Aprepitant and fosaprepitant use in children and adolescents at an academic medical center.

J Pediatr Pharmacol Ther

Department of Clinical Pharmacy, West Virginia University Healthcare, Morgantown, West Virginia.

Published: April 2014

Objective: To describe the use of aprepitant and fosaprepitant, a neurokinin 1 (NK-1) receptor inhibitor, in children and adolescents at a large academic medical center, for the prevention and management of chemotherapy-induced nausea and vomiting (CINV).

Methods: A retrospective chart review was conducted using an electronic medical record system to evaluate the use of aprepitant and fosaprepitant in all pediatric patients that were discharged from a single academic medical center between February 25, 2009 and May 25, 2012.

Results: Twenty-six patients were included in this review and received a total of 287 doses over the span of 114 cycles. Mean age was 10.1 years, with a range of 11 months to 17 years old. In 16 of 26 patients, aprepitant was used as the primary prophylaxis. Of those patients who received primary prophylaxis, 6 of 16 received it for highly emetogenic chemotherapy, and 10 of 16 received it for moderately emetogenic chemotherapy. Intravenous fosaprepitant was used in 7 of 26 patients, ages 13 to 17 (median 14) years old. No adverse effects attributable to aprepitant were reported.

Conclusions: Use of aprepitant and fosaprepitant in pediatric patients appeared to be well tolerated. No currently published reports data using aprepitant in a patient younger than 32 months old, whereas we reported its use in patients as young as 11 months old.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4093665PMC
http://dx.doi.org/10.5863/1551-6776-19.2.127DOI Listing

Publication Analysis

Top Keywords

aprepitant fosaprepitant
16
academic medical
12
medical center
12
children adolescents
8
fosaprepitant pediatric
8
pediatric patients
8
primary prophylaxis
8
emetogenic chemotherapy
8
aprepitant
7
patients
7

Similar Publications

: Cannabinoid Hyperemesis Syndrome (CHS), associated with long-term cannabinoid use, has been increasingly observed in emergency room visits as more states in the U.S. have legislatively permitted medical and recreational marijuana use.

View Article and Find Full Text PDF

Analyzing the adverse events of NK-1 receptor antagonists: a pharmacovigilance study from the FAERS database.

Sci Rep

December 2024

Department of Pharmacy, Suzhou Research Center of Medical School, Suzhou Hospital, Affiliated Hospital of Medical School, Nanjing University, Suzhou, 215153, China.

Background: NK-1 receptor antagonists (NK-1RAs) are proven to be successful in preventing chemotherapy-induced nausea and vomiting (CINV). The safety profile of NK-1RAs has not been systematically analyzed in the real world. This pharmacovigilance study investigated the differences in adverse events (AEs) between NK-1RAs.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the incidence of postoperative nausea and vomiting (PONV) in patients who underwent endoscopic bariatric and metabolic therapies (EBMT), focusing on the impact of neurokinin-1 receptor (NK-1) antagonists on PONV rates.
  • Out of 404 patients, 62.6% experienced PONV, with significant differences in rates between those who received NK-1 antagonists (35%) and those who did not (74%).
  • The findings suggest that using NK-1 antagonists as part of a comprehensive approach to prevent PONV significantly lowers the likelihood of this adverse event in patients recovering from EBMT.
View Article and Find Full Text PDF

Background: Sugammadex, aprepitant, and fosaprepitant are increasingly used perioperatively. These medications may interfere with the effectiveness of hormonal contraception. This study assessed anesthesia providers' use of sugammadex and aprepitant, their knowledge of interactions with hormonal birth control, and patient counseling practices to identify possible knowledge gaps or opportunities for practice improvement.

View Article and Find Full Text PDF

Background/aim: The frequency rate of injection site reactions (ISR) due to fosaprepitant meglumine (Fos APR) has been shown to vary depending on the types of combined anticancer drug. This study aimed to elucidate the impact of Fos APR on ISR in patients receiving paclitaxel and carboplatin, with and without bevacizumab therapy (TC±Bev).

Patients And Methods: This study focused on patients with gynecologic cancer (n=93) who received TC±Bev administration at Fujita Health University Hospital from March 2016 to February 2020, and monitored up to six cycles.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!