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Incidence of adverse events during intra-hospital transport of high-risk critically ill patients and the related risk factors: a prospective, single center, observational study

Incidence of adverse events during intra-hospital transport of high-risk critically ill patients and the related risk factors: a prospective, single center, observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054539
Enrollment
Unknown
Registered
2021-12-19
Start date
2021-12-20
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

critical illness

Interventions

Case series:none

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Elderly patients (aged >= 60 years); 2. Non-mechanical ventilation; 3. Mechanical ventilation; 4. Diagnosis of sepsis (3.0 diagnostic criteria); 5. Hyperlactatemia; 6. Continuous application of vasoactive drugs; 7. Diagnosis of ARDS (Berlin definition); 8. Decompensated acidosis or alkalosis; 9. Abnormal blood sugar; 10. APACHE II>=20; 11. ECMO transport.

Exclusion criteria

Exclusion criteria: 1. Emergency transport that requires emergency treatment; 2. Patients who are transferred to the operating room or general ward; 3. Patients or their families do not agree to be included in the study.

Design outcomes

Primary

MeasureTime frame
the incidence of adverse events during the intra-hospital transport;risk factors of adverse events during the intra-hospital transport ;—

Countries

China

Contacts

Public ContactJia Liu

The Second Affiliated Hospital of Harbin Medical University

jialiu179@163.com+86 13845076587

Outcome results

None listed

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