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W tym Artykule

  • Podsumowanie
  • Streszczenie
  • Wprowadzenie
  • Protokół
  • Wyniki
  • Dyskusje
  • Ujawnienia
  • Podziękowania
  • Materiały
  • Odniesienia
  • Przedruki i uprawnienia

Podsumowanie

We present a protocol to measure regional oxygen saturation (rSO2) in hemodialysis (HD) patients by using a near-infrared spectroscopy monitor. The rSO2 value is an index of tissue oxygenation. This noninvasive and real-time monitoring could be useful for confirming changes in organ oxygenation during HD.

Streszczenie

Near-infrared spectroscopy (NIRS) has recently been applied as a tool to measure regional oxygen saturation (rSO2), a marker of tissue oxygenation, in clinical settings including cardiovascular and brain surgery, neonatal monitoring and prehospital medicine. The NIRS monitoring devices are real-time and noninvasive, and have mainly been used for evaluating cerebral oxygenation in critically ill patients during an operation or intensive care. Thus far, the use of NIRS monitoring in patients with chronic kidney disease (CKD) including hemodialysis (HD) has been limited; therefore, we investigated rSO2 values in some organs during HD. We monitored rSO2 values using a NIRS device transmitting near-infrared light at 2 wavelengths of attachment. The HD patients were placed in a supine position, with rSO2 measurement sensors attached to the foreheads, the right hypochondrium and the lower legs to evaluate rSO2 in the brain, liver and lower leg muscles, respectively. NIRS monitoring could be a new approach to clarify changes in organ oxygenation during HD or factors affecting tissue oxygenation in CKD patients. This article describes a protocol to measure tissue oxygenation represented by rSO2 as applied in HD patients.

Wprowadzenie

Near-infrared spectroscopy (NIRS) has been used to evaluate regional oxygen saturation (rSO2), a marker of tissue oxygenation, especially cerebral oxygenation in various clinical settings1,2,3 and has recently been applied to patients undergoing hemodialysis (HD)4,5,6,7,8,9,10,11. Cerebral rSO2 is reportedly associated with cognitive function in patients undergoing HD or those with non-dialyzed chronic kidney disease (CKD)11,12. However, thus far, the use of NIRS monitoring has been limited in patients with CKD.

As NIRS monitoring is real-time and noninvasive, we assessed its usefulness as a monitoring device in patients undergoing HD. Although NIRS is mainly used to measure cerebral rSO2, we also investigated rSO2 values in other organs during HD. Specifically, the rSO2 measurement sensors were attached to the forehead, the right hypochondrium and the lower legs to evaluate rSO2 in the brain, liver and lower muscles, respectively. The results showed that NIRS monitoring could be a new approach to clarify changes in organ oxygenation during HD or factors affecting tissue oxygenation in CKD patients.

To date, continuous monitoring was performed during HD, blood volume monitoring, central venous oxygen saturation, thoracic admittance and electronic stethoscope-guided estimated blood pressure (BP) in clinical settings13,14,15; however, there are limitations for the prediction of hypotension or the wide use of devices. In contrast, the new noninvasive approach here could provide real-time information on intradialytic oxygen dynamics in individual organs. Therefore, this monitoring method may allow the detection of transient organ ischemia in the early phases of intradialytic hypotension and may also permit the safe performance of HD. This article describes a protocol to measure tissue oxygenation represented by rSO2, as applied in patients undergoing HD.

Protokół

All participants provided written informed consent. The study was approved by the Institutional Review Board of the Saitama Medical Center, Jichi Medical University, Japan (RIN 15–104).

1. Device for the monitoring of rSO2

  1. Prepare a NIRS device for measuring tissue oxygenation. This device has four channels and can perform measurement in up to four organs at the same time.
  2. Prepare a measurement sensor for NIRS monitoring, to evaluate rSO2 values in each organ via transmitting near-infrared light at two wavelengths of attachment.

2. Attaching the measurement sensor

  1. Allow each patient to rest in a supine position for at least 5 minutes before HD.
  2. Attach measurement sensors to the forehead, the right hypochondrium and lower legs to evaluate rSO2 in the brain, liver and lower leg muscles, respectively.
  3. Monitoring of cerebral oxygenation
    1. Attach measurement sensors to the forehead of the dominant hemisphere.
  4. Monitoring of hepatic oxygenation
    1. Prepare echography to measure the depth to the patients’ liver from the body surface. Confirm that this measurement is within 20–30 mm from the body surface. Next, attach the measurement sensors to the right hypochondrium.
      NOTE: In this device, rSO2 values should be obtained in deep tissue 20–30 mm from the body surface. In some instances, the liver may be located in more than 30 mm from the body surface due to the presence of thick subcutaneous fat.
  5. Monitoring of muscle oxygenation
    1. Attach measurement sensors to the right or bilateral lower legs.
  6. Sensor connection and powering the device
    1. Connect each sensor to the leads from the device. Next, turn on the device, and start measuring oxygenation.

3. Puncturing the dialysis shunt and starting monitoring

  1. Puncturing the dialysis shunt
    1. Puncture the patients’ dialysis shunt to start HD therapy. At this time, measure BP using a digital blood pressure monitor equipped with the dialysis machine and collect blood samples using syringes.
  2. Start monitoring
    1. After starting HD therapy, start monitoring the tissue oxygenation of the three organs: the brain, liver and lower leg muscle.
  3. Monitoring of rSO2 during HD
    1. Observe changes in rSO2 values of each organ and measure BP regularly in addition to the usual monitoring performed during HD therapy including heart rate, venous pressure and blood volume. Confirm the attachment area and connection between the sensors and leads.

Wyniki

Cerebral rSO2 values before HD were lower than those in healthy subjects and cerebral rSO2 in HD patients with diabetes mellitus (DM) were lower than those in HD patients without DM (Figure 1)16. Furthermore, although tissue oxygenation continues without a decrease of BP during HD, we incidentally observed changes in cerebral and hepatic rSO2 due to intradialytic hypotension (Figure 2). Due to the continuo...

Dyskusje

NIRS monitoring has been mainly used to evaluate cerebral rSO2, especially in cardiovascular or cerebrovascular surgeries, which require extracorporeal circulation. During extracorporeal circulation including HD therapy, some organs could show relative ischemia7,17,18; however, it remains unclear whether tissue oxygenation becomes low or not. Muscle cramps or abdominal pain during HD could be one of the prodromal symp...

Ujawnienia

No conflicts of interest.

Podziękowania

We thank the dialysis staffs and members of the department of nephrology in Saitama medical center of Jichi Medical University. We would like to thank Editage (www.editage.com) for English language editing.

Materiały

NameCompanyCatalog NumberComments
DBB-100NXNikkisoDBB-100NXDialysis machine
INVOS 5100cCovidien JapanINVOSTM 5100ctissue oxygenation device
SOMASENSERCovidien JapanCV-SAFB-SM/INTLNIRS sensor

Odniesienia

  1. Nishiyama, K., et al. Regional cerebral oxygen saturation monitoring for predicting interventional outcomes in patients following out-of-hospital cardiac arrest of presumed cardiac cause: A prospective, observational, multicentre study. Resuscitation. 96, 135-141 (2015).
  2. Kobayashi, K., et al. Factors associated with a low initial cerebral oxygen saturation value in patients undergoing cardiac surgery. Journal of Artificial Organs. 20 (2), 110-116 (2017).
  3. Cruz, S. M., et al. A novel multimodal computational system using near-infrared spectroscopy predicts the need for ECMO initiation in neonates with congenital diaphragmatic hernia. Journal of Pediatric Surgery. 53 (1), 152-158 (2018).
  4. MacEwen, C., Sutherland, S., Daly, J., Pugh, C., Tarassenko, L. Relationship between Hypotension and Cerebral Ischemia during Hemodialysis. Journal of the American Socociety of Nephrology. 28 (8), 2511-2520 (2017).
  5. Polinder-Bos, H. A., et al. Changes in cerebral oxygenation and cerebral blood flow during hemodialysis - A simultaneous near-infrared spectroscopy and positron emission tomography study. Journal of Cerebral Blood Flow & Metablism. 40 (2), 328-340 (2020).
  6. Ookawara, S., et al. Differences in tissue oxygenation and changes in total hemoglobin signal strength in the brain, liver, and lower-limb muscle during hemodialysis. Journal of Artificial Organs. 21 (1), 86-93 (2018).
  7. Malik, J., et al. Tissue ischemia worsens during hemodialysis in end-stage renal disease patients. The Journal of Vascular Access. 18 (1), 47-51 (2017).
  8. Ito, K., et al. Cerebral oxygenation improvement is associated with hemoglobin increase after hemodialysis initiation. TheInternational Journal of Artificial Organs. , (2020).
  9. Valerianova, A., et al. Factors responsible for cerebral hypoxia in hemodialysis population. Physiological Research. 68 (4), 651-658 (2019).
  10. Ookawara, S., et al. Associations of cerebral oxygenation with hemoglobin levels evaluated by near-infrared spectroscopy in hemodialysis patients. PLoS One. 15 (8), 0236720 (2020).
  11. Kovarova, L., et al. Low Cerebral Oxygenation Is Associated with Cognitive Impairment in Chronic Hemodialysis Patients. Nephron. 139 (2), 113-119 (2018).
  12. Miyazawa, H., et al. Association of cerebral oxygenation with estimated glomerular filtration rate and cognitive function in chronic kidney disease patients without dialysis therapy. PLoS One. 13 (6), 0199366 (2018).
  13. Locatelli, F., et al. Haemodialysis with on-line monitoring equipment: tools or toys. Nephrology Dialysis Transplantation. 20 (1), 22-33 (2005).
  14. Cordtz, J., Olde, B., Solem, K., Ladefoged, S. D. Central venous oxygen saturation and thoracic admittance during dialysis: new approaches to hemodynamic monitoring. Hemodialysis International. 12 (3), 369-377 (2008).
  15. Kamijo, Y., et al. Continuous monitoring of blood pressure by analyzing the blood flow sound of arteriovenous fistula in hemodialysis patients. Clinical and Experimental Nephrology. 22 (3), 677-683 (2018).
  16. Ito, K., et al. Factors affecting cerebral oxygenation in hemodialysis patients: cerebral oxygenation associates with pH, hemodialysis duration, serum albumin concentration, and diabetes mellitus. PLoS One. 10 (2), 0117474 (2015).
  17. Imai, S., et al. Deterioration of Hepatic Oxygenation Precedes an Onset of Intradialytic Hypotension with Little Change in Blood Volume during Hemodialysis. Blood Purification. 45 (4), 345-346 (2018).
  18. Cho, A. R., Kwon, J. Y., Kim, C., Hong, J. M., Kang, C. Effect of sensor location on regional cerebral oxygen saturation measured by INVOS 5100 in on-pump cardiac surgery. Journal of Anesthesia. 31 (2), 178-184 (2017).
  19. Ito, K., et al. Deterioration of cerebral oxygenation by aortic arch calcification progression in patients undergoing hemodialysis: A cross-sectional study. BioMed Research International. , 2852514 (2017).
  20. Ito, K., et al. Blood transfusion during haemodialysis improves systemic tissue oxygenation: A case report. Nefrologia. 37 (4), 435-437 (2017).
  21. Ito, K., et al. Improvement of bilateral lower-limb muscle oxygenation by low-density lipoprotein apheresis in a patient with peripheral artery disease undergoing hemodialysis. Nefrologia. 39 (1), 90-92 (2019).
  22. Kitano, T., et al. Changes in tissue oxygenation in response to sudden intradialytic hypotension. Journal of Artificial Organs. 23 (2), 187-190 (2020).
  23. Lemmers, P. M. A., Toet, M. C., van Bel, F. Impact of patent ductus arteriosus and subsequent therapy with indomethacin on cerebral oxygenation in preterm infants. Pediatrics. 121, 142-147 (2008).
  24. Ito, K., et al. Sleep apnea syndrome caused lowering of cerebral oxygenation in a hemodialysis patient: a case report and literature review. Renal Replacement Therapy. 4, 54 (2018).
  25. Minato, S., et al. Continuous monitoring of changes in cerebral oxygenation during hemodialysis in a patient with acute congestive heart failure. Journal of Artificial Organs. , (2019).

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Tissue OxygenationNear infrared SpectroscopyNIRSHemodialysisRegional Oxygen SaturationIntradialytic HypertensionCerebral Oxygen SaturationHepatic MeasurementsMuscle OxygenationMonitoring ProtocolNon invasive MeasurementReal time EvaluationDialysis PatientsOxygen DynamicsCognitive Impairment Diagnosis

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