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1.
J Oncol Pharm Pract ; 28(8): 1722-1730, 2022 Dec.
Article in English | MEDLINE | ID: mdl-34558367

ABSTRACT

BACKGROUND: Delivery of antineoplastic regimens in the pediatric setting is facilitated by a paper roadmap. Paper roadmaps are the key safety tool required for safe ordering. Electronic medical record systems offer technological solutions for ordering antineoplastic regimens, however, do not offer a solution that integrates paper roadmaps digitally. METHODS: A multidisciplinary project team implemented real-time clinician scanning of paper roadmaps into the electronic medical record. RESULTS: The rate of missing roadmaps decreased from an average of 1.6 to 0.8 per week. Pharmacists gained 3 h of productivity daily. Providers spend an average of 35-45 s and a total of seven clicks each time a roadmap is scanned. Overall, the clinical systems analyst spent less than 1 h of total build time. CONCLUSION: Implementing roadmap scanning decreased the rate of missing roadmaps, increased pharmacist productivity, and required a nominal amount of analyst and provider time. In addition, this solution allows for concurrent viewing of the roadmap files from any connected computer, facilitating an easier co-signature process for providers, pharmacists, and nurses. PRACTICE IMPLICATIONS: These results suggest that implementing real-time scanning of roadmaps can improve oncology care efficiency while maintaining the same safety rigor that paper roadmaps offer.


Subject(s)
Antineoplastic Agents , Neoplasms , Humans , Child , Electronic Health Records , Medical Oncology , Pharmacists , Neoplasms/drug therapy , Antineoplastic Agents/therapeutic use
2.
J Pediatr Hematol Oncol ; 43(7): e972-e974, 2021 10 01.
Article in English | MEDLINE | ID: mdl-33235157

ABSTRACT

COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is responsible for a global pandemic that can cause severe infections in children, especially those with comorbid conditions. Here, we report a case of a child with a newly diagnosed medulloblastoma, Fanconi Anemia, and SARS-CoV-2 infection. Through multidisciplinary care coordination and meticulous planning, we were able to safely initiate this patient's oncology care and implement a long-term model to address the patient's care. This approach could be replicated with any newly diagnosed pediatric patient that requires monitoring for signs of COVID-19 with concurrent oncology care.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , COVID-19/complications , Fanconi Anemia/drug therapy , Medulloblastoma/drug therapy , SARS-CoV-2/isolation & purification , COVID-19/transmission , COVID-19/virology , Child, Preschool , Fanconi Anemia/diagnosis , Fanconi Anemia/virology , Female , Humans , Medulloblastoma/diagnosis , Medulloblastoma/virology , Prognosis
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