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1.
Int J Lab Hematol ; 44(6): 1088-1093, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-36056688

RESUMO

INTRODUCTION: Established parameters for the investigation of suspected iron deficiency have recognized limitations that affect their sensitivity and specificity. Reticulocyte haemoglobin content (RHC) is an early biomarker of iron deficiency or restriction, which also demonstrates response to iron therapy. RHC parameters are offered on all major automated haematology analysers. There is no external quality assessment (EQA) for RHC in the UK, restricting its wider clinical application. The UK National External Quality Assessment Scheme (UKNEQAS) for Haematology has completed a pilot study on the use of stabilized blood for RHC EQA. METHODS: Blood was obtained from two JAK2 V617F mutation-positive, polycythaemia vera patients undergoing regular venesection, and from a healthy volunteer donor. Aliquots of each donation were distributed to users of Abbott, Horiba, Siemens and Sysmex automated analysers for RHC analysis on days 1, 3, 5 and 7. RESULTS: Results were received from 20 laboratories using four different platforms. The daily mean and standard deviation (SD) were calculated for each aliquot, by day of analysis and platform. With RHC there was no significant within-platform difference (p > 0.5) between testing days, although there were statistically significant differences (p < 0.001) between different platforms. The greatest difference was seen between Abbott MCHr and Horiba RhCc (-6.14 ± 1.25 pg). Despite inter-platform differences, it was possible to define iron deficient, borderline, and normal cut-offs to classify 95% of results correctly. CONCLUSIONS: The results demonstrate that it is possible to provide RHC EQA material using UKNEQAS standard procedures. The results are clinically relevant but indicate a requirement for inter-user comparison.


Assuntos
Hematologia , Deficiências de Ferro , Humanos , Reticulócitos , Projetos Piloto , Hemoglobinas , Ferro , Reino Unido
2.
Br J Haematol ; 181(3): 331-340, 2018 05.
Artigo em Inglês | MEDLINE | ID: mdl-29672840

RESUMO

Serum ferritin level is one of the most commonly requested investigations in both primary and secondary care. Whilst low serum ferritin levels invariably indicate reduced iron stores, raised serum ferritin levels can be due to multiple different aetiologies, including iron overload, inflammation, liver or renal disease, malignancy, and the recently described metabolic syndrome. A key test in the further investigation of an unexpected raised serum ferritin is the serum transferrin saturation. This guideline reviews the investigation and management of a raised serum ferritin level. The investigation and management of genetic haemochromatosis is not dealt with however and is the subject of a separate guideline.


Assuntos
Ferritinas/sangue , Sobrecarga de Ferro , Nefropatias , Hepatopatias , Síndrome Metabólica , Proteínas de Neoplasias/sangue , Neoplasias , Humanos , Inflamação/sangue , Inflamação/terapia , Sobrecarga de Ferro/sangue , Sobrecarga de Ferro/terapia , Nefropatias/sangue , Nefropatias/terapia , Hepatopatias/sangue , Hepatopatias/terapia , Síndrome Metabólica/sangue , Síndrome Metabólica/terapia , Neoplasias/sangue , Neoplasias/terapia , Guias de Prática Clínica como Assunto
4.
Leuk Lymphoma ; 46(4): 549-52, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16019483

RESUMO

Sixteen patients with relapsed mantle-cell lymphoma (MCL) were treated with the combination of fludarabine and cyclophosphamide (FC) with or without rituximab. All patients had received prior CHOP (cyclophosphamide, vincristine, doxorubicin, prednisone) chemotherapy, with a response rate of 63.5% (25% complete response), and a median duration of response of 10 months (range 1-32 months). Subsequent treatment with FC +/- rituximab produced a response rate of 75% with a higher complete response rate (56% P = 0.07 vs. CHOP), and a median duration of response of 11 months (4-25+ months). This study demonstrates that FC is a highly active regimen in patients relapsing following CHOP chemotherapy.


Assuntos
Anticorpos Monoclonais/administração & dosagem , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Ciclofosfamida/administração & dosagem , Linfoma de Célula do Manto/tratamento farmacológico , Vidarabina/análogos & derivados , Adulto , Idoso , Anticorpos Monoclonais Murinos , Ciclofosfamida/uso terapêutico , Intervalo Livre de Doença , Doxorrubicina/uso terapêutico , Humanos , Pessoa de Meia-Idade , Prednisona/uso terapêutico , Recidiva , Indução de Remissão , Estudos Retrospectivos , Rituximab , Resultado do Tratamento , Vidarabina/administração & dosagem , Vincristina/uso terapêutico
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