Postoperative outcomes of intravenous infusion port implantation
Conditions
Interventions
Investigation group:None
Sponsors
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients who received a venous port for long-term intravenous therapy with an indwelling duration of >=3 months. 2.Expected survival >=6 months. 3.Voluntarily participate in this study and sign the informed consent form. If a participant is unable to read and sign the informed consent form due to lack of capacity (e.g., cognitive impairment), their legal guardian shall complete the informed consent process and sign on their behalf. If a participant is unable to read the informed consent form (e.g., illiterate participants), an impartial witness shall observe the informed consent process and co-sign the form.?;
Exclusion criteria
Exclusion criteria: 1.patients with severe coagulation disorders. 2.Patients with systemic infections, such as sepsis or bacteremia.?; 3.Patients unable to complete all follow-up visits.?; 4.Other vulnerable populations excluding illiterate/elderly individuals, including but not limited to: patients with mental illness, cognitive impairment, critically ill patients, and pregnant women.?;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of complications; | — |
Countries
China
Contacts
Public ContactHu Hongjie
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Outcome results
None listed