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Tourniquet-induced tissue hypoxia characterized by near-infrared spectroscopy during ankle surgery: an observational study

BMC Anesthesiology volume 19, Article number: 70 (2019) Cite this article

Abstract

Background

Pneumatic tourniquet inflation during extremity surgery leads to profound and prolonged tissue ischemia. Its effect on tissue oxygenation is inadequately studied.

Methods

Patients undergoing elective ankle surgery with tourniquet application participated in this observational cohort study. Somatic and cerebral tissue oxygen saturation (SstO2 and SctO2) were monitored using tissue near-infrared spectroscopy. Oxygenation was monitored distally (SstO2-distal) and proximally to the tourniquet, on the contralateral leg, and the forehead (a total of 4 tissue beds). Tissue oxygenation at different time points was compared. The magnitude, duration, and load (product of magnitude and duration) of tissue desaturation during tourniquet inflation were correlated with tissue resaturation and hypersaturation after tourniquet deflation.

Results

Data of 26 patients were analyzed. The tourniquet inflation time was 120 ± 31 mins. Following a rapid desaturation from 77 ± 8% pre-inflation to 38 ± 20% 10 mins post-inflation, SstO2-distal slowly and continuously desaturated and reach the nadir (16 ± 11%) toward the end of inflation. After deflation, SstO2-distal rapidly resaturated from 16 ± 11% to 91 ± 5% (i.e., hypersaturation); SstO2 monitored proximally to the tourniquet and on contralateral leg had significant but small desaturation (~ 2–3%, p <  0.001); in contrast, SctO2 remained stable. The desaturation load had a significant correlation with resaturation magnitude (p <  0.001); while the desaturation duration had a significant correlation with hypersaturation magnitude (p = 0.04).

Conclusions

Tissue dys-oxygenation following tourniquet application can be reliably monitored using tissue oximetry. Its outcome significance remains to be determined.

Peer Review reports

Background

A pneumatic tourniquet is commonly employed during extremity surgery to reduce blood loss and facilitate the surgeon’s operation (i.e., a bloodless surgical field). It is intriguing when considering that, although the blood flow is completely or near-completely stopped for a prolonged period, the tissue beds distal to the tourniquet are still alive afterward. In theory, the ischemic tissue would become hypoxic, and the hypoxia would become progressively worse, following the interruption of blood flow as long as the tissue continues to consume oxygen albeit maybe at a much slower rate as a result of the adaptive changes or other factors such as anesthesia [1, 2]. It is enlightening if the change in tissue oxygenation following tourniquet inflation is continuously monitored. The modern tissue oximetry based on near-infrared spectroscopy enables non-invasive, bedside and continuous measurement of the hemoglobin oxygen saturation of the mixed arterial, capillary, and venous blood in the tissue bed that is ~ 2–2.5 cm below the probe. Cerebral tissue oxygen saturation (SctO2) monitored on the forehead has been used in clinical care for 20+ years in patients having surgery [3] and cardiac arrest [4]; in contrast, the clinical application of somatic tissue oxygen saturation (SstO2), monitored at a peripheral location, is relatively new [5, 6]. The goal of this prospective cohort study was to characterize the tissue dys-oxygenation related to tourniquet application during ankle surgery. The secondary objective was to correlate parameters derived during tourniquet inflation with parameters derived following tourniquet deflation to explore the potential direction for future research.

Methods

This observational analytic cohort study was approved by the Institutional Review Board for clinical investigations at Yale University, New Haven, Connecticut, USA. Consent to participate in the study was obtained from all patients before surgery.

Patients and anesthesia

The inclusion criteria were: 1) elective ankle surgery for non-diabetic-related injuries, 2) tourniquet application, and 3) American Society of Anesthesiologists (ASA) physical status score ≤ III. The exclusion criteria were: 1) patient refusal, 2) urgent or emergent surgery, 3) age < 18 years, 4) diabetic foot, 5) peripheral vascular disease, 6) skin condition unsuitable for adhesive oximetry probe, 7) pregnancy and 8) existing neuropathy or myopathy.

All patients received ultrasound-guided peripheral nerve blockade using an insulated needle before surgery. Patients were monitored with electrocardiogram, pulse oximetry, and non-invasive blood-pressure, supplemented with 2 l/min oxygen by nasal cannula, and pre-medicated with intravenous 1–2 mg midazolam and 50–100 μg fentanyl. A single-shot popliteal, sciatic, and saphenous nerve block were performed under in-plane technique with a total of 30 ml 0.5% ropivacaine. Upon arriving at the operating room and following anesthesia induction with intravenous lidocaine, fentanyl and propofol administration, either an endotracheal tube or laryngeal mask airway, at the discretion of the anesthesia team, was placed. Anesthesia was maintained using sevoflurane. The tourniquet was placed on the upper leg and inflated to 300 mmHg during surgery in all patients.

Tissue oxygenation monitoring

Tissue oxygenation was monitored using a tissue oximeter based on near-infrared spectroscopy (NIRS) (FORE-SIGHT Elite, CASMED, Inc., Branford, Connecticut). In essence, NIRS-measured tissue oxygenation is determined by the balanced between oxygen consumption and supply of the tissue bed which is about 2–2.5 cm below the interrogating probe. In this study, four different tissue beds were monitored in each patient: 1) SstO2 distal to the tourniquet (SstO2-distal) with the probe placed on the back of the lower leg and about 4 fingers below the popliteal crease; 2) SstO2 proximal to the tourniquet (SstO2-prox) with the probe placed on the front of the upper leg and about 6 fingers below the femoral crease; 3) SstO2 on the contralateral leg (SstO2-contra) at the same location as SstO2-distal; 4) SctO2 with the probe placed on the forehead. Monitoring and data recording started before anesthesia induction and stopped at the end of surgery.

Data recording and analysis

Tissue oxygenation of different tissue beds was simultaneously and continuously recorded into an excel worksheet by a research laptop at a frequency of one new data point every 2 s. The medians of tissue oxygenation within each minute were used in the analysis. The time points of interest were: immediately before tourniquet inflation (T0), 5 mins (T5), 10 mins (T10), 20 mins (T20), 30 mins (T30), and 60 mins (T60) after tourniquet inflation, immediately before tourniquet deflation (Tend), and 3–5 min after tourniquet deflation (Tpost). The hypoxic load, defined as the product of the magnitude and duration of tissue desaturation, is quantified by the area under the curve (AUC) encircled by the actual tracing and the straight line of the baseline value (T0).

Statistical analysis

As an exploratory observational study, a power analysis was not performed before the study. Data are expressed as mean ± SD. Paired Student's t-test was used when comparing the changes in tissue oxygenation of the same tissue bed. The correlation between the variables before tourniquet deflation (baseline oxygenation (T0), maximal hypoxia (Tend), hypoxic duration, and hypoxic load (AUC)) and the variables after tourniquet deflation (resaturation magnitude (∆Tpost-end), resaturation rate (%/second), and hyperemic response (∆Tpost-0)) was analyzed using Pearson’s correlation coefficient. The p value < 0.05 was considered significant. Statistical analyses were performed using SPSS software (ver. 22.0 for Windows; SPSS Inc., Chicago, IL).

Results

Thirty-one patients participated in this study. Five patients were excluded from the analysis due to incomplete data (n = 4) and conversion of ankle surgery to below-knee amputation (n = 1). Data of 26 patients were included in the final analysis. The patient’s demographic data and past medical history were summarized in Table 1. All patients had a tourniquet application, with an average duration of 120 ± 31 mins.

Table 1 Demographics, tourniquet time and co-morbidities of the study population (n = 26)
Full size table

Tissue oxygenation of different tissue beds was summarized in Table 2 and illustrated by Fig. 1. Tourniquet inflation led to a rapid decrease of SstO2-distal from 77 ± 8% pre-inflation to 38 ± 20% 10 mins post-inflation (51% relative decrease). SstO2-distal slowly, but continuously, trended downward (i.e., desaturation) throughout the rest of the inflation period and did not reach the nadir (16 ± 11, 79% relative decrease) until immediately before the tourniquet deflation. Following tourniquet deflation, there was a rapid increase (469% relative increase) of SstO2-distal from the nadir of 16 ± 11% to the peak of 91 ± 5% about 3–5 min post-deflation (i.e., resaturation). The difference between the post-deflation peak value (Tpost) and the pre-inflation baseline value (T0) of SstO2-distal was 14 ± 8% (18% relative increase) (i.e., hyperemia) (Table 3).

Table 2 Absolute values and changes of somatic tissue oxygen saturation (SstO2) and cerebral tissue oxygen saturation (SctO2) at different time points (n = 26)
Full size table
Fig. 1
figure 1

Group mean and standard deviation of somatic tissue oxygen saturation (SstO2) monitored distal (SstO2-distal) and proximal (SstO2-prox) to the tourniquet and on the contralateral leg (SstO2-contra) and cerebral tissue oxygen saturation (SctO2) monitored on the forehead at different time points. Tend = time point at the end of tourniquet inflation; Tpost = time point 3–5 min after tourniquet deflation

Full size image
Table 3 Association of representative variables of tissue oxygenation with variables of resaturation and hyperemia following tourniquet deflation (n = 26)
Full size table

The oxygenation of other tissue beds, including SstO2-prox, SstO2-contra and SctO2, remained stable throughout the ischemic period from T0 to Tend. The tourniquet deflation led to a relative decrease of both SstO2-prox and SstO2-contra of 3–4% (p <  0.05); in contrast, SctO2 remained relatively stable following tourniquet deflation, albeit it had a small increase in the 21-year old patient illustrated in Fig. 2.

Fig. 2
figure 2

Real-time tracing of somatic tissue oxygen saturation (SstO2) monitored distal (SstO2-distal) and proximal (SstO2-prox) to the tourniquet and on the contralateral leg (SstO2-contra) and cerebral tissue oxygen saturation (SctO2) monitored on the forehead in a 21-year old college student

Full size image

The resaturation magnitude (∆Tpost-end) had a significant correlation with maximal hypoxia (Tend) (p <  0.001) and hypoxic load (AUC) (p <  0.001). The resaturation rate (%/second) had a significant correlation with maximal hypoxia (Tend) (p = 0.03). The hyperemic response (∆Tpost-0) had a significant correlation with both baseline oxygenation (T0) (p <  0.001) and hypoxic duration (p = 0.04).

Discussion

This study showed that extreme tissue hypoxia incurred by tourniquet application can be reliably and continuously measured using NIRS-based tissue oximetry. The hypoxic load (AUC) is significantly associated with the magnitude of the reperfusion-related resaturation (∆Tpost-end), but not the rebound hyperemia (∆Tpost-0). In comparison, the ischemic time is significantly associated with the rebound hyperemia (∆Tpost-0), but not the magnitude of resaturation (∆Tpost-end). The magnitudes, durations, and loads of tissue hypoxia during tourniquet inflation vary among different patients; however, the clinical significance of these parameters remains to be determined.

In 1904, Harvey Cushing first described the clinical application of pneumatic tourniquet [7]. Tourniquet is currently widely used during upper and lower extremity surgery to facilitate the surgeon’s operation by rendering a bloodless surgical field. It is a milestone event in medical history. However, tourniquet is not risk-free. Various post-tourniquet complications have been reported such as nerve palsy [8], vascular injuries [9], wound hypoxia [10], abnormal electromyography and muscle weakness [11]. If given enough time, the tissues that are distal to the tourniquet will eventually die. However, the time limit of safe tourniquet inflation during extremity surgery remains controversial [12,13,14]. The dogma of 90 mins is based on animal studies [15, 16]. In patients undergoing knee surgery, Gidlöf et al. showed that tourniquet-induced prolonged ischemia (90–180 min) led to a progressively worsening endothelial injury [17]. Many other studies showed that tourniquet-induced extreme ischemia (> 4 h) can lead to irreversible skeletal muscle injury [18, 19].

The effect of tourniquet inflation on NIRS-measured tissue oxygenation in humans has been previously reported [20]. However, the tissue beds monitored and the research aims in these studies are different from our study. The study performed by Song et al. monitored cerebral, not somatic, tissue bed in patients undergoing total knee replacement surgery [21]. Tujjar et al. only monitored the tissue bed that was distal to the tourniquet in patients undergoing upper extremity surgery [22]. In healthy volunteers, Muellner et al. studied the effects of different tourniquet inflation pressures on tissue oxygenation based on the monitoring of the tissue bed distal to the tourniquet only [23]. In patients undergoing ankle fracture repair, Shadgan et al. studied the relationship between tissue oxygenation and oxidative muscle injury based on the monitoring of the tissue beds distal to the tourniquet and on the contralateral leg [24].

The reactive hyperemia following tourniquet release is a well-documented phenomenon [25]. De Backer and Durand advocated the use of reactive hyperemia as an indicator of the microvascular reserve [26], as corroborated by the observation that the magnitude of reactive hyperemia is reduced in septic patients compared with control subjects [27]. In a rat model, Kim et al. showed that NIRS-measured tissue oxygenation had an overshoot (i.e., higher than baseline) following a 2-h, not 3-h tourniquet inflation, suggesting an association between the duration of ischemia and the magnitude of hyperemic response [28].

The severity of tourniquet-induced ischemia is traditionally gauged by the duration of tourniquet inflation. However, this approach may have overlooked the dynamic nature of tissue ischemia in an individual patient and the variability of ischemic severity among different patients, as suggested by both our study and the previous studies [21,22,23,24]. Moreover, the consequence of tissue ischemia is determined not only by the ischemic duration, but also the metabolic demand as suggested by the association between slow energy consumption and delayed ultrastructural damage in the canine ischemic model [29]. Tissue oximetry, which measures the balance between tissue oxygen consumption and supply continuously and non-invasively, is a promising technology in assessing the severity of tourniquet-induced ischemia in individual patients.

Skeletal muscle can rapidly adjust its energy expenditure and production during acute ischemia [30, 31]. The ATPs reserved in muscle fibers only last for a few seconds [32]. However, the skeletal muscle can remarkably replenish energy via two distinctive anaerobic pathways. The pathway of anaerobic glycolysis can sustain muscle activity for a few minutes [33]; while the pathway of phosphocreatine degradation can sustain muscle activity from minutes to hours [34]. As a result, the ATPs in skeletal muscle fall at a very low rate during the first 3–4 h of ischemia [35, 36]. However, tissue damage characterized by cell necrosis and apoptosis eventually ensues about 6–7 h after the onset of ischemia when the glycogen and phosphocreatine reserves are exhausted [37].

An interesting observation of our study is the rapid desaturation for about 10 mins followed by a slow but continuous desaturation for the remaining ischemic period in the tissue bed distal to tourniquet. This phenomenon may be secondary to the adaptive adjustment of metabolic activity made by primarily muscular tissue. Although SctO2 remained stable following tourniquet deflation based on the average of all patients, the 21-year-old physically fit college student had a notable increase in SctO2, a change different to most other patients (Fig. 2). It may relate to the metabolites (including carbon dioxide) generated by the ischemic tissue which were flushed into cerebral circulation and led to cerebral vasodilation following tourniquet deflation. This 21-year-old young patient may have a more robust cerebral vasoreactivity to carbon dioxide than older patients (the average age of all patients = 48 years). Nonetheless, the exact cause and the clinical significance of this outlier remain to be elucidated.

This study did not evaluate the complications associated tourniquet application and thus cannot tell the relationship between tissue NIRS parameters and ischemia-related outcomes. This is a major limitation of our study. Also, all patients in our study had a peripheral nerve block, which makes it difficult to extrapolate the findings of this study in patients without nerve block. We found a considerable variation in both the rate and magnitude of tissue desaturation following tourniquet inflation. One of the potential causes of this inter-individual variation may relate to the thickness of the skin and subcutaneous tissue because thick superficial layers may preclude the near-infrared light from interrogating the deeper muscular tissue.

Conclusion

NIRS-based tissue oximetry can reliably and continuously measure tissue desaturation, resaturation and hypersaturation during tourniquet application. The desaturation load is associated the magnitude of resaturation; while the desaturation duration is associate with the magnitude of hypersaturation. The clinical value of tissue oximetry in patients receiving tourniquet application needs to be determined by future research.

Abbreviations

∆Tpost-0 :

Tpost – T0

∆Tpost-end :

Tpost – Tend

AUC:

Area under the curve

SctO2 :

Cerebral tissue oxygen saturation

SstO2 :

Somatic tissue oxygen saturation

SstO2-contra:

SstO2 on the contralateral leg

SstO2-distal:

SstO2 distal to the tourniquet

SstO2-prox:

SstO2 proximal to the tourniquet

T0 :

Immediately before tourniquet insufflation

Tend :

Immediately before tourniquet deflation

Tpost :

3–5 min after tourniquet deflation

References

  1. Mars M, Gregory MA. A histometric analysis of skeletal myofibers following 90 min of tourniquet ischemia and reperfusion. J Surg Res. 1991;50(2):191–5.

    Article  CAS  Google Scholar 

  2. Hogan MC, Kurdak SS, Arthur PG. Effect of gradual reduction in O2 delivery on intracellular homeostasis in contracting skeletal muscle. J Appl Physiol (1985). 1996;80(4):1313–21.

    Article  CAS  Google Scholar 

  3. Meng L, Gruenbaum SE, Dai F, Wang T. Physiology, intervention, and outcome: three critical questions about cerebral tissue oxygen saturation monitoring. Minerva Anestesiol. 2018;84(5):599–614.

    PubMed  Google Scholar 

  4. Sanfilippo F, Serena G, Corredor C, Benedetto U, Maybauer MO, Al-Subaie N, Madden B, Oddo M, Cecconi M. Cerebral oximetry and return of spontaneous circulation after cardiac arrest: a systematic review and meta-analysis. Resuscitation. 2015;94:67–72.

    Article  Google Scholar 

  5. Meng L, Xiao J, Gudelunas K, Yu Z, Zhong Z, Hu X. Association of intraoperative cerebral and muscular tissue oxygen saturation with postoperative complications and length of hospital stay after major spine surgery: an observational study. Br J Anaesth. 2017;118(4):551–62.

    Article  CAS  Google Scholar 

  6. Li G, Lin L, Dai F, Guo X, Meng L. Muscular tissue oxygen saturation during robotic hysterectomy and postoperative nausea and vomiting: exploring the potential therapeutic thresholds. J Clin Monit Comput. 2018.

  7. Bolton CF, McFarlane RM. Human pneumatic tourniquet paralysis. Neurology. 1978;28(8):787–93.

    Article  CAS  Google Scholar 

  8. Horlocker TT, Hebl JR, Gali B, Jankowski CJ, Burkle CM, Berry DJ, Zepeda FA, Stevens SR, Schroeder DR. Anesthetic, patient, and surgical risk factors for neurologic complications after prolonged total tourniquet time during total knee arthroplasty. Anesth Analg. 2006;102(3):950–5.

    Article  Google Scholar 

  9. Kumar SN, Chapman JA, Rawlins I. Vascular injuries in total knee arthroplasty. A review of the problem with special reference to the possible effects of the tourniquet. J Arthroplast. 1998;13(2):211–6.

    Article  CAS  Google Scholar 

  10. Clarke MT, Longstaff L, Edwards D, Rushton N. Tourniquet-induced wound hypoxia after total knee replacement. J Bone Joint Surg Br. 2001;83(1):40–4.

    Article  CAS  Google Scholar 

  11. Saunders KC, Louis DL, Weingarden SI, Waylonis GW. Effect of tourniquet time on postoperative quadriceps function. Clin Orthop Relat Res. 1979(143):194–9.

  12. Wakai A, Winter DC, Street JT, Redmond PH. Pneumatic tourniquets in extremity surgery. J Am Acad Orthop Surg. 2001;9(5):345–51.

    Article  CAS  Google Scholar 

  13. Chiu D, Wang HH, Blumenthal MR. Creatine phosphokinase release as a measure of tourniquet effect on skeletal muscle. Arch Surg. 1976;111(1):71–4.

    Article  CAS  Google Scholar 

  14. Appell HJ, Gloser S, Duarte JA, Zellner A, Soares JM. Skeletal muscle damage during tourniquet-induced ischaemia. The initial step towards atrophy after orthopaedic surgery? Eur J Appl Physiol Occup Physiol. 1993;67(4):342–7.

    Article  CAS  Google Scholar 

  15. Mohler LR, Pedowitz RA, Myers RR, Ohara WM, Lopez MA, Gershuni DH. Intermittent reperfusion fails to prevent posttourniquet neurapraxia. J Hand Surg Am. 1999;24(4):687–93.

    Article  CAS  Google Scholar 

  16. Heppenstall RB, Scott R, Sapega A, Park YS, Chance B. A comparative study of the tolerance of skeletal muscle to ischemia. Tourniquet application compared with acute compartment syndrome. J Bone Joint Surg Am. 1986;68(6):820–8.

    Article  CAS  Google Scholar 

  17. Gidlof A, Lewis DH, Hammersen F. The effect of prolonged total ischemia on the ultrastructure of human skeletal muscle capillaries. A morphometric analysis. Int J Microcirc Clin Exp. 1988;7(1):67–86.

    CAS  PubMed  Google Scholar 

  18. Harris K, Walker PM, Mickle DA, Harding R, Gatley R, Wilson GJ, Kuzon B, McKee N, Romaschin AD. Metabolic response of skeletal muscle to ischemia. Am J Phys. 1986;250(2 Pt 2):H213–20.

    CAS  Google Scholar 

  19. Paradis S, Charles AL, Meyer A, Lejay A, Scholey JW, Chakfe N, Zoll J, Geny B. Chronology of mitochondrial and cellular events during skeletal muscle ischemia-reperfusion. Am J Physiol Cell Physiol. 2016;310(11):C968–82.

    Article  Google Scholar 

  20. Palanca AA, Yang A, Bishop JA. The effects of limb elevation on muscle oxygen saturation: a near-infrared spectroscopy study in humans. PM R. 2016;8(3):221–4.

    Article  Google Scholar 

  21. Song I, Kim DY, Kim YJ. The effect of tourniquet deflation on hemodynamics and regional cerebral oxygen saturation in aged patients undergoing total knee replacement surgery. Korean J Anesthesiol. 2012;63(5):425–30.

    Article  Google Scholar 

  22. Tujjar O, De Gaudio AR, Tofani L, Di Filippo A. Effects of prolonged ischemia on human skeletal muscle microcirculation as assessed by near-infrared spectroscopy. J Clin Monit Comput. 2016.

  23. Muellner T, Nikolic A, Schramm W, Vecsei V. New instrument that uses near-infrared spectroscopy for the monitoring of human muscle oxygenation. J Trauma. 1999;46(6):1082–4.

    Article  CAS  Google Scholar 

  24. Shadgan B, Reid WD, Harris RL, Jafari S, Powers SK, O'Brien PJ. Hemodynamic and oxidative mechanisms of tourniquet-induced muscle injury: near-infrared spectroscopy for the orthopedics setting. J Biomed Opt. 2012;17(8):081408–1.

    Article  Google Scholar 

  25. Fahmy NR, Patel DG. Hemostatic changes and postoperative deep-vein thrombosis associated with use of a pneumatic tourniquet. J Bone Joint Surg Am. 1981;63(3):461–5.

    Article  CAS  Google Scholar 

  26. De Backer D, Durand A. Monitoring the microcirculation in critically ill patients. Best Pract Res Clin Anaesthesiol. 2014;28(4):441–51.

    Article  Google Scholar 

  27. Neviere R, Mathieu D, Chagnon JL, Lebleu N, Millien JP, Wattel F. Skeletal muscle microvascular blood flow and oxygen transport in patients with severe sepsis. Am J Respir Crit Care Med. 1996;153(1):191–5.

    Article  CAS  Google Scholar 

  28. Kim JG, Lee J, Roe J, Tromberg BJ, Brenner M, Walters TJ. Hemodynamic changes in rat leg muscles during tourniquet-induced ischemia-reperfusion injury observed by near-infrared spectroscopy. Physiol Meas. 2009;30(7):529–40.

    Article  CAS  Google Scholar 

  29. Murry CE, Richard VJ, Reimer KA, Jennings RB. Ischemic preconditioning slows energy metabolism and delays ultrastructural damage during a sustained ischemic episode. Circ Res. 1990;66(4):913–31.

    Article  CAS  Google Scholar 

  30. Timmons JA, Gustafsson T, Sundberg CJ, Jansson E, Hultman E, Kaijser L, Chwalbinska-Moneta J, Constantin-Teodosiu D, Macdonald IA, Greenhaff PL. Substrate availability limits human skeletal muscle oxidative ATP regeneration at the onset of ischemic exercise. J Clin Invest. 1998;101(1):79–85.

    Article  CAS  Google Scholar 

  31. Blei ML, Conley KE, Kushmerick MJ. Separate measures of ATP utilization and recovery in human skeletal muscle. J Physiol. 1993;465:203–22.

    Article  CAS  Google Scholar 

  32. Lewis SF, Haller RG. Skeletal muscle disorders and associated factors that limit exercise performance. Exerc Sport Sci Rev. 1989;17:67–113.

    CAS  PubMed  Google Scholar 

  33. Hultman E, Spriet LL. Skeletal muscle metabolism, contraction force and glycogen utilization during prolonged electrical stimulation in humans. J Physiol. 1986;374:493–501.

    Article  CAS  Google Scholar 

  34. Frontera WR, Ochala J. Skeletal muscle: a brief review of structure and function. Calcif Tissue Int. 2015;96(3):183–95.

    Article  CAS  Google Scholar 

  35. Walker PM. Ischemia/reperfusion injury in skeletal muscle. Ann Vasc Surg. 1991;5(4):399–402.

    Article  CAS  Google Scholar 

  36. Kuzon WM Jr, Walker PM, Mickle DA, Harris KA, Pynn BR, McKee NH. An isolated skeletal muscle model suitable for acute ischemia studies. J Surg Res. 1986;41(1):24–32.

    Article  Google Scholar 

  37. Troitzsch D, Moosdorf R, Hasenkam JM, Nygaard H, Vogt S. Effects of cyclosporine pretreatment on tissue oxygen levels and cytochrome oxidase in skeletal muscle ischemia and reperfusion. Shock. 2013;39(2):220–6.

    Article  CAS  Google Scholar 

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Acknowledgements

The authors would like to acknowledge CAS Medical Systems, Inc., Branford, Connecticut, USA, for providing the FORE-SIGHT ELITE Tissue Oximeter at no cost.

Funding

This study was funded solely by departmental resources.

Availability of data and materials

Study data is available upon contact of Dr. Lingzhong Meng by email.

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Authors and Affiliations

  1. Department of Anesthesiology, The First Affiliated Hospital, Xiamen University, Xiamen, Fujian Province, China

    Liang Lin

  2. Department of Anesthesiology, Peking University Third Hospital, Beijing, China

    Gang Li

  3. Department of Anesthesiology, Yale University School of Medicine, 333 Cedar Street, TMP 3, P.O. Box 208051, New Haven, CT, 06520, USA

    Jinlei Li & Lingzhong Meng

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Contributions

LL: Study design, data collection, data analysis, initial draft, approval of manuscript. GL: Data collection, critical revision and approval of manuscript. JL: Patient recruitment, critical revision and approval of manuscript. LM: Study design, patient recruitment, critical revision and approval of manuscript. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Lingzhong Meng.

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Ethics approval and consent to participate

This study was approved by the Internal Review Board at Yale University and patients gave written informed consent for study participation.

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Competing interests

Lingzhong Meng is a consultant to CAS Medical Systems, Inc. The other authors declare that they have no competing interests.

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Lin, L., Li, G., Li, J. et al. Tourniquet-induced tissue hypoxia characterized by near-infrared spectroscopy during ankle surgery: an observational study. BMC Anesthesiol 19, 70 (2019). https://doi.org/10.1186/s12871-019-0740-8

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Keywords

  • Tissue oxygenation
  • Tourniquet
  • Ischemia
  • Hypoxia

BMC Anesthesiology

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