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Incidence and Outcome of Reintubation in the PACU

Incidence and Outcome of Reintubation in the Postanesthesia Care Unit: a Single-center, Retrospective, Observational Matched Cohort Study in China

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05341596
Enrollment
121965
Registered
2022-04-22
Start date
2020-01-01
Completion date
2020-10-01
Last updated
2022-04-22

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

Conditions

Complication of Medical Care, Postoperative Complications

Keywords

general anesthesia, postanesthesia care unit, reintubation after planned extubation

Brief summary

This study evaluated the occurrence of reintubation after planned extubation (RAP), the impact of RAP on duration of PACU stay,length of stay,length of postoperative stay,inpatient healthcare costs, unanticipated ICU admission and readmission.

Detailed description

The study was carried out in Wuhan City, China at a general public university hospital with 62 clinical departments, 99 surgical rooms, and 38 beds in the PACU. The total number of operations performed in this hospital is more than 90,000/year. The study was approved by the hospital ethics committee and was deemed that written patient consent was not required. The adverse events, including RAP, in all patients in the PACU were recorded on a standardized form in a database by pre-trained qualified nurses and/or anesthesiologists at the time of care from January 1, 2017 to December 31, 2019. Data, including patient demographic and surgical and anesthesia parameters, were obtained from the anesthesia information system. Adverse events management and duration of PACU stay were also documented. For three years, all collected data were filed in a computer every day and were summarized and analyzed every month. Data, such as demographics, airway, oxygen saturation, consciousness, treatment, vital signs, and fast-track criteria scores, were recorded for all patients in the PACU. The first part contained preoperative and intraoperative data, which were entered into the database by the anesthesiologists involved in the patients' intraoperative care from the time of PACU admission. The second part were recorded by nurse and comprised postoperative data from the PACU to the ward or ICU. The third part were recorded by the surgeons and/ or surgical nurses and comprised postoperative data. The criteria for tracheal extubation in the operating room(OR) and the timing of transfer to the PACU were the responsibility of the anesthesiologist.

Interventions

PROCEDURErepeat endotracheal intubation

repeat endotracheal intubation in the PACU after planned extubation of the initial endotracheal intubation for general anesthesia or combined general anesthesia other than that performed in the operating room

Sponsors

Shangkun Liu (200966)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Patients requiring stay in PACU

Exclusion criteria

* Patients were transferred directly from the operating room to the ward or icu * non-postoperative patient

Design outcomes

Primary

MeasureTime frameDescription
Duration of PACU staythrough study completion, an average of three monthsFrom patient transfer into PACU to transfer out of PACU
Length of postoperative staythrough study completion, an average of three months
Unanticipated ICU admissionthrough study completion, an average of three monthsUnplanned transfer to the ICU

Secondary

MeasureTime frameDescription
Inpatient healthcare coststhrough study completion, an average of three monthsAny medical cost during hospital stay
Readmissionthrough study completion, an average of three monthsadmission after hospital discharge
Length of staythrough study completion, an average of three monthsThe time of hospital length of stay
Duration of postoperative monitoringthrough study completion, an average of three monthsThe time of postoperative monitoring

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026