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Chemotherapy-Inducted Nausea and Vomiting Guidelines for Adult ...

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Emetogenicity of Chemotherapeutic Agents<br />

Level 1 (60 mg/m 2 )<br />

Epirubicin hydrochloride (≤90 mg/m 2 )<br />

Mechlorethamine<br />

Idarubicin<br />

Pentostatin<br />

Ifosfamide<br />

Streptozocin<br />

Methenamine (oral)<br />

Methotrexate (250-1000 mg/m 2 )<br />

Mitoxantrone (≤15 mg/m 2 )<br />

*Intrathecal coadministration of methotrexate <strong>and</strong> cytarabine to pediatric patients increases the emetogenicity level to 3.<br />

Calculating Emetogenic Potential of Multiple-Agent Regimens<br />

Identify the agent with the highest emetogenic level, then determine the contribution of the remaining agents by using the<br />

following rules:<br />

Examples:<br />

(1) Level 1 agents do not contribute to emetogenicity. Level 1+1=0 2+1=2 3+1=3 4+1=4<br />

(2) Adding one or more level 2 agents increases the highest level by 1. Level 2+2=3 3+2=4 2+2+2=3 3+2+2=4<br />

(3) Adding level 3 or 4 agents increases the highest level by 1 per agent. Level 3+3=4 3+3+3=5 4+3=5<br />

PEDIATRIC GUIDELINES FOR CHEMOTHERAPY-INDUCED EMESIS<br />

Prevention of Acute Emesis<br />

Level 1<br />

Level 2-5<br />

Granisetron PO (patients able to take PO medications)<br />

OR<br />

Granisetron IV (patients who are not c<strong>and</strong>idates <strong>for</strong> PO)<br />

PLUS<br />

Dexamethasone PO or IV<br />

No preventative therapy necessary<br />

2 mg 30 minutes prior to chemotherapy<br />

10 mcg/kg IV 30 minutes prior to chemotherapy<br />

10 mg/m 2 PO or IV in single or divided doses<br />

Prevention of Acute Emesis – History of Refractory Emesis<br />

Ondansetron IV 0.15 mg/kg 30 minutes prior to chemotherapy <strong>and</strong> q4h x 2<br />

PLUS<br />

Dexamethasone PO or IV<br />

10 mcg/kg IV 30 minutes prior to chemotherapy<br />

Treatment of Breakthrough Emesis<br />

Dexamethasone<br />

OR<br />

Lorazepam (children >5 yrs only)<br />

OR<br />

Promethazine<br />

5-10 mg/m 2 PO or IV q12h prn<br />

0.05 mg/kg (max 2 mg) IV q12h prn<br />

0.25-0.5 mg/kg (max 25 mg) IV q6-8h prn<br />

Treatment of Refractory Emesis<br />

• Increase dose of current agent (within recommended range), OR<br />

• Add agent from different pharmacologic class, OR<br />

• Use a combination of above approaches

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