Haematology

Author(s):  
Dan Furmedge ◽  
Ricky Sinharay

Tackling haematology is never easy. Revision can be a struggle, as it may not always be obvious which topic areas will be directly relevant to clin­ical practice. We still, however, benefit from an understanding of these areas and an appreciation of how to do and interpret the basics and when more expertise is required. Sometimes the answers require a trip right back to the stem cell. A junior doctor’s most frequent contact with haematology is in interpreting a full blood count. In this task, the core skills of the chapter come to the fore— in response to an anaemia, we should be able to explore the possibilities of iron deficiency, vitamin deficiency, and haem­olysis. On seeing a thrombocytopenia or an abnormal clotting profile, we should be able to make a clinical assessment and perform further appropriate tests, with a view to suggesting differential diagnoses. The questions in this chapter aim to build confidence in these tasks. There is a lot more to haematology, however, than a blood count. As a junior doctor, there will be regular practical challenges such as pre­scribing and altering anticoagulation therapy, overseeing the safe delivery of a blood transfusion, and managing acute situations such as sickle- cell crises. The way forward is to be able to master these basics and start to see the bigger picture. This means developing a feel for the more subtle symptoms and signs of haematological disease and becoming proactive in the face of abnormal blood results. As with all of the chapters in this book, it is a way of thinking that is crucial— one that allows confident management of common situations and recognition of potentially catastrophic conditions, but also one that encourages creativity and initiative. When faced with a clinical conun­drum, we should have the knowledge and confidence to ask appropri­ately: ‘Is the answer in the blood?’

2018 ◽  
Vol 48 (4) ◽  
pp. 408-413 ◽  
Author(s):  
Lawrence J. Oh ◽  
Eugene Wong ◽  
Juliana Andrici ◽  
Peter McCluskey ◽  
James E. H. Smith ◽  
...  

2014 ◽  
Vol 23 (3) ◽  
pp. 799-806 ◽  
Author(s):  
Flávia Martinelli Pelegrino ◽  
Fabiana Bolela ◽  
Inaiara Scalçone de Almeida Corbi ◽  
Ariana Rodrigues da Silva Carvalho ◽  
Rosana Aparecida Spadoti Dantas

This is a report of experience on the construction and validation of an educational protocol for patients on oral anticoagulation therapy. Based on Bandura's Social Cognitive Theory, three phases were identified to construct the educational protocol. The literature review on oral anticoagulants was used to prepare the content of each phase of the protocol. As a result, verbal and written orientation in the phases of attention and retention were developed. In the reproduction and motivation phase, support through contact by telephone was provided. And finally, an improvement in the evaluation of the outcomes related to oral anticoagulant is expected in the performance phase. Once the educational protocol was defined, we proceeded with the face and content validity process, which allowed adaptations to the final version of the educational protocol constructed.


2020 ◽  
pp. 207-217
Author(s):  
Hugh C. Rayner ◽  
Mark E. Thomas ◽  
David V. Milford

2022 ◽  
Vol 22 (1) ◽  
Author(s):  
Gayani Shashikala Amarasinghe ◽  
Thilini Chanchala Agampodi ◽  
Vasana Mendis ◽  
Krishanthi Malawanage ◽  
Chamila Kappagoda ◽  
...  

Abstract Background The Sustainable development goals, which focus strongly on equity, aim to end all forms of malnutrition by 2030. However, a significant cause of intergenerational transfer of malnutrition, anaemia in pregnancy, is still a challenge. It is especially so in the low- and middle-income settings where possible context-specific aetiologies leading to anaemia have been poorly explored. This study explores the prevalence of etiological factors significantly contributing to anaemia in pregnancy in Sri Lanka, a lower-middle-income country with a high prevalence of malnutrition albeit robust public health infrastructure. Methods All first-trimester pregnant women registered in the public maternal care programme in the Anuradhapura district from July to September 2019 were invited to participate in Rajarata Pregnancy Cohort (RaPCo). After a full blood count analysis, high-performance liquid chromatography, peripheral blood film examination, serum B12 and folate levels were performed in anaemic participants, guided by an algorithm based on the red cell indices in the full blood count. In addition, serum ferritin was tested in a random subsample of 213 participants. Anaemic women in this subsample underwent B12 and folate testing. Results Among 3127 participants, 14.4% (95%CI 13.2–15.7, n = 451) were anaemic. Haemoglobin ranged between 7.4 to 19.6 g/dl. 331(10.6%) had mild anaemia. Haemoglobin ≥13 g/dl was observed in 39(12.7%). Microcytic, normochromic-normocytic, hypochromic-normocytic and macrocytic anaemia was observed in 243(54%), 114(25.3%), 80(17.8%) and two (0.4%) of full blood counts in anaemic women, respectively. Microcytic anaemia with a red cell count ≥5 * 106 /μl demonstrated a 100% positive predictive value for minor haemoglobinopathies. Minor hemoglobinopathies were present in at least 23.3%(n = 105) of anaemic pregnant women. Prevalence of iron deficiency, B12 deficiency and Southeast Asian ovalocytosis among the anaemic was 41.9% (95%CI 26.4–59.2), 23.8% (95%CI 10.6–45.1) and 0.9% (95%CI 0.3–2.3%), respectively. Folate deficiency was not observed. Conclusion Even though iron deficiency remains the primary cause, minor hemoglobinopathies, B 12 deficiency and other aetiologies substantially contribute to anaemia in pregnancy in this study population. Public health interventions, including screening for minor hemoglobinopathies and multiple micronutrient supplementation in pregnancy, should be considered in the national programme for areas where these problems have been identified.


2019 ◽  
Vol 7 (1) ◽  
pp. 34-45
Author(s):  
Irina Sokolovska ◽  
Nadezhda Maryukhnich ◽  
Valentyna Zarytska ◽  
Olena Kyrpychenko ◽  
Valentina Nechiporenko ◽  
...  

It has been stated that changes of lipid exchange and increasing of lipid peroxidation are accompanied by the inflammatory process, which show the increase of proatherogenic blood characteristics. In patients with chronic non-specific inflammatory diseases of genitals disorders of phagocytosis mechanisms, increasing of autointoxication and reaction of hypersensitivity of immediate type are revealed after full blood count index. On the basis of analyses results one can conclude that the increase of atherogenic properties of blood plasma in patients with chronic non-specific inflammatory diseases of genitals took place in accordance with vascular endothelium damage. The article is the first to show the effectiveness of complex treatment of different atherosclerotic pathogenesis links by means of correction of proatherogenic lipid fractions and antioxidative complexes.


2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Leonard Mutema ◽  
Zivanai Chapanduka ◽  
Fungai Musaigwa ◽  
Nomusa Mashigo

Background: The performance of laboratories can be objectively assessed using the overall turn-around time (TAT). However, TAT is defined differently by the laboratory and clinicians; therefore, it is important to determine the contribution of all the different components making up the laboratory test cycle.Objective: We carried out a retrospective analysis of the TAT of full blood count tests requested from the haematology outpatient department at Tygerberg Academic Hospital in Cape Town, South Africa, with an aim to assess laboratory performance and to identify critical steps influencing TAT.Methods: A retrospective audit was carried out, focused on the full blood count tests from the haematology outpatient department within a period of 3 months between 01 February and 30 April 2018. Data was extracted from the National Health Laboratory Service laboratory information system. The time intervals of all the phases of the test cycle were determined and total TAT and within-laboratory (intra-lab) TAT were calculated.Results: A total of 1176 tests were analysed. The total TAT median was 275 (interquartile range [IQR] 200.0–1537.7) min with the most prolonged phase being from authorisation to review by clinicians (median 114 min; IQR: 37.0–1338.5 min). The median intra-lab TAT was 55 (IQR 40–81) min and 90% of the samples were processed in the laboratory within 134 min of registration.Conclusion: Our findings showed that the intra-lab TAT was within the set internal benchmark of 3 h. Operational phases that were independent of the laboratory processes contributed the most to total TAT.


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