Skip to main content

ORIGINAL RESEARCH article

Front. Surg., 30 January 2023
Sec. Thoracic Surgery
Volume 10 - 2023 | https://doi.org/10.3389/fsurg.2023.1112675

Optimal discharge planning for esophagectomy patients with enhanced recovery after surgery: Recommendations

Kunzhi Li Kangning Wang Xing Wei Xuefeng Leng Qiang Fang*
  • Division of Thoracic Surgery, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China

Background: Studies have suggested that the postoperative length of stay (PLOS) of esophagectomy patients under the enhanced recovery after surgery (ERAS) pathway should be >10 days as against the previously recommended 7 days. We investigated the distribution and influencing factors of PLOS in the ERAS pathway in order to recommend an optimal planned discharge time.

Methods: This was a single-center retrospective study of 449 patients with thoracic esophageal carcinoma who underwent esophagectomy and perioperative ERAS between January 2013 and April 2021. We established a database to prospectively document the causes of delayed discharge.

Results: The mean and median PLOS were 10.2 days and 8.0 days (range: 5–97), respectively. Patients were divided into four groups: group A (PLOS ≤ 7 days), 179 patients (39.9%); group B (8 ≤ PLOS ≤ 10 days), 152 (33.9%); group C (11 ≤ PLOS ≤ 14 days), 68 (15.1%); group D (PLOS > 14 days), 50 patients (11.1%). The main cause of prolonged PLOS in group B was minor complications (prolonged chest drainage, pulmonary infection, recurrent laryngeal nerve injury). Severely prolonged PLOS in groups C and D were due to major complications and comorbidities. On multivariable logistic regression analysis, open surgery, surgical duration >240 min, age >64 years, surgical complication grade >2, and critical comorbidities were identified as risk factors for delayed discharge.

Conclusions: The optimal planned discharge time for patients undergoing esophagectomy with ERAS should be 7–10 days with a 4-day discharge observation window. Patients at risk of delayed discharge should be managed adopting PLOS prediction.

Introduction

Esophageal cancer is the seventh most commonly diagnosed cancer in the world and the sixth most common cause of cancer-associated mortality (1). More than 500,000 people die of this disease each year (1, 2). Currently, surgery is the cornerstone of multidisciplinary treatment for resectable esophageal cancer. The concept of enhanced recovery after surgery (ERAS) was first introduced by Professor Henrik Kehlet in Denmark in 1997. Over the subsequent years, the ERAS pathway has rapidly evolved and has been applied to all fields of surgery. ERAS model has been shown to significantly reduce the length of hospital stay without increasing complications (35). Most studies have demonstrated the safety, feasibility, and effectiveness of ERAS in patients with esophageal cancer (68); however, there is no clear consensus whether this approach can shorten the postoperative length of stay (PLOS). In the traditional perioperative pathway for esophageal cancer surgery, discharge time is usually determined according to the patient's postoperative status, and there is no emphasis on establishing a uniform, planned PLOS. In contrast, in the esophagectomy ERAS pathway, the currently accepted PLOS ends on postoperative day 7 (9). However, most studies have reported a mean or median PLOS of >10 days (6, 10, 11). As esophagectomy is a complex major surgery with many complications, a proportion of patients do not successfully complete the standard full perioperative protocol in the ERAS model of esophagectomy, resulting in delayed discharge. In the international esophageal cancer dataset (Esodata) study, in which our institution is a participating center, the overall rate of perioperative complications was as high as 60%, and only approximately 40% of patients experienced no complications (12). Esophagectomy ERAS does not significantly increase complications compared to conventional surgery, but the distribution of PLOS is not well characterized. Further research to develop a standardized PLOS for these patients is a key imperative. In addition, neoadjuvant therapy has gradually been introduced as a standard treatment option in esophageal cancer surgery (13, 14); however, its impact on the PLOS of ERAS is yet to be determined. In this study, we investigated the distribution and influencing factors of PLOS in patients undergoing ERAS esophagectomy from the beginning of the implementation of ERAS pathway at our institution in January 2013. Our findings may help establish a reasonable target PLOS for this population.

Methods

Data collection

This was a single-center retrospective cohort study of 449 patients with thoracic esophageal cancer who were treated at the Department of Thoracic Surgery between January 01, 2013 and April 30, 2021. All patients underwent surgery, and perioperative ERAS measurements were performed by the same team. The study was conducted according to the principles enshrined in the Declaration of Helsinki and the study protocol was approved by the Ethics Committee (EC) for Medical Research and New Medical Technology of Sichuan Cancer Hospital (SCCHEC-02-2022-042). Written informed consent of patients was waived by the EC. Data pertaining to clinical status, tumor characteristics, neoadjuvant therapy, surgical approach, surgical duration, intraoperative blood loss, anastomotic approach, anesthesia, PLOS, and perioperative complications (severity assessed using the Clavien-Dindo grading scale) were recorded. Causes of delayed discharge were monitored prospectively.

Diagnosis, treatment, and the standards for discharge from hospital

Clinical staging was based on preoperative contrast-enhanced cervicothoracic and abdominal CT, endoscopic ultrasound, fibreoptic bron choscopy, neck and abdominal ultrasound, and bone scan, with additional contrast-enhanced head MRI, and PET-CT scans to rule out distant metastases, if necessary. Tumor pathology was staged according to the 8th edition of the International Union Against Cancer (UICC). Neoadjuvant chemoradiotherapy, chemotherapy, or immunochemotherapy was administered according to the National Comprehensive Cancer Network guidelines, the Chinese Society of Clinical Oncology guidelines, registered clinical trials, and the patients’ wishes. Patients were treated with McKeown esophagectomy and three-field lymph node dissection if the tumor was located in the thoracic segment; the Ivor-Lewis or transhiatal surgical approach was used for tumors located at the esophagogastric junction. Clinical protocols of patients undergoing esophagectomy are shown in Table 1. The criteria for removal of the thoracic drainage tube were: no air leak, pleural drainage fluid <100 ml/day, and non-cloudy pleural drainage fluid. Patients were discharged when they qualified the following criteria: no need for intravenous rehydration, transoral semi-liquid diet with soft food that can meet physiological needs, normal body temperature, white blood cell count and neutrophil count within the normal range, wound healing grade A, ability to move freely when getting out of bed, no other serious complications, and willingness to be discharged.

TABLE 1
www.frontiersin.org

Table 1. Standardized ERAS protocol for perioperative.

Statistical analysis

Data analyses were performed using SPSS 24.0 software. Normally distributed continuous variables were expressed as mean ± standard deviation and between-group differences assessed using independent samples t test. Non-normally distributed continuous variables were expressed as median (range) and between-group differences assessed using the Mann-Whitney U test. Categorical variables were expressed as frequency (percentage) and between-group differences assessed using the Chi-squared test or Fisher's exact probability method. All statistically significant perioperative variables were included in a multifactorial analysis model using binary logistic stepwise regression analysis. Variables that were not statistically different were phased out until the model was explained by the lowest number of variables. P values < 0.05 were considered indicative of statistical significance.

Results

Descriptive characteristics

A total of 449 patients (358 men, 91 women; mean age: 63.1 ± 8.7 years) who were selected for the perioperative ERAS pathway were included in this study. The baseline characteristics are summarized in Table 2. Neoadjuvant therapy was used in 99 (22.0%) patients, and 82.8% of these patients had received neoadjuvant therapy within the past 4 years. Neoadjuvant chemoradiotherapy was administered to 75 patients, whereas 5 patients received neoadjuvant immunochemotherapy, 18 patients received neoadjuvant chemotherapy, and 1 patient received neoadjuvant radiotherapy. Esophagectomy was performed 4–8 weeks after neoadjuvant therapy.

TABLE 2
www.frontiersin.org

Table 2. Patient characteristics and preoperative data.

Distribution of PLOS

The distribution of the PLOS in our cohort is shown in Figure 1. The mean and median PLOS were 10.2 and 8.0 (range 5–97) days, respectively. Patients were divided into four groups according to their PLOS: group A (PLOS ≤ 7 days, n = 179, 39.9%); group B (8 ≤ PLOS ≤ 10 days, n = 152, 33.9%); group C (11 ≤ PLOS ≤ 14 days, n = 68, 15.1%); and group D (PLOS > 14 days, n = 50, 11.1%). The PLOS data had a skewed distribution. The PLOS of 73.8% patients was within the range of 3 days from the standard PLOS plan (5 ≤ PLOS ≤ 10 days, groups A and B).

FIGURE 1
www.frontiersin.org

Figure 1. Postoperative hospital length of stay, patient distribution. PLOS, postoperative length of stay; Patients (No.), the number of patients;.

Reasons for delayed discharge

The most important reason for delayed discharge was postoperative complications (Table 3). Patients in group B had mild complications, the most common of which were prolonged chest drainage time, pulmonary infection, recurrent laryngeal nerve injury, pulmonary air leak, and electrolyte abnormalities. Patients in group C had moderate complications, the most common of which were prolonged chest drainage, recurrent laryngeal nerve injury, poor incision healing, pulmonary infection, and gastrointestinal disorders. Pulmonary impairment was the most significant comorbidity leading to delayed discharge. More serious complications occurred in group D, most notably anastomotic fistulas and pulmonary infection. Prolonged chest drainage and pulmonary air leakage were important causes of complications, which may be closely related to the poor lung function experienced by those with preoperative comorbidity, leading to significant pulmonary and liver function impairment.

TABLE 3
www.frontiersin.org

Table 3. Reasons for delayed discharge.

Readmission

Six patients were readmitted within one month of discharge (readmission rate: 1.3%). Two patients were in group A, three in group B, and one in group C. All six patients were readmitted because of complications [anastomotic leakage (four patients), aspiration pneumonia (two patients), and recurrent laryngeal nerve injury (one patient)]. Clinical manifestations and blood indices of these patients were within the normal range, and all readmitted patients were eventually discharged (Table 4).

TABLE 4
www.frontiersin.org

Table 4. General clinical data of patients readmitted within 1 month after discharge.

Factors influencing PLOS

In this study, there were no significant differences between patients with PLOS ≤10 days and those with PLOS >10 days with respect to sex, tumor location, T stage, N stage, surgical approach, or neoadjuvant therapy. However, there were significant differences between the two groups with respect to age (P < 0.001), access modality (P = 0.04), American Society of Anesthesiologists (ASA) score (P = 0.01), intraoperative bleeding (P = 0.01), surgical duration (P = 0.04), classification of surgery-related complications (P < 0.001), and severe comorbidities (P < 0.001) (Table 5). There was no significant difference with respect to the PLOS between the neoadjuvant group (8 days, range, 5–97 days) and the non-neoadjuvant group (8 days, range 5–51 days, P = 0.88). PLOS score, operative time, intraoperative bleeding, and age were transformed into categorical variables.

TABLE 5
www.frontiersin.org

Table 5. Univariable analysis of delayed discharge.

Variables that showed significant differences in the univariable analysis were included in the multivariable binary logistic regression models. Multivariable binary logistic regression was performed after excluding patients with intraoperative blood loss of >150 ml (P = 0.515, OR = 1.180, 95% CI: 0.717–1.942) and ASA score >2 (P = 0.244, OR = 1.717, 95% CI: 0.692–4.261). The Hosmer-Lemeshow test revealed that the model explained 23.9% (Nagelkerke R2) of delayed discharges and correctly predicted 78.2% of discharges, with a sensitivity of 95.5%, specificity of 29.7%, positive predictive value of 79.2%, and a negative predictive value of 70.0%. The results of the multivariable binary logistic regression model are shown in Table 6; surgical duration >240 min [odds ratio (OR) = 1.903, 95% confidence interval (CI): 1.184–3.057], age >64 years (OR = 2.218, 95% CI: 1.376–3.575), surgery-related complication grade >2 (OR = 44.378, 95% CI: 9.719–202.632), and severe comorbidities (OR = 4.183, 95% CI: 2.199–7.985) were identified as significant factors affecting the PLOS.

TABLE 6
www.frontiersin.org

Table 6. Multivariable analysis of delayed discharge.

Discussion

The goal of the ERAS pathway is to enable patients to recover and approach a healthy physiological state as soon as possible after esophagectomy (15). Several studies have demonstrated the safety and efficacy of ERAS in esophagectomy (4, 8). Compared to the conventional esophagectomy protocol, the main intraoperative measures in the ERAS protocol include minimally-invasive surgery, pyloroplasty, no placement of drains near the anastomosis, no nasogastric tube, and no feeding tube. The main postoperative measures include early initiation of oral diet with parenteral nutrition, early postoperative removal of the nasogastric tube, and restriction of perioperative fluids (9). In the international multicentre Esodata study, the overall rate of surgery-related complications was approximately 60%, regardless of the surgical approach (minimally-invasive, hybrid, or open surgery). The incidence of Clavien-Dindo grade ≥ III b ranged from 15.7%–19.2%, with a mean length of stay of more than 10 days. Severe surgical complications affect the PLOS (16). Under the traditional clinical pathway, perioperative complications and mortality are core evaluation indicators, whereas PLOS is not (4, 17). In contrast, PLOS is the main indicator for evaluating the success of the standard ERAS pathway. Currently, in the ERAS pathway, the planned discharge time is set to 7 days after surgery. However, the timing and content of a standardized pathway based on this concept have not been well described. There are no specific reports on the number of patients who can successfully complete this pathway. The current lack of evidence prevents surgeons and patients from accurately developing individualized preoperative ERAS protocols and postoperative recovery goals. In this study, the mean and median PLOS were 10.2 days and 8.0 days, respectively. Only 39.9% of the patients were discharged within 7 days, and the majority of patients were unable to meet the planned discharge time according to the standard pathway. Approximately 40% of patients reached the planned standard PLOS without any complications, which is consistent with the results of the International Esodata Study. If the planned PLOS were extended by 3 days, 73.8% of patients would have successfully achieved the target PLOS with the ERAS protocol. The current target PLOS should be further optimized to improve its applicability. In our study, 15.1% and 11.1% of the patients were discharged after 11–14 days and 14 days, respectively. We identified the risk factors for increased PLOS, which may help determine the patient suitability for treatment with the standard ERAS protocol. Our results may help inform strategies for development of individualized ERAS clinical protocols for patients.

The readmission rate in our cohort was 1.3%, which is lower than that cited in the International Esodata Study statistical index (19.4%) (12). Five of the six patients readmitted after discharge belonged to groups A (2 patients) and B (3 patients), and these patients were readmitted because of anastomotic leak or aspiration pneumonia. Even when patients are discharged after successfully completing the standard ERAS pathway, there may be potential for undetectable anastomotic leaks. Four patients had a clinically significant anastomotic leak within 4 days of the planned PLOS discharge. However, the diagnosis of an anastomotic leak is time-related and is determined by leak characteristics. Therefore, patients at risk for anastomotic leak in any aspect of the perioperative period should be strictly evaluated for discharge criteria, with a possible extended discharge observation window, or additional testing to identify subtle clues of leakage. Optimal planning of the PLOS in the ERAS pathway for esophagectomy should be set within a window of approximately 4 days to provide a sufficient observation period for patients at potential risk. This would help maximize the timely detection of leak.

The database on which this study is based was primarily developed to address causes of impact-planned discharges. The database actively records impact events and causes. This is critical for an accurate analysis of the reasons for delayed discharge. Continuous analysis of these reasons can improve the quality of the ERAS protocol and provide a basis for developing the optimal PLOS plan for each patient. In this study, 33.9% of patients were discharged within 8–10 days; whether this group of patients could achieve the standard PLOS pathway (PLOS ≤ 7 days) warrants further analysis. In group B, the reasons for delayed discharge included prolonged chest drainage, pulmonary infection, and minor complications, such as recurrent laryngeal nerve injury, electrolyte disturbance, or pneumothorax. Esophagectomy and lymph node dissection result in large intrathoracic wounds that impede lymphatic return and produce more exudate (18, 19). Postoperative tissue repair and inflammation also increase capillary permeability inducing more drainage (20). Many factors contribute to the prolonged duration of chest drainage after esophagectomy. These factors vary among individual patients and are typically uncontrollable in advance despite being the main causes of prolonged chest drainage time. Pulmonary infection in post-esophagectomy patients is closely associated with advanced age, smoking history, underlying lung disease, and duration of surgery (21). The high incidence of pulmonary infection and individual differences make it difficult for patients in group B to fully meet the planned PLOS discharge criteria, even if they have successfully undergone the surgery and ERAS protocol. Patients tend to recover better if a discharge observation window is appropriately provided. This meets the requirements of ERAS and should be included in the PLOS plan.

In group C, more than 10% of patients had delayed discharge due to severely prolonged drainage, poor pulmonary function, recurrent laryngeal nerve injury, gastrointestinal disturbances, or poor wound healing. More than 5% had delayed discharge due to pulmonary infection. Patients in groups B and C had similar complications; however, complications in group C were more severe, and the patient's underlying condition tended to be worse. In patients with risk factors undergoing esophagectomy, it is particularly important to selectively dissect the lymph nodes surrounding the recurrent laryngeal nerve in order to avoid damage to it (22). This is a key surgical technique to avoid thermal and traction injury to the recurrent laryngeal nerve. The main reasons for delayed discharge in group D were severe anastomotic leak, pulmonary infection, prolonged chest drainage, impaired liver function, and prolonged postoperative air leak due to pleural adhesions and pulmonary bullae. For these patients, it is difficult to shorten the PLOS using ERAS. These patients should not be included in the standard ERAS protocol; however, their PLOS can be shortened using improved techniques and methodology.

We compared various factors in the perioperative period of the two subgroups (PLOS ≤10 days and PLOS >10 days), and factors with significant differences in univariable analysis were included in a multivariable logistic regression model. We found that a surgical duration >240 min, age >64 years, surgical complication grade >2, and severe comorbidities were risk factors for increased PLOS. This result is consistent with previous studies (5, 2225). Inclusion of these risk factors in the regression model would enable better prediction of delayed patient discharges and facilitate the development of personalized ERAS protocols by physicians and their patients. Patients with a high positive predictive value should be more carefully evaluated, and observed for longer periods of time, for each important ERAS measure to improve quality control rather than simply including them in the standard ERAS protocol.

Some limitations of our study should be considered while interpreting the results. This was a retrospective single-center study, and the conclusion was based on the single-center ERAS mode. Larger multicentre studies are required to investigate the applicability of our findings to other ERAS pathways.

Conclusions

The optimal planned discharge time for the ERAS pathway for esophagectomy should be between 7 and 10 days postoperatively, with a 4-day discharge observation window. For patients with risk factors for delayed discharge, prediction methods should be implemented to determine the planned PLOS. Individualized perioperative management protocols should also be provided.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Medical Research and New Medical Technology of Sichuan Cancer Hospital. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author contributions

KL: Conceptualization; Formal analysis; Methodology; Visualization; Investigation; Writing—original draft; Writing—review & editing; KW: Data curation; Writing—review & editing; XW: Conceptualization; Methodology; Writing—review & editing; XL; Data curation; Writing—review & editing; Funding acquisition; QF: Conceptualization; Formal analysis; Funding acquisition; Methodology; Project administration; Supervision; Visualization; Writing—original draft; Writing—review & editing. All authors contributed to the article and approved the submitted version.

Funding

This research was supported by Sichuan Province Science and Technology Support Program (No. 2021YJ0118 and No. 2020YFH0169).

Acknowledgments

The authors are grateful to all medical and nursing staff, enrolled patients and their families, and hospital committee members.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: gLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2021) 71:209–49. doi: 10.3322/caac.21660

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Zhang S, Sun K, Zheng R, Zeng H, Wang S, Chen R, et al. Cancer incidence and mortality in China, 2015. J Natl Cancer Center. (2021) 1:2–11. doi: 10.1016/j.jncc.2020.12.001

CrossRef Full Text | Google Scholar

3. Adamina M, Kehlet H, Tomlinson GA, Senagore AJ, Delaney CP. Enhanced recovery pathways optimize health outcomes and resource utilization: a meta-analysis of randomized controlled trials in colorectal surgery. Surgery. (2011) 149:830–40. doi: 10.1016/j.surg.2010.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Ljungqvist O, Scott M, Fearon KC. Enhanced recovery after surgery: a review. JAMA Surg. (2017) 152:292–8. doi: 10.1001/jamasurg.2016.4952

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Cerfolio RJ, Bryant AS, Bass CS, Alexander JR, Bartolucci AA. Fast tracking after Ivor Lewis esophagogastrectomy. Chest. (2004) 126:1187–94. doi: 10.1378/chest.126.4.1187

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Low DE, Kunz S, Schembre D, Otero H, Malpass T, Hsi A, et al. Esophagectomy–it's Not just about mortality anymore: standardized perioperative clinical pathways improve outcomes in patients with esophageal cancer. J Gastrointest Surg. (2007) 11:1395–402. doi: 10.1007/s11605-007-0265-1

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Chen L, Sun L, Lang Y, Wu J, Yao L, Ning J, et al. Fast-track surgery improves postoperative clinical recovery and cellular and humoral immunity after esophagectomy for esophageal cancer. BMC Cancer. (2016) 16:449. doi: 10.1186/s12885-016-2506-8

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Jiang K, Cheng L, Wang JJ, Li JS, Nie J. Fast track clinical pathway implications in esophagogastrectomy. World J Gastroenterol. (2009) 15:496–501. doi: 10.3748/wjg.15.496

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Parise P, Ferrari C, Cossu A, Puccetti F, Elmore U, De Pascale S, et al. Enhanced recovery after surgery (ERAS) pathway in esophagectomy: is a reasonable prediction of hospital stay possible? Ann Surg. (2019) 270:77–83. doi: 10.1097/SLA.0000000000002775

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Blom RL, van Heijl M, Bemelman WA, Hollmann MW, Klinkenbijl JH, Busch OR, et al. Initial experiences of an enhanced recovery protocol in esophageal surgery. World J Surg. (2013) 37:2372–8. doi: 10.1007/s00268-013-2135-1

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Ford SJ, Adams D, Dudnikov S, Peyser P, Rahamim J, Wheatley TJ, et al. The implementation and effectiveness of an enhanced recovery programme after oesophago-gastrectomy: a prospective cohort study. Int J Surg. (2014) 12:320–4. doi: 10.1016/j.ijsu.2014.01.015

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Kuppusamy MK, Low DE, International Esodata Study Group (IESG). Evaluation of international contemporary operative outcomes and management trends associated with esophagectomy: a 4-year study of >6000 patients using ECCG definitions and the online esodata database. Ann Surg. (2022) 275:515–25. doi: 10.1097/SLA.0000000000004309

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Burt BM, Groth SS, Sada YH, Farjah F, Cornwell L, Sugarbaker DJ, et al. Utility of adjuvant chemotherapy after neoadjuvant chemoradiation and esophagectomy for esophageal cancer. Ann Surg. (2017) 266:297–304. doi: 10.1097/SLA.0000000000001954

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Shah MA, Kennedy EB, Catenacci DV, Deighton DC, Goodman KA, Malhotra NK, et al. Treatment of locally advanced esophageal carcinoma: ASCO guideline. J Clin Oncol. (2020) 38:2677–94. doi: 10.1200/JCO.20.00866

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Ren L, Zhu D, Wei Y, Pan X, Liang L, Xu J, et al. Enhanced recovery after surgery (ERAS) program attenuates stress and accelerates recovery in patients after radical resection for colorectal cancer: a prospective randomized controlled trial. World J Surg. (2012) 36:407–14. doi: 10.1007/s00268-011-1348-4

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Van der Wilk BJ, Hagens ERC, Eyck BM, Gisbertz SS, van Hillegersberg R, Nafteux P, et al. Outcomes after totally minimally invasive versus hybrid and open Ivor Lewis oesophagectomy: results from the international esodata study group. Br J Surg. (2022) 109:283–90. doi: 10.1093/bjs/znab432

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Ni X, Jia D, Chen Y, Wang L, Suo J. Is the enhanced recovery after surgery (ERAS) program effective and safe in laparoscopic colorectal cancer surgery? A meta-analysis of randomized controlled trials. J Gastrointest Surg. (2019) 23:1502–12. doi: 10.1007/s11605-019-04170-8

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Yoshihara M, Shimono R, Tsuru S, Kitamura K, Sakuda H, Oguchi H, et al. Risk factors for late-onset lower limb lymphedema after gynecological cancer treatment: a multi-institutional retrospective study. Eur J Surg Oncol. (2020) 46:1334–8. doi: 10.1016/j.ejso.2020.01.033

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Younes RN, Gross JL, Aguiar S, Haddad FJ, Deheinzelin D. When to remove a chest tube? A randomized study with subsequent prospective consecutive validation. J Am Coll Surg. (2002) 195:658–62. doi: 10.1016/S1072-7515(02)01332-7

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Nakanishi R, Fujino Y, Yamashita T, Oka S. A prospective study of the association between drainage volume within 24 h after thoracoscopic lobectomy and postoperative morbidity. J Thorac Cardiovasc Surg. (2009) 137:1394–9. doi: 10.1016/j.jtcvs.2008.10.035

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Shimakawa T, Asaka S, Miyazawa M, Yamaguchi K, Murayama M, Yokomizo H, et al. Esophageal cancer surgery in elderly patients aged 80 years or older. Gan to Kagaku Ryoho. (2018) 45:2123–5. doi: 10.4993/acrt.18.50

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Li B, Zhang Y, Miao L, Ma L, Luo X, Zhang Y, et al. Esophagectomy with three-field versus two-field lymphadenectomy for middle and lower thoracic esophageal cancer: long-term outcomes of a randomized clinical trial. J Thorac Oncol. (2021) 16:310–7. doi: 10.1016/j.jtho.2020.10.157

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Yoshida N, Yamamoto H, Baba H, Miyata H, Watanabe M, Toh Y, et al. Can minimally invasive esophagectomy replace open esophagectomy for esophageal cancer? Latest analysis of 24,233 esophagectomies from the Japanese national clinical database. Ann Surg. (2020) 272:118–24. doi: 10.1097/SLA.0000000000003222

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Li J, Wang B, Liang T, Guo NN, Zhao M. Pre-embedded cervical circular stapled anastomosis in esophagectomy. Thorac Cancer. (2020) 11:723–7. doi: 10.1111/1759-7714.13324

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Schmidt HM, El Lakis MA, Markar SR, Hubka M, Low DE. Accelerated recovery within standardized recovery pathways after esophagectomy: a prospective cohort study assessing the effects of early discharge on outcomes, readmissions, patient satisfaction, and costs. Ann Thorac Surg. (2016) 102:931–9. doi: 10.1016/j.athoracsur.2016.04.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: esophageal cancer, esophagectomy, enhanced recovery after surgery, postoperative length of stay, complications, comorbidities

Citation: Li K, Wang K, Wei X, Leng X and Fang Q (2023) Optimal discharge planning for esophagectomy patients with enhanced recovery after surgery: Recommendations. Front. Surg. 10:1112675. doi: 10.3389/fsurg.2023.1112675

Received: 30 November 2022; Accepted: 10 January 2023;
Published: 30 January 2023.

Edited by:

Yi Shen, Nanjing General Hospital of Nanjing Military Command, China

Reviewed by:

Binhui Ren, Nanjing Medical University, China
Liwen Hu, Nanjing University, China

© 2023 Li, Wang, Wei, Leng and Fang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Qiang Fang drfangqiang311@163.com

ORCID Kunzhi Li orcid.org/0000-0002-2745-6126 Kangning Wang orcid.org/0000-0001-9376-9000 Xing Wei orcid.org/0000-0002-3035-5633 Xuefeng Leng orcid.org/0000-0002-5897-0419 Qiang Fang orcid.org/0000-0003-2518-745X

Specialty Section: This article was submitted to Thoracic Surgery, a section of the journal Frontiers in Surgery

Download