Rezan Abdul-Kadir
Royal Free Hospital
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Publication
Featured researches published by Rezan Abdul-Kadir.
American Journal of Obstetrics and Gynecology | 2009
Andra H. James; Peter A. Kouides; Rezan Abdul-Kadir; Mans Edlund; Augusto B. Federici; Susan Halimeh; Pieter Willem Kamphuisen; Barbara A. Konkle; Oscar Martínez-Perez; Claire McLintock; Flora Peyvandi; Rochelle Winikoff
Reproductive tract bleeding in women is a naturally occurring event during menstruation and childbirth. In women with menorrhagia, however, congenital bleeding disorders historically have been underdiagnosed. This consensus is intended to allow physicians to better recognize bleeding disorders as a cause of menorrhagia and consequently offer effective disease-specific therapies.
Transfusion | 2014
Rezan Abdul-Kadir; Claire McLintock; Anne Sophie Ducloy; Hazem El-Refaey; Adrian England; Augusto B. Federici; Chad A. Grotegut; Susan Halimeh; Jay H. Herman; Stefan Hofer; Andra H. James; Peter A. Kouides; Michael J. Paidas; Flora Peyvandi; Rochelle Winikoff
Postpartum hemorrhage (PPH) remains one of the leading causes of maternal morbidity and mortality worldwide, although the lack of a precise definition precludes accurate data of the absolute prevalence of PPH.
European Journal of Obstetrics & Gynecology and Reproductive Biology | 2011
Andra H. James; Peter A. Kouides; Rezan Abdul-Kadir; Jennifer E. Dietrich; Mans Edlund; Augusto B. Federici; Susan Halimeh; Pieter Willem Kamphuisen; Christine A. Lee; Oscar Martínez-Perez; Claire McLintock; Flora Peyvandi; Claire S. Philipp; Jeffrey Wilkinson; Rochelle Winikoff
Acute menorrhagia is a common gynecological disorder. Prevalence is high among women with inherited bleeding disorders and recent guidance for optimal management is lacking. Following a comprehensive review of the literature, an international expert panel in obstetrics, gynecology and hematology reached consensus on recommendations regarding the management of acute menorrhagia in women without a diagnosed bleeding disorder, as well as in patients with von Willebrand disease, platelet function disorders and other rare hemostatic disorders. The causes and predictors of acute menorrhagia are discussed and special consideration is given for the treatment of women on anticoagulation therapy. This review and accompanying recommendations will provide guidance for healthcare practitioners in the emergency management of acute menorrhagia.
Thrombosis and Haemostasis | 2011
Anne Riddell; Rezan Abdul-Kadir; Debra Pollard; Edward G. D. Tuddenham; Keith Gomez
Although factor XI (FXI) concentrate is an effective replacement therapy in severe FXI deficiency without inhibitors, some patients are unwilling to receive it because it is plasma-derived. We report on the use and monitoring of low dose, recombinant factor VIIa (rFVIIa, NovoSeven®), to cover surgery (caesarean section, cholecystectomy and abdominoplasty) in four female patients (FXI:C 2-4 IU/dl, aged 32-51 years) who wished to avoid exposure to plasma. None of our patients had inhibitors to FXI. Our aim was to find the optimal dose of rFVIIa by in vitro spiking of patient samples and to correlate this with the response to rFVIIa in vivo . Prior to surgery, venous blood was collected into sodium citrate with corn trypsin inhibitor and spiked with 0.25-1.0 μg/ml rFVIIa in vitro , equivalent to a 15-70 μg/kg dose of rFVIIa in vivo . Analysis using thromboelastometry and thrombin generation assays, triggered with tissue factor, showed that the thrombin generation assay was insufficiently sensitive to the haemostatic defect in these patients. A concentration of 0.5 μg/ml was as effective as 1.0 μg/ml FVIIa in normalising thromboelastometry in vitro in all four patients. Therefore, patients received 15-30 μg/kg rFVIIa at 2-4 hourly intervals with tranexamic acid 1g every six hours. Post treatment samples were taken at 10-240 minutes and showed initial normalisation of thromboelastometry with gradual return to baseline after 2-4 hours. In conclusion, low-dose rFVIIa therapy was successfully used in four patients with severe FXI deficiency undergoing surgery to prevent bleeding and can be monitored using thromboelastometry.
Expert Review of Hematology | 2018
Fadi Mirza; Rezan Abdul-Kadir; Christian Breymann; Ian S. Fraser; Ali Taher
ABSTRACT Introduction: Iron deficiency and iron deficiency anemia are highly prevalent among women throughout their lives. Some females are particularly vulnerable to iron deficiency/iron deficiency anemia, including those with heavy menstrual bleeding (HMB) and pregnant/postpartum women. Despite the high prevalence of iron deficiency/iron deficiency anemia in women, the condition is still underdiagnosed and therefore undertreated, with serious clinical consequences. Areas covered: The following review examines the impact of iron deficiency and iron deficiency anemia on clinical outcomes and quality of life in women from adolescence to post-menopause, paying particular attention to guidelines and current recommendations for diagnostic tests and management. Expert commentary: There are numerous adverse health consequences of an iron-deficient state, affecting all aspects of the physical and emotional health and well-being of women. Guidelines must be developed to help clinicians better identify and treat women at risk of iron deficiency or iron deficiency anemia, particularly those with HMB, or who are pregnant or postpartum. Replacement therapy with oral or intravenous iron preparations is the mainstay of treatment for iron deficiency/iron deficiency anemia, with red blood cell transfusion reserved for emergency situations. Each iron therapy type is associated with benefits and limitations which impact their use.
Transfusion | 2015
Rezan Abdul-Kadir; Claire McLintock; A. S. Ducloy; Hazem El-Refaey; Adrian England; Augusto B. Federici; Chad A. Grotegut; Susan Halimeh; Jay H. Herman; Stefan Hofer; Andra H. James; Peter A. Kouides; Michael J. Paidas; Flora Peyvandi; Rochelle Winikoff
Abdul-Kadir R, McLintock C, Ducloy A-S, El-Refaey H, England A, Federici AB, Grotegut CA, Halimeh S, Herman JH, Hofer S, James AH, Kouides PA, Paidas MJ, Peyvandi F, Winikoff R. Evaluation and management of postpartum hemorrhage: consensus from an international expert panel. Transfusion 2014;54:1756-68. The authors regret that an ergometrine dosage error was introduced within Table 7 (page 1762). It should read 200-500 mcg syntometrine given IV or IM, instead of 500 mg.
Journal of Applied Hematology | 2013
Rezan Abdul-Kadir; Joanna Davies; Susan Halimeh; Claudia Chi
Recent advances in prenatal diagnosis and multidisciplinary management has improved the reproductive outlook for carriers of hemophilia and their offspring. Pre-pregnancy planning allows the woman and her partner to explore reproductive options and prepares the family for the potential delivery of an affected male infant. Non-invasive methods of prenatal diagnosis are advancing, with the aim of providing a definitive test for hemophilia. Carriers of hemophilia have an increased risk of primary and secondary postpartum hemorrhage. The affected male offspring is potentially at risk of cranial bleeding during delivery. A multidisciplinary approach provides advanced planning for the optimum mode of delivery and provision of appropriate haemostatic cover to reduce the risk of bleeding complications. This review summarises current recommendations for pregnancy management in carriers of hemophilia, from the initial pre-pregnancy counseling through to delivery and care of the neonate.
In: Harper, A, (ed.) Haemorrhage and thrombosis for the MRCOG and beyond. (pp. 72-89). RCOG Press: London. (2005) | 2005
Rezan Abdul-Kadir; Christine A. Lee
© The Royal College of Obstetricians and Gynaecologists. Excessive or abnormal vaginal bleeding are the most common symptoms when women present to a gynaecologist. Undiagnosed bleeding disorders, especially Von Willebrands disorder, can be the under-lying cause of menorrhagia in a significant proportion of women. This chapter aims to increase awareness and provide basic information about these relatively uncommon disorders. Immune idiopathic thrombocytopenic purpura (lTP) in adults is usually a chronic disorder with an insidious onset of minor bleeding symptoms. Menorrhagia and dysmenorrhoea adversely affect womens quality of life and may have a major influence on lifestyle and employment. DDAVP (1-desamino-8-D-arginine vasopressin) nasal spray increases von Willebrand factor (VWF) and FVIII and can be used as a home treatment for some women with bleeding disorders. Increased awareness among clinicians of these problems and the treatment options available are essential to improve quality of life and avoid unnecessary surgical intervention.
Acta Obstetricia et Gynecologica Scandinavica | 2005
Claudia Chi; Alex Taylor; Nalini Munjuluri; Rezan Abdul-Kadir
Seminars in Hematology | 2005
Christine A. Lee; Rezan Abdul-Kadir
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Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
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