IVMP1IVIG raises platelet counts faster than IVIG alone: Results of a randomized, blinded trial in childhood ITP

Manuel Carcao, Mariana Silva, Michele David, Robert J. Klaassen, MacGregor Steele, Victoria Price, Cindy Wakefield, Lussia Kim, Derek Stephens, Victor S. Blanchette

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

14 Citas (Scopus)

Resumen

Children with immune thrombocytopenia (ITP) rarely suffer from life-threatening bleeds (eg, intracranial hemorrhage). In such settings, the combination of IV methylprednisolone (IVMP) with IV immune globulin (IVIG) is used to rapidly increase platelet counts (PCs). However, there are no controlled data to support using combination therapy over IVIG alone. We conducted a randomized, double-blind, placebo-controlled study to evaluate the rapidity of the PC increment and associated adverse events (AEs) between 2 regimens: A (IV placebo) and B (IVMP 30 mg/kg), both given over 1 hour, followed in both cases by IVIG (Gamunex 10%) 1 g/kg over 2-3 hours in children 1-17 years old with primary ITP and PCs ,20 3 109/L in whom physicians had decided to treat with IVIG. Thirty-two children (ages: median, 8 years; range, 1.2-17.5 years) with a mean baseline PC of 9.2 3 109/L participated. Eighteen were randomized to regimen A and 14 to regimen B. By 8 hours after initiating therapy, 55% of all children had a PC $20 3 109/L (no group difference). By 24 hours, mean PCs were 76.9 3 109/L (B) vs 55 3 109/L (A) (P 5 .06; P 5 .035 when adjusted for intergroup differences in patient ages). No patient experienced severe bleeding/unexpected severe AEs. There were statistically fewer IVIG-related headaches in the group receiving combination therapy (P 5 .046). Our findings show a rapid response to IVIG with/without steroids and provide evidence to support the use of IVMP1IVIG in life-threatening situations. This trial was registered at www.clinicaltrials.gov as #NCT00376077.

Idioma originalEnglish
Páginas (desde-hasta)1492-1500
Número de páginas9
PublicaciónBlood advances
Volumen4
N.º7
DOI
EstadoPublished - abr. 14 2020
Publicado de forma externa

Nota bibliográfica

Funding Information:
The authors thank the patients/families, nurses, and clinical research associates in our centers who participated in the study (Hospital for Sick Children, Toronto, ON, Canada; Children's Hospital of Eastern Ottawa, Ottawa, ON, Canada; Kingston General Hospital, Kingston, ON, Canada; Ste-Justine Hôpital, Montreal, QC, Canada; IWK Health Centre, Halifax, NS, Canada; and Alberta Children's Hospital, Calgary, AB, Canada). The authors also thank the members of the Data Monitoring Safety Board (Kaiser Ali, Sara Israels, and Shinya Ito). Funding for this study was provided through an investigator-initiated peer-reviewed grant submitted to the Bayer-Talecris-Canadian Blood Services Partnership fund.

Publisher Copyright:
© 2020 by The American Society of Hematology

ASJC Scopus Subject Areas

  • Hematology

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