Abstract:연구의 필요성2010년) administration in either the inpatient (N = 70) or outpatient setting (N = 70) from January to July 2012 were included. In the outpatient setting, HD-MTX was administered intravenously (IV) over 6 hours and included hydration with sodium bicarbonate (2000 ml/m 2 / for 12 hours). Daily visits to the outpatient setting followed. Leucovorin was given 24 hours after MTX at a standard dose (15 mg/m 2 IV bolus) every 6 hours. We compared the serum drug levels of MTX, hematologic and renal toxicity, hep… Show more
“…Current evidence is informative on the safety of ambulatory supportive care for HD MTX and its financial benefits. The transition to ambulatory care for HD MTX and supportive care is safe and effective (Choi et al, 2014;Holdsworth et al, 1997;Lange et al, 1988;Lashlee & O'Hanlon Curry, 2007;Lippert et al, 2017;Mahadeo et al, 2010;Newton & Ingram, 2014;Sive et al, 2012;Zelcer et al, 2008). Mahadeo et al (2010) identified that of the 97 ambulatory HD MTX administrations 99% were successfully completed outpatient; zero had elevated MTX levels at 24 hours, 26% experienced typical neutropenia, 4% experienced thrombocytopenia, and 1% experienced leukopenia.…”
The Children’s Oncology Group recommends children with high-risk acute lymphoblastic leukemia (ALL) receive high-dose methotrexate (HD MTX) throughout treatment. Historically, patients have been hospitalized for at least 54 hours for HD MTX. Literature supports the safety and efficacy of the transition of supportive care interventions of intravenous (IV) fluids and leucovorin to ambulatory care. The goal of this quality improvement (QI) project was to implement a system to support the safe delivery of supportive care in the home after inpatient HD MTX in children with high-risk ALL. An interdisciplinary team implemented system changes including an ambulatory supportive care protocol, standard computerized order sets, family education, and education of staff in the inpatient, outpatient, and home care setting. Measurements included laboratory results of renal function and medication clearance, length of hospitalization, and family-reported quality of life. During project implementation, 10 patients completed a total of 38 cycles. The system safely and effectively supported transition to the outpatient setting for all patients. Average length of stay was decreased by 37.8 hours per HD MTX cycle. Families reported that quality of life improved in most domains with family time and sleep having largest improvement, while level of stress remained the same. Ambulatory monitoring post-HD MTX requires a multidisciplinary approach to meet individualized patient needs. Future QI efforts should consider outpatient administration of HD MTX in addition to supportive care as a means to improved quality of life.
“…Current evidence is informative on the safety of ambulatory supportive care for HD MTX and its financial benefits. The transition to ambulatory care for HD MTX and supportive care is safe and effective (Choi et al, 2014;Holdsworth et al, 1997;Lange et al, 1988;Lashlee & O'Hanlon Curry, 2007;Lippert et al, 2017;Mahadeo et al, 2010;Newton & Ingram, 2014;Sive et al, 2012;Zelcer et al, 2008). Mahadeo et al (2010) identified that of the 97 ambulatory HD MTX administrations 99% were successfully completed outpatient; zero had elevated MTX levels at 24 hours, 26% experienced typical neutropenia, 4% experienced thrombocytopenia, and 1% experienced leukopenia.…”
The Children’s Oncology Group recommends children with high-risk acute lymphoblastic leukemia (ALL) receive high-dose methotrexate (HD MTX) throughout treatment. Historically, patients have been hospitalized for at least 54 hours for HD MTX. Literature supports the safety and efficacy of the transition of supportive care interventions of intravenous (IV) fluids and leucovorin to ambulatory care. The goal of this quality improvement (QI) project was to implement a system to support the safe delivery of supportive care in the home after inpatient HD MTX in children with high-risk ALL. An interdisciplinary team implemented system changes including an ambulatory supportive care protocol, standard computerized order sets, family education, and education of staff in the inpatient, outpatient, and home care setting. Measurements included laboratory results of renal function and medication clearance, length of hospitalization, and family-reported quality of life. During project implementation, 10 patients completed a total of 38 cycles. The system safely and effectively supported transition to the outpatient setting for all patients. Average length of stay was decreased by 37.8 hours per HD MTX cycle. Families reported that quality of life improved in most domains with family time and sleep having largest improvement, while level of stress remained the same. Ambulatory monitoring post-HD MTX requires a multidisciplinary approach to meet individualized patient needs. Future QI efforts should consider outpatient administration of HD MTX in addition to supportive care as a means to improved quality of life.
“…( 42 ) In extreme situations and with close monitoring, administration of high dose methotrexate on outpatient basis has also been found safe. ( 43 ) An individualized decision to continue subsequent cyclophosphamide, cytarabine or etoposide on outpatient basis can be made if patients are expected to comply with instructions on neutropenic care and regular follow up. ( 44 ) As ALL is curable disease in many age groups, it is recommended that priority be given to minimizing treatment delays.…”
The Coronavirus disease-2019 (COVID-19) pandemic is an unprecedented health care crisis and has led to over 1.5 million deaths worldwide. The risk of severe COVID-19 and mortality is markedly raised in patients with cancer, prompting several collaborative groups to issue guidelines to mitigate the risk of infection by delaying or de-escalating immunosuppressive therapy. However, delayed therapy is often not feasible for patients requiring treatment for acute leukemia or stem cell transplantation. We provide a focused review of the recommendations and evidence for managing this high-risk group of patients while minimizing the risk of COVID-19 infection, and provide a small snapshot of treatment data from our center.
“…8 This outpatient protocol presents the results of a quality improvement project conducted to analyze the methods used in our hospital to provide urinary alkalinization and hematological rescue to patients with NHL undergoing treatment with HDMTX. 11,12 In this study, the aim is to analyze the feasibility of an oral alkalinization and leucovorin rescue regimen that ensures the safety of outpatient treatment with HDMTX for CNS prophylaxis in NHL patients.…”
Background We describe the feasibility and safety of an oral administration schedule of hydration, alkalinization and leucovorin rescue with an ambulatory high-dose methotrexate regimen. Methods Single-centre prospective observational study conducted within a tertiary hospital where all patients have received systemic high-dose methotrexate (3.5 g/m2). Patients were instructed to keep an adequate ambulatory oral hydration and alkalinization to monitor urine pH and to adjust bicarbonate according to our institution's treatment protocol. High-dose methotrexate was infused over 4 h. Urine pH was checked before high-dose methotrexate administration, and for any value less than 7 a sodium bicarbonate bolus was given. Leucovorin at a standard dose was begun 24 h after high-dose methotrexate. methotrexate serum concentrations were monitored daily from 24 h after administration until clearance (level ≤ 0.1 µmol/L). Results From January 2016 to June 2018, 49 ambulatory high-dose methotrexate courses were given to 18 patients. No dose reduction was required afterwards. All patients completed succesfully the planned three doses in an outpatient basis, except four patients, one of them due to pneumonitis. Previous to methotrexate infusion, urinary pH > 7 was achieved in 35 (79.5%) cycles. Methotrexate clearance was achieved by 72 h in 35 courses (71.4%), and by 96 h in 100%. Neutropenia/trombocytopenia grades III/IV were observed in four cycles (8.16%) and two (4.08%) cycles, respectively. Around 20.40% were associated with stomatitis, 14.20% vomiting, 10.20% asthenia, 8.16% diarrhea and 6.12% with renal toxicity. Conclusions Ambulatory administration of high-dose methotrexate as CNS prophylaxis is safe and feasible following the described approach, allowing us to optimize healthcare resources.
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