Open-access To: Clinical outcomes of intensive care unit-acquired weakness in critically ill COVID-19 patients. A prospective cohort study

To the Editor

In a thought-provoking study, Werlang et al. prospectively evaluated the clinical outcomes of critically ill patients with coronavirus disease 2019 (COVID-19) complicated by intensive care unit-acquired weakness (ICUAW).(1) Citing the risk factors for neurological complications, the authors suggest similarities with regard to the predisposition to ICUAW between COVID-19 and non-COVID-19 cohorts.(1,2) In this context, we draw attention of the readership to relevant studies on the subject, highlighting a facet that was overlooked in the index study.

Wolfe et al. studied the impact of vasoactive medications on ICUAW in mechanically ventilated patients and obtained interesting results.(2) The use of vasoactive drugs in their setting increased the propensity to develop ICUAW, with an odds ratio (OR) and 95% confidence interval (95%CI) of 3.2 and 1.29 - 7.95, respectively (p value of 0.01) obtained with logistic regression analysis, independent of other established risk factors for weakness in critically ill patients. Notably, for every additional day that an ICU patient received a vasoactive agent, the odds of progressing to ICUAW increased by 35% (OR: 1.35; 95%CI: 1.1 - 1.65, p = 0.004). Moreover, when the role of the cumulative vasopressor dose was assessed, every 1µg/kg/d of norepinephrine administered resulted in a 1% increased odds of developing ICUAW (OR 1.01; 95%CI 1.001 - 1.02, p = 0.04), indicating a dose-dependent response.(2)

Even limiting the analysis to the use of vasopressors in patients with COVID-19, observational clinical studies have revealed that 35 - 94% of critically ill COVID-19 patients required hemodynamic support with vasopressors, with a weighted average of 66%.(3) Moreover, independent researchers such as Cavalleri et al., who have studied the 1-yr functional decline in COVID-19 and non-COVID-19 survivors, suggest that there is a prolonged duration of vasopressor support in the subset of critically ill patients with COVID-19 compared with the duration in the subset without COVID-19.(4) In addition, the data on vasopressor support in a recent systematic review and meta-analysis by Mermiri et al. on the greater prognostic implications of the use of vasopressors in the context of COVID-19 could elucidate the findings of Werlang et al., who evaluated the prognosis of ICUAW, and highlights the importance of these observations to current research.(1,5)

  • Publisher's note

REFERENCES

  • 1 Werlang AP, Boniatti VM, Neuenfeldt CT, Silva LC, Costa GM, Teixeira MC, et al. Clinical outcomes of intensive care unit-acquired weakness in critically ill COVID-19 patients. A prospective cohort study. Crit Care Sci. 2024;36:e20240003en.
  • 2 Wolfe KS, Patel BK, MacKenzie EL, Giovanni SP, Pohlman AS, Churpek MM, et al. Impact of vasoactive medications on ICU-acquired weakness in mechanically ventilated patients. Chest. 2018;154(4):781-7.
  • 3 Michard F, Vieillard-Baron A. Critically ill patients with COVID-19: are they hemodynamically unstable and do we know why? Intensive Care Med. 2021;47(2):254-5.
  • 4 Cavalleri J, Treguier D, Deliège T, Gurdebeke C, Ernst M, Lambermont B, et al. One-year functional decline in COVID-19 and non-COVID-19 critically ill survivors: a prospective study incorporating a pre-ICU status assessment. Healthcare (Basel). 2022;10(10):2023.
  • 5 Mermiri M, Mavrovounis G, Laou E, Papagiannakis N, Pantazopoulos I, Chalkias A. Association of vasopressors with mortality in critically ill patients with COVID-19: a systematic review and meta-analysis. APS. 2023;1(2):10.

Publication Dates

  • Publication in this collection
    22 Nov 2024
  • Date of issue
    2024

History

  • Received
    01 July 2024
  • Accepted
    03 July 2024
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E-mail: ccs@amib.org.br
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