Resuscitative efficacy of hemoglobin vesicles for severe postpartum hemorrhage in pregnant rabbits

We aimed to investigate the resuscitative efficacy of hemoglobin vesicles (HbVs) as a red blood cell (RBC) substitute for the initial treatment of severe postpartum hemorrhage (PPH). Twenty-five pregnant rabbits underwent cesarean section; uncontrolled hemorrhage was induced by transecting the right uterine artery to establish a severe PPH model. During the first 30 min, all rabbits were administered 6% hydroxyethyl starch (HES) of an equivalent volume to the hemorrhage every 5 min. Thereafter, they received any of the following three isovolemic fluids for resuscitation every 5 min: RBCs with platelet-poor plasma (RBC/PPP) (n = 8), 6% HES (n = 7), or HbVs with 25% human serum albumin (n = 10). After surgical hemostasis at 60 min, survival was monitored until 12 h. No rabbits receiving only HES infusion survived beyond 6 h, whereas all rabbits receiving RBC/PPP transfusion survived. The rabbits receiving HbV infusion showed significantly higher mean arterial pressure and hemoglobin levels than the HES-receiving rabbits, and 8 of 10 rabbits survived for 6 h. The HbV group showed significantly higher survival than the HES group but worse survival than the RBC/PPP group. In conclusion, HbV infusion for severe PPH effectively prevents lethal hemorrhagic shock in a pregnant rabbit model.

Severe postpartum hemorrhage (PPH) remains the leading cause of maternal morbidity and mortality worldwide 1,2 . At least 26% of PPH-related deaths result from insufficient and delayed blood transfusion 3 , and thus timely blood transfusions are essential. However, access to blood markedly differs between low-and high-income countries. Transfusion for severe PPH commonly involves red blood cells (RBCs) and other blood components. Every obstetrical facility should have an emergency strategy for severe PPH, including protocols for accessing packed RBCs 4 . However, blood transfusion services are highly resource intensive and require voluntary donations; donor screening, including blood-type antigen and cross-matching test; and a temperature-controlled system. Furthermore, the spread of epidemics, such as the COVID-19 infection, limits the available blood supply worldwide 5,6 . Thus, preparing adequate resources at small facilities is challenging.
To support the system, hemoglobin (Hb)-based oxygen carriers (HBOCs) were developed as blood substitutes for RBCs 7 . Cell-free typed HBOCs exert some side effects of bared Hbs, including nitric oxide (NO 2 − )-related vasoconstriction, hypertension, and higher infarction rates 8 . These results emphasize the significance of mimicking the cellular structure of RBCs. Therefore, many studies have attempted Hb encapsulation using liposomes to improve biocompatibility, storage stability, and oxygen-carrying capacity. Accordingly, hemoglobin vesicles (HbVs) were developed 9 . The liposomes in the structures of HbVs prevent the release of free Hb and avoid NO 2 related vasoconstrictive complications [10][11][12][13][14] . Blood substitutes including HbVs could be useful for hemorrhagic shock [15][16][17][18] . Furthermore, HbVs could be stored for at least 1 year; do not need donor screening, including blood-type antigen or cross-matching test; and have no risk of blood contamination 17,18 .
Scientific Reports | (2021) 11:22367 | https://doi.org/10.1038/s41598-021-01835-w www.nature.com/scientificreports/ Severe PPH is a type of hemorrhagic shock, and its treatment is basically similar to that of hemorrhagic shock 19 . However, no study has assessed the efficacy of HbVs for severe PPH. Moreover, animal models have been limited. Yu et al. 20 created a hemorrhagic shock model in pregnant rabbits; however, it was not a PPH model. This study aimed to investigate the resuscitative efficacy of HbVs for PPH. Toward this goal, we established a severe PPH model using pregnant rabbits based on top reflect clinical scenarios. Then we hypothesized in this study that HbVs could have a resuscitative effect on severe PPH as an alternative to blood transfusion.

Methods
Animal management. Female New Zealand white rabbits (weight: 3.5-3.9 kg, gestational age: 28 days [normal gestation period, 29-35 days]); Japan SLC, Hamamatsu, Japan) were used. They were given free access to standard feed and water during a 7-day adaptation period before the experiment. Male New Zealand white rabbits (weight: 2.6-2.8 kg; Japan SLC, Hamamatsu, Japan) were used as blood donors. The experimental protocol was approved by the Institutional Review Board for the Care of Animal Subjects of the National Defense Medical College (ethical approval number: #17032). All applicable international, national, and/or institutional guidelines for the care and use of animals were followed with strict adherence to ARRIVE guidelines 21,22 (Supplementary Note online).
Preparation of hemoglobin vesicles. HbVs were prepared as previously described 15,16 . Briefly, Hb was purified from outdated donor human blood provided by the Japanese Red Cross Society. Encapsulated carbonylhemoglobin (HbCO, 38 g/dL) contained 5.9 mM pyridoxal 5″-phosphate (Sigma Chemical, Saint Louis, USA) as an allosteric effector for regulating oxygen affinity. The lipid bilayer was a mixture of 1,2-dipalmitoyl-snglycero-3-phosphatidylcholine, cholesterol, and 1,5-bis-O-hexadecyl-N-succinyl-l-glutamate at a molar ratio of 5:4:0.9 and 1,2-distearoyl-sn-glycero-3-phosphatidyl-ethanolamine-N-polyethylene glycol (PEG) (0.3 mol%). HbV particles were suspended in isotonic saline; nitrogen gas was bubbled through the solution in a vial to remove the oxygen for ensuring product stability. Then, HbVs were stored in deoxygenated glass vials at 4 °C for 10-12 months. The HbV properties used in this experiment are shown in Table 1. The HbV solution showed no colloid osmotic pressure 23 , similar to RBCs when suspended in isotonic saline. Before the experiments, the HbV solution was mixed with 25% human serum albumin, which was concentrated by 5-6 times more than plasma (Benesis, Osaka, Japan) (vol/vol = 4:1), to adjust the albumin concentration of the vesicle-suspension medium to 5 g/dL and the colloid osmotic pressure to approximately 20 mmHg same as plasma.
Preparation of allogenic RBCs. Donor rabbits (n = 16) were anesthetized using an intramuscular injection of 25 mg/kg ketamine and 10 mg/kg xylazine. A 20-gauge catheter (polyethylene indwelling needle; Terumo, Tokyo, Japan) was aseptically introduced into the left femoral artery for blood sampling. Then, 50 mL/kg of donor blood was withdrawn from this artery. After removing platelet-poor plasma (PPP) from the blood by centrifugation (100×g for 15 min), the remaining RBCs were washed with acid citrate dextrose solution 16 . Subsequently, the same volume of mannitol adenine phosphate solution (1.457% [w/v%] d-mannitol, 0.014% adenine and 0.094% sodium dihydrogen phosphate [Terumo, Tokyo, Japan]) was added to prepare allogenic RBCs that were then stored at 4 °C. Before usage, we performed a cross-matching test between donor RBCs and recipient plasma and a test between donor plasma and recipient RBCs, same as clinical examination. PPP samples showed the following coagulation activity: fibrinogen, 121 mg/dL; antithrombin (AT) III activity, 81%; coagulation factor VIII, 388 ng/mL; prothrombin time (PT), 13.1 s; and activated partial thromboplastin time (APTT), 31.2 s, on average. Rabbit coagulation factor VIII in the rabbit PPP was measured using the Rabbit coagulation factor VIII ELISA kit (abx363389, Abbexa Ltd, Cambridge, UK). We showed the data of these coagulation parameters of rabbit PPP in Table 2.
Surgical procedures. Pregnant rabbits were anesthetized using an intramuscular injection of 25 mg/kg ketamine and 10 mg/kg xylazine, followed by intravenous injections of 15 mg/kg pentobarbital. Anaesthesia was maintained with additional doses as necessary. A local anaesthetic (3-5 mL of 1% lidocaine) was injected subcutaneously into the left inguinal area and mid-lower abdomen. The adequacy of general anaesthesia was monitored according to the loss of the ear pinch reflex. Rabbits were maintained in the supine position and  Severe postpartum haemorrhage model. We designed the severe PPH model and the actual clinical treatment after delivery. After lower midline laparotomy, we performed a caesarean section and delivered foetuses from the right side of the rabbit bicornuate uterus (Fig. 1A). Thereafter, uncontrolled haemorrhage was induced by transecting the right uterine artery (Fig. 1B). The bleeding was wiped off using a high-absorbent www.nature.com/scientificreports/ gauze (BEMCOT M-1, Asahikasei, Tokyo, Japan), and the absorbed blood volume was assessed based on the weight of gauze every 5 min. First, to compensate for the initial bleeding, an isovolemic infusion of 6% hydroxyethyl starch (HES) (Voluven 6%; Fresenius Kabi Deutschland, Bad Homburg, Germany) was repeated every 5 min through the femoral vein until 30 min or the bleeding volume reached 100 mL. The reason for setting the bleeding volume at 100 mL is as follows.
The need for blood transfusion was determined when the shock index (heart rate/systolic blood pressure) exceeded 1.5 based on a previous study, with a shock index of 1.5 corresponding to a blood loss volume of approximately 2.5 L 24 . In pregnant women weighing 60 kg, the circulating blood volume is approximately 4.6 L; thus, the blood loss rate in severe PPH is estimated at approximately 54% of circulating blood. According to the guidelines of the European Federation of Pharmaceutical Industries Associations and the European Centre for the Validation of Alternative Methods 25 , rabbit circulating blood is approximately 56 mL/kg. Considering that pregnant rabbits weighed approximately 3.5 kg, the bleeding volume corresponding to severe PPH was calculated at 106 mL (3.5 kg × 56 mL/kg × 0.54). Thus, we set the bleeding volume of severe PPH at 100 mL.
Fluid resuscitation with haemoglobin vesicles, RBCs, or 6% HES. Following the initial infusion of 6% HES, rabbits were randomized into three groups using the random function in Microsoft Excel (Supplementary Note online After progression to severe PPH, the rabbits in each group received an isovolemic fluid (allogenic RBC with PPP, 6% HES, or HbVs with 25% human serum albumin) for resuscitation, which was equivalent to the blood loss every 5 min until 60 min or when the bleeding volume reached over 200 mL (Fig. 1C), similar to the circulation volume in rabbits 23 . In pregnancy, such condition is lethal hemorrhagic shock class IV 26 . The fluid regimens consisted of allogenic RBC with PPP (vol/vol = 1:1, Hb concentration of 11.9 ± 1.6 g/dL) (RBC/ PPP group, n = 8) as a positive control, 6% HES infusion (HES group, n = 7) as a negative control, and HbVs with 25% human serum albumin (vol/vol = 4:1, Hb concentration of 8.0 g/dL) (HbV group, n = 10) (Fig. 1C). The selection of resuscitation fluid is controversial, and saline is the most commonly used fluid. Colloid solutions such as hydroxyethyl starch are possibly harmful in some patients. In contrast, these colloid solutions are used for many patients and many resuscitation episodes, including hemorrhagic shock, in several countries 27 . We selected HES infusion as a negative control for HbV infusion. After fluid resuscitation, the rabbits underwent a surgical hemostatic procedure via the ligation of a bleeding right uterine artery, followed by cesarean section to deliver the fetuses from the left side of the bicornate uterus. The laparotomy incisions were closed, and survival was monitored for at least 12 h. Postoperative analgesia was induced with intramuscular injections of buprenorphine (0.02 mg/kg) after 12 h for euthanasia.

Measurements of blood cell counts, coagulation factors, and blood gases.
Blood samples were obtained every 5 min for blood cell counting using an Erma PCE 170 hematology analyzer (Erma, Tokyo, Japan). Coagulation factors, except d-dimers, and blood gases were examined every 15 min. d-dimer levels were examined at 60 min. Hb concentration in the blood containing HbVs could not be accurately determined using the current analyzer because liposome capsules interfered with the spectrophotometric measurement of Hb absorbance. The actual Hb concentrations were estimated using a previous method 16 . To measure plasma AT III activity, PT, APTT, and D-dimers, blood samples were collected with a 3.2% sodium citrate solution and centrifuged at 50,000×g at 4 °C for 20 min to remove HbV particles. Measurements were conducted at Sanritsu Zelcova Laboratory (Tokyo, Japan). Plasma fibrinogen levels were measured using a rabbit fibrinogen enzyme-linked immunosorbent assay kit (LifeSpan BioSciences, Seattle, USA). Blood gas analyses, including plasma lactate and arterial oxygen content (CtO 2 ) levels, were performed using an ABL 80 blood gas analyzer (Radiometer, Copenhagen, Denmark).
Analyses of whole blood coagulation activity and plasma nitric oxide. Coagulation activity was measured every 15 min using a coagulation and platelet (PLT) function analyzer (Sonoclot) (Sienco Inc, Morrison, CO). The Sonoclot signal typically describes coagulation parameters, including activated clotting time (ACT) (which indicates the period up to the start of fibrinogen formation) and clot rate. Plasma NO 2 levels were measured every 15 min. Blood samples were collected with a heparinized syringe and centrifuged at 50,000×g at 4 °C for 20 min to remove HbV particles. The supernatant was stored at − 80 ℃ until analysis. Plasma NO 2 levels were measured using a high-performance liquid chromatography-Griess system in Eicom Laboratory (Eicom Inc Co, Kyoto, Japan).

Plasma biochemical test.
To evaluate haemolysis and acute kidney injury, plasma creatinine, iron, cellfree Hb, and cell-free heme levels were measured before the experiment and 60 min after bleeding. Plasma creatinine levels were measured using the Fuji Dry-Chem system (Fujifilm Medical, Saitama, Japan). Plasma iron levels were measured at Sanritsu Zelcova Laboratory (Tokyo, Japan). Plasma free Hb levels were measured using Plasma/Low Haemoglobin Hemocue (HemoCueAB, Angelholm, Sweden). Plasma cell-free heme levels were measured using the heme assay kit (BioChain Institute Inc, Newark, USA). All plasma samples were stored at − 80 ℃ until analysis.
Statistical analysis. The sample size for each group complied with the ARRIVE guidelines 21,22 (Supplementary Note online). In addition, statistical power analysis was performed using G*Power, version 3.1.9.4 software (https:// www. psych ologie. hhu. de/ arbei tsgru ppen/ allge meine-psych ologie-und-arbei tspsy cholo gie/ gpower. html) 28 . Survival curves were generated using the Kaplan-Meier method and compared using the logrank test. Statistical comparisons between two groups and among three groups were conducted using Student's t-test and one-way analysis of variance, followed by the Bonferroni post hoc test, respectively. Data are presented www.nature.com/scientificreports/ as the mean ± standard deviation (SD). All statistical analyses were performed using JMP software Pro 14.0.0 (SAS Institute Inc., Tokyo, Japan, https:// www. jmp. com/ ja_ jp/ softw are/ data-analy sis-softw are. html). P < 0.05 was considered statistically significant.

Results
Hemodynamic changes and rabbit survival. The rabbits developed postoperative severe anemia (Hb concentration < 6 g/dL) that progressed to severe PPH in the first 30 min. The time to severe PPH (bleeding volume > 100 mL) was 23 ± 7 min in the HES group, 24 ± 5 min in the HbV group, and 23 ± 4 min in the RBC/PPP group (Table 3), with no significant differences among the groups. There were also no significant differences in the total hemorrhage volume and total bleeding time (Table 3). Although the HES group showed progressively decreased mean arterial pressure (MAP) < 40 mmHg in the resuscitative phase (beyond 30 min), HbV and RBC/ PPP groups maintained significantly higher MAP than the HES group in this period (P < 0.05) ( Fig. 2A). Shock index was gradually increased in all groups; the shock index at 25-45 min was significantly higher in the HES group than in the other groups (P < 0.05), whereas no significant differences were observed among the three groups at 60 min (Fig. 2B). Within 6 h, all rabbits in the HES group died, whereas all rabbits in the RBC/PPP group survived, and 8 of the 10 rabbits in the HbV group survived. Regarding overall survival, the prognosis of the HbV group was significantly better than that of the HES group (P < 0.01), whereas it was significantly worse than that of RBC/PPP group (P = 0.01) (Fig. 2C).

Hematologic variables. The administration of HbVs and RBC/PPP following the initial HES infusion
gradually increased Hb concentration, and it was maintained over 6 g/dL in both groups, though the Hb concentration decreased under 2 g/dL at 60 min in the HES group (Fig. 3A). Unlike the Hb dynamics, the decrease in hematocrit (Hct) was similar between the HbV and HES groups, although the Hct level was higher in the RBC/PPP group (Fig. 3B). PLT counts could not be measured in the HbV group because the submicron HbV particle interfered with PLT counting with the current analyzer. Meanwhile, PLT counts gradually decreased in the RBC/PPP group but remained significantly higher than those in the HES group at 60 min ( Supplementary  Fig. S1online).
Blood gas analyses. The pH level was maintained above 7.35 in the HbV and RBC/PPP groups, whereas it was significantly decreased below 7.35 at 45 and 60 min in the HES group, which was significantly lower than in the other groups (P < 0.01) (Fig. 3C). The base excess and HCO 3 levels were significantly higher in the RBC/PPP group than in the other groups at 45 and 60 min (P < 0.05) (Figs. 3D and 4C). In contrast, no significant differences in the values of PaO 2 or PaCO 2 were observed among the groups throughout the experiment (Fig. 4A,B). During the initial 30 min, the concentration of total oxygen (CtO 2 ) (i.e., the sum of oxygen bound to Hb) decreased to approximately 6.5 vol% in all the three groups. RBC transfusion or HbV infusion restored the CtO 2 to 8.0 vol%. In contrast, the CtO 2 decreased to unmeasurable values at 60 min in the HES group (Fig. 3E). The lactate levels at baseline in the HbV group was statistically higher than that in other groups, but this value was clinically within the normal range. Meanwhile, lactate levels were maintained at approximately 2.0-3.0 mmol/L throughout the experiment in the HbV and RBC/PPP groups, whereas it was critically increased to 6 mmol/L at 60 min in the HES group, which was significantly higher than that in the other groups (P < 0.05) (Fig. 3F).
Coagulation variables and activity. The plasma fibrinogen levels in the RBC/PPP group gradually decreased but was maintained over 110 mg/dL even at 60 min because PPP contained a certain amount of coagulation factors, including fibrinogen (Fig. 5A). In contrast, the plasma fibrinogen levels continuously decreased and reached 20 mg/dL in both the HbV and HES groups (Fig. 5A). The values of AT III in both the HbV and HES groups were significantly lower than those in the RBC/PPP group at 45 (P < 0.05) and 60 min (P < 0.01) (Fig. 5B). Similarly, PT was significantly longer in the HbV and HES groups than in the RBC/PPP group at 60 min (P < 0.01) (Fig. 5C). APTT was prolonged beyond 75 s at 30-60 min in all three groups (Fig. 5D). In addition, plasma D-dimers levels were not elevated in any groups (< 0.2 μg/mL) at 60 min (not shown).
Regarding coagulation activity, ACT at 60 min was significantly longer in both the HbV and HES groups than in the RBC/PPP group (P < 0.05) (Fig. 5E). Regarding the clot rate, which indicated the slope of fibrin gel formation that was affected by both fibrinogen to fibrin conversion and the amount of fibrinogen, all three groups showed similar decreases in the clot rate with no significant differences (Fig. 5F).  (Table 4). HbV infusion did not induce hemolytic and acute renal dysfunction as indicated by the values of iron and creatinine being maintained within normal ranges. In addition, there was no significant increase in free Hb levels (Fig. 6A, Table 4). Meanwhile, although the cell-free heme levels were higher at 60 min after RBC transfusion or HbV infusion than at baseline, the increase in cell-free heme at 60 min was significantly lower in HbV infusion than in RBC transfusion (P < 0.05) (Fig. 6B).
Fetus survival after postpartum hemorrhage. The survival rates of the fetuses after PPH in the left side of the bicornate uterus was 38 ± 42%, 56 ± 49%, and 79 ± 40% in the HES, HbV, and RBC/PPP groups, respectively. There were no significant differences in survival rates among the three groups. In the HES group, the shock index from 25 to 45 min is significantly higher than in the other groups, whereas there is no significant difference at 60 min. (C) Survival of the HbV group is significantly better than that of the HES group (P < 0.01), whereas it is significantly worse than that of the RBC/PPP group (P = 0.01). *P < 0.05, value significantly different from the other groups. † P < 0.05, the prognosis of the RBC/PPP group is significantly different from that of the other groups. ‡ P < 0.05, the prognosis of the HbV group is significantly different from that of the HES group. Data shown are the mean ± standard deviation. HbV hemoglobin vesicles, HES hydroxyethyl starch, MAP mean arterial pressure, RBC/PPP red blood cells with platelet-poor plasma.

Discussion
This study developed a severe PPH model after caesarean section using pregnant rabbits. Total haemorrhage was approximately at least 50 mL/kg and led to severe PPH that became lethal within a few hours in the absence of any fluid resuscitation. Using the current PPH model, we demonstrated that HbVs helped to maintain hemodynamics during severe PPH. Consequently, maternal prognosis was better in HbV infusion than in HES infusion alone. Similarly, RBC and PPP transfusion achieved excellent prognosis. The pregnant rabbits receiving RBC transfusion achieved a target value of at least 8.0 g/dL for the Hb concentration, which is recommended after RBC transfusion for PPH 29 . Further, HbV infusion gradually increased the Hb concentration similar to that in transfusion. In contrast to the change in Hb levels, Hct levels were lower in the HbV group than in the RBC/ PPP group. The HbV particles used in this study did not affect the Hct level because their particle size (particle diameter: 250-280 nm) was extremely small 30 . To the best of our knowledge, this is the first report of an appropriate animal model requiring massive transfusion according to actual clinical practice. HbV infusion maintained the CtO 2 levels to those of the systemic tissues throughout the experiment. Maternal CtO 2 levels > 8 vol% were consequently achieved, which ensured adequate CtO 2 for fetal survival 31 . However, HbV infusion yielded a fetus survival rate of only 56%. The in vivo half-life of HbVs (47-72 h) is shorter than that of RBCs 32 , which may affect the maternal prognosis beyond 6 h. In addition, carbonic anhydrase is not incorporated www.nature.com/scientificreports/ into HbVs; consequently, plasma HCO 3 levels were significantly lower in the HbV group than in the RBC/PPP group. This might be critical because some studies have reported that low HCO 3 − , particularly < 16 mmol/L, independently predicted short-term prognosis 33 . The lactate levels at baseline in the HbV group was statistically higher than that in other groups. The average value of baseline in HbV group was 3.3 mmol/L (< 4.0 mmol/L). This value was clinically within the normal range and did not suggest a lactic acidosis, because the pH levels in the same time point (baseline) were higher than 7.35. In addition, the lactate levels in HbV group were not increased during the experiment. We think that the statistically significant difference in the baseline lactate levels was not clinically relevant difference.
Chemically modified, cell-free HBOCs, including glutaraldehyde-polymerized and PEG-conjugated Hbs, have advanced to clinical trials 34,35 . Nevertheless, such cell-free HBOCs showed toxicities caused by extravasation, oxidative stress, hypertension, and vasoconstriction. In contrast, the current HbVs compartmentalized a concentrated Hb solution in the inner aqueous phase of liposomes, analogous to erythrocytes, leading to reduced toxicities of bared Hb such as hemolysis or acute renal dysfunction 9,18 . HbVs could be stored for at least 12 months and thus may be used in clinical settings where transfusions would be insufficient or unavailable 17 . In the current study, HbV administration had no scavenging effect on plasma NO 2 levels. HbVs are metabolized by macrophages in the reticuloendothelial system as well as aging RBCs. Cholesterols, phospholipids, and β-lipoprotein transiently increase, peaking at 1 or 2 days, and return to the baseline level at 7 days 36 . HbVs do not cross the placental barrier 37 . However, the optimal strategy for improving acute placental hypoxia or shock stress due to hemorrhagic shock is an important issue that needs further research in the management of severe PPH.
Our findings should be interpreted with caution in the context of the principal limitations of this study. First, in this study, the efficacy of HbVs in severe PPH was evaluated in an animal model. As such, we used the transfusion of RBC + PPP (1:1) to maintain hemodynamics in severe PPH, as a positive control. Therefore, the recommended values of fibrinogen (200-400 mg/dL) in PPH was not reached. In addition, albumin preparation alone was not used for a negative control. Thus, the applicability of the findings in humans and the improved protocol for severe PPH need to be further verified. Second, we need to investigate the late toxicities of HbVs beyond the acute setting, such as the maternal effect in the late phase due to huge-volume infusions of HbVs for severe PPH in humans. Some studies, including this study, have reported the safety of huge-volume infusions of HbVs in animal models 36,38 , but not in humans. Third, we did not precisely investigate the effects of HbVs, including intrauterine fetal resuscitation, in this study. A previous study reported the efficacy of HbVs for chronic placental hypoxia and improvement in fetal growth restriction in a rat pre-eclampsia model 37 . However, there are no reports on the efficacy of intrauterine resuscitation for low uteroplacental blood flow due to acute massive peripartum haemorrhage, including placental abruption. In this study, HbV and HES groups showed Controlling coagulopathy should be further investigated using other blood substitutes with haemostatic capacity, including PLT substitutes 39 , or the combined resuscitation fluids of crystalloids, colloids, or albumin. Lastly,  Table 4. Plasma levels of nitric oxide, creatinine, and free Hb at 60 min by group. Data are expressed as the mean ± standard deviation. The HbV group does not show a significant reduction in the NO 2 − level. In addition, creatinine levels are maintained within normal ranges. There is also no significant increase in free Hb levels. Hb hemoglobin. Creatinine (mg/dL) 0.9 ± 0.1 0.9 ± 0.2 0.9 ± 0.2 0.9 ± 0. Despite these limitations, this study provides important baseline evidence in developing initial fluid treatment with HbV infusion for severe PPH. The remarkable resuscitative effect of HbV treatment in the first few hours reduced the elevation of plasma lactate levels. Thus, prompt HbV infusion might help stabilize the patients' hemodynamics and enable their transportation to secondary or tertiary facilities.
In conclusion, HbVs effectively prevented lethal haemorrhagic shock due to severe PPH in pregnant rabbit models. These findings support that these blood substitutes are possible alternative modalities for the initial and immediate treatment of severe PPH, particularly in institutions with limited availability of blood products, until transportation to a secondary or tertiary facility. The concentration of cell-free heme is increased after RBC transfusion or HbV infusion, with the increase being greater after RBC transfusion than after HbV infusion. ‡ P < 0.05, The concentration of cell-free hemoglobin increased after RBC transfusion than after HbV infusion. Data shown are the mean ± standard deviation. HbV hemoglobin vesicles, HES hydroxyethyl starch, RBC red blood cell, RBC/ PPP red blood cells with platelet-poor plasma.