Skip to main content
  • Research article
  • Open access
  • Published:

Intraoperative hypotension is a risk factor for postoperative acute kidney injury after femoral neck fracture surgery: a retrospective study

Abstract

Background

Hip fracture in elderly patients is a serious health concern due to the associated morbidity and mortality. Although acute kidney injury after hip fracture is known to be a significantly poor prognostic factor for morbidity and mortality, the literature regarding the risk factors for acute kidney injury after hip fracture is insufficient. This study aimed to investigate the incidence and associated risk factors for acute kidney injury in patients with femoral neck fracture.

Methods

A total of 248 patients who underwent an operation for femoral neck fracture between January 2011 and January 2015 were retrospectively analyzed. Acute kidney injury was defined according to the Kidney Disease: Improving Global Outcomes guidelines.

Results

The incidence of acute kidney injury was 17.7% (n = 44). Risk factors for acute kidney injury included diabetes mellitus, pre-existing renal disease, preoperative blood urea nitrogen (BUN), preoperative estimated glomerular filtration rate (eGFR), preoperative haemoglobin (Hb) level, type of operation, postoperative creatinine level and intraoperative hypotension (P <  0.05). After controlling for confounding variables, intraoperative hypotension was only the independent risk factor for acute kidney injury (P = 0.012).

Conclusions

Acute kidney injury was found to occur frequently after surgery for femur neck fracture. Surgeons should be aware of acute kidney injury when planning the management of patients with femoral neck fracture and consider that the duration of intraoperative hypotension is a risk factor for acute kidney injury.

Peer Review reports

Background

Hip fracture in elderly patients is a serious health concern due to the associated morbidity and mortality [1,2,3,4]. Complications such as deep vein thrombosis, pulmonary embolism, and myocardial infarction after hip fracture increase morbidity and mortality [5]. Of these, acute kidney injury (AKI) after hip fracture is known to be a significantly poor prognostic factor for morbidity and mortality. AKI is characterized by the sudden impairment of kidney function and can lead to potentially catastrophic complications after hip fracture surgery [2, 6, 7]. Although the exact definition of AKI has been subject to debate, a consensus definition of AKI according to the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines was established in 2012 and is widely used [8].

While several studies have reported that the postoperative development of AKI is associated with high morbidity and mortality after orthopedic operation, data regarding the risk factors for AKI after hip fracture are insufficient. Furthermore, the definition of AKI applied in the existing studies did not correspond to that specified by the KDIGO guidelines. Therefore, the purpose of this study was to investigate the incidence of and associated risk factors for AKI according to KDIGO guidelines in patients with femoral neck fracture.

Methods

This study was approved by our institutional review board. We retrospectively reviewed 312 patients who underwent surgery for femoral neck fracture between January 2011 and January 2015. All fractures were operated on by a single expert orthopedic surgeon. Of these, 24 patients were excluded due to insufficient medical records, and 36 patients were excluded as they were less than 65 years old. Finally, 248 patients (66 men and 182 women) were enrolled in this study. The mean age of the patients at operation was 77.6 years (range, 65–97 years) and the patients were followed for an average of 21.32 days (range, 5–96 days).

Demographic and clinical data including past medical history were thoroughly reviewed. The American Society of Anesthesiologists (ASA) score was determined to evaluate the general comorbidity of patients. Use of medications, such as angiotensin-converting enzyme inhibitors (ACE-Is), non-steroidal anti-inflammatory drugs, and contrast nephrotoxic antibiotics, which are known to affect renal function, was recorded, and preoperative hemoglobin (Hb) levels, electrolyte levels including blood urea nitrogen (BUN), and serum creatinine (SCr) were measured.

Additionally, intraoperative risk factors for AKI were assessed on the basis of the type of operation, operation time, intraoperative blood loss, and the presence of intraoperative hypotension (systolic blood pressure < 80 mmHg or a mean blood pressure < 55–60 mmHg) that persisted for more than 5 min [9].

AKI was diagnosed if any one of the following conditions was present, according to KDIGO 2012 [8]: an increase in SCr of ≥0.3 mg/dL (≥ 26.5 μmol/L) within 48 h, an increase in SCr of ≥1.5 times the baseline value within 7 days, or urine volume <  0.5 mL/kg/h for 6 h. SCr levels were measured at baseline and periodically over 3 days following the operation.

Statistical analysis

Patients were subdivided into 2 groups according to the presence or absence of AKI: the AKI and non-AKI groups. Quantitative variables are expressed as means ± standard deviation (SD) and qualitative variables as number and percentage. Student’s t-test was used for the comparison of quantitative variables and Fisher’s exact test was used for qualitative variables. We performed multivariable logistic regression analysis using the significant variables revealed by the univariate analysis as the independent variables and the presence of AKI as the dependent variable. The stepwise backward elimination method was used for multivariable logistic regression and the final model was selected according to the Akaike’s information criterion (AIC) value. All statistical analyses were conducted using SPSS software (IBM SPSS, version 21; SPSS, Chicago, IL) and a P-value < 0.05 was considered statistically significant.

Results

The demographic and clinical characteristics of patients are presented in Table 1. The overall incidence of AKI was 17.7% (n = 44) and the AKI group had a significantly higher rate of medical comorbidities, including diabetes (P <  0.001), pre-existing renal disease (P <  0.001), and medication with an ACE inhibitor (P = 0.037) than the non-AKI group. Preoperatively, the AKI group had a significantly lower preoperative Hb (P <  0.001), BUN (P <  0.001), preoperative (P = 0.034) and postoperative creatinine (P <  0.001), eGFR (P <  0.001), proteinuria (P = 0.029), ESR (P <  0.001), and CRP (P = 0.012) levels.

Table 1 Baseline characteristics of patients included in the study

The type of operation differed significantly between the AKI and non-AKI groups (P = 0.028). In a subgroup analysis according to the type of operation, including bipolar hemiarthroplasty (BH), total hip replacement (THR), and osteosynthesis, the prevalence of AKI was significantly different (Fig. 1). The incidence of intraoperative hypotension was significantly higher in the AKI group than in the non-AKI group (P = 0.42, Table 2).

Fig. 1
figure 1

Prevalence of AKI in different types of operation. The incidence of AKI was significantly higher in patients who underwent bipolar hemiarthroplasty than in those who underwent other types of operations

Table 2 Baseline laboratory and hemodynamic variables in the AKI and non-AKI groups

Univariable logistic regression analysis showed that type of operation, diabetes mellitus, pre-existing renal disease, ACE inhibitor, preoperative Hb level, preoperative BUN level, preoperative eGFR, postoperative Cr level and intraoperative hypotension were the significant risk factors for postoperative AKI. According to multivariable logistic regression analysis controlling for confounding variables, the presence of intraoperative hypotension was the only significant risk factor for postoperative AKI (Table 3).

Table 3 Multivariable logistic regression analysis for acute kidney injury

Discussion

AKI develops in 7.5% of patients undergoing noncardiac surgery [10] and the postoperative development of AKI is associated with an eight-fold increased probability of death within 30 days of surgery [11]. Interestingly, the previously reported incidence of AKI in patients undergoing cardiac surgery varies between 4 and 9% [12, 13], compared to between 15.3 and 16% for hip fracture surgery [2, 7]. Despite the significant association between AKI and hip fractures, the importance of AKI in patients with femoral neck fracture has only recently received attention. In the present study, the incidence of AKI in patients who underwent femoral neck fracture surgery was 17.7%, which was consistent with previous reports [2, 7]. There was a significant difference in the prevalence of diabetes, pre-existing renal disease, preoperative Hb level, preoperative BUN level, preoperative Cr level, type of operation, and intraoperative hypotension between the AKI and non-AKI groups. After controlling for confounding variables, intraoperative hypotension was the only independent risk factor for AKI.

Bipolar hemiarthroplasty, rather than THR, was significantly associated with an increased risk of AKI in this study, although THR leads to massive blood loss and prolonged operating time because of its invasive and meticulous surgical technique. One possible explanation is that the patients who underwent bipolar hemiarthroplasty were typically older and less ambulatory, owing to the presence of underlying disease. Several studies have demonstrated that the incidence of AKI increases with age and is most common in elderly patients [14, 15]. Additionally, diabetes and pre-existing renal disease have emerged as independent predictors of AKI [16]. Our study also showed independent risk factors, such as laboratory findings (BUN, postoperative serum creatinine, ESR) and diabetes, associated with AKI after femoral neck fracture surgery. Therefore, surgeons should be aware of the possibility of AKI when treating femoral neck fracture in patients with high morbidity.

The use of hypotensive anesthesia is generally recommended in the orthopedic department for decreasing intraoperative blood loss, transfusion requirements, and operation time, improving the quality of the surgical field, and preventing deep vein thrombosis. However, it may lead to intraoperative dehydration and hypotension and dehydration may in turn cause endothelial injury and the subsequent local release of endothelin, angiotensin II, and catecholamines, all of which cause vasoconstriction and exacerbate ischemia in the kidney [17, 18]. A clear relationship between hypotension during operation and the development of AKI was observed in this study. Therefore, clinicians should consider intraoperative hypotension among the various risk factors for AKI and prioritize intraoperative blood pressure control.

The major limitation of this study was that it did not investigate the total duration of intraoperative hypotension. Although the duration of hypotension required to incur damage is unclear, interest in the effects of the duration of intraoperative hypotension on AKI has recently increased [9, 19]. In addition, there are almost 50 different definitions of intraoperative hypotension in the recent literature [20], which may reduce the generalizability of our findings, although we used the most common definition [9]. Thus, future investigations that establish a clear definition of intraoperative hypotension and determine the critical duration of intraoperative hypotension are warranted.

Conclusions

In conclusion, AKI was found to occur frequently after surgery for femur neck fracture. Surgeons should be aware of acute kidney injury when planning the management of patients with femoral neck fracture and consider that the duration of intraoperative hypotension is a risk factor for acute kidney injury.

Abbreviations

ACE-Is:

Angiotensin-converting enzyme inhibitors

AKI:

Acute kidney injury

ASA:

American Society of Anesthesiologists

BH:

Bipolar hemiarthroplasty

BUN:

Blood urea nitrogen

Hb:

Hemoglobin

KDIGO:

Kidney Disease: Improving Global Outcomes

SCr:

Serum creatinine

THR:

Total hip replacement

References

  1. Bass E, French DD, Bradham DD, Rubenstein LZ. Risk-adjusted mortality rates of elderly veterans with hip fractures. Ann Epidemiol. 2007;17:514–9.

    Article  Google Scholar 

  2. Bennet SJ, Berry OM, Goddard J, Keating JF. Acute renal dysfunction following hip fracture. Injury. 2010;41:335–8.

    Article  Google Scholar 

  3. Choi HJSC, Ha Y-C, et al. Burden of osteoporosis in adults in Korea: a national health insurance database study. J Bone Miner Metab. 2012;30:54–8.

    Article  Google Scholar 

  4. Stewart NA, Chantrey J, Blankley SJ, Boulton C, Moran CG. Predictors of 5 year survival following hip fracture. Injury. 2011;42:1253–6.

    Article  Google Scholar 

  5. Fields AC, Dieterich JD, Buterbaugh K, Moucha CS. Short-term complications in hip fracture surgery using spinal versus general anaesthesia. Injury. 2015;46:719–23.

    Article  Google Scholar 

  6. Jafari SM, Huang R, Joshi A, Parvizi J, Hozack WJ. Renal impairment following total joint arthroplasty: who is at risk? J Arthroplast. 2010;25:49–53, e1-2.

    Article  Google Scholar 

  7. Ulucay C, Eren Z, Kaspar EC, et al. Risk factors for acute kidney injury after hip fracture surgery in the elderly individuals. Geriatr Orthop Surg Rehabil. 2012;3:150–6.

    Article  Google Scholar 

  8. KDIGO clinical practice guideline for acute kidney injury. Kidney Int Suppl. 2012;2:S1–S138.

    Article  Google Scholar 

  9. Bijker JB, van Klei WA, Kappen TH, Kappen TH, van Wolfswinkel L, Moons KG, Kalkman CJ. Incidence of intraoperative hypotension as a function of the chosen definition. Anesthesiology. 2007;107:213–20.

    Article  Google Scholar 

  10. Abelha FJ, Botelho M, Fernandes V, Barros H. Determinants of postoperative acute kidney injury. Crit Care. 2009;13:R79.

    Article  Google Scholar 

  11. Kheterpal S, Tremper KK, Heung M. Development and Validation of an acute kidney injury risk index for patients undergoing general surgery: results from a national data set. Anesthesiology. 2009;110:505–15.

  12. Dardashti A, Ederoth P, Algotsson L, Bronden B, Bjursten H. Incidence, dynamics, and prognostic value of acute kidney injury for death after cardiac surgery. J Thorac Cardiovasc Surg. 2014;147:800–7.

    Article  Google Scholar 

  13. Mariscalco GCM, Dominici C, et al. The effect of timing of cardiac catheterization on acute kidney injury after cardiac surgery is influenced by the type of operation. Int J Cardiol. 2014;173:46–54.

    Article  Google Scholar 

  14. Ali T, Khan I, Simpson W, et al. Incidence and outcomes in acute kidney injury: a comprehensive population-based study. J Am Soc Nephrol. 2007;18:1292–8.

    Article  CAS  Google Scholar 

  15. Coca SG. Acute kidney injury in elderly persons. Am J Kidney Dis. 2010;56:122–31.

    Article  Google Scholar 

  16. Thiele RH, Isbell JM, Rosner MH. AKI associated with cardiac surgery. Clin J Am Soc Nephrol. 2015;10:500–14.

    Article  Google Scholar 

  17. Caramelo C, Espinosa G, Manzarbeitia F, et al. Role of endothelium-related mechanisms in the pathophysiology of renal ischemia/reperfusion in normal rabbits. Circ Res. 1996;79:1031–8.

    Article  CAS  Google Scholar 

  18. Goligorsky MS, Noiri E, Tsukahara H, Budzikowski AS, Li H. A pivotal role of nitric oxide in endothelial cell dysfunction. Acta Physiol. 2000;168:33–40.

    Article  CAS  Google Scholar 

  19. Sun LY, Wijeysundera DN, Tait GA. Association of Intraoperative Hypotension with acute kidney injury after elective noncardiac surgery. Anesthesiology. 2015;123:515–23.

    Article  Google Scholar 

  20. Bijker JB, van Klei WA, Vergouwe Y, et al. Intraoperative hypotension and 1-year mortality after noncardiac surgery. Anesthesiology. 2009;111:1217–26.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research was supported by the NRF grant funded by the Korea government (NRF-2018R1C1B6005202).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Author information

Authors and Affiliations

Authors

Contributions

JKJ and DKL collected and analyzed the patient clinical and hematological data. WYJ and SBH interpreted data and were major contributors to writing the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Seung-Beom Han.

Ethics declarations

Ethics approval and consent to participate

The study protocol was approved by Korea University Anam Hospital Institutional Review Board (ED16357). Because of the study’s retrospective design, the need for consent to participate was waived.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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 distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jang, W.Y., Jung, JK., Lee, D.K. et al. Intraoperative hypotension is a risk factor for postoperative acute kidney injury after femoral neck fracture surgery: a retrospective study. BMC Musculoskelet Disord 20, 131 (2019). https://doi.org/10.1186/s12891-019-2496-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12891-019-2496-1

Keywords