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254
B.M.E. Hansson
:
d
b
Follow-
up
a
Recurrence
(%)
Mortality
Infection Other
No. complications (%)
5 2 0 29 (80.6) 31
>85%
nonabsorbable
b
Nonabsorbable 2 0 0 20 (74.1) 23
NS 4 3 1 7 (53.8) 7
Median
27
,
c
(59.7–78.3)
69.4%
3.8%
(1.0–9.4)
10.8%
(5.3–18.9)
NS NS 0 7 (53.8) 14
91%
(6.1–20.2)
nonabsorbable
Type of
stoma Type of sutures
EI
No.
repairs
Mod.
MINORS
index
10 36 EC, LC,
Time
period
1991
Reference
Table 23.2 Study characteristics and outcomes of suture repair of parastomal hernia
Rubin etal. [10] 1983–
11 16 EC, LC Nonabsorbable 0 5 3 6 (46.2) 38
1999
Cheung etal. [11] 1990–
10 14 EC, El,
Rieger etal. [12] 1990–
LI, LC
11 27 10 C,
1999–
2002
Riansuwan etal.
17 IC
2005
[13]
11 13 9 C, 4
– 106 – – 11.8%
2006
Weighted pooled
Pastor etal. [14] 1999–
% (95% CI)
Values are mean months follow-up unless otherwise stated
Excluding in-hospital deaths
C indicates colostomy, EC end colostomy, EI end ileostomy, IC ileal conduit, LC loop colostomy, LI loop ileostomy, NS not specied
a
Median of reported follow-up of studies with >12months follow-up
Weighted pooled proportion (xed effects model) using only studies with >12months mean follow-up
b
c
d
IC
23 Parastomal Hernia: Optimal Strategies forRepair
255
Fig. 23.2 Local repair with mesh
explained by the intra-abdominal pressure and the tangential forces working on the abdominal wall leading to ongoing widening of the keyhole according to Laplace’s law (T=P×R/2) [17]. Therefore, the Keyhole technique is no longer advised.
With the Sugarbaker technique, a mesh without a hole is used after lateralization
of the bowel.
The technique was rst described by Sugarbaker in 1985 [16]. At that time, the mesh was only sutured to the fascial edges. As we have learned from incisional hernia repair, an overlap of 3–5cm between the mesh and the adjacent fascia is mandatory to prevent recurrent hernias [18]. Therefore, the Sugarbaker technique was modied according to Fig.23.4.
256
B.M.E. Hansson
:
c
a
Follow-
up
Median
36
b
Recurrence
(%)
Mortality
Mesh
infection Other
No. complications (%)
Wound
infection
Type of
stoma Material; technique
2 0 9 0 15 (25.9) 51
PPM; ‘Stove pipe
hat’
24 EI,
3 LI
0 1 1 NS 3 (18.8) 33
PPM (7), PE (6),
PPM; KH 0 0 0 0 0 (0) 7
Vicryl (1); KH (14),
CRE-PPM (2)
IC
EI
PPM; KH 0 0 0 0 1 (20.0) 12
EI
17.2%
(11.9–23.4)
0%
(0.0–
2.3)
8.3%
(4.5–
13.7)
2.6%
(0.7–
6.4)
(0.4–5.5)
No.
repairs
Amin etal. [20] 1999 9 9 1 C, 8
10 5 4 C, 1
2000
Kald etal. [21] 1999–
– 157 – – 1.9%
Weighted
pooled% (95-CI)
C indicates colostomy, CRE-PPM central ring enforced polypropylene mesh, EC end colostomy, El end ileostomy, IC ileal conduit, LC loop colostomy, LI loop
11 16 12 C, 3
2002
9 8 EC PPM; KH 1 0 0 0 0 (0) 38
1997–
1993–
Venditti etal.
2006
1996
Lüning and
Spillenaar-
[18]
Bilgen [19]
Mod.
Table 23.3 Study characteristics and outcomes of onlay mesh repair of parastomal hernia
11 15 IC PPM; KH 0 0 2 0 1 (6.7) 15
MINORS
index
1982–
Time
period
Ho and Fawcett
Reference
1988–
2002
2001
De Ruiter and
Bijnen [16]
[15]
Steele etal. [17] 1988–
11 58 31 EC,
11 46 C CRE-PPM 0 3 1 0 7 (15.2) 51
Weighted pooled proportion (xed effects model) using only studies with >12months mean follow-up
Values are mean months follow-up unless otherwise stated
ileostomy, NS not specied
Median of reported follow-up of studies with >12months follow-up
a
b
c
23 Parastomal Hernia: Optimal Strategies forRepair
Fig. 23.3 Keyhole technique
257
Fig. 23.4 Sugarbaker technique
258
B.M.E. Hansson
The Sugarbaker technique has a recurrence rate of 10.2% when repaired with a ePTFE mesh [11, 13, 19]. No publications on long-term outcome of other meshes are available so far.
Berger and coworkers reported on the use of a Sandwich technique, which com­bines both Keyhole and Sugarbaker techniques using PVDF-PP mesh (Dynamesh
®
[17]. After a follow-up of 20months, one out of 47 (2.1%) had a recurrence. While outcome is positive, more studies are needed to validate these results [19].
Meta-analysis of all studies on laparoscopic repair shows that the Sugarbaker technique has the best results and is recommended when patient and surgeon are t for laparoscopy [11, 13, 20–22].
Open Repair
The open modied Sugarbaker technique is an excellent alternative when a laparoscopic approach is not suitable. Reviewing the literature showed only one study reporting on 20 repairs. No mesh infections occurred and 3 out of 20 hernias recurred (15%) [22].

Conclusion

Parastomal hernia continues to be a common complication of stoma surgery that can have a signicant impact on quality of life and may even carry life-threatening risk. An organized approach to these patients with multidisciplinary management is essential. Choice of surgical repair depends on patient factors; however, a mini­mally invasive approach is feasible in many circumstances (Fig.23.5).
)
Fig. 23.5 Flowsheet
23 Parastomal Hernia: Optimal Strategies forRepair
259

References

1. Pearl RK.Parastomal hernias. World J Surg. 1989;13:569–72.
2. Cingi A, Carik T, Sever A, Aktan AO.Enterostomy site hernias: a clinical and computerized
tomographic evaluation. Dis Colon Rectum. 2006;49:1559–63.
3. Moreno-Matias J, Serra-Aracil X, Darnell-Martin A, Bonbardo- Junca J, Mora-Lopez L,
Alcantara-Moral M, Ayguavives-Garnica I, Navarro-Soto S.The prevalence of parastomal hernia after formation of an end colostomy. Color Dis. 2009;11:173–7.
4. Pilgrim CHC, McIntyre R, Bailey M.Prospective audit of parastomal hernia: prevalence and
associates comorbidities. Dis Colon Rectum. 2010;53:71–6.
5. Nastro P, Knowles CH, McGrath A, Porrett TRC, Lunniss PJ.Complications of intestinal sto-
mas. Br JSurg. 2010;97:1885–9.
6. Janes A, Weisby L, Israelsson LA. Parastomal hernia: clinical and radiological denitions.
Hernia. 2011;15:189–92.
7. Nasvall P, Wikner F, Gunnarsson U, Rutegard J, Stringard K. A comparision between 3D
ultrasonography, CT scanning and ndings at surgery in patients with stomal complaints. Int JColor Dis. 2014;29:1263–6.
8. Smietanski M, Szczepkowski M, Alexandre JA, Berger D, Bury K, Conze J, Hansson B, Janes
A, Miserez M, Mandala V, Montgamery A, Morales-Conde S, Muysoms F.European Hernia Society classication of parastomal hernias. Hernia. 2014;18:1–6.
9. Stravos AA, Muysoms F etal. EHS parastomal hernia guidelines. Submitted in Hernia.
10. Krogsgaard M, Pilsgaard B, Borglit TB, Bentzen J, Balleby L, Krarup PM.Symptom load and
individual symptoms before and after repair of parastomal hernia: a prospective single centre study. Color Dis. 2017;19:200.
11. Hansson BME, Slater NJ, Schouten van der Velden AP, Groenewoud HMM, Buyne OR, de
Hingh IJT, Bleichrodt RP. Surgical techniques for parastomal hernia repair: a systematic review of the literature. Ann Surg. 2012;255:685–95.
12. Rosin JD, Bonardi RA.Paracolostomy hernia repair with Marlex mesh: a new technique. Dis
Colon Rectum. 1977;20:299–302.
13. Hansson BME, Morales-Conde S, Mussack T, Valdes J, Muysoms FE, Bleichrodt
RP.Laparoscopic modied Sugarbaker technique is safe and has a low recurrence rate: a mul­ticenter cohort study. Surg Endosc. 2013;27:494–500.
14. Hansson BME, de Hingh IHJT, Bleichrodt RP.Laparoscopic parastomal hernia repair is fea-
sible and safe: early results of a prospective clinical study including 55 consecutive patients. Surg Endosc. 2007;21:989–93.
15. Hansson BME, van Nieuwenhoven EJ, Bleichrodt RP.Promising new technique in the repair
of parastomal hernia. Surg Endosc. 2003;17:1789–91.
16. Sugarbaker PH.Peritoneal approach to prosthetic mesh repair of paraostomy hernias. Ann
Surg. 1985;201:344–6.
17. Berger D, Bientzle M. Polyvinylidene uoride: a suitable mesh material for laparoscopic
incisional and parastomal hernia repair! A prospective, observational study with 344 patients. Hernia. 2009;13:167–72.
18. de Vries Reilingh TS, van Geldere D, Langenhorst B, de Jong D, van der Wilt GJ, van Goor H,
Bleichrodt RP.Repair of large midline incisional hernias with polypropylene mesh: compari­son of three operative techniques. Hernia. 2004;8:56–9.
19. Stelzner S, Hellmich G, Ludwig K.Repair of paracolostomy hernias with a prosthetic mesh in the
intraperitoneal onlay position: modied Sugarbaker technique. Dis Colon Rectum. 2004;47:185–91.
20. Levy S, Plymale MA, Miller MT, Davenport DL, Roth JS.Laparoscopic parastomal hernia
repair: no different than a laparoscopic ventral hernia repair? Surg Endosc. 2016;30:1542–6.
21. DeAsis F, Lapin B, Gitelis M, Ujiki M.Current state of laparoscopic parastomal hernia repair:
a meta-analysis. World JGastroenterol. 2015;21:8670–7.
22. DeAsis FJ, Linn JG, Lapin B, Denham W, Carbray JM. Modied laparoscopic Sugarbaker
repair decreases recurrence rates of parastomal hernia. Surgery. 2015;158:954–9.
23. Hansson BME, Bleichrodt RP, De Hingh IH. Laparoscopic parastomal hernia repair using a
keyhole technique results in a high recurrence rate. Surg Endosc. 2009;23:1456–9.
Part VII
Optimizing Pelvic Dissection for Rectal Cancer
Proctectomy forAdvanced Rectal Cancer: APE or ELAPE?
TorbjörnHolm

Introduction

Ernest Miles’ paper “A method of performing abdomino-perineal excision for car­cinoma of the rectum and of the terminal portion of the pelvic colon” was published in The Lancet in 1908 [1]. This description of an abdominoperineal excision of the rectum has since been called “the Miles’ operation” and had a strong impact on rectal cancer surgery. In the original description of the procedure, the rectum was bluntly mobilized down to the sacrococcygeal articulation, to the prostate, and to “the upper surface of the levatores ani” laterally, thus leaving the mesorectum attached to the pelvic oor. After mobilization of the rectum, a colostomy was cre­ated, and the abdominal wall was closed. The patient was turned over and placed in the right lateral and semi-prone position. Miles emphasized that the levator muscles should be divided “as far outwards as their origin from the white line so as to include the lateral zone of spread,” and as a result the perineal part of the operation included a wide excision of skin, fat, and pelvic oor (levator muscles).
The Lancet paper had an enormous impact on the surgical community, and for many decades, the “Miles operation” was the gold standard procedure for all rectal carcino­mas. However, the concept of removing the entire rectum, the anus, and the perineum in all patients with rectal cancer was gradually abandoned. An increasing experience with bowel reconstruction, including developments of stapling instruments, led to a new concept of anterior resection (AR) and low anterior resection (LAR), which became the standard procedures for tumors of the upper and mid- rectum [2–6].
For tumors of the lower rectum, most surgeons continued to perform abdomino­perineal excision (APE), although the extensive perineal approach described by Miles was more or less neglected and the synchronous combined APE was
24
T. Holm (*) Section of Coloproctology, Department of Surgical Gastroenterology, Karolinska University Hospital, Stockholm, Sweden e-mail: torbjorn.holm@ki.se
© Springer International Publishing AG 2018 C.M. Schlachta, P. Sylla (eds.), Current Common Dilemmas in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-70117-2_24
263
264
T. Holm
introduced as a feasible procedure which became popular and gained widespread use in the treatment of low rectal cancer [7]. During the synchronous combined operation, the perineal part is carried out simultaneously with the pelvic part of the abdominal procedure, with the patient in the supine lithotomy or Lloyd-Davies position; the rectum with its mesorectum is rst mobilized down to the pelvic oor, and the perineal surgeon then enters the pelvic cavity just in front of the coccyx, the levator muscles are divided on both sides, and nally the rectum is dissected off the prostate or the vagina, and the specimen is delivered through the perineum.
Although there were gradual improvements in the treatment of rectal cancer dur­ing the twentieth century, local control remained a major problem after surgery, with local recurrence rates of up to 40% after potentially curative resections [8] (Fig.24.1).
With the development of total mesorectal excision (TME), as described by Bill Heald, treatment results improved dramatically, both concerning local control and survival. Heald reported a local recurrence rate around 5% and a cancer-specic survival around 70% at 5years, without radiotherapy [9, 10]. During the recent two decades, the TME technique has been introduced in many countries, and subse­quently the results with regard to local control and cancer survival have improved signicantly. Local recurrence rates are now reported to be less than 10% in population- based studies [11, 12].
Consequently, teaching rectal cancer surgery has mainly focused on the opera­tive technique of TME and AR. Although the technique used for the abdominal part of an APE was modied along the lines of TME, little attention was given to the perineal part of the procedure. Thus, most surgeons adopted the technique of sharp dissection under direct vision outside the mesorectal fascia down to the pelvic oor, with the aim to save autonomic nerves and to create a perfect specimen with an
Fig. 24.1 Patient with a large local recurrence growing in the perineum after a standard APR
24 Proctectomy forAdvanced Rectal Cancer: APE or ELAPE?
265
intact mesorectal fascia. The perineal part, however, was often completed in the conventional way, with dissection close to the external sphincter and with the divi­sion of the levator muscles close to the rectal wall. With the patient in the supine lithotomy position, it is difcult to achieve an optimal view, especially anteriorly, and therefore parts of the perineal dissection are often done with blunt dissection when this approach is used.
Problems Related totheConventional APE
With an increasing focus on oncological outcomes and improved audit, several authors have acknowledged the fact that local control and survival after APE have not improved to the same degree as that seen after AR.In one study based on 561 patients from Leeds, UK, it was reported that patients undergoing APE had a higher local failure rate (22.3 vs. 13.5%) and a poorer survival (52.3 vs. 65.8%) compared with patients who had an AR during the same time period [13].
In another paper based on data from ve different European trials, it was reported that the APE procedure was associated with an increased risk of circumferential resection margin (CRM) involvement, an increased local recurrence rate, and a decreased cancer-specic survival [14]. A large cohort study from Norway also reported a higher local recurrence rate (15 vs. 10%) and a poorer 5-year survival (55 vs. 68%) after APE than after AR [12].
These differences in oncological outcomes between the two procedures may be explained by several factors, including anatomical difculties and the surgical tech­nique associated with standard APE surgery. In the lower rectum, the surrounding mesorectum is reduced in size and disappears at the top of the sphincters. Below this level, the sphincter muscle forms the circumferential resection margin (CRM). As mentioned above, the abdominal dissection during a conventional APE is often car­ried out along the mesorectum, all the way down to the pelvic oor and the top of the puborectalis muscle, with the mesorectum being mobilized off the levator mus­cles. The perineal dissection then follows the external sphincter to meet the pelvic dissection at the top of the anal canal (Fig.24.2). With this technique the retrieved specimen often has a typical “waist” at 3–5cm from the distal end, corresponding to the top of the external sphincter at the level of the puborectalis muscle and the lowest part of the mesorectum (Fig.24.3).
The inward coning at the pelvic oor carries the dissection close to the rectal wall, and several studies have reported higher rates of bowel perforation and tumor involvement of the CRM after APE as compared with AR.Nagtegaal etal. assessed 846 AR specimens and 373 APE specimens from the Dutch TME trial and found that the plane of resection was within the sphincter muscle, the submucosa or lumen in more than 1/3 of the APE cases, and in the remainder was on the sphincter mus­cles. This resulted in a positive CRM rate of 30.4% after APE versus 10.7% after AR and a perforation rate of 13.7% after APE versus 2.5% after AR [15]. Similarly, population-based reports from Sweden, Norway, and Holland have shown a three­fold increase in perforation rates after APE compared to AR (14–15% vs. 3–4%)