Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5591
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dc.contributor.authorNoun, Peteren_US
dc.contributor.authorInati, Adletteen_US
dc.contributor.authorRaffoul, Ranaen_US
dc.contributor.authorYounes, Jennifer Abien_US
dc.contributor.authorMardini, Joelleen_US
dc.contributor.authorKhalife, Hassanen_US
dc.date.accessioned2022-05-16T09:39:49Z-
dc.date.available2022-05-16T09:39:49Z-
dc.date.issued2022-03-12-
dc.identifier.issn09395555-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5591-
dc.description.abstractAbout 20% to 30% of pediatric patients with immune thrombocytopenia (ITP) develop chronic or refractory disease lasting 12 months or more that can be challenging to treat. Eltrombopag is being used after failure of previous lines of therapy with good results at tertiary healthcare centers in Lebanon, a developing country with available multidisciplinary treatment modalities. This is a retrospective multicenter observational study that analyzed data on pediatric patients with chronic or refractory ITP who were given eltrombopag as second- or third-line therapy in 6 large referral hospitals in Beirut (country capital located in mid Lebanon), South, North, and Mount Lebanon between October 2016 and May 2020. The primary end point of the study was a proportion of patients achieving platelet counts of ≥ 50 × 109/L for at least 6 weeks without requiring rescue therapy during the observation period. Data from 36 patients treated for chronic and refractory ITP, 20 (55.6%) males and 16 (44.4%) females, were analyzed. The median age at the eltrombopag dose was 11 years (2-18 years). All the patients had failure of the first-line therapy with steroids, 3 patients received eltrombopag as second-line therapy, and the remaining patients had failure of at least 2 previous lines of therapy, including steroids. The primary end point was achieved in 21 (58.3%) of 36 patients. The treatment was discontinued in 3 patients due to no response. Hepatotoxicity and all other adverse events (headache, weakness, and diarrhea) were mild and transient. All the patients who achieved the target platelet count of ≥ 50 × 109/L maintained the response for the treatment duration, which was a minimum of 5 months up to 3 years, with median/mean observation periods of 12 months and 14 months, respectively. This study confirms the findings of randomized controlled trials that eltrombopag as second- or third-line therapy in pediatric patients with chronic and refractory ITP is effective and safe, reinforcing its role in the real-world management of these patients.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.subjectBleeding disordersen_US
dc.subjectChronic and refractory ITP, immune thrombocytopeniaen_US
dc.subjectEltrombopagen_US
dc.subjectPediatricen_US
dc.subjectRetrospective studyen_US
dc.titleEltrombopag in pediatric chronic and refractory ITP: data from a retrospective multicenter study from Lebanonen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1007/s00277-022-04804-z-
dc.identifier.pmid35278100-
dc.identifier.scopus2-s2.0-85126234381-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85126234381-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume101en_US
dc.description.issue5en_US
dc.description.startpage991en_US
dc.description.endpage997en_US
dc.date.catalogued2022-05-16-
dc.description.statusPublisheden_US
dc.identifier.openURLhttps://link.springer.com/article/10.1007/s00277-022-04804-zen_US
dc.relation.ispartoftextAnnals of Hematologyen_US
dc.description.campusSGH campusen_US
Appears in Collections:Faculty of Medicine
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