Skip to main content
Cureus logoLink to Cureus
. 2021 Sep 5;13(9):e17733. doi: 10.7759/cureus.17733

Relationship Between Neutrophil/Albumin Ratio and Early Mortality After Major Lower Extremity Amputation

Ali Eray Günay 1,, Mehmet Ekici 1
Editors: Alexander Muacevic, John R Adler
PMCID: PMC8491629  PMID: 34659947

Abstract

Introduction

Diabetic foot infection is a condition that affects the patient's life, may cause limb loss, and has a high mortality. Too many parameters were used for predicting early mortality but the gold standard method wasn't described. Neutrophil lymphocyte ratio (NLR) is universally accepted as a predictive value for amputation-free survival and mortality. NLR increases due to inflammation-induced neutrophilia and lymphopenia related to cortisol-induced stress. Increasing in the neutrophil albumin ratio is expected due to decreasing albumin levels because albumin is a negative acute-phase reactant. The aim of this study is to investigate the sensitivity and value of the neutrophil albumin ratio (NAR) for early mortality after major lower extremity amputation (LEA).

Methods 

Following the approval of the ethics committee, 87 patients who underwent major LEA between May 2018 and May 2020 were analyzed for the study. White blood cell (WBC), neutrophil, lymphocyte, C-reactive protein (CRP), creatinine, albumin, platelet, and hemoglobin values on the day prior to surgery were recorded. NLR was calculated as the ratio of neutrophil count to lymphocyte count, NAR as the ratio of neutrophil count to albumin value, CRP/albumin ratio (CAR) as the ratio of CRP value to albumin value, and platelet lymphocyte ratio (PLR) as the ratio of platelet count to lymphocyte count. Each parameter was also recorded in the postoperative second week.

Results

Of the patients included in the study, 52 were men (59.8%) and 35 were women (40.2%). It was determined that 29 of 87 patients (33.3%) died within the first year. The relationship between post-operative NAR value and early mortality is examined. The area under the curve was calculated as 0.873. When the cut-off value was applied as 0.265, the sensitivity was found as 88% and specificity as 76%.

Conclusions

Higher neutrophil/albumin ratio after lower extremity amputation was associated with early mortality after extremity amputation. This parameter can help predict mortality. The cut-off value was determined as 0.265, the sensitivity was found as 88%, and specificity as 76%.

Keywords: nar, limb amputation, lea, diabetic foot infection, neutrophil, albumin

Introduction

Amputations performed at the proximal ankle level are called major lower extremity amputation (LEA) [1]. Major LEA is a surgical procedure with high morbidity and mortality rates. The incidence of nontraumatic major lower extremity amputation is 12-50 per 100000 annually [2]. After non-traumatic major amputation, the five-year mortality rate reaches 40% [3].

Patients requiring major amputation on the basis of atherosclerosis and diabetes mellitus are generally elderly and have multiple comorbidities [4]. Critical limb ischemia is a clinical condition characterized by nonhealing ulcers especially in the lower extremities, gangrene, and pain in tissues other than the ischemic area [2]. Severe inflammation occurs in case of ischemic tissue damage. In this case, the neutrophil lymphocyte ratio (NLR) increases due to inflammation-induced neutrophilia and lymphopenia related to cortisol-induced stress [5-7]. Similar to the NLR, the platelet/lymphocyte ratio is also one of the inflammatory response values that increase with systemic inflammation. They have previously been used as a prognostic biomarker in various diseases [4,8]. Limb ischemia is an atherosclerotic disease associated with an inflammatory response. In previous studies, C-reactive protein (CRP), platelet aggregation, and NLR were defined as effective predictive values for limb ischemia [9,10]. In addition, NLR is universally accepted as a predictive value for amputation-free survival and mortality [11].

Serum albumin level is a negative acute-phase reactant. Its level in the blood decreases with systemic inflammatory response [12]. Although the neutrophil/albumin ratio (NAR) has been used as a prognostic factor in different areas, there is no study on the predictive effect of NAR on limb ischemia and related amputations [13,14].

The hypothesis of this study is that increased systemic response is associated with early mortality following major LEA. The rising level of NAR may predict mortality risk. The aim of this study is to investigate the sensitivity and value of the NAR for early mortality after major LEA.

Materials and methods

Following the approval of the local ethics committee, 163 patients who underwent major LEA at our institution between May 2018 and May 2020 were retrospectively analyzed for the study.

Patients who did not benefit from conservative treatment and other surgical procedures (i.e., revascularization) and had undergone major amputation due to diabetic foot ulcer or peripheral artery disease (PAD) were included in the study. Patients who underwent amputation secondary to trauma, underwent bilateral amputation, had sepsis, had a history of malignancy, used corticosteroids, and patients whose blood white blood cell (WBC) count was less than 4x109/L or more than 25x109/L before surgery were excluded from the study. A total of 76 patients were excluded from the study due to exclusion criteria.

As surgical procedures, below-knee amputation, above-knee amputation, or knee disarticulation were performed on the patients. Demographic data, such as age, gender, follow-up time, postoperative survival was evaluated.

Patients were divided into two groups according to the cut-off value of NAR level found by receiver operating characteristic (ROC) analysis after surgery. Those with NAR levels below the cut-off value were named group one, and those with a higher cut-off value were named group two.

WBC, neutrophils, lymphocyte count, CRP, creatinine, albumin, platelets (PLT), and hemoglobin (HGB) values from the venous blood sample drawn on the day prior to surgery were retracted from the records. Venous blood sample results drawn in the second week after surgery were determined as a control value. NLR was calculated as the ratio of neutrophil count to lymphocyte count, NAR as the ratio of neutrophil count to albumin value, CRP/albumin ratio (CAR) as the ratio of CRP value to albumin value, and PLR as the ratio of platelet count to lymphocyte count. Each parameter was recorded separately as pre-op and post-op second week.

The data was transferred to the computer environment and analyzed with IBM Corp. Released 2013. IBM SPSS Statistics for Windows, Version 22.0. Armonk, NY: IBM Corp. The compliance of quantitative data to normal distribution was tested with the Shapiro-Wilk test. Pearson’s Chi-Square was used for the analysis of categorical data, and Mann-Whitney U and Kruskal-Wallis tests were used for the analysis of quantitative data that did not show normal distribution. ROC analysis was used to calculate the predictive value of pre-operative and post-operative NAR, PLR, CAR, and NLR specificity and sensitivity ratios. Results with a p-value less than 0.05 were considered statistically significant. 

Results

Of the 87 patients included in the study, 52 were men (59.8%) and 35 were women (40.2%). The mean age of the patients was found to be 70.63 ± 1.27 (44-92) years. 23 patients (26.4%) were amputated due to PAD and 64 patients (73.6%) were amputated due to diabetic foot ulcers. The mean hospital stay was 21.95 ± 1.79 days.

It was determined that 19 patients (21.8%) died in the first month after surgery, nine died in the first to sixth months, and one patient died in the 12th month, 29 of 87 patients (33.3%) died within the first year. It was determined that two of the patients who died in the first month died within the first 24 hours after the operation, 16 died in the hospital before discharge, and three died at home after discharge. The mean follow-up period of the patients who did not die was found to be 15.6 ± 1.13 months.

As a surgical procedure, 73 patients (83.9%) underwent below-knee amputation, 12 patients (13.8%) underwent above-knee amputation, and two (2.3%) underwent knee disarticulation. The mean operation time was 68.28 ± 2.59 minutes.

Pre-op and post-op blood parameters of the patients are shown in Table 1. Pre-op and post-op NAR, CAR, NLR, and PLR cut-off values of the patients were calculated for early mortality. Post-op mortality numbers for each value, including the patients below and above the cut-off value, are given in the table. Since two patients died within 24 hours postoperatively, albumin values were not found in the records (Table 2).

Table 1. Comparision of the pre-operative and post-operative blood parameters .

NLR: Neutrophil/Lymphocyte ratio, NAR: Neutrophil /Albumin ratio, CAR: CRP/Albumin ratio, PLR: Platelet/ Lymphocyte ratio, g: gram, dL: deciliter, mg: milligram, L: Liter, WBC: White Blood Cell

    Preop     Postop   p
Median Min Max Median Min Max
WBC (x109/L) 12.36 6.53 24.10 8.48 4.04 15.29 <0.001
Neutrophil (x109/L) 9.58 3.96 22.33 5.95 2.05 13.15 <0.001
Lymphocyte(x109/L) 1.51 0.57 3.14 1.56 0.54 2.86 0.930
Hemoglobin (g/dL) 10.20 7.1 13.4 9.8 7.4 13.4 0.041
Platelet (103/mm3) 320 73 631 325 147 846 <0.001
CRP (mg/L) 136.1 20.20 379.4 51.5 7.8 211.2 <0.001
Albumin (g/dL) 25.4 14 36.4 27 22.7 37 0.390
Creatinine (mg/L) 0.95 0.45 5.36 0.88 0.37 6.07 0.045
NLR 6.04 1.62 19.93 3.39 1.21 24.35 <0.001
PLR 207.79 100 555.91 218.18 115.54 409.41 0.876
NAR 0.34 0.10 1.08 0.20 0.07 0.52 <0.001
CAR 5.24 0.65 20.50 1.96 0.26 8.1 <0.001

Table 2. ROC analysis results and cut-off values of preoperative and postoperative NAR, CAR, PLR, NLR, and post-operative mortality rates .

AUC: Area under curve, NLR: Neutrophil/Lymphocyte ratio, NAR: Neutrophil/Albumin ratio, CAR: CRP/Albumin ratio, PLR: Platelet/ Lymphocyte ratio

          Mortality Total p
  AUC Cut-off Sensitivity Spesivity No n (%) Yes n (%)
NAR                
Pre-operative 0.707 0.365≥ 62 63 36 (%62.0) 11 (%38.9) 47 0.041
0.365< 22 (%38.0) 18 (%61.1) 40
Post-operative 0.865 0.265≥ 88 76 43 (%74.1) 3 (%11.1) 46 <0.001
0.265< 15(%25.9) 24(%88.9) 39
NLR                
Pre-operative 0.746 6.37≥ 93 52 30 (%51.7) 2 (%6.9) 32 0.041
6.37< 28 (%48.3) 27 (%93.1) 55
Post-operative 0.883 7.06≥ 81 85 49 (%84.5) 5 (%18.5) 54 <0.001
7.06< 9 (%15.5) 22 (%71.5) 31
PLR                
Pre-operative 0.547 247.28≥ 51 64 37 (%63.8) 13 (%44.8) 50 0.176
247.28< 21 (%36.2) 16 (%55.2) 37
Post-operative 0.611 191.71≥ 74 44 25 (%43.1) 7 (%25.9) 32 0.154
191.71< 33 (%56.9) 20 (%74.1) 53
CAR                
Pre-operative 0.540 2.79≥ 82 23 13 (%24.1) 6 (%22.2) 19 0.778
2.79< 41 (%75.9) 21 (%77.8) 62
Post-operative 0.790 3.07≥ 78 71 34 (%69.4) 6 (%25.0) 40 <0.001
3.07< 15 (%30.6) 18 (%75.0) 33

The relationship between post-op NAR value and early mortality is shown in Figure 1.

Figure 1. ROC analysis graphic for post-op NAR.

Figure 1

NAR: Neutrophil/Albumin ratio ROC: Receiver operating characteristic

The area under the curve was calculated as 0.873. When the cut-off value was applied as 0.265, the sensitivity was found as 88% and specificity as 76%. For the NLR pre-op cut-off value, sensitivity was calculated as 93% and specificity as 52% (Table 2). According to logistic regression analysis results, it was observed that a postoperative NAR value over 0.265 increases the risk of death 11.5 times (Table 3). Distributions of demographic and laboratory results after grouping with post-operative NAR cut-off values are shown in Table 4 and Table 5

Table 3. Effect of postoperative NAR value on mortality according to logistic regression analysis.

NAR: Neutrophil/Albumin Ratio, CAR: C-reactive protein/Albumin Ratio, OR: Odds Ratio, CI: Confidence Interval

  Cut Off n Mortality (%) OR (CI 95%)
NAR postoperative 0.265≥ 46 3 (6.5%) 1.0
0.265< 39 24 (61.5%) 11.5 (2.6 – 50.3)
CAR postoperative 3.070≥ 40 6 (15.0%) 1.0
3.070< 33 18 (54.5%) 2.3 (0.6 – 8.9)

Table 4. Distributions of demographic and laboratory results after grouping with post-operative NAR cut off value.

NLR: Neutrophil/Lymphocyte ratio, NAR: Neutrophil/Albumin ratio, CAR: CRP/Albumin ratio, PLR: Platelet/Lymphocyte ratio, g: gram, dL: deciliter, mg: milligram, L: Liter, WBC: White Blood Cell, CRP: C-reactive protein

  Group 1 (n=46) Group 2 (n=39)  
  Median Min Mix Median Min Max p
Age (years) 67.50 44 91 77 49 92 0.050
Surgery Duration (min) 72 25 140 64 30 170 0.148
Follow Up Time (months) 15.50 1 31 15.5 1 31 <0.001
Hospitalization (day) 20.50 4 78 21 6 53 0.251
WBC Pre-op (x109/L) 11.67 6.53 24.10 12.90 6.61 19.36 0.027
WBC Post-op (x109/L) 7.71 4.04 11.40 10.61 8.50 14.95 <0.001
Neutrophil Pre-op (x109/L) 8.71 3.96 22.33 10.09 1.67 17.24 0.022
Neutrophil Post-op (x109/L) 4.88 2.05 8.55 7.97 5.40 12.44 <0.001
Lymphocyte Pre-op(x109/L) 1.48 0.32 3.14 1.50 0.42 3.40 0.195
Lymphocyte Post-op(x109/L) 1.63 0.49 2.86 1.56 0.73 2.60 0.006
NAR Pre-op 0.34 0.10 1.08 0.37 0.07 1.01 0.060
NAR Post-op 0.17 0.07 0.25 0.32 0.26 0.41 <0.001
Hb Pre-op (g/L) 10.60 7.10 14.40 9.70 9.10 13.40 0.774
Hb Post-op (g/L) 9.80 7.40 13.40 9.70 8.20 13.30 0.478
PLT Pre-op (103/mm3) 319 66 664 272 145 570 0.815
PLT Post-op (103/mm3) 297 53 846 312 100 629 0.161
Creatinine Pre-op (mg/L) 0.92 0.44 8.02 1.18 0.63 5.36 0.031
Creatinine Post-op (mg/L) 0.82 0.28 7.45 1.00 0.66 6.07 0.013
CRP Pre-op (mg/L) 121.10 16.50 393.50 162.00 88.80 322.00 0.167
CRP Post-op (mg/L) 49.20 7.00 175.40 88.15 40.40 211.20 <0.001
Albumin Pre-op (g/dL) 25.00 16.00 36.20 25.00 17.00 33.10 0.965
Albumin Post-op (g/dL) 26.90 19.00 37.00 24.50 16.00 31.00 <0.001

Table 5. Distribution of gender, diabetes mellitus prevalence, amputation level, and mortality day.

  Group 1 Group 2 p
Gender      
            Male 26 25 0.512
            Female 20 14
Diabetes Mellitus 36/46 27/39 0.457
Amputation      
            Below Knee 41 30 0.152
            Above and Knee 6 9
Mortality      
            30 Days> 1 16 0.535
            30 Days≤ 2 8

Discussion

Mortality after major LEA is a serious issue. It is important to be able to predict this situation in order to prevent medicolegal problems and to manage treatment. Mortality in the first 30 days after major LEA was reported between 7%-30%, and one-year mortality was reported between 19% and 48% [15-20]. In our study, the first-month mortality after surgery was 21.8%, and the one-year mortality was 33.3%.

NLR is a known proinflammatory parameter. Luo et al. showed that the NLR value on the seventh day after treatment in critical limb ischemia is an independent predictive value for the risk of amputation [21]. Teperman et al. [8] showed that there is a significant relationship between NLR and the severity of lower extremity PAD. Fest et al. [22] showed that the NLR value is an underlying disease-independent risk factor for mortality in the whole population. In our study, the cut-off value of NLR for early mortality was 6.37 (93% sensitivity, 52% specificity) for preoperative values and 7.06 (81% sensitivity, 85% specificity) for postoperative values. These values demonstrate that the postoperative NLR value is a strong predictor of early mortality.

In this study, the ratio of postoperative NAR value was found to have an independent predictive value for early mortality. NAR postop cut-off value for early mortality was found to be 0.265 (88% sensitivity, 76% specificity). The sensitivity and specificity of the preop NAR value were found to be lower than the postop NAR value. Earlier NAR has been used in few studies. Hwang et al. [23] showed that patients with severe sepsis with high delta neutrophil/serum albumin ratio (DNI/A) had higher 28-day early mortality rates, and Peng et al. [24] showed the relationship between NAR value and mortality after cardiogenic shock.

Decrease in neutrophil value and increase in albumin level result in a decrease in NAR value. It was observed that the neutrophil value was lower and the albumin value was higher in patients with low NAR values after surgery, and these differences were considered statistically significant. Serum albumin level is a nutritional marker and a negative acute phase reactant for inflammation [11, 25]. Yeşil et al. found that in patients who were followed up for diabetic foot ulcers, serum albumin levels of patients who underwent amputation were lower than patients who recovered [26].

Thrombocytosis and lymphopenia correlate with the severity of systemic infection, and PLR is a new infection marker that includes both hematological values. Taşoğlu et al. reported that the extremity survival time was significantly reduced in patients with a PLR value >160 in PAD-induced extremity ischemia [27]. Yaprak et al. concluded that PLR is a superior marker to NLR in determining early mortality in patients with end-stage renal disease [28]. In our study, the sensitivity of preoperative PLR value for early mortality was 51% and its specificity was 64%. The sensitivity of postop PLR was 74% and its specificity was 44%.

CRP is an acute phase reactant. It has been shown that there is a potential relationship between rising CRP value and major amputation [23,29]. CAR in critically ill patients and malignancies is a prognostic factor based on systemic infection [29]. Süleymanoğlu et al. [30] showed the CAR value as an independent predictor in the prognosis of PAD. In our study, the cut-off value for preop CAR was 2.79 (sensitivity 82%, specificity 23%), and the postop CAR cut-off value was 3.07 (sensitivity 78%, specificity 71%). NLR value is a superior marker for mortality after major amputation compared to CAR and PLR.

The limitations of the study were that it was conducted on a relatively small group and was a single center retrospective study.

Conclusions

In conclusion, a higher neutrophil/albumin ratio after lower extremity amputation was associated with early mortality after extremity amputation. When the cut-off value for NAR was accepted as 0.265, the sensitivity was found to be 88% and the specificity as 76%. Prospective studies with larger case series aiming to reveal which of the factors that increase this rate are more effective on mortality are needed.

The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.

The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained or waived by all participants in this study. Kayseri City Hospital Clinical Research Ethics Committee issued approval 311

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

References

  • 1.Comparing the incidence of lower extremity amputations across the world: the global lower extremity amputation study. Unwin N. http://onlinelibrary.wiley.com/doi/abs/10.1111/j.1464-5491.1995.tb02055.x. Diabet Med. 1995;12:14–18. [PubMed] [Google Scholar]
  • 2.Inter-society consensus for the management of peripheral arterial disease (TASC II) Norgren L, Hiatt WR, Dormandy JA, Nehler MR, Harris KA, Fowkes FG. J Vasc Surg. 2007;45:0–67. doi: 10.1016/j.jvs.2006.12.037. [DOI] [PubMed] [Google Scholar]
  • 3.Fifteen-year trends in lower limb amputation, revascularization, and preventive measures among medicare patients. Goodney PP, Tarulli M, Faerber AE, Schanzer A, Zwolak RM. JAMA Surg. 2015;150:84–86. doi: 10.1001/jamasurg.2014.1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Prognostic significance of combination of preoperative platelet count and neutrophil-lymphocyte ratio (COP-NLR) in patients with non-small cell lung cancer: based on a large cohort study. Zhang H, Zhang L, Zhu K, et al. PLoS One. 2015;10:0. doi: 10.1371/journal.pone.0126496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Neutrophil-lymphocyte ratio predicts medium-term survival following elective major vascular surgery: a cross-sectional study. Bhutta H, Agha R, Wong J, Tang TY, Wilson YG, Walsh SR. Vasc Endovascular Surg. 2011;45:227–231. doi: 10.1177/1538574410396590. [DOI] [PubMed] [Google Scholar]
  • 6.The role of inflammation, humoral and cell mediated autoimmunity in the pathogenesis of atherosclerosis. Pereira IA, Borba EF. http://smw.ch/article/doi/smw.2008.12287. Swiss Med Wkly. 2008;138:534–539. doi: 10.4414/smw.2008.12287. [DOI] [PubMed] [Google Scholar]
  • 7.Preoperative neutrophil-lymphocyte ratio and outcome from coronary artery bypass grafting. Gibson PH, Croal BL, Cuthbertson BH, et al. Am Heart J. 2007;154:995–1002. doi: 10.1016/j.ahj.2007.06.043. [DOI] [PubMed] [Google Scholar]
  • 8.Relationship between neutrophil-lymphocyte ratio and severity of lower extremity peripheral artery disease. Teperman J, Carruthers D, Guo Y, et al. Int J Cardiol. 2017;228:201–204. doi: 10.1016/j.ijcard.2016.11.097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Comparison of the neutrophil/lymphocyte ratio and C-reactive protein levels in patients with amputation for diabetic foot ulcers. Metineren H, Dülgeroğlu TC. Int J Low Extrem Wounds. . 2017;16:23–28. doi: 10.1177/1534734617696729. [DOI] [PubMed] [Google Scholar]
  • 10.Evaluation of major and minor lower extremity amputation in diabetic foot patients. Ozan F, Gürbüz K, Çelik İ, Beştepe Dursun Z, Uzun E. Turk J Med Sci. 2017;47:1109–1116. doi: 10.3906/sag-1601-58. [DOI] [PubMed] [Google Scholar]
  • 11.Clinical predictors of long-term outcomes in patients with critical limb ischemia who have undergone endovascular therapy. Chang SH, Tsai YJ, Chou HH, Wu TY, Hsieh CA, Cheng ST, Huang HL. Angiology. 2014;65:315–322. doi: 10.1177/0003319713515544. [DOI] [PubMed] [Google Scholar]
  • 12.Prognostic significance of an elevated neutrophil-lymphocyte ratio in the amputation-free survival of patients with chronic critical limb ischemia. González-Fajardo JA, Brizuela-Sanz JA, Aguirre-Gervás B, Merino-Díaz B, Del Río-Solá L, Martín-Pedrosa M, Vaquero-Puerta C. Ann Vasc Surg. 2014;28:999–1004. doi: 10.1016/j.avsg.2013.06.037. [DOI] [PubMed] [Google Scholar]
  • 13.Risk factors for lower extremity amputation in diabetic foot disease categorized by Wagner classification. Sun JH, Tsai JS, Huang CH, et al. Diabetes Res Clin Pract. 2012;95:358–363. doi: 10.1016/j.diabres.2011.10.034. [DOI] [PubMed] [Google Scholar]
  • 14.Preprocedural neutrophil to albumin ratio predicts in-stent restenosis following carotid angioplasty and stenting. Shen H, Dai Z, Wang M, Gu S, Xu W, Xu G, Liu X. J Stroke Cerebrovasc Dis. 2019;28:2442–2447. doi: 10.1016/j.jstrokecerebrovasdis.2019.06.027. [DOI] [PubMed] [Google Scholar]
  • 15.Early post-operative mortality after major lower limb amputation: a systematic review of population and regional based studies. van Netten JJ, Fortington LV, Hinchliffe RJ, Hijmans JM. Eur J Vasc Endovasc Surg. 2016;51:248–257. doi: 10.1016/j.ejvs.2015.10.001. [DOI] [PubMed] [Google Scholar]
  • 16.Usefulness of neutrophil/lymphocyte ratio as a predictor of amputation after embolectomy for acute limb ischemia. Taşoğlu I, Çiçek OF, Lafcı G, et al. Annals of Vascular Surgery. 2014;28:606–613. doi: 10.1016/j.avsg.2012.12.009. [DOI] [PubMed] [Google Scholar]
  • 17.Major lower extremity amputations at a Veterans Affairs hospital. Cruz CP, Eidt JF, Capps C, Kirtley L, Moursi MM. Am J Surg. 2003;186:449–454. doi: 10.1016/j.amjsurg.2003.07.027. [DOI] [PubMed] [Google Scholar]
  • 18.Rates of lower-extremity amputation and arterial reconstruction in the United States, 1979 to 1996. Feinglass J, Brown JL, LoSasso A, Sohn MW, Manheim LM, Shah SJ, Pearce WH. Am J Public Health. 1999;89:1222–1227. doi: 10.2105/ajph.89.8.1222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Nontraumatic amputation: incidence and cost analysis. Jindeel A, Narahara KA. Int J Low Extrem Wounds. 2012;11:177–179. doi: 10.1177/1534734612457031. [DOI] [PubMed] [Google Scholar]
  • 20.A meta-analysis of long-term mortality and associated risk factors following lower extremity amputation. Stern JR, Wong CK, Yerovinkina M, et al. Ann Vasc Surg. 2017;42:322–327. doi: 10.1016/j.avsg.2016.12.015. [DOI] [PubMed] [Google Scholar]
  • 21.Post-treatment neutrophil-lymphocyte ratio independently predicts amputation in critical limb ischemia without operation. Luo H, Yuan D, Yang H, et al. Clinics (Sao Paulo) 2015;70:273–277. doi: 10.6061/clinics/2015(04)09. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.The neutrophil-to-lymphocyte ratio is associated with mortality in the general population: the Rotterdam study. Fest J, Ruiter TR, Groot Koerkamp B, Rizopoulos D, Ikram MA, van Eijck CH, Stricker BH. Eur J Epidemiol. 2019;34:463–470. doi: 10.1007/s10654-018-0472-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Newly designed delta neutrophil index-to-serum albumin ratio prognosis of early mortality in severe sepsis. Hwang YJ, Chung SP, Park YS, et al. Am J Emerg Med. 2015;33:1577–1582. doi: 10.1016/j.ajem.2015.06.012. [DOI] [PubMed] [Google Scholar]
  • 24.Association between neutrophil-to-albumin ratio and mortality in patients with cardiogenic shock: a retrospective cohort study. Peng Y, Xue Y, Wang J, Xiang H, Ji K, Wang J, Lin C. BMJ Open. 2020;10:0. doi: 10.1136/bmjopen-2020-039860. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Serum albumin: relationship to inflammation and nutrition. Don BR, Kaysen G. Semin Dial. 2004;17:432–437. doi: 10.1111/j.0894-0959.2004.17603.x. [DOI] [PubMed] [Google Scholar]
  • 26.Predictors of amputation in diabetics with foot ulcer: single center experience in a large Turkish cohort. Yesil S, Akinci B, Yener S, et al. Hormones (Athens) 2009;8:286–295. doi: 10.14310/horm.2002.1245. [DOI] [PubMed] [Google Scholar]
  • 27.Neutrophil-lymphocyte ratio and the platelet-lymphocyte ratio predict the limb survival in critical limb ischemia. Taşoğlu İ, Sert D, Colak N, Uzun A, Songur M, Ecevit A. Clin Appl Thromb Hemost. 2014;20:645–650. doi: 10.1177/1076029613475474. [DOI] [PubMed] [Google Scholar]
  • 28.Platelet-to-lymphocyte ratio predicts mortality better than neutrophil-to-lymphocyte ratio in hemodialysis patients. Yaprak M, Turan MN, Dayanan R, Akın S, Değirmen E, Yıldırım M, Turgut F. Int Urol Nephrol. 2016;48:1343–1348. doi: 10.1007/s11255-016-1301-4. [DOI] [PubMed] [Google Scholar]
  • 29.Evaluation of a modified early warning system for acute medical admissions and comparison with C-reactive protein/albumin ratio as a predictor of patient outcome. Fairclough E, Cairns E, Hamilton J, Kelly C. Clin Med (Lond) 2009;9:30–33. doi: 10.7861/clinmedicine.9-1-30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Assessment of the relation between C-reactive protein to albumin ratio and the severity and complexity of peripheral arterial disease. Süleymanoğlu M, Burak C, Gümüşdağ A, et al. Vascular. 2020;28:731–738. doi: 10.1177/1708538120925952. [DOI] [PubMed] [Google Scholar]

Articles from Cureus are provided here courtesy of Cureus Inc.

RESOURCES