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10.1245/ASO.2005.11.923
Annals of Surgical Oncology 12:91-94 (2005)
© 2005 Society of Surgical Oncology
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Editorial

Pelvic Reconstruction After Abdominoperineal Resection: Is It Worthwhile?

Charles E. Butler, MD, FACS1 and Miguel A. Rodriguez-Bigas, MD, FACS2

1 Department of Plastic Surgery, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030
2 Department of Surgical Oncology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 444, Houston, Texas 77030

Correspondence: Address correspondence and reprint requests to: Miguel A. Rodriguez-Bigas, MD, FACS; E-mail: mrodbig{at}mdanderson.org.

The management of the perineal wound after an abdominoperineal resection (APR) has represented a challenge to surgeons. Perineal wound complications after APR have been reported to occur in 25% to 60% of cases,1,2 and rates are higher after resection of multiple visceral organs. Thus, general, oncological, colorectal, and other pelvic surgeons, in conjunction with plastic and reconstructive surgeons, have sought innovative ways to reduce perineal wound morbidity. Post-APR reconstruction of the pelvis with a vertical rectus abdominis musculocutaneous (VRAM) flap has been one such method.3

In this issue of Annals of Surgical Oncology, Chessin et al.4 report a modest-sized cohort study comparing patients who underwent reconstruction with a VRAM flap after APR with patients whose perineal wound was closed primarily after APR. All patients in both groups received preoperative chemoradiation. Perineal wound complications were significantly less frequent in the flap group than in the primary closure group (16% vs. 44%, respectively). There were no significant differences between groups in hospital stay or time to perineal wound healing. However, in patients who developed perineal wound complications, the time to perineal wound healing was shorter in the patients who had VRAM reconstruction than in those who had primary closure.

The experience reported by Chessin et al.4 is not unique. In fact, other authors have reported similar results with musculocutaneous flaps such as the rectus abdominis, gracilis, and gluteus maximus flaps.1,2,5 The advantages of musculocutaneous flap reconstruction of the irradiated pelvis and perineal wound include reduction of dead space, interposition of wellvascularized, nonirradiated tissue, and replacement of resected skin. The disadvantages of these flaps include the added time for the surgical procedure, the added costs, and the potential morbidity (such as infections, flap loss, seroma, ventral and perineal hernia, and abdominal bulge) of such procedures. These disadvantages are usually offset by the lower rates of perineal wound complications.

On the basis of the literature and the substantial experience with perineal reconstruction after radiation therapy at our institution, we emphatically agree that the inferiorly based VRAM flap is extremely valuable for post-APR reconstructions, for the reasons proposed by Chessin et al. In fact, its use is becoming the rule rather than the exception at our institution. As the authors point out, the VRAM flap has several advantages over unilateral or bilateral thigh-based flaps such as the gracilis musculocutaneous, posterior thigh, and anterolateral thigh flaps. These advantages include more reliable vascularity and skin viability, greater reduction of dead space, and absence of a separate donor site.

Chessin et al. report several important findings in their study, particularly, the improved perineal wound healing and absence of increased overall and abdominal wall complications with the VRAM flap. An additional benefit of VRAM flap reconstruction that we have observed with prolonged follow-up is a reduction in the incidence of perineal bulge and hernia, which can occur years after APR. As we have experienced in our ongoing study of more than 60 patients who have undergone VRAM flap reconstruction of perineal defects, the design of such a study is challenging and subject to several shortcomings. Despite review over a 12-year period, Chessin et al. identified only 19 patients who had reconstruction with a VRAM flap. This represented only 9% of the 206 patients who underwent APR after chemoradiation. At our institution, the indications for VRAM flap reconstruction of APR defects have expanded over the past 5 years, with a greater percentage of APR cases having VRAM flap reconstruction. Identification of an appropriate control population is difficult. The indications and patientselection criteria for VRAM flap reconstruction may have differed between operations performed early versus later in the period studied. In addition, several important wound-healing factors were not controlled for, including body mass index, tobacco use, nutritional status, and the condition of the surrounding perineal and buttock skin; however, data on these variables may not have been available in this retrospective analysis. There was also no description of the methods used or the follow-up period for detection of abdominal wall complications. Abdominal bulge or hernia frequently occur as late complications, and accurate assessment of these complications would require extended follow-up.

Sound surgical judgment and technique are absolutely critical for the success of VRAM flap reconstruction. Numerous preventable complications can occur because of inexperience and technical imperfection. In addition to techniques described by Chessin et al., we believe that several technical aspects of VRAM perineal reconstruction improve outcome and reduce complications. A detailed discussion of reconstructive techniques is beyond the scope of this editorial, but some concepts deserve mention. Chessin et al. illustrate a vertical skin paddle design that includes the upper abdominal skin. This design is often used because it enables the flap to reach and be positioned into the perineal defect without tension in most patients. Regardless of the skin paddle location and orientation (vertical or oblique), the paddle should include the periumbilical musculofasciocutaneous perforating vessels to ensure adequate vascularity. We have found that extending the skin paddle superolaterally, toward the axilla and just below the inframammary fold (Fig. 1Go), is remarkably useful when additional skin and/or bulk is required, particularly at the distal reach of the flap, such as the sacral region. The vascularity of the distal flap segment is usually robust when correctly designed and elevated.



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FIG. 1. (A) Elevation of an extended vertical rectus abdominis musculocutaneous flap. The extension, including skin and subcutaneous fat, traverses the costal margin and is positioned just below the inframammary fold. (B) The donor site scar is concealed below the breast (© 2004 Charles Butler).

 
VRAM flaps can be inset in two different orientations. The anterior surface of the flap can be positioned facing the sacral prominence with the flap tip located at the anterior aspect of the perineal skin defect; alternatively, the anterior flap surface can be positioned toward the vagina or prostate (if not resected) with the flap tip near the coccyx. In many circumstances, either orientation is acceptable, and the choice is made by determining which orientation provides the greatest pelvic dead space obliteration and best skin paddle fit into the perineal skin defect with the least flap tension, compression, and twist. The latter orientation is preferred when the skin paddle is used for partial or complete vaginal reconstruction.

Even when well-vascularized flap tissue is interposed into the perineal skin defect, wound complications can occur. We have found a vest-overpants skin inset to be helpful in reducing wound complications. The peripheral circumference of the skin paddle is de-epithelialized for several centimeters (Fig. 2Go), and the de-epithelialized skin edge is secured to the remnant pelvic floor elements, perineal fascia, or both. The perineal skin defect edges are then sutured to the central (epithelialized) aspect of the flap skin paddle. This reliably reinforces the pelvic floor defect and helps prevent wound dehiscence. Furthermore, the early postoperative use of a foam thigh abduction pillow is helpful to prevent compression and congestion of the skin paddle.



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FIG. 2. (A) The flap skin paddle has been transposed into the perineal skin defect, and the peripheral margin has been de-epithelialized. (B) The de-epithelialized flap edges are sutured to the pelvic floor defect edges, and the perineal skin defect edges are sutured to the epithelialized (central) area of the flap, creating a vest-over-pants closure (© 2004 Charles Butler).

 
Meticulous flap design and harvest and abdominal donor site closure are paramount in reducing abdominal wall complications. Sparing viable fascia during flap harvest can minimize tension on the fascial closure. We prefer to include only the section of anterior rectus sheath fascia that contains the medial and lateral rows of perforating vessels to the skin paddle. To accomplish this, the laparotomy skin incision is made along the midline, and the medial side of the flap skin paddle is then elevated from the fascia to the medial row of perforating vessels. The anterior sheath is incised just medial to the medial row of perforating vessels to spare the medial portion of the anterior rectus sheath fascia. This medial anterior rectus sheath fascia is elevated o. the rectus muscle, and the peritoneal cavity is entered by exposure of and incision through the posterior rectus sheath fascia 1 to 2 cm lateral to the midline (Fig. 3Go). The anterior fascial incision is transitioned medially to a standard midline (linea alba) incision inferior to the periumbilical region (below the location of the skin paddle). The lateral anterior rectus sheath fascia is incised just lateral to the lateral perforating vessels to spare fascia laterally.



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FIG. 3. To minimize the amount of fascia removed with the flap, the anterior rectus sheath is incised 1 to 2 cm lateral to the linea alba in the periumbilical area. The medial edge of the rectus abdominis muscle is retracted laterally for exposure of and incision through the posterior sheath to enter the peritoneal cavity. Alice clamps have been placed on the spared medial anterior rectus sheath fascia (© 2004 Charles Butler).

 
Chessin et al. are to be congratulated, because this study provides objective evidence to justify the use of rectus abdominis flap reconstruction of irradiated APR defects. They have reminded us that immediate pelvic reconstruction in selected patients is appropriate, can be done safely, and is beneficial. On the basis of the literature and the experience at our institution, we believe that patients undergoing multivisceral resections after irradiation or with intraoperative irradiation and patients with recurrent disease are prime candidates for such reconstructions. Future studies will be important to define the specific indications for this approach so that the patients who will benefit most can be properly selected. Long-term outcome and cost data will be also be important to further refine these indications.

Received for publication November 11, 2004. Accepted for publication December 7, 2004.

REFERENCES

  1. Khoo AKM, Skibber JM, Nabawi AS, et al. Indications for immediate tissue transfer for soft tissue reconstruction in visceral pelvic surgery. Surgery 2001;130:463–9.[Medline]
  2. Buchel EW, Finical S, Johnson C. Pelvic reconstruction using rectus abdominis musculocutaneous flaps. Ann Plast Surg 2004;52:22–6.[Medline]
  3. Kroll SS, Pollock R, Jessup JM, Ota D. Transpelvic rectus abdominis flap reconstruction following abdominoperineal resection. Am J Surg 1989;55:632–7.[CrossRef]
  4. Chessin DB, Hartley J, Cohen AM, et al. Rectus flap reconstruction decreases perineal wound complications following pelvic chemoradiation and surgery: a cohort study. Ann Surg Oncol (in press).
  5. Shibata D, Hyland W, Busse P, et al. Immediate reconstruction of the perineal wound with gracilis muscle flaps following abdominoperineal resection and intraoperative radiation therapy for recurrent carcinoma of the rectum. Ann Surg Oncol 1999;6:33–7.[Abstract]




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