There is a need for a structured registry to collect real-world data on patient characteristics, surgical strategies, perioperative outcomes, and long-term results. Such a registry will provide insights into quality of care, support benchmarking, and form the basis for clinical and translational research.

The objective of this study is to collect and register all clinical data on patients undergoing pancreatic surgery at Antwerp University Hospital. Data collection will include demographic information, medical history, preoperative workup, surgical details, postoperative outcomes, lab results, pathology results and long-term follow-up.

There is no intervention in this study; patient care will be done according to the current standard of care. The data will be used to further improve patient outcomes, identify risk factors for complications (both patient-specific and procedure-specific), investigate oncological outcomes and long-term patient survival, help predict exocrine and endocrine insufficiency, and identify patient populations in which specific screening for this is indicated.

Inclusion Criteria:

• benign indications for pancreatic surgery, including chronic pancreatitis, cystic lesions and IPMN
• malignant indications for pancreatic surgery, including PDAC, duodenal carcinoma, pancreatic neuro-endocrine tumours, distal cholangiocarcinoma.

Exclusion criteria:

• indications for pancreatic resection caused by acute pancreatitis
• pancreatic resection after abdominal trauma

Patients undergoing pancreatic surgery

Full access to the dataset will be limited to the PI, co-PI and study coordinator.

Site investigators may access the full dataset upon formal request, subject to approval by the steering group. Requests must include a description of their research plans for consideration.

IPD would be available depending on the study...

Full access to the dataset will be limited to the PI, co-PI and study coordinator.

Site investigators may access the full dataset upon formal request, subject to approval by the steering group. Requests must include a description of their research plans for consideration.