BackgroundEndoscopic retrograde cholangiopancreatography (ERCP) is an interventional procedure that requires deep sedation or general anaesthesia. the purpose of this prospective observational study was to assess the feasibility and safety of deep sedation in ERCP to maintain spontaneous breathing.methodsThis is a single-centre observational prospective cohort study conducted in a tertiary referral university hospital. all consecutive patients who needed sedation or general anaesthesia for ERCP were included from January 2021 to June 2021. Deep sedation was achieved and maintained by continuous infusion of an association of propofol and remifentanil. the primary endpoint was to assess the prevalence of major anaesthesia-related complications, such as arrhythmias, hypotension, gas exchange dysfunction, and vomiting (safety endpoint). secondary endpoints were: (a) to assess the prevalence of signs of an insufficient level of sedation, such as movement, cough, and hiccups (feasibility endpoint): (b) time needed to achieve the target level of sedation and for recovery from anaesthesia. In order to do so we collect the following parameters: peripheral oxygen saturation, fraction of inspired oxygen, noninvasive systemic blood pressure, heart rate, number of breaths per minute, neurological functions with the use of the bispectral index to determine depth of anaesthesia, and partially exhaustive CO2 end pressure to continuously assess the ventilatory status. the collected data were analysed by several tests: shapiro-wilk, student's t, Tuckey post-hoc, wilcoxon rank-sum and kruskall-wallis ran. statistical analysis was performed using Stata/BE 17.0 (StataCorp LLC).Results114 patients were enroled. Eeght patients were excluded because they did not meet the inclusion criteria. we found that all patients were hemodynamically stable: intraoperative mean systolic blood pressure was 139,23 mmHg, mean arterial pressure was on average 106,66 mmHg, mean heart rate was 74,471 bpm. The mean time to achieve the target level of sedation was 63 s, while the mean time for the awakening after having stopped drug infusion was 92 s.ConclusionsDuring ERCP, deep sedation and analgesia using the association of propofol and remifentanil and maintaining spontaneous breathing are safe and feasible, allowing for a safe and quick recovery from anaesthesia.

De Vico, P., Biasucci, D.g., Aversano, L., Polidoro, R., Zingaro, A., Millarelli, F.r., et al. (2023). Feasibility and safety of deep sedation with propofol and remifentanil in spontaneous breathing during endoscopic retrograde cholangiopancreatography: an observational prospective study. BMC ANESTHESIOLOGY, 23(1), 260 [10.1186/s12871-023-02218-6].

Feasibility and safety of deep sedation with propofol and remifentanil in spontaneous breathing during endoscopic retrograde cholangiopancreatography: an observational prospective study

De Vico, Pasquale;Biasucci, Daniele G;Aversano, Lucia;Polidoro, Roberto;Zingaro, Alessia;Millarelli, Francesca Romana;Del Vecchio Blanco, Giovanna;Troncone, Edoardo;Dauri, Mario
2023-08-04

Abstract

BackgroundEndoscopic retrograde cholangiopancreatography (ERCP) is an interventional procedure that requires deep sedation or general anaesthesia. the purpose of this prospective observational study was to assess the feasibility and safety of deep sedation in ERCP to maintain spontaneous breathing.methodsThis is a single-centre observational prospective cohort study conducted in a tertiary referral university hospital. all consecutive patients who needed sedation or general anaesthesia for ERCP were included from January 2021 to June 2021. Deep sedation was achieved and maintained by continuous infusion of an association of propofol and remifentanil. the primary endpoint was to assess the prevalence of major anaesthesia-related complications, such as arrhythmias, hypotension, gas exchange dysfunction, and vomiting (safety endpoint). secondary endpoints were: (a) to assess the prevalence of signs of an insufficient level of sedation, such as movement, cough, and hiccups (feasibility endpoint): (b) time needed to achieve the target level of sedation and for recovery from anaesthesia. In order to do so we collect the following parameters: peripheral oxygen saturation, fraction of inspired oxygen, noninvasive systemic blood pressure, heart rate, number of breaths per minute, neurological functions with the use of the bispectral index to determine depth of anaesthesia, and partially exhaustive CO2 end pressure to continuously assess the ventilatory status. the collected data were analysed by several tests: shapiro-wilk, student's t, Tuckey post-hoc, wilcoxon rank-sum and kruskall-wallis ran. statistical analysis was performed using Stata/BE 17.0 (StataCorp LLC).Results114 patients were enroled. Eeght patients were excluded because they did not meet the inclusion criteria. we found that all patients were hemodynamically stable: intraoperative mean systolic blood pressure was 139,23 mmHg, mean arterial pressure was on average 106,66 mmHg, mean heart rate was 74,471 bpm. The mean time to achieve the target level of sedation was 63 s, while the mean time for the awakening after having stopped drug infusion was 92 s.ConclusionsDuring ERCP, deep sedation and analgesia using the association of propofol and remifentanil and maintaining spontaneous breathing are safe and feasible, allowing for a safe and quick recovery from anaesthesia.
4-ago-2023
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/41
English
Deep sedation
Endoscopic retrograde cholangiopancreatography
Nonoperating room anaesthesia
Total intravenous anesthesia
De Vico, P., Biasucci, D.g., Aversano, L., Polidoro, R., Zingaro, A., Millarelli, F.r., et al. (2023). Feasibility and safety of deep sedation with propofol and remifentanil in spontaneous breathing during endoscopic retrograde cholangiopancreatography: an observational prospective study. BMC ANESTHESIOLOGY, 23(1), 260 [10.1186/s12871-023-02218-6].
De Vico, P; Biasucci, Dg; Aversano, L; Polidoro, R; Zingaro, A; Millarelli, Fr; Del Vecchio Blanco, G; Paoluzi, Oa; Troncone, E; Monteleone, G; Dauri, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/342703
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