Next Article in Journal
Predictors of the Development of Protracted Bacterial Bronchitis following Presentation to Healthcare for an Acute Respiratory Illness with Cough: Analysis of Three Cohort Studies
Previous Article in Journal
Preterm Birth and Small-for-Gestational Age Neonates among Prepregnancy Underweight Women: A Case-Controlled Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Efficacy of Intraoperative Blood Salvage in Cerebral Aneurysm Surgery

1
Department of Neurosurgery, University Hospital Frankfurt, Goethe University, 60528 Frankfurt am Main, Germany
2
Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, Goethe University, 60528 Frankfurt am Main, Germany
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2021, 10(24), 5734; https://doi.org/10.3390/jcm10245734
Submission received: 18 September 2021 / Revised: 11 November 2021 / Accepted: 3 December 2021 / Published: 7 December 2021
(This article belongs to the Section Clinical Neurology)

Abstract

:
Background. The use and effectiveness of intraoperative cell salvage has been analyzed in many surgical specialties. Until now, no data exist evaluating the efficacy of intraoperative cell salvage in cerebral aneurysm surgery. Aim. To evaluate the efficacy and cost effectiveness of intraoperative cell salvage in cerebral aneurysm surgery. Methods. Data were collected retrospectively for all the patients who underwent cerebral aneurysm surgery at our institution between 2013 and 2019. Routinely, we apply blood salvage through autotransfusion. The cases were divided into a ruptured cerebral aneurysm group and a unruptured cerebral aneurysm group. Results. A total of 241 patients underwent cerebral aneurysm clipping. Of all the cerebral aneurysms, 116 were ruptured and 125 were unruptured and clipped electively. Age, location of the aneurysm, postoperative red blood cell count, intraoperative blood loss, and number of allogenic blood cell transfusions were statistically significantly different between the groups. The autotransfusion of salvaged blood could only be facilitated in eight cases with ruptured cerebral aneurysms and in none with unruptured cerebral aneurysms clipped electively (p < 0.01). Additionally, 35 patients with ruptured cerebral aneurysms and one patient with unruptured cerebral aneurysm required allogenic red blood cell transfusion after surgery, and 71 vs. 2 units of blood were transfused (p < 0.0001). In terms of cost effectiveness, a total of EUR 45,189 in 241 patients was spent to run the autotransfusion system, while EUR 13,797 was spent for allogenic blood transfusion. Conclusions. The use of cell salvage in patients with unruptured cerebral aneurysm, undergoing elective surgery, is not effective.

1. Introduction

Intraoperative cell salvage is widely used in many surgical specialties. Cell salvage seems to be efficacious in reducing the need for allogeneic red blood cell (RBC) transfusion in adults, and also in pediatric elective surgical procedures [1,2,3,4,5,6]. Although some studies report the advantage of using cell salvage in spine surgery, little evidence exists to support the use of intraoperative cell salvage in intracranial surgical procedures [7,8,9,10,11]. Overall, cohort studies including all types of neurosurgical procedures have reported rates of allogeneic transfusion ranging between 10 and 45% [12,13,14]. The rate of transfusion also varies depending on the procedure, from 10% in complex skull base neurosurgical procedures to 36% in patients with TBI, and as high as 45% in pediatric craniosynostosis surgery [13,15,16,17]. In patients undergoing open neurosurgical intervention for intracranial aneurysm, the occurrence of major intraoperative morbidity and complications was an independent risk factor for perioperative red blood cell (RBC) transfusion [18].
The aim of the present study was to evaluate the efficacy and cost effectiveness of intraoperative cell salvage and autotransfusion in cerebral aneurysm surgery.

2. Materials and Methods

Data, medical history, intraoperative protocols of all patients who underwent neurosurgical clipping for cerebral aneurysm repair between 2013 and 2019 in the University Hospital Frankfurt am Main were included in this retrospective study. Patients were stratified into two groups, depending on the cause of aneurysm surgery, in a ruptured or unruptured aneurysm group. Cell salvage using an autotransfusion system (CellSaver®, Haemonetics Co., Signy, Switzerland) was used in all surgical cases. Pre- and postoperative hemoglobin and hematocrit, intraoperative blood loss, duration of surgery, body mass index (BMI), habitual use of anticoagulants or non-steroidal anti-inflammatory drug (NSAID), amount of autotransfused RBCs and allogenic RBC transfusion were analyzed. Patient comorbidities were assessed according to the Charlson comorbidity index (CCI) [19].
Additionally, we looked at the costs directly associated with the routine use of autotransfusion in the setting of cerebral aneurysm clipping. Before treatment, cerebral angiography was performed in all patients and a decision in favor of clipping or coiling was made interdisciplinary. Blood transfusion was carried out in accordance with the recommendations of the Federal Medical Association; blood transfusion is recommended in all patients with a hemoglobin level below 6 g/dL. An RBC transfusion is only recommended in patients with a hemoglobin level between 6 and 8 g/dL, and limited compensation, such as coronary heart disease, heart failure and cerebrovascular disease. Furthermore, if the hemoglobin level is between 6 and 8 g/dL, blood should be given if obvious transfusion triggers, such as tachycardia, hypotension, ECG signs of ischemia and lactic acidosis, which reflect anemic hypoxia, are present.
Allogenic blood donation in patients with a hemoglobin level between 8 and 10 g/dL is only recommended with signs of anemic hypoxia.

Statistical Analysis

Comparison of important baseline characteristics and surgical parameters between the study groups was made using Fisher’s exact test for categorical variables. Tests for normal distribution were performed using the Shapiro–Wilk test. Nonparametric tests included the Mann–Whitney U and Kruskal–Wallis tests to compare groups of data that did not follow the normal distribution. p < 0.05 (2-tailed) was deemed significant. All calculations were made with standard commercial software (SPSS version 22, Chicago, IL, USA).

3. Results

In the study period, 241 patients underwent cerebral aneurysm surgery and were included in the present study. Out of all the aneurysms, 116 were ruptured prior to (emergency) surgery and 125 were unruptured, and these patients underwent elective clipping. Table 1 entails the main baseline characteristics, and the significant differences revealed regarding age, intraoperative blood loss, autologous RBC transfusion, postoperative RBC count, and amount of allogenic red blood cell transfusion between both groups.
The patients harboring an unruptured cerebral aneurysm were significantly younger compared to the patients undergoing cerebral aneurysm repair after subarachnoid hemorrhage (p = 0.03). The gender distribution in both groups, level of pre- and postoperative hematocrit, BMI, habitual use of anticoagulants or NSAIDs, hemoglobin level, and duration of surgery did not differ significantly. The amount of blood loss was significantly higher in patients with ruptured cerebral aneurysms compared to those with unruptured aneurysms (p < 0.0001). The number of comorbidities was significantly higher in patients with ruptured cerebral aneurysms (18% vs. 6.4%; p = 0.006). The likelihood of allogenic RBC transfusion was significantly higher in patients suffering from subarachnoid hemorrhage, undergoing cerebral aneurysm repair, compared to patients with unruptured cerebral aneurysm clipping. The autotransfusion of salvaged blood could be facilitated in eight patients with ruptured cerebral aneurysms compared to none of the patients with unruptured cerebral aneurysms (p = 0.007). The mean blood loss in these 8 patients was 1981.3 mL, compared to 416.4 mL in the remaining 108 patients without autotransfusion (p < 0.0001). The mean amount of blood salvaged and retransfused through the cell saver was 353.8 ± 226 mL. More autotransfused patients received additional RBC transfusion than those patients who were not autotransfused (p = 0.04). The BMI, CCI, and habitual use of anticoagulants or NSAID were not significantly different between the groups (Table 2).

Cost Analysis

The autotransfusion system was set up in all the surgical cases. Setting up the system was warranted in all the cases of the 125 patients undergoing elective clipping for aneurysm repair,. No patient in this group required autotransfusion of RBCs. The average cost, per procedure, of running the autotransfusion system was calculated to be EUR 189. Hence, a total of EUR 23,625 was invested in these cases. In the patients with aneurysmal subarachnoid hemorrhage, blood could be salvaged and autotransfused in eight patients; the cost of running the cell saver in the remaining 108 patients was EUR 20,412. Thus, overall, EUR 44,037 was invested without regaining blood for autotransfusion. At our institution, one unit of RBC costs EUR 86; thus, EUR 6106 was spent for 71 transfused units of RBCs.

4. Discussion

High intraoperative blood loss and consecutive allogenic RBC transfusion are associated with severe pathological complications, such as immunomodulation, infectious and allergic complications, transfusion-associated lung injury, and circulatory overload. These complications result in an increased risk of respiratory failure, prolonged intubation, acute respiratory distress syndrome, wound infection, sepsis, cardiac events, increased length of hospital stay, and death [20]. Blood salvage strategies in individual patients, such as preoperative correction of underlying coagulopathy and anemia, have been proposed to reduce allogenic blood donation (Meybohm P. et al., 2016, Ann Surg). Moreover, the use of intraoperative cell salvage demonstrated a significantly positive effect on reducing blood transfusion [1,3,5,6,7,8,9,10,11].
The beneficial effects of the use of intraoperative cell salvage have been investigated in many surgical specialties, such cardiac surgery, vascular surgery, spine and orthopedic surgical procedures, and many others [1,2,4,5,6,8,10] (Keding 2018 World J. Surg. Oncol.). According to the results of a recent meta-analysis published by Meyboehm et al., reviewing data from 47 studies, an overall reduction in allogeneic RBC transfusion, by a relative 39%, was observed by using washed cell salvaged blood, with the most significant result in orthopedic surgery, where the use of cell salvage reduced the exposure by 57% in 15 trials [21].
In neurosurgery, the overall RBC transfusion risk is increased in patients with aneurysmal subarachnoid hemorrhage, especially when intraoperative aneurysmal rupture occurs, or in patients with a lower preoperative hemoglobin level and higher WFNS classification [15,22]. Therefore, in accordance with our institutional standard of care, the use of intraoperative cell salvage was introduced for all patients selected for microsurgical aneurysm clipping, either electively or acutely. However, the beneficial effect of cell salvage has not been investigated until now.
Unfortunately, there are a lack of scientific data evaluating the efficacy of intraoperative cell salvage in cranial neurosurgery, except one publication from 1997. The authors of this publication concluded that the use of intraoperative cell salvage was safe and decreased the amount of allogenic blood transfusion [23]. Furthermore, almost 20% of the patients required transfusion and were operated on for different pathologies, such as unruptured cerebral aneurysms, meningiomas, and other benign and malignant brain tumors. In contrast, in our study, which only comprised patients undergoing aneurysm surgery, we found that there was hardly a need for RBC transfusion in non-ruptured compared to ruptured aneurysms (approximately 1% vs. 33%, respectively). Further, 0.8% of the patients in our investigated cohort, who were undergoing elective cerebral aneurysm surgery, required allogenic blood transfusion. Therefore, a direct comparison of our patients with the previously published data is not candidly possible.
Here, we found significant differences between both groups. First of all, the age was significantly higher in patients with ruptured cerebral aneurysms, and the ruptured aneurysms were more often located in the posterior circulation. Furthermore, there was an increase in comorbidities among the patients with SAH, undergoing emergency aneurysm clipping. The body weight, and habitual use of anticoagulants and NSIAD were almost similar in both groups. The RBCs, hemoglobin level, and hematocrit level were reduced in patients suffering from SAH. The reason for this could be the initial pretreatment with a fluid donation before the first blood test and before undergoing surgery. As expected, the amount of intraoperative blood loss was significantly higher in patients with ruptured cerebral aneurysm. Autologous blood transfusion could be facilitated in only eight patients. Due to the principle of cell salvage, consisting of blood collection, separation, washing, and filtrating, only a small part of the lost blood can be collected and retransfused [24].
Despite the abovementioned advantages of cell salvage, there are many potential complications associated with this technique, such as non-immune hemolysis, air embolus, febrile non-hemolytic transfusion reactions, mistransfusion, coagulopathy, contamination with drugs, cleaning solutions and infectious agents, and incomplete washing, leading to contamination with activated leucocytes, cytokines, and other microaggregates [25].
Since the cell saver is very rarely used in aneurysm surgery, the main problems are associated with the handling of the technique, cleaning solution, and adequate transfer. Suctioning of RBCs may cause sheer stress injury, which can result in hemolysis or damaged RBCs, and, therefore, a reduction in the return of RBCs [26,27].
An important reason for the difference in the need for transfusion between both patient groups is most likely the significant volume of blood loss. Patients with ruptured aneurysms, who are undergoing repair, are at a much higher risk for substantial intraoperative blood loss due to intraoperative rupture and renewed bleeding than patients without previous subarachnoid hemorrhage. Our findings underline the assumption that the use of cell salvage is beneficial in cases with an anticipated blood loss of more than 1000 mL.
Nevertheless, high blood loss cannot be predicted. The cell saver is a safety measure and, although only used in a few cases, reduces the administration of allogenic blood. A cost analysis of safety measures is always difficult and should primarily be viewed as a necessary measure to protect the patient. The cost of cell salvage is an important consideration, and must take into account the financial and biological benefits of autologous transfusion. Previously published data remain elusive as to whether the use of cell salvage is associated with increased or decreased costs [5,7,26,27,28,29]. Reviewing our data, we conclude that the use of cell salvage only in patients with unruptured cerebral aneurysm is not effective. In elective surgery of aneurysms, there is often no significant blood loss due to the presence of proximal control of the parent artery. In patients undergoing surgery for unruptured aneurysms, EUR 23,189 was spent for less than 1% of the patients requiring transfusion, and autotransfusion could not be facilitated to spare allogenic RBC transfusion. This underscores the limited value of regular autotransfusion in this patient group.
The effectiveness of a safety measure cannot primarily be related to costs alone. It has been shown that the use of a cell saver brings benefits and, even if rarely used, leads to the saving of allogenic blood donations.

5. Conclusions

The use of cell salvage in patients with unruptured cerebral aneurysms, undergoing elective surgery, is not effective. Further prospective studies are necessary to evaluate the effect of cell salvage in patients with ruptured cerebral aneurysms.

Author Contributions

B.B.: study enrollment, writing and formatting manuscript, submission; F.G.: interpretation of the data; B.B., F.G., E.A., U.S., S.-Y.W., D.D. and J.K.: data collection; V.S.: Supporting, supervising the study; C.S.: follow-up examination, senior surgeon. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board of the University of Frankfurt am Main.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data available on request from the authors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Klein, A.A.; Nashef, S.A.; Sharples, L.; Bottrill, F.; Dyer, M.; Armstrong, J.; Vuylsteke, A. A randomized controlled trial of cell salvage in routine cardiac surgery. Anesth. Analg. 2008, 107, 1487–1495. [Google Scholar] [CrossRef]
  2. Odak, S.; Raza, A.; Shah, N.; Clayson, A. Clinical efficacy and cost effectiveness of intraoperative cell salvage in pelvic trauma surgery. Ann. R. Coll. Surg. Engl. 2013, 95, 357–360. [Google Scholar] [CrossRef] [Green Version]
  3. Carless, P.A.; Henry, D.A.; Moxey, A.J.; O’Connell, D.; Brown, T.; Fergusson, D.A. Cell salvage for minimising perioperative allogeneic blood transfusion. Cochrane Database Syst. Rev. 2010, CD001888. [Google Scholar] [CrossRef]
  4. Bowley, D.M.; Barker, P.; Boffard, K.D. Intraoperative blood salvage in penetrating abdominal trauma: A randomised, controlled trial. World J. Surg. 2006, 30, 1074–1080. [Google Scholar] [CrossRef]
  5. Damgaard, S.; Steinbrüchel, D.A. Autotransfusion with cell saver for off-pump coronary artery bypass surgery: A randomized trial. Scand. Cardiovasc. J. SCJ 2006, 40, 194–198. [Google Scholar] [CrossRef] [PubMed]
  6. Elawad, A.A.; Ohlin, A.K.; Berntorp, E.; Nilsson, I.M.; Fredin, H. Intraoperative autotransfusion in primary hip arthroplasty. A randomized comparison with homologous blood. Acta Orthop. Scand. 1991, 62, 557–562. [Google Scholar] [CrossRef]
  7. Liang, J.; Shen, J.; Chua, S.; Fan, Y.; Zhai, J.; Feng, B.; Cai, S.; Li, Z.; Xue, X. Does intraoperative cell salvage system effectively decrease the need for allogeneic transfusions in scoliotic patients undergoing posterior spinal fusion? A prospective randomized study. Eur. Spine J. 2015, 24, 270–275. [Google Scholar] [CrossRef] [PubMed]
  8. Djurasovic, M.; McGraw, K.E.; Bratcher, K.; Crawford, C.H., III; Dimar, J.R., II; Puno, R.M.; Glassman, S.D.; Owens, R.K., II; Carreon, L.Y. Randomized trial of Cell Saver in 2- to 3-level lumbar instrumented posterior fusions. J. Neurosurg. Spine 2018, 29, 582–587. [Google Scholar] [CrossRef] [PubMed]
  9. Reitman, C.A.; Watters, W.C.; Sassard, W.R. The Cell Saver in adult lumbar fusion surgery: A cost-benefit outcomes study. Spine 2004, 29, 1580–1583, discussion 1584. [Google Scholar] [CrossRef] [PubMed]
  10. Oliveira, J.A.A.; Façanha Filho, F.A.M.; Fernandes, F.V.; Almeida, P.C.; de Oliveira, V.F.; Lima Verde, S.R. Is cell salvage cost-effective in posterior arthrodesis for adolescent idiopathic scoliosis in the public health system? J. Spine Surg. 2017, 3, 2–8. [Google Scholar] [CrossRef] [Green Version]
  11. Gakhar, H.; Bagouri, M.; Bommireddy, R.; Klezl, Z. Role of intraoperative red cell salvage and autologus transfusion in metastatic spine surgery: A pilot study and review of literature. Asian Spine J. 2013, 7, 167–172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Linsler, S.; Ketter, R.; Eichler, H.; Schwerdtfeger, K.; Steudel, W.-I.; Oertel, J. Red blood cell transfusion in neurosurgery. Acta Neurochir. 2012, 154, 1303–1308. [Google Scholar] [CrossRef]
  13. Rolston, J.D.; Han, S.J.; Lau, C.Y.; Berger, M.S.; Parsa, A.T. Frequency and predictors of complications in neurological surgery: National trends from 2006 to 2011. J. Neurosurg. 2014, 120, 736–745. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Vassal, O.; Desgranges, F.; Tosetti, S.; Burgal, S.; Dailler, F.; Javouhey, E.; Mottolese, C.; Chassard, D. Risk factors for intraoperative allogeneic blood transfusion during craniotomy for brain tumor removal in children. Paediatr. Anaesth. 2016, 26, 199–206. [Google Scholar] [CrossRef] [PubMed]
  15. Luostarinen, T.; Lehto, H.; Skrifvars, M.B.; Kivisaari, R.; Niemelä, M.; Hernesniemi, J.; Randell, T.; Niemi, T. Transfusion Frequency of Red Blood Cells, Fresh Frozen Plasma, and Platelets During Ruptured Cerebral Aneurysm Surgery. World Neurosurg. 2015, 84, 446–450. [Google Scholar] [CrossRef]
  16. Mebel, D.; Akagami, R.; Flexman, A.M. Use of Tranexamic Acid Is Associated with Reduced Blood Product Transfusion in Complex Skull Base Neurosurgical Procedures: A Retrospective Cohort Study. Anesth. Analg. 2016, 122, 503–508. [Google Scholar] [CrossRef]
  17. Boutin, A.; Chassé, M.; Shemilt, M.; Lauzier, F.; Moore, L.; Zarychanski, R.; Griesdale, D.; Desjardins, P.; Lacroix, J.; Fergusson, D.; et al. Red Blood Cell Transfusion in Patients With Traumatic Brain Injury: A Systematic Review and Meta-Analysis. Transfus. Med. Rev. 2016, 30, 15–24. [Google Scholar] [CrossRef] [PubMed]
  18. Seicean, A.; Alan, N.; Seicean, S.; Neuhauser, D.; Selman, W.R.; Bambakidis, N.C. Risks associated with preoperative anemia and perioperative blood transfusion in open surgery for intracranial aneurysms. J. Neurosurg. 2015, 123, 91–100. [Google Scholar] [CrossRef] [Green Version]
  19. Charlson, M.E.; Pompei, P.; Ales, K.L.; MacKenzie, C.R. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J. Chronic Dis. 1987, 40, 373–383. [Google Scholar] [CrossRef]
  20. Kisilevsky, A.; Gelb, A.W.; Bustillo, M.; Flexman, A.M. Anaemia and red blood cell transfusion in intracranial neurosurgery: A comprehensive review. Br. J. Anaesth. 2018, 120, 988–998. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Meybohm, P.; Choorapoikayil, S.; Wessels, A.; Herrmann, E.; Zacharowski, K.; Spahn, D.R. Washed cell salvage in surgical patients: A review and meta-analysis of prospective randomized trials under PRISMA. Medicine 2016, 95, e4490. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Le Roux, P.D. Participants in the International Multi-disciplinary Consensus Conference on the Critical Care Management of Subarachnoid Hemorrhage. Anemia and transfusion after subarachnoid hemorrhage. Neurocritical Care 2011, 15, 342–353. [Google Scholar] [CrossRef] [PubMed]
  23. Cataldi, S.; Bruder, N.; Dufour, H.; Lefevre, P.; Grisoli, F.; François, G. Intraoperative autologous blood transfusion in intracranial surgery. Neurosurgery 1997, 40, 765–771, discussion 771-2. [Google Scholar] [CrossRef] [PubMed]
  24. Ashworth, A.; Klein, A.A. Cell salvage as part of a blood conservation strategy in anaesthesia. Br. J. Anaesth. 2010, 105, 401–416. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Fong, J.; Gurewitsch, E.D.; Kang, H.-J.; Kump, L.; Mack, P.F. An analysis of transfusion practice and the role of intraoperative red blood cell salvage during cesarean delivery. Anesth. Analg. 2007, 104, 666–672. [Google Scholar] [CrossRef] [PubMed]
  26. Yazer, M.H.; Waters, J.H.; Elkin, K.R.; Rohrbaugh, M.E.; Kameneva, M.V. A comparison of hemolysis and red cell mechanical fragility in blood collected with different cell salvage suction devices. Transfusion 2008, 48, 1188–1191. [Google Scholar] [CrossRef] [PubMed]
  27. Waters, J.H.; Williams, B.; Yazer, M.H.; Kameneva, M.V. Modification of Suction-Induced Hemolysis During Cell Salvage. Anesth. Analg. 2007, 104, 684–687. [Google Scholar] [CrossRef] [PubMed]
  28. Waters, J.R.; Meier, H.H.; Waters, J.H. An economic analysis of costs associated with development of a cell salvage program. Anesth. Analg. 2007, 104, 869–875. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Goel, P.; Pannu, H.; Mohan, D.; Arora, R. Efficacy of cell saver in reducing homologous blood transfusions during OPCAB surgery: A prospective randomized trial. Transfus. Med. 2007, 17, 285–289. [Google Scholar] [CrossRef] [PubMed]
Table 1. Patients’ characteristics.
Table 1. Patients’ characteristics.
VariablesRupturedUnrupturedp-Value
No. of patients116125
Age (mean)55.4 ± 14.352 ± 110.003
Sex
Male42 (36.2%)39 (31.2%)0.4
Aneurysm location
Anterior circulation100 (86.2%)121 (96.8%)0.004
Posterior circulation16 (13.8%)4 (3.2%)
Hunt & Hess Grade
I26 (22.4%)
II19 (16.4%)
III23 (19.8%)
IV25 (21.5%)
V23 (19.8%)
Red blood cells (/pL)
Preoperative4.2 ± 0.44.5 ± 0.40.2
Postoperative3.5 ± 0.53.8 ± 0.50.009
Hematocrit (%)
Preoperative37.6 ± 3.940.1 ± 4.20.1
Postoperative31.4 ± 4.933.3 ± 4.80.1
Hemoglobin (g/dL)
Preoperative12.9 ± 1.513.7 ± 1.20.1
Postoperative10.6 ± 1.611.4 ± 1.40.2
Median BMI25260.4
Median CCI210.05
CCI 0-295 (82%)117 (94%)0.006
NSAID4 (3.4%)5 (4%)1.0
Anticoagulation (n/%)11 (9.4%)7 (5.6%)0.3
Intraoperative blood loss (mL)601 ± 809244.1 ± 1970.00001
Operation time (min)200 ± 53.9201.5 ± 50.10.7
Allogenic RBC transfusion(n [%])35 (32.4%)1 (0.8%)0.0001
Allogenic blood units (n)71 (61.2%)2 (1.6%)
Autotransfusion (n)8 (6.9%)00.007
Costs for CS setup€21,924 €23,625
Table 2. Data of patients in the ruptured group stratified by RBC retransfusion and no retransfusion.
Table 2. Data of patients in the ruptured group stratified by RBC retransfusion and no retransfusion.
CellsaverNo Cellsaverp Value
No. of patients8108
Age (mean)52.4 y56.1 y0.4
Sex
Male2 (25%)40 (37%)0.7
Female6 (75%)68 (63%)
Anterior circulation6 (75%)95 (88%)0.3
Posterior circulation2 (25%)14 (13%)
Hunt & Hess Grade
I1 (12.5%)25 (23.1%)1.0
II1 12.5%)18 (16.7%)1.0
III3 (37.5%)21(19.4%)0.15
IV2 (25%)22 (20.3%)0.7
V1 (12.5%)22 (20.4%)1.0
Red blood cells (/pL)
Preoperative4.0 ± 0.44.2 ± 0.40.8
Postoperative3.2 ± 0.33.5 ± 0.50.5
Hematocrit (%)
Preoperative37.8 ± 4.137.8 ± 3.80.2
Postoperative29.0 ± 3.131.5 ± 5.00.4
Hemoglobin (g/dL)
Preoperative12.1 ± 1.513.0 ± 1.50.2
Postoperative9.4 ± 1.310.7 ± 1.70.9
Median BMI25250.4
Median CCI220.5
CCI 0-27 (87.5%)88 (81.5%)1.0
NSAID04 (3.7%)
Anticoagulation (n/%)011 (10.2%)
Intraoperative blood loss (mL)1981.3 ± 1587.4416.4 ± 315.00.00001
Operation time (min)182.5 ± 51.1200.8 ± 53.90.4
Allogenic blood cell transfusion (n [%])5 (62.5%)30 (26.9%)0.04
Allogenic RBC units (n)2645
Amount of autotransfusion (mL)353.8±2260
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Behmanesh, B.; Gessler, F.; Adam, E.; Strouhal, U.; Won, S.-Y.; Dubinski, D.; Seifert, V.; Konczalla, J.; Senft, C. Efficacy of Intraoperative Blood Salvage in Cerebral Aneurysm Surgery. J. Clin. Med. 2021, 10, 5734. https://doi.org/10.3390/jcm10245734

AMA Style

Behmanesh B, Gessler F, Adam E, Strouhal U, Won S-Y, Dubinski D, Seifert V, Konczalla J, Senft C. Efficacy of Intraoperative Blood Salvage in Cerebral Aneurysm Surgery. Journal of Clinical Medicine. 2021; 10(24):5734. https://doi.org/10.3390/jcm10245734

Chicago/Turabian Style

Behmanesh, Bedjan, Florian Gessler, Elisabeth Adam, Ulrich Strouhal, Sae-Yeon Won, Daniel Dubinski, Volker Seifert, Juergen Konczalla, and Christian Senft. 2021. "Efficacy of Intraoperative Blood Salvage in Cerebral Aneurysm Surgery" Journal of Clinical Medicine 10, no. 24: 5734. https://doi.org/10.3390/jcm10245734

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop