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Obesity and postoperative outcomes of the patients with laparoscopic adrenalectomy: a systematic review and meta-analysis

Abstract

Background

Studies have suggested differences in postoperative outcomes between patients with obesity and those without following adrenalectomy, but these remained to be ascertained with synthesis of available evidence. The aim of this systematic review and meta-analysis was to investigate the association between obesity and outcomes of patients after laparoscopic adrenalectomy.

Methods

We searched EMBASE, PubMed, Global Index Medicus, and Web of Science, without language restriction, to identify cohort studies published between January 1, 2000 and November 6, 2019. We considered studies with data comparing outcomes of adults with and without obesity after laparoscopic adrenalectomy. Random-effects meta-analysis was used to pool study-specific estimates. This review was registered with PROSPERO, CRD42018117070.

Results

Five studies with data on a pooled sample of 353 patients with obesity and 828 without were included in the meta-analysis. The risk of bias was moderate to low. We found no association between obesity and the various stages of postoperative complications: Clavien-Dindo grade 1 (OR = 1.57; 95%CI = 0.55–4.48; I2 = 44.6%), grade 2 (OR = 1.12; 95%CI = 0.54–2.32; I2 = 0.0%), grade 3 (OR = 1.79; 95%CI = 0.58–5.47; I2 = 0.0%;), grade 4 (OR = 0.43; 95%CI = 0.05–3.71; I2 = 0.0%), and grade 5 (death) (OR = 0.43; 95% CI = 0.02–14.31). Furthermore, no association was found between obesity and readmission rates (OR = 0.7; 95% CI = 0.13–3.62) and conversion of laparoscopic to open surgery (OR = 0.62; 95% CI = 0.16–2.34; I2 = 19.5%).

Conclusions

This study suggests that obesity is not associated with complications following laparoscopic adrenalectomy. This meta-analysis might have been underpowered to detect a true association between obesity and patient outcome after laparoscopic adrenalectomy due to the small number of included studies. Larger studies are needed to clarify the role of obesity in patients undergoing laparoscopic adrenalectomy.

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Background

Obesity is a global public health concern, with rising prevalence over the last forth decade [1,2,3,4]. Low- and middle-income countries are experiencing an epidemiologic transition from communicable to chronic non-communicable diseases [3]. Hypertension, diabetes, tobacco, and obesity are among the leading risk factors for non-communicable disease [3, 4]. According to the World Health Organization (WHO), over 1.9 billion adults were overweight in 2016 [2, 5]. Of these over 650 million were obese. Moreover, 39% of adults aged 18 years and over were overweight and 13% were obese during the same year [2, 5]. Thus, obesity represents a global public health and clinical concern face by teams working in both the medical and surgical fields.

The role of obesity in the outcome of patients after surgery in general, and after abdominal and adrenal surgery in particular is unclear [6,7,8,9,10,11,12]. Some studies suggested that obesity has a detrimental effect on the outcomes of patients after abdominal surgery [8, 13,14,15]. It is argued that patients with obesity would have higher postoperative morbidity than patients without [16,17,18]. On the other hand, other studies evoked the absence of association between obesity and occurrence of post-operative complication, and even a protective effect of obesity on postoperative mortality after digestive surgery, and this phenomenon has been named the ‘obesity paradox’ [7, 19, 20]. Unfortunately, most of these studies either focused on surgery of intraperitoneal organs or a particular type of surgery (cancer surgery or bariatric surgery), leaving aside the surgical procedures of retro-peritoneal structures such as adrenal glands and benign tumors.

Adrenal glands are two retroperitoneal structures located on the kidneys, divided in two part: cortex and medulla [21]. Tumors such as adenomas and adrenocortical carcinomas that need surgical interventions can originate from the adrenal glands [22]. During the last two decades, surgery of adrenal gland has been widely vulgarized, and the number of published studies on this topic has increased significantly. This phenomenon is partly due to the ageing of the global population and improved access to modern medical imaging such as computed tomography and magnetic resonance imaging which allow a more frequent fortuitous discovery of adrenal tumors named incidentalomas [23,24,25,26,27]. These tumors are among the most common indications of adrenalectomies, regardless of the suspected histological nature [28]. Laparoscopic surgery has gradually replaced open surgery as gold standard for the management of adrenal tumors [17, 29,30,31,32,33]. Although indications for this approach were initially limited to benign tumors, they gradually expanded to include malignant tumors, making laparoscopy the preferred approach for adrenal gland surgery [30,31,32, 34, 35]. However, laparoscopic adrenalectomy is said to be technically difficult in patients with obesity given the retroperitoneal localization of adrenal glands. Furthermore, several recent studies suggested a difference in outcome of patients having laparoscopic adrenalectomy when stratified according to obesity status [17, 20]. Hitherto, no study has ascertained this hypothesis by the mean of a meta-analysis of available published data. With the increased number of adrenal gland surgery worldwide, performed especially in obese patients, there is a need to generate reliable evidence on the effect of obesity on patient outcome following laparoscopic adrenalectomy. Thus, the present systematic review and meta-analysis aimed at assessing the association between obesity and postoperative outcomes of patients after laparoscopic adrenalectomy.

Methods

This review was registered in the International Prospective Register of Systematic Reviews (PROSPERO) under the registration number CRD42018117070. We used Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines as template for reporting this systematic review with meta-analysis [36].

Search strategy and selection criteria

Global Index Medicus, Excerpta Medica Database (EMBASE), Medline through PubMed, and Web of Science (Web of Science Core Collection, Current Contents Connect, KCI-Korean Journal Database, SciELO Citation Index, Russian Science Citation Index) were searched to identify studies published between January 1, 2000 and November 6, 2019. No language restriction was applied. The initial search strategy was designed for EMBASE and was adapted for use in other databases (Supplementary Table 1). The search strategy was based on the combination of relevant text words and medical subject headings related to adrenalectomy and obesity. Moreover, the references of all relevant articles found were scrutinized for potential additional data sources. For studies published in more than one report, the one reporting the largest sample size was considered.

Our population of interest was patients with adrenalectomy regardless of age, sex, and geographic location. Exposure considered for this review was obesity defined as body mass index (BMI) ≥ 30 Kg/m2 or central obesity for waist circumference or waist-to-hip ratio as per WHO guidelines or according to country specific guidelines [5, 37]. Outcomes of interest included overall deaths, surgical site infection, conversion from laparoscopy to open surgery, and complications classified according to Clavien-Dindo grades [38]. We considered prospective and retrospective cohort studies. We excluded letters, reviews, commentaries, editorials, studies lacking key data and/or explicit method description as well as studies in which relevant data on obesity and outcomes of patients after adrenalectomy was not possible to extract even after contacting the corresponding author.

Two reviewers (CD and VNA) independently screened the titles and abstract of articles for eligibility. Full texts of potentially eligible articles were retrieved and screened for final inclusion. Disagreements between the two reviewers were solved by discussion and when a consensus was not reached, a third reviewer (JJB) resolved discrepancies.

Data synthesis and analysis

A standardized data extraction sheet was used by two reviewers (VNA and CD) to independently extract data from individual studies. The last name of the first author, year of publication, country, study design, sample size, mean or median age, proportion of males, mean/median duration of hospital stay, mean/median BMI, mean/median WC, definition of obesity, total number of obese and non-obese patients included, number of patients with outcomes of interest.

A meta-analysis was used to summarize evidence. Study-specific estimates were pooled through a Dersimonian and Laird random-effects meta-analysis model to obtain an overall summary estimate with inverse variance method [39]. Odds ratio (OR), with their 95% confidence interval (95%CI), was used as the effect size. The presence of heterogeneity was assessed with the χ2 test of Cochrane and, quantified by I2 values, assuming that I2 of 25, 50 and 75% represent low, medium and high heterogeneity respectively [40]. A p value < 0.05 was indicative of significant difference. Inter-rater agreement for study inclusion was assessed using Cohen’s κ coefficient [41]. The methodological quality of included study was assessed by two reviewers (VNA and CD) using an adapted version of the risk of bias in non-randomized studies of interventions (Supplementary Table 2) [42].

Results

Study selection

In total, 387 citations were identified from database searches. Twenty-four eligible full texts were assessed for eligibility after duplicate citations have been removed and records eliminated following screening of title and abstract. Five studies met the inclusion criteria and were included in this systematic review and meta-analysis [20, 43,44,45,46]. Supplementary Figure 1 displays the process of study selection including the reasons of study exclusion of full texts assessed for eligibility. The Cohen’s coefficients for the inclusion of studies based on titles and abstract and full text were 0.91 and 0.94, respectively.

Characteristics of included studies

Studies included were published between 2011 and 2018 and conducted between 1997 and 2016. Studies were from China, Japan, Norway, Poland, and USA; one study per country. The timing of data collection was retrospective for three studies, prospective for one, and unclear for one study. All studies considered adult participants (≥ 18 years) with the mean/median age varying from 44 to 59 years for patients with obesity and from 49 to 57 years for those without. Male proportion varied from 29.3 to 54.0% in patients with obesity and from 33.1 to 54.8% for those without obesity. The mean duration for surgical procedures varied from 1.5 to 3.8 h for patients with obesity and from 1.2 to 3.5 h for non-obese patients. The mean duration for hospital staying after surgery varied from 2 to 6 days for participants with obesity and from 1 to 6 days for non-obese ones. All studies defined obesity with BMI ≥ 30 mg/m2. There were various indications for adrenalectomy (Supplementary Table 3).

For all the five included studies, there was high risk of confounding bias for one study, high risk for selection bias in two studies, high risk of bias due to missing data in one study. All studies had low risk of classification bias and unclear risk of bias in outcome measurement (Supplementary Figure 2).

Postoperative complications of laparoscopic adrenalectomy

In total, five studies were included for this analysis [20, 43,44,45,46]. There was no association between obesity and all Clavien-Dindo grades for postoperative complications (Fig. 1): Clavien-Dindo grade 1 (OR 1.57; 95%CI: 0.55–4.48), Clavien-Dindo grade 2 (OR 1.12; 95%CI: 0.54–2.32), Clavien-Dindo garde 3 (OR 1.79; 95%CI: 0.58–5.47), Clavien-Dindo grade 4 (OR 0.43; 95%CI: 0.05–3.71), and Clavien-Dindo grade (death) 5 (OR 0.43; 95%CI: 0.02–14.31). Three out of five study reported no difference in intervention time between patients with and those without obesity. Furthermore, there was no substantial heterogeneity for all these analyses.

Fig. 1
figure 1

Meta-analysis of postoperative complications after laparoscopic adrenalectomy in patients with and without obesity

Conversion from laparoscopic to open adrenalectomy

Three studies were eligible for this analysis [43, 45, 46]. There was no association between obesity and conversion of laparoscopy to open adrenalectomy (OR 1.07; 95%CI: 0.34–3.35) (Fig. 2).

Fig. 2
figure 2

Association between obesity and conversion from laparoscopic to open surgery and readmission within 30 days after surgery

Readmission within 30 days after surgery

One study provided data on readmission as a complication of laparoscopic adrenalectomy [46]. We found no association between obesity and the risk of readmission within 30 days of surgery (OR 0.7; 95%CI: 0.13–3.62) (Fig. 2).

Discussion

From five cohort studies with 353 patients with obesity and 828 without obesity, we found that obesity was not associated with the occurrence of postoperative complications, risk of death, conversion during laparoscopic adrenalectomy to open surgery and, the readmission within 30 days after surgery. Definitively, evidence suggesting that obesity is a risk factor for increased postoperative morbidity during and after surgery are contradictory [6, 11, 16, 19, 47, 48].

The observed absence of difference in outcome between obese and non-obese patients following laparoscopic adrenalectomy is probably multifactorial and related to the timing of this type of surgery, mechanical constraints and postoperative management [33, 49]. In fact, laparoscopic adrenalectomy is usually performed as a planned surgery. Thus, tailored preoperative preparation can be done to minimize the surgical risk by taking into consideration the particularity of each patient in terms of co-morbidities and obesity [50, 51]. Furthermore, during laparoscopic adrenalectomy, parietal thickness is not really a major factor. Regardless of wall thickness, the incision is minimal and is associated with minimal exposure and manipulation of subcutaneous tissue and muscle, reducing the risk of post-operative infection and pain, regardless of BMI [7, 52]. Moreover, after a laparoscopic adrenalectomy, feeding is quickly resumed and rapid recovery is expected for both obese and non-obese patients [53]. Which reduced significantly the risk of complication related to prolong bed rest and fasting in patients with obesity.

One of the most important elements related to patient outcomes during and after laparoscopic surgery is the visceral fat mass rather than obesity estimated with BMI [54,55,56]. It is argued that some populations such as Asians may have a BMI in the normal range, but a high visceral fat content that may compromise the per- and postoperative outcomes [55]. Because laparoscopic adrenalectomy is performed within the intracorporeal field, it is more sensitive to element that can modify intra or retroperitoneal environment like visceral fat. This may explain why we observed to evidence of an association between BMI and patient outcome following laparoscopic adrenalectomy when stratified according to obesity status, but a difference may be observe if those patients are stratified instead according to their visceral fat mass [55, 57, 58].

Our findings were similar to those of previous studies which found no difference in post-operative outcomes between patients with and without obesity after digestive tract surgery [10, 48, 59, 60], gynecologic surgery [61, 62], vascular surgery [63, 64], neurosurgery [9], or orthopedic surgery [12, 65, 66], even among those admitted in intensive care unit [67]. In most of these studies, a minimal invasive surgical method was used like in studies included in the current meta-analysis, allowing less damages for surrounding tissues, rapid post-operative rehabilitation,

Elsewhere, an increased risk of morbidity in postoperative period in patients with obesity has been widely documented in recent years in both oncology and non-oncology surgery. In the field of oncological surgery of the digestive tract, recent studies suggested obesity as risk factor of postoperative complications such as anastomosis leakage, surgical site infection, cardiovascular complications, however without an increased risk of mortality [7, 14, 15, 18, 19].

The results of this meta-analysis should be considered in the context of some limitations. The first is the small number of studies included in the meta-analysis. Indeed, only five were eligible for the meta-analysis. Therefore, this study might have been underpowered to detect an association if one truly exists. The high cost related to equipment necessary for laparoscopic surgery could explain the low number of eligible studies done in low-incomes countries; this can hinder the generalizability of the findings. However, this is the first systematic review and meta-analysis to summarized current evidence on the effect of obesity on outcome of patients after laparoscopic surgery. No substantial heterogeneity was found in all analyses.

Conclusions

This study suggests that obesity is not associated with adverse outcomes following laparoscopic adrenalectomy. However, larger scale studies are needed to ascertain the impact of obesity on postoperative outcomes among patients undergoing adrenalectomy.

Availability of data and materials

All data generated or analyzed during this study are included in this published article and its supplementary information files.

Abbreviations

BMI:

Body mass index

WHO:

World Health Organization

References

  1. Berghöfer A, Pischon T, Reinhold T, Apovian CM, Sharma AM, Willich SN. Obesity prevalence from a European perspective: a systematic review. BMC Public Health. 2008;8(1):200.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Obesity and overweight [Internet]. [cited 2019 Feb 13]. Available from: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight.

  3. National Research Council (US). The Continuing Epidemiological Transition in Sub-Saharan Africa: A Workshop Summary. Washington (DC): National Academies Press (US); 2012. [cited 2019 Feb 11]. (The National Academies Collection: Reports funded by National Institutes of Health). Available from: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/books/NBK105418/.

    Google Scholar 

  4. Tremmel M, Gerdtham U-G, Nilsson PM, Saha S. Economic burden of obesity: a systematic literature review. Int J Environ Res Public Health. 2017;19:14(4).

    Google Scholar 

  5. Obesity and overweight [Internet]. World Health Organization. [cited 2018 Nov 11]. Available from: http://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight.

  6. Pan W, Sun Z, Xiang Y, Fang W. The correlation between high body mass index and survival in patients with esophageal cancer after curative esophagectomy: evidence from retrospective studies. Asia Pac J Clin Nutr. 2015;24(3):480–8.

    CAS  PubMed  Google Scholar 

  7. Mullen JT, Moorman DW, Davenport DL. The obesity paradox: body mass index and outcomes in patients undergoing nonbariatric general surgery. Ann Surg. 2009;250(1):166–72.

    Article  PubMed  Google Scholar 

  8. Hussan H, Gray DM, Hinton A, Krishna SG, Conwell DL, Stanich PP. Morbid obesity is associated with increased mortality, surgical complications, and incremental health care utilization in the Peri-operative period of colorectal Cancer surgery. World J Surg. 2016;40(4):987–94.

    Article  PubMed  Google Scholar 

  9. Schultheiss KE, Jang YG, Yanowitch RN, Tolentino J, Curry DJ, Lüders J, et al. Fat and neurosurgery: does obesity affect outcome after intracranial surgery? Neurosurgery. 2009;64(2):316–26 discussion 326-327.

    Article  PubMed  Google Scholar 

  10. Chisholm JA, Jamieson GG, Lally CJ, Devitt PG, Game PA, Watson DI. The effect of obesity on the outcome of laparoscopic antireflux surgery. J Gastrointest Surg Off J Soc Surg Aliment Tract. 2009;13(6):1064–70.

    Article  Google Scholar 

  11. He Y, Wang J, Bian H, Deng X, Wang Z. BMI as a predictor for perioperative outcome of laparoscopic colorectal surgery: a pooled analysis of comparative studies. Dis Colon Rectum. 2017;60(4):433–45.

    Article  PubMed  Google Scholar 

  12. Cavaignac E, Lafontan V, Reina N, Pailhé R, Wargny M, Warmy M, et al. Obesity has no adverse effect on the outcome of unicompartmental knee replacement at a minimum follow-up of seven years. Bone Jt J. 2013;95-B(8):1064–8.

    Article  CAS  Google Scholar 

  13. Duan X-F, Tang P, Shang X-B, Jiang H-J, Zhao Q, Yu Z-T. High body mass index worsens survival in patients with esophageal squamous cell carcinoma after Esophagectomy. Dig Surg. 2017;34(4):319–27.

    Article  PubMed  Google Scholar 

  14. Mathur AK, Ghaferi AA, Osborne NH, Pawlik TM, Campbell DA, Englesbe MJ, et al. Body mass index and adverse perioperative outcomes following hepatic resection. J Gastrointest Surg Off J Soc Surg Aliment Tract. 2010;14(8):1285–91.

    Article  Google Scholar 

  15. Zhang SS, Yang H, Luo KJ, Huang QY, Chen JY, Yang F, et al. The impact of body mass index on complication and survival in resected oesophageal cancer: a clinical-based cohort and meta-analysis. Br J Cancer. 2013;109(11):2894–903.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Ri M, Aikou S, Seto Y. Obesity as a surgical risk factor. Ann Gastroenterol Surg. 2017;2(1):13–21.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Fazeli-Matin S, Gill IS, Hsu TH, Sung GT, Novick AC. Laparoscopic renal and adrenal surgery in obese patients: comparison to open surgery. J Urol. 1999;162(3 Pt 1):665–9.

    Article  CAS  PubMed  Google Scholar 

  18. Struecker B, Biebl M, Dadras M, Chopra S, Denecke C, Spenke J, et al. The impact of obesity on outcomes following resection for gastric Cancer. Dig Surg. 2017;34(2):133–41.

    Article  PubMed  Google Scholar 

  19. Mullen JT, Davenport DL, Hutter MM, Hosokawa PW, Henderson WG, Khuri SF, et al. Impact of body mass index on perioperative outcomes in patients undergoing major intra-abdominal cancer surgery. Ann Surg Oncol. 2008;15(8):2164–72.

    Article  PubMed  Google Scholar 

  20. Kazaryan AM, Marangos IP, Røsok BI, Rosseland AR, Edwin B. Impact of body mass index on outcomes of laparoscopic adrenal surgery. Surg Innov. 2011;18(4):358–67.

    Article  PubMed  Google Scholar 

  21. Cesmebasi A, Du Plessis M, Iannatuono M, Shah S, Tubbs RS, Loukas M. A review of the anatomy and clinical significance of adrenal veins. Clin Anat N Y N. 2014;27(8):1253–63.

    Article  Google Scholar 

  22. Delozier OM, Stiles ZE, Deschner BW, Drake JA, Deneve JL, Glazer ES, et al. Implications of Conversion during Attempted Minimally Invasive Adrenalectomy for Adrenocortical Carcinoma. Ann Surg Oncol. 2020. https://0-link-springer-com.brum.beds.ac.uk/article/10.1245/s10434-020-08824-9#citeas.

  23. Chatzellis E, Kaltsas G. Adrenal Incidentalomas. In: De Groot LJ, Chrousos G, Dungan K, Feingold KR, Grossman A, Hershman JM, et al., editors. Endotext. South Dartmouth: MDText.com, Inc.; 2000. [cited 2018 Nov 11]. Available from: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/books/NBK279021/.

    Google Scholar 

  24. O’Sullivan JW, Muntinga T, Grigg S, Ioannidis JPA. Prevalence and outcomes of incidental imaging findings: umbrella review. BMJ. 2018;361:k2387.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Kastelan D, Kraljevic I, Dusek T, Knezevic N, Solak M, Gardijan B, et al. The clinical course of patients with adrenal incidentaloma: is it time to reconsider the current recommendations? Eur J Endocrinol. 2015;173(2):275–82.

    Article  CAS  PubMed  Google Scholar 

  26. Hitzeman N, Cotton E. Incidentalomas: initial management. Am Fam Physician. 2014;90(11):784–9.

    PubMed  Google Scholar 

  27. Gheorghisan-Galateanu AA, Carsote M, Valea A. Incidentaloma: from general practice to specific endocrine frame. JPMA J Pak Med Assoc. 2017;67(6):917–22.

    PubMed  Google Scholar 

  28. Azzi AS, Driessens N. Adrenal disease diagnosis: management of adrenal incidentaloma. Rev Med Brux. 2017;38(4):325–33.

    CAS  PubMed  Google Scholar 

  29. Aziz O, Athanasiou T, Tekkis PP, Purkayastha S, Haddow J, Malinovski V, et al. Laparoscopic versus open appendectomy in children: a meta-analysis. Ann Surg. 2006;243(1):17–27.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Chiang PH, Yu CJ, Lee WC, Wang HJ, Hsu WC. Comparison of retroperitoneoscopic and transperitoneal laparoscopic adrenalectomy for right-sided benign tumors: a single-institute experience. Urol Int. 2015;94(2):144–8.

    Article  PubMed  Google Scholar 

  31. Shen ZJ, Chen SW, Wang S, Jin XD, Chen J, Zhu Y, et al. Predictive factors for open conversion of laparoscopic Adrenalectomy: a 13-year review of 456 cases. J Endourol. 2007;21(11):1333–8.

    Article  CAS  PubMed  Google Scholar 

  32. Maestroni U, Vicente D, Del Rio P, Ziglioli F, Dinale F, Campobasso D, et al. Laparoscopic adrenalectomy for large adrenal masses: a challenge or a routine? Minerva Chir. 2014;69(2):59–64.

    CAS  PubMed  Google Scholar 

  33. Mellon MJ, Sethi A, Sundaram CP. Laparoscopic adrenalectomy: Surgical techniques. Indian J Urol IJU J Urol Soc India. 2008;24(4):583–9.

    Article  Google Scholar 

  34. Popov Z, Jankulovski N, Stankov O, Stavridis S, Saidi S, Kuzmanoski M, et al. Laparoscopic Adrenalectomy: first single-center experience in the Balkans. Pril Makedon Akad Na Nauk Umet Oddelenie Za Med Nauki. 2015;36(3):27–33.

    Google Scholar 

  35. Hirano D, Hasegawa R, Igarashi T, Satoh K, Mochida J, Takahashi S, et al. Laparoscopic adrenalectomy for adrenal tumors: a 21-year single-institution experience. Asian J Surg. 2015;38(2):79–84.

    Article  PubMed  Google Scholar 

  36. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097.

    Article  PubMed  PubMed Central  Google Scholar 

  37. World Health Organization. Waist circumference and waist-hip ratio: report of a WHO expert consultation, Geneva, 8–11 December 2008. Geneva: World Health Organization; 2011.

    Google Scholar 

  38. Dindo D, Demartines N, Clavien P-A. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240(2):205–13.

    Article  PubMed  PubMed Central  Google Scholar 

  39. DerSimonian R, Laird N. Meta-analysis in clinical trials revisited. Contemp Clin Trials. 2015;45(Pt A):139–45.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Higgins JPT, Altman DG, Gøtzsche PC, Jüni P, Moher D, Oxman AD, et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011;343:d5928.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Viera AJ, Garrett JM. Understanding interobserver agreement: the kappa statistic. Fam Med. 2005;37(5):360–3.

    PubMed  Google Scholar 

  42. Risk of bias tools - ROBINS-I tool [Internet]. [cited 2019 Mar 12]. Available from: https://sites.google.com/site/riskofbiastool/welcome/home.

  43. Dancea HC, Obradovic V, Sartorius J, Woll N, Blansfield JA. Increased complication rate in obese patients undergoing laparoscopic Adrenalectomy. JSLS. 2012;16(1):45–9.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Hu Q, Hang Z, Ho Y, Sun C, Xu K, Xia G, et al. Impact of obesity on perioperative outcomes of retroperitoneal laparoscopic Adrenalectomy. Urol Int. 2015;95(3):361–6.

    Article  PubMed  Google Scholar 

  45. Inaishi T, Kikumori T, Takeuchi D, Ishihara H, Miyajima N, Shibata M, et al. Obesity does not affect peri- and postoperative outcomes of transabdominal laparoscopic adrenalectomy. Nagoya J Med Sci. 2018;80(1):21–8.

    PubMed  PubMed Central  Google Scholar 

  46. Pędziwiatr M, Major P, Pisarska M, Natkaniec M, Godlewska M, Przęczek K, et al. Laparoscopic transperitoneal adrenalectomy in morbidly obese patients is not associated with worse short-term outcomes. Int J Urol Off J Jpn Urol Assoc. 2017;24(1):59–63.

    Google Scholar 

  47. Bregendahl S, Nørgaard M, Laurberg S, Jepsen P. Risk of complications and 30-day mortality after laparoscopic and open appendectomy in a Danish region, 1998-2007; a population-based study of 18,426 patients. Pol Przegl Chir. 2013;85(7):395–400.

    Article  PubMed  Google Scholar 

  48. Miao L, Chen H, Xiang J, Zhang Y. A high body mass index in esophageal cancer patients is not associated with adverse outcomes following esophagectomy. J Cancer Res Clin Oncol. 2015;141(5):941–50.

    Article  PubMed  Google Scholar 

  49. Gill IS. The case for laparoscopic adrenalectomy. J Urol. 2001;166(2):429–36.

    Article  CAS  PubMed  Google Scholar 

  50. Mullen MG, Michaels AD, Mehaffey JH, Guidry CA, Turrentine FE, Hedrick TL, et al. Risk associated with complications and mortality after urgent surgery vs elective and emergency surgery: implications for defining “quality” and reporting outcomes for urgent surgery. JAMA Surg. 2017;152(8):768–74.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Havens JM, Peetz AB, Do WS, Cooper Z, Kelly E, Askari R, et al. The excess morbidity and mortality of emergency general surgery. J Trauma Acute Care Surg. 2015;78(2):306–11.

    Article  PubMed  Google Scholar 

  52. Alfa-Wali M, Osaghae S. Practice, training and safety of laparoscopic surgery in low and middle-income countries. World J Gastrointest Surg. 2017;9(1):13–8.

    Article  PubMed  PubMed Central  Google Scholar 

  53. TAUPYK Y, CAO X, ZHAO Y, WANG C, WANG Q. Fast-track laparoscopic surgery: a better option for treating colorectal cancer than conventional laparoscopic surgery. Oncol Lett. 2015;10(1):443–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  54. Erbil Y, Barbaros U, Sari S, Agcaoglu O, Salmaslioglu A, Ozarmagan S. The effect of retroperitoneal fat mass on surgical outcomes in patients performing laparoscopic adrenalectomy: the effect of fat tissue in adrenalectomy. Surg Innov. 2010;17(2):114–9.

    Article  PubMed  Google Scholar 

  55. Tsujinaka S, Konishi F, Kawamura YJ, Saito M, Tajima N, Tanaka O, et al. Visceral obesity predicts surgical outcomes after laparoscopic colectomy for sigmoid colon cancer. Dis Colon Rectum. 2008;51(12):1757–65 discussion 1765-1767.

    Article  PubMed  Google Scholar 

  56. Yanishi M, Kinoshita H, Koito Y, Taniguchi H, Mishima T, Sugi M, et al. Adherent Perinephric fat is a surgical risk factor in laparoscopic single-site donor nephrectomy: analysis using Mayo adhesive probability score. Transplant Proc. 2020;52(1):84–8.

    Article  PubMed  Google Scholar 

  57. Ishii Y, Hasegawa H, Nishibori H, Watanabe M, Kitajima M. Impact of visceral obesity on surgical outcome after laparoscopic surgery for rectal cancer. Br J Surg. 2005;92(10):1261–2.

    Article  CAS  PubMed  Google Scholar 

  58. Evaluation of the technical difficulty performing laparoscopic resection of a rectosigmoid carcinoma: visceral fat reflects technical difficulty more accurately than body mass index [Internet]. springermedizin.de. [cited 2019 Aug 14]. Available from: https://www.springermedizin.de/evaluation-of-the-technical-difficulty-performing-laparoscopic-r/8531170.

  59. Salem AI, Thau MR, Strom TJ, Abbott AM, Saeed N, Almhanna K, et al. Effect of body mass index on operative outcome after robotic-assisted Ivor-Lewis esophagectomy: retrospective analysis of 129 cases at a single high-volume tertiary care center. Dis Esophagus Off J Int Soc Dis Esophagus. 2017;30(1):1–7.

    Google Scholar 

  60. Blom RLGM, Lagarde SM, Klinkenbijl JHG, Busch ORC, van Berge Henegouwen MI. A high body mass index in esophageal cancer patients does not influence postoperative outcome or long-term survival. Ann Surg Oncol. 2012;19(3):766–71.

    Article  CAS  PubMed  Google Scholar 

  61. Wysham WZ, Kim KH, Roberts JM, Sullivan SA, Campbell SB, Roque DR, et al. Obesity and perioperative pulmonary complications in robotic gynecologic surgery. Am J Obstet Gynecol. 2015;213(1):33.e1–7.

    Article  Google Scholar 

  62. Bohlin KS, Ankardal M, Nüssler E, Lindkvist H, Milsom I. Factors influencing the outcome of surgery for pelvic organ prolapse. Int Urogynecology J. 2018;29(1):81–9.

    Article  Google Scholar 

  63. Saratzis A, Saedon M, Melas N, Kitas GD, Mahmood A. Obesity as an independent predictor of outcome after endovascular abdominal aortic aneurysm repair. Ann Vasc Surg. 2014;28(4):816–22.

    Article  PubMed  Google Scholar 

  64. Shahabuddin S, Perveen S, Furnaz S, Fatimi S, Sami S, Sharif H. Body mass index--predictor of outcome after coronary artery bypass grafting. Asian Cardiovasc Thorac Ann. 2013;21(2):176–80.

    Article  PubMed  Google Scholar 

  65. Plate JF, Augart MA, Seyler TM, Bracey DN, Hoggard A, Akbar M, et al. Obesity has no effect on outcomes following unicompartmental knee arthroplasty. Knee Surg Sports Traumatol Arthrosc Off J ESSKA. 2017;25(3):645–51.

    Article  Google Scholar 

  66. Shetty GM, Mullaji AB, Bhayde S, Lingaraju AP. No effect of obesity on limb and component alignment after computer-assisted total knee arthroplasty. Knee. 2014;21(4):862–5.

    Article  PubMed  Google Scholar 

  67. Gupta R, Villa M, Agaba E, Ritter G, Sison C, Marini CP, et al. The effect of body mass index on the outcome of critically ill surgical patients. JPEN J Parenter Enteral Nutr. 2013;37(3):368–74.

    Article  PubMed  Google Scholar 

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This review received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

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CD and JJB conceived the idea of the study and developed the protocol with VNA. JJB and CD did the literature search. CD and VNA selected the studies. CD and VNA extracted the relevant information. JJB synthesized the data. CD and VNA wrote the first draft of the paper. CD, VNA and JJB critically revised successive drafts of the paper and approved the final version. CD and JJB are the guarantors of the review. All Authors read and approved the final version of the manuscript.

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Correspondence to Celestin Danwang.

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Danwang, C., Agbor, V.N. & Bigna, J.J. Obesity and postoperative outcomes of the patients with laparoscopic adrenalectomy: a systematic review and meta-analysis. BMC Surg 20, 194 (2020). https://0-doi-org.brum.beds.ac.uk/10.1186/s12893-020-00848-y

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