Vancomycin-resistant enterococci in acute myeloid leukemia and myelodysplastic syndrome patients undergoing induction chemotherapy with idarubicin and cytarabine

2017 ◽  
Vol 58 (11) ◽  
pp. 2565-2572 ◽  
Author(s):  
Ronald W. Heisel ◽  
Robert R. Sutton ◽  
Gerard P. Mascara ◽  
Daniel G. Winger ◽  
David R. Weber ◽  
...  
2020 ◽  
Vol 4 (4) ◽  
pp. 611-616
Author(s):  
Frances Linzee Mabrey ◽  
Kelda M. Gardner ◽  
Kathleen Shannon Dorcy ◽  
Andrea Perdue ◽  
Heather A. Smith ◽  
...  

Abstract To improve patient quality of life and reduce health care costs, many conditions formerly thought to require inpatient care are now treated in the outpatient setting. Outpatient induction chemotherapy for acute myeloid leukemia (AML) may confer similar benefits. This possibility prompted a pilot study to explore the safety and feasibility of intensive outpatient initial or salvage induction chemotherapy administration for adults with AML and high-risk myelodysplastic syndrome (MDS). Patients with no significant organ dysfunction and a treatment-related mortality (TRM) score corresponding to a day 28 mortality rate of <5% to 10% were eligible for study. Patients were treated as outpatients with daily evaluation by providers and only admitted to the hospital if mandated by complications. Twenty patients were consented, and 17 were treated. Eight patients received initial induction chemotherapy and 9 received salvage induction chemotherapy. Fourteen patients completed induction chemotherapy administration in the outpatient setting (82.4%; exact 95% confidence interval [CI], 55.8-95.3). Three patients were admitted during the course of chemotherapy administration, 2 for neutropenic fever and 1 for grade 3 mucositis. No patients died within 14 days of the initiation of induction chemotherapy (exact 95% CI, 0-22.9). Results of this pilot study suggest it is feasible to complete outpatient induction chemotherapy in select patients with AML and high-risk MDS. A team including nurses, social workers, medical providers, and pharmacists was key to the successful implementation of outpatient induction.


Cancer ◽  
2010 ◽  
Vol 117 (7) ◽  
pp. 1463-1469 ◽  
Author(s):  
Celeste Bello ◽  
Daohai Yu ◽  
Rami S. Komrokji ◽  
Weiwei Zhu ◽  
Gene A. Wetzstein ◽  
...  

2021 ◽  
Vol 1 (8) ◽  
Author(s):  
Reimbursement Team

CADTH recommends that Venclexta in combination with azacitidine should be reimbursed for the treatment of patients with newly diagnosed acute myeloid leukemia (AML) who are 75 years or older, or who have comorbidities that preclude use of intensive induction chemotherapy, only if certain conditions are met. Venclexta plus azacitidine should only be reimbursed if prescribed by clinicians who have expertise in managing patients with AML and are familiar with the toxicity profile of this regimen, and if the costs of Venclexta and azacitidine are reduced. Venclexta plus azacitidine should only be covered to treat adult patients who are considered ineligible for standard intensive induction chemotherapy and have not been treated with venetoclax or chemotherapy for myelodysplastic syndrome.


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