High tie versus low tie of the inferior mesenteric artery: a protocol for a systematic review
- Roberto Cirocchi†1Email author,
- Eriberto Farinella†1,
- Stefano Trastulli†1,
- Jacopo Desiderio†1,
- Giorgio Di Rocco†2,
- Piero Covarelli†3,
- Alberto Santoro†2,
- Giammario Giustozzi†1,
- Adriano Redler†2,
- Nicola Avenia†3,
- Antonio Rulli†3,
- Giuseppe Noya†3 and
- Carlo Boselli†3
© Cirocchi et al; licensee BioMed Central Ltd. 2011
Received: 11 August 2011
Accepted: 9 November 2011
Published: 9 November 2011
In anterior resection of rectum, the section level of inferior mesenteric artery is still subject of controversy between the advocates of high and low tie. The low tie is the division and ligation to the branching of the left colic artery and the high tie is the division and ligation at its origin at the aorta. We intend to assess current scientific evidence in literature and to establish the differences comparing technique, anatomy and physiology. The aim of this protocol is to achieve a meta-analysis that tests safety and feasibility of the two procedures with several types of outcome measures.
Nowadays surgery for rectal cancer (anterior resection or abdomino-perineal amputation) has been well standardized both ways in open and laparoscopic approach .
Neither of these techniques assures to be superior to another, this is the opinion of two experts and of two literature reviews [19, 20]. Recently a systematic review of the literature has displayed a significant advantage to accomplish the high tie .
The aim of our systematic review is to appraise the real advantages of the high and low tie of the IMA.
Materials and methods
All aspects of the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement will be followed.
We will consider both ways, randomized and non-randomized studies which compare high tie (ligation at the aortic origin) versus low tie (ligation below the origin of the left colic artery) of the IMA for sigmoid or rectal resection for cancer. Furthermore, in order to be considered for inclusion, studies have to report outcomes for sigmoid (left colectomy) or rectal cancer surgery (anterior resection/sphincter-sparing surgery or abdomino - perineal resection) and to compare high tie versus low tie. We will not impose any language or publication status restrictions.
Exclusion criteria for study
The studies will be excluded from analysis if the outcomes of interest will not report the two techniques or whether it will be not possible to extrapolate them from the published results, also studies will be about benign lesions or inflammatory bowel disease without a distinct group of patients with cancer.
Types of participants
Patients of any age and sex with sigmoid or rectal cancer will be considered.
Types of surgery
Both sigmoid or rectal resection with high and low IMA tie.
Types of outcome measures
The following outcomes will be observed:
Overall colonic cancer at 5 year survival rate
Overall rectal cancer at 5 year survival rate
Disease free survival colonic cancer at 5 year survival rate
Disease free survival rectal cancer at 5 year survival rate
Information sources and search
A systematic search will be conducted in: Medline, Embase, Cochrane Central Register of Controlled Trials, CINAHL, BioMed Central, Science Citation Index and performed on all studies for potentially relevant trials comparing high with low IMA tie. A secondary search will be conducted reviewing unpublished literature databases including: Greynet, SIGLE, National Technological Information Service, British Library Integrated catalogue, Current Controlled Trials and the Cochrane Central Register of Controlled Trials
Combinations of the following search terms will be used: inferior mesenteric artery'; 'lymph node' or 'lymph nodes'; 'colon' or 'rectum'; 'cancer', 'neoplasia', 'tumour', or 'tumor'.
We will search the related article of Pub Med and all references.
To minimize retrieval bias we will perform a new manual search method that utilize the Google Scholar database and manually searched seven high-impact journals, chosen on the basis of the frequency of articles and on expert opinion.
The reference lists of all potentially eligible studies will be reviewed. Researchers who may have carried out relevant studies will be contacted. Animal trials will be excluded.
Two authors (RC and CB) will assess titles or abstracts of all identified studies independently and exclude all the irrelevant ones. Full text articles of potentially relevant studies will be obtained. These studies will be assess independently in an unblended standardized manner by the two authors (GDR and AS) as to whether they met the inclusion criteria for this review.
Data collection process
We will develop a data extraction sheet (based on the Cochrane Consumers and Communication Review Group's data extraction template), pilot tested it on ten randomly-selected included studies and refined it accordingly. One author (ST) will extract the data from the included study and the second author (GN) will check the extracted data. Disagreements will be solved through discussion, if necessary, by involving an independent third author (AR).
Year and language of publication.
Country in which the trial was conducted.
Year of conduct of trial.
Single-center or multicenter trial.
Characteristics of trial participants
Inclusion and exclusion criteria.
Two authors (ST and EF) will perform the statistical analysis in line with recommendations from the PRISMA statement  and the Cochrane Handbook for systematic reviews . Statistical analysis for categorical variables will be performed by using the odds ratio (OR) as summary statistic. This ratio represents the odds of an adverse event occurring in the high tie group compared with the low tie. The Mantel-Haenszel method will be used to combine the ORS for the outcomes of interest) [24, 25]. For continuous variables statistical analysis, we will use the weighted mean difference (WMD). A negative WMD favored the high tie group and subgroups, and the estimated point of the WMD will be considered statistically significant with P < 0.05, if 95% confidence interval (CI) did not include the value zero.
Fixed effect models and Random effect model will be initially calculated for all outcomes. Then we will test the homogeneity among the studies by calculating the chi2 and I2. I2 or "inconsistency" describes the proportion of total variation in studies and it is independent from the number of combined studies. If the test rejects the assumption of homogeneity of the studies, then it is not appropriate to use a fixed effect model, and random effect analysis will be reported. Sensitivity analyses will also lead to explore the statistical heterogeneity .
If the studies report their continuous variables as medians with ranges that a meta-analysis cannot use, we will assume the mean to be equal to the median value itself and estimated the standard deviation (SD) as a quarter of the range (samples = 70) or one sixth of the range (samples > 70) . If neither range nor other measure of dispersion will be reported, it will be impossible to estimate the mean and the SD based on the published data and the corresponding continuous variables will be excluded from the statistical pool.
Statistical analysis will be conducted by using the statistical software Review Manager Version 5.0.
Assessment of quality and bias risk of the included studies
Two authors will assess the risk of bias of the trials independently (ST, JD) using for the RCTs the instructions given in the Cochrane Handbook for Systematic Reviews of Interventions and for CCTs the modified Newcastle-Ottawa scale [28, 29]. Graphical exploration with funnel plots will be used to evaluate publication bias .
Strategy for data synthesis
A narrative synthesis of the included studies, risk of bias and results will be performed. If heterogeneity will present a I2 < 50% will reported the outcome results using a random effects meta-analysis. We will conduct sensitivity analyses based on study quality.
The article will be submitted to a peer-reviewed journal.
Organizational affiliation of the review
University of Perugia
Anticipated or actual start date
1 September 2011
Anticipated completion date
1 December 2011
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