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Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre

OBJECTIVE: The study aimed to demonstrate the pattern of clinical presentations and outcome of acute Immune Thrombocytopenia (ITP) in our Centre. METHODS: A descriptive, observational study was conducted by collecting and analysing the data of 103 patients of acute ITP, ageing between 1-14 years, at...

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Autores principales: Zafar, Huma, Anwar, Saadia, Faizan, Mahwish, Riaz, Shazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191794/
https://www.ncbi.nlm.nih.gov/pubmed/30344575
http://dx.doi.org/10.12669/pjms.345.15687
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author Zafar, Huma
Anwar, Saadia
Faizan, Mahwish
Riaz, Shazia
author_facet Zafar, Huma
Anwar, Saadia
Faizan, Mahwish
Riaz, Shazia
author_sort Zafar, Huma
collection PubMed
description OBJECTIVE: The study aimed to demonstrate the pattern of clinical presentations and outcome of acute Immune Thrombocytopenia (ITP) in our Centre. METHODS: A descriptive, observational study was conducted by collecting and analysing the data of 103 patients of acute ITP, ageing between 1-14 years, at The Children’s Hospital, Lahore from January 2016 to December 2016. We collected the data regarding age, sex, clinical presentations, history of preceding viral infections, vaccination history, laboratory values, different treatment options used, and response to the treatment concerning complete response, partial response and poor responders. Statistical analysis performed by using IBM SPSS statistics version 20. RESULTS: We retrospectively, reviewed total 103 patients cases. The median age, at the time of presentation, was 5±3.4 years while mean age was 4.5±2.9 years. The male to female ratio was 1.28:1. Mean platelet count on presentation was 7 x 10(9)/L (range: 0-24). Twenty three (22.3%), patients had the history of preceding illness. Bruises, petechiae, epistaxis and hematemesis remained the common presentations. Six (5.8%) patients showed spontaneous recovery while 97 (94%) patients received treatment for ITP. Overall, 71 (68.9%) showed a response after treatment. Sixty-two patients (59.22%) showed loss of response and received treatment again. Among these patients, thirty-four patients (33%) developed chronic disease. CONCLUSION: Majority of patients presenting to our tertiary care centre had severe acute ITP on presentation. After management and follow-up, almost 1/3 of the patients develop chronic disease hence the incidence of developing chronic disease remained high as compared to the other centers.
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spelling pubmed-61917942018-10-19 Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre Zafar, Huma Anwar, Saadia Faizan, Mahwish Riaz, Shazia Pak J Med Sci Original Article OBJECTIVE: The study aimed to demonstrate the pattern of clinical presentations and outcome of acute Immune Thrombocytopenia (ITP) in our Centre. METHODS: A descriptive, observational study was conducted by collecting and analysing the data of 103 patients of acute ITP, ageing between 1-14 years, at The Children’s Hospital, Lahore from January 2016 to December 2016. We collected the data regarding age, sex, clinical presentations, history of preceding viral infections, vaccination history, laboratory values, different treatment options used, and response to the treatment concerning complete response, partial response and poor responders. Statistical analysis performed by using IBM SPSS statistics version 20. RESULTS: We retrospectively, reviewed total 103 patients cases. The median age, at the time of presentation, was 5±3.4 years while mean age was 4.5±2.9 years. The male to female ratio was 1.28:1. Mean platelet count on presentation was 7 x 10(9)/L (range: 0-24). Twenty three (22.3%), patients had the history of preceding illness. Bruises, petechiae, epistaxis and hematemesis remained the common presentations. Six (5.8%) patients showed spontaneous recovery while 97 (94%) patients received treatment for ITP. Overall, 71 (68.9%) showed a response after treatment. Sixty-two patients (59.22%) showed loss of response and received treatment again. Among these patients, thirty-four patients (33%) developed chronic disease. CONCLUSION: Majority of patients presenting to our tertiary care centre had severe acute ITP on presentation. After management and follow-up, almost 1/3 of the patients develop chronic disease hence the incidence of developing chronic disease remained high as compared to the other centers. Professional Medical Publications 2018 /pmc/articles/PMC6191794/ /pubmed/30344575 http://dx.doi.org/10.12669/pjms.345.15687 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zafar, Huma
Anwar, Saadia
Faizan, Mahwish
Riaz, Shazia
Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title_full Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title_fullStr Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title_full_unstemmed Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title_short Clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
title_sort clinical features and outcome in paediatric newly diagnosed immune thrombocytopenic purpura in a tertiary care centre
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191794/
https://www.ncbi.nlm.nih.gov/pubmed/30344575
http://dx.doi.org/10.12669/pjms.345.15687
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