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dvt prophylaxis, in icu, deep venous thrombosis prophylaxis ,
1.
2. INTRODUCTION
⢠Venous thromboembolism (VTE) includes the spectrum of deep vein
thrombosis (DVT) and pulmonary embolism (PE).
⢠Extraordinarily common in hospitalized patients.
⢠Estimating the frequency of DVT is problematic.
⢠Nonspecific clinical findings and high rate of undiagnosed events
underestimate the true incidence of disease.
⢠Autopsy data may overestimate meaningful events by detecting
asymptomatic cases.
3. Incidence And Natural History
⢠The incidence of VTE is thought to be in excess of 600,000 cases per
year in the united states
⢠In a study of critically ill patients,10% to 30% of medical/surgical
intensive care unit (ICU) patients experienced DVT within the first
week of admission.
⢠Approximately 60% of trauma patients had DVT within the first 2
weeks, most of which were clinically silent .
⢠The prevalence of VTE as a cause of critical illness is also uncertain.
Attia J, Ray JG,Cook DJ, et al: Deep vein thrombosis and its prevention in critically
illadults. Arch Intern Med161:1268,2001
7. Increasing Evidence:
DVT risk factors reflect these underlying pathophysiologic processes
VTE does not usually develop in their absence.
Convincing evidence that risk increases in proportion to the number of
predisposing factors
8. ⢠Strong risk factors (odds ratio>
10)
⢠Hip or leg fracture
⢠Hip or knee replacement
⢠Major general surgery
⢠Major trauma, including spinal cord
injury
⢠Moderate risk factors (odds
ratio2â9)
⢠Arthroscopic knee surgery
⢠Central venous catheterization
⢠Congestive heart or respiratory
failure
⢠Hormone replacement and oral
contraceptive therapy
⢠Malignancy (active or recently
treated)
⢠Pregnancy
⢠Paralytic stroke
⢠Prior VTE
⢠Thrombophilia (inherited or acquired
9. ⢠Weak risk factors (odds ratio <2)
⢠Bed rest > 3d
⢠Prolonged immobility due to sitting (e.g.,car or air travel)
⢠Increasing age
⢠Laparoscopic surgery
⢠Obesity
⢠Pregnancy
⢠Varicose veins
⢠Anderson FA Jr,Spencer FA: Risk factors for venous thromboembolism
Circulation107[23, Suppl 1]:I9,2003.
10.
11. ⢠Critically ill patients may be at especially high risk for VTE due to
⢠Severe underlying disease
⢠Immobility
⢠Veno invasive catheters
⢠Incidence of VTE increases correspondingly with the number of risk
factors present
⢠Thrombosis may occur in up to 67%of patients with invasive
catheters .
⢠The frequency of clinically meaningful complications due to cvc-
related thrombosis remains unclear.
14. ⢠The Padua Prediction Score was used
⢠to determine VTE risk in 1180 consecutive medical patients. Patients
were followed for up to 90 days following admission to assess the
occurrence of symptomatic VTE . The percent of subjects developing
VTE was as follows:
⢠â˘âLow riskâ patients (711): 0.3 percent
⢠â˘âHigh riskâ patients receiving adequate in-hospital
thromboprophylaxis (186): 2.2 percent
⢠â˘âHigh riskâ patients not receiving adequate in-hospital
thromboprophylaxis (283): 11.0 percent
A risk assessment model for the identification of hospitalized medical patients at risk for venous
thromboembolism: the Padua Prediction Score.Barbar S, Noventa F, Rossetto V, Ferrari A, Brandolin B,
Perlati M, De Bon E, Tormene D, Pagnan A, Prandoni PJ Thromb Haemost. 2010;8(11):2450.
15.
16. ⢠âThe IMPROVE risk score was used to determine VTE risk in 15,156
medical patients enrolled in the observational International Medical
Prevention Registry on Venous Thromboembolism (IMPROVE) study .
⢠The observed rate of VTE within 92 days of admission was 0.4 to 0.5
percent if none of these risk factors was present, and was in the range
of 8 to 11 percent in those with the highest risk score.
17.
18. ⢠The GENEVA risk score was subject to a
⢠multicentre validation study , 1478 hospitalized medical patients,
⢠43% did not receive thromboprophylaxis.
⢠Over three percent of high-risk score subjects developed
symptomatic VTE or VTE-related death at 90 days, compared to 0.6
percent of low-risk score patients.
⢠When only patients who did not receive prophylaxis were considered,
these risks were 3.5 and 1.1 percent respectively
19. Prediction scores
⢠Require validation from independent, prospective studies before they
can be used in routine practice.
⢠Despite the absence of a prospectively validated risk model, the
following conclusions can be reached:
⢠In general, VTE prophylaxis should be considered in medical patients
older than age 40 who have limited mobility for âĽ3 days, and have
at least one thrombotic risk factor .
⢠All patients admitted to intensive care units are considered high risk
for VTE , even after routine prophylactic anticoagulation .
20. Bleeding risk assessment
⢠Validated models are lacking
⢠Makes it difficult for the clinician to fully assess the risks and benefits
of prophylactic anticoagulation
⢠Retrospective analysis of data from (IMPROVE) has been used
⢠to assess in-hospital bleeding incidence
⢠to identify risk factors at the time of admission associated with in-hospital
bleeding risk in acutely ill medical patients
21.
22. ⢠The cumulative incidence of major and non-major in-hospital
bleeding within 14 days of admission was 3.2 percent.
⢠Active gastroduodenal ulcer (OR 4.15; 95% ci 2.21-7.77)
⢠Bleeding within the three months prior to admission (OR 3.64; 95%
ci 2.21-5.99), and a
⢠Platelet count <50,000/microl (OR 3.37; 95% ci 1.84-6.18)
Strongest independent risk factors for bleeding at the time of
admission.
⢠Other bleeding risk factors included increased age,
hepatic and/or renal failure, intensive care unit stay, presence of a
central venous catheter, rheumatic disease, cancer, and male sex
23. ⢠If this model is validated in other patient populations, it may assist
clinicians in estimating the risks of prophylactic anticoagulation in
patients at risk for VTE
25. Overall Approaches
⢠Primary prophylaxis âcarried out using either drugs or physical
methods that are effective for preventing deep vein thrombosis
(DVT).
⢠Secondary prevention â Secondary prevention involves the early
detection and treatment of subclinical venous thrombosis by
screening medical patients with objective tests that are sensitive for
the presence of DVT.
26. ⢠Primary prophylaxis :
⢠preferred in most clinical circumstances
⢠more cost effective than treatment of complications once they occur
Secondary prevention with screening is reserved for patients in whom
primary prophylaxis is either contraindicated or shown to be ineffective
27. ⢠The characteristics of an ideal primary prophylactic
method includes ease of administration,
effectiveness, safety (particularly with respect to
bleeding), and cost-effectiveness or at least cost-
neutrality when compared with current standards.
29. Indicated in patients :
At high risk of bleeding or in whom anticoagulation is contraindicated
(eg, gastrointestinal or intracranial hemorrhage) .
Transition to a pharmacologic agent should be considered as
soon as the bleeding risk becomes acceptably low or has
been reversed
30. Intermittent Pneumatic Compression (IPC) Devices
⢠Prevents deep vein thrombosis (DVT) by enhancing blood flow in the
deep veins of the legs, thereby preventing venous stasis .
⢠IPC also reduces plasminogen activator inhibitor-1 (PAI-1), thereby
increasing endogenous fibrinolytic activity.
⢠Roberts VC, Sabri S, Beeley AH, Cotton LT. The effect of intermittently applied external
pressure on the haemodynamics of the lower limb in man. Br J Surg 1972; 59:223.
⢠Comerota AJ, Chouhan V, Harada RN, et al. The fibrinolytic effects of intermittent pneumatic
compression: mechanism of enhanced fibrinolysis. Ann Surg 1997; 226:306.
31. ⢠Alternative for VTE prevention in medical patients with a high risk of
bleeding .
⢠Complications:
⢠Skin breakdown is a known complication, especially in the frail older
adult population.
⢠No data available on skin complications
⢠Contraindication
Patients with evidence of leg ischemia due to peripheral vascular
disease.
Attention must be paid to optimal compliance, as well as proper fit of
the ipc device.
32. ⢠Data on the efficacy and safety of IPCs are limited.
⢠one large randomized trial in patients with stroke suggested that IPCs reduce the
incidence of VTE .
Effectiveness of intermittent pneumatic compression in reduction of risk of deep vein thrombosis in patients who have
had a stroke (CLOTS 3): a multicentre randomised controlled trial.
CLOTS (Clots in Legs Or sTockings after Stroke) Trials Collaboration, Dennis M, Sandercock P, Reid J, Graham C,
Forbes J, Murray G
.
33. A multicenter, randomized trial of 2876 immobile patients with acute
stroke (CLOTS 3) reported that, compared to no device, IPC use was
associated with a lower rate of VTE at 30 days (12 versus 8.5 percent;
absolute risk reduction 3.6 percent; 95% CI 1.4 to 5.8) without altering
mortality (13 versus 11 percent).
Lancet. 2013;382(9891):516
34. Graduated compression stockings and venous
foot pump
⢠There is less convincing evidence regarding the efficacy of graduated
compression stockings (GCS) and venous foot pump (VFP) in randomized
clinical trials.
⢠In a meta-analysis, GCS was found to be ineffective in the prevention of
VTE in patients with ischemic stroke.
⢠Amaragiri SV, Lees TA. Elastic compression stockings for prevention of deep vein thrombosis. Cochrane Database
Syst Rev 2000; :CD001484.
⢠AndrÊ C, de Freitas GR, Fukujima MM. Prevention of deep venous thrombosis and pulmonary embolism following
stroke: a systematic review of published articles. Eur J Neurol 2007; 14:21
35. ⢠One randomized trial showed that thigh-length GCS was associated
with no benefit with respect to reduction of VTE, along with a
fourfold increase in skin ulcers and necrosis .
⢠Similarly, there are few convincing studies showing the efficacy of VFP
devices.
1.CLOTS Trials Collaboration, Dennis M, Sandercock PA, et al. Effectiveness of thigh-length graduated
compression stockings to reduce the risk of deep vein thrombosis after stroke (CLOTS trial 1): a multicentre,
randomised controlled trial. Lancet 2009; 373:1958
38. ⢠The 2012 ACCP Guidelines suggest the use of either IPC or GCS rather than no
mechanical prophylaxis in acutely ill hospitalized medical patients at increased
risk for thrombosis who are bleeding or are at high risk for major bleeding .
39. Mechanical Compression and Pharmacologic
Prophylaxis:
⢠No studies that have compared mechanical compression vs
anticoagulants to prevent VTE in hospitalized medical
patients
⢠Indirect evidence from various orthopedic and non
orthopedic surgical populations.
⢠Meta-analysis by Eppsteiner of 16 trials (3,887 patients) of
various compression modalities tested against LDUH or
LMWH
40.
41.
42. Mechanical Compression and Pharmacologic
Prophylaxis
⢠Trials in postsurgical patients that compared the combination of
intermittent pneumatic compression devices with a pharmacologic
method to pharmacologic therapy used alone showed a strong trend
toward fewer dvts with combination therapy
⢠Indirect data derived primarily from surgical populations suggest that
GCS may be modestly effective at preventing asymptomatic DVT and
possibly PE in hospitalized medical patients
43. Mechanical Thromboprophylaxis
⢠May be preferable to no prophylaxis in patients at
appreciable risk for VTE who are also at high risk for
bleeding
⢠Costs related to purchase and maintenance and the
time and vigilance required to ensure optimal
compliance
⢠Must ensure that the correct size is used, that they are
properly applied, and that they are worn at all times
44. ⢠Devices are often not functioning when patients are out of
bed or being transported, either due to
⢠Improperly applied sleeves or nonfunctioning compression
pump
⢠Devices were properly functioning in ,50% of postoperative
patients in one study and only 19% of trauma patients in
another.
⢠Newer battery-powered portable devices are available, and a
recent study reported better compliance with these devices
than with traditional plug-in devices
46. Selection of agent
⢠In hospitalized and immobilized medical patients, especially those at
high risk for VTE (eg, stroke, myocardial infarction, and critically ill),
pharmacologic prophylaxis with unfractionated heparin (UFH), low
molecular weight (LMW) heparin, or fondaparinux have all been
shown to be superior to placebo or mechanical devices in preventing
deep venous thrombosis (DVT) and pulmonary embolism (PE)
49. UNFRACTIONATED HEPARIN
⢠Heparin is an Indirect Thrombin Inhibitor that complexes with
Antithrombin (AT, formerly known as AT III), converting this circulating
cofactor from a slow to a rapid inactivator of thrombin, factor Xa, and
to a lesser extent, factors XIIa, XIa, and Ixa
⢠The usual dose is 5000 units subcutaneously every 8 or 12 hours.
⢠Bleeding, heparin-induced thrombocytopenia (HIT), and osteoporosis
⢠Relatively low side effect profile, relatively inexpensive and easily
administered.
⢠Anticoagulant monitoring is also not required, the platelet count
should be monitored regularly.
50. In a meta-analysis of 12 randomized studies of
UFH given either two (BID) or three (TID) times
daily for the prevention of VTE in medical
patients, the following findings were noted :
51. ⢠No significant difference in the overall rate of VTE between
BID (5.4/1000 patient-days) and TID (3.5/1000 patient-days) UFH
heparin dosing.
⢠TID heparin showed a trend toward a decrease in PE
(bid 1.5/1000 patient-days, TID 0.5/100 patient-days) and in proximal
DVT plus PE (BID 2.3/1000 patient-days, TID 0.9/1000 patient-days).
⢠The risk for major bleeding was significantly greater with TID than
with BID UFH dosing (BID 0.35/1000 patient-days,
TID 0.96/1000 patient-days).
53. LOW MOLECULAR WEIGHT HEPARINS
⢠Three LMW heparins have been approved for clinical use in the
United States : ENOXAPARIN, DALTEPARIN,TINZAPARIN.
⢠Additional LMW heparin products are either commercially available in
Europe and other countries or are in phase III clinical trials .
⢠These include REVIPARIN, NADROPARIN, BEMIPARIN, AND
CERTOPARIN
54. Advantages
⢠They have greater bioavailability
⢠The duration of the anticoagulant effect is greater because of
reduced binding to macrophages and endothelial cells, permitting
administration only once or twice daily.
⢠The anticoagulant response (anti-Xa activity) is highly correlated with
body weight, permitting administration of a fixed dose.
⢠However, the dose may have to be adjusted for patients who are
extremely obese or have renal insufficiency
55. ⢠Laboratory monitoring is not necessary
⢠Much less likely to induce immune-mediated thrombocytopenia (ie,
heparin-induced thrombocytopenia) than UFH
⢠They do not increase osteoclast number and activity as much as UFH,
and may therefore produce less bone loss .
56. ⢠Medical patients with severely-restricted mobility during acute
illness: 40 mg once daily; continue until risk of DVT has diminished
(usually 6 to 11 days).
⢠Obesity: In morbidly-obese patients (BMI âĽ40 kg/m2), increasing the
prophylactic dose by 30% may be appropriate for some indications.
⢠Abdominal surgery: 40 mg once daily, with initial dose given 2 hours
prior to surgery; continue until risk of DVT has diminished (usually 7
to 10 days).
57. ⢠Knee replacement surgery: 30 mg every 12 hours, with initial dose within 12 to
24 hours after surgery, and every 12 hours for at least 10 days or until risk of
DVT has diminished. The ACCP recommends initiation âĽ12 hours
preoperatively or âĽ12 hours postoperatively; extended duration of up to 35
days suggested
⢠Bariatric surgery : Roux-en-Y gastric bypass: Appropriate dosing strategies have
not been clearly defined (Borkgren-Okonek, 2008; Scholten, 2002):
⢠BMI â¤50 kg/m2: 40 mg every 12 hours
⢠BMI >50 kg/m2: 60 mg every 12 hours
58. ⢠Hip replacement surgery:
⢠Twice-daily dosing: 30 mg every 12 hours, with initial dose within 12 to 24
hours after surgery, and every 12 hours for at least 10 days or until risk of DVT
has. The ACCP recommends initiation âĽ12 hours preoperatively or âĽ12 hours
postoperatively; extended duration of up to 35 days suggested
⢠Once-daily dosing: 40 mg OD, with initial dose within 9 to 15 hours before
surgery, and daily for at least 10 days (or up to 35 days postoperatively) or
until risk of DVT has diminished. The ACCP recommends initiation âĽ12 hours
preoperatively or âĽ12 hours postoperatively; extended duration of up to 35
days suggested .
59. ⢠Crcl âĽ30 ml/minute: No dose change .Monitor closely for bleeding.
⢠Crcl <30 ml/minute:clcr 20 to 29 ml/min: dvt prophylaxis in abdominal
surgery, hip replacement, knee replacement, or in medical patients
during acute illness:
⢠Subq: 30 mg once daily. ( The canadian labeling recommends 20 to
30 mg once daily (based on risk/benefit assessment) for prophylaxis in
abdominal or colorectal surgery or in medical patients during acute
illness).
73. Fondaparinux (Arixtra)
Adult DVT prophylaxis: SubQ: Adults âĽ50 kg: 2.5 mg OD.
⢠Prophylactic use contraindicated in patients <50 kg.
⢠DVT prophylaxis with history of HIT (off-label use): SubQ: 2.5 mg OD
⢠Fondaparinux is a highly sulfated pentasaccharide.
⢠Indirect factor xa inhibitor
⢠Acts indirectly on factor xa by binding to antithrombin (at), inducing a conformational
change in at that increases the ability of at to inactivate factor xa.
⢠Binds to at with a higher affinity than the native pentasaccharide of unfractionated
heparin or low molecular weight heparin
⢠100 percent bioavailable after subcutaneous injection,
⢠Half-maximal and peak serum concentrations reached in 25 minutes and 1.7 hours
following subcutaneous injection, respectively .
⢠Longer half-life (15 to 17 hours) allowing it to be given once daily
74. Using the composite end point of
asymptomatic or symptomatic DVT and
non-fatal or fatal PE, fondaparinux was
compared with placebo for 6 to 14 days in
644 hospitalized medical patients.
VTE was detected in 5.6 percent of
patients treated with fondaparinux versus
10.5 percent of patients given placebo, for
a relative risk reduction of 47 percent
(95% Cl 7.7-69)
75. In comparison studies
⢠Fondaparinux in recommended doses has shown lesser efficacy
than enoxaparin 30 mg twice daily, (the enoxaparin regimen used in
north america).
⢠Fondaparinux in recommended doses appears to have the same
efficacy as enoxaparin 40 mg once daily (the enoxaparin regimen
favored in europe).
⢠50 percent reduction in the dose with reduced renal function (ie,
creatinine clearances in the range of 30 to 50 ml/min) .
76. The safety and efficacy of reduced dosing was tested in a multicenter
prospective cohort study in 206 acutely ill older medical patients (mean age 82
years; mean creatinine clearance 33 mL/minute [range 20 to 50]) at high risk
for both bleeding and thrombosis. Subjects received 1.5 mg/day of
fondaparinux for 6 to 15 days as thromboprophylaxis. Results included the
following :
âMajor bleeding occurred in one subject (0.49 percent)
âClinically relevant non-major bleeding occurred in eight subjects (3.88
percent)
âSymptomatic VTE developed in three subjects (1.46 percent)
77. ASPIRIN
⢠Highly effective in reducing major arterial thrombotic events .
⢠Little evidence that aspirin has a significant effect on the prevention
of venous thromboembolic events in medical patients.
⢠An early meta-analysis and a later literature review indicated
that aspirin reduced the incidence of VTE by approximately 20
percent compared with placebo or no treatment
⢠Collins R, Baigent C, Sandercock P, Peto R. Antiplatelet therapy for thromboprophylaxis: the need for careful
consideration of the evidence from randomised trials. Antiplatelet Trialists' Collaboration. BMJ 1994;
309:1215
78. However, other studies
have shown either no
significant benefit or
inferiority when compared
with other modalities such
as LMW heparin .
79. As a result, the 2012 ACCP Guidelines do not recommend the
use of aspirin, either alone or in combination, as prophylaxis
against VTE in any medical patient group
80. WARFARIN
⢠Not appropriate for immediate and short-term prevention of VTE for
two reasons :
⢠The ultimate anticoagulant effect of warfarin is delayed, does not
occur until 36 to 72 hours after drug administration.
⢠Achieving targeted levels of anticoagulation may be problematic
due to comorbidities (eg, impaired liver function)
⢠Medications that interact with it (eg, antibiotics) that may lead to
supratherapeutic anticoagulation.
93. Retrospective observational study of 175,665
critically ill adult patients .
The crude ICU and hospital mortality rates in
those who received early
thromboprophylaxis were 6.3 and 10.6
percent, respectively.
Rates were significantly lower than in those
who did not receive thromboprophylaxis
within 24 hours of icu admission (7.6 and
11.2 percent, respectively) .
94. ⢠Pharmacological prophylaxis prevents deep vein thrombosis (strong
evidence)
⢠It prevents pulmonary embolism (strong evidence)
⢠Does it prevent ICU mortality? â Observational studies suggest it
may ; but these studies are not robust enough to address this
question
⢠Which agent to use? Fairly strong evidence to suggest that LMWH
may be more efficacious in preventing pulmonary embolism
compared to UFH
⢠Fondaparinux may be more efficacious in selected subgroups of
patients (post operative hip/knee surgery)
⢠Mechanical devices may not be effective when used in isolation
95.
96. ⢠However, while thromboprophylaxis has been shown to reduce the
risk of VTE in hospitalized medical and surgical patients, and to
reduce the risk of death in surgical patients [20,29], most studies and
a meta-analysis have not been able to show a consistent beneficial
effect of thromboprophylaxis on reducing overall mortality in
hospitalized medical patients [30-37]. The reasons for this difference
between medical and surgical patients are unclear but may be related
to a greater number of comorbidities in medical patients that
contribute to overall deaths.
Hinweis der Redaktion
of stasis, venous injury And hypercoagulability described nearly 150 years ago
(not plugged in, power switch not turned on, or air hose compressed).
Couple of rcts looked at placebo and lmwh
Several end points they looked at. Dvt by Doppler. Judt plain dvt. Significantly reduces dvt irrespective of anything. It does reduce dvt
Very strong trend that favors the use of heparin even though its not statis sign
In an assorted gp f medical surgical pts use of both did not change the incidence
Only two rcts very hard to draw coclusios but it probably says that it favors may reduce the incidence o pe
Significant less pe
Vry strong trend which favors lmwh
in patients who are at risk or who have established atherosclerotic disease.
Initiating warfarin in patients who are not already anticoagulated is
HERE ALSO----NO ANTIDOTE, NO MONITORING OF OVERDOSE----SO IT BECOMES VERY DIFFICULT IN ACUTE TRAUMA OR EMERGENCY SURGERY
The function of these drugs is often misunderstood because they are sometimes referred to as blood thinners; they do not in fact thin the blood
These drugs will not dissolve clots also that already have formed, but it will stop an existing clot from becoming worse and prevent future clots