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Written by expert consultants and clinical scientists currently practising in the UK, the BSH Guidelines provide up-to-date evidence-based guidance on the diagnosis and treatment of haematological diseases. Self accreditation Listen to two podcasts and earn one CPD point via self-accreditation Join our Guidelines Newsletter to be notified when new guidelines/good practice papers are published by going into your members account under MyBSH. Non members can email bshguidelines@b-s-h.org.uk to sign up for updates.
Episodes

Friday Apr 19, 2024
Diagnosis and management of heparin-induced thrombocytopenia: Third edition
Friday Apr 19, 2024
Friday Apr 19, 2024
A podcast recording by Dr Deepa J. Arachchillage on the guideline: Diagnosis and management of heparin-induced thrombocytopenia: Third edition.

Monday Apr 08, 2024
Diagnosis and management of marginal zone lymphomas
Monday Apr 08, 2024
Monday Apr 08, 2024
The objective of this podcast presented by Kim Linton and Renata Walewska is to provide healthcare professionals with clear guidance on the diagnosis and management of patients with marginal zone lymphoma (MZL).

Thursday Apr 04, 2024
Guideline on the Investigation and management of a raised serum ferritin
Thursday Apr 04, 2024
Thursday Apr 04, 2024
Guideline on the Investigation and management of a raised serum ferritin: A podcast recording of a conversation between Dr Jenny Tam and Dr Wayne Thomas.

Wednesday Nov 29, 2023
Significant Haemoglobinopathies: a guideline for screening and diagnosis
Wednesday Nov 29, 2023
Wednesday Nov 29, 2023
Antenatal screening/testing of pregnant women should be carried out according to the guidelines of the National Health Service (NHS) Sickle Cell and Thalassaemia Screening Programme. Newborn screening and, when necessary, follow-up testing and referral, should be carried out according to the guidelines of the NHS Sickle Cell and Thalassaemia Screening Programme. All babies under 1 year of age arriving in the United Kingdom should be offered screening for sickle cell disease (SCD). Preoperative screening for SCD should be carried out in patients from ethnic groups in which there is a significant prevalence of the condition. Emergency screening with a sickle solubility test must always be followed by definitive analysis. Laboratories performing antenatal screening should utilise methods that are capable of detecting significant variants and are capable of quantitating haemoglobins A2 and F at the cut-off points required by the national antenatal screening programme. The laboratory must ensure a provisional report is available for antenatal patients within three working days from sample receipt.

Tuesday Nov 21, 2023
Diagnosis and management of Mantle Cell Lymphoma
Tuesday Nov 21, 2023
Tuesday Nov 21, 2023
The objective of this guideline is to provide healthcare professionals with clear guidance on the diagnosis and management of patients with mantle cell lymphoma.

Wednesday Aug 02, 2023
Wednesday Aug 02, 2023
This Good Practice Paper podcast provides recommendations for the diagnosis, risk stratification and management of the monoclonal gammopathy of undetermined significance (MGUS). It describes the recently recognised entity of the monoclonal gammopathy of clinical significance (MGCS), and recommends how it should be managed. The potential for targeted population screening for MGUS is also discussed.

Wednesday Jul 12, 2023
Guideline on the investigation and management of acute transfusion reactions
Wednesday Jul 12, 2023
Wednesday Jul 12, 2023

Wednesday Jun 07, 2023
Haematological management of major haemorrhage
Wednesday Jun 07, 2023
Wednesday Jun 07, 2023
Haematological management of major haemorrhage: A podcast recording of a conversation between Prof Simon Stanworth and Dr Heidi Doughty.

Friday May 26, 2023
Friday May 26, 2023
A BSH Guideline on the Anticoagulant management of pregnant individuals with mechanical heart valves presented by Dr Will Lester.

Wednesday Dec 21, 2022
Wednesday Dec 21, 2022
Guideline session at EHA Conference 2022 on The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper