Publication:
Effectiveness of the Analgesia Nociception Index Monitoring in Patients Who Undergo Colonoscopy with Sedo-Analgesia

dc.contributor.authorsSoral, Merve; Altun, Gulbin Tore; Dinccr, Pelin Corman; Arslantas, Mustafa Kemal; Aykac, Zuhal
dc.date.accessioned2022-03-14T10:10:46Z
dc.date.accessioned2026-01-10T17:03:34Z
dc.date.available2022-03-14T10:10:46Z
dc.date.issued2020-01-31
dc.description.abstractObjective: The objective of this study was to improve the patient comfort and safety during procedures done under anaesthesia and sedation. The analgesia nociception index (ANI) noninvasively provides information on the nociception-antinociception balance, and it can be used to assess analgesia objectively. We aimed to compare the effects of analgesia management with conventional methods and with ANI monitoring on total opioid consumption, sedation and analgesia levels in patients who underwent colonoscopy using sedo-analgesia. Methods: Adult patients (n=102), scheduled for procedural sedation, were prospectively analysed. After the induction with propofol and ketamine, infusions of propofol (2 mg kg(-1) h(-1)) and remifentanil (0.05 mcg kg(-1) min(-1)) were started. In Group A, remifentanil infusions were titrated to maintain the ANI value between 50 and 70, whereas in Group C, analgesic requirements were met according to the attending anaesthetist's intention. The heart rate, blood pressure, respiratory rate, SpO(2), BIS, Numeric Rating Scale (NRS) and Ramsay Sedation Scale were monitored. Complications, analgesics consumption, duration of the procedure, demographic information, NRS and the Modified Aldrete Score were evaluated. Results: A total remifentanil amount used in Group A was 66.51 +/- 47.87 mcg and 90.15 +/- 58.17 mcg in Group C (p=0.011); there was no difference in total amounts of ketamine and propofol given. There was a negative correlation between ANI and NRS scores of Group A patients at Minute 0 at the level of 0.402, which was significant statistically (p=0.003). Conclusion: Opioid consumption was diminished when ANI monitoring was used, and thus the patient safety was improved. Further studies with longer procedure times and with a greater number of patients are required to demonstrate whether there is a difference in side effects and recovery times.
dc.identifier.doi10.5152/TJAR.2019.45077
dc.identifier.eissn2667-6370
dc.identifier.pubmed32076680
dc.identifier.urihttps://hdl.handle.net/11424/244163
dc.identifier.wosWOS:000512301900009
dc.language.isoeng
dc.publisherAVES
dc.relation.ispartofTURKISH JOURNAL OF ANAESTHESIOLOGY AND REANIMATION
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnalgesia nociception index
dc.subjectcolonoscopy
dc.subjectsedation
dc.subjectsedo-analgesia
dc.subjectTOTAL INTRAVENOUS ANESTHESIA
dc.subjectHEART-RATE-VARIABILITY
dc.subjectANALGESIA/NOCICEPTION INDEX
dc.subjectPOSTOPERATIVE PAIN
dc.subjectREMIFENTANIL
dc.subjectPROPOFOL
dc.subjectPREDICTION
dc.subjectPARAMETER
dc.subjectSEDATION
dc.subjectKETAMINE
dc.titleEffectiveness of the Analgesia Nociception Index Monitoring in Patients Who Undergo Colonoscopy with Sedo-Analgesia
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage57
oaire.citation.issue1
oaire.citation.startPage50
oaire.citation.titleTURKISH JOURNAL OF ANAESTHESIOLOGY AND REANIMATION
oaire.citation.volume48

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