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Inicio Cirugía Española (English Edition) Single-Port Colectomy vs Multi-Port Laparoscopic Colectomy. Systematic Review an...
Información de la revista
Vol. 93. Núm. 5.
Páginas 307-319 (mayo 2015)
Visitas
4431
Vol. 93. Núm. 5.
Páginas 307-319 (mayo 2015)
Original article
Acceso a texto completo
Single-Port Colectomy vs Multi-Port Laparoscopic Colectomy. Systematic Review and Meta-Analysis of More Than 2800 Procedures
Colectomía mediante puerto único vs. colectomía mediante laparoscopia multipuerto. Revisión sistemática y metaanálisis de más de 2.800 procedimientos
Visitas
4431
Juan Antonio Lujána,
Autor para correspondencia
juanlujan@telefonica.net

Corresponding author.
, María Teresa Sorianoa, Jesús Abrisquetaa, Domingo Pérezb, Pascual Parrillaa
a Departamento de Cirugía General, Unidad de Coloproctología, Hospital Clínico Universitario Virgen de la Arrixaca, Universidad de Murcia, Murcia, Spain
b Departamento de Estadística, Universidad de Murcia, Murcia, Spain
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Table 1. Demographic Characteristics of Studies Included.
Table 2. Variables Collected From the Studies Included.
Table 3. Complications According to Clavien–Dindo.
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Abstract
Objective

Multiport laparoscopic surgery in colon pathology has been demonstrated as a safe and effective technique. Interest in reducing aggressiveness has led to other procedures being described, such as SILS. The aim of this meta-analysis is to evaluate feasibility and security of SILS technique in colonic surgery.

Material and methods

A meta-analysis of 27 observational studies and one prospective randomised trial has been conducted by the use of random-effects models.

Results

A total amount of 2870 procedures was analysed: 1119 SILS and 1751 MLC. We did not find statistically significant differences between SILS and MLC in age (WMD 0.28 [−1.13, 1.68]; P=.70), BMI (WMD −0.63 [−1.34, 0.08]; P=.08), ASA score (WMD −0.02 [−0.08, 0.04]; P=.51), length of incision (WMD −1.90 [−3.95, 0.14]; P=.07), operating time (WMD −2.69 (−18.33, 12.95]; P=.74), complications (OR=0.89 [0.69, 1.15]; P=.37), conversion to laparotomy (OR=0.59 [0.33, 1.04]; P=.07), mortality (OR=0.91 [0.36, 2.34]; P=.85) or number of lymph nodes harvested (WMD 0.13 [−2.52, 2.78]; P=.92). The blood loss was significantly lower in the SILS group (WMD −42.68 [−76.79, −8.57]; P=.01) and the length of hospital stay was also significantly lower in the SILS group (WMD −0.73 [−1.18, −0.28]; P=.001).

Conclusion

Single-port laparoscopic colectomy is a safe and effective technique with additional subtle benefits compared to multiport laparoscopic colectomy. However, further prospective randomised studies are needed before single-port colectomy can be considered an alternative to multiport laparoscopic surgery of the colon.

Keywords:
Colon
SILS
Laparoscopy
Resumen
Objetivos

La cirugía laparoscópica multipuerto (CLM) ha demostrado su seguridad y efectividad en la cirugía del colon. Con la intención de reducir la agresividad surgen otras técnicas como la cirugía por puerto único (SILS). El objetivo de este metaanálisis es evaluar la seguridad y la viabilidad de la técnica SILS en la cirugía del colon.

Material y métodos

Se realiza un metaanálisis de 27 estudios observacionales y uno prospectivo aleatorizado mediante el modelo de efectos aleatorios.

Resultados

Se han analizado 2.870 procedimientos: 1.119 SILS y 1.751 CLM. No se han encontrado diferencias estadísticamente significativas en la edad (DMP 0,28 [−1,13, 1,68]; p=0,70), IMC (DMP −0,63 [−1,34, 0,08]), ASA (DMP −0,02 [−0,08, 0,04]; p=0,51), longitud de incisión (DMP −1,90 [−3,95, 0,14]; p=0,07), tiempo operatorio (DMP −2,69 [−18,33, 12,95]; p=0,74), complicaciones (OR=0,89 [0,69, 1,15]]; p=0,37), conversión a laparotomía (OR=0,59 [0,33, 1,04]; p=0,07), mortalidad (OR=0,91 [0,36, 2,34]; p=0,85) o número de ganglios obtenidos (DMP 0,13 [−2,52, 2,78]; p=0,92). La pérdida de sangre (DMP −42,68 [−76,79, −8,57]; p=0,01) y la estancia hospitalaria (DMP −0,73 [−1,18, −0,28]; p=0,001) son significativamente menores en el grupo SILS.

Conclusiones

La cirugía colorrectal mediante SILS es segura y efectiva, con ligeros beneficios respecto a la CLM. Sin embargo, se necesitan más estudios aleatorizados antes de que la SILS se pueda considerar una alternativa a la CLM.

Palabras clave:
Colon
SILS
Laparoscopia
Texto completo
Introduction

Multiport laparoscopic colectomy (MLC) is a safe and effective technique, a fact that has been confirmed by many prospective randomised studies that have shown a lower level of blood loss, a better postoperative recovery, a shorter length of hospital stay, and similar oncological results when compared to open colectomy.1–4 With the aim of reducing aggressiveness and improving MLC results, other procedures have been described, such as mini-laparoscopic surgery, natural orifice transluminal endoscopic surgery (NOTES)5 and single-incision laparoscopic surgery (SILS). Due to its similarity to MLC, only SILS has been adopted by a wide group of surgeons, mainly in appendectomy and cholecystectomy, as well as in more complex procedures, such as colectomy, showing the safety and effectiveness of the intervention.6,7 In comparison with MLC, SILS could offer potential benefits like better aesthetics, less trauma to the abdominal wall, and a reduction in postoperative pain. However, some disadvantages are that it requires a learning curve, adequate technology, a longer operating time, it is difficult to expose and visualise and it may potentially compromise the oncological results of the malignant disease. This is why some surgeons question whether it is possible for SILS colectomy to offer tangible benefits in comparison with MLC, due to the lack of sufficient scientific evidence to that effect. Although there is an increasing number of studies reporting on SILS colectomy results, few of them compare SILS to MLC, making it necessary to rigorously evaluate the safety, the efficacy, and the oncological results in colorectal cancer before SILS methodology is used in a widespread manner.

The main purpose of this article is to review the published literature on SILS colectomy, using meta-analysis to evaluate comparative studies between MLC and SILS in colorectal disease.

Method

This meta-analysis was prepared following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA).8

Search Strategy

We have conducted a systematic search of the major databases, including MEDLINE and PUBMED, articles, clinical trials, reviews and works related to single-port laparoscopic colorectal surgery. The date of the last search was April 30, 2014. Only articles in English and Spanish have been included; papers in other languages have been excluded. The key words searched were: “single incision”, “single port”, “single access”, “colectomy”, “colorectal surgery.” Abstracts have been independently scrutinised by 2 authors (JL and MTS) to determine the eligibility for inclusion in the study. Disagreements were solved by means of a third author. The references mentioned in the selected articles have been analysed to identify possible relevant studies.

Criteria of Selection and Eligibility of the Studies

The articles were selected if the abstract contained information about patients treated via SILS for colorectal diseases, benign and malignant. Prospective randomised and non-randomised studies have been included, as well as comparative case–control and cohort studies. Articles related to natural orifice transluminal endoscopic surgery (NOTES), meta-analyses, reviews, editorials, case series, expert opinions and letters to the director have been excluded, as well as articles referring to series of patients with ≤15 SILS procedures. Multicentric studies containing units and hospitals data, already included in the studies, have also been excluded to avoid duplicating patients.

Data Extraction Process

Three authors (JL, MTS, and JA) obtained the following data from each study, and then entered them in a database: year of publication, type of study, number of patients treated with each technique, demographic characteristics of the study population (age, gender, ASA score, body mass index [BMI], indication for surgery [benign pathology, malignant pathology, or both], type of surgical procedure, average operating time in minutes [min], blood loss measured in millilitres [ml], conversion to open surgery, length of the incision in centimetres [cm], postoperative complications, average length of hospital stay in days, and mortality. In the studies where oncological procedures have been conducted, the number of lymph nodes harvested was also obtained. The data analysed come exclusively from the published articles. No author was contacted to complete the information.

The parameters analysed in the meta-analysis were: BMI, ASA score, length of the incision, blood loss, operating time, postoperative complications, length of hospital stay, number of lymph nodes, and mortality.

A postoperative complication was defined as a complication that developed within 30 days of the intervention as a direct result of the surgery. The complications were classified by degree of severity, according to the Clavien–Dindo scale.9

The conversion to open surgery was defined as the performance of a laparotomy in both SILS and MLC.

Assessment of the Methodological Quality and of Bias

The quality of the articles included in this meta-analysis was assessed according to the revised and modified Scottish Intercollegiate Guidelines Network,10,11 where the maximum punctuation is 20. A score of <8 equals poor quality; a score between 8 and 14 equals intermediate quality, and a score ≥15 equals very good quality.

Statistical Analysis

All the data were extracted from the selected articles, tables, and figures, and then entered into an SPSS spreadsheet (SPSS version 19, Inc., Chicago, IL, USA). The odds ratio (OR) was calculated for binary and qualitative variables according to the random effects method of Mantel–Haenszel. OR is the probability of an event occurring in a group in relation with the probability of that event occurring in another group. This ratio was calculated for the studies that informed the occurrences and non-occurrences of events. The studies where the event did not occur in any of the groups were excluded. An OR<1 was favourable to the SILS group and the OR point estimation of P<.05 was considered to be statistically significant if 95% of the confidence interval (CI) did not include the value 1. The weighted mean difference (WMD) was used for the quantitative variables in the studies that included the mean and the standard deviation. Those studies that did not contain that information were excluded. A WMD<0 was favourable to the SILS group and was considered statistically significant with P<.05, if 95% of the CI did not include the value 0.

The degree of heterogeneity among studies was also analysed (the variation in the results among them), by means of τ2, χ2 (Cochrane Q) and I2, where τ2 values >1.00, χ2 values associated to P<.01 and I2 values >50 were indicators of heterogeneity.

Statistical analysis was performed with the statistical software Review Manager (REVMAN), version 5.0 (The Nordic Cochrane Centre, Copenhagen, The Cochrane Collaboration, 2008).

ResultsBibliographic Search

From January, 2008 to April, 2014, we collected 267 articles using the inclusion criteria for the search. After the exclusion criteria was used, we obtained 28 comparative articles to be included in the meta-analysis12–39: 27 comparative studies, and one prospective randomised study29 (Fig. 1).

Fig. 1.

Flow chart of the systematic review of the literature.

(0.2MB).
Characteristics of the Studies

According to the modified Scottish Intercollegiate Guidelines Network classification,10,11 the average quality of the methodology used in the articles included in the meta-analysis was 13.21±1.87 with a range of (9–16). This means they are intermediate to good quality studies. The 28 studies of this meta-analysis included 2870 patients: 1119 treated via SILS and 1751 via MLC. Out of 28 studies, 11 compared malignant disease17,19,21–23,29,32,35,37–39; 2 compared benign diseases,25,33 and 15 compared benign and malignant diseases.12–16,18,20,24,26–28,30,31,34,36 The type of colectomy more frequently performed was the right hemicolectomy. Table 1 shows the demographic characteristics of all the procedures included. Table 2 shows the data collected individually from each study included in the meta-analysis.

Table 1.

Demographic Characteristics of Studies Included.

Study  Year  No.GenderAgeBMIASA ScoreIndication  Procedure
    SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC    SILS  MLC 
Adair  2010  17  17  M5/F12  M5/F12  66.6±10  66.7±13  26.2±4.3  25.2±5  –  –  Bo  LARHC  LARHC 
Chen  2010  18  21  M10/F8  M14/F7  69.44  66.19  23.34  23.92  –  –  Bo  LARHC  LARHC 
Gandhi  2010  24  24  M12/F12  M12/F12  54.1±8.6  56±11.1  28.5±7.2  28.5±6  2.3±0.6  2.3±0.5  Bo  Various  Various 
Waters  2010  16  27  M4/F6  M15/F12  65 (39–82)  67 (40–91)  29 (20–41)  29 (18–45)  –  –  Bo  LARHC  LARHC 
Champagne  2011  29  29  M10/F19  M10/F19  61.2  63.5  27.4  28.8  –  –  Bo  Various  Various 
Fujii  2011  23  23  M10/F13  M13/F10  63.9±9.9  65.2±9.6  21.6±2.9  22.9±4.5  1.52±0.51  1.61±0.5  Various  Various 
Gaujoux  2011  25  50  M8/F17  M22/F28  56 (32–69)  55 (38–61)  22.6 (21.2–24.7)  22.6 (20–25)  –  –  Bo  Various  Various 
Kim  2011  73  106  –  –  67 (35–87)  63 (27–88)  22.7±4  25.6±20.7  2±0.69  1.93±0.68  Various  Various 
Lee  2011  46  46  M17/F29  M21/F25  58 (16–84)  61 (16–85)  24 (16–42)  25 (16–36)  –  –  Bo  Various  Various 
Lu  2011  27  68  M16/F11  M36/F32  60.26±15.69  64.29±15.06  –  –  –  –  Various  Various 
McNally  2011  27  46  M13/F14  M21/F25  67 (26–86)  73 (48–92)  27 (18.3–39.9)  26 (16.6–71.4)  2.44±0.62  2.5±0.62  Various  Various 
Papaconstantinou  2011  26  26  M11/F15  M11/F15  65±13  66±12  28±5  28±5  2.54±0.51  2.54±0.51  Various  Various 
Ramos-Valadez  2011  20  20  M11/F9  M11/F9  59±10  56.4±12.6  25.9±3.9  29.6±5.4  –  –  Bo  Sigm  Sigm 
Rickjen  2011  20  20  M6/F14  M6/F14  31.6±10.8  31.7±10.7  21.5±2.6  21.2±2.5  1.7±0.57  1.85±0.49  Be  IR  IR 
Champagne  2012  165  165  M58/F107  M65/F99  58  57.6  27  27.4  –  –  Bo  Various  Various 
Chew  2012  40  104  M22/F18  M60/F44  63 (41–48)  67 (23–88)  22.3 (16.1–34.9)  23.1 (14–36.6)  1.93±0.35  1.9±0.45  Bo  LARHC  LARHC 
Costedio  2012  24  24  M9/F15  M10/F14  43.2±12.5  42.3±12.7  24.8±4.8  25.3±4.3  –  –  Bo  Total  Total 
Huscher  2012  16  16  M6/F10  M9/F7  70±11  70±13  –  –  1.94±0.68  2.13±0.81  Various  Various 
Kanakala  2012  40  78  M22/F18  M49/F29  54.1 (17–86)  64.8 (23–84)  26.2 (18–37)  28 (21–45)  2.23±0.62  2.18±0.68  Bo  Various  Various 
Osborne  2012  55  327  M27/F28  –  63±13  –  26 (17–41)  –  –  –  Bo  HAR  HAR 
Park  2012  37  54  M21/F16  M26/F28  63.8±10.4  59.9±10.6  24.7±2.8  23.9±3.2  –  –  Sigm  Sigm 
Vasilakis  2012  20  20  M12/F8  M12/F8  58.3±10.7  57.9±10.8  28.5±4.9  29±5.2  2.35±0.49  2.35±0.49  Be  Sigm  Sigm 
Velthuis  2012  50  50  M21/F29  M22/F28  73±13.2  71±11.8  25 (20–32)  25 (20–36)  –  –  Bo  LARHC  LARHC 
Woo Lim  2012  40  123  M21/F19  M62/F61  62.8±10.5  64.4±11.2  22.7±3.6  23.7±3.4  1.78±0.42  1.8±0.49  Various  Various 
Keshava  2013  75  74  M35/F40  M36/F38  68 (18–99)  74 (34–96)  27 (19–42)  27.3 (20–45.1)  –  –  Bo  LARHC  LARHC 
Pedraza  2013  50  50  M25/F25  M23/F27  64.6±12.4  66.3±12.9  27.2±5.7  31±8.1  2.5±0.7  2.7±0.6  Various  Various 
Rosati  2013  50  50  M17/F33  M26/F24  65 (36–88)a  65 (44–87)a  –  –  –  –  LARHC  LARHC 
Yun  2013  66  93  M33/F33  M55/F38  61±11  59±11  23.82±2.81  24.23±2.7  1.65±0.54  1.7±0.55  LARHC  LARHC 

Bo: both; Be: benign; LARHC: laparoscopically assisted right hemicolectomy; HAR: anterior resection; M: malignant; IR: ileocolic resection; Sigm: sigmoidectomy.

a

Mean.

Table 2.

Variables Collected From the Studies Included.

Study  Year  No.Length of incision (cm)Operating time (min)ConversionBlood loss (ml)Lymph nodesComplicationsLength of hospital stay (days)Mortality
    SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC  SILS  MLC 
Adair  2010  17  17  3.8  5.1  139±29.7  134±32.3      20.1±11.3  18.6±4.1  3.9±3.7  4.1±2.2 
Chen  2010  18  21  4 (3–6)  4 (3–6)  175 (145–280)  165 (120–340)  75 (20–700)  50 (20–300)  19.5 (3–42)  19 (15–57)  5 (3–15)  5 (3–38)     
Gandhi  2010  24  24  3.3±1.1  6.6±2.1  143.2±37.2  112.8±44.8  62.5±37.6  90.6±60.6  24.6±12.3  18.6±5.7  2.7±0.8  3.3±1.1 
Waters  2010  16  27  2.5–4.5  2.5–4.5  106 (71–223)  100 (65–215)  54 (25–120)  90 (25–300)  18 (13–22)  16 (10–21)  5 (2–24)  6 (2–28) 
Champagne  2011  29  29  3.80  4.50  103.80  134.40      19.4  21.6  3.70  3.90     
Fujii  2011  23  23  3.3±1.2  5.5±2.4  174±37  179±40  9±9  109±391  19.9±5.2  23.3±11.5  8.2±3.4  12.7±12.9     
Gaujoux  2011  25  50      130 (110–185)  180 (110–200)  100 (50–150)  90 (50–100)      6 (6–7)  7 (6–9) 
Kim  2011  73  106      274 (105–405)  254 (80–470)  282 (105–405)  418 (100–2.600)  29.3±16  23.2±15.4  23  39  9.60  15.50 
Lee  2011  46  46  5.1±1.8  6.4±2.4  135±21  134±39              11  12  4.6±1.6  4.3±0.8     
Lu  2011  27  68  4.07±1.18  4.77±1.19  180 (150–205)  185 (155–230)      35 (30–50)  50 (30–80)      7 (5–8)  7 (6–9)     
McNally  2011  27  46      114 (59–268)  135 (45–314)  50 (5–100)  50 (5–250)  15 (3–32)  17 (0–35)  16  3 (2–17)  5 (2–11) 
Papaconstantinou  2011  26  26      144±24  144±51  57±40  87±70  18±6  17±12      3.6±1.6  5±2.2     
Ramos-Valadez  2011  20  20      159.2±29.9  162.1±40.3  58.3±34.3  98.8±52.1  20.3±3.8  18.3±6.8  3.2±1  3.8±2.1     
Rickjen  2011  20  20  3.8 (2.5–5)    137.4±28.4  166.4±37.5          9±3.4  9.2±5.9     
Champagne  2012  165  165      135.4±45  133.2±56  47.20  63.50      43  48  4.3±1.6  4.6±1.4 
Chew  2012  40  104  5 (3–12)  6 (3–25)  95 (45–180)  100 (55–190)      19 (10–43)  18 (6–54)  21  5 (4–15)  5 (3–109) 
Costedio  2012  24  24      125.9±39.3  230±117.4  95.8±65  241.7±135.5      11  19  6.08±4.2  6.3±3.05 
Huscher  2012  16  16      147±61  129±46      200    18±6  16±5  6±3  7±2 
Kanakala  2012  40  78      162  170      22.9 (11–41)  13.8 (0–28)  10  4 (2–11)  4 (2–20) 
Osborne  2012  55  327      79±37  113±44      18 (2–34)  14 (5–53)  12  27  1 (1–8)  3 (1–24)     
Park  2012  37  54  3.3±0.9  9.1±1.4  118.1±41.5  140±42.2  92  131  14.6±6.8  23.4±11.4  5.5±2.3  7.7±4.2     
Vasilakis  2012  20  20  4.9±1.9  5.1±1.9  175, 5±40.2  178.7±50.7  74.5±55.3  81.3±54.9      3.9±1.6  5.5±2 
Velthuis  2012  50  50      97 (60–148)  112 (70–225)      14 (10–28)  12.5 (10–34)  17  17  6 (2–41)  6 (2–103) 
Woo Lim  2012  40  123  4.6±0.7  4.4±0.9  225.5±48.3  144.6±32.6  109.2±80.3  96±58.4  25.3±11.9  28.3±13.2  18  7.7±1.1  7.8±2.8 
Keshava  2013  75  74  4.3 (3–6)  5 (4–9)          17.00  17.00  13  5 (3–43)  8 (4–33) 
Pedraza  2013  50  50      127.9±37.6  126.7±63.3  64.4±64.7  87.2±89.8  21.4±8.4  19.2±7.6  4.5±3.7  4±1.7     
Rosati  2013  50  50      160 (115–210)a  152 (110–215)a      21 (13–34)a  22 (8–38)a  11  6 (4–16)a  8 (4–34)a 
Yun  2013  66  93      131±27  143±54      24±11  27±13  14  8±4  9±5     

min: minutes; ml: millilitres.

a

Mean.

Body Mass Index

The meta-analysis did not show statistically significant differences between both groups, with a WMD: −0.63 (−1.34, 0.08); P=.08 (Fig. 2).

Fig. 2.

Analysis of body mass index.

(0.39MB).
Age

The meta-analysis estimation did not show statistically significant differences between both groups. WMD: 0.28 (−1.13, 1.68); P=.70 (Fig. 3).

Fig. 3.

Analysis of age.

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ASA Score

The ASA score was informed in 22 studies. Thirteen articles were included in the meta-analysis after the mean and SD were calculated in studies where it was possible to do so.14,17,19,22,23,25,27,29,30,33,35,37,39 The meta-analysis did not show statistically significant differences between both groups. WMD: −0.02 (−0.08, 0.04); P=.51 (Fig. 4).

Fig. 4.

Analysis of ASA score.

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Length of Incision

The meta-analysis did not show statistically significant differences for both groups. WMD: −1.90 (−3.95, 0.14); P=.07 (Fig. 5).

Fig. 5.

Analysis of length of incision.

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Conversion

Out of 1119 SILS procedures, conversion to laparotomy was necessary in 15 (1.34%) patients. Out of 1751 MLC cases, conversion to open surgery was necessary in 45 (2.56%) patients. No statistically significant differences were shown with OR=0.59 (0.33, 1.04); P=.07 (Fig. 6).

Fig. 6.

Analysis of conversion.

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Operating Time

The meta-analysis estimation did not show statistically significant differences between both groups. WMD: −2.69 (−18.33, 12.95); P=.74 (Fig. 7).

Fig. 7.

Analysis of operating time.

(0.47MB).
Blood Loss

The meta-analysis showed a significantly lower blood loss in the SILS group. WMD: −42.68 (−76.79, −8.57); P=.01 (Fig. 8).

Fig. 8.

Analysis of blood loss.

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Postoperative Complications

Postoperative complications were reported in all studies but one.23 There were 199 (17.78%) postoperative complications in the SILS group and 311 (17.76%) in the MLC group. Table 3 shows complications according to the Clavien–Dindo classification.9 The most frequent complications in both groups were graded type I, excluding studies that did not contribute enough data to grade the complications. There were no differences in the postoperative complications with OR=0.89 (0.69, 1.15); P=.37 (Fig. 9).

Table 3.

Complications According to Clavien–Dindo.

Degree  SILS  MLC 
59  71 
II  32  55 
IIIa  11 
IIIb  16  40 
IVa 
IVb 
Fig. 9.

Analysis of postoperative complications.

(0.58MB).
Postoperative Pain

Postoperative pain was reported in 6 articles.13,17,19,21,25,33 No statistical study was conducted due to the variability in the type of analgesia and the pain scale grading. Only 2 studies found significant differences: one with less pain in SILS colectomy during the first and second postoperative days, with no repercussions in the length of hospital stay33; and the other, with less pain in MLC colectomy,21 which is attributed to a longer length of umbilical incision in SILS, and to the fact that in the MLC, the specimen is extracted by means of McBurney's incision, which is less painful.

Hospital Stay

The meta-analysis showed that the length of hospital stay was also significantly lower in the SILS group. WMD: −0.73 (−1.18, −0.28); P=.001 (Fig. 10).

Fig. 10.

Analysis of length in hospital stay.

(0.41MB).
Mortality

Out of 1119 SILS cases, there were 5 (0.44%) deaths. Out of 1751 MLC interventions, 9 (0.51%) patients died. No statistically significant differences were shown with OR=0.91 (0.36, 2.34); P=.85 (Fig. 11).

Fig. 11.

Analysis of mortality.

(0.32MB).
Isolated Lymph Nodes

The meta-analysis did not show statistically significant differences. WMD: 0.13 (−2.52, 2.78); P=.92 (Fig. 12).

Fig. 12.

Analysis of the number of isolated lymph nodes.

(0.34MB).
Discussion

Colon surgery via SILS, as well as in other diseases, is a surgeon's attempt to diminish surgery aggressiveness by reducing the number of ports of entry. The aim is to diminish postoperative pain, reduce complications, improve the time of recovery, and obtain a better aesthetic result, without jeopardising the safety and efficiency of the surgery. The vast majority of these advantages are based on cohort series studies, non-randomised comparative studies, sometimes with contradictory results which may raise more questions than answers. This meta-analysis has intended to answer whether SILS offers benefits as compared to MLC, using the best of the evidence available at present.

Operating time is similar in both groups, although longer in some MLC cases. It is difficult to explain how the operating time could be shorter in SILS colectomy. One possible explanation to this is that MLC procedures, most of the times, are performed by surgeons in training, while SILS are exclusively performed by surgeons with experience in laparoscopic procedures.18,34 Another argument could be the very nature of the patient selection, as with patients with a stoma, which is generally placed at the end of the intervention, since it could be time-saving as the stoma orifice is already made and protected by a wound retractor, so there is no need to close the fascia or the skin in the additional ports, as in the MLC.18 These two arguments, patient selection and the surgeon's expertise, could also be the cause of the increased blood loss in MLC patients.

Among the potential benefits of SILS over MLC is the shorter length of incision, which could contribute to an improvement in the aesthetics of the procedure and a reduction in postoperative pain. In this meta-analysis, the length of the incision was similar in both procedures. This could be so because in the laparoscopic colectomy, the length of the incision is not determined by the access path, whether it is SILS or MLC, but by the specimen size, the obesity and the depth of the abdominal wall, the mobility and thickness of the mesentery and omentum, and the amount of stool in the colon.

On the other hand, the advantage of better aesthetics attributed to SILS could be relevant for patients who underwent SILS cholecystectomy, but it is not clear, and it would probably be an irrelevant advantage for colon cancer patients.

The length of hospital stay was shorter in the SILS colectomy group. Discharge from hospital depends on the recovery programme implemented by each institution, on the operating time, the complexity of the surgery, and the morbidity associated to it. All of these parameters are very difficult to assess in non-prospective randomised studies. In a Cochrane review, comparing “fast track” surgery vs conventional postoperative care in colorectal surgery, the length of hospital stay was found to be shorter in health care centres that provided fast-track recovery programmes.40 Therefore, it is a variable that strongly depends on the centre that performs the study and, although this meta-analysis showed a statistically significant shorter length of hospital stay, results have to be taken with caution.

The majority of studies show that SILS colectomy is a safe technique when compared to MLC. In this meta-analysis, the complications have been similar in both surgical techniques. This shows the technique is safe. In the vast majority of the studies, the selected SILS patients had a low BMI. In addition, the surgeons performing the interventions were skilled in laparoscopic surgery. It is unknown whether the safety and effectiveness will remain the same when operating on patients with more complex health profiles and a higher BMI. Moreover, regarding BMI, the results obtained by meta-analysis show that patients intervened via SILS technique have lower BMIs. It leads to think that there is a selection bias, although the results obtained are not statistically significant. On the other hand, one of the theoretical advantages of the SILS interventions is that there are fewer complications related to trocar ports of entry. MLC requires 4–6 ports. Each port represents a potential risk of bleeding, hernia, or intraperitoneal organ lesions. SILS reduces invasiveness since it only performs a single incision, and this could consequently reduce complication rates. However, there are no conclusive clinical studies that show the actual incidence of these complications, among other things, due to the low incidence of complications related to trocars.

In patients with colon cancer, the number of isolated lymph nodes is relevant for staging, determining a prognosis, and defining therapeutic implications. At present, there are no prospective randomised studies or cohort studies to determine oncological results with SILS, in the long run. In 3 studies (2 retrospective studies,23,39 and one prospective randomised study29), the oncological results in adenocarcinoma of colon are compared in the short run, in both techniques: SILS colectomy and MLC. It is shown that in expert hands it is feasible to achieve a correct oncological resection with SILS, although there is no scientific evidence that proves the benefits via this intervention and no study has been able to show SILS colectomy advantages so far.29 In this meta-analysis, the oncological parameters available in the short run, as the number of isolated lymph nodes, have been the same in both groups: with a mean of 19.22 isolated lymph nodes in SILS colectomy, and 18.55 in MLC. Literature suggests that, for a correct oncological study, there should be a minimum of 12 isolated lymph nodes in colectomies performed for cancer.41 This leads to believe that SILS colectomy is as effective in oncology as MLC, provided the principles of laparoscopic resection of colorectal cancer are maintained: to perform an early ligation of the vascular pedicle, to avoid manipulating the tumour, and to protect the surgical wound for the specimen extraction.

This meta-analysis includes more studies and a larger amount of patients than other meta-analyses conducted before. The results indicated in those meta-analyses are surprising, in some respects: larger number of isolated lymph nodes during oncological resection performed by SILS, giving SILS colectomy a major improvement when compared to MLC.42 The authors are aware that this meta-analysis has some methodological limitations. Thus, in the design of the comparative studies, only one study was prospective randomised29 and the rest were observational studies. This may reduce the quality of the results.

The meta-analyses based on good quality observational studies generally produce estimates similar to those of meta-analyses based on prospective randomised studies,43 which is why observational studies should not be excluded from meta-analyses, as it was demonstrated by the meta-analyses conducted with non-randomised comparative studies of laparoscopic resection of colorectal cancer.44 Other biases in this meta-analysis is that in the majority of SILS colectomy studies, the intervention was conducted by surgeons with experience in laparoscopic surgery, while MLC is performed by surgeons in the process of being trained in laparoscopic colectomy. In addition, SILS studies select patients with lower BMIs, as obese and morbidly obese patients are a difficult population to be treated via SILS due to potential additional traction requirements. For this reason, the results obtained in this meta-analysis should be taken with caution.

In conclusion, based on the results of this meta-analysis, SILS is a safe and effective technique, with additional subtle benefits in comparison with MLC. Development in this area should continue, and prospective randomised studies are needed to be able to consider single-port laparoscopic colectomy an alternative to multi-port laparoscopic colectomy, as the evidence available at present is not enough to determine whether this practice should be a standard in laparoscopic colectomy.

Authors’ Contributions

J. Luján: study design, data collection, draft of the manuscript; M.T. Soriano: data collection, draft of the manuscript; J. Abrisqueta: data collection, draft of the manuscript, statistical analysis; D. Pérez: data collection, statistical analysis; P. Parrilla: data collection, draft and review of the manuscript.

Conflict of Interests

The authors declare that there are no conflicts of interests.

References
[1]
R. Veldkamp, E. Kuhry, W.C. Hop, J. Jeekel, G. Kazemier, H.J. Bonjer, COlon cancer Laparoscopic or Open Resection Study Group (COLOR), et al.
Laparoscopic surgery versus open surgery for colon cancer: short-term outcomes of a randomised trial.
Lancet Oncol, 6 (2005), pp. 477-484
[2]
Clinical Outcomes of Surgical Therapy Study Group.
A comparison of laparoscopically assisted and open colectomy for colon cancer.
N Engl J Med, 350 (2004), pp. 2050-2059
[3]
A.M. Lacy, J.C. García-Valdecasas, S. Delgado, A. Castells, P. Taurá, J.M. Piqué, et al.
Laparoscopy-assisted colectomy versus open colectomy for treatment of non-metastatic colon cancer: A randomised trial.
Lancet, 359 (2002), pp. 2224-2229
[4]
J. Lujan, G. Valero, Q. Hernandez, A. Sanchez, M.D. Frutos, P. Parrilla.
Randomized clinical trial comparing laparoscopic and open surgery in patients with rectal cancer.
Br J Surg, 96 (2009), pp. 982-989
[5]
J.P. Pearl, J.L. Ponsky.
Natural orifice translumenal endoscopic surgery: a critical review.
J Gastrointest Surg, 12 (2008), pp. 1293-1300
[6]
M.D. Frutos, J. Abrisqueta, J. Lujan, I. Abellan, P. Parrilla.
Randomized prospective study to compare laparoscopic appendectomy versus umbilical single-incision appendectomy.
Ann Surg, 257 (2013), pp. 413-418
[7]
B.A. Boone, P. Wagner, E. Ganchuk, L. Evans, H.J. Zeh, D.L. Bartlett, et al.
Single-incision laparoscopic right colectomy in an unselected patient population.
Surg Endosc, 26 (2012), pp. 1595-1601
[8]
D. Moher, A. Liberati, J. Tetzlaff, D.G. Altman.
PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
Int J Surg, 8 (2010), pp. 336-341
[9]
D. Dindo, N. Demartines, P.A. Clavien.
Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey.
Ann Surg, 240 (2004), pp. 205-213
[10]
Scottish Intercollegiate Guidelines Network (SIGN) guidelines. Available from: http://www.sign.ac.uk/guidelines/fulltext/50/checklist3 [accessed 30.04.13].
[11]
N. Vettoretto, R. Cirocchi, J. Randolph, A. Parisi, E. Farinella, G. Romano.
Single incision laparoscopic right colectomy: a systematic review and meta-analysis.
Colorectal Dis, 16 (2014), pp. O123-O132
[12]
J. Adair, M.A. Gromski, R.B. Lim, D. Nagle.
Single-incision laparoscopic right colectomy: experience with 17 consecutive cases and comparison with multiport laparoscopic right colectomy.
Dis Colon Rectum, 53 (2010), pp. 1549-1554
[13]
W.T. Chen, S.C. Chang, H.C. Chiang, W.Y. Lo, L.B. Jeng, C. Wu, et al.
Single incision laparoscopic versus conventional laparoscopic right hemicolectomy: a comparison of short-term surgical results.
Surg Endosc, 25 (2011), pp. 1887-1892
[14]
D.P. Gandhi, M. Ragupathi, C.B. Patel, D.I. Ramos-Valadez, T.B. Pickron, E.M. Haas.
Single-incision versus hand-assisted laparoscopic colectomy: a case-matched series.
Br J Surg, 97 (2010), pp. 1881-1883
[15]
J.A. Waters, M.J. Guzman, A.D. Fajardo, D.J. Selzer, E.A. Wiebke, B.W. Robb, et al.
Single-port laparoscopic right hemicolectomy: a safe alternative to conventional laparoscopy.
Dis Colon Rectum, 53 (2010), pp. 1467-1472
[16]
B.J. Champagne, E.C. Lee, F. Leblanc, S.L. Stein, C.P. Delaney.
Single-incision vs straight laparoscopic segmental colectomy: a case-controlled study.
Dis Colon Rectum, 54 (2011), pp. 183-186
[17]
S. Fujii, K. Watanabe, M. Ota, J. Watanabe, Y. Ichikawa, S. Yamagishi, et al.
Single-incision laparoscopic surgery using colon-lifting technique for colorectal cancer: a matched case–control comparison with standard multiport laparoscopic surgery in terms of short-term results and access instrument cost.
Surg Endosc, 26 (2012), pp. 1403-1411
[18]
S. Gaujoux, L. Maggiori, F. Bretagnol, M. Ferron, Y. Panis.
Safety, feasibility, and short-term outcomes of single port access colorectal surgery: a single institutional case-matched study.
J Gastrointest Surg, 16 (2012), pp. 629-634
[19]
S.J. Kim, G.O. Ryu, B.J. Choi, J.G. Kim, K.J. Lee, S.C. Lee, et al.
The short-term outcomes of conventional and single-port laparoscopic surgery for colorectal cancer.
Ann Surg, 254 (2011), pp. 933-940
[20]
S.W. Lee, J.W. Milsom, G.M. Nash.
Single-incision versus multiport laparoscopic right and hand-assisted left colectomy: a case-matched comparison.
Dis Colon Rectum, 54 (2011), pp. 1355-1361
[21]
C.C. Lu, S.E. Lin, K.C. Chung, K.M. Rau.
Comparison of clinical outcome of single-incision laparoscopic surgery using a simplified access system with conventional laparoscopic surgery for malignant colorectal disease.
Colorectal Dis, 14 (2012), pp. e171-e176
[22]
M.E. McNally, B. Todd Moore, K.M. Brown.
Single-incision laparoscopic colectomy for malignant disease.
Surg Endosc, 25 (2011), pp. 3559-3565
[23]
H.T. Papaconstantinou, J.S. Thomas.
Single-incision laparoscopic colectomy for cancer: Assessment of oncologic resection and short-term outcomes in a case-matched comparison with standard laparoscopy.
Surgery, 150 (2011), pp. 820-827
[24]
D.I. Ramos-Valadez, M. Ragupathi, J. Nieto, C.B. Patel, S. Miller, T.B. Pickron, et al.
Single-incision versus conventional laparoscopic sigmoid colectomy: a case-matched series.
Surg Endosc, 26 (2012), pp. 96-102
[25]
E. Rijcken, R. Mennigen, I. Argyris, N. Senninger, M. Bruewer.
Single-incision laparoscopic surgery for ileocolic resection in Crohn's disease.
Dis Colon Rectum, 55 (2012), pp. 140-146
[26]
B.J. Champagne, H.T. Papaconstantinou, S.S. Parmar, D.A. Nagle, T.M. Young-Fadok, E.C. Lee, et al.
Single-incision versus standard multiport laparoscopic colectomy: a multicenter, case-controlled comparison.
[27]
M.H. Chew, M.H. Chang, W.S. Tan, M.T. Wong, C.L. Tang.
Conventional laparoscopic versus single-incision laparoscopic right hemicolectomy: a case cohort comparison of short-term outcomes in 144 consecutive cases.
Surg Endosc, 27 (2013), pp. 471-477
[28]
M.M. Costedio, E. Aytac, E. Gorgun, R.P. Kiran, F.H. Remzi.
Reduced port versus conventional laparoscopic total proctocolectomy and ileal J pouch-anal anastomosis.
Surg Endosc, 26 (2012), pp. 3495-3499
[29]
C.G. Huscher, A. Mingoli, G. Sgarzini, A. Mereu, B. Binda, G. Brachini.
Standard laparoscopic versus single-incision laparoscopic colectomy for cancer: early results of a randomized prospective study.
Am J Surg, 204 (2012), pp. 115-120
[30]
V. Kanakala, D.W. Borowski, A.K. Agarwal, M.A. Tabaqchali, D.K. Garg, T.S. Gill.
Comparative study of safety and outcomes of single-port access versus conventional laparoscopic colorectal surgery.
Tech Coloproctol, 16 (2012), pp. 423-428
[31]
A.J. Osborne, J. Lim, K.J. Gash, B. Chaudhary, A.R. Dixon.
Comparison of single-incision laparoscopic high anterior resection with standard laparoscopic high anterior resection.
Colorectal Dis, 15 (2013), pp. 329-333
[32]
S.J. Park, K.Y. Lee, B.M. Kang, S.I. Choi, S.H. Lee.
Initial experience of single-port laparoscopic surgery for sigmoid colon cancer.
World J Surg, 37 (2013), pp. 652-656
[33]
V. Vasilakis, C.E. Clark, L. Liasis, H.T. Papaconstantinou.
Non cosmetic benefits of single-incision laparoscopic sigmoid colectomy for diverticular disease: a case-matched comparison with multiport laparoscopic technique.
J Surg Res, 180 (2013), pp. 201-207
[34]
S. Velthuis, P.B. van den Boezem, D.J. Lips, H.A. Prins, M.A. Cuesta, C. Sietses.
Comparison of short-term surgical outcomes after single-incision laparoscopic versus multiport laparoscopic right colectomy: a two-center, prospective case-controlled study of 100 patients.
Dig Surg, 29 (2012), pp. 477-483
[35]
S.W. Lim, H.J. Kim, C.H. Kim, J.W. Huh, Y.J. Kim, H.R. Kim.
Umbilical incision laparoscopic colectomy with one additional port for colorectal cancer.
Tech Coloproctol, 17 (2013), pp. 193-199
[36]
A. Keshava, C.J. Young, G.L. Richardson, K. De-Loyde.
A historical comparison of single incision and conventional multiport laparoscopic right hemicolectomy.
Colorectal Dis, 15 (2013), pp. e618-e622
[37]
R. Pedraza, A. Aminian, J. Nieto, C. Faraj, T.B. Pickron, E.M. Haas.
Single-incision laparoscopic colectomy for cancer: short-term outcomes and comparative analysis.
Minim Invasive Surg, 2013 (2013), pp. 283438
[38]
C.M. Rosati, L. Boni, G. Dionigi, E. Cassinotti, L. Giavarini, G. David, et al.
Single port versus standard laparoscopic right colectomies: results of a case–control retrospective study on one hundred patients.
Int J Surg, 11 (2013), pp. S50-S53
[39]
J.A. Yun, S.H. Yun, Y.A. Park, Y.B. Cho, H.C. Kim, W.Y. Lee, et al.
Single-incision laparoscopic right colectomy compared with conventional laparoscopy for malignancy: assessment of perioperative and short-term oncologic outcomes.
Surg Endosc, 27 (2013), pp. 2122-2130
[40]
W.R. Spanjersberg, J. Reurings, F. Keus, C.J. van Laarhoven.
Fast track surgery versus conventional recovery strategies for colorectal surgery.
Cochrane Database Syst Rev, 16 (2011), pp. CD007635
[41]
H. Nelson, N. Petrelli, A. Carlin, J. Couture, J. Fleshman, J. Guillem, et al.
National Cancer Institute Expert Panel. Guidelines 2000 for colon and rectal cancer surgery.
J Natl Cancer Inst, 93 (2001), pp. 583-596
[42]
L. Maggiori, S. Gaujoux, E. Tribillon, F. Bretagnol, Y. Panis.
Single-incision laparoscopy for colorectal resection: a systematic review and meta-analysis of more than a thousand procedures.
Colorectal Dis, 14 (2012), pp. e643-e654
[43]
I. Shrier, J.F. Boivin, R.J. Steele, R.W. Platt, A. Furlan, R. Kakuma, et al.
Should meta-analyses of interventions include observational studies in addition to randomized controlled trials? A critical examination of underlying principles.
Am J Epidemiol, 166 (2007), pp. 1203-1209
[44]
N.S. Abraham, C.M. Byrne, J.M. Young, M.J. Solomon.
Meta-analysis of non-randomized comparative studies of the short-term outcomes of laparoscopic resection for colorectal cancer.
ANZ J Surg, 77 (2007), pp. 508-516

Please cite this article as: Luján JA, Soriano MT, Abrisqueta J, Pérez D, Parrilla P. Colectomía mediante puerto único vs. colectomía mediante laparoscopia multipuerto. Revisión sistemática y metaanálisis de más de 2.800 procedimientos. Cir Esp. 2015;93:307–319.

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