
==== Front
Ann Surg Open
Ann Surg Open
AS9
Annals of Surgery Open
2691-3593
Wolters Kluwer Health, Inc. Two Commerce Square, 2001 Market Street, Philadelphia, PA 19103

AOSO-D-24-00119
00006
10.1097/AS9.0000000000000458
3
Original Study
How to Reduce Delayed Gastric Emptying After Pancreatoduodenectomy: A Systematic Literature Review and Meta-Analysis
Rebelo Artur MD *
Kresse Randi *
Sunami Yoshiaki PhD *
Ronellenfitsch Ulrich MD *
Kleeff Jörg MD *
Klose Johannes MD *
From the * Department of Visceral, Vascular and Endocrine Surgery, University Hospital Halle (Saale), Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Reprints: Artur Rebelo, MD, MHBA, FEBVS, Department of Visceral, Vascular and Endocrine Surgery, University Hospital Halle (Saale), Martin-Luther-University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120 Halle (Saale), Germany. E-mail: artur.rebelo@uk-halle.de.
28 6 2024
9 2024
5 3 e458e458
29 5 2024
2 6 2024
Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.
2024
https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

Introduction:

The occurrence of delayed gastric emptying (DGE) following pancreatoduodenectomy is of high clinical relevance. Despite the pivotal nature of this topic, the existing evidence is limited and often conflicting. This meta-analysis aims to assess the impact of various interventions, such as the type of surgical reconstruction (specifically pylorus resection or preservation), enhanced recovery after surgery (ERAS), epidural anesthesia (EA), as well as strategies involving nasogastric decompression on DGE.

Methods:

Following the PRISMA guidelines, a systematic search was conducted. Studies that compared patients undergoing pancreatoduodenectomy regarding one of the following interventions were included: pylorus-preserving pancreaticoduodenectomy (ppPD) versus pylorus-resecting pancreaticoduodenectomy (prPD), ERAS versus no ERAS, epidural anesthesia EA versus no EA, nasogastric decompression versus no nasogastric decompression and jejunostomy/nasojejunal feeding tube placement (J/NJF) versus no J/NJF.

Results:

The analysis included 5930 patients from 29 studies. Patients undergoing ppPD exhibited a higher incidence of DGE compared with those undergoing prPD (logOR, −0.95; 95% CI = −1.57 to −0.34; P = 0.002). Additionally, patients in the ERAS group showed reduced rates of DGE (logOR, −0.712; 95% CI = −1.242 to −0.183; P = 0.008). Lower rates of DGE were observed in patients without a J/NJF (logOR, −0.618; 95% CI, 0.39–0.84; P < 0.001).

Conclusion:

In summary, our meta-analysis reveals that pylorus resection, adherence to ERAS protocols, and the absence of a J/NJF are associated with lower rates of DGE after pancreatoduodenectomy. Although these results are partially based on observational studies, they contribute valuable insights to the current understanding of interventions impacting DGE in these complex procedures.

delayed gastric emptying
meta-analysis
pancreatic surgery
OPEN-ACCESSTRUE
SDCT
==== Body
pmcINTRODUCTION

Pancreatoduodenectomy is the surgical therapy of choice for malignant and benign conditions in the pancreatic head region. Postoperative complications include pancreatic fistula, bleeding, and delayed gastric emptying (DGE). DGE occurs in up to two-thirds of the patients, even in high-volume centers.1

Although harmless in nature, DGE compromises patients’ quality of life, prolongs hospital stay, postpones discharge, and increases total hospital costs. DGE was defined by the International Study Group of Pancreatic Surgery (ISGPS) as the inability to normal oral food uptake by the end of the first postoperative week.2 This condition also includes prolonged or new nasogastric tube placement. DGE can be classified into 3 different grades (A, B, C) depending on its duration and the required medical provisions.

Risk factors for the occurrence of DGE include pylorus preservation, the type of surgical reconstruction, and the occurrence of pancreatic or bile fistula or chyle leak.3,4 Understanding the factors influencing DGE is vital for effective management or prevention. Despite the crucial nature of the topic, the evidence remains limited and often conflicting. Pylorus preservation is regularly accused of being associated with DGE. Several meta-analyses suggested that pylorus resection was associated with a decreased rate of DGE.5–7 In contrast, Klaiber and co-workers have shown in their meta-analysis that pylorus resection is not superior compared to pylorus preservation to prevent DGE after surgery.8

Beside pylorus preservation, numerous risk factors for DGE were identified.6 Due to the heterogeneity of the data, strategies to prevent DGE are not clear. The effectiveness of enhanced recovery after surgery (ERAS) protocols following pancreatoduodenectomy in reducing the rate of DGE is still unclear.9 Research on DGE after pancreatic surgery spans various aspects, from defining the condition to identifying risk factors and evaluating the impact of surgical techniques. While several meta-analyses have been published on the topic,5–8,10 our meta-analysis is the first to analyze multiple interventions for DGE.

We aimed to assess the outcome of several interventions with the potential to reduce DGE in pancreatic surgery, including pylorus resection or preservation, the type of surgical reconstruction, the use of ERAS protocols, epidural anesthesia, nasogastric decompression, and jejunostomy or nasojejunal feeding tube placement.

METHODS

The literature search and data analysis were conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 statement.11 The study has been registered in the PROSPERO (International Prospective Register of Systematic Reviews) database (CRD42023405721).12

SEARCH STRATEGY

We searched the databases PubMed/MEDLINE, Web of Science Core Collection, Cochrane Library, and ClinicalTrials.gov using their respective online search engines. The search covered studies published from the inception of each database until February 2, 2023. The search strategies employed are detailed in Supplemental Material 1, http://links.lww.com/AOSO/A366. Two authors (R.K. and A.R.) independently assessed the titles and abstracts following a standardized procedure to determine eligibility for inclusion. Identified studies were categorized as either “retrieve” (eligible, potentially eligible, or unclear) or “do not retrieve.” For studies labeled as “retrieve,” two reviewers (R.K. and A.R.) independently reviewed the full text and provided recommendations for inclusion or exclusion. Discrepancies between the reviewers were resolved through consensus; in cases of unresolved disagreements, a third reviewer (J.Klo.) made the decision on whether to include the respective study. Additionally, the reference lists of the included studies were manually scrutinized to identify any additional relevant articles.

INCLUSION AND EXCLUSION CRITERIA

We only considered articles in English for inclusion. Studies that compared patients undergoing pancreatoduodenectomy regarding one of the following interventions and provided information on DGE were included: pylorus-preserving pancreaticoduodenectomy (ppPD) versus pylorus-resecting pancreaticoduodenectomy (prPD), ERAS no ERAS, versus epidural anesthesia (EA) versus no EA, nasogastric decompression (NGD) versus no nasogastric decompression and jejunostomy/nasojejunal feeding tube placement (J/NJF) versus no J/NJF. Excluded from consideration were review articles, case reports, case series with fewer than 5 patients, commentaries, and letters. A flowchart summarizing the study selection process was created following the guidelines outlined in the PRISMA 2020 statement (Fig. 1).

FIGURE 1. PRISMA 2020 flow chart.

DATA COLLECTION

Data from the included studies were extracted separately by two authors (R.K. and A.R.) and stored in a dedicated database. The following descriptive data were documented for each selected study: first author, year of publication, sample size, group, study type, inclusion period, country where the study was conducted, score used, and mean or median follow-up time. The distribution of the following patient characteristics was documented: type of surgery, type of reconstruction, duration of surgery (minutes), blood loss (ml), patients age (mean), patients’ gender (masculine and feminine), American Society of Anesthesiologists classification,13 body mass index, and diabetes (Yes/No). The following predefined outcomes were extracted: DGE (ISGPS definition, ≥2),2 postoperative pancreatic fistula (ISGPS definition, ≥2),14 postpancreatectomy hemorrhage (ISGPS definition, any degree),14 intraabdominal fluid or abscess, chyle leak, bile leak, wound infection, pulmonary complications and mortality. Meta-analysis was performed for the type of intervention: ppPD and prPD, ERAS, EA, NGD and J/NFJ.

In every observational study, the evaluation of risk of bias employed the ROBINS-I tool, while for randomized controlled trials (RCTs), the Cochrane Risk of Bias 2 (RoB 2) tool was utilized for assessment.15,16

STATISTICAL ANALYSIS

The study employed SPSS software17 for analysis. Forest plots were utilized to visually represent the effect estimate’s magnitude. Log odds ratios (logORs) were computed for binary data, while weighted mean differences and relative standard deviation (SD) differences were determined for continuous data. Random-effect models were employed in the calculation of ORs. Each outcome was accompanied by reporting 95% confidence intervals (CI) and statistical significance. A P value of less than 0.05 was considered statistically significant.

RESULTS

In total 29 studies18–46 from 10 countries published between 2007 and 2022, were included in the meta-analysis (Fig. 1). The enrolment periods of these studies ranged from 1981 to 2020. In these studies, a total of 5930 patients were included (ppPD: 908, prPD: 1371, ERAS: 346, No ERAS: 207, EA: 364, No EA: 172, NGD: 430, No NGD: 223, J/NFJ: 953, No J/NFJ: 956).

The study features, patient characteristics, and outcomes are presented in Supplemental Material 2, http://links.lww.com/AOSO/A367.

Patients undergoing ppPD experienced more DGE when compared with patients undergoing prPD (logOR, −0.95; 95% CI = −1.57 to −0.34; P = 0.002) (Fig. 2). In a separate analysis of the 4 available RCTs comparing the effect of pylorus resection or preservation on DGE, this effect could be observed as well but did not reach statistical significance (logOR, −0.28; 95% CI = −1.05 to 0.48; P = 0.47) (Fig. 3).

FIGURE 2. Forest plot of odds ratio (logOR) with 95% CI for DGE. The logORs presented are pylorus-preserving pancreaticoduodenectomy (ppPD) vs. pylorus-resecting pancreaticoduodenectomy (prPD).

FIGURE 3. Forest plot of odds ratio (logOR) with 95% CI for DGE (only RCTs). The logORs presented are pylorus-preserving pancreaticoduodenectomy (ppPD) vs. pylorus-resecting pancreaticoduodenectomy (prPD).

Concerning the other pancreas- and surgery-specific outcomes, there was no statistically significant difference between the 2 groups (Table 1).

TABLE 1. Meta-analysis Including (logOR) With 95% CI for All Investigated Outcomes

Outcome	Effect Size (logOR)	95% CI	P value	
POPF	−0.26	−0.58 to 0.09	0.14	
PPHR	0.11	−0.47 to 0.70	0.7	
IAF	−0.238	−0.600 to 0.124	0.197	
CL	0.184	−0.545 to 0.913	0.621	
BL	1.005	−0.272 to 2.282	0.123	
WI	0.043	−0.633 to 0.719	0.902	
PC	0.478	−0.335 to 1.292	0.249	
Mortality	−0.057	−0.956 to 0.843	0.902	
Reoperation	0.085	−0.708 to 0.878	0.833	
Duration of Surgery	0.040	−0.136 to 0.216	0.654	
Blood Loss	0.058	−0.173 to 0.290	0.621	
Length of Stay	−0.196	−0.418 to 0.026	0.083	
The logORs presented are pylorus-preserving pancreaticoduodenectomy (ppPD) vs. pylorus-resecting pancreaticoduodenectomy (prPD).

BL, bile leak; CL, chyle leak; IAF, intraabdominal fluid; PC, pulmonary complications; POPF, postoperative pancreatic fistula; PPHR, postpancreatectomy hemorrhage; WI, wound infection.

When comparing patients with ERAS and no ERAS, patients in the ERAS group experienced lower rates of DGE (logOR, −0.712; 95% CI = −1.242 to −0.183; P = 0.008) (Fig. 4). Concerning the other above-mentioned outcomes, there was no statistically significant difference between the 2 groups (Table 2). A meta-analysis could not be conducted for the remaining above-mentioned outcomes due to a lack of data.

TABLE 2. Meta-analysis Including (logOR) With 95% CI for All Investigated Outcomes

Outcome	Effect Size (logOR)	95% CI	P Value	
POPF	−0.185	−0.709 to 0.340	0.490	
PPHR	−0.504	−1.406 to 0.399	0.274	
IAF	−1.345	−3.246 to 0.556	0.166	
BL	−1.026	−2.496 to 0.444	0.171	
WI	−0.588	−1.305 to 0.129	0.108	
Mortality	0.042	−1.352 to 1.436	0.953	
Readmission	−0.422	−1.654 to 0.810	0.502	
Duration of Surgery	−0.049	−0.309 to 0.210	0.709	
Blood Loss	−0.559	−1.730 to 0.612	0.349	
Length of Hospital Stay	−0.930	−2.738 to 0.879	0.314	
The logORs presented are Enhanced Recovery after Surgery protocols (ERAS) vs no ERAS.

BL, bile leak; IAF, intraabdominal fluid; POPF, postoperative pancreatic fistula; PPHR, postpancreatectomy haemorrhage; WI, wound infection.

FIGURE 4. Forest plot of odds ratio (logOR) with 95% CI for DGE. The logORs presented are enhanced recovery after surgery protocols (ERAS) vs. no ERAS.

Regarding EA and NGD there was no statistically significant difference between any of the reported outcomes between the 2 groups (Supplemental Material 3, http://links.lww.com/AOSO/A368).

Concerning J/NJF, lower rates of DGE were observed in the no J/NJF group (logOR, −0.618; 95% CI = 0.39–0.84; P < 0.001) (Fig. 5). Concerning the other investigated outcomes there was no statistically significant difference between the 2 groups (Table 3). A comprehensive meta-analysis could not be performed for the remaining above-mentioned outcomes due to insufficient data availability.

TABLE 3. Meta-analysis Including (logOR) With 95% CI for All Investigated Outcomes

Outcome	Effect Size (logOR)	95% CI	P Value	
POPF	0.7	−0.28 to 0.43	0.70	
IAF	−0.05	−0.33 to 0.23	0.74	
WI	0.033	−0.31 to 0.37	0.85	
Mortality	0.17	−1.5 to 1.8	0.83	
Readmission	0.19	−0.05 to 0.43	0.12	
Length of Hospital Stay	0.32	−0.03 to 0.66	0.07	
The logORs presented are jejunal/nasojejunal feeding tube (J/NJF) vs no J/NJF.

IAF, intraabdominal fluid; POPF, postoperative pancreatic fistula; WI, wound infection.

FIGURE 5. Forest plot of odds ratio (logOR) with 95% CI for DGE. The logORs presented are jejunal/nasojejunal feeding tube (J/NJF) vs. no J/NJF.

We did not conduct separate analyses for RCTs regarding ERAS, EA, and J/NJF because only 1 RCT was conducted for each intervention. No RCTs were available regarding NGD.

For the non-RCTs, ROBINS-I analysis revealed that the majority of studies (18/22) did not systematically control confounding via a regression analysis or the Cochrane-Mantel-Haenszel method. Four studies12,19,35,42 analyzed potential confounding factors, but did not systematically adjust data. All studies except Akizuki et al18 were categorized as “low risk of bias” for domains “bias in classification of interventions” and “bias in selection of participants into the study”. For the domains “bias due to deviations from intended interventions”, “bias in measurement of the outcome”, and “bias in selection of the reported result”, all studies were categorized as “low risk of bias”. For the RCTs, all studies were categorized as “low risk of bias” for domains “bias due to missing outcome data” and “bias in measurement of the outcome”. For “bias arising from the randomization process”, 3 studies were categorized as “high risk of bias”, because they did not conduct external institutional randomization or they did not use sealed envelopes.24,29,33 For the domain “bias due to deviations from intended intervention”, 2 studies were categorized as “high risk of bias”. For the domain “bias in selection of the reported result”, all studies were categorized as “low risk of bias” except Ergenc et al24 (“some concerns”), because there was no prepublished study protocol or preregistered clinical study publicly available. (Supplemental Material 4, http://links.lww.com/AOSO/A369 and 5, http://links.lww.com/AOSO/A370).

DISCUSSION

In this comprehensive systematic review and meta-analysis, we investigated the impact of various surgical and perioperative approaches on DGE after pancreatoduodenectomy. Our meta-analysis yielded 3 primary findings: (1) patients undergoing ppPD had a higher incidence of DGE compared with those undergoing prPD; (2) patients in the enhanced recovery after surgery group exhibited reduced rates of DGE; and (3) patients without placement of a feeding jejunostomy showed lower rates of delayed gastric emptying compared with the group with jejunostomy formation.

The significance of DGE in pancreatoduodenectomy cannot be overstated. Patients afflicted with DGE frequently experience extended hospitalization periods, leading to escalated healthcare expenses and heightened utilization of medical resources. Moreover, patients with DGE often necessitate supplementary medical interventions and nutritional support, thereby prolonging the recovery process and placing additional strain on both patients and healthcare systems. Additionally, DGE can impede the timely initiation of adjuvant therapies leading to impaired long-term outcomes.

The choice of ppPD versus prPD is comparable to Goethe’s Gretchenfrage among hepatio-pancreato-biliary surgeons: how do you deal with it? Since decades, there has been an ongoing debate about whether preservation or resection of the pylorus is associated with lower rates or even prevention of DGE after pancreatoduodenectomy. Initially described in 2007, the first trial on DGE examined the effects of erythromycin on gastric emptying following pancreatoduodenectomy. This prospective, randomized, placebo-controlled trial demonstrated that erythromycin administration accelerated gastric emptying in patients undergoing pancreatic surgery.47 Afterwards numerous randomized and non-randomized studies addressed this question and several systematic reviews and meta-analyses summarized their results.

The latest meta-analysis included 3 RCTs and 8 nonrandomized studies, comprising a total of 992 patients. In this study, the superiority of prPD versus ppPD concerning DGE (OR, 2.71; 95% CI = 1.48–4.96; P = 0.001) was observed when both RCTs and non-RCTs were included.8 In contrast, no significant difference was observed in a subgroup analysis only including RCTs (OR, 1.60; 95% CI = 0.57–4.47; P = 0.37).8 As referred, in our analysis, ppPD was associated with higher rates of DGE. In our subgroup analysis including 4 RCTs, this trend could be observed but did not reach statistical significance.

Of note, compared to the meta-analysis of Klaiber and co-workers, we were able to include one more RCT concerning the comparison between ppPD and prPD. The inclusion of 4 studies underlines the value of the data obtained in our study. Hence, we conclude that pylorus resection should be performed during pancreatoduodenectomy. This is in line with the recent data on minimally invasive pancreatic surgery. De Graaf and co-workers demonstrated in their retrospective cohort study that robotic pancreatoduodenectomy (where pylorus resection is commonly performed) is not associated with an increased rate of DGE compared with open (pylorus-preserving) pancreaticoduodenectomy.48

In our study, the ERAS group exhibited reduced rates of DGE. This correlates to the available evidence concerning other surgical specialties. The implementation of ERAS protocols has consistently been associated with reduced rates of DGE in various surgical procedures. Studies in gynecologic and colorectal procedures,49–53 distal pancreatectomy,54 and abdominal wall reconstruction55 have all reported shorter hospital stays, reduced opioid use, and improved patient satisfaction, which are all factors that can contribute to a lower risk of DGE. The specific components of ERAS pathways, such as patient education, multimodal analgesia, and early ambulation, have been shown to facilitate early recovery and discharge, further reducing the risk of DGE.56,57 Kuemmerli and co-workers demonstrated the favorable effects of ERAS protocols on DGE after pancreatoduodenectomy before. They discovered that ERAS was linked to reduced rates of DGE (risk difference, −0.11; 95% CI = −0.22 to −0.01; P = 0.039) with earlier oral food intake and reduced time to pass first stool.58 In line with these findings are the data from an early meta-analysis from 2018 regarding the effect of ERAS on DGE. The authors also describe reduced rates of DGE in the ERAS group compared with conventionally treated patients after pancreatoduodenectomy.59

Finally, patients without the placement of a feeding jejunostomy showed lower rates of delayed gastric emptying. The use of jejunostomy in pancreatic surgery has been explored in various studies. Jejunostomy can be safely used for enteral nutrition in patients with severe acute pancreatitis and those undergoing pancreatic surgery.60,61 However, Waliye et al62 suggested that routine placement of jejunostomy tubes during pancreatoduodenectomy may not be necessary, as it did not significantly decrease morbidity or mortality. In a propensity score case-matched analysis, feeding jejunostomy was associated with increased rates of DGE compared with surgery without feeding tube placement (26.8% vs. 16.4%; P < 0.001).43 These findings corroborate our analysis and collectively suggest that while jejunostomy can be a useful tool in highly selected cases, its routine use may not be necessary during pancreatoduodenectomy.

This meta-analysis has several limitations. Primarily, it relies not only on RCTs but also on observational studies, introducing heterogeneity in outcome definitions and treatments. The retrospective design across multiple studies raises concerns about potential selection bias. The results stem from nonrandomized, uncontrolled comparisons of patients with diverse backgrounds, lacking a clear distinction between groups receiving several therapies across all studies. Despite adhering to PRISMA guidelines (Supplemental Material 6, http://links.lww.com/AOSO/A371) for transparency and standardized reporting, a notable risk of bias persists. Therefore, caution is warranted in the interpretation and application of the data. This study is also subject to confounding variables and bias and is hampered by the quality of the pooled studies underlying the analysis. Regarding ERAS, a protective effect was observed, aligning with contemporary practices aimed at minimizing NGD, promoting early ambulation, and reducing narcotic use—though the exact definition of ERAS was not explicitly stated across the studies. Interestingly, NGD and epidural anesthesia did not impact DGE rates when analyzed independently, suggesting a synergistic effect with bundled ERAS care. It is important to note that insufficient RCTs were available for ERAS, epidural anesthesia, NGD use, or J/NJ tube feeds, highlighting the limitations in interpreting the data and drawing well-supported conclusions. The meta-analysis’ strength lies in its inclusion of all available studies providing comparative information on various approaches to reduce DGE in patients undergoing pancreatoduodenectomy, encompassing a large number of patients.

In conclusion, our meta-analysis demonstrates that factors such as pylorus resection, adherence to ERAS protocols, and the absence of jejunostomy are linked to reduced occurrences of delayed gastric emptying in patients undergoing pancreatoduodenectomy. These results provide valuable insights that contribute to the ongoing comprehension of interventions influencing delayed gastric emptying in individuals undergoing pancreatic surgery.

ACKNOWLEDGMENT

We greatly thank Professor Jonathan Sterne for the revised version (January 2022) of the ROBINS-I tool.

AUTHOR CONTRIBUTIONS

Conceptualization and design: A.R., J.Kle. J.Klo. initiated the meta-analysis, outlining the research questions, objectives, and methodology, and ensuring the study’s design was robust and comprehensive. Literature search and data collection: A.R. and R.K. were responsible for conducting a thorough literature search and identifying relevant studies for inclusion. J.Klo. assisted in screening the studies and extracting critical data, ensuring accuracy and consistency. Data analysis: A.R. took the lead on statistical analysis. Original draft preparation: A.R. and J.Klo. drafted the initial manuscript, focusing on articulating the study’s findings and integrating the data analysis into a cohesive narrative. Y.S. contributed to the writing of specific sections, such as bias analysis. All authors participated in reviewing and editing the manuscript.

Supplementary Material

Disclosure: The authors declare that they have nothing to disclose.

This work was partially supported by the Advanced Clinician Scientist Program of the Medical Faculty of the Martin-Luther University Halle-Wittenberg, Halle (Saale) to A.R. The content is solely the responsibility of the authors and does not represent the official views of the funding agencies.

The study has been registered in the PROSPERO ID CRD42023405721.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s Web site (www.annalsofsurgery.com).
==== Refs
REFERENCES

1. Welsch T Borm M Degrate L . Evaluation of the international study group of pancreatic surgery definition of delayed gastric emptying after pancreatoduodenectomy in a high-volume centre. Br J Surg. 2010;97 :1043–1050.20632270
2. Wente MN Bassi C Dervenis C . Delayed gastric emptying (DGE) after pancreatic surgery: a suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery. 2007;142 :761–768.17981197
3. Park Y-C Kim S-W Jang J-Y . Factors influencing delayed gastric emptying after pylorus-preserving pancreatoduodenectomy. J Am Coll Surg. 2003;196 :859–865.12788421
4. Malleo G Crippa S Butturini G . Delayed gastric emptying after pylorus-preserving pancreaticoduodenectomy: validation of international study group of pancreatic surgery classification and analysis of risk factors. HPB (Oxford). 2010;12 :610–618.20961369
5. Hanna MM Gadde R Tamariz L . Delayed gastric emptying after pancreaticoduodenectomy: is subtotal stomach preserving better or pylorus preserving? J Gastrointest Surg. 2015;19 :1542–1552.25862001
6. Huang MQ Li M Mao JY . Braun enteroenterostomy reduces delayed gastric emptying: a systematic review and meta-analysis. Int J Surg. 2015;23 (Pt A ):75–81.26384836
7. Hu HL Zhou XD Zhang Q . Factors influencing delayed gastric emptying after pancreaticoduodenectomy - a meta-analysis. Hepatogastroenterology. 2014;61 :1539–1545.25436339
8. Klaiber U Probst P Strobel O . Meta-analysis of delayed gastric emptying after pylorus-preserving versus pylorus-resecting pancreatoduodenectomy. Br J Surg. 2018;105 :339–349.29412453
9. Balzano G Zerbi A Braga M . Fast-track recovery programme after pancreatico-duodenectomy reduces delayed gastric emptying. Br J Surg. 2008;95 :1387–1393.18844251
10. Dai S Peng Y Wang G . Risk factors of delayed gastric emptying in patients after pancreaticoduodenectomy: a comprehensive systematic review and meta-analysis. Int J Surg. 2023;109 :2096–2119.37073540
11. Page MJ McKenzie JE Bossuyt PM . The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372 :n71.33782057
12. Available at: https://www.crd.york.ac.uk/prospero/
13. Doyle DJ Hendrix JM Garmon EH . American Society of Anesthesiologists Classification. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2023 Aug 17.
14. Bassi C Marchegiani G Dervenis C . The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 years after. Surgery. 2017;161 :584–591.28040257
15. Sterne JA Hernán MA Reeves BC . ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ. 2016;355 :i4919.27733354
16. Sterne JAC Savović J Page MJ . RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366 :l4898.31462531
17. SPSS Inc. SPSS for Windows, Version 16.0. Chicago: SPSS Inc; Released 2007
18. Akizuki E Kimura Y Nobuoka T . Prospective nonrandomized comparison between pylorus-preserving and subtotal stomach-preserving pancreaticoduodenectomy from the perspectives of DGE occurrence and postoperative digestive functions. J Gastrointest Surg. 2008;12 :1185–1192.18427904
19. Arango NP Prakash LR Chiang Y-J . Risk-stratified pancreatectomy clinical pathway implementation and delayed gastric emptying. J Gastrointest Surg. 2021;25 :2221–2230.33236322
20. Aristizabal Linares JP Estrada Quiroz JJ Gómez CH . Analysis of complications after Whippleʼs procedure using ERAS protocols. Rev Colomb Anestesiol. 2019;47 :219–225.
21. Bilgiç C Sobutay E Bilge O . Risk factors for delayed gastric emptying after pancreaticoduodenectomy. Pancreas. 2022;51 :496–501.35835110
22. Busquets J Martín S Secanella L . Delayed gastric emptying after classical Whipple or pylorus-preserving pancreatoduodenectomy: a randomized clinical trial (QUANUPAD). Langenbecks Arch Surg. 2022;407 :2247–2258.35786739
23. Cai X Zhang M Liang C . Delayed gastric emptying after pancreaticoduodenectomy: a propensity score-matched analysis and clinical nomogram study. BMC Surg. 2020;20 :149.32646466
24. Ergenc M Karpuz S Ergenc M . Enhanced recovery after pancreatic surgery: a prospective randomized controlled clinical trial. J Surg Oncol. 20211070;124 :1070–1076.
25. Flick KF Soufi M Yip-Schneider MT . Routine gastric decompression after pancreatoduodenectomy: treating the surgeon? J Gastrointest Surg. 2021;25 :2902–2907.33772404
26. Fujii T Kanda M Kodera Y . Preservation of the pyloric ring has little value in surgery for pancreatic head cancer: a comparative study comparing three surgical procedures. Ann Surg Oncol. 2012;19 :176–183.21735323
27. Gaignard E Bergeat D Courtin-Tanguy L . Is systematic nasogastric decompression after pancreaticoduodenectomy really necessary? Langenbecks Arch Surg. 2018;403 :573–580.29943225
28. Hackert T Hinz U Hartwig W . Pylorus resection in partial pancreaticoduodenectomy: impact on delayed gastric emptying. Am J Surg. 2013;206 :296–299.23806827
29. Hackert T Probst P Knebel P . Pylorus resection does not reduce delayed gastric emptying after partial pancreatoduodenectomy: a blinded randomized controlled trial (PROPP Study, DRKS00004191). Ann Surg. 2018;267 :1021–1027.28885510
30. Hayashibe A Kameyama M Shinbo M . The surgical procedure and clinical results of subtotal stomach preserving pancreaticoduodenectomy (SSPPD) in comparison with pylorus preserving pancreaticoduodenectomy (PPPD). J Surg Oncol. 2007;95 :106–109.17262740
31. Hufkens A-S van Cleven S de Carvalho LA . Evaluation of an enhanced recovery program for outcome improvement after pancreaticoduodenectomy: a retrospective cohort study. Int J Surg Open. 2021;28 :8–16.
32. Kawai M Tani M Hirono S . Pylorus ring resection reduces delayed gastric emptying in patients undergoing pancreatoduodenectomy: a prospective, randomized, controlled trial of pylorus-resecting versus pylorus-preserving pancreatoduodenectomy. Ann Surg. 2011;253 :495–501.21248633
33. Klotz R Hofer S Schellhaaß A . Intravenous versus epidural analgesia to reduce the incidence of gastrointestinal complications after elective pancreatoduodenectomy (the PAKMAN trial, DRKS 00007784): study protocol for a randomized controlled trial. Trials. 2016;17 :194.27068582
34. Kurahara H Takao S Shinchi H . Subtotal stomach-preserving pancreaticoduodenectomy (SSPPD) prevents postoperative delayed gastric emptying. J Surg Oncol. 2010;102 :615–619.20721956
35. Lee YH Hur YH Kim HJ . Is delayed gastric emptying associated with pylorus ring preservation in patients undergoing pancreaticoduodenectomy? Asian J Surg. 2021;44 :137–142.32951961
36. Daniel SK Thornblade LW Mann GN . Standardization of perioperative care facilitates safe discharge by postoperative day five after pancreaticoduodenectomy. PLoS One. 2018;13 :e0209608.30592736
37. Li A Shah R Han X . Pancreaticoduodenectomy and placement of operative enteral access: better or worse? Am J Surg. 2019;217 :458–462.30538033
38. Liu X Chen Q Fu Y . Early nasojejunal nutrition versus early oral feeding in patients after pancreaticoduodenectomy: a randomized controlled trial. Front Oncol. 2021;11 :656332.33996579
39. Matsumoto I Shinzeki M Asari S . A prospective randomized comparison between pylorus- and subtotal stomach-preserving pancreatoduodenectomy on postoperative delayed gastric emptying occurrence and long-term nutritional status. J Surg Oncol. 2014;109 :690–696.24619624
40. Moris D Lim JJ Cerullo M . Empiric nasogastric decompression after pancreaticoduodenectomy is not necessary. HPB (Oxford). 2021;23 :1906–1913.34154924
41. Nanashima A Abo T Sumida Y . Comparison of results between pylorus-preserving pancreaticoduodenectomy and subtotal stomach-preserving pancreaticoduodenectomy: report at a single cancer institute. Hepatogastroenterology. 2013;60 :1182–1188.23803381
42. Negrini D Ihsan M Freitas K . The clinical impact of the perioperative epidural anesthesia on surgical outcomes after pancreaticoduodenectomy: a retrospective cohort study. Surg Open Sci. 2022;10 :91–96.36062076
43. Soufi M Al-Temimi M Nguyen TK . Friend or foe? Feeding tube placement at the time of pancreatoduodenectomy: propensity score case-matched analysis. Surg Endosc. 2022;36 :2994–3000.34165639
44. Zhao R Chang Y Wang X . Pylorus-preserving pancreaticoduodenectomy versus standard pancreaticoduodenectomy in the treatment of duodenal papilla carcinoma. Oncol Lett. 2018;15 :6368–6376.29725396
45. Zhou Y Lin L Wu L . A case-matched comparison and meta-analysis comparing pylorus-resecting pancreaticoduodenectomy with pylorus-preserving pancreaticoduodenectomy for the incidence of postoperative delayed gastric emptying. HPB (Oxford). 2015;17 :337–343.25388024
46. Zhu I Li X Li H . Enhanced recovery after surgery pathways benefit patients with soft pancreatic texture following pancreaticoduodenectomy. Am J Surg. 2020;219 :1019–1023.31409454
47. Yeo CJ Barry MK Sauter PK . Erythromycin accelerates gastric emptying after pancreaticoduodenectomy. a prospective, randomized, placebo-controlled trial. Ann Surg. 1993;218 :229–37; discussion 237.8103982
48. de Graaf N Zwart MJW van Hilst J . Early experience with robotic pancreatoduodenectomy versus open pancreatoduodenectomy: nationwide propensity-score-matched analysis. Br J Surg. 2024;111 :znae043.38415878
49. Peters A Siripong N Wang L . Enhanced recovery after surgery outcomes in minimally invasive nonhysterectomy gynecologic procedures. Am J Obstet Gynecol. 2020;223 :234.e1-234.e8.
50. Chapman JS Roddy E Ueda S . Enhanced recovery pathways for improving outcomes after minimally invasive gynecologic oncology surgery. Obstet Gynecol. 2016;128 :138–144.27275797
51. Kalogera E Bakkum-Gamez JN Jankowski CJ . Enhanced recovery in gynecologic surgery. Obstet Gynecol. 2013;122 :319–328.23969801
52. Carter-Brooks CM Du AL Ruppert KM . Implementation of a urogynecology-specific enhanced recovery after surgery (ERAS) pathway. Am J Obstet Gynecol. 2018;219 :495.e1-495.e10.
53. Gustafsson UO Scott MJ Hubner M . Guidelines for perioperative care in elective colorectal surgery: enhanced recovery after surgery (ERAS®) society recommendations: 2018. World J Surg. 2019;43 :659–695.30426190
54. Pecorelli N Capretti G Balzano G . Enhanced recovery pathway in patients undergoing distal pancreatectomy: a case-matched study. HPB (Oxford). 2017;19 :270–278.27914764
55. Colvin J Rosen M Prabhu A . Enhanced recovery after surgery pathway for patients undergoing abdominal wall reconstruction. Surgery. 2019;166 :849–853.31262568
56. Simpson JC Moonesinghe SR Grocott MP ; National Enhanced Recovery Partnership Advisory Board. Enhanced recovery from surgery in the UK: an audit of the enhanced recovery partnership programme 2009-2012. Br J Anaesth. 2015;115 :560–568.25926312
57. Kim HJ Steinhaus M Punyala A . Enhanced recovery pathway in adult patients undergoing thoracolumbar deformity surgery. Spine J. 2021;21 :753–764.33434650
58. Kuemmerli C Tschuor C Kasai M . Impact of enhanced recovery protocols after pancreatoduodenectomy: meta-analysis. Br J Surg. 2022;109 :256–266.35037019
59. Ji HB Zhu WT Wei Q . Impact of enhanced recovery after surgery programs on pancreatic surgery: a meta-analysis. World J Gastroenterol. 2018;24 :1666–1678.29686474
60. Weimann A Braunert M Müller T . Feasibility and safety of needle catheter jejunostomy for enteral nutrition in surgically treated severe acute pancreatitis. JPEN J Parenter Enteral Nutr. 2004;28 :324–327.15449571
61. Thodiyil PA El-Masry NS Williamson RCN . Ttube jejunostomy feeding after pancreatic surgery: a safe adjunct. Asian J Surg. 2004;27 :80–84.15140657
62. Waliye HE Wright GP McCarthy C . Utility of feeding jejunostomy tubes in pancreaticoduodenectomy. Am J Surg. 2017;213 :530–533.27863719
