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40138 Management of Presacral/Pelvic Bleeding
stressed. The literature has consistently demon­strated that checklists improve outcomes in a stressful situation [8]. As such, it is important to have a structured plan.
Prior to engaging in specific technical ma­noeuvres described below, the situation first needs to be acknowledged. Troublesome bleed­ing in the pelvis is a constant hindrance but does not impede progress nor compromise the pa­tient. Significant bleeding, however, should be verbally acknowledged. This is important since all members in operating room may not be able to see the operation or may not be aware of the gravity of the situation. It is possible that the fel­low or resident either performing or assisting in the operation may not have encountered signifi­cant pelvic haemorrhage before [9]. It will thus be necessary for the surgeon to take over the operation and organise the assistants in the most useful position (e.g. opposite the surgeon or in between the patient’s legs) as per their seniority. An escalation in hierarchy should also be con­ducted with other members of staff in theatre. The most senior nurse should take over as the scrub nurse if not already involved, and multiple unscrubbed nurses should be available as a num­ber of uncommonly used tools may need to be acquired expediently. Similarly, the anaesthesi­ologist should be informed directly.
Role of the Anaesthesiologist
Once the anaesthesiologist has been informed, acute circulatory support can be considered to have been delegated. Though the practical role of the surgeon is to control the bleeding, it is im­portant to be familiar with the strategies at the disposal of the anaesthesiologist.
The focus of the anaesthesiologist will include initial measures including ensuring optimal in­travenous access and volume resuscitation. This may lead to more intensive monitoring for the acute period and also in anticipation of the likely necessity of admission to the high dependency unit or intensive care unit.
Volume replacement may include activation of the massive transfusion protocol or component blood replacement in line with institutional prac­tice. Serial thromboelastograph measurements may also be important to guide blood product replacement alongside advice from a haematolo­gist [10].
Tranexamic acid may also help limit the mag­nitude of bleeding. Recent evidence suggests that tranexamic acid reduces bleeding in gastrointes­tinal surgery with no increase in the incidence of thromboembolic events [11]. Anecdotal experi­ence also suggests that use during pelvic exen­teration decreases surgical ‘ooze’.
Role of the Surgeon
Once the operating team has been suitably organ­ised, the pelvis should be packed. At this time, more help should be obtained from a colleague if possible. The importance of an experienced first assistant and the potential advantage of a hitherto uninvolved person cannot be overstated.
The injury now needs to be localised and il­lumination and proper exposure is crucial espe­cially since a hallmark of this type of bleeding is gushing blood form the pelvic floor with a near­undetectable bleeding point. A practical solution to obtain optimal illumination is that the operat­ing surgeon should utilise a headlight. Exposure can also be facilitated by expedient removal of the specimen whilst the area remains tampon­aded with packs. If the bleeding point cannot be reliably detected, pressure should be maintained for 15–20 min. The temptation to re-examine the area ahead of this interval should be resisted, and the time should be used to formulate a plan and obtain necessary equipment. The pressure ef­fects of packing may also be complemented with commercially available fibrin-based haemostatic agents [12]. A combination of haemostatic ma­trices (e.g. FloSeal, Baxter, USA) and absorb­able haemostatic products (e.g. Surgicel Fibrillar, Ethicon, USA) may be used.
It is important to determine whether the bleed­ing has resulted from an injury to the presacral
402 S. Srinivasa and A. G. Hill
venous plexus or to a basovertebral vein. If the bleeding point can be controlled by compressing the surrounding veins, there has been an injury to the presacral veins. If the bleeding is abated only by direct compression, it is from an injury to a fine or large-calibre basivertebral vein.
Injury to the presacral venous plexus can often be successfully managed with suture ligation en­suring that it is performed over intact presacral fascia and the bites are deep enough to contain presacral veins but also surrounding deep con­nective tissue so that the stitches hold traction [13].
Injury to the basivertebral veins can be man­aged with thumbtacks over the sacral foramen or by breaking the sacral foramen with a blunt­ended instrument [4]. A number of authors have reported the successful use of thumbtacks to stop presacral bleeding [14, 15]. It is inexpensive and technically straightforward unless the bleeding arises from veins near S3 or S4 as the curvature of the distal sacrum can make access difficult. Thumbtack displacement and chronic pain have been reported though these are secondary issues when confronted with life-threatening bleeding [16, 17].
Lou et al. have also described “welding” an epiploic appendix to the bleeding point with cau­tery whilst Saurabh et al. have reported success­ful management of bleeding with the use of argon plasma coagulation [2, 18]. Both techniques have been reported in the context of open surgery but could be applicable to minimal-access surgery. Rectus muscle tamponade has also been de­scribed as a strategy and is broadly similar to the use of the epiploic appendix though the former has been reported to lead to subsequent necrosis and abscess development [19].
Other strategies that have been successfully used include the application of bone wax, Tef­lon pledgets, expandable breast implant sizers or saline bags and haemostatic agents [16, 17, 20,
21]. Ligation of the internal iliac veins is usually
futile since this will obstruct blood flow in the pelvic venous plexus, obturator veins and gluteal veins. As a result, blood flow will be redirected to
the injured veins via the lateral or anterior sacral veins.
A number of strategies have been described in the literature. However, practical application of these techniques in an individual situation is limited by the surgeon’s familiarity and comfort and availability of required tools within the in­stitution. The listed strategies cannot be exhaus­tively worked through due to the rapidity of the bleeding. Rather, it is up to the individual to de­cide upon a few which he/she can employ in a systematic manner.
If the bleeding cannot be controlled despite all attempts, the pelvis should be packed and the op­eration abandoned. The patient should be trans­ferred to the intensive care unit with a planned re­look laparotomy when the patient has stabilised. Assistance from interventional radiologists may also be helpful for angioembolising any vessel showing extravasation of contrast though this is unlikely to be helpful due to the bidirectional na­ture of flow and redundant pathways contributing to bleeding.
Minimal-Access Surgery
Many of the techniques described above can be utilised during laparoscopic or robotic resection. The initial differences upon encountering signifi­cant presacral bleeding relate to the view, which may in fact be superior to open surgery, and iden­tification of the bleeding point (Fig. 38.2). Port placement may preclude direct pressure over the sacrum, and extra ports should be inserted as appropriate to maintain direct pressure in an ergonomic fashion. Since the view during laparo­scopic or robotic surgery may be highly magni­fied, the bleeding may appear even more volumi­nous. The other disadvantage is that it may not be possible to remove the operative specimen as quickly as during open surgery.
The specific strategies used successfully in the literature include argon plasma coagulation in a ‘point and shoot’ manner [18]. Germanos et al. have described the use of haemostatic agents to
40338 Management of Presacral/Pelvic Bleeding
Fig. 38.2 Presacral bleeding. MSV middle sacral vein, IIV internal iliac vein, LSV lateral sacral vein, BVV ba-
sivertebral vein, PSVP presacral venous plexus, IVVS in-
control presacral bleeding [16]. Although their case reports are in the context of open surgery, a similar strategy of using haemostatic matrixes and fibrin-based haemostatic gauze may be ap­plicable and technically straightforward in mini­mal-access surgery.
Suture ligation may also be used but will only be useful if the bleeding arises from the presacral venous plexus. It also requires advanced laparo­scopic skills, and its applicability may be limited by unfavourable, non-ergonomic working angles with conventional port placement.
A simple algorithm reported in the literature involves a trial of local compression with gauze or an absorbable haemostat followed by attempt­ed sealing of the bleeding point with either an omentum or an epiploic appendix. The graft is obtained using bipolar diathermy and then held in place with grasping forceps with monopolar diathermy to seal it in place. The third stage of the authors’ algorithm was to use a bovine peri­cardial graft and attach it to the source of bleed­ing with endoscopic tacking devices [22].
Strategies used in minimal-access surgery are broadly similar to those used in open surgery, and the principles have been partially derived from liver bleeding during laparoscopic chole­cystectomy. Although presacral bleeding can be safely managed laparoscopically or robotically, prolonged periods of time should not be spent
tervertebral venous system. (Reproduced with permission from [13] © Springer 2013)
attempting to control the bleeding without con­verting to open surgery.
The Postoperative Period
The patient should remain in a monitored envi­ronment, and their ongoing fluid and blood re­quirements should be managed to prevent the le­thal triad of hypothermia, coagulopathy and aci­dosis. Patients may benefit from ongoing doses of tranexamic acid and antibiotics (though there is no evidence for this). Anticoagulation with heparin or equivalent should be withheld. The family should be informed.
Lastly, given the rarity of the event, a debrief­ing session should be held for all members in­volved. This is particularly valuable for junior members of staff. The benefit of an even an in­formal debriefing session is to discuss prevention and management in detail whilst also potentially resulting in system improvements as necessary.
Summary
Presacral bleeding is a rare but clinically sig­nificant event in open- or minimal-access pelvic surgery. It usually results from injury to either the presacral venous plexus or the basivertebral
404 S. Srinivasa and A. G. Hill
veins. Conventional means to stop bleeding are usually unsuccessful. The management of this problem requires the active participation of the whole operating theatre team. Successful tech­nical strategies involve localising the bleeding point, identifying whether the bleeding has arisen from the presacral venous plexus or basivertebral veins and employing appropriate strategies in a systematic manner in line with the surgeon’s preference and availability of necessary tools within the institution.
Key Points
1. Correct identification of the TME plane, espe­cially posteriorly
2. Pack the pelvis and identify source of bleed­ing
3. Inform operating room staff and get additional help if possible
4. Differentiate between injury to the presacral venous plexus and basivertebral veins
5. Follow a structured plan based on injury type—suture ligation/haemostatic agents/ thumbtacks etc.
References
1. van der Vurst TJ, Bodegom ME, Rakic S. Tamponade of presacral hemorrhage with hemostatic sponges fixed to the sacrum with endoscopic helical tackers: report of two cases. Dis Colon Rectum. 2004;47(9):1550–3.
2. Lou Z, Zhang W, Meng R, Fu C. Massive pre­sacral bleeding during rectal surgery: from anat­omy to clinical practice. World J Gastroenterol. 2013;19(25):4039–44.
Baque P, Karimdjee
3. Benchimol D, et plexus: implications for rectal surgery. Surg Radiol Anatomy. 2004;26(5):355–8.
4. Qinyao W, Weijin S, Youren Z, Wenqing Z, Zhengrui H. New concepts in severe presacral hemorrhage dur­ing proctectomy. Arch Surg. 1985;120(9):1013–20.
Heald RJ, Husband EM, Ryall RDH. The mesorectum
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6. Sammour T, Kahokehr Hill AG. Laparoscopic colorectal surgery is associ­ated with a higher intraoperative complication rate than open surgery. Ann Surg. 2011;253(1):35–43. doi:10.1097/SLA.0b013e318204a8b4.
7. The Beyond TME Collaborative Group. Consensus statement patients with recurrent and primary rectal cancer beyond total mesorectal excision planes. Br J Surg. 2013;100(8):1009–14.
8. Weiser TG, Haynes AB, Dziekan G, Berry WR, Lipsitz SR, Gawande AA, et safety checklist during urgent operations in a global patient population. Ann Surg. 2010;251(5):976–80. doi:10.1097/SLA.0b013e3181d970e3.
9. Bell RH Jr, Biester RS, Cofer JB, Britt LD, et rience of residents in US general surgery pro­grams: a gap between expectation and experience. Ann Surg. 2009;249(5):719–24. doi:10.1097/ SLA.0b013e3181a38e59.
Bolliger D, Seeberger MD, Tanaka KA. Principles
10. and practice of thromboelastography in clinical coagulation management and transfusion practice. Transfus Med Rev. 2012;26(1):1–13.
11. Ker K, Prieto-Merino D, Roberts I. Systematic review, meta-analysis and meta-regression of the effect of tranexamic acid on surgical blood loss. Br J Surg. 2013;100(10):1271–9.
Fischer CP,
12. Hart JC. A prospective, randomized, controlled trial
of the efcacy and safety of brin pad as an adjunct
to control soft tissue bleeding during abdominal, ret­roperitoneal, pelvic, and thoracic surgery. J Am Coll Surg. 2013;217(3):385–93.
13. Jiang J, Li X, Wang Y, Qu H, Jin Z, Dai Y. Circular suture ligation of presacral venous plexus to control presacral venous bleeding during rectal mobiliza­tion. J Gastrointest Surg. 2013;17(2):416–20.
14. Stol VM, Milsom JW, Lavery IC, Oakley JR,
Church JM, Fazio VW. Newly designed occluder pin for presacral hemorrhage. Dis Colon Rectum. 1992;35(2):166–9.
15. Arnaud JP, Tuech JJ, Pessaux P. Management of pre­sacral venous bleeding with the use of thumbtacks. Dig Surg. 2000;17(6):651–2.
16. Germanos S, Bolanis I, Saedon M, Baratsis S. Con­trol of presacral gery. Am J Surg. 2010;200(2):e33–5.
17. Joseph P, Perakath B. Control of presacral venous bleeding with helical tacks on PTFE pledgets combined with pelvic packing. Tech Coloproctol. 2011;15(1):79–80.
18. Saurabh S, Strobos EH, Patankar S, Zinkin A, Snyder M. The argon beam coagulator: a more effective and expeditious way to address presacral bleeding. Tech Coloproctol. 2012;18(1):1–4.
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40538 Management of Presacral/Pelvic Bleeding
19. Remzi F, Oncel M, Fazio V. Muscle tamponade to control presacral venous bleeding. Dis Colon Rectum. 2002;45(8):1109–11.
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20. Khatri VP. Controlled tamponade of severe presacral venous hemorrhage: use of a breast implant sizer. Dis Colon Rectum. 2002;45(1):140–2.
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21. to control massive presacral bleeding. Surg Today. 2002;32(10):944–5.
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C,
Breakdown/Non-healing ofPerineal Wound
Justin M. Broyles, Jonathan E. Efron andJustinM.Sacks
39
Introduction
Malignancies of the anorectum, vagina, and other soft tissues in anogenital region are the most com­mon reason for perineal resection. Commonly employed procedures include the traditional ab­dominoperineal resection (APR), intersphincteric resection, pelvic exenteration, and low anterior resection (LAR). Although there is a trend to­ward more sphincter preserving surgery for rectal cancer, traditional APR is still used in 15–25 % of patients with rectal cancer [1].
The perineum is one of the more difficult sites in the human body to reconstruct after surgical obliteration due to the significant volume of dead space, close proximity of multiple organs, high bacterial counts, and the subjection to direct pres­sure in both the sitting and recumbent positions. Cancer patients receiving tumor extirpation in
Disclosures: Dr. Justin M. Sacks is a speaker/consultant for LifeCell Corporation. Branchburg, NJ.
J. M. Sacks () · J. M. Broyles Department of Plastic and Reconstructive Surgery, The Johns Hopkins Hospital Outpatient Center, 601N. Caroline St., Suite 2114C, Baltimore, MD 21287, USA e-mail: jmsacks@jhmi.edu
J. E. Efron Department of Surgery, The Johns Hopkins University, Baltimore, MD, USA e-mail: jefron1@jhmi.edu
this anatomic location often have undergone neo­adjuvant chemotherapy and/or radiotherapy to downstage their disease, which further impacts wound healing. As a result, wound complications are frequently encountered in these patients, with rates ranging from 40 to 65 % (Fig. 39.1) [14].
Primary closure of large perineal defects can be associated with unacceptable wound-healing complications ranging as high as 65 % [24]. Other common surgical complications include hematoma, seroma, abdominal and/or perineal hernia, fistulization, and nonhealing wounds [1]. Such complications can lengthen hospital stays, decrease mobility, prolong time to adjuvant ther­apy, and increase patient morbidity.
In an attempt to mitigate the occurrence of such complications, many plastic and reconstruc­tive surgeons advocate the use of a pedicled, vascularized soft-tissue flap coverage to close large perineal defects [3, 4]. Utilizing a vascu­larized, soft-tissue flap will assist in obliterat­ing dead space and this has shown to improve wound-healing outcomes by decreasing inci­sional tension while increasing vascular sup­ply, oxygenation, and delivery of cytokines and growth factors. In the current chapter, we aim to provide a comprehensive overview of the various reconstructive options for perineal defects to ed­ucate the reader on how to prevent as well as treat perineal wounds in an effort to maximize patient outcomes in these challenging cases.
T. M. Pawlik et al. (eds.), Gastrointestinal Surgery, DOI 10.1007/978-1-4939-2223-9_39, © Springer Science+Business Media New York 2015
407
408 J. M. Broyles et al.
Fig. 39.1 Large perineal defect demonstrating vast dead space and exposed viscera
Preoperative Evaluation
The physiologic status of the patient must be con­sidered and balanced with the overall reconstruc­tive plan. The long-term prognosis of the patient must also be taken into account as well. Recon­struction to improve quality of life should be con­sidered even in a palliative scenario. If possible, an accurate assessment of the wound or planned surgical site should be performed in the preopera­tive setting and may be facilitated by an examina­tion under anesthesia.
Medical Comorbidities
A thorough review of the patient’s past medical history should be performed to risk-stratify each patient using conditions that increase the relative risk of infection and/or wound-healing problems. Smoking has been shown to affect microcircu­latory blood flow and soft-tissue healing and should be discontinued a minimum of 4 weeks prior to surgical intervention if possible [5]. Pa­tients undergoing major reconstructive efforts re­quire optimization of nutritional parameters prior to intervention [68]. If enteral feeding is not possible preoperatively, postoperative enteral or parenteral nutrition should be administered with protein supplementation.
Radiation Therapy
Radiation therapy induces tissue injury through changes in the microcirculation of the defect and its surrounding areas, leading to decreased perfusion and impaired wound healing [4]. The reconstructive surgeon should be cognizant of the timing, dosage, and location of any prior or planned radiation and not limit debridement of radiated tissue. Additionally, the surgeon should utilize tissue outside the field of radiation for flap reconstruction.
Chemotherapy
Neoadjuvant chemotherapy can significantly impair wound healing and should be consid­ered when selecting reconstructive options. The plastic and reconstructive surgeon should work closely with the medical oncology team to deter­mine if and when the patient will require adju­vant chemotherapy, as wound-healing complica­tions can potentially delay onset to therapy.
Imaging
Preoperative evaluation with imaging modali­ties such as computed tomography (CT) and/or magnetic resonance imaging (MRI) could be ob­tained to evaluate the integrity of the surround­ing soft tissue and vascular anatomy. While these adjuncts are not essential, they can assist the sur­geon in surgical planning.
Timing of Reconstruction
The timing of perineal reconstruction is most often dictated by the status of the tumor and sur­gical margins. Certain factors such as advanced age, multiple comorbidities, or the need for loco­regional control with adjuvant radiotherapy must also be considered in the timing. Primary recon­struction carries a significantly decreased rate of
Table 39.1 Classication of perineal defects by anatomic location
Anatomic structure(s) involved Missing tissue components Vaginal vault S, MS, ST Vulvoperineal surface MS, ST Scrotum S, ST Penis S, MS, ST Perineum and pelvic support musculature S, ST (extensive) Sacrum/pelvic rim S, ST, +/− osseous involvement S skin, MS mucosal surface, ST soft tissue
40939 Breakdown/Non-healing of Perineal Wound
wound-healing complications and is preferred to delayed reconstruction in defects located in other areas of the body [9, 10]. Delayed reconstruction, while not optimal, is occasionally unavoidable for defects with extensive soft-tissue deficits or patient instability. If a patient requires delayed reconstruction, a negative pressure closure de­vice is the preferred temporizing measure until definitive reconstruction can be performed at a later time.
Classification of Defect
Acquired perineal defects should be classified according to what structures are missing and/or compromised. This will allow the reconstructive surgeon to employ the correct reconstructive mo­dality in an effort to replace damaged tissue with tissue that is most similar to that which is miss­ing. The classification of perineal defects is listed in Table 39.1.
The size of the defect and types of missing tis­sue should be assessed for viability. Potential flap donor sites should be evaluated for adequate rota­tional length. If there is a potential for microvas­cular free tissue transfer, recipient donor vessels should be evaluated for patency. If these vessels are unavailable or greater length is required, ar­teriovenous loop can be created if needed. How­ever, most perineal defects can be reconstructed with the use of local flaps typically from the ab­dominal wall, thigh, or buttock region.
Reconstructive Surgical Tenants
The core principles underlying reconstructive algorithms used by plastic and reconstructive surgeons are to progress from simple to more complex reconstructions on the basis of the spe­cific wound requirements. The goal for each re­construction is to provide a tension-free closure that obliterates all dead space which replaces the defect with tissue that is most similar to what is missing. The adage is “like with like.”
Local tissue flaps enable surgeons to recon­struct soft-tissue defects with similar tissue from an adjacent location. Axial pattern flaps are based on named blood vessels and are the mainstay of perineal reconstruction. Axial pattern flaps can be fasciocutaneous (deep muscle fascia with overly­ing skin), myocutaneous (muscle with skin), and myofasciocutaneous (muscle with deep fascia and overlying skin), which will enable recon­structive surgeons to repair defects with tissue that is similar to the resected tissue.
Microvascular free tissue transfer involves harvesting a tissue construct and its named blood supply from a distant region of the body and placing it into a defect using microvascular anas­tomosis between the flap’s donor vessels and the patient’s recipient vessels. Most cases are per­formed under magnification provided by a surgi­cal microscope. The decision to use a particular flap is based on the requirements for replacing missing skin, adipose tissue, fascia, and muscle. The primary advantage of microvascular free
410 J. M. Broyles et al.
tissue transfer is that tissue of a quality similar to that of the resected tissue can be moved from a remote part of the body, thereby enabling optimal aesthetic and functional outcomes. This also al­lows irradiated or infected tissue to be removed and replaced with soft, pliable, and vascularized tissue from a different part of the body, outside of the field of injury. Drawbacks of free tissue transfer are related to donor site morbidity and the potential for longer operative times.
Adjuncts to Flap Surgery
Negative Pressure Wound Therapy
Negative pressure-assisted closure can provide for temporary coverage in soft-tissue perineal de­fects when definitive reconstruction is either de­layed or not required. When utilized appropriate­ly, this device can promote neo-vascularization, decrease edema, and increase local granulation tissue as well as providing contractile force at wound edges [11]. This modality is often used to prepare the wound bed for definitive reconstruc­tion with soft-tissue flaps in a delayed fashion if immediate surgical intervention is not possible. Additionally, it can also be used to promote heal­ing by secondary intention in partial-thickness defects.
hollow viscous or neurovascular structures. Risks of tissue expansion include infection, extrusion, and rupture of the implant [12]. Additionally, the sequential expansion of the prosthesis can be un­comfortable to the patient and requires multiple office visits to obtain satisfactory expansion.
Biologic Tissue Matrices
Commercially available biologic tissue matri­ces (BTMs) currently come from five different sources: human dermis, porcine dermis, porcine small intestinal submucosa, bovine dermis, and bovine pericardium [13]. BTMs claim to induce early revascularization capacity in an effort to provide soft-tissue coverage and resist infection. For perineal reconstruction, BTMs can be used in a multitude of capacities including the creation of pelvic diaphragms to prevent visceral herniation into low perineal defects. Additionally, BTMs can be used to reinforce abdominal site donor defects in an effort to decrease bulge and hernia formation in the face or prior irradiation or con­current ostomy placement.
Characterization of Axial Pattern Flaps (Table39.2)
Rectus Abdominis Muscle
Tissue Expansion
Tissue expansion is a process in which an inflat­able prosthetic implant with a silicone shell is used to expand local and regional tissues so that they can eventually be advanced into the wound in a delayed fashion. The inflatable implant is in­serted at the time of tumor extirpation or during a second procedure. At subsequent office visits, saline is injected through an integrated or remote port to gradually expand the implant. Once the tissue has been sufficiently expanded, it can be advanced into the defect in a second surgical pro­cedure. Because tissue expansion takes time, the method is not feasible for immediate perineal re­construction that requires immediate coverage of
The pedicled vertical rectus abdominis (VRAM) flap is a versatile flap based on the deep inferior epigastric system. The flap can be harvested as a muscle-only, myocutaneous flap, or perforator flap with a large skin paddle. All but the largest of myocutaneous flaps can still allow for primary closure of the donor site. However, as previously mentioned, synthetic or BTM reinforcement may be required to prevent subsequent complications. The flap has a robust vascularity and abundant soft-tissue bulk that can be used to obliterate the vast amounts of dead space seen with large APR defects [1417]. Butler et al. demonstrated that despite the overall complication rate not being significantly different between primary closure and VRAM flap reconstruction, patients who
Table 39.2 Commonly employed pedicled ap options for perineal reconstruction
Flap name Blood supply Area of use Rectus abdominis Inferior epigastric artery Total perineal reconstruction/poste-
rior vaginal wall Gracilis Medial circumflex femoral artery Smaller perineal defects Gluteus maximus Superior gluteal artery Posterior/inferior perineal defects Pudendal Posterior labial artery Vaginal vault defects Anteriolateral thigh Descending branch of lateral circumflex femoral artery Total perineal reconstruction
41139 Breakdown/Non-healing of Perineal Wound
underwent VRAM reconstruction experienced significantly lower incidences of perineal ab­scesses (9 vs. 37 (9 vs. 30 %) (Fig. 39.2) [
%) and major wound dehiscence
17].
Advantages of the VRAM are seen in the abil­ity to provide robust, vascularized tissue into the defect that is outside of the field of radiation. The large, vertical skin paddle is particularly useful when reconstructing the contour of the posterior vaginal wall. Alternatively, this flap can be tubed to create a neovagina if the entire vaginal vault has been obliterated. In many cases, the donor site is already exposed during tumor extirpation
Fig. 39.2 Surface anatomy of VRAM (vertical rectus ab- dominis) flap displaying arterial pedicle
negating the need for a second incision and donor site (Fig. 39.3).
Disadvantages of this flap are inherently re­lated to the anatomic location of the donor site. If the patient is not undergoing a concurrent mid­line laparotomy, flap harvest obligates the patient to undergo an anterior approach, which can lead to herniation, bulge formation, wound-healing complications, and/or injury to the surrounding viscera. Furthermore, this flap should not be har­vested at the site of planned ostomy placement to allow the new stoma to be anchored into the rectus abdominis muscle. Finally, the vascularity of the VRAM is questionable in the presence of prior ostomy placement through the rectus ab­dominis muscle and should be avoided if at all possible.
Gracilis Muscle Flap
The pedicled gracilis muscle flap is a versatile flap based on the medial circumflex femoral ar­tery in the proximal thigh. The flap can be har­vested as a muscle-only or a myocutaneous flap with a small skin paddle. The flap has minimal donor site morbidity and can be harvested bilat­erally if additional soft-tissue bulk is required.
Advantages of the gracilis flap include a rela­tive ease of dissection with minimal donor site morbidity. The ample pedicle length coupled with a relatively linear muscle design allows for the flap to be tailored fitting a variety of defects. It is particularly useful for obliterating fistulous tracts between the rectum and vagina or urethra with an excellent success record [18, 19].
Disadvantages of the gracilis muscle flap are related to flap size and dimension. Often times, even when harvested bilaterally, the gracilis flap