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Double Stenting for Malignant Biliary and Duodenal Obstruction: A Systematic Review and Meta-Analysis

Fábián, Anna MD1; Bor, Renáta MD1; Gede, Noémi MSc2; Bacsur, Péter1; Pécsi, Dániel MD2; Hegyi, Péter MD, PhD, DSc2; Tóth, Barbara MPharm, PhD3; Szakács, Zsolt MD2; Vincze, Áron MD, PhD4; Ruzsics, István MD5; Rakonczay, Zoltán Jr MD, PhD, DSc6; Erőss, Bálint MD2; Sepp, Róbert MD, PhD, DSc7; Szepes, Zoltán MD, PhD1

Author Information
Clinical and Translational Gastroenterology: April 2020 - Volume 11 - Issue 4 - p e00161
doi: 10.14309/ctg.0000000000000161



Unresectable pancreatobiliary, gastroduodenal, and metastatic malignancies can lead to concomitant biliary and duodenal obstruction. Biliary obstruction may occur in 51%–72% of advanced pancreatobiliary cancers (1,2), and duodenal obstruction rate has also risen to 38% because of oncologic advances and consequently longer patient survival (3).

Historically applied double surgical bypass (gastroenterostomy with biliodigestive anastomosis) (4) is often associated with substantial perioperative mortality and morbidity (2) because of poor performance status and frequent comorbidities (5). Because duodenal obstruction usually develops after biliary obstruction and it may occur in up to 20% of those who underwent single biliary bypass, creation of prophylactic gastroenteric anastomosis (GEA) was proposed in patients with unresectable disease confirmed at surgical exploration (2,6). Prophylactic GEA use reduces the chance for developing duodenal obstruction without impairing the short-term outcomes in pancreatic and periampullary cancer (6,7). Therefore, most studies reporting double bypass involve cases where biliary bypass was combined with prophylactic GEA (8–10).

Endoscopic placement of plastic or self-expandable metal stents has offered a minimal invasive palliation alternative for patients unsuitable for surgery. Currently, transpapillary stenting via endoscopic retrograde cholangiopancreatography (ERCP) is the standard treatment of malignant biliary obstruction alone (11,12). In the case of ERCP failure (reported in approximately 10% because of altered anatomy or duodenal obstruction), biliary stenting can be performed via percutaneous transhepatic drainage (PTD) or endoscopic ultrasound-guided biliary drainage (EUS-BD) (13). Recently, the first-line use of EUS-BD in malignant biliary obstruction was also proposed based on comparable technical and clinical success and favorable adverse event and reintervention rates over ERCP (14). In 2018, a Cochrane Database Systematic Review comparing stent placement and surgical palliation for malignant gastric outlet obstruction found quicker resumption of oral intake and reduced hospital stay as benefits and higher reintervention rate as a drawback of duodenal stenting over surgery (15).

Combined biliary and duodenal stent placement (double stenting) was first reported in 1994 (16). Adequate modality for double stenting should be chosen based on duodenal obstruction type (located above [type I], at the level [type II], or below the ampulla [type III]) and sequence of biliary and duodenal stenting (biliary first, duodenal first, or simultaneous). Although technically challenging, biliary stenting can also be performed through the mesh of a duodenal stent (11). Nevertheless, the efficacy data of double stenting are limited, as usually there are few such cases in a single center (17), partly because of the sequential development of biliary and duodenal obstruction, and its place in the therapeutic algorithm is not clearly specified.


This systematic review and meta-analysis aimed to assess efficiency and safety of double stenting in malignant duodenobiliary obstruction compared with surgical double bypass in terms of technical and clinical success, survival, adverse events, and reintervention rate and determine the optimal method for double stenting: duodenal stenting combined with ERCP vs PTD vs EUS-BD.


Protocol and registration

This work was reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2009 Statement (18). The study protocol was registered at the International Prospective Register of Systematic Reviews (PROSPERO) with the registration number CRD42018103101.

Eligibility criteria

We included studies reporting the following outcome measures in patients with concomitant malignant biliary and duodenal obstruction treated either with combined duodenal and biliary stenting (via ERCP, PTD, or EUS-BD) or with double surgical bypass (gastroenterostomy with biliodigestive anastomosis): technical and clinical success, survival, adverse events, and reintervention rates. Studies reporting about temporary stenting were excluded. Studies reporting about prophylactic GEA were included; however, technical and clinical success could only be interpreted as that of biliary bypass in such cases.

Both experimental and observational studies (either prospective or retrospective) without respect to their primary objectives were included. Conference abstracts were included to minimize publication bias. Case reports and case series reporting about less than 5 patients were excluded from quantitative analysis. Eligible articles were written in English or had an English abstract (data were obtained from the abstract in such cases).

Information sources and search strategy

A systematic literature search limited to human studies without language filters was performed by 2 reviewers in the PubMed (MEDLINE), EMBASE, Web of Science, and Cochrane Central Register of Controlled Trials (CENTRAL) databases with the terms “([biliary obstruction AND duodenal obstruction] OR bilio-duodenal obstruction) AND (stent OR surgery).” The final search was performed on July 17, 2018. Reference lists of included articles were also investigated to capture all relevant studies.

Study selection and data collection process

After the removal of duplicates, the following data were extracted by 2 independent authors: age, gender, type of underlying malignancy, type of duodenal obstruction, method of biliary drainage, type of biliary and duodenal stents, timing of stent placement, technical and clinical success, adverse events, reintervention rate, survival, and follow-up.

Risk of bias assessment

Risk of bias was assessed using a modified version of the Newcastle–Ottawa Scale (NOS) by 2 independent review authors. Disagreements were resolved by discussion, with involvement of a third review author, when needed.

The modified NOS contained 7 items covering 2 main domains (selection and outcome) as comparability domain was not applicable because of the lack of head-to-head comparative studies: representativeness of the exposed cohort, selection of the nonexposed cohort, ascertainment of exposure, demonstration that the outcome of interest was not present at the study's start (selection domain), assessment of outcome, and length and adequacy of follow-up (outcome domain). Studies could be awarded a maximum of one star for each item. Each item was rated as “high risk” (zero stars) or “low risk” (one star).

Data synthesis and statistical methods

Pooled event rate was calculated for events, and pooled mean was calculated for continuous data with 95% confidence intervals (CIs). A random-effect model was applied in all analyses with the DerSimonian–Laird estimation. Statistical heterogeneity was analyzed using the I2 and χ2 tests to gain probability values; P < 0.10 was defined to indicate significant heterogeneity. The I2 test represents the percentage of total variability across studies because of heterogeneity. I2 values of 30%–60%, 50%–90%, and 75%–100% corresponded to moderate, substantial, and considerable heterogeneity, respectively, based on Cochrane's handbook (19). Statistical analyses were performed with Comprehensive Meta-Analysis Software and STATA. Forest plots displayed the results of the meta-analysis.

Outcome measures

Overall technical success was defined as adequate placement of both biliary and duodenal stents or successful performance of double bypass in the case of manifest gastric outlet and biliary obstruction (4,20,21). Clinical success of biliary stenting was usually defined as a postprocedural reduction in serum bilirubin level within 2 weeks. However, this definition varied remarkably across studies: One study required normalization of serum bilirubin level (22), whereas others considered clinical success when a 25% or 50% reduction in bilirubin was observed (17,21,23) or only stated improvement of biliary obstruction symptoms without further clarification (4,24). Clinical success of duodenal stenting, when clarified other than clinical improvement of symptoms (4,24), mainly referred to a better score on the gastric outlet obstruction scoring system (21,23). Technical and clinical success was determined for that of biliary stenting/bypass and duodenal stenting/bypass together and separately as well.

Cases of prophylactic GEA were also included in the meta-analysis because it is recommended and commonly applied in the surgical treatment of pancreatic tumors. However, when prophylactic GEA was included in the surgical group, technical and clinical success could only be interpreted as that of biliary bypass, and accordingly, this was compared with technical and clinical success of biliary stenting.

Survival was determined as the time to death from both stents' placement (or creation of double bypass). For sequential biliary and duodenal stenting, survival was calculated from placement of the later stent. The following adverse events were investigated: pancreatitis, cholangitis, cholecystitis, bleeding, bile leakage, perforation, pneumoperitoneum, abdominal pain, wound infection, pneumonia, and others (including symptomless amylasemia, atrial fibrillation, cardiac arrest, aspiration, intra-abdominal abscess, and deep vein thrombosis). Stent migration, recurrent biliary obstruction (RBO; defined mostly as per the Tokyo criteria (25)), and recurrent duodenal obstruction (RDO; reoccurrence of gastric outlet obstruction symptoms) were also investigated. Adverse event rate was given as the number of patients with one or more adverse events. Reintervention rate was defined as the number of patients who required endoscopic or surgical intervention to treat RBO or RDO.


Study selection and characteristics

A total of 2,765 records were identified through a database search: 833 in PubMed, 1,531 in EMBASE, 382 in Web of Science, and 19 in CENTRAL. Nine additional records were found from the reference list of relevant articles. After removing duplicates and irrelevant records, 121 studies were found eligible. From these, 41 case reports and case series were excluded from quantitative synthesis (Figure 1). Therefore, 80 studies were included in the pooled analysis: 8 prospective and 72 retrospective observational studies (Tables 1 and 2). No randomized controlled trials were available. Fifty-five studies including 5,026 patients reported about double stenting, 22 with 1,080 patients about double bypass, and only 3 about both the techniques (including 64 patients who underwent double stenting and 93 with double bypass) (8,22,26). However, insufficient outcome reporting hindered the direct comparison of outcomes.

Figure 1.
Figure 1.:
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses flowchart.
Table 1.
Table 1.:
Characteristics of included studies dealing with endoscopic double stenting
Table 1-A.
Table 1-A.:
Characteristics of included studies dealing with endoscopic double stenting
Table 1-B.
Table 1-B.:
Characteristics of included studies dealing with endoscopic double stenting
Table 2.
Table 2.:
Characteristics of included studies dealing with surgical double bypass

Underlying malignancy was specified in 73% of cases: pancreatobiliary cancer in 4,149, gastroduodenal cancer in 212, metastatic cancer in 49, and other malignancies in 144 cases. Duodenal stenosis was located above and at the ampullary level in 43.7% each and below the ampulla in 12.5% of reported cases. Seventeen studies reported about prophylactic GEA, and it was applied in 69% of surgical cases. In case of double stenting, biliary stenting was performed via ERCP in 69%, PTD in 17%, and EUS-BD in 14% of patients. Biliary and duodenal stents were placed simultaneously in 25.5% of reported cases; biliary stenting preceded duodenal in 45.7% and followed it in 28.8%. The mean interval between stent placements was 114 ± 106 days (201 ± 173 days for biliary first and 74 ± 75 days for duodenal first).

In post hoc analysis, the mean age of patients who underwent double stenting was significantly higher (67.9 years [95% CI: 67.0–68.9 years; I2 = 88.0%]) than that of those who underwent double bypass (63.7 years [95% CI: 62.3–65.0 years; I2 = 89.2%]). Gender distribution showed no difference between the groups.

Risk of bias assessment

Risk of bias of individual studies was assessed with the NOS (see Table, Supplementary Digital Content 1, Baseline characteristics were reported in almost all journal articles but were only partially available in conference abstracts (Tables 1 and 2). Clinical success rate's definition varied, and other outcome measures were defined mostly uniformly (4,17,21–24). Although assessment of different outcomes was reported reliably in more than 90% (Figure 2), outcomes were reported heterogeneously (see Tables, Supplementary Digital Content 2 and 3, and Adequate follow-up data were available in only approximately 40%, but the length of follow-up was appropriate for assessment of outcomes, when reported (Figure 2).

Figure 2.
Figure 2.:
Risk of bias assessment of individual studies according to the modified Newcastle–Ottawa Scale. (a) Endoscopic studies and (b) surgical studies. Each item was rated as “high risk” (zero stars) or “low risk” (one star). Selection domain: (i) representativeness of the exposed cohort, (ii) selection of the nonexposed cohort, (iii) ascertainment of exposure, and (iv) demonstration that the outcome of interest was not present at the start of study. Outcome domain: (v) assessment of outcome, (vi) length of follow-up, and (vii) adequacy of follow-up.

Meta-analytical calculations

Technical and clinical success

Overall technical and clinical success rates of double stenting were 97% (95% CI: 95%–99%) and 92% (95% CI: 89%–95%), respectively. Subgroup analysis of different biliary stenting modalities found no difference in technical and clinical success (see Figures, Supplementary Digital Content 4 and 5, and

Considering frequent prophylactic GEA use during surgical double bypass, technical and clinical success in this group could only be assessed for biliary bypass. No difference was found between technical success of endoscopic stenting and surgical biliary bypass (see Figure, Supplementary Digital Content 6,, whereas clinical success of endoscopic biliary stenting was higher (97% [95% CI: 94%–99%; I2 = 67.3%] vs 86% [95% CI: 78%–92%; I2 = 19.9%], respectively) (Figure 3). Technical and clinical success of duodenal stenting was 99% (95% CI: 97%–100%) and 97% (95% CI: 94%–99%), respectively.

Figure 3.
Figure 3.:
Clinical success of biliary bypass in case of double stenting and double surgical bypass (including cases with prophylactic GEA). CI, confidence interval; ES, effect size; GEA, gastroenteric anastomosis.

Adverse event rate

Double stenting was associated with less adverse events compared with surgical double bypass (13% [95% CI: 8%–19%; I2 = 86.3%] vs 28% [95% CI: 19%–38%; I2 = 89.3%]) (Figure 4). See Table (Supplementary Digital Content 7, for details of adverse events associated with double stenting and double bypass. Adverse events occurred at 67.8 days on average (95% CI: 5.1–128.4 days) postprocedure. There was no difference between adverse events' occurrence time after double stenting and double bypass (52.8 days [95% CI: 23.7–129.3 days] vs 108.7 days [95% CI: 123.2–340.6 days], respectively).

Figure 4.
Figure 4.:
Adverse events related to double stenting and double surgical bypass. CI, confidence interval; ES, effect size.

ERCP was associated with the least adverse events (3% [95% CI: 1%–6%; I2 = 42.8%]), followed by PTD (10% [95% CI: 0%–37%; I2 = 90.2%]) and EUS-BD (23% [95% CI: 15%–33%; I2 = 1.8%]) (Figure 5). The difference was significant between ERCP and EUS-BD.

Figure 5.
Figure 5.:
Adverse events related to ERCP, EUS-BD, and PTD. CI, confidence interval; ERCP, endoscopic retrograde cholangiopancreatography; ES, effect size; EUS-BD, endoscopic ultrasound-guided biliary drainage; PTD, percutaneous transhepatic drainage.

Reintervention rate

More reinterventions were needed after double stenting than after double bypass (21% [95% CI: 16%–27%; I2 = 79.4%] vs 10% [95% CI: 4%–19%; I2 = 90.2%]) (see Figure, Supplementary Digital Content 8, In subgroup analysis, reinterventions were least likely to be necessary after PTD (4% [95% CI: 0%–15%]), followed by ERCP and EUS-BD (16% [95% CI: 9%–24%] and 32% [95% CI: 15%–50%], respectively) (Figure 6).

Figure 6.
Figure 6.:
Reintervention rate related to ERCP, PTD, and EUS-BD. CI, confidence interval; ERCP, endoscopic retrograde cholangiopancreatography; ES, effect size; EUS-BD, endoscopic ultrasound-guided biliary drainage; PTD, percutaneous transhepatic drainage.

Although only 2 surgical studies specified whether reintervention was necessary because of RBO or RDO (26,27), several endoscopic studies investigated RBO and RDO separately (see Table, Supplementary Digital Content 2, RBO was reported in a total of 285 cases, whereas RDO was reported in 100 cases. The mean time until the occurrence of RBO and RDO was 167.3 days (95% CI: 93.0–241.6 days; I2 = 96.0%) and 106.0 days (95% CI: 56.7–155.3 days; I2 = 51.1%), respectively.


Cumulative mean survival of patients after double stenting was 156.4 days (95% CI: 128.3–184.5 days). Subgroup analysis of the different biliary stenting methods as part of double stenting revealed no difference in mean survival (see Figure, Supplementary Digital Content 9, A small number of surgical studies and frequent GEA use in the surgical cohort prevented comparison of survival in the endoscopic and surgical cohorts.


Although double stenting for combined malignant biliary and duodenal obstruction has been a treatment option for 25 years (16), its place in the therapeutic algorithm has not been clearly specified, and reliable efficacy data are still lacking because of the rare concomitant occurrence of these conditions (17). To the best of our knowledge, this is the first systematic review and meta-analysis dealing with the feasibility of double endoscopic stenting in this scenario.

According to our findings, high cumulative technical and clinical success rates can be achieved with double stenting in this difficult-to-treat population. Success rates were comparable with traditionally applied surgical bypass regarding biliary bypass; moreover, clinical success rate of endoscopic biliary bypass was even higher than that of surgery. The importance of this finding lies in the fact that those underwent double stenting were significantly older compared with those with double bypass, suggesting a potential superiority of double stenting in the elderly.

The adverse event profile of double stenting was favorable over that of double bypass in terms of not only numbers but also severity (death was only reported in the surgical cohort). However, the occurrence of adverse events depends on the method of biliary stenting: ERCP was associated with significantly fewer adverse events than EUS-BD. A previous meta-analysis about EUS-BD reported a similarly high cumulative adverse event rate (23.32%) (28). The high proportion of ERCPs in the double stenting cohort may also contribute to the overall adverse event rate.

However, double stenting was associated with higher reintervention rate independently of the biliary stenting method. Duodenal stent placement alone was found to require more reinterventions than surgery (15), and a recent multicenter randomized controlled trial comparing ERCP and EUS-BD as the primary treatment modality of malignant biliary obstruction reported reintervention rates of 42.6% and 15.6%, respectively (14). These facts, and plastic biliary stents' use in numerous studies and inclusion of early studies dealing with double stenting, might also contribute to high reintervention rates (29). Considering cumulative survival and mean time until RBO or RDO, generally one reintervention will be necessary for patients undergoing double stenting. Nevertheless, PTD and EUS-BD were mostly second-line treatments after ERCP failure, and the exact number of sessions required to stent placement (especially for PTD, when stenting is often performed in a second session after temporary external biliary drainage) was generally not reported; therefore, complete burden of interventions cannot be reliably assessed.

Common prophylactic GEA use in double bypass also needs to be considered. Because it is associated with a lower risk of development of duodenal stenosis (6,7), lower rates of reinterventions for RDO are expected in the surgical cohort, which consists mostly of cases with prophylactic GEA. Therefore, cumulative overall reintervention rates might also be lower; however, details of conditions requiring reintervention in this cohort were generally not reported. Another aspect related to prophylactic GEA use is the impossibility to compare overall success rates of the cohorts because technical and clinical success of duodenal bypass is not applicable in such cases.


The main limitation was the lack of head-to-head comparative studies assessing double stenting and double bypass; therefore, only an indirect comparison could be provided with significant heterogeneity between studies. Different timing of biliary and duodenal interventions and frequent second-line use of PTD and EUS-BD increase heterogeneity further. Numerous studies were retrospective or not available as full text, and being a relatively rare entity, a huge part of literature (particularly for EUS-BD) consists of case reports and case series.

Results of double stenting and double bypass must be compared with caution because the cohorts may not consist of the exact same population (double stenting was traditionally an alternative for patients unfit for surgery). The higher age of those underwent double stenting seems to be confirming this; however, objective measures to assess operative risk (e.g., the American Society of Anesthesiologists classification system), which might serve as a basis for such a distinction, were not reported.

Implications for practice

A crucial clinical question regarding malignant duodenobiliary obstruction is whether to refer patients to surgery or endoscopy for palliation. According to our meta-analysis, high technical and clinical success rates, especially the higher clinical success rate of endoscopic biliary stenting compared with surgical bypass, and the lower adverse event rate suggest a justification of minimally invasive techniques in this setting, but high reintervention rates should also be acknowledged. Based on the adverse event profile, when technically feasible, ERCP can be recommended as the first-choice method for biliary stenting also in case of duodenobiliary stenosis, but high reintervention rates and frequent sequential development of duodenal stenosis do not allow to make general recommendations. Caution should be taken because of the limited and substantially heterogeneous available evidence.

Implications for research

To define the cohorts that can benefit most from double stenting, there is a pressing need for multicentric, prospective, comparative studies with well-defined outcome measures and carefully chosen cohorts. Aspects such as prophylactic GEA use, selection of patients “unfit for surgery” based on the well-defined scoring systems for risk stratification, and the possible use of EUS-BD as the primary treatment option should also be considered.


Guarantor of the article: Anna Fábián, MD.

Specific author contributions: A.F., R.B, and Z. Szepes designed the study. A.F., R.B., and P.B. acquired the data. A.F., R.B., N.G., P.B., D.P., and Z. Szakács analyzed and interpreted the data. N.G. performed the statistical analysis. A.F. and N.G. wrote the paper. D.P., P.H., B.T., Z. Szakács, Á.V., I.R., Z.R., B.E., R.S., and Z. Szepes provided critical revision. All authors read and approved the final manuscript.

Financial support: The study was supported by the University of Szeged Open Access Fund (grant number: 4630), the Economic Development and Innovation Operational Programme Grant (GINOP 2.3.2-15-2016-00048) and by the Human Resources Development Operational Programme Grant (EFOP-3.6.2-16-2017-00006 and EFOP-3.6.3-VEKOP-16-2017-00009) from the National Research, Development and Innovation Office.

Potential competing interests: None to report.


1. Manuel-Vázquez A, Latorre-Fragua R, Ramiro-Pérez C, et al. Laparoscopic gastrojejunostomy for gastric outlet obstruction in patients with unresectable hepatopancreatobiliary cancers: A personal series and systematic review of the literature. World J Gastroenterol 2018;24(18):1978–88.
2. Laquente B, Calsina-Berna A, Carmona-Bayonas A, et al. Supportive care in pancreatic ductal adenocarcinoma. Clin Transl Oncol 2017;19(11):1293–302.
3. Shah A, Fehmi A, Savides TJ. Increased rates of duodenal obstruction in pancreatic cancer patients receiving modern medical management. Dig Dis Sci 2014;59(9):2294–8.
4. Hori Y, Naitoh I, Hayashi K, et al. Covered duodenal self-expandable metal stents prolong biliary stent patency in double stenting: The largest series of bilioduodenal obstruction. J Gastroenterol Hepatol 2018;33(3):696–703.
5. Bartlett EK, Wachtel H, Fraker DL, et al. Surgical palliation of pancreatic malignancy: Practice patterns and predictors of morbidity and mortality. J Gastrointest Surg 2014;18:1292–8.
6. Hüser N, Michalski CW, Schuster T, et al. Systematic review and meta-analysis of prophylactic gastroenterostomy for unresectable advanced pancreatic cancer. Br J Surg 2009;96:711–9.
7. Gurusamy KS, Kumar S, Davidson BR. Prophylactic gastrojejunostomy for unresectable periampullary carcinoma. Cochrane Database Syst Rev 2013;(2):CD008533.
8. Williamson C, Wennerblom J, Tingstedt B, et al. A wait-and-see strategy with subsequent self-expanding metal stent on demand is superior to prophylactic bypass surgery for unresectable periampullary cancer. HPB (Oxford) 2016;18(1):107–12.
9. Kohan G, Ocampo CG, Zandalazini HI, et al. Laparoscopic hepaticojejunostomy and gastrojejunostomy for palliative treatment of pancreatic head cancer in 48 patients. Surg Endosc 2015;29(7):1970–5.
10. Lyons JM, Karkar A, Correa-Gallego CC, et al. Operative procedures for unresectable pancreatic cancer: Does operative bypass decrease requirements for postoperative procedures and in-hospital days? HPB (Oxford) 2012;14(7):469–75.
11. Nakai Y, Hamada T, Isayama H, et al. Endoscopic management of combined malignant biliary and gastric outlet obstruction: A narrative review. Dig Endosc 2017;29(1):16–25.
12. Dumonceau J-M, Tringali A, Blero D, et al. Biliary stenting: Indications, choice of stents and results: European Society of Gastrointestinal Endoscopy (ESGE) clinical guideline. Endoscopy 2012;44(3):277–98.
13. Ardengh JC, Lopes CV, Kemp R, et al. Different options of endosonography-guided biliary drainage after endoscopic retrograde cholangio-pancreatography failure. World J Gastrointest Endosc 2018;10(5):99–108.
14. Paik WH, Lee TH, Park DH, et al. EUS-guided biliary drainage versus ERCP for primary palliation of malignant biliary obstruction: A multicenter randomized clinical trial. Am J Gastroenterol 2018;113(7):987–97.
15. Upchurch E, Ragusa M, Cirocchi R. Stent placement versus surgical palliation for adults with malignant gastric outlet obstruction. Cochrane Database Syst Rev 2018;5:CD012506.
16. Maetani I, Ogawa S, Hoshi H, et al. Self-expandable metal stents for palliative treatment of malignant biliary and duodenal stenoses. Endoscopy 1994;26:701–4.
17. Hamada T, Nakai Y, Lau JY, et al. International study of endoscopic management of distal malignant biliary obstruction combined with duodenal obstruction. Scand J Gastroenterol 2018;53(1):46–55.
18. Moher D, Liberati A, Tetzlaff J, et al.; The PRISMA Group (2009). Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA statement. PLoS Med 2009;6(7):e1000097.
19. Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA (eds). Cochrane Handbook for Systematic Reviews of Interventions version 6.0 ( (2019).
20. Staub J, Siddiqui A, Taylor LJ, et al. ERCP performed through previously placed duodenal stents: A multicenter retrospective study of outcomes and adverse events. Gastrointest Endosc 2018;87(6):1499–504.
21. Matsumoto K, Kato H, Tsutsumi K, et al. Long-term outcomes and risk factors of biliary stent dysfunction after endoscopic double stenting for malignant biliary and duodenal obstructions. Dig Endosc 2017;29(5):617–25.
22. Fu Q, Chen Y, Liu X. The choice of palliative treatment for biliary and duodenal obstruction in patients with unresectable pancreatic cancer: Is surgery bypass better? Int Surg 2016;101(1-2):58–63.
23. Canena J, Coimbra J, Carvalho D, et al. Endoscopic bilio-duodenal bypass: Outcomes of primary and revision efficacy of combined metallic stents in malignant duodenal and biliary obstructions. Dig Dis Sci 2014;59(11):2779–89.
24. Sato T, Hara K, Mizuno N, et al. Type of combined endoscopic biliary and gastroduodenal stenting is significant for biliary route maintenance. Intern Med 2016;55(16):2153–61.
25. Isayama H, Hamada T, Yasuda I, et al. TOKYO criteria 2014 for transpapillary biliary stenting. Dig Endosc 2015;27(2):259–64.
26. Valeshabad AK, Leung WD, Camilo J, et al. Multicenter experience with performance of ERCP in patients with an indwelling duodenal stent. Gastrointest Endosc 2013;77(5 Suppl):AB296.
27. Lesurtel M, Dehni N, Tiret E, et al. Palliative surgery for unresectable pancreatic and periampullary cancer: A reappraisal. J Gastrointest Surg 2006;10(2):286–91.
28. Wang K, Zhu J, Xing L, et al. Assessment of efficacy and safety of EUS-guided biliary drainage: A systematic review. Gastrointest Endosc 2016;83(6):1218–27.
29. Bliss LA, Eskander MF, Kent TS, et al. Early surgical bypass versus endoscopic stent placement in pancreatic cancer. HPB (Oxford) 2016;18(8):671–7.
30. Kaw M, Singh S, Gagneja H. Clinical outcome of simultaneous self-expandable metal stents for palliation of malignant biliary and duodenal obstruction. Surg Endosc 2003;17(3):457–61.
    31. Vanbiervliet G, Demarquay JF, Dumas R, et al. Endoscopic insertion of biliary stents in 18 patients with metallic duodenal stents who developed secondary malignant obstructive jaundice. Gastroenterol Clin Biol 2004;28(12):1209–13.
      32. Choi HJ, Park SJ, Lee KM, et al. Clinical outcome of consecutive non-operative management for palliation of malignant biliary and duodenal obstruction. Gastrointest Endosc 2015;61(5):AB202.
        33. Olsen E, Kiil J, Petersen JB. [Self-expanding metal stents as pallative treatment of a malign obstruction in the distal part of the ventricle or duodenum]. Ugeskr Laeger 2005;167(39):3678–81. Danish.
          34. Maire F, Hammel P, Ponsot P, et al. Long-term outcome of biliary and duodenal stents in palliative treatment of patients with unresectable adenocarcinoma of the head of pancreas. Am J Gastroenterol 2006;101(4):735–42.
            35. Sulieman BM, Bardia A, Silverman WB. Efficacy and safety of self expanding metal stents (SEMS) in alleviating combined malignant biliary and duodenal obstruction: A nine year tertiary center experience. Gastrointest Endosc 2006;63(5):AB305.
              36. Wang F, Ji DH, Liu YS, et al. Combined biliary and duodenal stenting for palliation of biliary and duodenal obstructions. J Interv Radiol 2006;15(3):157–9.
                37. Akinci D, Akhan O, Ozkan F, et al. Palliation of malignant biliary and duodenal obstruction with combined metallic stenting. Cardiovasc Intervent Radiol 2007;30(6):1173–7.
                  38. Hou GX, Zhang HJ, Wang YF, et al. Application of metallic self-expanding stent in the treatment of malignant biliary obstruction associated with duodenal obstruction. Chin J Interv Imaging Ther 2007;4(2):129–31.
                    39. Mutignani M, Tringali A, Shah SG, et al. Combined endoscopic stent insertion in malignant biliary and duodenal obstruction. Endoscopy 2007;39(5):440–7.
                      40. Moon JH, Choi HJ, Ko BM, et al. Combined endoscopic stent-in-stent placement for malignant biliary and duodenal obstruction by using a new duodenal metal stent (with videos). Gastrointest Endosc 2009;70(4):772–7.
                        41. Katsinelos P, Kountouras J, Germanidis G, et al. Sequential or simultaneous placement of self-expandable metallic stents for palliation of malignant biliary and duodenal obstruction due to unresectable pancreatic head carcinoma. Surg Laparosc Endosc Percutan Tech 2010;20(6):410–5.
                          42. Keranen I, Udd M, Lepisto A, et al. Outcome for self-expandable metal stents in malignant gastroduodenal obstruction: Single-center experience with 104 patients. Surg Endosc Other Interv Tech 2010;24(4):891–6.
                            43. Iwamuro M, Kawamoto H, Harada R, et al. Combined duodenal stent placement and endoscopic ultrasonography-guided biliary drainage for malignant duodenal obstruction with biliary stricture. Dig Endosc 2010;22(3):236–40.
                              44. Zheng SJ, Ji PT, Ru LX, et al. Dual stent placement of biliary and duodenal tract for the treatment of malignant obstruction. J Interv Radiol 2010;19(5):392–4.
                                45. Li LP, Yu YT, Zhang JY, et al. Combined stent insertion in the treatment of malignant biliary and duodenal obstruction. Chin J Interv Imaging Ther 2011;8(3):189–92.
                                  46. Price C, Krige J, Shaw J, et al. Combined palliative stenting for malignant biliary and duodenal obstruction. HPB (Oxford) 2011;13:44.
                                    47. Ardengh JC, Micelli-Neto O, Bertani CG, et al. Unresectable pancreatic head carcinoma: The simultaneous diagnosis and sequential treatment of jaundice, pain, and duodenal obstruction can improve the quality of life these patients? A prospective study. Gastrointest Endosc 2012;75(4):AB291.
                                      48. Hamada T, Nakai Y, Isayama H, et al. Duodenal metal stent placement is a risk factor for biliary metal stent dysfunction: An analysis using a time-dependent covariate. Surg Endosc 2013;27(4):1243–8.
                                        49. Kanno Y, Ito K, Fujita N, et al. Endoscopic double stenting for biliary obstruction and duodenal obstruction caused by pancreatobiliary malignancies. J Gastroenterol Hepatol 2012;27:112.
                                          50. Khashab MA, Fuji LL, Baron TH, et al. EUS-guided biliary drainage for patients with malignant biliary obstruction with an indwelling duodenal stent (with videos). Gastrointest Endosc 2012;76(1):209–13.
                                            51. Kim KO, Kim TN, Lee HC. Effectiveness of combined biliary and duodenal stenting in patients with malignant biliary and duodenal obstruction. Scand J Gastroenterol 2012;47(8-9):962–7.
                                              52. Maluf-Filho F, Retes FA, Neves CZ, et al. Transduodenal endosonography-guided biliary drainage and duodenal stenting for palliation of malignant obstructive jaundice and duodenal obstruction. J Pancreas 2012;13(2):210–4.
                                                53. Kushnir VM, Almaskeen SA, Bill J, et al. Minimally invasive therapy for concomitant malignant biliary and duodenal strictures: Outcomes of a multidisciplinary approach. Gastrointest Endosc 2013;77(5):AB309.
                                                  54. Pan YM, Wang TT, Gao DJ, et al. Simultaneous stenting in bile duct and duodenum under endoscope for treatment of malignant biliary and duodenal obstruction. Acad J Second Mil Med Univ 2013;34(3):261–5.
                                                    55. Tonozuka R, Itoi T, Sofuni A, et al. Endoscopic double stenting for the treatment of malignant biliary and duodenal obstruction due to pancreatic cancer. Dig Endosc 2013;25(Suppl 2):100–8.
                                                      56. Waidmann O, Trojan J, Friedrich-Rust M, et al. SEMS vs cSEMS in duodenal and small bowel obstruction: High risk of migration in the covered stent group. World J Gastroenterol 2013;19(37):6199–206.
                                                        57. Carvalho DFB, Canena J, Coimbra J, et al. Outcomes of primary and revision efficacy of combined metallic stents in malignant duodenal and biliary obstructions. United Eur Gastroenterol J 2014;2(1):A192.
                                                          58. Hamada T, Isayama H, Nakai Y, et al. Transmural biliary drainage can be an alternative to transpapillary drainage in patients with an indwelling duodenal stent. Dig Dis Sci 2014;59(8):1931–8.
                                                            59. Khashab MA, Valeshabad AK, Leung W, et al. Multicenter experience with performance of ERCP in patients with an indwelling duodenal stent. Endoscopy 2014;46(3):252–5.
                                                              60. Lee E, Gwon DI, Ko GY, et al. Percutaneous biliary covered stent insertion in patients with malignant duodenobiliary obstruction. Acta Radiol 2014;56(2):166–73.
                                                                61. Yu JF, Hao JY, Wu DF, et al. Retrospective evaluation of endoscopic stenting of combined malignant common bile duct and gastric outlet-duodenum obstructions. Exp Ther Med 2014;8(4):1173–7.
                                                                  62. Di Mitri R, Mocciaro F, Pecoraro GM. Double endoscopic self-expanding metal stent placement for the treatment of malignant duodenal and biliary obstruction: A large series of patients from a referral center for palliative care. Gastrointest Endosc 2015;81(5):AB576.
                                                                    63. Kubo A, Tamaki H, Noda T, et al. Double stent placement for biliary and duodenal obstruction caused by unresectable pancreatobiliary cancer. HPB (Oxford) 2015;17:42.
                                                                      64. Manta R, Conigliaro R, Mangiafico S, et al. A multimodal, one-session endoscopic approach for management of patients with advanced pancreatic cancer. Surg Endosc 2016;30(5):1863–8.
                                                                        65. Matsumoto K, Kato H, Tsutsumi K, et al. Clinical outcome of endoscopic double stenting for the treatment of malignant biliary and duodenal obstruction due to pancreatic cancer. J Gastroenterol Hepatol 2015;30:225.
                                                                          66. Sanchez-Ocana R, Santos-Santamarta F, Penas-Herrero I, et al. Long-term clinical outcomes of palliative dual endoscopic stenting in patients with concurrent biliary and gastric outlet obstruction. United Eur Gastroenterol J 2015;3(5):A579.
                                                                            67. Sano I, Katanuma A, Maguchi H, et al. Endoscopic double stenting for biliary and duodenal obstruction due to unresectable pancreatic cancer. J Gastroenterol Hepatol 2015;30:228.
                                                                              68. Ogura T, Chiba Y, Masuda D, et al. Comparison of the clinical impact of endoscopic ultrasound-guided choledochoduodenostomy and hepaticogastrostomy for bile duct obstruction with duodenal obstruction. Endoscopy 2016;48(2):156–63.
                                                                                69. Paik KH, Kim HW, Lee JC, et al. Comparison of endoscopic and percutaneous biliary stenting in patients with pyloric obstruction. J Gastroenterol Hepatol 2016;31:342–3.
                                                                                  70. Yao JF, Zhang L, Wu H. Analysis of high risk factors for endoscopic retrograde cholangiopancreatography biliary metallic stenting after malignant duodenal SEMS implantation. J Biol Regul Homeost Agents 2016;30(3):743–8.
                                                                                    71. Zhao L, Xu HT, Zhang YB. Palliation double stenting for malignant biliary and duodenal obstruction. Exp Ther Med 2016;11(1):348–52.
                                                                                      72. Bulut E, Ciftci T, Akhan O, et al. Palliation of malignant gastroduodenal obstruction: Fluoroscopic metallic stent placement with different approaches. Diagn Interv Radiol 2017;23(3):211–6.
                                                                                        73. Fukushima T, Hamanaka J, Sano Y, et al. Accumulation of double stenting for malignant gastroduodenal and biliary obstruction. Dig Endosc 2017;29:153.
                                                                                          74. Brewer Gutierrez OI, Nieto J, Irani S, et al. Double endoscopic bypass for gastric outlet obstruction and biliary obstruction: Double endoscopic bypass for gastric outlet obstruction and biliary obstruction. Endosc Int Open 2017;5(9):E893–9.
                                                                                            75. Kim KY, Tsauo J, Kim PH, et al. Acute biliary obstruction after gastroduodenal covered self-expanding metallic stent placement in patients with previous biliary stent placement for periampullary cancer: Frequency and protective factors. Cardiovasc Intervent Radiol 2018;41(4):603–9.
                                                                                              76. Lee JJ, Hyun JJ, Choe JW, et al. Endoscopic biliary stent insertion through specialized duodenal stent for combined malignant biliary and duodenal obstruction facilitated by stent or PTBD guidance. Scand J Gastroenterol 2017;52(11):1258–62.
                                                                                                77. Rai AA, Laeeq SM, Luck NH. The experience of simultaneous and sequential double stenting in combined malignant biliary and duodenal obstructions. Dig Endosc 2017;29:146.
                                                                                                  78. Yamao K, Kitano M, Takenaka M, et al. Outcomes of endoscopic biliary drainage in pancreatic cancer patients with an indwelling gastroduodenal stent: A multicenter cohort study in West Japan. Gastrointest Endosc 2018;88(1):66.
                                                                                                    79. Levi JU, Zeppa R, Hutson D, et al. A rapid technique for biliary and duodenal bypass in nonresectable pancreatic carcinoma. Arch Surg 1982;117(3):375–6.
                                                                                                      80. Wongsuwanporn T, Basse E. Palliative surgical treatment of sixty-eight patients with carcinoma of the head of the pancreas. Surg Gynecol Obstet 1983;156(1):73–5.
                                                                                                        81. Lee YTNM. Surgery for carcinoma of the pancreas and periampullary structures: Complications of resectional and palliative procedures. J Surg Oncol 1984;27(4):280–5.
                                                                                                          82. Parker GA, Postlethwaite RW. The continuing problem of carcinoma of the pancreas. J Surg Oncol 1985;28(1):36–8.
                                                                                                            83. La Ferla G, Murray WR. Carcinoma of the head of the pancreas: Bypass surgery in unresectable disease. Br J Surg 1987;74(3):212–3.
                                                                                                              84. Singh SM, Longmire WP Jr, Reber HA. Surgical palliation for pancreatic cancer: The UCLA experience. Ann Surg 1990;212(2):132–9.
                                                                                                                85. Casaccia M, Diviacco P, Molinello P, et al. Laparoscopic palliation of unresectable pancreatic cancers: Preliminary results. Eur J Surg 1999;165(6):556–9.
                                                                                                                  86. Hamade AM, Al-Bahrani AZ, Owera AM, et al. Therapeutic, prophylactic, and preresection applications of laparoscopic gastric and biliary bypass for patients with periampullary malignancy. Surg Endosc 2005;19(10):1333–40.
                                                                                                                    87. Hao CY, Su XQ, Ji JF, et al. Stomach-interposed cholecystogastrojejunostomy: A palliative approach for periampullary carcinoma. World J Gastroenterol 2005;11(13):2009–12.
                                                                                                                      88. Khan AZ, Miles WF, Singh KK. Initial experience with laparoscopic bypass for upper gastrointestinal malignancy: A new option for palliation of patients with advanced upper gastrointestinal tumors. J Laparoendosc Adv Surg Tech A 2005;15(4):374–8.
                                                                                                                        89. Mortenson MM, Ho HS, Bold RJ. An analysis of cost and clinical outcome in palliation for advanced pancreatic cancer. Am J Surg 2005;190(3):406–11.
                                                                                                                          90. Tang CN, Siu WT, Ha JPY, et al. Endo-laparoscopic approach in the management of obstructive jaundice and malignant gastric outflow obstruction. Hepato-Gastroenterology 2005;52(61):128–34.
                                                                                                                            91. Ghanem AM, Hamade AM, Sheen AJ, et al. Laparoscopic gastric and biliary bypass: A single-center cohort prospective study. J Laparoendosc Adv Surg Tech A 2006;16(1):21–6.
                                                                                                                              92. Mann CD, Thomasset SC, Johnson NA, et al. Combined biliary and gastric bypass procedures as effective palliation for unresectable malignant disease. Anz J Surg 2009;79(6):471–5.
                                                                                                                                93. Ausania F, Vallance AE, Manas DM, et al. Double bypass for inoperable pancreatic malignancy at laparotomy: Postoperative complications and long-term outcomes. Ann R Coll Surg Engl 2012;94:563–8.
                                                                                                                                  94. Malde DJ, Brown R, Menon KV, et al. Palliative double bypass in unresectable pancreatic carcinoma: Single centre experience. HBP (Oxford) 2012;14:671.
                                                                                                                                    95. Kofokotsios A, Papzisis K, Andronikidis I, et al. Palliation with endoscopic metal stents may be preferable to surgical intervention for patients with obstructive pancreatic head adenocarcinoma. Int Surg 2015;100(6):1104–10.
                                                                                                                                      96. Giuliani J, Bonetti A. The role of palliative surgery in the management of advanced pancreatic cancer in patients with biliary and duodenal obstruction. Eur J Surg Oncol 2016;42(4):581–3.

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