Risk factors associated with nausea and vomiting in children with cancer receiving chemotherapy

被引:7
|
作者
Eliasen, Astrid [1 ,2 ,3 ]
Kornholt, J. [1 ,3 ]
Mathiasen, R. [2 ]
Brok, J. [2 ]
Rechnitzer, C. [2 ]
Schmiegelow, K. [2 ,3 ]
Dalhoff, K. [1 ,3 ]
机构
[1] Bispebjerg & Frederiksberg Univ Hosp, Dept Clin Pharmacol, Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Dept Paediat & Adolescent Med, Rigshosp, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Med, Inst Clin Med, Copenhagen, Denmark
关键词
Chemotherapy-induced nausea; mobile health; nausea; paediatrics; risk factors; HIGHLY EMETOGENIC CHEMOTHERAPY; DOUBLE-BLIND; PEDIATRIC-PATIENTS; PREVENTION; APREPITANT; VALIDATION; PHASE-3;
D O I
10.1177/10781552221122026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Despite treatment with antiemetic medications, nausea remains uncontrolled for many children receiving chemotherapy. One reason is that risk factors for nausea in children remain poorly explored. The purpose of this study was to identify risk factors for chemotherapy-induced nausea (CIN) in children. Methods Prospective, observational study including 101 children (median age 6.4 years, range 0.8-17.9) with cancer receiving moderately or highly emetogenic chemotherapy. Primary endpoints were complete control of acute and delayed CIN, defined as no nausea in the acute phase 0-24 h after chemotherapy and in the delayed phase starting after the acute phase and ending 5 days later. Multivariable analyses included age, sex, cancer type, susceptibility to motion sickness, chemotherapy duration, numbers of antiemetics, co-administration with opioids or tricyclic antidepressants, and previously uncontrolled nausea or vomiting. Results Acute CIN was associated with susceptibility to motion sickness (odds ratio [OR] 5.73, 95% confidence interval [CI] 1.36-33.7) and older age (OR 4.19, 95% CI 1.30-14.7), comparing age group 8-18 years with 0-3 years. Delayed CIN was associated with uncontrolled acute nausea or vomiting (OR 10.3, 95% CI 2.65-50.9), highly emetogenic chemotherapy (OR 8.26, 95% CI 1.17-76.8), and having a hematologic cancer type (OR 7.81, 95% CI 1.05-79.2). Conclusions Susceptibility to motion sickness and age can influence the risk of acute CIN. More research is needed on how best to integrate risk information in preventive antiemetic strategies. Sufficient acute nausea and vomiting control are crucial to prevent delayed CIN.
引用
收藏
页码:1361 / 1368
页数:8
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