Nausea after surgery may negatively influence patient satisfaction, may delay discharge, and cause unexpected hospital admissions. The trend toward ambulatory surgery has increased the focus on postoperative nausea, but published evidence is not based on standardized criteria for assessment. Therefore, the results for postoperative nausea are very diverse, especially reports on nausea incidence after regional anesthesia, i.e. spinal anesthesia. When peripheral nerve blocks have been applied for postoperative pain control, they significantly reduce postoperative pain, opioid consumption and side effects; patients receiving general anesthesia (GA) and nerve blocks are thought likely to have less nausea than patients receiving GA alone. This study is a pilot study looking at the incidence and intensity of nausea after orthopedic surgery under nerve blocks in foot and ankle (FA) patients and under nerve blocks with either sedation or GA in total shoulder arthroplasty (TSA) patients. The results of this study will help power a future randomized controlled trial, comparing the incidence and intensity of nausea in FA patients receiving GA through laryngeal mask airway (LMA) versus spinal anesthesia.
Nausea after surgery may negatively influence patient satisfaction, may delay discharge, and cause unexpected hospital admissions. The trend toward ambulatory surgery has increased the focus on postoperative nausea, but published evidence is not based on standardized criteria for assessment. Therefore, the results for postoperative nausea are very diverse, especially reports on nausea incidence after regional anesthesia, i.e. spinal anesthesia. This is due to varying data sources, such as nurse notes and/or patient reports, and a lack of a consistent antiemetic and pain medication protocol. The results of this study will help power a future randomized controlled trial, comparing the incidence and intensity of nausea in FA patients receiving GA through laryngeal mask airway (LMA) versus spinal anesthesia. When peripheral nerve blocks have been applied for postoperative pain control, they significantly reduce postoperative pain, opioid consumption and side effects; patients receiving GA and nerve blocks are thought likely to have less nausea than patients receiving GA alone, due a reduction in pain leading to reduction in need for emetogenic opioids. This study is a pilot study looking at the incidence and intensity of nausea after orthopedic surgery under nerve blocks in foot and ankle (FA) patients and under nerve blocks with either sedation or GA in total shoulder arthroplasty (TSA) patients. At the author's institution, TSA is commonly performed with a brachial plexus block and either GA or intravenous sedation. TSA patients represent a model system for the effect of GA on nausea among patients receiving nerve blocks.
Study Type
OBSERVATIONAL
Enrollment
55
Hospital for Special Surgery, New York
New York, New York, United States
Number of Participants With Nausea 1 Hour After Post-anesthesia Care Unit (PACU) Admission
Yes/no response to whether patient had nausea in the PACU 1 hour after admission. If yes, investigators will seek out intensity
Time frame: 1 hour after surgery
Number of Participants With Nausea
Yes/no question. If yes, the investigators will then seek intensity of nausea.
Time frame: Average 2 hours after surgery (at discharge from the recovery room after surgery)
Intensity of Nausea
On an 11 grade Likert scale (0=no nausea, 10=worst possible nausea)
Time frame: 1 hour after surgery
Intensity of Nausea
On a 11 grade Likert scale (0=no nausea, 10=worst possible nausea)
Time frame: 2 hours after surgery
Antiemetic Consumption
Yes/no question if antiemetic consumption occured.
Time frame: Duration of stay in recovery room after surgery (average 2 hours)
Number of Participants With Emesis
Yes/no question. If yes, the investigators will then seek intensity of emesis
Time frame: 1 hour after surgery
Number of Participants With Emesis
Yes/no question. If yes, the investigators will then seek intensity of emesis
Time frame: Average 2 hours after surgery (at discharge from the recovery room after surgery)
Number of Participants Satisfied With Anesthesia
Lowest satisfaction score on a 11 grade Likert scale (0=no satisfaction, 10=maximal satisfaction).
Time frame: PACU before discharge, an average of 2 hours
Patients Receiving Opioids in the PACU
Yes/no for patients that were given opioids for pain management in the PACU. If opioids were consumed, the oral morphine equivalents for the patients taking opioids was totaled.
Time frame: PACU stay before discharge (average 2 hours)
Opioid Dose Among Patients Receiving Opioids in the PACU
Total opioid dose taken by patients who took any opioids in the PACU, measured in oral morphine equivalents (mg OME)
Time frame: Duration of PACU stay (Average 2 hours)
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