To date, numerous studies have sought to identify reliable predictors of developing postoperative complications; demanding challenges for general thoracic surgeons in their daily practice [1, 2]. Oesophagectomy, both for benign and malignant diseases, is a complex surgical procedure characterized by relevant rates of mortality and morbidity, along with the worse quality of life [3, 4]. Although current postoperative mortality is <5% at high-volume centres, major complications remain significant, from 26% to 31% [5]. These translate into longer hospital stays and higher overall patient costs, which increase according to their severity [6]. Finally, the overall morbidity associated with the operation has not been significantly reduced yet, even with the minimally invasive approach, thus suggesting that the pathogenesis of complications associated with oesophagectomy is multifactorial [7].
Efforts have been made to identify patient-related prognostic factors for major comorbidities and anastomotic leakage. In a recent meta-analysis, van Kooten and colleagues [5] found male sex [odds ratio (OR) 4.50; 95% confidence interval (CI) 1.21–16.64; P = 0.02], cardiac comorbidity (OR 1.53; 95% CI 1.25–1.87; P = 0.01) and diabetes (OR 1.93; 95% CI 1.14–3.26; P = 0.01) to be significantly associated with major complications. Moreover, 9 risk factors for anastomotic leakage have also been identified, with the renal disease being the most prominent.
Although much attention has been centred on preoperative conditions, the present article by Zheng et al. [8] focuses on intraoperative risk factors which might be useful for clinicians to decrease complications. In ‘Surgical Apgar score could predict complications after oesophagectomy: a systematic review and meta-analysis’, the authors sought to shed light on the role of surgical Apgar score (SAS) in predicting adverse events after oesophagectomy. Concerning the secondary outcomes, the meta-analysis of 4 studies concluded that SAS could predict the incidence of pulmonary complications (OR = 2.32, 95% CI: 1.61–3.36, P < 0.001); whereas the association between SAS and 5-year survival rate, as well as perioperative mortality, was not investigated since they were reported only in one study each.
This stimulating paper helps to clarify the role of the SAS in predicting major complications after oesophagectomy. Indeed, since Gawande first applied the SAS score calculated on 3 intraoperative variables, estimated blood loss, lowest mean arterial pressure and lowest heart rate, several studies on this topic have been carried out leading to inconsistent results [9]. While it has been proven to be an effective tool in predicting complications after surgery in some urological, gynaecological and digestive operations, regarding oesophagectomy for cancer, this has failed to be confirmed. Why should surgeons be interested in the findings of this meta-analysis?
The implications of these reported results include that we might be able to better screen for patients who are at a high risk of developing postoperative complications. With this exceedingly simple scoring system, clinicians could optimize the individual perioperative management by applying closer postoperative surveillance or delayed enteral feeding in high-risk patients, so to decrease the probability of postoperative complications. If so, this would have an impact on shortening hospital stays and reducing overall patient costs.
Future high-quality, prospective studies aimed at confirming these findings would be beneficial in assessing the usefulness of the SAS in reliably predicting complications after oesophagectomy. Zheng et al. are to be congratulated on their contribution to this field of understanding. Their findings will certainly prove to be most beneficial to the surgical community if confirmed in larger studies.
Conflict of interest: none declared.
REFERENCES
- 1. Cagini L, Capozzi R, Tassi V, Savignani C, Quintaliani G, Reboldi G. et al. Fluid and electrolyte balance after major thoracic surgery by bioimpedance and endocrine evaluation. Eur J Cardiothorac Surg 2011;40:e71–6. [DOI] [PubMed] [Google Scholar]
- 2. Cagini L, Andolfi M, Potenza R, Ceccarelli S, Vannucci J, Berti V. et al. Microalbuminuria assessment after thoracic surgery: early identification of complication risks. Clin Respir J 2020;14:564–70. [DOI] [PubMed] [Google Scholar]
- 3. Orringer MB, Marshall B, Iannettoni MD.. Transhiatal esophagectomy for treatment of benign and malignant esophageal disease. World J Surg 2001;25:196–203. [PubMed] [Google Scholar]
- 4. Tassi V, Lugaresi M, Mattioli B, Daddi N, Pilotti V, Ferruzzi L. et al. Quality of life after operation for end-stage achalasia: pull-down Heller-Dor versus esophagectomy. Ann Thorac Surg 2022;113:271–8. [DOI] [PubMed] [Google Scholar]
- 5. van Kooten RT, Voeten DM, Steyerberg EW, Hartgrink HH, van Berge Henegouwen MI, van Hillegersberg R. et al. Patient-related prognostic factors for anastomotic leakage, major complications, and short-term mortality following esophagectomy for cancer: a systematic review and meta-analyses. Ann Surg Oncol 2022;29:1358–73. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Löfgren A, Åkesson O, Johansson J, Persson J.. Hospital costs and health-related quality of life from complications after esophagectomy. Eur J Surg Oncol 2021;47:1042–7. [DOI] [PubMed] [Google Scholar]
- 7. Bonavina L, Asti E, Sironi A, Bernardi D, Aiolfi A.. Hybrid and total minimally invasive esophagectomy: how I do it. J Thorac Dis 2017;9:S761–72. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Zheng C, Luo C, Xie, Jiang-Shan K, Zhou H, Hu L-W. et al. Surgical Apgar score could predict complications after esophagectomy: a systematic review and meta-analysis. Interact CardioVasc Thorac Surg. https://doi.org/10.1093/icvts/ivac045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Gawande A, Kwaan M, Regenbogen S, Lipsitz S, Zinner M.. An Apgar score for surgery. J Am Coll Surg 2007;204:201–8. [DOI] [PubMed] [Google Scholar]
