Morbid obesity / metabolic syndrome
Conditions
Interventions
Group 1: 304 Patients who have undergone a Roux-en-Y Gastric Bypass as a primary surgical intervention at the St. Marien Hospital in Friesoythe from the 1st of January 2019 until the 31st of December
Sponsors
St.-Marien-Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients included in this retrospective study have been diagnosed with the ICD-Code E66.02: „Obesity from excess caloric intake Obesity Grade III (WHO) obesity in patients 18 years of age and older “and undergone a primary gastric bypass (Roux-en-Y), registered under: Ø OPS: 5-445.41 (Other surgery on the stomach: gastroenterostomy without gastric resection (Bypass procedure): With stapled suture or transaction (Obesity): with gastrojejunostomy through Roux-Y-anastomosis: laparoscopic (based on data 2021) Moreover, patient selection and indication for a bariatric procedure strictly follow the S-3 Guideline under section 4.2.3 Indication of metabolic surgery of the S3-Guideline Surgery of Obesity and metabolic diseases (Version 2.3 – February 2018 – AWMF-Register Nr. 088-001). On the surgery date, all patients suffer from morbid obesity with a BMI of more than 40 kg/m2.
Exclusion criteria
Exclusion criteria: All patients underwent pre-operatively an endocrinological exclusion diagnostic and a psychiatric assessment. Deficiencies of vitamin and trace elements have been balanced out pre-operatively. Patients without a psychiatric recommendation of a bariatric procedure have been excluded and received no surgical procedure. In addition, all patients attended sessions of professional nutrition advice minimum of 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Digital workflow management-systems in the OR generate positive outcome on process costs. | — |
Secondary
| Measure | Time frame |
|---|---|
| Digital workflow management-systems in the OR generate posi&ve outcome on process quality (intraopera&ve complica&ons and post-OR complica&ons up to 30 days) and on OR-time. | — |
Countries
Germany
Contacts
Public ContactRalf Weise
St.-Marien-Hospital
Outcome results
None listed