TY - JOUR
T1 - A comparative prospective observational study of children and adults with immune thrombocytopenia
T2 - 2-year follow-up
AU - Intercontinental Cooperative ITP Study Group (ICIS)
AU - Schifferli, Alexandra
AU - Holbro, Andreas
AU - Chitlur, Meera
AU - Coslovsky, Michael
AU - Imbach, Paul
AU - Donato, Hugo
AU - Elalfy, Mohsen
AU - Graciela, Elena
AU - Grainger, John
AU - Holzhauer, Susanne
AU - Riccheri, Cecilia
AU - Rodeghiero, Francesco
AU - Ruggeri, Marco
AU - Tamary, Hannah
AU - Uglova, Tatjana
AU - Wu, Runhui
AU - Kühne, Thomas
N1 - Funding Information:
We thank all patients who continue to participate in the PARC-ITP Registry and the staff of the participating institutions. We thank all investigators of the PARC-ITP Registry who supported ICIS and generously provided us with their patient data. A complete membership list appears in “Appendix”. We are indebted to Verena Stahel, Caroline Asal Martin, and Monika Imbach for data administration and secretarial work. The registry is supported in part by grants from the ITP Foundation, Darien, CT, USA; Eduard Waeffler-Ludwig-Stiftung, Basel, Switzerland; Stiftung zur Fo€rderung medizinischer und biolo-gischer Forschung, Basel, Switzerland; and University Children’s Hospital Basel, University of Basel, Switzerland. We thank Enago for editorial assistance.
Funding Information:
We thank all patients who continue to participate in the PARC-ITP Registry and the staff of the participating institutions. We thank all investigators of the PARC-ITP Registry who supported ICIS and generously provided us with their patient data. A complete membership list appears in “Appendix”. We are indebted to Verena Stahel, Caroline Asal Martin, and Monika Imbach for data administration and secretarial work. The registry is supported in part by grants from the ITP Foundation, Darien, CT, USA; Eduard Waeffler-Ludwig-Stiftung, Basel, Switzerland; Stiftung zur Förderung medizinischer und biologischer Forschung, Basel, Switzerland; and University Children's Hospital Basel, University of Basel, Switzerland. We thank Enago for editorial assistance.
Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2018/6
Y1 - 2018/6
N2 - Comparative clinical studies of children and adults with immune thrombocytopenia (ITP) are poorly covered in the literature. However, the accepted classification of ITP—childhood ITP and adult ITP—results in considerable differences in treatment protocols and practice guidelines. The analysis of the Pediatric and Adult Registry on Chronic ITP (PARC-ITP) of patients at first presentation demonstrated fewer differences in clinical and laboratory findings at initial diagnosis between children and adults than expected. The present report of 2-year follow-up data supports the hypothesis that there are common aspects of childhood and adult ITP. Data of 3360 children and 420 adults were collected during the time of 2004 until 2015 at initial diagnosis. Follow-up information was available for 51% and 33% of children and 66% and 49% of adults at 12- and 24-months, respectively. Similarities were found in unexpected areas of ITP, such as the rate of late remission at 12 and 24 months, reported bleeding sites, platelet count in bleeders, and the frequency of treated patients with persistent or chronic ITP. Differences were confirmed for the overall rate of remission and treatment modalities. Unexpected differences were found in the percentage of nonbleeders, with more adults in the nonbleeder group. More studies are needed to investigate different age groups with the aim to optimize their management.
AB - Comparative clinical studies of children and adults with immune thrombocytopenia (ITP) are poorly covered in the literature. However, the accepted classification of ITP—childhood ITP and adult ITP—results in considerable differences in treatment protocols and practice guidelines. The analysis of the Pediatric and Adult Registry on Chronic ITP (PARC-ITP) of patients at first presentation demonstrated fewer differences in clinical and laboratory findings at initial diagnosis between children and adults than expected. The present report of 2-year follow-up data supports the hypothesis that there are common aspects of childhood and adult ITP. Data of 3360 children and 420 adults were collected during the time of 2004 until 2015 at initial diagnosis. Follow-up information was available for 51% and 33% of children and 66% and 49% of adults at 12- and 24-months, respectively. Similarities were found in unexpected areas of ITP, such as the rate of late remission at 12 and 24 months, reported bleeding sites, platelet count in bleeders, and the frequency of treated patients with persistent or chronic ITP. Differences were confirmed for the overall rate of remission and treatment modalities. Unexpected differences were found in the percentage of nonbleeders, with more adults in the nonbleeder group. More studies are needed to investigate different age groups with the aim to optimize their management.
UR - http://www.scopus.com/inward/record.url?scp=85044527660&partnerID=8YFLogxK
U2 - 10.1002/ajh.25086
DO - 10.1002/ajh.25086
M3 - Article
C2 - 29516627
AN - SCOPUS:85044527660
SN - 0361-8609
VL - 93
SP - 751
EP - 759
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 6
ER -