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European Society of Thoracic
Surgeons and The American
Association for Thoracic Surgery
guidelines for the prevention of
cancer-associated venous
thromboembolism in thoracic
surgery
Background :
Venous thromboembolism (VTE), which includes
both deep vein thrombosis (DVT) and
pulmonary embolism (PE), is a potentially fatal
but preventable perioperative complication.
PE is the third most common cause of
cardiovascular death after myocardial infarction
and stroke, the most common preventable
cause of hospital death, and the risk of
occurrence can be significantly mitigated
through prophylaxis.
Despite thoracic oncology patients undergoing
surgical resection being considered amongst the
highest risk for VTE in the perioperative period,
specific VTE prophylaxis guidelines have not
been defined for this population.
*These joint evidence-based guidelines from
The American Association for Thoracic Surgery
(AATS) and the European Society of Thoracic
Surgeons (ESTS) were conducted with guidance
from the McMaster University GRADE Center.
*European Journal of Cardio-Thoracic Surgery
2022.
*Received 10 September 2021; received in
revised form 21 April 2022; accepted 9 May
2022
Description of the Health Problem
*VTE, comprising DVT and PE, is a potentially fatal
but largely preventable postoperative complication.
Without thromboprophylaxis, the incidence of
objectively confirmed DVT is 10% to 40% in general
medical and surgical patients.
*Thrombotic complications are the most common
cause of 30- day postoperative mortality
*Compared with the noncancer surgical
populations, cancer patients who have undergone
surgical resection have a 2- to 3- fold increased risk
for postoperative DVT, a 3-fold increased risk for
fatal PE.
Thoracic surgery patients undergoing cancer
resections are considered a uniquely high-risk
population based on risk assessment models. A PE
in particular is associated with a high mortality
rate in patients with an already compromised
pulmonary status .
Lobectomy/Segmentectomy:
• Parenteral Anticoagulation Versus No
Anticoagulation.
• LMWH Versus UFH.
• Mechanical Prophylaxis Versus No Prophylaxis.
• Combined Mechanical and Pharmacological
Prophylaxis Versus Pharmacological Prophylaxis
Alone.
• Extended Versus In-Hospital Prophylaxis
• Pre- Versus Postoperative Administration of
Prophylaxis.
• Routine Postoperative Screening for VTE.
Parenteral Anticoagulation Versus No
Anticoagulation
*We identified 52 randomized controlled trials that fulfilled our
inclusion criteria and measured outcomes relevant to this context.
• 20 of the trials included patients undergoing major general surgery,
• 13 of the trials included patients undergoing major abdominal
surgery,
• 7 of the trials included patients undergoing gynecological surgery,
• 5 of the trials included patients undergoing urological surgery,
• 3 of the trials included patients undergoing gastrointestinal or
colorectal surgery,
• 2 trials included patients undergoing laparoscopic cholecystectomy,
• 1 trial included patients undergoing liver resection, and
• 1 trial included patients undergoing lobectomy.
• 20 trials reported on the effect of parenteral
anticoagulants (LMWH or UFH given
subcutaneously) on mortality
• 37 on symptomatic PE
• 8 on proximal DVT , 13 on distal DVT
• 30 on major bleeding, 9 on reoperation, 15 on
wound hematoma, 4 on wound infection, and 6
on heparin-induced thrombocytopenia (HIT).
Benefits:
The panel considered these health benefits to
be moderate. At a lower baseline risk of VTE in
this patient population the anticipated desirable
effects with reductions in PE and DVT would
probably be considered small
Harms and burden:
• Parenteral anticoagulation as compared to not using
anticoagulation may increase major bleeding ,this
corresponds to 6 more major bleeds per 1000
patients.
• Use of anticoagulants may have no impact on
reoperation.
• The occurrence of wound hematoma may be
increased with use of anticoagulants.
• The use of parenteral anticoagulants was also found
to have no influence on HIT.
**(The guideline panel considered the size of these
adverse effects to be small.)
Conclusions:
• Based on the body of available evidence, it is likely
that parenteral anticoagulation reduces the risk of
mortality, PE and DVT.
• The certainty was low due to indirectness of the
research evidence coming from older studies
primarily on other surgery types.
• The panel noted that the use of parenteral
anticoagulants in this population is highly
acceptable but the magnitude of beneficial effects
may not be clear in patients with cancer
undergoing lung resection.
• The panel noted the uncertainty about risks of
outcomes due to cancer versus due to surgery
LMWH Versus UFH
We identified 17 randomized controlled trials that fulfilled
our inclusion criteria and measured outcomes relevant to
this context .
All the trials included a study population consisting of
patients with cancer undergoing major surgeries, including
abdominal, pelvic, gynecological, gastrointestinal or
colorectal surgery, with 2 trials including patients
undergoing thoracic surgery or lung surgery.
Eight trials reported on the effect of LMWH versus UFH on
mortality, 15 on symptomatic PE, 8 on symptomatic DVT,
10 on major bleeding, 4 on reoperation, 6 on wound
hematoma, 3 on wound infection, and 2 on HIT.
Benefits:
• LMWH compared with UFH probably reduces
mortality ,this corresponds to 2 fewer deaths per
1000 patients.
• LMWH probably reduces PE ,this corresponds to
1 fewer symptomatic PE per 1000 patients.
• %. LMWH probably reduces symptomatic DVT,
this corresponds to 4 fewer DVT per 1000
patients.
**The panel considered these health benefits to
be small.
Harms and burden.
• LMWH compared with UFH probably has little
influence on major bleeding, this corresponds to 1
more major bleed per 1000 patients.
• Use of LMWH may reduce reoperation.
• The rate of wound hematoma is probably reduced
with LMWH.
• The rate of wound infections is probably
increased with LMWH.
**The guideline panel considered the size of the
anticipated undesirable effects to be small.
Conclusions:
• The conditional recommendation for use of
LMWH as thromboprophylaxis in patients with
cancer undergoing lung resection is due to a
balance of effects that probably favors LMWH.
• The panel made a conditional recommendation
for use of LMWH rather than a strong
recommendation given varying costs of the
intervention and issues regarding access to the
specific anticoagulants in different settings, with
both options being acceptable.
• The panel did not identify any further research
priorities for this guideline question.
Combined Mechanical and
Pharmacological Prophylaxis Versus
Pharmacological Prophylaxis Alone
*We identified 15 randomized controlled trials
that fulfilled our inclusion criteria and measured
outcomes relevant to this context.
Benefits
*Use of combined prophylaxis compared with
pharmacological prophylaxis alone may reduce
mortality ,this corresponds to 9 fewer deaths per 1000
patients.
*Combined prophylaxis may reduce PE ,this
corresponds to 1 fewer symptomatic PE per 1000
patients .
*Use of combined prophylaxis probably reduces
proximal DVT (RR, 0.14; 95% CI, 0.01-2.63; very low
certainty in the evidence of effects); this corresponds
to 10 fewer proximal DVT per 1000 patients.
*The panel considered these health benefits to be
small.
Harms and burden.
• For the effect of using combined prophylaxis on
major bleeding there were very serious concerns
about imprecision due to a small number of
events in the included trials and we are uncertain
about this effect
Conclusions:
*The conditional recommendation for use of
combined mechanical and pharmacological
prophylaxis in patients with cancer undergoing lung
resection is due to a balance of effects that probably
favors combined prophylaxis based on very low
certainty in the evidence, negligible costs for the in-
patient setting, and the intervention being viewed as
acceptable and feasible.
*Despite the very low uncertainty in the evidence, the
panel did not identify the use of combined prophylaxis
as a research priority
Mechanical Prophylaxis Versus No
Prophylaxis
• We identified 20 randomized controlled trials that
fulfilled our inclusion criteria and measured
outcomes relevant to this context.
• Mechanical prophylaxis compared with no
prophylaxis may reduce PE,this corresponds to 4
fewer symptomatic PE per 1000 patients.
• Use of mechanical prophylaxis may reduce
proximal ,this corresponds to 2 fewer proximal
DVT per 1000 patients.
• The panel considered these health benefits to be
small
Harms and burden
• The panel judged that overall the undesirable
anticipated effects of using mechanical
prophylaxis would be trivial.
Conclusions:
• The conditional recommendation for use of
mechanical prophylaxis in patients undergoing
lung resection, who do not receive
pharmacological prophylaxis, is due to a small
benefit and overall balance of efficacy and
safety that probably favors the intervention in
the context of very low certainty of evidence,
likely acceptability and feasibility, as well as
negligible costs.
Extended Versus In-Hospital
Prophylaxis
• We identified 7 randomized controlled trials
that fulfilled our inclusion criteria and
measured outcomes relevant to this context.
• All of the trials addressed use of extended
prophylaxis with LMWH for a duration up to
28 to 35 days compared with LMWH for a
duration of 6 to 10 days.
Benefits:
• The effect of using extended prophylaxis compared
with in-hospital prophylaxis on mortality was
uncertain ,with 2 more (3 fewer to 9 more) deaths
per 1000 patient.
• Extended prophylaxis probably reduces PE ,this
corresponds to 11 fewer symptomatic PE per 1000
patients.
• Use of extended prophylaxis probably reduces
proximal DVT ,this corresponds to 9 fewer proximal
DVT per 1000 patients.
• The panel considered these health benefits to be
small.
Harms and burden.
• s extended prophylaxis may result in a
reduction in major bleeding ,this corresponds
to 5 fewer major bleeds per 1000 patients.
• No data was reported in the included trials on
wound infection, wound hematoma, or
reoperation.
Conclusion:
• The panel judged that within the
heterogenous population of patients
undergoing lung resection, for those at higher
risk of thrombosis the balance of effects
probably favors use of extended prophylaxis,
whereas for those at lower risk the balance
probably favors in-hospital prophylaxis only.
Pre- Versus Postoperative
Administration of Prophylaxis
• We identified 3 randomized controlled trials
that fulfilled our inclusion criteria and
measured outcomes relevant to this context
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx
European Society of Thoracic Surgeons and The American.pptx

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European Society of Thoracic Surgeons and The American.pptx

  • 1. European Society of Thoracic Surgeons and The American Association for Thoracic Surgery guidelines for the prevention of cancer-associated venous thromboembolism in thoracic surgery
  • 2. Background : Venous thromboembolism (VTE), which includes both deep vein thrombosis (DVT) and pulmonary embolism (PE), is a potentially fatal but preventable perioperative complication. PE is the third most common cause of cardiovascular death after myocardial infarction and stroke, the most common preventable cause of hospital death, and the risk of occurrence can be significantly mitigated through prophylaxis.
  • 3. Despite thoracic oncology patients undergoing surgical resection being considered amongst the highest risk for VTE in the perioperative period, specific VTE prophylaxis guidelines have not been defined for this population.
  • 4. *These joint evidence-based guidelines from The American Association for Thoracic Surgery (AATS) and the European Society of Thoracic Surgeons (ESTS) were conducted with guidance from the McMaster University GRADE Center. *European Journal of Cardio-Thoracic Surgery 2022. *Received 10 September 2021; received in revised form 21 April 2022; accepted 9 May 2022
  • 5. Description of the Health Problem *VTE, comprising DVT and PE, is a potentially fatal but largely preventable postoperative complication. Without thromboprophylaxis, the incidence of objectively confirmed DVT is 10% to 40% in general medical and surgical patients. *Thrombotic complications are the most common cause of 30- day postoperative mortality *Compared with the noncancer surgical populations, cancer patients who have undergone surgical resection have a 2- to 3- fold increased risk for postoperative DVT, a 3-fold increased risk for fatal PE.
  • 6. Thoracic surgery patients undergoing cancer resections are considered a uniquely high-risk population based on risk assessment models. A PE in particular is associated with a high mortality rate in patients with an already compromised pulmonary status .
  • 8. • Parenteral Anticoagulation Versus No Anticoagulation. • LMWH Versus UFH. • Mechanical Prophylaxis Versus No Prophylaxis. • Combined Mechanical and Pharmacological Prophylaxis Versus Pharmacological Prophylaxis Alone. • Extended Versus In-Hospital Prophylaxis • Pre- Versus Postoperative Administration of Prophylaxis. • Routine Postoperative Screening for VTE.
  • 9. Parenteral Anticoagulation Versus No Anticoagulation *We identified 52 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context. • 20 of the trials included patients undergoing major general surgery, • 13 of the trials included patients undergoing major abdominal surgery, • 7 of the trials included patients undergoing gynecological surgery, • 5 of the trials included patients undergoing urological surgery, • 3 of the trials included patients undergoing gastrointestinal or colorectal surgery, • 2 trials included patients undergoing laparoscopic cholecystectomy, • 1 trial included patients undergoing liver resection, and • 1 trial included patients undergoing lobectomy.
  • 10. • 20 trials reported on the effect of parenteral anticoagulants (LMWH or UFH given subcutaneously) on mortality • 37 on symptomatic PE • 8 on proximal DVT , 13 on distal DVT • 30 on major bleeding, 9 on reoperation, 15 on wound hematoma, 4 on wound infection, and 6 on heparin-induced thrombocytopenia (HIT).
  • 11. Benefits: The panel considered these health benefits to be moderate. At a lower baseline risk of VTE in this patient population the anticipated desirable effects with reductions in PE and DVT would probably be considered small
  • 12. Harms and burden: • Parenteral anticoagulation as compared to not using anticoagulation may increase major bleeding ,this corresponds to 6 more major bleeds per 1000 patients. • Use of anticoagulants may have no impact on reoperation. • The occurrence of wound hematoma may be increased with use of anticoagulants. • The use of parenteral anticoagulants was also found to have no influence on HIT. **(The guideline panel considered the size of these adverse effects to be small.)
  • 13. Conclusions: • Based on the body of available evidence, it is likely that parenteral anticoagulation reduces the risk of mortality, PE and DVT. • The certainty was low due to indirectness of the research evidence coming from older studies primarily on other surgery types. • The panel noted that the use of parenteral anticoagulants in this population is highly acceptable but the magnitude of beneficial effects may not be clear in patients with cancer undergoing lung resection. • The panel noted the uncertainty about risks of outcomes due to cancer versus due to surgery
  • 14. LMWH Versus UFH We identified 17 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context . All the trials included a study population consisting of patients with cancer undergoing major surgeries, including abdominal, pelvic, gynecological, gastrointestinal or colorectal surgery, with 2 trials including patients undergoing thoracic surgery or lung surgery. Eight trials reported on the effect of LMWH versus UFH on mortality, 15 on symptomatic PE, 8 on symptomatic DVT, 10 on major bleeding, 4 on reoperation, 6 on wound hematoma, 3 on wound infection, and 2 on HIT.
  • 15. Benefits: • LMWH compared with UFH probably reduces mortality ,this corresponds to 2 fewer deaths per 1000 patients. • LMWH probably reduces PE ,this corresponds to 1 fewer symptomatic PE per 1000 patients. • %. LMWH probably reduces symptomatic DVT, this corresponds to 4 fewer DVT per 1000 patients. **The panel considered these health benefits to be small.
  • 16. Harms and burden. • LMWH compared with UFH probably has little influence on major bleeding, this corresponds to 1 more major bleed per 1000 patients. • Use of LMWH may reduce reoperation. • The rate of wound hematoma is probably reduced with LMWH. • The rate of wound infections is probably increased with LMWH. **The guideline panel considered the size of the anticipated undesirable effects to be small.
  • 17. Conclusions: • The conditional recommendation for use of LMWH as thromboprophylaxis in patients with cancer undergoing lung resection is due to a balance of effects that probably favors LMWH. • The panel made a conditional recommendation for use of LMWH rather than a strong recommendation given varying costs of the intervention and issues regarding access to the specific anticoagulants in different settings, with both options being acceptable. • The panel did not identify any further research priorities for this guideline question.
  • 18. Combined Mechanical and Pharmacological Prophylaxis Versus Pharmacological Prophylaxis Alone *We identified 15 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context.
  • 19. Benefits *Use of combined prophylaxis compared with pharmacological prophylaxis alone may reduce mortality ,this corresponds to 9 fewer deaths per 1000 patients. *Combined prophylaxis may reduce PE ,this corresponds to 1 fewer symptomatic PE per 1000 patients . *Use of combined prophylaxis probably reduces proximal DVT (RR, 0.14; 95% CI, 0.01-2.63; very low certainty in the evidence of effects); this corresponds to 10 fewer proximal DVT per 1000 patients. *The panel considered these health benefits to be small.
  • 20. Harms and burden. • For the effect of using combined prophylaxis on major bleeding there were very serious concerns about imprecision due to a small number of events in the included trials and we are uncertain about this effect
  • 21. Conclusions: *The conditional recommendation for use of combined mechanical and pharmacological prophylaxis in patients with cancer undergoing lung resection is due to a balance of effects that probably favors combined prophylaxis based on very low certainty in the evidence, negligible costs for the in- patient setting, and the intervention being viewed as acceptable and feasible. *Despite the very low uncertainty in the evidence, the panel did not identify the use of combined prophylaxis as a research priority
  • 22. Mechanical Prophylaxis Versus No Prophylaxis • We identified 20 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context. • Mechanical prophylaxis compared with no prophylaxis may reduce PE,this corresponds to 4 fewer symptomatic PE per 1000 patients. • Use of mechanical prophylaxis may reduce proximal ,this corresponds to 2 fewer proximal DVT per 1000 patients. • The panel considered these health benefits to be small
  • 23. Harms and burden • The panel judged that overall the undesirable anticipated effects of using mechanical prophylaxis would be trivial.
  • 24. Conclusions: • The conditional recommendation for use of mechanical prophylaxis in patients undergoing lung resection, who do not receive pharmacological prophylaxis, is due to a small benefit and overall balance of efficacy and safety that probably favors the intervention in the context of very low certainty of evidence, likely acceptability and feasibility, as well as negligible costs.
  • 25. Extended Versus In-Hospital Prophylaxis • We identified 7 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context. • All of the trials addressed use of extended prophylaxis with LMWH for a duration up to 28 to 35 days compared with LMWH for a duration of 6 to 10 days.
  • 26. Benefits: • The effect of using extended prophylaxis compared with in-hospital prophylaxis on mortality was uncertain ,with 2 more (3 fewer to 9 more) deaths per 1000 patient. • Extended prophylaxis probably reduces PE ,this corresponds to 11 fewer symptomatic PE per 1000 patients. • Use of extended prophylaxis probably reduces proximal DVT ,this corresponds to 9 fewer proximal DVT per 1000 patients. • The panel considered these health benefits to be small.
  • 27. Harms and burden. • s extended prophylaxis may result in a reduction in major bleeding ,this corresponds to 5 fewer major bleeds per 1000 patients. • No data was reported in the included trials on wound infection, wound hematoma, or reoperation.
  • 28. Conclusion: • The panel judged that within the heterogenous population of patients undergoing lung resection, for those at higher risk of thrombosis the balance of effects probably favors use of extended prophylaxis, whereas for those at lower risk the balance probably favors in-hospital prophylaxis only.
  • 29. Pre- Versus Postoperative Administration of Prophylaxis • We identified 3 randomized controlled trials that fulfilled our inclusion criteria and measured outcomes relevant to this context