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DOI: 10.1055/a-2388-3298
Predeposit Autologous Blood Donation in Rh(D)-Negative Pregnant Women: A Single-Center Study
Abstract
Objective The primary purpose of this study was to assess the practicability of predeposit autologous blood donation (PABD) in the practice of Rh(D)-negative pregnant women.
Materials and Methods A cohort of 405 Rh(D)-negative pregnant women who had a delivery in the comprehensive tertiary hospital in Nanjing was analyzed retrospectively, over 10 years.
Results After PABD, 203 women experienced a slight drop in mean hemoglobin of 5.32 ± 0.5 g/L (PABD-associated anemia was not featured in our study). Thirteen women who received allogeneic blood might benefit from PABD practically.
Conclusion PABD is applicable for Rh(D)-negative pregnant women, as it ensures the availability of the patient's blood in the event of perinatal hemorrhage, thus minimizing the need for transfusion from external sources. Despite the autologous blood reinfusion of low proportion, PABD could still serve as an alternative when allogeneic blood resources are scarce. However, one challenge in the future is to identify candidates who may benefit most from PABD. Also, more attention is needed to raise awareness of patient blood management. Recommended strategies include early screening and treatment of anemia, hemostasis promotion, and blood loss reduction. Replacement of allogeneic transfusion with autotransfusion could be referred to where feasible. We believe that PABD still has a promising potential for application in Rh(D)-negative pregnant women.
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Keywords
predeposit autologous blood donation - postpartum hemorrhage - gestational anemia - patient blood managementThe Rh blood group is the most intricate and polymorphic in human blood group systems, arguably second only to the ABO system in clinical significance and it exhibits high immunogenicity, especially the D antigen. In transfusion medicine, D antigen deletion is typically termed as Rh (D) negative. Earlier studies uncovered that D antigen distribution differs considerably from ethnicities. Approximately 15% of Caucasians express D negative phenotype, and 8% of Africans. Comparatively, there is a lower prevalence of only 0.4% in Asians.[1] [2] Sparse Rh(D)-negative population poses difficulty in obtaining adequate blood resources from donors. In real life, blood transfusion services are often challenged to promptly provide Rh (D) negative blood products.
On the other side, all over the world, maternal death is primarily caused by severe obstetric bleeding and blood transfusion is an irreplaceable rescue measure. Consistently, obstetricians and transfusionists face the vexing issue of how to ensure safe delivery in such groups. The lives of puerpera and fetus could be threatened when severe postpartum hemorrhage (PPH) happens during a blood resources shortage. Therefore, appropriate blood products should be prepared beforehand in anticipation of such an emergency.
As concerns for transfusion safety and blood shortage become increasingly prominent, autotransfusion has garnered widespread attention. Autotransfusion is an alternative of allogeneic transfusion, which consists of three modalities: predeposit autologous blood donation (PABD), acute normovolemic hemodilution (ANH), and intraoperative cell salvage (ICS). ANH and ICS have been limited in some areas with underdeveloped medical conditions owing to higher technically demanding. In comparison, PABD is praised for its low cost and simplicity. It could not only stimuli erythrocyte regeneration but also avoid immune responses associated with allogenic transfusion and prevent blood-transmissible diseases. Since 1980, PABD has been extensively applied in some high-bleeding-risk surgeries, including cardiac surgery, liver surgery, and orthopaedic surgery. It is considered as a good alternative to the allogeneic transfusion. Nevertheless, controversy regarding its safety and availability are retained in obstetric.[3] The study was conducted to evaluate its application in Rh(D)-negative pregnant women, aiming to provide reference for perinatal blood management in this special group.
Materials and Methods
The medical records of all Rh(D)-negative pregnant women who had delivered in the comprehensive tertiary hospital in Nanjing, China from January 1, 2012, to January 31, 2022, were reviewed retrospectively. Only pregnancies with complete clinical data and transfusion records were included in this study. The indicated population for PABD was Rh (D)-negative pregnant women in our institution. All eligible women were encouraged to carry out PABD. The participants corresponded with the following conditions: (1) The patient had a hemoglobin (Hb) value ≥110 g/L or hematocrit ≥33%. (2) The patients who experienced cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, blood system disease, and other serious complications were excluded. (3) Every patient was advised of associated risks and then signed an informed consent. PABD was scheduled to initiate beyond 37 weeks' gestation with a blood collection volume of 200 mL each time and no more than twice throughout the program. All procedures were performed by experienced transfusionists, and blood collection was completed within 5 minutes. The whole blood was collected into a blood bag with CPDA1 preservation solution and stored in the dedicated refrigerator at 4°C in the blood transfusion branch for up to 35 days.
Vital signs, including oxygen saturation, respiratory rate, blood pressure, heart rate, and body temperature, were monitored consistently throughout blood sampling, and fetal heart monitoring was performed to assess fetal well-being by obstetricians simultaneously. Hb values at separate stages (before PABD, before delivery, and 24 hours after delivery) were recorded. Blood loss within postpartum 24 hours and the amount of transfused blood, autologous or allogeneic, or both were documented. Triggers are the same for allogeneic and autogenous transfusion. Transfusion measures were taken for patients with PPH (defined as blood loss exceeding 500 mL within 24 hours following a vaginal delivery or exceeding 1,000 mL following cesarean delivery) or postpartum anemia (defined as Hb < 10 g/dL). Unused autologous blood was scrapped in accordance with medical waste by the blood transfusion branch.
Statistical analysis for obtained data was done with IBM SPSS Statistics version 23.0. Continuous variables were analyzed by independent two-sample t-test, while categorical variables were analyzed by chi-square test. A p-value of < 0.05 was accepted as statistical significance. Figures were drawn using GraphPad Prism 8.0 software.
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Results
Data on 405 Rh(D)-negative women were enrolled in this study, after the exclusion of 34 women who had either suffered a miscarriage at less than 28 weeks' gestation (n = 2) or were found to have missing data in one or more laboratory records (n = 32). Among all (n = 344) women who fulfilled the PABD criterion, 141 women declined to participate because of various reasons, either not being supported by individual religiosity or having psychological fear when confronted with blood donation ([Fig. 1]). A total of 203 women underwent PABD, vital signs were maintained well, and no adverse blood donation reactions were observed, such as lightheadedness, shortness of breath, fatigue, palpitations, or syncope caused by vagal nerve. Fetal heart monitoring indicated no appreciable abnormality.
The mean Hb before blood collection and predelivery of 203 women who underwent PABD were 123.59 ± 8.81 and 118.27 ± 9.31 g/L, respectively, with declining by only 5.32 ± 0.5 g/L ([Fig. 2]). The predelivery mean Hb of 141 women who met the criteria for PABD but did not undergo was 122.04 ± 9.59 g/L. Comparison of the predelivery Hb was statistically difference in two groups (118.27 ± 9.31 vs. 122.04 ± 9.59 g/L, p = 0.001). Among these 203 individuals, 146 women had one unit and 57 women had two units of autologous blood, respectively, 25 women reinfused one unit and 16 women reinfused two units of autologous blood, and another 2 women reinfused one unit autologous blood and required additional allogeneic blood due to excessive postpartum bleeding ([Fig. 3]). Forty-one women received autologous of 273.17 ± 96.33 mL, with predelivery Hb of 115.49 ± 11.87 g/L and blood loss of 447.46 ± 237.07 mL. Of the remaining 160 women, the collected autologous blood units were not used, with predelivery Hb of 119.13 ± 8.30 g/L and blood loss of 380.97 ± 118.61 mL. Among these 141 women who met the criteria for PABD but failed to engage, 128 women who required no transfusion had predelivery Hb of 122.38 ± 9.85 g/L and blood loss of 418.77 ± 140.01 mL. Thirteen women received allogeneic blood of 376.92 ± 147.56 mL, with predelivery Hb of 118.77 ± 5.34 g/L and blood loss of 569.62 ± 282.17 mL. In the population of 61 women who were ineligible for PABD, 35 women did not need transfusion, with predelivery Hb of 103.43 ± 4.64 g/L and blood loss of 488.67 ± 153.47 mL, and 26 women received allogeneic blood transfusion of 892.31 ± 989.14 mL, with predelivery Hb of 89.81 ± 15.57 g/L and blood loss of 814.81 ± 1,085.45 mL ([Table 1]) ([Figs. 4] and [5]).
Abbreviations: Hb, hemoglobin; PABD, predeposit autologous blood donation.
The primary indications for transfusion cases were assayed below. Forty-one women received only autologous blood and 2 women who required extra allogeneic blood were incorporated in the same autologous transfusion group. Of these 43 women, 16 women also experienced hypertension, diabetes, macrosomia, or twin pregnancies, which were indicated as PPH induced by uterine atony. Seven women with the indication of postpartum Hb <100 g/L and nine women with a scarred uterus received autologous blood. There were no apparent transfusion indications for the remaining 10 patients. Among 39 women who received allogeneic blood, gestational anemia accounted for 19, uterine atony accounted for 6, scarred uterus accounted for 5, and placenta previa accounted for 4 ([Table 2]).
Abbreviation: Hb, hemoglobin.
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Discussion
PABD is a technique that involves collecting and storing the patient's blood prior to surgery or other medical procedures, to use this blood if a transfusion is needed. PABD is proven to be safe both theoretically and empirically. In theory, during the pregnancy process, total blood volume normally increases by ∼1,450 mL, not only offers the essential nutrients for fetal growth but also acts as a native protection mechanism to cope with delivery bleeding. Typically, blood loss within the range of 1,000 to 1,500 mL would have no undesirable theoretically consequence for the pregnant women with normal Hb value.[4] Hence, PABD is possible to be performed safely. Empirically, PABD has been confirmed to be a safe and feasible therapy measure in our study, which is consistent with conclusions from various previous research projects.[5] [6] [7] Vital signs of 203 women during PABD presented well and no unfavorable blood donation reaction was observed. The fetal heart monitoring recordings revealed normal. PABD-associated anemia almost did not occur, with merely a slight decline in mean Hb of 5.32 ± 0.5 g/L. Additionally, no adverse transfusion reactions, such as fever, skin rash palpitations, and chest tightness, were observed during autologous blood reinfusion. Our findings demonstrated that PABD could be added as a viable transfusion practice.
In the autotransfusion cohort, uterine factors take up a proportion of 58.1% (25/43). Uterine atony after parturition causes uterine spiral artery dilation and then ultimately ends up with excessive bleeding, which is the main contributor to PPH.[8] Precipitating factors for uterine atony emerged in the present study included fetal macrosomia, twin pregnancy, gestational diabetes, and scarred uterus. In addition, placenta factors and birth canal laceration are also high-risk factors for inducing PPH. All pregnant women practically could have the potential probability of PPH. The latest guideline proposed that 60% of women with PPH had no preexisting known risk factors.[9] Rh(D)-negative blood products are not routinely available due to extreme blood resources shortage in our country, especially where access to proper medical services is limited. Thus, blood preparation in advance is imperative in this specific population. PABD could serve as a proper alternative in the context of allogeneic blood resources shortage.
Among 344 patients who met the criteria for PABD, pre-PABD Hb and postpartum blood loss were similar between the autotransfusion group (n = 41) and the untransfused group (n = 128). After checking medical records, we noted that 10 patients in autotransfusion group indeed lacked justifiable transfusion indications. We concluded that they might not truly need transfusion. Admittedly, transfusion triggers vary widely from medical institutions and are affected by the experience and subjective judgments from physicians. Some patients insisted upon being reinfused with their blood, although lacked the indication for transfusion. One explanation is that predeposit autologous blood may inspire liberal transfusion policy, consistent with a prior study.[10]
Among the allogeneic transfusion group, we contemplated that 13 patients were virtually beneficiary population of PABD since they met the criteria for PABD but failed to attend, such patients were accompanied by comorbidities including scarred uterine, twin pregnancies, or macrosomia, which represented good indication of PABD. It was noteworthy that pregnancies solely with anemia accounted for 48.7% (19/39) of the allogeneic transfusion group. Compared with nonanemic patients, anemia patients could be more prone to developing PPH and peripartum transfusion because of poorer tolerance for blood loss.[11] [12] According to the WHO data, ∼40% pregnancies were accompanied by anemia all over the world.[13] About 15.1% patients (61/405) in this study had anemia of mild to moderate severity, and even severe anemia. Gestational anemia can trigger a series of adverse perinatal outcomes, including premature rupture of membranes, preterm delivery, and increased maternal and fetal mortality.[14] Furthermore, in the absence of PPH, blood transfusion can chiefly be attributed to predelivery anemia. Iron deficiency anemia (IDA) is the commonest type of anemia during pregnancy, which is characterized by depleted iron stores and impaired iron supply to tissues.[15] Guidelines set forth by American College of Obstetricians and Gynecologists (2021a) recommend screening for anemia in all pregnant women and iron supplementation should be promptly administered once IDA is diagnosed.[16] Anemia is a modifiable risk factor since sufficient time is available to optimize Hb value before delivery. Early identification and management of anemia may be favorable to improve maternal and neonatal outcomes.
PABD has a prominent advantage in that it minimizes exposure to allogeneic blood. PABD reduces the risk of infectious diseases that can be transmitted through blood transfusions, such as hepatitis B and C and human immunodeficiency virus. The mother is assured that the blood she receives will be safe and compatible, as it is her blood. Autologous blood protects pregnant women from being sensitized by exogenous erythrocyte antigens that will be conducive to another pregnancy.[17] In addition to its potential use in Rh(D)-negative pregnant women, PABD may also be used in other clinical scenarios where blood transfusions are anticipated. For example, it may be used in patients undergoing elective surgeries, such as joint replacement, where blood transfusions are common. PABD may also be used in patients with rare blood types or who have developed alloantibodies to common blood antigens.
However, the use of PABD is not without controversy. There are drawbacks to conduct PABD, including the potential for inadequate blood volume or Hb concentration at the time of delivery. If the mother experiences significant bleeding during delivery, she may require a transfusion of additional blood products, which may not be available if the PABD was insufficient or if the mother does not meet the donation criteria. In addition, PABD can be a time-consuming process that requires multiple visits to the blood donation center. This can be a burden to the mother, who may already be busy dealing with the stresses of pregnancy and preparing for childbirth. It is important to note that the procedure itself carries certain risks, such as anemia, infection, and venous thrombosis. Patients who undergo PABD should be closely monitored for potential complications, and appropriate interventions should be taken if needed. There are also concerns that PABD may promote unnecessary blood transfusions and contribute to overuse of health care resources. Additionally, the costs associated with PABD, including the cost of the blood tests and the cost of storage and processing, can be a barrier for some women. Thus, some critics argue that the costs and risks associated with PABD may outweigh the benefits.
Ultimately, the decision to undergo PABD should be based on individual risk factors and medical history. Women with a history of hemolytic disease of the newborn, multiple pregnancies, or previous blood transfusions may be considered risky in allogeneic transfusion and could benefit from PABD. PABD may also be recommended in cases where a planned cesarean section is scheduled, as these procedures can result in significant blood loss. Certain medical conditions such as placenta previa, placental abruption, or fetal distress may increase the risk of PPH and the need for blood transfusions during or after delivery.[11] [18] In some geographic areas or health care systems, Rh(D)-negative blood products are limited and PABD may be considered as a way to ensure that the patient has access to Rh(D)-negative blood if needed.
Health care providers need to provide adequate education and counseling to women who are considering PABD. This includes explaining the benefits and risks of PABD, discussing the donation process, and addressing any concerns or questions patients may have. Women who choose to undergo PABD should also be given clear instructions on how to prepare for the donation, such as maintaining a healthy diet and hydration, and avoiding medications that may affect the blood donation process. Finally, health care providers need to ensure that the PABD process is well-coordinated with the hospital or birthing center. This includes assuring that the donated blood is properly labeled and stored, and that hospital staff are aware of the mother's PABD status and prepared to use the donated blood if necessary. In conclusion, adequate education, counseling, and coordination with the hospital or birthing center can help ensure a safe and successful PABD process.
Furthermore, the use of PABD requires adequate resources and infrastructure, including trained personnel, appropriate storage and processing facilities, and access to blood testing and transfusion services. In some health care settings, these resources may be limited, which may impact the feasibility of using PABD. To address potential shortages of PABD, health care providers may consider alternative strategies, such as intraoperative blood salvage, where blood lost during surgery is collected, processed, and reinfused back into the patient. This technique may be particularly useful in surgeries with high blood loss, such as cardiac or orthopaedic surgeries.[19] [20] The overall use of blood transfusions has been declining in recent years due to efforts to reduce unnecessary transfusions and improve patient outcomes. For example, the use of restrictive transfusion strategies, which aim to maintain lower Hb levels before transfusing blood, has been shown to reduce the need for transfusions and improve outcomes in certain patient populations.[21] [22] Health care providers may also consider other strategies to optimize patient outcomes, such as reducing surgical blood loss through the use of hemostatic agents, optimizing preoperative Hb levels through iron supplementation or erythropoietin therapy, and improving patient blood management (PBM) practices.[23] Furthermore, health care providers may also consider the use of nonblood alternatives to transfusions, such as intravenous fluids, medications, and oxygen therapies, which may be effective in certain clinical scenarios.
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Conclusion
In summary, PABD is applicable for Rh(D)-negative pregnant women, as it minimizes the risk of transfusion from external sources by utilizing the availability of the patient's blood in the event of perinatal hemorrhage. Although it is not without defects, health care providers can work to address these challenges by exploring alternative strategies, collaborating with blood banks to improve the availability of Rh(D)-negative blood products, and implementing PBM practices to optimize patient outcomes and reduce the need for transfusions.
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Conflict of Interest
None declared.
* Juan Xie and Yu Ling contributed equally to this work.
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References
- 1 Kanko TK, Woldemariam MK. Prevalence of Rhesus D negativity among reproductive age women in Southern Ethiopia: a cross-sectional study. BMC Womens Health 2021; 21 (01) 161
- 2 Zonneveld R, Schmitz P, Eppink J. et al. RhD negativity among pregnant women in multiethnic Suriname. Transfusion 2016; 56 (02) 321-324
- 3 Zhou J. A review of the application of autologous blood transfusion. Braz J Med Biol Res 2016; 49 (09) e5493
- 4 Yamamoto Y, Yamashita T, Tsuno NH. et al. Safety and efficacy of preoperative autologous blood donation for high-risk pregnant women: experience of a large university hospital in Japan. J Obstet Gynaecol Res 2014; 40 (05) 1308-1316
- 5 Manuel SP, Roberts JP, Bakhtary S. Preoperative autologous blood collection in adult living liver donors: are we wasting donor blood and increasing exposure to risk?. Transplantation 2019; 103 (02) 387-391
- 6 Lim MH, Je HG, Ju MH, Lee JH, Oh HR, Kim YR. Effects of preoperative autologous blood donation in patients undergoing minimally invasive cardiac surgery. Korean J Thorac Cardiovasc Surg 2019; 52 (06) 385-391
- 7 Arora K, Kelley J, Martinez F, Tholpady A. Preoperative autologous blood collection before bone marrow harvests in haploidentical related donors: is it justified?. Transfusion 2018; 58 (07) 1618-1625
- 8 Kroh S, Waters JH. Obstetrical hemorrhage. Anesthesiol Clin 2021; 39 (04) 597-611
- 9 Surbek D, Vial Y, Girard T. et al. Patient blood management (PBM) in pregnancy and childbirth: literature review and expert opinion. Arch Gynecol Obstet 2020; 301 (02) 627-641
- 10 Ćatić D, Milojković A, Steblovnik L. Preoperative autologous blood donation in placenta previa patients. Transfus Apher Sci 2018; 57 (06) 793-796
- 11 Stephens B, Sethna F, Crispin P. Postpartum obstetric red cell transfusion practice: a retrospective study in a tertiary obstetric centre. Aust N Z J Obstet Gynaecol 2018; 58 (02) 170-177
- 12 Nair M, Chhabra S, Choudhury SS. et al; MaatHRI collaborators. Relationship between anaemia, coagulation parameters during pregnancy and postpartum haemorrhage at childbirth: a prospective cohort study. BMJ Open 2021; 11 (10) e050815
- 13 Anemia in pregnancy: screening and clinical management strategies. MCN Am J Matern Child Nurs 2022; 47 (01) E2
- 14 James AH. Iron deficiency anemia in pregnancy. Obstet Gynecol 2021; 138 (04) 663-674
- 15 Imai K. Parity-based assessment of anemia and iron deficiency in pregnant women. Taiwan J Obstet Gynecol 2020; 59 (06) 838-841
- 16 Stanley AY, Wallace JB, Hernandez AM, Spell JL. Anemia in pregnancy: screening and clinical management strategies. MCN Am J Matern Child Nurs 2022; 47 (01) 25-32
- 17 Greenawalt JA, Zernell D. Autologous blood transfusion for postpartum hemorrhage. MCN Am J Matern Child Nurs 2017; 42 (05) 269-275
- 18 Nigam A, Prakash A, Saxena P. Blood transfusion in obstetrics. Kathmandu Univ Med J 2013; 11 (44) 355-359 (KUMJ)
- 19 Côté CL, Yip AM, MacLeod JB. et al. Efficacy of intraoperative cell salvage in decreasing perioperative blood transfusion rates in first-time cardiac surgery patients: a retrospective study. Can J Surg 2016; 59 (05) 330-336
- 20 van der Merwe M, Lightfoot NJ, Munro JT, Boyle MJ. Intraoperative cell salvage use reduces the rate of perioperative allogenic blood transfusion in patients undergoing periacetabular osteotomy. J Hip Preserv Surg 2019; 6 (03) 277-283
- 21 Wang L, Wang Z, Huang Y. et al. Expanding restrictive transfusion evidence in surgical practice: a multicentre, prospective cohort study. Blood Transfus 2022; 20 (05) 382-394
- 22 Yoon BH, Lee BS, Won H, Kim HK, Lee YK, Koo KH. Preoperative iron supplementation and restrictive transfusion strategy in hip fracture surgery. Clin Orthop Surg 2019; 11 (03) 265-269
- 23 Franchini M, Marano G, Veropalumbo E. et al. Patient blood management: a revolutionary approach to transfusion medicine. Blood Transfus 2019; 17 (03) 191-195
Address for correspondence
Publikationsverlauf
Eingereicht: 03. Mai 2024
Angenommen: 04. August 2024
Accepted Manuscript online:
14. August 2024
Artikel online veröffentlicht:
30. August 2024
© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Kanko TK, Woldemariam MK. Prevalence of Rhesus D negativity among reproductive age women in Southern Ethiopia: a cross-sectional study. BMC Womens Health 2021; 21 (01) 161
- 2 Zonneveld R, Schmitz P, Eppink J. et al. RhD negativity among pregnant women in multiethnic Suriname. Transfusion 2016; 56 (02) 321-324
- 3 Zhou J. A review of the application of autologous blood transfusion. Braz J Med Biol Res 2016; 49 (09) e5493
- 4 Yamamoto Y, Yamashita T, Tsuno NH. et al. Safety and efficacy of preoperative autologous blood donation for high-risk pregnant women: experience of a large university hospital in Japan. J Obstet Gynaecol Res 2014; 40 (05) 1308-1316
- 5 Manuel SP, Roberts JP, Bakhtary S. Preoperative autologous blood collection in adult living liver donors: are we wasting donor blood and increasing exposure to risk?. Transplantation 2019; 103 (02) 387-391
- 6 Lim MH, Je HG, Ju MH, Lee JH, Oh HR, Kim YR. Effects of preoperative autologous blood donation in patients undergoing minimally invasive cardiac surgery. Korean J Thorac Cardiovasc Surg 2019; 52 (06) 385-391
- 7 Arora K, Kelley J, Martinez F, Tholpady A. Preoperative autologous blood collection before bone marrow harvests in haploidentical related donors: is it justified?. Transfusion 2018; 58 (07) 1618-1625
- 8 Kroh S, Waters JH. Obstetrical hemorrhage. Anesthesiol Clin 2021; 39 (04) 597-611
- 9 Surbek D, Vial Y, Girard T. et al. Patient blood management (PBM) in pregnancy and childbirth: literature review and expert opinion. Arch Gynecol Obstet 2020; 301 (02) 627-641
- 10 Ćatić D, Milojković A, Steblovnik L. Preoperative autologous blood donation in placenta previa patients. Transfus Apher Sci 2018; 57 (06) 793-796
- 11 Stephens B, Sethna F, Crispin P. Postpartum obstetric red cell transfusion practice: a retrospective study in a tertiary obstetric centre. Aust N Z J Obstet Gynaecol 2018; 58 (02) 170-177
- 12 Nair M, Chhabra S, Choudhury SS. et al; MaatHRI collaborators. Relationship between anaemia, coagulation parameters during pregnancy and postpartum haemorrhage at childbirth: a prospective cohort study. BMJ Open 2021; 11 (10) e050815
- 13 Anemia in pregnancy: screening and clinical management strategies. MCN Am J Matern Child Nurs 2022; 47 (01) E2
- 14 James AH. Iron deficiency anemia in pregnancy. Obstet Gynecol 2021; 138 (04) 663-674
- 15 Imai K. Parity-based assessment of anemia and iron deficiency in pregnant women. Taiwan J Obstet Gynecol 2020; 59 (06) 838-841
- 16 Stanley AY, Wallace JB, Hernandez AM, Spell JL. Anemia in pregnancy: screening and clinical management strategies. MCN Am J Matern Child Nurs 2022; 47 (01) 25-32
- 17 Greenawalt JA, Zernell D. Autologous blood transfusion for postpartum hemorrhage. MCN Am J Matern Child Nurs 2017; 42 (05) 269-275
- 18 Nigam A, Prakash A, Saxena P. Blood transfusion in obstetrics. Kathmandu Univ Med J 2013; 11 (44) 355-359 (KUMJ)
- 19 Côté CL, Yip AM, MacLeod JB. et al. Efficacy of intraoperative cell salvage in decreasing perioperative blood transfusion rates in first-time cardiac surgery patients: a retrospective study. Can J Surg 2016; 59 (05) 330-336
- 20 van der Merwe M, Lightfoot NJ, Munro JT, Boyle MJ. Intraoperative cell salvage use reduces the rate of perioperative allogenic blood transfusion in patients undergoing periacetabular osteotomy. J Hip Preserv Surg 2019; 6 (03) 277-283
- 21 Wang L, Wang Z, Huang Y. et al. Expanding restrictive transfusion evidence in surgical practice: a multicentre, prospective cohort study. Blood Transfus 2022; 20 (05) 382-394
- 22 Yoon BH, Lee BS, Won H, Kim HK, Lee YK, Koo KH. Preoperative iron supplementation and restrictive transfusion strategy in hip fracture surgery. Clin Orthop Surg 2019; 11 (03) 265-269
- 23 Franchini M, Marano G, Veropalumbo E. et al. Patient blood management: a revolutionary approach to transfusion medicine. Blood Transfus 2019; 17 (03) 191-195