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General Hematology

M-A | Direct oral anticoagulants versus warfarin across the spectrum of kidney function in patients with AF

3 May, 2023 | 15:32h | UTC

Direct Oral Anticoagulants Versus Warfarin Across the Spectrum of Kidney Function: Patient-Level Network Meta-Analyses From COMBINE AF – Circulation (free for a limited period)

 

Commentary on Twitter

 


Scientific Statement | Iron deficiency in heart failure

3 May, 2023 | 15:25h | UTC

Iron Deficiency in Heart Failure: A Scientific Statement from the Heart Failure Society of America – Journal of Cardiac Failure

 


Clinical practice guidelines on hemochromatosis

3 May, 2023 | 15:23h | UTC

Clinical practice guidelines on hemochromatosis: Asian Pacific Association for the Study of the Liver – Hepatology International

 


ASCO Guideline Update | Venous thromboembolism prophylaxis and treatment in patients with cancer

25 Apr, 2023 | 14:49h | UTC

Venous Thromboembolism Prophylaxis and Treatment in Patients With Cancer: ASCO Guideline Update – Journal of Clinical Oncology

Commentary: ASCO Updates Guideline on Venous Thromboembolism Prophylaxis and Treatment in Patients With Cancer – ASCO Daily News

 


RCT | Blood donor’s sex does not impact transfusion recipients’ survival

19 Apr, 2023 | 13:20h | UTC

Effect of Donor Sex on Recipient Mortality in Transfusion – New England Journal of Medicine (link to abstract – $ for full-text)

News release: Sex of blood donor has no effect on recipient survival – Ottawa Hospital

 

Commentary on Twitter

 


Phase 2 RCT | Dersimelagon in erythropoietic protoporphyrias

17 Apr, 2023 | 13:05h | UTC

Dersimelagon in Erythropoietic Protoporphyrias – News England Journal of Medicine (link to abstract – $ for full-text)

 

Commentary on Twitter

 


M-A | Efficacy of postpartum pharmacologic thromboprophylaxis

17 Apr, 2023 | 12:55h | UTC

Efficacy of Postpartum Pharmacologic Thromboprophylaxis: A Systematic Review and Meta-analysis – Obstetrics and Gynecology

 


RCT | Hydroxyurea for secondary stroke prevention in children with sickle cell anemia

17 Apr, 2023 | 12:48h | UTC

Hydroxyurea for secondary stroke prevention in children with sickle cell anemia in Nigeria: a randomized controlled trial – Blood

 


Review | Inappropriate prescriptions of direct oral anticoagulants (DOACs) in hospitalized patients

12 Apr, 2023 | 13:14h | UTC

Inappropriate prescriptions of direct oral anticoagulants (DOACs) in hospitalized patients: A narrative review – Thrombosis Research

 


Review | Anticoagulation in patients with liver cirrhosis: friend or foe?

11 Apr, 2023 | 14:17h | UTC

Anticoagulation in Patients with Liver Cirrhosis: Friend or Foe? – Digestive Diseases and Sciences

 


Cohort Study | Antiphospholipid antibodies’ prevalence & link to cardiovascular events

10 Apr, 2023 | 13:59h | UTC

Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events – JAMA Network Open

News Release: Antiphospholipid antibodies may increase heart disease risk in healthy people – Michigan Medicine

 


Guidelines on diagnosis and management of chronic neutropenia in adults and children

10 Apr, 2023 | 13:25h | UTC

The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action – HemaSphere

 

Commentary on Twitter

 


Hydroxyurea use in youths with sickle cell anemia: underused despite updated 2014 guidelines

5 Apr, 2023 | 13:16h | UTC

Changes in Hydroxyurea Use Among Youths Enrolled in Medicaid With Sickle Cell Anemia After 2014 Revision of Clinical Guidelines – JAMA Network Open

Original Guideline: National Heart, Lung, and Blood Institute. Evidence-based management of sickle cell disease: expert panel report, 2014

 

Commentary on Twitter

 


RCTs | Fitusiran prophylaxis reduces bleeding in people with hemophilia A or hemophilia B

3 Apr, 2023 | 13:44h | UTC

Efficacy and safety of fitusiran prophylaxis in people with haemophilia A or haemophilia B with inhibitors (ATLAS-INH): a multicentre, open-label, randomised phase 3 trial – The Lancet (link to abstract – $ for full-text)

Fitusiran prophylaxis in people with severe haemophilia A or haemophilia B without inhibitors (ATLAS-A/B): a multicentre, open-label, randomised, phase 3 trial – The Lancet Haematology (link to abstract – $ for full-text)

News Release: Monthly injections of fitusiran reduces bleeds in patients with haemophilia A and B – The Lancet

 


Position Paper | Prehospital hemorrhage control and treatment by clinicians

27 Mar, 2023 | 13:20h | UTC

Prehospital Hemorrhage Control and Treatment by Clinicians: A Joint Position Statement – Prehospital Emergency Care

 


Study shows increased bleeding complications in ESKD patients undergoing AF ablation

24 Mar, 2023 | 13:09h | UTC

Summary: The study analyzed 347 procedures in 307 patients with end-stage kidney disease (ESKD) undergoing atrial fibrillation (AF) catheter ablation in 12 referral centers in Japan.

Despite a vast majority of patients having subtherapeutic international normalized ratio (INR) values during the peri-procedural period, 35 patients (10%) experienced major complications, with the majority being major bleeding events (19 patients; 5.4%), including 11 cases of cardiac tamponade (3.2%). There were also two peri-procedural deaths (0.6%), both related to bleeding events. A pre-procedural INR value of 2.0 or higher was identified as the only independent predictor of major bleeding.

Current peri-procedural anticoagulation guidelines state that patients undergoing AF ablation should be under therapeutic anticoagulation throughout the peri-procedural period. The findings of this study suggest that these guidelines may not be appropriate for ESKD patients undergoing the procedure, and the role of peri-procedural anticoagulation in this population should be further investigated.

Article: Peri-procedural anticoagulation in patients with end-stage kidney disease undergoing atrial fibrillation ablation: results from the multicentre end-stage kidney disease–atrial fibrillation ablation registry – EP Europace

 

Commentary on Twitter

 


RCT | 4F-PCC fails to reduce blood product consumption and raises thromboembolic events in trauma patients

22 Mar, 2023 | 13:41h | UTC

Summary: The PROCOAG Randomized Clinical Trial aimed to investigate the efficacy and safety of 4-factor prothrombin complex concentrate (4F-PCC) in trauma patients at risk of massive transfusion. Conducted in 12 French trauma centers, this double-blind, randomized, placebo-controlled superiority trial involved 324 patients. All patients were treated according to European traumatic hemorrhage guidelines and received early ratio-based transfusion (packed red blood cells:fresh frozen plasma ratio of 1:1 to 2:1). The primary outcome measured was 24-hour blood product consumption (efficacy), while arterial or venous thromboembolic events were assessed as a secondary outcome (safety).

The trial revealed no significant difference in 24-hour blood product consumption between the 4F-PCC and placebo groups, with median consumption of 12 units and 11 units, respectively. However, the study identified a statistically significant higher risk of thromboembolic events in the 4F-PCC group, with 35% of patients experiencing at least one event compared to 24% in the placebo group.

In conclusion, the study found no beneficial effect of incorporating 4F-PCC into a ratio-based transfusion strategy for patients with severe trauma at risk of massive transfusion. Furthermore, the higher rate of thromboembolic events in the 4F-PCC group indicated potential harm. The findings do not support the routine use of 4F-PCC in patients experiencing trauma who are at risk for extensive transfusion.

Article: Efficacy and Safety of Early Administration of 4-Factor Prothrombin Complex Concentrate in Patients With Trauma at Risk of Massive Transfusion: The PROCOAG Randomized Clinical Trial – JAMA (free for a limited period)

See also: Visual Abstract

 


Review | Gene Therapy for Hemophilia — Opportunities and Risks

21 Mar, 2023 | 13:25h | UTC

Gene Therapy for Hemophilia—Opportunities and Risks – Deutsches Ärzteblatt International

 


ISCCM Consensus Statement | Prevention of venous thromboembolism in the critical care unit

13 Mar, 2023 | 14:53h | UTC

Indian Society of Critical Care Medicine Consensus Statement for Prevention of Venous Thromboembolism in the Critical Care Unit – Indian Journal of Critical Care Medicine

 


Minimum platelet count threshold before invasive procedures in cirrhosis: evolution of the guidelines

13 Mar, 2023 | 14:36h | UTC

Minimum platelet count threshold before invasive procedures in cirrhosis: Evolution of the guidelines – World Journal of Gastrointestinal Surgery

 


Single-arm study | Gene therapy with Etranacogene Dezaparvovec for Hemophilia B

9 Mar, 2023 | 14:07h | UTC

Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B – New England Journal of Medicine (link to abstract – $ for full-text)

Commentary: Gene Therapy Beneficial for Patients With Hemophilia B – HealthDay

 


Guideline | Management of severe peri-operative bleeding

8 Mar, 2023 | 14:18h | UTC

Management of severe peri-operative bleeding: Guidelines from the European Society of Anaesthesiology and Intensive Care – European Journal of Anaesthesiology

 


M-A | Oral iron supplementation and anemia in children according to schedule, duration, dose and cosupplementation

7 Mar, 2023 | 12:53h | UTC

Summary:

The article is a systematic review and meta-analysis of 129 randomized trials on iron supplementation and anemia in children. The study aimed to identify the optimal schedule, duration, dose, and cosupplementation regimen for iron supplementation in children and adolescents aged under 20 years.

The results showed that frequent (3-7 times/week) and intermittent (1-2 times/week) iron supplementation could be equally effective at increasing hemoglobin and decreasing anemia, iron deficiency, and iron deficiency anemia.

The study supports WHO recommendations regarding the frequency, duration, and dose of iron supplementation, including 3 months annually of daily oral iron supplementation for children aged 6 months to 12 years living in regions with a high burden of anemia. However, it also suggests that weekly iron supplementation might be considered an alternative to the recommended daily regimen in some contexts, given evidence of similar efficacy.

Article: Oral iron supplementation and anaemia in children according to schedule, duration, dose and cosupplementation: a systematic review and meta-analysis of 129 randomised trials – BMJ Global Health

 


Consensus Statement on the definition and classification of metabolic hyperferritinemia

3 Mar, 2023 | 13:58h | UTC

Consensus Statement on the definition and classification of metabolic hyperferritinaemia – Nature Reviews Endocrinology (if the link is paywalled, try this one)

 


Review | Practical guide for anticoagulant and antiplatelet reversal in clinical practice

3 Mar, 2023 | 13:42h | UTC

Practical Guide for Anticoagulant and Antiplatelet Reversal in Clinical Practice – Pharmacy

 


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