COVID-19 Clinical Trial
Official title:
Effect of Post-traumatic Stress Disorder (PTSD) of Surgeons and Anesthesiologists on Postoperative Complications of Surgical Patients Under the Background of the COVID-19 Pandemic
The objective of this prospective cohort study is to explore the association between the development of post-traumatic stress disorder (PTSD) in surgeons and anesthesiologists and postoperative prognosis in surgical patients they care for during the COVID-19 pandemic. There are 2 cohorts included in this study. The first cohort consists of registered surgeons and anesthesiologists in the study center. The development of PTSD will be evaluated with a series of questionnaires and scales. This cohort defines exposure (with PTSD). The second cohort consists of surgical patients managed by the surgeons and anesthesiologists in the first cohort. The postoperative outcome of these patients will be evaluated thus to explore the association between PTSD in physicians and adverse patient outcomes. The second cohort defines the outcomes( response).
Status | Recruiting |
Enrollment | 10000 |
Est. completion date | October 31, 2024 |
Est. primary completion date | May 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Registered Surgeons and anesthesiologists in the study center Exclusion Criteria: - Surgeons and anesthesiologists with potential practice location changes during the study periods - Refuse to sign written informed consent and fill out the evaluation questionnaire |
Country | Name | City | State |
---|---|---|---|
China | Ningbo NO.2 hospital | Ningbo | Zhejiang |
China | Xijing Hospital | Xi'an |
Lead Sponsor | Collaborator |
---|---|
Xijing Hospital | Ningbo No.2 Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | postoperative complications of surgical patients cared by these surgeons and anesthesiologists | postoperarive complications of patients whose surgery was performed by surgeons or anesthesiologists who participates in the study | During hospitalization or within 7 days postoperatively, whichever comes first | |
Secondary | postoperative pulmonary complications of surgical patients cared by these surgeons and anesthesiologists | Postoperative pulmonary related adverse events, including respiratory infection, respiratory failure, pleural effusion, atelectasis, pneumothorax, bronchospasm, and aspiration pneumonitis. | During hospitalization or within 7 days postoperatively, whichever comes first | |
Secondary | postoperative length of hospital stay of surgical patients cared by these surgeons and anesthesiologists | the duration between end of surgery to discharge from hospital | From the date of surgery until patients discharged from hospital, assessed up to 30 days | |
Secondary | postoperative unplanned ICU admission rate of surgical patients cared by these surgeons and anesthesiologists | Percentage of patients admission to ICU for which is unexpected before surgery. | From the date of surgery until patients discharged from hospital, assessed up to 30 days | |
Secondary | all cause in-hospital mortality of surgical patients cared by these surgeons and anesthesiologists | defined as comfirmed death or discharge to hospice. | From the date of surgery until patients discharged from hospital, assessed up to 30 days | |
Secondary | Incidence of serious adverse events after operation of surgical patients cared by these surgeons and anesthesiologists | including acute kidney injury, myocardial infarction and stroke | During hospitalization or within 7 days postoperatively,whichever comes first |
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