|Year : 2020 | Volume
| Issue : 1 | Page : 74-78
|Patient blood management in a patient with multiple red cell antibodies (anti-C, anti-e, and anti-K) undergoing liver transplant in South India: A team approach
Deepti Sachan1, Aseem K Tiwari2, Ravi Dara3, Dinesh Jothimani4, Ilankumaran Kaliamoorthy4, Srinivas Mettu Reddy4, Mohamed Rela4
1 Department of Transfusion Medicine, Gleneagles Global Health City, Chennai, Tamil Nadu, India
2 Department of Transfusion Medicine, Medanta – The Medicity, Gurgaon, Haryana, India
3 Department of Transfusion Medicine, Manipal Hospitals, Jaipur, Rajasthan, India
4 Institute of Liver Disease and Transplantation, Gleneagles Global Health City, Chennai, Tamil Nadu, India
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|Date of Submission||24-Apr-2018|
|Date of Acceptance||03-Mar-2019|
|Date of Web Publication||24-Jul-2020|
| Abstract|| |
End-stage liver disease (ESLD) patients undergoing liver transplant (LT) surgery are often multiply alloimmunized and pose significant challenges to the transfusion services in terms of red cell cross-match incompatibility, unpredictable blood requirements, and often lead to significant delays in availing compatible red cell units. We report a case of a 64-year-old female from Bahrain, a known case of hepatitis C-related ESLD referred for LT surgery. She had a history of multiple uneventful transfusions in the preceding year. Her blood group was A-positive, direct antiglobulin test, and cold antibodies were negative. Indirect antiglobulin test was positive, and antibody identification confirmed the presence of anti-C, anti-e, and anti-K. Her red cell phenotype was R2R2and Kell negative (C-c+E+e-K-). The patient was started on erythropoietin. Requests for R2R2and Kell negative units were sent to various blood banks across the country. After >800 A/O group units phenotyping and a waiting period of 6 weeks, two compatible R2R2phenotypes and Kell negative could be arranged in-house and three units were received from Gurgaon, North India. Intraoperative management included blood preservation techniques including cell salvage, antifibrinolytic drug, and monitoring using thromboelastography. The estimated blood loss was 350 ml with pre- and postoperative Hb 10.4 gm% and 9.2 gm%, respectively. She received intraoperatively two units of single-donor platelet and four units of fresh frozen plasma and postoperatively one unit of leukocyte-depleted-packed red cells and doing well at 12-month follow-up. This case highlights the importance of advance immunohematology for timely detection of alloimmunization and providing antigen-negative compatible units, proper communication between the transfusion specialists, and the clinical team for proper patient blood management as well as the need for central rare donor registry program to avoid delays in providing compatible blood in such inevitable cases.
Keywords: Alloimmunization, liver transplant, R2R2, rare donor registry, rare group
|How to cite this article:|
Sachan D, Tiwari AK, Dara R, Jothimani D, Kaliamoorthy I, Reddy SM, Rela M. Patient blood management in a patient with multiple red cell antibodies (anti-C, anti-e, and anti-K) undergoing liver transplant in South India: A team approach. Asian J Transfus Sci 2020;14:74-8
|How to cite this URL:|
Sachan D, Tiwari AK, Dara R, Jothimani D, Kaliamoorthy I, Reddy SM, Rela M. Patient blood management in a patient with multiple red cell antibodies (anti-C, anti-e, and anti-K) undergoing liver transplant in South India: A team approach. Asian J Transfus Sci [serial online] 2020 [cited 2020 Aug 7];14:74-8. Available from: http://www.ajts.org/text.asp?2020/14/1/74/290643
| Introduction|| |
Liver transplantation has provided a favorable change to the outcome of patients with end-stage liver disease (ESLD). These patients are often multiply transfused, alloimmunized, and need proper and timely immunohematological workup to avoid any immune hemolysis-related morbidity and mortality.
Transfusion requirements have been reduced significantly in the past few decades; still, the transfusion therapy for liver transplant (LT) patients remains a challenge in patient with multiple red cell antibodies. We present a case of multiple alloimmunized female patient and her blood management during live-related donor LT (LDLT) surgery.
| Case Report|| |
A 64-year-old female from Bahrain, a case of hepatitis C-related ESLD, Child-B cirrhosis. She had a history of multiple episodes of gastrointestinal bleed, encephalopathy, and ascites for the past 12 months requiring frequent interventions in the form of large-volume therapeutic paracentesis. She also had a history of multiple uneventful transfusions and the last transfusion was received from the first-degree relatives around 1-year back. She was referred to our hospital for LDLT. On admission, patient's hemoglobin was 7.5 g/dl, hematocrit – 25%, total leukocyte count – 2230/cmm, platelet – 34,400/cmm, T. bilirubin – 1.06 g/dL, direct bilirubin – 0.12 g/dL, T protein – 6.8 g/dL, albumin – 2.6 g/dL, PT – 16.5 s, and INR – 1.36.
Blood group was A Rh (D) positive. Direct antiglobulin test was negative. Indirect antiglobulin test was performed using commercially available three cell panel (ID Diacell, Biorad) which showed positive agglutination in P1 (3+), P2 (0), and P3 (3+). Antibody identification was performed using 11 cell panels (ID-Diapanel, Biorad) which were suggestive of anti-C, anti-e, and anti-K antibodies. Cold Antibodies were not detected. Extended antigen phenotyping of patient was done using Biorad Rh + K phenotype cards, and the patient was found to be R2R2(C-c+E+e-K-) phenotype. Antibody titer was performed using conventional tube method and using select cells and was anti-e: 1:32, anti-e + C: 1:1024, and anti-e + K: 1:128. On cross-matching, all the units showed incompatibility. The liver team was informed and the search for A or O group, C negative, e negative, K negative, and Rh(D) positive or negative units was initiated. The patient's relatives and children, ten in number who had come to India, were also screened. They were all “A positive,” were incompatible with the patient.
Random cross-matching and Rh and Kell phenotyping was initiated in all blood units in our inventory. The segments of blood units were collected from other neighboring blood banks for Rh and Kell phenotyping and cross-matching. Samples were also sent to another hospital Medanta – The Medicity, Gurgaon, and the National Institute of Immunohematology, Mumbai, for confirmation of antibody and requests for compatible units. We also contacted various centers in India for rare donor registry or availability of R2R2 and Kell (K)-negative units. More than 500 units among our inventory and other blood banks in the city, only two units could be identified with same phenotype and were compatible.
Meanwhile, the patient was put on erythropoietin and iron therapy to increase the preoperative hemoglobin level. The patient received erythropoietin 4000 units twice weekly for 6 weeks. Folic acid, iron sulfate, and multivitamins were also administered. The hematocrit at the beginning of the treatment was 25%. The hematocrit raised to 28% and 33% after 4 weeks and 8 weeks of treatment respectively.
Three O Rh(D)-positive units with R2R2 and Kell-negative phenotype were received from the Department of Transfusion Medicine, Medanta – The Medicity, Gurgaon, North India, (two from their rare-donor registry, one unit from random screening of >300 units in their inventory). The units were collected and transported maintaining cold chain. The transplant was done successfully. The liver graft was obtained from live-donor with blood group “A positive” individual with C+e+K− phenotype.
Before the surgery, the baseline hemoglobin was 10.4 g/dL, platelet count – 44,000/cmm, and INR-1.46. Intraoperative monitoring was done using thromboelastography. Cell saver was also used to salvage the intraoperative blood that was shed. Single-adult dose of tranexamic acid was also administered. Approximate blood loss during the surgery is 350 ml. Two units of single-donor platelet (SDP) and three units of fresh frozen plasma were transfused intraoperatively. No leukocyte-depleted-packed red cells (LDPRC) transfusion was given intraoperatively.
At the end of the procedure, the hematocrit was 9.2 and the patient had no intraoperative complications. During the postoperative period, she had a drop in her hemoglobin and received one unit of LDPRCs and one unit SDP uneventfully. [Figure 1] shows hospital course of patient with change in hemoglobin and platelet count and blood transfusions. The intensive care unit and hospital stay were 5 and 16 days, respectively. At discharge, the liver function tests were normal and she is doing well at 12-month follow-up.
|Figure 1: Hospital course of patient waiting for transplant with the trend of hemoglobin and platelet count|
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| Discussion|| |
The present case highlights many important aspects of patient blood management in a multiply alloimmunized patient undergoing LT surgery in India. The case is an excellent example of team approach between transplant surgeons, hepatologist, anesthesiologists, and transfusion specialists across various blood banks in city as well as across the country.
From a transfusion specialist point of view, preoperative immuno-hematological workup is critical involving identifying clinically significant alloantibodies, availing antigen-negative compatible blood, and meeting demands of major surgeries such as liver transplantation.
Red cell alloimmunization can lead to several problems varying from delay in getting compatible blood to hemolytic transfusion reactions. The frequency of red cell alloantibodies varies considerably depending on numerous factors, for example, demographics, previous transfusions, pregnancy, genetic constitution, immune status, disease factors, time and frequency of screening, and sensitivity of methodology. UK single-center survey had reported 6.8% clinically significant red cell antibodies in adults undergoing liver transplantation and the most commonly reported alloantibodies in alloimmunized patients are alloantibodies against Rh and Kell antigens. Luzo et al. have shown a high incidence of 23% in Sao Paulo, due to ethnic heterogeneity. Studies have also reported the negative influence of the history of red cell antibodies on patient survival after LT highlighting the importance of appropriate patient blood management for alloimmunized patients.
To arrange multiple antigen negative or rare blood group units, there is a need to develop a centralized rare donor database involving voluntary donor organizations as well as reference laboratories and organize the information about rare donors in India. In the era of medical tourism, the centralized donor database will help patients in communities throughout the country and in some cases around the world. In the present case study, two units were sourced from a local registry of around 300 donors maintained by a hospital in Gurgaon. It is desirable to have a national level registry for wider access and shorter turnaround time (TAT). Since we depended largely (three out of five) on typing of units in inventory and to small extent (two out of five) on a local registry, our TAT to arrange the compatible units were over 50 days. Readily accessible large national database could have shortened this TAT, considerably.
Screening of all donors, however, is not often performed due to limiting resources such as antisera, staff, and costs. Some facilities identify rare blood type donors by performing mass antigen screening. At present, there are many studies from India which has shown red cell minor antigen profiles of blood donors and have shown Rh and Kell antigen frequencies as shown in [Table 1].,,,,,,,,,
|Table 1: Indian studies showing Rh and Kell prevalence in the Indian donor population|
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However, no much data are available regarding any active registry and follow-up of the typed donors. Knowledge of red cell antigen phenotype frequencies in a population is definitely the first step in understanding the ethnic distribution, in creating a donor data bank for the preparation of indigenous cell panels, and providing antigen-negative compatible blood to patients with multiple alloantibodies. Most transfusion centers rely on random cross-matching and searching in existing inventories; rather than accessing rare donors' registry. Before searching the antigen-negative compatible units, the prevalence of compatible donors should be determined. To calculate the prevalence, the prevalence of donors who are negative for one antigen should be multiplied with the prevalence of donors who are negative for other antigens. For example, if the prevalence of C antigen 85%, e antigen 98%, and Kell Antigen 2%. The prevalence of compatible donors (C negative, e negative and Kell negative, A positive) as in our case would be 0.15 (C-) X 0.02 (e-) X0.98 (K-) = 0.002 or 2 in 1000 donors.
Other strategies include screening of family members, intraoperative blood salvage, and collection and freezing of autologous blood units when the patient's condition permits.
Preoperative red cell augmentation with erythropoietin, intraoperative cell saver, and postoperative blood conservation through judicious control of laboratory testing should be planned. The use of erythropoietin before surgery allowed us to raise the total red cell mass in our patient. The feasibility of using intraoperative hemodilution and intraoperative red blood cell (RBC) salvage, as well as ways of minimizing hemostatic derangements intraoperatively must be discussed and planned ahead of time. For the transfusion service, this might require reserving additional units of platelets, plasma, and cryoprecipitate for the transplant. Intraoperative blood salvage can also be of benefit in transplant cases with difficult RBC antibodies.
The risk of alloimmunization can be minimized by routine typing the donors and patients for clinically significant antigens. The proactive use of Rh- and K-typed units may prevent some of these patients from being immunized. This extended matching would be an ultimate solution, although the associated logistics and cost will raise the serious concern, especially in resource-limited countries such as India. Due to the different distribution of blood groups in patient and general populations, managing inventory in the face of extended cross-matching further poses serious challenges.
To minimize the risk of hemolysis, alloimmunized patients are often managed with antigen-negative PRBC units for the first 5–10 units when the antibody is still present. They may be switched to antigen-unscreened units during massive blood loss when there is hemodilution of antibody/ies, and switched back to antigen-negative units for the last 5–10 units transfused when transfusion returns to small volumes and transfused cells are expected to remain in the circulation. In patients with multiple antibodies, for whom sufficient quantities of antigen-negative blood cannot be found, consideration is given first to avoid antibodies that fix complement with the potential to cause intravascular hemolysis., However, the time to switch back to the use of compatible blood is not always clearly delineated, potentially putting the patient at risk for a delayed hemolytic transfusion reaction, and increased postoperative morbidity.
Most unusual alloantibodies are predicted to cause shortened red cell survival, but transfusion of incompatible blood may or may not result in clinical or laboratory signs of hemolytic transfusion reaction. A balance is required between pretransfusion estimation of clinical significance and search for expensive and rare phenotype blood for patients with alloantibodies to high-incidence antigens or multiple antigens. In India, RBC survival studies or cellular assays (e.g., the monocyte monolayer assay and chemiluminescence test) are not widely developed which can aid in the decision to transfuse RBCs incompatible with antibodies to high-incidence antigens.
Still, situations like this can lead us in a near but not impossible situation where we are forced to think about the need of centralized (and not just local) registry of donors with rare antigen profile.
The transfusion medicine has advanced significantly in the past few years preventing many hemolytic reactions by timely antibody screening and providing antigen-negative and compatible units. Complete screening of alloantibodies combined with rational blood transfusion policy is mandatory to prevent RBC alloimmunization among LT candidates. We recommend the transfusion of Rh and Kell antigen-matched blood to patients with high transfusion requirements in the future and enforce the need to have a national donor registry for rare blood groups.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
The authors express thanks to all staff in the Department of Transfusion Medicine, Gleneagles Global Health City, Medanta – The Medicity, Gurgaon, the National Institute of Immunohematology, and various Chennai blood banks for their greatest cooperation and technical assistance for finding rare units among inventory.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Mushkbar M, Watkins E, Doughty H. A UK single-centre survey of red cell antibodies in adult patients undergoing liver transplantation. Vox Sang 2013;105:341-5.
Luzo AC, Pereira FB, de Oliveira RC, Azevedo PR, Cunha RD, Leonardi MI, et al.
Red blood cell antigen alloimmunization in liver transplant recipients. Transplant Proc 2010;42:494-5.
Boyd SD, Stenard F, Lee DK, Goodnough LT, Esquivel CO, Fontaine MJ. Alloimmunization to red blood cell antigens affects clinical outcomes in liver transplant patients. Liver Transpl 2007;13:1654-61.
Basu D, Datta SS, Montemayor C, Bhattacharya P, Mukherjee K, Flegel WA. ABO, rhesus, and kell antigens, alleles, and haplotypes in West Bengal, India. Transfus Med Hemother 2018;45:62-6.
Pachaury R, Arya DR, Mahawar NL, Bharti A, Das PK. Frequency of Rh Phenotypes in voluntary blood donors. J Med Sci Clin Res 2017;5:25083-8.
Gundrajukuppam DK, Vijaya SB, Rajendran A, Sarella JD. Prevalence of principal Rh blood group antigens in blood donors at the blood bank of a tertiary care hospital in Southern India. J Clin Diagn Res 2016;10:EC07-10.
Garg N, Singh DK, Tomar R, Singh B. Phenotype prevalence of blood group systems (ABO, Rh, Kell) in voluntary, healthy donors-experience of a tertiary care hospital in Delhi, North India. J Blood Disord Transfus 2015;6:297.
Kahar MA, Patel RD. Phenotype frequencies of blood group systems (Rh, Kell, Kidd, Duffy, MNS, P, Lewis, and Lutheran) in blood donors of South Gujarat, India. Asian J Transfus Sci 2014;8:51-5.
] [Full text]
Lamba DS, Kaur R, Basu S. Clinically significant minor blood group antigens amongst North Indian donor population. Adv Hematol 2013;2013:215454.
Makroo RN, Bhatia A, Gupta R, Phillip J. Prevalence of Rh, Duffy, Kell, Kidd and MNSs blood group antigens in the Indian blood donor population. Indian J Med Res 2013;137:521-6.
] [Full text]
Sharma DC, Singhal S, Rai S, Iyenger S, Sao S, Jain B. Incidence of Rh antigens, phenotype and probable genotype in the population of Gwalior and Chambal region, central India. Int Blood Res Rev 2013;1:29-43.
Agarwal N, Thapliyal RM, Chatterjee K. Blood group phenotype frequencies in blood donors from a tertiary care hospital in North India. Blood Res 2013;48:51-4.
Thakral B, Saluja K, Sharma RR, Marwaha N. Phenotype frequencies of blood group systems (Rh, Kell, Kidd, Duffy, MNS, P, Lewis, and Lutheran) in North Indian blood donors. Transfus Apher Sci 2010;43:17-22.
Dzik WH, Jenkins R. Use of intraoperative blood salvage during orthotopic liver transplantation. Arch Surg 1985;120:946-8.
Ramsey G, Cornell FW, Hahn LF, Fonzi F, Starzl TE. Incompatible blood transfusions in liver transplant patients with significant red cell alloantibodies. Transplant Proc 1989;21:3531.
Thompson JC, Shulman IA, Nelson JM, Okamoto M, Strautz R. Lifesaving incompatible blood transfusion. Lab Med1987;18:385.
Dr. Deepti Sachan
Department of Transfusion Medicine, Gleneagles Global Health City, #439, Cheran Nagar, Perumbakkam, Chennai, Tamil Nadu
Source of Support: None, Conflict of Interest: None
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