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Predictive factors of response to IVIG in pediatric immune thrombocytopenic purpura.
Higashide, Yukiko; Hori, Tsukasa; Yoto, Yuko; Kabutoya, Hiroyuki; Honjo, Saho; Sakai, Yoshiyuki; Nojima, Masanori; Yoda, Minami; Yamamoto, Masaki; Tsutsumi, Hiroyuki.
Afiliación
  • Higashide Y; Department of Pediatrics, Hakodate Municipal Hospital, Hakodate, Japan.
  • Hori T; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Yoto Y; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Kabutoya H; Department of Pediatrics, Hakodate Municipal Hospital, Hakodate, Japan.
  • Honjo S; Department of Pediatrics, Hakodate Municipal Hospital, Hakodate, Japan.
  • Sakai Y; Department of Pediatrics, Hakodate Municipal Hospital, Hakodate, Japan.
  • Nojima M; Center for Translational Research, Institute of Medical Science Hospital, University of Tokyo, Tokyo, Japan.
  • Yoda M; Department of Pediatrics, Hakodate Municipal Hospital, Hakodate, Japan.
  • Yamamoto M; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Tsutsumi H; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
Pediatr Int ; 60(4): 357-361, 2018 Apr.
Article en En | MEDLINE | ID: mdl-29297955
ABSTRACT

BACKGROUND:

Immune thrombocytopenic purpura (ITP) is commonly treated with i.v. immunoglobulin (IVIG).

METHODS:

We retrospectively evaluated whether pretreatment clinical and laboratory finding could predict the short- and long-term response to IVIG.

RESULTS:

Short-term response was estimated by platelet count 2 weeks after IVIG, and long-term response was assessed on thrombocytopenia-free survival (TFS). TFS was defined as the probability of survival without treatment failure after initial IVIG, such as relapse, requirement for additional therapeutic interventions, or progressing to chronic ITP. Seventy-six patients with newly diagnosed ITP who were initially treated with IVIG were evaluated. Fifty-three patients (69.7%) were determined as responders at 2 weeks after IVIG. On multivariate analysis, age ≥23 months (P = 0.020) and platelet count <9.0 × 109 /L (P = 0.018) were considered to be unfavorable factors for short-term response. Cumulative proportion of long-term (1 year) good prognosis was estimated at 53.0% (95%CI 40.8-65.2). On multivariate analysis of unfavorable factors for long-term response, age ≥23 months (P = 0.020) was the only significant factor.

CONCLUSIONS:

For new-onset ITP in patients aged >2 years, corticosteroid therapy in addition to IVIG may be considered as the initial treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Púrpura Trombocitopénica Idiopática / Inmunoglobulinas Intravenosas / Factores Inmunológicos Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Púrpura Trombocitopénica Idiopática / Inmunoglobulinas Intravenosas / Factores Inmunológicos Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Japón