Microsurgery Flashcards

1
Q

What is the average tissue survival rate for a microvascular free flap?

A

95% or better

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2
Q

What is the reexploration rate for flap compromise?

A

Approximately 10%.

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3
Q

What is the salvage rate for microvascular free flaps that require reexploration for flap ischemia?

A

50% to 85%.

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4
Q

What is the maximum warm ischemia time tolerated by muscle flaps?

A

Less than 3 hours.

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5
Q

What is the maximum warm ischemia time tolerated by bone flaps?

A

Less than 3 hours.

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6
Q

What is the maximum warm ischemia time tolerated by skin and fasciocutaneous flaps?

A

Approximately 4 to 6 hours.

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7
Q

What is the warm ischemia time tolerated by jejunal flaps?

A

Less than 2 hours.

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8
Q

How can the maximum tolerated ischemia time be increased?

A

Cooling of tissues: up to 12 hours of ischemia tolerated for fasciocutaneous tissues, 8 hours for muscle, and
24 hours for bone.

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9
Q

Which results higher flap survival rates, end-to-end or end-to-side anastomoses?

A

Most studies demonstrate similar patencies.

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10
Q

Which type of arteriotomy, slit or circular/oval, is more successful?

A

Most studies demonstrate similar patencies.

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11
Q

Under what circumstances might an end-to-side anastomosis be advantageous?

A

Vessel size discrepancy (larger donor vessel), only one artery or vein available and needed for distal organ/tissue
perfusion, limited exposure/availability of similar size donor vessels.

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12
Q

What anastomotic angles are thought to be the most desirable and result in the greatest amount of blood flow to the recipient vessel in an end-to-side anastomosis?

A

Based on technical factors and blood flow rates, angles of 45◦ to 90◦ result in greater arterial flow than obtuse angles up to 135◦.

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13
Q

What methods relieve vasospasm?

A

Topical anesthetics (eg, lidocaine), topical papaverine, dilation, adventitial stripping, sympathetic nerve block (eg,
epidural anesthesia for lower extremity reconstruction).

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14
Q

What is the reason for adventitial stripping?

A

To relieve vasospasm and to prevent loose adventitia from being caught in the vessel lumen, a potential trigger for
thrombosis.

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15
Q

Which method of adventitial stripping is preferred, blunt or sharp?

A

Sharp adventitial stripping is associated with less vessel trauma resulting less vasospasm and improved blood flow to
the flap.

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16
Q

What are the characteristics of a viable flap?

A

Warmth, color, softness, capillary refill, and detectable pulse (eg, Doppler).

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17
Q

What are signs of inadequate arterial flow?

A

Pale, cool flap with slow (>2 second) capillary refill and decreased tissue turgor.

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18
Q

What are signs of inadequate venous flow?

A

Cyanotic or dusky flap with fast (<1 second) capillary refill and increased tissue turgor.

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19
Q

What are the most reliable methods of free flap monitoring?

A

Clinical observation, Doppler ultrasound flowmetry, pinprick or scratch testing, pulse oximetry, quantitative
fluorometry, surface temperature probing.

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20
Q

How can buried flaps, such as those used for pharyngeal reconstruction, be monitored?

A

A segment of the flap can be pedicled on separate perforating blood vessels and exteriorized. Alternately, an implantable Doppler can be placed on the vein or artery or both, distal to the anastomosis.

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21
Q

How long before a pseudointima forms at the anastomotic site?

A

Approximately 5 days.

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22
Q

How long before a new intima forms at the anastomotic site?

A

Approximately 1 to 2 weeks.

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23
Q

What types of sutures are typically used for microvascular surgery?

A

Nylon or polypropylene sutures ranging from 8-0 to 12-0.

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24
Q

How is the microvascular suture selected?

A

Thicker sutures with larger needles are indicated for larger vessels. Thinner sutures with finer needles are indicated for smaller vessels. In general, 9-0 sutures are used for vessels of 2 mm or more in diameter and 10-0 sutures are used for vessels of 1 to 2 mm.

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25
Q

In an end-to-end anastomosis, what is the maximum size discrepancy between vessels that can be accommodated?

A

Between 2:1 and 3:1

26
Q

What are some strategies for performing an anastomosis between vessels with a size mismatch?

A

Other than placing sutures farther apart on the larger vessel, strategies include beveling or spatulating the smaller vessel, partially closing or narrowing the larger vessel lumen with sutures, or using an interposition graft that is intermediate in diameter between the two vessels (see Figure 75-1). When the recipient vessel is larger, an end-to-side anastomosis into the recipient vessel can be performed. Strategiesfordealingwithavesselsizemismatchincludenarrowingthelargervesselwithsutures,bevelingthesmaller vessel, using an interposition graft of intermediate diameter, and performing an end-to-side anastomosis when the recipient vessel is larger.)

27
Q

Under what circumstances can microvascular coupling anastomotic devices generally be used?

A

Coupling devices are usually used for minimally discrepant, soft, pliable venous microvascular anastomoses.

28
Q

Which has superior patency rates, coupled or hand-sewn anastomoses?

A

They are similar when used appropriately.

29
Q

Can coupling devices be used on arteries?

A

Yes, but they generally do not work well on thick-walled or inelastic, atherosclerotic vessels.

30
Q

What is the maximum closing pressure of vascular clips that should be used to minimize damage to vessels?

A

30 g/mm2.

31
Q

What are some key points when performing an anastomosis for preventing exposure of subendothelium and thereby inducing platelet aggregation?

A

Use small needles, avoid repeated needle punctures, equal placement of sutures, avoid tying sutures too loose or too tight, avoid use of too many sutures, which can cause endothelial slough.

32
Q

How does heparin prevent coagulation?

A

Primarily by increasing the action of antithrombin-3, which inactivates thrombin. It also decreases platelet adhesion
and inhibits the conversion of fibrinogen to fibrin.

33
Q

What risks are associated with heparin use?

A

In addition to bleeding and hematoma formation, heparin can cause thrombocytopenia. Heparin-induced
thrombocytopenia is thought to be caused by antibodies to the complex formed by heparin and platelet factor 4.

34
Q

How does aspirin function to prevent platelet aggregation?

A

Aspirin blocks the endothelial cyclooxygenase pathway with subsequent blockage of thromboxane A2 preventing
vasoconstriction and thrombus formation.

35
Q

Is high-dose aspirin more effective than low-dose aspirin to prevent platelet aggregation?

A

No. At low doses, aspirin selectively inhibits thromboxane A2, a platelet aggregator and vasoconstrictor. At high doses, prostaglandin I2, a vasodilator and inhibitor of platelet aggregation are also inhibited. For example, aspirin in doses of 81 and 325 mg has been shown to be more effective in preventing cerebrovascular accidents, myocardial infarction, and death after carotid endarterectomy than doses of 650 and 1300 mg.

36
Q

How does dextran work to prevent clotting?

A

Dextran is a volume expander that prevents platelet adhesion by increasing the negative electric charge of platelets, erythroctyes, and endothelial cells, resulting in a destabilization of fibrin polymerization. Dextran is also an inactivator of von Willebrand factor, a major contributor to platelet aggregation and adhesion to vessel wall collagen.

37
Q

What are some possible complications associated with the use of low-molecular-weight dextran?

A

Bleeding, pulmonary edema, and allergic reaction including anaphylaxis.

38
Q

What is the mechanism of the no-reflow phenomenon?

A

Ischemia results in cellular swelling in the vascular endothelium with subsquent intravascular platelet agregation and leakage of intravascular fluid into the interstitial space.

39
Q

What pharmacologic agents can be used to rescue some free flaps in which anastomotic revision fails to restore flap perfusion or is associated with recurrent thrombosis?

A

Thrombolytic agents such as streptokinase, urokinase, tissue plasminogen activator.

40
Q

How do thrombolytic agents work?

A

Thrombolytic agents, such as streptokinase, urokinase, and tissue plasminogen activator, function by directly or indirectly activating plasminogen to form plasmin, which cleaves fibrin in clots as well as fibrinogen and coagulation factors V, VIII, IX, XI, and XII.

41
Q

What are the risks associated with using streptokinase?

A

In addition to bleeding and hematoma formation, streptokinase is antigenic and can result in an allergic response (6% incidence) with a 0.1% incidence of anaphylactic reaction. Streptokinase can also result in a “lytic state,” causing diffuse bleeding when administered in high doses. Unlike streptokinase, urokinase and tissue plasminogen activator do not appear to be antigenic.

42
Q

What is the mechanism of thrombosis in microvascular anastomosis?

A

Exposure of subendothelial collagen-containing surfaces to which platelets adhere eventually leading to fibrin
deposition, vasospasm, stenosis, and thrombosis, causing loss of blood flow.

43
Q

What is Virchow’s triad?

A

Virchow’s triad refers to risk factors for thrombosis and includes stasis, intimal injury, and hypercoagulability

44
Q

Why is bipolar electocautery preferable to monopolar electrocautery in the control of bleeding from or around a recipient or donor blood vessel used in microvascular free tissue transfer?

A

Bipolar cautery damages tissue, including endothelium and media, over a much more limited distance (approximately 1–2 mm) compared to unipolar cautery.

45
Q

Why is the number of sutures placed in an anastomosis critical?

A

Too few sutures result in excessive bleeding and thrombus formation; too many result in increased damage to the
endothelium and thrombus formation.

46
Q

Which anastomotic technique demonstrates greater success rates, interrupted suture placement or continuous sutures?

A

In experienced hands, similar success rates are observed.

47
Q

Does smoking tobacco increase free flap failure rate?

A

Most retrospective studies demonstrate similar (nondigital) flap survival and thrombosis rates between smokers and nonsmokers, although smokers have a higher incidence of healing complications at the flap interface and at the donor-site wound.

48
Q

What happens to vein grafts when they are used to bridge intra-arterial gaps?

A

There is ingrowth of smooth muscle cells and creation of a neointima that results in significant thickening of the vein wall. Also, graft length decreases by 26% to 30% when used as an intra-arterial or intravenous graft.

49
Q

In addition to excellent vascular and neural anastomoses what other factor determines the success of functional free skeletal muscle transfer?

A

Reestablishment of the correct resting tension since very small decreases in resting tension can markedly reduce the power and amplitude of muscle contraction.

50
Q

Name some commonly used donor sites for free osseous and osseocutaneous flaps.

A

Rib, fibula, iliac crest, second metatarsal, radius, calvarium, scapula.

51
Q

In what ways are vascularized bone transfers superior to nonvascularized bone grafts?

A

Vascularized bone grafts demonstrate earlier incorporation, bone hypertrophy, mechanical strength to failure,
osseous mass retention, and resistance to local infection.

52
Q

What techniques can be used to prolong ischemia time in limb replantation?

A

Cooling and AV shunting.

53
Q

What are the major contraindications to replantation?

A

Concomitant life-threatening injury, multiple segmental injuries to the amputated part, severe crushing or avulsion of the tissues, extreme contamination, inhibiting systemic illness (small vessel disease, diabetes mellitus, etc), prior surgery or trauma to the amputated part precluding replantation.

54
Q

How do leeches function to relieve venous congestion?

A

By secreting hirudin, a selective thrombin inhibitor that is injected into the hosts tissue as they feed on host blood.

55
Q

What pathogenic bacterium do leeches commonly transmit?

A

Aeromonas hydrophila.

56
Q

What antibiotics should be used in the prophylaxis or treatment of bacterial infections associated with the use of leeches?

A

Ciprofloxacin, tetracycline, trimethoprim-sulfamethoxazole, or second- and third-generation cephalosporins.

57
Q

Does the order of anastomosis and microvascular clamp removal affect the survival of free flaps?

A

There are no significant differences in flap survival based on the order of anastomosis or microvascular clamp removal seen in an animal model, although early, transient venous congestion does develop if the artery is anastomosed first and the clamp on the artery is removed prior to venous anastomosis and clamp removal.

58
Q

Can loupe magnification be safely used for microvascular anastomoses?

A

High-power loupes have been used for anastomosing vessels greater than 1 mm in diameter with success rates comparable to those achieved using a microscope.

59
Q

Can microvascular surgery be successfully performed in children?

A

Yes. A success rate of 93% has been observed in children younger than 15 years, despite smaller blood vessel size.

60
Q

Can microvascular surgery be successfully performed in the elderly?

A

Yes. Age has not been found to be an independent predictor of flap loss in several studies. However, older age is frequently associated with medical comorbidities, including cardiac and peripheral vascular disease, as well as development of other complications related to long surgeries.