Extended Sedation With Continuous Midazolam or Dexmedetomidine Infusion for Young Children Receiving 131I‐MIBG Radiopharmaceutical Therapy for Advanced Neuroblastoma. Issue 3 (19th November 2015)

• Record Type: Journal Article
• Authors: Lee, Jean S.; Wu, Rebecca; Wong, Thalia; DuBois, Steven G.; Matthay, Katherine; Gustafson, Clay; Hawkins, Randall; Roy‐Burman, Arup
• Is Part Of: Pediatric blood & cancer. Volume 63:Issue 3(2016)
• Page Start: 471
• Page End: 478
• Publication Date: 2015-11-19
• Subjects: MIBG -- neuroblastoma -- sedation; Tumors in children -- Periodicals; Blood -- Diseases -- Periodicals; Cancer in children -- Periodicals; 618.92
• DOI: 10.1002/pbc.25827
• Languages: English
• ISSNs: 1545-5009

Abstract

Abstract : Background: 131 I‐MIBG is increasingly used for treating neuroblastoma; however, administration requires careful adherence to radiation safety guidelines. We describe our experience using continuous sedation to facilitate safe 131 I‐MIBG therapy for young children. Procedure: Patients were included in this case series if they received continuous midazolam or dexmedetomidine infusion for sedation during 131 I‐MIBG therapy from November 1, 2012, to October 1, 2014. Key outcomes included adequacy of sedation for both 131 I‐MIBG infusion and the duration of radioactive isolation, as well as sedative‐related toxicities. Additionally, nuclear medicine scans before and after 131 I‐MIBG therapy were assessed using the Curie score. These scores were compared qualitatively between midazolam, dexmedetomidine, and control (no sedative infusion) groups. Results: Of the 13 patients receiving continuous sedation for 131 I‐MIBG therapy, seven achieved adequate sedation with midazolam, five achieved adequate sedation with dexmedetomidine, one patient (1.6 years old) failed to achieve adequate sedation with either medication and did not receive 131 I‐MIBG therapy. Sedation was generally well tolerated. Common side effects for dexmedetomidine infusion included hypotension and relative bradycardia. Both treatment and control groups had multiple patients with increased Curie scores post‐ 131 I‐MIBG therapy. However, one patient in the midazolam group and two in the dexmedetomidine group had decreased Curie scores after 131 I‐MIBG therapy, while none decreased in the control group. Conclusions: Although we cannot exclude the possibility of some inhibition of 131 I‐MIBG uptake by midazolam or dexmedetomidine, this case series suggests that continuous infusions of either agent can provide effective sedation to allow safe administration of 131 I‐MIBG to young patients.