• Pediatric blood & cancer · Apr 2019

    Randomized Controlled Trial Multicenter Study

    Risk factors for chemotherapy-induced nausea in pediatric patients receiving highly emetogenic chemotherapy.

    • L Lee Dupuis, Roy N Tamura, Kara M Kelly, Jeffrey P Krischer, Anne-Marie Langevin, Lu Chen, E Anders Kolb, Nicole J Ullrich, Sahler Olle Jane Z OJZ Pediatric Hematology/Oncology, Golisano Children's Hospital, University of Rochester Medical Center, Rochester, New York., Eleanor Hendershot, Ann Stratton, Lillian Sung, and Thomas W McLean.
    • Department of Pharmacy and Research Institute, The Hospital of Sick Children, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
    • Pediatr Blood Cancer. 2019 Apr 1; 66 (4): e27584.

    BackgroundLittle is known regarding risk factors for chemotherapy-induced nausea (CIN) in pediatric patients.ProcedureA secondary analysis was conducted of a previously published multicenter, prospective, randomized, single-blind, sham-controlled trial assessing the efficacy of acupressure in preventing CIN in pediatric patients receiving highly emetogenic chemotherapy. The primary outcome was nausea severity, self-reported using the Pediatric Nausea Assessment Tool. The relationships between acute and delayed nausea severity and patient- (sex, race, age, and cancer diagnosis) and treatment-related (chemotherapy, antiemetic prophylaxis, CIN, and vomiting control) factors were analyzed by a proportional odds generalized estimating equation approach. The acute phase started with administration of the first and continued for 24 hours after the last chemotherapy dose. The delayed phase started at the end of the acute phase and continued until the next chemotherapy block (maximum seven days).ResultsIn the acute and delayed phases, 165 and 144 patients provided data for analysis, respectively. Nonwhite race was significantly associated with higher acute phase nausea severity (OR, 1.7; 95% CI, 1.1-2.6). Poor CIN control in the acute phase (OR, 16; 95% CI, 4.0-64.6), diagnosis of a cancer other than a central nervous system (CNS) tumor (OR, 2.5; 95% CI, 1.2-5.3), and cisplatin administration (OR, 3.7; 95% CI, 2.1-6.0) were significantly associated with higher delayed phase nausea severity.ConclusionAcute phase CIN was associated with nonwhite race. Delayed phase CIN was associated with poor acute phase CIN control, diagnosis of non-CNS cancer, and receipt of cisplatin. These findings will inform future antiemetic trial design.© 2018 Wiley Periodicals, Inc.

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