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PubMed:21188127 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 102-108 HP_0002018 denotes nausea
T2 113-121 HP_0002013 denotes vomiting
T3 166-172 HP_0002664 denotes cancer
T4 234-240 HP_0002013 denotes emesis
T5 906-912 HP_0002018 denotes nausea
T6 917-925 HP_0002013 denotes vomiting

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 88-216 DRI_Background denotes Prevention of nausea and vomiting is the main goal of antiemetic treatment in cancer patients scheduled to receive chemotherapy.
T2 217-384 DRI_Approach denotes To prevent acute emesis, antiemetics should be administered just before chemotherapy and patients should be protected for up to 24 hours after chemotherapy initiation.
T3 385-507 DRI_Background denotes The emetogenic potential of chemotherapeutic agents guides clinicians towards the most appropriate antiemetic prophylaxis.
T4 508-693 DRI_Background denotes Current guidelines recommend the use of 5-HT(3) receptor antagonist (RA) either alone or in combination with dexamethasone and/or a neurokinin-1 RA both in the acute and delayed phases.
T5 694-820 DRI_Background denotes The second-generation 5-HT(3)RA palonosetron exhibits a longer half-life and a higher binding affinity than older antagonists.
T6 821-1095 DRI_Background denotes Palonosetron has been approved by the FDA for the prevention of chemotherapy-induced nausea and vomiting (CINV) in patients scheduled to receive either moderately (MEC) or highly emetogenic chemotherapy (HEC) and for the prevention of delayed CINV in patients receiving MEC.