2016
DOI: 10.7860/jcdr/2016/20347.8976
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High dose Intravenous Anti-D Immune Globulin is More Effective and Safe in Indian Paediatric Patients of Immune Thrombocytopenic Purpura

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Cited by 3 publications
(3 citation statements)
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“…Revisiting the data surrounding hemolysis, ~15% patients suffer from hemolysis, defined differently among studies, following anti-D immunoglobulin. [36][37][38] Less clear, however, is the severity of hemolytic episodes as well as the clinical impact, since magnitude of anti-D immunoglobulin-associated hemolysis is unclassified in the majority of reports. Further, there is a paucity of reported data on prioritized patient-related outcomes, making full determination of balance between desirable and undesirables unknown.…”
Section: Table 2 Evidence-to-decision Frameworkmentioning
confidence: 99%
“…Revisiting the data surrounding hemolysis, ~15% patients suffer from hemolysis, defined differently among studies, following anti-D immunoglobulin. [36][37][38] Less clear, however, is the severity of hemolytic episodes as well as the clinical impact, since magnitude of anti-D immunoglobulin-associated hemolysis is unclassified in the majority of reports. Further, there is a paucity of reported data on prioritized patient-related outcomes, making full determination of balance between desirable and undesirables unknown.…”
Section: Table 2 Evidence-to-decision Frameworkmentioning
confidence: 99%
“…Although ITP is commonly seen clinically, its pathogenesis remains unclear. There are many ways in which the disease can be treated with much improvement, but no concrete method to eliminate it has been found (Swain et al, 2016). The choice drug for ITP is glucocorticoid, which serves to reduce the production of autoantibody and effectively inhibit immunoreaction, but it has a great adverse reaction (Guenno et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…ITP is a relatively common hemorrhagic disease in children. While acute ITP typically resolves within 3 months, chronic refractory ITP has characteristic long disease course ( Swain et al, 2016 ; Queliza et al, 2017 ). Adrenocortical hormone therapy (prednisone acetate, cortisone, etc.)…”
Section: Introductionmentioning
confidence: 99%