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Department of Anesthesiology and Pain Management, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas
Address correspondence and reprint requests to Dr. Paul F. White, Department of Anesthesiology and Pain Management, University of Texas Southwestern Medical Center at Dallas, 5161 Harry Hines Boulevard, CS 2. 282, Dallas, TX 75235-9068. Address e-mail to pwhite{at}mednet.swmed.edu
| Introduction |
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We hypothesized that using this new scoring system to determine a patient's fast-track eligibility would reduce the need for nursing interventions to administer parenteral medications in the Phase II recovery area. The times to fast-track eligibility were compared using the modified Aldrete and new fast-track criteria in outpatients undergoing laparoscopic surgery with one of three standardized general anesthetic techniques.
| Methods |
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All patients were premedicated with midazolam 2 mg IV. Anesthesia was induced with propofol 2 mg/kg IV and remifentanil 1 µg/kg IV (for LT) or with fentanyl 2 µg/kg IV (for LC). Laryngoscopy and tracheal intubation were facilitated with either succinylcholine 1 mg/kg IV (for LT) or with rocuronium 0.6 mg/kg IV (for LC). After tracheal intubation, anesthesia was maintained with one of the three anesthetics: desflurane 2%8% (inspired), sevoflurane 0.6%2.4% (inspired), or propofol 50200 µg · kg -1 · min-1, in combination with nitrous oxide 67% in oxygen. Supplemental bolus doses of fentanyl 2550 µg IV were administered for persistent hypertension or/and tachycardia that did not respond to increases in the dose of the maintenance anesthetic. Muscle relaxation was maintained with bolus doses of either mivacurium 0.04 mg/kg (for LT) or rocuronium 0.15 mg/kg IV (for LC). All patients received both analgesic and antiemetic prophylaxis with ketorolac 30 (for LT) to 60 (for LC) mg IV and droperidol 0.625 mg IV 1530 min before the end of surgery.
Early recovery status was evaluated at 1-min intervals after discontinuation of the maintenance anesthetics using both the modified Aldrete scoring system (1) and the new fast-track scoring system (Appendix 1) (4). In calculating the fast-track score, the recorded visual analog scale (VAS) scores for pain, nausea, and vomiting (0 = none to 10 = maximal) were assigned a descriptive term. A VAS score
3 was considered "mild," 47 represented "moderate," and
8 was classified as "severe." Patients were considered fast-trackeligible if they achieved a score of 10 using the modified Aldrete scoring system or a score of
12 (with no score <1 in any individual category) using the new scoring system. Times from discontinuation of the maintenance anesthetics to fast-track eligibility using the two scoring systems were recorded at 1-min intervals until 5 min after arrival in the PACU, and subsequently at 5-min intervals until the patient achieved fast-track eligibility using both scoring systems.
Data were analyzed using one-way analysis of variance for continuous variables and
2 test for discrete variables. These data are expressed as means ± SD or percentages, with P values <0.05 considered statistically significant.
| Results |
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| Discussion |
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The modified Aldrete's scoring system is a highly acceptable criteria for discharging patients from the PACU. However, this scoring system was not designed to assess the patient's ability to bypass the PACU after major ambulatory procedures under general anesthesia. The results from this data evaluation demonstrated that 22%29% of outpatients judged fast-trackeligible using the modified Aldrete scoring system subsequently required IV analgesics and antiemetics. Although these patients were fully oriented and had stable vital signs, they would have added to the workload of the Phase II nursing staff and may have necessitated the use of more extensive monitoring in the step-down unit. Although the new fast-track scoring system should be useful for determining which outpatients can safely bypass the PACU, these criteria were not designed for determining home-readiness after ambulatory surgery (7,8).
The new fast-track scoring system takes into consideration pain and emetic symptoms, as well as Aldrete's assessments of consciousness, physical activity, and hemodynamic and respiratory stability. Using the new fast-track criteria, significantly fewer outpatients would require IV medication for the management of pain and emesis in the step-down unit after laparoscopic surgery. Although the modified Aldrete scoring system provided a useful starting point in assessing the fast-tracking eligibility of patients in the ambulatory setting (2), using the new scoring system should help to limit the number of additional nursing interventions required in the step-down unit. Additional prospective clinical studies are required to validate the utility of this new scoring system in the clinical fast-track situation.
In conclusion, the new fast-track scoring system seems to offer advantages over the modified Aldrete's scoring system in evaluating the suitability of outpatients for bypassing the PACU after undergoing ambulatory surgery with general anesthesia.
| Appendix 1 |
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| Acknowledgments |
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| References |
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