Tolerability of Daratumumab Amongst Asian Patients with Plasma Cell Dyscrasias - A Single Centre Experience [0.03%]
daratumumab治疗亚洲浆细胞异常患者的耐受性：一项单中心研究
Allison C Y Tso,Samuel S Y Wang,Christian A Gallardo et al.
Allison C Y Tso et al.
Daratumumab is increasingly incorporated into the standard treatment regimens for patients with plasma cell dyscrasias in Asia, especially with cost-containment measures implemented by various regional health authorities. This analysis aime...
Celebrating five years of "Hematology without Borders" by the International Academy for Clinical Hematology (IACH) [0.03%]
国际临床血液学研究院(IACH)庆祝"无界血液学"五周年纪念日
Mohamad Mohty,Arnon Nagler,Bipin Savani
Mohamad Mohty
A Retrospective Review of Secondary Hemophagocytic Lymphohistiocytosis (HLH) and Dengue-associated HLH from a Teaching Hospital in Singapore [0.03%]
新加坡教学医院继发性噬血细胞性淋巴组织细胞增生症(HLH)和登革热相关HLH病例的回顾性研究
Allison C Y Tso,Sanchalika Acharyya,Sing Zern Fong et al.
Allison C Y Tso et al.
Real-world data on the outcome of Asian patients with secondary hemophagocytic lymphohistiocytosis (HLH), especially on dengue-associated HLH, are limited to small case series. This is a retrospective records review of adult patients with s...
Sinus bradycardia as a rare adverse event in patients receiving cyclosporine A after allogeneic hematopoietic stem cell transplantation [0.03%]
allo-HSCT后接受环孢素A治疗患者出现窦性心动过缓的一项罕见不良反应
Magdalena Karasek,Maciej Majcherek,Bartłomiej Kuszczak et al.
Magdalena Karasek et al.
Cyclosporine A (CSA) is a commonly used immunosuppressive agent for the prophylaxis of graft-versus-host disease following allogeneic hematopoietic stem cell transplantation (alloHSCT). While tachycardia is a known adverse effect of CSA, br...
Mohamad Mohty,Kenneth C Anderson
Mohamad Mohty
Walking ability in adults with severe hemophilia: A cross-sectional study [0.03%]
重度甲型血友病成人患者步行能力的横断面研究
Malika Jhandai,Dimple Choudhry,Sudhir Kumar Atri et al.
Malika Jhandai et al.
A lack of factor VIII (FVIII) or factor IX (FIX) results in hemophilia, a blood-clotting illness. The mode of inheritance is chromosome X-linked and recessive. The primary symptom of severe hemophilia is spontaneous and recurrent bleeding i...
Wolfgang P Rennert,Jenna Smith M,Katie A Cormier et al.
Wolfgang P Rennert et al.
Supportive care needs for hematopoietic stem cell recipients have been studied. Less is known about the care needs of stem cell donors. Care challenges arise at donor selection, preparation for the donation, the donation procedure and the i...
The Role of Vertebral Augmentation Procedures in the Management of Multiple Myeloma [0.03%]
多发性骨髓瘤治疗中椎体成型术的作用
Nishanth Thalambedu,Mudassar Kamran,Samer Al-Hadidi
Nishanth Thalambedu
Approximately 90% of patients with multiple myeloma experience significant pain from osseous involvement during their lifetime. Untreated osseous involvement results in vertebral compression fractures, leading to negative consequences for q...
Early de-escalation of antibiotic therapy in hospitalized cellular therapy adult patients with febrile neutropenia [0.03%]
有关发热性中性粒细胞减少成人细胞治疗住院患者抗生素降阶梯治疗的时机探索研究
Mariana Lucena,Kelly J Gaffney,Theresa Urban et al.
Mariana Lucena et al.
Febrile neutropenia (FN) is an oncologic emergency frequently encountered in hematopoietic cell transplant (HCT) and chimeric antigen receptor (CAR) T-cell therapy patients, which requires immediate initiation of broad-spectrum antibiotics....
Incidence and Risk of Secondary Malignancy in Patients with Waldenström Macroglobulinemia: A Population-Based Analysis [0.03%]
华氏巨球蛋白血病继发恶性肿瘤的发病及风险分析：基于人口的队列研究
Mohammad Ebad Ur Rehman,Maha Hameed,Zunairah Shah et al.
Mohammad Ebad Ur Rehman et al.
Waldenström macroglobulinemia (WM) is a rare lymphoplasmacytic lymphoma which may predispose individuals to development of secondary malignancies (SMs). The Surveillance, Epidemiology, and End Results (SEER) database is a comprehensive reg...