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Featured researches published by Bethan Myers.


British Journal of Haematology | 2012

UK guidelines on the management of iron deficiency in pregnancy

Sue Pavord; Bethan Myers; Susan Robinson; Shubha Allard; Jane Strong; Christina Oppenheimer

Iron deficiency is the most common deficiency state in the world, affecting more than 2 billion people globally. Although it is particularly prevalent in less‐developed countries, it remains a significant problem in the developed world, even where other forms of malnutrition have already been almost eliminated. Effective management is needed to prevent adverse maternal and pregnancy outcomes, including the need for red cell transfusion. The objective of this guideline is to provide healthcare professionals with clear and simple recommendations for the diagnosis, treatment and prevention of iron deficiency in pregnancy and the postpartum period. This is the first such guideline in the UK and may be applicable to other developed countries. Public health measures, such as helminth control and iron fortification of foods, which can be important to developing countries, are not considered here. The guidance may not be appropriate to all patients and individual patient circumstances may dictate an alternative approach.


Blood Reviews | 2011

Bleeding and thrombotic complications of kidney disease

Sue Pavord; Bethan Myers

With the rising prevalence of kidney disease, clinicians are increasingly faced with concerns about potential thrombotic and bleeding complications. Thrombotic risk, both arterial and venous, predominates with all severities of kidney disease but bleeding manifestations become an additional concern particularly with uraemia. This article reviews these contrasting problems and discusses strategies for prevention and management in the context of renal impairment, renal replacement therapy and renal transplantation.


British Journal of Haematology | 2012

Diagnosis and management of maternal thrombocytopenia in pregnancy

Bethan Myers

Thrombocytopenia is a common finding in pregnancy, occurring in approximately 7–10% of pregnancies. It may be a diagnostic and management problem, and has many causes, some of which are specific to pregnancy. Although most cases of thrombocytopenia in pregnancy are mild, and have no adverse outcome for either mother or baby, occasionally a low platelet count may be part of a more complex disorder with significant morbidity and may be life‐threatening. Overall, about 75% of cases are due to gestational thrombocytopenia, 15–20% secondary to hypertensive disorders; 3–4% due to an immune process, and the remaining 1–2% made up of rare constitutional thrombocytopenias, infections and malignancies. In this review, a diagnostic approach to investigating thrombocytopenia in pregnancy is presented, together with antenatal, anaesthetic and peri‐natal management issues for mother and baby, followed by a detailed discussion on the specific causes of thrombocytopenia and the management options in each case.


British Journal of Haematology | 1995

Hepatitis C virus infection in multi-transfused children with haematological malignancy

Bethan Myers; W. Irving; R. Holungsworth; D. Readett; J. S. Lilleyman; G. Dolan

Summary. Transmission of hepatitis C virus (HCV) is an important hazard of blood transfusion and may result in chronic liver disease. 98 children from Nottingham and Sheffield with haematological malignancies were studied to determine the prevalence of HCV infection by enzyme immunoassay and RT/PCR techniques. The children had been exposed to up to 184 donors through red cell and platelet transfusion, the majority prior to routine testing for HCV infection in blood donors. Only one sample showed evidence of HCV infection being both FXISA and RT/PCR positive. None of the samples taken since donor screening were positive. This provides reassurance as to the low rate of HCV acquisition in multi‐transfused patients in this part of the U.K. compared to other parts of the world.


Arteriosclerosis, Thrombosis, and Vascular Biology | 2005

Leukocytosis, Vascular Disease, and Adenine Nucleotide Metabolism

S. Heptinstall; Jacqueline R. Glenn; Andrew D. Johnson; Bethan Myers; Ann E. White; Lian Zhao

To the Editor: We read with interest the paper by Barry S. Coller on leukocytosis and its relationship with vascular disease morbidity and mortality1 and the subsequent correspondence.2,3 We are intrigued to learn that relative leukocytopenia may be associated with increased morbidity and mortality in patients with acute myocardial infarction1,4 and in those undergoing percutaneous coronary intervention.5 We note the discussion on whether leukocyte count is merely a marker of general disturbances in inflammation and general poor health, or whether leukocytes might contribute directly to thrombosis and atherosclerosis. Although several mechanisms through which leukocytes may contribute to thrombosis and atherosclerosis were discussed,1–3 nothing has been said about the role of leukocytes in adenine nucleotide metabolism. Adenosine diphosphate (ADP) is, of course, a major contributor to the thrombotic mechanism as evidenced by the successful use of ADP antagonists which reduce ADP-induced platelet activation and aggregation and thereby act as anti-thrombotic agents.6 It was recognized that leukocytes are active in the metabolism of adenine nucleotides many years …


British Journal of Haematology | 2001

Lack of response to thalidomide in plasmacytomas.

Bethan Myers; Charlotte Grimley; D. Crouch; G. Dolan


British Journal of Haematology | 2001

Thalidomide and low-dose dexamethasone in myeloma treatment.

Bethan Myers; Charlotte Grimley; G. Dolan


British Journal of Haematology | 2008

Incidence and management of 82 cases of pregnancy-associated venous thromboembolism occurring at a single centre -comparison with Voke et al

Hamish Lyall; Bethan Myers


British Journal of Haematology | 2000

Thalidomide treatment in advanced refractory myeloma.

Bethan Myers; D. Crouch; G. Dolan


British Journal of Haematology | 2001

Audit of laboratory investigation of antiphospholipid syndrome

Bethan Myers; G. Dolan; J. Gould

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D. Crouch

University of Nottingham

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Hamish Lyall

University of Nottingham

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Ann E. White

University of Nottingham

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Beverley Hunt

Luton and Dunstable Hospital

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J. Gould

University of Nottingham

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