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Dexamethasone versus 5-HT3 receptor antagonists in preventing nausea during awake craniotomy: a propensity score matching study. | LitMetric

AI Article Synopsis

  • Nausea and vomiting during awake craniotomy can lead to serious complications, prompting the use of 5-HT3 receptor antagonists like granisetron and dexamethasone to prevent these issues.* -
  • A study involving 170 patients examined the effectiveness of dexamethasone compared to granisetron in reducing nausea after AC, focusing on a subset of 82 patients matched for analysis.* -
  • Results showed that dexamethasone significantly reduced the incidence of nausea (9.8%) compared to granisetron (41.5%), indicating that dexamethasone is a more effective option for managing nausea during these procedures.*

Article Abstract

Background: Nausea and vomiting during awake craniotomy (AC) can increase cerebral pressure and cause asphyxia and aspiration. 5-HT3 receptor antagonists, such as granisetron, are often administered before awakening to prevent nausea during AC. Recently, dexamethasone was reported to prevent nausea and vomiting during AC; however, the efficacy of both drugs in preventing nausea has not yet been investigated.

Methods: We examined the frequency of nausea and vomiting in AC patients (n = 170) treated at our hospital until the end of September 2019. We divided patients as those who received dexamethasone (n = 71) and or granisetron (n = 99) before awakening and examined the frequency of nausea and vomiting after propensity score (PS) matching.

Result: Eighty-two patients were selected after PS matching. The incidence of nausea was significantly lower in the dexamethasone group than in the granisetron group (9.8% vs 41.5%, p = 0.002). In the logistic regression analysis after matching, the incidence of nausea significantly reduced with dexamethasone treatment (odds ratio: 0.12, 95% confidence interval: 0.029-0.499, p = 0.03).

Conclusion: In conclusion, dexamethasone was more effective than granisetron in preventing nausea during AC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11458841PMC
http://dx.doi.org/10.1186/s40981-024-00746-9DOI Listing

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