Pancreatic Surgery Patients
Conditions
Interventions
Experimental group:According to the "Consensus of Chinese Experts on Whole-process Nutritional Management in Pancreatic Surgery Perioperative Period", individualized nutritional treatment plans are gi
Control group:Based on the clinical experience of physicians, patient conditions, and dietary habits, traditional nutritional treatment models are given before and after surgery
Sponsors
900TH Hospital of Joint Logistics Support Force
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: (1) Age = 18 years old, regardless of gender. (2) Nutrition risk screening score (NRS 2002) = 3. (3) Patients undergoing elective pancreatic surgery, such as pancreatoduodenectomy, pancreatectomy, total pancreatectomy, pancreatectomy preserving the duodenum, local pancreatectomy, and various drainage surgeries for chronic pancreatitis. (4) Informed consent from patients or relatives and signing of a research informed consent form. (5) Good medication compliance, complete case data, and ability to cooperate with follow-up. (6) Able to communicate and communicate normally.
Exclusion criteria
Exclusion criteria: (1) There are contraindications for parenteral and enteral nutrition (unstable vital signs, coagulation disorders, severe gastrointestinal dysfunction, metabolic diseases that cannot be corrected, etc.). (2) Allergies to any components of parenteral or enteral nutrition preparations used for research. (3) Not suitable for measuring human body composition. The measurement of human body composition is not suitable for the following population: those who install pacemakers cannot undergo bioelectrical impedance measurement; If the stratum corneum of the ankle is too thick, body composition data cannot be measured; Unconscious and unable to cooperate with the examination; Metal substances in the body, such as artificial joints and internal fixators, may affect the measurement results. (4) Incomplete case data, failure to follow educational plans, failure to follow up and complete examinations as required. (5) Withdrawal of the researcher for other reasons. (6) Patients deemed unsuitable by the researchers to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Human body composition; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nutritional indicator;Length of hospital stay;Time of first postoperative exhaust and defecation; | — |
Countries
China
Contacts
Public ContactQing Chen
900TH Hospital of Joint Logistics Support Force
Outcome results
None listed