 85:958965.
4 Monroe DM, Hoffman M. What does it take to make
the perfect clot? Arterioscler Thromb Vasc Biol. 2006; 26:
4148.
5 Rapaport SI, Rao LV. The tissue factor pathway: How it
has become a prima ballerina. Thromb Haemost. 1995;
74:717.
6 Frank RD, Weber J, Dresbach H, Thelen H, Weiss C,
Floege J. Role of contact system activation in hemo-
dialyzer-induced thrombogenicity. Kidney Int. 2001; 60:
19721981.
7 Noris M, Remuzzi G. Uremic bleeding: Closing the circle
after 30 years of controversies? Blood. 1999; 94:
25692574.
8 Tveit DP, Hypolite IO, Hshieh P, et al. Chronic dialysis
patients have high risk for pulmonary embolism. Am J
Kidney Dis. 2002; 39:10111017.
9 Nampoory MR, Das KC, Johny KV, et al. Hypercoagula-
bility, a serious problem in patients with ESRD on main-
tenance hemodialysis, and its correction after kidney
transplantation. Am J Kidney Dis. 2003; 42:797805.
10 Culp K, Flanigan M, Taylor L, Rothstein M. Vascular
access thrombosis in new hemodialysis patients. Am J
Kidney Dis. 1995; 26:341346.
11 Pawlak K, Borawski J, Naumnik B, et al. Relationship
between oxidative stress and extrinsic coagulation path-
way in hemodialyzed patients. Thromb Res. 2003;
109:247251.
12 Naumnik B, Borawski J, Pawlak K, et al. Effect of hemo-
dialysis on plasma levels of vascular endothelial markers.
Clin Appl Thromb Hemost. 2002; 8:245250.
Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 187
13 Mercier E, Branger B, Vecina F, et al. Tissue factor co-
agulation pathway and blood cells activation state in re-
nal insufciency. Hematol J. 2001; 2:1825.
14 Ando M, Iwata A, Ozeki Y, et al. Circulating platelet-de-
rived microparticles with procoagulant activity may be a
potential cause of thrombosis in uremic patients. Kidney
Int. 2002; 62:17571763.
15 Kushiya F, Wada H, Sakakura M, et al. Atherosclerotic
and hemostatic abnormalities in patients undergoing he-
modialysis. Clin Appl Thromb Hemost. 2003; 9:5360.
16 Vaziri ND, Gonzales EC, Wang J, et al. Blood coagula-
tion, brinolytic, and inhibitory proteins in end-stage
renal disease: Effect of hemodialysis. Am J Kidney Dis.
1994; 23:828835.
17 Faioni EM, Franchi F, Krachmalnicoff A, et al. Low levels
of the anticoagulant activity of protein C in patients with
chronic renal insufciency: An inhibitor of protein C is
present in uremic plasma. Thromb Haemost. 1991; 66:
420425.
18 Ambu hl PM, Wu thrich RP, Korte W, Schmid L, Krapf R.
Plasma hypercoagulability in hemodialysis patients: Im-
pact of dialysis and anticoagulation. Nephrol Dial Trans-
plant. 1997; 12:23552364.
19 Bo hler J, Fischer KG. Thrombogenesis and anticoagula-
tion in patients undergoing chronic hemodialysis. In:
Ho rl WH, Koch KM, Lindsay RM, Ronco C, Winchester
JF. eds. Replacement of Renal Function by Dialysis. 5th ed.
Lancaster, Great Britain: Lancaster Publishing; 2004:
259271.
20 Spijker HT, Graaff R, Boonstra PW, et al. On the inu-
ence of ow conditions and wettability on blood material
interactions. Biomaterials. 2003; 24:47174727.
21 OBrien JR. Shear-induced platelet aggregation. Lancet.
1990; 335:711713.
22 Gawaz MP, Mujais SK, Schmidt B, et al. Platelet-leukocyte
aggregation during hemodialysis. Kidney Int. 1994; 46:
489495.
23 Bonomini M, Sirolli V, Stuard S, et al. Interactions be-
tween platelets and leukocytes during hemodialysis. Artif
Organs. 1999; 23:2328.
24 Gawaz MP, Mujais SK, Schmidt B, et al. Platelet-leukocyte
aggregates during hemodialysis: Effect of membrane
type. Artif Organs. 1999; 23:2936.
25 Gorbet MB, Sefton MV. Leukocyte activation and leuko-
cyte procoagulant activities after blood contact with
polystyrene and polyethylene glycol-immobilized poly-
styrene beads. J Lab Clin Med. 2001; 137:345355.
26 Basmadjian D, Sefton MV, Baldwin SA. Coagulation on
biomaterials in owing blood: Some theoretical consid-
erations. Biomaterials. 1997; 18:15111522.
27 Fischer KG. Mechanism and clinical presentation of hep-
arin-induced thrombocytopenia. Hemodial Int. 2001; 5:
7480.
28 Fischer KG. Hemodialysis in heparin-induced thrombo-
cytopenia. In: Warkentin TE, Greinacher A. eds. Heparin-
Induced Thrombocytopenia. 3rd ed. New York: Marcel
Dekker; 2003:509530.
29 European best practice guidelines for hemodialysis
(part 1). Nephrol Dial Transplant. 2002; 17(Suppl 7):
6371.
30 Greiber S, Weber U, Galle J, Bramer P, Schollmeyer P.
Activated clotting time is not a sensitive parameter to
monitor anticoagulation with low molecular weight hep-
arin in haemodialysis. Nephron. 1997; 76:1519.
31 Frank RD, Brandenburg VM, Lanzmich R, Floege J. Fac-
tor Xa-activated whole blood clotting time (Xa-ACT)
for bedside monitoring of dalteparin anticoagulation
during hemodialysis. Nephrol Dial Transplant. 2004; 19:
15521558.
32 Warkentin TE, Kelton JG. A 14-year study of hep-
arin-induced thrombocytopenia. Am J Med. 1996; 101:
502507.
33 Magnani HN, Gallus A. Heparin-induced thrombocyto-
penia (HIT): A report of 1,478 clinical outcomes of
patients treated with danaparoid (Orgaran) from 1982
to mid-2004. Thromb Haemost. 2006; 95:967981.
34 Tardy-Poncet B, Tardy B, Reynaud J, et al. Efcacy and
safety of danaparoid sodium (ORG 10172) in critically ill
patients with heparin-associated thrombocytopenia. Chest.
1999; 115:16161620.
35 Fischer KG. Hirudin in renal insufciency. Semin Thromb
Haemost. 2002; 28:467482.
36 Kern H, Ziemer S, Kox WJ. Bleeding after intermittent or
continuous r-hirudin during CVVH. Intens Care Med.
1999; 25:13111314.
37 Vanholder RC, Camez A, Veys N, et al. Pharmacokinetics
of recombinant hirudin in hemodialyzed end-stage renal
failure patients. Thromb Haemost. 1997; 77:650655.
38 Fischer KG, van de Loo A, Bo hler J. Recombinant hiru-
din (lepirudin) as anticoagulant in intensive care patients
treated with continuous hemodialysis. Kidney Int. 1999;
56(Suppl 72):S4650.
39 Bauersachs RM, Lindhoff-Last E, Ehrly AM, et al. Treat-
ment of hirudin overdosage in a patient with chronic
renal failure. Thromb Haemost. 1999; 81:323324.
40 Fischer KG, Weiner SM, Benz K, Nauck M, Bo hler J.
Treatment of hirudin overdose with hemoltration. Blood
Purif. 2000; 18:8081.
41 Eichler P, Friesen HJ, Lubenow N, et al. Antihirudin an-
tibodies in patients with heparin-induced thrombocyto-
penia treated with lepirudin: Incidence, effects on aPTT,
and clinical relevance. Blood. 2000; 96:23732378.
42 Huhle G, Hoffmann U, Song X, et al. Immunologic re-
sponse to recombinant hirudin in HIT type II patients
during long-term treatment. Br J Haematol. 1999; 106:
195201.
43 Huhle G, Liebe V, Hudek R, et al. Anti-r-hirudin anti-
bodies reveal clinical relevance through direct functional
inactivation of r-hirudin or prolongation of r-hirudins
plasma half-life. Thromb Haemost. 2001; 85:936938.
Fischer
Hemodialysis International 2007; 11:178189 188
44 Fischer KG, Liebe V, Hudek R, et al. Anti-hirudin anti-
bodies alter pharmacokinetics and pharmacodynamics of
recombinant hirudin. Thromb Haemost. 2003; 89:973
982.
45 Hafner G, Roser M, Nauck M. Methods for the monitor-
ing of direct thrombin inhibitors. Semin Thromb Hemost.
2002; 28:425430.
46 Swan SK, Hursting MJ. The pharmacokinetics and phar-
macodynamics of argatroban: Effects of age, gender, and
hepatic or renal dysfunction. Pharmacotherapy. 2000;
20:318329.
47 Reddy BV, Grossman EJ, Trevino SA, Hursting MJ,
Murray PT. Argatroban anticoagulation in patients with
heparin-induced thrombocytopenia requiring renal
replacement therapy. Ann Pharmacother. 2005; 39:
16011605.
48 Murray PT, Reddy BV, Grossman EJ, et al. A prospective
comparison of three argatroban treatment regimens dur-
ing hemodialysis in end-stage renal disease. Kidney Int.
2004; 66:24462453.
49 Tang IY, Cox DS, Patel K, et al. Argatroban and renal re-
placement therapy in patients with heparin-induced
thrombocytopenia. Ann Pharmacother. 2005; 39:231236.
50 Guzzi LM, McCollum DA, Hursting MJ. Effect of renal
function on argatroban therapy in heparin-induced
thrombocytopenia. J Thromb Thrombolysis. 2006; 22:
169176.
51 Arpino PA, Hallisey RK. Effect of renal function on the
pharmacodynamics of argatroban. Ann Pharmacother.
2004; 38:2529.
52 Turpie AG, Gallus AS, Hoek JA. A synthetic pentasac-
charide for the prevention of deep-vein thrombosis
after total hip replacement. N Engl J Med. 2001; 344:
619625.
53 Flanigan MJ, Von Brecht J, Freeman RM, Lim VS.
Reducing the hemorrhagic complications of hemodialy-
sis: A controlled comparison of low-dose heparin
and citrate anticoagulation. Am J Kidney Dis. 1987; 9:
147153.
54 Bo hler J, Schollmeyer P, Dressel B, Dobos G, Ho rl WH.
Reduction of granulocyte activation during hemodialysis
with regional citrate anticoagulationdissociation of
complement activation and neutropenia from neutrophil
degranulation. J Am Soc Nephrol. 1996; 7:234241.
55 Hofbauer R, Moser D, Frass M, et al. Effect of anticoag-
ulation on blood membrane interactions during hemo-
dialysis. Kidney Int. 1999; 56:15781583.
56 Apsner R, Buchmayer H, Lang T, et al. Simplied citrate
anticoagulation for high-ux hemodialysis. Am J Kidney
Dis. 2001; 38:979987.
Anticoagulation in hemodialysis
Hemodialysis International 2007; 11:178189 189