Acute immune thrombocytopenia (ITP) in childhood: Retrospective and prospective survey in Germany

被引:68
作者
Sutor, AH [1 ]
Harms, A [1 ]
Kaufmehl, K [1 ]
机构
[1] Univ Freiburg, Kinderklin, D-79106 Freiburg, Germany
关键词
immune thrombocytopenia (ITP); children; incidence; symptoms; platelet count; treatment; side effects of treatment; survey;
D O I
10.1055/s-2001-15255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Treatment of acute childhood immune thrombocytopenia (ITP) is controversial. For information on the present situation in Germany, a retrospective and a prospective survey were carried out. Tn the retrospective survey, questionnaires were sent to all German pediatric hospitals asking about local policies for handling ITP and whether in the preceding year (starting on October 1995) death or ICH had occurred; 86% answered. In the prospective survey, 94% responded to the mailings ("have you seen a case of ITP?") sent in monthly intervals between October 1, 1996 and September 30, 1997; 89% of the questionnaires were retrieved. In the retrospective survey, no deaths and no ICH were reported. If only mild bleedings, such as skin bleeds alone (or additional. mild mucous membrane bleeding) were present, 20.5% (26.4%) preferred the "watchful waiting" regimen (supportive care), irrespective of the platelet count; 79.5% (73.6%) would treat if the platelet counts were <5 X 10(9)/L, 73.5% (67.9%) if < 10, 35.9% (33.6%) if < 20, and 4.2% (2.6%) if < 30. Of the treaters, 50.5% would prefer immunoglobulins (Ig), 24.4% glucocorticosteroids (GC), and 20.5% GC and/or Ig. Generally, a rise in platelets, most frequently > 50 X 10(9)/L was considered as therapeutic success. In the prospective survey, from the reported 323 children an annual incidence of 2.16 per 100,000 children was calculated. The incidence depended on age and gender, being highest for boys younger than 2 years with 5.8 (girls 3.42) and low with 0.44 for boys (girls 0.89) older than 14 years. About 60% of the patients had a preceding infection. Although 83% had a platelet count < 20 X 10(9)/L (56% < 10 x 10(9)/L), almost all (97.5%) had only mild bleeding symptoms; 2.5% had serious bleeding symptoms requiring blood transfusion or nasal packing, none had ICH, and no death was reported. The mean platelet count on admission was 11.348 (lowest count 8.253) X 10(9)/L. Sixty-one percent received Ig, 19% GC (both either alone or as first choice), 6% Ig plus GC, and 14% no treatment. Side effects were reported in 22% of the children treated with Ig. The retrospective survey mirrored the uncertainty in regard to treatment. The prospective survey provided new aspects on incidence, age, and gender distribution. Although almost all patients had only mild bleeding; symptoms, most received Ig and/or GC. The decision to treat depended mainly on the platelet count. From these surveys, conclusions about the effectiveness of treatment cannot be drawn. Recommendations based primarily on platelet counts must be reconsidered.
引用
收藏
页码:253 / 267
页数:15
相关论文
共 72 条
[1]  
Baronci C, 1998, Ann Ist Super Sanita, V34, P457
[2]  
BEDRI A, 1995, ETHIOPIAN MED J, V33, P75
[3]   Neutropenia as a complication of intravenous immunoglobulin (IVIG) therapy in children with immune thrombocytopenic purpura: common and non-alarming [J].
Berkovitch, M ;
Dolinski, G ;
Tauber, T ;
Aladjem, M ;
Kaplinsky, C .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1999, 21 (06) :411-415
[4]   A PROSPECTIVE, RANDOMIZED TRIAL OF HIGH-DOSE INTRAVENOUS IMMUNE GLOBULIN G THERAPY, ORAL PREDNISONE THERAPY, AND NO THERAPY IN CHILDHOOD ACUTE IMMUNE THROMBOCYTOPENIC PURPURA [J].
BLANCHETTE, VS ;
LUKE, B ;
ANDREW, M ;
SOMMERVILLENIELSEN, S ;
BARNARD, D ;
DEVEBER, B ;
GENT, M .
JOURNAL OF PEDIATRICS, 1993, 123 (06) :989-995
[5]  
Böcher A, 1998, MED KLIN, V93, P707
[6]   Idiopathic thrombocytopenic purpura [J].
Bolton-Maggs, PHB .
ARCHIVES OF DISEASE IN CHILDHOOD, 2000, 83 (03) :220-222
[7]  
BoltonMaggs PHB, 1997, BLOOD, V89, P1465
[8]   Assessment of UK practice for management of acute childhood idiopathic thrombocytopenic purpura against published guidelines [J].
BoltonMaggs, PHB ;
Moon, I .
LANCET, 1997, 350 (9078) :620-623
[9]  
Buchanan GR, 1997, BLOOD, V89, P1464, DOI 10.1182/blood.V89.4.1464
[10]   IMMUNE HEMOLYSIS, DISSEMINATED INTRAVASCULAR COAGULATION, AND SERUM SICKNESS AFTER LARGE DOSES OF IMMUNE GLOBULIN GIVEN INTRAVENOUSLY FOR KAWASAKI-DISEASE [J].
COMENZO, RL ;
MALACHOWSKI, ME ;
MEISSNER, HC ;
FULTON, DR ;
BERKMAN, EM .
JOURNAL OF PEDIATRICS, 1992, 120 (06) :926-928