Overview
This retrospective study investigates the relationship between cardiopulmonary bypass (CPB) duration and the incidence of gastrointestinal complications (GICs) in patients undergoing heart valve replacement. Patients will be grouped into a normal CPB group (CPB <120 minutes) and a prolonged CPB group (CPB ≥120 minutes). The study aims to determine whether prolonged CPB time is associated with a higher risk of GICs and to evaluate the outcomes and recovery process for patients who develop GICs postoperatively.
Description
Heart valve replacement with CPB carries a risk of GICs due to potential ischemia-reperfusion injury to the gastrointestinal tract. GICs in the postoperative period can lead to increased morbidity and prolong recovery. Prolonged CPB time may serve as a predictive factor for the development of GICs following heart valve replacement. This study will utilize established diagnostic criteria to define GICs, which include clinical symptoms, laboratory tests, and imaging as necessary, based on standards from critical care and gastrointestinal surgery guidelines. By understanding this correlation, the study aims to reduce the incidence and severity of postoperative GICs and improve surgical outcomes.
Eligibility
Inclusion Criteria:
- Patients undergoing heart valve replacement with CPB
- Age ≥ 18 years and ≤ 75 years
Exclusion Criteria:
- Have received major gastrointestinal surgery within 5 years.
- History of severe infection (e.g., pneumonia, urinary tract infection) requiring hospitalization within 1 month prior to surgery.
- Inflammatory bowel disease (IBD), including ulcerative colitis, Crohn's disease, or colitis.
- Acute gastroenteritis.
- Clostridium difficile or Helicobacter pylori infection.
- Chronic constipation.
- Peptic ulcer.
- Polyps in the stomach or intestines.
- Gastrointestinal neoplasms.
- Abdominal hernia.
- Irritable bowel syndrome.
- Acute or chronic cholecystitis, hepatitis.
- Patients who died intraoperatively or within 24 hours postoperatively.
- Patients with digestive system tumors.
- Pregnancy or breastfeeding could affect postoperative medication use and study observations.
- Involvement in other studies that may interfere with the objective results of this study.