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N. Patel et al.
replantation [85], and the use of LMWH has been described in salvage of free aps. Injection of LMWH directly into areas of the congested ap in a subcutaneous fashion has been described, with the onset of action and time to visible effect reported to be about 2h, with peak effect occurring at about 4–5 h and duration of effect of about 12–24 h. It has been recommended that doses of 20–40mg every 4–6h should be implemented for the rst 1–3days, decreasing to 10–20mg every 24 h around the 10–14-day mark [86]. Therapy should be continued for a minimum of 10days, as studies have identied the time frame for the re­establishment of neovascularization to be around 7–10days [87]. As with Rt-PA, the use of LMWH can be useful in cases of thrombosis both at the level of the pedicle and within the microcirculation of the ap, which may not be amenable to surgical exploration. In addition to its anticoagulant effects, heparin has been shown to reduce endothelial dys­function within the microcirculation of postisch­emic aps, thus providing a protection against reperfusion injury that is independent of its sys­temic anticoagulant effects, though the exact mech­anism of this effect is yet unknown. It has been postulated to be linked to effects such as inhibition of leukocyte adhesion to postischemic endothelium via increases in nitric oxide synthesis, reduction of free radicals due to its capacity to release superox­ide dismutase from the endothelium, as well as direct anti-inammatory effects [8890].
Leeches (hirudotherapy) have shown promise in the management of venous congested aps, particularly as a bridge to formal surgical explo­ration and revision [91, 92]. Leech therapy is only useful, however, in cases where arterial inow is patent and sufcient, and therapy is tar­geted at decreasing the accumulating venous pressure within the ap (Fig. 6.9). Leeches
secrete a non-heparin anticoagulant called hiru­din, which aids in the feeding process. Leeches are kept in refrigerated distilled water with Hirudo salt. Prior to application, any blood clots should be cleaned off with dry gauze (use of alco­hol swabs may interfere with latching). The leech is grasped with gloves or non-toothed forceps and placed onto the ap. If the leech does not latch, the ap can be pricked to induce bleeding to encourage the leech to latch. The leech will generally detach once it is fully distended and must be monitored to prevent migration of the leech to other areas, with treatment lasting any­where from 30 min to 4–5 h. Leeches are then euthanized in 70% isopropyl alcohol and dis­carded. All patients are placed on antibiotics pro­phylaxis for Aeromonas hydrophila for the duration of leech therapy, which consists of dox­ycycline, ciprooxacin, ceftriaxone, or Bactrim, with prophylaxis continuing for 14 days after cessation of leech therapy. Furthermore, the patient’s hemoglobin levels must be monitored throughout the treatment period every 6h, and transfusion should be considered if levels drop below 10g/dL in symptomatic patients [93]. It should be noted that leech therapy has not been shown to help salvage all venous congested tis­sues and as such should not be used as a primary method of ap salvage [94, 95].
HBOT has been shown to improve the sur­vival of free ap failures in the setting of arterial, venous, and combined arteriovenous insuf­ciency; however, it has been validated primarily in animal models [96]. In contrast to leech ther­apy, HBOT has been shown to impact ap sur­vival greatest in cases of arterial insufciency, secondary to its ability to enhance broblasts and collagen synthesis, promote neovascularization, and reduce local hypoxic insults [97, 98]. Further
Fig. 6.9 Use of medicinal leeches on venous congested ap. Note the improvement of central portion of ap, with necrosis of limited to lateral edge and distal tip
6 Free Flap Considerations andComplications
107
investigation in human subjects is necessary at this time to better evaluate the efcacy of HBOT as an accepted mode of free ap salvage in head and neck reconstructive surgery.
Hematomas
The formation of hematomas not only compro­mises tissues by the extrinsic pressure effect they elicit, but they also induce a complex sequence of interrelated biochemical and cellular events, including neutrophil inltration, cytokine­mediated inammation, and a prothrombotic state, which leads to synthesis of reactive oxygen species and activation of the complement system, resulting in tissue injury, as well as vascular thrombosis [99, 100]. Sources of bleeding may include the vascular pedicle, tissue bed, as well as bleeding from ap edges. Postoperative hematoma formation (Fig. 6.10) accounts for anywhere between 0.2% and 30% [101] of post­operative complications relating to free aps in head and neck reconstruction, representing the second most common postoperative complica­tion in free aps, just behind vascular thrombosis [102]. This is higher than other regions of the body, likely relating to increased dead space in the head and neck with more anatomical con­straints, more complex vascular anatomy, as well as difculty in immobilization and autonomic reexes such as gagging and coughing, as well as vomiting, resulting in inadvertent pedicle disrup­tion or vascular leakage [103]. Studies have shown that free aps are compromised by hema­tomas 2–4% of the time within this cohort, most commonly resulting from compromise of venous outow and ap congestion [104]. As such, early
recognition of hematoma formation and manage­ment are crucial to free ap salvage. A study by Chen etal. concluded that if return to the OR for re-exploration and salvage was within 36h, sal­vage rates were signicantly higher at 84% as compared to 50% if return to OR was after this time frame, with salvage rates especially higher in cases where there was an absence of thrombo­sis [105]. Other studies have shown salvage rates of 93.3% if return to OR was within 5h of detec­tion, and 100% in the absence of thrombosis, as compared to 58.3% in the presence of vascular thrombosis [106]. The use of postoperative anti­coagulation to decrease vascular thrombosis rates in free aps remains a debated topic with no con­sensus as of yet. Studies have shown that in cases where no anticoagulation therapy was used, rates of free ap failure, thrombosis, as well as rates of hematoma formation were similar to rates of var­ious anticoagulation therapies [107, 108]. However, a study by Kroll etal. demonstrated a statistically signicant increase in rates of hema­toma formation in patients who received high­dose heparin for pedicle thrombosis prophylaxis at 20% [109]. Moreover, other studies have shown that the use of NSAIDs postoperatively has been associated with higher rates of hema­toma formation in this cohort, with aspirin show­ing the lowest rates of hematomas [110, 111]. All this may suggest that anticoagulation postopera­tively offers no or minimal improvement in ap survival and minimal effect on ap-related com­plications in the postoperative setting [112]. Despite this, patients often require chemopro­phylaxis for reasons other than prevention of ap thrombosis, such as prevention of VTE, and thus
Fig. 6.10 Formation of postoperative hematomas in free ap patients
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N. Patel et al.
this should be taken into consideration. It has also been suggested that postoperative blood pressure control can inuence rates of hematoma formation and should ideally be <150 mmHg systolic, as rates of hematoma formation can increase with even transient increases of about 165mmHg systolic [113]. Despite this, maintain­ing a high enough blood pressure to maintain good ap perfusion and avoiding signicant peri­ods of hypotension are essential, with systolic blood pressure ideally maintained above 100mmHg for this purpose [114].
Signs of the presence of a hematoma can sometimes be subtle, with just the localized development of ecchymosis in the cervical region or just the presence of a mild amount of edema. Other times, evidence of hematoma formation is more obvious, with the presence of a large swell­ing, ecchymosis, bleeding from between sutures, compression of the vascular pedicle, and venous outow blockage.
One method by which to manage hematoma formation is the removal of sutures at bedside with evacuation of the hematoma. Some authors however have stated that given the cytotoxic nature of the effects of a hematoma, as well as the potential for incomplete hematoma evacuation, performing this maneuver is not sufcient and return to the OR for exploration and formal evac­uation is recommended (Fig. 6.11) [115]. Additionally, formal exploration is often war­ranted in order to identify and obtain surgical control of bleeders if present, and to examine the vascular pedicle for potential thrombosis. If re­exploration is performed prior to the formation of
vascular thrombosis, salvage rates are signi­cantly higher, underscoring the importance of early detection.
Salvage Reconstruction
Unfortunately, there are the rare instances where ap salvage appears to be unlikely, and surgeons are left to make a tough decision, namely when to terminate salvage efforts and what steps to take next. In the case of partial ap failure, options for management depend primarily on the amount of residual defect after partial ap debridement or excision, location of the defect, as well as tissue availability. In cases where a small defect remains, local tissue rearrangement sometimes sufces for the purposes of wound coverage, whereas larger defects may necessitate the use of a regional ap. If the defect involves a communi­cation of the oral cavity to the neck, salivary leak into the cervical tissues becomes a signicant consideration, given the increased risk of infec­tion and stula formation. In the setting of total ap failure, one must balance the needs of the wound or defect for reconstruction with a goal of restoring form and function, with the ability of the patient to tolerate another extensive proce­dure and to decide what additional procedure should be undertaken. The reconstructive options remain similar, a second free tissue transfer, regional ap, or local tissue rearrangement (Fig.6.12) [4]. In addition to the tolerance of a secondary procedure, consideration should be made for extended hospital stay with potential for
Fig. 6.11 Complete evacuation of hematoma during exploratory surgery in OR
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Fig. 6.12 Unsalvageable necrotic free ap with removal of ap, and salvage supraclavicular ap performed for cheek reconstruction
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Fig. 6.12 (continued)
additional morbidity, as well as the timing of radiation, if applicable, as a delay in this treat­ment modality is not favorable. The decision of what type of secondary reconstruction should be done at this time depends on several factors, including the type and location of the original defect, number and amount of available tissues or ap options, and patient comorbidities and stabil­ity. The simplest reconstruction should be under­taken, one that has the highest chance of success and the minimum amount of additional patient morbidity. For example, in the case of maxillo­mandibular reconstruction with a free osteocuta­neous bula ap, in the event of bula ap failure, the ideal salvage ap would be a second free b­ula ap, as that has the highest chance of meeting the reconstructive requirements. However, if a second bula ap cannot be harvested due to ana­tomic restrictions (lack of adequate three-vessel runoff), or due to the patient’s fragility or inabil­ity to tolerate a second lengthy procedure, one should consider a soft tissue ap such as an anterolateral thigh ap or radial forearm free ap to obtain wound coverage, which would provide a shorter procedure and thus less morbidity for the patient. If the patient will be obtaining dental implants, secondary bone grafting can be consid­ered at a later stage. Another option in this case can be a pedicled ap, such as a pectoralis myo­cutaneous ap if the surgeon chooses to avoid
N. Patel et al.
another free ap procedure because of a vessel­depleted neck, patient stability issues, diagnosis of thrombophilic disorder, severe infection, etc. Salvage reconstruction often presents a challenge as it occurs in a previously operated wound bed, often contaminated or infected, and the ideal ap has already been utilized. As such, success rates in the salvage setting often drop as compared to the primary reconstruction setting. Bozikov and Arnez found that ap failures in the salvage oper­ation were 4.6× more likely, with a success rate of only 53.3% [116]. Salvage reconstruction can be done either in the immediate setting or in a delayed fashion, depending on these factors, though most surgeons will opt to perform it immediately. In the head and neck, this presents a particular challenge as specic issues come into consideration, such as dealing with vessel­depleted necks, salivary contamination/leak if a composite defect of the oral cavity is involved, patients having a history of prior radiation, patients with head and neck cancer who are often malnourished with poor wound healing, and need for coverage of the great vessels, among others [117]. In cases of limited availability of adequate vessels for anastomosis, due to radiation damage or depletion from previous free ap surgery, sur­geons can consider options such as vein grafting; use of the internal mammary, thoracoacromial vessels, or transverse cervical vessels; and use of the contralateral neck vessels, or end-to-side anastomoses, in particular with the internal jugu­lar vein, as this provides reliable drainage, good caliber, and consistent anatomy [118121]. Though surgeons often desire to provide patients with the best reconstructive option possible, one must also consider that sometimes the best recon­struction … is no reconstruction. The use of syn­thetic prostheses, when available, often can represent excellent alternatives as prosthetic reconstruction, for patients in whom surgical reconstruction is not an option. A wide variety of options exist for orbital, nasal, maxillary, and auricular reconstruction, with or without implants for support and retention [122].
6 Free Flap Considerations andComplications
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Conclusion
Free ap reconstruction of the head and neck rep­resents a complex surgical endeavor and can be wrought with complications at any stage of patient care. Surgeons must be mindful and must employ careful patient selection and workup, as well as demonstrate excellent surgical technique, and patients should be carefully and constantly monitored in the immediate postoperative period to help mitigate, and ideally avoid, these compli­cations. Surgeons must be adept at recognizing issues early that could potentially compromise ap viability and be prepared to perform addi­tional salvage procedures to maximize success rates.
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Part III
Post-operative Considerations
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