Results 11 to 20 of about 7,837 (201)

Successful Desensitization Protocol in an Infant Following Anaphylaxis Secondary to Recombinant Factor VIIa. [PDF]

open access: greenPediatr Allergy Immunol Pulmonol, 2020
Ulusoy Severcan E   +6 more
europepmc   +3 more sources

Medication-Use Evaluation of Recombinant Human Factor VIIa [PDF]

open access: yesGlobal Journal on Quality and Safety in Healthcare, 2020
Introduction: Medication-use evaluation (MUE) is a performance improvement method used to achieve optimal patient outcomes. The recombinant human factor VIIa (rFVIIa) (NovoSeven) is an expensive agent approved by the U.S.
Abrar Al-Subhi   +2 more
doaj   +1 more source

Dental Management of Glanzmann's Thrombasthenia in a 4-Year-Old Child With Rampant Caries: A Case Report and Literature Review. [PDF]

open access: yesClin Case Rep
ABSTRACT Glanzmann's Thrombasthenia (GT) is a rare congenital bleeding disorder in children, caused by the absence or dysfunction of glycoprotein (GP) IIb/IIIa, a receptor located on the platelet membrane. Proper oral health and regular dental appointments are crucial for these patients. However, maintaining good oral hygiene is challenging among them.
Nazemisalman B   +3 more
europepmc   +2 more sources

The prophylactic use of recombinant factor VIIa in a patient with DeBakey type III aortic dissection -A case report- [PDF]

open access: yesKorean Journal of Anesthesiology, 2011
Little is known about the prophylactic use of recombinant factor VIIa (rFVIIa) in patients undergoing surgery for a bleeding aorta employing cardiopulmonary bypass.
Wook Jong Kim   +7 more
doaj   +1 more source

The international, prospective Glanzmann Thrombasthenia Registry: treatment and outcomes in surgical intervention

open access: yesHaematologica, 2015
Standard treatment for Glanzmann thrombasthenia, a severe inherited bleeding disorder, is platelet transfusion. Recombinant factor VIIa is reported to be effective in Glanzmann thrombasthenia with platelet antibodies and/or refractoriness to platelet ...
Man-Chiu Poon   +5 more
doaj   +1 more source

Factor VII deficiency-related recurrent hemarthrosis in a female child – When to suspect?

open access: yesIraqi Journal of Hematology, 2021
Recurrent hemarthrosis is a common entity in children. Although recurrent hemarthrosis most often associated with hemophilia (VIII or IX deficiency), but rarely it can be associated with factor VII deficiency (FVIID).
Siyaram Didel   +4 more
doaj   +1 more source

Successful Treatment of Intractable Hemothorax with Recombinant Factor VIIa in a Nonhemophilic Patient

open access: yesJournal of the Formosan Medical Association, 2006
Recombinant factor VIIa (rFVIIa) was developed for the treatment of bleeding in hemophilic patients with inhibitors. It has also been used to stop bleeding in nonhemophilic patients who fail to respond to conventional treatment.
Yu-Feng Wei   +4 more
doaj   +1 more source

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