Skip to main content

The association between admission mean corpuscular volume and preoperative deep venous thrombosis in geriatrics hip fracture: a retrospective study

Abstract

Objective

This study evaluated the association between admission MCV and preoperative deep vein thrombosis (DVT) in geriatric hip fractures.

Methods

Older adult patients with hip fractures were screened between January 2015 and September 2019. The demographic and clinical characteristics of the patients were collected at the largest trauma center in northwest China. MCV was measured at admission and converted into a categorical variable according to the quartile. Multivariate binary logistic regression and generalized additive model were used to identify the linear and nonlinear association between MCV and preoperative DVT. Analyses were performed using EmpowerStats and the R software.

Results

A total of 1840 patients who met the criteria were finally enrolled and divided into four groups according to their MCV levels. The mean MCV was 93.82 ± 6.49 (80.96 to 105.91 fL), and 587 patients (31.9%) were diagnosed with preoperative DVT. When MCV was a continuous variable, the incidence of preoperative DVT increased with mean corpuscular volume. In the fully adjusted model, admission MCV was positively correlated with the incidence of preoperative DVT (OR: 1.03; 95% CI: 1.01–1.05; P = 0.0013). After excluding the effect of other factors, each additional 1fL of MCV increased the prevalence of preoperative DVT by 1.03 times as a continuous variable.

Conclusion

MCV was linearly associated with preoperative DVT in geriatric patients with hip fractures and could be considered a predictor of DVT risk. The MCV may contribute to risk assessment and preventing adverse outcomes in the elderly.

Study registration

This study is registered on the website of the Chinese Clinical Trial Registry (ChiCTR: ChiCTR2200057323).

Peer Review reports

Introduction

Hip fractures are one of the most common types of fractures in the elderly population [1]. The global number of hip fractures is expected to increase from 1.26 million in 1990 to 4.5 million by 2050 [1]. Meanwhile, deep venous thrombosis (DVT) is the most dangerous complication of hip fracture. Medical studies have generally shown that DVT can lead to pulmonary embolism and even death in patients with fracture trauma [2,3,4]. In addition, functional recovery in patients with DVT will be delayed, resulting in heavier financial and treatment burdens than those without DVT [5]. Therefore, it is of great significance for clinical work to understand the risk factors and epidemiological characteristics of deep vein thrombosis and prevent the occurrence of deep vein thrombosis.

The incidence of preoperative DVT is higher in elderly patients with hip fractures due to senility, medication, and underlying diseases [6,7,8,9]. Thrombosis formation is a complex process that requires the combined action of red blood cells, platelets, and white blood cells, which has been widely recognized. In recent years, more and more basic researches support red blood cell plays an essential role in thrombus formation. The red blood cell indexes in routine blood tests include MCV, MCH, and MCHC, which were used to determine red blood cells' size and hemoglobin content. MCV measures the mean size of red blood cells and is proportional to hematocrit [10]. It has been reported that high MCV was correlated with high mortality in patients with acute myocardial infarction, acute decompensated heart failure, and consecutive patients subjected to percutaneous coronary intervention [11,12,13]. Zhang et al. found that higher admission MCV was an independent predictor of long-term major adverse cardiovascular events [14]. They believe that the possible reason is that the high MCV value leads to the imbalance between the cytoplasm and the nucleus, hinders the flow of red blood cells with poor flexibility through the microcirculation, and damages the antioxidant properties of the red blood cell membrane. In addition, Weisel et al. pointed out that the increase of MCV and erythrocyte membrane hardness would lead to the change of rheological effect, which promotes the adhesion of platelets to the vascular wall, enhances the interaction between platelets and endothelial cells, and enhances the possibility of thrombosis [15].

Unfortunately, clinical studies on the association between admission MCV and preoperative DVT are limited to our knowledge. In addition, the incidence of DVT increases with age, and the relationship has not been explored in the elderly with hip fractures.

Therefore, we aimed to explore the relationship between MCV at admission and preoperative DVT in elderly with a hip fracture through this retrospective study, which will help surgeons to ensure surgical safety, reduce mortality, help individualized risk assessment, and prevent adverse outcomes.

Materials and methods

Study design

In this retrospective cohort study, we recruited older adults who had a hip fracture from 1 Jan 2015 to 30 Sep 2019 at the largest trauma center in Northwest China.

This retrospective study was approved by the Ethics Committee of Xi’an Honghui Hospital (No. 202201009). All patients provided informed consent. All human-related procedures followed the 1964 Declaration of Helsinki and its later amendments. The study has been reported according to the STROCSS 2021 guidelines [16].

Participants

Demographic and clinical data of the patients were obtained from their original medical records. The inclusion criteria were as follows:

(1) Age ≥ 65 years, (2) X-ray or computed tomography diagnosis of the femoral neck, intertrochanteric, or subtrochanteric fracture, (3) patients who were receiving surgical or conservative treatment in the hospital. Informed consent has been signed and agreed to receive anticoagulant therapy to prevent thrombosis, (4) patients with hip fractures were evaluated by a senior orthopedic surgeon based on physical examination and imaging (including X-ray, CT, or MRI).

Exclusion criteria were as follows:

(1) No preoperative ultrasound result on DVT, (2) no MCV results at admission.

Hospital treatment

Patients were examined using blood tests to prepare for surgery. Prophylaxis for DVT was initiated at admission. Mechanical thromboprophylaxis (foot intermittent pneumatic compression sleeve, 20 min twice a day) was used to prevent DVT. Low molecular weight heparin was injected subcutaneously for patients without contraindications to prevent DVT.

Endpoint events

The endpoint event in this study was DVT before operation. We used Doppler ultrasonography to diagnose the DVT. The diagnostic criteria are the presence of a constant intraluminal filling defect. Patients were examined preoperatively. All patients underwent ultrasonography of bilateral lower extremities the day before the scheduled surgery.

Variables

The variables collected in this study were as follows: age, sex, occupation, history of allergy, injury mechanism, fracture classification, hypertension, diabetes, coronary heart disease (CHD), arrhythmia, hemorrhagic stroke, ischemic stroke, cancer, associated injuries, dementia, chronic obstructive pulmonary disease (COPD), hepatitis, gastritis, age-adjusted Charlson comorbidity index (aCCI), time from injury to admission, admission glomerular filtration rate (GFR), admission D-dimer and MCV.

The dependent variable was preoperative DVT, and the independent variable was the MCV. Other variables were potentially confounding factors.

Statistics analysis

Continuous variables are reported as mean ± standard deviation (SD) (Gaussian distribution) or median (min, max) (Skewed distribution), and categorical variables are given as frequencies and percentages. We used χ2 (categorical variables), the One-way ANOVA test (normal distribution), or the Kruskal-Whallis H test (skewed distribution) to test for differences among different MCV (quartile). We used a univariate and multivariate binary logistic regression model to test the association between MCV and preoperative DVT with three distinct models by stand linear regression. Model 1 was not adjusted for covariates. Model 2 was a minimally adjusted model with only sex adjusted. Model 3 was a fully adjusted model with meaningful variables in univariate analyses and some bias factors (such as diabetes, hypertension and ischemic stroke) generated by univariate analyses.

To account for the nonlinear relationship between MCV and preoperative DVT, we used a generalized additive model and the smooth curve fitting (penalized spline method) to address nonlinearity. Besides, the two-piecewise binary logistic regression model was also used to explain the nonlinearity further. To test the robustness of our results, we performed a sensitivity analysis. We converted MCV into a categorical variable according to the quartile. We calculated the P for trend to verify the results of MCV as the continuous variable and to examine the possibility of nonlinearity.

All analyses were performed using statistical software packages R. (http://www.R-project.org, R Foundation) and EmpowerStats (http://www. empowerstats.com, X&Y Solutions Inc., Boston, MA, USA). Odds ratios (OR) and 95%CI were calculated. A P-value < 0.05 (two-sided) was considered to represent statistical significance.

Results

Patient characteristics

A total of 1840 patients were included in the study according to the inclusion and exclusion criteria from 1 Jan 2015 to 30 Sep 2019 (Fig. 1). We divided the patients into four groups according to MCV level. The general information of patients is shown in Table 1. Among them, 558 were male, and 1282 were female, with a mean age of 79.40 ± 6.88 (72.52–86.28 years). The injury mechanism included 1773 (96.36%) falls, 53 (2.88%) accidents, and 14 (0.76%) multiple injuries. There were 1106 intertrochanteric fractures, 701 femoral neck fractures, and 33 subtrochanteric fractures. Multiple injuries were in 131 patients. Combined medical diseases: 950 cases of CHD, 924 cases of hypertension, 367 cases of diabetes, 32 cases of hemorrhagic stroke, and 583 cases of arrhythmia. No pulmonary embolism occurred in the preoperative period.

Fig. 1
figure 1

The flow chart of including patient cohort

Table 1 The Demographic and clinical characteristics according to MCV quartiles

Univariate analysis of the association between variates and DVT

Based on the results of univariate analysis (Table 2), according to the criteria of P < 0.1, we found six confounding factors: sex, fracture classification, multiple injuries, time to operation, dementia, and admission D-dimer.

Table 2 Effects of factors on DVT measured by univariate analysis

Multivariate analysis between preoperative MCV and DVT

We used a binary logistic regression model to assess the correlation between admission MCV and preoperative DVT incidence. We showed the non-adjusted model, the minimally-adjusted model, and the fully-adjusted model in Table 3. In the unadjusted model, MCV was associated with preoperative DVT incidence (OR: 1.02; 95% CI: 1.01–1.04; P = 0.0067). In the minimally-adjusted model, the results were positively correlated (OR: 1.02; 95% CI: 1.01–1.04; P = 0.0041). The results were positively correlated in the fully adjusted model (OR: 1.03; 95% CI: 1.01–1.05; P = 0.0013).

Table 3 Univariate and multivariate results by linear regression

Curve fitting and analysis of threshold effect

As shown in Fig. 2, there was a linear association between admission MCV and DVT after adjusting for confounding factors. We compared the binary logistic regression model (by stand linear regression) and generalized additive model (two-piecewise linear regression) to explain this association (Table 4), and we observed the inflection point value was 97.9 in the model. However, the P for the log-likelihood ratio test was 0.110. It was better to explain the relationship between MCV and DVT by the linear association at present.

Fig. 2
figure 2

Curve fitting between preoperative MCV and DVT. They were adjusted for sex, fracture classification, multiple injuries, dementia, and time to operation, admission D-dimer, hypertension, diabetes and ischemic stroke

Table 4 The binary logistic regression model (by stand linear regression) and generalized additive model of preoperative MCV and DVT

Discussion

First, this retrospective study found that higher MCV was a risk factor for preoperative DVT. There was a linear association between the admission of MCV and preoperative DVT in geriatric patients with hip fractures. Further, when analyzing as a continuous variable, each additional 1fL of MCV increased the prevalence of preoperative DVT by 1.03 times after excluding the effect of other confounding factors.

As far as we know, Previous studies have shown that the incidence of preoperative lower extremity deep venous thrombosis in elderly patients with hip fracture in China is about 30% [17, 18], similar to our results (31.9%). However, Cho [6] et al. from South Korea reported that 152 elderly patients with a minimum incidence of 2.6% received ultrasound or CT scans, which they attributed to early hospitalization ( 90.1% within three days after injury). This is not easy to achieve in Northwest China. The health resource supply shortage, uneven distribution, and the lack of relevant knowledge of patients lead to delayed admission to hospitals for treatment [19]. Vascular injury caused by fracture activates the coagulation system, and long-term bedridden fixation after fracture can lead to venous congestion and increase the possibility of thrombosis. In addition, the incidence of preoperative DVT in patients with hip fracture is also related to the diagnosis method (including venography, computed tomography, ultrasonography, D-dimer, etc.). Relevant literature points out that the diagnostic rate of different diagnostic methods is from 2.6% to 60% [20]. We used Doppler ultrasound to diagnose deep vein thrombosis, which may impact the incidence of DVT.

This is the first retrospective study on the association between admission MCV and preoperative DVT in geriatrics with hip fractures. Previous studies suggested age, sex, hyperlipidemia, dementia, movement disorder, bedridden time, diabetes, pulmonary disease, d-dimer, and kidney disease as risk factors for developing DVT after fractures [9, 21,22,23,24]. Meantime, many studies have found that laboratory indicators of blood routine, such as RDW (red cell distribution width), blood monocyte count, and hematocrit, were risk factors for postoperative deep vein thrombosis in patients with hip fracture [25,26,27]. There was limited understanding of the risk factors of preoperative DVT after hip fractures, especially the red blood cell indices. Other studies evaluated the relationship between MCV at admission and adverse events in patients with hip fractures and showed varied and conflicting results. The following study by Braekkan SK et al. [28]. found that elevated mean corpuscular volume at admission was not associated with postoperative adverse outcomes in patients with hip fracture. By contrast, Eischer L et al. demonstrated that high hematocrit is a risk factor for Venous thromboembolism (VTE) recurrence in women [27]. Rezende SM et al. found an association between high MCV (above 101.5 fL) and high MCH (above 2.15 fmol) and venous thrombosis [26]. However, for hip fracture patients waiting for surgery, there is limited information on the association between high MCV at admission and preoperative deep vein thrombosis. In this study, we found that MCV was associated with preoperative DVT, and there was a linear relationship between the two factors.

MCV is part of the whole blood count. The calculation method of MCV is the ratio of hematocrit to red blood cell count per liter of blood (Hematocrit is directly proportional to the MCV). They are mainly used for the clinical diagnosis of anemia. According to the relationship between MCV and hematocrit [10] and growing evidence from basic research, we found a potential biological mechanism of high MCV causing DVT. (1) Red blood cells have a typical rheological effect during blood coagulation: The circulation of red blood cells and platelets in blood vessels has specific rules, and red blood cells preferentially move to the center of blood vessels when circulating in blood vessels, resulting in the movement of platelets to endothelial cells (margination), where platelets and blood vessel walls can interact and form a temporary blockage when injured [29,30,31]. When MCV increases, hematocrit also increases; one consequence of elevated hematocrit is increased margination of platelets, enhancing the interaction between platelets and endothelial cells and promoting thrombosis. (2) MCV is inversely proportional to the deformability of red blood cells. The excellent deformability of red blood cells is mainly the result of their double concave shape, especially the high surface area and volume ratio. Therefore, with the increase of MCV, the degeneration ability of red blood cells decreases, and the rigidity of the red blood cell membrane increases [32, 33], which makes it difficult for red blood cells to squeeze through the microvascular system and strengthens the movement of platelets to the edge, thus promoting the formation of thrombus. The second possibility is that elevated MCV will increase blood viscosity, and viscosity increases exponentially with MCV in large vessels [34], which hinders the speed of blood flow. These hemorheological effects of red blood cells may be a factor that promotes thrombosis because blood flow damage is a component of Virchow’s triad that explains the pathophysiological mechanism of thrombosis through a combination of hypercoagulability, blood flow disorders, and endothelial damage [10].

Furthermore, MCV was affected by many factors, such as age, genetic conditions (such as sickle cell disease and thalassemia), malnutrition (iron, folic acid, or vitamin B12 deficiency), and inflammation [35, 36]. Our study mainly discussed hip fractures in geriatrics. Recently, Hoffmann et al. showed a mean age-related increase in MCV of 6.6% over the entire age range [37], and the MCV was more significant in the elderly. So MCV could be considered a predictor for the risk of DVT.

MCV can be observed in routine blood tests. A blood routine test is a cheap and readily available detection method in most hospitals. Elderly patients with hip fractures after admission were generally required to have a routine blood test, which contains the MCV results. We can use MCV to predict preoperative DVT. MCV can also be used as an indicator in the preoperative DVT prediction model. However, the causal relationship between MCV and DVT needs further exploration. Thus, future research and clinical work should assess the potential role of MCV in preventing and treating thrombosis.

This study has the following notable strengths: First, with a large sample size, we recruited 1840 patients who meet the criteria. To the best of our knowledge, this is the first study of the correlation between admission MCV and preoperative DVT in elderly with hip fractures. Second, we corrected various factors and explored the linear and curvilinear relationships. Through multiple methods, we determine the reliability of the linear relationship. However, the study still has some limitations. (1) We use univariate analysis to select covariates for the model, which is prone to bias. Confounders are associated with both the “independent” and “dependent” variables. We only considered covariates associated with the outcomes. (2) Our data came from one hospital in one region, and there may be selection bias in the study population. Therefore, the extrapolation of the results needed to be confirmed in other populations.

Conclusion

Taken together, the MCV was associated linearly with preoperative DVT in geriatric patients with hip fractures, and it could be considered a predictor of DVT risk. Further study on the factors that affect the formation of preoperative DVT in geriatrics with hip fractures is conducive to formulating a more appropriate diagnosis and treatment plan.

Availability of data and materials

Xi’an Honghui Hospital implemented the data. According to relevant regulations, the data could not be shared but could request from the corresponding author.

References

  1. Cauley J, et al. Geographic and ethnic disparities in osteoporotic fractures. Nat Rev Endocrinol. 2014;10(6):338–51.

    Article  PubMed  Google Scholar 

  2. Drescher F, et al. Aspirin versus anticoagulation for prevention of venous thromboembolism major lower extremity orthopedic surgery: a systematic review and meta-analysis. J Hosp Med. 2014;9(9):579–85.

    Article  PubMed  Google Scholar 

  3. Forster R, Stewart M. Anticoagulants (extended duration) for prevention of venous thromboembolism following total hip or knee replacement or hip fracture repair. Cochrane Database Syst Rev. 2016;3(3):CD004179.

    PubMed  Google Scholar 

  4. Veronese N, Maggi S. Epidemiology and social costs of hip fracture. Injury. 2018;49(8):1458–60.

    Article  PubMed  Google Scholar 

  5. Trivedi N, et al. The incremental cost of inpatient venous thromboembolism after hip fracture surgery. J Orthop Trauma. 2020;34(4):169–73.

    Article  PubMed  Google Scholar 

  6. Cho Y, et al. Preoperative incidence of deep vein thrombosis after hip fractures in Korean. Clin Orthop Surg. 2015;7(3):298–302.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Zhang L, et al. Incidence and risk factors of admission deep vein thrombosis in patients with traumatic fracture: a multicenter retrospective study. Clin Appl Thromb Hemost. 2023;29:10760296231167144.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Pan S, et al. Preoperative prevalence and risk factors for calf muscular vein thrombosis in elderly patients with hip fracture. Orthop Surg. 2023;15(7):1806–13.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Yao W, et al. Association between hyperglycemia on admission and preoperative deep venous thrombosis in patients with femoral neck fractures. BMC Musculoskelet Disord. 2022;23(1):899.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  10. Maner, B.S. and L. Moosavi, Mean Corpuscular Volume, in StatPearls. 2022: Treasure Island (FL).

  11. Franczuk P, et al. Could an analysis of mean corpuscular volume help to improve risk stratification in non-anemic patients with acute myocardial infarction? Cardiol J. 2015;22(4):421–7.

    Article  PubMed  Google Scholar 

  12. Ueda T, et al. High mean corpuscular volume is a new indicator of prognosis in acute decompensated heart failure. Circ J. 2013;77(11):2766–71.

    Article  PubMed  CAS  Google Scholar 

  13. Myojo M, et al. Prognostic implication of macrocytosis on adverse outcomes after coronary intervention. Atherosclerosis. 2012;221(1):148–53.

    Article  PubMed  CAS  Google Scholar 

  14. Zhang Z, et al. Relationship between Red Blood Cell Indices (MCV, MCH, and MCHC) and Major Adverse Cardiovascular Events in Anemic and Nonanemic Patients with Acute Coronary Syndrome. Dis Markers. 2022;2022:2193343.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Weisel J, Litvinov R. Red blood cells: the forgotten player in hemostasis and thrombosis. J Thromb Haemost. 2019;17(2):271–82.

    Article  PubMed Central  CAS  Google Scholar 

  16. Mathew G, Agha R. STROCSS 2021 guidelines: What is new? Int J Surg (London, England). 2021;96:106185.

    Article  Google Scholar 

  17. Cong Y, et al. The correlation between preoperative lower extremity Deep Vein Thrombosis (DVT) and the Time from Injury to Surgery (TFITS). Clin Appl Thromb Hemost. 2022;28:10760296221108960.

    Article  PubMed Central  Google Scholar 

  18. Xing F, et al. Admission prevalence of deep vein thrombosis in elderly Chinese patients with hip fracture and a new predictor based on risk factors for thrombosis screening. BMC Musculoskelet Disord. 2018;19(1):444.

    Article  PubMed Central  CAS  Google Scholar 

  19. Wang Y, et al. The disequilibrium in the distribution of the primary health workforce among eight economic regions and between rural and urban areas in China. International Journal for equity in health. 2020;19(1):28.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Kobayashi T, Akiyama T, Mawatari M. Predictors of preoperative deep vein thrombosis in hip fractures: a systematic review and meta-analysis. J Orthop Sci. 2023;28(1):222–32.

    Article  PubMed  Google Scholar 

  21. He S, et al. Incidence and risk factors of preoperative deep venous thrombosis following hip fracture: a retrospective analysis of 293 consecutive patients. Eur J Trauma Emerg Surg. 2022;48(4):3141–7.

    Article  PubMed  Google Scholar 

  22. Luo Z, et al. Preoperative incidence and locations of deep venous thrombosis (DVT) of lower extremity following ankle fractures. Sci Rep. 2020;10(1):10266.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Wang T, et al. Risk factors for preoperative deep venous thrombosis in hip fracture patients: a meta-analysis. J Orthop Traumatol. 2022;23(1):19.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Zhou Y, et al. Computational analysis of the related factors of Deep Vein Thrombosis (DVT) formation in patients undergoing hip fracture surgery. Evidence-based complementary and alternative medicine : eCAM. 2022;2022:1127095.

    PubMed  Google Scholar 

  25. Cheng X, et al. Red cell distribution width-to-high-density lipoprotein Cholesterol Ratio (RHR): a promising novel predictor for preoperative deep vein thrombosis in geriatric patients with hip fracture. Clin Interv Aging. 2022;17:1319–29.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  26. Rezende S, et al. Hematologic variables and venous thrombosis: red cell distribution width and blood monocyte count are associated with an increased risk. Haematologica. 2014;99(1):194–200.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Eischer L, et al. Hematocrit and the risk of recurrent venous thrombosis: a prospective cohort study. PLoS One. 2012;7(6):e38705.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. Braekkan S, et al. Hematocrit and risk of venous thromboembolism in a general population. The Tromso study. 2010;95(2):270–5.

    Google Scholar 

  29. Flamm M, Diamond S. Multiscale systems biology and physics of thrombosis under flow. Ann Biomed Eng. 2012;40(11):2355–64.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Farina, A., F. Rosso, and A.J.J.o.b.p. Fasano, A continuum mechanics model for the Fåhræus-Lindqvist effect. 2021. 47(3): p. 253–270.

  31. Leo F, et al. Red blood cell and endothelial eNOS independently regulate circulating nitric oxide metabolites and blood pressure. Circulation. 2021;144(11):870–89.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  32. Barabino G, Platt M, Kaul D. Sickle cell biomechanics. Annu Rev Biomed Eng. 2010;12:345–67.

    Article  PubMed  CAS  Google Scholar 

  33. Takeishi N, et al. Deformation of a red blood cell in a narrow rectangular microchannel. Micromachines (Basel). 2019;10(3):199.

    Article  Google Scholar 

  34. Sorlie P, et al. Hematocrit and risk of coronary heart disease: the Puerto Rico Health Program. Am Heart J. 1981;101(4):456–61.

    Article  CAS  Google Scholar 

  35. DeLoughery T. Microcytic anemia. N Engl J Med. 2014;371(14):1324–31.

    Article  PubMed  Google Scholar 

  36. Christensen R, et al. Whole-blood viscosity in the neonate: effects of gestational age, hematocrit, mean corpuscular volume and umbilical cord milking. J Perinatol. 2014;34(1):16–21.

    Article  PubMed  CAS  Google Scholar 

  37. Hoffmann J, Nabbe K, van den Broek N. Effect of age and gender on reference intervals of red blood cell distribution width (RDW) and mean red cell volume (MCV). Clin Chem Lab Med. 2015;53(12):2015–9.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This work was supported by the Foundation of Xi’an Municipal Health Commission (Grant Number: 2024ms15).

Author information

Authors and Affiliations

Authors

Contributions

Bin-Fei Zhang and Yu-Min Zhang conceived and designed the study. Shuai-Liang Xu, Wen-Wen Cao and Shao-Hua Chen, Shang-Bo Ren performed the study. Bin-Fei Zhang, Shuai-Liang Xu, Wen-Wen Cao, Shao-Hua Chen, Shang-Bo Ren analyzed the data. Shuai-Liang Xu and Kun Li wrote the manuscript.

Corresponding author

Correspondence to Bin-Fei Zhang.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the Ethics Committee of the Honghui Hospital, Xi'an Jiaotong University (No. 202201009). All patients provided informed consent. All human-related procedures followed the 1964 Declaration of Helsinki and its later amendments. The study has been reported according to the STROCSS 2021 guidelines.

Consent for publication

Not applicable. The work described has not been published before (except in the form of an abstract or as part of a published lecture, review, or thesis); it is not under consideration for publication elsewhere, and all co-authors have approved its publication.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, SL., Li, K., Cao, WW. et al. The association between admission mean corpuscular volume and preoperative deep venous thrombosis in geriatrics hip fracture: a retrospective study. BMC Musculoskelet Disord 25, 40 (2024). https://0-doi-org.brum.beds.ac.uk/10.1186/s12891-023-07147-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12891-023-07147-6

Keywords