Table 1.

Clinical activities of the hematology unit before and during the COVID-19 pandemic

ServicesBaseline, nWeek 1 (24 Feb)Week 2 (2 Mar)Week 3 (9 Mar)Week 4 (16 Mar)Week 5 (23 Mar)Week 6 (30 Mar)
Total services 743.8 672 (−10) 686 (−8) 738 (−1) 712 (−4) 634 (−15) 599 (−19) 
Outpatients visits 446.2 312 (−30) 317 (−29) 256 (−43) 208 (−53) 181 (−59) 193 (−57) 
Day-hospital care accesses 288.6 239 (−17) 270 (−6) 276 (−4) 236 (−18) 198 (−31) 201 (−30) 
Transfusions* 70.3 60 (−15) 55 (−22) 63 (−10) 54 (−23) 53 (−25) 49 (−30) 
Therapies 136.6 102 (−25) 174 (+27) 157 (+15) 123 (−10) 107 (−22) 102 (−25) 
Bone marrow 32.6 23 (−29) 22 (−32) 25 (−23) 25 (−23) 15 (−54) 15 (−54) 
Other§ 40.3 54 (+34) 19 (−53) 31 (−23) 34 (−16) 23 (−43) 35 (−13) 
New admissions to hematology ward 5 (0) 4 (−20) 8 (+60) 6 (+20) 6 (+20) 6 (+20) 
New admissions to transplant ward 3 (−25) 5 (+25) 2 (−50) 3 (−25) 2 (−50) 4 (0) 
ServicesBaseline, nWeek 1 (24 Feb)Week 2 (2 Mar)Week 3 (9 Mar)Week 4 (16 Mar)Week 5 (23 Mar)Week 6 (30 Mar)
Total services 743.8 672 (−10) 686 (−8) 738 (−1) 712 (−4) 634 (−15) 599 (−19) 
Outpatients visits 446.2 312 (−30) 317 (−29) 256 (−43) 208 (−53) 181 (−59) 193 (−57) 
Day-hospital care accesses 288.6 239 (−17) 270 (−6) 276 (−4) 236 (−18) 198 (−31) 201 (−30) 
Transfusions* 70.3 60 (−15) 55 (−22) 63 (−10) 54 (−23) 53 (−25) 49 (−30) 
Therapies 136.6 102 (−25) 174 (+27) 157 (+15) 123 (−10) 107 (−22) 102 (−25) 
Bone marrow 32.6 23 (−29) 22 (−32) 25 (−23) 25 (−23) 15 (−54) 15 (−54) 
Other§ 40.3 54 (+34) 19 (−53) 31 (−23) 34 (−16) 23 (−43) 35 (−13) 
New admissions to hematology ward 5 (0) 4 (−20) 8 (+60) 6 (+20) 6 (+20) 6 (+20) 
New admissions to transplant ward 3 (−25) 5 (+25) 2 (−50) 3 (−25) 2 (−50) 4 (0) 

Unless otherwise noted, all data are n (percentage change from baseline). The mean for the 3 weeks preceding the COVID-19 pandemic was used as the baseline value.

*

Transfusions are intended as the number of patients receiving transfusions.

Therapies performed included the following drugs or schemes: adriamycin, bleomycin, vinblastine, and dacarbazine (ABVD), bendamustine, gemcitabine, and vinorelbine (BEGEV), cyclophosphamide, doxorubicine, etoposide, vincristine, and prednisolone (CHEOP), rituximab, cyclophosphamide, doxorubicine, vincristine, and prednisolone (R-CHOP), rituximab, cyclophosphamide, lyposomial doxorubicine, vincristine, and prednisolone (R-COMP), gemcitabine, oxalyplatinum, and prednisolone (GDP), carfilzomib, lenalidomide, dexamethazone (KRD), rituximab, bendamustine, blinatumomab, bortezomib, brentuximab, daratumumab, decitabine, azacitidine, obinutuzumab, cyclophosphamide, elotuzumab, and arsenic trioxide (TRISENOX), and eculizumab. The following therapies were deferred: 3 chemoimmunotherapy cycles for indolent NHL, 17 biologic drugs (4 bortezomib, 12 carfilzomib, 1 daratumumab) for MM and amyloidosis, and 2 hypomethylating agents (azacitidine) for high-risk myelodysplastic syndrome (MDS). Lenalidomide maintenance was interrupted in 5 MM patients, all in long-term remission.

Reasons for bone marrow deferral were routine follow-up of AL (n = 2) and myeloproliferative neoplasms (n = 4), staging of indolent NHL (n = 5), evaluation of monoclonal gammopathy of undetermined significance (n = 3), and reevaluation of immune thrombocytopenia, aplastic anemia, and low-risk MDS (n = 1 each).

§

Other procedures included IV hydration, phlebotomy, IV immunoglobulin, albumin infusions, lumbar punctures, and venetoclax ramp-up.

Two allogeneic nonurgent transplants for cutaneous NHL were postponed (1 because of the inability to receive the donor’s stem cells from Australia, and 1 because of the temporary unavailability of ICU support). However, 4 allogeneic transplants for acute myeloid leukemia (3 haploidentical and 1 matched unrelated donor) and 5 autologous transplants for MM were performed during the study period.

Close Modal

or Create an Account

Close Modal
Close Modal