Sanda Stojanović Stipić

Dr. Sanda Stojanović Stipić

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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 August 2017 in European Archives of Oto-Rhino-Laryngology
Verified
Journal Article
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SSSanda Stojanović Stipić
Sanda Stojanović Stipić
MCMladen Carev
Mladen Carev
ŽBŽarko Bajić
Žarko Bajić
DDDaniela Supe Domic
Daniela Supe Domic
ZRZeljka Roje
Zeljka Roje
TSTonci Stipic
Tonci Stipic

10 March 2026 in Medical Sciences
Verified
Journal Article
Open access
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GPGrgur Prižmić
Grgur Prižmić
FPFilip Peris
Filip Peris
MPMarinela Jozeljić Pešić
Marinela Jozeljić Pešić
Ana Maria MitarAna Maria Mitar
Ana Maria Mitar
ABAna Bego
Ana Bego
SSSanda Stojanović Stipić
Sanda Stojanović Stipić
Background/Objectives: Emergence agitation (EA) is common after rhinologic surgery and may cause self-injury, bleeding, and prolonged post-anesthesia care unit (PACU) stay. Remimazolam is an ultra-short-acting benzodiazepine that may reduce EA without delaying recovery. The objective of this study was to evaluate the effect of a single dose of remimazolam administered at the end of surgery on the incidence of EA in adult patients undergoing nasal surgery. Methods: In this prospective, randomized, triple-blind, placebo-controlled trial, 62 adults undergoing elective rhinologic surgery under sevoflurane anesthesia received either remimazolam 0.1 mg/kg or saline immediately after sevoflurane discontinuation and before extubation. EA was assessed using the Richmond Agitation–Sedation Scale (RASS) at extubation and every 5 min for 30 min in the PACU. The primary outcome was presence of EA (RASS ≥ 2) at extubation. Secondary outcomes included Aldrete recovery scores, VAS, PONV incidence and safety outcomes. The study was registered at ClinicalTrials.gov (NCT06398275; 3 May 2024). Results: EA occurred in 12/32 patients (37.5%) in the control group and 0/30 (0%) in the remimazolam group (p < 0.001). Extubation time and operative durations were similar between groups. More patients in the remimazolam group achieved an Aldrete score ≥ 9 at extubation (76.7% vs. 50.0%, p = 0.030). Severe agitation (RASS ≥ 3) requiring rescue sedation occurred in 6/32 control-group patients and in 0/30 patients in the remimazolam group (p = 0.025). Pain scores were low (no VAS > 2). PONV occurred in one patient per group. Clinically relevant postoperative nasal bleeding requiring intervention occurred in 2/32 control-group patients and in 0/30 remimazolam-group patients. No laryngospasm or respiratory complications within 24 h were observed. Conclusions: A single remimazolam bolus given at the end of surgery prevented clinically relevant EA after rhinologic surgery without delaying early recovery.


9 May 2017
Verified
Conference Paper
Closed access
SSSanda Stojanović Stipić
Sanda Stojanović Stipić
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