key: cord-0885759-0ar3r299 authors: Sahi, Puneet Kaur; Chandra, Jagdish title: Pediatric Hemato-Oncology Care Amid the COVID-19 Pandemic date: 2021-01-09 journal: Indian J Pediatr DOI: 10.1007/s12098-020-03577-5 sha: 02a9e76c3239139279502d406d9133f1db6e6cb0 doc_id: 885759 cord_uid: 0ar3r299 nan The Coronavirus disease (COVID-19) pandemic has created a parallel world of neglected non-COVID patients, especially, children with cancer and chronic blood disorders with several barriers to continuing care. Challenges to Continuing Care 1. Hospital resource (e.g., hospital staff, hospital beds, ventilators, blood components) re-allocation to manage COVID-19 infection has severely curbed services to pediatric hematology-oncology patients. Several tertiarycare hospitals have been designated as exclusive COVID-19 treatment centres without any suitable alternative centres being allotted for pediatric hematooncology patients [1, 2] . 2. Interrupted drug supply chains have resulted from travel restrictions and shutting of several pharmacies in highrisk areas. 3. Blood component shortage has resulted from reduced voluntary blood donations due to restricted travel and fear of getting exposed to COVID-19 during hospital visit. Transmission of SARS-CoV-2 via blood product transfusion is controversial. Despite insufficient data, certain International organizations advise deferral of blood donation for 28 d after symptom resolution in a COVID-19 positive case and for 21 d after exposure to a confirmed case of COVID-19 [3] . 4. Fear of contracting COVID-19 during hospital visits may reduce access of healthcare by patients during 'seemingly stable' clinical condition. Restricted travel may result in treatment default by outstation patients receiving treatment from pediatric hematooncology centres concentrated in major cities in India. 6. Financial crisis may cause significant treatment defaults in low-income groups due to redirection of limited money to provision of basic necessities (food/clothing/house rent) and inability to afford private local treatment. functioning may impact fund-raising and organizing care in LMICs. 8. Un-lockdown would bring challenges of increased COVID-19 cross-infection rates in patients and doctors, sudden cumulative surge of newly diagnosed hematooncology patients (likely in more advanced stages of disease), pending chemo-radiotherapy and surgery patients, and complicated cases (tumor relapses, treatment failures). COVID-19 testing strategy and quarantine prior to intense therapy especially for outstation patients will need attention. Apart from the universal infection prevention practices such as screening of patients and caregivers, isolation of patients, ensuring 'social distancing' and use of masks, the following measures may help: [4] [5] [6] [7] i) Tele-consultation as substitute for follow-up visits for stable patients ii) Patient tracking for those lost to follow-up by dedicated hospital staff and treatment advise per feasibility iii) Courier methods to deliver oral chemotherapy for home administration. iv) Follow-up visits in person should be limited, drugs should be dispensed in buffer amounts to cover for delays in scheduled visit Conversion of our centre at the pandemic-onset, to an exclusive COVID-19 care hospital, entailed coordinated transfer of hemato-oncology patients to other hospitals. Listing of all patients with stage and phase of treatment, stratification on the basis of urgency of treatment continuation and feasibility of transfer to other nearby government/private hospitals was worked upon. Networking was done with all pediatric hemato-oncologists in Delhi, and with involvement from the NGO's, the patient transfer was implemented. Outstation patients were additionally tagged with local healthcare facilities. Throughout, treatment from other centres, regular tele-consultation was ensured between the primary and transfer-center hemato-oncologists as well as the patient. Transport, residence and medical finances were supported by NGOs. In return, a large number of COVID-19 positive hematooncology patients were treated at our centre. 3. Dissemination of hospital policy using social media platforms, email, personal communication to update patients of available services and working days, avoiding unnecessary visits [4] . 4. Blood donations/transfusion may be continued as follows: Facilitation of blood transfusion at nearby healthcare facility ii) Mobile unit services for facilitating blood donation at doorstep iii) Special social media drives to encourage blood donations iv) Special travel passes for donors, issued by e-mail or WhatsApp to facilitate travel to the blood banks v) Advertise safety of blood collection areas The following principles may be applied with local modifications: 1. Diagnostic investigations and response evaluation may be adapted to available resources. For example: If sincere attempts to get baseline flow cytometry/ molecular genetics in an acute leukemia child significantly delays treatment, initiation of therapy may be based on morphology. If possible, standard protocols for diagnosis and treatment of cancer patients "unmodified" should be continued. If resource constraints mandate treatment modification, a whole-service approach over individual clinical decision-making should be preferred [5] . This should be done after discussion with the family explaining proposed modifications/ alternatives and possible consequences. Documentation should be done on the case records with a revised consent. 2. A triage system may be used to tailor treatment per patient disease, stage, phase of treatment and prognosis [6] . For example: very-low-risk patients (cancer survivors) may be advised to stay home and tele-consult regularly, low-risk patients (receiving less intense chemotherapy like acute lymphoblastic leukemia maintenance, Hodgkin lymphoma, etc.) may be given chemotherapy at a nearby hospital and monitored with necessary investigations via teleconsultation. Intermediate-risk patients (those requiring surgery/radiation/stem-cell transplant) may be given an additional chemotherapy cycle awaiting the deferred procedure. High-risk patients (like induction/ consolidation of acute leukemia, Non-Hodgkin lymphoma) should be given chemotherapy via in-house admission/day-care facility [6] . 3. Measures like drug-dose reductions, delay of intensive chemotherapy regimens, increased duration between cycles and conversion to oral agents may be adopted to reduce patient visits [5, 7] . Following disease-specific modifications may be made [7] : a). Acute lymphoblastic leukemia (ALL) i) Deferral of Intrathecal chemotherapy during maintenance ii) Capizzi interim maintenance instead of high dose methotrexate therapy iii) Pegylated L-asparaginase instead of Escherichia coli-asparaginase b). Acute myeloid leukemia (AML): Consolidation chemotherapy instead of BMT in high-risk disease iii) Reduction of intensive cycle cytarabine dose from 18 to 12 g/m 2 c). Non-Hodgkin lymphoma: Less myelosuppressive regimen (Ex: MCP842 for non-CNS disease) d). Solid tumors: Oral metronomic therapy (palliative intent) for advanced stage ii) Dose compressed three weekly chemotherapy cycles for Ewings sarcoma iii) Use of non-high dose methotrexate protocols in osteosarcoma iv) Switch from ifosfamide to cyclophosphamide for rhabdomyosaroma reducing inpatient admission by 24 h v) Use of prophylactic pegylated G-CSF Consider surgical delays if tumor is benign/low grade [5] . 5. Consider disease-specific modified radiotherapy protocols to minimize treatment duration and complications [8] , like hypofractionation of radiotherapy for brain tumors 6. Enlist cases with treatment modification and review on priority on return of normal service capacity. 7. Febrile neutropenia -Administer antimicrobials near place of patients stay and consider early switch to oral antimicrobials to reduce hospital visits. Avoid throat examination and aerosol generating procedures. 8. Undertake interdepartmental teleconsultation to help shared decision-making without in-person meetings With phased un-lockdown, catching-up on delayed diagnosis and acute treatment may become priority, and treatment modifications and deferrals may be needed in fewer cases. The above-mentioned triage system may be modified to resume treatment for both highrisk and intermediate-risk patients while deferred highrisk transplants, essential surgeries and radiotherapy sessions may be resumed. Blood Disorder Specific Measures [9] 1. Monitor thalassaemia patients with crucial tests like hemogram and serum ferritin as usual 2. Emphasize extra-caution in thalassemia children with comorbidities such as good glycemic control in patients with secondary diabetes 3. Postpone annual routine monitoring tests like Ferriscan in stable patients 4. Continue low-dose hydroxyurea in sickle cell children as it prevents stroke, acute chest syndrome and vasoocclusive crisis in under-transfused SCD [9] 5. Defer stem-cell transplantation 6. Ensure up-to-date vaccinations COVID-19 in children is milder with lower mortality and predominance of gastrointestinal and respiratory manifestations. Limited data show SARS-CoV-2 infection is mild in children with cancer and chronic blood disorders except when associated with co-morbidities (splenectomized, iron overload, etc.) [9] [10] [11] . In SCD, COVID-19 infection may act as a trigger for acute chest syndrome [9] . Testing Policy for COVID-19 in pediatric hematooncology patients is the same as that for the general population [10, 12] , although certain centers may prefer a cautionary test prior to invasive procedures. Chemotherapy/radiotherapy/surgery may be deferred for symptomatic COVID-19 positive patients [13] . For COVID-19 positive asymptomatic patients, chemotherapy may be continued in the intensive phases (e.g., induction of ALL) but may be withheld in less intense phase of chemotherapy (like maintenance of ALL) [13, 14] . Hydroxychloroquine prophylaxis has been used in asymptomatic COVID-19 positive patients [14] . Azithromycin has been used in patients with mild respiratory disease. Broad-spectrum antibiotics and anti-viral drugs like remdesevir have been used in COVID-19 positive moderately to severely symptomatic lymphopenic patients [13, 14] . Stringent monitoring for disease progression and check on drug contraindications, interactions and side-effects are required. For symptomatic COVID-19 positive thalassemics, deferiprone (side effectslymphopenia and agranulocytosis) may be withheld [15] . During an acute febrile episode, chelation should be stopped until detailed patient evaluation [15] . No changes in transfusion thresholds have been advised. All-in-all, strategies for care of pediatric hemato-oncology patients need to be adapted locally in line with available resources, updated researches and the dynamic nature of the pandemic. 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