Capnodynamic monitoring of lung volume and blood flow in response to increased positive end-expiratory pressure in moderate to severe COVID-19 pneumonia: an observational study

Luis Schulz, Antony Stewart, William O'Regan, Peter McCanny, Danielle Austin, Magnus Hallback, Mats Wallin, Anders Aneman, Luis Schulz, Antony Stewart, William O'Regan, Peter McCanny, Danielle Austin, Magnus Hallback, Mats Wallin, Anders Aneman

Abstract

Background: The optimal level of positive end-expiratory pressure (PEEP) during mechanical ventilation for COVID-19 pneumonia remains debated and should ideally be guided by responses in both lung volume and perfusion. Capnodynamic monitoring allows both end-expiratory lung volume ([Formula: see text]) and effective pulmonary blood flow (EPBF) to be determined at the bedside with ongoing ventilation.

Methods: Patients with COVID-19-related moderate to severe respiratory failure underwent capnodynamic monitoring of [Formula: see text] and EPBF during a step increase in PEEP by 50% above the baseline (PEEPlow to PEEPhigh). The primary outcome was a > 20 mm Hg increase in arterial oxygen tension to inspired fraction of oxygen (P/F) ratio to define responders versus non-responders. Secondary outcomes included changes in physiological dead space and correlations with independently determined recruited lung volume and the recruitment-to-inflation ratio at an instantaneous, single breath decrease in PEEP. Mixed factor ANOVA for group mean differences and correlations by Pearson's correlation coefficient are reported including their 95% confidence intervals.

Results: Of 27 patients studied, 15 responders increased the P/F ratio by 55 [24-86] mm Hg compared to 12 non-responders (p < 0.01) as PEEPlow (11 ± 2.7 cm H2O) was increased to PEEPhigh (18 ± 3.0 cm H2O). The [Formula: see text] was 461 [82-839] ml less in responders at PEEPlow (p = 0.02) but not statistically different between groups at PEEPhigh. Responders increased both [Formula: see text] and EPBF at PEEPhigh (r = 0.56 [0.18-0.83], p = 0.03). In contrast, non-responders demonstrated a negative correlation (r = - 0.65 [- 0.12 to - 0.89], p = 0.02) with increased lung volume associated with decreased pulmonary perfusion. Decreased (- 0.06 [- 0.02 to - 0.09] %, p < 0.01) dead space was observed in responders. The change in [Formula: see text] correlated with both the recruited lung volume (r = 0.85 [0.69-0.93], p < 0.01) and the recruitment-to-inflation ratio (r = 0.87 [0.74-0.94], p < 0.01).

Conclusions: In mechanically ventilated patients with moderate to severe COVID-19 respiratory failure, improved oxygenation in response to increased PEEP was associated with increased end-expiratory lung volume and pulmonary perfusion. The change in end-expiratory lung volume was positively correlated with the lung volume recruited and the recruitment-to-inflation ratio. This study demonstrates the feasibility of capnodynamic monitoring to assess physiological responses to PEEP at the bedside to facilitate an individualised setting of PEEP.

Trial registration: NCT05082168 (18th October 2021).

Keywords: COVID-19; Lung perfusion; Lung volume; Mechanical ventilation; Monitoring; Positive end-expiratory pressure.

Conflict of interest statement

MH is a current and MW is a former employee of Maquet Critical Care AB. None of the other authors have any conflicts of interest do declare.

© 2022. The Author(s).

Figures

Fig. 1
Fig. 1
Capnodynamic monitoring of changes in end-expiratory lung volume (∆EELVCO2) and effective pulmonary blood flow (∆EPBF) in patients with (solid dots, black lines) or without (open squares, grey lines) an increase in PaO2/FiO2 by > 20 mm Hg following increased PEEP level (left hand graph). Changes in end-expiratory lung volume (∆EELVCO2) and effective pulmonary blood flow (∆EPBF) are also shown in patients with (stars, black lines) or without (open circles, grey lines) an improvement in Vd/Vt following increased PEEP (right hand graph). Correlations are shown as Pearson’s regression (solid line) with the 95% confidence intervals (dashed lines)
Fig. 2
Fig. 2
Changes in end-expiratory lung volume by capnodynamic monitoring (∆EELVCO2) and the recruited lung volume (∆Volrec) assessed based on the exhaled tidal volume at the rapid reduction from PEEPhigh to PEEPlow as previously described [19]. The correlation is shown as Pearson’s regression (solid line) with the 95% confidence intervals (dashed lines)
Fig. 3
Fig. 3
Changes in end-expiratory lung volume by capnodynamic monitoring (∆EELVCO2) and the recruitment-to-inflation ratio assessed at the rapid reduction from PEEPhigh to PEEPlow as previously described [19]. The correlation is shown as Pearson’s regression (solid line) with the 95% confidence intervals (dashed lines)

References

    1. Nasa P, Azoulay E, Khanna AK, Jain R, Gupta S, Javeri Y, Juneja D, Rangappa P, Sundararajan K, Alhazzani W, et al. Expert consensus statements for the management of COVID-19-related acute respiratory failure using a Delphi method. Crit Care. 2021;25(1):106. doi: 10.1186/s13054-021-03491-y.
    1. Alhazzani W, Evans L, Alshamsi F, Moller MH, Ostermann M, Prescott HC, Arabi YM, Loeb M, Ng Gong M, Fan E, et al. Surviving sepsis campaign guidelines on the management of adults with coronavirus disease 2019 (COVID-19) in the ICU: first update. Crit Care Med. 2021;49(3):e219–e234. doi: 10.1097/CCM.0000000000004899.
    1. Li Bassi G, Suen JY, Dalton HJ, White N, Shrapnel S, Fanning JP, Liquet B, Hinton S, Vuorinen A, Booth G, et al. An appraisal of respiratory system compliance in mechanically ventilated covid-19 patients. Crit Care. 2021;25(1):199. doi: 10.1186/s13054-021-03518-4.
    1. Cronin JN, Camporota L, Formenti F. Mechanical ventilation in COVID-19: a physiological perspective. Exp Physiol. 2021;107:683–693. doi: 10.1113/EP089400.
    1. Camporota L, Cronin JN, Busana M, Gattinoni L, Formenti F. Pathophysiology of coronavirus-19 disease acute lung injury. Curr Opin Crit Care. 2022;28(1):9–16. doi: 10.1097/MCC.0000000000000911.
    1. Chiumello D, Bonifazi M, Pozzi T, Formenti P, Papa GFS, Zuanetti G, Coppola S. Positive end-expiratory pressure in COVID-19 acute respiratory distress syndrome: the heterogeneous effects. Crit Care. 2021;25(1):431. doi: 10.1186/s13054-021-03839-4.
    1. Rossi S, Palumbo MM, Sverzellati N, Busana M, Malchiodi L, Bresciani P, Ceccarelli P, Sani E, Romitti F, Bonifazi M, et al. Mechanisms of oxygenation responses to proning and recruitment in COVID-19 pneumonia. Intensive Care Med. 2022;48(1):56–66. doi: 10.1007/s00134-021-06562-4.
    1. Gibot S, Conrad M, Courte G, Cravoisy A. Positive end-expiratory pressure setting in COVID-19-related acute respiratory distress syndrome: comparison between electrical impedance tomography, PEEP/FiO2 tables, and transpulmonary pressure. Front Med (Lausanne) 2021;8:720920. doi: 10.3389/fmed.2021.720920.
    1. van der Zee P, Somhorst P, Endeman H, Gommers D. Electrical impedance tomography for positive end-expiratory pressure titration in COVID-19-related acute respiratory distress syndrome. Am J Respir Crit Care Med. 2020;202(2):280–284. doi: 10.1164/rccm.202003-0816LE.
    1. Stevic N, Chatelain E, Dargent A, Argaud L, Cour M, Guerin C. Lung recruitability evaluated by recruitment-to-inflation ratio and lung ultrasound in COVID-19 acute respiratory distress syndrome. Am J Respir Crit Care Med. 2021;203(8):1025–1027. doi: 10.1164/rccm.202012-4447LE.
    1. Tusman G, Wallin M, Acosta C, Santanera B, Portela F, Viotti F, Fuentes N, Hallback M, Suarez-Sipmann F. Positive end-expiratory pressure individualization guided by continuous end-expiratory lung volume monitoring during laparoscopic surgery. J Clin Monit Comput. 2021 doi: 10.1007/s10877-021-00800-2.
    1. Suarez-Sipmann F, Tusman G, Wallin M. Continuous non-invasive monitoring of cardiac output and lung volume based on CO2 kinetics. In: Vincent J-L, editor. Annual update in intensive care and emergency medicine. Berlin: Springer; 2019. pp. 215–229.
    1. Sigmundsson TS, Ohman T, Hallback M, Suarez-Sipmann F, Wallin M, Oldner A, Hallsjo-Sander C, Bjorne H. Comparison between capnodynamic and thermodilution method for cardiac output monitoring during major abdominal surgery: an observational study. Eur J Anaesthesiol. 2021;38(12):1242–1252. doi: 10.1097/EJA.0000000000001566.
    1. Ohman T, Sigmundsson TS, Hallback M, Suarez Sipmann F, Wallin M, Oldner A, Bjorne H, Hallsjo Sander C. Clinical and experimental validation of a capnodynamic method for end-expiratory lung volume assessment. Acta Anaesthesiol Scand. 2020;64(5):670–676. doi: 10.1111/aas.13552.
    1. von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP, Initiative S. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Int J Surg. 2014;12(12):1495–1499. doi: 10.1016/j.ijsu.2014.07.013.
    1. Tusman G, Acosta CM, Wallin M, Hallback M, Esperatti M, Peralta G, Gonzalez ME, Suarez-Sipmann F. Perioperative continuous noninvasive cardiac output monitoring in cardiac surgery patients by a novel capnodynamic method. J Cardiothorac Vasc Anesth. 2022;36:2900–2907. doi: 10.1053/j.jvca.2022.02.002.
    1. Acute Respiratory Distress Syndrome N. Brower RG, Matthay MA, Morris A, Schoenfeld D, Thompson BT, Wheeler A. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med. 2000;342(18):1301–1308. doi: 10.1056/NEJM200005043421801.
    1. Enghoff H. Volumen inefficax, Bemerkungen zur Frage des schadlichen Raumes. Upsala Lakareforen Forh. 1938;44:191–218.
    1. Chen L, Del Sorbo L, Grieco DL, Junhasavasdikul D, Rittayamai N, Soliman I, Sklar MC, Rauseo M, Ferguson ND, Fan E, et al. Potential for lung recruitment estimated by the recruitment-to-inflation ratio in acute respiratory distress syndrome. A clinical trial. Am J Respir Crit Care Med. 2020;201(2):178–187. doi: 10.1164/rccm.201902-0334OC.
    1. Tusman G, Sipmann FS, Borges JB, Hedenstierna G, Bohm SH. Validation of Bohr dead space measured by volumetric capnography. Intensive Care Med. 2011;37(5):870–874. doi: 10.1007/s00134-011-2164-x.
    1. Langer T, Brioni M, Guzzardella A, Carlesso E, Cabrini L, Castelli G, Dalla Corte F, De Robertis E, Favarato M, Forastieri A, et al. Prone position in intubated, mechanically ventilated patients with COVID-19: a multi-centric study of more than 1000 patients. Crit Care. 2021;25(1):128. doi: 10.1186/s13054-021-03552-2.
    1. Smit MR, Beenen LFM, Valk CMA, de Boer MM, Scheerder MJ, Annema JT, Paulus F, Horn J, Vlaar APJ, Kooij FO, et al. Assessment of lung reaeration at 2 levels of positive end-expiratory pressure in patients with early and late COVID-19-related acute respiratory distress syndrome. J Thorac Imaging. 2021;36(5):286–293. doi: 10.1097/RTI.0000000000000600.
    1. Beloncle FM, Pavlovsky B, Desprez C, Fage N, Olivier PY, Asfar P, Richard JC, Mercat A. Recruitability and effect of PEEP in SARS-Cov-2-associated acute respiratory distress syndrome. Ann Intensive Care. 2020;10(1):55. doi: 10.1186/s13613-020-00675-7.
    1. Protti A, Santini A, Pennati F, Chiurazzi C, Cressoni M, Ferrari M, Iapichino GE, Carenzo L, Lanza E, Picardo G, et al. Lung response to a higher positive end-expiratory pressure in mechanically ventilated patients with COVID-19. Chest. 2021;161:979–988. doi: 10.1016/j.chest.2021.10.012.
    1. Chiumello D, Cressoni M, Chierichetti M, Tallarini F, Botticelli M, Berto V, Mietto C, Gattinoni L. Nitrogen washout/washin, helium dilution and computed tomography in the assessment of end expiratory lung volume. Crit Care. 2008;12(6):R150. doi: 10.1186/cc7139.
    1. Caravita S, Baratto C, Di Marco F, Calabrese A, Balestrieri G, Russo F, Faini A, Soranna D, Perego GB, Badano LP, et al. Haemodynamic characteristics of COVID-19 patients with acute respiratory distress syndrome requiring mechanical ventilation. An invasive assessment using right heart catheterization. Eur J Heart Fail. 2020;22(12):2228–2237. doi: 10.1002/ejhf.2058.
    1. Becker A, Seiler F, Muellenbach RM, Danziger G, Kamphorst M, Lotz C, Group PAS, Bals R, Lepper PM. Pulmonary hemodynamics and ventilation in patients with COVID-19-related respiratory failure and ARDS. J Intensive Care Med. 2021;36(6):655–663. doi: 10.1177/0885066621995386.
    1. Dell'Anna AM, Carelli S, Cicetti M, Stella C, Bongiovanni F, Natalini D, Tanzarella ES, De Santis P, Bocci MG, De Pascale G, et al. Hemodynamic response to positive end-expiratory pressure and prone position in COVID-19 ARDS. Respir Physiol Neurobiol. 2022;298:103844. doi: 10.1016/j.resp.2022.103844.
    1. Hallsjo Sander C, Lonnqvist PA, Hallback M, Sipmann FS, Wallin M, Oldner A, Bjorne H. Capnodynamic assessment of effective lung volume during cardiac output manipulations in a porcine model. J Clin Monit Comput. 2016;30(6):761–769. doi: 10.1007/s10877-015-9767-7.
    1. Suarez-Sipmann F, Villar J, Ferrando C, Sanchez-Giralt JA, Tusman G. Monitoring expired CO2 kinetics to individualize lung-protective ventilation in patients with the acute respiratory distress syndrome. Front Physiol. 2021;12:785014. doi: 10.3389/fphys.2021.785014.
    1. Zerbib Y, Lambour A, Maizel J, Kontar L, De Cagny B, Soupison T, Bradier T, Slama M, Brault C. Respiratory effects of lung recruitment maneuvers depend on the recruitment-to-inflation ratio in patients with COVID-19-related acute respiratory distress syndrome. Crit Care. 2022;26(1):12. doi: 10.1186/s13054-021-03876-z.
    1. Pan C, Chen L, Lu C, Zhang W, Xia JA, Sklar MC, Du B, Brochard L, Qiu H. Lung Recruitability in COVID-19-associated acute respiratory distress syndrome: a single-center observational study. Am J Respir Crit Care Med. 2020;201(10):1294–1297. doi: 10.1164/rccm.202003-0527LE.
    1. Gattinoni L, Chiumello D, Caironi P, Busana M, Romitti F, Brazzi L, Camporota L. COVID-19 pneumonia: Different respiratory treatments for different phenotypes? Intensive Care Med. 2020;46(6):1099–1102. doi: 10.1007/s00134-020-06033-2.
    1. Grasselli G, Tonetti T, Protti A, Langer T, Girardis M, Bellani G, Laffey J, Carrafiello G, Carsana L, Rizzuto C, et al. Pathophysiology of COVID-19-associated acute respiratory distress syndrome: a multicentre prospective observational study. Lancet Respir Med. 2020;8(12):1201–1208. doi: 10.1016/S2213-2600(20)30370-2.

Source: PubMed

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