Skip to main content

A nomogram model based on SII, AFR, and NLR to predict infectious complications of laparoscopic hysterectomy for cervical cancer

Abstract

Background

This study aimed to investigate the potential risk factors associated with postoperative infectious complications following laparoscopic hysterectomy for cervical cancer and to develop a prediction model based on these factors.

Methods

This study enrolled patients who underwent selective laparoscopic hysterectomy for cervical cancer between 2019 and 2024. A multivariate regression analysis was performed to identify independent risk factors associated with postoperative infectious complications. A nomogram prediction model was subsequently constructed and evaluated using R software.

Results

Out of 301 patients were enrolled and 38 patients (12.6%) experienced infectious complications within one month postoperatively. Six variables were independent risk factors for postoperative infectious complications: age ≥ 60 (OR: 3.06, 95% confidence interval (CI): 1.06–8.79, P = 0.038), body mass index (BMI) ≥ 24.0 (OR: 3.70, 95%CI: 1.4–9.26, P = 0.005), diabetes (OR: 2.91, 95% CI: 1.10–7.73, P = 0.032), systemic immune-inflammation index (SII) ≥ 830 (OR: 6.95, 95% CI: 2.53–19.07, P < 0.001), albumin-to-fibrinogen ratio (AFR) < 9.25 (OR: 4.94, 95% CI: 2.02–12.07, P < 0.001), and neutrophil-to-lymphocyte ratio (NLR) ≥ 3.45 (OR: 7.53, 95% CI: 3.04–18.62, P < 0.001). Receiver operator characteristic (ROC) curve analysis indicated an area under the curve (AUC) of this nomogram model of 0.928, a sensitivity of 81.0%, and a specificity of 92.1%.

Conclusions

The nomogram model, incorporating age, BMI, diabetes, SII, AFR, and NLR, demonstrated strong predictive capabilities for postoperative infectious complications following laparoscopic hysterectomy for cervical cancer.

Introduction

Cervical cancer ranks as the fourth worldwide [1] with approximately 660,000 new cases and 350,000 deaths in 2022 by the World Health Organization (WHO). In China, cervical cancer is the fourth most common cancer among women and poses a significant threat to public health [2]. Laparoscopic radical hysterectomy is indeed a major treatment strategy for cervical cancer, particularly for early-stage disease. This minimally invasive surgical approach offers reduced morbidity, quicker recovery, and better cosmetic outcomes than traditional laparotomy [3].

However, postoperative complications have significant adverse impacts on the prognosis of patients after surgery for cervical cancer. Infection complications are very common postoperative complications after laparoscopic hysterectomy, associated with delayed recovery, extended hospital stays, increased costs, and even elevated postoperative morbidity [4]. Therefore, it is crucial to investigate the potential valid predictive factors for infectious complications to improve prognosis. Risk factors for the developing postoperative infectious complications include smoking, obesity, uncontrolled diabetes, compromised immune function, and prolonged hospital stays [5]. Despite ongoing efforts by the researchers to explore predictive factors, significant gaps remain in this area. This study aimed to investigate the potential predictors and construct a nomogram prediction model for postoperative infectious complications.

Materials and methods

This retrospective cohort study included individuals who underwent consecutive selective laparoscopic hysterectomy for cervical cancer at The Affiliated Taizhou People’s Hospital of Nanjing Medical University, between 2019 and 2024. The inclusion criteria were as follows: (1) patients diagnosed with cervical cancer supported by pathological evidence; (2) patients who underwent laparoscopic hysterectomy under general anesthesia; and (3) patients with follow-up for at least one month. The exclusion criteria were as follows: (1) Incomplete clinical data or follow-up; (2) patients who underwent laparotomy or laparoscopic conversion to laparotomy; (3) patients who were recently treated with immunosuppressants; (4) patients with pre-existing infection before the surgery; (5) patients who underwent neoadjuvant therapy for advanced cervical cancer; (6) patients who underwent radiotherapy after the surgery. The study received approval from the hospital’s ethics committee, and all enrolled patients provided written informed consent.

The enrolled patients underwent surgery under general anesthesia for surgery, with induction achieved using sufentanil, propofol, rocuronium bromide, and midazolam. Anesthesia was maintained using sevoflurane, remifentanil, and dexmedetomidine. To prevent infection, the patients in the study were routinely administered antibiotics both pre- and post-surgery antibiotics. Furthermore, a drainage tube was consistently inserted before the completion of the surgical procedure.

The following data were collected: (1) Demographic information, including age, body mass index (BMI), and presence of pausimenia; (2) clinically relevant details, including pathological type, International Federation of Gynecology and Obstetrics (FIGO) stage, American Society of Anesthesiologists (ASA) score, comorbidities of hypertension, diabetes, chronic obstructive pulmonary disease (COPD), history of abdominal surgery, operation time, and lymph node dissection; (3) preoperative laboratory variables, including white blood cells (WBC), hemoglobin, platelets, C-reactive protein (CRP), albumin, fibrinogen, monocytes, neutrophils, and lymphocytes.

The primary outcome of this study was the incidence of infectious complications within one month post-surgery. The diagnosis of postoperative infectious complications (mainly including surgical site, respiratory, and urinary tract infections) typically follows clinical criteria that include a combination of symptoms (fever, tachycardia, and others), laboratory findings (white blood cells and others), sometimes urine and blood cultures, and radiological examinations (chest X-ray). As reported in previous studies [6, 7], the systemic immune-inflammation index (SII) was calculated using the following formula: SII = platelets × neutrophils/lymphocytes (×10^9/L). The albumin-to-fibrinogen ratio (AFR) was derived by dividing fibrinogen by albumin, whereas the neutrophil-to-lymphocyte ratio (NLR) was derived by dividing the number of neutrophils by lymphocytes.

Statistical analysis

Statistical analyses were conducted using SPSS (version 23.0) and GraphPad (version 9.0) software, employing t-tests, Mann-Whitney U tests, and chi-square tests. Online receiver operator characteristic (ROC) curves [8] were used to evaluate the predictive value of the quantitative data for postoperative infectious complications. Binary logistic regression analysis was employed to explore independent risk factors, which were then incorporated into a nomogram predictive model using R (version 4.0.1). A two-sided P<0.05 was considered statistically significant.

Results

Based on the inclusion and exclusion criteria, 301 patients who had undergone laparoscopic hysterectomy for cervical cancer were enrolled. Within one month postoperatively, 38 patients experienced infectious complications, resulting in an overall incidence rate of 12.6%. Table 1 presents the demographic, clinical, and laboratory variables associated with postoperative infectious complications. No statistically significant differences were observed in the presence of pausimenia, pathological type, FIGO stage, history of abdominal surgery, comorbidities of hypertension and COPD, or lymph node dissection between patients with and without infectious complications (P > 0.05). Patients ≥ 60 years of age (P = 0.019), BMI ≥ 24.0 (P = 0.001), or with diabetes (P = 0.007) showed a significant association with the development of postoperative infectious complications. Additionally, operation time ≥ 3 h (P < 0.001) and CRP level ≥ 8 mg/L (P = 0.035) correlated with an increased risk of infectious complications. Furthermore, patients in the complication group exhibited significantly higher levels of SII (P < 0.001) and NLR (P < 0.001) and lower levels of AFR (P < 0.001) thanthose in the non-complication group.

Table 1 Demographic and clinical variables associated with postoperative infectious complications

Three continuous variables (SII, AFR, and NLR), identified as potential risk factors for infectious complications (P < 0.05; Table 1), were further evaluated using ROC curves. The SII (AUC: 0.732, P < 0.001, cut-off value: 830), AFR (AUC: 0.755, P < 0.001, cut-off value: 9.25), and NLR (AUC: 0.805, P < 0.001, cut-off value: 3.45) were all significant predictors for postoperative infectious complications (Fig. 1). According to the cut-off points, these three continuous variables were classified into two groups: high (≥ cut-off value) and low (< cut-off value).

Fig. 1
figure 1

Predictive values of the SII (A), AFR (B), and NLR (C) for postoperative infectious complications by ROC curve analysis. ROC, receiver operating characteristic; SII, systemic immune-inflammation index; AFR, albumin/fibrinogen ratio; NLR, neutrophil-to-lymphocyte ratio; AUC, area under the curve

Eight variables (P < 0.05; Table 1) were analyzed using a binary multivariate logistic regression model. Six variables were identified to be independent risk factors for postoperative infectious complications (Table 2): Age ≥ 60 (OR: 3.06, 95%CI: 1.06–8.79, P = 0.038), BMI ≥ 24.0 (OR: 3.70, 95%CI: 1.48–9.26, P = 0.005), diabetes (OR: 2.91, 95% CI: 1.10–7.73, P = 0.032), SII ≥ 830 (OR: 6.95, 95%CI: 2.53–19.07, P < 0.001), AFR < 9.25 (OR: 4.94, 95%CI: 2.02–12.07, P < 0.001), and NLR ≥ 3.45 (OR: 7.53, 95%CI: 3.04–18.62, P < 0.001). Furthermore, these six factors were incorporated into a nomogram prediction model using R The scores of SII, AFR, and NLR were significantly higher than those of age, BMI, and diabetes, indicating that they carry more weight in the predictive model (Fig. 2A). Evaluation of the nomogram model by ROC curve analysis indicated an AUC of 0.928, a sensitivity of 81.0%, and a specificity of 92.1%, respectively (Fig. 2B). Moreover, the decision curve analysis (DCA) demonstrated that this model provides superior benefits for predicting infectious complications in comparison with the “treat all” or “treat none” strategies (Fig. 3B). Furthermore, the calibration curve confirmed that the nomogram predictions (actual and bias-corrected curves) were closely aligned with the ideal curve (Fig. 3C). These findings support the strong predictive performance of our nomogram model.

Table 2 Binary multivariate logistic regression analysis of postoperative infectious complications
Fig. 2
figure 2

A nomogram model for postoperative infectious complications (A) and evaluated using ROC curve analysis (B). BMI, body mass index; SII, systemic immune-inflammation index; AFR, albumin-to-fibrinogen ratio; NLR, neutrophil-to-lymphocyte ratio; ROC, receiver operating characteristic; AUC, area under the curve

Fig. 3
figure 3

Evaluation of nomogram model using DCA (A) and calibration (B) curve analyses. DCA, decision curve analysis

Discussion

Cervical cancer has become a global health threat, and its early diagnosis and treatment are crucial for patient prognosis. Several studies support the use of specific biomarkers (carcinoembryonic antigen, squamous cell carcinoma antigen, and CD44) to identify early-stage cervical cancer and, therefore, offer a better prognosis for patients [9, 10]. Infectious complications are very common postoperative complications after cervical cancer, which severely affect patients’ outcomes [11]. Consequently, identifying predictive factors for infectious complications is extremely important. The incidence of infectious complications among patients enrolled in this study was 12.6%, which is higher than the 5.8% reported by Capozzi’s group [12]. A previous study reported variable incidence rates of infectious complications after hysterectomy: 13.0% in vaginal hysterectomy, 10.5% in abdominal hysterectomy, and 9.0% in laparoscopic hysterectomy [13]. As the reported incidence of complications varies with different surgical approaches, this study chose to focused on laparoscopic hysterectomy for cervical cancer.

Despite these advancements, hysterectomy remains a compelling and challenging area of research for the surgical teams. Minimally invasive approaches have the following advantages: reduced trauma associated with surgery in terms of hospital stay, recovery time, and aesthetic outcomes. Given the improvements in patient outcomes and benefits to healthcare systems, minimally invasive surgery should be preferred when feasible and safe [14]. Some studies have shown that different surgical approaches can lead to varying complications and outcomes in the treatment of cervical cancer. A recent meta-analysis found that laparoscopic radical hysterectomy is associated with a higher risk of perioperative urologic complications compared to abdominal radical hysterectomy [15]. However, Pecorino et al. reported no significant differences in intraoperative and postoperative complication rates, follow-up death, or recurrence rates between patients who underwent abdominal or laparoscopic radical hysterectomy [16]. Another study by Corrado et al. also revealed no statistically significant difference regarding disease-free survival and overall survival between minimally invasive and abdominal radical hysterectomy [17]. Considering the potential impact of different surgical approaches on the results, we only included, patients who underwent laparoscopic hysterectomy for cervical cancer.

This study identified six independent risk factors (age ≥ 60, BMI ≥ 24.0, diabetes, SII ≥ 830, AFR < 9.25, and NLR ≥ 3.45) for postoperative infectious complications. Age is a well-recognized risk factor for postoperative complications (including infectious complications), particularly in patients aged > 60 years old [18]. Elderly patients, often experience a decline in immune function, impairing their body’s ability to fight infections. Additionally, elderly patients are more likely to have comorbid conditions (e.g., diabetes, cardiovascular diseases, and reduced renal function), which can further compromise their immune responses and wound-healing capabilities [19]. BMI ≥ 24.0 (overweight or obese in China) is usually associated with many physiological changes that can compromise surgical recovery and increase the likelihood of infections [20]. A previous study by Mullen et al. [21] showed that patients with a BMI of 25 or higher had a significantly higher rate of surgical site infections following various surgical procedures, consistent with our results. Diabetes has also been widely recognized as a risk factor for postoperative infectious complications due to its effects on the immune system and wound healing processes [22, 23]. Diabetes is associated with both microvascular and macrovascular alterations that impair blood flow, leading to decreased oxygen and nutrient supply to tissues, which are critical for healing [24, 25]. Additionally, hyperglycemia can inhibit various immune functions, including neutrophil activity, which is crucial for preventing and controlling infections [26].

The SII has emerged as a potential biomarker for predicting inflammatory status and has been associated with outcomes in various medical conditions, including cancer [27] and cardiovascular diseases [28]. A higher SII level usually indicates a pro-inflammatory state, and an imbalanced immune response, potentially leading to increased susceptibility to infections or a weakened immune defense mechanism [29, 30]. An emerging biomarker, AFR, is calculated using albumin and fibrinogen levels, and it evaluates the balance between nutritional status and the inflammatory response. AFR has been investigated in various clinical settings to predict outcomes, including cancer prognosis [31] and cardiovascular events [32]. A study by Maimaiti et al. [33] indicated that preoperative AFR can effectively predict septic failure and periprosthetic joint infection in patients who underwent revision total joint arthroplasty. All these studies support the predictive value of a low AFR level for postoperative infectious complications in this study. A widely researched biomarker, NLR, measures the balance between neutrophils and lymphocytes in the blood and has become an important prognostic indicator in various clinical diseases, including sepsis [34], Mycoplasma pneumoniae pneumonia [35], and cancer [36]. Neutrophils are key players in acute inflammatory responses and infections, whereas lymphocytes represent the regulatory elements of the immune system [37]. Accordingly, an elevated NLR often suggests a heightened inflammatory state and a potentially compromised immune response [37], which can predispose patients to infections.

Based on these six independent risk factors, we constructed a nomogram prediction model and the evaluation results indicated its accuracy in predicting postoperative infectious complications. This model can aid in identifying high-risk patients who may benefit from closer monitoring and pre-emptive interventions. Moreover, if complications arise, high-risk patients identified by the model could receive more intensive prophylactic antibiotic regimens, enhanced postoperative surveillance, and earlier interventions. Furthermore, early identification and management of potential infectious complications can lead to quicker interventions, reduced morbidity, and improved overall patient outcomes. In summary, this predictive tool can estimate a patient’s risk of developing infections after surgery, enabling personalized medical decision-making and improving patient outcomes.

The strength of this study lies in identifying six novel independent risk factors for postoperative infectious complications through multivariate analysis and constructing an effective individualized risk prediction model based on these factors. However, the limitations include the single-center retrospective nature of the study and the relatively small sample size, which may have omitted some important risk factors.

Data availability

No datasets were generated or analysed during the current study.

References

  1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    Article  PubMed  Google Scholar 

  2. Chen W, Zheng R, Baade PD, et al. Cancer statistics in China, 2015. CA Cancer J Clin. 2016;66(2):115–32.

    Article  PubMed  Google Scholar 

  3. Ramirez PT, Frumovitz M, Pareja R, et al. Minimally invasive versus Abdominal Radical Hysterectomy for Cervical Cancer. N Engl J Med. 2018;379(20):1895–904.

    Article  PubMed  Google Scholar 

  4. Jaiyeoba O. Postoperative infections in obstetrics and gynecology. Clin Obstet Gynecol. 2012;55(4):904–13.

    Article  PubMed  Google Scholar 

  5. Clarke-Pearson DL, Geller EJ. Complications of hysterectomy. Obstet Gynecol. 2013;121(3):654–73.

    Article  PubMed  Google Scholar 

  6. Zhao J, Jiang Y, Qian J, et al. A nomogram model based on the combination of the systemic immune-inflammation index and prognostic nutritional index predicts weight regain after laparoscopic sleeve gastrectomy. Surg Obes Relat Dis. 2023;19(1):50–8.

    Article  PubMed  Google Scholar 

  7. Zhu S, Cheng Z, Hu Y, et al. Prognostic value of the systemic Immune-inflammation index and Prognostic Nutritional Index in patients with Medulloblastoma Undergoing Surgical Resection. Front Nutr. 2021;8:754958.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Robin X, Turck N, Hainard A, et al. pROC: an open-source package for R and S + to analyze and compare ROC curves. BMC Bioinformatics. 2011;12:77.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Valenti G, Vitale SG, Tropea A, Biondi A, Laganà AS. Tumor markers of uterine cervical cancer: a new scenario to guide surgical practice. Updates Surg. 2017;69(4):441–9.

    Article  PubMed  Google Scholar 

  10. Giannini A, D’Oria O, Chiantera V, et al. Minimally invasive surgery for cervical Cancer: should we look beyond squamous cell carcinoma. J Invest Surg. 2022;35(7):1602–3.

    Article  PubMed  Google Scholar 

  11. Kumarasamy S, Kumar H, Sharma V, Mandavdhare H, Ram S, Singh H. Role of Interleukin-6 in prediction of early complications after minimally invasive Oesophagectomy-a pilot study. Indian J Surg Oncol. 2023;14(3):694–8.

    Article  PubMed  Google Scholar 

  12. Capozzi VA, De Finis A, Scarpelli E, et al. Infectious complications in laparoscopic gynecologic oncology surgery within an ERAS-Compliant setting. J Pers Med. 2024;14(2):147.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Mäkinen J, Johansson J, Tomás C, et al. Morbidity of 10 110 hysterectomies by type of approach. Hum Reprod. 2001;16(7):1473–8.

    Article  PubMed  Google Scholar 

  14. Giannini A, D’Oria O, Bogani G, et al. Hysterectomy: Let’s step up the ladder of evidence to look over the Horizon. J Clin Med. 2022;11(23):6940.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Hwang JH, Kim BW. Laparoscopic radical hysterectomy has higher risk of perioperative urologic complication than abdominal radical hysterectomy: a meta-analysis of 38 studies. Surg Endosc. 2020;34(4):1509–21.

    Article  PubMed  Google Scholar 

  16. Pecorino B, D’Agate MG, Scibilia G, et al. Evaluation of Surgical outcomes of Abdominal Radical Hysterectomy and Total Laparoscopic Radical Hysterectomy for Cervical Cancer: a retrospective analysis of data collected before the LACC Trial. Int J Environ Res Public Health. 2022;19(20):13176.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Corrado G, Anchora LP, Bruni S, et al. Patterns of recurrence in FIGO stage IB1-IB2 cervical cancer: comparison between minimally invasive and abdominal radical hysterectomy. Eur J Surg Oncol. 2023;49(11):107047.

    Article  PubMed  Google Scholar 

  18. Wang Y, Li H, Ye H, et al. Postoperative infectious complications in elderly patients after elective surgery in China: results of a 7-day cohort study from the International Surgical outcomes Study. Psychogeriatrics. 2021;21(2):158–65.

    Article  PubMed  Google Scholar 

  19. Stevens LA, Li S, Wang C, et al. Prevalence of CKD and comorbid illness in elderly patients in the United States: results from the kidney early evaluation program (KEEP). Am J Kidney Dis. 2010;55(3 Suppl 2):S23–33.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Jin X, Qiu T, Li L, et al. Pathophysiology of obesity and its associated diseases. Acta Pharm Sin B. 2023;13(6):2403–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Mullen JT, Moorman DW, Davenport DL. The obesity paradox: body mass index and outcomes in patients undergoing nonbariatric general surgery. Ann Surg. 2009;250(1):166–72.

    Article  PubMed  Google Scholar 

  22. Rifkin WJ, Kantar RS, Cammarata MJ, et al. Impact of diabetes on 30-Day complications in Mastectomy and Implant-based breast Reconstruction. J Surg Res. 2019;235:148–59.

    Article  PubMed  Google Scholar 

  23. Lorenzo Soriano L, Ordaz Jurado DG, Pérez Ardavín J, et al. Predictive factors of infectious complications in the postoperative of percutaneous nephrolithotomy. Actas Urol Esp (Engl Ed). 2019;43(3):131–6.

    Article  CAS  PubMed  Google Scholar 

  24. Cade WT. Diabetes-related microvascular and macrovascular diseases in the physical therapy setting. Phys Ther. 2008;88(11):1322–35.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Skyler JS, Bakris GL, Bonifacio E, et al. Differentiation of diabetes by Pathophysiology, Natural History, and prognosis. Diabetes. 2017;66(2):241–55.

    Article  CAS  PubMed  Google Scholar 

  26. Jafar N, Edriss H, Nugent K. The effect of short-term hyperglycemia on the Innate Immune System. Am J Med Sci. 2016;351(2):201–11.

    Article  PubMed  Google Scholar 

  27. Tian BW, Yang YF, Yang CC, et al. Systemic immune-inflammation index predicts prognosis of cancer immunotherapy: systemic review and meta-analysis. Immunotherapy. 2022;14(18):1481–96.

    Article  CAS  PubMed  Google Scholar 

  28. Ye Z, Hu T, Wang J, et al. Systemic immune-inflammation index as a potential biomarker of cardiovascular diseases: a systematic review and meta-analysis. Front Cardiovasc Med. 2022;9:933913.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Marchi F, Pylypiv N, Parlanti A, et al. Systemic Immune-inflammation index and systemic inflammatory response index as predictors of Mortality in ST-Elevation myocardial infarction. J Clin Med. 2024;13(5):1256.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Xia Y, Xia C, Wu L, Li Z, Li H, Zhang J. Systemic Immune inflammation index (SII), system inflammation response index (SIRI) and risk of all-cause Mortality and Cardiovascular Mortality: a 20-Year Follow-Up Cohort Study of 42,875 US adults. J Clin Med. 2023;12(3):1128.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Sun DW, An L, Lv GY. Albumin-fibrinogen ratio and fibrinogen-prealbumin ratio as promising prognostic markers for cancers: an updated meta-analysis. World J Surg Oncol. 2020;18(1):9.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Hou XG, Wu TT, Zheng YY, et al. The fibrinogen-to-albumin ratio is Associated with poor prognosis in patients with coronary artery disease: findings from a large cohort. J Cardiovasc Transl Res. 2023;16(5):1177–83.

    Article  CAS  PubMed  Google Scholar 

  33. Maimaiti Z, Xu C, Fu J, et al. A novel biomarker to screen for Malnutrition: Albumin/Fibrinogen ratio predicts septic failure and Acute infection in patients who underwent Revision Total Joint Arthroplasty. J Arthroplasty. 2021;36(9):3282–8.

    Article  PubMed  Google Scholar 

  34. Huang Z, Fu Z, Huang W, Huang K. Prognostic value of neutrophil-to-lymphocyte ratio in sepsis: a meta-analysis. Am J Emerg Med. 2020;38(3):641–7.

    Article  PubMed  Google Scholar 

  35. Li D, Gu H, Chen L, et al. Neutrophil-to-lymphocyte ratio as a predictor of poor outcomes of Mycoplasma pneumoniae pneumonia. Front Immunol. 2023;14:1302702.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Mosca M, Nigro MC, Pagani R, De Giglio A, Di Federico A. Neutrophil-to-lymphocyte ratio (NLR) in NSCLC, gastrointestinal, and other solid tumors: Immunotherapy and Beyond. Biomolecules. 2023;13(12):1803.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Buonacera A, Stancanelli B, Colaci M, Malatino L. Neutrophil to lymphocyte ratio: an emerging marker of the relationships between the Immune System and diseases. Int J Mol Sci. 2022;23(7):3636.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

None.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

HL X, DL Y, and YB Z participated in the conception and design, data collection, statistical analysis. HL X, and L J wrote the manuscript, participated in the conception and design and data collection.

Corresponding author

Correspondence to Lin Jiang.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the ethics committee of The Affiliated Taizhou People’s Hospital of Nanjing Medical University, Taizhou School of Clinical Medicine, Nanjing Medical University. All methods were carried out in accordance with Declaration of Helsinki. Written Informed consent was obtained from all participants/patients.

Consent for publication

Not applicable.

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

Xing, H., Yuan, D., Zhu, Y. et al. A nomogram model based on SII, AFR, and NLR to predict infectious complications of laparoscopic hysterectomy for cervical cancer. World J Surg Onc 22, 190 (2024). https://doi.org/10.1186/s12957-024-03489-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12957-024-03489-0

Keywords