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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Cell. Infect. Microbiol.</journal-id>
<journal-title>Frontiers in Cellular and Infection Microbiology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Cell. Infect. Microbiol.</abbrev-journal-title>
<issn pub-type="epub">2235-2988</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fcimb.2023.1220456</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Cellular and Infection Microbiology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Analysis of risk factors for deep vein thrombosis after spinal infection surgery and construction of a nomogram preoperative prediction model</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Xu</surname>
<given-names>Dongcheng</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2308810"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hu</surname>
<given-names>Xiaojiang</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1980947"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Hongqi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1021828"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gao</surname>
<given-names>Qile</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1549229"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guo</surname>
<given-names>Chaofeng</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liu</surname>
<given-names>Shaohua</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2095624"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tang</surname>
<given-names>Bo</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Guang</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Chengran</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Tang</surname>
<given-names>Mingxing</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2301581"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Spine Surgery and Orthopaedics, Xiangya Hospital, Central South University</institution>, <addr-line>Changsha</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>China for Geriatric Disorders, Xiangya Hospital, Central South University</institution>, <addr-line>Changsha</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Hongyi Shao, Beijing Jishuitan Hospital, China</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Andreas G. Tsantes, National and Kapodistrian University of Athens, Greece; Yang Lv, Peking University Third Hospital, China</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Mingxing Tang, <email xlink:href="mailto:Tangmingxing2018@163.com">Tangmingxing2018@163.com</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>03</day>
<month>08</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>13</volume>
<elocation-id>1220456</elocation-id>
<history>
<date date-type="received">
<day>10</day>
<month>05</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>07</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Xu, Hu, Zhang, Gao, Guo, Liu, Tang, Zhang, Zhang and Tang</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Xu, Hu, Zhang, Gao, Guo, Liu, Tang, Zhang, Zhang and Tang</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec>
<title>Objective</title>
<p>To investigate the differences in postoperative deep venous thrombosis (DVT) between patients with spinal infection and those with non-infected spinal disease; to construct a clinical prediction model using patients&#x2019; preoperative clinical information and routine laboratory indicators to predict the likelihood of DVT after surgery.</p>
</sec>
<sec>
<title>Method</title>
<p>According to the inclusion criteria, 314 cases of spinal infection (SINF) and 314 cases of non-infected spinal disease (NSINF) were collected from January 1, 2016 to December 31, 2021 at Xiangya Hospital, Central South University, and the differences between the two groups in terms of postoperative DVT were analyzed by chi-square test. The spinal infection cases were divided into a thrombotic group (DVT) and a non-thrombotic group (NDVT) according to whether they developed DVT after surgery. Pre-operative clinical information and routine laboratory indicators of patients in the DVT and NDVT groups were used to compare the differences between groups for each variable, and variables with predictive significance were screened out by least absolute shrinkage and operator selection (LASSO) regression analysis, and a predictive model and nomogram of postoperative DVT was established using multi-factor logistic regression, with a Hosmer- Lemeshow goodness-of-fit test was used to plot the calibration curve of the model, and the predictive effect of the model was evaluated by the area under the ROC curve (AUC).</p>
</sec>
<sec>
<title>Result</title>
<p>The incidence of postoperative DVT in patients with spinal infection was 28%, significantly higher than 16% in the NSINF group, and statistically different from the NSINF group (P &lt; 0.000). Five predictor variables for postoperative DVT in patients with spinal infection were screened by LASSO regression, and plotted as a nomogram. Calibration curves showed that the model was a good fit. The AUC of the predicted model was 0.8457 in the training cohort and 0.7917 in the validation cohort.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>In this study, a nomogram prediction model was developed for predicting postoperative DVT in patients with spinal infection. The nomogram included five preoperative predictor variables, which would effectively predict the likelihood of DVT after spinal infection and may have greater clinical value for the treatment and prevention of postoperative DVT.</p>
</sec>
</abstract>
<kwd-group>
<kwd>spine</kwd>
<kwd>infection</kwd>
<kwd>deep vein thrombosis</kwd>
<kwd>risk factors</kwd>
<kwd>predictive model</kwd>
<kwd>LASSO</kwd>
<kwd>nomogram</kwd>
<kwd>mNGS (metagenomic next-generation sequencing)</kwd>
</kwd-group>
<counts>
<fig-count count="4"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="49"/>
<page-count count="11"/>
<word-count count="4705"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Clinical Microbiology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<label>1</label>
<title>Introduction</title>
<p>Spinal infection is a rare disease. Its incidence rate is 0.001%~0.004% and its estimated mortality rate ranges between 2 and 4% (<xref ref-type="bibr" rid="B17">Duarte and Vaccaro, 2013</xref>). In recent years, the incidence rate and mortality rate of spinal infection is on the rise (<xref ref-type="bibr" rid="B2">Babic and Simpfendorfer, 2017</xref>; <xref ref-type="bibr" rid="B36">Sato et&#xa0;al., 2019</xref>). The main reason of spinal infection is the colonization of pathogens in the spine, and its pathogens mainly include various bacteria and viruses. Diagnosis of spinal infection is mainly based on clinical symptoms and signs, laboratory tests and imaging examinations. Routine microbial culture as direct evidence for infection diagnosis is the gold standard for diagnosis of spinal infection (<xref ref-type="bibr" rid="B42">Urrutia and Bono, 2022</xref>). Antibiotics are the main treatment for spinal infection. Surgical treatment should be used for patients with severe illness and no significant improvement (<xref ref-type="bibr" rid="B24">Herren et&#xa0;al., 2017</xref>; <xref ref-type="bibr" rid="B38">Scheyerer et&#xa0;al., 2022</xref>).</p>
<p>Deep venous thrombosis (DVT) is a well-known and feared surgical complication, as well as a leading cause of death. The incidence of venous thrombosis following spinal surgery varies between 0.31% and 31%. DVT may result in substantial morbidity, poor quality of life, and even death. It may also lead to increased medical costs and a considerable financial burden on individuals and their families (<xref ref-type="bibr" rid="B43">Wang and Wu, 2022</xref>). Studies have showed that risk factors for venous thrombosis following spinal surgery are associated with high age, female, spinal fusion, big volume blood loss patients, operation time, and hypertension, diabetes, and walking issue. A series of risk prediction models for deep venous thrombosis after surgery for patients with spinal surgery and fracture (<xref ref-type="bibr" rid="B13">Cheng et&#xa0;al., 2022</xref>; <xref ref-type="bibr" rid="B25">Hu et&#xa0;al., 2022</xref>; <xref ref-type="bibr" rid="B46">Yan et&#xa0;al., 2022</xref>).</p>
<p>Recently, the association between infection and venous thrombosis has long been recognized (<xref ref-type="bibr" rid="B15">Colling et&#xa0;al., 2021</xref>). Systemic or localized infections increase the risk of thrombosis about 2~20 times and are independent risk factors for thromboembolic diseases (<xref ref-type="bibr" rid="B6">Beristain-Covarrubias et&#xa0;al., 2019</xref>). Neutrophils, monocytes, and platelets interact with each other and the endothelium in host defense and also play critical roles in the formation of venous thromboembolism (<xref ref-type="bibr" rid="B6">Beristain-Covarrubias et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B15">Colling et&#xa0;al., 2021</xref>). However, clinical research on thrombosis after spinal infection surgery has not received much attention yet. It is generally believed that the incidence of thrombosis should be higher than that of a single spinal surgery or infection. Study has showed that patients with spine infections requiring irrigation and d&#xe9;bridement may be at considerably increased risk for DVT. Lambrechts MJ et&#xa0;al. found that 14.3% of patients undergoing spine irrigation and d&#xe9;bridement with subsequent peripherally inserted central catheter (PICC) placement developed postoperative DVT (<xref ref-type="bibr" rid="B28">Lambrechts et&#xa0;al., 2022</xref>). In this study, we compared the incidence of DVT after surgery for spinal infection, analysed the risk factors for DVT after surgery for spinal infection, screened the predictor variables by LASSO regression and developed a predictive model for the prediction of postoperative DVT in patients with spinal infection.</p>
</sec>
<sec id="s2">
<label>2</label>
<title>Method</title>
<sec id="s2_1">
<label>2.1</label>
<title>Study subjects</title>
<p>314 cases of spinal infection from January 2016 to December 2021 were collected from Xiangya Hospital of Central South University; 314 cases of non-infected spinal disease from January 2016 to December 2021 were randomly selected from Xiangya Hospital of Central South University. The spinal infection cases included 126 cases tested by metagenomic next-generation sequencing (mNGS). Ethical approval: Institutional ethics review board approval was obtained (IRB#: 201303232). This study was approved by the Ethics Committee of Xiangya Hospital Central South University.</p>
<sec id="s2_1_1">
<label>2.1.1</label>
<title>Inclusion criteria</title>
<p>Inclusion criteria for spinal infection cases: (1) complete clinical information, including gender, age and temperature; (2) routine preoperative laboratory indices; (3) patients treated surgically; (4) lesion specimens identified as pathogenic microbial infections by pathological examination, bacterial culture and staining, DNA testing of Mycobacterium tuberculosis flora and macrogenome sequencing; (5) postoperative vascular ultrasound results of both lower limbs.</p>
<p>Inclusion criteria for non-infected spinal disease cases: (1) complete clinical information, including gender and age; (2) patients were treated surgically; (3) patients did not have infectious diseases or signs of infection (e.g. fever, elevated blood count, etc.); (4) postoperative vascular ultrasound findings in both lower limbs.</p>
</sec>
<sec id="s2_1_2">
<label>2.1.2</label>
<title>Exclusion criteria</title>
<p>Patients meeting the following criteria will be excluded: (1) patients with infections elsewhere in the body; (2) patients with previous bleeding disorders (e.g. haemophilia, thrombocytopenic purpura, etc.) or vascular disorders (e.g. varicose veins, thrombophlebitis, etc.) (<xref ref-type="bibr" rid="B8">Boender et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B11">Chang et&#xa0;al., 2018</xref>); (3)Patients treated with preoperative anticoagulation or antiplatelet drugs; (4) patients with preoperative tests suggestive of DVT; (5) patients with critical multi-organ failure; (6) patients with malignancies (<xref ref-type="bibr" rid="B21">Falanga et&#xa0;al., 2013</xref>; <xref ref-type="bibr" rid="B20">Falanga et&#xa0;al., 2015</xref>).</p>
</sec>
</sec>
<sec id="s2_2">
<label>2.2</label>
<title>Research methods</title>
<sec id="s2_2_1">
<label>2.2.1</label>
<title>Pathogenic microbial detection methods</title>
<p>One of the following diagnostic criteria can be met: (1) pathological examination of the spinal lesion suggests a spinal infection (including inflammatory lesions, septicemia, etc.); (2) bacterial culture or staining of the spinal lesion detects bacteria or fungi (<xref ref-type="bibr" rid="B5">Berbari et&#xa0;al., 2015</xref>); (3) mNGS of the spinal lesion (<xref ref-type="bibr" rid="B45">Xu et&#xa0;al., 2022</xref>): high quality sequences are screened by FastQC software, removing sequences with connectors, low quality bases and too short (&lt;50bp) sequences. BowtiE2 was used for inter-sequence comparison and to remove host-associated reads. The processed sequences were compared with the Guangzhou Sage pathogenic microbial database for BWA analysis to obtain the number of detected sequences of pathogenic microorganisms; (4) positive spinal lesions for Mycobacterium tuberculosis cluster DNA detection (Xpert MTB/RIF) (<xref ref-type="bibr" rid="B16">Dorman et&#xa0;al., 2018</xref>).</p>
</sec>
<sec id="s2_2_2">
<label>2.2.2</label>
<title>Routine laboratory test result data collection</title>
<p>Patient&#x2019;s preoperative platelet (PLT), plateletcrit (PCT), prothrombin time (PT), activeated partial thromboplastin time (APTT), international normalized ratio (INR), D-dimer (DD), white blood cell (WBC), red blood cell (RBC), hemoglobin (HGB), neutrophil (Neut), lymphocyte (Lymph), eosinophil (EO), basophil (BASO), monocyte (Mono), neutrophil% (Neut%), lymphocyte% (Lymph%), basophil% (BASO%), eosinophil% (EO%), monocyte% (Mono%), red blood cell distribution width (RDW), mean platelet volume (MPV), total protein (TP), albumin (A), globulin (G), albumin to globulin ratio (A/G), alanine transaminase (ALT), aspartate transaminase (AST), blood urea nitrogen (BUN), creatinine (Cr), triglyceride (TG), cholesterol (Chol), high density lipoprotein (HDL), low density lipoprotein (LDL), glucose (GLU), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), procalcitonin (PCT).</p>
</sec>
<sec id="s2_2_3">
<label>2.2.3</label>
<title>DVT diagnostic criteria</title>
<p>The diagnosis was confirmed on the basis of postoperative vascular ultrasound findings in both lower limbs (<xref ref-type="bibr" rid="B29">Lim et&#xa0;al., 2018</xref>).</p>
</sec>
</sec>
<sec id="s2_3">
<label>2.3</label>
<title>Statistical methods</title>
<p>Measures that conformed to a normal distribution were described using the mean &#xb1; standard deviation and t-tests for two independent samples were used for comparisons between groups. Measures that did not conform to a normal distribution were described using the median and percentile, and comparisons between groups were made using a non-parametric test. The chi-square test was used for inter-group comparisons of the count data. Predictors were screened using the least absolute shrinkage and operator selection (LASSO) regression technique, and postoperative D-dimer prediction models and column line plots (nomograms) were developed using multifactorial logistic regression. The calibration curve of the model was plotted using the Hosmer-Lemeshow goodness-of-fit test. The predictive effect of the model was evaluated by calculating the area under the ROC curve (AUC). 60% of spinal infection cases were randomly selected as the training set and the remaining spinal infection cases were included in the validation set for internal validation of the prediction model. Statistical analyses and image plotting were performed using R software (version 4.2.2; R Foundation for Statistical Computing, Vienna, Austria) and differences were considered statistically significant when p&lt;0.05.</p>
</sec>
</sec>
<sec id="s3" sec-type="result">
<label>3</label>
<title>Result</title>
<p>A total of 314 cases of all patients with spinal infection (SINF) and 314 cases of randomly selected patients with non-infected spinal disease (NSINF) who met the inclusion criteria and were admitted to Xiangya Hospital of Central South University from 1 January 2016 to 31 December 2021 were included in the study. The general data of patients in the SINF and NSINF groups are analysed in <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>. There was no statistical difference in age and gender between the SINF and NSINF, The results of the chi-square test for postoperative DVT between the SINF and NSINF groups are shown in <xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref>. There was a significant difference in the incidence of postoperative DVT between the two groups (p &lt; 0.000), and the incidence of postoperative DVT was significantly higher in SINF than in NSINF.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Characteristics of the clinical data of each group of patients.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Variables</th>
<th valign="top" align="left">SINF (n=314)</th>
<th valign="top" align="left">NSINF (n=314)</th>
<th valign="top" align="left">p value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Age, years</td>
<td valign="top" align="left">55 (46.25, 64)</td>
<td valign="top" align="left">54 (46, 63)</td>
<td valign="top" align="left">0.453</td>
</tr>
<tr>
<td valign="top" align="left">Gender, n (%)</td>
<td valign="top" align="left"/>
<td valign="top" align="left"/>
<td valign="top" align="left">0.936</td>
</tr>
<tr>
<td valign="top" align="left">female</td>
<td valign="top" align="left">132 (42)</td>
<td valign="top" align="left">133 (42)</td>
<td valign="top" align="left"/>
</tr>
<tr>
<td valign="top" align="left">male</td>
<td valign="top" align="left">182 (58)</td>
<td valign="top" align="left">181 (58)</td>
<td valign="top" align="left"/>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Results of the chi-square test analysis of postoperative DVT for each group of patients.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" rowspan="2" align="center">Group</th>
<th valign="top" colspan="2" align="center">DVT, n (%)</th>
<th valign="middle" rowspan="2" align="center">Total</th>    <th valign="middle" rowspan="2" align="center">&#x3c7;<sup>2</sup>
</th>
<th valign="middle" rowspan="2" align="center">p value</th>
</tr>
<tr>
<th valign="top" align="center">positive</th>
<th valign="top" align="center">negative</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="center">SINF group</td>
<td valign="top" align="center">89 (28)</td>
<td valign="top" align="center">225 (72)</td>
<td valign="top" align="center">314</td>
<td valign="middle" rowspan="3" align="center">14.053</td>
<td valign="middle" rowspan="3" align="center">&lt; 0.000</td>
</tr>
<tr>
<td valign="top" align="center">NSINF group</td>
<td valign="top" align="center">50 (16)</td>
<td valign="top" align="center">264 (84)</td>
<td valign="top" align="center">314</td>
</tr>
<tr>
<td valign="top" align="center">Total</td>
<td valign="top" align="center">139 (22)</td>
<td valign="top" align="center">489 (78)</td>
<td valign="top" align="center">628</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The SINF consisted of 126 cases tested by mNGS, including 110 bacterial infections (including 28 tuberculosis infections and 9 brucellosis infections), 6 fungal infections, 5 viral infections, 2 rickettsial infections, 1 mycoplasma infection and 2 undetected cases. See <xref ref-type="supplementary-material" rid="SM1"><bold>Supplementary Information</bold></xref> for specific microbial species.</p>
<p>The SINF cases were divided into a thrombotic group (DVT) and a non-thrombotic group (NDVT) based on postoperative lower limb vascular ultrasound findings. There were 89 patients in the DVT and 225 patients in the NDVT. The general data and each preoperative serological index of the two groups are shown in <xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>. The two groups differed in Age, T, PCT, Plateletcrit, MPV, A, AG and APTT (p&lt;0.05). In this study, univariate ROC curves were plotted by these variables (<xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) and their AUC results were plotted (<xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1B</bold>
</xref>).</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Univariate analysis of patients and variables for spinal infection cases.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="left">Variables</th>
<th valign="middle" align="center">Total (n = 314)</th>
<th valign="middle" align="center">NDVT (n = 225)</th>
<th valign="middle" align="center">DVT (n = 89)</th>
<th valign="middle" align="center">p value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">Gender, n (%)</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.983</td>
</tr>
<tr>
<td valign="middle" align="left">female</td>
<td valign="middle" align="center">132 (42)</td>
<td valign="middle" align="center">94 (42)</td>
<td valign="middle" align="center">38 (43)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="left">male</td>
<td valign="middle" align="center">182 (58)</td>
<td valign="middle" align="center">131 (58)</td>
<td valign="middle" align="center">51 (57)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="left">Age, years</td>
<td valign="middle" align="center">55 (46.25, 64)</td>
<td valign="middle" align="center">53 (44, 63)</td>
<td valign="middle" align="center">60 (53, 69)</td>
<td valign="middle" align="center">&lt; 0.001</td>
</tr>
<tr>
<td valign="middle" align="left">T, &#xb0;C</td>
<td valign="middle" align="center">36.6 (36.5, 36.8)</td>
<td valign="middle" align="center">36.5 (36.5, 36.8)</td>
<td valign="middle" align="center">36.6 (36.6, 36.9)</td>
<td valign="middle" align="center">&lt; 0.001</td>
</tr>
<tr>
<td valign="middle" align="left">WBC, 10^9/L</td>
<td valign="middle" align="center">6.25 (4.8, 7.7)</td>
<td valign="middle" align="center">6.3 (5, 7.7)</td>
<td valign="middle" align="center">6.2 (4.5, 7.7)</td>
<td valign="middle" align="center">0.146</td>
</tr>
<tr>
<td valign="middle" align="left">RBC, 10^12/L</td>
<td valign="middle" align="center">4.07 &#xb1; 0.6</td>
<td valign="middle" align="center">4.08 &#xb1; 0.63</td>
<td valign="middle" align="center">4.06 &#xb1; 0.51</td>
<td valign="middle" align="center">0.836</td>
</tr>
<tr>
<td valign="middle" align="left">HGB, g/L</td>
<td valign="middle" align="center">117 (106.25, 132)</td>
<td valign="middle" align="center">117 (105, 132)</td>
<td valign="middle" align="center">119 (108, 133)</td>
<td valign="middle" align="center">0.249</td>
</tr>
<tr>
<td valign="middle" align="left">PLT, 10^9/L</td>
<td valign="middle" align="center">241 (188.25, 310.75)</td>
<td valign="middle" align="center">253 (190, 323)</td>
<td valign="middle" align="center">225 (184, 277)</td>
<td valign="middle" align="center">0.046</td>
</tr>
<tr>
<td valign="middle" align="left">Neut, 10^9/L</td>
<td valign="middle" align="center">4 (3, 5.4)</td>
<td valign="middle" align="center">4 (3, 5.5)</td>
<td valign="middle" align="center">3.8 (2.9, 5)</td>
<td valign="middle" align="center">0.339</td>
</tr>
<tr>
<td valign="middle" align="left">Lymph, 10^9/L</td>
<td valign="middle" align="center">1.31 (1, 1.79)</td>
<td valign="middle" align="center">1.4 (1, 1.7)</td>
<td valign="middle" align="center">1.3 (0.9, 1.8)</td>
<td valign="middle" align="center">0.332</td>
</tr>
<tr>
<td valign="middle" align="left">EO, 10^9/L</td>
<td valign="middle" align="center">0.1 (0.08, 0.2)</td>
<td valign="middle" align="center">0.1 (0.08, 0.2)</td>
<td valign="middle" align="center">0.1 (0.1, 0.2)</td>
<td valign="middle" align="center">0.566</td>
</tr>
<tr>
<td valign="middle" align="left">BASO, 10^9/L</td>
<td valign="middle" align="center">0 (0, 0.03)</td>
<td valign="middle" align="center">0 (0, 0.03)</td>
<td valign="middle" align="center">0 (0, 0.02)</td>
<td valign="middle" align="center">0.328</td>
</tr>
<tr>
<td valign="middle" align="left">Mono, 10^9/L</td>
<td valign="middle" align="center">0.5 (0.4, 0.7)</td>
<td valign="middle" align="center">0.5 (0.4, 0.7)</td>
<td valign="middle" align="center">0.5 (0.4, 0.7)</td>
<td valign="middle" align="center">0.917</td>
</tr>
<tr>
<td valign="middle" align="left">Neut%, %</td>
<td valign="middle" align="center">65.85 (58.82, 72.1)</td>
<td valign="middle" align="center">66 (58.3, 72.5)</td>
<td valign="middle" align="center">65.6 (60.5, 70.9)</td>
<td valign="middle" align="center">0.855</td>
</tr>
<tr>
<td valign="middle" align="left">Lymph%, %</td>
<td valign="middle" align="center">21.65 (16.72, 27.6)</td>
<td valign="middle" align="center">21.8 (16.8, 27.9)</td>
<td valign="middle" align="center">21.5 (16.7, 26.3)</td>
<td valign="middle" align="center">0.486</td>
</tr>
<tr>
<td valign="middle" align="left">BASO%, %</td>
<td valign="middle" align="center">0.5 (0.3, 0.7)</td>
<td valign="middle" align="center">0.5 (0.3, 0.6)</td>
<td valign="middle" align="center">0.5 (0.3, 0.7)</td>
<td valign="middle" align="center">0.325</td>
</tr>
<tr>
<td valign="middle" align="left">EO%, %</td>
<td valign="middle" align="center">1.8 (0.9, 3.2)</td>
<td valign="middle" align="center">1.7 (0.9, 3.1)</td>
<td valign="middle" align="center">2 (1.1, 3.3)</td>
<td valign="middle" align="center">0.27</td>
</tr>
<tr>
<td valign="middle" align="left">Mono%, %</td>
<td valign="middle" align="center">8.8 (7.2, 10.5)</td>
<td valign="middle" align="center">8.8 (6.8, 10.5)</td>
<td valign="middle" align="center">8.8 (7.6, 10.3)</td>
<td valign="middle" align="center">0.27</td>
</tr>
<tr>
<td valign="middle" align="left">RDW, %</td>
<td valign="middle" align="center">13.8 (12.9, 14.8)</td>
<td valign="middle" align="center">13.8 (12.9, 14.9)</td>
<td valign="middle" align="center">14.1 (13.1, 14.7)</td>
<td valign="middle" align="center">0.266</td>
</tr>
<tr>
<td valign="middle" align="left">Plateletcrit<sup>*</sup>, %</td>
<td valign="middle" align="center">0.2 (0.16, 0.26)</td>
<td valign="middle" align="center">0.22 (0.17, 0.28)</td>
<td valign="middle" align="center">0.17 (0.14, 0.2)</td>
<td valign="middle" align="center">&lt; 0.001</td>
</tr>
<tr>
<td valign="middle" align="left">MPV, fL</td>
<td valign="middle" align="center">8.35 (7.52, 9.5)</td>
<td valign="middle" align="center">8.71 (7.76, 9.9)</td>
<td valign="middle" align="center">7.81 (6.8, 8.35)</td>
<td valign="middle" align="center">&lt; 0.001</td>
</tr>
<tr>
<td valign="middle" align="left">TP, g/L</td>
<td valign="middle" align="center">69.83 &#xb1; 6.72</td>
<td valign="middle" align="center">70.26 &#xb1; 6.77</td>
<td valign="middle" align="center">68.73 &#xb1; 6.52</td>
<td valign="middle" align="center">0.066</td>
</tr>
<tr>
<td valign="middle" align="left">A, g/L</td>
<td valign="middle" align="center">36.86 &#xb1; 4.47</td>
<td valign="middle" align="center">37.43 &#xb1; 4.48</td>
<td valign="middle" align="center">35.4 &#xb1; 4.12</td>
<td valign="middle" align="center">&lt; 0.001</td>
</tr>
<tr>
<td valign="middle" align="left">G, g/L</td>
<td valign="middle" align="center">32.4 (28.6, 36.9)</td>
<td valign="middle" align="center">32.7 (28, 36.9)</td>
<td valign="middle" align="center">31.8 (29.3, 36.9)</td>
<td valign="middle" align="center">0.773</td>
</tr>
<tr>
<td valign="middle" align="left">A/G</td>
<td valign="middle" align="center">1.15 (0.97, 1.31)</td>
<td valign="middle" align="center">1.2 (1, 1.4)</td>
<td valign="middle" align="center">1.07 (0.91, 1.29)</td>
<td valign="middle" align="center">0.029</td>
</tr>
<tr>
<td valign="middle" align="left">ALT, U/L</td>
<td valign="middle" align="center">17.8 (11.4, 28.25)</td>
<td valign="middle" align="center">17.9 (11.9, 28.6)</td>
<td valign="middle" align="center">17.3 (10.3, 27.7)</td>
<td valign="middle" align="center">0.296</td>
</tr>
<tr>
<td valign="middle" align="left">AST, U/L</td>
<td valign="middle" align="center">21.1 (16.8, 29.7)</td>
<td valign="middle" align="center">21 (17.1, 30.3)</td>
<td valign="middle" align="center">21.6 (16.5, 27)</td>
<td valign="middle" align="center">0.424</td>
</tr>
<tr>
<td valign="middle" align="left">BUN, mmol/L</td>
<td valign="middle" align="center">4.85 (3.81, 6.12)</td>
<td valign="middle" align="center">4.68 (3.81, 5.98)</td>
<td valign="middle" align="center">5 (3.82, 6.35)</td>
<td valign="middle" align="center">0.333</td>
</tr>
<tr>
<td valign="middle" align="left">Cr, mmol/L</td>
<td valign="middle" align="center">72 (61, 82.2)</td>
<td valign="middle" align="center">72 (61, 82.2)</td>
<td valign="middle" align="center">72.4 (62, 82.2)</td>
<td valign="middle" align="center">0.430</td>
</tr>
<tr>
<td valign="middle" align="left">TG, mmol/L</td>
<td valign="middle" align="center">1.23 (0.88, 1.65)</td>
<td valign="middle" align="center">1.23 (0.86, 1.68)</td>
<td valign="middle" align="center">1.25 (0.95, 1.62)</td>
<td valign="middle" align="center">0.729</td>
</tr>
<tr>
<td valign="middle" align="left">Chol, mmol/L</td>
<td valign="middle" align="center">4.26 (3.6, 5.07)</td>
<td valign="middle" align="center">4.21 (3.58, 4.94)</td>
<td valign="middle" align="center">4.36 (3.7, 5.14)</td>
<td valign="middle" align="center">0.299</td>
</tr>
<tr>
<td valign="middle" align="left">HDL, mmol/L</td>
<td valign="middle" align="center">1.02 (0.86, 1.21)</td>
<td valign="middle" align="center">1.02 (0.87, 1.2)</td>
<td valign="middle" align="center">1.01 (0.85, 1.23)</td>
<td valign="middle" align="center">0.706</td>
</tr>
<tr>
<td valign="middle" align="left">LDL, mmol/L</td>
<td valign="middle" align="center">2.68 (2.25, 3.24)</td>
<td valign="middle" align="center">2.67 (2.2, 3.25)</td>
<td valign="middle" align="center">2.73 (2.32, 3.19)</td>
<td valign="middle" align="center">0.491</td>
</tr>
<tr>
<td valign="middle" align="left">GLU, mmol/L</td>
<td valign="middle" align="center">5.19 (4.77, 5.8)</td>
<td valign="middle" align="center">5.23 (4.74, 5.88)</td>
<td valign="middle" align="center">5.16 (4.8, 5.61)</td>
<td valign="middle" align="center">0.446</td>
</tr>
<tr>
<td valign="middle" align="left">PT, s</td>
<td valign="middle" align="center">12.8 (12, 13.7)</td>
<td valign="middle" align="center">12.7 (12, 13.7)</td>
<td valign="middle" align="center">12.9 (12, 13.7)</td>
<td valign="middle" align="center">0.695</td>
</tr>
<tr>
<td valign="middle" align="left">APTT, s</td>
<td valign="middle" align="center">32.6 (29.2, 36.35)</td>
<td valign="middle" align="center">32.9 (29.4, 36.9)</td>
<td valign="middle" align="center">31.2 (28.7, 35.3)</td>
<td valign="middle" align="center">0.044</td>
</tr>
<tr>
<td valign="middle" align="left">INR</td>
<td valign="middle" align="center">1.02 (0.96, 1.09)</td>
<td valign="middle" align="center">1.02 (0.96, 1.09)</td>
<td valign="middle" align="center">1.02 (0.96, 1.09)</td>
<td valign="middle" align="center">0.951</td>
</tr>
<tr>
<td valign="middle" align="left">DD, mg/L</td>
<td valign="middle" align="center">0.3 (0.17, 0.54)</td>
<td valign="middle" align="center">0.3 (0.17, 0.52)</td>
<td valign="middle" align="center">0.29 (0.19, 0.57)</td>
<td valign="middle" align="center">0.493</td>
</tr>
<tr>
<td valign="middle" align="left">ESR, mm/h</td>
<td valign="middle" align="center">70.5 (40.25, 103.75)</td>
<td valign="middle" align="center">70 (38, 105)</td>
<td valign="middle" align="center">71 (51, 102)</td>
<td valign="middle" align="center">0.561</td>
</tr>
<tr>
<td valign="middle" align="left">CRP, mg/L</td>
<td valign="middle" align="center">17.3 (6.65, 41.88)</td>
<td valign="middle" align="center">17.3 (6.57, 42.2)</td>
<td valign="middle" align="center">17.5 (6.81, 37.4)</td>
<td valign="middle" align="center">0.755</td>
</tr>
<tr>
<td valign="middle" align="left">Procalcitonin<sup>**</sup>, n (%)</td>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center"/>
<td valign="middle" align="center">0.337</td>
</tr>
<tr>
<td valign="middle" align="left">negative</td>
<td valign="middle" align="center">226 (72)</td>
<td valign="middle" align="center">158 (70)</td>
<td valign="middle" align="center">68 (76)</td>
<td valign="middle" align="center"/>
</tr>
<tr>
<td valign="middle" align="left">positive</td>
<td valign="middle" align="center">88 (28)</td>
<td valign="middle" align="center">67 (30)</td>
<td valign="middle" align="center">21 (24)</td>
<td valign="middle" align="center"/>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>*Plateletcrit (PCT) and Procalcitonin (PCT) have the same abbreviation, so their full names are used in this study.</p>
</fn>
<fn>
<p>**The Procalcitonin is defined as a count data because there are multiple clinical assays with different normal values between methods.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Single variables on DVT predictive capability: <bold>(A)</bold> ROC curve of single variables on DVT prediction; <bold>(B)</bold> AUC of single variables for DVT prediction.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcimb-13-1220456-g001.tif"/>
</fig>
<p>In this study, five non-zero coefficient variables (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>), including Plateletcrit, MPV, APTT, T and Age, were selected from 40 variables in patients with spinal infection by LASSO regression, and the corresponding postoperative DVT prediction model was developed by multifactorial logistic regression analysis based on these five variables. In this study, a nomogram of postoperative DVT in patients with spinal infection (<xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>) was constructed based on the prediction model, and the results of the prediction model were presented visually to facilitate the preoperative assessment of patients with spinal infection.</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Screening variables by LASSO regression: <bold>(A)</bold> LASSO regression model graph. In this study, five non-zero coefficients were screened using Lambda.min as the criterion.; <bold>(B)</bold> Lambda (adjustment parameter) was obtained by cross-validated LASSO regression. The left dashed line is Lambda at minimum error (Lambda.min), the right dashed line is Lambda at standard error (Lambda.1-SE).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcimb-13-1220456-g002.tif"/>
</fig>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Nomogram and scoring method for postoperative DVT in patients with spinal infection. The corresponding score (top line) is found according to the value of each predictor variable (the line after each variable), then the values of the individual scores are summed to obtain the total score, and the corresponding predicted probability is based on the total score(bottom line).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcimb-13-1220456-g003.tif"/>
</fig>
<p>The Hosmer-Lemeshow goodness of fit test (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4A</bold>
</xref>) shows a good fit between the nomogram predicted probabilities and the actual probabilities. This indicates that there is no deviation from a perfect fit between the predicted and observed values. In addition, this study plotted the ROC curve for the model, which had an AUC of 0.8457 (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4B</bold>
</xref>) in the training cohort and 0.7917 (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4C</bold>
</xref>) in the validation cohort.</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>Evaluation of nomogram clinical prediction model: <bold>(A)</bold> Calibration curve of the model; <bold>(B)</bold> ROC curve of the model for the training cohort, and its AUC was 0.8457; <bold>(C)</bold> ROC curve of the model for the validation cohort, and its AUC was 0.7917.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcimb-13-1220456-g004.tif"/>
</fig>
</sec>
<sec id="s4" sec-type="discussion">
<label>4</label>
<title>Discussion</title>
<p>In this study, a clinical prediction model for postoperative DVT in patients with spinal infection was developed using LASSO regression and visualised by nomogram. The nomogram had five preoperative predictor variables including Plateletcrit, MPV, APTT, T and Age. The goodness of fit test shows a good fit between the nomogram predicted probabilities and the actual probabilities. In addition, the ROC curve of the model was plotted in this study. Its AUC was 0.8457 in the training cohort and 0.7917 in the validation cohort. The prediction model nomogram showed good preoperative predictive ability and clinical value.</p>
<p>In recent years, with the progression of an ageing population and the misuse of antibiotics, there has been an upward trend in the incidence of spinal infections (<xref ref-type="bibr" rid="B2">Babic and Simpfendorfer, 2017</xref>; <xref ref-type="bibr" rid="B18">Dunn and Ben Husien, 2018</xref>), particularly with various drug-resistant bacterial infections, leading to an increased probability of serious complications. Patients with spinal infections who experience spinal bone destruction often experience skeletal related events (SREs) such as severe bone pain, pathological fractures, spinal cord compression and hypercalcaemia. Surgical treatment is usually required in this case. DVT is one of the most common complications of surgery and one of the most common causes of death in surgical patients (<xref ref-type="bibr" rid="B7">Blitzer and Eisenstein, 2021</xref>). Numerous studies have shown that the incidence of postoperative venous thromboembolism is significantly higher in surgical patients than preoperatively (<xref ref-type="bibr" rid="B48">Zhang et&#xa0;al., 2021</xref>; <xref ref-type="bibr" rid="B26">Jiang et&#xa0;al., 2022</xref>). Patients undergoing spinal surgery are more likely to develop postoperative DVT due to the need for prolonged bed rest after surgery, as evidenced by the study by Hengyan <xref ref-type="bibr" rid="B48">Zhang et&#xa0;al. (2021)</xref>. The occurrence of postoperative DVT in patients has been associated with several preoperative factors, such as advanced age and infection. Studies have shown that infection is an important factor influencing the development of DVT, and that the dysfunction of haemostasis and vascular barrier dysfunction caused by infection promotes thrombosis (<xref ref-type="bibr" rid="B15">Colling et&#xa0;al., 2021</xref>). In this study, 314 SINF and 314 NSINF cases were included. There were no significant differences between SINF and NSINF in terms of age and gender, while there were statistically significant differences in terms of postoperative DVT. Therefore, for patients with spinal infection, the likelihood of postoperative DVT would be significantly increased.</p>
<p>This study included 126 cases that were tested for mNGS. The 2018 guidelines of the Infectious Diseases Society of America and the American Society for Microbiology continue to use microbiological culture of spinal lesions as a criterion for laboratory diagnosis of spinal infections (<xref ref-type="bibr" rid="B33">Miller et&#xa0;al., 2018</xref>). However, studies have shown that positive microbial cultures of spinal infection lesions are low (<xref ref-type="bibr" rid="B49">Zhang et&#xa0;al., 2023</xref>), making it difficult to meet clinical diagnostic needs, and the long culture period for some microorganisms (e.g. Mycobacterium tuberculosis) may lead to delays in treatment. mNGS is extremely sensitive and specific for the detection of pathogenic microorganisms (<xref ref-type="bibr" rid="B49">Zhang et&#xa0;al., 2023</xref>), and with advances in technology, a rapid 50-minute median time mNGS assays (<xref ref-type="bibr" rid="B23">Gu et&#xa0;al., 2021</xref>). Therefore, mNGS may become an effective clinical tool for accurate and rapid diagnosis of infections.</p>
<p>In this study, a total of 314 patients with spinal infections were included. They were divided into 89 cases of DVT and 225 cases of NDVT according to the results of the vascular ultrasound of both lower limbs. univariate analysis of 40 preoperative data from both groups showed significant differences in Age, T, PLT, Plateletcrit, MPV, A, AG and APTT. By plotting ROC curves and calculating AUC, we found that all individual variables did not show significant value for predicting DVT (AUC &lt; 0.75), suggesting that a single variable is difficult to accurately predict the likelihood of postoperative DVT. Therefore, to more accurately predict postoperative DVT, this study used LASSO regression to screen out five variables, including Plateletcrit, MPV, APTT, T and Age, and construct a DVT prediction model by logistic regression. The model achieved an AUC of 0.8457 in the training cohort and 0.7917 in the validation cohort, indicating that the model has relatively good predictive value. The fitted curves also showed a good fit. This study found that a decrease in preoperative Plateletcrit, MPV and APTT levels predicted an increased likelihood of DVT in patients postoperatively, while an increase in T and Age predicted an increased likelihood of DVT in patients postoperatively.</p>
<p>Marina Panova-Noeva et&#xa0;al. observed that MPV was lower in cases where thrombosis occurred compared to controls (<xref ref-type="bibr" rid="B34">Panova-Noeva et&#xa0;al., 2020</xref>), a phenomenon that has been validated in other studies on thrombosis (<xref ref-type="bibr" rid="B30">Lippi et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B9">Braester et&#xa0;al., 2021</xref>). In infectious diseases, MPV levels can help to indicate the onset of inflammation. For example, in cases of acute appendicitis, MPV levels were significantly lower than in controls (<xref ref-type="bibr" rid="B22">Fan et&#xa0;al., 2017</xref>). Plateletcrit, which is the percentage of platelet volume in peripheral blood to whole blood volume, is the product of PLT and MPV, and decreased levels of Plateletcrit have been suggested to be associated with sepsis and poor prognosis in systemic inflammatory diseases in established studies (<xref ref-type="bibr" rid="B37">Sayed et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B47">Yard&#x131;mc&#x131; et&#xa0;al., 2021</xref>). Shortening of APTT as an indicator of coagulation is usually indicative of a hypercoagulable state, and APTT light transmission waveform analysis is currently used by some investigators as a tool to detect infection and assess its prognosis (<xref ref-type="bibr" rid="B14">Chopin et&#xa0;al., 2006</xref>). The correlation between fever and infection has been well documented (<xref ref-type="bibr" rid="B31">Lu et&#xa0;al., 2015</xref>), and clinically, in non-serious patients, an increase in temperature is also often indicative of the onset or exacerbation of infection. A clinical trial has shown that fever is common in patients with DVT and has a worse prognosis (<xref ref-type="bibr" rid="B3">Barba et&#xa0;al., 2011</xref>). Advanced age is known to be an independent risk factor for thrombosis (<xref ref-type="bibr" rid="B1">Abad Rico et&#xa0;al., 2010</xref>). Recent studies have also shown that age has shown greater value in the diagnosis and prediction of DVT. Kelly Broen et&#xa0;al. used age-adjusted DD, and the adjusted DD threshold showed higher specificity and negative predictive value for the exclusion diagnosis of DVT (<xref ref-type="bibr" rid="B10">Broen et&#xa0;al., 2016</xref>). Jian Xiang Wu et&#xa0;al. used a similar approach and used age-adjusted-DD for preoperative DVT screening (<xref ref-type="bibr" rid="B44">Wu et&#xa0;al., 2021</xref>). Advanced age is also a risk factor for various infectious diseases, and studies have shown that the risk of urinary tract and surgical site infections will increase with age (<xref ref-type="bibr" rid="B12">Cheadle, 2006</xref>; <xref ref-type="bibr" rid="B39">Tandogdu and Wagenlehner, 2016</xref>). The morbidity and mortality of sepsis also increases significantly with age (<xref ref-type="bibr" rid="B27">Kingren et&#xa0;al., 2021</xref>). A large number of previous studies as well as clinical practice have shown that DD is highly sensitive for the diagnosis of DVT exclusion and guidelines published by the American Society of Hematology have identified DD as a preferred screening indicator for thrombosis (<xref ref-type="bibr" rid="B29">Lim et&#xa0;al., 2018</xref>). However, in the present study, we observed that preoperative DD levels did not show good predictive value for postoperative DVT in patients with spinal infections. We speculate that this may be related to the short half-life of DD. However, whether this phenomenon exists in other diseases still needs to be verified by more studies.</p>
<p>In the existing study, we noted that Xin Yan et&#xa0;al. predicted the risk of postoperative DVT progression in patients undergoing spinal surgery by plotting a nomogram, and they eventually screened five preoperative and intraoperative indicators, which included the time of surgery (<xref ref-type="bibr" rid="B46">Yan et&#xa0;al., 2022</xref>). Unlike their study, firstly, the present study included a large number of cases for calculation in patients with spinal infection, making the nomogram more relevant. Secondly, the present study included more routine preoperative serological indicators, which made it easier for clinicians to assess. Of course, there are differences in the outcomes we predict, with the present study predicting the occurrence rather than progression of DVT. Kimon Bekelis et&#xa0;al. analysed several risk factors for postoperative complications of spinal surgery, including DVT, and presented them in the form of an odds ratio (OR) (<xref ref-type="bibr" rid="B4">Bekelis et&#xa0;al., 2014</xref>). However, they did not present the predictive model visually, and in this respect, nomogram showed a greater advantage. In addition, we note that several studies have explored new methods for the diagnosis and prediction of DVT. A pilot study has shown that patients with musculoskeletal tumors can be defined as hypercoagulable by preoperative thromboelastography. And patients with a preoperative defined hypercoagulable state are more likely to develop DVT postoperatively (<xref ref-type="bibr" rid="B35">Sabharwal et&#xa0;al., 2023</xref>). Andreas G Tsantes et&#xa0;al. analyzed preoperative and postoperative rotational thromboelastometry parameters in patients with malignant bone tumors. Their accuracy for postoperative thrombus prediction was found to be significantly better than that of DD (<xref ref-type="bibr" rid="B40">Tsantes et&#xa0;al., 2023</xref>). Another study on rotational thromboelastometry analyzed data from patients with hip fractures and found a number of abnormal rotational thromboelastometry abnormalities associated with the development of venous thromboembolism (VTE), with preoperative clot formation time showing good performance in detecting symptomatic VTE (<xref ref-type="bibr" rid="B41">Tsantes et&#xa0;al., 2021</xref>). A study on spinal fractures analyzed risk factors for preoperative DVT, which included DD, and the adjusted optimal threshold for DD was 1.08ug/ml (<xref ref-type="bibr" rid="B32">Ma et&#xa0;al., 2021</xref>).</p>
<p>In this study, clinical data were retrospectively collected from patients undergoing surgery for spinal infection in Hunan Province, but there are geographical differences in the incidence of spinal infection, for example, Mycobacterium tuberculosis infection may be related to regional economic level and climatic environment (<xref ref-type="bibr" rid="B19">European Centre for Disease Prevention and Control and WHO Regional Office for Europe, 2022</xref>). Therefore, the applicability of this prediction model to other regions still needs further validation. This is a retrospective study and due to the absence of some preoperative data, this study excluded some indicators, such as height and weight, which may have value for preoperative prediction of DVT. Therefore, we intend to conduct further prospective studies based on this study to improve the accuracy of preoperative prediction of DVT.</p>
</sec>
<sec id="s5" sec-type="conclusion">
<label>5</label>
<title>Conclusion</title>
<p>In this study, a nomogram was developed to predict postoperative DVT in patients with spinal infection. The nomogram includes five preoperative predictor variables, which will effectively predict the likelihood of DVT after surgery. This nomogram is valuable in predicting postoperative DVT and will help clinicians to decide whether early intervention is needed based on the preoperative prediction results and the patient&#x2019;s specific situation.</p>
</sec>
<sec id="s6" sec-type="data-availability">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s7" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The studies involving humans were approved by Ethics Committee of Xiangya Hospital Central South University. The studies were conducted in accordance with the local legislation and institutional requirements. The ethics committee/institutional review board waived the requirement of written informed consent for participation from the participants or the participants&#x2019; legal guardians/next of kin because All subjects signed a consent form.</p>
</sec>
<sec id="s8" sec-type="author-contributions">
<title>Author contributions</title>
<p>DX and MT designed research, performed research, analyzed data, and wrote the paper. XH, HZ, QG, CG and SL developed the idea for the study. XH, BT, GZ and CZ collected the data. All authors contributed to the article and approved the submitted version.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgments</title>
<p>A special thanks to Xiangya Medical Big Data of Central South University.</p>
</ack>
<sec id="s9" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s10" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s11" sec-type="supplementary-material"><title>Supplementary material</title><p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fcimb.2023.1220456/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fcimb.2023.1220456/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Table_1.docx" id="SM1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document"/>
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