Red Blood Cell (RBC) Survival Following Transfusion in Infants

Neonatal Anemia Clinical Trial

Official title:

Red Blood Cell Survival Following Transfusion in Infants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00731588
• Other study ID #: 200710747
• Secondary ID: 2P01HL046925
• Status: Completed
• Phase: Phase 2
• Start date: June 2008
• Est. completion date: March 2, 2018

Study information

• Verified date: August 2021
• Source: University of Iowa
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

OUR OVERALL HYPOTHESIS is that post-transfusion survival of allogeneic and autologous RBCs can be accurately quantified in anemic human infants using biotin-labeled RBCs combined with mathematical modeling that adjusts for confounding factors commonly encountered in neonates. These confounding factors include 1) dilution of labeled RBC as a result of growth stimulated erythropoiesis, anemia stimulated erythropoiesis, and blood transfusion; 2) loss of labeled RBC due to laboratory phlebotomy; and 3) variable RBC life spans resulting from RBCs having been produced at different developmental periods and under varying rates of erythropoiesis. In contrast to infants, adjustment for these factors is not necessary in healthy adults under conditions of steady state erythropoiesis. Instead in adults, RBC survival is typified by a linear decline in concentration of labeled RBCs over time. When this line is extrapolated to zero concentration, the intercept with the time axis represents the mean potential lifespan (MPL) of RBCs. (<7 d) and stored (>21 d) allogeneic adult RBCs transfused in the same infant.

Description:

Phase I: Includes only Aim #1 from Thrasher Foundation Grant in which adult subjects will be studied.

SPECIFIC AIM #1 (Thrasher Foundation Grant): To develop in vitro and validate in vivo in adult humans and anemic infants the capability of biotinylating RBCs at up to 5 discrete densities for simultaneously determining RBC kinetics of multiple, distinct RBC populations. This requires expansion of the RBC biotin labeling technology we have previously developed. After refinement, the method will be applied in the subsequent aims conducted in anemic infants receiving clinically ordered RBC transfusions.

As suggested by our previous RBC survival studies, we anticipate that the heaviest biotin labeling will alter the intrinsic RBC structural properties of RBCs, shortening their long term survival. The in vitro and in vivo validation studies we propose in adults are necessary because the conditions for reproducibly obtaining discrete RBC biotin densities at appropriate, closely spaced intervals have not been conclusively worked out, nor have we determined empirically which of the five densities will not artifactually shorten long-term RBC survival. We can use the lighter densities for RBC survival measurements and the heavier densities for the simultaneous RBC volume measurements needed to account for RBC volume increases caused by growth. It is important to perform these feasibility studies in both adults and infants because of the vastly different physiologic states, ie, normal, healthy adults are in steady state erythropoiesis while critically ill, anemic infants experience multiple clinical circumstances which perturb RBC survival, eg, growth, phlebotomy, intervening transfusion, etc.

In addition to the biotin labeling of RBC method, the "differential agglutination, antigenic method" using flow cytometry will be applied for infants receiving allogeneic RBC transfusions. The results of the two methods will be compared with one another. The differential agglutination method utilizes differences in the RBC surface antigens between the donor and the recipient for determining short- and long-term RBC survival. Genotyping results of adult donor and the infant recipient RBC antigens (performed at the Mississippi Valley Regional Blood Center) permits identification of minor blood group differences between donor and recipient RBCs so that appropriately labeled minor RBC antibodies (available commercially and used by blood banks for minor blood group RBC typing) can be used in flow cytometric determination of RBC survival. RBC survival determined for each of the biotin labels and for the RBC antigenic differences will all be compared among one other. The differential agglutination/antigen method will considered the "gold standard" as the RBCs are labeled ex-vivo, AFTER the RBC transfusion, thus without modifying the RBC membrane surface proteins as biotinylation does. Our hypothesis is that the addition of too much biotin can lead to artifactually shortened in vivo RBC survival, but that lower doses of biotin to not. By also including the differential agglutination/antigen method RBC survival results, we will be able to better validate our multi-density biotin hypothesis.

Our overall objective in this research is to improve red blood cell (RBC) transfusion practices for anemic, critically ill infants. This project has received support from two granting agencies: 1) The Thrasher Foundation, entitled, "Red Blood Cell Recovery and Survival Following Transfusion in Infants;" and 2) NIH PPG Grant P01 HL046925, Project 1 entitled, "Red Blood Cell Survival Following Transfusion In Infants." Abstracts for both are included below. This project will be completed in two phases:

Phase I includes studies of autologous biotinylated RBCs transfused into normal, health adult human volunteers (see Specific Aim #1 in Thrasher Foundation Abstract below); and

Phase II includes studies of infants requiring physician order red blood cell transfusions (see Specific Aims #2, #3, and #4 in Thrasher Foundation Abstract below; and see Specific Aim #4 in NIH which is included in its entirety in the three Thrasher Grant specific aims).

The Phase I studies are completed and we are no longer enrolling adults. We are enrolling infants for Phase II studies. We are adding these phases sequentially based on the recommendation of Martha Jones at the time our proposal was first submitted to the IRB. We have applied the knowledge we have gained from the Phase I studies in adult subject volunteers to make modifications of our study design for Phase II to be performed in infant study subjects receiving clinically ordered RBC transfusions. At the end of Phase II, justification for including a new, comparison "gold standard" method for determining RBC survival in infants (the "differential agglutination, antigenic method") is included. We have completed enrollment of all adult subjects for phase I.

ABSTRACT I (FOR THRASHER FOUNDATION GRANT)

Background:

Anemic, critically ill newborn infants are among the most frequently transfused groups of patients in the US. An estimated 130,000 infants annually receive approximately 1,000,000 RBC transfusions. Unlike adults, important data are lacking regarding the transfusion product for optimal RBC survival in infants. Contributing to this lack are two major recent changes in neonatal blood banking and transfusion practices. These are 1) the use of transfused adult donor blood stored for up to the 42 day FDA limit instead of only using blood stored for less than 7 days as had been done previously; and 2) potential use of the infant's own blood harvested from the placenta to avoid the risks of viral infections and immune transfusion reactions from donor blood. Unfortunately, there are no definitive infant studies that address these changes by directly measuring RBC survival. Such infant studies have been hampered by technical problems. Specifically, RBC survival data must be adjusted for growth, laboratory phlebotomy loss, and intervening additional RBC transfusions but in practice have not. Moreover, safety issues have precluded many infant RBC survival studies (eg, exposure to 51Cr radioactivity and removal of too much blood from today's tiny, premature infants). Indeed, prior to 1970 (the end of using 51Cr as a RBC label in infant RBC survival studies), infants weighing less than 1,500 g at birth did not often survive, and RBC survival data do not exist for today's smallest, most frequently transfused infants whose birth weights are 500-1,000 g.

Specific Aims:

Specific Aim #1: To develop in vitro and validate in vivo in adults the capability for biotinylating RBCs at up to 5 discrete densities that are measurable by flow cytometry. These five RBC biotin density labels will be used in Specific Aims #2, 3, and 4 to simultaneously determine RBC survival of multiple, distinct populations of transfused RBCs in premature infants.

Specific Aim #2. To determine whether RBC survival of donor and placental RBCs are significantly longer when adjusted by mathematical modeling. We anticipate that the unmodeled values substantially underestimate RBC survival.

Specific Aim #3. To compare long-term RBC survival results for transfused adult donor and fetal/placental RBCs in anemic newborn infants. We anticipate that more rapid growth in fetuses will result in greater stress erythropoiesis leading to intrinsic RBC "defects" and shortened RBC survival compared to adult donor RBCs.

Specific Aim #4. To quantify the effects of storage on model adjusted RBC survival of adult donor RBCs transfused into newborn infants. We anticipate that storage of donor RBCs will not alter RBC survival.

Study Design:

The studies proposed here build on biotinylation and mathematical modeling methods that our research group has developed for accurately measuring RBC survival without exposing the infant to radioactivity. The biotin RBC labeling method is well suited to newborn infants because it permits the simultaneous tracking of multiple RBC populations on <10 µL blood. Survival of RBCs labeled at multiple biotin densities will be quantified using the standard RBC survival parameters, ie, post-transfusion short-term 24 h RBC recovery and long-term modeled RBC survival, ie, until 50 and 100% of biotin-labeled RBCs have disappeared from the circulation. The latter two measurements will be calculated using the required mathematical adjustments for growth, laboratory phlebotomy loss, and intervening RBC transfusions.

Only Specific Aim #4 in the Thrasher Foundation Abstract involves human infant study subjects. Specific Aim #4) USE THE RBC BIOTINYLATION AND MATHEMATICAL MODELING METHODOLOGIES VALIDATED IN ADULT SHEEP AND NEWBORN LAMBS TO ACCURATELY MEASURE POST-TRANSFUSION RBC KINETICS IN ANEMIC NEWBORN INFANTS TRANSFUSED WITH FRESH AUTOLOGOUS, FRESH ALLOGENEIC AND STORED ALLOGENEIC RBCS. The use of biotin, a non-toxic, non-radioactive B vitamin, to distinguish among different RBC populations simultaneously by flow cytometry is critical for accomplishing our aims and holds clear advantages over other RBC labeling methods in both safety and accuracy. In utilizing the four Specific Aims to achieve our goal of establishing more effective transfusion practices by identifying the optimal RBC transfusion product for use in anemic INFANTS.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 140
• Est. completion date: March 2, 2018
• Est. primary completion date: March 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 6 Months

Eligibility

Adult Study:

Inclusion Criteria:

• Males or post-menopausal females

• 18-65 years of age.

• Weight >110 lbs.

• Healthy- the subject feels well and can perform normal activities.

• Hemoglobin at or above 12.5 g/dL or hematocrit at or above 38%.

• Note: Members of the research team that are not supervised or under the employee of the PI may participate in the study.

Exclusion Criteria:

• Presence of chronic illness unless the subject is being treated and the condition is under control.

• Consumption of biotin supplements or raw eggs.

• Premenopausal women.

• Blood donation in the previous 8 weeks (single donation) or 16 weeks (double red cell donation).

• Blood loss in the previous 8 weeks due to epistaxis, gastrointestinal blood loss, trauma, significant diagnostic phlebotomy loss (i.e., > 30 mL total), or other significant bleeding

• Treatment with antibiotics within the last 7 days. Antibiotics for prevention of an infection or treatment of acne are not exclusion criteria.

• Note: If study subjects experience any of these conditions associated with blood loss or donate any blood products, they will not be included in the primary analysis but will be replaced.

Infant Study:

MOTHERS FOR PLACENTAL BLOOD COLLECTION AND MOTHERS OF INFANT STUDY SUBJECTS

Inclusion Criteria:

1. >/= 24 weeks gestation

2. mothers who deliver through the birth canal or by c-section can be included in the study.

Exclusion Criteria:

1. Pregnant with fetus with major congenital anomaly.

2. Clinically suspected or documented maternal chorioamnionitis (This only applies to infant study subjects receiving autologous RBCs from the placenta).

3. Viral or bacterial infection (e.g. HIV, Hepatitis B, Hepatitis C, Primary Herpes, Tuberculosis) based on clinically available prenatal or postnatal test results in the mother's medical record. (This only applies to infant study subjects receiving autologous RBCs from the placenta.)

4. minor mothers (<18 years old) are excluded from the study.

INFANT STUDY SUBJECTS

Inclusion Criteria:

Newborns >/=24 weeks gestation who are patients in the Neonatal Intensive Care Unit (NICU) at UIHC that:

1) Are being treated with the expectation of survival.

Exclusion Criteria:

1. Difference of more than 5% in the percentage of HbF cells (measured by flow cytometry in the Widness lab) between blood harvested from the placenta and that from discarded neonatal blood in the first day of life and before the first neonatal blood transfusion. This is done to exclude the rare possibility of transfusing newborns with blood that is contaminated with a significant proportion of their mother's blood if a maternal-to-placenta bleed occurs after umbilical cord clamping is done. (This only applies to infant study subjects receiving autologous RBCs from the placenta.)

2. Need of emergent blood transfusion as determined by the subject's medical care team.

3. Hematological diseases (except for anemia associated with phlebotomy loss and prematurity)

4. Alloimmune hemolytic anemia, diffuse intravascular coagulation, and thrombosis.

5. Major congenital anomaly.

6. Sepsis with positive blood or spinal fluid culture.

7. Receiving treatment with erythropoietin (r-HuEPO) or cardiorespiratory bypass support (ECMO).

8. Overt clinical bleeding.

Related Conditions & MeSH terms

• Anemia, Neonatal
• Neonatal Anemia

Intervention

Biological:
• Transfused Biotin RBCs - Adults Phase I
A 3 mL venous blood sample is obtained. 250 mL of blood will be drawn to a blood collection bag containing the anticoagulant CPD. Separate equal volumes of RBCs are labeled with up to five different densities of biotin. The biotinylated RBCs are resuspended in autologous plasma to achieve a 60 to 70% hematocrit. An IV is inserted for the reinfusion of the biotinylated RBCs. Three mL aliquots of blood are sampled at 5, 10, 20, and 60 minutes after infusion. The subject returns ~24 hours and 3 days after the RBC infusion to obtain a 3 mL venous blood sample. Subjects return for weekly 3 mL blood sampling.
• Transfused Biotin RBCs - Infants Phase II
After the infant's clinical care team decides that a RBC transfusion is needed, a 15mL/kilogram of body weight is ordered. Transfusion will be given in 2 parts: 1) approximately 80% of the total transfusion to be transfused over 3-4 hours and 2) approximately 20% of the total transfusion will be marked with biotin to be transfused upon completion of the first part. The bedside nurse maintains constant observation of the infant as appropriate for the infant's condition, assessing for signs and symptoms of a transfusion reaction.
• Transfused Biotin RBCs - Infants Phase III
Phase III (infants) to be determined upon completion of Phase II (infants).

Locations

Country	Name	City	State
United States	University of Iowa	Iowa City	Iowa
United States	University of Iowa Hospitals and Clinics	Iowa City	Iowa

Sponsors (4)

Lead Sponsor	Collaborator
John A Widness	National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Thrasher Research Fund

Country where clinical trial is conducted

United States, 

References & Publications (9)

Mock DM, Lankford GL, Matthews NI, Burmeister LF, Kahn D, Widness JA, Strauss RG. Accelerated removal of antibody-coated red blood cells from the circulation is accurately tracked by a biotin label. Transfusion. 2012 May;52(5):1097-105. doi: 10.1111/j.153 — View Citation

Mock DM, Matthews NI, Strauss RG, Burmeister LF, Schmidt R, Widness JA. Red blood cell volume can be independently determined in vitro using sheep and human red blood cells labeled at different densities of biotin. Transfusion. 2009 Jun;49(6):1178-85. doi — View Citation

Mock DM, Matthews NI, Zhu S, Burmeister LF, Zimmerman MB, Strauss RG, Schmidt RL, Nalbant D, Cress GA, Widness JA. Red blood cell (RBC) volume can be independently determined in vivo in humans using RBCs labeled at different densities of biotin. Transfusi — View Citation

Mock DM, Matthews NI, Zhu S, Strauss RG, Schmidt RL, Nalbant D, Cress GA, Widness JA. Red blood cell (RBC) survival determined in humans using RBCs labeled at multiple biotin densities. Transfusion. 2011 May;51(5):1047-57. doi: 10.1111/j.1537-2995.2010.02 — View Citation

Mock DM, Widness JA, Strauss RG, Franco RS. Posttransfusion red blood cell (RBC) survival determined using biotin-labeled RBCs has distinct advantages over labeling with (51) Cr. Transfusion. 2012 Jul;52(7):1596-8. doi: 10.1111/j.1537-2995.2012.03588.x. — View Citation

Nalbant D, Bhandary P, Matthews NI, Schmidt RL, Bogusiewicz A, Cress GA, Zimmerman MB, Strauss RG, Mock DM, Widness JA. Comparison of multiple red cell volume methods performed concurrently in premature infants following allogeneic transfusion. Pediatr Re — View Citation

Schmidt RL, Mock DM, Franco RS, Cohen RM, North AK, Cancelas JA, Geisen C, Strauss RG, Vlaar AP, Nalbant D, Widness JA. Antibodies to biotinylated red blood cells in adults and infants: improved detection, partial characterization, and dependence on red b — View Citation

Widness JA, Kuruvilla DJ, Mock DM, Matthews NI, Nalbant D, Cress GA, Schmidt RL, Strauss RG, Zimmerman MB, Veng-Pedersen P. Autologous Infant and Allogeneic Adult Red Cells Demonstrate Similar Concurrent Post-Transfusion Survival in Very Low Birth Weight — View Citation

Widness JA, Nalbant D, Matthews NI, Strauss RG, Schmidt RL, Cress GA, Zimmerman MB, Mock DM. Tracking donor RBC survival in premature infants: agreement of multiple populations of biotin-labeled RBCs with Kidd antigen-mismatched RBCs. Pediatr Res. 2013 De — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Discrete Biotinylated RBC Densities (up to 5 Discrete Densities) That Can be Accurately Measured by Flow Cytometry, i.e., Without Overlap.	The biotin-labeled RBCs that were studied were: 2, 6, 18, 54, and 162 µg NHS-biotinylating reagent per mL of packed RBCs. Here we report the number of discrete biotin densities without overlap as determined in vitro.	from day of blood draw this can be accomplished in 4 hours
Primary	RBC Survival (Life Span) in Days of Multiple, Distinct BioRBC Density Populations of Transfused Autologous RBCs in Adults and Premature Infants.	Using flow cytometry was measured for each RBC biotin density in days as determined when RBC measurement was no longer detectable.	for up to 5 months
Primary	RBC Survival (Life Span) in Days of Multiple, Distinct BioRBC Density Populations of Transfused Allogeneic RBCs in Premature Infants.	Using flow cytometry was measured for each RBC biotin density in days as determined when RBC measurement was no longer detectable.	for up to 4 months
Secondary	Number of Participants With Positive Antibody Screen in Response to Biotin-labeled RBCs.	IgG gel card agglutination test that was developed in our laboratory	4 to 5 mo post transfusion of biotin RBCs
Secondary	Survival of Allogeneic RBCs in Days as Measured by the Antigenic Method Using Flow Cytometry for Comparison With BioRBC in Premature Infants		4 months