| Literature DB >> 35387223 |
Abstract
Background: Postoperative nausea and vomiting (PONV) is a typical and unpleasant physical symptom that occurs in patients after surgery, and it may be one of the most challenging elements of the recovery process. PONV can be caused by a variety of factors, including surgery itself, anesthesia, or medications. Palonosetron is a medication that is now licensed by the Food and Drug Administration for the treatment of this ailment. The efficacy of palonosetron in reducing physical symptoms in patients following surgery was investigated in this meta-analysis and comprehensive review.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35387223 PMCID: PMC8977333 DOI: 10.1155/2022/7474053
Source DB: PubMed Journal: Comput Math Methods Med ISSN: 1748-670X Impact factor: 2.238
Figure 1Process of literature screening.
Figure 2Summary of the results of the risk of bias.
Summary of 10 studies: author (years) participant surgery/anesthesia outcome.
| Author (years) | Participants | Surgery/anesthesia | Outcomes |
|---|---|---|---|
| Adis (2009) | 70 patients with cancer | Laparoscopic cholecystectomy under isoflurane/nitrous oxide GA | Headache and constipation were among the most commonly reported adverse events with the use of palonosetron |
| Ahn et al. (2016) | 695 patients were included in the final analysis | Laparoscopic abdominal and pelvic surgeries under sevoflurane GA | Palonosetron was more effective than ramosetron, when the administration time for the 5-HT3 receptor antagonist was during the early phase of the operation |
| Srivastava et al. (2020) | 64 patients, scheduled for middle ear surgery, were randomized into two groups | Laparoscopic cholecystectomy under sevoflurane GA | The combination of palonosetron-dexamethasone is superior to ondansetron-dexamethasone for the prevention of postoperative nausea and vomiting after middle ear surgeries |
| Fonseca et al. (2020) | 60 individuals who underwent video cholecystectomy were randomized into three groups | Sevoflurane þ remifentanil | The present study showed evidence that palonosetron is superior to the drugs compared regarding a protracted antiemetic effect and less requirement of rescue drugs, mainly related to its ability to completely inhibit the uncomfortable symptom of nausea |
| Liu et al. (2018) | 129 patients were included in the final analysis | Laparoscopic cholecystectomy under isoflurane/nitrous oxide GA | Palonosetron is not more efficacious than ondansetron in the prevention of early PONV. However, palonosetron was more efficacious than ondansetron in the prevention of vomiting after laparoscopic surgery |
| Lee et al. (2019) | 51 adult patients | Bariatric surgery under sevoflurane GA | LBW-based dosing might be suitable for high-weight patients to avoid possible underdosing. Nevertheless, the current fixed dosing of palonosetron is acceptable for adult patients with normal weight |
| Grigio et al. (2020) | 100 patients according to a random number generator | Laparoscopic cholecystectomy under isoflurane/nitrous oxide GA | The addition of aprepitant as a third antiemetic resulted in no significant reduction in the incidence of PONV in this population. However, the incidence of PONV was reduced in relation to the general population |
| Gouveia et al. (2020) | Involving 80 female patients | Thyroid surgery under sevoflurane/nitrous oxide GA | A body weight-adjusted dose of palonosetron was as effective as 75 |
| Song et al. (2017) | 146 patients were randomly allocated | Laparoscopic abdominal or pelvic surgery under sevoflurane GA | Compared with palonosetron, ramosetron may be superior for reducing PONV severity, especially in patients with ABCB1 3435TT or 2677TT genotype |
| Kang et al. (2018) | 274 adults | Laparoscopic surgeries under sevoflurane GA | The combined use of prophylactic palonosetron before anesthetic induction and sugammadex as a reversal of neuromuscular blockade are associated with a reduction in the incidence of PONV in patients undergoing MVD under propofol-maintained anesthesia |
Figure 3Effect of palonosetron on PONV after 24 hours.
Figure 4Different doses of palonosetron RIDIT.
Figure 5Incidence rate of PONV after 48 hours.
Figure 6Comparison of PONV risk of dexamethasone combination.
Figure 7Comparison of 6-hour PONV.
Figure 8Effect of palonosetron concentration on plasma motilin.
Figure 9Comparison of adverse reactions.
Figure 10Risk of bias assessment.