Post-Chemotherapy Titer Status and Need for Revaccination After Treatment for Childhood Cancer

2020 ◽  
Vol 59 (6) ◽  
pp. 606-613
Author(s):  
Lindy Zhang ◽  
Clifton P. Thornton ◽  
Kathy Ruble ◽  
Stacy L. Cooper

Objectives. To evaluate the strategy of checking vaccine titers after completion of chemotherapy. Study Design. Retrospective review of pediatric oncology patients who completed chemotherapy. Demographics, post-chemotherapy titers, and absolute lymphocyte counts (ALCs) were analyzed. Results. Ninety patients met inclusion criteria, and 87% of patients had at least one titer checked. Comparing patients <7 years and those ≥7 years at diagnosis, there was no difference in incidence of negative titers except mumps; those <7 years old were more likely to have negative titers (58% vs 20%, P = .003). Comparing those <13 years old to ≥13 years old, there was no difference in negative titers except mumps (45% vs 19%, P = .02) and tetanus (44% vs 0%, P = .002). No patient maintained all protective titers after completion of chemotherapy. Time to ALC recovery was not predictive of positive titers. Conclusion. Checking titers after chemotherapy is not recommended. Providers should assume loss of immunity.

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. e21030-e21030
Author(s):  
Vicky Rowena Breakey ◽  
Dena Zeraatkar ◽  
Burke Baird ◽  
Brian Timmons

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 4037-4037
Author(s):  
Henna Butt ◽  
Natalie Davis ◽  
Regina A. Macatangay

Abstract Background: Once diagnosis of malignancy is made in pediatric patients, it can be important to initiate therapy to prevent delay in benefits derived from treatment. In certain diagnoses, prompt initiation of chemotherapy can help reduce complications such as hyperleukocytosis, mass effect from solid tumors, and spread of malignancy. These patients require provision of central vascular access in order to begin treatment. In children's hospitals patients often receive central venous catheters in the operating room under general anesthesia. However, this requires scheduling for the operating room, availability of pediatric surgeons, appropriate anesthesia consent and examination ahead of time for safety of proceeding. The benefit of having a pediatric vascular access team (PVAT) is that these providers are flexible with their availability, the time required to place the lines is often less and it eliminates the need for general anesthesia as well as the cost of the operating room. The aim of this study was to compare vascular access provision by a designated pediatric vascular access team with surgical placement of central venous access in pediatric oncology patients. Methods: This was an IRB-approved retrospective medical record review of subjects diagnosed with an oncologic malignancy with inclusion criteria: ages 0-21 years of age, treatment for pediatric malignancy at the University of Maryland Children's Hospital between 1/1/2017-12/31/2019. We performed bivariate analyses comparing variables between patients who had line placement by PVAT vs surgical placement. Analyses was performed using SAS 9.4. Results: We identified 69 patients who met inclusion criteria with 39% (n=27) having undergone line placement by PVAT. Surgical placement occurred for 55% (n=38), with interventional radiology (IR) or other placement making up the remainder 6% of patients (n=4). The mean age was noted to be younger in the surgical group (8.6 +/- 6 years) in comparison to the PVAT group (13+/-6.3 years), p=0.0061. The mean time from consult to line placement was 10 (+/-9) hours in the PVAT group vs 76 (+/-56) hours in the surgery group (p&lt;0.0001). There was a statistically significant difference in procedure duration, with PVAT placement requiring less time (27+/-12 minutes) vs surgical placement (48+/-19 minutes), p=0.0005. There were no statistically significant differences among groups in race, sex, time-to-initiation of treatment after line placement, or complications. There was a small difference in mean number of attempts, with surgical requiring 1 (+/-0) vs. PVAT 1.2 (+/-0.4) attempts. Compared to complications of surgical line placement, the complications experienced by our PVAT team were largely related to need for revision of line placement, although not frequent enough to be statistically significant. Conclusion: Data show that having a PVAT for central line insertions demonstrates good safety profiles, successful insertion and low complication rates. PVAT has also increased the efficiency of vascular access at large academic institutions. The presence of vascular access teams allows for initiation of therapy in a timely fashion and allows central line placement under anesthesia to occur at a safer time. At our institution, having a PVAT in house has allowed for more efficient line placements, shorter time to provision of access and transition to placement of surgical lines when more stable. This allows for not only patients to receive care faster, but also to have lines placed in shorter times while optimizing patient safety. Schultz TR, Durning S, Niewinski M, Frey AM. A multidisciplinary approach to vascular access in children. J Spec Pediatr Nurs. 2006;11(4):254-256. doi:10.1111/j.1744-6155.2006.00078. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 2682-2682 ◽  
Author(s):  
Nicole Giamanco ◽  
Anne B. Warwick ◽  
Gary Crouch

Abstract Background. Intensive therapy for childhood cancer is possible in large part due to improvements in supportive care that are currently available. Blood product transfusions, including red blood cell transfusions, are supportive care measures which are important in the tolerability of this therapy, and are frequently used in the majority of patients receiving therapy for childhood cancer. Although it is well recognized that frequent red blood cell transfusions in pediatric hematological disorders, such as sickle cell disease and thalassemia major, lead to iron overload and its complications (ie, organ dysfunction), pediatric oncology patients receiving numerous red blood cell transfusions are not routinely screened or evaluated for risk of iron overload or its consequences. This study was done to identify pediatric oncology patients with iron overload in a general pediatric hematology/oncology clinic. Methods. A retrospective blood bank records review was performed of pediatric hematology/oncology patients treated in our clinic in the last 10 years (2003-2013) to identify those patients receiving >10 packed red blood cell (PRBC) transfusions. These patients’ medical records were reviewed to determine which patients had been assessed for iron overload with a serum ferritin level. If a serum ferritin was obtained and the result was >1000 ug/L, records were reviewed to determine if patients received therapy for iron overload. Results. For the time period 2003-2013, blood bank records were screened on 144 patients. Fifty patients (34.7%) were identified as receiving >10 PRBC transfusions. Of these patients, 22 (44%; M/F = 12/10; age range = 2-23 y/o) were patients who had received therapy or were on active therapy for childhood cancer; 14 with leukemia (5 AML, 9 ALL), 8 with solid tumors (5 sarcomas, 1 hepatoblastoma, 1 lymphoma). Of these 22 patients, 6 (27%) patients had a serum ferritin level that was obtained and the remaining 16 (73%) had not. All the patients (100%) with a serum ferritin result had a serum ferritin level >1000 ug/L (range 1048-22021). Only one patient (off-therapy sarcoma patient, serum ferritin =1788 ug/L) was on therapy for iron overload (Exjade and phlebotomy). Conclusions. Pediatric oncology patients receiving numerous PRBC transfusions are at risk for iron overload. Routine risk screening and assessment for iron overload should be accomplished in all pediatric oncology patients as part of their off therapy follow-up management. For those identified as having iron overload, appropriate therapy should be considered as indicated. Disclosures No relevant conflicts of interest to declare.


2006 ◽  
Author(s):  
Kristina K. Hardy ◽  
Melanie J. Bonner ◽  
Katherine C. Hutchinson ◽  
Victoria W. Willard

2007 ◽  
Author(s):  
Stephen R. Lassen ◽  
Brent Collett ◽  
Stan Whitsett ◽  
Debra Friedman

2007 ◽  
Vol 83 (7) ◽  
pp. 54-63 ◽  
Author(s):  
Ana Verena Almeida Mendes ◽  
Roberto Sapolnik ◽  
Núbia Mendonça

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