Highlights
-
•
The modified Blumgart anastomosis (mBA) was associated with a lower POPF rate.
-
•
mBA was associated with a shorter anastomotic time.
-
•
The incidence of postpancreatectomy hemorrhage was lower in the mBA group.
-
•
Lower POPF rates with mBA persisted after propensity score matching.
-
•
The simplicity of mBA may facilitate surgical standardization.
Keywords: Blumgart anastomosis, Pancreatic fistula, Pancreaticoduodenectomy, Pancreaticojejunostomy
Abstract
Introduction
The modified Blumgart anastomosis (mBA) is widely used for pancreaticojejunostomy; however, its clinical benefits remain uncertain.
Methods
We prospectively enrolled 179 consecutive patients scheduled to undergo pancreaticoduodenectomy (PD) at our institution between February 2016 and December 2018; 125 underwent PD with mBA and were included in the analysis. Short-term outcomes were compared with those of a historical cohort of 103 patients who underwent conventional anastomosis (CA) between April 2012 and January 2016.
Results
Baseline demographic characteristics did not differ significantly between the two groups. The incidences of clinically relevant postoperative pancreatic fistula (POPF) and grade B/C postpancreatectomy hemorrhage (PPH) were significantly lower in the mBA group than in the CA group (7.2%vs. 24.3%, p < 0.001; 4.0% vs. 11.7%, p = 0.028, respectively). The anastomotic time was also significantly shorter in the mBA group (p < 0.001), whereas the overall operative time did not differ significantly (p = 0.206). Multivariable analysis showed that mBA was independently associated with lower odds of clinically relevant POPF, and the incidence remained significantly lower after propensity score matching (PSM).
Discussion
The mBA technique may reduce shear stress on the pancreatic parenchyma, potentially contributing to the lower incidences of POPF and PPH.
Conclusions
The mBA was associated with lower incidences of clinically relevant POPF and PPH and with a shorter anastomotic time, suggesting potential clinical advantages of this technique.
1. Introduction
Pancreaticoduodenectomy (PD) is the standard surgical procedure for neoplasms of the pancreatic head and periampullary region, including tumors of the distal bile duct, duodenum, and ampulla of Vater [[1], [2], [3]]. The procedure was first reported by Whipple in 1935, with an operative mortality rate of 25% in the initial series [1]. PD is a complex procedure associated with substantial postoperative morbidity [4]. Advances in surgical techniques, perioperative care, and centralization have improved its safety [5,6], and recent reports indicate mortality rates below 3% at high-volume centers [7,8]. Nevertheless, PD remains associated with a substantial risk of postoperative complications, including postoperative pancreatic fistula (POPF), hemorrhage, and POPF-related intra-abdominal abscess [9,10].
The reported incidence of POPF after pancreaticojejunostomy (PJ) ranges from 9.9% to 28.5% according to the definitions of the International Study Group of Pancreatic Surgery (ISGPS) [[11], [12], [13]]. Clinically relevant POPF often requires intensive postoperative management and prolongs hospitalization. Established risk factors include a soft pancreatic texture, a small main pancreatic duct (MPD; < 3 mm), and substantial intraoperative blood loss (> 500 mL) [14,15]. A high body mass index (BMI), advanced age, and male sex may also increase the risk of POPF [14,16].
PJ is a technically demanding component of PD [17], and various techniques have been developed to reduce the incidence of POPF [[18], [19], [20], [21], [22]]. Blumgart and colleagues described a duct-to-mucosa PJ reinforced with transpancreatic U-shaped mattress sutures [20,21]. Fujii et al. subsequently simplified this technique, creating what is now known as the modified Blumgart anastomosis (mBA) [22]. Recent studies have reported favorable outcomes with mBA, including a lower incidence of POPF [17,[22], [23], [24], [25], [26], [27], [28]].
At our institution, we introduced mBA in February 2016 and prospectively collected outcomes thereafter. In this study, we evaluated the surgical outcomes of mBA by comparing them with those of CA, the technique used in nearly all patients undergoing PD at our institution through January 2016.
2. Methods
2.1. Ethics
This study was conducted in accordance with the Declaration of Helsinki and was approved by the Institutional Review Board of Tohoku University on January 25, 2016 (approval no. 2015-1-689). The study was registered in the UMIN Clinical Trials Registry (UMIN000020813).
2.2. Patients and study outline
Patients in the mBA group were prospectively enrolled between February 2016 and December 2018. Initially, 179 consecutive patients scheduled to undergo PD were assessed for eligibility; 125 patients who underwent PD with mBA were included in the final analysis. The remaining 54 patients were excluded because the planned resection was not performed, they underwent total pancreatectomy or minimally invasive surgery (MIS), a non-mBA technique was used, or data were insufficient. MIS cases were excluded to maintain comparability with the historical cohort because MIS had not been widely adopted as a standard approach at our institution through 2015. The mBA data were collected prospectively, whereas the historical control group comprised 103 patients who underwent CA between April 2012 and January 2016. Thus, 228 patients who underwent PD at Tohoku University Hospital between April 2012 and December 2018 were included (Fig. 1). Sex was recorded as male or female according to the medical records. Morbidity was defined as Clavien-Dindo grade IIIa or higher [29]. POPF was defined and graded according to the 2016 ISGPS criteria [30], and postpancreatectomy hemorrhage (PPH) was defined and graded according to the ISGPS criteria [31]. Mortality was defined as in-hospital death. To account for baseline pancreatic fistula risk, the Fistula Risk Score (FRS) was calculated for each patient from four intraoperative variables: pancreatic texture, MPD diameter, pathology, and blood loss [32]. This study was reported in accordance with the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement.
Fig. 1.

Case selection flowchart.
2.3. Surgical technique
At our institution, subtotal stomach-preserving pancreaticoduodenectomy (SSPPD) was the standard form of PD. Lymph node dissection was performed as indicated and included nodes in the hepatoduodenal ligament, around the celiac axis and superior mesenteric artery, and around the pancreatic head. The pancreatic parenchyma was transected using electrocautery or an ultrasonic coagulating and cutting device. For reconstruction, the jejunum was brought up through a retrocolic route, and the modified Child method was used in all cases. An external pancreatic duct stent was generally preferred; however, the decision to place a stent was based on intraoperative findings, including pancreatic texture and MPD diameter, and the stent could be omitted in selected cases. Internal pancreatic stents were not used during the study period. All procedures were performed by dedicated gastrointestinal and hepatobiliary-pancreatic (HBP) surgical teams. To maintain technical consistency across the two periods, the primary surgeons were either board-certified HBP surgeons with 10–25 years of experience or senior residents. When a senior resident served as the primary surgeon, a board-certified HBP surgeon served as the first assistant and provided direct supervision.
2.4. Conventional anastomosis
The CA technique consisted of a two-layer, end-to-side anastomosis between the pancreas and jejunum. A small jejunotomy was created on the antimesenteric side of the jejunum. First, the posterior pancreatic parenchyma was sutured to the jejunum using interrupted 5–0 nonabsorbable monofilament sutures. The pancreatic duct was then anastomosed circumferentially to the jejunal mucosa using eight interrupted 6–0 absorbable monofilament sutures. Finally, the anterior pancreatic parenchyma was sutured to the jejunum using interrupted 5–0 nonabsorbable monofilament sutures. An external pancreatic duct stent was placed when the MPD diameter was ≤ 3 mm and omitted when it was > 3 mm [33].
2.5. Modified Blumgart anastomosis
The mBA was an end-to-side PJ originally described by Blumgart [20] and subsequently modified by Fujii [22]. A small jejunotomy was created on the antimesenteric side of the jejunum. Six transpancreatic jejunal seromuscular stitches were placed using three double-armed 3-0 nonabsorbable monofilament sutures. A duct-to-mucosa anastomosis was then constructed circumferentially using eight interrupted 6-0 absorbable monofilament sutures, as in the CA technique. After completion of the duct-to-mucosa anastomosis, the anterior jejunal wall was secured to the anterior surface of the pancreatic remnant using the same three double-armed 3-0 nonabsorbable monofilament sutures in a mattress fashion. An external pancreatic duct stent was routinely placed.
2.6. Statistical analysis
All statistical analyses were performed using JMP® Student Edition 18.2.2 for Macintosh (SAS Institute Inc., Cary, NC, USA). Continuous variables were compared using the Wilcoxon rank-sum test, and categorical variables were compared using Fisher's exact test or the chi-square test. Factors associated with clinically relevant POPF were examined using univariable and multivariable logistic regression analyses. PSM was used to adjust for potential clinical and intraoperative confounders. The propensity score model included patient characteristics (age, sex, BMI, diabetes mellitus [DM], and hypertension [HT]) and surgical factors (operative time, blood loss, MPD diameter, pancreatic texture, and pancreatic stent use). One-to-one nearest-neighbor matching was performed with a caliper width of 0.2. A p value < 0.05 was considered statistically significant.
3. Results
3.1. Characteristics of the patients
Patient characteristics are shown in Table 1. A total of 228 patients who underwent PD were included (125 in the mBA group and 103 in the CA group). The median age of the entire cohort was 68 years (range, 19–84 years), and 148 patients (64.9%) were male. Baseline clinicodemographic characteristics did not differ significantly between the groups, including sex, age, preoperative BMI, history of DM or HT, antithrombotic drug use, diagnosis, and receipt of neoadjuvant therapy. The mBA group comprised 85 male and 40 female patients, with a median age of 67 years (range, 19–84 years); the CA group comprised 63 male and 40 female patients, with a median age of 68 years (range, 19–82 years). Pancreatic cancer was the most common diagnosis in both groups, occurring in 53 (42.4%) and 49 patients (47.6%) in the mBA and CA groups, respectively.
Table 1.
Demographics and clinical characteristics of 228 patients.
| Group p | mBA | CA |
|---|---|---|
| Number (case) | 125 (54.8%) | 103 (45.2%) |
| Age (year) 0.482 | 67 (19–84) | 68 (19–82) |
| Sex (male/female) 0.282 | 85 / 40 | 63 / 40 |
| BMI (kg/m2) 0.161 | 22.6 (16.9–32.5) | 21.9 (15.8–29.6) |
| DM (case) 0.910 | 44 (35.2%) | 37 (35.9%) |
| HT (case) 0.317 | 69 (55.2%) | 50 (48.5%) |
| Antithrombotic (case) 0.738 | 24 (19.2%) | 18 (17.5%) |
| Disease (case) | 0.681 | |
| Pancreatic Cancer | 53 (42.4%) | 49 (47.6%) |
| IPMN or IPMC | 18 (14.4%) | 11 (10.7%) |
| Cholangiocarcinoma | 24 (19.2%) | 16 (15.5%) |
| Other | 30 (24.0%) | 27 (26.2%) |
| Neoadjuvant therapy 0.615 | 34 (27.2%) | 25 (24.3%) |
*Values are medians (range).
Abbreviations are BMI, body mass index; DM, diabetes mellitus; HT, hypertension; IPMN, intraductal papillary mucinous neoplasm; IPMC, intraductal papillary mucinous carcinoma.
3.2. Surgical outcomes
Surgical outcomes are summarized in Table 2. Operative time, blood loss, MPD diameter, pancreatic texture, FRS (p = 0.947), and postoperative anticoagulant therapy did not differ significantly between the groups. By contrast, the rates of combined vascular resection and pancreatic stent use and the anastomotic time differed significantly. In the mBA group, 27 patients (21.6%) underwent vascular resection and 124 (99.2%) received a pancreatic stent, compared with 37 (35.9%) and 55 (53.4%), respectively, in the CA group (p = 0.017 and p < 0.001, respectively). Despite the higher rate of vascular resection in the CA group, operative time and blood loss did not differ significantly. The anastomotic time was significantly shorter in the mBA group than in the CA group (median, 33 min [range, 13–55] vs. 44 min [range, 23–73]; p < 0.001) (Fig. 2).
Table 2.
Surgical outcomes of 228 patients.
| Group p | mBA (n = 125) | CA (n = 103) |
|---|---|---|
| Operative time (min) 0.206 | 516 (209–1345) | 534 (295–1021) |
| Blood loss (mL) 0.275 | 1006 (100–4813) | 1120 (150–9695) |
| Vascular resection (case) 0.017 | 27 (21.6%) | 37 (35.9%) |
| MPD (mm) 0.749 | 4 (1–8) | 4 (1–15) |
| Texture (soft / hard) 0.232 | 73 / 52 | 52 / 51 |
| Pancreatic stent (case) < 0.001 | 124 (99.2%) | 55 (53.4%) |
| Anticoagulants (case) 0.068 | 71 (56.8%) | 46 (44.7%) |
| Anastomotic time (min) < 0.001 | 33 (13–55) | 44 (23–73) |
| Fistula risk score 0.947 | 6 (1–9) | 5 (1–10) |
*Values are medians (range).
Abbreviations are MPD, main pancreatic duct.
Fig. 2.

Comparison of anastomotic time between the mBA and CA groups. Anastomotic time was significantly shorter in the mBA group than in the CA group.
3.3. Postoperative outcomes
Postoperative outcomes are presented in Table 3. The rates of clinically relevant POPF and grade B/C PPH were significantly lower in the mBA group than in the CA group (7.2%vs. 24.3%, p < 0.001; 4.0% vs. 11.7%, p = 0.028, respectively). The rates of drain reinsertion and Clavien-Dindo grade III or higher morbidity were also significantly lower in the mBA group (4.0%vs. 14.6%, p = 0.005; 21.6% vs. 37.9%, p = 0.007, respectively). No significant differences were observed in biliary leakage, time to drain removal, or postoperative hospital stay. One patient in each group died during the hospital stay.
Table 3.
Postoperative outcomes of 228 patients.
| Group p | mBA (n = 125) | CA (n = 103) |
|---|---|---|
| C-D ≥ III (case) 0.007 | 27 (21.6%) | 39 (37.9%) |
| DGE | 8 (6.4%) | 12 (11.7%) |
| Abdominal abscess | 11 (8.8%) | 20 (19.4%) |
| Reoperation | 3 (2.4%) | 4 (3.9%) |
| POPF (case) 0.097 | 61 (48.8%) | 39 (37.9%) |
| None | 64 (51.2%) | 64 (62.1%) |
| BL | 52 (41.6%) | 14 (13.6%) |
| CR | 9 (7.2%) | 25 (24.3%) |
| < 0.001 | ||
| PPH grade B/C (case) 0.028 | 5 (4.0%) | 12 (11.7%) |
| Biliary leakage (case) 0.336 | 4 (3.2%) | 6 (5.8%) |
| Drain removal day (day) 0.212 | 6 (4–124) | 6 (4–275) |
| Drain reinsertion (case) 0.005 | 5 (4.0%) | 15 (14.6%) |
| Hospital stays (day) 0.140 | 31 (13–113) | 34 (5–419) |
| Mortality (case) 0.891 | 1 (0.8%) | 1 (1.0%) |
*Values are medians (range).
Abbreviations are C-D, Clavien-Dindo classification; DGE, delayed gastric emptying; POPF, postoperative pancreatic fistula; BL, biochemical leak; CR, clinically relevant; PPH, postpancreatectomy hemorrhage.
3.4. Factors associated with clinically relevant POPF
Factors associated with clinically relevant POPF are shown in Table 4. Univariable analysis identified BMI < 25 kg/m² (odds ratio [OR], 0.355; p = 0.028), absence of DM (OR, 0.420; p = 0.041), mBA (OR, 0.242; p < 0.001), and pancreatic stent use (OR, 0.311; p = 0.034) as factors associated with lower odds of clinically relevant POPF. In multivariable analysis, BMI < 25 kg/m² (OR, 0.271; 95% confidence interval [CI], 0.10–0.76; p = 0.014), mBA (OR, 0.117; 95% CI, 0.04–0.27; p < 0.001), and pancreatic stent use (OR, 0.123; 95% CI, 0.03–0.41; p < 0.001) remained independently associated with lower odds of clinically relevant POPF.
Table 4.
Univariable and multivariable analyses of factors associated with clinically relevant POPF.
| Univariable analysis | Multivariable analysis |
||||
|---|---|---|---|---|---|
| N | OR | p | OR | CI (95%) p | |
| Male | 148 | 0.989 | 0.978 | ||
| BMI < 25 kg/m2 | 197 | 0.355 | 0.028 | 0.271 | [0.10, 0.76] 0.014 |
| Pancreatic cancer | 102 | 0.541 | 0.111 | ||
| Neoadjuvant therapy | 59 | 0.570 | 0.219 | ||
| Non-DM | 147 | 0.420 | 0.041 | 0.546 | [0.19, 1.44] 0.227 |
| Non-HT | 109 | 0.965 | 0.925 | ||
| No use of antithrombotic | 186 | 0.691 | 0.417 | ||
| mBA | 125 | 0.242 | <0.001 | 0.117 | [0.04, 0.27] <0.001 |
| Pancreatic stent | 179 | 0.311 | 0.034 | 0.123 | [0.03, 0.41] <0.001 |
| Combined vascular resection | 64 | 0.502 | 0.127 | ||
Abbreviations are BMI, body mass index; DM, diabetes mellitus; HT, hypertension; mBA, modified Blumgart anastomosis.
3.5. Postoperative outcomes after PSM
Patient characteristics after PSM are shown in Supplementary Table 1, and postoperative outcomes are presented in Supplementary Table 2. PSM matched 47 of 125 patients in the mBA group with 47 of 103 patients in the CA group, forming the mBA-PSM and CA-PSM groups, respectively. After matching, clinicodemographic variables did not differ significantly between the groups, including age, sex, preoperative BMI, DM, HT, antithrombotic drug use, diagnosis, and receipt of neoadjuvant therapy. No significant between-group differences were observed in surgical factors, including MPD diameter, pancreatic texture, pancreatic stent use, and postoperative anticoagulant therapy (Supplementary Table 1). The rates of clinically relevant POPF and grade B/C PPH were significantly lower in the mBA-PSM group than in the CA-PSM group (8.5%vs. 42.6%, p < 0.001; 2.1% vs. 19.1%, p = 0.004, respectively). The rates of Clavien-Dindo grade III or higher morbidity and drain reinsertion were also significantly lower in the mBA-PSM group (25.5%vs. 51.1%, p = 0.010; 4.3% vs. 27.7%, p = 0.002, respectively).
4. Discussion
Several studies have reported favorable surgical outcomes with mBA after PD [[22], [23], [24], [25], [26], [27]], including less intraoperative blood loss, shorter operative time, a lower incidence of POPF, and shorter hospitalization [17,[22], [23], [24], [25], [26]]. In the present study, although overall morbidity and postoperative hospital stay did not differ significantly between the groups, the rates of clinically relevant POPF, grade B/C PPH, and drain reinsertion were significantly lower and the anastomotic time was significantly shorter in the mBA group than in the CA group. Unlike most previous reports, which were retrospective observational studies [[24], [25], [26], [27], [28]], data for the mBA cohort in the present study were collected prospectively.
The mBA technique may reduce shear stress on the fragile pancreatic parenchyma by using transpancreatic U-shaped mattress sutures to approximate the jejunal seromuscular layer to the pancreatic remnant during knot tying [20]. Leakage at the PJ site may result from tangential tension and shear forces on the pancreatic parenchyma, potentially disrupting the pancreatic capsule or tissue at the suture or knot sites. In high-risk patients with a soft pancreas and a small MPD, anastomotic integrity may be compromised by geometric mismatch and tissue fragility [34]. Among the available PJ techniques, mBA may therefore offer a technical advantage by limiting these stresses. In the present study, mBA was associated with a significantly lower incidence of clinically relevant POPF.
Although previous studies have reported shorter overall operative times with mBA [[24], [25], [26]], these findings may also reflect broader advances in surgical techniques and devices. Differences in total operative time therefore cannot be attributed to the anastomotic method alone. In our cohort, however, mBA was associated with a significantly shorter anastomotic time. A simpler and faster anastomosis may facilitate procedural standardization and surgical training.
In the CA group, a pancreatic duct stent was placed when the MPD diameter was ≤ 3 mm, whereas a stent was routinely placed in the mBA group. Consequently, pancreatic stent use was significantly more frequent in the mBA group. Pancreatic stenting, particularly in patients with a narrow MPD, has been reported to reduce the incidence of POPF [9,33]. After PSM, which included pancreatic stent use in the propensity score model, the incidence of clinically relevant POPF remained significantly lower in the mBA group. Nevertheless, because of the nonrandomized historical-control design, these findings demonstrate an association but do not establish an independent causal effect of mBA.
Although mBA was associated with a lower incidence of clinically relevant POPF, it was not associated with a shorter postoperative hospital stay. In Japan, the timing of postoperative discharge may be influenced by the healthcare system and patient preferences. In this cohort, postoperative hospital stay was approximately 30 days in both groups, and many patients were discharged after drain removal and recovery to their preoperative functional status. Thus, a lower incidence of POPF alone may not directly translate into a shorter hospital stay in this setting.
The incidence of PPH in this study was higher than that in previous reports. Fewer than half of the patients had pancreatic cancer, and more than half had a soft pancreas, indicating that the cohort included a high proportion of patients at risk of POPF and related hemorrhage. Nevertheless, only one in-hospital death occurred in each group, suggesting acceptable perioperative safety.
This study has several limitations. First, it was a single-center study comparing a prospectively collected mBA cohort from February 2016 to December 2018 with a historical CA cohort from April 2012 to January 2016. This nonrandomized historical comparison introduced potential temporal, selection, and perioperative-care biases. Although the standardized perioperative management protocol remained fundamentally consistent throughout the study period, advances in surgical proficiency, techniques, and devices may have favorably influenced outcomes in the more recent mBA group. Second, the sample size was relatively small, even though our institution is a high-volume pancreatic surgery center in Japan. Third, changes in primary surgeons between the two periods may have introduced surgeon-related confounding. Fourth, pancreatic stent use differed substantially between the groups, and multivariable analysis identified stent use as independently associated with lower odds of POPF. Although pancreatic stent use was included in the PSM model, residual confounding cannot be excluded, and the lower incidence of POPF cannot be attributed solely to the anastomotic technique. Finally, intraoperative blood loss was relatively high compared with recent benchmarks, likely reflecting the complexity of cases treated at our tertiary referral center, including those requiring extensive retroperitoneal dissection or major vascular reconstruction. A large, multicenter randomized controlled trial would be needed to address these limitations and evaluate the effects of mBA more definitively.
In conclusion, mBA was associated with lower incidences of clinically relevant POPF and PPH and with a shorter anastomotic time. Its technical simplicity may facilitate skill acquisition and procedural standardization, potentially improving surgical outcomes.
Ethics statements
This study was conducted in accordance with the Declaration of Helsinki and was approved by the Institutional Review Board of Tohoku University on January 25, 2016 (approval no. 2015-1-689). Written informed consent for the use of clinical data was obtained from all patients.
Declaration of generative AI and AI-assisted technologies in the manuscript preparation process
During the preparation of this work, the authors used ChatGPT and Gemini (Google) for language editing, translation, and text formatting. After using these tools, the authors reviewed and edited the content as needed and take full responsibility for the content of the published article.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
CRediT authorship contribution statement
Hideaki Sato: Writing – original draft, Investigation, Data curation, Conceptualization. Shuichi Aoki: Validation, Project administration, Formal analysis, Data curation, Conceptualization. Ryosuke Kashiwagi: Data curation. Mika Ando: Data curation. Yuichiro Umino: Data curation. Mitsuhiro Shimura: Data curation. Koetsu Inoue: Data curation. Masahiro Iseki: Data curation. Daisuke Douchi: Data curation. Takayuki Miura: Data curation. Shimpei Maeda: Data curation. Masaharu Ishida: Data curation. Masamichi Mizuma: Data curation. Michiaki Unno: Data curation.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
The authors thank all surgeons involved in the surgical care of these patients, as well as the gastroenterologists and radiologists in the Departments of Gastroenterology and Diagnostic Radiology at Tohoku University Hospital.
Footnotes
Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.sipas.2026.100360.
Appendix. Supplementary materials
Data availability
The datasets analyzed in this study are not publicly available because of hospital regulations governing patient privacy and institutional data protection. De-identified clinical data supporting the findings are available from the corresponding author upon reasonable academic request.
References
- 1.Whipple A.O., Parsons W.B., Mullins C.R. Treatment of carcinoma of the ampulla of Vater. Ann Surg. 1935;102(4):763–779. doi: 10.1097/00000658-193510000-00023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Li Y., Wu W., Zhang T., Liao Q., Zhao Y., Dai M. Comparison of long-term benefits of organ-preserving pancreatectomy techniques for benign or low-grade malignant tumors at the pancreatic head. Medicine (Baltimore) 2017;96(51) doi: 10.1097/MD.0000000000009420. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Whipple A.O. The rationale of radical surgery for cancer of the pancreas and ampullary region. Ann Surg. 1941;114(4):612–615. doi: 10.1097/00000658-194111440-00008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.DeOliveira M.L., Winter J.M., Schafer M., Cunningham S.C., Cameron J.L., Yeo C.J., et al. Assessment of complications after pancreatic surgery: a novel grading system applied to 633 patients undergoing pancreaticoduodenectomy. Ann Surg. 2006;244(6):931–939. doi: 10.1097/01.sla.0000246856.03918.9a. discussion 937-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Balcom J.H., 4th, Rattner D.W., Warshaw A.L., Chang Y., Fernandez-del Castillo C. Ten-year experience with 733 pancreatic resections: changing indications, older patients, and decreasing length of hospitalization. Arch Surg. 2001;136(4):391. doi: 10.1001/archsurg.136.4.391. [DOI] [PubMed] [Google Scholar]
- 6.Hata T., Motoi F., Ishida M., Naitoh T., Katayose Y., Egawa S., et al. Effect of hospital volume on surgical outcomes after pancreaticoduodenectomy: a systematic review and meta-analysis. Ann Surg. 2016;263(4):664–672. doi: 10.1097/SLA.0000000000001437. [DOI] [PubMed] [Google Scholar]
- 7.Glasgow R.E., Jackson H.H., Neumayer L., Schifftner T.L., Khuri S.F., Henderson W.G., et al. Pancreatic resection in veterans affairs and selected university medical centers: results of the patient safety in surgery study. J Am Coll Surg. 2007;204(6):1252–1260. doi: 10.1016/j.jamcollsurg.2007.03.015. [DOI] [PubMed] [Google Scholar]
- 8.Mizuma M., Endo H., Yamamoto H., Shimura M., Iseki M., Unno M., et al. Updated risk prediction model for pancreaticoduodenectomy using data from the National clinical database in Japan. Ann Gastroenterol Surg. 2025;9(3):559–568. doi: 10.1002/ags3.12883. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Poon R.T., Fan S.T., Lo C.M., Ng K.K., Yuen W.K., Yeung C., et al. External drainage of pancreatic duct with a stent to reduce leakage rate of pancreaticojejunostomy after pancreaticoduodenectomy: a prospective randomized trial. Ann Surg. 2007;246(3):425–435. doi: 10.1097/SLA.0b013e3181492c28. discussion 433-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Kawai M., Tani M., Terasawa H., Ina S., Hirono S., Nishioka R., et al. Early removal of prophylactic drains reduces the risk of intra-abdominal infections in patients with pancreatic head resection: prospective study for 104 consecutive patients. Ann Surg. 2006;244(1):1–7. doi: 10.1097/01.sla.0000218077.14035.a6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Keck T., Wellner U.F., Bahra M., Klein F., Sick O., Niedergethmann M., et al. Pancreatogastrostomy versus pancreatojejunostomy for RECOnstruction after PANCreatoduodenectomy (RECOPANC, DRKS 00000767): perioperative and long-term results of a multicenter randomized controlled trial. Ann Surg. 2016;263(3):440–449. doi: 10.1097/SLA.0000000000001240. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Bassi C., Butturini G., Molinari E., Mascetta G., Salvia R., Falconi M., et al. Pancreatic fistula rate after pancreatic resection. The importance of definitions. Dig Surg. 2004;21(1):54–59. doi: 10.1159/000075943. [DOI] [PubMed] [Google Scholar]
- 13.Aoki S., Miyata H., Konno H., Gotoh M., Motoi F., Kumamaru H., et al. Risk factors of serious postoperative complications after pancreaticoduodenectomy and risk calculators for predicting postoperative complications: a nationwide study of 17,564 patients in Japan. J Hepatobiliary Pancreat Sci. 2017;24(5):243–251. doi: 10.1002/jhbp.438. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Nahm C.B., Connor S.J., Samra J.S., Mittal A. Postoperative pancreatic fistula: a review of traditional and emerging concepts. Clin Exp Gastroenterol. 2018;Volume 11:105–118. doi: 10.2147/CEG.S120217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Fu S.J., Shen S.L., Li S.Q., Hu W.J., Hua Y.P., Kuang M., et al. Risk factors and outcomes of postoperative pancreatic fistula after pancreatico-duodenectomy: an audit of 532 consecutive cases. BMC Surg. 2015;15:34. doi: 10.1186/s12893-015-0011-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Fujii T., Kanda M., Nagai S., Suenaga M., Takami H., Yamada S., et al. Excess weight adversely influences treatment length of postoperative pancreatic fistula: a retrospective study of 900 patients. Pancreas. 2015;44(6):971–976. doi: 10.1097/MPA.0000000000000352. [DOI] [PubMed] [Google Scholar]
- 17.Li Z., Wei A., Xia N., Zheng L., Yang D., Ye J., et al. Blumgart anastomosis reduces the incidence of pancreatic fistula after pancreaticoduodenectomy: a systematic review and meta-analysis. Sci Rep. 2020;10(1) doi: 10.1038/s41598-020-74812-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Schoellhammer H.F., Fong Y., Gagandeep S. Techniques for prevention of pancreatic leak after pancreatectomy. Hepatobiliary Surg Nutr. 2014;3(5):276–287. doi: 10.3978/j.issn.2304-3881.2014.08.08. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Kakita A., Takahashi T., Yoshida M., Furuta K. A simpler and more reliable technique of pancreatojejunal anastomosis. Surg Today. 1996;26(7):532–535. doi: 10.1007/BF00311562. [DOI] [PubMed] [Google Scholar]
- 20.Kleespies A., Rentsch M., Seeliger H., Albertsmeier M., Jauch K.W., Bruns C.J. Blumgart anastomosis for pancreaticojejunostomy minimizes severe complications after pancreatic head resection. Br J Surg. 2009;96(7):741–750. doi: 10.1002/bjs.6634. [DOI] [PubMed] [Google Scholar]
- 21.Grobmyer S.R., Kooby D.A., Hochwald S.N., Blumgart L.H. Blumgart anastomosis for pancreaticojejunostomy minimizes severe complications after pancreatic head resection (Br J Surg 2009; 96: 741-750) Br J Surg. 2010;97(1):134. doi: 10.1002/bjs.6953. author reply 134-5. [DOI] [PubMed] [Google Scholar]
- 22.Fujii T., Sugimoto H., Yamada S., Kanda M., Suenaga M., Takami H., et al. Modified Blumgart anastomosis for pancreaticojejunostomy: technical improvement in matched historical control study. J Gastrointest Surg. 2014;18(6):1108–1115. doi: 10.1007/s11605-014-2523-3. [DOI] [PubMed] [Google Scholar]
- 23.Ricci C., Ingaldi C., Alberici L., Pagano N., Mosconi C., Marasco G., et al. Blumgart anastomosis after pancreaticoduodenectomy. A comprehensive systematic review, Meta-analysis, and meta-regression. World J Surg. 2021;45(6):1929–1939. doi: 10.1007/s00268-021-06039-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Li Y.T., Zhang H.Y., Xing C., Ding C., Wu W.M., Liao Q., et al. Effect of Blumgart anastomosis in reducing the incidence rate of pancreatic fistula after pancreatoduodenectomy. World J Gastroenterol. 2019;25(20):2514–2523. doi: 10.3748/wjg.v25.i20.2514. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Kalev G., Marquardt C., Matzke H., Matovu P., Schiedeck T. The modified Blumgart anastomosis after pancreaticoduodenectomy: a retrospective single center cohort study. Innov Surg Sci. 2021;5(3–4):105–109. doi: 10.1515/iss-2020-0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Lee Y.N., Kim W.Y. Comparison of Blumgart versus conventional duct-to-mucosa anastomosis for pancreaticojejunostomy after pancreaticoduodenectomy. Ann Hepatobiliary Pancreat Surg. 2018;22(3):253. doi: 10.14701/ahbps.2018.22.3.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Revoredo Rego F., Reaño Paredes G., Kometter Barrios F., Wang T., Herrera Chávez G., Villanueva Alegre L., et al. Does modified Blumgart pancreatojejunostomy compared with original Blumgart pancreatojejunostomy decrease the rate of clinically relevant postoperative pancreatic fistula? A single-center propensity score-matched analysis. Ann Hepatobiliary Pancreat Surg. 2026;30(2):234–243. doi: 10.14701/ahbps.26-044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Ye L., Jian Z., Yue W., Weng J., Mo Q., Li G., et al. Novel modified blumgart anastomosis reduces clinically relevant pancreatic fistula after pancreaticoduodenectomy: a retrospective study using inverse probability of treatment weighting. Front Surg. 2025;12:1610561. doi: 10.3389/fsurg.2025.1610561. [DOI] [PMC free article] [PubMed]
- 29.Dindo D., Demartines N., Clavien P.A. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240(2):205–213. doi: 10.1097/01.sla.0000133083.54934.ae. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Bassi C., Marchegiani G., Dervenis C., Sarr M., Abu Hilal M., Adham M., et al. The 2016 update of the international study group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 years after. Surgery. 2017;161(3):584–591. doi: 10.1016/j.surg.2016.11.014. Epub 2016 Dec 28. Erratum in: Surgery. 2024 Sep;176(3):988-9. [DOI] [PubMed] [Google Scholar]
- 31.Wente M.N., Veit J.A., Bassi C., Dervenis C., Fingerhut A., Gouma D.J., et al. Postpancreatectomy hemorrhage (PPH): an international study group of pancreatic surgery (ISGPS) definition. Surgery. 2007;142(1):20–25. doi: 10.1016/j.surg.2007.02.001. [DOI] [PubMed] [Google Scholar]
- 32.Callery M.P., Pratt W.B., Kent T.S., Chaikof E.L., Vollmer C.M. A prospectively validated clinical risk score accurately predicts pancreatic fistula after pancreatoduodenectomy. J Am Coll Surg. 2013;216(1):1–14. doi: 10.1016/j.jamcollsurg.2012.09.002. [DOI] [PubMed] [Google Scholar]
- 33.Motoi F., Egawa S., Rikiyama T., Katayose Y., Unno M. Randomized clinical trial of external stent drainage of the pancreatic duct to reduce postoperative pancreatic fistula after pancreaticojejunostomy. Br J Surg. 2012;99(4):524–531. doi: 10.1002/bjs.8654. [DOI] [PubMed] [Google Scholar]
- 34.Marcucci F., Fassari A., Amariutei A., Rosso E. The mismatch point: a modified technique to prevent and overcome duct-enterotomy discrepancy in high-risk pancreaticojejunostomy. World J Surg. 2026;50(4):1075–1081. doi: 10.1002/wjs.70311. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets analyzed in this study are not publicly available because of hospital regulations governing patient privacy and institutional data protection. De-identified clinical data supporting the findings are available from the corresponding author upon reasonable academic request.
