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Risk factors for gastrointestinal complications after cardiac surgery: A retrospective study

Risk factors for gastrointestinal complications after cardiac surgery: A retrospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101207
Enrollment
Unknown
Registered
2025-04-22
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal complications

Interventions

Experimental groups1:None
Control groups1:None
Experimental groups 2:None
Control groups2:None
Experimental groups 3:None
Control groups 3:None

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with severe gastrointestinal complications, enrollment conditions: (1) Fecal occult blood to two or more consecutive times after cardiac surgery, and transfusion of blood products due to gastrointestinal bleeding, and/or bleeding affecting circulation; (2) Patients with gastrointestinal bleeding and abdominal pain, diarrhea and abdominal distension after cardiac surgery; (3) Patients with abdominal distension and diarrhea after cardiac surgery, combined with fecal occult blood (or above) for more than 3 days, and patients who are not relieved by drug treatment; (4) Patients with mild abdominal distension or fecal occult blood after cardiac surgery, but sudden abdominal pain and intestinal necrosis/perforation diagnosed by imaging examination; 2. Enrollment conditions for general gastrointestinal complications: postoperative cardiac surgery patients with abdominal distension for 3-5 days but rapid improvement after treatment; Control group of gastrointestinal complications after aortic type A dissection: patients with type A dissection who did not have serious gastrointestinal complications during the time period (2017 to 2021) were selected.

Exclusion criteria

Exclusion criteria: 1. Patients with small gastrointestinal bleeding (/, no transfusion of blood products due to gastrointestinal bleeding) and rapid improvement after conservative drug treatment; 2. Patients whose abdominal distension improves rapidly after treatment; 3. Patients with gastrointestinal complications (non-gastrointestinal factors) who have been hospitalized again or more after surgery.

Design outcomes

Primary

MeasureTime frame
Risk factors for non occlusive mesenteric ischemia (NOMI);

Secondary

MeasureTime frame
Whether there is A difference in NOMI between postoperative and elective postoperative acute type A aortic dissection, and the treatment methods.;Diagnosis and treatment of NOMI: The diagnostic methods of NOMI are different abroad. The diagnosis of NOMI in our center is based on clinical manifestations, and different examination methods, mainly gastrointestinal endoscopy, are used.;

Countries

China

Contacts

Public ContactCheng Hao

Shanghai Changhai Hospital

haocheng3746@126.com+86 150 0061 5140

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026