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vol. 13
Systematic review/Meta-analysis

Laparoscopic and open liver resection – a literature review with meta-analysis

Andrzej L. Komorowski
Jerzy W. Mituś
Wojciech M. Wysocki
Małgorzata M. Bała

Arch Med Sci 2017; 13, 3: 525–532
Online publish date: 2016/12/13
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With the advent of minimally invasive surgical techniques the interest in laparoscopic resection of the liver increased significantly [1]. Following the initial report on the applicability of laparoscopy in liver surgery in 1993, several authors reported their experience [2]. The first published series dealt with relatively simple liver resections, which left major liver resection for the traditional, open approach [3]. However, with growing experience more surgeons started to perform all types of liver surgery laparoscopically [4]. Unfortunately, the scientific evidence supporting this approach is scarce [5]. In this review we have looked at the available data comparing open and laparoscopic approaches to liver resection.

Material and methods

Literature search strategies

A literature search was conducted using MEDLINE, Embase and the Cochrane Library from the inception to February 2014. Search terms were “liver” AND “laparoscopy”. All papers with English abstracts were evaluated by two authors (ALK and WMW). Relevant journals that were not well abstracted were hand-searched for full text articles and retrieved as appropriate. Overlapping search results from different databases were excluded.

Inclusion criteria and definitions

Articles were included if the English abstract contained information on comparison of the frequency of complications of open and laparoscopic liver resection, regardless of the underlying disease or study design. Randomized clinical trials, clinical controlled trials and observational studies with a control group were all considered eligible for this review.
We excluded studies evaluating techniques other than conventional laparoscopy (i.e. hand-assisted laparoscopy, robotic surgery), studies on pyogenic abscess, hydatid cyst, cystic disease and hepatolithiasis management and studies evaluating living donor hepatectomy. In order to limit our review to studies performed by highly experienced teams, we also excluded all observational studies with less than 30 patients in any of the study arms. The odds of postoperative surgical and general complications as well as oncologic results (if applicable) were compared between open and laparoscopy groups.

Statistical analysis

Binary data (odds ratio) on complications were pooled using the Mantel-Haenszel method fixed or random effect model (in the case of unexplained moderate heterogeneity) or Peto fixed methods (in the case of event rates below 1%) [6–8]. Continuous data (means with SD) were pooled using inverse variance random effects models and in cases of missing SD they were calculated (whenever possible) using the range rule. The meta-analysis was performed using the Review Manager (RevMan) computer program, version 5.2 (Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2012).
The main results are presented in the form of forest plots. For each study odds ratios with 95% CI are presented. The horizontal line represents 95% CI and the effects estimates are presented as black squares. The size of those squares represents the weight that the study has in the overall effect estimate. The pooled odds ratio with its 95% CI is displayed as a diamond at the bottom of the figure. For each meta-analysis the number of studies for which results for reported outcomes were available is summarized in Table I.
Heterogeneity between the studies was calculated using the I2 test, and it was defined as low if I2 was below 30%, moderate if I2 was up to 50%, and substantial if I2 was above 50% [9]. Heterogeneity between the studies was explored. In case of substantial heterogeneity study results were not pooled.


The first search resulted in 489 abstracts. All were revised by two authors (ALK and WMW) for the inclusion criteria. At this stage 416 abstracts were rejected. The remaining 73 studies were retrieved and evaluated in full text versions. At this stage studies were excluded because they were: studies evaluating techniques other than laparoscopy (6) or only laparoscopy with no comparison to open technique (2), studies evaluating synchronous liver and colon resections (2), hydatid cyst resections (3), pyogenic abscess management (2), liver cyst (2), living donor hepatectomies (3), meta-analysis (4), hepatolithiasis resections (3) and one study protocol. A further 31 studies were excluded because in one of the study arms there were less than 30 patients.
Sixteen studies were included in the final analysis [1, 10–24]. Three of the included studies were prospective and 13 were retrospective cohort studies. The flow chart is presented in Figure 1.

Description of included studies

Study quality was assessed using the Newcastle-Ottawa Scale part for cohort studies [25]. Three major domains were evaluated: selection of the study groups, comparability and assessment of the outcome. The maximum score that could be achieved was 9 stars. Two authors (MMB and JWM) independently assessed scale components for each study. All of the differences between authors were resolved by discussion until a consensus was reached. Table II presents the characteristics of the selected studies.
Results of the quality evaluation showed that two out of 16 studies were of good quality in all domains, 11 studies were of good quality in two domains and eight studies were of poor quality in one domain [26].
The basic characteristics of patients included in the reviewed studies are presented in Table III.

Blood loss

The difference in the mean intraoperative blood loss was evaluated in seven studies. The blood loss was significantly lower in the laparoscopy group (MD = –244.93 ml (–300.37, –189.5), p < 0.00001). Heterogeneity between the studies was low (I2 = 25%).
The study by Hu et al. was analyzed separately as they reported blood loss in grams instead of ml (40.00 g (20.35, 59.65)) [16].

Blood transfusion

Twelve studies provided data on perioperative blood transfusion for meta-analysis. The odds of blood transfusion was lower in the laparoscopy group (OR = 0.35, 95% CI: 0.20–0.61, p = 0.0002). The forest plot of odds ratio of perioperative blood transfusion is presented in Figure 2.

Positive resection margin

The odds of leaving a positive margin on pathology examination after liver resection was evaluated in eight studies. The odds of a positive margin was significantly lower in the laparoscopy group: OR = 0.22, 95% CI: 0.12–0.43, p < 0.00001). The forest plot of probability of a positive margin on pathology examination is presented in Figure 3.


Readmissions defined as admission of a patient discharged 30 days or less postoperatively were reported in three studies. The odds of readmission were lower in the laparoscopy group (OR = 0.36, 95% CI: 0.13–0.97, p = 0.04).

Pulmonary complications

Eleven studies provided data on pulmonary complications for meta-analysis. The odds of pulmonary complications were significantly lower in the laparoscopy group (OR = 0.38, 95% CI: 0.20–0.72, p = 0.003).
The forest plot of probability of perioperative pulmonary complications is presented in Figure 4.

Cardiac complications

Six studies provided data on cardiac complications for meta-analysis. The odds of cardiac complications were significantly lower in the laparoscopy group (OR = 0.30, 95% CI: 0.11–0.83, p = 0.02).

Risk of liver failure

Six studies provided data which could be used in the meta-analysis of the odds of postoperative liver failure. The odds were lower for the laparoscopy group (OR = 0.24, 95% CI: 0.10–0.58, p = 0.001). The forest plot of risk of liver failure is presented in Figure 5.


Four perioperative deaths occurred in the laparoscopic group and 18 deaths in the open group. The number of deaths was low; six studies reported no deaths, six studies reported single deaths in one or both groups, and four studies reported more than one death.

Length of stay

Data on the length of stay were available for fourteen studies. There was no difference in the length of stay between the study groups, but there was substantial heterogeneity between the studies, so their results were not pooled. The mean differences reported in the studies varied from –0.8 days (–1.66, 0.06) to –7.0 days (–8.37, –5.63) and median values varied between –1.0 day (–4.39, 2.39) and –4.0 days (–7.95, –0.05).
There was no difference between the groups in the odds of: postoperative bleeding (OR = 0.33, 95% CI: 0.08–1.33, p = 0.12), operative time (MD = –3.75 min (–16.56, 9.07), p = 0.57), bile leak (OR = 0.51, 95% CI: 0.22–1.22, p = 0.13), intraabdominal abscess formation (OR = 1, 95% CI: 0.32–3.16, p = 1.00), postoperative ascites (OR = 0.39, 95% CI: 0.14–1.07, p = 0.07), 30 days reoperation rate (OR = 0.77, 95% CI: 0.14–4.11, p = 0.76), or local recurrence (OR = 0.89, 95% CI: 0.58–1.37, p = 0.76), however in many case numbers of events reported in the studies were low.


In the recent decades we have witnessed an important rise in the indications for curative liver resections [27]. At the same time, with the advent of minimally invasive techniques, liver resection is performed by many surgeons laparoscopically [4, 28]. However, we do not have results of any randomized clinical trial directly comparing these two approaches. Results of the two ongoing trials are expected [5]. Current evidence is based on case-series and cohort studies.
At the beginning of the liver laparoscopy learning curve, the surgeons tend to choose less technically demanding resections for laparoscopy. However, the current cumulative experience in liver laparoscopy has risen to the point that we need to have a higher level of evidence to decide whether laparoscopic liver resection is equal to the open approach. According to the 2015 Morioka statement, the indication for laparoscopic liver resections depends on the technical expertise of the surgeon [29].
In the current review we have looked for papers comparing laparoscopy with the open approach to liver resection performed by highly experienced teams with at least 30 patients in each study arm. Such centers represent the best platform to compare the technique, as they have important experience in both open liver surgery and liver laparoscopy [20]. The current review has some important limitations. It was limited to English abstracts, and there were only two key words used as search terms. This approach may have resulted in missing some studies. In addition, we have not found any randomized trial, only three studies were prospective, and a significant number of studies (31) were excluded based on the number of participating patients. Also, the overall quality of the included studies was poor, with only two studies evaluated as having good quality in all domains. Furthermore, most studies did not provide definition for the outcomes reported. For several of analysed outcomes the numbers of events were low and in several studies no events were reported.
Ten studies did not report any events for the liver failure, so the effect of the surgical approach on that was also not estimable. The pooled odds ratio of postoperative liver failure for patients undergoing laparoscopic resections was significantly lower than for open resections , but this was based on small number of events reported in six studies. These are interesting findings, and one of the explanations for this phenomenon is selection bias. Even in experienced centers the surgeons tend to choose fitter patients for a technique still considered as a novelty [17]. This bias could have been eliminated by a prospective randomized trial comparing open and laparoscopic liver resections. However, as stated before, we have failed to find such a study in our review. Also, the number of the available studies is too small to perform a meta-analysis of only one type of liver resection.
Contrary to the findings on postoperative liver failure, ascites has been found with similar frequency in both groups. In the pooled studies the laparoscopy group had lower intraoperative blood loss and required less blood transfusion. This finding may be explained by an augmented surgical view offered by modern high definition laparoscopy optics, as well as meticulous surgical technique [24]. However, one study (Hu) which reported blood loss in grams showed the opposite effect in blood loss, while another study (Bhojani) which reported intra- and postoperative transfusions separately did not find a significant difference between the groups [15, 16].
The laparoscopy patients less frequently suffered from pulmonary and cardiac complications (low number of events reported in six studies). There was no difference in the frequency of intraabdominal abscess formation between the groups (low number of events reported in five studies), and the odds of postoperative bile leak and bleeding were similar in both study groups; however, the number of events was low, and most studies did not report any events, so they had no influence on the results of the meta-analysis.
The odds of a positive resection margin on pathology examination after liver resection for malignancy were lower in the laparoscopy group. Probably patient selection bias can also play a role here, as bigger tumors and/or more technically demanding cases were more frequently scheduled for open surgery. However, local recurrence rates were found to be similar in both laparoscopy and open surgery groups.
Surprisingly, operative time was similar for both groups. This probably reflects our inclusion criteria, which favored papers with at least 30 patients in each study arm. That approach eliminated papers from centers with a low laparoscopy case load. The risk of readmission was lower for the laparoscopy group, this result was based on such events reported in only 3 studies, but the risk of reoperation did not differ between the groups this was based on such events reported in only 2 studies. And finally, the length of stay in most studies was shorter in laparoscopy groups, but substantial heterogeneity precluded us from pooling the results of those studies.
In conclusion, the results of this review with meta-analysis of available data should be interpreted with caution. We have not found any randomized clinical trial on the subject. Included studies were observational, of low quality, most likely with high risk of selection bias and heterogeneous. However, the pooled results showed that the laparoscopic approach to liver resection may be at least equally safe for patients as the open technique in experienced centers.

Conflict of interest

The authors declare no conflict of interest.


1. Tranchart H, Di Giuro G, Lainas P, et al. Laparoscopic resection for hepatocellular carcinoma: a matched-pair comparative study. Surg Endosc 2010; 24: 1170-6.
2. Wayand W, Woisetschlager R. [Laparoscopic resection of liver metastasis]. Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen 1993; 64: 195-7.
3. Abdel-Atty MY, Farges O, Jagot P, Belghiti J. Laparoscopy extends the indications for liver resection in patients with cirrhosis. Br J Surg 1999; 86: 1397-400.
4. Vibert E, Kouider A, Gayet B. Laparoscopic anatomic liver resection. HPB 2004; 6: 222-9.
5. Rao AM, Ahmed I. Laparoscopic versus open liver resection for benign and malignant hepatic lesions in adults. Cochrane Database Syst Rev 2013; 5: CD010162.
6. Greenland S, Robins JM. Estimation of a common effect parameter from sparse follow-up data. Biometrics 1985; 41: 55-68.
7. Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959; 22: 719-48.
8. Yusuf S, Peto R, Lewis J, Collins R, Sleight P. Beta blockade during and after myocardial infarction: an overview of the randomized trials. Progress Cardiovasc Dis 1985; 27: 335-71.
9. Higgins JPT, Green S, Cochrane Collaboration. Cochrane handbook for systematic reviews of interventions. Chichester, England; Hoboken, NJ: Wiley-Blackwell; 2009; 649.
10. Cheung TT, Poon RT, Yuen WK, et al. Long-term survival analysis of pure laparoscopic versus open hepatectomy for hepatocellular carcinoma in patients with cirrhosis: a single-center experience. Ann Surg 2013; 257: 506-11.
11. Guerron AD, Aliyev S, Agcaoglu O, et al. Laparoscopic versus open resection of colorectal liver metastasis. Surg Endosc 2013; 27: 1138-43.
12. Tranchart H, Di Giuro G, Lainas P, et al. Laparoscopic liver resection with selective prior vascular control. Am J Surg 2013; 205: 8-14.
13. Cannon RM, Scoggins CR, Callender GG, McMasters KM, Martin RC 2nd. Laparoscopic versus open resection of hepatic colorectal metastases. Surgery 2012; 152: 567-74.
14. Slim A, Garancini M, Di Sandro S, et al. Laparoscopic versus open liver surgery: a single center analysis of post-operative in-hospital and post-discharge results. Langenbeck’s Arch Surg 2012; 397: 1305-11.
15. Bhojani FD, Fox A, Pitzul K, et al. Clinical and economic comparison of laparoscopic to open liver resections using a 2-to-1 matched pair analysis: an institutional experience. J Am Coll Surg 2012; 214: 184-95.
16. Hu BS, Chen K, Tan HM, Ding XM, Tan JW. Comparison of laparoscopic vs open liver lobectomy (segmentectomy) for hepatocellular carcinoma. World J Gastroenterol 2011; 17: 4725-8.
17. Abu Hilal M, Di Fabio F, Teng MJ, Lykoudis P, Primrose JN, Pearce NW. Single-centre comparative study of laparoscopic versus open right hepatectomy. J Gastrointest Surg 2011; 15: 818-23.
18. Ito K, Ito H, Are C, et al. Laparoscopic versus open liver resection: a matched-pair case control study. J Gastrointest Surg 2009; 13: 2276-83.
19. Belli G, Limongelli P, Fantini C, et al. Laparoscopic and open treatment of hepatocellular carcinoma in patients with cirrhosis. Br J Surg 2009; 96: 1041-8.
20. Castaing D, Vibert E, Ricca L, Azoulay D, Adam R, Gayet B. Oncologic results of laparoscopic versus open hepatectomy for colorectal liver metastases in two specialized centers. Ann Surg 2009; 250: 849-55.
21. Cai XJ, Yang J, Yu H, et al. Clinical study of laparoscopic versus open hepatectomy for malignant liver tumors. Surg Endosc 2008; 22: 2350-6.
22. Koffron AJ, Auffenberg G, Kung R, Abecassis M. Evaluation of 300 minimally invasive liver resections at a single institution: less is more. Ann Surg 2007; 246: 385-94.
23. Morino M, Morra I, Rosso E, Miglietta C, Garrone C. Laparoscopic vs open hepatic resection: a comparative study. Surg Endosc 2003; 17: 1914-8.
24. Topal B, Fieuws S, Aerts R, Vandeweyer H, Penninckx F. Laparoscopic versus open liver resection of hepatic neoplasms: comparative analysis of short-term results. Surg Endosc 2008; 22: 2208-13.
25. Wells GA, Shea B, O’Connell D, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. Ottawa Health Research Institute: Ottawa Health Research Institute; 2014 [cited 2014 30/Aug/2014]. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.htm.
26. McPheeters ML, Kripalani S, Peterson NB, et al. Closing the quality gap: revisiting the state of the science (vol. 3: quality improvement interventions to address health disparities). Evidence Report/Technology Assessment 2012 (208.3): 1-475.
27. Treska V, Skalicky T, Sutnar A, et al. Prognostic importance of some clinical and therapeutic factors for the effect of portal vein embolization in patients with primarily inoperable colorectal liver metastases. Arch Med Sci 2013; 9: 47-54.
28. Alba Mesa F, Amaya Cortijo A, Romero Fernandez JM, et al. Transvaginal sigmoid cancer resection: first case with 12 months of follow-up--technique description. J Laparoendosc Adv Surg Techn A 2012; 22: 587-90.
29. Wakabayashi G, Cherqui D, Geller DA, et al. Recommendations for laparoscopic liver resection: a report from the second international consensus conference held in Morioka. Ann Surg 2015; 261: 619-29.
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