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The Association Between Anesthetic and Surgical Practices and Patient Length of Stay in the Post Anesthesia Care Unit

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What is being collected

Data Collection

Collected from past medical records and data - Retrospective
No Sample Retained
Who is being recruted

Over 18 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: November 2012
See protocol details

Summary

Principal SponsorUniversity of California, Davis
Last updated: April 19, 2017
Sourced from a government-validated database.Claim as a partner

Study start date: November 1, 2012

Actual date on which the first participant was enrolled.

We are conducting a retrospective, cross-sectional chart review of patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main (Pavilion) post anesthesia care unit between January 1, 2012 and March 31, 2012. We are excluding patients less than 18-years of age, patients transferred to the intensive care unit, and patients for whom data is not reported. Charts will be reviewed and data will be collected by the primary and co-investigator(s). Analysis will consist of cross-tabulation counts across independent variables, univariate analysis (outcome variable PACU length of stay), and regression analysis (outcome variable PACU length of stay). We aim to measure patient length of stay in the post anesthesia care unit (PACU) as the outcome variable. The following patient, operative, and post operative factors will be recorded as covariates: age, gender, height, weight, American Society of Anesthesiologists physical status classification, pre-operative use of pain medication, pre-operative pain score, whether the patient is non-English speaking, history of smoking, surgical service, anesthetic time, surgical time, urgency of surgery, use of general anesthetic or monitored anesthesia care, use of regional anesthetic, regional anesthetic type, use of inhalational or total intravenous anesthetic maintenance, intraoperative use of dexmedetomidine, intraoperative use of dexamethasone, intraoperative use of ondansetron, intraoperative use of remifentanyl, intraoperative use of ketamine, total volume of crystalloid or colloid administered, intraoperative use of endotracheal tube, natural airway, or laryngeal mask airway, time of PACU arrival, initial pain score in the PACU, episode of post operative nausea or vomiting, administration of antiemetic in the PACU, post operative temperature, time of anesthesiologist sign out in the PACU, time of patient transfer from the PACU, location of transfer from PACU, preoperative placement of scopolamine patch, history of postoperative nausea and vomiting, type of surgery (including categories of major abdominal-open, orthopedic, ear nose and throat, thoracic, vascular, ophthalmology, abdominal-laparoscopic, urology, minor, neurology, and plastics), intra operative estimated blood loss, intra operative administration of the following medications: dexamethasone, antiemetics including dexamethasone, acetaminophen, ketorolac, muscle relaxant (i.e. paralytics), muscle relaxant reversal agents, and morphine equivalent dosage of opioids; intra operative volume of colloid administered, intra operative volume of blood products administered, morphine equivalent dosage of opioids administered in the post anesthesia care unit, times of admission and discharge from the post anesthesia care unit. The data will be labeled with a code that the research team can link to personal identifying information when acquired. The code sheet will be secured and kept separate from the dataset. The primary and co-investigator(s) will be the only individuals who have access to the password protected database stored on a secure server at the University of California Davis Medical Center.

Principal SponsorUniversity of California, Davis
Last updated: April 19, 2017
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

1 inclusion criteria required to participate
Patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main post anesthesia care unit between January 1, 2012 and March 31, 2012

3 exclusion criteria prevent from participating
Patients for whom data is not reported

Patients less than 18-years of age

Patients transferred to the intensive care unit, and

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

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