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Complications of cutaneous surgery in patients taking clopidogrel-containing anticoagulation
Robert H Cook-Norris1, Jason D Michaels2, Amy L Weaver3
1Department of Dermatology, Mayo Clinic, Rochester, Minnesota.
Background:
Most anticoagulants are not associated with increased risk of severe complications during cutaneous surgery, but no data exist on clopidogrel.
Objective:
We sought to determine frequency and severity of perioperative complications in patients taking clopidogrel-containing anticoagulation.
Methods:
This was a retrospective review of medical records of patients undergoing Mohs micrographic surgery at Mayo Clinic, Rochester, MN, while taking clopidogrel-containing anticoagulation between 2004 and 2008, compared with control subjects taking aspirin monotherapy or no anticoagulants.
Results:
In all, 220 patients taking clopidogrel-containing anticoagulation underwent 363 surgical procedures on 268 occasions. Severe complications occurred in 11 of 363 surgical sites in 10 cases. Clopidogrel-containing anticoagulation was 28 times more likely than no anticoagulation and 6 times more likely than aspirin monotherapy to result in severe complications after Mohs procedures (P < .001 and P = .022, respectively). Severe complications were 8 times more likely after Mohs procedures in patients taking both clopidogrel and aspirin than in control subjects taking aspirin monotherapy (P = .009). No statistically significant difference was found between patients taking clopidogrel monotherapy and control subjects not taking anticoagulants (P = .15). Patients experiencing severe complications were more likely to have larger postoperative surgical sites (P < .001). No thrombotic complications were encountered with discontinuation of clopidogrel-containing anticoagulation; a postoperative thrombotic complication occurred in one patient whose clopidogrel-containing anticoagulation regimen was modified.
Limitations:
Retrospective nature of study, possible recall bias as a result of telephone contact, and small number of severe complications were limitations, which reduced study power.
Conclusion:
Cutaneous surgery in patients taking clopidogrel-containing anticoagulation is associated with an increased risk of nonlife-threatening severe complications.
Insights
Patients taking clopidogrel for anticoagulation face a higher risk of severe complications during cutaneous surgery. This risk is significantly elevated compared to aspirin or no anticoagulation, particularly for larger surgical sites.
Area of Science:
- Dermatology
- Cardiology
- Surgical Oncology
Background:
- Most anticoagulants do not increase severe complications during cutaneous surgery.
- Limited data exists on clopidogrel's association with surgical complications.
Purpose of the Study:
- To determine the frequency and severity of perioperative complications in patients undergoing cutaneous surgery while on clopidogrel-containing anticoagulation.
- To compare complication rates between clopidogrel users, aspirin monotherapy users, and non-anticoagulated patients.
Main Methods:
- Retrospective review of medical records of patients undergoing Mohs micrographic surgery.
- Comparison of patients on clopidogrel-containing anticoagulation with control groups on aspirin monotherapy or no anticoagulation.
- Data collected between 2004 and 2008 at Mayo Clinic, Rochester, MN.
Main Results:
- Clopidogrel-containing anticoagulation was associated with a significantly higher risk of severe complications (28x vs. no anticoagulation, 6x vs. aspirin monotherapy).
- Patients on both clopidogrel and aspirin had an 8x higher risk of severe complications compared to aspirin monotherapy.
- Larger postoperative surgical sites were linked to a higher likelihood of severe complications.
Conclusions:
- Cutaneous surgery in patients on clopidogrel-containing anticoagulation is linked to an increased risk of severe, non-life-threatening complications.
- Limitations include the retrospective design, potential recall bias, and a small number of severe complications.
- No thrombotic complications occurred upon discontinuation of clopidogrel; one occurred with regimen modification.
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