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Table 1 Study characteristics

From: Interventions to decrease the risk of adverse cardiac events for patients receiving chemotherapy and serotonin (5-HT3) receptor antagonists: a systematic review

Reference

Study period, country

Study design, # of patients

5-HT3 dose/day

Intervention, examination timing

Outcomes examined

Hesketh [18]

NR, USA

Non-RCT, 44

IV dolasetron 1.2 mg/kg, 1.8 mg/kg, 2.4 mg/kg 30 mins before chemotherapy

ECG, 1–2 hrs and 24–48 hrs

PR, QT

Gralla [19]

August 2000 to October 2001, Germany, Italy, UK, Netherlands, Russia

RCT, 98

IV palonosetron 0.25 mg, IV palonosetron 0.75 mg, IV ondansetron 32 mg 30 mins before chemotherapy

ECG, 15 mins, 24 hrs, 1 wk

Mortality, QT

Kim [20]

April 2002 to October 2002, South Korea

RCT, 114

IV dolasetron 100 mg 30 mins before and 200 mg p.o. 2-5 days after chemotherapy, IV ondansetron 8 mg 30 mins before and IV ondansetron 16 mg 2–4 hrs plus an additional 16 mg/day p.o. 2-5 days after chemotherapy

ECG, 15 mins, 24 hrs, 1 wk

ECG findings unspecified

  1. ECG: electrocardiogram; IV: intravenous; NR: not reported; Non-RCT: non-randomized clinical trial; p.o.: administered orally; RCT: randomized controlled trial.