Duodenum-preserving pancreatic head resection compared to pancreaticoduodenectomy: A systematic review and network meta-analysis of surgical outcomes

Objectives: In this systemic review and network meta-analysis, we investigated pancreaticoduodenectomy (PD), pylorus-preserving pancreaticoduodenectomy (PPPD), and different modifications of duodenum-preserving pancreatic head resection (DPPHR) to evaluate the efficacy of different surgical procedures.

Methods: A systemic search of six databases was conducted to identify studies comparing PD, PPPD, and DPPHR for treating pancreatic head benign and low-grade malignant lesions. Meta-analyses and network meta-analyses were performed to compare different surgical procedures.

Results: A total of 44 studies were enrolled in the final synthesis. Three categories of a total of 29 indexes were investigated. The DPPHR group had better working ability, physical status, less loss of body weight, and less postoperative discomfort than the Whipple group, while both groups had no differences in quality of life (QoL), pain scale scores, and other 11 indexes. Network meta-analysis of a single procedure found that DPPHR had a larger probability of best performance in seven of eight analyzed indexes than PD or PPPD.

Conclusion: DPPHR and PD/PPPD have equal effects on improving QoL and pain relief, while PD/PPPD has more severe symptoms and more complications after surgery. PD, PPPD, and DPPHR procedures exhibit different strengths in treating pancreatic head benign and low-grade malignant lesions.

Systematic Review Registration: https://www.crd.york.ac.uk/prospero/, identifier: CRD42022342427.

1. Introduction

As a part of the pancreas, the pancreatic head has exocrine and endocrine functions. Numerous benign and low-grade malignant lesions involving the pancreatic head require surgical intervention (1). Chronic pancreatitis (CP) or CP with pancreatolithiasis comprises a large part of a pancreatic head benign lesion, and it causes parenchymal or intraductal calcifications, pancreatic fibrosis, and exocrine and endocrine pancreatic insufficiency. With the progression of CP, lots of patients often need to undergo surgical intervention due to severe abdominal pain, reduced quality of life (QoL), occlusion of the portal vein, obstruction of the duodenum, common bile duct (CBD), main pancreatic duct, and so on (2, 3). Low-grade malignant lesions in the pancreatic head generally include intraductal mucinous neoplasms, solid pseudopapillary neoplasm, neuroendocrine tumor, and serous/mucinous cystadenoma, while these have a low incidence of metastasis and good prognosis with surgical resection (4, 5).

Pancreaticoduodenectomy (PD) and pylorus-reserving pancreaticoduodenectomy (PPPD) are traditional surgical approaches for treating lesions involving the pancreatic head and periampullary regions (6). Although PD and PPPD completely remove the primary lesions, their disadvantages remain significant, including great changes to the digestive tract, procedural complexity, and more complications based on anatomic and physiologic complexity (7).

Many surgeons designed and performed various novel procedures to further improve the efficacy and reduce the complications of surgical procedures. Beger et al. (8) reported a new surgical strategy for benign and low-grade malignant lesions. Since then, duodenum-preserving pancreatic head resection (DPPHR) and its modifications have been employed in treating pancreatic head lesions (1, 7, 9). These surgical procedures can potentially preserve the adjacent organs and exocrine/endocrine functions of the pancreas while reducing complications and mortality (10). Diener et al. stressed that DPPHR procedures had superiority over PD in hospital stay, weight gain, exocrine insufficiency, QoL, and other postoperative outcome parameters (11). DPPHR had better short-term results and a longer survival time than PD (12). The clinical evidence may be the verification of DPPHR advantages. Previous studies have compared different DPPHR procedures (13–15). However, they explored only a few parameters. The advantages and disadvantages of different DPPHR procedures need to be further investigated. Also, there is no study comparing different DPPHR procedures and systemically direct/indirect comparing PD/PPPD/DPPHR simultaneously. In this study, we developed meta-analyses and network meta-analyses to compare different surgical procedures directly/indirectly for pancreatic head benign/low-grade malignant lesions in terms of postoperative outcomes.

2. Methods

2.1. Search strategies and selection criteria

Because our study was a systemic review of the published literature, ethical approval, and written consent were not required. Before the literature search, we determined to review PICO: “P” for patients with pancreatic head lesions, “I” for operations involving the pancreatic head, “C” for different surgical procedures, and “O” for multiple postoperative outcomes. A computerized search was performed using databases PubMed, Web of Science, Embase, Cochrane Library, CNKI, and WANFANG DATA in August 2021 with the combination of keywords “benign lesion or low-grade malignant lesion,” “chronic pancreatitis,” “pancreatolithiasis,” “duodenum preserving,” “organ sparing,” “organ preserving,” and “pancreatic head resection.” Results were limited to human studies and English papers but not meeting abstracts, case reports, and reviews. Articles and meta-analyses were included. Basic information including title, authors, abstract, and publication information was exported for primary review.

Two authors reviewed/selected the literature, extracted data, and assessed the bias of enrolled literature independently. We kept papers closely related to the subject of this research for following detailed reading after the first review of the title and abstract. Studies in non-English writing, without access to the full paper, having insufficient statistics, or suspicious of redundant publication were excluded. Resting studies were included in quality assessment and data extraction.

2.2. Data extraction and assessment for risk of bias

After fully evaluating enrolled papers, we extracted the data related to postoperative function assessment, postoperative symptom investigation, surgical and hospitalization parameters, and baseline of studies. The specific indexes are listed in the following tables. Continuous data were presented in means with standard deviations (±SDs) or medians with ranges/interquartile ranges (ranges/IQRs); dichotomous data were expressed in numbers. All data were extracted for the same trial reported in different follow-up periods, and only the latest data were used for the overall comparison.

The risk of bias in randomized controlled studies (RCTs) was evaluated according to the Cochrane Handbook for Systematic Reviews of Interventions (16). The evaluation of observational studies was scored based on the Newcastle–Ottawa scale (NOS) (17). Low-quality literature was excluded based on risk assessment. If there were discordance in literature selection, data extraction, and bias assessment between reviewers, we rechecked the course or consulted another author until an agreement was reached.

2.3. Data synthesis and analysis

We analyzed dichotomous data (e.g., morbidity, pancreatic fistula) as a risk ratio (RR) with a 95% confidence interval (CI) and continuous data as a mean difference (MD) with 95% CI when the outcome was reported or converted to the same units (e.g., hospital stay) or as a standardized mean difference (SMD) with 95% CI when scales were used (e.g., QoL). We converted the medians (IQRs/ranges) into the means (±SDs) through a method published by Luo et al. (18).

We assessed heterogeneity using the I² tests to evaluate the overlap of 95% CIs. The fixed-effects model was adopted for low heterogeneity (I² ≤ 50%), the random-effects model was adopted for greater heterogeneity (I² > 75%), and subgroup analysis was explored. We developed a funnel plot to explore potential publication biases if the subgroup included more than five trials.

Our research is reported in line with PRISMA (19). All the syntheses and analyses were conducted in Revman 5.4 and STATA 14 software. A p-value less than 0.05 could be of statistical significance. This work has been registered in PROSPERO (ID: CRD42022342427).

3. Results

3.1. Search results

Following our search strategy, 2,409 pieces of literature (809 PubMed studies, 923 Web of Science studies, 77 Embase studies, 60 Cochrane Library studies, 234 CNKI studies, 306 WANFANG DATA studies, and 10 records identified through other sources) were exported. Only 44 studies (Supplementary List S1) were enrolled in the final data synthesis after full paper reading and quality assessment by two authors. Figure 1 shows the flowchart of this study.

FIGURE 1

Figure 1. Flowchart of literature screening.

3.2. Included studies

Characteristics of the enrolled non-randomized studies are shown in Table 1, and those of RCTs and long-term follow-ups of RCT are presented in Table 2. This study included seven RCTs, six long-term follow-ups of RCT, 30 retrospective and prospective cohort studies, and one long-term follow-up of a prospective study. All of the studies included 3,471 patients, of which 14 studies involving 350 patients investigated benign or low-grade malignant lesions and 30 studies (including all RCTs and long-term follow-up of RCTs) investigated CP. However, only five retrospective studies and one RCT had ≥50 patients per subgroup. No RCTs were excluded from our study. NOS scores of 8, 7, and 6 were assigned to 13, 13, and 5 nonrandomized studies, respectively. The gender distribution, age range, and follow-up duration varied among studies. Studies were excluded with reasons and presented in the flowchart (Supplementary Figure S1).

TABLE 1

Table 1. Characteristics of enrolled non-randomized studies.

TABLE 2

Table 2. Characteristics of the enrolled randomized studies.

3.3. Risk of bias in enrolled studies

None of the RCTs was a low risk or high risk. Supplementary Figure S1A shows the specific evaluation terms of RCT and results. Supplementary Figure S1B shows the summary of the risk of bias in the individual domains. The evaluation of nonrandomized studies was presented as NOS scores, as shown in Table 1. The scores of included nonrandomized studies ranged from 6 to 8. Five studies were excluded due to low quality (NOS score <6).

3.4. Meta-analysis of enrolled studies

We defined the treatment options of conventional pancreatoduodenectomy or Whipple procedure as PD, pylorus-preserving PD as PPPD, duodenum-preserving pancreatic head resection as DPPHR, and DPPHR procedure of pancreatic head resection with segmental duodenectomy as PHRSD. Specific DPPHR procedures were named after the reporter's name, such as Beger. Some modifications of DPPHR procedures with total/partial pancreatic head resection were named as mDPPHRt/p. If there was no detailed description of the DPPHR procedure or a mixture of DPPHR, a general DPPHR treatment label was allocated.

We collected three categories of indexes: disease-specific risks, symptom scale scores, and function scale scores (20). The latter two categories were developed for and mostly reported in the postdischarge assessment of general and pancreatic disease-related QoL (20, 21). Patients who underwent PD and PPPD were classified into the Whipple group, and patients who underwent all DPPHR procedures into the DPPHR group. Each category consisted of several indexes, as shown in Figure 2.

FIGURE 2

Figure 2. Meta-analysis of collected indexes. Meta-analysis of three categories of indexes: functioning scale scores, symptom scale scores, and disease-specific risks. The last 10 indexes of the third category were analyzed by RR. QoL, quality of life; DPPHR, duodenum-preserving pancreatic head resection; MD, mean difference.

For the function scale score after discharge from the hospital, our meta-analyses showed that there were no significant differences between the two groups in QoL, social function, emotional function, and cognitive function. However, DPPHR had better working ability and physical status (Figure 2).

For the postdischarge symptom scale score, we found that the Whipple group had more severe symptoms than the DPPHR group in diarrhea, constipation, insomnia, loss of appetite, nausea, and fatigue. Financial worries, dyspnea, and pain were comparable between the two groups (Figure 2).

We collected frequently reported disease-specific risk indexes. Body weight change, intraoperative blood loss, length of hospital stay, and operation time were presented as continuous variables. The remaining indexes of this category were presented as binary variables. The meta-analyses revealed that the Whipple group had more body weight loss, intraoperative blood loss, longer hospital stay, longer operation time, and more complications, especially in delayed gastric emptying and endocrine and exocrine insufficiency. Postoperative infection, pancreatic leakage, bile duct fistula, hemorrhage, rehospitalization, and mortality were comparable between the two groups (Figure 2).

The heterogeneity test showed that most meta-analyses of the indexes had low and moderate heterogeneity (I² ≤ 50%, 50% < I² ≤ 75%). Only working ability, body weight change, length of hospital stay, and operation time had obvious heterogeneity (I² > 75%). Each group consisted of several procedures that might contribute to the heterogeneity. These indexes were analyzed in the following network meta-analysis.

3.5. Publication bias of meta-analysis

Considering that the meta-analyses of most indexes included more than 10 studies except for three indexes, we constructed funnel plots to assess the publication bias of the studies enrolled in each meta-analysis. By observing the distribution of enrolled studies in the funnel plots, we found that all studies had a rough symmetric funnel shape, indicating no obvious publication bias in each meta-analysis.

3.6. Network meta-analysis

Several surgical procedures have been applied to treat pancreatic head benign and low-grade malignant lesions. However, the potential advantages of these surgical procedures remain unclear. We conducted network meta-analyses of indexes that had obvious heterogeneity in meta-analysis and that were mostly reported (nearly half of the enrolled literature in our study) and had significant differences in the meta-analysis (Table 3). Only a single procedure was compared in this part.

TABLE 3

Table 3. Subgroups of network meta-analysis.

3.6.1. Operation time

We identified 20 studies including seven procedures that were eligible for the analysis. Owing to the consistency test showing p = 0.008, only 12 direct comparisons of 21 comparisons in the network analysis were kept. The surface under the cumulative ranking curve (SUCRA) was used to provide the probability of the best treatment. The result showed that Berne (55.9%), PPPD (36.8%), and Frey (3.3%) procedures had the largest probability of the shortest operation time (Table 3). The forest plot also supported that DPPHR procedures were shorter than PD (Figure 3A).

FIGURE 3

Figure 3. Network meta-analysis. (A) Operation time, (B) length of hospital stay, (C) body weight change, and (D) complication morbidity.

3.6.2. Length of hospital stay

Sixteen studies including seven procedures were analyzed in this part. The consistency test showed p < 0.001. The eligible 11 direct comparisons in the network analysis found that PPPD, Berne, DPPHRt, and PHRSD were shorter than PD and PPPD was shorter than Berne in terms of the length of hospital stay (Figure 3B). The SUCRA rank result also had a similar trend that PPPD (84.8%), DPPHRt (13.9%), and Frey (1.2%) had the most possible and shortest hospital stay than other procedures (Table 3).

3.6.3. Body weight change

Five studies including six procedures were analyzed in this part. The consistency test showed p = 0.495. The network meta-analysis results found that eight out of 15 comparisons had statistically significant difference. PHRSD [MD: 5.64 (0.87, 10.41)] and PPPD [MD: 6.45 (1.69, 11.22)] lost more weight than Beger. PPPD [MD: 11.05 (5.74, 16.37)], PHRSD [MD: 10.24 (4.92, 15.56)], Beger [MD: −4.60 (−6.96, −2.24)], and Frey [MD: 9.66 (4.04, 15.29)] lost more body weight than Berne. However, PPPD had no difference compared to PHRSD [MD: 0.82 (−1.53, 3.16)] (Figure 3C). The SUCRA rank result indicated that PPPD (69.7%), PHRSD (23.9%), and Frey (6%) had the largest probability of remarkably losing body weight after surgery (Table 3).

3.6.4. Complication morbidity

Sixteen studies including seven procedures were analyzed in this part. The consistency test showed p = 0.096. The network meta-analysis results found that the advantage of DPPHRt, PHRSD, Frey, Berne, and Beger in complication morbidity gradually decreased in order. In contrast, the comparison between PPPD/PD and DPPHRt/PHRSD needs further validation (Figure 3D). The SUCRA rank result indicated that DPPHRt (44.5%), Berne (34.5%), and PHRSD (10%) had the largest probability of least complication morbidity (Table 3).

3.6.5. Endocrine insufficiency

Seventeen studies including seven procedures were analyzed in this part. The consistency test showed p = 0.082. Beger had less endocrine insufficiency than PPPD [RR: −0.17 (−1.21, 0.86)] and PD [RR: 0.14 (−0.34, 0.63)]. DPPHRt, Frey, and Berne have relative advantages over each other in order (Figure 4A). Frey (62.7%), Beger (21.3%), and Berne (9.3%) had the largest probability of least endocrine insufficiency morbidity (Table 3).

FIGURE 4

Figure 4. Network meta-analysis. (A) Endocrine insufficiency, (B) exocrine insufficiency, (C) working ability, and (D) qualify of life.

3.6.6. Exocrine insufficiency

Twelve studies including six procedures were analyzed in this part. The consistency test showed p = 0.005. The network meta-analysis showed that Berne, Frey, and PPPD had less morbidity than Beger. PPPD and PHRSD had less morbidity than PD (Figure 4B). PHRSD (79.2%), Berne (16.3%), and Frey (3.2%) had the largest probability of least exocrine insufficiency morbidity (Table 3).

3.6.7. Working ability

Eleven studies including six procedures were analyzed in this part. The consistency test showed p = 0.085. The network meta-analysis showed that only one comparison had statistical significance. PPPD was better than PD [SMD: 1.42 (0.08, 2.77)] (Figure 4C). PHRSD (66.7%), PPPD (16.5%), and Berne (11.8%) had the most possible best working ability after discharge than other procedures (Table 3).

3.6.8. Quality of life

Ten studies including five procedures were analyzed in this part. The consistency test showed p = 0.682. The network meta-analysis found that all comparisons had no statistical significance, which might mean that all procedures had a similar effect on improving the postoperative QoL of patients (Figure 4D). However, the SUCRA rank still showed a potential trend that Berne (81.1%), Berger (12.7%), and Frey (2.7%) had a larger possibility of improving QoL than PPPD (1.7%) and PD (1.2%) (Table 3).

3.7. Publication bias of network meta-analysis

All network meta-analysis subgroups had at least six direct comparisons. We constructed funnel plots to assess publication bias in each subgroup. We observed a rough symmetric funnel shape, which indicated that there was no obvious publication bias in each subgroup (Supplementary Figure S2).

4. Discussion

To deeply investigate the surgical treatment of pancreatic head benign and low-grade malignant lesions, this study contained accessible literature including large amounts of retrospective and prospective cohort studies, RCTs, and long-term follow-ups of RCT from six databases and enrolled many more legal literature works than any previous meta-analysis publications (11, 22–26). We provided multidimensional comprehensive comparisons among surgical procedures.

Through meta-analyses, we found that PD/PPPD and DPPHR had equal ability to improve postoperative QoL, pain relief, and other functions. This consisted of the latest RCT (27) and previous meta-analysis of RCTs (22). Different literature works reported outcomes in short-term or long-term follow-ups, comparing PD/PPPD with DPPHR. In contrast, our synthesis had moderate heterogeneity for QoL (60.0%) and symptom of pain (67.3%). Pooled data also showed that these two interventions had no differences in improving short-term and long-term QoL and pain relief (22, 26). Subgroup meta-analysis of RCTs or observational studies supported that PD/PPPD and DPPHR had no difference in postoperative pain relief (25). All evidence indicated that both interventions could have equal effects on improving QoL and pain relief in short-term and long-term discharge days.

Each intervention may have different disadvantages and advantages. The advantages of DPPHR included improved working ability, physical status, and body weight compared with PD/PPPD. PD/PPPD had more severe symptoms and more disease-specific risks such as more intraoperative blood loss, longer length of hospital stay, longer operation time, and more complications. Although we disagreed with Strate et al. (28) and Bachmann et al. (12) in terms of working ability and physical status, our results had the same tendency as Zhao et al. (26) with meta-analysis of RCTs and Möbius et al. (29) with a long-term follow-up of a prospective cohort study. In addition, the short-term and long-term effects of these interventions were consistent (26). For the comparison of symptom scale scores and disease-specific risks, our pooled results were generally consistent with most results of previous meta-analyses (11, 25, 26). Endocrine and exocrine insufficiency morbidity after surgery have different definitions in various literature works. More uniformed oral glucose tolerance test (OGTT) was tested for endocrine insufficiency, and fecal elastase concentration measurement was used for exocrine function examination (29–34); however, other methods were mentioned (35–39) or could not find descriptions in some articles. These reasons together with article enrollment discrepancy may cause inconsistency of pooled results compared to former partial meta-analyses (24–26).

Owing to good quantification methods defined by pioneer studies, pooled results of the function and symptom scales did not have obvious heterogeneity. Other indexes like endocrine and exocrine insufficiency reports in the literature may have different definitions or cutoff values or classifications. Our study enrolled 44 pieces of literature, but these studies had various baseline characteristic contents and most had a small sample size. What is more, data were presented in an inconsistent format. These would contribute to heterogeneity. However, we observed that only four of 29 indexes had obvious heterogeneity, 10 of 29 indexes had moderate heterogeneity, and more than half had low heterogeneity. Although not all pooled results were consistent with the previous meta-analyses, we included all studies of their enrollment and more legal pieces of literature to get more exact and representative results.

Another heterogeneity source found that we included multiple procedures in each Whipple/DPPHR group and each procedure had individual properties. In this study, we enrolled Beger, Frey, Berne, mDPPHRt, mDPPHRp, and PHRSD in the DPPHR group. Since Beger et al. presented DPPHR, many modifications have been reported. We made a list and summary of them in Supplementary Table S1. We could see that excision extension differed from specific consideration. These procedures involved resection of the duodenum, partial/total pancreatic head tissue, pancreatic body/tail tissue, common bile duct, and pancreatoduodenal artery arch with the corresponding anastomosis. As time went by, new surgical techniques emerged. Laparoscopy (Supplementary Table S1) and robot-assisted (also called minimally invasive) (39, 40) pancreas surgeries have been done, but their strengths and weaknesses needed further investigation (41–44). In addition, Wang et al. (45) recently designed and performed one novel surgical procedure (Duodenum-CBD-Oddi's Sphincter-preserving Pancreatic Head en bloc Total Resection, DCOPPHTR, Wang's procedure) for CP and CP with pancreatolithiasis, while Wang's procedure was also extended to treat benign or low-grade malignant tumors of the pancreatic head. They performed a series of cases and made 9-year long-term follow-ups for all patients who underwent Wang's procedure. It confirmed that Wang's procedure broke through DPPHR's principles, while the efficacy and safety were excellent. Open and laparoscopic mDPPHRt were achieved in our and other centers (Supplementary Table S1) due to a comprehensive understanding of pancreatic anatomy (46, 47), while the investigation of the differences between DPPHR procedures was still deficient (13, 14).

We conducted eight subgroups of network meta-analyses of indexes holding obvious heterogeneity and most frequently reported in our meta-analyses. We found that PPPD/PD and DPPHR procedures had distinct strengths. DPPHR procedures had a larger probability of best performance in seven of eight analyzed indexes. PD showed the lowest probability of getting the best outcomes, but it could potentially remove pre-/minimal malignant lesions. Although SUCRA rank gave us an intuitional judgment of the best choice, pooled results presented in the forest plot found that not all procedures significantly differed from the others.

Network meta-analysis detected an obvious inconsistency in operation time, length of hospital stays, and exocrine insufficiency, which may also indicate heterogeneity among comparisons derived from different studies. The previous meta-analysis also detected obvious heterogeneity in the pooled results of operation time (11, 23, 24). More uniform objective research designed for these indexes in single-procedure comparison could bring us more solid evidence. Meta-analysis and network meta-analysis had the same outcome that PD/PPPD and DPPHR were equal in improving QoL, while network analysis overturned the result of meta-analysis in working ability. It stressed the necessity of exploring heterogeneity and equality in the working ability improvement of interventions (12, 28). Generally, we provided delicate comparisons for clinical reference.

Both parts of our analysis had an unapparent publication bias. Data in different formats from the enrolled literature were collected and converted, which may add uncertainty to the results. However, more usable data could provide more confirmed and elaborate subgroup analysis. Different studies had different definitions for one parameter, such as loss of body weight and weight gain. This contributed to reducing the availability of limited published data.

5. Conclusion

Our analysis found that DPPHR and PD/PPPD had equality in improving QoL and pain relief, while PD/PPPD had more severe symptoms and more complications after surgery. PD, PPPD, and DPPHR procedures had different strengths in treating pancreatic head benign and low-grade malignant lesions. Surgeons should pay more attention to identifying characteristics of procedures and patients' clinical features to provide precision treatment with individualized surgical procedures.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author/.

Author contributions

SG, QZ, and HW designed this research. SG and QZ searched and selected literature. QZ and JY extracted data. SG, QZ, and JT analyzed the data. JZ and HW checked the enrolled articles and data. QZ wrote the first manuscript and SG corrected the first manuscript. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by grants from the National Natural Science Foundation of China [grant no. 82072723], the Natural Science Foundation of Chongqing [grant no. cstc2020jcyj-msxmX0707], the Science and Health Research Project of Chongqing [grant no. 2021MSXM344], and the Natural Science Foundation of Yuzhong District of Chongqing [grant no. 20210160].

Acknowledgments

The authors thank professor Lei Cai of their department for manuscript writing assistance. The authors also appreciate support from their colleagues who helped conduct DPPHR and patients' corporation during treatment.

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsurg.2023.1107613/full#supplementary-material.

References

1. Beger HG, Mayer B, Rau BM. Parenchyma-sparing, limited pancreatic head resection for benign tumors and low-risk periampullary cancer—a systematic review. J Gastrointest Surg. (2016) 20(1):206–17. doi: 10.1007/s11605-015-2981-2

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Beyer G, Habtezion A, Werner J, Lerch MM, Mayerle J. Chronic pancreatitis. Lancet. (2020) 396(10249):499–512. doi: 10.1016/s0140-6736(20)31318-0

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Kempeneers MA, Issa Y, Ali UA, Baron RD, Besselink MG, Buechler M, et al. International consensus guidelines for surgery and the timing of intervention in chronic pancreatitis. Pancreatology. (2020) 20(2):149–57. doi: 10.1016/j.pan.2019.12.005

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Beger HG. Surgical treatment of benign, premalignant and low-risk tumors of the pancreas: standard resection or parenchyma preserving, local extirpation. Chirurg. (2016) 87(7):579–84. doi: 10.1007/s00104-016-0159-4

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Beger HG, Poch B, Vasilescu C. Benign cystic neoplasm and endocrine tumours of the pancreas—when and how to operate—an overview. Int J Surg. (2014) 12(6):606–14. doi: 10.1016/j.ijsu.2014.03.020

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Hüttner FJ, Fitzmaurice C, Schwarzer G, Seiler CM, Antes G, Büchler MW, et al. Pylorus-preserving pancreaticoduodenectomy (pp Whipple) versus pancreaticoduodenectomy (classic Whipple) for surgical treatment of periampullary and pancreatic carcinoma. Cochrane Database Syst Rev. (2016) 2(2):CD006053. doi: 10.1002/14651858.CD006053.pub6

CrossRef Full Text | Google Scholar

7. Beger HG, Mayer B, Yang Y, Poch B. Duodenum-preserving pancreatic head resection for benign tumors, cystic neoplasms and neuroendocrine adenomas—an overview. Chin J Surg. (2021) 59(7):608–17. doi: 10.3760/cma.j.cn112139-20210519-00218

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Mihaljevic AL, Kleeff J, Friess H. Beger’s operation and the Berne modification: origin and current results. J Hepatobiliary Pancreat Sci. (2010) 17(6):735–44. doi: 10.1007/s00534-009-0179-2

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Bachmann K, Izbicki JR, Yekebas EF. Chronic pancreatitis: modern surgical management. Langenbecks Arch Surg. (2011) 396(2):139–49. doi: 10.1007/s00423-010-0732-0

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Andersen DK, Frey CF. The evolution of the surgical treatment of chronic pancreatitis. Ann Surg. (2010) 251(1):18–32. doi: 10.1097/SLA.0b013e3181ae3471

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Diener MK, Rahbari NN, Fischer L, Antes G, Büchler MW, Seiler CM. Duodenum-preserving pancreatic head resection versus pancreatoduodenectomy for surgical treatment of chronic pancreatitis: a systematic review and meta-analysis. Ann Surg. (2008) 247(6):950–61. doi: 10.1097/SLA.0b013e3181724ee7

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Bachmann K, Tomkoetter L, Kutup A, Erbes J, Vashist Y, Mann O, et al. Is the Whipple procedure harmful for long-term outcome in treatment of chronic pancreatitis? 15-Years follow-up comparing the outcome after pylorus-preserving pancreatoduodenectomy and Frey procedure in chronic pancreatitis. Ann Surg. (2013) 258(5):815–20. doi: 10.1097/SLA.0b013e3182a655a8; discussion 20–1.24096767

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kleeff J, Stoess C, Mayerle J, Stecher L, Maak M, Simon P, et al. Evidence-based surgical treatments for chronic pancreatitis a systematic review and meta-analysis of randomized controlled trials. Dtsch Arztebl Int. (2016) 113:489–96. doi: 10.3238/arztebl.2016.0489

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Ratnayake CBB, Kamarajah SK, Loveday BPT, Nayar M, Oppong K, White S, et al. A network meta-analysis of surgery for chronic pancreatitis: impact on pain and quality of life. J Gastrointest Surg. (2020) 24(12):2865–73. doi: 10.1007/s11605-020-04718-z

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Jawad ZAR, Tsim N, Pai M, Bansi D, Westaby D, Vlavianos P, et al. Short and long-term post-operative outcomes of duodenum preserving pancreatic head resection for chronic pancreatitis affecting the head of pancreas: a systematic review and meta-analysis. HPB (Oxford). (2016) 18(2):121–8. doi: 10.1016/j.hpb.2015.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Cumpston M, Li T, Page MJ, Chandler J, Welch VA, Higgins JP, et al. Updated guidance for trusted systematic reviews: a new edition of the Cochrane Handbook for Systematic Reviews of Interventions. Cochrane Database Syst Rev. (2019) 10:ED000142. doi: 10.1002/14651858.Ed000142

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Stang A. Critical evaluation of the Newcastle–Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. (2010) 25(9):603–5. doi: 10.1007/s10654-010-9491-z

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Luo D, Wan X, Liu J, Tong T. How to estimate the sample mean and standard deviation from the sample size, median, extremes or quartiles? Chin J Evid-Based Med. (2017) 17(11):1350–6. doi: 10.7507/1672-2531.201706060

CrossRef Full Text | Google Scholar

19. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. Int J Surg. (2021) 88:105906. doi: 10.1016/j.ijsu.2021.105906

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European Organization for Research and Treatment of Cancer Qlq-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. (1993) 85(5):365–76. doi: 10.1093/jnci/85.5.365

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Fitzsimmons D, Johnson CD, George S, Payne S, Sandberg AA, Bassi C, et al. Development of a disease specific quality of life (QoL) questionnaire module to supplement the EORTC core cancer QoL questionnaire, the QLQ-C30 in patients with pancreatic cancer. EORTC study group on quality of life. Eur J Cancer. (1999) 35(6):939–41. doi: 10.1016/s0959-8049(99)00047-7

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Gurusamy KS, Lusuku C, Halkias C, Davidson BR. Duodenum-preserving pancreatic resection versus pancreaticoduodenectomy for chronic pancreatitis. Cochrane Database Syst Rev. (2016) 2(2):CD011521. doi: 10.1002/14651858.CD011521.pub2

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Jiang K, Wu K, Liao Y, Tu B. A meta-analysis of surgery treatment of chronic pancreatitis with an inflammatory mass in the head of pancreas: duodenum-preserving pancreatic head resection versus pancreatoduodenectomy. Chin J Surg. (2014) 52(9):668–74. doi: 10.3760/cma.j.issn.0529-5815.2014.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Yin Z, Sun J, Yin D, Wang J. Surgical treatment strategies in chronic pancreatitis: a meta-analysis. Arch Surg. (2012) 147(10):961–8. doi: 10.1001/archsurg.2012.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Zhao Y, Zhang J, Lan Z, Jiang Q, Zhang S, Chu Y, et al. Duodenum-preserving resection of the pancreatic head versus pancreaticoduodenectomy for treatment of chronic pancreatitis with enlargement of the pancreatic head: systematic review and meta-analysis. Biomed Res Int. (2017) 2017:3565438. doi: 10.1155/2017/3565438

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Zhao X, Cui N, Wang X, Cui Y. Surgical strategies in the treatment of chronic pancreatitis: an updated systematic review and meta-analysis of randomized controlled trials. Medicine. (2017) 96(9):e6220. doi: 10.1097/md.0000000000006220

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Diener MK, Hüttner FJ, Kieser M, Knebel P, Dörr-Harim C, Distler M, et al. Partial pancreatoduodenectomy versus duodenum-preserving pancreatic head resection in chronic pancreatitis: the multicentre, randomised, controlled, double-blind ChroPac trial. Lancet. (2017) 390(10099):1027–37. doi: 10.1016/s0140-6736(17)31960-8

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Strate T, Bachmann K, Busch P, Mann O, Schneider C, Bruhn JP, et al. Resection vs drainage in treatment of chronic pancreatitis: long-term results of a randomized trial. Gastroenterology. (2008) 134(5):1406–11. doi: 10.1053/j.gastro.2008.02.056

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Möbius C, Max D, Uhlmann D, Gumpp K, Behrbohm J, Horvath K, et al. Five-year follow-up of a prospective non-randomised study comparing duodenum-preserving pancreatic head resection with classic Whipple procedure in the treatment of chronic pancreatitis. Langenbecks Arch Surg. (2007) 392(3):359–64. doi: 10.1007/s00423-007-0175-4

CrossRef Full Text | Google Scholar

30. Strate T, Taherpour Z, Bloechle C, Mann O, Bruhn JP, Schneider C, et al. Long-term follow-up of a randomized trial comparing the Beger and Frey procedures for patients suffering from chronic pancreatitis. Ann Surg. (2005) 241(4):591–8. doi: 10.1097/01.sla.0000157268.78543.03

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Keck T, Adam U, Makowiec F, Riediger H, Wellner U, Tittelbach-Helmrich D, et al. Short- and long-term results of duodenum preservation versus resection for the management of chronic pancreatitis: a prospective, randomized study. Surgery. (2012) 152(3 Suppl 1):S95–102. doi: 10.1016/j.surg.2012.05.016

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Witzigmann H, Max D, Uhlmann D, Geissler F, Schwarz R, Ludwig S, et al. Outcome after duodenum-preserving pancreatic head resection is improved compared with classic Whipple procedure in the treatment of chronic pancreatitis. Surgery. (2003) 134(1):53–62. doi: 10.1067/msy.2003.170

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Izbicki JR, Bloechle C, Knoefel WT, Kuechler T, Binmoeller KF, Broelsch CE. Duodenum-preserving resection of the head of the pancreas in chronic pancreatitis. A prospective, randomized trial. Ann Surg. (1995) 221(4):350–8. doi: 10.1097/00000658-199504000-00004

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Izbicki JR, Bloechle C, Broering DC, Knoefel WT, Kuechler T, Broelsch CE. Extended drainage versus resection in surgery for chronic pancreatitis: a prospective randomized trial comparing the longitudinal pancreaticojejunostomy combined with local pancreatic head excision with the pylorus-preserving pancreatoduodenectomy. Ann Surg. (1998) 228(6):771–9. doi: 10.1097/00000658-199812000-00008

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Klaiber U, Alldinger I, Probst P, Bruckner T, Contin P, Köninger J, et al. Duodenum-preserving pancreatic head resection: 10-year follow-up of a randomized controlled trial comparing the Beger procedure with the Berne modification. Surgery. (2016) 160(1):127–35. doi: 10.1016/j.surg.2016.02.028

PubMed Abstract | CrossRef Full Text | Google Scholar

36. McClaine RJ, Lowy AM, Matthews JB, Schmulewitz N, Sussman JJ, Ingraham AM, et al. A comparison of pancreaticoduodenectomy and duodenum-preserving head resection for the treatment of chronic pancreatitis. HPB (Oxford). (2009) 11(8):677–83. doi: 10.1111/j.1477-2574.2009.00118.x

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Kelemen D, Horváth OP. Clinical experience with different techniques of pancreatic head resection for chronic pancreatitis. Dig Surg. (2002) 19(1):28–35. doi: 10.1159/000052002

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Pedrazzoli S, Canton SA, Sperti C. Duodenum-preserving versus pylorus-preserving pancreatic head resection for benign and premalignant lesions. J Hepatobiliary Pancreat Sci. (2011) 18(1):94–102. doi: 10.1007/s00534-010-0317-x

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Jiang Y, Jin JB, Zhan Q, Deng XX, Peng CH, Shen BY. Robot-assisted duodenum-preserving pancreatic head resection with pancreaticogastrostomy for benign or premalignant pancreatic head lesions: a single-centre experience. Int J Med Robot. (2018) 14(4):e1903. doi: 10.1002/rcs.1903

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Jin JB, Qin K, Yang Y, Shi YS, Wu ZC, Deng XX, et al. Robotic pancreatectomy for solid pseudopapillary tumors in the pancreatic head: a propensity score-matched comparison and analysis from a single center. Asian J Surg. (2020) 43(1):354–61. doi: 10.1016/j.asjsur.2019.05.016

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Belfiori G, Wiese D, Partelli S, Wächter S, Maurer E, Crippa S, et al. Minimally invasive versus open treatment for benign sporadic insulinoma comparison of short-term and long-term outcomes. World J Surg. (2018) 42(10):3223–30. doi: 10.1007/s00268-018-4628-4

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Hwang HK, Song KB, Park M, Kwon W, Jang JY, Heo JS, et al. Minimally invasive versus open pancreatectomy for right-sided and left-sided G1/G2 nonfunctioning pancreatic neuroendocrine tumors: a multicenter matched analysis with an inverse probability of treatment-weighting method. Ann Surg Oncol. (2021) 28(12):7742–58. doi: 10.1245/s10434-021-10092-0

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Issa Y, Kempeneers MA, Bruno MJ, Fockens P, Poley J-W, Ahmed Ali U, et al. Effect of early surgery vs endoscopy-first approach on pain in patients with chronic pancreatitis the escape randomized clinical trial. JAMA. (2020) 323(3):237–47. doi: 10.1001/jama.2019.20967

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Cahen DL, Gouma DJ, Nio Y, Rauws EAJ, Boermeester MA, Busch OR, et al. Endoscopic versus surgical drainage of the pancreatic duct in chronic pancreatitis. N Engl J Med. (2007) 356(7):676–84. doi: 10.1056/NEJMoa060610

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Shixiang G, Huaizhi W. Duodenum-CBD-Oddi’s sphincter-preserving pancreatic head en bloc total resection (DCOPPHTR). Chin J Oper Proc Gen Surg. (2021) 15(4):374. doi: 10.3877/cma.j.issn.1674-3946.2021.04.005

CrossRef Full Text | Google Scholar

46. Yamaguchi H, Wakiguchi S, Murakami G, Hata F, Hirata K, Shimada K, et al. Blood supply to the duodenal papilla and the communicating artery between the anterior and posterior pancreaticoduodenal arterial arcades. J Hepatobiliary Pancreat Surg. (2001) 8(3):238–44. doi: 10.1007/s005340170023

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Guangwei W, Yuanlong G, Niankuan Z, Minfeng L. Relative anatomic research around pancreatic interfascial space and safe surgical plane-regard pancreas as axis. Chin J Bases Clin General Surg. (2012) 19(2):177–80.

Google Scholar