Successful management of the potentially fatal hyperhaemolysis syndrome of sickle cell anaemia with a regimen including bortezomib and Hemopure-Reference-Cited by-同舟云学术

Successful management of the potentially fatal hyperhaemolysis syndrome of sickle cell anaemia with a regimen including bortezomib and Hemopure

Published:2019-06-25 Issue:5 Volume:44 Page:815-818
ISSN:0269-4727
Container-title:Journal of Clinical Pharmacy and Therapeutics
language:en
Short-container-title:J Clin Pharm Ther

Author:

Epstein Stacy S.¹^ORCID,Hadley Terence J.¹

Affiliation:

1. Norton Cancer Institute, Norton HealthCare Louisville Kentucky

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcpt.12998

Reference14 articles.

1. Pathological basis of symptoms and crises in sickle cell disorder: implications for counseling and psychotherapy;Oluwatoyin OI;Hematology reports,2010

2. Challenges of alloimmunization in patients with haemoglobinopathies

3. Hyperhemolysis syndrome in sickle cell disease

4. Hyperhaemolysis in sickle cell disease — an unusual and potentially life‐threatening complication

5. Hyperhemolysis in Patients With Hemoglobinopathies: A Single-Center Experience and Review of the Literature

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3. “Don’t Add Fuel to the Fire”– Hyperhemolysis Syndrome in a Pregnant Woman with Compound Sickle Cell Disease/β0-Thalassemia: Case Report and Review of the Literature;Acta Haematologica;2023-10-13

4. Epidemiological and clinical features, therapeutic strategies and outcomes in patients with hyperhaemolysis: A systematic review;British Journal of Haematology;2023-04-19

5. Use of cell salvage and HBOC-201 in a pregnant Jehovah’s Witness with sickle beta+thalassaemia undergoing emergency caesarean section;BMJ Case Reports;2022-11