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İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi

Yıl 2019, Cilt: 17 Sayı: 3, 350 - 358, 02.12.2019

Öz

GİRİŞ ve AMAÇ:
İmmun Trombositopeni (İTP) tanılı çocuklarda intravenöz immunoglobulin
tedavisini etkileyen prognostik faktörler ve tedavinin kronikleşme üzerine
etkisi belirlenmek istenmiştir.





YÖNTEM ve GEREÇLER: Çalışmaya;
2010-2016 yılları arasında başvuran, 3 ay- 16 yaş aralığındaki 80 hasta
alınmıştır. Her hastanın cinsiyeti, yaşı, tanı öncesin varsa enfeksiyon ve
aşılanma öyküsü, kanama bulguları, tanı anındaki laboratuvar değeri, IVIG
tedavisine yanıt süresi, tanıdan 1 yıl sonraki trombosit değeri incelenmiştir.
Akut ve kronik İTP tanısı alan gruplar arasında veriler karşılaştırılmıştır.





BULGULAR: İTP tanısı alan ve IVIG tedavisi verilen 80 olgunun
sosyodemografik ve laboratuvar özellikleri değerlendirildi. Yaş ortalaması
71,40±46,18 ay idi. Olgularımızda erkek/kız oranı 1,0 olarak tespit edildi. 32
olguda başvurudan önceki 6 hafta içerisinde, viral enfeksiyon geçirme öyküsü
vardı. Akut İTP’ lerin %11 inde trompositopeni gelişmeden önceki 6 hafta içinde
aşı olma öyküsü varken kronik İTP ‘lerde son 6 hafta içinde aşı öyküsü
saptanmadı. Akut İTP olgularının en çok sonbahar aylarında, kronik İTP
olgularının ön planda kış ve yaz aylarında tanı aldığı görüldü. Tüm hastaların
ortalama trombosit
sayıları,WBC, MPV, PDW,
PCT, CRP, PT, aPTT değerleri
değerlendirildiğinde
benzer sonuçlar elde edildi (p>0.05).



TARTIŞMA ve SONUÇ: İmmun Trombositopeni’de kronikleşmeyi ön görebilmek için demografik
özellikler, klinik bulgular, laboratuvar bulguları ve tedavi şekillerinden
ziyade otoantikorlar ve immun trompositopeninin genetik mekanizmalarına yönelik
ileri çalışmalara ihtiyaç olduğunu saptadık.

Kaynakça

  • 1. Lanzkowsy P , Lipton JM, Fish, JD. Disorders of Platelets. In: Manual of Pediatric Hematology and Oncology. 6th ed. New York: Elsevier; 2016:254-260.
  • 2. Fogarty PF, Segal JB. The epidemiology of immune thrombocytopenic purpura. Curr Opin Hematol. 2007;14(5):515-519
  • 3. Terrell DR, Beebe LA, Vesely SK, Neas BR, Segal JB, George JN. The incidence of immune thrombocytopenic purpura in children and adults: A critical review of published reports. Am J Hematol. 2010;85(3):174-180.
  • 4. Pels SG. Current therapies in primary immune thrombocytopenia. Semin Thromb Hemost. 2011;37(6):621-630.
  • 5. Shirahata A, Ishii E, Eguchi H, Okawa H, Ohta S, Kanekoet T et al. Consensus guideline for diagnosis and treatment of childhood idiopathic thrombocytopenic purpura. Int J Hematol. 2006;83(1):29-38.
  • 6. Klaassen RJ, Blanchette VS, Barnard D, Wakefield CD, Curtis C, Bradley CS, et al. Validity, Reliability, and Responsiveness of a New Measure of Health-Related Quality of Life in Children with Immune Thrombocytopenic Purpura: The Kids’ ITP Tools. J Pediatr. 2007;150(5): 510-515.
  • 7. Zilber R, Bortz AP, Yacobovich J, Yaniv I, Tamary H. Analysis of health-related quality of life in children with immune thrombocytopenia and their parents using the kids’ ITP tools. J Pediatr Hematol Oncol. 2012;34(1):2-5.
  • 8. Heitink-Pollé KMJ, Nijsten J, Boonacker CWB, De Haas M, Bruin MCA. Clinical and laboratory predictors of chronic immune thrombocytopenia in children: A systematic review and meta-analysis. Blood. 2014;124(22):3295-3307.
  • 9. Tamminga R, Berchtold W, Bruin M, Buchanan GR, Kühne T. Possible lower rate of chronic ITP after IVIG for acute childhood ITP an analysis from registry I of the Intercontinental Cooperative ITP Study Group (ICIS). Br J Haematol. 2009;146(2):180-184.
  • 10. Imbach P, Kühne T, Müller D, Berchtold W, Zimmerman S, Elalfy M et al. Childhood ITP: 12 Months follow-up data from the prospective registry I of the Intercontinental Childhood ITP Study Group (ICIS). Pediatr Blood Cancer. 2006;46(3):351-356.
  • 11. Rohmer B, Valla F V, Baleydier F, Launay V, Dommange-Romero F, Pondarré C. Newly diagnosed immune thrombocytopenic purpura in childhood: Successful implementation of a limited intervention strategy in the setting of pediatric emergency care. J Pediatr. 2015;166(2):480-482.
  • 12. Morimoto Y, Yoshida N, Kawashima N, Matsumoto K, Kato K. Identification of predictive factors for response to intravenous immunoglobulin treatment in children with immune thrombocytopenia. Int J Hematol. 2014;99(5):597-602.
  • 13. Kühne T, Imbach P, Bolton-Maggs PHB, Berchtold W, Blanchette V, Buchanan GR. Newly diagnosed idiopathic thrombocytopenic purpura in childhood: An observational study. Lancet. 2001;358(9299):2122-2125.
  • 14. Glanz J, France E, Xu S, Hayes T, Hambidge S. A population-based, multisite cohort study of the predictors of chronic idiopathic thrombocytopenic purpura in children. Pediatrics. 2008;121(3):10-15.
  • 15. Buchanan GR, Adix L. Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. J Pediatr. 2002;141(5):683-688.
  • 16. Celik M, Bulbul A, Aydogan G, Tugcu D, Can E, Uslu S et al. Comparison of anti-D immunoglobulin, methylprednisolone, or intravenous immunoglobulin therapy in newly diagnosed pediatric immune thrombocytopenic purpura. J Thromb Thrombolysis. 2013;35(2):228-233.
  • 17. Choi HS, Ji MH, Kim SJ, Ahn HS. Platelet count recovery after intravenous immunoglobulin predicts a favorable outcome in children with immune thrombocytopenia. Blood Res. 2016;51(2):95-101.
  • 18. Donato H, Picón A, Martinez M, Rapetti MC, Rosso A, Gomez S et al. Demographic data, natural history, and prognostic factors of idiopathic thrombocytopenic purpura in children: A multicentered study from argentina. Pediatr Blood Cancer. 2009;52(4):491-496.

Prognostic Factors Affecting Intravenous Immunglobulin Therapy in Children Diagnosed Immune Thrombocytopenic Purpura and Effect of Treatment on Chronicity

Yıl 2019, Cilt: 17 Sayı: 3, 350 - 358, 02.12.2019

Öz

INTRODUCTION:
Main purpose of this study is to evaluate the prognostic factors affecting
intravenous immunglobulin therapy in children diagnosed immune thrombocytopenic
purpura and effect of treatment on chronicity.

METHODS: 80
children who are 3 months-16 years old diagnosed with immune thrombocytopenia
during 2000-2016 were included in this study. The gender of each patient, age,
history of infection and vaccination before diagnosis, bleeding findings,
laboratory values at diagnosis, duration of response to IVIG treatment, and
thrombocyte counts after 1 year were examined. Data were compared between acute
and chronic ITP groups.

RESULTS:
Sociodemographic and laboratory characteristics of totally 80 children were
evaluated. The average age of children was 71.40±46.18 months. In our cases,
the ratio of male to female was 1,0. Thirty two of our cases (53.33%) had a
history of viral infection within 6 weeks prior to admission. 11% of acute ITPs
had a story of vaccination within 6 weeks prior to thrombocytopenia, whereas no
vaccination was detected within 6 weeks of chronic ITP. Acute ITP was diagnosed
in 22 cases in autumn at most, and chronic ITP was diagnosed in 7 cases in
winter and summer months. Similar results were obtained when tthe mean platelet
counts, WBC, MPV, PDW, PCT, CRP, PT, aPTT values of the patients were
evaluated.







DISCUSSION
AND CONCLUSION:
We
need further studies on the genetic mechanism and autoantibodies in immune
thrombocytopenia with respect to demographics, clinical findings, laboratory
findings and treatment modalities to predict chronicity

Kaynakça

  • 1. Lanzkowsy P , Lipton JM, Fish, JD. Disorders of Platelets. In: Manual of Pediatric Hematology and Oncology. 6th ed. New York: Elsevier; 2016:254-260.
  • 2. Fogarty PF, Segal JB. The epidemiology of immune thrombocytopenic purpura. Curr Opin Hematol. 2007;14(5):515-519
  • 3. Terrell DR, Beebe LA, Vesely SK, Neas BR, Segal JB, George JN. The incidence of immune thrombocytopenic purpura in children and adults: A critical review of published reports. Am J Hematol. 2010;85(3):174-180.
  • 4. Pels SG. Current therapies in primary immune thrombocytopenia. Semin Thromb Hemost. 2011;37(6):621-630.
  • 5. Shirahata A, Ishii E, Eguchi H, Okawa H, Ohta S, Kanekoet T et al. Consensus guideline for diagnosis and treatment of childhood idiopathic thrombocytopenic purpura. Int J Hematol. 2006;83(1):29-38.
  • 6. Klaassen RJ, Blanchette VS, Barnard D, Wakefield CD, Curtis C, Bradley CS, et al. Validity, Reliability, and Responsiveness of a New Measure of Health-Related Quality of Life in Children with Immune Thrombocytopenic Purpura: The Kids’ ITP Tools. J Pediatr. 2007;150(5): 510-515.
  • 7. Zilber R, Bortz AP, Yacobovich J, Yaniv I, Tamary H. Analysis of health-related quality of life in children with immune thrombocytopenia and their parents using the kids’ ITP tools. J Pediatr Hematol Oncol. 2012;34(1):2-5.
  • 8. Heitink-Pollé KMJ, Nijsten J, Boonacker CWB, De Haas M, Bruin MCA. Clinical and laboratory predictors of chronic immune thrombocytopenia in children: A systematic review and meta-analysis. Blood. 2014;124(22):3295-3307.
  • 9. Tamminga R, Berchtold W, Bruin M, Buchanan GR, Kühne T. Possible lower rate of chronic ITP after IVIG for acute childhood ITP an analysis from registry I of the Intercontinental Cooperative ITP Study Group (ICIS). Br J Haematol. 2009;146(2):180-184.
  • 10. Imbach P, Kühne T, Müller D, Berchtold W, Zimmerman S, Elalfy M et al. Childhood ITP: 12 Months follow-up data from the prospective registry I of the Intercontinental Childhood ITP Study Group (ICIS). Pediatr Blood Cancer. 2006;46(3):351-356.
  • 11. Rohmer B, Valla F V, Baleydier F, Launay V, Dommange-Romero F, Pondarré C. Newly diagnosed immune thrombocytopenic purpura in childhood: Successful implementation of a limited intervention strategy in the setting of pediatric emergency care. J Pediatr. 2015;166(2):480-482.
  • 12. Morimoto Y, Yoshida N, Kawashima N, Matsumoto K, Kato K. Identification of predictive factors for response to intravenous immunoglobulin treatment in children with immune thrombocytopenia. Int J Hematol. 2014;99(5):597-602.
  • 13. Kühne T, Imbach P, Bolton-Maggs PHB, Berchtold W, Blanchette V, Buchanan GR. Newly diagnosed idiopathic thrombocytopenic purpura in childhood: An observational study. Lancet. 2001;358(9299):2122-2125.
  • 14. Glanz J, France E, Xu S, Hayes T, Hambidge S. A population-based, multisite cohort study of the predictors of chronic idiopathic thrombocytopenic purpura in children. Pediatrics. 2008;121(3):10-15.
  • 15. Buchanan GR, Adix L. Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. J Pediatr. 2002;141(5):683-688.
  • 16. Celik M, Bulbul A, Aydogan G, Tugcu D, Can E, Uslu S et al. Comparison of anti-D immunoglobulin, methylprednisolone, or intravenous immunoglobulin therapy in newly diagnosed pediatric immune thrombocytopenic purpura. J Thromb Thrombolysis. 2013;35(2):228-233.
  • 17. Choi HS, Ji MH, Kim SJ, Ahn HS. Platelet count recovery after intravenous immunoglobulin predicts a favorable outcome in children with immune thrombocytopenia. Blood Res. 2016;51(2):95-101.
  • 18. Donato H, Picón A, Martinez M, Rapetti MC, Rosso A, Gomez S et al. Demographic data, natural history, and prognostic factors of idiopathic thrombocytopenic purpura in children: A multicentered study from argentina. Pediatr Blood Cancer. 2009;52(4):491-496.
Toplam 18 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Araştırma
Yazarlar

Kadriye Nil Kaptan Bu kişi benim 0000-0001-8326-8798

Emine Türkkan Bu kişi benim 0000-0002-5126-7843

Yayımlanma Tarihi 2 Aralık 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 17 Sayı: 3

Kaynak Göster

APA Kaptan, K. N., & Türkkan, E. (2019). İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi. Güncel Pediatri, 17(3), 350-358. https://doi.org/10.32941/pediatri.647116
AMA Kaptan KN, Türkkan E. İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi. Güncel Pediatri. Aralık 2019;17(3):350-358. doi:10.32941/pediatri.647116
Chicago Kaptan, Kadriye Nil, ve Emine Türkkan. “İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler Ve Tedavinin Kronikleşme Üzerine Etkisi”. Güncel Pediatri 17, sy. 3 (Aralık 2019): 350-58. https://doi.org/10.32941/pediatri.647116.
EndNote Kaptan KN, Türkkan E (01 Aralık 2019) İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi. Güncel Pediatri 17 3 350–358.
IEEE K. N. Kaptan ve E. Türkkan, “İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi”, Güncel Pediatri, c. 17, sy. 3, ss. 350–358, 2019, doi: 10.32941/pediatri.647116.
ISNAD Kaptan, Kadriye Nil - Türkkan, Emine. “İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler Ve Tedavinin Kronikleşme Üzerine Etkisi”. Güncel Pediatri 17/3 (Aralık 2019), 350-358. https://doi.org/10.32941/pediatri.647116.
JAMA Kaptan KN, Türkkan E. İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi. Güncel Pediatri. 2019;17:350–358.
MLA Kaptan, Kadriye Nil ve Emine Türkkan. “İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler Ve Tedavinin Kronikleşme Üzerine Etkisi”. Güncel Pediatri, c. 17, sy. 3, 2019, ss. 350-8, doi:10.32941/pediatri.647116.
Vancouver Kaptan KN, Türkkan E. İmmun Trombositopenik Purpura Tanılı Çocuklarda İntravenöz İmmunoglobulin Tedavisini Etkileyen Prognostik Faktörler ve Tedavinin Kronikleşme Üzerine Etkisi. Güncel Pediatri. 2019;17(3):350-8.