Article Text
Abstract
Objective Lumen-apposing metal stents (LAMS) are believed to clinically improve endoscopic transluminal drainage of infected necrosis when compared with double-pigtail plastic stents. However, comparative data from prospective studies are very limited.
Design Patients with infected necrotising pancreatitis, who underwent an endoscopic step-up approach with LAMS within a multicentre prospective cohort study were compared with the data of 51 patients in the randomised TENSION trial who had been assigned to the endoscopic step-up approach with double-pigtail plastic stents. The clinical study protocol was otherwise identical for both groups. Primary end point was the need for endoscopic transluminal necrosectomy. Secondary end points included mortality, major complications, hospital stay and healthcare costs.
Results A total of 53 patients were treated with LAMS in 16 hospitals during 27 months. The need for endoscopic transluminal necrosectomy was 64% (n=34) and was not different from the previous trial using plastic stents (53%, n=27)), also after correction for baseline characteristics (OR 1.21 (95% CI 0.45 to 3.23)). Secondary end points did not differ between groups either, which also included bleeding requiring intervention—5 patients (9%) after LAMS placement vs 11 patients (22%) after placement of plastic stents (relative risk 0.44; 95% CI 0.16 to 1.17). Total healthcare costs were also comparable (mean difference −€6348, bias-corrected and accelerated 95% CI −€26 386 to €10 121).
Conclusion Our comparison of two patient groups from two multicentre prospective studies with a similar design suggests that LAMS do not reduce the need for endoscopic transluminal necrosectomy when compared with double-pigtail plastic stents in patients with infected necrotising pancreatitis. Also, the rate of bleeding complications was comparable.
- endoscopy
- acute pancreatitis
Data availability statement
Data are available on reasonable request. Request for data can be made to the corresponding author (r.p.voermans@amsterdamumc.nl) and will first be discussed during a meeting of the Dutch Pancreatitis Study Group.
Statistics from Altmetric.com
Data availability statement
Data are available on reasonable request. Request for data can be made to the corresponding author (r.p.voermans@amsterdamumc.nl) and will first be discussed during a meeting of the Dutch Pancreatitis Study Group.
Footnotes
Twitter @marcbesselink
Collaborators The Dutch Pancreatitis Study Group.
Contributors This study was primarily designed by LB, RCV, MGB, JEvH, J-WP, FPV, MBo, PF and RPV, and was subsequently discussed in research meetings with all authors. The study was conducted by LB, RCV, MGB, MAB, TLB, SAWB, VCC, WC, CHD, SMvD, HMvD, CvE, E-JvG, MH, WLH, PH, JEvH, MAJMJ, JECK, MPMK, EK, SK, ML, VBN, LP, J-WP, RQ, RJdR, HCvS, CJSW, MS, HCT, BW, DSU, NGV, FV, RLJvW, MBr, PF and RPV. The data were collected and analysed by LB who also drafted the manuscript under supervision of RPV. All authors contributed to the interpretation of the data and to the draft of the manuscript. All authors have approved of the final manuscript. The guarantor of the article is RPV.
Funding This study was funded by Boston Scientific Corporation (grand number: ISREND00028) and Amsterdam UMC (grand number: not applicable).
Competing interests MGB reports grants from Intuitive, grants from Ethicon Endo-Surgery, grants from Medtronic, outside the submitted work; MBo reports grants and personal fees from Johnson & Johnson, grants and personal fees from Acelity/KCI, grants and personal fees from Bard, grants from Ipsen, grants from New Compliance, grants from Mylan, personal fees from Gore, personal fees from Smith & Newphew, outside the submitted work; MBr reports grants and personal fees from Boston Scientific, grants and personal fees from Cook Medical, grants from Pentax Medical, grants from Mylan, grants from 3M, grants from InterScope, outside the submitted work; PF reports personal fees from Cook Medical, personal fees from Olympus, personal fees from Ethicon Endo-Surgery, outside the submitted work; J-WP reports personal fees and other from Cook Endoscopy, personal fees and other from Boston Scientific, personal fees and other from Pentax Medical, outside the submitted work; E-JvG reports grants from Mylan, grants from Olympus, personal fees from MTW-Endoskopie, outside the submitted work; JEvH reports personal fees from Olympus Endoscopy, grants from Cook Medical, personal fees from Boston Scientific, personal fees from Medtronic, outside the submitted work; FV reports grants from Boston Scientific, outside the submitted work; RPV reports grants and personal fees from Boston Scientific, grants from Zambon, outside the submitted work.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.